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Sample records for adsorbed water film

  1. Hydraulic properties of adsorbed water films in unsaturated porous media

    SciTech Connect

    Tokunaga, Tetsu K.

    2009-03-01

    Adsorbed water films strongly influence residual water saturations and hydraulic conductivities in porous media at low saturations. Hydraulic properties of adsorbed water films in unsaturated porous media were investigated through combining Langmuir's film model with scaling analysis, without use of any adjustable parameters. Diffuse double layer influences are predicted to be important through the strong dependence of adsorbed water film thickness (f) on matric potential ({Psi}) and ion charge (z). Film thickness, film velocity, and unsaturated hydraulic conductivity are predicted to vary with z{sup -1}, z{sup -2}, and z{sup -3}, respectively. In monodisperse granular media, the characteristic grain size ({lambda}) controls film hydraulics through {lambda}{sup -1} scaling of (1) the perimeter length per unit cross sectional area over which films occur, (2) the critical matric potential ({Psi}{sub c}) below which films control flow, and (3) the magnitude of the unsaturated hydraulic conductivity when {Psi} < {Psi}{sub c}. While it is recognized that finer textured sediments have higher unsaturated hydraulic conductivities than coarser sands at intermediate {Psi}, the {lambda}{sup -1} scaling of hydraulic conductivity predicted here extends this understanding to very low saturations where all pores are drained. Extremely low unsaturated hydraulic conductivities are predicted under adsorbed film-controlled conditions (generally < 0.1 mm y{sup -1}). On flat surfaces, the film hydraulic diffusivity is shown to be constant (invariant with respect to {Psi}).

  2. Adsorbed Water Illustration

    NASA Technical Reports Server (NTRS)

    2008-01-01

    The Thermal and Electrical Conductivity Probe on NASA's Phoenix Mars Lander detected small and variable amounts of water in the Martian soil.

    In this schematic illustration, water molecules are represented in red and white; soil minerals are represented in green and blue. The water, neither liquid, vapor, nor solid, adheres in very thin films of molecules to the surfaces of soil minerals. The left half illustrates an interpretation of less water being adsorbed onto the soil-particle surface during a period when the tilt, or obliquity, of Mars' rotation axis is small, as it is in the present. The right half illustrates a thicker film of water during a time when the obliquity is greater, as it is during cycles on time scales of hundreds of thousands of years. As the humidity of the atmosphere increases, more water accumulates on mineral surfaces. Thicker films behave increasingly like liquid water.

    The Phoenix Mission is led by the University of Arizona, Tucson, on behalf of NASA. Project management of the mission is by NASA's Jet Propulsion Laboratory, Pasadena, Calif. Spacecraft development is by Lockheed Martin Space Systems, Denver.

  3. Aging of the nanosized photochromic WO3 films and the role of adsorbed water in the photochromism

    NASA Astrophysics Data System (ADS)

    Gavrilyuk, A. I.

    2016-02-01

    Here it has been reported on aging of the nanosized WO3 film, which is revealed is continuous reduction of the photochromic sensitivity over time. Water molecules physically adsorbed on the film surface from ambient air form donor-acceptor and hydrogen bonds, changing gradually the adsorption state to chemisorption which prevents an access of organic molecules that serve as hydrogen donors by the photochromism. The mechanism of the process has been investigated and discussed. The role of water in the photochromism has been highlighted. The difference in the efficiency for being of a hydrogen donor in the photochromic process between water and organic molecules is discussed.

  4. The Effect of monoglycerides on structural and topographical characteristics of adsorbed beta-casein films at the air-water interface.

    PubMed

    Fernández, Marta Cejudo; Sánchez, Cecilio Carrera; Rodríguez Niño, M Rosario; Rodríguez Patino, Juan M

    2006-02-01

    The effect of monoglycerides (monopalmitin and monoolein) on the structural and topographical characteristics of beta-casein adsorbed film at the air-water interface has been analyzed by means of surface pressure (pi)-area (A) isotherms and Brewster angle microscopy (BAM). At surface pressures lower than that for the beta-casein collapse (pi(c)(beta-casein)), attractive interactions between beta-casein and monoglycerides were observed. At higher surface pressures, the collapsed beta-casein is partially displaced from the interface by monoglycerides. However, beta-casein displacement by monoglycerides is not quantitative at the monoglyceride concentrations studied in this work. From the results derived from these experiments, we have concluded that interactions, miscibility, and displacement of proteins by monoglycerides in adsorbed mixed monolayers at the air-water interface depend on the particular protein-monoglyceride system, the interactions between film-forming components being higher for adsorbed than for spread films. The adsorbed films are more segregated than spread films, and both collapsed protein domains and monoglyceride domains in adsorbed films are smaller than for spread films.

  5. Infrared spectroscopy of water clusters co-adsorbed with hydrogen molecules on a sodium chloride film

    NASA Astrophysics Data System (ADS)

    Yamakawa, Koichiro; Fukutani, Katsuyuki

    2016-06-01

    Hydrogen gas containing a trace of water vapor was dosed on a vacuum-evaporated sodium chloride film at 13 K, and water clusters formed on the substrate were investigated by infrared absorption spectroscopy. Absorption bands due to (H2O)n clusters with n = 3-6 and an induced absorption band due to hydrogen were clearly observed. With increasing gas dosage, the intensities of the cluster bands increased linearly while the intensity of the hydrogen band was constant. This suggests that the water clusters were formed in two-dimensional matrices of hydrogen. We found that the water clusters did exist on the surface upon heating even after the hydrogen molecules had desorbed. A further rise of the substrate temperature up to 27 K yielded the formation of larger clusters, (H2O)n with n > 6 . We also discuss the origins of the two bands of the trimer in terms of pseudorotation and a metastable isomer.

  6. Morphological changes in adsorbed protein films at the air-water interface subjected to large area variations, as observed by brewster angle microscopy.

    PubMed

    Xu, Rong; Dickinson, Eric; Murray, Brent S

    2007-04-24

    Adsorbed films of proteins at the air-water interface have been imaged using Brewster angle microscopy (BAM). The proteins beta-lactoglobulin (beta-L) and ovalbumin (OA) were studied at a range of protein concentrations and surface ages at 25.0 degrees C and two pH values (7 and 5) in a Langmuir trough. The adsorbed films were periodically subjected to compression and expansion cycles such that the film area was typically varied between 125% and 50% of the original film area. With beta-L on its own, no structural changes were observable at pH 7. When a low-area fraction (less than 0.01%) of 20 mum polystyrene latex particles was spread at the interface before adsorption of beta-L, the particles became randomly distributed throughout the interface, but after protein adsorption and compression/expansion, the particles highlighted notable structural features not visible in their absence. Such features included the appearance of long (several hundred micrometers or more) folds and cracks in the films, generally oriented at right angles to the direction of compression, and also aggregates of protein and/or particles. Such structuring was more visible the longer the film was aged or at higher initial protein concentrations for shorter adsorption times. At pH 5, close to the isoelectric pH of beta-L, such features were just noticeable in the absence of particles but were much more pronounced than at pH 7 in the presence of particles. Similar experiments with OA revealed even more pronounced structural features, both in the absence and presence of particles, particularly at pH 5 (close to the isoelectric pH of OA also), producing striking stripelike and meshlike domains. Changes in the dilatational elasticity of the films could be correlated with the variations in the structural integrity of the films as observed via BAM. The results indicate that interfacial area changes of this type, typical of those that occur in food colloid processing, will lead to highly

  7. Interaction of magnetic nanoparticles with phospholipid films adsorbed at a liquid/liquid interface.

    PubMed

    Cámara, C I; Monzón, L M A; Coey, J M D; Yudi, L M

    2015-01-07

    The interaction of Co hexagonal magnetic nanoparticles (MNPs) with distearoyl phosphatidyl glycerol (DSPG) and distearoyl phosphatidic acid (DSPA) films adsorbed at a water/1,2-dichloroethane interface is studied employing cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), capacity curves and interfacial pressure-area isotherms. DSPA and DSPG adsorb at the interface forming homogenous films and producing a blocking effect on the transfer process of tetraethyl ammonium (TEA(+)), used as a probe cation. In the presence of Co NPs this effect is reversed and the reversible transfer process for TEA(+) is reestablished, to a greater or lesser extent depending on the structuration of the film. Co-DSPA hybrid films have a homogeneous structure while Co-DSPG films present different domains. Moreover, the presence of Co on DSPA film modifies the partition coefficient of the organic electrolyte into the hydrocarbon layer.

  8. Activity of alkaline phosphatase adsorbed and grafted on "polydopamine" films.

    PubMed

    Ball, Vincent

    2014-09-01

    The oxidation of dopamine in slightly basic solutions and in the presence of oxygen as an oxidant allows for the deposition of dopamine-eumelanin ("polydopamine") films on almost all kinds of materials allowing for an easy secondary functionalization. Molecules carrying nucleophilic groups like thiols and amines can be easily grafted on those films. Herein we show that alkaline phosphatase (ALP), as a model enzyme, adsorbs to "polydopamine" films and part of the adsorbed enzyme is rapidly desorbed in contact with Tris buffer. However a significant part of the enzyme remains irreversibly adsorbed and keeps some enzymatic activity for at least 2 weeks whereas ALP adsorbed on quartz slides is rapidly and quantitatively deactivated. In addition we estimated the Michaelis constant Km of the enzyme irreversibly bound to the "polydopamine" film. The Michaelis constant, and hence the affinity constant between paranitrophenol phosphate and ALP are almost identical between the enzyme bound on the film and the free enzyme in solution. Complementarily, it was found that "polydopamine" films display some phosphatase like catalytic activity.

  9. The condensation of water on adsorbed viruses.

    PubMed

    Alonso, José María; Tatti, Francesco; Chuvilin, Andrey; Mam, Keriya; Ondarçuhu, Thierry; Bittner, Alexander M

    2013-11-26

    The wetting and dewetting behavior of biological nanostructures and to a greater degree single molecules is not well-known even though their contact with water is the basis for all biology. Here, we show that environmental electron microscopy (EM) can be applied as a means of imaging the condensation of water onto viruses. We captured the formation of submicrometer water droplets and filaments on single viral particles by environmental EM and by environmental transmission EM. The condensate structures are compatible with capillary condensation between adsorbed virus particles and with known droplet shapes on patterned surfaces. Our results confirm that such droplets exist down to <50 nm. The viruses preserved their shape after a condensation/evaporation cycle as expected from their stability in air and water. Moreover we developed procedures that overcome problems of beam damage and of resolving structures with a low atomic number.

  10. Anomalous conformational transitions in cytochrome C adsorbing to Langmuir-Blodgett films

    NASA Astrophysics Data System (ADS)

    Sankaranarayanan, Kamatchi; Nair, B. U.; Dhathathreyan, A.

    2013-05-01

    Helix to beta conformational transitions in proteins has attracted much attention due to their relevance to fibril formation which is implicated in many neurological diseases. This study reports on unusual conformational transition of cytochrome C adsorbing to hydrophilic surface containing pure cationic lipid and mixed Langmuir-Blodgett films (LB films) of cationic and neutral lipids. Evidence for conformational changes of the protein from its native helical state to beta sheet comes from Circular dichroic spectroscopy (CD spectroscopy). Analysis of these samples using High resolution TEM (HRTEM) shows a typical fibrillar pattern with each strand spacing of about 0.41 nm across which can be attributed to the repeat distance of interdigitated neighboring hydrogen-bonded ribbons in a beta sheet. Changes in contact angles of protein adsorbing to the LB films together with the increased mass uptake of water using quartz crystal microbalance (QCM) confirm the role of positive charges in the conformational transition. Dehydration of the protein resulting from the excess water entrainment in the polar planes of the cationic lipid in hydrophilic surface seems to trigger the refolding of the protein to beta sheet while it retains its native conformation in hydrophobic films. The results suggest that drastic conformational changes in CytC adsorbing to cationic lipids may be of significance in its role as a peripheral membrane protein.

  11. Liquid 4He Adsorbed Films on Very Attractive Substrates

    NASA Astrophysics Data System (ADS)

    Urrutia, Ignacio; Szybisz, Leszek

    Adsorbed films of liquid 4He are analized, in the framework of Density functionals Theories (DF). In these systems, when the substrate becomes increasingly attractive, the thin films of 4He approaches the quasi-bidimensional limit. We study this strongly attractive substrate regime with two DF, the Orsay-Trento (OT) and a recent Hybrid proposal (Hyb), focusing in the energy behavior. It is showed that OT does not reproduce the correct limiting energy curve, and it implies that this functional could not provide reliable results for very strongly attractive substrates like Graphite (Gr). In other hand, with the Hyb DF, the correct energy behavior is found for the adsorption energy of 4He on Gr. These results show that OT should not be applied to quasi 2D (confinement) situations, and that Hyb DF provides a much more realistic description.

  12. Liquid 4He Adsorbed Films on Very Attractive Substrates

    NASA Astrophysics Data System (ADS)

    Urrutia, Ignacio; Szybisz, Leszek

    2006-09-01

    Adsorbed films of liquid 4He are analized, in the framework of Density Functional Theories (DF). In these systems, when the substrate becomes increasingly attractive, the thin films of 4He approaches the quasi-bidimensional limit. We study this strongly attractive substrate regime with two DF, the Orsay-Trento (OT) and a recent Hybrid proposal (Hyb), focusing in the energy behavior. It is showed that OT does not reproduce the correct limiting energy curve, and it implies that this functional could not provide reliable results for very strongly attractive substrates like Graphite (Gr). In other hand, with the Hyb DF, the correct energy behavior is found for the adsorption energy of 4He on Gr. These results show that OT should not be applied to quasi 2D (confinement) situations, and that Hyb DF provides a much more realistic description.

  13. Adsorbed Methane Film Properties in Nanoporous Carbon Monoliths

    NASA Astrophysics Data System (ADS)

    Soo, Yuchoong; Chada, Nagaraju; Beckner, Matthew; Romanos, Jimmy; Burress, Jacob; Pfeifer, Peter

    2013-03-01

    Carbon briquetting can increase methane storage capacity by reducing the useless void volume resulting in a better packing density. It is a robust and efficient space-filling form for an adsorbed natural gas vehicle storage tank. To optimize methane storage capacity, we studied three fabrication process parameters: carbon-to-binder ratio, compaction temperature, and pyrolysis temperature. We found that carbon-to-binder ratio and pyrolysis temperature both have large influences on monolith uptakes. We have been able to optimize these parameters for high methane storage. All monolith uptakes (up to 260 bar) were measured by a custom-built, volumetric, reservoir-type instrument. The saturated film density and the film thickness was determined using linear extrapolation on the high pressure excess adsorption isotherms. The saturated film density was also determined using the monolayer Ono-Kondo model. Film densities ranged from ca. 0.32 g/cm3 - 0.37 g/cm3.The Ono-Kondo model also determines the binding energy of methane. Binding energies were also determined from isosteric heats calculated from the Clausius-Clapeyron equation and compared with the Ono-Kondo model method. Binding energies from Ono-Kondo were ca. 7.8 kJ/mol - 10 kJ/mol. Work funded by California Energy Commission Contract #500-08-022.

  14. Structure of water adsorbed on a single graphene sheet

    NASA Astrophysics Data System (ADS)

    Gordillo, M. C.; Martí, J.

    2008-08-01

    We present the result of molecular-dynamics simulations of water adsorbed on top of a single graphene layer at temperatures between 25 and 50°C . The analysis of the energy per particle and the density profiles indicate that the behavior of the adsorbed liquid is similar to the case of multiple graphene layers (graphite) with the only difference being the values of configurational energy. Other structural properties, such as stability ranges, hydrogen bond distributions, and molecular orientations are also presented.

  15. Influence of ionic strength changes on the structure of pre-adsorbed salivary films. A response of a natural multi-component layer.

    PubMed

    Macakova, Lubica; Yakubov, Gleb E; Plunkett, Mark A; Stokes, Jason R

    2010-05-01

    Salivary films coating oral surfaces are critically important for oral health. This study focuses on determining the underlying nature of this adsorbed film and how it responds to departures from physiological conditions due to changes in ionic strength. Under physiological conditions, it is found that pre-adsorbed in vitro salivary film on hydrophobic surfaces is present as a highly hydrated viscoelastic layer. We follow the evolution of this film in terms of its effective thickness, hydration and viscoelastic properties, as well as adsorbed mass of proteins, using complementary surface characterisation methods: a Surface Plasmon Resonance (SPR) and a Quartz Crystal Microbalance with Dissipation Monitoring (QCM-D). Our results support a heterogeneous model for the structure of the salivary film with an inner dense anchoring layer and an outer highly extended hydrated layer. Further swelling of the film was observed upon decreasing the salt concentration down to 1mM NaCl. However, upon exposure to deionised water, a collapse of the film occurs that was associated with the loss of water contained within the adsorbed layer. We suggest that the collapse in deionised water is driven by an onset of electrostatic attraction between different parts of the multi-component salivary film. It is anticipated that such changes could also occur when the oral cavity is exposed to food, beverage, oral care and pharmaceutical formulations where drastic changes to the structural integrity of the film is likely to have implications on oral health, sensory perception and product performance.

  16. Mechanical properties of hexadecane-water interfaces with adsorbed hydrophobic bacteria

    NASA Astrophysics Data System (ADS)

    Kang, Zhewen

    Certain strains of hydrophobic bacteria are known to play critical roles in petroleum-related applications. The aim of this study was to investigate how hydrophobic bacteria in their stationary phase could adsorb onto the hexadecane-water interface and alter its mechanical properties. The two strains of bacteria used in forming the interfacial films were Acinetobacter venetianus RAG-1 (a Gram-negative bacterium) and Rhodococcus erythropolis 20S-E1-c (Gram-positive). Experiments at two different length scales (millimetre and micrometre) were conducted and the results were compared. In addition, a simple flow experiment was designed in a constricted channel and the results were related to the intrinsic mechanical properties of bacteria-adsorbed films. On the millimetre scale, using the pendant drop technique, the film interfacial tension was monitored as the surface area was made to undergo changes. Under static conditions, both types of bacteria showed no significant effect on the interfacial tension. When subjected to transient excitations, the two bacterial films exhibited qualitatively similar, yet quantitative distinct rheological properties (including film elasticities and relaxation times). Under continuous reduction of surface area, the RAG-1 system showed a "paper-like" interface, while the interface of the 20S-E1-c system was "soap film-like." These macroscopic observations could be explained by the surface ultrastructures of the two cell strains. On the micrometre scale, using the micropipette technique, colloidal stability of the bacteria-coated oil droplets was examined through direct-contact experiments. Both types of bacteria were seen to function as effective stabilizers. In addition, the adsorbed bacteria also interacted with one another at the interface, giving rise to higher order 2-D rheological properties. A technique of directly probing the mechanical properties of the emulsion drop surfaces revealed that (a) the films behaved as purely elastic

  17. Detection of adsorbed water and hydroxyl on the Moon.

    PubMed

    Clark, Roger N

    2009-10-23

    Data from the Visual and Infrared Mapping Spectrometer (VIMS) on Cassini during its flyby of the Moon in 1999 show a broad absorption at 3 micrometers due to adsorbed water and near 2.8 micrometers attributed to hydroxyl in the sunlit surface on the Moon. The amounts of water indicated in the spectra depend on the type of mixing and the grain sizes in the rocks and soils but could be 10 to 1000 parts per million and locally higher. Water in the polar regions may be water that has migrated to the colder environments there. Trace hydroxyl is observed in the anorthositic highlands at lower latitudes.

  18. Detection of adsorbed water and hydroxyl on the moon

    USGS Publications Warehouse

    Clark, R.N.

    2009-01-01

    Data from the Visual and Infrared Mapping Spectrometer (VIAAS) on Cassini during its flyby of the AAoon in 1999 show a broad absorption at 3 micrometers due to adsorbed water and near 2.8 micrometers attributed to hydroxyl in the sunlit surface on the AAoon. The amounts of water indicated in the spectra depend on the type of mixing and the grain sizes in the rocks and soils but could be 10 to 1000 parts per million and locally higher. Water in the polar regions may be water that has migrated to the colder environments there. Trace hydroxyl is observed in the anorthositic highlands at lower latitudes.

  19. Adsorbent selection for endosulfan removal from water environment.

    PubMed

    Sudhakar, Y; Dikshit, A K

    1999-01-01

    In the present study, an attempt was made to select a low cost adsorbing material for the removal of endosulfan [C,C'-(1,4,5,6,7,7-hexachloro-8,9,10- trinorborn-5-en-2,3-ylene)(dimethylsulphite)] from water. Various low cost adsorbents like wood charcoal, kimberlite tailings, silica, macro fungi sojar caju were tried with activated charcoal as reference material. The above materials were selected from various sources encompassing organic, inorganic, clayey, and biological sources. For the selection of suitable adsorbent for endosulfan uptake, maximum adsorption capacity (Qmax) was chosen as the parameter. Kinetic profiles of removal were generated for all the materials to assess the equilibrium time. Equilibrium studies were carried out for all materials to assess the adsorption equilibrium model that they followed. The model that gave the best correlation coefficient by linear regression analysis, was adopted for the calculation of Qmax of the corresponding adsorbent material. Using linearised forms of equilibrium models like Langmuir, BET, and Freundlich, maximum adsorptive capacities were determined. Activated charcoal showed the best adsorptive capacity with Qmax of 2.145 mg/g followed by wood charcoal 1.773 mg/g, sojar caju 1.575 mg/g, kimberlite tailings 0.8821 mg/g, and silica 0.3231 mg/g. Albeit activated charcoal gave better performance, it was not considered as a candidate material because of its high cost. Wood charcoal was the next best adsorbent with Qmax 1.773 mg/g. Therefore, wood charcoal was chosen as the best material for endosulfan removal. The study of physical and chemical characteristics of wood charcoal revealed that it is a potential adsorbent and can even be improved further.

  20. Heat capacity measurements of atoms and molecules adsorbed on evaporated metal films

    SciTech Connect

    Kenny, T.W.

    1989-05-01

    Investigations of the properties of absorbed monolayers have received great experimental and theoretical attention recently, both because of the importance of surface processes in practical applications such as catalysis, and the importance of such systems to the understanding of the fundamentals of thermodynamics in two dimensions. We have adapted the composite bolometer technology to the construction of microcalorimeters. For these calorimeters, the adsorption substrate is an evaporated film deposited on one surface of an optically polished sapphire wafer. This approach has allowed us to make the first measurements of the heat capacity of submonolayer films of /sup 4/He adsorbed on metallic films. In contrast to measurements of /sup 4/He adsorbed on all other insulating substrates, we have shown that /sup 4/He on silver films occupies a two-dimensional gas phase over a broad range of coverages and temperatures. Our apparatus has been used to study the heat capacity of Indium flakes. CO multilayers, /sup 4/He adsorbed on sapphire and on Ag films and H/sub 2/ adsorbed on Ag films. The results are compared with appropriate theories. 68 refs., 19 figs.

  1. Unusual Morphologies of Poly(vinyl alcohol) Thin Films Adsorbed on Poly(dimethylsiloxane) Substrates.

    PubMed

    Karki, Akchheta; Nguyen, Lien; Sharma, Bhanushee; Yan, Yan; Chen, Wei

    2016-04-05

    Adsorption of poly(vinyl alcohol) (PVOH), 99% and 88% hydrolyzed poly(vinyl acetate), to poly(dimethylsiloxane) (PDMS) substrates was studied. The substrates were prepared by covalently attaching linear PDMS polymers of 2, 9, 17, 49, and 116 kDa onto silicon wafers. As the PDMS molecular weight/thickness increases, the adsorbed PVOH thin films progressively transition from continuous to discontinuous morphologies, including honeycomb and fractal/droplet. The structures are the result of thin film dewetting that occurs upon exposure to air. The PVOH film thickness does not vary significantly on these PDMS substrates, implicating the PDMS thickness as the cause for the morphology differences. The adsorbed PVOH thin films are less stable and have a stronger tendency to dewet on thicker, more liquid-like PDMS layers. When PVOH(99%) and PVOH(88%) thin films are compared, fractal and droplet morphologies are observed on high molecular weight PDMS substrates, respectively. The formation of the unique fractal features in the PVOH(99%) thin films as well as other crystalline and semicrystalline thin films is most likely driven by crystallization during the dehydration process in a diffusion-limited aggregation fashion. The only significant enhancement in hydrophilicity via PVOH adsorption was obtained on PDMS(2k), which is completely covered with a PVOH thin film. To mimic the lower receding contact angle and less liquid-like character of the PDMS(2k) substrate, light plasma treatment of the higher molecular weight PDMS substrates was carried out. On the treated PDMS substrates, the adsorbed PVOH thin films are in the more continuous honeycomb morphology, giving rise to significantly enhanced wettability. Furthermore, hydrophobic recovery of the hydrophilized PDMS substrates was not observed during a 1 week period. Thus, light plasma oxidation and subsequent PVOH adsorption can be utilized as a means to effectively hydrophilize conventional PDMS substrates. This study

  2. Utility of adsorbents in the purification of drinking water: a review of characterization, efficiency and safety evaluation of various adsorbents.

    PubMed

    Dubey, Shashi Prabha; Gopal, Krishna; Bersillon, J L

    2009-05-01

    Clean drinking water is one of the implicit requisites fora healthy human population. However the growing industrialization and extensive use of chemicals for various concerns, has increased the burden of unwanted pollutants in the drinking water of developing countries like India. The entry of potentially hazardous substances into the biota has been magnifying day by day. In the absence of a possible stoppage of these, otherwise, useful chemicals, the only way to maintain safer water bodies is to develop efficient purifying technologies. One such immensely beneficial procedure that has been in use is that of purification of water using 'adsorbents'. Indigenous minerals and natural plants products have potential for removing many pollutants viz. fluoride, arsenic, nitrate, heavy metals, pesticides as well as trihalomethanes. Adsorbents which are derived from carbon, alumina, zeolite, clay minerals, iron ores, industrial by products, and natural products viz. parts of the plants, herbs and algal biomass offer promising potential of removal. In the recent years attention has been paid to develop process involving screening/pretreatment/activation/impregnation using alkalies, acids, alum, lime, manganese dioxide, ferric chloride and other chemicals which are found to enhance their adsorbing efficiency. Chemical characterization of these adsorbents recapitulates the mechanism of the process. It is imperative to observe that capacities of the adsorbents may vary depending on the characteristics, chemical modifications and concentration of the individual adsorbent. Removal kinetics is found to be based on the experimental conditions viz. pH, concentration of the adsorbate, quantity of the adsorbent and temperature. It is suggested that isotherm model is suitable tool to assess the adsorption capacities in batch and column modes. Safety evaluation and risk assessment of the process/products may be useful to provide guidelines for its sustainable disposal.

  3. Spectrophotochemical and electrochemical characterization of perylene derivatives adsorbed on nanoporous metaloxide films

    NASA Astrophysics Data System (ADS)

    Kus, M.; Demic, S.; Zafer, C.; Saygili, G.; Bilgili, H.; Icli, S.

    2007-03-01

    Electrochemistry of perylene imide and anhydride derivatives adsorbed on semiconductor TiO{2} (NT) and insulator Al{2}O{3} (NA) metal oxide films were presented. Adsorption rates on metal oxide surface are observed to be strongly depending on molecular structure. Monoanhydride-monoimide derivatives show two reversible reductions in solution and one reversible reduction in films. Color change from red to blue and violet is observed indicating the formation of monoanion and dianion radicals. Spectroelectrochemical measurements support this interpretation. The color reversal is quite stable in NA films in comparison with NT films. This paper has been presented at “ECHOS06”, Paris, 28 30 juin 2006.

  4. In situ ATR and DRIFTS studies of the nature of adsorbed CO₂ on tetraethylenepentamine films.

    PubMed

    Wilfong, Walter Christopher; Srikanth, Chakravartula S; Chuang, Steven S C

    2014-08-27

    CO2 adsorption/desorption onto/from tetraethylenepentamine (TEPA) films of 4, 10, and 20 μm thicknesses were studied by in situ attenuated total reflectance (ATR) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) techniques under transient conditions. Molar absorption coefficients for adsorbed CO2 were used to determine the CO2 capture capacities and amine efficiencies (CO2/N) of the films in the DRIFTS system. Adsorption of CO2 onto surface and bulk NH2 groups of the 4 μm film produced weakly adsorbed CO2, which can be desorbed at 50 °C by reducing the CO2 partial pressure. These weakly adsorbed CO2 exhibit low ammonium ion intensities and could be in the form of ammonium-carbamate ion pairs and zwitterions. Increasing the film thickness enhanced the surface amine-amine interactions, resulting in strongly adsorbed ion pairs and zwitterions associated with NH and NH2 groups of neighboring amines. These adsorbed species may form an interconnected surface network, which slowed CO2 gas diffusion into and diminished access of the bulk amine groups (or amine efficiency) of the 20 μm film by a minimum of 65%. Desorption of strongly adsorbed CO2 comprising the surface network could occur via dissociation of NH3(+)/NH2(+)···NH2/NH ionic hydrogen bonds beginning from 60 to 80 °C, followed by decomposition of NHCOO(-)/NCOO(-) at 100 °C. These results suggest that faster CO2 diffusion and adsorption/desorption kinetics could be achieved by thinner layers of liquid or immobilized amines.

  5. Titanate-based adsorbents for radioactive ions entrapment from water.

    PubMed

    Yang, Dongjiang; Liu, Hongwei; Zheng, Zhanfeng; Sarina, Sarina; Zhu, Huaiyong

    2013-03-21

    This feature article reviews some titanate-based adsorbents for the removal of radioactive wastes (cations and anions) from water. At the beginning, we discuss the development of the conventional ion-exchangeable titanate powders for the entrapment of radioactive cations, such as crystalline silicotitanate (CST), monosodium titanate (MST), peroxotitanate (PT). Then, we specially emphasize the recent progress in the uptake of radioactive ions by one-dimensional (1D) sodium titanate nanofibers and nanotubes, which includes the synthesis and phase transformation of the 1D nanomaterials, adsorption ability (capacity, selectivity, kinetics, etc.) of radioactive cations and anions, and the structural evolution during the adsorption process.

  6. Water depth penetration film test

    NASA Technical Reports Server (NTRS)

    Lockwood, H. E.; Perry, L.; Sauer, G. E.; Lamar, N. T.

    1974-01-01

    As part of the National Aeronautics and Space Administration Earth Resources Program, a comparative and controlled evaluation of nine film-filter combinations was completed to establish the relative effectiveness in recording water subsurface detail if exposed from an aerial platform over a typical water body. The films tested, with one exception, were those which prior was suggested had potential. These included an experimental 2-layer positive color film, a 2-layer (minus blue layer) film, a normal 3-layer color film, a panchromatic black-and-white film, and a black-and-white infrared film. Selective filtration was used with all films.

  7. Stability and interface properties of thin cellulose ester films adsorbed from acetone and ethyl acetate solutions.

    PubMed

    Amim, Jorge; Kosaka, Priscila M; Petri, Denise F S; Maia, Francisco C B; Miranda, Paulo B

    2009-04-15

    Stability and interface properties of cellulose acetate propionate (CAP) and cellulose acetate butyrate (CAB) films adsorbed from acetone or ethyl acetate onto Si wafers have been investigated by means of contact angle measurements and atomic force microscopy (AFM). Surface energy (gamma(S)(total)) values determined for CAP adsorbed from acetone are larger than those from ethyl acetate. In the case of CAB films adsorbed from ethyl acetate and acetone were similar. Dewetting was observed by AFM only for CAP films prepared from ethyl acetate. Positive values of effective Hamaker constant (A(eff)) were found only for CAP prepared from ethyl acetate, corroborating with dewetting phenomena observed by AFM. On the contrary, negative values of A(eff) were determined for CAP and CAB prepared from acetone and for CAB prepared from ethyl acetate, corroborating with experimental observations. Sum frequency generation (SFG) vibrational spectra indicated that CAP and CAB films prepared from ethyl acetate present more alkyl groups oriented perpendicularly to the polymer-air interface than those films prepared from acetone. Such preferential orientation corroborates with macroscopic contact angle measurements. Moreover, SFG spectra showed that acetone binds strongly to Si wafers, creating a new surface for CAP and CAB films.

  8. Miscibility of sodium chloride and sodium dodecyl sulfate in the adsorbed film and aggregate.

    PubMed

    Iyota, Hidemi; Krastev, Rumen

    2009-04-01

    The adsorption, micelle formation, and salting out of sodium dodecyl sulfate in the presence of sodium chloride were studied from the viewpoint of their mixed adsorption and aggregate formation. The surface tension of aqueous solutions of a sodium chloride-sodium dodecyl sulfate mixture was measured as a function of the total molality and composition of the mixture. Phase diagrams of adsorption and aggregate formation were obtained by applying thermodynamic equations to the surface tension. Judging from the phase diagrams, sodium chloride and sodium dodecyl sulfate are miscible in the adsorbed film at very large composition of sodium chloride and in the salted-out crystalline particle, while they are immiscible in the micelle. The miscibilities in the adsorbed film, micelle, and crystalline particle increase in the following order: particle > adsorbed film > micelle. The difference in miscibility among the oriented states was ascribed to the difference in geometry between the adsorbed film and micelle and to the interaction between bilayer surfaces in the particle.

  9. Forsterite Carbonation in Wet-scCO2: Dependence on Adsorbed Water Concentration

    NASA Astrophysics Data System (ADS)

    Loring, J.; Benezeth, P.; Qafoku, O.; Thompson, C.; Schaef, T.; Bonneville, A.; McGrail, P.; Felmy, A.; Rosso, K.

    2013-12-01

    Capturing and storing CO2 in basaltic formations is one of the most promising options for mitigating atmospheric CO2 emissions resulting from the burning of fossil fuels. These geologic reservoirs have high reactive potential for CO2-mineral trapping due to an abundance of divalent-cation containing silicates, such as forsterite (Mg2SiO4). Recent studies have shown that carbonation of these silicates under wet scCO2 conditions, e. g. encountered near a CO2 injection well, proceeds along a different pathway and is more effective than in CO2-saturated aqueous fluids. The presence of an adsorbed water film on the forsterite surface seems to be key to reactivity towards carbonation. In this study, we employed in situ high pressure IR spectroscopy to investigate the dependence of adsorbed water film thickness on forsterite carbonation chemistry. Post reaction ex situ SEM, TEM, TGA, XRD, and NMR measurements will also be discussed. Several IR titrations were performed of forsterite with water at 50 °C and 90 bar scCO2. Aliquots of water were titrated at 4-hour reaction-time increments. Once a desired total water concentration was reached, data were collected for about another 30 hours. One titration involved 10 additions, which corresponds to 6.8 monolayers of adsorbed water. Clearly, a carbonate was precipitating, and its spectral signature matched magnesite. Another titration involved 8 aliquots, or up to 4.4 monolayers of water. The integrated absorbance under the CO stretching bands of carbonate as a function of time after reaching 4.4 monolayers showed an increase and then a plateau. We are currently unsure of the identity of the carbonate that precipitated, but it could be an amorphous anhydrous phase or magnesite crystals with dimensions of only several nanometers. A third titration only involved 3 additions, or up to 1.6 monolayers of water. The integrated absorbance under the CO stretching bands of carbonate as a function of time after reaching 1.6 monolayers

  10. Removal of acutely hazardous pharmaceuticals from water using multi-template imprinted polymer adsorbent.

    PubMed

    Venkatesh, Avinash; Chopra, Nikita; Krupadam, Reddithota J

    2014-05-01

    Molecularly imprinted polymer adsorbent has been prepared to remove a group of recalcitrant and acutely hazardous (p-type) chemicals from water and wastewaters. The polymer adsorbent exhibited twofold higher adsorption capacity than the commercially used polystyrene divinylbenzene resin (XAD) and powdered activated carbon adsorbents. Higher adsorption capacity of the polymer adsorbent was explained on the basis of high specific surface area formed during molecular imprinting process. Freundlich isotherms drawn showed that the adsorption of p-type chemicals onto polymer adsorbent was kinetically faster than the other reference adsorbents. Matrix effect on adsorption of p-type chemicals was minimal, and also polymer adsorbent was amenable to regeneration by washing with water/methanol (3:1, v/v) solution. The polymer adsorbent was unaltered in its adsorption capacity up to 10 cycles of adsorption and desorption, which will be more desirable in cost reduction of treatment compared with single-time-use activated carbon.

  11. Adsorbate-induced demagnetization and restructuring of ultrathin magnetic films: CO chemisorbed on γ-Fe/Cu(100)

    NASA Astrophysics Data System (ADS)

    Spišák, D.; Hafner, J.

    2001-09-01

    First-principles local-spin-density (LSD) investigations of the structural, magnetic, and electronic properties of clean and CO-adsorbed ultrathin γ-iron films epitaxially grown on Cu(100) surfaces demonstrate that both the geometrical and the magnetic structures of the films are profoundly modified by the adsorption of CO. The enhanced magnetic moments of the top-layer atoms are strongly quenched by the presence of the adsorbate. Due to the pronounced magnetovolume effect, this leads also to a correlated change in the interlayer relaxations. Strikingly, the adsorbate-induced demagnetization is primarily limited to those surface atoms directly bonded to the adsorbate. This leads to the formation of an in-plane magnetic pattern in a partially adsorbate-covered film. The comparison of the calculated vibrational eigenfrequencies of the CO adsorbate with experiment confirms the picture based on the LSD calculations.

  12. Smooth deuterated cellulose films for the visualisation of adsorbed bio-macromolecules

    PubMed Central

    Su, Jielong; Raghuwanshi, Vikram S.; Raverty, Warwick; Garvey, Christopher J.; Holden, Peter J.; Gillon, Marie; Holt, Stephen A.; Tabor, Rico; Batchelor, Warren; Garnier, Gil

    2016-01-01

    Novel thin and smooth deuterated cellulose films were synthesised to visualize adsorbed bio-macromolecules using contrast variation neutron reflectivity (NR) measurements. Incorporation of varying degrees of deuteration into cellulose was achieved by growing Gluconacetobacter xylinus in deuterated glycerol as carbon source dissolved in growth media containing D2O. The derivative of deuterated cellulose was prepared by trimethylsilylation(TMS) in ionic liquid(1-butyl-3-methylimidazolium chloride). The TMS derivative was dissolved in toluene for thin film preparation by spin-coating. The resulting film was regenerated into deuterated cellulose by exposure to acidic vapour. A common enzyme, horseradish peroxidase (HRP), was adsorbed from solution onto the deuterated cellulose films and visualized by NR. The scattering length density contrast of the deuterated cellulose enabled accurate visualization and quantification of the adsorbed HRP, which would have been impossible to achieve with non-deuterated cellulose. The procedure described enables preparing deuterated cellulose films that allows differentiation of cellulose and non-deuterated bio-macromolecules using NR. PMID:27796332

  13. Smooth deuterated cellulose films for the visualisation of adsorbed bio-macromolecules.

    PubMed

    Su, Jielong; Raghuwanshi, Vikram S; Raverty, Warwick; Garvey, Christopher J; Holden, Peter J; Gillon, Marie; Holt, Stephen A; Tabor, Rico; Batchelor, Warren; Garnier, Gil

    2016-10-31

    Novel thin and smooth deuterated cellulose films were synthesised to visualize adsorbed bio-macromolecules using contrast variation neutron reflectivity (NR) measurements. Incorporation of varying degrees of deuteration into cellulose was achieved by growing Gluconacetobacter xylinus in deuterated glycerol as carbon source dissolved in growth media containing D2O. The derivative of deuterated cellulose was prepared by trimethylsilylation(TMS) in ionic liquid(1-butyl-3-methylimidazolium chloride). The TMS derivative was dissolved in toluene for thin film preparation by spin-coating. The resulting film was regenerated into deuterated cellulose by exposure to acidic vapour. A common enzyme, horseradish peroxidase (HRP), was adsorbed from solution onto the deuterated cellulose films and visualized by NR. The scattering length density contrast of the deuterated cellulose enabled accurate visualization and quantification of the adsorbed HRP, which would have been impossible to achieve with non-deuterated cellulose. The procedure described enables preparing deuterated cellulose films that allows differentiation of cellulose and non-deuterated bio-macromolecules using NR.

  14. Smooth deuterated cellulose films for the visualisation of adsorbed bio-macromolecules

    NASA Astrophysics Data System (ADS)

    Su, Jielong; Raghuwanshi, Vikram S.; Raverty, Warwick; Garvey, Christopher J.; Holden, Peter J.; Gillon, Marie; Holt, Stephen A.; Tabor, Rico; Batchelor, Warren; Garnier, Gil

    2016-10-01

    Novel thin and smooth deuterated cellulose films were synthesised to visualize adsorbed bio-macromolecules using contrast variation neutron reflectivity (NR) measurements. Incorporation of varying degrees of deuteration into cellulose was achieved by growing Gluconacetobacter xylinus in deuterated glycerol as carbon source dissolved in growth media containing D2O. The derivative of deuterated cellulose was prepared by trimethylsilylation(TMS) in ionic liquid(1-butyl-3-methylimidazolium chloride). The TMS derivative was dissolved in toluene for thin film preparation by spin-coating. The resulting film was regenerated into deuterated cellulose by exposure to acidic vapour. A common enzyme, horseradish peroxidase (HRP), was adsorbed from solution onto the deuterated cellulose films and visualized by NR. The scattering length density contrast of the deuterated cellulose enabled accurate visualization and quantification of the adsorbed HRP, which would have been impossible to achieve with non-deuterated cellulose. The procedure described enables preparing deuterated cellulose films that allows differentiation of cellulose and non-deuterated bio-macromolecules using NR.

  15. Influence of fluoride-detergent combinations on the visco-elasticity of adsorbed salivary protein films.

    PubMed

    Veeregowda, Deepak H; van der Mei, Henny C; Busscher, Henk J; Sharma, Prashant K

    2011-02-01

    The visco-elasticity of salivary-protein films is related to mouthfeel, lubrication, biofilm formation, and protection against erosion and is influenced by the adsorption of toothpaste components. The thickness and the visco-elasticity of hydrated films (determined using a quartz crystal microbalance) of 2-h-old in vitro-adsorbed salivary-protein films were 43.5 nm and 9.4 MHz, respectively, whereas the dehydrated thickness, measured using X-ray photoelectron spectroscopy, was 2.4 nm. Treatment with toothpaste slurries decreased the thickness of the film, depending on the fluoride-detergent combination involved. Secondary exposure to saliva resulted in a regained thickness of the film to a level similar to its original thickness; however, no association was found between the thickness of hydrated and dehydrated films, indicating differences in film structure. Treatment with stannous fluoride/sodium lauryl sulphate (SnF(2)/SLS)-containing toothpaste slurries yielded a strong, immediate two-fold increase in characteristic film frequency (f(c)) with respect to untreated films, indicating cross-linking in adsorbed salivary-protein films by Sn(2+) that was absent when SLS was replaced with sodium hexametaphosphate (NaHMP). Secondary exposure to saliva of films treated with SnF(2) caused a strong, six-fold increase in f(c) compared with primary salivary-protein films, regardless of whether SLS or NaHMP was the detergent. This suggests that ionized stannous is not directly available for cross-linking in combination with highly negatively charged NaHMP, but becomes slowly available after initial treatment to cause cross-linking during secondary exposure to saliva.

  16. Photoelectron decay kinetics of cubic silver chloride microcrystal film adsorbing plentiful dye excited by laser

    NASA Astrophysics Data System (ADS)

    Zhang, Rongxiang; Zhang, Jixian; Lai, Weidong; Hu, Yanxia; Dai, Xiuhong; Han, Li; Li, Xiaowei

    2007-12-01

    There will be large numbers of carriers coming into being in the interior of silver chloride microcrystals when illumination acts on it. Microwave absorption and dielectric spectrum detection technology with high temporal resolution (1ns) can detect instantaneous decay process of photoelectrons. In this work, the photoelectron decay action of spectral sensitized silver chloride emulsion is measured by microwave absorption and dielectric spectrum detection technology. By analyzing the measured results, it is found that when plentiful dye adsorb on silver chloride microcrystals film, the photoelectron decay of silver chloride emulsion becomes faster than that of pure emulsion. However it is not that the more the dye is adsorbed, the faster the photoelectron decay will be. When the adsorbed dye reaches a certain level, the photoelectron decay becomes slower than the fastest instance. Combining with photoelectron decay kinetics theory it is found that the above results are induced by two kinds of effect from dye adsorption.

  17. Contribution of Adsorbed Protein Films to Nanoscopic Vibrations Exhibited by Bacteria Adhering through Ligand-Receptor Bonds.

    PubMed

    Song, Lei; Sjollema, Jelmer; Norde, Willem; Busscher, Henk J; van der Mei, Henny C

    2015-09-29

    Bacteria adhering to surfaces exhibit nanoscopic vibrations that depend on the viscoelasticity of the bond. The quantification of the nanoscopic vibrations of bacteria adhering to surfaces provides new opportunities to better understand the properties of the bond through which bacteria adhere and the mechanisms by which they resist detachment. Often, however, bacteria do not adhere to bare surfaces but to adsorbed protein films, on which adhesion involves highly specific ligand-receptor binding next to nonspecific DLVO interaction forces. Here we determine the contribution of adsorbed salivary protein and fibronectin films to vibrations exhibited by adhering streptococci and staphylococci, respectively. The streptococcal strain used has the ability to adhere to adsorbed salivary proteins films through antigen I/II ligand-receptor binding, while the staphylococcal strain used adheres to adsorbed fibronectin films through a proteinaceous ligand-receptor bond. In the absence of ligand-receptor binding, electrostatic interactions had a large impact on vibration amplitudes of adhering bacteria on glass. On an adsorbed salivary protein film, vibration amplitudes of adhering streptococci depended on the film softness as determined by QCM-D and were reduced after film fixation using glutaraldehyde. On a relatively stiff fibronectin film, cross-linking the film in glutaraldehyde hardly reduced its softness, and accordingly fibronectin film softness did not contribute to vibration amplitudes of adhering staphylococci. However, fixation of the staphylococcus-fibronectin bond further decreased vibration amplitudes, while fixation of the streptococcus bond hardly impacted vibration amplitudes. Summarizing, this study shows that both the softness of adsorbed protein films and the properties of the bond between an adhering bacterium and an adsorbed protein film play an important role in bacterial vibration amplitudes. These nanoscopic vibrations reflect the viscoelasticity of the

  18. Film morphology and orientation of amino silicone adsorbed onto cellulose substrate

    NASA Astrophysics Data System (ADS)

    Xu, Yingjun; Yin, Hong; Yuan, Shenfeng; Chen, Zhirong

    2009-07-01

    A series of amino silicones with different amino values were synthesized and adsorbed onto surfaces of cotton fibers and cellulose substrates. The film morphology, hydrophobic properties and surface composition of the silicones are investigated and characterized by field emission scanning electron microscope (FESEM), atomic force microscope (AFM), contact angle measurement, X-ray photoelectron spectroscopy (XPS) and attenuated total reflectance infrared (ATR-IR). The results of the experiments indicate that the amino silicone can form a hydrophobic film on both cotton fibers and cellulose substrates and reduce the surface roughness significantly. Furthermore, the roughness becomes smaller with an increase in the amino value. All these results suggest that the orientation of amino silicone molecule is with the amino functional groups of amino silicone molecule adsorbed onto the cellulose interface while the main polymer chains and the hydrophobic Si-CH 3 groups extend toward the air.

  19. Aggregate formation of eosin-Y adsorbed on nanocrystalline TiO2 films

    NASA Astrophysics Data System (ADS)

    Yaguchi, Kaori; Furube, Akihiro; Katoh, Ryuzi

    2012-11-01

    We have studied the adsorption of eosin-Y on nanocrystalline TiO2 films with two different solvents namely acetonitrile (ACN) and ethanol (EtOH). A Langmuir-type adsorption isotherm was observed with ACN. In contrast, a Freundlich-type adsorption isotherm was observed with EtOH, suggesting that EtOH molecules co-adsorbed on TiO2 surface. Absorption spectra of the dye adsorbed films clearly show aggregate formation at high concentrations of dye in the solutions. From the analysis of the spectra, we conclude that head-to-tail type aggregates are observed with ACN, whereas various types of aggregates, including H-type and head-to-tail type aggregates, are observed with EtOH.

  20. The National Shipbuilding Research Program, Heavy Metal Adsorbents for Storm Water Pollution Prevention

    DTIC Science & Technology

    1997-12-01

    Heavy Metal Adsorbents for Storm Water Pollution Prevention U.S. DEPARTMENT OF THE NAVY CARDEROCK DIVISION, NAVAL SURFACE WARFARE CENTER in...National Shipbuilding Research Program, Heavy Metal Adsorbents for Storm Water Pollution Prevention 5a. CONTRACT NUMBER 5b. GRANT NUMBER 5c. PROGRAM...States Navy. ANY POSSIBLE IMPLIED WARRANTIES OF MERCHANTABILITY AND/OR FITNESS FOR PURPOSE ARE SPECIFICALLY DISCLAIMED. FINAL REPORT HEAVY METAL ADSORBENTS

  1. In situ investigations of Fe3+ induced complexation of adsorbed Mefp-1 protein film on iron substrate.

    PubMed

    Zhang, Fan; Sababi, Majid; Brinck, Tore; Persson, Dan; Pan, Jinshan; Claesson, Per M

    2013-08-15

    A range of in situ analytical techniques and theoretical calculations were applied to gain insights into the formation and properties of the Mefp-1 film on iron substrate, as well as the protein complexation with Fe(3+) ions. Adsorption kinetics of Mefp-1 and the complexation were investigated using QCM-D. The results suggest an initially fast adsorption, with the molecules oriented preferentially parallel to the surface, followed by a structural change within the film leading to molecules extending toward solution. Exposure to a diluted FeCl3 solution results in enhanced complexation within the adsorbed protein film, leading to water removal and film compaction. In situ Peak Force Tapping AFM was employed for determining morphology and nano-mechanical properties of the surface layer. The results, in agreement with the QCM-D observations, demonstrate that addition of Fe(3+) induces a transition from an extended and soft protein layer to a denser and stiffer one. Further, in situ ATR-FTIR and Confocal Raman Micro-spectroscopy (CRM) techniques were utilized to monitor compositional/structural changes in the surface layer due to addition of Fe(3+) ions. The spectroscopic analyses assisted by DFT calculations provide evidence for formation of tri-Fe(3+)/catechol complexes in the surface film, which is enhanced by Fe(3+) addition.

  2. Comparative FTIR spectroscopy of HX adsorbed on solid water: Ragout-jet water clusters vs ice nanocrystal arrays.

    PubMed

    Devlin, J P; Farník, M; Suhm, M A; Buch, V

    2005-02-17

    In addition to revealing the stretch-mode bands of the smallest mixed clusters of HCl and HBr (HX) with water, the ragout-jet FTIR spectra of dense mixed water-acid supersonic jets include bands that result from the interaction of HX with larger water clusters. It is argued here that low jet temperatures prevent the water-cluster-bound HX molecules from becoming sufficiently solvated to induce ionic dissociation. The molecular nature of the HX can be deduced directly from the observed influence of changing from HCl to HBr and from replacing H2O with D2O. Furthermore, the band positions of HX are roughly coincidental with bands assigned to molecular HCl and HBr adsorbed on ice nanocrystal surfaces at temperatures below 100 K. It is also interesting that the HX band positions and widths approximate those of HX bound to the surface of amorphous ice films at <60 K. Though computational results suggest the adsorbed HX molecules observed in the jet expansions are weakly distorted by single coordination with surface dangling-oxygen atoms, on-the-fly trajectories indicate that the cluster skeletons undergo large-amplitude low-frequency vibrations. Local HX solvation, the extent of proton sharing, and the HX vibrational spectra undergo serious modulation on a picosecond time scale.

  3. Thermodynamic formalism of water uptakes on solid porous adsorbents for adsorption cooling applications

    NASA Astrophysics Data System (ADS)

    Sun, Baichuan; Chakraborty, Anutosh

    2014-05-01

    This Letter presents a thermodynamic formulation to calculate the amount of water vapor uptakes on various adsorbents such as zeolites, metal organic frameworks, and silica gel for the development of an advanced adsorption chiller. This formalism is developed from the rigor of the partition distribution function of each water vapor adsorptive site on adsorbents and the condensation approximation of adsorptive water molecules and is validated with experimental data. An interesting and useful finding has been established that the proposed model is thermodynamically connected with the pore structures of adsorbent materials, and the water vapor uptake highly depends on the isosteric heat of adsorption at zero surface coverage and the adsorptive sites of the adsorbent materials. Employing the proposed model, the thermodynamic trends of water vapor uptakes on various adsorbents can be estimated.

  4. Miscibility and interaction between 1-alkanol and short-chain phosphocholine in the adsorbed film and micelles.

    PubMed

    Takajo, Yuichi; Matsuki, Hitoshi; Kaneshina, Shoji; Aratono, Makoto; Yamanaka, Michio

    2007-09-01

    The miscibility and interaction of 1-hexanol (C6OH) and 1-heptanol (C7OH) with 1,2-dihexanoyl-sn-glycero-3-phosphocholine (DHPC) in the adsorbed films and micelles were investigated by measuring the surface tension of aqueous C6OH-DHPC and aqueous C7OH-DHPC solutions. The surface density, the mean molecular area, the composition of the adsorbed film, and the excess Gibbs energy of adsorption g(H,E), were estimated. Further, the critical micelle concentration of the mixtures was determined from the surface tension versus molality curves; the micellar composition was calculated. The miscibility of the 1-alkanols and DHPC molecules in the adsorbed film and micelles was examined using the phase diagram of adsorption (PDA) and that of micellization (PDM). The PDA and the composition dependence of g(H,E) indicated the non-ideal mixing of the 1-alkanols and DHPC molecules due to the attractive interaction between the molecules in the adsorbed film, while the PDM indicated that the 1-alkanol molecules were not incorporated in the micelles within DHPC rich region. The dependence of the mean molecular area of the mixtures on the surface composition suggested that the packing property of the adsorbed film depends on the chain length of 1-alkanol: C6OH expands the DHPC adsorbed film more than C7OH.

  5. Oil palm biomass-based adsorbents for the removal of water pollutants--a review.

    PubMed

    Ahmad, Tanweer; Rafatullah, Mohd; Ghazali, Arniza; Sulaiman, Othman; Hashim, Rokiah

    2011-07-01

    This article presents a review on the role of oil palm biomass (trunks, fronds, leaves, empty fruit bunches, shells, etc.) as adsorbents in the removal of water pollutants such as acid and basic dyes, heavy metals, phenolic compounds, various gaseous pollutants, and so on. Numerous studies on adsorption properties of various low-cost adsorbents, such as agricultural wastes and its based activated carbons, have been reported in recent years. Studies have shown that oil palm-based adsorbent, among the low-cost adsorbents mentioned, is the most promising adsorbent for removing water pollutants. Further, these bioadsorbents can be chemically modified for better efficiency and can undergo multiple reuses to enhance their applicability at an industrial scale. It is evident from a literature survey of more than 100 recent papers that low-cost adsorbents have demonstrated outstanding removal capabilities for various pollutants. The conclusion is been drawn from the reviewed literature, and suggestions for future research are proposed.

  6. Selection and evaluation of adsorbents for the removal of anionic surfactants from laundry rinsing water.

    PubMed

    Schouten, Natasja; van der Ham, Louis G J; Euverink, Gert-Jan W; de Haan, André B

    2007-10-01

    Low-cost adsorbents were tested to remove anionic surfactants from laundry rinsing water to allow re-use of water. Adsorbents were selected corresponding to the different surfactant adsorption mechanisms. Equilibrium adsorption studies of linear alkyl benzene sulfonate (LAS) show that ionic interaction results in a high maximum adsorption capacity on positively charged adsorbents of 0.6-1.7 gLAS/g. Non-ionic interactions, such as hydrophobic interactions of LAS with non-ionic resins or activated carbons, result in a lower adsorption capacity of 0.02-0.6 gLAS/g. Negatively charged materials, such as cation exchange resins or bentonite clay, have negligible adsorption capacities for LAS. Similar results are obtained for alpha olefin sulfonate (AOS). Cost comparison of different adsorbents shows that an inorganic anion exchange material (layered double hydroxide) and activated carbons are the most cost-effective materials in terms of the amount of surfactant adsorbed per dollar worth of adsorbent.

  7. Miscibility of Hydrocarbon and Fluorocarbon Surfactants in Adsorbed Film and Micelle.

    PubMed

    Villeneuve, Masumi; Nomura, Teruko; Matsuki, Hitoshi; Kaneshina, Shoji; Aratono, Makoto

    2001-02-01

    We investigated the miscibility of nonionic hydrocarbon and fluorocarbon surfactants in the adsorbed film and the micelle by surface tension measurements of the aqueous solution. The combination of tetraethyleneglycol monodecyl ether (C10E4) and tetraethyleneglycol mono-1,1,7-trihydrododecafluoroheptyl ether (FC7E4) was chosen because they have the same hydrophilic groups and about the same surface activity. The extent of nonideal mixing was estimated quantitatively in terms of the excess Gibbs energy in the adsorbed film g(H,E) and that in the micelle g(M,E). The excess area per adsorbed molecule, A(H,E), was also evaluated and discussed. The ionic hydrocarbon and fluorocarbon mixed surfactant systems, lithium dodecyl sulfate (LiDS)/lithium perfluorooctane sulfonate (LiFOS) and lithium tetradecyl sulfate (LiTS)/LiFOS systems are also investigated from the standpoint of excess Gibbs energy and excess area. It is also clearly shown that the regular solution approach does not fit in the systems that contain ionic species. Copyright 2001 Academic Press.

  8. AC microcalorimetry of adsorbates on evaporated metal films: Orientational ordering of H{sub 2} multilayers

    SciTech Connect

    Phelps, R.B.

    1991-11-01

    We have improved and extended a novel ac calorimetric technique for measuring the heat capacity of adsorbates on evaporated metal films. Metallic substrates are of particular interest in current studies of the thermodynamics of adsorbed molecules. The method described in the present work is only calorimetric technique which allows measurements of molecules on simple metallic surfaces. Among other improvements, we have achieved significant progress in the preparation and characterization of the evaporated metal film. We have applied this novel technique to a study of hydrogen multilayers on gold and sapphire substrates. We have shown that samples of normal-hydrogen with a nominal coverage n of approximately 25 monolayers (ML) undergo a bulk-like orientational ordering transition. The transition is suppressed as the coverage is decreased, and no sign of the transition remains above 1.6 K for n {approx} 1 ML. For n {approx_lt} 8 ML, the peak in the heat capacity exhibits signs of finite-size effects. At higher coverages, finite-size effects are not observed, and the shape of the peak depends strongly on the substrate. We conclude that the peak is inhomogeneously broadened for n {approx_lt} 8 ML. This work represents the first measurements of the heat capacity due to orientational ordering in adsorbed hydrogen. The results of an earlier experiment involving vibrational spectroscopy of adsorbed molecules are included in the Appendix. In this work, we have used infrared emission spectroscopy to study the spectral region in the vicinity of the C=O stretch vibration of bridge-bonded CO on Pt(111).

  9. AC microcalorimetry of adsorbates on evaporated metal films: Orientational ordering of H sub 2 multilayers

    SciTech Connect

    Phelps, R.B.

    1991-11-01

    We have improved and extended a novel ac calorimetric technique for measuring the heat capacity of adsorbates on evaporated metal films. Metallic substrates are of particular interest in current studies of the thermodynamics of adsorbed molecules. The method described in the present work is only calorimetric technique which allows measurements of molecules on simple metallic surfaces. Among other improvements, we have achieved significant progress in the preparation and characterization of the evaporated metal film. We have applied this novel technique to a study of hydrogen multilayers on gold and sapphire substrates. We have shown that samples of normal-hydrogen with a nominal coverage n of approximately 25 monolayers (ML) undergo a bulk-like orientational ordering transition. The transition is suppressed as the coverage is decreased, and no sign of the transition remains above 1.6 K for n {approx} 1 ML. For n {approx lt} 8 ML, the peak in the heat capacity exhibits signs of finite-size effects. At higher coverages, finite-size effects are not observed, and the shape of the peak depends strongly on the substrate. We conclude that the peak is inhomogeneously broadened for n {approx lt} 8 ML. This work represents the first measurements of the heat capacity due to orientational ordering in adsorbed hydrogen. The results of an earlier experiment involving vibrational spectroscopy of adsorbed molecules are included in the Appendix. In this work, we have used infrared emission spectroscopy to study the spectral region in the vicinity of the C=O stretch vibration of bridge-bonded CO on Pt(111).

  10. Application of 1H NMR spectroscopy method for determination of characteristics of thin layers of water adsorbed on the surface of dispersed and porous adsorbents.

    PubMed

    Turov, V V; Leboda, R

    1999-02-01

    The paper presents 1H NMR spectroscopy as a perspective method of the studies of the characteristics of water boundary layers in the hydrated powders and aqueous dispergated suspensions of the adsorbents. The method involves measurements of temperature dependence proton signals intensity in the adsorbed water at temperatures lower than 273 K. Free energy of water molecules at the adsorbent/water interface is diminished due to the adsorption interactions causing the water dosed to the adsorbent surface freezes at T < 273 K. Thickness of a non-freezing layer of water can be determined from the intensity of the water signal of 1H NMR during the freezing-thawing process. Due to a disturbing action of the adsorbent surface, water occurs in the quasi-liquid state. As a result, it is observed in the 1H NMR spectra as a relatively narrow signal. The signal of ice is not registered due to great differences in the transverse relaxation times of the adsorbed water and ice. The method of measuring the free surface energy of the adsorbents from the temperature dependence of the signal intensity of non-freezing water is based on the fact that the temperature of water freezing decreases by the quantity which depends on the surface energy and the distance of the adsorbed molecules from the solid surface. The water at the interface freezes when the free energies of the adsorbed water and ice are equal. To illustrate the applicability of the method under consideration the series of adsorption systems in which the absorbents used differed in the surface chemistry and porous structure. In particular, the behaviour of water on the surface of the following adsorbents is discussed: non-porous and porous silica (aerosils, silica gels); chemically and physically modified non-porous and porous silica (silanization, carbonization, biopolymer deposition); and pyrogeneous Al2O3 and aluminasilicas. The effect of preliminary treatment of the adsorbent (thermal, high pressure, wetting with polar

  11. Gold nanoparticle-aluminum oxide adsorbent for efficient removal of mercury species from natural waters.

    PubMed

    Lo, Sut-I; Chen, Po-Cheng; Huang, Chih-Ching; Chang, Huan-Tsung

    2012-03-06

    We report a new adsorbent for removal of mercury species. By mixing Au nanoparticles (NPs) 13 nm in diameter with aluminum oxide (Al(2)O(3)) particles 50-200 μm in diameter, Au NP-Al(2)O(3) adsorbents are easily prepared. Three adsorbents, Al(2)O(3), Au NPs, and Au NP-Al(2)O(3), were tested for removal of mercury species [Hg(2+), methylmercury (MeHg(+)), ethylmercury (EtHg(+)), and phenylmercury (PhHg(+))]. The Au NP adsorbent has a higher binding affinity (dissociation constant; K(d) = 0.3 nM) for Hg(2+) ions than the Al(2)O(3) adsorbent (K(d) = 52.9 nM). The Au NP-Al(2)O(3) adsorbent has a higher affinity for mercury species and other tested metal ions than the Al(2)O(3) and Au NP adsorbents. The Au NP-Al(2)O(3) adsorbent provides a synergic effect and, thus, is effective for removal of most tested metal ions and organic mercury species. After preconcentration of mercury ions by an Au NP-Al(2)O(3) adsorbent, analysis of mercury ions down to the subppq level in aqueous solution was performed by inductively coupled plasma mass spectrometry (ICP-MS). The Au NP-Al(2)O(3) adsorbent allows effective removal of mercury species spiked in lake water, groundwater, and seawater with efficiencies greater than 97%. We also used Al(2)O(3) and Au NP-Al(2)O(3) adsorbents sequentially for selectively removing Hg(2+) and MeHg(+) ions from water. The low-cost, effective, and stable Au NP-Al(2)O(3) adsorbent shows great potential for economical removal of various mercury species.

  12. Quantitative time-of-flight secondary ion mass spectrometry for the characterization of multicomponent adsorbed protein films

    NASA Astrophysics Data System (ADS)

    Wagner, M. S.; Shen, M.; Horbett, T. A.; Castner, David G.

    2003-01-01

    Time-of-flight secondary ion mass spectrometry (ToF-SIMS) is ideal for the characterization of adsorbed proteins due to its chemical specificity and surface sensitivity. We have employed ToF-SIMS and multivariate analysis to determine the surface composition of adsorbed protein films from binary mixtures, blood serum, and blood plasma. Good correlation between ToF-SIMS data and independent radiolabeling studies was achieved for binary mixtures, though these results depended on the substrate. Qualitative insight into the composition of the serum and plasma protein films was obtained via comparison to standard single protein film spectra. ToF-SIMS and multivariate analysis were able to measure the surface composition of multicomponent adsorbed protein films.

  13. ToF-SIMS and XPS Characterization of Protein Films Adsorbed onto Bare and Sodium Styrenesulfonate-Grafted Gold Substrates.

    PubMed

    Foster, Rami N; Harrison, Elisa T; Castner, David G

    2016-04-05

    The adsorption of single-component bovine serum albumin (BSA), bovine fibrinogen (Fgn), and bovine immunoglobulin G (IgG) films as well as multicomponent bovine plasma films onto bare and sodium styrenesulfonate (NaSS)-grafted gold substrates was characterized. The adsorption isotherms, measured via X-ray photoelectron spectroscopy, showed that at low solution concentrations all three single-component proteins adsorb with higher affinity onto gold surfaces compared to NaSS surfaces. However, at higher concentrations, NaSS surfaces adsorb the same or more total protein than gold surfaces. This may be because proteins that adsorb onto NaSS undergo structural rearrangements, resulting in a larger fraction of irreversibly adsorbed species over time. Still, with the possible exception of BSA adsorbed onto gold, neither surface appeared to have saturated at the highest protein solution concentration studied. Principal component (PC) analysis of amino acid mass fragments from time-of-flight secondary ion mass spectra distinguished between the same protein adsorbed onto NaSS and gold surfaces, suggesting that proteins adsorb differently on NaSS and gold surfaces. Explored further using peak ratios for buried/surface amino acids for each protein, we found that proteins denature more on NaSS surfaces than on gold surfaces. Also, using peak ratios for asymmetrically distributed amino acids, potential structural differences were postulated for BSA and IgG adsorbed onto NaSS and gold surfaces. PC modeling, used to track changes in plasma adsorption with time, suggests that plasma films on NaSS and Au surfaces become more Fgn-like with increasing adsorption time. However, the PC models included only three proteins, where plasma is composed of hundreds of proteins. Therefore, while both gold and NaSS appear to adsorb more Fgn with time, further study is required to confirm that this is representative of the final state of the plasma films.

  14. The effect of mineral bond strength and adsorbed water on fault gouge frictional strength

    USGS Publications Warehouse

    Morrow, C.A.; Moore, Diane E.; Lockner, D.A.

    2000-01-01

    Recent studies suggest that the tendency of many fault gouge minerals to take on adsorbed or interlayer water may strongly influence their frictional strength. To test this hypothesis, triaxial sliding experiments were conducted on 15 different single-mineral gouges with various water-adsorbing affinities. Vacuum dried samples were sheared at 100 MPa, then saturated with water and sheared farther to compare dry and wet strengths. The coefficients of friction, μ, for the dry sheet-structure minerals (0.2-0.8), were related to mineral bond strength, and dropped 20-60% with the addition of water. For non-adsorbing minerals (μ = 0.6-0.8), the strength remained unchanged after saturation. These results confirm that the ability of minerals to adsorb various amounts of water is related to their relative frictional strengths, and may explain the anomalously low strength of certain natural fault gouges.

  15. Atomic force microscopy of AgBr crystals and adsorbed gelatin films

    SciTech Connect

    Haugstad, G.; Gladfelter, W.L.; Keyes, M.P.; Weberg, E.B.

    1993-06-01

    Atomic force microscopy of the (111) surface of macroscopic AgBr crystals revealed steps ranging in height from two atomic layers up to 10 nm, lying predominantly along the (110) and (112) families of crystal directions. Rods of elemental Ag, formed via photoreduction, were observed along the (110) family of directions. Images of adsorbed gelatin films revealed circular pores with diameters of order 10-100 nm, extending to the AgBr surface. The length of deposition time, the pH and concentration of the gelatin solution, and the presence of steps on the AgBr surface were observed to affect the size, number, and location of pores in the gelatin films. 12 refs., 7 figs.

  16. Liquid 4He Adsorbed Films on Very Attractive Substrates

    NASA Astrophysics Data System (ADS)

    Urrutia, Ignacio; Szybisz, Leszek

    Adsorbed films of liquid 4He are analized, in the framework of Density Functional Theories (DF). In these systems, when the substrate becomes increasingly attractive, the thin films of 4He approaches the quasi-bidimensional limit. We study this strongly attractive substrate regime with two DF, the Orsay-Trento (OT) and a recent Hybrid proposal (Hyb), focusing in the energy behavior. It is showed that OT does not reproduce the correct limiting energy curve, and it implies that this functional could not provide reliable results for very strongly attractive substrates like Graphite (Gr). In other hand, with the Hyb DF, the correct energy behavior is found for the adsorption energy of 4He on Gr. These results show that OT should not be applied to quasi 2D (confinement) situations, and that Hyb DF provides a much more realistic description.

  17. Hydration level dependence of the microscopic dynamics of water adsorbed in ultramicroporous carbon

    SciTech Connect

    Mamontov, Eugene; Yue, Yanfeng; Bahadur, Jitendra; Guo, Junjie; Contescu, Cristian I.; Gallego, Nidia C.; Melnichenko, Yuri B.

    2016-10-20

    Even when not functionalized intentionally, most carbon materials are not hydrophobic and readily adsorb water molecules from atmospheric water vapor. We have equilibrated an ultramicroporous carbon at several levels of relative humidity, thereby attaining various hydration levels. The water molecules were adsorbed on the pore walls (but did not fill completely the pore volume) and thus could be better described as hydration, or surface, rather than confined, water. We used quasielastic neutron scattering to perform a detailed investigation of the dependence of microscopic dynamics of these adsorbed water species on the hydration level and temperature. The behavior of hydration water in ultramicroporous carbon clearly demonstrates the same universal traits that characterize surface (hydration) water in other materials that are surface-hydrated. In addition, unless special treatment is intentionally applied to ultramicroporous carbon, the species filling its pores in various applications, ranging from hydrogen molecules to electrolytes, likely find themselves in contact with non-freezing water molecules characterized by rich microscopic dynamics.

  18. Retention of radium from thermal waters on sand filters and adsorbents.

    PubMed

    Elejalde, C; Herranz, M; Idoeta, R; Legarda, F; Romero, F; Baeza, A

    2007-06-18

    This study was focussed on laboratory experiences of retention of radium from one thermal water on sand filters and adsorbents, trying to find an easy method for the elimination in drinkable waters polluted with this natural radio-nuclide. A thermal water from Cantabria (Spain) was selected for this work. Retention experiences were made with columns of 35 mm of diameter containing 15 cm layers of washed river sand or 4 cm layers of zeolite A3, passing known volumes of thermal water at flows between 4 and 40 ml/min with control of the retained radium by determining the amount in the water after the treatment. The statistical analysis of data suggests that retention depends on the flow and the volume passed through the columns. As additional adsorbents were used kaolin and a clay rich in illite. Jar-test experiences were made agitating known weights of adsorbents with the selected thermal water, with addition of flocculants and determination of radium in filtrated water after the treatment. Data suggest that retention is related to the weight of adsorbent used, but important quantities of radium seem remain in solution for higher amounts of adsorbents, according to the statistical treatment of data. The elution of retained radium from columns or adsorbents, previously used in experiences, should be the aim of a future research.

  19. Removal of arsenic from water using nano adsorbents and challenges: A review.

    PubMed

    Lata, Sneh; Samadder, S R

    2016-01-15

    Many researchers have used nanoparticles as adsorbents to remove water pollutants including arsenic after modifying the properties of nanoparticles by improving reactivity, biocompatibility, stability, charge density, multi-functionalities, and dispersibility. For arsenic removal, nano adsorbents emerged as the potential alternatives to existing conventional technologies. The present study critically reviewed the past and current available information on the potential of nano adsorbents for arsenic removal from contaminated water and the challenges involved in that. The study discussed the separation and regeneration techniques of nano adsorbents and the performance thereof. The study evaluated the adsorption efficiency of the various nanoparticles based on size of nanoparticles, types of nano adsorbents, method of synthesis, separation and regeneration of the nano adsorbents. The study found that more studies are required on suitable holding materials for the nano adsorbents to improve the permeability and to make the technology applicable at the field condition. The study will help the readers to choose suitable nanomaterials and to take up further research required for arsenic removal using nano adsorbents.

  20. Thermodynamic properties of adsorbed water on silica gel - Exergy losses in adiabatic sorption processes

    NASA Astrophysics Data System (ADS)

    Worek, W. M.; Zengh, W.; San, J.-Y.

    1991-09-01

    In order to perform exergy analyses to optimize the transient heat and mass transfer processes involving sorption by solid adsorbents, the thermodynamic properties of adsorbed water must be determined. In this paper, the integral enthalpy and entropy are determined directly from isotherm data of water adsorbed on silica gel particles and silica gel manufactured in the form of a felt with 25 percent cotton as a support and Teflon as a binder. These results are then used to evaluate the exergy losses, due to the sorption and the convective heat and mass transfer processes, that occur in each portion of an adiabatic desiccant dehumidificaton cycle.

  1. Submerged membrane adsorption hybrid system using four adsorbents to remove nitrate from water.

    PubMed

    Kalaruban, Mahatheva; Loganathan, Paripurnanda; Kandasamy, Jaya; Vigneswaran, Saravanamuthu

    2017-04-05

    Nitrate contamination of ground and surface waters causes environmental pollution and human health problems in many parts of the world. This study tests the nitrate removal efficiencies of two ion exchange resins (Dowex 21K XLT and iron-modified Dowex 21K XLT (Dowex-Fe)) and two chemically modified bio-adsorbents (amine-grafted corn cob (AG corn cob) and amine-grafted coconut copra (AG coconut copra)) using a dynamic adsorption treatment system. A submerged membrane (microfiltration) adsorption hybrid system (SMAHS) was used for the continuous removal of nitrate with a minimal amount of adsorbents. The efficiency of membrane filtration flux and replacement rate of adsorbent were studied to determine suitable operating conditions to maintain the effluent nitrate concentration below the WHO drinking standard limit of 11.3 mg N/L. The volume of water treated and the amount of nitrate adsorbed per gramme of adsorbent for all four flux tested were in the order Dowex-Fe > Dowex > AG coconut copra > AG corn cob. The volumes of water treated (L/g adsorbent) were 0.91 and 1.85, and the amount of nitrate removed (mg N/g adsorbent) were 9.8 and 22.2 for AG corn cob and Dowex-Fe, respectively, at a flux of 15 L/(m(2)/h).

  2. Evaluating of arsenic(V) removal from water by weak-base anion exchange adsorbents.

    PubMed

    Awual, M Rabiul; Hossain, M Amran; Shenashen, M A; Yaita, Tsuyoshi; Suzuki, Shinichi; Jyo, Akinori

    2013-01-01

    Arsenic contamination of groundwater has been called the largest mass poisoning calamity in human history and creates severe health problems. The effective adsorbents are imperative in response to the widespread removal of toxic arsenic exposure through drinking water. Evaluation of arsenic(V) removal from water by weak-base anion exchange adsorbents was studied in this paper, aiming at the determination of the effects of pH, competing anions, and feed flow rates to improvement on remediation. Two types of weak-base adsorbents were used to evaluate arsenic(V) removal efficiency both in batch and column approaches. Anion selectivity was determined by both adsorbents in batch method as equilibrium As(V) adsorption capacities. Column studies were performed in fixed-bed experiments using both adsorbent packed columns, and kinetic performance was dependent on the feed flow rate and competing anions. The weak-base adsorbents clarified that these are selective to arsenic(V) over competition of chloride, nitrate, and sulfate anions. The solution pH played an important role in arsenic(V) removal, and a higher pH can cause lower adsorption capacities. A low concentration level of arsenic(V) was also removed by these adsorbents even at a high flow rate of 250-350 h(-1). Adsorbed arsenic(V) was quantitatively eluted with 1 M HCl acid and regenerated into hydrochloride form simultaneously for the next adsorption operation after rinsing with water. The weak-base anion exchange adsorbents are to be an effective means to remove arsenic(V) from drinking water. The fast adsorption rate and the excellent adsorption capacity in the neutral pH range will render this removal technique attractive in practical use in chemical industry.

  3. Physicochemical controls on absorbed water film thickness in unsaturated geological media

    SciTech Connect

    Tokunaga, T.

    2011-06-14

    Adsorbed water films commonly coat mineral surfaces in unsaturated soils and rocks, reducing flow and transport rates. Therefore, it is important to understand how adsorbed film thickness depends on matric potential, surface chemistry, and solution chemistry. Here, the problem of adsorbed water film thickness is examined through combining capillary scaling with the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory. Novel aspects of this analysis include determining capillary influences on film thicknesses, and incorporating solution chemistry-dependent electrostatic potential at air-water interfaces. Capillary analysis of monodisperse packings of spherical grains provided estimated ranges of matric potentials where adsorbed films are stable, and showed that pendular rings within drained porous media retain most of the 'residual' water except under very low matric potentials. Within drained pores, capillary contributions to thinning of adsorbed films on spherical grains are shown to be small, such that DLVO calculations for flat surfaces are suitable approximations. Hamaker constants of common soil minerals were obtained to determine ranges of the dispersion component to matric potential-dependent film thickness. The pressure component associated with electrical double layer forces was estimated using the compression and linear superposition approximations. The pH-dependent electrical double layer pressure component is the dominant contribution to film thicknesses at intermediate values of matric potential, especially in lower ionic strength solutions (< 10 mol m{sup -3}) on surfaces with higher magnitude electrostatic potentials (more negative than - 50 mV). Adsorbed water films are predicted to usually range in thickness from 1 to 20 nm in drained pores and fractures of unsaturated environments.

  4. Low-cost magnetic adsorbent for As(III) removal from water: adsorption kinetics and isotherms.

    PubMed

    Kango, Sarita; Kumar, Rajesh

    2016-01-01

    Magnetite nanoparticles as adsorbent for arsenic (As) were coated on sand particles. The coated sand was used for the removal of highly toxic element 'As(III)' from drinking water. Here, batch experiments were performed with the variation of solution pH, adsorbent dose, contact time and initial arsenic concentration. The adsorbent showed significant removal efficiency around 99.6 % for As(III). Analysis of adsorption kinetics revealed that the adsorbent follows pseudo-second-order kinetics model showing R (2) = 0.999, whereas for pseudo-first-order kinetics model, the value of R (2) was 0.978. In the case of adsorption equilibrium, the data is well fitted with Langmuir adsorption isotherm model (R (2) > 0.99), indicating monolayer adsorption of As(III) on the surface of adsorbent. The existence of commonly present ions in water influences the removal efficiency of As(III) minutely in the following order PO4 (3-) > HCO3 (-) > Cl(-) > SO4 (2-). The obtained adsorbent can be used to overcome the problem of water filtration in rural areas. Moreover, as the nano-magnetite is coated on the sand, it avoids the problem of extraction of nanoparticles from treated water and can easily be removed by a simple filtration process.

  5. Adsorption and Desorption of Carbon Dioxide and Water Mixtures on Synthetic Hydrophobic Carbonaceous Adsorbents

    NASA Technical Reports Server (NTRS)

    Finn, John E.; Harper, Lynn D. (Technical Monitor)

    1994-01-01

    Several synthetic carbonaceous adsorbents produced through pyrolysis of polymeric materials are available commercially. Some appear to have advantages over activated carbon for certain adsorption applications. In particular, they can have tailored hydrophobicities that are significantly greater than that of activated carbon, while moderately high surfaces areas are retained. These sorbents are being investigated for possible use in removing trace contaminants and excess carbon dioxide from air in closed habitats, plant growth chambers, and other applications involving purification of humid gas streams. We have analyzed the characteristics of a few of these adsorbents through adsorption and desorption experiments and standard characterization techniques. This paper presents pure and multicomponent adsorption data collected for carbon dioxide and water on two synthetic carbonaceous adsorbents having different hydrophobicities and capillary condensation characteristics. The observations are interpreted through consideration of the pore structure and surface chemistry of the solids and interactions between adsorbed carbon dioxide, water, and the solvent gas.

  6. The formation of standing cylinders in block copolymer films by irreversibly adsorbed polymer layers on substrates

    NASA Astrophysics Data System (ADS)

    Shang, Jun; Jiang, Naisheng; Endoh, Maya; Koga, Tadanori

    2013-03-01

    Block copolymers offer a simple and effective route to produce standing cylindrical nanostructures with regularity on the order of 10-100 nm, the length scale that is desirable for many advanced applications. However, these formations have been especially troublesome due to the fact that preferential interactions between one of the blocks and the surfaces will induce parallel alignment of the cylinders in order to minimize interfacial and surface energy. Here we introduce an alternative simple method utilizing an irreversibly adsorbed polymer layer (a ``Guiselin'' brush) as a neutral ``substrate'' formed on solid substrates for the arrangement of standing cylindrical nanostructures. The effect of polymer adsorbed layer on the long range ordering of asymmetric cylinder forming poly(styrene-block-ethylene/butylene-block-styrene) (SEBS) triblock copolymer thin films were investigated by using a combination of grazing incidence small angle x-ray scattering and atomic force microscopy techniques. We found that the SEBS, which forms cylinders lying parallel to the surface when prepared on silicon substrates, show standing cylindrical structures on selected Guiselin brush layers after prolong thermal annealing. The details will be discussed in the presentation. We acknowledges the financial support from NSF Grant No. CMMI-084626

  7. Friction and transfer of copper, silver, and gold to iron in the presence of various adsorbed surface films

    NASA Technical Reports Server (NTRS)

    Buckley, D. H.

    1979-01-01

    Sliding friction experiments were conducted with the noble metals copper, silver, and gold and two binary alloys of these metals contacting iron in the presence of various adsorbates including, oxygen, methyl mercaptan, and methyl chloride. A pin on disk specimen configuration was used with a load of 100 grams, sliding velocity of 60 mm/min; at 25 C with the surfaces saturated with the adsorbates. Auger emission spectroscopy was used to monitor surface films. Results of the experiments indicate that friction and transfer characteristics are highly specific with respect to both the noble metal and surface film present. With all three metals and films transfer of the noble metal to iron occurred very rapidly. With all metals and films transfer of the noble metal to iron continuously increased with repeated passes except for silver and copper sliding on iron sulfide.

  8. Mesoscopic Hamiltonian for the fluctuations of adsorbed Lennard-Jones liquid films.

    PubMed

    Fernández, Eva M; Chacón, Enrique; MacDowell, Luis G; Tarazona, Pedro

    2015-06-01

    We use Monte Carlo simulations of a Lennard-Jones fluid adsorbed on a short-range planar wall substrate to study the fluctuations in the thickness of the wetting layer, and we get a quantitative and consistent characterization of their mesoscopic Hamiltonian, H[ξ]. We have observed important finite-size effects, which were hampering the analysis of previous results obtained with smaller systems. The results presented here support an appealing simple functional form for H[ξ], close but not exactly equal to the theoretical nonlocal proposal made on the basis a generic density-functional analysis by Parry and coworkers. We have analyzed systems under different wetting conditions, as a proof of principle for a method that provides a quantitative bridge between the molecular interactions and the phenomenology of wetting films at mesoscopic scales.

  9. Sputtering and secondary ion emission properties of alkali metal films and adsorbed monolayers

    SciTech Connect

    Krauss, A R; Gruen, D M

    1980-01-01

    The secondary ion emission of alkali metal adsorbed monlayer and multilayer films has been studied. Profiling with sub-monolayer resolution has been performed by Auger, x-ray photoemission and secondary ion mass spectroscopy. Characteristic differences in the sputtering yields, and ion fraction have been observed which are associated with both the surface bonding properties and the mechanism leading to the formation of secondary ions. By sputtering with a negative bias applied to the sample, positive secondary ions are returned to the surface, resulting in a reduced sputter-induced erosion rate. Comparison with the results obtained with K and Li overlayers sputtered without sample bias provides an experimental value of both the total and secondary ion sputtering yields. The first and second monolayers can be readily identified and the first monolayer exhibits a lower sputtering yield and higher secondary ion fraction. This result is related to adsorption theory and measured values are compared with those obtained by thermal desorption measurements.

  10. Relaxation dynamics of surface-adsorbed water molecules in nanoporous silica probed by terahertz spectroscopy

    NASA Astrophysics Data System (ADS)

    Huang, Yu-Ru; Liu, Kao-Hsiang; Mou, Chung-Yuan; Sun, Chi-Kuang

    2015-08-01

    Relaxation dynamics of an exclusively adsorbed water molecule in mesoporous silica MCM-41-S was studied by using terahertz spectroscopy. With the temperature controlled from 0 to 50 °C, we observed strongly frequency- and temperature-dependent dielectric relaxation responses, implying that, unlike ice, surface-adsorbed water molecules retained flourishing picosecond dynamics. Based on the Debye relaxation model, a relaxation time constant was found to increase from 1.77 to 4.83 ps when the water molecule was cooled from 50 to 0 °C. An activation energy of ˜15 kJ/mol, which was in close agreement with a hydrogen-bonding energy, was further extracted from the Arrhenius analysis. Combined with previous molecular dynamics simulations, our results indicate that the reorientation relaxation originated from the "flip-flop" rotation of a three hydrogen-bonded surface-adsorbed water molecule.

  11. Interactions between glycine and amorphous solid water nanoscale films

    NASA Astrophysics Data System (ADS)

    Tzvetkov, George; Koller, Georg; Netzer, Falko P.

    2012-12-01

    The interactions of glycine (Gly) with amorphous solid water (ASW) nanolayers (≤ 100 ML), vapor-deposited on single crystalline AlOx surfaces at 100 K, have been investigated by near-edge X-ray absorption fine structure spectroscopy (NEXAFS) at the oxygen K-edge, temperature-programmed thermal desorption (TPD), X-ray photoelectron spectroscopy (XPS), and temperature-dependent work function measurements. Gly-on-ASW, ASW-on-Gly, and Gly on top of ASW-on-Gly ultrathin films have been fabricated. In contrast to the uniform ASW films grown directly on the hydrophilic AlOx, water molecules adsorb on the hydrophobic Gly films in the form of 3D ASW clusters. This leads to significant differences in the NEXAFS and work function data obtained from ASW-on-AlOx and ASW-on-Gly films, respectively. Furthermore, these structural differences influence the chemical state of Gly molecules (neutral vs. zwitterionic) adsorbed on top of ASW films. N1s XPS measurements revealed an increased amount of neutral Gly molecules in the film top-deposited on the ASW-on-Gly structure in comparison to the neutral Gly in the films directly condensed on AlOx or grown on the ASW substrate. H2O TPD spectra demonstrate that the crystallization and desorption processes of ASW are affected in a different way by the Gly layers, top-deposited on to ASW-on-AlOx and ASW-on-Gly films. At the same time, Gly adlayers sink into the ASW film during crystallization/desorption of the latter and land softly on the alumina surface in the form of zwitterionic clusters.

  12. Adsorption and removal kinetics of phosphonate from water using natural adsorbents.

    PubMed

    Kumar, R Anil; Velayudhan, K T; Ramachandran, V; Bhai, R Susheela; Unnikrishnan, G; Vasu, K

    2010-01-01

    The removal of phosphonate from water was studied using some natural adsorbents. Potassium phosphonate is a fungicide used for the control of Phytophthora capsici, which is prevalent in black pepper (Piper nigrum L.). Batch adsorption kinetic experiments were conducted on the adsorption of phosphonate onto the adsorbents. The concentration of phosphonate was measured on a high-performance liquid chromatograph fitted with a conductivity detector. The percentage removal of phosphonate by powdered laterite stone (PLS) from water was 40.4%, within a residence time of 15 minutes. The mechanisms of the rate of adsorption were analyzed and compared using the pseudo-second-order, Elovich, and intraparticle diffusion models. The experimental data was found to correlate well with the pseudo-second-order kinetic model, indicating adsorption as a chemisorption process. A possible reaction in the phosphonate-PLS system also has been proposed. The PLS can be used as a low-cost natural adsorbent for phosphonate removal from water.

  13. Preliminary results on the immobilisation of radionuclides from waters with specific adsorbers based on phosphate salts.

    PubMed

    Valentini Ganzerli, Maria Teresa; Maggi, Luigino; Crespi Caramella, Vera; Berzero, Antonella

    2004-11-01

    The present paper is focused on the ability of aluminium phosphate (ALPC), magnesium ammonium phosphate (MGPC), magnesium hydrogen phosphate (MGHPC), and calcium hydrogenphosphate (CAHPC), adsorbed onto charcoal, to immobilise actinides by adsorption from natural waters. The objective of this process is to evaluate the environmental pollution due to the actinides. Europium, thorium, protactinium, neptunyl, and uranyl ions were chosen to simulate actinides in the +3, +4, +5 and +6 oxidation state. The adsorbers were tested using natural waters samples. The adsorption trends and capacities were analysed. ALPC and MGPC exhibited a similar behaviour and adsorbed demonstrating that the +5, +4 and +3 actinide ions can be easily immobilised from natural waters and may be successfully used at pH 7-8. MGHPC may be used at a higher pH, whereas CAHPC is effective in the whole pH range. In all cases, thorium, protactinium and europium were strongly

  14. Structure of water adsorbed on a mica surface

    SciTech Connect

    Park, Sung-Ho; Sposito, Garrison

    2002-01-29

    Monte Carlo simulations of hydration water on the mica (001) surface under ambient conditions revealed water molecules bound closely to the ditrigonal cavities in the surface, with a lateral distribution of approximately one per cavity, and water molecules interposed between K{sup +} counter ions in a layer situated about 2.5 {angstrom} from a surface O along a direction normal to the (001) plane. The calculated water O density profile was in quantitative agreement with recent X-ray reflectivity measurements indicating strong lateral ordering of the hydration water but liquid-like disorder otherwise.

  15. Structural study and wetting behavior of ethane and tetrafluoromethane thick films adsorbed on graphite (0001)

    NASA Astrophysics Data System (ADS)

    Gay, Jean-Marc; Suzanne, Jean; Pepe, Gérard; Meichel, Thierry

    1988-10-01

    We present a quantitative study of the diffraction patterns (LEED, RHEED and neutron) of ethane and tetrafluoromethane thick films adsorbed on graphite (0001). We propose to interpret the streak-like RHEED patterns of C 2H 6 and CF 4 with tabular crystallites epitaxially grown on the thin underlying film. The growth of flat ethane crystallites is explained by a partial agreement of the lattice parameters, the symmetry and the molecule orientations between the bilayer structure deduced from static energy calculations and the structure within the 3D (011) plane which appears as the interfacial plane. The change in the CF 4 RHEED pattern observed at T = 37 K and previously considered as the signature of a wetting transition might be due to a change of interfacial plane. It could be the 3D (100) or (001) plane in which a hexagonal or quasi-hexagonal symmetry in the molecule packing appears for T > 37 K. At lower temperature, T < 37 K, this symmetry could be lost with the (101¯) interfacial plane which presents a quasi-square molecule packing. We would like to emphasize the caution necessary for interpreting RHEED results. The determination of the growth mode requires the combination of different methods of measurements in order to draw conclusions without ambiguities. These two molecular systems show rather well the difficulties for interpreting experimental results on the wetting phenomenon.

  16. Preparation of dye-adsorbing ZnO thin films by electroless deposition and their photoelectrochemical properties.

    PubMed

    Nagaya, Satoshi; Nishikiori, Hiromasa

    2013-09-25

    Dye-adsorbing ZnO thin films were prepared on ITO films by electroless deposition. The films were formed in an aqueous solution containing zinc nitrate, dimethylamine-borane, and eosin Y at 328 K. The film thickness was 1.2-2.0 μm. Thinner and larger-plane hexagonal columns were produced from the solution containing a higher concentration of eosin Y. A photocurrent was observed in the electrodes containing such ZnO films during light irradiation. The photoelectrochemical performance of the film was improved by increasing the concentration of eosin Y because of increases in the amount of absorbed photons and the electronic conductivity of ZnO.

  17. Ion Diffusion Within Water Films in Unsaturated Porous Media.

    PubMed

    Tokunaga, Tetsu K; Finsterle, Stefan; Kim, Yongman; Wan, Jiamin; Lanzirotti, Antonio; Newville, Matthew

    2017-04-05

    Diffusion is important in controlling local solute transport and reactions in unsaturated soils and geologic formations. Although it is commonly assumed that thinning of water films controls solute diffusion at low water contents, transport under these conditions is not well understood. We conducted experiments in quartz sands at low volumetric water contents (θ) to quantify ion diffusion within adsorbed films. At the lowest water contents, we employed fixed relative humidities to control water films at nm thicknesses. Diffusion profiles for Rb(+) and Br(-) in unsaturated sand packs were measured with a synchrotron X-ray microprobe, and inverse modeling was used to determine effective diffusion coefficients, De, as low as ∼9 × 10(-15) m(2) s(-1) at θ = 1.0 × 10(-4) m(3) m(-3), where the film thickness = 0.9 nm. Given that the diffusion coefficients (Do) of Rb(+) and Br(-) in bulk water (30 °C) are both ∼2.4 × 10(-9) m(2) s(-1), we found the impedance factor f = De/(θDo) is equal to 0.03 ± 0.02 at this very low saturation, in agreement with the predicted influence of interface tortuosity (τa) for diffusion along grain surfaces. Thus, reduced cross-sectional area (θ) and tortuosity largely accounted for the more than 5 orders of magnitude decrease in De relative to Do as desaturation progressed down to nanoscale films.

  18. Enhanced removal of nitrate from water using surface modification of adsorbents--a review.

    PubMed

    Loganathan, Paripurnanda; Vigneswaran, Saravanamuthu; Kandasamy, Jaya

    2013-12-15

    Elevated concentration of nitrate results in eutrophication of natural water bodies affecting the aquatic environment and reduces the quality of drinking water. This in turn causes harm to people's health, especially that of infants and livestock. Adsorbents with the high capacity to selectively adsorb nitrate are required to effectively remove nitrate from water. Surface modifications of adsorbents have been reported to enhance their adsorption of nitrate. The major techniques of surface modification are: protonation, impregnation of metals and metal oxides, grafting of amine groups, organic compounds including surfactant coating of aluminosilicate minerals, and heat treatment. This paper reviews current information on these techniques, compares the enhanced nitrate adsorption capacities achieved by the modifications, and the mechanisms of adsorption, and presents advantages and drawbacks of the techniques. Most studies on this subject have been conducted in batch experiments. These studies need to include continuous mode column trials which have more relevance to real operating systems and pilot-plant trials. Reusability of adsorbents is important for economic reasons and practical treatment applications. However, only limited information is available on the regeneration of surface modified adsorbents.

  19. Adsorption of methylene blue using modified adsorbents from drinking water treatment sludge.

    PubMed

    Nageeb Rashed, M; El-Daim El Taher, M A; Fadlalla, Somaya M M

    2016-10-01

    This study aims to explore the preparation and application of alum sludge (AS) and mud sludge (MS) from a drinking water treatment plant to remove methylene blue (MB) dye from aqueous solution. The sludge (MS and AS) was treated by chemical and physical activation to obtain new adsorbents. The adsorption experiments were carried out under different conditions of initial dye concentration (50-100 mg/L) adsorbent dosage (0.05-0.25 g), solution pH (3-9), temperature (20-60 °C) and contact time (20-90 min). Scanning electron microscopy (SEM) and X-ray diffraction instruments were used for characterization of the developed adsorbents. The results show that sludge activated by nitric acid (0.25 M HNO3) and pyrolysis at 700 °C were the best chemically and physically activated adsorbents. The optimum adsorption conditions for the adsorption of MB are 100 ppm initial dye concentration, 1 hour contact time, 250 °C solution temperature, pH 7 and 0.25 g adsorbent dosage. Application of the Langmuir and Freundlich Isotherm models showed that adsorbents fitted the Langmuir model well. SEM studies indicated the porous structural aspects of sludge suitable for removing MB dye.

  20. Denaturation resistance of beta-lactoglobulin in monomolecular films at the air-water interface.

    PubMed

    Lin, Jhih-Min; White, John W

    2009-10-29

    Using X-ray reflectometry we report strong differences in the denaturation response of beta-lactoglobulin adsorbed as a monomolecular film at the air-water interface from that observed in mixed denaturant/beta-lactoglobulin bulk solutions. Using the "flow trough" technique an isolated monomolecular film of the protein showed little change in structure when subjected to a 4.0 M guanidinium hydrochloride substrate. Unlike the bulk solution where a new protein layer structure appears, small changes in the protein packing and the roughness of the film are the only evidence of change. These parameters have been studied as a function of denaturant concentration and film quality. The strength of the response depends on the degree of perfection of the originally formed film; quickly formed films are more easily denatured. As the response is so subtle, possible interfering effects such as denaturant release of protein adsorbed on the trough have been quantified.

  1. Role(s) of adsorbed water in the surface chemistry of environmental interfaces.

    PubMed

    Rubasinghege, Gayan; Grassian, Vicki H

    2013-04-18

    The chemistry of environmental interfaces such as oxide and carbonate surfaces under ambient conditions of temperature and relative humidity is of great interest from many perspectives including heterogeneous atmospheric chemistry, heterogeneous catalysis, photocatalysis, sensor technology, corrosion science, and cultural heritage science. As discussed here, adsorbed water plays important roles in the reaction chemistry of oxide and carbonate surfaces with indoor and outdoor pollutant molecules including nitrogen oxides, sulfur dioxide, carbon dioxide, ozone and organic acids. Mechanisms of these reactions are just beginning to be unraveled and found to depend on the details of the reaction mechanism as well as the coverage of water on the surface. As discussed here, adsorbed water can: (i) alter reaction pathways and surface speciation relative to the dry surface; (ii) hydrolyze reactants, intermediates and products; (iii) enhance surface reactivity by providing a medium for ionic dissociation; (iv) inhibit surface reactivity by blocking sites; (v) solvate ions; (vi) enhance ion mobility on surfaces and (vii) alter the stability of surface adsorbed species. In this feature article, drawing on research that has been going on for over a decade on the reaction chemistry of oxide and carbonate surfaces under ambient conditions of temperature and relative humidity, a number of specific examples showing the multi-faceted roles of adsorbed water are presented.

  2. Turning things downside up: Adsorbate induced water flipping on Pt(111)

    SciTech Connect

    Kimmel, Greg A. E-mail: bruce.kay@pnnl.gov; Zubkov, Tykhon; Smith, R. Scott; Petrik, Nikolay G.; Kay, Bruce D. E-mail: bruce.kay@pnnl.gov

    2014-11-14

    We have examined the adsorption of the weakly bound species N{sub 2}, O{sub 2}, CO, and Kr on the (√(37)×√(37))R25.3{sup ∘} water monolayer on Pt(111) using a combination of molecular beam dosing, infrared reflection absorption spectroscopy, and temperature programmed desorption. In contrast to multilayer crystalline ice, the adsorbate-free water monolayer is characterized by a lack of dangling OH bonds protruding into the vacuum (H-up). Instead, the non-hydrogen-bonded OH groups are oriented downward (H-down) to maximize their interaction with the underlying Pt(111) substrate. Adsorption of Kr and O{sub 2} have little effect on the structure and vibrational spectrum of the “√(37)” water monolayer while adsorption of both N{sub 2}, and CO are effective in “flipping” H-down water molecules into an H-up configuration. This “flipping” occurs readily upon adsorption at temperatures as low as 20 K and the water monolayer transforms back to the H-down, “√(37)” structure upon adsorbate desorption above 35 K, indicating small energy differences and barriers between the H-down and H-up configurations. The results suggest that converting water in the first layer from H-down to H-up is mediated by the electrostatic interactions between the water and the adsorbates.

  3. Turning things downside up: Adsorbate induced water flipping on Pt(111)

    SciTech Connect

    Kimmel, Gregory A.; Zubkov, Tykhon; Smith, R. Scott; Petrik, Nikolay G.; Kay, Bruce D.

    2014-11-14

    We have examined the adsorption of the weakly bound species N2, O2, CO and Kr on the water monolayer on Pt(111) using a combination of molecular beam dosing, infrared reflection absorption spectroscopy (IRAS), and temperature programmed desorption (TPD). In contrast to multilayer crystalline ice, the adsorbate-free water monolayer is characterized by a lack of dangling OH bonds protruding into the vacuum (H-up). Instead, the non-hydrogen-bonded OH groups are oriented downward (H-down) to maximize their interaction with the underlying Pt(111) substrate. Adsorption of Kr and O2 have little effect on the structure and vibrational spectrum of the “ ” water monolayer while adsorption of both N2, and CO are effective in “flipping” H-down water molecules into an H-up configuration. This “flipping” occurs readily upon adsorption at temperatures as low as 20 K and the water monolayer transforms back to the H-down, “ ” structure upon adsorbate desorption above 35 K, indicating small energy differences and barriers between the H-down and H-up configurations. The results suggest that converting water in the first layer from H-down to H-up is mediated by the electrostatic interactions between the water and the adsorbates.

  4. Formation of 1D adsorbed water structures on CaO(001)

    NASA Astrophysics Data System (ADS)

    Zhao, Xunhua; Bhattacharya, Saswata; Ghiringhelli, Luca M.; Levchenko, Sergey V.; Scheffler, Matthias

    2015-03-01

    Understanding the interaction of water with oxide surfaces is of fundamental importance for basic and engineering sciences. Recently, a spontaneous formation of one-dimensional (1D) adsorbed water structures have been observed on CaO(001). Interestingly, at other alkaline earth metal oxides, in particular MgO(001) and SrO(001), such structures have not been found experimentally. We calculate the relative stability of adsorbed water structures on the three oxides using density-functional theory combined with the ab initio atomistic thermodynamics. Low-energy structures at different coverages are obtained with a first-principles genetic algorithm. Finite-temperature vibrational spectra are calculated using ab initio molecular dynamics. We find a range of (T, p) conditions where 1D structures are thermodynamically stable on CaO(001). The orientation and vibrational spectra of the 1D structures are in agreement with the experiments. The formation of the 1D structures is found to be actuated by a symmetry breaking in the adsorbed water tetramer, as well as by a balance between water-water and water-substrate interactions, determined by the lattice constant of the oxide.

  5. Hydration level dependence of the microscopic dynamics of water adsorbed in ultramicroporous carbon

    DOE PAGES

    Mamontov, Eugene; Yue, Yanfeng; Bahadur, Jitendra; ...

    2016-10-20

    Even when not functionalized intentionally, most carbon materials are not hydrophobic and readily adsorb water molecules from atmospheric water vapor. We have equilibrated an ultramicroporous carbon at several levels of relative humidity, thereby attaining various hydration levels. The water molecules were adsorbed on the pore walls (but did not fill completely the pore volume) and thus could be better described as hydration, or surface, rather than confined, water. We used quasielastic neutron scattering to perform a detailed investigation of the dependence of microscopic dynamics of these adsorbed water species on the hydration level and temperature. The behavior of hydration watermore » in ultramicroporous carbon clearly demonstrates the same universal traits that characterize surface (hydration) water in other materials that are surface-hydrated. In addition, unless special treatment is intentionally applied to ultramicroporous carbon, the species filling its pores in various applications, ranging from hydrogen molecules to electrolytes, likely find themselves in contact with non-freezing water molecules characterized by rich microscopic dynamics.« less

  6. Removal of lead and zinc ions from water by low cost adsorbents.

    PubMed

    Mishra, P C; Patel, R K

    2009-08-30

    In this study, activated carbon, kaolin, bentonite, blast furnace slag and fly ash were used as adsorbent with a particle size between 100 mesh and 200 mesh to remove the lead and zinc ions from water. The concentration of the solutions prepared was in the range of 50-100 mg/L for lead and zinc for single and binary systems which are diluted as required for batch experiments. The effect of contact time, pH and adsorbent dosage on removal of lead and zinc by adsorption was investigated. The equilibrium time was found to be 30 min for activated carbon and 3h for kaolin, bentonite, blast furnace slag and fly ash. The most effective pH value for lead and zinc removal was 6 for activated carbon. pH value did not effect lead and zinc removal significantly for other adsorbents. Adsorbent doses were varied from 5 g/L to 20 g/L for both lead and zinc solutions. An increase in adsorbent doses increases the percent removal of lead and zinc. A series of isotherm studies was undertaken and the data evaluated for compliance was found to match with the Langmuir and Freundlich isotherm models. To investigate the adsorption mechanism, the kinetic models were tested, and it follows second order kinetics. Kinetic studies reveals that blast furnace slag was not effective for lead and zinc removal. The bentonite and fly ash were effective for lead and zinc removal.

  7. Copper ions removal from water using functionalized carbon nanotubes–mullite composite as adsorbent

    SciTech Connect

    Tofighy, Maryam Ahmadzadeh; Mohammadi, Toraj

    2015-08-15

    Highlights: • CNTs–mullite composite was prepared via chemical vapor deposition (CVD) method. • The prepared composite was modified with concentrated nitric acid and chitosan. • The modified CNTs–mullite composites were used as novel adsorbents. • Copper ion removal from water by the prepared adsorbents was performed. • Langmuir and Freundlich isotherms and two kinetic models were applied to fit the experimental data. - Abstract: Carbon nanotubes–mullite composite was synthesized by direct growth of carbon nanotubes on mullite particles via chemical vapor deposition method using cyclohexanol and ferrocene as carbon precursor and catalyst, respectively. The carbon nanotubes–mullite composite was oxidized with concentrated nitric acid and functionalized with chitosan and then used as a novel adsorbent for copper ions removal from water. The results demonstrated that modification with concentrated nitric acid and chitosan improves copper ions adsorption capacity of the prepared composite, significantly. Langmuir and Freundlich isotherms and two kinetic models were applied to fit the experimental data. The carbon nanotubes growth on mullite particles to form the carbon nanotubes–mullite composite with further modification is an inherently safe approach for many promising environmental applications to avoid some concerns regarding environment, health and safety. It was found that the modified carbon nanotubes–mullite composite can be considered as an excellent adsorbent for copper ions removal from water.

  8. Melt crystallization/dewetting of ultrathin PEO films via carbon dioxide annealing: the effects of polymer adsorbed layers.

    PubMed

    Asada, Mitsunori; Jiang, Naisheng; Sendogdular, Levent; Sokolov, Jonathan; Endoh, Maya K; Koga, Tadanori; Fukuto, Masafumi; Yang, Lin; Akgun, Bulent; Dimitriou, Michael; Satija, Sushil

    2014-09-14

    The effects of CO2 annealing on the melting and subsequent melt crystallization processes of spin-cast poly(ethylene oxide) (PEO) ultrathin films (20-100 nm in thickness) prepared on Si substrates were investigated. By using in situ neutron reflectivity, we found that all the PEO thin films show melting at a pressure as low as P = 2.9 MPa and at T = 48 °C which is below the bulk melting temperature (Tm). The films were then subjected to quick depressurization to atmospheric pressure, resulting in the non-equilibrium swollen state, and the melt crystallization (and/or dewetting) process was carried out in air via subsequent annealing at given temperatures below Tm. Detailed structural characterization using grazing incidence X-ray diffraction, atomic force microscopy, and polarized optical microscopy revealed two unique aspects of the CO2-treated PEO films: (i) a flat-on lamellar orientation, where the molecular chains stand normal to the film surface, is formed within the entire film regardless of the original film thickness and the annealing temperature; and (ii) the dewetting kinetics for the 20 nm thick film is much slower than that for the thicker films. The key to these phenomena is the formation of irreversibly adsorbed layers on the substrates during the CO2 annealing: the limited plasticization effect of CO2 at the polymer-substrate interface promotes polymer adsorption rather than melting. Here we explain the mechanisms of the melt crystallization and dewetting processes where the adsorbed layers play vital roles.

  9. A simplified density functional theory method for investigating charged adsorbates on an ultrathin, insulating film supported by a metal substrate.

    PubMed

    Scivetti, Ivan; Persson, Mats

    2014-04-02

    A simplified density functional theory (DFT) method for investigating charged adsorbates on an ultrathin, insulating film supported by a metal substrate is developed and presented. This new method is based on a previous DFT development that uses a perfect conductor (PC) model to approximate the electrostatic response of the metal substrate, while the film and the adsorbate are both treated fully within DFT (Scivetti and Persson 2013 J. Phys.: Condens. Matter 25 355006). The missing interactions between the metal substrate and the insulating film in the PC approximation are modelled by a simple force field (FF). The parameters of the PC model and the force field are obtained from DFT calculations of the film and the substrate, here shown explicitly for a NaCl bilayer supported by a Cu(100) surface. In order to obtain some of these parameters and the polarizability of the force field, we have to include an external, uniformly charged plane in the DFT calculations, which has required the development of a periodic DFT formalism to include such a charged plane in the presence of a metal substrate. This extension and implementation should be of more general interest and applicable to other challenging problems, for instance, in electrochemistry. As illustrated for the gold atom on the NaCl bilayer supported by a Cu(100) surface, our new DFT-PC-FF method allows us to handle different charge states of adsorbates in a controlled and accurate manner with a considerable reduction of the computational time. In addition, it is now possible to calculate vertical transition and reorganization energies for the charging and discharging of adsorbates that cannot be obtained by current DFT methodologies that include the metal substrate. We find that the computed vertical transition energy for charging of the gold adatom is in good agreement with experiments.

  10. Laser tracks in rainbow films on water

    SciTech Connect

    Startsev, Aleksandr V; Stoilov, Yurii Yu

    2012-08-31

    It is found that narrow non-diverging laser tracks, earlier studied in free soap films, can also arise in thin rainbow films, e.g., of petrol, on water. (laser applications and other topics in quantum electronics)

  11. The Impact of Adsorbed Triethylene Glycol on Water Wettability of the {1014} Calcium Carbonate Surface

    NASA Astrophysics Data System (ADS)

    Olsen, R.

    2015-12-01

    Water flooding is increasingly being used as a method of enhanced oil recovery and frequently involves calcium carbonate reservoirs. Very often, thermodynamic conditions in the upper few hundred meters allow for hydrate formation. One possible method of preventing hydrates is to inject hydrate inhibitors such as triethylene glycol (TEG) into the reservoir. Thus, it is of importance to know how such glycols affect water wettability, which is an important factor defining the oil behavior in such reservoirs. Wettability of a surface is defined by the contact angle of a liquid drop on the surface. The stronger the liquid is attracted to the surface, the smaller the wetting angle becomes, implying an increased degree of wetting. Therefore, it is possible to gain qualitative knowledge of the change in wetting properties with respect to external influences by studying corresponding changes in free energy of adsorption of the liquid. In our work [1], we used molecular dynamics (MD) and Born-Oppenheimer molecular dynamics (BOMD) to study how adsorbed TEG on the {1014} calcium carbonate surface affected adsorbed water. We used the changes in density profiles of water to estimate changes in adsorption free energy of water. The adaptive biasing force (ABF) method was applied to TEG to calculate the adsorption free energy of TEG on the calcium carbonate surface. We found that water wetting of the calcium carbonate surface decreased in the presence of adsorbed TEG. [1] - Olsen, R.; Leirvik, K.; Kvamme, B.; Kuznetsova, T. Adsorption Properties of Triethylene Glycol on a Hydrated {1014} Calcite Surface and Its Effect on Adsorbed Water, Langmuir 2015, DOI: 10.1021/acs.langmuir.5b02228

  12. Far-Infrared Dielectric Properties Of Adsorbed Water In A Cellulose-Air Matrix

    NASA Astrophysics Data System (ADS)

    Bernard, Pierre; Belanger, Pierre-Andre; Boulay, Russel; Drouin, Bernard; Gagnon, Richard

    1986-09-01

    A standard three components mixture model for the dielectric constant is compared to the measured transmittance and reflectance of FIR radiation through a wet cellulose matrix. This model reproduces, at least qualitatively, the peculiar behaviour of the reflectance versus water content curve. However, the absorption coefficient for water content above 5% can only be reproduced if we postulate that the water adsorbed between 5% and 10% in volume possesses an anomalously high absorption coefficient. This is interpreted in terms of the flickering clusters model for water and the structure breaking role of the cellulose surface.

  13. First-principles study of the dielectric functions of carbon nanotubes with adsorbed water

    NASA Astrophysics Data System (ADS)

    Iwasaki, Daisuke; Suzuki, Yasumitsu; Watanabe, Kazuyuki

    2017-04-01

    A recent study demonstrated adsorption of water molecules on the surfaces of carbon nanotubes (CNTs). Importantly, it was reported that the peak positions in the absorption and photoluminescence spectra of the CNTs were shifted to lower energy as the number of adsorbed water molecules increased. Here, we investigated the mechanism by which this redshift occurs by calculating the dielectric functions of CNTs following water adsorption using density functional theory. Our calculations reproduced the redshifts and demonstrated that they can be attributed to decreases in the band gaps, which result from electronic coupling between the CNTs and the water molecules.

  14. Arsenic removal from water using a novel amorphous adsorbent developed from coal fly ash.

    PubMed

    Zhang, Kaihua; Zhang, Dongxue; Zhang, Kai

    2016-01-01

    A novel effective adsorbent of alumina/silica oxide hydrate (ASOH) for arsenic removal was developed through simple chemical reactions using coal fly ash. The iron-modified ASOH with enhancing adsorption activity was further developed from raw fly ash based on the in situ technique. The adsorbents were characterized by X-ray diffraction, Fourier transform infrared spectrometry, scanning electron micrograph, laser particle size and Brunauer-Emmet-Teller surface area. The results show that the adsorbents are in amorphous and porous structure, the surface areas of which are 8-12 times that of the raw ash. The acidic hydrothermal treatment acts an important role in the formation of the amorphous structure of ASOH rather than zeolite crystal. A series of adsorption experiments for arsenic on them were studied. ASOH can achieve a high removal efficiency for arsenic of 96.4% from water, which is more than 2.5 times that of the raw ash. Iron-modified ASOH can enhance the removal efficiency to reach 99.8% due to the in situ loading of iron (Fe). The condition of synthesis pH = 2-4 is better for iron-modified ASOH to adsorb arsenic from water.

  15. Adsorption of prototypical amino acids on silica: Influence of the pre-adsorbed water multilayer

    NASA Astrophysics Data System (ADS)

    Remesal, Elena R.; Amaya, Javier; Graciani, Jesús; Márquez, Antonio M.; Sanz, Javier Fdez.

    2016-04-01

    We explore the interaction between acetic acid, some typical α-amino acids (α-AAs), and a fully hydroxylated (0001) surface of α-quartz by means of theoretical calculations based on the density functional theory (DFT) under periodic boundary conditions. The influence of microsolvation, represented by a water multilayer, and dispersion forces is analyzed. All the considered molecules strongly adsorb on the hydroxylated surface and prefer to adsorb molecularly. The inclusion of dispersion forces increases the interaction energies by 15-30 kJ/mol, without significant changes in structure and mode of adsorption except for histidine where the interaction is improved through protonation of the α-amine group. When the water multilayer is included a decrease in the surface-adsorbate interaction energies is observed. Also, some α-AAs, glycine and alanine, change their adsorption mode and, now, the more stable structure is the zwitterion. Adsorption as zwitterions is always favored with respect to molecular interaction when dispersion forces are taken into account. Comparing the energies of adsorbed and solvated α-AA zwitterions, it turns out that inclusion of dispersion forces predicts that solvated zwitterions are the lower energy configurations.

  16. Role of Adsorbed Water on Charge Carrier Dynamics in Photoexcited TiO2

    PubMed Central

    2017-01-01

    Overall photocatalytic water splitting is one of the most sought after processes for sustainable solar-to-chemical energy conversion. The efficiency of this process strongly depends on charge carrier recombination and interaction with surface adsorbates at different time scales. Here, we investigated how hydration of TiO2 P25 affects dynamics of photogenerated electrons at the millisecond to minute time scale characteristic for chemical reactions. We used rapid scan diffuse-reflectance infrared Fourier transform spectroscopy (DRIFTS). The decay of photogenerated electron absorption was substantially slower in the presence of associated water. For hydrated samples, the charge carrier recombination rates followed an Arrhenius-type behavior in the temperature range of 273–423 K; these became temperature-independent when the material was dehydrated at temperatures above 423 K or cooled below 273 K. A DFT+U analysis revealed that hydrogen bonding with adsorbed water stabilizes surface-trapped holes at anatase TiO2(101) facet and lowers the barriers for hole migration. Hence, hole mobility should be higher in the hydrated material than in the dehydrated system. This demonstrates that adsorbed associated water can efficiently stabilize photogenerated charge carriers in nanocrystalline TiO2 and suppress their recombination at the time scale up to minutes.

  17. Removal of arsenate from water by adsorbents: a comparative case study.

    PubMed

    Bang, Sunbaek; Pena, Maria E; Patel, Manish; Lippincott, Lee; Meng, Xiaoguang; Kim, Kyoung-Woong

    2011-01-01

    Laboratory and field filtration experiments were conducted to study the effectiveness of As(V) removal for five types of adsorbent media. The media included activated alumina (AA), modified activated alumina (MAA), granular ferric hydroxide (GFH), granular ferric oxide (GFO), and granular titanium dioxide (TiO₂). In laboratory batch and column experiments, the synthetic challenge water was used to evaluate the effectiveness for five adsorbents. The results of the batch experiments showed that the As(V) adsorption decreased as follows at pH 6.5: TiO₂ > GFO > GFH > MAA > AA. At pH 8.5, however, As(V) removal decreased in the following order: GFO = TiO₂ > GFH > MAA > AA. In column experiments, at pH 6.5, the adsorbed As(V) for adsorbents followed the order: TiO₂ > GFO > GFH, whereas at pH 8.5 the order became: GFO = TiO₂ > GFH when the challenge water containing 50 μg/L of As(V) was used. Field filtration experiments were carried out in parallel at a wellhead in New Jersey. Before the effluent arsenic concentration increased to 10 μg/L, approximately 58,000 and 41,500 bed volumes of groundwater containing an average of 47 μg/L of As(V) were treated by the filter system packed with GFO and TiO₂, respectively. The As(V) adsorption decreased in the following sequence: GFO > TiO₂ > GFH > MAA > AA. Filtration results demonstrated that GFO and TiO₂ adsorbents could be used as media in small community filtration systems for As(V) removal.

  18. A multifunctional azobenzene-based polymeric adsorbent for effective water remediation

    NASA Astrophysics Data System (ADS)

    Wan, Decheng; Chen, Feng; Geng, Qingrui; Lu, Hang; Willcock, Helen; Liu, Qiuming; Wang, Fangyingkai; Zou, Kaidian; Jin, Ming; Pu, Hongting; Du, Jianzhong

    2014-12-01

    The efficient removal of trace carcinogenic organic pollutants, such as polycyclic aromatic hydrocarbons (PAHs) and ionic dyes, from water is an important technical challenge. We report a highly effective recyclable multifunctional azobenzene (AZ)-based silica-supported polymeric adsorbent which can simultaneously remove both PAHs and anionic dyes from water to below parts per billion (ppb) level based on multiple interactions such as the hydrophobic effect, π-π stacking and electrostatic interactions, thus providing a new strategy for designer water remediation materials.

  19. A multifunctional azobenzene-based polymeric adsorbent for effective water remediation.

    PubMed

    Wan, Decheng; Chen, Feng; Geng, Qingrui; Lu, Hang; Willcock, Helen; Liu, Qiuming; Wang, Fangyingkai; Zou, Kaidian; Jin, Ming; Pu, Hongting; Du, Jianzhong

    2014-12-03

    The efficient removal of trace carcinogenic organic pollutants, such as polycyclic aromatic hydrocarbons (PAHs) and ionic dyes, from water is an important technical challenge. We report a highly effective recyclable multifunctional azobenzene (AZ)-based silica-supported polymeric adsorbent which can simultaneously remove both PAHs and anionic dyes from water to below parts per billion (ppb) level based on multiple interactions such as the hydrophobic effect, π-π stacking and electrostatic interactions, thus providing a new strategy for designer water remediation materials.

  20. Removal of antibiotics from water using sewage sludge- and waste oil sludge-derived adsorbents.

    PubMed

    Ding, Rui; Zhang, Pengfei; Seredych, Mykola; Bandosz, Teresa J

    2012-09-01

    Sewage sludge- and waste oil sludge-derived materials were tested as adsorbents of pharmaceuticals from diluted water solutions. Simultaneous retention of eleven antibiotics plus two anticonvulsants was examined via batch adsorption experiments. Virgin and exhausted adsorbents were examined via thermal and FTIR analyses to elucidate adsorption mechanisms. Maximum adsorption capacities for the 6 materials tested ranged from 80 to 300 mg/g, comparable to the adsorption capacities of antibiotics on various activated carbons (200-400 mg/g) reported in the literature. The performance was linked to surface reactivity, polarity and porosity. A large volume of pores similar in size to the adsorbate molecules with hydrophobic carbon-based origin of pore walls was indicated as an important factor promoting the separation process. Moreover, the polar surface of an inorganic phase in the adsorbents attracted the functional groups of target molecules. The presence of reactive alkali metals promoted reaction with acidic groups, formation of salts and their precipitation in the pore system.

  1. Chemical characterization of organic carbon dissolved in natural waters using inorganic adsorbents.

    PubMed

    Sugiyama, Y; Kumagai, T

    2001-01-01

    Dissolved organic carbon (DOC) in water samples from Lake Biwa was chemically characterized by two inorganic adsorbents with completely different surface characteristics. The two adsorbents were HIO (hydrous iron oxide) and SG (silica gel). Solutions of reference standard materials were analyzed concerning their adsorption behavior to HIO and SG for bovine serum albumin (BSA), fulvic acid extracted from the bottom sediments of Lake Biwa, phthalic acid, and starch. The adsorption of DOC to HIO was mainly controlled by ligand exchange and electrostatic interaction; that of SG was by electrostatic interaction. It was found that in a weak acid solution of around pH 5, BSA adsorbs to both HIO and SG, but that fulvic acid, phthalic acid and starch only show adsorption to HIO. Using these characteristics, DOC samples in natural water samples were characterized into pro-DOC, which adsorbs to both HIO and SG at pH 5, and car-DOC, which only adsorbs to HIO at pH 5. The DOC samples in Lake Biwa on October 7, 1997, at sampling sites Nb-2 and Nb-5 (south basin of Lake Biwa, the depths were about 2 and 4 m), and Ie-1 (north basin of Lake Biwa, the depth was about 75 m) were characterized. The pro-DOC has different values, depending on their sampling sites and depths, and had the maximum value of 0.42 mg C l(-1) at the surface water of Ie-1, and had the lowest values at middle to deeper water depths (0.18-0.27 mg C l(-1)). The car-DOC showed a relatively stable value at Ie-1 regardless of the depth (0.63-0.83 mg C l(-1)), and the maximum value was observed in Nb-2 and Nb-5 (1.2 and 1.3 mg C l(-1)). The ratios between car-DOC and pro-DOC concentrations were 0.2-0.5, and had different values for different sampling sites and depths. The ratios were significantly different for surface water samples where the biological activities are high and for bottom water samples where decomposition predominates.

  2. Arsenic removal from water/wastewater using adsorbents--A critical review.

    PubMed

    Mohan, Dinesh; Pittman, Charles U

    2007-04-02

    Arsenic's history in science, medicine and technology has been overshadowed by its notoriety as a poison in homicides. Arsenic is viewed as being synonymous with toxicity. Dangerous arsenic concentrations in natural waters is now a worldwide problem and often referred to as a 20th-21st century calamity. High arsenic concentrations have been reported recently from the USA, China, Chile, Bangladesh, Taiwan, Mexico, Argentina, Poland, Canada, Hungary, Japan and India. Among 21 countries in different parts of the world affected by groundwater arsenic contamination, the largest population at risk is in Bangladesh followed by West Bengal in India. Existing overviews of arsenic removal include technologies that have traditionally been used (oxidation, precipitation/coagulation/membrane separation) with far less attention paid to adsorption. No previous review is available where readers can get an overview of the sorption capacities of both available and developed sorbents used for arsenic remediation together with the traditional remediation methods. We have incorporated most of the valuable available literature on arsenic remediation by adsorption ( approximately 600 references). Existing purification methods for drinking water; wastewater; industrial effluents, and technological solutions for arsenic have been listed. Arsenic sorption by commercially available carbons and other low-cost adsorbents are surveyed and critically reviewed and their sorption efficiencies are compared. Arsenic adsorption behavior in presence of other impurities has been discussed. Some commercially available adsorbents are also surveyed. An extensive table summarizes the sorption capacities of various adsorbents. Some low-cost adsorbents are superior including treated slags, carbons developed from agricultural waste (char carbons and coconut husk carbons), biosorbents (immobilized biomass, orange juice residue), goethite and some commercial adsorbents, which include resins, gels, silica

  3. Theoretical Study on Surface-Enhanced Raman Spectra of Water Adsorbed on Noble Metal Cathodes of Nanostructures

    NASA Astrophysics Data System (ADS)

    Wu, De-Yin; Pang, Ran; Tian, Zhong-Qun

    2016-06-01

    The observed surface-enhanced Raman scattering (SERS) spectra of water adsorbed on metal film electrodes of silver, gold, and platinum nanoparticles were used to infer interfacial water structures. The basis is the change of the electrochemical vibrational Stark tuning rates and the relative Raman intensity of the stretching and bending modes. How it is not completely understood the reason why the relative Raman intensity ratio of the bending and stretching vibrations of interfacial water increases at the very negative potential region. Density functional theory calculations provide the conceptual model. The specific enhancement effect for the bending mode was closely associated with the water adsorption structure in a hydrogen bonded configuration through its H-end binding to surface sites with large polarizability due to strong cathodic polarization. The present theoretical results allow us to propose that interfacial water molecules exist on these metal cathodes with different hydrogen bonding interactions, the HO-H…Ag(Au) for silver and gold. In acidic solution, a surface electron-hydronium ion-pair was proposed as an adsorption configuration of interfacial water structures on silver and gold cathodes based on density functional theory (DFT) calculations. The EHIP is in the configuration of H3O+(H2O)ne-, where the hydronium H3O+ and the surface electron is separated by water layers. The electron bound in the EHIP can first be excited under light irradiation, subsequently inducing a structural relaxation into a hydrated hydrogen atom. Thus, Raman intensities of the interfacial water in the EHIP species are signifcantly enhanced due to the cathodic polarization on silver and gold electrodes.

  4. Zinc peroxide nanomaterial as an adsorbent for removal of Congo red dye from waste water.

    PubMed

    Chawla, Sneha; Uppal, Himani; Yadav, Mohit; Bahadur, Nupur; Singh, Nahar

    2017-01-01

    In the past decade, various natural byproducts, advanced metal oxide composites and photocatalysts have been reported for removal of dyes from water. Although these materials are useful for select applications, they have some limitations such as use at fixed temperature, ultra violet (UV) light and the need for sophisticated experimental set up. These materials can remove dyes up to a certain extent but require long time. To overcome these limitations, a promising adsorbent zinc peroxide (ZnO2) nanomaterial has been developed for the removal of Congo red (CR) dye from contaminated water. ZnO2 is highly efficient even in the absence of sunlight to remove CR from contaminated water upto the permissible limits set by the World Health Organization (WHO) and the United States- Environmental Protection Agency (US-EPA). The adsorbent has a specific property to adjust the pH of the test solution within 6.5-7.5 range irrespective of acidic or basic nature of water. The adsorption capacity of the material for CR dye was 208mgg(-1) within 10min at 2-10pH range. The proposed material could be useful for the industries involved in water purification. The removal of CR has been confirmed by spectroscopic and microscopic techniques. The adsorption data followed a second order kinetics and Freundlich isotherm.

  5. SiO(2)-LiBr Nanocomposite Sol-Gel Adsorbents of Water Vapor: Preparation and Properties.

    PubMed

    Mrowiec-Bialoń; Lachowski; Jarz&ecedil;bski; Gordeeva; Aristov

    1999-10-15

    Water vapor adsorption on SiO(2)-LiBr sol-gel materials strongly depends on bromide content. Adsorption capacities exhibited by these materials at higher relative pressures can be as high as 0.8 kg of water/kg of adsorbent. These adsorbents can be regenerated by heating at 473 K and reused. However, a gradual decay of adsorption properties occurs during repeated adsorption-desorption cycles. Thus, this family of adsorbents seems to be less attractive than the corresponding SiO(2)-CaCl(2) composites. Copyright 1999 Academic Press.

  6. The role of adsorbed water on the friction of a layer of submicron particles

    USGS Publications Warehouse

    Sammis, Charles G.; Lockner, David A.; Reches, Ze’ev

    2011-01-01

    Anomalously low values of friction observed in layers of submicron particles deformed in simple shear at high slip velocities are explained as the consequence of a one nanometer thick layer of water adsorbed on the particles. The observed transition from normal friction with an apparent coefficient near μ = 0.6 at low slip speeds to a coefficient near μ = 0.3 at higher slip speeds is attributed to competition between the time required to extrude the water layer from between neighboring particles in a force chain and the average lifetime of the chain. At low slip speeds the time required for extrusion is less than the average lifetime of a chain so the particles make contact and lock. As slip speed increases, the average lifetime of a chain decreases until it is less than the extrusion time and the particles in a force chain never come into direct contact. If the adsorbed water layer enables the otherwise rough particles to rotate, the coefficient of friction will drop to μ = 0.3, appropriate for rotating spheres. At the highest slip speeds particle temperatures rise above 100°C, the water layer vaporizes, the particles contact and lock, and the coefficient of friction rises to μ = 0.6. The observed onset of weakening at slip speeds near 0.001 m/s is consistent with the measured viscosity of a 1 nm thick layer of adsorbed water, with a minimum particle radius of approximately 20 nm, and with reasonable assumptions about the distribution of force chains guided by experimental observation. The reduction of friction and the range of velocities over which it occurs decrease with increasing normal stress, as predicted by the model. Moreover, the analysis predicts that this high-speed weakening mechanism should operate only for particles with radii smaller than approximately 1 μm. For larger particles the slip speed required for weakening is so large that frictional heating will evaporate the adsorbed water and weakening will not occur.

  7. The adsorption of water on Cu2O and Al2O3 thin films

    SciTech Connect

    Deng, Xingyi; Herranz, Tirma; Weis, Christoph; Bluhm, Hendrik; Salmeron, Miquel

    2008-06-27

    The initial stages of water condensation, approximately 6 molecular layers, on two oxide surfaces, Cu{sub 2}O and Al{sub 2}O{sub 3}, have been investigated by using ambient pressure X-ray photoelectron spectroscopy at relative humidity values (RH) from 0 to >90%. Water adsorbs first dissociatively on oxygen vacancies producing adsorbed hydroxyl groups in a stoichiometric reaction: O{sub lattic} + vacancies + H{sub 2}O = 2OH. The reaction is completed at {approx}1% RH and is followed by adsorption of molecular water. The thickness of the water film grows with increasing RH. The first monolayer is completed at {approx}15% RH on both oxides and is followed by a second layer at 35-40% RH. At 90% RH, about 6 layers of H{sub 2}O film have been formed on Al{sub 2}O{sub 3}.

  8. Selective capture of water using microporous adsorbents to increase the lifetime of lubricants.

    PubMed

    Ng, Eng-Poh; Delmotte, Luc; Mintova, Svetlana

    2009-01-01

    Long live lubricants: The selective capture of water from lubricants using nanosized microporous aluminophosphate (AEI) and aluminosilicate materials was studied. Nearly 98 % of the moisture was removed from the lubricating oil under ambient conditions, resulting in a significant improvement in the lubricating service lifetime. Moreover, both the lubricant and the microporous sorbents can be recovered and reused.The selective capture of water from lubricants using nanosized microporous aluminophosphate and aluminosilicate materials was studied with an aim to increase the lifetime of the lubricating mineral oil. The amount of water present in oxidized lubricating oil before and after treatment with microporous materials was studied by FTIR spectroscopy and determined quantitatively using the Karl Fischer titration method. Nanosized aluminophosphate revealed a high selectivity for water without adsorbing other additives, in contrast to nanosized aluminosilicates which also adsorb polar oxidation products and ionic additives. About 98 % of the initial moisture could be removed from the lubricating oil under ambient conditions, resulting in a significant improvement in the lubricating service lifetime. Moreover, no by-products are formed during the process and both the lubricant and the sorbents can be recovered and reused, thus the method is environmentally friendly.

  9. Feasibility of using drinking water treatment residuals as a novel chlorpyrifos adsorbent.

    PubMed

    Zhao, Yuanyuan; Wang, Changhui; Wendling, Laura A; Pei, Yuansheng

    2013-08-07

    Recent efforts have increasingly focused on the development of low-cost adsorbents for pesticide retention. In this work, the novel reuse of drinking water treatment residuals (WTRs), a nonhazardous ubiquitous byproduct, as an adsorbent for chlorpyrifos was investigated. Results showed that the kinetics and isothermal processes of chlorpyrifos sorption to WTRs were better described by a pseudo-second-order model and by the Freundlich equation, respectively. Moreover, compared with paddy soil and other documented absorbents, the WTRs exhibited a greater affinity for chlorpyrifos (log Koc = 4.76-4.90) and a higher chlorpyrifos sorption capacity (KF = 5967 mg(1-n)·L·kg(-1)) owing to the character and high content of organic matter. Further investigation demonstrated that the pH had a slight but statistically insignificant effect on chlorpyrifos sorption to WTRs; solution ionic strength and the presence of low molecular weight organic acids both resulted in concentration-dependent inhibition effects. Overall, these results confirmed the feasibility of using WTRs as a novel chlorpyrifos adsorbent.

  10. Interaction of acetonitrile with thin films of solid water

    SciTech Connect

    Bahr, S.; Kempter, V.

    2009-06-07

    Thin films of water were prepared on Ag at 124 K. Their properties were studied with metastable impact electron spectroscopy, reflection absorption infrared spectroscopy, and temperature programmed desorption. The interaction of acetonitrile (ACN) with these films was studied with the abovementioned techniques. From the absence of any infrared activity in the initial adsorption stage, it is concluded that ACN adsorbs linearly and that the C{identical_to}N axis is aligned parallel to the water surface (as also found on neat Ag). Initially, the interaction with water surface species involves their dangling OD groups. During the completion of the first adlayer the ACN-ACN lateral interaction becomes of importance as well, and the ACN molecules become tilted with respect to the water surface. ACN shows propensity to stay at the surface after surface adsorption even during annealing up to the onset of desorption. The present results for the ACN-water interaction are compared with available classical molecular dynamics calculations providing the orientation profile for ACN on water as well as the ACN bonding properties.

  11. Interaction of acetonitrile with thin films of solid water.

    PubMed

    Bahr, S; Kempter, V

    2009-06-07

    Thin films of water were prepared on Ag at 124 K. Their properties were studied with metastable impact electron spectroscopy, reflection absorption infrared spectroscopy, and temperature programmed desorption. The interaction of acetonitrile (ACN) with these films was studied with the abovementioned techniques. From the absence of any infrared activity in the initial adsorption stage, it is concluded that ACN adsorbs linearly and that the C identical withN axis is aligned parallel to the water surface (as also found on neat Ag). Initially, the interaction with water surface species involves their dangling OD groups. During the completion of the first adlayer the ACN-ACN lateral interaction becomes of importance as well, and the ACN molecules become tilted with respect to the water surface. ACN shows propensity to stay at the surface after surface adsorption even during annealing up to the onset of desorption. The present results for the ACN-water interaction are compared with available classical molecular dynamics calculations providing the orientation profile for ACN on water as well as the ACN bonding properties.

  12. Interaction of acetonitrile with thin films of solid water

    NASA Astrophysics Data System (ADS)

    Bahr, S.; Kempter, V.

    2009-06-01

    Thin films of water were prepared on Ag at 124 K. Their properties were studied with metastable impact electron spectroscopy, reflection absorption infrared spectroscopy, and temperature programmed desorption. The interaction of acetonitrile (ACN) with these films was studied with the abovementioned techniques. From the absence of any infrared activity in the initial adsorption stage, it is concluded that ACN adsorbs linearly and that the C≡N axis is aligned parallel to the water surface (as also found on neat Ag). Initially, the interaction with water surface species involves their dangling OD groups. During the completion of the first adlayer the ACN-ACN lateral interaction becomes of importance as well, and the ACN molecules become tilted with respect to the water surface. ACN shows propensity to stay at the surface after surface adsorption even during annealing up to the onset of desorption. The present results for the ACN-water interaction are compared with available classical molecular dynamics calculations providing the orientation profile for ACN on water as well as the ACN bonding properties.

  13. A review of the use of red mud as adsorbent for the removal of toxic pollutants from water and wastewater.

    PubMed

    Bhatnagar, Amit; Vilar, Vítor J P; Botelho, Cidália M S; Boaventura, Rui A R

    2011-01-01

    Red mud (an aluminium industry waste) has received wide attention as an effective adsorbent for water pollution control, showing significant adsorption potential for the removal of various aquatic pollutants. In this review, an extensive list of red-mud-based adsorbents has been compiled and their adsorption capacities (maximum uptake value of the adsorbent for the pollutant or adsorbate being removed) for various aquatic pollutants (metal ions, dyes, phenolic compounds, inorganic anions) are presented. The review provides a summary of recent information obtained using batch studies and deals with the adsorption mechanisms involved. It is evident from the literature survey that red mud has been found to be efficient for the removal of various aquatic pollutants, especially arsenic and phosphate. However, there is still a need to investigate the practical utility of these adsorbents on a commercial scale.

  14. Determination of anisotropic optical constants and surface coverage of molecular films using polarized visible ATR spectroscopy. Application to adsorbed cytochrome c films.

    PubMed

    Runge, Anne F; Rasmussen, Nicole C; Saavedra, S Scott; Mendes, Sergio B

    2005-01-13

    This article describes a method to determine the anisotropic optical constants and surface coverage of molecular films using polarized attenuated total reflectance (ATR) absorbance measurements. We have extended the transfer-matrix formalism to describe birefringent and dichroic films in ATR geometries and have combined it with an iterative numerical procedure to determine the anisotropic values of both the real (n) and imaginary (k) parts of the complex refractive index of the film under investigation. Anisotropic values of the imaginary part of the refractive index (k) allow for the determination of the surface coverage and one order parameter of the film. To illustrate this approach, we have used cytochrome c (cyt c) protein films adsorbed to glass and indium tin oxide (ITO) surfaces. Experimental results show that cyt c films on these surfaces, which were formed under identical conditions, have significant differences in their surface coverages (11.2 +/- 0.4 pmol/cm(2) on glass and 21.7 +/- 0.9 pmol/cm(2) on ITO); however, their order parameters are similar (0.30 +/- 0.02 on glass and 0.36 +/- 0.04 on ITO).

  15. Adsorption characteristics of water vapor on gear-pellet and honeycomb-pellet types of adsorbents containing A-type zeolite

    SciTech Connect

    Nakamura, A.; Munakata, K.; Hara, K.; Narita, S.; Sugiyama, T.; Kotoh, K.; Tanaka, M.; Uda, T.

    2015-03-15

    It is necessary to recover or process tritiated species that are extensively coexistent in nuclear fusion installations. A conventional way to recover tritium release to atmosphere is catalytic oxidation of tritiated species and adsorption of tritiated water vapor on adsorbents with high surface areas. Therefore, new adsorbents with low pressure loss and high surface areas need to be developed and utilized for such large-scale adsorption systems. In this study, attention was focused on new adsorbents, which are gear-type pellet MS5A adsorbent, gear-type pellet MS4A adsorbent and honeycomb-type pellet MS5A adsorbent. The adsorption characteristics of the new adsorbent were comparatively studied with conventional type of adsorbents (pellet-type MS5A adsorbent and pebble-type MS5A adsorbent), in terms of adsorption capacity, pressure loss and adsorption rate. It was found that the adsorption capacity of water vapor on the gear-type adsorbents is higher than that on a honeycomb-type adsorbent. The experimental breakthrough curves indicate that the adsorption rates of water vapor on gear-type and honeycomb-type adsorbents are smaller than that on conventional type adsorbents. Various adsorption models were also tested to correlate the experimental isotherms. It was found that the Langmuir-Freundlich model could properly correlate the experimental adsorption isotherms.

  16. Fluoride removal in water by a hybrid adsorbent lanthanum-carbon.

    PubMed

    Vences-Alvarez, Esmeralda; Velazquez-Jimenez, Litza Halla; Chazaro-Ruiz, Luis Felipe; Diaz-Flores, Paola E; Rangel-Mendez, Jose Rene

    2015-10-01

    Various health problems associated with drinking water containing high fluoride levels, have motivated researchers to develop more efficient adsorbents to remove fluoride from water for beneficial concentrations to human health. The objective of this research was to anchor lanthanum oxyhydroxides on a commercial granular activated carbon (GAC) to remove fluoride from water considering the effect of the solution pH, and the presence of co-existing anions and organic matter. The activated carbon was modified with lanthanum oxyhydroxides by impregnation. SEM and XRD were performed in order to determine the crystal structure and morphology of the La(III) particles anchored on the GAC surface. FT-IR and pK(a)'s distribution were determined in order to elucidate both the possible mechanism of the lanthanum anchorage on the activated carbon surface and the fluoride adsorption mechanism on the modified material. The results showed that lanthanum ions prefer binding to carboxyl and phenolic groups on the activated carbon surface. Potentiometric titrations revealed that the modified carbon (GAC-La) possesses positive charge at a pH lower than 9. The adsorption capacity of the modified GAC increased five times in contrast to an unmodified GAC adsorption capacity at an initial F(-) concentration of 20 mg L(-1). Moreover, the presence of co-existing anions had no effect on the fluoride adsorption capacity at concentrations below 30 mg L(-1), that indicated high F(-) affinity by the modified adsorbent material (GAG-La).

  17. Water hyacinth (Eichhornia crassipes) waste as an adsorbent for phosphorus removal from swine wastewater.

    PubMed

    Chen, Xi; Chen, Xiuxia; Wan, Xianwei; Weng, Boqi; Huang, Qin

    2010-12-01

    Both live plants and dried straw of water hyacinth were applied to a sequential treatment of swine wastewater for nitrogen and phosphorus reduction. In the facultative tank, the straw behaved as a kind of adsorbent toward phosphorus. Its phosphorus removal rate varied considerably with contact time between the straw and the influent. In the laboratory, the straw displayed a rapid total phosphorus reduction on a KH(2)PO(4) solution. The adsorption efficiency was about 36% upon saturation. At the same time, the water hyacinth straw in the facultative tank enhanced NH(3)-N removal efficiency as well. However, no adsorption was evident. This study demonstrated an economically feasible means to apply water hyacinth phosphorus straw for the swine wastewater treatment. The sequential system employed significantly reduced the land use, as compared to the wastewater stabilization pond treatment, for pollution amelioration of swine waste.

  18. Adsorbent materials from paper industry waste materials and their use in Cu(II) removal from water.

    PubMed

    Méndez, A; Barriga, S; Fidalgo, J M; Gascó, G

    2009-06-15

    This paper deals with the removal of Cu(2+) from water using adsorbent materials prepared from paper industry waste materials (one de-inking paper sludge and other sludge from virgin pulp mill). Experimental results showed that de-inking paper sludge leads to mesoporous materials (V(mic)/V(T)=0.13 and 0.14), whereas the sludge from virgin pulp mill produces high microporous adsorbents (V(mic)/V(T)=0.39 and 0.41). Adsorbent materials were then used for Cu(2+) removal from water at acid pH. During water treatment, heavy metals lixiviation from adsorbent materials was not produced. However, important Ca and Mg leaching was observed. Final pH significantly increases after treatment of water with adsorbent materials probably due to their elevated CaCO(3) content. In general, highest Cu(2+) removal was obtained using adsorbent materials from de-inking paper sludge. This result could be due to their higher content in oxygenated surface groups, high average pore diameter, elevated superficial charge density, high CaCO(3) amount and high Ca and Mg exchange content.

  19. A study of the alumina-silica gel adsorbent for the removal of silicic acid from geothermal water: increase in adsorption capacity of the adsorbent due to formation of amorphous aluminosilicate by adsorption of silicic acid.

    PubMed

    Yokoyama, Takushi; Ueda, Akira; Kato, Koichi; Mogi, Katsumi; Matsuo, Shorin

    2002-08-01

    Two kinds of adsorbents (Si adsorbent and Al adsorbent) for the removal of silicic acid from geothermal water to retard the formation of silica scales were prepared using silicic acid contained in geothermal water. The Si adsorbent was prepared by evaporating geothermal water, and the Al adsorbent was prepared by evaporating geothermal water after the addition of aluminum chloride. The specific surface area of the Si adsorbent was small and it's adsorption capacity of silicic acid was low. Although the specific surface area of the Al adsorbent was also small, it was significantly increased by the adsorption of silicic acid and it's adsorption capacity was high. Based on the change in the local structure of aluminum ion by the adsorption of silicic acid, the Al adsorbent was considered to be silica particles covered with crystalline aluminum hydroxide. Moreover, it was concluded that the increase in the specific surface area of the Al adsorbent and the decrease in the zeta potential were due to the formation of an amorphous aluminosilicate with a large surface area and a negative charge (one 4-coordinated Al) by the reaction between aluminum ions and silicic acids.

  20. Investigation of interparticle forces in natural waters: effects of adsorbed humic acids on iron oxide and alumina surface properties.

    PubMed

    Sander, Sylvia; Mosley, Luke M; Hunter, Keith A

    2004-09-15

    The nature of interparticle forces acting on colloid particle surfaces with adsorbed surface films of the internationally used humic acid standard material, Suwannee River Humic Acid (SHA), has been investigated using an atomic force microscope (AFM). Two particle surfaces were used, alumina and a hydrous iron oxide film coated onto silica particles. Adsorbed SHA dominated the interactive forces for both surface types when present. At low ionic strength and pH > 4, the force curves were dominated by electrostatic repulsion of the electrical double layers, with the extent of repulsion decreasing as electrolyte (NaCl) concentration increased, scaling with the Debye length (kappa(-1)) of the electrolyte according to classical theory. At pH approximately 4, electrostatic forces were largely absent, indicating almost complete protonation of carboxylic acid (-COOH) functional groups on the adsorbed SHA. Under these conditions and also at high electrolyte concentration ([NaCl] > 0.1 M), the absence of electrostatic forces allowed observation of repulsion forces arising from steric interaction of adsorbed SHA as the oxide surfaces approached closely to each other (separation < 10 nm). This steric barrier shrank as electrolyte concentration increased, implying tighter coiling of the adsorbed SHA molecules. In addition, adhesive bridging between surfaces was observed only in the presence of SHA films, implying a strong energy barrier to spontaneous detachment of the surfaces from each other once joined. This adhesion was especially strong in the presence of Ca2+ which appears to bridge SHA layers on each surface. Overall, our results show that SHA is a good model for the NOM adsorbed on colloids.

  1. Ceria modified activated carbon: an efficient arsenic removal adsorbent for drinking water purification

    NASA Astrophysics Data System (ADS)

    Sawana, Radha; Somasundar, Yogesh; Iyer, Venkatesh Shankar; Baruwati, Babita

    2016-03-01

    Ceria (CeO2) coated powdered activated carbon was synthesized by a single step chemical process and demonstrated to be a highly efficient adsorbent for the removal of both As(III) and As(V) from water without any pre-oxidation process. The formation of CeO2 on the surface of powdered activated carbon was confirmed by X-ray diffraction, Raman spectroscopy and X-ray photoelectron spectroscopy. The percentage of Ce in the adsorbent was confirmed to be 3.5 % by ICP-OES. The maximum removal capacity for As(III) and As(V) was found to be 10.3 and 12.2 mg/g, respectively. These values are comparable to most of the commercially available adsorbents. 80 % of the removal process was completed within 15 min of contact time in a batch process. More than 95 % removal of both As(III) and As(V) was achieved within an hour. The efficiency of removal was not affected by change in pH (5-9), salinity, hardness, organic (1-4 ppm of humic acid) and inorganic anions (sulphate, nitrate, chloride, bicarbonate and fluoride) excluding phosphate. Presence of 100 ppm phosphate reduced the removal significantly from 90 to 18 %. The equilibrium adsorption pattern of both As(III) and As(V) fitted well with the Freundlich model with R 2 values 0.99 and 0.97, respectively. The material shows reusability greater than three times in a batch process (arsenic concentration reduced below 10 ppb from 330 ppb) and a life of at least 100 L in a column study with 80 g material when tested under natural hard water (TDS 1000 ppm, pH 7.8, hardness 600 ppm as CaCO3) spiked with 330 ppb of arsenic.

  2. New diffusive gradients in a thin film technique for measuring inorganic arsenic and selenium(IV) using a titanium dioxide based adsorbent.

    PubMed

    Bennett, William W; Teasdale, Peter R; Panther, Jared G; Welsh, David T; Jolley, Dianne F

    2010-09-01

    A new diffusive gradients in a thin film (DGT) technique, using a titanium dioxide based adsorbent (Metsorb), has been developed and evaluated for the determination of dissolved inorganic arsenic and selenium. As(III), As(V), and Se(IV) were found to be quantitatively accumulated by the adsorbent (uptake efficiencies of 96.5-100%) and eluted in 1 M NaOH (elution efficiencies of 81.2%, 75.2%, and 88.7%). Se(VI) was not quantitatively accumulated by the adsorbent (<20%). Laboratory DGT validation experiments gave linear mass uptake over time (R(2) >or= 0.998) for As(III), As(V), and Se(IV). Consistent uptake occurred over pH (3.5-8.5) and ionic strength (0.0001-0.75 mol L(-1) NaNO(3)) ranges typical of natural waters, including seawater. Field deployments of DGT probes with various diffusive layer thicknesses confirmed the use of the technique in situ, allowing calculation of the diffusive boundary layers and an accurate measurement of inorganic arsenic. Reproducibility of the technique in field deployments was good (relative standard deviation <8%). Limits of detection (4 day deployments) were 0.01 microg L(-1) for inorganic arsenic and 0.05 microg L(-1) for Se(IV). The results of this study confirmed that DGT with Metsorb was a reliable and robust method for the measurement of inorganic arsenic and the selective measurement of Se(IV) within useful limits of accuracy.

  3. Hydrophobic but hygroscopic polymer films--identifying interfacial species and understanding water ingress behavior.

    PubMed

    Hsiao, Erik; Barnette, Anna L; Bradley, Laura C; Kim, Seong H

    2011-11-01

    The hydrophobic but hygroscopic nature of polydimethylsiloxane (PDMS) with quaternary ammonium cationic side chains adsorbed on a SiO(2) surface was investigated with sum frequency generation vibration spectroscopy (SFG) and attenuated total reflectance infrared spectroscopy (ATR-IR). PDMS with cationic side chains, named cationic polymer lubricant (CPL), forms a self-healing boundary lubrication film on SiO(2). It is interesting that CPL films are externally hydrophobic but internally hydrophilic. The comparison of SFG and ATR-IR data revealed that the methyl groups of the PDMS backbone are exposed at the film/air interface and the cationic side groups and counterions are embedded within the film. The hydrophobicity must originate from the surface CH(3) groups, while the ionic groups inside the film must be responsible for water uptake. The surface hydrophobicity can alleviate the capillary adhesion while the hygroscopic property enhances the mobility and self-healing capability of the CPL boundary lubrication film.

  4. Optical and electrical characterizations of nanocomposite film of titania adsorbed onto oxidized multiwalled carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Feng, Wei; Feng, Yiyu; Wu, Zigang; Fujii, Akihiko; Ozaki, Masanori; Yoshino, Katsumi

    2005-07-01

    Composite film containing titania electrostatically linked to oxidized multiwalled carbon nanotubes (TiO2-s-MWNTs) was prepared from a suspension of TiO2 nanoparticles in soluble carbon nanotubes. The structure of the film was analysed principally by Fourier transform infrared spectroscopy, scanning electron micrography and x-ray diffraction. The optical and electrical characterizations of the film were investigated by UV-vis spectrum, photoluminescence and photoconductivity. The enhancement of photocurrent in the TiO2-s-MWNT film is discussed by taking the photoinduced charge transfer between the MWNT and TiO2 into consideration.

  5. Impacts of surface adsorbed catechol on tropospheric aerosol surrogates: heterogeneous ozonolysis and its effects on water uptake.

    PubMed

    Woodill, Laurie A; O'Neill, Erinn M; Hinrichs, Ryan Z

    2013-07-11

    Surface adsorbed organics are ubiquitous components of inorganic tropospheric aerosols and have the potential to alter aerosol chemical and physical properties. To assess the impact of adsorbed organics on water uptake by inorganic substrates, we used diffuse reflectance infrared spectroscopy to compared water adsorption isotherms for uncoated NaCl and α-Al2O3 samples, samples containing a monolayer of adsorbed catechol, and adsorbed catechol samples following ozonolysis. Adsorption of gaseous catechol on to the inorganic substrates produced vibrational features indicating physisorption on NaCl and displacement of surface hydroxyl groups forming binuclear bidentate catecholate on α-Al2O3, with surface concentrations of 2-3 × 10(18) molecules m(-2). Subsequent heterogeneous ozonolysis produced muconic acid at a rate 4-5 times faster on NaCl compared to α-Al2O3, with predicted atmospheric lifetimes of 4.3 and 18 h, respectively, assuming a tropospheric ozone concentration of 40 ppb. Water adsorption isotherms for all NaCl samples were indistinguishable within experimental uncertainty, indicating that these organic monolayers had negligible impact on coadsorbed water surface concentrations for these systems. α-Al2O3-catechol samples exhibited dramatically less water uptake compared to uncoated α-Al2O3, while oxidation of surface adsorbed catechol had no effect on the extent of water uptake. For both substrates, adsorbed organics increased the relative abundance of "ice-like" versus "liquid-like" water, with the effect larger for catechol than oxidized ozonolysis products. These results highlight the importance of aerosol substrate in understanding the heterogeneous ozonolysis of adsorbed polyphenols and suggest such coatings may impair ice nucleation by aluminosilicate mineral aerosol.

  6. Removal of cadmium and lead ions from water by sulfonated magnetic nanoparticle adsorbents.

    PubMed

    Chen, Kai; He, Junyong; Li, Yulian; Cai, Xingguo; Zhang, Kaisheng; Liu, Tao; Hu, Yi; Lin, Dongyue; Kong, Lingtao; Liu, Jinhuai

    2017-05-15

    A new adsorbent, Fe3O4 sulfonated magnetic nanoparticle (Fe3O4-SO3H MNP), was developed for heavy metal ions removal from water, which could be effectively separated from the solution owing to the superparamagnetic property. The nanoparticles can be used to remove heavy metal ions due to the additional active site, "sulfo-group", introduced by the AMPS branches grafted onto the iron oxide. The as-synthesized materials were characterized by SEM, TEM, FT-IR and BET. The FTIR, XPS and Zeta potential were used to describe the adsorption mechanism. The Fe3O4-SO3H MNPs showed rapid removal for Pb(2+) and Cd(2+) with maximum of adsorption capacity of 108. 93 and 80.9mg/g at 25°C, respectively. The adsorption isotherms for Pb(2+) and Cd(2+) fitted better with Langmuir than Freundlich models, indicated that the processes of the removal of Pb(2+) and Cd(2+) could follow a kind of similar adsorption manner. The adsorption kinetic was consistent with pseudo-second-order model. Furthermore, the reuse experiments results showed the adsorbent might have potential in treating heavy metal ions pollution in water.

  7. Water and ion transport in ultra-adsorbing porous magnesium carbonate studied by dielectric spectroscopy

    NASA Astrophysics Data System (ADS)

    Pochard, Isabelle; Frykstrand, Sara; Ahlström, Olle; Forsgren, Johan; Strømme, Maria

    2014-01-01

    Porous materials are used in application areas ranging from drug and vaccine delivery, medical implants, molecular sieves and cosmetics to catalysis and humidity control. In the present work, we employed an alternative approach to gain in-depth understanding about water interaction properties in such materials by the use of dielectric spectroscopy and thereby show that it is possible to obtain information that is not accessible from the more commonly employed water interaction analysis techniques. Specifically, the complex dielectric response of Upsalite, a novel, super-hydroscopic, high-surface area, porous magnesium carbonate material was measured in isothermal frequency scans between 10-3 and 106 Hz at controlled relative humidity (RH). We found the dielectric constant of the dry material to be 1.82. The ratio of bound to free water present in Upsalite after adsorption at room temperature was found to be high irrespective of the surrounding humidity with values ranging from ˜67% to ˜90%. We further found that OH- ions are the charge carriers responsible for the electrode polarization observed in the dielectric response and that the amount of these ions that are free to move in the material corresponds to a concentration of the order of 1-10 μmol l-1 independent of RH. Finally, the OH- diffusion coefficient displayed a drastic decrease with decreasing RH, typical of transport in unsaturated conditions. The presented results provide detailed insight about water interactions in the novel water adsorbing material under study and it is foreseen that the employed analysis methods can be used to evaluate other types of moisture adsorbing materials as well as the movement of functional species in the pores of inorganic drug delivery materials and materials tailored for adsorption of harmful charged species.

  8. Adsorption Characteristics of Different Adsorbents and Iron(III) Salt for Removing As(V) from Water

    PubMed Central

    Ćurko, Josip; Matošić, Marin; Crnek, Vlado; Stulić, Višnja

    2016-01-01

    Summary The aim of this study is to determine the adsorption performance of three types of adsorbents for removal of As(V) from water: Bayoxide® E33 (granular iron(III) oxide), Titansorb® (granular titanium oxide) and a suspension of precipitated iron(III) hydroxide. Results of As(V) adsorption stoichiometry of two commercial adsorbents and precipitated iron(III) hydroxide in tap and demineralized water were fitted to Freundlich and Langmuir adsorption isotherm equations, from which adsorption constants and adsorption capacity were calculated. The separation factor RL for the three adsorbents ranged from 0.04 to 0.61, indicating effective adsorption. Precipitated iron(III) hydroxide had the greatest, while Titansorb had the lowest capacity to adsorb As(V). Comparison of adsorption from tap or demineralized water showed that Bayoxide and precipitated iron(III) hydroxide had higher adsorption capacity in demineralized water, whereas Titansorb showed a slightly higher capacity in tap water. These results provide mechanistic insights into how commonly used adsorbents remove As(V) from water. PMID:27904416

  9. Novel Anionic Clay Adsorbents for Boiler-Blow-Down Waters Reclaim and Reuse

    SciTech Connect

    Muhammad Sahimi; Theodore Tsotsis

    2010-01-08

    Arsenic (As) and Selenium (Se) are found in water in the form of oxyanions. Relatively high concentrations of As and Se have been reported both in power plant discharges, as well as, in fresh water supplies. The International Agency for Research on Cancer currently classifies As as a group 1 chemical, that is considered to be carcinogenic to humans. In Phase I of this project we studied the adsorption of As and Se by uncalcined and calcined layered double hydroxide (LDH). The focus of the present work is a systematic study of the adsorption of As and Se by conditioned LDH adsorbents. Conditioning the adsorbent significantly reduced the Mg and Al dissolution observed with uncalcined and calcined LDH. The adsorption rates and isotherms have been investigated in batch experiments using particles of four different particle size ranges. As(V) adsorption is shown to follow a Sips-type adsorption isotherm. The As(V) adsorption rate on conditioned LDH increases with decreasing adsorbent particle size; the adsorption capacity, on the other hand, is independent of the particle size. A homogeneous surface diffusion model (HSDM) and a bi-disperse pore model (BPM) - the latter viewing the LDH particles as assemblages of microparticles and taking into account bulk diffusion in the intraparticle pore space, and surface diffusion within the microparticles themselves - were used to fit the experimental kinetic data. The HSDM estimated diffusivity values dependent on the particle size, whereas the BPM predicted an intracrystalline diffusivity, which is fairly invariant with particle size. The removal of As(V) on conditioned LDH adsorbents was also investigated in flow columns, where the impact of important solution and operational parameters such as influent As concentration, pH, sorbent particle size and flow rate were studied. An early breakthrough and saturation was observed at higher flow rates and at higher influent concentrations, whereas a decrease in the sorbent particle

  10. Removal of atrazine from water by low cost adsorbents derived from agricultural and industrial wastes.

    PubMed

    Sharma, Rajendra Kumar; Kumar, Anoop; Joseph, P E

    2008-05-01

    In the present study six adsorbents viz. wood charcoal, fly ash, coconut charcoal, saw dust, coconut fiber and baggasse charcoal were studied for their capacity to remove atrazine from water. The removal efficiency of different adsorbents varied from 76.5% to 97.7% at 0.05 ppm concentration and 78.5% to 95.5% at 0.1 ppm concentration of atrazine solution, which was less than removal efficiency of activated charcoal reported as 98% for atrazine (Adams and Watson, J Environ Eng ASCE 39:327-330, 1996). Wood charcoal was a cheap (Rs 15 kg(-1)) and easily available material in house holds. Since wood charcoal was granular in nature, it could be used for the removal of atrazine from water to the extent of 95.5%-97.7%. Fly ash is a waste product of thermal plant containing 40%-50% silica, 20%-35% alumina, 12%-30% carbon and unburnt minerals having a high pH of 9-10. It is very cheap and abundant material and has comparatively good adsorption capacity. It was found that fly ash effectively removed about 84.1%-88.5% atrazine from water at 0.05 and 0.1 ppm levels. Coconut shell is also waste product. Therefore, both are inexpensive. The removal efficiency of atrazine from water was 92.4%-95.2% by coconut shell charcoal and 85.9%-86.3% by coconut fiber. Sawdust is generally used as domestic fuel and found everywhere. It is also very cheap (Re. 1 kg(-1)). Baggasse charcoal is a waste product of sugar mill and abundant material. Its cost is due to transport expense, which depends upon distance from the sugar mill. The removal efficiency of sawdust and baggasse charcoal was found 78.5-80.5 and 76.5-84.6, respectively. The efficacy of chemically treated adsorbents for the removal of atrazine from water is in the order: wood charcoal > coconut shell charcoal > fly ash > coconut fiber charcoal > baggasse charcoal > sawdust.

  11. Effect of peptide secondary structure on adsorption and adsorbed film properties on end-grafted polyethylene oxide layers.

    PubMed

    Binazadeh, M; Zeng, H; Unsworth, L D

    2014-01-01

    Poly-l-lysine (PLL), in α-helix or β-sheet configuration, was used as a model peptide for investigating the effect of secondary structures on adsorption events to poly(ethylene oxide) (PEO) modified surfaces formed using θ solvents. Circular dichroism results showed that the secondary structure of PLL persisted upon adsorption to Au and PEO modified Au surfaces. Quartz crystal microbalance with dissipation (QCM-D) was used to characterize the chemisorbed PEO layer in different solvents (θ and good solvents), as well as the sequential adsorption of PLL in different secondary structures (α-helix or β-sheet). QCM-D results suggest that chemisorption of PEO 750 and 2000 from θ solutions led to brushes 3.8 ± 0.1 and 4.5 ± 0.1 nm thick with layer viscosities of 9.2 ± 0.8 and 4.8 ± 0.5 cP, respectively. The average number of H2O per ethylene oxides, while in θ solvent, was determined as ~0.9 and ~1.2 for the PEO 750 and 2000 layers, respectively. Upon immersion in good solvent (as used for PLL adsorption experiments), the number of H2O per ethylene oxides increased to ~1.5 and ~2.0 for PEO 750 and 2000 films, respectively. PLL adsorbed masses for α-helix and β-sheet on Au sensors was 231 ± 5 and 1087 ± 14 ng cm(-2), with layer viscosities of 2.3 ± 0.1 and 1.2 ± 0.1 cP, respectively; suggesting that the α-helix layer was more rigid, despite a smaller adsorbed mass, than that of β-sheet layers. The PEO 750 layer reduced PLL adsorbed amounts to ~10 and 12% of that on Au for α-helices and β-sheets respectively. The PLL adsorbed mass to PEO 2000 layers dropped to ~12% and 4% of that on Au, for α-helix and β-sheet respectively. No significant differences existed for the viscosities of adsorbed α-helix and β-sheet PLL on PEO surfaces. These results provide new insights into the fundamental understanding of the effects of secondary structures of peptides and proteins on their surface adsorption.

  12. A method for preparing ferric activated carbon composites adsorbents to remove arsenic from drinking water.

    PubMed

    Zhang, Qiao Li; Lin, Y C; Chen, X; Gao, Nai Yun

    2007-09-30

    Iron oxide/activated carbon (FeO/AC) composite adsorbent material, which was used to modify the coal-based activated carbon (AC) 12 x 40, was prepared by the special ferric oxide microcrystal in this study. This composite can be used as the adsorbent to remove arsenic from drinking water, and Langmuir isotherm adsorption equation well describes the experimental adsorption isotherms. Then, the arsenic desorption can subsequently be separated from the medium by using a 1% aqueous NaOH solution. The apparent characters and physical chemistry performances of FeO/AC composite were investigated by X-ray diffraction (XRD), nitrogen adsorption, scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Batch and column adsorption experiments were carried out to investigate and compare the arsenic removal capability of the prepared FeO/AC composite material and virgin activated carbon. It can be concluded that: (1) the main phase present in this composite are magnetite (Fe(3)O(4)), maghemite (gamma-Fe(2)O(3)), hematite (alpha-Fe(2)O(3)) and goethite (alpha-FeO(OH)); (2) the presence of iron oxides did not significantly affect the surface area or the pore structure of the activated carbon; (3) the comparisons between the adsorption isotherms of arsenic from aqueous solution onto the composite and virgin activated carbon showed that the FeO/AC composite behave an excellent capacity of adsorption arsenic than the virgin activated carbon; (4) column adsorption experiments with FeO/AC composite adsorbent showed that the arsenic could be removed to below 0.01 mg/L within 1250 mL empty bed volume when influent concentration was 0.5mg/L.

  13. Water films, asphaltenes, and wettability alteration

    SciTech Connect

    Kaminsky, R.; Radke, C.J.

    1998-06-01

    We present a transport model for asphaltene diffusion from an oil/water interface through a water film followed by adsorption at a solid/water interface. Using a Langmuir adsorption isotherm, the effect of asphaltene aqueous solubility and adsorption constant K on equilibration time are established. For K greater than 1 nm and asphaltene solubilities down to 0.1 ppb, adsorption equilibrium, taken to be 1 mg/m{sup 2}, occurs within a few hours. Negligible asphaltene solubility does not explain why a water film prevents asphaltene adsorption and wettability alteration in reservoir rock.

  14. Development of long-life-cycle tablet ceramic adsorbent for geosmin removal from water solution

    NASA Astrophysics Data System (ADS)

    Chen, Rongzhi; Xue, Qiang; Zhang, Zhenya; Sugiura, Norio; Yang, Yingnan; Li, Miao; Chen, Nan; Ying, Zhao; Lei, Zhongfang

    2011-01-01

    In this study, the tablet ceramic adsorbent (TCA), a silica/iron(III) oxide composite material, has been developed for geosmin (GSM) removal from the water solution. The physicochemical characteristics of TCA were examined with XRD, SEM, EDX and BET analyses. The sorption characteristics of GSM on TCA were investigated in a batch system. Attempts have been made to understand the adsorption kinetics, the effect of initial GSM concentration, solution pH, and reaction time. The batch experiments equilibrium data were well fitted to the Lagergren kinetic equation, which indicate the first-order nature adsorption. Over 82% of the GSM was removed by the TCA within 600 min at an initial concentration of 200 ng/L with 20 g/L of TCA dose. The batch and regeneration study indicated that the TCA is a cost-effective GSM adsorbent with sufficient mechanical strength to retain its physical integrity after long-time adsorption, and high regeneration performance for long-life-cycle application. Almost no second contamination (toxic sludge or leached iron) was observed after adsorption, and the gas resultant of thermal regeneration is harmless to atmospheric environment.

  15. Activated carbons and low cost adsorbents for remediation of tri- and hexavalent chromium from water.

    PubMed

    Mohan, Dinesh; Pittman, Charles U

    2006-09-21

    Hexavalent chromium is a well-known highly toxic metal, considered a priority pollutant. Industrial sources of Cr(VI) include leather tanning, cooling tower blowdown, plating, electroplating, anodizing baths, rinse waters, etc. The most common method applied for chromate control is reduction of Cr(VI) to its trivalent form in acid (pH approximately 2.0) and subsequent hydroxide precipitation of Cr(III) by increasing the pH to approximately 9.0-10.0 using lime. Existing overviews of chromium removal only cover selected technologies that have traditionally been used in chromium removal. Far less attention has been paid to adsorption. Herein, we provide the first review article that provides readers an overview of the sorption capacities of commercial developed carbons and other low cost sorbents for chromium remediation. After an overview of chromium contamination is provided, more than 300 papers on chromium remediation using adsorption are discussed to provide recent information about the most widely used adsorbents applied for chromium remediation. Efforts to establish the adsorption mechanisms of Cr(III) and Cr(VI) on various adsorbents are reviewed. Chromium's impact environmental quality, sources of chromium pollution and toxicological/health effects is also briefly introduced. Interpretations of the surface interactions are offered. Particular attention is paid to comparing the sorption efficiency and capacities of commercially available activated carbons to other low cost alternatives, including an extensive table.

  16. Cross-linked chitosan thin film coated onto glass plate as an effective adsorbent for adsorption of reactive orange 16.

    PubMed

    Jawad, Ali H; Azharul Islam, Md; Hameed, B H

    2017-02-01

    Fabrication of an immobilized cross-linked chitosan-epichlorohydrine thin film (CLCETF) onto glass plate for adsorption of reactive orange 16 (RO16) dye was successfully studied using the direct casting technique. Adsorption experiments were performed as a function of contact time, initial dye concentration (25mg/L to 350mg/L), and pH (3-11). The adsorption isotherm followed the Langmuir model. The adsorption capacity of CLECTF for RO16 was 356.50mg/g at 27±2°C. The kinetics closely followed the pseudo-second-order model. Results supported the potential use of an immobilized CLECTF as effective adsorbent for the treatment of reactive dye without using filtration process.

  17. Dynamic mechanical properties of a polyelectrolyte adsorbed insoluble lipid monolayer at the air-water interface.

    PubMed

    Park, Chang Young; Kim, Mahn Won

    2015-04-23

    Polymers have been used to stabilize interfaces or to tune the mechanical properties of interfaces in various contexts, such as in oil emulsions or biological membranes. Although the structural properties of these systems are relatively well-studied, instrumental limitations continue to make it difficult to understand how the addition of polymer affects the dynamic mechanical properties of thin and soft films. We have solved this challenge by developing a new instrument, an optical-tweezer-based interface shear microrheometer (ISMR). With this technique, we observed that the interface shear modulus, G*, of a dioctadecyldimethylammonium chloride (DODAC) monolayer at the air-water interface significantly increased with adsorption of polystyrenesulfonate (PSS). In addition, the viscous film (DODAC monolayer) became a viscoelastic film with PSS adsorption. At a low salt concentration, 10 mM of NaCl in the subphase, the viscoelasticity of the DODAC/PSS composite was predominantly determined by a particular property of PSS, that is, it behaves as a Gaussian chain in a θ-solvent. At a high salt concentration, 316 mM of NaCl, the thin film behaved as a polymer melt excluding water molecules.

  18. Rapid removal of aniline from contaminated water by a novel polymeric adsorbent.

    PubMed

    Huang, Yunhong; Xu, Yang; He, Qinghua; Cao, Yusheng; Du, Bibai

    2014-01-01

    Dummy molecularly imprinted polymers (DMIPs) for aniline were synthesized by a thermal polymerization method using acrylamide as a functional monomer, ethylene dimethacrylate as a crosslinker, 2,2-azobisisobutyronitrile as a free radical initiator, acetonitrile as a porogenic solvent, and analogues of aniline, namely sulfadiazine, as the template. The DMIPs that were obtained showed a high affinity to aniline compared to non-imprinted polymers. It was proven that the DMIPs obtained using sulfadiazine as the template were much better than the molecularly imprinted polymers using aniline as the template. The results indicated that the Freundlich model was fit for the adsorption model of DMIP for aniline and the adsorption model of the DMIP for aniline was multilayer adsorption. Furthermore, the results showed that the DMIP synthesized by bulk polymerization could be used as a novel adsorbent for removal of aniline from contaminated water.

  19. Arsenic adsorption and speciation in drinking water by GAC-based iron-containing adsorbents

    NASA Astrophysics Data System (ADS)

    Gim, Yewon; Terry, Jeff; Gu, Zhimang; Hua, B.; Deng, Baolin

    2008-04-01

    Granular Activated Carbon (GAC) with Iron adsorbents were developed for effective removal of arsenic from drinking water. The structure and proposed mechanism for As removal was studied using X-ray absorption spectroscopy. The oxidation state of As(III)GAC sample was calculated using XANES spectra and verified to be predominantly As(V). The structure was determined using EXAFS spectra of As(V) and Fe. The Fe spectra suggested thin layer of Fe oxide formation on GAC surface. As data showed As oxide formed bond on the Fe oxide surface. The spectra were calculated using multiple geometrically optimized models calculated using density functional theory. Further calculations were done to verify the structure, and further examine the structure.

  20. Study for Reduction of Outgassing Property of Adsorbed Water Gas for Improved Surface Finished Titanium Material

    NASA Astrophysics Data System (ADS)

    Takeda, Masatoshi; Kurisu, Hiroki; Uchida, Takashi; Yamamoto, Setsuo; Ishizawa, Katsunobu; Nomura, Takeru; Eda, Takahiro; Murashige, Nobuyuki

    This paper addresses the development of the surface finishing for a titanium material and the study for the reduction of outgassing property of adsorbed water (H2O) molecules. Developed surface finishing is composed of the buffing for the reduction of the surface roughness and improved chemical polishing for the thick surface oxide layer compared with the chemical polishing so far. The surface roughness of the surface finished titanium material is reduced 35% and the thickness of the surface oxide layer increases by 30%. The total amount of thermal desorbed H2O gas for the new surface finished titanium is reduced 30%. It is considered that the origin for the decrease of the amount of desorption H2O gas is the reduction of the adsorption sites due to the decrease of the surface roughness and the reduction of adsorption energy of H2O gas due to the strong surface oxidation for a titanium material.

  1. Removal efficiency of water purifier and adsorbent for iodine, cesium, strontium, barium and zirconium in drinking water.

    PubMed

    Sato, Itaru; Kudo, Hiroaki; Tsuda, Shuji

    2011-01-01

    The severe incident of Fukushima Daiichi Nuclear Power Station has caused radioactive contamination of environment including drinking water. Radioactive iodine, cesium, strontium, barium and zirconium are hazardous fission products because of the high yield and/or relatively long half-life. In the present study, 4 pot-type water purifiers and several adsorbents were examined for the removal effects on these elements from drinking water. Iodide, iodate, cesium and barium were removed by all water purifiers with efficiencies about 85%, 40%, 75-90% and higher than 85%, respectively. These efficiencies lasted for 200 l, which is near the recommended limits for use of filter cartridges, without decay. Strontium was removed with initial efficiencies from 70% to 100%, but the efficiencies were slightly decreased by use. Zirconium was removed by two models, but hardly removed by the other models. Synthetic zeolite A4 efficiently removed cesium, strontium and barium, but had no effect on iodine and zirconium. Natural zeolite, mordenite, removed cesium with an efficiency as high as zeolite A4, but the removal efficiencies for strontium and barium were far less than those of zeolite A4. Activated carbon had little removal effects on these elements. In case of radioactive contamination of tap water, water purifiers may be available for convenient decontamination of drinking water in the home.

  2. Entropy-Driven Conformational Control of α,ω-Difunctional Bidentate-Dithiol Azo-Based Adsorbates Enables the Fabrication of Thermally Stable Surface-Grafted Polymer Films.

    PubMed

    Lee, Han Ju; Jamison, Andrew C; Lee, T Randall

    2016-06-22

    Thermally stable radical initiator monolayers were prepared from uniquely designed α,ω-difunctional adsorbates with bidentate headgroups for the growth of nanoscale polymer films on metal surfaces. The length of the spacer separating the bidentate headgroups was varied to afford 4,4'-(diazene-1,2-diyl)bis(N-(16-(3,5-bis(mercaptomethyl)phenoxy)hexadecyl)-4-cyanopentanamide) (B16), 4,4'-(diazene-1,2-diyl)bis(N-(16-(3,5-bis(mercapto-methyl)phenoxy)decyl)-4-cyanopentanamide) (B10), and 4,4'-(diazene-1,2-diyl)bis(N-(4-(3,5-bis(mercaptomethyl)phenoxy)butyl)-4-cyanopentanamide) (B4). The structural features of the self-assembled monolayers (SAMs) derived from B16, B10, and B4 were characterized by X-ray photoelectron spectroscopy (XPS), ellipsometry, and polarization modulation infrared reflection-absorption spectroscopy (PM-IRRAS) and compared to those derived from an analogous α,ω-difunctional adsorbate with monodentate headgroups, 4,4'-(diazene-1,2-diyl)bis(4-cyano-N-(16-mercaptohexadecyl)pentanamide (M). These studies demonstrate that the conformation (i.e., hairpin vs standing up) of the bidentate initiator adsorbates on gold surfaces was easily controlled by adjusting the concentration of the adsorbates in solution. The results of solution-phase thermal desorption tests revealed that the radical initiator monolayers generated from B16, B10, and B4 exhibit an enhanced thermal stability when compared to those generated from M. Furthermore, a study of the growth of polymer films was performed to evaluate the utility of these new bidentate adsorbate SAMs as film-development platforms for new functional materials and devices. Specifically, surface-grafted polystyrene films were successfully generated from SAMs derived from B16. In contrast, attempts to grow polystyrene films from SAMs derived from M under a variety of analogous conditions were unsuccessful.

  3. Surface-induced solid-liquid phase transitions in ultra-thin water films at T > 0 ^oC

    NASA Astrophysics Data System (ADS)

    Chakraborty, Animesh; Gellman, Andrew; Baker, Layton; Broitman, Estebahn

    2008-03-01

    We report here the measurements of both the adsorption isotherms and the dissipation in ultra-thin films of water adsorbed on the surfaces of SiO2 . The measurements were made in a small high vacuum chamber in which we have mounted a QCM. The chamber was evacuated to ˜10-8 Torr and then filled with water vapor at pressures ranging from 10-3 -- 40 Torr (the vapor pressure of water at room temperature is ˜22 Torr). In addition the temperature of the apparatus can be varied in the range 10 -- 60^oC. This is sufficient to measure the adsorption isotherm and to probe the phase of adsorbed water films over the range of conditions. Recently published work studying the adsorption of water on the SiO2 layer formed on Si single crystals has suggested that the phase of the water at temperatures well above 0^oC is actually that of a solid, ice-like structure rather than liquid water [1]. That work is based on the comparison of the vibrational spectrum of thin water films with those of liquid water and ice. In our study we are using the QCM to investigate the possibility of formation of Ice-like structures on SiO2. [1] Asay, D. B. and Kim, S.H., Evolution of the Adsorbed Water Layer Structure on Silicon Oxide at Room Temperature. J. Phys. Chem. B. 2005, 109, 16760-16763

  4. Water clusters adsorbed on polycyclic aromatic hydrocarbons: Energetics and conformational dynamics

    NASA Astrophysics Data System (ADS)

    Simon, Aude; Spiegelman, Fernand

    2013-05-01

    In this work, we present some classical molecular dynamics (MD) simulations and finite temperature infrared (IR) spectra of water clusters adsorbed on coronene (C24H12), a compact polycyclic aromatic hydrocarbon (PAH). The potential energy surface is obtained within the self-consistent-charge density-functional based tight-binding approach with modifications insuring the correct description of water-water and water-PAH interactions. This scheme is benchmarked for the minimal energy structures of (C24H12)(H2O)n (n = 3-10) against density-functional theory (DFT) calculations and for the low-energy isomers of (H2O)6 and (C6H6)(H2O)3 against correlated wavefunction and DFT calculations. A detailed study of the low energy isomers of (C24H12)(H2O)3, 6 complexes is then provided. On-the-fly Born-Oppenheimer MD simulations are performed in the temperature T range 10-350 K for (C24H12)(H2O)n (n = 3-7) complexes. The description of the evolution of the systems with T is provided with emphasis on (C24H12)(H2O)n (n = 3,6). For T in the range 50-150 K, isomerisation processes are observed and when T increases, a solid-to-liquid phase-change like behavior is shown. The desorption of one water molecule is frequently observed at 300 K. The isomerisation processes are evidenced on the finite temperature IR spectra and the results are presented for (C24H12)(H2O)n (n = 3,6). A signature for the edge-coordination of the water cluster on the PAH is also proposed.

  5. Anisotropic orientational motion of molecular adsorbates at the air-water interface

    SciTech Connect

    Zimdars, D.; Dadap, J.I.; Eisenthal, K.B.; Heinz, T.F.

    1999-04-29

    The ultrafast orientational motions of coumarin 314 (C314) adsorbed at the air/water interface were investigated by time-resolved surface second harmonic generation (TRSHG). The theory and method of using TRSHG to detect both out-of-plane and in-plane orientational motions are discussed. The interfacial solute motions were found to be anisotropic, with differing out-of-plane and in-plane reorientation time constants. This report presents the first direct observation of in-plane orientational motion of a molecule (C314) at the air/water interface using TRSHG. The in-plane reorientation time constant is 600 {+-} 40 ps. The out-of-plane reorientation time constant is 350 {+-} 20 ps. The out-of-plane orientational motion of C314 is similar to the previous results on rhodamine 6G at the air/water interface which indicated increased interfacial friction compared with bulk aqueous solution. The surface reorientation times are 2--3 times slower than the bulk isotropic orientational diffusion time.

  6. Sulfonated graphene nanosheets as a superb adsorbent for various environmental pollutants in water.

    PubMed

    Shen, Yi; Chen, Baoliang

    2015-06-16

    Graphene nanosheets, as a novel nanoadsorbent, can be further modified to optimize the adsorption capability for various pollutants. To overcome the structural limits of graphene (aggregation) and graphene oxide (hydrophilic surface) in water, sulfonated graphene (GS) was prepared by diazotization reaction using sulfanilic acid. It was demonstrated that GS not only recovered a relatively complete sp(2)-hybridized plane with high affinity for aromatic pollutants but also had sulfonic acid groups and partial original oxygen-containing groups that powerfully attracted positively charged pollutants. The saturated adsorption capacities of GS were 400 mg/g for phenanthrene, 906 mg/g for methylene blue and 58 mg/g for Cd(2+), which were much higher than the corresponding values for reduced graphene oxide and graphene oxide. GS as a graphene-based adsorbent exhibits fast adsorption kinetic rate and superior adsorption capacity toward various pollutants, which mainly thanks to the multiple adsorption sites in GS including the conjugate π region sites and the functional group sites. Moreover, the sulfonic acid groups endow GS with the good dispersibility and single or few nanosheets which guarantee the adsorption processes. It is great potential to expose the adsorption sites of graphene nanosheets for pollutants in water by regulating their microstructures, surface properties and water dispersion.

  7. Study on nicotinamide adenine dinucleotide adsorbed at nano-boehmite/water and nano-corundum/water interfaces.

    PubMed

    Li, Li; Xie, Yanfang; Wang, Yanping; Yang, Xiaodi; Chen, Rong Fu; Shen, Ren Fang

    2013-02-01

    In this study, the adsorption behaviors of nicotinamide adenine dinucleotide (NAD(+)) on nano-boehmite (γ-AlOOH) and nano-corundum (γ-Al(2)O(3)) surfaces were investigated. The results showed that NAD(+) was predominantly adsorbed at the boehmite/water and corundum/water interfaces in outer-sphere fashions by electrostatic interaction between NAD(+) phosphate and surface hydroxyl groups. However, the features of ATR-FTIR spectra suggested that some minor inner-sphere complex should be considered at low pH conditions on corundum surface, which was consistent with the effect of NAD(+) on dissolution rate of corundum. In addition, the adsorption data well fitted with Langmuir and Freundlich isotherms on the boehmite and corundum surfaces, respectively. Also, the Gibbs adsorption energy was negative on the boehmite surface, which indicated that the adsorption behavior was spontaneous.

  8. Conductivity of copper phthalocyanine-polystyrene composite films in the presence of adsorbed oxygen

    NASA Astrophysics Data System (ADS)

    Pochtennyi, A. E.; Misevich, A. V.; Dolgii, V. K.

    2014-09-01

    The electrical conductivity and adsorption-resistive response to nitrogen dioxide of composite films containing copper phthalocyanine nanoparticles dispersed into the polystyrene matrix are investigated experimentally. The results are analyzed using the two-level model of hopping conductivity. The contributions to the conductivity from intrinsic and impurity localization centers are singled out, and the concentrations of the localization centers in copper phthalocyanines free of impurities as well as the electron localization radii in impurity and intrinsic states are determined.

  9. Kosterlitz-Thouless transition for 4He films adsorbed to rough surfaces.

    PubMed

    Luhman, D R; Hallock, R B

    2004-08-20

    We report the study of adsorption isotherms of 4He on several well characterized rough CaF2 surfaces using a quartz crystal microbalance technique at 1.672 K. The signature of decoupled mass observed on crossing the Kosterlitz-Thouless transition as a function of 4He film thickness decreases and becomes increasingly difficult to identify as the surface roughness is increased. A peak in the dissipation, indicative of the onset of superfluidity, changes little with roughness.

  10. Effect of adsorbed films on friction of Al2O3-metal systems

    NASA Technical Reports Server (NTRS)

    Pepper, S. V.

    1976-01-01

    The kinetic friction of polycrystalline Al2O3 sliding on Cu, Ni, and Fe in ultrahigh vacuum was studied as a function of the surface chemistry of the metal. Clean metal surfaces were exposed to O2, Cl2, C2H4, and C2H3Cl, and the change in friction due to the adsorbed species was observed. Auger electron spectroscopy assessed the elemental composition of the metal surface. It was found that the systems exposed to Cl2 exhibited low friction, interpreted as the van der Waals force between the Al2O3 and metal chloride. The generation of metal oxide by oxygen exposures resulted in an increase in friction, interpreted as due to strong interfacial bonds established by reaction of metal oxide with Al2O3 to form the complex oxide (spinel). The only effect of C2H4 was to increase the friction of the Fe system, but C2H3Cl exposures decreases friction in both Ni and Fe systems, indicating the dominance of the chlorine over the ethylene complex on the surface

  11. Polymer composite adsorbents using particles of molecularly imprinted polymers or aluminium oxide nanoparticles for treatment of arsenic contaminated waters.

    PubMed

    Önnby, L; Pakade, V; Mattiasson, B; Kirsebom, H

    2012-09-01

    Removal of As(V) by adsorption from water solutions was studied using three different synthetic adsorbents. The adsorbents, (a) aluminium nanoparticles (Alu-NPs, <50 nm) incorporated in amine rich cryogels (Alu-cryo), (b) molecular imprinted polymers (<38 μm) in polyacrylamide cryogels (MIP-cryo) and (c) thiol functionalised cryogels (SH-cryo) were evaluated regarding material characteristics and arsenic removal in batch test and continuous mode. Results revealed that a composite design with particles incorporated in cryogels was a successful means for applying small particles (nano- and micro- scale) in water solutions with maintained adsorption capacity and kinetics. Low capacity was obtained from SH-cryo and this adsorbent was hence excluded from the study. The adsorption capacities for the composites were 20.3 ± 0.8 mg/g adsorbent (Alu-cryo) and 7.9 ± 0.7 mg/g adsorbent (MIP-cryo) respectively. From SEM images it was seen that particles were homogeneously distributed in Alu-cryo and heterogeneously distributed in MIP-cryo. The particle incorporation increased the mechanical stability and the polymer backbones of pure polyacrylamide (MIP-cryo) were of better stability than the amine containing polymer backbone (Alu-cryo). Both composites worked well in the studied pH range of pH 2-8. Adsorption tested in real wastewater spiked with arsenic showed that co-ions (nitrate, sulphate and phosphate) affected arsenic removal for Alu-cryo more than for MIP-cryo. Both composites still adsorbed well in the presence of counter-ions (copper and zinc) present at low concentrations (μg/l). The unchanged and selective adsorption in realistic water observed for MIP-cryo was concluded to be due to a successful imprinting, here controlled using a non-imprinted polymer (NIP). A development of MIP-cryo is needed, considering its low adsorption capacity.

  12. Natural attenuation of pesticide water contamination by using ecological adsorbents: Application for chlorinated pesticides included in European Water Framework Directive

    NASA Astrophysics Data System (ADS)

    El Bakouri, Hicham; Morillo, José; Usero, José; Ouassini, Abdelhamid

    2009-01-01

    SummaryIn this work, a series of experiments were performed to demonstrate the potential use of natural organic substances (NOS) as an ecological technique to prevent pesticide contamination of ground water resources. A preliminary test has been carried out for determining the potentialities of ten NOS in the elimination of alachlor, aldrin, atrazine, chlorpyrifos, chlorfenvinphos, dieldrin, alpha-endosulfan, endrin, hexachlorobenzene, beta-HCH, gamma-HCH (lindane), simazine and trifluralin. The best adsorbents that present higher removal efficiency were date and olives stones, and in minor measurement Raphanus raphanistrum and Cistus ladaniferus. Experimental results showed that the pH and temperature of pesticide solutions negatively affect the adsorption process. According to adsorption kinetic data, 8 h were considered as the equilibrium time for realizing adsorption isotherms. Adsorption data were fit with Freundlich isotherm model which describes better the adsorption process. The K f values depended mainly on the nature of each adsorbent and ranged from 4.53 for Eucalyptus gomphocephala to 13.54 for date stones.

  13. Determination of surface properties of iron hydroxide-coated alumina adsorbent prepared for removal of arsenic from drinking water.

    PubMed

    Hlavay, József; Polyák, Klára

    2005-04-01

    A novel type adsorbent was prepared by in situ precipitation of Fe(OH)3 on the surface of activated Al2O3 as a support material. The iron content of the adsorbent was 0.31+/-0.003% m/m (56.1 mmol/g); its mechanical and chemical stability proved to be appropriate in solutions. The total capacity of the adsorbent was 0.12 mmol/g, and the pH of zero point of charge, pH(zpc) = 6.9+/-0.3. Depending on the pH of solutions, the adsorbent can be used for binding of both anions and cations, if pH(eq) < pH(zpc) anions are sorbed on the surface of adsorbent (S) through [SOH2+] and [SOH] groups. A graphical method was used for the determination of pH(iep) (isoelectric points) of the adsorbent and values of pH(iep) = 6.1+/-0.3 for As(III) and pH(iep) = 8.0+/-0.3 for As(V) ions were found. The amount of surface charged groups (Q) was about zero within the a pH range of 6.5-8.6, due to the practically neutral surface formed on the adsorption of As(V) ions. At acidic pH (pH 4.7), Q = 0.19 mol/kg was obtained. The adsorption of arsenate and arsenite ions from solutions of 0.1-0.4 mmol/L was represented by Langmuir-type isotherms. A great advantage of the adsorbent is that it can be used in adsorption columns, and low waste technology for removal of arsenic from drinking water can be developed.

  14. Thick-Film Carbon Dioxide Sensor via Anodic Adsorbate Stripping Technique and Its Structural Dependence.

    PubMed

    Photinon, Kanokorn; Wang, Shih-Han; Liu, Chung-Chiun

    2009-01-01

    A three-electrode based CO(2) sensor was fabricated using thick-film technology. The performance of this sensor was further enhanced by incorporating platinum nanoparticles onto the working electrode surface. An eight-fold increase in the signal output was obtained from the electrode with the platinum nanoparticles. The sensing output was linearly related to the CO(2) presented. Stability measurements demonstrated that the decline of the active surface area and the sensitivity of the sensor were 8% and 13%, respectively, over a two week period of time. The sensor response appeared to be a structural dependence of the crystallographic orientation of platinum electrode.

  15. Soluble hydrocarbons uptake by porous carbonaceous adsorbents at different water ionic strength and temperature: something to consider in oil spills.

    PubMed

    Flores-Chaparro, Carlos E; Ruiz, Luis Felipe Chazaro; Alfaro-De la Torre, Ma Catalina; Rangel-Mendez, Jose Rene

    2016-06-01

    Nowadays, petrochemical operations involve risks to the environment and one of the biggest is oil spills. Low molecular aromatics like benzene, toluene, and naphthalene dissolve in water, and because of their toxicological characteristics, these produce severe consequences to the environment. The oil spill cleanup strategies are mainly designed to deal with the heavy fractions accumulated on the water surface. Unfortunately, very limited information is available regarding the treatment of dissolved fractions.A commercial (Filtrasorb 400) and modified activated carbons were evaluated to remove benzene, toluene, and naphthalene from water, which are the most soluble aromatic hydrocarbons, at different ionic strengths (I) and temperatures (0-0.76 M and 4-25 °C, respectively). This allowed simulating the conditions of fresh and saline waters when assessing the performance of these adsorbents. It was found that the hydrocarbons adsorption affinity increased 12 % at a I of 0.5 M, due to the less negative charge of the adsorbent, while at a high I (≃0.76 M) in a synthetic seawater, the adsorption capacity decreased 21 % that was attributed to the adsorbent's pores occlusion by water clusters. Approximately, 40 h were needed to reach equilibrium; however, the maximum adsorption rate occurred within the first hour in all the cases. Moreover, the hydrocarbons adsorption and desorption capacities increased when the temperature augmented from 4 to 25 °C. On the other hand, thermally and chemically modified materials showed that the interactions between adsorbent-contaminant increased with the basification degree of the adsorbent surface.

  16. Control of the electrostatic effect on DAM-adsorbent for the water-soluble compounds by HPLC.

    PubMed

    Kamichatani, Waka; Inoue, Yoshinori; Yamamoto, Atsushi

    2012-01-01

    The effect of the mobile phase pH on the control of the electrostatic interaction was evaluated on a column packed with water-holding adsorbent on which diallylamine-maleic acid copolymers were immobilizing. The adsorbent showed extraordinary retention behaviors of water-soluble solutes under acidic conditions, however, their behavior became stable along with increasing pH. Hydrating water contents tended to level off at pH above 8. Thus, the electrostatic interaction with the stationary phase can be controlled by adjusting the mobile phase pH above 8. In this region, the retention of water-soluble solutes appears to be mainly governed by the hydrophilic partition interaction.

  17. Valorization of solid waste products from olive oil industry as potential adsorbents for water pollution control--a review.

    PubMed

    Bhatnagar, Amit; Kaczala, Fabio; Hogland, William; Marques, Marcia; Paraskeva, Christakis A; Papadakis, Vagelis G; Sillanpää, Mika

    2014-01-01

    The global olive oil production for 2010 is estimated to be 2,881,500 metric tons. The European Union countries produce 78.5% of the total olive oil, which stands for an average production of 2,136,000 tons. The worldwide consumption of olive oil increased of 78% between 1990 and 2010. The increase in olive oil production implies a proportional increase in olive mill wastes. As a consequence of such increasing trend, olive mills are facing severe environmental problems due to lack of feasible and/or cost-effective solutions to olive-mill waste management. Therefore, immediate attention is required to find a proper way of management to deal with olive mill waste materials in order to minimize environmental pollution and associated health risks. One of the interesting uses of solid wastes generated from olive mills is to convert them as inexpensive adsorbents for water pollution control. In this review paper, an extensive list of adsorbents (prepared by utilizing different types of olive mill solid waste materials) from vast literature has been compiled, and their adsorption capacities for various aquatic pollutants removal are presented. Different physicochemical methods that have been used to convert olive mill solid wastes into efficient adsorbents have also been discussed. Characterization of olive-based adsorbents and adsorption mechanisms of various aquatic pollutants on these developed olive-based adsorbents have also been discussed in detail. Conclusions have been drawn from the literature reviewed, and suggestions for future research are proposed.

  18. Photoassisted oxidation of oil films on water

    SciTech Connect

    Heller, A.; Brock, J.R.

    1990-10-01

    The objective of the project is to develop a method for the solar assisted oxidation of oil slicks. A semiconducting photocatalyst, titanium dioxide, is used. Upon absorbing a photon, an electron-hole pair is generated in the TiO{sub 2} microcrystal. The electron reacts with surface-adsorbed oxygen, reducing it to hydrogen peroxide; the hole directly oxidizes adsorbed organic compounds. Titanium dioxide is denser than either oil or seawater; the density of its anatase phase is 3.8 and that of its rutile phase is 4.3. In order to keep the titanium dioxide at the air/oil interface, it is attached to a low density, floating material. The particles of the latter are sufficiently small to make the system economical. Specifically, the photocatalyst particles are attached to inexpensive hollow glass microbeads of about 100{mu}m diameter. Those areas of the microbeads that are not covered by photocatalyst are made oleophilic, so that the microbeads will follow the oil slick and not migrate to either the air/water or the water/oil interface.

  19. Bio-photovoltaic conversion device using chlorine-e6 derived from chlorophyll from Spirulina adsorbed on a nanocrystalline TiO2 film electrode.

    PubMed

    Amao, Yutaka; Komori, Tasuku

    2004-03-15

    A bio-photovoltaic conversion device based on dye-sensitised solar cell (DSSC) using the visible light sensitisation of chlorine-e6 (Chl-e6) derived from chlorophyll from Spirulina adsorbed on a nanocrystalline TiO2 film was developed. Form fluorescence spectrum of Chl-e6 adsorbed on a nanocrystalline TiO2 film, the emission of Chl-e6 was effectively quenched by TiO2 nanocrystalline indicating that the effective electron injection from the excited singlet state of Chl-e6 into the conduction band of TiO2 particles occurred. The short-circuit photocurrent density (Isc). the open-circuit photovoltage (Voc). and the fill factor (FF) of solar cell using Chl-e6 adsorbed on a nanocrystalline TiO2 film electrode were estimated to be 0.305 +/- 0.012 mA cm(-2), 426 +/- 10 mV, and 45.0%, respectively. IPCE values were reached a maximum around the wavelength of absorption maximum (7.40% at 400 nm; 1.44% at 514 nm and 2.91% at 670 nm), indicating that the DSSC using visible light sensitisation of nanocrystalline TiO2 film by Chl-e6 was developed.

  20. Adsorbent synthesis of polypyrrole/TiO2 for effective fluoride removal from aqueous solution for drinking water purification: Adsorbent characterization and adsorption mechanism.

    PubMed

    Chen, Jie; Shu, Chiajung; Wang, Ning; Feng, Jiangtao; Ma, Hongyu; Yan, Wei

    2017-06-01

    More than 20 countries are still suffering problems of excessive fluoride containing water, and greater than 8mg/L fluoride groundwater has been reported in some villages in China. In order to meet the challenge in the drinking water defluoridation engineering, a high efficiency and affinity defluoridation adsorbent PPy/TiO2 composite was designed and synthetized by in-situ chemical oxidative polymerization. Fourier Transform Infrared Spectroscopy (FTIR), X-ray diffraction Investigator (XRD), X-ray photoelectron spectroscopy (XPS), Thermogravimetric analysis (TG), N2 isotherm analysis, Scanning Electron Microscopy (SEM) and Zeta potential analysis were conducted to characterize surface and textural properties of the as-prepared PPy/TiO2, and the possibility of fluoride adsorption was carefully estimated by adsorption isotherm and kinetic studies. Characterization investigations demonstrate the uniqueness of surface and textural properties, such as suitable specific surface area and abundant positively charged nitrogen atoms (N(+)), which indicate the composite is a suitable material for the fluoride adsorption. Adsorption isotherms and kinetics follow better with Langmuir and pseudo-second-order model, respectively. The maximum adsorption capacity reaches 33.178mg/g at 25°C according to Langmuir model, and particular interest was the ability to reduce the concentration of fluoride from 11.678mg/L to 1.5mg/L for drinking water at pH of 7 within 30min. Moreover, the adsorbent can be easily recycled without the loss of adsorption capacity after six cycles, greatly highlighting its outstanding affinity to fluoride, low-cost and novel to be used in the purification of fluoride containing water for drinking. Furthermore, the adsorption mechanism was extensively investigated and discussed by FTIR investigation and batch adsorption studies including effect of pH, surface potential and thermodynamics. The adsorption is confirmed to be a spontaneous and exothermic process

  1. Preparation of Al-Ce hybrid adsorbent and its application for defluoridation of drinking water.

    PubMed

    Liu, Han; Deng, Shubo; Li, Zhijian; Yu, Gang; Huang, Jun

    2010-07-15

    A novel Al-Ce hybrid adsorbent with high sorption capacity for fluoride was prepared through the coprecipitation method in this study, and its preparation conditions were optimized. X-ray diffraction (XRD) and scanning electron microscope (SEM) results showed that the hybrid adsorbent was of amorphous structure and constituted by some aggregated nanoparticles. As the adsorbent had the zero point of zeta potential at pH 9.6, it was very effective in fluoride removal from aqueous solution via electrostatic interaction. The results of sorption experiments including sorption kinetics, isotherms, and the effect of solution pH showed that the sorption of fluoride on the Al-Ce adsorbent was fast and pH-dependent. Especially, the adsorbent had high sorption capacity up to 27.5 mg g(-1) for fluoride at the equilibrium fluoride concentration of 1 mg L(-1), much higher than that of the conventional adsorbents. Fourier transform infrared (FTIR) analysis and zeta potential measurement showed that the hydroxyl groups and the protonated hydroxyl groups on the adsorbent surface were involved in the fluoride adsorption.

  2. Cellulose based cationic adsorbent fabricated via radiation grafting process for treatment of dyes waste water.

    PubMed

    Goel, Narender Kumar; Kumar, Virendra; Misra, Nilanjal; Varshney, Lalit

    2015-11-05

    A cationized adsorbent was prepared from cellulosic cotton fabric waste via a single step-green-radiation grafting process using gamma radiation source, wherein poly[2-(methacryloyloxy) ethyl]trimethylammonium chloride (PMAETC) was covalently attached to cotton cellulose substrate. Radiation grafted (PMAETC-g-cellulose) adsorbent was investigated for removal of acid dyes from aqueous solutions using two model dyes: Acid Blue 25 (AB25) and Acid Blue 74 (AB74). The equilibrium adsorption data was analyzed by Langmuir and Freundlich isotherms, whereas kinetic data was analyzed by pseudo first order, pseudo second order, intra particle diffusion and Boyd's models. The PMAETC-g-cellulose adsorbent with 25% grafting yield exhibited equilibrium adsorption capacities of ∼ 540.0mg/g and ∼ 340.0mg/g for AB25 and AB74, respectively. Linear and nonlinear fitting of adsorption data suggested that the equilibrium adsorption process followed Langmuir adsorption isotherm model, whereas, the kinetic adsorption process followed pseudo-second order model. The multi-linearities observed in the intra-particle kinetic plots suggested that the intraparticle diffusion was not the only rate-controlling process in the adsorption of acid dyes on the adsorbent, which was further supported by Boyd's model. The adsorbent could be regenerated by eluting the adsorbed dye from the adsorbent and could be repeatedly used.

  3. Coordination structure of adsorbed Zn(II) at Water-TiO2 interfaces

    SciTech Connect

    He, G.; Pan, G.; Zhang, M.; Waychunas, G.A.

    2011-01-15

    The local structure of aqueous metal ions on solid surfaces is central to understanding many chemical and biological processes in soil and aquatic environments. Here, the local coordination structure of hydrated Zn(II) at water-TiO{sub 2} interfaces was identified by extended X-ray absorption fine structure (EXAFS) and X-ray absorption near-edge structure (XANES) spectroscopy combined with density functional theory (DFT) calculations. A nonintegral coordination number of average {approx}4.5 O atoms around a central Zn atom was obtained by EXAFS analysis. DFT calculations indicated that this coordination structure was consistent with the mixture of 4-coordinated bidentate binuclear (BB) and 5-coordinated bidentate mononuclear (BM) metastable equilibrium adsorption (MEA) states. The BB complex has 4-coordinated Zn, while the monodentate mononuclear (MM) complex has 6-coordinated Zn, and a 5-coordinated adsorbed Zn was found in the BM adsorption mode. DFT calculated energies showed that the lower-coordinated BB and BM modes were thermodynamically more favorable than the higher-coordinated MM MEA state. The experimentally observed XANES fingerprinting provided additional direct spectral evidence of 4- and 5-coordinated Zn-O modes. The overall spectral and computational evidence indicated that Zn(II) can occur in 4-, 5-, and 6-oxygen coordinated sites in different MEA states due to steric hindrance effects, and the coexistence of different MEA states formed the multiple coordination environments.

  4. A Comprehensive Study of Hydrogen Adsorbing to Amorphous Water ice: Defining Adsorption in Classical Molecular Dynamics

    NASA Astrophysics Data System (ADS)

    Dupuy, John L.; Lewis, Steven P.; Stancil, P. C.

    2016-11-01

    Gas-grain and gas-phase reactions dominate the formation of molecules in the interstellar medium (ISM). Gas-grain reactions require a substrate (e.g., a dust or ice grain) on which the reaction is able to occur. The formation of molecular hydrogen (H2) in the ISM is the prototypical example of a gas-grain reaction. In these reactions, an atom of hydrogen will strike a surface, stick to it, and diffuse across it. When it encounters another adsorbed hydrogen atom, the two can react to form molecular hydrogen and then be ejected from the surface by the energy released in the reaction. We perform in-depth classical molecular dynamics simulations of hydrogen atoms interacting with an amorphous water-ice surface. This study focuses on the first step in the formation process; the sticking of the hydrogen atom to the substrate. We find that careful attention must be paid in dealing with the ambiguities in defining a sticking event. The technical definition of a sticking event will affect the computed sticking probabilities and coefficients. Here, using our new definition of a sticking event, we report sticking probabilities and sticking coefficients for nine different incident kinetic energies of hydrogen atoms [5-400 K] across seven different temperatures of dust grains [10-70 K]. We find that probabilities and coefficients vary both as a function of grain temperature and incident kinetic energy over the range of 0.99-0.22.

  5. Selective concentration of aromatic bases from water with a resin adsorbent

    USGS Publications Warehouse

    Stuber, H.A.; Leenheer, J.A.

    1983-01-01

    Aromatic bases are concentrated from water on columns of a resin adsorbent and recovered by aqueous-acid elution. The degree of concentration attainable depends on the ratio of the capacity factor (k) of the neutral form of the amine to that of the ionized form. Capacity factors of ionic forms of amines on XAD-8 resin (a methylacrylic ester polymer) are greater than zero, ranging from 20 to 250 times lower than those of their neutral forms; they increase with increasing hydrophobicity of the amine. Thus, desorption by acid is an edition (k during desorption >0) rather than a displacement (k during desorption = 0) process. The degree of concentration attainable on XAD-8 resin varies with the hydrophobicity of the amine, being limited for hydrophilic solutes (for example, pyridine) by small neutral-form k's, reaching a maximum for amines of intermediate hydrophobicity (for example, quinoline), and decreasing for more hydrophobc solutes (for example, acridine) because of their large ionic-form k's.

  6. David Adler Lectureship Award Talk: Friction and energy dissipation mechanisms in adsorbed molecules and molecularly thin films

    NASA Astrophysics Data System (ADS)

    Krim, Jacqueline

    2015-03-01

    Studies of the fundamental origins of friction have undergone rapid progress in recent years, with the development of new experimental and computational techniques for measuring and simulating friction at atomic length and time scales. The increased interest has sparked a variety of discussions and debates concerning the nature of the atomic-scale and quantum mechanisms that dominate the dissipative process by which mechanical energy is transformed into heat. Measurements of the sliding friction of physisorbed monolayers and bilayers can provide information on the relative contributions of these various dissipative mechanisms. Adsorbed films, whether intentionally applied or present as trace levels of physisorbed contaminants, moreover are ubiquitous at virtually all surfaces. As such, they impact a wide range of applications whose progress depends on precise control and/or knowledge of surface diffusion processes. Examples include nanoscale assembly, directed transport of Brownian particles, material flow through restricted geometries such as graphene membranes and molecular sieves, passivation and edge effects in carbon-based lubricants, and the stability of granular materials associated with frictional and frictionless contacts. Work supported by NSFDMR1310456.

  7. Removal of microcystin-LR from drinking water using a bamboo-based charcoal adsorbent modified with chitosan.

    PubMed

    Zhang, Hangjun; Zhu, Guoying; Jia, Xiuying; Ding, Ying; Zhang, Mi; Gao, Qing; Hu, Ciming; Xu, Shuying

    2011-01-01

    A new kind of low-cost syntactic adsorbent from bamboo charcoal and chitosan was developed for the removal of microcystin-LR from drinking water. Removal efficiency was higher for the syntactic adsorbent when the amount of bamboo charcoal was increased. The optimum dose ratio of bamboo charcoal to chitosan was 6:4, and the optimum amount was 15 mg/L; equilibrium time was 6 hr. The adsorption isotherm was non-linear and could be simulated by the Freundlich model (R2 = 0.9337). Adsorption efficiency was strongly affected by pH and natural organic matter (NOM). Removal efficiency was 16% higher at pH 3 than at pH 9. Efficiency rate was reduced by 15% with 25 mg/L NOM (UV254 = 0.089 cm(-1)) in drinking water. This study demonstrated that the bamboo charcoal modified with chitosan can effectively remove microcystin-LR from drinking water.

  8. Adsorption removal of cesium from drinking waters: a mini review on use of biosorbents and other adsorbents.

    PubMed

    Liu, Xiang; Chen, Guan-Ru; Lee, Duu-Jong; Kawamoto, Tohru; Tanaka, Hisashi; Chen, Man-Li; Luo, Yu-Kuo

    2014-05-01

    Radiocesium (Cs) removal from waters becomes an emerging issue after the Fukushima Daiichi Nuclear Power Plant Disaster, during which a total of approximately 3.3×10(16) Bq Cs was released to contaminate the environment. This mini-review provided a summary on literature works to develop efficient adsorbent for removing Cs from waters. Adsorbent made of raw and modified minerals, composites particles, and biosorbents that are highly specific to Cs in the presence of other alkali and alkali earth metals were summarized. Development of Prussian blue (PB) nanoparticles on Cs removal and its potential use in drinking waterworks was discussed. This review is a unique report for adsorption removal of Cs from contaminated waters.

  9. Tribochemical synthesis of nano-lubricant films from adsorbed molecules at sliding solid interface: Tribo-polymers from α-pinene, pinane, and n-decane

    NASA Astrophysics Data System (ADS)

    He, Xin; Barthel, Anthony J.; Kim, Seong H.

    2016-06-01

    The mechanochemical reactions of adsorbed molecules at sliding interfaces were studied for α-pinene (C10H16), pinane (C10H18), and n-decane (C10H22) on a stainless steel substrate surface. During vapor phase lubrication, molecules adsorbed at the sliding interface could be activated by mechanical shear. Under the equilibrium adsorption condition of these molecules, the friction coefficient of sliding steel surfaces was about 0.2 and a polymeric film was tribochemically produced. The synthesis yield of α-pinene tribo-polymers was about twice as much as pinane tribo-polymers. In contrast to these strained bicyclic hydrocarbons, n-decane showed much weaker activity for tribo-polymerization at the same mechanical shear condition. These results suggested that the mechanical shear at tribological interfaces could induce the opening of the strained ring structure of α-pinene and pinane, which leads to polymerization of adsorbed molecules at the sliding track. On a stainless steel surface, such polymerization reactions of adsorbed molecules do not occur under typical surface reaction conditions. The mechanical properties and boundary lubrication efficiency of the produced tribo-polymer films are discussed.

  10. Application of ultradisperse magnetic adsorbents for removal of small concentrations of pollutants from large volumes of water

    NASA Astrophysics Data System (ADS)

    Nechitailo, Galina S.; Kuznetsov, Anatoli; Kuznetsov, Oleg

    2016-07-01

    Pollution of natural bodies of water (rivers, lakes, ground water, etc) is unfortunately very common, both from natural sources like volcanic activity; and, even more importantly, from human activity, including disposal of industrial and municipal waste, mining, etc. Many toxic substances are harmful for humans and other organisms even in very low concentrations (e.g., less than 1 µg/L of cadmium is harmful, for Hg it is 0.5 µg/L, for phenol - 1 µg/L), and can remain in water for decades or longer. Cleaning large volumes of water even from low concentrations of pollutants is a challenging technological task and is very expensive. We propose to use suspension of ultradisperse magnetic adsorbents, for example, nanostructured ferro-carbon particles, produced by plasmachemical technique, for removing small concentrations of pollutants from large volumes of water. The suspension is introduced into the water. Due to their small sizes and densities similar to water (we measured the density of FC-4 ferro-carbon to be about 1 g/cm3; presumably due to porosity) the particles do not sediment for a long time (hours, days or longer), move due to Brownian motion and adsorb a variety of substances from the water. The particle surface can be modified to provide selectivity of the adsorption. Sorption capacities of ferro-carbon adsorbents is in dozens of percent. Therefore, to collect 1 kg of a pollutant, 2 to 20 kg of the adsorbents is required. Then the particles with the adsorbed contaminant can be collected (e.g., downstream of the river) using a variety of magnetic traps. The traps can consist of ferromagnetic wires and permanent magnets, a variety of simple and inexpensive designs are available. As a model system, the kinetics of adsorption of a highly diluted (0.002 mg/ml) aqueous solution of a low molecular weight compound (toluidine blue) by a small concentration of a ferro-carbon powder (FC-4) was studied by spectrophotometry. Before each measurement, the particles

  11. Novel insights in Al-MCM-41 precursor as adsorbent for regulated haloacetic acids and nitrate from water.

    PubMed

    Bruzzoniti, Maria Concetta; De Carlo, Rosa Maria; Sarzanini, Corrado; Caldarola, Dario; Onida, Barbara

    2012-11-01

    High concentration of NO (3) (-) in groundwater has raised concern over possible contamination of drinking water supplies. In addition, the formation of haloacetic acids (HAAs) as by-products during disinfection with chlorine-based agents is still a relevant issue, since HAAs pose serious health hazard. In this work, we investigated the affinity of a precursor of Al-MCM-41 (a mesostructured hexagonal aluminosilicate containing the template surfactant) towards nitrate and HAAs, for its possible application in the removal of these pollutants from natural and drinking waters. Additionally, adsorption kinetics and isotherms were studied. The adsorbent was synthesized using cetyltrimethylammonium bromide as surfactant and characterized by physico-chemical techniques. Simulated drinking water was spiked with the EPA-regulated HAAs (monochloroacetic (MCAA), monobromoacetic (MBAA), dichloroacetic (DCAA), dibromoacetic (DBAA), and trichloroacetic (TCAA) acids) and placed in contact with the adsorbent. The effect of matrix composition was studied. Adsorption kinetic studies were performed testing three kinetics models. For the adsorption studies, three adsorption isotherm approaches have been tested to experimental data. The pollutant recoveries were evaluated by suppressed ion chromatography. The affinity of the adsorbent was TCAA = DBAA = DCAA > MBAA > MCAA with DCAA, DBAA, and TCAA completely removed. A removal as high as 77 % was achieved for 13 mg/L nitrate. The adsorption isotherms of NO (3) (-) and monochloroacetic acid can be modeled by the Freundlich equation, while their adsorption kinetics follow a pseudo-second-order rate mechanism. The adsorbent exhibited high affinity towards HAAs in simulated drinking water even at relevant matrix concentrations, suggesting its potential application for water remediation technologies.

  12. A new polymeric ionic liquid-based magnetic adsorbent for the extraction of inorganic anions in water samples.

    PubMed

    Chen, Lei; Huang, Xiaojia; Zhang, Yong; Yuan, Dongxing

    2015-07-17

    In this work, a novel type of polymeric ionic liquid (PIL)-based magnetic adsorbent was successfully synthesized and applied for the extraction and determination of seven inorganic anions in water samples by coupling with ion chromatography. The new adsorbent was synthesized by simple free radical copolymerization of 1-ally-3-vinylimidazolium chloride, ethylene glycol dimethacrylate and silica-coated magnetite. The adsorbent exhibited well-defined core-shell structure and good magnetic response ability. Furthermore, due to the presence of abundant anion-exchange groups in the PIL, the adsorbent displayed expected extraction performance for anions including F(-), Cl(-), Br(-), NO2(-), NO3(-), PO4(3-) and SO4(2-). Various experimental parameters that could affect the extraction performance, such as the amount of adsorbent, desorption solvent, extraction and desorption time, the pH value of sample solution were investigated in detail. Under the optimized conditions, low limits of detection (S/N=3) and quantification limits (S/N=10) of the proposed method for the target anions were achieved within the range of 0.061-0.73μg/L and 0.19-2.41μg/L, respectively. The repeatability was investigated by evaluating the intra-day, inter-day precisions and batch-to-batch reproducibility with relative standard deviations (RSDs) lower than 11%. At the same time, the method also showed high extraction speed, simplicity, practicality and low cost for the extraction inorganic anions. Finally, the proposed method was used to detect anions in different water samples successfully. The recoveries were in the range of 71.0-111%, and the RSDs were below 12% in the all cases.

  13. Water absorbance and thermal properties of sulfated wheat gluten films

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Wheat gluten films of varying thicknesses formed at 30C to 70C were treated with cold sulfuric acid to produce sulfated gluten films. Chemical, thermal, thermal stability, and water uptake properties were characterized for neat and sulfated films. The sulfated gluten films were able ...

  14. Development of high efficiency silica coated β-cyclodextrin polymeric adsorbent for the removal of emerging contaminants of concern from water.

    PubMed

    Bhattarai, Bikash; Muruganandham, M; Suri, Rominder P S

    2014-05-30

    This article reports the removal of several emerging contaminants (ECs) from water using novel adsorbent comprising of β-cyclodextrin (β-CD) coated on silica. Fourteen different adsorbents were synthesized under different experimental conditions using two different crosslinking agents (hexamethylene diisocyanate (HMDI) and epichlorohydrin (EPI)) and co-polymers (glycidoxypropyl trimethoxysilane (GPTS) and aminopropyl triethoxysilane (APTES). The adsorption capacities of the synthesized adsorbents were initially evaluated using 17β-estradiol, perfluorooctanoic acid (PFOA), and bisphenol-A (BPA) as adsorbates. The adsorbent prepared by using HMDI as crosslinking agent with DMSO as solvent was observed to perform the best, and removed more than 90% of 17β-estradiol, PFOA, and BPA. Furthermore, the β-CD loading on the ECs removal was studied which showed that the adsorbate removal increases with increase in loading of β-CD on the substrate. The best adsorbent was resynthesized in seven batches and its performance was reproducible for the removal of ten steroid hormones. The adsorbent showed very good regeneration potential for four successive adsorption-regeneration cycles to remove steroid hormones and PFOA. A plausible mechanism of adsorption is proposed. The synthesized best adsorbent is characterized using FTIR, HR-TEM, TGA and nitrogen adsorption analysis. The TGA results showed that the adsorbent has thermal stability of upto 300°C.

  15. Expanded graphite loaded with lanthanum oxide used as a novel adsorbent for phosphate removal from water: performance and mechanism study.

    PubMed

    Zhang, Ling; Gao, Yan; Li, Mengxue; Liu, Jianyong

    2015-01-01

    A novel adsorbent of expanded graphite (EG) loaded with lanthanum oxide (EG-LaO) was prepared for phosphate removal from water and characterized by scanning electron microscopy (SEM) and Fourier transform infrared (FT-IR) spectroscopy. The effects of impregnation time, La3+ concentration, activation time, and activation temperature on the phosphate removal performance of the adsorbent were studied for optimization of preparation conditions. Isothermal adsorption studies suggested that the Langmuir model fits the experimental data well. Adsorption kinetics investigation showed that the pseudo-second-order model fits the experimental data quite well, indicating that the adsorption process is mainly a process of chemical adsorption, and chloride ions compete to react with the active sites of the adsorbent but do not prevent phosphate from adsorbing onto EG-LaO. The adsorption mechanism studies were performed by a pH dependence study of the adsorption amount. The results demonstrated that the probable mechanisms of phosphate adsorption on EG-LaO were electrostatic and Lewis acid-base interactions in addition to ion exchange.

  16. Toward 3D graphene oxide gels based adsorbents for high-efficient water treatment via the promotion of biopolymers.

    PubMed

    Cheng, Chong Sage; Deng, Jie; Lei, Bei; He, Ai; Zhang, Xiang; Ma, Lang; Li, Shuang; Zhao, Changsheng

    2013-12-15

    Recent studies showed that graphene oxide (GO) presented high adsorption capacities to various water contaminants. However, the needed centrifugation after adsorption and the potential biological toxicity of GO restricted its applications in wastewater treatment. In this study, a facile method is provided by using biopolymers to mediate and synthesize 3D GO based gels. The obtained hybrid gels present well-defined and interconnected 3D porous network, which allows the adsorbate molecules to diffuse easily into the adsorbent. The adsorption experiments indicate that the obtained porous GO-biopolymer gels can efficiently remove cationic dyes and heavy metal ions from wastewater. Methylene blue (MB) and methyl violet (MV), two cationic dyes, are chosen as model adsorbates to investigate the adsorption capability and desorption ratio; meanwhile, the influence of contacting time, initial concentration, and pH value on the adsorption capacity of the prepared GO-biopolymer gels are also studied. The GO-biopolymer gels displayed an adsorption capacity as high as 1100 mg/g for MB dye and 1350 mg/g for MV dye, respectively. Furthermore, the adsorption kinetics and isotherms of the MB were studied in details. The experimental data of MB adsorption fitted well with the pseudo-second-order kinetic model and the Langmuir isotherm, and the results indicated that the adsorption process was controlled by the intraparticle diffusion. Moreover, the adsorption data revealed that the porous GO-biopolymer gels showed good selective adsorbability to cationic dyes and metal ions.

  17. From illite/smectite clay to mesoporous silicate adsorbent for efficient removal of chlortetracycline from water.

    PubMed

    Wang, Wenbo; Tian, Guangyan; Zong, Li; Zhou, Yanmin; Kang, Yuru; Wang, Qin; Wang, Aiqin

    2017-01-01

    A series of mesoporous silicate adsorbents with superior adsorption performance for hazardous chlortetracycline (CTC) were sucessfully prepared via a facile one-pot hydrothermal reaction using low-cost illite/smectite (IS) clay, sodium silicate and magnesium sulfate as the starting materials. In this process, IS clay was "teared up" and then "rebuilt" as new porous silicate adsorbent with high specific surface area of 363.52m(2)/g (about 8.7 folds higher than that of IS clay) and very negative Zeta potential (-34.5mV). The inert SiOSi (Mg, Al) bonds in crystal framework of IS were broken to form Si(Al) O(-) groups with good adsorption activity, which greatly increased the adsorption sites served for holding much CTC molecules. Systematic evaluation on adsorption properties reveals the optimal silicate adsorbent can adsorb 408.81mg/g of CTC (only 159.7mg/g for raw IS clay) and remove 99.3% (only 46.5% for raw IS clay) of CTC from 100mg/L initial solution (pH3.51; adsorption temperature 30°C; adsorbent dosage, 3g/L). The adsorption behaviors of CTC onto the adsorbent follows the Langmuir isotherm model, Temkin equation and pseudo second-order kinetic model. The mesopore adsorption, electrostatic attraction and chemical association mainly contribute to the enhanced adsorption properties. As a whole, the high-efficient silicate adsorbent could be candidates to remove CTC from the wastewater with high amounts of CTC.

  18. Abiotic properties of landfill leachate controlling arsenic release from drinking water adsorbents.

    PubMed

    Stuckman, Mengling Y; Lenhart, John J; Walker, Harold W

    2011-10-15

    In this study, As leaching from five arsenic bearing solid residuals (ABSRs) comprised of the iron hydroxide adsorbent Bayoxide E33 used in long-term operations was evaluated in leaching trials using California Waste Extraction Test (CalWET) and Toxicity Characteristic Leaching Protocol (TCLP) leachate solutions, a landfill leachate (LL), and synthetic leachate (SL). The initial As loading of the media, which reflects the influence of source water chemistry and varying treatment conditions at the point of removal, strongly influenced the magnitude of As release. The chemical composition of the leachate also influenced As release and demonstrated the relative importance of different release mechanisms, namely media dissolution, pH-dependent sorption/desorption, and ion exchange. The CalWET solution, which partially dissolved the iron-based media, resulted in 100 times more As release than did the TCLP solution, which did not dissolve the media. The LL had a higher pH than the TCLP solution, and even though its organic carbon content was lower it tended to release more As. Tests with the SL were conducted to determine the influence of variations in leachate pH, phosphate, bicarbonate, sulfate, silicate, and natural organic matter (NOM). Release increased at high pH, in the presence of high concentrations of phosphate and bicarbonate, and in the presence of high NOM concentrations. For pH, this reflects the pH-dependence of sorption reactions, whereas for the anions and NOM, direct competition appeared important. Similar to the CalWET solution, excess NOM dissolved portions of the media thereby facilitating As release. In general, our results suggest that estimating As release into landfills will remain a challenge as it depends upon As loading, which reflects site-specific properties, and the composition of the leachate, which varies from landfill to landfill.

  19. Pore distribution effect of activated carbon in adsorbing organic micropollutants from natural water.

    PubMed

    Ebie, K; Li, F; Azuma, Y; Yuasa, A; Hagishita, T

    2001-01-01

    Adsorption isotherms of organic micropollutants in coexistence with natural organic matter (NOM) were analyzed to evaluate the impacts of pore size distribution of activated carbon (AC) on the competition effects of the NOM. Single solute adsorption experiments and simultaneous adsorption experiments with NOM contained in a coagulation-pretreated surface water were performed for four agricultural chemicals and three coal-based activated carbons (ACs) having different pore distributions. The results showed that, for all the carbons used, the adsorption capacity of the chemicals was reduced distinctly in the presence of NOM. Such a reduction was more apparent for AC with a larger portion of small pores suitable for the adsorption of small organic molecules and for the agricultural chemicals with a more hydrophilic nature. Ideal adsorbed solution theory (IAST) incorporated with the Freundlich isotherm expression (IAST-Freundlich model) could not interpret the impact of NOM on the adsorption capacity of the chemicals unless a pore blockage effect caused by the adsorption of NOM was also considered. By taking into account this effect, the adsorption isotherm of the chemicals in the presence of NOM was well described, and the capacity reduction caused by the NOM was quantitatively assessed from the viewpoints of the site competition and the pore blockage. Analytical results clearly indicated that pore blockage was an important competition mechanism that contributed to 10-99% of the total capacity reductions of the chemicals, the level depended greatly on the ACs, the chemicals and the equilibrium concentrations, and could possibly be alleviated by broadening the pore size distributions of the ACs to provide a large volume percentage for pores with sizes above 30 A.

  20. Novel Anionic Clay Adsorbents for Boiler-Blow Down Waters Reclaim and Reuse

    SciTech Connect

    Muhammad Sahimi; Theodore T. Tsotsis

    2005-12-01

    Our goal in this study is to utilize novel anionic clay sorbents for treating and reclaiming/reusing power-plant effluents, in particular, boiler blow-down waters containing heavy metals, such as As and Se. Developing and using novel materials for such application is dictated by the challenge posed by reclaiming and recycling these too-clean-to-clean effluent streams, generated during electricity production, whose contaminant levels are in the ppm/ppb (or even less) trace levels. During the study model blow-down streams have been treated in batch experiments. Adsorption isotherms as a function of pH/temperature have been established for both As and Se. Adsorption rates have also measured as a function of concentration, temperature, pH, and space time. For both the equilibrium and rate measurements, we have studied the As/Se interaction, and competition from background anions. A homogeneous surface diffusion model is used to describe the experimental kinetic data. The estimated diffusivity values are shown to depend on the particle size. On the other hand, a model taking into account the polycrystalline nature of these adsorbent particles, and the presence of an intercrystallite porous region predicts correctly that the surface diffusivity is particle size independent. A mathematical model to describe flow experiments in packed-beds has also been developed during phase I of this project. The goal is to validate this model with flow experiments in packed-beds during the phase II of this project, to determine the adsorption capacity under flow conditions, and to compare it with the capacity estimated from the adsorption isotherms determined from the batch studies.

  1. Water-based oxygen-sensor films.

    PubMed

    Habibagahi, Arezoo; Mébarki, Youssef; Sultan, Yasir; Yap, Glenn P A; Crutchley, Robert J

    2009-08-01

    The luminescent cyclometalated iridium complex [Ir(fppy)(2)(t-Bu-iCN)(2)]CF(3)SO(3), 1 (fppy = 4-(2-pyridyl)benzaldehyde, and t-Bu-iCN = tert-butyl isocyanide), was synthesized and characterized by X-ray crystallography and (1)H NMR, absorption, and emission spectroscopies. Complex 1 was quantitatively bound to the water-soluble amine-functionalized polymer Silamine D208-EDA by reductive amination, to produce 2. The quantum yield of emission and excited state lifetime of 2 (varphi(em) = 0.23 and tau = 20.6 mus) are comparable to that of the model complex [Ir(tpy)(2)(t-Bu-iCN)(2)]CF(3)SO(3), 3 (tpy = 2-(p- tolyl) pyridine) with varphi(em) = 0.28 and tau = 35.6 mus. Aqueous blends of 2 with Silamine and colloidal microcrystalline cellulose (MC) were used to prepare oxygen-sensor films. Oxygen sensitivities of these films were determined as a function of Silamine:MC ratio and obeyed Stern-Volmer kinetics. The optimum oxygen-sensor film composition was 2 in 1:1 Silamine:MC, which had an oxygen sensitivity of 0.502 over an atmospheric pressure range of 0.007-45 psi. Temperature sensitivity (percentage loss of intensity per degrees C) of this film was determined to be -1.1 and -1.4% degrees C(-1) at vacuum and 1 bar atmospheric pressure, respectively. These results were compared to those of films incorporating dispersions of 1 and 3. Luminescence microscopy of 9:1, 1:1, and 1:5 Silamine:MC films of 2 show that the charged iridium complex in 2 associates with the surface of MC and lifetime measurements of these films show an increase in lifetime with increasing MC fraction. The optimum quenching sensitivity observed for the 1:1 Silamine:MC film suggests that the diffusion of oxygen must decrease with increasing fraction of MC and thereby decrease oxygen sensitivity. These novel materials offer an environmentally friendly alternative to the preparation of oxygen-sensor films.

  2. Ionic strength affects tertiary structure and aggregation propensity of a monoclonal antibody adsorbed to silicone oil-water interfaces.

    PubMed

    Gerhardt, Alana; Bonam, Kurt; Bee, Jared S; Carpenter, John F; Randolph, Theodore W

    2013-02-01

    Therapeutic proteins formulated in prefilled syringes lubricated with silicone oil come in contact with silicone oil-water interfaces for their entire shelf lives. Thus, the interactions between protein and silicone oil were studied to determine the effect of silicone oil on a monoclonal antibody's stability, both at the interface and in the bulk solution. The influence of ionic strength on these interactions was also investigated through the addition of various monovalent and divalent salts to sample formulations. The tertiary structure of the antibody was perturbed when it adsorbed to the silicone oil-water interface in solutions at low ionic strength. However, the tertiary structure of the antibody at the interface was not perturbed when the ionic strength of the formulation was increased. Even at low ionic strength, the secondary structure of the antibody adsorbed to the silicone oil-water interface was retained, suggesting that at low ionic strength, the adsorbed antibody assumes a molten globule-like conformation. This partially unfolded species was aggregation-prone, especially during agitation. Silicone oil-induced aggregation of the antibody was inhibited at higher ionic strength.

  3. Novel deep eutectic solvent-functionalized carbon nanotubes adsorbent for mercury removal from water.

    PubMed

    AlOmar, Mohamed Khalid; Alsaadi, Mohammed Abdulhakim; Jassam, Taha M; Akib, Shatirah; Ali Hashim, Mohd

    2017-07-01

    Due to the interestingly tolerated physicochemical properties of deep eutectic solvents (DESs), they are currently in the process of becoming widely used in many fields of science. Herein, we present a novel Hg(2+) adsorbent that is based on carbon nanotubes (CNTs) functionalized by DESs. A DES formed from tetra-n-butyl ammonium bromide (TBAB) and glycerol (Gly) was used as a functionalization agent for CNTs. This novel adsorbent was characterized using Raman spectroscopy, Fourier transform infrared (FTIR) spectroscopy, XRD, FESEM, EDX, BET surface area, and Zeta potential. Later, Hg(2+) adsorption conditions were optimized using response surface methodology (RSM). A pseudo-second order model accurately described the adsorption of Hg(2+). The Langmuir and Freundlich isotherm models described the absorption of Hg(2+) on the novel adsorbent with acceptable accuracy. The maximum adsorption capacity was found to be 177.76mg/g.

  4. Removal of 1,2-dichlorobenzene from water emulsion using adsorbent catalysts and its regeneration.

    PubMed

    Netskina, O V; Tayban, E S; Moiseenko, A P; Komova, O V; Mukha, S A; Simagina, V I

    2015-03-21

    Purification of emulsions of 1,2-dichlorobenzene (1,2-DCB) by carbon-based adsorbent catalysts has been studied. The cycle of purification includes: (1) adsorption of 1,2-DCB from the aqueous phase and (II) reductive regeneration by hydrodechlorination of the adsorbed 1,2-DCB by molecular hydrogen in the liquid phase. 1,2-DCB adsorption from aqueous solutions has been found to proceed by the mechanism of volume filling of pores. The rate of hydrodechlorination was shown to correlate with the particle size of the active component: the finer the particles, the higher the activity of the adsorbent catalyst. Pd/FAS with an average Pd particle size of 2.8 nm was found to be the most efficient catalyst.

  5. Optimal Electromagnetic (EM) Geophysical Techniques to Map the Concentration of Subsurface Ice and Adsorbed Water on Mars and the Moon

    NASA Astrophysics Data System (ADS)

    Stillman, D. E.; Grimm, R. E.

    2013-12-01

    Water ice is ubiquitous in our Solar System and is a probable target for planetary exploration. Mapping the lateral and vertical concentration of subsurface ice from or near the surface could determine the origin of lunar and martian ice and quantify a much-needed resource for human exploration. Determining subsurface ice concentration on Earth is not trivial and has been attempted previously with electrical resistivity tomography (ERT), ground penetrating radar (GPR), airborne EM (AEM), and nuclear magnetic resonance (NMR). These EM geophysical techniques do not actually detect ice, but rather the absence of unfrozen water. This causes a non-unique interpretation of frozen and dry subsurface sediments. This works well in the arctic because most locations are not dry. However, for planetary exploration, liquid water is exceedingly rare and subsurface mapping must discriminate between an ice-rich and a dry subsurface. Luckily, nature has provided a unique electrical signature of ice: its dielectric relaxation. The dielectric relaxation of ice creates a temperature and frequency dependence of the electrical properties and varies the relative dielectric permittivity from ~3.1 at radar frequencies to >100 at low frequencies. On Mars, sediments smaller than silt size can hold enough adsorbed unfrozen water to complicate the measurement. This is because the presence of absorbed water also creates frequency-dependent electrical properties. The dielectric relaxation of adsorbed water and ice can be separated as they have different shapes and frequency ranges as long as a spectrum spanning the two relaxations is measured. The volume concentration of ice and adsorbed water is a function of the strength of their relaxations. Therefore, we suggest that capacitively-coupled dielectric spectroscopy (a.k.a. spectral induced polarization or complex resistivity) can detect the concentration of both ice and adsorbed water in the subsurface. To prove this concept we have collected

  6. Amorphous boron-doped sodium titanates hydrates: Efficient and reusable adsorbents for the removal of Pb(2+) from water.

    PubMed

    di Bitonto, Luigi; Volpe, Angela; Pagano, Michele; Bagnuolo, Giuseppe; Mascolo, Giuseppe; La Parola, Valeria; Di Leo, Paola; Pastore, Carlo

    2017-02-15

    Amorphous titanium hydroxide and boron-doped (B-doped) sodium titanates hydrates were synthetized and used as adsorbents for the removal of Pb(2+) from water. The use of sodium borohydride (NaBH4) and titanium(IV) isopropoxide (TTIP) as precursors permits a very easy synthesis of B-doped adsorbents at 298K. The new adsorbent materials were first chemically characterized (XRD, XPS, SEM, DRIFT and elemental analysis) and then tested in Pb(2+) adsorption batch experiments, in order to define kinetics and equilibrium studies. The nature of interaction between such sorbent materials and Pb(2+) was also well defined: besides a pure adsorption due to hydroxyl interaction functionalities, there is also an ionic exchange between Pb(2+) and sodium ions even working at pH 4.4. Langmuir model presented the best fitting with a maximum adsorption capacity up to 385mg/g. The effect of solution pH and common ions (i.e. Na(+), Ca(2+) and Mg(2+)) onto Pb(2+) sorption were also investigated. Finally, recovery was positively conducted using EDTA. Very efficient adsorption (>99.9%) was verified even using tap water spiked with traces of Pb(2+) (50ppb).

  7. Halloysite Nanotubes as a New Adsorbent for Solid Phase Extraction and Spectrophotometric Determination of Iron in Water and Food Samples

    NASA Astrophysics Data System (ADS)

    Samadi, A.; Amjadi, M.

    2016-07-01

    Halloysite nanotubes (HNTs) have been introduced as a new solid phase extraction adsorbent for preconcentration of iron(II) as a complex with 2,2-bipyridine. The cationic complex is effectively adsorbed on the sorbent in the pH range of 3.5-6.0 and efficiently desorbed by trichloroacetic acid. The eluted complex has a strong absorption around 520 nm, which was used for determination of Fe(II). After optimizing extraction conditions, the linear range of the calibration graph was 5.0-500 μg/L with a detection limit of 1.3 μg/L. The proposed method was successfully applied for the determination of trace iron in various water and food samples, and the accuracy was assessed through the recovery experiments and analysis of a certified reference material (NIST 1643e).

  8. Enhanced adsorption of phenol from water by a novel polar post-crosslinked polymeric adsorbent.

    PubMed

    Zeng, Xiaowei; Fan, Yunge; Wu, Guolin; Wang, Chunhong; Shi, Rongfu

    2009-09-30

    A novel post-crosslinked polymeric adsorbent PDM-2 was prepared by Friedel-Crafts reaction of pendant vinyl groups without external crosslinking agent. Both the specific surface area and the pore volume of starting copolymer PDM-1 increased significantly after post-crosslinking. Batch adsorption runs of phenol from aqueous solution onto PDM-1 and PDM-2 were investigated. Commercial macroporous resins XAD-4 and AB-8 were chosen as the comparison. Experimental results showed that isotherms of phenol adsorption onto these four polymeric adsorbents could be represented by Freundlich model reasonably. PDM-2 exhibited higher adsorption capacity of phenol than other three adsorbents, which resulted from synergistic effect of larger specific surface area and polar groups on the network. The adsorption process for phenol was proved to be exothermic and spontaneous in nature. Thermodynamic parameters such as Gibb's free energy (DeltaG), change in enthalpy (DeltaH) and change in entropy (DeltaS) were calculated. Kinetics studies indicated that phenol uptake onto PDM-1 and PDM-2 followed the pseudo-second order model and the intraparticle diffusion process was a rate-controlling step. Column adsorption runs demonstrated that nearly 100% regeneration efficiency for PDM-2 by 3BV industrial alcohol and the adsorbate phenol can be easily recovered by further distilling. Continuous column adsorption-regeneration cycles indicated negligible capacity loss of PDM-2 during operation.

  9. In situ STM imaging of bis-3-sodiumsulfopropyl-disulfide molecules adsorbed on copper film electrodeposited on Pt(111) single crystal electrode.

    PubMed

    Tu, HsinLing; Yen, PoYu; Chen, Sihzih; Yau, ShuehLin; Dow, Wei-Ping; Lee, Yuh-Lang

    2011-06-07

    The adsorption of bis-3-sodiumsulfopropyldi-sulfide (SPS) on metal electrodes in chloride-containing media has been intensively studied to unveil its accelerating effect on Cu electrodeposition. Molecular resolution scanning tunneling microscopy (STM) imaging technique was used in this study to explore the adsorption and decomposition of SPS molecules concurring with the electrodeposition of copper on an ordered Pt(111) electrode in 0.1 M HClO(4) + 1 mM Cu(ClO(4))(2) + 1 mM KCl. Depending on the potential of Pt(111), SPS molecules could react, adsorb, and decompose at chloride-capped Cu films. A submonolayer of Cu adatoms classified as the underpotential deposition (UPD) layer at 0.4 V (vs Ag/AgCl) was completely displaced by SPS molecules, possibly occurring via RSSR (SPS) + Cl-Cu-Pt → RS(-)-Pt(+) + RS(-) (MPS) + Cu(2+) + Cl(-), where MPS is 3-mercaptopropanesulfonate. By contrast, at 0.2 V, where a full monolayer of Cu was presumed to be deposited, SPS molecules were adsorbed in local (4 × 4) structures at the lower ends of step ledges. Bulk Cu deposition driven by a small overpotential (η < 50 mV) proceeded slowly to yield an atomically smooth Cu deposit at the very beginning (<5 layers). On a bilayer Cu deposit, the chloride adlayer was still adsorbed to afford SPS admolecules arranged in a unique 1D striped phase. SPS molecules could decompose into MPS upon further Cu deposition, as a (2 × 2)-MPS structure was observed with prolonged in situ STM imaging. It was possible to visualize either SPS admolecules in the upper plane or chloride adlayer sitting underneath upon switching the imaging conditions. Overall, this study established a MPS molecular film adsorbed to the chloride adlayer sitting atop the Cu deposit.

  10. Development of a novel polystyrene/metal-organic framework-199 electrospun nanofiber adsorbent for thin film microextraction of aldehydes in human urine.

    PubMed

    Liu, Feilong; Xu, Hui

    2017-01-01

    In this work, electrospun polystyrene/metal-organic frameworks-199 (PS/MOF-199) nanofiber film was synthesized and investigated as a novel adsorbent for thin film microextraction (TFME) of aldehydes in human urine. Some properties of the prepared PS/MOF-199 nanofiber film, including morphology, structure, wettability, solvent stability and extraction performance were studied systematically. Porous fibrous structure, large surface area, good stability, strong hydrophobicity and excellent extraction efficiency were obtained for the film. Based on the PS/MOF-199 film, a thin film microextraction-high performance liquid chromatography (TFME-HPLC) method was developed, and the experimental parameters that affected the extraction and desorption were optimized. Under the optimal conditions, the limits of detection (LODs) were in the range of 4.2-17.3nmolL(-1) for the analysis of six aldehydes. Good linearity was achieved with correlation coefficients (R(2)) being lager than 0.9943. Satisfactory recovery (82-112%) and acceptable reproducibility (relative standard deviation: 2.1-13.3%) were also obtained for the method. The developed TFME-HPLC method has been successfully applied to the analysis of aldehyde metabolites in the urine samples of lung cancer patients and healthy people. The method possesses the advantages of simplicity, rapidity, cost-effective, sensitivity and non-invasion, it provides an alternative tool for the determination of aldehydes in complex sample matrices.

  11. Host and adsorbate dynamics in silicates with flexible frameworks: Empirical force field simulation of water in silicalite

    NASA Astrophysics Data System (ADS)

    Bordat, Patrice; Cazade, Pierre-André; Baraille, Isabelle; Brown, Ross

    2010-03-01

    Molecular dynamics simulations are performed on the pure silica zeolite silicalite (MFI framework code), maintaining via a new force field both framework flexibility and realistic account of electrostatic interactions with adsorbed water. The force field is similar to the well-known "BKS" model [B. W. H. van Beest et al., Phys. Rev. Lett. 64, 1955 (1990)], but with reduced partial atomic charges and reoptimized covalent bond potential wells. The present force field reproduces the monoclinic to orthorhombic transition of silicalite. The force field correctly represents the hydrophobicity of pure silica silicalite, both the adsorption energy, and the molecular diffusion constants of water. Two types of adsorption, specific and weak unspecific, are predicted on the channel walls and at the channel intersection. We discuss molecular diffusion of water in silicalite, deducing a barrier to crossing between the straight and the zigzag channels. Analysis of the thermal motion shows that at room temperature, framework oxygen atoms incurring into the zeolite channels significantly influence the dynamics of adsorbed water.

  12. Immobilized smart RNA on graphene oxide nanosheets to specifically recognize and adsorb trace peptide toxins in drinking water.

    PubMed

    Hu, Xiangang; Mu, Li; Wen, Jianping; Zhou, Qixing

    2012-04-30

    The contaminations of peptide toxins in drinking water lead directly to sickness and even death in both humans and animals. A smart RNA as aptamer is covalently immobilized on graphene oxide to form a polydispersed and stable RNA-graphene oxide nanosheet. RNA-graphene oxide nanosheets can resist nuclease and natural organic matter, and specifically adsorb trace peptide toxin (microcystin-LR) in drinking water. The adsorption data fit the pseudo-second-order kinetics and the Langmuir isotherm model. The adsorption capacity of RNA-graphene oxide nanosheets decreases at extreme pH, temperature, ionic strength and natural organic matter, but it is suitable to adsorb trance pollutants in contaminated drinking water. Compared with other chemical and biological sorbents, RNA-graphene oxide nanosheets present specific and competitive adsorption, and are easily synthesized and regenerated. Aptamer (RNA) covalently immobilized on graphene oxide nanosheets is a potentially useful tool in recognizing, enriching and separating small molecules and biomacromolecules in the purification of contaminated water and the preparation of samples.

  13. Water-insoluble sericin/β-cyclodextrin/PVA composite electrospun nanofibers as effective adsorbents towards methylene blue.

    PubMed

    Zhao, Rui; Wang, Yong; Li, Xiang; Sun, Bolun; Jiang, Ziqiao; Wang, Ce

    2015-12-01

    A novel water-insoluble sericin/β-cyclodextrin/poly (vinyl alcohol) composite nanofiber adsorbent was prepared by electrospinning and followed by thermal crosslinking for removal of cationic dye methylene blue from aqueous solution. Fourier transform infrared spectroscopy and solubility experiments confirmed that sericin and β-cyclodextrin were incorporated into the nanofibers and the crosslinking reaction occurred successfully. Kinetics, isotherms and thermodynamics analysis were studied for adsorption of methylene blue. The adsorption process is better fitted with the pseudo-second-order model and Langmuir isotherm model. The maximum adsorption capacities are 187.97, 229.89, and 261.10mg/g at the temperatures 293, 313 and 333 K, respectively. Thermodynamic parameters showed that methylene blue adsorption was endothermic and spontaneous. In addition, the fiber membrane adsorbent could be easily separated from dye solution and showed high recyclable removal efficiency. All these results suggest that crosslinked sericin/β-cyclodextrin/poly(vinyl alcohol) composite nanofibers could be potential recyclable adsorbents in dye wastewater treatment.

  14. Water-evaporation reduction by duplex films: application to the human tear film.

    PubMed

    Cerretani, Colin F; Ho, Nghia H; Radke, C J

    2013-09-01

    Water-evaporation reduction by duplex-oil films is especially important to understand the physiology of the human tear film. Secreted lipids, called meibum, form a duplex film that coats the aqueous tear film and purportedly reduces tear evaporation. Lipid-layer deficiency is correlated with the occurrence of dry-eye disease; however, in-vitro experiments fail to show water-evaporation reduction by tear-lipid duplex films. We review the available literature on water-evaporation reduction by duplex-oil films and outline the theoretical underpinnings of spreading and evaporation kinetics that govern behavior of these systems. A dissolution-diffusion model unifies the data reported in the literature and identifies dewetting of duplex films into lenses as a key challenge to obtaining significant evaporation reduction. We develop an improved apparatus for measuring evaporation reduction by duplex-oil films including simultaneous assessment of film coverage, stability, and temperature, all under controlled external mass transfer. New data reported in this study fit into the larger body of work conducted on water-evaporation reduction by duplex-oil films. Duplex-oil films of oxidized mineral oil/mucin (MOx/BSM), human meibum (HM), and bovine meibum (BM) reduce water evaporation by a dissolution-diffusion mechanism, as confirmed by agreement between measurement and theory. The water permeability of oxidized-mineral-oil duplex films agrees with those reported in the literature, after correction for the presence of mucin. We find that duplex-oil films of bovine and human meibum at physiologic temperature reduce water evaporation only 6-8% for a 100-nm film thickness pertinent to the human tear film. Comparison to in-vivo human tear-evaporation measurements is inconclusive because evaporation from a clean-water surface is not measured and because the mass-transfer resistance is not characterized.

  15. Potassium Niobate Nanolamina: A Promising Adsorbent for Entrapment of Radioactive Cations from Water

    PubMed Central

    Sun, Jin; Yang, Dongjiang; Sun, Cuihua; Liu, Long; Yang, Shuanglei; (Alec) Jia, Yi; Cai, Rongsheng; Yao, Xiangdong

    2014-01-01

    Processing and managing radioactive waste is a great challenge worldwide as it is extremely difficult and costly; the radioactive species, cations or anions, leaked into the environment are a serious threat to the health of present and future generations. We report layered potassium niobate (K4Nb6O17) nanolamina as adsorbent to remove toxic Sr2+, Ba2+ and Cs+ cations from wastewater. The results show that K4Nb6O17 nanolamina can permanently confine the toxic cations within the interlayer spacing via a considerable deformation of the metastable layered structure during the ion exchange process. At the same time, the nanolaminar adsorbent exhibits prompt adsorption kinetics, high adsorption capacity and selectivity, and superior acid resistance. These merits make it be a promising material as ion exchanger for the removal of radioactive cations from wastewater. PMID:25472721

  16. Phase transitions in films of lung surfactant at the air-water interface.

    PubMed Central

    Nag, K; Perez-Gil, J; Ruano, M L; Worthman, L A; Stewart, J; Casals, C; Keough, K M

    1998-01-01

    45 mN/m. It also induced formation of large amounts of novel, nearly circular domains containing probe above pi of 50 mN/m, these domains being different in appearance than any seen at lower pressures with calcium or higher pressures in the absence of calcium. Surfactant protein-A (SP-A) adsorbed from the subphase onto solvent-spread LSE films, and aggregated condensed domains in presence of calcium. This study indicates that spread or adsorbed lung surfactant films can undergo expanded to condensed, and possibly other, phase transitions at the air-water interface as lateral packing density increases. These phase transitions are affected by divalent cations and SP-A in the subphase, and possibly by loss of material from the surface upon cyclic compression and expansion. PMID:9635752

  17. Functionalized paper--A readily accessible adsorbent for removal of dissolved heavy metal salts and nanoparticles from water.

    PubMed

    Setyono, Daisy; Valiyaveettil, Suresh

    2016-01-25

    Paper, a readily available renewable resource, comprises of interwoven cellulosic fibers, which can be functionalized to develop interesting low-cost adsorbent material for water purification. In this study, polyethyleneimine (PEI)-functionalized paper was used for the removal of hazardous pollutants such as Au and Ag nanoparticles, Cr(VI) anions, Ni(2+), Cd(2+), and Cu(2+) cations from spiked water samples. Compared to untreated paper, the PEI-coated paper showed significant improvement in adsorption capacities toward the pollutants investigated in this study. Kinetics, isotherm models, pH, and desorption studies were carried out to study the adsorption mechanism of pollutants on the adsorbent surface. Adsorption of pollutants was better described by pseudo-second order kinetics and Langmuir isotherm model. Maximum adsorption of anionic pollutants was achieved at pH 5 while that of cations was at pH>6. Overall, the PEI-functionalized paper showed interesting Langmuir adsorption capacities for heavy metal ions such as Cr(VI) (68 mg/g), Ni(2+) (208 mg/g), Cd(2+) (370 mg/g), and Cu(2+) (435 mg/g) ions at neutral pH. In addition, the modified paper was also used to remove Ag-citrate (79 mg/g), Ag-PVP (46 mg/g), Au-citrate (30 mg/g), Au-PVP (17 mg/g) nanoparticles from water. Desorption of NPs from the adsorbent was done by washing with 2 M HCl or thiourea solution, while heavy metal ions were desorbed using 1 M NaOH or HNO3 solution. The modified paper retained its extraction efficiencies upon desorption of pollutants.

  18. Pectin-blended anionic polysaccharide films for cationic contaminant sorption from water.

    PubMed

    Li, Mei; Buschle-Diller, Gisela

    2017-03-17

    Substantial amounts of industrial, agricultural, medical and domestic water worldwide are polluted by different types of contaminants. Removing these contaminants from effluent by adsorbent materials made from abundant, inexpensive polysaccharides is a feasible and promising approach to deal with this problem. In the present study, pectin blended with four other types of anionic polysaccharides, including alginate, carrageenan, xylan and xanthan, were crosslinked with zinc acetate and formed into thin films. In addition, a negatively charged polyelectrolyte, poly(4-styrenesulfonic acid-co-maleic acid) sodium salt (PSSMA) was coated on the film surface with the goal of increasing the capture of cationic contaminants. The average film thickness was measured by a digital micrometer. Surface morphologies and element analysis were obtained by energy dispersive spectroscopy connected with scanning electron microscopy. The swelling ratio and the mechanical properties of the films were investigated in relationship to their composition and PSSMA coating. The sorption of model cationic pollutants clearly improved for coated films and showed to be predominantly based on the interaction of positively and negatively charged groups between film/coating and contaminants.

  19. Water Sorption Isotherm of Pea Starch Edible Films and Prediction Models

    PubMed Central

    Saberi, Bahareh; Vuong, Quan V.; Chockchaisawasdee, Suwimol; Golding, John B.; Scarlett, Christopher J.; Stathopoulos, Costas E.

    2015-01-01

    The moisture sorption isotherm of pea starch films prepared with various glycerol contents as plasticizer was investigated at different storage relative humidities (11%–96% RH) and at 5 ± 1, 15 ± 1, 25 ± 1 and 40 ± 1 °C by using gravimetric method. The results showed that the equilibrium moisture content of all films increased substantially above aw = 0.6. Films plasticized with glycerol, under all temperatures and RH conditions (11%–96%), adsorbed more moisture resulting in higher equilibrium moisture contents. Reduction of the temperature enhanced the equilibrium moisture content and monolayer water of the films. The obtained experimental data were fitted to different models including two-parameter equations (Oswin, Henderson, Brunauer–Emmitt–Teller (BET), Flory–Huggins, and Iglesias–Chirife), three-parameter equations Guggenhiem–Anderson–deBoer (GAB), Ferro–Fontan, and Lewicki) and a four-parameter equation (Peleg). The three-parameter Lewicki model was found to be the best-fitted model for representing the experimental data within the studied temperatures and whole range of relative humidities (11%–98%). Addition of glycerol increased the net isosteric heat of moisture sorption of pea starch film. The results provide important information with estimating of stability and functional characteristics of the films in various environments. PMID:28231096

  20. Why can water cages adsorb aqueous methane? A potential of mean force calculation on hydrate nucleation mechanisms.

    PubMed

    Guo, Guang-Jun; Li, Meng; Zhang, Yi-Gang; Wu, Chang-Hua

    2009-11-28

    By performing constrained molecular dynamics simulations in the methane-water system, we successfully calculated the potential of mean force (PMF) between a dodecahedral water cage (DWC) and dissolved methane for the first time. As a function of the distance between DWC and methane, this is characterized by a deep well at approximately 6.2 A and a shallow well at approximately 10.2 A, separated by a potential barrier at approximately 8.8 A. We investigated how the guest molecule, cage rigidity and the cage orientation affected the PMF. The most important finding is that the DWC itself strongly adsorbs methane and the adsorption interaction is independent of the guests. Moreover, the activation energy of the DWC adsorbing methane is comparable to that of hydrogen bonds, despite differing by a factor of approximately 10% when considering different water-methane interaction potentials. We explain that the cage-methane adsorption interaction is a special case of the hydrophobic interaction between methane molecules. The strong net attraction in the DWC shell with radii between 6.2 and 8.8 A may act as the inherent driving force that controls hydrate formation. A cage adsorption hypothesis for hydrate nucleation is thus proposed and discussed.

  1. Natural cotton fibers as adsorbent for solid-phase extraction of polycyclic aromatic hydrocarbons in water samples.

    PubMed

    Wang, Jianping; Liu, Shengquan; Chen, Chunyan; Zou, Ying; Hu, Huiping; Cai, Qingyun; Yao, Shouzhuo

    2014-07-21

    A natural material, cotton fiber, has been applied as a solid-phase extraction (SPE) adsorbent for sample preparation for the analysis of polycyclic aromatic hydrocarbons (PAH) in water samples using high-performance liquid chromatography. The cotton fiber was used directly without any chemical modifications, which avoided a complex synthesis process and consumption of a large volume of organic solvent. The conditions affecting the extraction efficiency were optimized to achieve high detection sensitivity, and included elution solvent, ultrasonic elution time, extraction time, sample volume, salt concentration and organic modifier addition. Under the optimal conditions, the detection limits for seven PAH compounds could reach up to 0.1-2.0 ng L(-1). The method accuracy was evaluated using recovery measurements in standard spiked samples and good recoveries of 70.69-110.04% with relative standard deviations of less than 10% have been achieved. Consequently, the method developed was successfully applied for determining PAH in environmental samples: snow water, metal-fabrication factory wastewater and Xiangjiang River water, with PAH contents ranging from 13.2 to 83.1 ng L(-1). Therefore, using cotton fiber as a new SPE adsorbent, was easy to prepare, had a low cost and great reusability, and this implies it is a promising method for sample preparation.

  2. Reliable determination of oxygen and hydrogen isotope ratios in atmospheric water vapour adsorbed on 3A molecular sieve.

    PubMed

    Han, Liang-Feng; Gröning, Manfred; Aggarwal, Pradeep; Helliker, Brent R

    2006-01-01

    The isotope ratio of atmospheric water vapour is determined by wide-ranging feedback effects from the isotope ratio of water in biological water pools, soil surface horizons, open water bodies and precipitation. Accurate determination of atmospheric water vapour isotope ratios is important for a broad range of research areas from leaf-scale to global-scale isotope studies. In spite of the importance of stable isotopic measurements of atmospheric water vapour, there is a paucity of published data available, largely because of the requirement for liquid nitrogen or dry ice for quantitative trapping of water vapour. We report results from a non-cryogenic method for quantitatively trapping atmospheric water vapour using 3A molecular sieve, although water is removed from the column using standard cryogenic methods. The molecular sieve column was conditioned with water of a known isotope ratio to 'set' the background signature of the molecular sieve. Two separate prototypes were developed, one for large collection volumes (3 mL) and one for small collection volumes (90 microL). Atmospheric water vapour was adsorbed to the column by pulling air through the column for several days to reach the desired final volume. Water was recovered from the column by baking at 250 degrees C in a dry helium or nitrogen air stream and cryogenically trapped. For the large-volume apparatus, the recovered water differed from water that was simultaneously trapped by liquid nitrogen (the experimental control) by 2.6 per thousand with a standard deviation (SD) of 1.5 per thousand for delta(2)H and by 0.3 per thousand with a SD of 0.2 per thousand for delta(18)O. Water-vapour recovery was not satisfactory for the small volume apparatus.

  3. Water absorption and transport in bis-silane films.

    PubMed

    Wang, Yimin; Wang, Peng; Kohls, Doug; Hamilton, William A; Schaefer, Dale W

    2009-01-07

    Water (D2O) ingress in bis-amino silane and bis-sulfur silane films was studied by in situ neutron reflectivity. Bis-amino silane film absorbs substantially more D2O (33 vol%) than the bis-sulfur silane film (4.6 vol%) at equilibrium. The volume increase (swelling) of both films, however, is much smaller than the total volume of D2O absorbed in the films. The results suggest that the absorbed water exists in two populations: one is dissolved in the polymer matrix (Henry's mode) while the other occupies unrelaxed free volume existing in the polymer (Langmuir mode). The dominance of Langmuir mode accounts for the small film thickness change during the water absorption. Dual-mode sorption is also consistent with the observed two-stage swelling process whereby an initial rapid increase in film thickness is followed by a slower process extending over 11 h.

  4. A novel adsorbent obtained by inserting carbon nanotubes into cavities of diatomite and applications for organic dye elimination from contaminated water.

    PubMed

    Yu, Hongwen; Fugetsu, Bunshi

    2010-05-15

    A novel approach is described for establishing adsorbents for elimination of water-soluble organic dyes by using multi-walled carbon nanotubes (MWCNTs) as the adsorptive sites. Agglomerates of MWCNTs were dispersed into individual tubes (dispersed-MWCNTs) using sodium n-dodecyl itaconate mixed with 3-(N,N-dimethylmyristylammonio)-propanesulfonate as the dispersants. The resultant dispersed-MWCNTs were inserted into cavities of diatomite to form composites of diatomite/MWCNTs. These composites were finally immobilized onto the cell walls of flexible polyurethane foams (PUF) through an in situ PUF formation process to produce the foam-like CNT-based adsorbent. Ethidium bromide, acridine orange, methylene blue, eosin B, and eosin Y were chosen to represent typical water-soluble organic dyes for studying the adsorptive capabilities of the foam-like CNT-based adsorbent. For comparisons, adsorptive experiments were also carried out by using agglomerates of the sole MWCNTs as adsorbents. The foam-like CNT-based adsorbents were found to have higher adsorptive capacities than the CNT agglomerates for all five dyes; in addition, they are macro-sized, durable, flexible, hydrophilic and easy to use. Adsorption isotherms plotted based on the Langmuir equation gave linear results, suggesting that the foam-like CNT-based adsorbent functioned in the Langmuir adsorption manner. The foam-like CNT-based adsorbents are reusable after regeneration with aqueous ethanol solution.

  5. Conformation of adsorbed bovine serum albumin governing its desorption behavior at alumina-water interfaces.

    PubMed

    Urano, H; Fukuzaki, S

    2000-01-01

    The mode of initial adsorption of bovine serum albumin (BSA) onto positively charged Al2O3 particles was studied as a function of surface coverage (theta). The adsorption isotherm of BSA exhibited saturation (theta = 1) and the existence of an inflection point at theta of 0.82. The relative numbers of ionic groups on a BSA molecule interacting with the Al2O3 surface at various theta were monitored by measuring the relative adsorption density of H+ and OH-, ([gamma(H+) - gamma(OH-)]), for BSA-adsorbed Al2O3 using potentiometric titration. The [gamma(H+) - gamma(OH-)] curves for Al2O3, BSA, and BSA-adsorbed Al2O3 at various KNO3 concentrations showed a common intersection point (cip) which was the pH giving the acid-base equivalence point, respectively. Compared with the cip's of Al2O3 (5.6) and BSA (5.2), the cip's of BSA-adsorbed Al2O3 were situated at points corresponding to more alkaline pH values over the theta range of 0.13 to 1.0. These results suggested that negatively charged groups, mainly carboxyl groups, on the BSA molecule electrostatically interacted with the Al2O3 surface. The degree of shift in the cip increased gradually with increasing theta from 0.13 to 0.70, while it decreased markedly over the theta range of 0.82 to 1.0. The variation in the cip reflected the change in the total number of ion pairs formed between BSA molecules and Al2O3. The initial rates of BSA desorption during alkali cleaning were low and almost constant over the theta range of 0.13 to 0.70, but increased markedly at theta higher than 0.82. It is suggested that the conformational changes of BSA adsorbed on Al2O3, involving changes in the relative magnitude of electrostatic interaction forces, occur discretely at theta of approximately 0.8.

  6. Optimization of tetravalent manganese feroxyhyte's negative charge density: A high-performing mercury adsorbent from drinking water.

    PubMed

    Kokkinos, E; Simeonidis, K; Pinakidou, F; Katsikini, M; Mitrakas, M

    2017-01-01

    This study demonstrates an optimization procedure for the development of an Hg-specified adsorbent able to comply with the regulation limit for drinking water of 1μg/L. On this purpose, the synthesis of Mn(IV)-feroxyhyte was modified to achieve high negative charge density by combining alkaline and extreme oxidizing conditions. In particular, precipitation of FeSO4 at pH9 and excess of KMnO4 follows a very fast nucleation step providing a product with very small nanocrystal size (1-2nm), high specific surface area (300m(2)/g) and maximum negative charge density (1.8mmol H(+)/g). The adsorbent was validated for Hg removal in batch experiments and column tests using natural-like water indicating an adsorption capacity as high as 2.5μg/mg at equilibrium concentration 1μg/L under reliable conditions of application. Importantly, the adsorption is an exothermic spontaneous process, resulting in the formation of inner sphere complexes by sharing both A-type and B-type oxygen atoms with the metal surface octahedral as revealed by the X-ray absorption fine structure results.

  7. In situ x-ray photoelectron spectroscopic and density-functional studies of Si atoms adsorbed on a C60 film.

    PubMed

    Onoe, Jun; Nakao, Aiko; Hara, Toshiki

    2004-12-08

    The interaction between C(60) and Si atoms has been investigated for Si atoms adsorbed on a C(60) film using in situ x-ray photoelectron spectroscopy (XPS) and density-functional (DFT) calculations. Analysis of the Si 2p core peak identified three kinds of Si atoms adsorbed on the film: silicon suboxides (SiO(x)), bulk Si crystal, and silicon atoms bound to C(60). Based on the atomic percent ratio of silicon to carbon, we estimated that there was approximately one Si atom bound to each C(60) molecule. The Si 2p peak due to the Si-C(60) interaction demonstrated that a charge transfer from the Si atom to the C(60) molecule takes place at room temperature, which is much lower than the temperature of 670 K at which the charge transfer was observed for C(60) adsorbed on Si(001) and (111) clean surfaces [Sakamoto et al., Phys. Rev. B 60, 2579 (1999)]. The number of electrons transferred between the C(60) molecule and Si atom was estimated to be 0.59 based on XPS results, which is in good agreement with the DFT result of 0.63 for a C(60)Si with C(2v) symmetry used as a model cluster. Furthermore, the shift in binding energy of both the Si 2p and C 1s core peaks before and after Si-atom deposition was experimentally obtained to be +2.0 and -0.4 eV, respectively. The C(60)Si model cluster provides the shift of +2.13 eV for the Si 2p core peak and of -0.28 eV for the C 1s core peak, which are well corresponding to those experimental results. The covalency of the Si-C(60) interaction was also discussed in terms of Mulliken overlap population between them.

  8. Wetting and absorption of water drops on Nafion films.

    PubMed

    Goswami, Sharonmoyee; Klaus, Shannon; Benziger, Jay

    2008-08-19

    Water drops on Nafion films caused the surface to switch from being hydrophobic to being hydrophilic. Contact angle hysteresis of >70 degrees between advancing and receding values were obtained by the Wilhelmy plate technique. Sessile drop measurements were consistent with the advancing contact angle; the sessile drop contact angle was 108 degrees . Water drop adhesion, as measured by the detachment angle on an inclined plane, showed much stronger water adhesion on Nafion than Teflon. Sessile water and methanol drops caused dry Nafion films to deflect. The flexure went through a maximum with time. Flexure increased with contact area of the drop, but was insensitive to the film thickness. Methanol drops spread more on Nafion and caused larger film flexure than water. The results suggest that the Nafion surface was initially hydrophobic but water and methanol drops caused hydrophilic sulfonic acid domains to be drawn to the Nafion surface. Local swelling of the film beneath the water drop caused the film to buckle. The maximum flexure is suggested to result from motion of a water swelling front through the Nafion film.

  9. Artificial neural network modeling in competitive adsorption of phenol and resorcinol from water environment using some carbonaceous adsorbents.

    PubMed

    Aghav, R M; Kumar, Sunil; Mukherjee, S N

    2011-04-15

    This paper illustrates the application of artificial neural network (ANN) for prediction of performances in competitive adsorption of phenol and resorcinol from aqueous solution by conventional and low cost carbonaceous adsorbent materials, such as activated carbon (AC), wood charcoal (WC) and rice husk ash (RHA). The three layer's feed forward neural network with back propagation algorithm in MATLAB environment was used for estimation of removal efficiencies of phenol and resorcinol in bi-solute water environment based on 29 sets of laboratory batch study results. The input parameters used for training of the neural network include amount of adsorbent (g/L), initial concentrations of phenol (mg/L) and resorcinol (mg/L), contact time (h), and pH. The removal efficiencies of phenol and resorcinol were considered as an output of the neural network. The performances of the developed ANN models were also measured using statistical parameters, such as mean error, mean square error, root mean square error, and linear regression. The comparison of the removal efficiencies of pollutants using ANN model and experimental results showed that ANN modeling in competitive adsorption of phenolic compounds reasonably corroborated with the experimental results.

  10. Subharmonic excitation in amplitude modulation atomic force microscopy in the presence of adsorbed water layers

    SciTech Connect

    Santos, Sergio; Barcons, Victor; Verdaguer, Albert; Chiesa, Matteo

    2011-12-01

    In ambient conditions, nanometric water layers form on hydrophilic surfaces covering them and significantly changing their properties and characteristics. Here we report the excitation of subharmonics in amplitude modulation atomic force microscopy induced by intermittent water contacts. Our simulations show that there are several regimes of operation depending on whether there is perturbation of water layers. Single period orbitals, where subharmonics are never induced, follow only when the tip is either in permanent contact with the water layers or in pure noncontact where the water layers are never perturbed. When the water layers are perturbed subharmonic excitation increases with decreasing oscillation amplitude. We derive an analytical expression which establishes whether water perturbations compromise harmonic motion and show that the predictions are in agreement with numerical simulations. Empirical validation of our interpretation is provided by the observation of a range of values for apparent height of water layers when subharmonic excitation is predicted.

  11. Adsorption of drinking water fluoride on a micron-sized magnetic Fe3O4@Fe-Ti composite adsorbent

    NASA Astrophysics Data System (ADS)

    Zhang, Chang; Li, Yingzhen; Wang, Ting-Jie; Jiang, Yanping; Wang, Haifeng

    2016-02-01

    A micron-sized magnetic adsorbent (MMA) for fluoride removal from drinking water was prepared by spray drying and subsequent calcination of a magnetic Fe3O4@Fe-Ti core-shell nanoparticle slurry. The MMA granules had high mechanical strength and stability against water scouring, can be easily separated from the water by a magnet, and had a high selectivity for fluoride versus common co-existing ions and high fluoride removal efficiency in a wide range of initial pH of 3-11. Abundant hydroxyl groups on the MMA surface acted as the active sites for fluoride adsorption, which resulted in a high affinity of the MMA for fluoride. The pH in the adsorption process affected the adsorption significantly. At neutral initial pH, the adsorption isotherm was well fitted with the Langmuir model, and the maximum adsorption capacity reached a high value of 41.8 mg/g. At a constant pH of 3, multilayer adsorption of fluoride occurred due to the abundant positive surface charges on the MMA, and the adsorption isotherm was well fitted with the Freundlich model. The MMA had a fast adsorption rate, and adsorption equilibrium was achieved within 2 min. The adsorption kinetics followed a quasi-second order model. The regeneration of the MMA was easy and fast, and can be completed within 2 min. After 10 recycles, the fluoride removal efficiency of the MMA still remained high. These properties showed that the MMA is a promising adsorbent for fluoride removal.

  12. Experimental Measurement of Water Bands in Anhydrous Minerals to Improve Modeling of Adsorbed and Bound Water on the Regoliths of Inner Solar System Airless Bodies

    NASA Astrophysics Data System (ADS)

    Young, B. C.

    2015-12-01

    Investigating the characteristics of H2O/OH-absorption bands is critical for understanding their abundance and adherence to remotely observed surfaces. Our goal is to experimentally measure the spectra of anhydrous minerals in thin section and as powders to distinguish between internal H2O, surface adsorbed H2O, adsorbed OH, and OH that was formed as a result of irradiation. From these spectra, we are developing a model that will allow us to better deconvolve the abundance of adsorbed H2O and internally bound OH-/H2O in these materials. With this model, we aim to be able to remove the effects of terrestrial adsorbed H2O, thus enabling us to use the dry spectra to model these materials in the regoliths of airless bodies found in the inner solar system. To complete this task, we created un-mounted thin sections of two ordinary chondrite meteorites (Kilabo - LL6 and Gao-Guenie - H5) and eight ultramafic and banded rocks collected at the Stillwater Intrusion to serve as analogs for the Earth's moon. These rocks host an abundance of three key mineral series of interest: olivine, pyroxene, and plagioclase. We conducted EDS scans of each rock to create an elemental map and assess the specific mineral composition of phases in each sample. Transmittance spectra of each thin section were also collected from the visible through mid-IR range using the FTIR microscope to characterize bound water in each sample. These thin sections will be heated up to ~1000°C in a vacuum to remove any internal water and will be measured in transmission for a second time to determine their true anhydrous spectral baseline. Subsets of the samples have been powdered and will be measured under ultra-high vacuum conditions at temperatures ranging from ~293K to 650K to examine the spectral parameters for adsorbed terrestrial water on each sample. Ultimately, these powdered samples will be used for space weathering experiments to examine the nature of the OH- bands induced by irradiation.

  13. Oxygen isotope fractionation effects in soil water via interaction with cations (Mg, Ca, K, Na) adsorbed to phyllosilicate clay minerals

    NASA Astrophysics Data System (ADS)

    Oerter, Erik; Finstad, Kari; Schaefer, Justin; Goldsmith, Gregory R.; Dawson, Todd; Amundson, Ronald

    2014-07-01

    In isotope-enabled hydrology, soil and vadose zone sediments have been generally considered to be isotopically inert with respect to the water they host. This is inconsistent with knowledge that clay particles possessing an electronegative surface charge and resulting cation exchange capacity (CEC) interact with a wide range of solutes which, in the absence of clays, have been shown to exhibit δ18O isotope effects that vary in relation to the ionic strength of the solutions. To investigate the isotope effects caused by high CEC clays in mineral-water systems, we created a series of monominerallic-water mixtures at gravimetric water contents ranging from 5% to 32%, consisting of pure deionized water of known isotopic composition with homoionic (Mg, Ca, Na, K) montmorillonite. Similar mixtures were also created with quartz to determine the isotope effect of non-, or very minimally-, charged mineral surfaces. The δ18O value of the water in these monominerallic soil analogs was then measured by isotope ratio mass spectrometry (IRMS) after direct headspace CO2 equilibration. Mg- and Ca-exchanged homoionic montmorillonite depleted measured δ18O values up to 1.55‰ relative to pure water at 5% water content, declining to 0.49‰ depletion at 30% water content. K-montmorillonite enriched measured δ18O values up to 0.86‰ at 5% water content, declining to 0.11‰ enrichment at 30% water. Na-montmorillonite produces no measureable isotope effect. The isotope effects observed in these experiments may be present in natural, high-clay soils and sediments. These findings have relevance to the interpretation of results of direct CO2-water equilibration approaches to the measurement of the δ18O value of soil water. The adsorbed cation isotope effect may bear consideration in studies of pedogenic carbonate, plant-soil water use and soil-atmosphere interaction. Finally, the observed isotope effects may prove useful as molecular scale probes of the nature of mineral-water

  14. Adsorbent phosphates

    NASA Technical Reports Server (NTRS)

    Watanabe, S.

    1983-01-01

    An adsorbent which uses as its primary ingredient phosphoric acid salts of zirconium or titanium is presented. Production methods are discussed and several examples are detailed. Measurements of separating characteristics of some gases using the salts are given.

  15. Novel adhesive properties of poly(ethylene-oxide) adsorbed nanolayers

    NASA Astrophysics Data System (ADS)

    Zeng, Wenduo

    Solid-polymer interfaces play crucial roles in the multidisciplinary field of nanotechnology and are the confluence of physics, chemistry, biology, and engineering. There is now growing evidence that polymer chains irreversibly adsorb even onto weakly attractive solid surfaces, forming a nanometer-thick adsorbed polymer layer ("adsorbed polymer nanolayers"). It has also been reported that the adsorbed layers greatly impact on local structures and properties of supported polymer thin films. In this thesis, I aim to clarify adhesive and tribological properties of adsorbed poly(ethylene-oxide) (PEO) nanolayers onto silicon (Si) substrates, which remain unsolved so far. The adsorbed nanolayers were prepared by the established protocol: one has to equilibrate the melt or dense solution against a solid surface; the unadsorbed chains can be then removed by a good solvent, while the adsorbed chains are assumed to maintain the same conformation due to the irreversible freezing through many physical solid-segment contacts. I firstly characterized the formation process and the surface/film structures of the adsorbed nanolayers by using X-ray reflectivity, grazing incidence X-ray diffraction, and atomic force microscopy. Secondly, to compare the surface energy of the adsorbed layers with the bulk, static contact angle measurements with two liquids (water and glycerol) were carried out using a optical contact angle meter equipped with a video camera. Thirdly, I designed and constructed a custom-built adhesion-testing device to quantify the adhesive property. The experimental results provide new insight into the microscopic structure - macroscopic property relationship at the solid-polymer interface.

  16. AFM observation of monatomic step movements on NaCl(001) with the help of adsorbed water

    NASA Astrophysics Data System (ADS)

    Shindo, H.; Ohashi, M.; Baba, K.; Seo, A.

    1996-06-01

    AFM observation of cleaved NaCl(001) surface in air at room temperature revealed spontaneous motion of monatomic steps, depending on relative humidity, to minimize one-dimensional surface free energy. While step motion was recognized only at the parts having large positive curvature at 52% humidity, even straight steps moved at 57%. The motion was accelerated toward higher humidity. It is suggested that adsorbed water having 2-dimensional nature transports ions at the surface. By holding the AFM tip at one place, salt solution was collected beneath the tip by capillary action. Upon removal of the tip, the solution droplet turned into a bell-shaped hillock of salt as high as 78 nm. Although the hillocks gradually flattened spontaneously, the method has potential application in pattern formation.

  17. Single-walled carbon nanohorn as new solid-phase extraction adsorbent for determination of 4-nitrophenol in water sample.

    PubMed

    Zhu, Shuyun; Niu, Wenxin; Li, Haijuan; Han, Shuang; Xu, Guobao

    2009-10-15

    Single-walled carbon nanohorn (SWCNH) was developed as new adsorbent for solid-phase extraction using 4-nitrophenol as representative. The unique exoteric structures and high surface area of SWCNH allow extracting a large amount of 4-nitrophenol over a short time. Highly sensitive determination of 4-nitrophenol was achieved by linear sweep voltammetry after only 120s extraction. The calibration plot for 4-nitrophenol determination is linear in the range of 5.0x10(-8) M-1.0x10(-5) M under optimum conditions. The detection limit is 1.1x10(-8) M. The proposed method was successfully employed to determine 4-nitrophenol in lake water samples, and the recoveries of the spiked 4-nitrophenol were excellent (92-106%).

  18. Electron transporting water-gated thin film transistors

    NASA Astrophysics Data System (ADS)

    Al Naim, Abdullah; Grell, Martin

    2012-10-01

    We demonstrate an electron-transporting water-gated thin film transistor, using thermally converted precursor-route zinc-oxide (ZnO) intrinsic semiconductors with hexamethyldisilazene (HMDS) hydrophobic surface modification. Water gated HMDS-ZnO thin film transistors (TFT) display low threshold and high electron mobility. ZnO films constitute an attractive alternative to organic semiconductors for TFT transducers in sensor applications for waterborne analytes. Despite the use of an electrolyte as gate medium, the gate geometry (shape of gate electrode and distance between gate electrode and TFT channel) is relevant for optimum performance of water-gated TFTs.

  19. Magnetic nanoporous carbon as an adsorbent for the extraction of phthalate esters in environmental water and aloe juice samples.

    PubMed

    Liu, Li; Hao, Yunhui; Ren, Yiqian; Wang, Chun; Wu, Qiuhua; Wang, Zhi

    2015-05-01

    In this work, magnetic nanoporous carbon with high surface area and ordered structure was synthesized using cheap commercial silica gel as template and sucrose as the carbon source. The prepared magnetic nanoporous carbon was firstly used as an adsorbent for the extraction of phthalate esters, including diethyl phthalate, diallyl phthalate, and di-n-propyl-phthalate, from lake water and aloe juice samples. Several parameters that could affect the extraction efficiency were optimized. Under the optimum conditions, the limit of detection of the method (S/N = 3) was 0.10 ng/mL for water sample and 0.20 ng/mL for aloe juice sample. The linearity was observed over the concentration range of 0.50-150.0 and 1.0-200.0 ng/mL for water and aloe juice samples, respectively. The results showed that the magnetic nanoporous carbon has a high adsorptive capability toward the target phthalate esters in water and aloe juice samples.

  20. Oscillating electric-field effects on adsorbed-water at rutile- and anatase-TiO2 surfaces

    NASA Astrophysics Data System (ADS)

    Futera, Zdenek; English, Niall J.

    2016-11-01

    We have performed non-equilibrium molecular dynamics simulations of various TiO2/water interfaces at ambient temperature in presence of oscillating electric fields in frequency range 20-100 GHz and RMS intensities 0.05-0.25 V/Å. Although the externally applied fields are by one order of magnitude lower than the intrinsic electric field present on the interfaces (˜1.5-4.5 V/Å), significant non-thermal coupling of rotational and translational motion of water molecules was clearly observed. Enhancement of the motion, manifested by increase of diffusivity, was detected in the first hydration layer, which is known to be heavily confined by adsorption to the TiO2 surface. Interestingly, the diffusivity increases more rapidly on anatase than on rutile facets where the adsorbed water was found to be more organized and restrained. We observed that the applied oscillating field reduces number of hydrogen bonds on the interface. The remaining H-bonds are weaker than those detected under zero-field conditions; however, their lifetime increases on most of the surfaces when the low-frequency fields are applied. Reduction of adsorption interaction was observed also in IR spectra of interfacial water where the directional patterns are smeared as the intensities of applied fields increase.

  1. Use of industrial by-products and natural media to adsorb nutrients, metals and organic carbon from drinking water.

    PubMed

    Grace, Maebh A; Healy, Mark G; Clifford, Eoghan

    2015-06-15

    Filtration technology is well established in the water sector but is limited by inability to remove targeted contaminants, found in surface and groundwater, which can be damaging to human health. This study optimises the design of filters by examining the efficacy of seven media (fly ash, bottom ash, Bayer residue, granular blast furnace slag (GBS), pyritic fill, granular activated carbon (GAC) and zeolite), to adsorb nitrate, ammonium, total organic carbon (TOC), aluminium, copper (Cu) and phosphorus. Each medium and contaminant was modelled to a Langmuir, Freundlich or Temkin adsorption isotherm, and the impact of pH and temperature (ranging from 10 °C to 29 °C) on their performance was quantified. As retention time within water filters is important in contaminant removal, kinetic studies were carried out to observe the adsorption behaviour over a 24h period. Fly ash and Bayer residue had good TOC, nutrient and Cu adsorption capacity. Granular blast furnace slag and pyritic fill, previously un-investigated in water treatment, showed adsorption potential for all contaminants. In general, pH or temperature adjustment was not necessary to achieve effective adsorption. Kinetic studies showed that at least 60% of adsorption had occurred after 8h for all media. These media show potential for use in a multifunctional water treatment unit for the targeted treatment of specific contaminants.

  2. Complete wetting of Pt(111) by nanoscale liquid water films

    SciTech Connect

    Xu, Yuntao; Dibble, Collin J.; Petrik, Nikolay G.; Smith, R. Scott; Kay, Bruce D.; Kimmel, Gregory A.

    2016-02-04

    The melting and wetting of nanoscale crystalline ice films on Pt(111) that are transiently heated above the melting point using nanosecond laser pulses are studied with infrared refection absorption spectroscopy (IRAS) and Kr temperature programmed desorption (TPD). The as-grown crystalline ice films consist of isolated nanoscale ice crystallites embedded in a hydrophobic water monolayer. Upon heating above the melting point, these ice crystallites rapidly melt to form nanoscale droplets of liquid water. Rapid cooling of the system to cryogenic temperatures after each laser pulse quenches the water films and allows them to be interrogated with IRAS, Kr TPD and other ultrahigh vacuum surface science techniques. With each successive heat pulse, these liquid drops spread across the surface until it is entirely covered with multilayer water films after several pulses. These results, which show that nanoscale water films completely wet Pt(111), are in contrast to molecular dynamics simulations predicting partial wetting of nanoscale water drops on a hydrophobic water monolayer. The results provide valuable new insights into the wetting characteristics of nanoscale water films on a clean, well-characterized single crystal surface.

  3. Cleaning Water Contaminated with Heavy Metal Ions Using Pyrolyzed Biochar Adsorbents

    EPA Science Inventory

    The extraction of pollutants from water using activated biochar materials is a low cost, sustainable approach for providing safe water in developing countries. The adsorption of copper ions, Cu (II), onto banana peels that were dried, pyrolyzed and activated was studied and compa...

  4. Wire Frame Holds Water-Soap Film in Space

    NASA Technical Reports Server (NTRS)

    2003-01-01

    Expedition 6 astronaut Dr. Don Pettit photographed a cube shaped wire frame supporting a thin film made from a water-soap solution during his Saturday Morning Science aboard the International Space Station's (ISS) Destiny Laboratory. Food coloring was added to several faces to observe the effects of diffusion within the film.

  5. Surfactant-modified alumina: an efficient adsorbent for malachite green removal from water environment.

    PubMed

    Das, Asit K; Saha, Sandip; Pal, Anjali; Maji, Sanjoy K

    2009-07-15

    Surface of alumina was modified with sodium dodecyl sulfate (SDS), an anionic surfactant. The surfactant-modified alumina (SMA) was characterized by FTIR and thermal analysis. The SMA was then used for the removal of malachite green (MG; Basic Green 4), a well-known toxic cationic dye from aqueous environment. The removal of MG takes place in the micellar structure formed on alumina surface, and the process is called adsolubilization. All the studies were carried out in batch mode. The kinetic studies showed that 1 h contact time was sufficient to attain equilibrium. SMA was very efficient to remove MG up to 99% under optimum conditions. The concentration range of MG was 20-100 mg/L. The isotherm studies showed that it follows Langmuir model better than the Freundlich model. The maximum adsorption capacity was 185 mg/g. The effects of various parameters such as pH, presence of interfering ions (Cl-, NO3-, H2PO4-, SO4(2-), Fe2+, Ca2+) and organics (pesticides such as 2,4-dichlorophenoxyacetic acid, atrazine, endosulfan, and humic acid) are evaluated. It was observed that H2PO4-, Fe2+, endosulfan, and humic acid have maximum interference. Desorption of MG from exhausted SMA using acetone, and its reuse was studied. The regenerated adsorbent shows approximately 80% efficiency on the removal of MG. The usability of SMA for the removal of MG from real wastewater was also examined. The kinetic equilibrium was attained within 1 h and the removal could be achieved up to approximately 95% at a dose of 20 g/L. The adsorption followed Freundlich isotherm model better than the Langmuir model.

  6. The origin of the low efficiency of carbon removal from the Nickel/Yttrium-Stabilized Zirconia triple-phase boundary by adsorbed water

    NASA Astrophysics Data System (ADS)

    Zhang, Yanxing; Yang, Zongxian

    2015-04-01

    Carbon removal from the anode triple-phase boundary (TPB) of solid oxide fuel cells (SOFCs) by adsorbed water molecule was studied using the density functional calculations, and a detailed dynamic picture was presented. It is found that the adsorbed H2O molecule can dissociate easily at the Ni/YSZ interface and on the YSZ part compared with the Ni part and react with the interface carbon to form the CHO species. The dissociation process of CHO to CH and O is more favorable as compared with that of CHO to CO and H. The CH fragment can easily diffuse to the O vacancy formed in the dynamic reaction processes and dissociate into C and H, which regenerates carbon at the interface. This might be the main reasons for the low efficiency of carbon removal from the TPB of Ni/YSZ by adsorbed water.

  7. Photoassisted oxidation of oil films on water

    SciTech Connect

    Heller, A.; Brock, J.R.

    1991-08-01

    The objective of the project is to develop TiO{sub 2}-based photocatalysts for the solar assisted oxidative dissolution of oil slicks. In a TiO{sub 2} crystal, absorption of a photon generates an electron-hole pair. The electron reacts with surface-adsorbed oxygen, reducing it to hydrogen peroxide; the hole directly oxidizes adsorbed organic compounds, usually via an intermediate OH radical. Since the density of TiO{sub 2} (3.8g/cc for anatase, 4.3 g/cc for rutile) is greater than that of either oil or seawater, TiO{sub 2} crystals are attached to inexpensive, engineered hollow glass microspheres to ensure flotation on the oil slick surface. Portions of the microsphere surface not covered by TiO{sub 2} are made oleophilic so that the microbeads will be preferentially attracted to the oil-air interface.

  8. Nanoscale confinement and interfacial effects on the dynamics and glass transition/crystallinity of thin adsorbed films on silica nanoparticles

    NASA Astrophysics Data System (ADS)

    Madathingal, Rajesh Raman

    The research investigated in this dissertation has focused on understanding the structure-property-function relationships of polymer nanocomposites. The properties of composite systems are dictated by the properties of their components, typically fillers in a polymer matrix. In nanocomposites, the polymer near an interface has significantly different properties compared with the bulk polymer, and the contribution of the adsorbed polymer to composite properties becomes increasingly important as the filler size decreases. Despite many reports of highly favorable properties, the behavior of polymer nanocomposites is not generally predictable, and thus requires a better understanding of the interfacial region. The ability to tailor the filler/matrix interaction and an understanding of the impact of the interface on macroscopic properties are keys in the design of nanocomposite properties. In this original work the surface of silica nanoparticles was tailored by: (a) Changing the number of sites for polymer attachment by varying the surface silanols and, (b) By varying the size/curvature of nanoparticles. The effect of surface tailoring on the dynamic properties after the adsorption of two model polymers, amorphous polymethyl methacrylate (PMMA) and semicrystalline polyethylene oxide (PEO) was observed. The interphase layer of polymers adsorbed to silica surfaces is affected by the surface silanol density as well as the relative size of the polymer compared with the size of the adsorbing substrate. The non-equilibrium adsorption of PMMA onto individual colloidal Stober silica (SiO2) particles, where Rparticle (100nm) > RPMMA (˜6.5nm) was compared with the adsorption onto fumed silica, where Rparticle (7nm) ˜ RPMMA (6.5nm) < Raggregate (˜1000nm), both as a function of silanol density [SiOH] and hydrophobility. In the former case, TEM images showed that the PMMA adsorbed onto individual nanoparticles, so that the number of PMMA chains/bead could be calculated, whereas

  9. Phosphate Remediation and Recovery from Lake Water using Modified Iron Oxide-based Adsorbents

    EPA Science Inventory

    Adsorption behavior of Bayoxide ® E33 (E33) and three E33-modified sorbents for the removal of phosphate from lake water was investigated in this study. E33-modified sorbents were synthesized by coating with manganese and nanoparticles. Characterization was done by X-ray diffract...

  10. Proton magnetic relaxation study of the thermodynamic characteristics of water adsorbed by cellulose fibers

    NASA Astrophysics Data System (ADS)

    Grunin, Yu. B.; Grunin, L. Yu.; Masas, D. S.; Talantsev, V. I.; Sheveleva, N. N.

    2016-11-01

    The possibility of determining the thermodynamic parameters that characterize the sorption properties of cellulose and the state of water associated with its fibers is demonstrated using modern concepts of the structure of this vegetable polymer and methods based on theories of adsorption and NMR relaxation in heterogeneous systems.

  11. Water-insoluble Silk Films with Silk I Structure

    SciTech Connect

    Lu, Q.; Hu, X; Wang, X; Kluge, J; Lu, S; Cebe, P; Kaplan, D

    2010-01-01

    Water-insoluble regenerated silk materials are normally produced by increasing the {beta}-sheet content (silk II). In the present study water-insoluble silk films were prepared by controlling the very slow drying of Bombyx mori silk solutions, resulting in the formation of stable films with a predominant silk I instead of silk II structure. Wide angle X-ray scattering indicated that the silk films stabilized by slow drying were mainly composed of silk I rather than silk II, while water- and methanol-annealed silk films had a higher silk II content. The silk films prepared by slow drying had a globule-like structure at the core surrounded by nano-filaments. The core region was composed of silk I and silk II, surrounded by hydrophilic nano-filaments containing random turns and {alpha}-helix secondary structures. The insoluble silk films prepared by slow drying had unique thermal, mechanical and degradative properties. Differential scanning calorimetry results revealed that silk I crystals had stable thermal properties up to 250 C, without crystallization above the T{sub g}, but degraded at lower temperatures than silk II structure. Compared with water- and methanol-annealed films the films prepared by slow drying had better mechanical ductility and were more rapidly enzymatically degraded, reflecting the differences in secondary structure achieved via differences in post processing of the cast silk films. Importantly, the silk I structure, a key intermediate secondary structure for the formation of mechanically robust natural silk fibers, was successfully generated by the present approach of very slow drying, mimicking the natural process. The results also point to a new mode of generating new types of silk biomaterials with enhanced mechanical properties and increased degradation rates, while maintaining water insolubility, along with a low {beta}-sheet content.

  12. Magnetic spherical carbon as an efficient adsorbent for the magnetic extraction of phthalate esters from lake water and milk samples.

    PubMed

    Wu, Juanjuan; Wang, Chenhuan; Liang, Xinyu; Yang, Xiumin; Wang, Chun; Wu, Qiuhua; Wang, Zhi

    2017-03-29

    Magnetic spherical carbon was synthesized by a facile hydrothermal carbonization procedure with biomass glucose as the carbon precursor and nanoclusters iron colloid as magnetic precursor. The textures of the as-prepared magnetic spherical carbon were characterized by nitrogen adsorption-desorption isotherms, X-ray diffraction, transmission electron microscopy, scanning electron microscopy and vibration sample magnetometry. Results indicated that the magnetic spherical carbon possessed high surface area as well as strong magnetism, which endows the material with good adsorption capability and easy separation property. To assess its absorption performance, the magnetic spherical carbon was employed as adsorbent for the extraction and preconcentration of phthalate esters from lake water and milk samples before high-performance liquid chromatographic analysis. Some key parameters that could influence the enrichment efficiency were investigated. Under the optimum conditions, a good linearity was achieved with the linear correlation coefficients higher than 0.9973. The limits of detection (S/N = 3) were 0.05-0.08 ng mL(-1) for lake water and 0.1-0.2 ng mL(-1) for milk samples. The recoveries of the analytes for the method were in the range 80.1-112.6%. This article is protected by copyright. All rights reserved.

  13. Nano-silica fabricated with silver nanoparticles: antifouling adsorbent for efficient dye removal, effective water disinfection and biofouling control

    NASA Astrophysics Data System (ADS)

    Das, Sujoy K.; Khan, Md. Motiar R.; Parandhaman, T.; Laffir, Fathima; Guha, Arun K.; Sekaran, G.; Mandal, Asit Baran

    2013-05-01

    A nano-silica-AgNPs composite material is proposed as a novel antifouling adsorbent for cost-effective and ecofriendly water purification. Fabrication of well-dispersed AgNPs on the nano-silica surface, designated as NSAgNP, has been achieved through protein mediated reduction of silver ions at ambient temperature for development of sustainable nanotechnology. The coated proteins on AgNPs led to the formation of stable NSAgNP and protected the AgNPs from oxidation and other ions commonly present in water. The NSAgNP exhibited excellent dye adsorption capacity both in single and multicomponent systems, and demonstrated satisfactory tolerance against variations in pH and dye concentration. The adsorption mainly occurred through electrostatic interaction, though π-π interaction and pore diffusion also contributed to the process. Moreover, the NSAgNP showed long-term antibacterial activity against both planktonic cells and biofilms of Gram-negative Escherichia coli and Pseudomonas aeruginosa. The antibacterial activity of AgNPs retarded the initial attachment of bacteria on NSAgNP and thus significantly improved the antifouling properties of the nanomaterial, which further inhibited biofilm formation. Scanning electron and fluorescence microscopic studies revealed that cell death occurred due to irreversible damage of the cell membrane upon electrostatic interaction of positively charged NSAgNP with the negatively charged bacterial cell membrane. The high adsorption capacity, reusability, good tolerance, removal of multicomponent dyes and E. coli from the simulated contaminated water and antifouling properties of NSAgNP will provide new opportunities to develop cost-effective and ecofriendly water purification processes.A nano-silica-AgNPs composite material is proposed as a novel antifouling adsorbent for cost-effective and ecofriendly water purification. Fabrication of well-dispersed AgNPs on the nano-silica surface, designated as NSAgNP, has been achieved through

  14. Spectromicroscopy of C60 and azafullerene C59N: Identifying surface adsorbed water

    PubMed Central

    Erbahar, Dogan; Susi, Toma; Rocquefelte, Xavier; Bittencourt, Carla; Scardamaglia, Mattia; Blaha, Peter; Guttmann, Peter; Rotas, Georgios; Tagmatarchis, Nikos; Zhu, Xiaohui; Hitchcock, Adam P.; Ewels, Chris P.

    2016-01-01

    C60 fullerene crystals may serve as important catalysts for interstellar organic chemistry. To explore this possibility, the electronic structures of free-standing powders of C60 and (C59N)2 azafullerenes are characterized using X-ray microscopy with near-edge X-ray adsorption fine structure (NEXAFS) spectroscopy, closely coupled with density functional theory (DFT) calculations. This is supported with X-ray photoelectron spectroscopy (XPS) measurements and associated core-level shift DFT calculations. We compare the oxygen 1s spectra from oxygen impurities in C60 and C59N, and calculate a range of possible oxidized and hydroxylated structures and associated formation barriers. These results allow us to propose a model for the oxygen present in these samples, notably the importance of water surface adsorption and possible ice formation. Water adsorption on C60 crystal surfaces may prove important for astrobiological studies of interstellar amino acid formation. PMID:27748425

  15. Spectromicroscopy of C60 and azafullerene C59N: Identifying surface adsorbed water

    NASA Astrophysics Data System (ADS)

    Erbahar, Dogan; Susi, Toma; Rocquefelte, Xavier; Bittencourt, Carla; Scardamaglia, Mattia; Blaha, Peter; Guttmann, Peter; Rotas, Georgios; Tagmatarchis, Nikos; Zhu, Xiaohui; Hitchcock, Adam P.; Ewels, Chris P.

    2016-10-01

    C60 fullerene crystals may serve as important catalysts for interstellar organic chemistry. To explore this possibility, the electronic structures of free-standing powders of C60 and (C59N)2 azafullerenes are characterized using X-ray microscopy with near-edge X-ray adsorption fine structure (NEXAFS) spectroscopy, closely coupled with density functional theory (DFT) calculations. This is supported with X-ray photoelectron spectroscopy (XPS) measurements and associated core-level shift DFT calculations. We compare the oxygen 1s spectra from oxygen impurities in C60 and C59N, and calculate a range of possible oxidized and hydroxylated structures and associated formation barriers. These results allow us to propose a model for the oxygen present in these samples, notably the importance of water surface adsorption and possible ice formation. Water adsorption on C60 crystal surfaces may prove important for astrobiological studies of interstellar amino acid formation.

  16. Banana peel as an adsorbent for removing atrazine and ametryne from waters.

    PubMed

    Silva, Claudineia R; Gomes, Taciana F; Andrade, Graziela C R M; Monteiro, Sergio H; Dias, Ana C R; Zagatto, Elias A G; Tornisielo, Valdemar L

    2013-03-13

    The feasibility of using banana peel for removal of the pesticides atrazine and ametryne from river and treated waters has been demonstrated, allowing the design of an efficient, fast, and low-cost strategy for remediation of polluted waters. The conditions for removal of these pesticides in a laboratory scale were optimized as sample volume = 50 mL, banana mass = 3.0 g, stirring time = 40 min, and no pH adjustment necessary. KF(sor) values for atrazine and ametryne were evaluated as 35.8 and 54.1 μg g(-1) (μL mL(-1)) by using liquid scintillation spectrometry. Adsorption was also evaluated by LC-ESI-MS/MS. As quantification limits were 0.10 and 0.14 μg L(-1) for both pesticides, sample preconcentration was not needed. Linear analytical curves (up to 10 μg L(-1)), precise results (RSD < 4.5%), good recoveries (82.9-106.6%), and a > 90% removal efficiency were attained for both pesticides. Water samples collected near an intensively cultivated area were adequately remedied.

  17. Cu-Zn powders as potential Cr(VI) adsorbents for drinking water.

    PubMed

    Kaprara, E; Seridou, P; Tsiamili, V; Mitrakas, M; Vourlias, G; Tsiaoussis, I; Kaimakamis, G; Pavlidou, E; Andritsos, N; Simeonidis, K

    2013-11-15

    This work examines the possibility of applying CuZn alloys as a reducing medium for the efficient removal of hexavalent chromium from drinking water. In an effort to develop a route for producing powders of CuZn alloys under mild conditions and investigate the optimum composition for such application, a series of alloys in the form of powders were prepared, by a sequence of Cu and Zn ball-milling and low temperature annealing. Batch Cr(VI) removal tests, performed to evaluate and compare the efficiency of the products under typical natural water parameters (pH 7 and natural-like water), indicated that the best performing material have a composition around 50 wt% Cu. The dominant reduction mechanisms are both the corrosion of the alloy surface and the electron transfer to the solution. The behavior of granulated CuZn media was tested in rapid-scale column tests using the commercial KDF which verified the high potential of CuZn alloys in Cr(VI) removal. Nevertheless, Cu and Zn leaching problems should be also considered.

  18. Modelling and experimental investigation on the application of water super adsorbents in waste air biofilters.

    PubMed

    Danaee, Soroosh; Fazaelipoor, Mohammad Hassan; Gholami, Abdollah; Ataei, Seyed Ahmad; Afzali, Daryoush

    2015-01-01

    In this research work, a synthetic water super absorbent polymer was included in the bed of a perlite-based biofilter for the removal of ethanol from air. The performance of this biofilter was compared with the performance of a control perlite-based biofilter lacking the water super absorbent. With the empty bed residence time of 2 min, both biofilters were able to remove more than 90% of the entering pollutant with the concentration of 1 g /m3, when regular moistening was applied. After last irrigation on day 23, the performance of the control biofilter was unchanged until day 35. From day 36 onwards, the control biofilter lost its activity gradually and became totally inactive on day 45. The performance of the super absorbent containing biofilter, however, was unchanged until day 58 before starting to lose its activity. A mechanistic model was developed to describe the performance of a biofilter under drying effects. The model could predict the trends of experimental results reasonably well. The model was also applied to predict the trends of experimental data from a published paper on the removal of hexane in a perlite/super absorbent containing biofilter.

  19. Electrospun polystyrene/graphene nanofiber film as a novel adsorbent of thin film microextraction for extraction of aldehydes in human exhaled breath condensates.

    PubMed

    Huang, Jing; Deng, Hongtao; Song, Dandan; Xu, Hui

    2015-06-09

    In the current study, we introduced a novel polystyrene/graphene (PS/G) composite nanofiber film for thin film microextraction (TFME) for the first time. The PS/G nanofiber film was fabricated on the surface of filter paper by a facile electrospinning method. The morphology and extraction performance of the resultant composite film were investigated systematically. The PS/G nanofiber film exhibited porous fibrous structure, large surface area and strong hydrophobicity. A new thin film microextraction-high performance liquid chromatography (TFME-HPLC) method was developed for the determination of six aldehydes in human exhaled breath condensates. The method showed high enrichment efficiency and fast analysis speed. Under the optimal conditions, the linear ranges of the analytes were in the range of 0.02-30 μmol L(-1) with correlation coefficients above 0.9938, and the recoveries were between 79.8% and 105.6% with the relative standard deviation values lower than 16.3% (n=5). The limits of quantification of six aldehydes ranged from 13.8 to 64.6 nmol L(-1). The established method was successfully applied for the quantification of aldehyde metabolites in exhaled breath condensates of lung cancer patients and healthy people. Taken together, the TFME-HPLC method provides a simple, rapid, sensitive, cost-effective, non-invasion approach for the analysis of linear aliphatic aldehydes in human exhaled breath condensates.

  20. Incorporation and thermal evolution of rhodamine 6G dye molecules adsorbed in porous columnar optical SiO2 thin films.

    PubMed

    Sánchez-Valencia, Juan R; Blaszczyk-Lezak, Iwona; Espinós, Juan P; Hamad, Said; González-Elipe, Agustín R; Barranco, Angel

    2009-08-18

    Rhodamine 6G (Rh6G) dye molecules have been incorporated into transparent and porous SiO2 thin films prepared by evaporation at glancing angles. The porosity of these films has been assessed by analyzing their water adsorption isotherms measured for the films deposited on a quartz crystal monitor. Composite Rh6G/SiO2 thin films were prepared by immersion of a SiO2 thin film into a solution of the dye at a given pH. It is found that the amount of Rh6G molecules incorporated into the film is directly dependent on the pH of the solution and can be accounted for by a model based on the point of zero charge (PZC) concepts originally developed for colloidal oxides. At low pHs, the dye molecules incorporate in the form of monomers, while dimers or higher aggregates are formed if the pH increases. Depending on the actual preparation and treatment conditions, they also exhibit high relative fluorescence efficiency. The thermal stability of the composite films has been also investigated by characterizing their optical behavior after heating in an Ar atmosphere at increasing temperatures up to 275 degrees C. Heating induces a progressive loss of active dye molecules, a change in their agglomeration state, and an increment in their relative fluorescence efficiency. The obtained Rh6G/SiO2 composite thin films did not disperse the light and therefore can be used for integration into optical and photonic devices.

  1. Growth and structure of water on SiO2 films on Si investigated byKelvin probe microscopy and in situ X-ray Spectroscopies

    SciTech Connect

    Verdaguer, A.; Weis, C.; Oncins, G.; Ketteler, G.; Bluhm, H.; Salmeron, M.

    2007-06-14

    The growth of water on thin SiO{sub 2} films on Si wafers at vapor pressures between 1.5 and 4 torr and temperatures between -10 and 21 C has been studied in situ using Kelvin Probe Microscopy and X-ray photoemission and absorption spectroscopies. From 0 to 75% relative humidity (RH) water adsorbs forming a uniform film 4-5 layers thick. The surface potential increases in that RH range by about 400 mV and remains constant upon further increase of the RH. Above 75% RH the water film grows rapidly, reaching 6-7 monolayers at around 90% RH and forming a macroscopic drop near 100%. The O K-edge near-edge X-ray absorption spectrum around 75% RH is similar to that of liquid water (imperfect H-bonding coordination) at temperatures above 0 C and ice-like below 0 C.

  2. Adsorption depth profile of water on thermoplastic starch films

    SciTech Connect

    Bonno, B.; Laporte, J.L.; Paris, D.; D'Leon, R.T.

    2000-01-01

    It is well known that petroleum derived polymers are primary environmental contaminants. The study of new packing biodegradable materials has been the object of numerous papers in past years. Some of these new materials are the thermoplastic films derived from wheat starch. In the present paper, the authors study some of properties of wheat starch thermoplastic films, with various amounts of absorbed water, using photoacoustic spectroscopy techniques. The absorption depth profile of water in the starch substrate is determined for samples having a variable water level.

  3. Absorption depth profile of water on thermoplastic starch films

    SciTech Connect

    Bonno, B.; Laporte, J.L.; Paris, D.; D'Leon, R.T.

    2000-01-01

    It is well known that petroleum derived polymers are primary environmental contaminants. The study of new packing biodegradable materials has been the object of numerous papers in past years. Some of these new materials are the thermoplastic films derived from wheat starch. In the present paper, the authors study some of properties of wheat starch thermoplastic films, with various amounts of absorbed water, using photoacoustic spectroscopy techniques. The absorption depth profile of water in the starch substrate is determined for samples having a variable water level.

  4. Spontaneously adsorbed monolayer films: Fabrication, characterization, and application of monolayers of alkanethiol and sulfur-bearing cyclodestrin derivatives

    SciTech Connect

    Chinkap, Chung.

    1991-03-12

    Monolayers of n-alkanethiols (CH{sub 3}(CH{sub 2}){sub n}SH, n=1--17) and sulfur-bearing cyclodextrin derivatives spontaneously adsorbed on Ag and Au have been studied with a variety of surface characterization methods, such as infrared inflection spectroscopy, contact angle measurements, electro-chemistry, optical ellipsometry, and scanning tunneling microscopy. Long chain n-alkanethiols monolayers on Ag and Au are insulating to electron transfer and have contact angles indicative of well-ordered hydrocarbon terminated structures. Infrared and contact angle data indicate a different orientation of the methyl group with respect to the surface for chains with odd and even numbers of methylene groups. Compared to monolayers on Au, the alkanethiol monolayers on Ag are oriented more towards the surface normal. The observed odd-even effect methyl group orientation for these monolayers on Ag is offset by a methylene group from that on Au. The relationships between the structure and packing of the monolayers on Ag and Au and the composition, roughness, and crystallinity of the substrate are also discussed. Monolayers of sulfur-bearing cyclodextrin derivatives on Au and Ag are fabricated by spontaneous adsorption and characterized by the above techniques. Size-selectively and molecular recognition of the {alpha}- and {beta}- cyclodextrin cavity are shown with our monolayers. Because of molecular recognition, p-nitrophenol is retained preferrentially by the cyclodextrin monolayers over o-nitrophenol. 146 refs., 44 figs., 5 tabs.

  5. Nature of corrosion films in simulated LWR water. Final report

    SciTech Connect

    Lumsden, J.B.

    1985-06-01

    Passive films on Alloy 600 and Type 304 stainless steel were characterized using surface analysis instruments. The films were formed under conditions suspected of causing cracking in nuclear systems and compared to those formed under conditions where cracking does not occur. Alloy 600 was investigated in the boric acid-lithium hydroxide thiosulfate solution. Susceptibility to stress corrosion cracking was correlated with the occurrence of a film containing sulfide ions. Environmental conditions which produce an oxide film do not cause stress corrosion cracking of Alloy 600 in the system studied. Type 304 stainless steel was investigated in high purity water at 288/sup 0/C having levels of dissolved O/sub 2/ where Type 304 stainless steel is susceptible and not susceptible to stress corrosion cracking. A correlation was found between passive film chemistry and susceptibility to stress corrosion cracking.

  6. Regenerable adsorbents for removal of arsenic from contaminated waters and synthesis and characterization of multifunctional magnetic nanoparticles for environmental and biomedical applications

    NASA Astrophysics Data System (ADS)

    Verdugo Gonzalez, Brenda

    The present work is divided into two sections. The first section deals with the synthesis of regenerable adsorbents for the removal of arsenic from contaminated waters. An adsorbent based on carboxymethylated polyethylenimine grafted agarose gels was synthesized and characterized as a regenerable synthetic ferric oxide adsorbent with high capacity for arsenate ions at pH 3.0. Similarly, four metal ion chelating adsorbents based on dipicolylamine were synthesized and characterized with respect to their Cu(II), Fe(III) and As(V) adsorption capacities. The most efficient adsorbents were Nov-PEI-DPA and Nov-TREN-DPA. Additionally, a commercial ion exchange resin was modified with permanganate to oxidize arsenite into arsenate. A complete oxidation-adsorption system was proposed in which a column packed with the oxidation resin was connected in series with an adsorbent column composed of the polyethylenimine grafted agarose gels. The second section involved work with magnetic nanoparticles. First, composite adsorbents consisting of magnetic particles encapsulated within agarose beads with and without grafted iminodiacetic acid (IDA) chelating groups were synthesized. The adsorption capacity of the adsorbents for Cu(II), Fe(III) and As(V) at different concentrations was investigated. Batch experiments were carried out to determine the Fe(III) and As(V) adsorption isotherms for the magnetic Novarose-IDA. Regenerability of the adsorbent was achieved with a pH change of the inlet solution, without affecting its magnetic or adsorption properties. Magnetic composite particles were synthesized for biomedical applications. First, magnetic nanoparticles were coated with silica and then used for gold nanoshell production. These nanoshells were functionalized with a Brij S10 derivative, containing carboxylic groups, using dodecanethiol as a bridging agent to incorporate a fluorescent biomolecule. Finally, magnetic and gold particles were encapsulated in PLGA nanoparticles

  7. 21 CFR 177.1400 - Hydroxyethyl cellulose film, water-insoluble.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Hydroxyethyl cellulose film, water-insoluble. 177... cellulose film, water-insoluble. Water-insoluble hydroxyethyl cellulose film may be safely used for... cellulose film consists of a base sheet manufactured by the ethoxylation of cellulose under...

  8. 21 CFR 177.1400 - Hydroxyethyl cellulose film, water-insoluble.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Hydroxyethyl cellulose film, water-insoluble. 177... cellulose film, water-insoluble. Water-insoluble hydroxyethyl cellulose film may be safely used for... cellulose film consists of a base sheet manufactured by the ethoxylation of cellulose under...

  9. 21 CFR 177.1400 - Hydroxyethyl cellulose film, water-insoluble.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Hydroxyethyl cellulose film, water-insoluble. 177... cellulose film, water-insoluble. Water-insoluble hydroxyethyl cellulose film may be safely used for... cellulose film consists of a base sheet manufactured by the ethoxylation of cellulose under...

  10. 21 CFR 177.1400 - Hydroxyethyl cellulose film, water-insoluble.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Hydroxyethyl cellulose film, water-insoluble. 177... cellulose film, water-insoluble. Water-insoluble hydroxyethyl cellulose film may be safely used for... cellulose film consists of a base sheet manufactured by the ethoxylation of cellulose under...

  11. Thin Water Films at Multifaceted Hematite Particle Surfaces.

    PubMed

    Boily, Jean-François; Yeşilbaş, Merve; Uddin, Munshi Md Musleh; Baiqing, Lu; Trushkina, Yulia; Salazar-Alvarez, Germàn

    2015-12-08

    Mineral surfaces exposed to moist air stabilize nanometer- to micrometer-thick water films. This study resolves the nature of thin water film formation at multifaceted hematite (α-Fe2O3) nanoparticle surfaces with crystallographic faces resolved by selected area electron diffraction. Dynamic vapor adsorption (DVA) in the 0-19 Torr range at 298 K showed that these particles stabilize water films consisting of up to 4-5 monolayers. Modeling of these data predicts water loadings in terms of an "adsorption regime" (up to 16 H2O/nm(2)) involving direct water binding to hematite surface sites, and of a "condensation regime" (up to 34 H2O/nm(2)) involving water binding to hematite-bound water nanoclusters. Vibration spectroscopy identified the predominant hematite surface hydroxo groups (-OH, μ-OH, μ3-OH) through which first layer water molecules formed hydrogen bonds, as well as surface iron sites directly coordinating water molecules (i.e., as geminal η-(OH2)2 sites). Chemometric analyses of the vibration spectra also revealed a strong correspondence in the response of hematite surface hydroxo groups to DVA-derived water loadings. These findings point to a near-saturation of the hydrogen-bonding environment of surface hydroxo groups at a partial water vapor pressure of ∼8 Torr (∼40% relative humidity). Classical molecular dynamics (MD) resolved the interfacial water structures and hydrogen bonding populations at five representative crystallographic faces expressed in these nanoparticles. Simulations of single oriented slabs underscored the individual roles of all (hydro)oxo groups in donating and accepting hydrogen bonds with first layer water in the "adsorption regime". These analyses pointed to the preponderance of hydrogen bond-donating -OH groups in the stabilization of thin water films. Contributions of μ-OH and μ3-OH groups are secondary, yet remain essential in the stabilization of thin water films. MD simulations also helped resolve crystallographic

  12. Synthesis, characterization, and evaluation of simple aluminum-based adsorbents for fluoride removal from drinking water.

    PubMed

    Du, Junyi; Sabatini, David A; Butler, Elizabeth C

    2014-04-01

    Simple aluminum (hydr)oxides and layered double hydroxides were synthesized using common chemicals and equipment by varying synthesis temperature, concentrations of extra sulfate and citrate, and metal oxide amendments. Aluminum (hydr)oxide samples were aged at either 25 or 200°C during synthesis and, in some cases, calcined at 600 °C. Despite yielding increased crystallinity and mineral phase changes, higher temperatures had a generally negative effect on fluoride adsorption. Addition of extra sulfate during synthesis of aluminum (hydr)oxides led to significantly higher fluoride adsorption capacity compared to aluminum (hydr)oxides prepared with extra citrate or no extra ligands. X-ray diffraction results suggest that extra sulfate led to the formation of both pseudoboehmite (γ-AlOOH) and basaluminite (Al4SO4(OH)10⋅4H2O) at 200 °C; energy dispersive X-ray spectroscopy confirmed the presence of sulfur in this solid. Treatment of aluminum (hydr)oxides with magnesium, manganese, and iron oxides did not significantly impact fluoride adsorption. While layered double hydroxides exhibited high maximum fluoride adsorption capacities, their adsorption capacities at dissolved fluoride concentrations close to the World Health Organization drinking water guideline of 1.5 mg L(-1) were much lower than those for the aluminum (hydr)oxides.

  13. Regenerative adsorbent heat pump

    NASA Technical Reports Server (NTRS)

    Jones, Jack A. (Inventor)

    1991-01-01

    A regenerative adsorbent heat pump process and system is provided which can regenerate a high percentage of the sensible heat of the system and at least a portion of the heat of adsorption. A series of at least four compressors containing an adsorbent is provided. A large amount of heat is transferred from compressor to compressor so that heat is regenerated. The process and system are useful for air conditioning rooms, providing room heat in the winter or for hot water heating throughout the year, and, in general, for pumping heat from a lower temperature to a higher temperature.

  14. Driving force behind adsorption-induced protein unfolding: a time-resolved X-ray reflectivity study on lysozyme adsorbed at an air/water interface.

    PubMed

    Yano, Yohko F; Uruga, Tomoya; Tanida, Hajime; Toyokawa, Hidenori; Terada, Yasuko; Takagaki, Masafumi; Yamada, Hironari

    2009-01-06

    Time-resolved X-ray reflectivity measurements for lysozyme (LSZ) adsorbed at an air/water interface were performed to study the mechanism of adsorption-induced protein unfolding. The time dependence of the density profile at the air/water interface revealed that the molecular conformation changed significantly during adsorption. Taking into account previous work using Fourier transform infrared (FTIR) spectroscopy, we propose that the LSZ molecules initially adsorbed on the air/water interface have a flat unfolded structure, forming antiparallel beta-sheets as a result of hydrophobic interactions with the gas phase. In contrast, as adsorption continues, a second layer forms in which the molecules have a very loose structure having random coils as a result of hydrophilic interactions with the hydrophilic groups that protrude from the first layer.

  15. The origin of 1560 cm-1 band in experimental IR spectra of water adsorbed on TiO2 surface: Ab initio assessment

    NASA Astrophysics Data System (ADS)

    Kevorkyants, Ruslan; Rudakova, Aida V.; Chizhov, Yuri V.; Bulanin, Kirill M.

    2016-10-01

    We present DFT study on vibrational spectrum of water layer on a surface of TiO2 which is modeled via Ti8O16 nanocluster. In contrast to ν2 mode's frequency of liquid water (1645 cm-1) for the water layer theory predicts considerably lower ν2 frequency (1570 cm-1) which matches experimentally observed shoulder in IR spectrum (1560 cm-1). We demonstrate that the calculated ν2 frequencies depend linearly on a distance between adsorbed water molecules and a surface of Ti8O16 nanocluster! We also show that hydrogen bonding strongly affects ν1 vibrational frequencies but leaves ν2 and ν3 ones almost intact.

  16. Preparation and characterization of γ-AlOOH @CS magnetic nanoparticle as a novel adsorbent for removing fluoride from drinking water.

    PubMed

    Wan, Zhen; Chen, Wei; Liu, Cheng; Liu, Yu; Dong, Changlong

    2015-04-01

    For this study, a novel adsorbent of γ-AlOOH @CS (pseudoboehmite and chitosan shell) magnetic nanoparticles (ACMN) with magnetic separation capabilities was developed to remove fluoride from drinking water. The adsorbent was first characterized, and then its performance in removing fluoride was evaluated. Kinetic data demonstrated rapid fluoride adsorption with more than 80% fluoride adsorption within the initial 20 min and equilibrium reached in 60 min. Based on the results of kinetic and isotherm models, the fluoride adsorption process on the ACMN's surface was a monolayer adsorption on a homogeneous surface. Thermodynamic parameters presented that the adsorption process is spontaneous and endothermic in nature. The mechanism for the adsorption involved electrostatic interaction and hydrogen bonding. Moreover, the calculated adsorption capacity of the ACMN for fluoride using the Langmuir model was 67.5 mg/g (20°C, pH=7.0±0.1), higher than other fluoride removal adsorbents. This nanoadsorbent performed well over a pH range of 4-10. The study found that PO4(3-) was the co-existing anion most able to hinder the nanoparticle's fluoride adsorption, followed by NO3(-) then Cl(-). Experimental results suggest that ACMN is a promising adsorbent for treating fluoride-contaminated water.

  17. First-Principles Study of the Electric Field Effect on the Water-Adsorbed Rutile Titanium Dioxide Surface

    NASA Astrophysics Data System (ADS)

    Hmiel, Abraham L.

    TiO2 is a semiconducting material that has been used extensively in many industrial applications, and recently has become a candidate for photocatalytic water splitting, fuel cell anode support materials, sensors, and other novel nanodevices. The interface of TiO2 with water, historically well-studied but still poorly understood, presents a ubiquitous environmental challenge towards the ultimate practical usefulness of these technologies. Ground-state density functional theory (DFT) calculations studying the characteristics of molecular adsorption on model surfaces have been studied for decades, showing constant improvement in the description of the energetics and electronic structure at interfaces. These simulations are invaluable in the materials science innovation pipeline because they can interpret the results of experiments and investigate properties at the nanoscale that traditional methods cannot reach. In this work, spin-polarized DFT calculations within the generalized gradient approximation and with the recent self-consistent opt-B88 van der Waals functional have been applied to investigate the problem of molecularly adsorbed water on the rutile (110) TiO2 surface under the influence of an applied electric field. The effective screening medium theory is used to break the symmetry of the simulation in the slab normal direction and implement a metal-like boundary condition at the edges of the simulation cell to model the charged capacitor in a real electrochemical device. This study begins with an investigation of bulk and surface properties of TiO2 to obtain a sound theoretical baseline. Following that, an attempt to obtain simple and meaningful structure-property relationships of rectangular TiO 2 nanowires with (110) facets resulting from quantum confinement. Finally, a systematic study of energetics, geometrical configuration, charge partitioning, and electronic structure of water in monomer coverage up to monolayer coverage provides insight into the

  18. Surface-enhanced Raman scattering of 4-aminothiophenol adsorbed on silver nanosheets deposited onto cubic boron nitride films.

    PubMed

    Zhou, Yanli; Zhi, Jinfang; Zhao, Jianwen; Xu, Maotian

    2010-01-01

    A simple method was found for the fabrication of silver nanosheets (AgNS) by the catalysis of gold nanoparticles (AuNP) on an amine-terminated cubic boron nitride (cBN) surface deposited on a Si(001) substrate in the presence of reductant. The morphology of the AgNS/AuNP/NH(2)-cBN/Si(001) sample was characterized by scanning electron microscopy and X-ray diffraction. The performance of the AgNS/AuNP/NH(2)-cBN/Si(001) sample as surface-enhanced Raman scattering (SERS) active substrate was evaluated by using 4-aminothiophenol (PATP) as the probe molecule. The SERS measurements showed that the maximum intensity was obtained on the AgNS/AuNP/NH(2)-cBN/Si(001) sample for 5 min silver deposition. Compared with the AuNP/NH(2)-cBN/Si(001) sample and a silver film/cBN/Si(001) prepared by the mirror reaction, the SERS signal of PATP was obviously improved on the above AgNS/AuNP/NH(2)-cBN/Si(001) film. The sensitivity and the stability of the AgNS/AuNP/NH(2)-cBN/Si(001) sample were also investigated.

  19. Strain-induced water dissociation on supported ultrathin oxide films

    PubMed Central

    Song, Zhenjun; Fan, Jing; Xu, Hu

    2016-01-01

    Controlling the dissociation of single water molecule on an insulating surface plays a crucial role in many catalytic reactions. In this work, we have identified the enhanced chemical reactivity of ultrathin MgO(100) films deposited on Mo(100) substrate that causes water dissociation. We reveal that the ability to split water on insulating surface closely depends on the lattice mismatch between ultrathin films and the underlying substrate, and substrate-induced in-plane tensile strain dramatically results in water dissociation on MgO(100). Three dissociative adsorption configurations of water with lower energy are predicted, and the structural transition going from molecular form to dissociative form is almost barrierless. Our results provide an effective avenue to achieve water dissociation at the single-molecule level and shed light on how to tune the chemical reactions of insulating surfaces by choosing the suitable substrates. PMID:26953105

  20. Polydopamine Films from the Forgotten Air/Water Interface.

    PubMed

    Ponzio, Florian; Payamyar, Payam; Schneider, Anne; Winterhalter, Mathias; Bour, Jérôme; Addiego, Frédéric; Krafft, Marie-Pierre; Hemmerle, Joseph; Ball, Vincent

    2014-10-02

    The formation of polydopamine under mild oxidation conditions from dopamine solutions with mechanical agitation leads to the formation of films that can functionalize all kinds of materials. In the absence of stirring of the solution, we report the formation of polydopamine films at the air/water interface (PDA A/W) and suggest that it arises from an homogeneous nucleation process. These films grow two times faster than in solution and can be deposited on hydrophilic or hydrophobic substrates by the Langmuir-Schaeffer technique. Thanks to this new method, porous and hydrophobic materials like polytetrafluoroethylene (PTFE) membranes can be completely covered with a 35 nm thick PDA A/W film after only 3h of reaction. Finally the oxidation of a monomer followed by a polymerization in water is not exclusive to polydopamine since we also transferred polyaniline functional films from the air/water interface to solid substrates. These findings suggest that self-assembly from a solution containing hydrophilic monomers undergoing a chemical transformation (here oxidation and oligomerization) could be a general method to produce films at the liquid/air interface.

  1. Hexagonal boron nitride nanosheets as adsorbents for solid-phase extraction of polychlorinated biphenyls from water samples.

    PubMed

    Jia, Shiliang; Wang, Zhenhua; Ding, Ning; Elaine Wong, Y-L; Chen, Xiangfeng; Qiu, Guangyu; Dominic Chan, T-W

    2016-09-14

    The adsorptive potential of hexagonal boron nitride nanosheets (h-BNNSs) for solid-phase extraction (SPE) of pollutants was investigated for the first time. Seven indicators of polychlorinated biphenyls (PCBs) were selected as target analytes. The adsorption of PCBs on the surface of the h-BNNSs in water was simulated by the density functional theory and molecular dynamics. The simulation results indicated that the PCBs are adsorbed on the surface by π-π, hydrophobic, and electrostatic interactions. The PCBs were extracted with an h-BNNS-packed SPE cartridge, and eluted by dichloromethane. Gas chromatography-tandem mass spectrometry working in the multiple reaction monitor mode was used for the sample quantification. The effect of extraction parameters, including the flow rate, pH value, breakthrough volume, and the ionic strength, were investigated. Under the optimal working conditions, the developed method showed low limits of detection (0.24-0.50 ng L(-1); signal-to-noise ratio = 3:1), low limits of quantification (0.79-1.56 ng L(-1); signal-to-noise ratio = 10:1), satisfactory linearity (r > 0.99) within the concentration range of 2-1000 ng L(-1), and good precision (relative standard deviation < 12%). The PCBs concentration in environmental water samples was determined by the developed method. This results demonstrate that h-BNNSs have high analytical potential in the enrichment of pollutants.

  2. Methyl red removal from water by iron based metal-organic frameworks loaded onto iron oxide nanoparticle adsorbent

    NASA Astrophysics Data System (ADS)

    Dadfarnia, S.; Haji Shabani, A. M.; Moradi, S. E.; Emami, S.

    2015-03-01

    The objective followed by this research is the synthesis of iron based metal organic framework loaded on iron oxide nanoparticles (Fe3O4@MIL-100(Fe)) and the study of its capability for the removal of methyl red. Effective parameters in the selection of a new adsorbent, i.e. adsorption capacity, thermodynamics, and kinetics were investigated. All the studies were carried out in batch experiments. Removal of methyl red from aqueous solutions varied with the amount of adsorbent, methyl red contact time, initial concentration of dye, adsorbent dosage, and solution pH. The capability of the synthesized adsorbent in the removal of methyl red was compared with the metal organic framework (MIL-100(Fe)) and iron oxide nanoparticles. The results show that Fe3O4@MIL-100(Fe) nanocomposite exhibits an enhanced adsorption capacity.

  3. A comparison of different concentration methods for the detection of viruses present in bottled waters and those adsorbed to water bottle surfaces.

    PubMed

    Huguet, L; Carteret, C; Gantzer, C

    2012-04-01

    This study aimed to provide a tool for selecting the best approach to virological testing of bottled waters. Different methods were investigated. Method A examined the recovery of virus RNA following in situ lysis of virus particles in the aqueous phase and of those adhered to the bottle wall, method B examined the recovery of virus RNA following lysis of virus particles in the aqueous phase, and method C examined the recovery of intact virus particles. Method C generated the lowest genome recovery rate regardless of the water and virus type used, therefore comparison was mainly conducted between methods A and B.The effects of independent variables on the viral RNA recovery rate were determined by full factorial design. These independent variables included three waters (differing in mineral composition), four viruses (poliovirus 1, hepatitis A virus, Norovirus, and the MS2 phage), three incubation times (0, 10, and 20 days), and two methods (A and B). According to the results, each factor influenced the recovery rate of viral RNA with the exception of incubation time. Statistical analysis identified interactions between the factors. The strongest interactions involved the water and virus types, as well as the methods. The results suggested that method A should be used for the concentration and detection of hepatitis A virus, regardless of the divalent cation concentration of the bottled water. Method A was most suitable for water with the highest mineral content (divalent cation concentration of 250 mgL(-1)) and for the analysis of viruses capable of adsorbing onto the bottle walls (Poliovirus 1). Method B could be recommended for the analysis of water whose cation concentration is unknown.

  4. Isothermal dehydration of thin films of water and sugar solutions

    SciTech Connect

    Heyd, R.; Rampino, A.; Bellich, B.; Elisei, E.; Cesàro, A.; Saboungi, M.-L.

    2014-03-28

    The process of quasi-isothermal dehydration of thin films of pure water and aqueous sugar solutions is investigated with a dual experimental and theoretical approach. A nanoporous paper disk with a homogeneous internal structure was used as a substrate. This experimental set-up makes it possible to gather thermodynamic data under well-defined conditions, develop a numerical model, and extract needed information about the dehydration process, in particular the water activity. It is found that the temperature evolution of the pure water film is not strictly isothermal during the drying process, possibly due to the influence of water diffusion through the cellulose web of the substrate. The role of sugar is clearly detectable and its influence on the dehydration process can be identified. At the end of the drying process, trehalose molecules slow down the diffusion of water molecules through the substrate in a more pronounced way than do the glucose molecules.

  5. Adsorption of organic matter at mineral/water interfaces: I. ATR-FTIR spectroscopic and quantum chemical study of oxalate adsorbed at boehmite/water and corundum/water interfaces

    NASA Astrophysics Data System (ADS)

    Yoon, Tae Hyun; Johnson, Stephen B.; Musgrave, Charles B.; Brown, Gordon E.

    2004-11-01

    The types and structures of adsorption complexes formed by oxalate at boehmite (γ-AlOOH)/water and corundum (α-Al 2O 3)/water interfaces were determined using in situ attenuated total reflectance fourier transform infrared (ATR-FTIR) spectroscopy and quantum chemical simulation methods. At pH 5.1, at least four different oxalate species were found at or near the boehmite/water interface for oxalate surface coverages (Γ ox) ranging from 0.25 to 16.44 μmol/m 2. At relatively low coverages (Γ ox < 2.47), strongly adsorbed inner-sphere oxalate species (IR peaks at 1286, 1418, 1700, and 1720 cm -1) replace weakly adsorbed carbonate species, and a small proportion of oxalate anions are adsorbed in an outer-sphere mode (IR peaks at 1314 and 1591 cm -1). IR peaks indicative of inner-sphere adsorbed oxalate are also observed for oxalate at the corundum/water interface at Γ ox = 1.4 μmol/m 2. With increasing oxalate concentration (Γ ox > 2.47 μmol/m 2), the boehmite surface binding sites for inner-sphere adsorbed oxalate become saturated, and excess oxalate ions are present dominantly as aqueous species (IR peaks at 1309 and 1571 cm -1). In addition to these adsorption processes, oxalate-promoted dissolution of boehmite following inner-sphere oxalate adsorption becomes increasingly pronounced with increasing Γ ox and results in an aqueous Al(III)-oxalate species, as indicated by shifted IR peaks (1286 → 1297 cm -1 and 1418 → 1408 cm -1). At pH 2.5, no outer-sphere adsorbed oxalate or aqueous oxalate species were observed. The similarity of adsorbed oxalate spectral features at pH 2.5 and 5.1 implies that the adsorption mechanism of aqueous HOx - species involves loss of protons from this species during the ligand-exchange reaction. As a consequence, adsorbed inner-sphere oxalate and aqueous Al(III)-oxalate complexes formed at pH 2.5 have coordination geometries very similar to those formed at pH 5.1. The coordination geometry of inner-sphere adsorbed oxalate

  6. Application of near infrared spectroscopy for the determination of adsorbed p-nitrophenol on HDTMA organoclay--implications for the removal of organic pollutants from water.

    PubMed

    Zhou, Qin; Xi, Yunfei; He, Hongping; Frost, Ray L

    2008-03-01

    NIR spectroscopy has been used to measure the adsorption of p-nitrophenol on untreated montmorillonite and surfactant exchanged montmorillonite. p-Nitrophenol is characterised by an intense NIR band at 8890 cm(-1) which shifts to 8840 cm(-1) upon adsorption on organoclay. The band was not observed for p-nitrophenol adsorbed on untreated montmorillonite. Both the montmorillonite and the surfactant modified montmorillonite are characterised by NIR bands at 7061 and 6791 cm(-1). The organoclay is characterised by two prominent bands at 5871 and 5667 cm(-1) assigned to the fundamental overtones of the mid-IR bands at 2916 and 2850 cm(-1). A band at 6017 cm(-1) is attributed to the p-nitrophenol adsorbed on the organoclay. The band is not observed for the montmorillonite with adsorbed p-nitrophenol. It is concluded that p-nitrophenol is adsorbed to significantly greater amounts on the organoclay compared with the untreated montmorillonite. The implication is that organoclays are most useful for removing organic molecules from water through adsorption.

  7. A study of the potential application of nano-Mg(OH)2 in adsorbing low concentrations of uranyl tricarbonate from water.

    PubMed

    Cao, Qing; Huang, Feng; Zhuang, Zanyong; Lin, Zhang

    2012-04-07

    This work aims at the investigation of nano-Mg(OH)(2) as a promising adsorbent for uranium recovery from water. Systematic analysis including the uranium adsorption isotherm, the kinetics and the thermodynamics of adsorption of low concentrations of uranyl tricarbonate (0.1-20 mg L(-1)) by nano-Mg(OH)(2) was carried out. The results showed a spontaneous and exothermic uranium adsorption process by Mg(OH)(2), which could be well described with pseudo second order kinetics. Surface site calculation and zeta potential measurement further demonstrated that UO(2)(CO(3))(3)(4-) was a monolayer adsorbed onto nano-Mg(OH)(2) by electrostatic forces. Accordingly, the adsorption behavior met the conditions of the Langmuir isotherm. Moreover, in most of the reported literature, nano-Mg(OH)(2) had a higher UO(2)(CO(3))(3)(4-) adsorption affinity b, which implied a higher adsorption amount at equilibrium in a dilute adsorbate system. The significance of the adsorption affinity b for choosing and designing adsorbents with respect to low concentration of resources/pollutants treatment has also been assessed.

  8. Development of magnetic graphene oxide adsorbent for the removal and preconcentration of As(III) and As(V) species from environmental water samples.

    PubMed

    Rashidi Nodeh, Hamid; Wan Ibrahim, Wan Aini; Ali, Imran; Sanagi, Mohd Marsin

    2016-05-01

    New-generation adsorbent, Fe3O4@SiO2/GO, was developed by modification of graphene oxide (GO) with silica-coated (SiO2) magnetic nanoparticles (Fe3O4). The synthesized adsorbent was characterized using Fourier transform infrared spectroscopy, X-ray diffractometry, energy-dispersive X-ray spectroscopy, and field emission scanning electron microscopy. The developed adsorbent was used for the removal and simultaneous preconcentration of As(III) and As(V) from environmental waters prior to ICP-MS analysis. Fe3O4@SiO2/GO provided high adsorption capacities, i.e., 7.51 and 11.46 mg g(-1) for As(III) and As(V), respectively, at pH 4.0. Adsorption isotherm, kinetic, and thermodynamic were investigated for As(III) and As(V) adsorption. Preconcentration of As(III) and As(V) were studied using magnetic solid-phase extraction (MSPE) method at pH 9.0 as the adsorbent showed selective adsorption for As(III) only in pH range 7-10. MSPE using Fe3O4@SiO2/GO was developed with good linearities (0.05-2.0 ng mL(-1)) and high coefficient of determination (R (2) = 0.9992 and 0.9985) for As(III) and As(V), respectively. The limits of detection (LODs) (3× SD/m, n = 3) obtained were 7.9 pg mL(-1) for As(III) and 28.0 pg mL(-1) for As(V). The LOD obtained is 357-1265× lower than the WHO maximum permissible limit of 10.0 ng mL(-1). The developed MSPE method showed good relative recoveries (72.55-109.71 %) and good RSDs (0.1-4.3 %, n = 3) for spring water, lake, river, and tap water samples. The new-generation adsorbent can be used for the removal and simultaneous preconcentration of As(III) and As(V) from water samples successfully. The adsorbent removal for As(III) is better than As(V).

  9. Water Films: Moisture that Extends Beyond the Capillary Wetting Front

    NASA Astrophysics Data System (ADS)

    Dragila, M. I.; Ambrowiak, G.

    2015-12-01

    Imbibition dynamics were investigated by measuring upward imbibition rates in laboratory vertical columns that were filled with sandy loam soil media. The contribution of films and capillary water which drives the infiltrating wetting front was successfully quantified. It was demonstrated that films move ahead of the wetting front only after capillary water has ceased driving percolation, and that the hydraulic diffusion coefficient (Dh) of film flow varied from 10-70% of the hydraulic diffusion coefficient of capillary water. The magnitude of Dh depended upon particle size distribution, surface roughness and initial moisture content of the media. What is the potential value of this mechanism in soil moisture dynamics research? (1) In coarse textured soils with low capillary potential, film that stretches well beyond the capillary wetting front can provide moisture to microbiota and mycorhyza, thereby increasing nutrient diffusion to a broader area than by capillary based models (e.g., modeling of drip irrigation systems). Even though the potential role of films in these processes has been previously discussed, the magnitude of potential moisture delivery has not been measured. (2) Films surging ahead of a decelerating capillary front may reduce the effect of subsurface water repellency. It is known that over time, moisture decreases both the contact angle of water against silica and water repellent soils. Therefore, in time, a film may predispose sandy soil to greater imbibition capacity. (3) The need to maximize water efficiency becomes exceedingly important in drought threatened, semi-arid irrigated agriculture. A thoughtful, yet realistic balance must be reached between water conservation and crop production. As our climate changes and water needs increase, protecting against crop failure will require a more comprehensive understanding of the mechanisms that control soil moisture dynamics. This study adds to this conversation by investigating higher level

  10. Preliminary indications of water film distribution and thickness on an airfoil in a water spray

    NASA Technical Reports Server (NTRS)

    Hastings, E. C., Jr.; Weinstein, L. M.

    1984-01-01

    A sensor for measuring water film thickness is evaluated. The test is conducted in a small flow apparatus with a 1 ft chord model wing in a water spray. Photographic and visual observations are made of the upper wing surface and film thickness is measured on the upper and lower wing surfaces. The performance of the sensor appears highly satisfactory, and where valid comparisons can be made, repeatable results are obtained.

  11. Amino-functionalized mesoporous MCM-41 silica as an efficient adsorbent for water treatment: batch and fixed-bed column adsorption of the nitrate anion

    NASA Astrophysics Data System (ADS)

    Ebrahimi-Gatkash, Mehdi; Younesi, Habibollah; Shahbazi, Afsaneh; Heidari, Ava

    2015-11-01

    In the present study, amino-functionalized Mobil Composite Material No. 41 (MCM-41) was used as an adsorbent to remove nitrate anions from aqueous solutions. Mono-, di- and tri-amino functioned silicas (N-MCM-41, NN-MCM-41 and NNN-MCM-41) were prepared by post-synthesis grafting method. The samples were characterized by means of X-ray powder diffraction, FTIR spectroscopy, thermogravimetric analysis, scanning electron microscopy and nitrogen adsorption-desorption. The effects of pH, initial concentration of anions, and adsorbent loading were examined in batch adsorption system. Results of adsorption experiments showed that the adsorption capacity increased with increasing adsorbent loading and initial anion concentration. It was found that the Langmuir mathematical model indicated better fit to the experimental data than the Freundlich. According to the constants of the Langmuir equation, the maximum adsorption capacity for nitrate anion by N-MCM-41, NN-MCM-41 and NNN-MCM-41 was found to be 31.68, 38.58 and 36.81 mg/g, respectively. The adsorption kinetics were investigated with pseudo-first-order and pseudo-second-order model. Adsorption followed the pseudo-second-order rate kinetics. The coefficients of determination for pseudo-second-order kinetic model are >0.99. For continuous adsorption experiments, NNN-MCM-41 adsorbent was used for the removal of nitrate anion from solutions. Breakthrough curves were investigated at different bed heights, flow rates and initial nitrate anion concentrations. The Thomas and Yan models were utilized to calculate the kinetic parameters and to predict the breakthrough curves of different bed height. Results from this study illustrated the potential utility of these adsorbents for nitrate removal from water solution.

  12. Dielectric Characterization of Confined Water in Chiral Cellulose Nanocrystal Films.

    PubMed

    Natarajan, Bharath; Emiroglu, Caglar; Obrzut, Jan; Fox, Douglas M; Pazmino, Beatriz; Douglas, Jack F; Gilman, Jeffrey W

    2017-04-10

    A known deterrent to the large-scale development and use of cellulose nanocrystals (CNCs) in composite materials is their affinity for moisture, which has a profound effect on dispersion, wetting, interfacial adhesion, matrix crystallization, water uptake and hydrothermal stability. To quantify and control the hydration and confinement of absorbed water in CNCs we studied sulfated-CNCs neutralized with sodium cations and CNCs functionalized with less hydrophilic methyl(triphenyl)phosphonium cations. Films were cast from water suspensions at 20 ○C under controlled humidity and drying rate, yielding CNC materials with distinguishably different dielectric properties and cholesteric structures. By controlling the evaporation rate, we obtained self-assembled chiral CNC films with extended uniformity, having helical modulation length (nominal pitch) tunable from 1300 nm to 600 nm. SEM imaging, and UV-Vis-NIR total reflectance spectra revealed tighter and more uniform CNC packing in films cast at slow evaporation rates or having lower surface energy when modified with phosphonium. The dielectric constant was measured by a non-contact microwave cavity perturbation method and fitted to a classical mixing model employing randomly oriented ellipsoidal water inclusions. The dielectric constant of absorbed water was found to be significantly smaller than that for free liquid indicating a limited mobility due to binding with the CNC "matrix". In the case of hydrophilic Na modified CNCs, a decreasing pitch led to greater anisotropy in the shape of moisture inclusions (spherical to platelet-like) and greater confinement. In contrast, the structure of hydrophobic phosphonium modified CNC films was found to reduce the pitch considerably, yet the shape of confined water remained predominantly spherical. These results provide a useful perspective on the current state of understanding of CNC-water interactions as well as on CNC self-assembly mechanisms. More broadly we believe that

  13. MTBE adsorption on alternative adsorbents and packed bed adsorber performance.

    PubMed

    Rossner, Alfred; Knappe, Detlef R U

    2008-04-01

    Widespread use of the fuel additive methyl tertiary-butyl ether (MTBE) has led to frequent MTBE detections in North American and European drinking water sources. The overall objective of this research was to evaluate the effectiveness of a silicalite zeolite, a carbonaceous resin, and a coconut-shell-based granular activated carbon (GAC) for the removal of MTBE from water. Isotherm and short bed adsorber tests were conducted in ultrapure water and river water to obtain parameters describing MTBE adsorption equilibria and kinetics and to quantify the effect of natural organic matter (NOM) on MTBE adsorption. Both the silicalite zeolite and the carbonaceous resin exhibited larger MTBE adsorption uptakes than the tested GAC. Surface diffusion coefficients describing intraparticle MTBE mass transfer rates were largest for the GAC and smallest for the carbonaceous resin. Pilot tests were conducted to verify MTBE breakthrough curve predictions obtained with the homogeneous surface diffusion model and to evaluate the effect of NOM preloading on packed bed adsorber performance. Results showed that GAC was the most cost-competitive adsorbent when considering adsorbent usage rate only; however, the useful life of an adsorber containing silicalite zeolite was predicted to be approximately 5-6 times longer than that of an equally sized adsorber containing GAC. Pilot column results also showed that NOM preloading did not impair the MTBE removal efficiency of the silicalite zeolite. Thus, it may be possible to regenerate spent silicalite with less energy-intensive methods than those required to regenerate GAC.

  14. Synthesis of an attapulgite clay@carbon nanocomposite adsorbent by a hydrothermal carbonization process and their application in the removal of toxic metal ions from water.

    PubMed

    Chen, Li-Feng; Liang, Hai-Wei; Lu, Yang; Cui, Chun-Hua; Yu, Shu-Hong

    2011-07-19

    A new kind of attapulgite clay@carbon (ATP@C) nanocomposite adsorbent has been synthesized by a one-pot hydrothermal carbonization process under mild conditions using two cheap, ecofriendly materials (i.e., attapulgite clay (ATP), which is a magnesium aluminum silicate that is abundant in nature, and glucose, which is a green chemical obtained from biomass). Compared to carbon-based materials, this new ATP@C nanocomposite exhibits a high adsorption ability for Cr(VI) and Pb(II) ions with maximum adsorption capacities of 177.74 and 263.83 mg·g(-1), respectively. The results demonstrate that this nanocomposite is an exceptionally promising candidate as a low-cost, sustainable, and effective adsorbent for the removal of toxic ions from water.

  15. Thin water film formation on metal oxide crystal surfaces.

    PubMed

    Gilbert, Benjamin; Katz, Jordan E; Rude, Bruce; Glover, T E; Hertlein, Marcus P; Kurz, Charles; Zhang, Xiaoyi

    2012-10-09

    Reactions taking place at hydrated metal oxide surfaces are of considerable environmental and technological importance. Surface-sensitive X-ray methods can provide structural and chemical information on stable interfacial species, but it is challenging to perform in situ studies of reaction kinetics in the presence of water. We have implemented a new approach to creating a micrometer-scale water film on a metal oxide surface by combining liquid and gas jets on a spinning crystal. The water films are stable indefinitely and sufficiently thin to allow grazing incidence X-ray reflectivity and spectroscopy measurements. The approach will enable studies of a wide range of surface reactions and is compatible with interfacial optical-pump/X-ray-probe studies.

  16. 21 CFR 177.1400 - Hydroxyethyl cellulose film, water-insoluble.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Hydroxyethyl cellulose film, water-insoluble. 177... Repeated Use Food Contact Surfaces § 177.1400 Hydroxyethyl cellulose film, water-insoluble. Water-insoluble hydroxyethyl cellulose film may be safely used for packaging food in accordance with the following...

  17. Preparation, characterization and application of Saussurea tridactyla Sch-Bip as green adsorbents for preconcentration of rare earth elements in environmental water samples

    NASA Astrophysics Data System (ADS)

    Zhang, Qiangying; He, Man; Chen, Beibei; Hu, Bin

    2016-07-01

    This paper deals with preparation, characterization and application of the Saussurea tridactyla Sch-Bip (STSB) as a new green adsorbent for separation of matrix elements and preconcentration of rare earth elements (REEs) in environmental water samples. The pretreated STSB adsorbent with 2 mol L- 1 NaOH is characterized with higher surface area and adsorption capacities in comparison with a raw STSB material. The new adsorbent was used for the development of on-line solid phase extraction (SPE) for the determination of REEs by radial viewing 27 MHz inductively coupled plasma optical emission spectrometry (ICP-OES). Various parameters affecting the adsorption/desorption procedure were optimized. The adsorption capacities for the STSB were found to be 62.2 (Y)-153 mg g- 1 (Tm). Under the optimized conditions, the limits of detection (LODs, 3σ) for REEs were in the range of 0.06 (Yb)-8.77 (Sm) ng mL- 1. The relative standard deviations (RSDs) for 7 replicate determinations of target REEs at low concentration level ranged from 2.4 (Yb) to 8.9 (Sm)%. The adsorption isotherm fitted Langmuir model and the adsorption kinetics fitted well with both Pseudo-first order and Pseudo-second order models. The predominant adsorption mechanism is ion exchange. The STSB pretreated with 2 mol L- 1 NaOH has been demonstrated to be low cost, green and environment friendly adsorbent, featuring with high adsorption capacity, wide pH range, and fast adsorption/desorption kinetics for target REEs with long lifetime. The proposed method was applied to the determination of REEs in East Lake, Yangtze River and rain water samples.

  18. Sulfate-doped Fe3O4/Al2O3 nanoparticles as a novel adsorbent for fluoride removal from drinking water.

    PubMed

    Chai, Liyuan; Wang, Yunyan; Zhao, Na; Yang, Weichun; You, Xiangyu

    2013-08-01

    A novel adsorbent of sulfate-doped Fe3O4/Al2O3 nanoparticles with magnetic separability was developed for fluoride removal from drinking water. The nanosized adsorbent was characterized and its performance in fluoride removal was evaluated. Kinetic data reveal that the fluoride adsorption was rapid in the beginning followed by a slower adsorption process, nearly 90% adsorption can be achieved within 20 min and only 10-15% additional removal occurred in the following 8 h. The fluoride adsorption isotherm was well described by Elovich model. The calculated adsorption capacity of this nanoadsorbent for fluoride by two-site Langmuir model was 70.4 mg/g at pH 7.0. Moreover, this nanoadsorbent performed well over a considerable wide pH range of 4-10, and the fluoride removal efficiencies reached up to 90% and 70% throughout the pH range of 4-10 with initial fluoride concentrations of 10 mg/L and 50 mg/L, respectively. The observed sulfate-fluoride displacement and decreased sulfur content on the adsorbent surface reveal that anion exchange process was an important mechanism for fluoride adsorption by the sulfate-doped Fe3O4/Al2O3 nanoparticles. Moreover, a shift of the pH of zero point charge (pHPZC) of the nanoparticles and surface analysis based on X-ray photoelectron spectroscopy (XPS) suggest the formation of inner-sphere fluoride complex at the aluminum center as another adsorption mechanism. With the exception of PO4(3-), other co-existing anions (NO3(-), Cl(-) and SO4(2-)) did not evidently inhibit fluoride removal by the nanoparticles. Findings of this study demonstrate the potential utility of the nanoparticles as an effective adsorbent for fluoride removal from drinking water.

  19. Uptake of CO2, SO2, HNO3 and HCl on calcite (CaCO3) at 300 K: mechanism and the role of adsorbed water.

    PubMed

    Santschi, Ch; Rossi, M J

    2006-06-01

    All experimental observations of the uptake of the four title compounds on calcite are consistent with the presence of a reactive bifunctional surface intermediate Ca(OH)(HCO3) that has been proposed in the literature. The uptake of CO2 and SO2 occurs on specific adsorption sites of crystalline CaCO3(s) rather than by dissolution in adsorbed water, H2O(ads). SO2 primarily interacts with the bicarbonate moiety whereas CO2, HNO3 and HCl all react first with the hydroxyl group of the surface intermediate. Subsequently, the latter two react with the bicarbonate group to presumably form Ca(NO3)2 and CaCl2.2H2O. The effective equilibrium constant of the interaction of CO2 with calcite in the presence of H2O(ads) is kappa = deltaCO2/(H2O(ads)[CO2]) = 1.62 x 10(3) bar(-1), where CO2 is the quantity of CO2 adsorbed on CaCO3. The reaction mechanism involves a weakly bound precursor species that is reversibly adsorbed and undergoes rate-controlling concurrent reactions with both functionalities of the surface intermediate. The initial uptake coefficients gamma0 on calcite powder depend on the abundance of H2O(ads) under the present experimental conditions and are on the order of 10(-4) for CO2 and 0.1 for SO2, HNO3 and HCl, with gamma(ss) being significantly smaller than gamma0 for HNO3 and HCl, thus indicating partial saturation of the uptake. At 33% relative humidity and 300 K there are 3.5 layers of H2O adsorbed on calcite that reduce to a fraction of a monolayer of weakly and strongly bound water upon pumping and/or heating.

  20. Characterization of Thin Film Dissolution in Water with in Situ Monitoring of Film Thickness Using Reflectometry.

    PubMed

    Yersak, Alexander S; Lewis, Ryan J; Tran, Jenny; Lee, Yung C

    2016-07-13

    Reflectometry was implemented as an in situ thickness measurement technique for rapid characterization of the dissolution dynamics of thin film protective barriers in elevated water temperatures above 100 °C. Using this technique, multiple types of coatings were simultaneously evaluated in days rather than years. This technique enabled the uninterrupted characterization of dissolution rates for different coating deposition temperatures, postdeposition annealing conditions, and locations on the coating surfaces. Atomic layer deposition (ALD) SiO2 and wet thermally grown SiO2 (wtg-SiO2) thin films were demonstrated to be dissolution-predictable barriers for the protection of metals such as copper. A ∼49% reduction in dissolution rate was achieved for ALD SiO2 films by increasing the deposition temperatures from 150 to 300 °C. ALD SiO2 deposited at 300 °C and followed by annealing in an inert N2 environment at 1065 °C resulted in a further ∼51% reduction in dissolution rate compared with the nonannealed sample. ALD SiO2 dissolution rates were thus lowered to values of wtg-SiO2 in water by the combination of increasing the deposition temperature and postdeposition annealing. Thin metal films, such as copper, without a SiO2 barrier corroded at an expected ∼1-2 nm/day rate when immersed in room temperature water. This measurement technique can be applied to any optically transparent coating.

  1. Thin Water and Ice Films at Mineral Surfaces

    NASA Astrophysics Data System (ADS)

    Yeşilbaş, Merve; Boily, Jean-François

    2016-04-01

    Mineral-water and ice interactions play important roles in atmospheric cloud formation. They also affect soil biogeochemistry as well as outer-space processes. In this study, thin water and ice films formed on minerals of varied bulk and surface structure, shape, size and surface roughness were probed by Fourier Transform Infrared Spectroscopy (FTIR) and by Dynamic Vapor Adsorption (DVA). Measurements on several types of iron (oxyhydr)oxides, phyllosilicates, orthosilicates, tectosilicates as well as Arizona Test Dust (ATD) and Icelandic volcanic ash constrained our understanding of the molecular-level nature of mineral surface-water and ice interactions. DVA experiments showed that particle size is the key feature controlling water loadings at 25 ° C. Under this condition, nano-sized particles stabilized the equivalence of no more than ˜6 monolayers of water at the near saturation of water vapor while sub-micron sized particles stabilized several thousand layers. This result can be explained by the greater ability of larger sized particles at driving water condensation reactions. Cryogenic FTIR measurements at -10 and -50 ° C revealed that most minerals acquired the thin ice films with similar hydrogen bonding environments as those formed at room temperature.[1,2] These thin ice films have weaker hydrogen bond environments than hexagonal ice (νOH ≈ 3130 cm-1), a result seen by FTIR through predominant O-H stretching modes at νOH ≈ 3408-3425 cm-1. The water bending region (˜1630 cm-1) also reveals that most thin ice films are rather supercooled forms of water. Only the materials with greatest levels of heterogeneity, namely ATD and volcanic ash, stabilized solid forms of water reminiscent to hexagonal ice. This work thus constrains further our understanding of how interfacial ice is stabilized at mineral surfaces, and opens possibilities for future studies focused on atmospheric gas uptake on mineral- water and ice admixtures. [1] Song, X. and Boily, J

  2. Bioinspired molecular adhesive for water-resistant oxygen indicator films.

    PubMed

    Vu, Chau Hai Thai; Won, Keehoon

    2013-01-01

    Mussels can attach themselves to nearly all types of hard surfaces in wet environments. Such attractive adhesive ability of mussels is believed to rely on the amino acid composition of proteins found near the plaque-substrate interface. Dopamine (DA) is identified as a simplified mimic of mussel proteins, which are rich in 3,4-dihydroxy-L-phenylalanine and lysine, because it contains both catechol and amine functional groups. In this work, we have first applied this bioinspired adhesive to tackle a dye leaching problem of colorimetric oxygen indicator films, which are widely used to ensure the absence of oxygen inside the package of oxygen-sensitive materials. Simple immersion of packaging films into a DA solution resulted in poly(DA) deposition, decreasing the water contact angle of the films from 105° to 65°. The poly(DA) coating could reduce the thionine leakage of the UV-activated oxygen indicator film. The effects of poly(DA) coating were found to be dependent on the DA solution pH, the coating time, and the DA concentration. The film resistant to dye leaching lost its dye color by 5 min UVB irradiation and regained the color in the presence of oxygen, demonstrating that it functioned successfully as UV-activated oxygen indicators.

  3. Magnetic metal-organic framework-titanium dioxide nanocomposite as adsorbent in the magnetic solid-phase extraction of fungicides from environmental water samples.

    PubMed

    Su, Hao; Lin, Yunliang; Wang, Zhenhua; Wong, Y-L Elaine; Chen, Xiangfeng; Chan, T-W Dominic

    2016-09-30

    In this work, a core-shell Fe3O4@SiO2@MOF/TiO2 nanocomposite was synthesized and used to as adsorbent for magnetic solid-phase extraction (MSPE) of triazole fungicides from environmental water samples. Five triazole fungicides, namely, triadimenol, hexaconazole, diniconazole, myclobutanil, and tebuconazole, were selected as target analytes for MSPE. These analytes were quantitatively adsorbed on microspheres, and the sorbents were separated from the solution by using a magnet. The analytes were desorbed by methanol and determined through liquid-chromatography coupled with tandem mass spectrometry. The extraction parameters affecting the extraction efficiency were optimized through response surface methodology. The limits of detection and limits of quantification for the selected fungicides were 0.19-1.20ngL(-1) and 0.61-3.62ngL(-1), respectively. The proposed method was applied to determine the concentration of fungicides in actual environmental water samples. The accuracy of the proposed method was evaluated by measuring the recovery of the spiked samples. The satisfying recoveries of the four water samples ranged from 90.2% to 104.2%. Therefore, the magnetic metal-organic framework/TiO2 nanocomposite based MSPE is a potential approach to analyze fungicides in actual water samples.

  4. Adsorptive Removal of Pharmaceuticals and Personal Care Products from Water with Functionalized Metal-organic Frameworks: Remarkable Adsorbents with Hydrogen-bonding Abilities

    PubMed Central

    Seo, Pill Won; Bhadra, Biswa Nath; Ahmed, Imteaz; Khan, Nazmul Abedin; Jhung, Sung Hwa

    2016-01-01

    Adsorption of typical pharmaceuticals and personal care products (PPCPs) (such as naproxen, ibuprofen and oxybenzone) from aqueous solutions was studied by using the highly porous metal-organic framework (MOF) MIL-101 with and without functionalization. Adsorption results showed that MIL-101s with H-donor functional groups such as –OH and –NH2 were very effective for naproxen adsorption, despite a decrease in porosity, probably because of H-bonding between O atoms on naproxen and H atoms on the adsorbent. For this reason, MIL-101 with two functional groups capable of H-bonding (MIL-101-(OH)2) exhibited remarkable adsorption capacity based on adsorbent surface area. The favorable contributions of –OH and –(OH)2 on MIL-101 in the increased adsorption of ibuprofen and oxybenzone (especially based on porosity) confirmed again the importance of H-bonding mechanism. The adsorbent with the highest adsorption capacity, MIL-101-OH, was very competitive when compared with carbonaceous materials, mesoporous materials, and pristine MIL-101. Moreover, the MIL-101-OH could be recycled several times by simply washing with ethanol, suggesting potential application in the adsorptive removal of PPCPs from water. PMID:27695005

  5. Wide pH range for fluoride removal from water by MHS-MgO/MgCO₃ adsorbent: kinetic, thermodynamic and mechanism studies.

    PubMed

    Zhang, Kaisheng; Wu, Shibiao; Wang, Xuelong; He, Junyong; Sun, Bai; Jia, Yong; Luo, Tao; Meng, Fanli; Jin, Zhen; Lin, Dongyue; Shen, Wei; Kong, Lingtao; Liu, Jinhuai

    2015-05-15

    A novel environment friendly adsorbent, micro-nano hierarchical structured flower-like MgO/MgCO3 (MHS-MgO/MgCO3), was developed for fluoride removal from water. The adsorbent was characterized and its defluoridation properties were investigated. Adsorption kinetics fitted well the pseudo-second-order model. Kinetic data revealed that the fluoride adsorption was rapid, more than 83-90% of fluoride could be removed within 30 min, and the adsorption equilibrium was achieved in the following 4 h. The fluoride adsorption isotherm was well described by Freundlich model. The maximum adsorption capacity was about 300 mg/g at pH=7. Moreover, this adsorbent possessed a very wide available pH range of 5-11, and the fluoride removal efficiencies even reached up to 86.2%, 83.2% and 76.5% at pH=11 for initial fluoride concentrations of 10, 20 and 30 mg/L, respectively. The effects of co-existing anions indicated that the anions had less effect on adsorption of fluoride except phosphate. In addition, the adsorption mechanism analysis revealed that the wide available pH range toward fluoride was mainly resulted from the exchange of the carbonate and hydroxyl groups on the surface of the MHS-MgO/MgCO3 with fluoride anions.

  6. Adsorptive Removal of Pharmaceuticals and Personal Care Products from Water with Functionalized Metal-organic Frameworks: Remarkable Adsorbents with Hydrogen-bonding Abilities

    NASA Astrophysics Data System (ADS)

    Seo, Pill Won; Bhadra, Biswa Nath; Ahmed, Imteaz; Khan, Nazmul Abedin; Jhung, Sung Hwa

    2016-10-01

    Adsorption of typical pharmaceuticals and personal care products (PPCPs) (such as naproxen, ibuprofen and oxybenzone) from aqueous solutions was studied by using the highly porous metal-organic framework (MOF) MIL-101 with and without functionalization. Adsorption results showed that MIL-101s with H-donor functional groups such as –OH and –NH2 were very effective for naproxen adsorption, despite a decrease in porosity, probably because of H-bonding between O atoms on naproxen and H atoms on the adsorbent. For this reason, MIL-101 with two functional groups capable of H-bonding (MIL-101-(OH)2) exhibited remarkable adsorption capacity based on adsorbent surface area. The favorable contributions of –OH and –(OH)2 on MIL-101 in the increased adsorption of ibuprofen and oxybenzone (especially based on porosity) confirmed again the importance of H-bonding mechanism. The adsorbent with the highest adsorption capacity, MIL-101-OH, was very competitive when compared with carbonaceous materials, mesoporous materials, and pristine MIL-101. Moreover, the MIL-101-OH could be recycled several times by simply washing with ethanol, suggesting potential application in the adsorptive removal of PPCPs from water.

  7. Effect of Amine Surface Coverage on the Co-Adsorption of CO2 and Water: Spectral Deconvolution of Adsorbed Species.

    PubMed

    Didas, Stephanie A; Sakwa-Novak, Miles A; Foo, Guo Shiou; Sievers, Carsten; Jones, Christopher W

    2014-12-04

    Three primary amine materials functionalized onto mesoporous silica with low, medium, and high surface amine coverages are prepared and evaluated for binary CO2/H2O adsorption under dilute conditions. Enhancement of amine efficiency due to humid adsorption is most pronounced for low surface amine coverage materials. In situ FT-IR spectra of adsorbed CO2 on these materials suggest this enhancement may be associated with the formation of bicarbonate species during adsorption on materials with low surface amine coverage, though such species are not observed on high surface coverage materials. On the materials with the lowest amine loading, bicarbonate is observed on longer time scales of adsorption, but only after spectral contributions from rapidly forming alkylammonium carbamate species are removed. This is the first time that direct evidence for bicarbonate formation, which is known to occur in liquid aqueous amine solutions, has been presented for CO2 adsorption on solid amine adsorbents.

  8. Heat transfer to the adsorbent in solar adsorption cooling device

    NASA Astrophysics Data System (ADS)

    Pilat, Peter; Patsch, Marek; Papucik, Stefan; Vantuch, Martin

    2014-08-01

    The article deals with design and construction of solar adsorption cooling device and with heat transfer problem in adsorber. The most important part of adsorption cooling system is adsorber/desorber containing adsorbent. Zeolith (adsorbent) type was chosen for its high adsorption capacity, like a coolant was used water. In adsorber/desorber occur, at heating of adsorbent, to heat transfer from heat change medium to the adsorbent. The time required for heating of adsorber filling is very important, because on it depend flexibility of cooling system. Zeolith has a large thermal resistance, therefore it had to be adapted the design and construction of adsorber. As the best shows the tube type of adsorber with double coat construction. By this construction is ensured thin layer of adsorbent and heating is quick in all volume of adsorbent. The process of heat transfer was experimentally measured, but for comparison simulated in ANSYS, too.

  9. A small angle neutron scattering study of the adsorbed asphaltene layer in water-in-hydrocarbon emulsions: structural description related to stability.

    PubMed

    Jestin, Jacques; Simon, Sébastien; Zupancic, Lina; Barré, Loïc

    2007-10-09

    We have developed a specific protocol to study with SANS measurements, the structure of the interfacial film layer in water-in-oil emulsions stabilized by asphaltene. Using the contrast matching technique available for neutron scattering, we have access to both the composition and the quantity of interface. The results obtained give us a view of the asphaltene aggregates in the interfacial film, which are structured as a monolayer and show a direct correlation between the size of asphaltene aggregates in solution and the thickness of the film layer. The organization of the interface has been studied as a function of several parameters such as the quantity of resins, i.e., the size of aggregates, the pH of the aqueous phase, and the aging time of the emulsions and the consequences of these variations on the macroscopic stability of these emulsions. We show that the key parameter for the stability is the inter-asphaltene aggregate interaction inside the film layer. Changing the attractive/repulsive balance between the aggregates in the film at the microscopic scale, by changing the aggregate's size or the aggregate's ionization, has a direct incidence on the quantity of water recovered after centrifugation: the stronger the attraction between aggregates in the film, the more stable the emulsion is.

  10. Water Storage in Thin Films Maintaining the Total Film Thickness as Probed with in situ Neutron Reflectivity.

    PubMed

    Wang, Weinan; Metwalli, Ezzeldin; Perlich, Jan; Troll, Kordelia; Papadakis, Christine M; Cubitt, Robert; Müller-Buschbaum, Peter

    2009-01-16

    We investigate a new type of thin film material which allows for water storage without an increase in film thickness, whereas typically water storage in polymers and polymer films is accompanied with a strong swelling of the film, i.e., a strong increase in the film thickness. So these films will avoid problems related to strains which are caused by swelling. The basic key for the preparation of such thin films is the installation of a glassy network by the use of an asymmetric diblock copolymer polystyrene-block-poly(N-isopropylacrylamide) [P(S-b-NIPAM)] with a long PS and short PNIPAM block in combination with a solvent which is more equal in interaction with both the blocks as compared to water. With in situ neutron reflectivity the water storage and removal are probed. The total film thickness increases only by 2.5% by allowing for a total water storage of 17.4%. Thus the material can be used for coatings to reduce humidity in nano-applications, which might suffer from changes in the water content of the surrounding environment.

  11. Impact of temperature and electrical potentials on the stability and structure of collagen adsorbed on the gold electrode

    NASA Astrophysics Data System (ADS)

    Meiners, Frank; Ahlers, Michael; Brand, Izabella; Wittstock, Gunther

    2015-01-01

    The morphology and structure of collagen type I adsorbed on gold electrodes were studied as a function of electrode potential and temperature by means of capacitance measurements, polarization modulation infrared reflection-absorption spectroscopy and scanning force microscopy at temperatures of 37 °C, 43 °C and 50 °C. The selected temperatures corresponded to the normal body temperature, temperature of denaturation of collagen molecules and denaturation of collagen fibrils, respectively. Independently of the solution temperature, collagen was adsorbed on gold electrodes in the potential range - 0.7 V < E < 0.4 V vs. Ag/AgCl, where the protein film was very stable. Fragments of collagen molecules made a direct contact to the gold surface and water was present in the film. Protein molecules were oriented preferentially with their long axis towards the gold surface. Collagen molecules in the adsorbed state preserved their native triple helical structure even at temperatures corresponding to collagen denaturation in aqueous solutions. Application of E < - 0.75 V vs. Ag/AgCl leads to the swelling of the protein film by water and desorption from the electrode surface. IR spectra provided no evidence of the thermal denaturation of adsorbed collagen molecules. A temperature increase to 50 °C leads to a distortion of the collagen film. The processes of aggregation and fibrilization were preferred over thermal denaturation for collagen adsorbed on the electrode surface and exposed to changing potentials.

  12. Preparation and characterization of polar polymeric adsorbents with high surface area for the removal of phenol from water.

    PubMed

    Zeng, Xiaowei; Yu, Tingjun; Wang, Peng; Yuan, Ronghua; Wen, Qing; Fan, Yunge; Wang, Chunhong; Shi, Rongfu

    2010-05-15

    Preparation of methyl methacrylate (MMA)/divinylbenzene (DVB) and ethylene glycol dimethacrylate (EGDMA)/DVB copolymers via suspension polymerization yielded precursors which possess residual vinyl groups. Post-crosslinking of appropriate dichloroethane swollen precursors without external crosslinking agent in the presence of anhydrous ferric chloride (FeCl(3)) yielded post-crosslinked resins with high surface area and suitable polarity. FT-IR spectrum indicated that increasing the proportion of MMA or EGDMA in monomer mixtures notably reduces the amount of the pendant vinyl groups onto the matrix of the precursors. Furthermore, the pendant vinyl groups of precursors were almost absent when the content of MMA and EGDMA increased to 40 mol% and 20 mol% in the monomers, respectively. The specific surface areas and pore volumes of copolymers showed a remarkable increase after post-crosslinking. Experimental results showed that isotherms of phenol adsorption onto these polymeric adsorbents could be represented by Freundlich model and Langmuir model reasonably. PDE-5 pc exhibited higher adsorption capacity of phenol than other adsorbents, which resulted from synergistic effect of larger specific surface area and polar groups onto the network. Column adsorption/desorption dynamic curves suggested that PDE-5 pc is a potential candidate for treatment of chemical effluent containing phenol and phenolic pollutants.

  13. Arsenic Re-Mobilization in Water Treatment Adsorbents Under Reducing Conditions: Part II, XAS and Modeling Study

    SciTech Connect

    Liu,S.; Jing, C.; Meng, X.

    2008-01-01

    The mechanism of arsenic re-mobilization in spent adsorbents under reducing conditions was studied using X-ray absorption spectroscopy and surface complexation model calculations. X-ray absorption near edge structure (XANES) spectroscopy demonstrated that As(V) was partially reduced to As(III) in spent granular ferric hydroxide (GFH), titanium dioxide (TiO2), activated alumina (AA) and modified activated alumina (MAA) adsorbents after 2 years of anaerobic incubation. As(V) was completely reduced to As(III) in spent granular ferric oxide (GFO) under 2-year incubation. The extended X-ray absorption fine structure (EXAFS) spectroscopy analysis showed that As(III) formed bidentate binuclear surface complexes on GFO as evidenced by an average As(III)-O bond distance of 1.78 Angstroms and As(III)-Fe distance of 3.34 Angstroms . The release of As from the spent GFO and TiO2 was simulated using the charge distribution multi-site complexation (CD-MUSIC) model. The observed redox ranges for As release and sulfate mobility were described by model calculations.

  14. Sum Frequency Generation Vibrational Spectroscopy of Adsorbed Amino Acids, Peptides and Proteins of Hydrophilic and Hydrophobic Solid-Water Interfaces

    SciTech Connect

    Holinga IV, George Joseph

    2010-09-01

    Sum frequency generation (SFG) vibrational spectroscopy was used to investigate the interfacial properties of several amino acids, peptides, and proteins adsorbed at the hydrophilic polystyrene solid-liquid and the hydrophobic silica solid-liquid interfaces. The influence of experimental geometry on the sensitivity and resolution of the SFG vibrational spectroscopy technique was investigated both theoretically and experimentally. SFG was implemented to investigate the adsorption and organization of eight individual amino acids at model hydrophilic and hydrophobic surfaces under physiological conditions. Biointerface studies were conducted using a combination of SFG and quartz crystal microbalance (QCM) comparing the interfacial structure and concentration of two amino acids and their corresponding homopeptides at two model liquid-solid interfaces as a function of their concentration in aqueous solutions. The influence of temperature, concentration, equilibration time, and electrical bias on the extent of adsorption and interfacial structure of biomolecules were explored at the liquid-solid interface via QCM and SFG. QCM was utilized to quantify the biological activity of heparin functionalized surfaces. A novel optical parametric amplifier was developed and utilized in SFG experiments to investigate the secondary structure of an adsorbed model peptide at the solid-liquid interface.

  15. Evaluation of the use of performance reference compounds in an oasis-HLB adsorbent based passive sampler for improving water concentration estimates of polar herbicides in freshwater

    USGS Publications Warehouse

    Mazzella, N.; Lissalde, S.; Moreira, S.; Delmas, F.; Mazellier, P.; Huckins, J.N.

    2010-01-01

    Passive samplers such as the Polar Organic Chemical Integrative Sampler (POCIS) are useful tools for monitoring trace levels of polar organic chemicals in aquatic environments. The use of performance reference compounds (PRC) spiked into the POCIS adsorbent for in situ calibration may improve the semiquantitative nature of water concentration estimates based on this type of sampler. In this work, deuterium labeled atrazine-desisopropyl (DIA-d5) was chosen as PRC because of its relatively high fugacity from Oasis HLB (the POCIS adsorbent used) and our earlier evidence of its isotropic exchange. In situ calibration of POCIS spiked with DIA-d5was performed, and the resulting time-weighted average concentration estimates were compared with similar values from an automatic sampler equipped with Oasis HLB cartridges. Before PRC correction, water concentration estimates based on POCIS data sampling ratesfrom a laboratory calibration exposure were systematically lower than the reference concentrations obtained with the automatic sampler. Use of the DIA-d5 PRC data to correct POCIS sampling rates narrowed differences between corresponding values derived from the two methods. Application of PRCs for in situ calibration seems promising for improving POCIS-derived concentration estimates of polar pesticides. However, careful attention must be paid to the minimization of matrix effects when the quantification is performed by HPLC-ESI-MS/MS. ?? 2010 American Chemical Society.

  16. Graphene-modified TiO2 nanotube arrays as an adsorbent in micro-solid phase extraction for determination of carbamate pesticides in water samples.

    PubMed

    Zhou, Qingxiang; Fang, Zhi

    2015-04-15

    Graphene is a good adsorbent for organic pollutants, especially for compounds containing benzene rings. When used in TiO2 nanotube arrays for micro-solid phase extraction (μ-SPE), the combination of graphene's strong adsorptive properties with its good separation capabilities results in excellent sample preconcentration performance. In the present study, graphene-modified TiO2 nanotube arrays were prepared by electrodeposition using a cyclic voltammetric reduction method. Four carbamate pesticides, including metolcarb, carbaryl, isoprocarb, and diethofencarb, were used as model analytes to validate the enrichment properties of the prepared adsorbent in μ-SPE. Factors affecting the enrichment efficiency of the μ-SPE procedure were optimized and included sample pH, elution solvents, salting-out effect, adsorption time and desorption time. Under optimal conditions, graphene-modified TiO2 nanotube arrays exhibited excellent enrichment efficiency for carbamate pesticides. The detection limits of these carbamate pesticides ranged from 2.27 to 3.26 μg L(-1). The proposed method was validated using four environmental water samples, and yields of pesticides recovered from spiked test samples of the four analytes were in the range of 83.9-108.8%. These results indicate that graphene-modified TiO2 nanotube arrays exhibit good adsorption to the target pollutants, and the method described in this work could be used as a faster and easier alternative procedure for routine analysis of carbamate pesticides in real water samples.

  17. Determination of triazine herbicides in environmental water samples by high-performance liquid chromatography using graphene-coated magnetic nanoparticles as adsorbent.

    PubMed

    Zhao, Guangying; Song, Shuangju; Wang, Chun; Wu, Qiuhua; Wang, Zhi

    2011-12-05

    In this paper, a graphene-based Fe(3)O(4) magnetic nanoparticles (G-Fe(3)O(4) MNPs) was used as the adsorbent for the magnetic solid-phase extraction of some triazine herbicides (atrazine, prometon, propazine and prometryn) in environmental water samples followed by high performance liquid chromatography-diode array detection (HPLC-DAD). After the extraction, the adsorbent can be conveniently separated from the aqueous samples by an external magnet. The main factors influencing the extraction efficiency including the amount of the MNPs, the extraction time, the pH of sample solution, and desorption conditions were studied and optimized. Under the optimized experimental conditions, a good linearity was observed in the range of 0.1-50.0 ng mL(-1) for all the analytes, with the correlation coefficients (r) ranging from 0.9996 to 0.9999. The limits of detection of the method ranged between 0.025 and 0.040 ng mL(-1). Good reproducibility was obtained with the relative standard deviations below 5.2%. The developed method was applied to the analysis of the triazine herbicides in different water samples (lake, river and reservoir). The recoveries of the method were in the range between 89.0% and 96.2%.

  18. Magnetized graphene layers synthesized on the carbon nanofibers as novel adsorbent for the extraction of polycyclic aromatic hydrocarbons from environmental water samples.

    PubMed

    Rezvani-Eivari, Mostafa; Amiri, Amirhassan; Baghayeri, Mehdi; Ghaemi, Ferial

    2016-09-23

    The application of magnetized graphene (G) layers synthesized on the carbon nanofibers (CNFs) (m-G/CNF) was investigated as novel adsorbent for the magnetic solid-phase extraction (MSPE) of polycyclic aromatic hydrocarbons (PAHs) in water samples followed by gas chromatography-flame ionization detector (GC-FID). Six important parameters, affecting the extraction efficiency of PAHs, including: amount of adsorbent, adsorption and desorption times, type and volume of the eluent solvent and salt content of the sample were evaluated. The optimum extraction conditions were obtained as: 5min for extraction time, 20mg for sorbent amount, dichloromethane as desorption solvent, 1mL for desorption solvent volume, 5min for desorption time and 15% (w/v) for NaCl concentration. Good performance data were obtained at the optimized conditions. The calibration curves were linear over the concentration ranges from 0.012 to 100ngmL(-1) with correlation coefficients (r) between 0.9950 and 0.9967 for all the analytes. The limits of detection (LODs, S/N=3) of the proposed method for the studied PAHs were 0.004-0.03ngmL(-1). The relative standard deviations (RSDs) for five replicates at two concentration levels (0.1 and 50ngmL(-1)) of PAHs were ranged from 3.4 to 5.7%. Appropriate relative recovery values, in the range of 95.5-99.9%, were also obtained for the real water sample analysis.

  19. Ice-Accretion Scaling Using Water-Film Thickness Parameters

    NASA Technical Reports Server (NTRS)

    Anderson, David N.; Feo, Alejandro

    2003-01-01

    Studies were performed at INTA in Spain to determine water-film thickness on a stagnation-point probe inserted in a simulated cloud. The measurements were correlated with non-dimensional parameters describing the flow and the cloud conditions. Icing scaling tests in the NASA Glenn Icing Research Tunnel were then conducted using the Ruff scaling method with the scale velocity found by matching scale and reference values of either the INTA non-dimensional water-film thickness or a Weber number based on that film thickness. For comparison, tests were also performed using the constant drop-size Weber number and the average-velocity methods. The reference and scale models were both aluminum, 61-cm-span, NACA 0012 airfoil sections at 0 deg. AOA. The reference had a 53-cm-chord and the scale, 27 cm (1/2 size). Both models were mounted vertically in the center of the IRT test section. Tests covered a freezing fraction range of 0.28 to 1.0. Rime ice (n = 1.0) tests showed the consistency of the IRT calibration over a range of velocities. At a freezing fraction of 0.76, there was no significant difference in the scale ice shapes produced by the different methods. For freezing fractions of 0.40, 0.52 and 0.61, somewhat better agreement with the reference horn angles was typically achieved with the average-velocity and constant-film thickness methods than when either of the two Weber numbers was matched to the reference value. At a freezing fraction of 0.28, the four methods were judged equal in providing simulations of the reference shape.

  20. Water/carbonate stripping for CO.sub.2 capture adsorber regeneration and CO.sub.2 delivery to photoautotrophs

    DOEpatents

    Chance, Ronald; Koros, William J.; McCool, Benjamin; Noel, James

    2015-08-11

    The invention provides systems and methods for the delivery of carbon to photoautotrophs. The invention utilizes low energy regeneration of adsorbent for CO.sub.2 capture and provides for effective CO.sub.2 loading into liquids useful for photoautotroph growth and/or production of photosynthetic products, such as biofuels, via photoautotrophic culture media. The inventive system comprises a fluid/membrane/fluid contactor that provides selective transfer of molecular CO.sub.2 via a dense (non-porous) membrane from a carbonate-based CO.sub.2 snipping solution to a culture medium where the CO.sub.2 is consumed by a photoautotroph for the production of biofuels, biofuel precursors or other commercial products.

  1. Simultaneous removal of multiple pesticides from water: effect of organically modified clays as coagulant aid and adsorbent in coagulation-flocculation process.

    PubMed

    Shabeer, T P Ahammed; Saha, Ajoy; Gajbhiye, V T; Gupta, Suman; Manjaiah, K M; Varghese, Eldho

    2014-01-01

    Contamination of drinking water sources with agrochemical residues became a major concern in the twenty-first century. Coagulation-flocculation is the most widely used water-treatment process, but the efficiency to remove pesticides and other organic pollutants are limited compared to adsorption process. Thus, simultaneous action of adsorption on normal bentonite or organo-modified montmorillonite clays [modified with octadecylamine (ODA-M) and octadecylamine + amino-propyltriethoxysilane (ODAAPS-M)] followed by coagulation-flocculation by alum and poly aluminium chloride has been evaluated for removal of 10 different pesticides, namely atrazine, lindane, metribuzin, aldrin, chlorpyriphos, pendimethalin, alpha-endosulphan, beta-endosulphan, p,p'-DDT, cypermethrin and two of its metabolites, endosulphan sulphate and p,p'-DDE, from water. The coagulation without integration of adsorption was less effective (removal % varies from 12 to 49) than the adsorption-coagulation integrated system (removal % varies from 71 to 100). Further, coagulation integrated with adsorption was more effective when organically modified montmorillonite was used as adsorbent compared to normal bentonite. The removal efficiency of organic clay depends upon the concentration of pesticides, doses of clay minerals, and efficiency was more for ODAAPS-M as compared to ODA-M. The combination of ODAAPS-M-clay with coagulants was also used efficiently for the removal of pesticides from natural and fortified natural water collected and the results exhibit the usefulness of this remediation technique for application in water decontamination and in treatment of industrial and agricultural waste waters.

  2. Degradation Of 4-Chlorophenol Using Water Falling Film Dbd Reactor

    NASA Astrophysics Data System (ADS)

    Dojcinovic, B.; Roglic, G.; Obradovic, B. M.; Kuraica, M. M.; Puric, J.; Natic, M.; Tosti, T.; Manojlovic, D.

    2010-07-01

    In this paper we present experimental results of degradation of 4-chlorphenol using falling film dielectric barrier discharge (DBD) reactor. Degradation of 100 ml/L water solution of 4-chlorphenol was examined using catalysts in four different set of conditions: DBD, DBD/H2O2, DBD/TiO2 i DBD/Fe2+. Kinetics of the 4-chlorophenol degrada- tion in several successive passes trough the reactor was monitored using HPLC. Changes in concentrations of carbon that originate from products of degradations like acetic, formic and oxalic acids and changes in concentrations of carbon calculated on basis of degraded 4-chlorophenole are presented.

  3. The configuration of water on rough natural surfaces: Implications for understanding air-water interfacial area, film thickness, and imaging resolution

    NASA Astrophysics Data System (ADS)

    Kibbey, Tohren C. G.

    2013-08-01

    Previous studies of air-water interfacial areas in unsaturated porous media have often distinguished between interfacial area corresponding to water held by capillary forces between grains and area corresponding to water associated with solid surfaces. The focus of this work was on developing a better understanding of the nature of interfacial area associated with solid surfaces following drainage of porous media. Stereoscopic scanning electron microscopy was used to determine surface elevation maps for eight different surfaces of varying roughness. An algorithm was developed to calculate the true configuration of an air-water interface in contact with the solid surface as a function of capillary pressure. The algorithm was used to calculate surface-associated water configurations for capillary pressures ranging from 10 to 100 cm water. The results of the work show that, following drainage, the configuration of surface-associated water is dominated by bridging of macroscopic surface roughness features over the range of capillary pressures studied, and nearly all of the surface-associated water is capillary held. As such, the thicknesses of surface-associated water were found to be orders-of-magnitude greater than might be expected at the same capillary pressures based on calculations of adsorbed film thickness. The fact that capillary forces in air-water interfaces dominate surface-associated water configuration means that interface shapes are largely unaffected by microscopic surface roughness, and interfaces are considerably smoother than the underlying solid. As such, calculations suggest that microscopic surface roughness likely has minimal impact on the accuracy of surface-associated air-water interfacial areas determined by limited-resolution imaging methods such as computed microtomography.

  4. A Multi-technique Characterization of Adsorbed Protein Films: Orientation and Structure by ToF-SIMS, NEXAFS, SFG, and XPS

    NASA Astrophysics Data System (ADS)

    Baio, Joseph E.

    immobilization schemes. This protein contained both a hexahistidine tag and a cysteine residue, introduced at opposite ends of the HuLys Fv, for immobilization onto nitrilotriacetic acid (NTA) and maleimide oligo- (ethylene glycol) (MEG)-terminated substrates. The thiol group on the cysteine residue selectively binds to the MEG groups, while the his-tag selectively binds to the Ni-loaded NTA groups. XPS was used to monitor protein coverage on both surfaces by following the change in the nitrogen atomic %. The ToF-SIMS data provided a clear differentiation between the two samples due to the intensity differences of secondary ions originating from asymmetrically located amino acids in HuLys Fv. Indicating that the HuLys Fv fragment when adsorbed into the NTA and MEG substrates will be induced into two different orientations. On the NTA substrate the protein's binding site is accessible, while on the MEG substrate the binding site is oriented towards the surface. By taking advantage of the electron pathway through the heme group in cytochrome c (CytoC) electrochemists have built sensors based upon CytoC immobilized onto functionalized metal electrodes. When immobilized onto a charged surface, CytoC, with its distribution of lysine and glutamate residues around its surface, should orient and form a well-ordered protein film. Here a detailed examination of CytoC orientation when electrostatically immobilized onto both amine (NH 3+) and carboxyl (COO-) functionalized gold is presented. Again, protein coverage, on both surfaces, was monitored by the change in the atomic % N, as determined by XPS. ToF-SIMS data demonstrated a clear separation between the two samples based on the intensity differences of secondary ions stemming from amino acids located asymmetrically within CytoC, indicating opposite orientations of the protein on the two different surfaces. Spectral features within the in situ sum frequency generation vibrational spectra, acquired for the protein interacting with

  5. A novel fiber-based adsorbent technology

    SciTech Connect

    Reynolds, T.A.

    1997-10-01

    In this Phase I Small Business Innovation Research program, Chemica Technologies, Inc. is developing an economical, robust, fiber-based adsorbent technology for removal of heavy metals from contaminated water. The key innovation is the development of regenerable adsorbent fibers and adsorbent fiber cloths that have high capacity and selectivity for heavy metals and are chemically robust. The process has the potential for widespread use at DOE facilities, mining operations, and the chemical process industry.

  6. Gas-film coefficients for the volatilization of ethylene dibromide from water

    USGS Publications Warehouse

    Rathbun, R.E.; Tal, D.Y.

    1986-01-01

    Gas-film coefficients for the volatilization of ethylene dibromide (EDB) and water were determined in the laboratory as a function of wind speed and temperature. The ratio of the coefficients was independent of wind speed and increased slightly with temperature. Use of this ratio with an environmentally determined gas-film coefficient for the evaporation of water permits determination of the gas-film coefficient for the volatilization of EDB from environmental waters.

  7. Properties of amphiphilic oligonucleotide films at the air/water interface and after film transfer.

    PubMed

    Keller, R; Kwak, M; de Vries, J W; Sawaryn, C; Wang, J; Anaya, M; Müllen, K; Butt, H-J; Herrmann, A; Berger, R

    2013-11-01

    The self-assembly of amphiphilic hybrid materials containing an oligonucleotide sequence at the air/water interface was investigated by means of pressure-molecular area (Π-A) isotherms. In addition, films were transferred onto solid substrates and imaged using scanning force microscopy. We used oligonucleotide molecules with lipid tails, which consisted of a single stranded oligonucleotide 11 mer containing two hydrophobically modified 5-(dodec-1-ynyl)uracil nucleobases (dU11) at the 5'-end of the oligonucleotide sequence. The air/water interface was used as confinement for the self-assembling process of dU11. Scanning force microscopy of films transferred via Langmuir-Blodgett technique revealed mono-, bi- (Π ≥ 2 mN/m) and multilayer formation (Π ≥ 30 mN/m). The first layer was 1.6 ± 0.1 nm thick. It was oriented with the hydrophilic oligonucleotide moiety facing the hydrophilic substrate while the hydrophobic alkyl chains faced air. In the second layer the oligonucleotide moiety was found to face the air. The second layer was found to cover up to 95% of the sample area. Our measurements indicated that the rearrangement of the molecules into bi- and multiple bilayers happened already at the air/water interface. Similar results were obtained with a second type of oligonucleotide amphiphile, an oligonucleotide block copolymer, which was composed of an oligonucleotide 11 mer covalently attached at the terminus to polypropyleneoxide (PPO).

  8. A 2D-g-C3N4 nanosheet as an eco-friendly adsorbent for various environmental pollutants in water.

    PubMed

    Cai, Xingguo; He, Junyong; Chen, Liang; Chen, Kai; Li, Yulian; Zhang, Kaisheng; Jin, Zhen; Liu, Jinyun; Wang, Chengming; Wang, Xuguang; Kong, Lingtao; Liu, Jinhuai

    2017-03-01

    A novel graphitic carbon nitride (g-C3N4) nanosheet adsorbent with a large surface area, remarkable hydrophilicity and high adsorption capacity, was presented for the removal of cadmium ions (Cd(2+)) and methylene blue (MB) from aqueous solution. Adsorption measurements were conducted systematically to study the influences of the contact time, initial concentrations of Cd(2+) and MB, temperature, and pH value. The maximum adsorption capacities of g-C3N4 towards Cd(2+) and MB were 94.4 and 42.1 mg g(-1), respectively, at 318.5 K when the initial concentrations of Cd(2+) and MB were 200 and 20 mg L(-1), respectively. The adsorption kinetics fit a pseudo-second-order model. The high adsorption performance of the g-C3N4 adsorbent can be attributed to the multiple adsorption sites on g-C3N4, including the π-π conjugate interactions and electrostatic attractions with pollutants in water. In addition, it is significant to achieve high adsorption performance of g-C3N4 nanosheets by efficiently exposing the adsorption sites by adjusting the microstructure surface properties and dispersity in solution.

  9. Interactions of organic contaminants with mineral-adsorbed surfactants.

    PubMed

    Zhu, Lizhong; Chen, Baoliang; Tao, Shu; Chiou, Cary T

    2003-09-01

    Sorption of organic contaminants (phenol, p-nitrophenol, and naphthalene) to natural solids (soils and bentonite) with and without myristylpyridinium bromide (MPB) cationic surfactant was studied to provide novel insightto interactions of contaminants with the mineral-adsorbed surfactant. Contaminant sorption coefficients with mineral-adsorbed surfactants, Kss, show a strong dependence on surfactant loading in the solid. At low surfactant levels, the Kss values increased with increasing sorbed surfactant mass, reached a maximum, and then decreased with increasing surfactant loading. The Kss values for contaminants were always higher than respective partition coefficients with surfactant micelles (Kmc) and natural organic matter (Koc). At examined MPB concentrations in water the three organic contaminants showed little solubility enhancement by MPB. At low sorbed-surfactant levels, the resulting mineral-adsorbed surfactant via the cation-exchange process appears to form a thin organic film, which effectively "adsorbs" the contaminants, resulting in very high Kss values. At high surfactant levels, the sorbed surfactant on minerals appears to form a bulklike medium that behaves essentially as a partition phase (rather than an adsorptive surface), with the resulting Kss being significantly decreased and less dependent on the MPB loading. The results provide a reference to the use of surfactants for remediation of contaminated soils/sediments or groundwater in engineered surfactant-enhanced washing.

  10. Interactions of organic contaminants with mineral-adsorbed surfactants

    USGS Publications Warehouse

    Zhu, L.; Chen, B.; Tao, S.; Chiou, C.T.

    2003-01-01

    Sorption of organic contaminants (phenol, p-nitrophenol, and naphthalene) to natural solids (soils and bentonite) with and without myristylpyridinium bromide (MPB) cationic surfactant was studied to provide novel insight to interactions of contaminants with the mineral-adsorbed surfactant. Contaminant sorption coefficients with mineral-adsorbed surfactants, Kss, show a strong dependence on surfactant loading in the solid. At low surfactant levels, the Kss values increased with increasing sorbed surfactant mass, reached a maximum, and then decreased with increasing surfactant loading. The Kss values for contaminants were always higher than respective partition coefficients with surfactant micelles (Kmc) and natural organic matter (Koc). At examined MPB concentrations in water the three organic contaminants showed little solubility enhancement by MPB. At low sorbed-surfactant levels, the resulting mineral-adsorbed surfactant via the cation-exchange process appears to form a thin organic film, which effectively "adsorbs" the contaminants, resulting in very high Kss values. At high surfactant levels, the sorbed surfactant on minerals appears to form a bulklike medium that behaves essentially as a partition phase (rather than an adsorptive surface), with the resulting Kss being significantly decreased and less dependent on the MPB loading. The results provide a reference to the use of surfactants for remediation of contaminated soils/sediments or groundwater in engineered surfactant-enhanced washing.

  11. Let's Talk About Water: Film Screenings as an Entrée to Water Science

    NASA Astrophysics Data System (ADS)

    Hooper, R. P.; Lilienfeld, L.; Arrigo, J.

    2011-12-01

    "Let's Talk about Water" is a film symposium designed to bring together experts and the public to talk about the complex water issues facing society. The format of the event is quite simple: a panel of experts and the audience view a water documentary (such as "FLOW", "Liquid Assets", or "Gasland") together and there is an extended moderated discussion period following the film between the panel and the audience. Properly handled, this simple format can be very effective. A film creates a context of subject and language for the discussion--it gets the audience and the panel on the same page. The moderators must actively manage the discussion, both challenging the panelists with follow up questions, asking questions to simplify the language the expert is using, and passing a question among panelists to bring out different points of view. The panelists are provided with the film in advance to view and, most importantly, meet the day before the event to discuss the film. This makes for a much more convivial discussion at the event. We have found that these discussions can easily be sustained for 90 to 120 minutes with active audience participation. This format has been applied at college campuses with a target audience of lower-level undergraduates. Student clubs are engaged to help with publicity before the event and to assist with registration and ushering during the event. Appropriate classes offer extra credit for student attendance to ensure a strong turnout. A Hollywood film ("Chinatown" in southern California, "A Civil Action" in Boston) is shown on campus during the week preceding the event to help advertise the event. The event itself is typically held on a Saturday with a morning screening of the film. The audience is provided with index cards and pencils to write down questions they have about the film. A lunch is provided during which the questions are organized and used to initiate different discussion themes. The discussion begins with points raised by

  12. Water vapor barrier and sorption properties of edible films from pullulan and rice wax.

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Edible films were prepared by using various ratios of pullulan and rice wax. Freestanding composite films were obtained with up to 46.4% rice wax. Water vapor barrier properties of the film were improved with increased addition of rice wax. Moisture sorption isotherms were also studied to examine...

  13. Effect of rice wax on water vapor permeability and sorption properties of edible pullulan films

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Edible pullulan films were prepared by substituting the pullulan with various ratios of rice wax. Freestanding composite films were obtained with up to 50% rice wax. Water vapor barrier properties of the film were improved with increased addition of the rice wax. Moisture sorption isotherms were ...

  14. Predicting the film and lens water volume between soil particles using particle size distribution data

    NASA Astrophysics Data System (ADS)

    Mohammadi, M. H.; Meskini-Vishkaee, F.

    2012-12-01

    SummaryWe develop four conceptual approaches to quantify the volume of water lenses between soil particles (ɛi) and adsorbed water films (δi) coating soil particles based on soil Particle Size Distribution (PSD) data. Method 1 is based on expression of the ɛi as matric suction independent pendular rings and method 2 is based on expression of the ɛi as function of matric suction. Methods 3 and 4 are based on the coupling of δi estimated with van der Waals and electrostatic forces, with ɛi estimated with methods 1 and 2 respectively. We show that the filling angle of the lens water is independent of surface tension but increases with the porosity. The four methods are applied to predict effects of ɛi and δi on Soil Moisture Characteristics (SMC) in eighty soil samples selected from UNSODA database. The total component of the ɛi in soil water content ranged from 0.0111 (L3 L-3) to 0.1604 (L3 L-3), with the average of 0.0703 (L3 L-3) for method 1 and from 0.0082 (L3 L-3) to 0.0523 (L3 L-3), with the average of 0.0237 (L3 L-3) for method 2. The component of δi is less than 0.0121 of each pore water content. Results showed that for methods 1 and 2, the component of the ɛi in the soil water content was partially relevant for the prediction of SMC, especially in dry range. Moreover, the accuracy of the method 1 was slightly greater than that of the method 2. We attribute the methods error to the roughness of soil particles, high surface energy content of clay particles and, to the simplified pore geometric concepts that does not effectively reflect the pore geometry. We conclude that the main advantage of the present approaches is developing two different methods for estimation of the volume of the lens water by using only the PSD data and bulk density which are measured easily.

  15. Drainage of the air-water-quartz film: experiments and theory.

    PubMed

    Manica, Rogerio; Chan, Derek Y C

    2011-01-28

    Experimental results of the kinetics of drainage of the trapped water film between an approaching air bubble and a quartz plate have been analysed using recent theoretical advances in formulating and solving the flow problem in deformable films. Excellent agreement is obtained between experimental data and a model that assumes the bubble-water interface is tangentially immobile in its hydrodynamic response. The coupling between hydrodynamic pressure, disjoining pressure and film deformation is critical in determining the dynamic behaviour of the drainage process. The Reynolds parallel film model that omits the effects of film deformation predicts results that are qualitatively incorrect.

  16. Effect of film morphology on oxygen and water interaction with copper phthalocyanine

    NASA Astrophysics Data System (ADS)

    Muckley, Eric S.; Miller, Nicholas; Gredig, Thomas; Ivanov, Ilia N.

    2016-09-01

    Copper phthalocyanine (CuPc) films of thickness 25 nm and 100 nm were grown by thermal sublimation at 25°C, 150°C, and 250°C in order to vary morphology. Using a source-measure unit and a quartz crystal microbalance (QCM), we measured changes in electrical resistance and film mass in situ during exposure to controlled pulses of O2 and H2O vapor. Mass loading by O2 was enhanced by a factor of 5 in films deposited at 250°C, possibly due to the 200°C CuPc α->β transition which allows higher O2 mobility between stacked molecules. While gas/vapor sorption occurred over timescales of < 10 minutes, resistance change occurred over timescales < 1 hour, suggesting that mass change occurs by rapid adsorption at active surface sites, whereas resistive response is dominated by slow diffusion of adsorbates into the film bulk. Resistive response generally increases with film deposition temperature due to increased porosity associated with larger crystalline domains. The 25 nm thick films exhibit higher resistive response than 100 nm thick films after an hour of O2/H2O exposure due to the smaller analyte diffusion length required for reaching the film/electrode interface. We found evidence of decoupling of CuPc from the gold-coated QCM crystal due to preferential adsorption of O2/H2O molecules on gold, which is consistent with findings of other studies.

  17. Effect of film morphology on oxygen and water interaction with copper phthalocyanine

    SciTech Connect

    Miller, Nicholas; Gredig, Thomas; Ivanov, Ilia N

    2016-01-01

    Copper phthalocyanine (CuPc) films of thickness 25 nm and 100 nm were grown by thermal sublimation at 25 C, 150 C, and 250 C in order to vary morphology. Using a source-measure unit and a quartz crystal microbalance (QCM), we measured changes in electrical resistance and film mass in situ during exposure to controlled pulses of O2 and H2O vapor. Mass loading by O2 was enhanced by a factor of 5 in films deposited at 250 C, possibly due to the ~200 C CuPc transition which allows higher O2 mobility between stacked molecules. While gas/vapor sorption occurred over timescales of < 10 minutes, resistance change occurred over timescales > 1 hour, suggesting that mass change occurs by rapid adsorption at active surface sites, whereas resistive response is dominated by slow diffusion of adsorbates into the film bulk. Resistive response generally increases with film deposition temperature due to increased porosity associated with larger crystalline domains. The 25 nm thick films exhibit higher resistive response than 100 nm thick films after an hour of O2/H2O exposure due to the smaller analyte diffusion length required for reaching the film/electrode interface. We found evidence of decoupling of CuPc from the gold-coated QCM crystal due to preferential adsorption of O2/H2O molecules on gold, which is consistent with findings of other studies.

  18. Effect of addition of water-soluble chitin on amylose film.

    PubMed

    Suzuki, Shiho; Shimahashi, Katsumasa; Takahara, Junichi; Sunako, Michihiro; Takaha, Takeshi; Ogawa, Kozo; Kitamura, Shinichi

    2005-01-01

    Amylose films blended with chitosan, which were free from additives such as acid, salt, and plasticizer, were prepared by casting mixtures of an aqueous solution of an enzymatically synthesized amylose and that of water-soluble chitin (44.1% deacetylated). The presence of a small amount of chitin (less than 10%) increased significantly the permeability of gases (N2, O2, CO2, C2H4) and improved the mechanical parameters of amylose film; particularly, the elastic modulus and elongation of the blend films were larger than those of amylose or chitin films. No antibacterial activity was observed with either amylose or water-soluble chitin films. But amylose films having a small amount of chitin showed strong antibacterial action, suggesting a morphological change in water-soluble chitin on the film surface by blending with amylose molecule. These facts suggested the presence of a molecular complex of amylose and chitosan.

  19. Zeolite-loaded poly(dimethylsiloxane) hybrid films for highly efficient thin-film microextraction of organic volatiles in water.

    PubMed

    Wang, Tao; Ansai, Toshihiro; Lee, Seung-Woo

    2017-01-15

    ZSM-5 zeolite-loaded poly(dimethylsiloxane) (PDMS) hybrid thin films were demonstrated for efficient thin-film microextraction (TFME) coupled with gas chromatography-mass spectrometry for analyzing organic volatiles in water. The extraction efficiency for a series of aliphatic alcohols and two aromatic compounds was significantly improved owing to the presence of ZSM-5 zeolites. The extraction efficiency of the hybrid films was increased in proportion to the content of ZSM-5 in the PDMS film, with 20wt% of ZSM-5 showing the best results. The 20wt% ZSM-5/PDMS hybrid film exhibited higher volatile organic content extraction compared with the single-component PDMS film or PDMS hybrid films containing other types of zeolite (e.g., SAPO-34). Limits of detection and limits of quantitation for individual analytes were in the range of 0.0034-0.049ppb and of 0.010-0.15 ppb, respectively. The effects of experimental parameters such as extraction time and temperature were optimized, and the molecular dispersion of the zeolites in/on the hybrid film matrix was confirmed with scanning electron microscopy and atomic force microscopy. Furthermore, the optimized hybrid film was preliminarily tested for the analysis of organic volatiles contained in commercially available soft drinks.

  20. High-pressure homogenization lowers water vapor permeability of soybean protein isolate-beeswax films.

    PubMed

    Zhang, Chao; Ma, Yue; Guo, Kuan; Zhao, Xiaoyan

    2012-03-07

    Soybean-protein isolate (SPI) has excellent film-forming capacity. However, the water vapor permeability of SPI film is high, which will cause the moisture lose of packaged products. The effect of high-pressure homogenization (HPH) on the water vapor permeability of SPI-beeswax films was evaluated. The HPH was effective at lowering the water vapor permeability of SPI-beeswax films to about 50% of the control. The HPH reduced the particle size of films and made their matrix more compact. The HPH improved the hydrophobicity of SPI-beeswax films. For the first time, we proved that the HPH improved the bound-beeswax content in SPI-beeswax films. The bound beeswax was effective at lowering the water vapor permeability of films rather than the free beeswax in the film matrix. In summary, the HPH lowered water vapor permeability of SPI-beeswax films by reducing their particle size and raising their hydrophobicity and bound-beeswax content.

  1. Determination of copper in tap water using solid-phase spectrophotometry

    NASA Technical Reports Server (NTRS)

    Hill, Carol M.; Street, Kenneth W.; Philipp, Warren H.; Tanner, Stephen P.

    1994-01-01

    A new application of ion exchange films is presented. The films are used in a simple analytical method of directly determining low concentrations of Cu(2+) in aqueous solutions, in particular, drinking water. The basis for this new test method is the color and absorption intensity of the ion when adsorbed onto the film. The film takes on the characteristic color of the adsorbed cation, which is concentrated on the film by many orders of magnitude. The linear relationship between absorbance (corrected for variations in film thickness) and solution concentration makes the determinations possible. These determinations agree well with flame atomic absorption determinations.

  2. Structure of water at zwitterionic copolymer film-liquid water interfaces as examined by the sum frequency generation method.

    PubMed

    Kondo, Takuya; Nomura, Kouji; Gemmei-Ide, Makoto; Kitano, Hiromi; Noguchi, Hidenori; Uosaki, Kohei; Saruwatari, Yoshiyuki

    2014-01-01

    A copolymer film composed of zwitterionic carboxymethylbetaine (CMB) and n-butyl methacrylate (BMA), Poly(CMB-r-BMA), was cast on a flat plane of an octadecyltrichlorosilane (ODS)-modified fused quartz prism with a semi-cylindrical shape. CH stretching of the polymer film and O-H stretching of water at the surface of the film were examined using the sum frequency generation (SFG) technique. The C-H stretching band of the cast film, indicating a gauche defect of the film, was affected by the contact medium including dry nitrogen, water vapor-saturated nitrogen and liquid water. In contrast, the C-H stretching of an octadecyl group introduced onto the quartz prism for stable attachment of the cast film was not significantly changed by the contact medium. The O-H stretching band indicated that water molecules at the surface of the Poly(CMB-r-BMA) film in contact with liquid water were not greatly oriented in comparison with those at the surfaces of a bare prism, an ODS SAM-modified prism, and a prism covered with a PolyBMA film or a copolymer film of BMA and methacrylic acid or 2-(dimethylamino)ethyl methacrylate. A similar small perturbation of the structure of water was previously observed in the vicinity of water-soluble zwitterionic polymers and zwitterionic copolymer films using Raman and attenuated total reflection infrared spectroscopies, respectively. A distinct effect of charge neutralization to diminish the perturbation of the structure of interfacial water around polymer materials was suggested.

  3. Photovoltaic cells based on sequentially adsorbed multilayers of conjugated poly(p-phenylene ethynylene)s and a water-soluble fullerene derivative.

    PubMed

    Mwaura, Jeremiah K; Pinto, Mauricio R; Witker, David; Ananthakrishnan, Nisha; Schanze, Kirk S; Reynolds, John R

    2005-10-25

    We describe the layer-by-layer (LBL) fabrication of multilayer films and photovoltaic cells using poly(phenylene ethynylene)-based anionic conjugated polyelectrolytes as electron donors and water-soluble cationic fullerene C60 derivatives as acceptors. LBL film deposition was found to be linearly related to the number of bilayers as monitored by UV-vis absorption. Atomic force microscopy (AFM) and scanning electron microscopy (SEM) of the multilayer films revealed an aggregated but relatively uniform morphology devoid of any long-range phase separation. The maximum incident monochromatic photon to current conversion efficiency (IPCE) of the photovoltaic cells was 5.5%, the highest efficiency reported to date for cells fabricated by using the LBL fabrication technique, and since the thin film cells do not provide complete absorption of the incident light, the current generation per photon absorbed may be as much as 10%. The cells exhibited open circuit voltages of 200-250 mV with highest measured short circuit currents up to 0.5 mA/cm2 and fill factors around 30%. The power conversion efficiencies measured at AM 1.5 solar conditions (100 mW/cm2) varied between 0.01 and 0.04%, and similar to the IPCE results, the efficiency is a function of the thickness of the PV active layer.

  4. Rapid visible color change and physical swelling during water exposure in triethanolamine-metalcone films formed by molecular layer deposition

    SciTech Connect

    Lemaire, Paul C.; Oldham, Christopher J.; Parsons, Gregory N.

    2016-01-15

    Molecular layer deposition (MLD) of “metalcones,” including alucone, zincone, titanicone, and others, involves self-limiting half-reactions between organic and organometallic (or metal-halide) reactants. Studies have typically focused on metal precursors reacting with ethylene glycol or glycerol to form the films' polymeric O-M-O-(CH{sub x}){sub y}-O-M-O repeat units. The authors report new MLD materials that incorporate tertiary amine groups into the organic linkage. Specifically, reacting triethanolamine (TEA) with either trimethylaluminum or titanium tetrachloride produces TEA-alucone (Al-TEA) and TEA-titanicone (Ti-TEA), respectively, and the amine group leads to unique physical and optical properties. Fourier-transform infrared (FTIR) analysis confirms that the films have prominent C-H, C-N, and M-O-C peaks, consistent with the expected bond structure. When exposed to vapors, including water, alcohol, or ammonia, the Ti-TEA films changed their visible color within minutes and increased physical thickness by >35%. The Al-TEA showed significantly less response. X-ray photoelectron spectroscopy and FTIR suggest that HCl generated during MLD coordinates to the amine forming a quaternary ammonium salt that readily binds adsorbates via hydrogen bonding. The visible color change is reversible, and ellipsometry confirms that the color change results from vapor absorption. The unique absorptive and color-changing properties of the TEA-metalcone films point to new possible applications for MLD materials in filtration, chemical absorption, and multifunctional chemical separations/sensing device systems.

  5. Assessment of carbon nanotubes and silver nanoparticles loaded clays as adsorbents for removal of bacterial contaminants from water sources.

    PubMed

    Hassouna, M E M; ElBably, M A; Mohammed, Asmaa N; Nasser, M A G

    2017-02-01

    This work evaluated the antimicrobial efficacy of kaolin clay and its loaded forms with carbon nanotubes (CNTs) and silver nanoparticles (AgNPs) against bacterial isolates from different water supplies (tap, underground and surface water) in addition to wastewater. A total of 160 water samples were collected from different water sources in the investigated districts. Samples were cultured for isolation and serological identification of pathogenic bacteria. AgNPs were synthesized by a typical one-step synthesis protocol, where CNTs were carried out in a reactor employing the double bias-assisted hot filament chemical vapor deposition method. Both were characterized using transmission electron microscopy, infrared and X-ray fluorescence (XRF) spectroscopy. The antimicrobial efficacy of each of natural kaolin clay, AgNPs- and CNTs-loaded clays were evaluated by their application in four concentrations (0.01, 0.03, 0.05 and 0.1 ppm) at different contact times (5 min, 15 min, 30 min and 2 h). AgNPs-loaded clays at concentrations of 0.05 and 0.1 mg/l for 2 h contact time exhibited a higher bactericidal efficacy on Escherichia coli and Salmonella spp. (70, 70, 80 and 90%, respectively) compared to CNTs-loaded clay. Concluding, the application of AgNPs-loaded clay for removal of water bacterial contaminants at a concentration of 0.1 ppm for 2 h contact times resulted in highly effective removals.

  6. Nitrogen cycling between sediment and the shallow-water column in the transition zone of the Potomac River and Estuary. II. The role of wind-driven resuspension and adsorbed ammonium

    USGS Publications Warehouse

    Simon, N.S.

    1989-01-01

    During periods of sediment resuspension, desorption of ammonium from sediment solids can be the major pathway for enriching the water column with the ammonium that is produced by bacterial degradation of organic matter in the bottom material. This hyopthesis is based on a three-year study of diffusive flux in the transition zone of the Potomac River at a site 35 m from the Virginia shore where the average water-column depth is approximately 1 m over sandy sediment. A diffusion-controlled sampler was used to collect water samples at the interface between the water column and sediment and at several tens of centimeters into the sediment. Interstitial water concentration gradients showed that diffusive flux of ammonium from the sandy shallow-water sediments was approximately 1% of the diffusive flux of ammonium from the silty channel sediments in the same zone of the Potomac River. Organic nitrogen and bound or adsorbed ammonium were the predominant nitrogen forms in the sediment. Adsorbed ammonium concentrations ranged from nondetectable to 3??7 ??mol g-1 of sediment. Concentrations of adsorbed ammonium per gram of sediment were one to three orders of magnitude more than interstitial water ammonium concentrations. Desorption of ammonium from sediment solids appeared to be the controlling factor in the degree of water-column ammonium enrichment. In laboratory experiments that simulated sediment resuspension, 40-80% of the adsorbed ammonium predicted to desorb did so after approximately 30 min of mixing. Based on calculations for 1 m2 to a depth of 4 cm, one resuspenion event lasting minutes could mix more ammonium into the water column from desorption of ammonium from sediment solids than could be delivered to the water column by diffusive flux from shallow-water sediments in 10-1000 days and would be comparable to enrichment by ammonium diffusive flux for 5-50 days from channel sediments in the same river zone. ?? 1989.

  7. Gliadins polymerized with cysteine: effects on the physical and water barrier properties of derived films.

    PubMed

    Hernández-Muñoz, Pilar; Lagarón, José M; López-Rubio, Amparo; Gavara, Rafael

    2004-01-01

    To study the effects of disulfide bonds on certain functional properties of films made from the wheat gluten proteins gliadin and glutenin, cysteine was used to promote the formation of interchain disulfide bridges between gliadins in 70% ethanolic solution. Disulfide-mediated polymerization of gliadins was confirmed by means of SDS-PAGE analysis. After chemical treatment of gliadins, films were solution cast and the effects of both glycerol (used as a plasticizer) and relative humidity were studied on water vapor permeability, moisture sorption isotherms at 23 degrees C, and the optical properties of the films. The results were compared with those obtained from analogous films made from untreated glutenin macromolecules. Cysteine-mediated polymerization of gliadins improved the water vapor resistance of films achieving values close to those obtained for glutenin films. Development of intra- and interchain disulfide bonds did not change the moisture sorption capacity of the films but transparency was slightly diminished.

  8. Thin films, asphaltenes, and reservoir wettability

    SciTech Connect

    Kaminsky, R.; Bergeron, V.; Radke, C.J. |

    1993-04-01

    Reservoir wettability impacts the success of oil recovery by waterflooding and other methods. To understand wettability and its alteration, thin-film forces in solid-aqueous-oil systems must be elucidated. Upon rupture of thick aqueous films separating the oil and rock phases, asphaltene components in the crude oil adsorb irreversibly on the solid surface, changing it from water-wet to oil-wet. Conditions of wettability alteration can be found by performing adhesion tests, in which an oil droplet is brought into contact with a solid surface. Exceeding a critical capillary pressure destabilizes the film, causing spontaneous film rupture to a molecularly adsorbed layer and oil adhesion accompanied by pinning at the three-phase contact line. The authors conduct adhesion experiments similar to those of Buckley and Morrow and simultaneously examine the state of the underlying thin film using optical microscopy and microinterferometry. Aqueous thin films between an asphaltic Orcutt crude oil and glass surfaces are studied as a function of aqueous pH and salinity. For the first time, they prove experimentally that strongly water-wet to strongly oil-wet wettability alteration and contact-angle pinning occur when thick aqueous films thin to molecularly adsorbed films and when the oil phase contains asphaltene molecules.

  9. Mechanical and water barrier properties of glutenin films influenced by storage time.

    PubMed

    Hernández-Muñoz, Pilar; López-Rubio, Amparo; Del-Valle, Valeria; Almenar, Eva; Gavara, Rafael

    2004-01-14

    The goal of this work was to study the effect of storage time on the functional properties of glutenin films plasticized with selected hydrophilic low molecular weight compounds: glycerol (GL), triethanolamine (TEA), and sorbitol (S). Glutenins were extracted from wheat gluten, and films were cast from film-forming solutions. The glutenin-based films were homogeneous, flexible, translucent, and easy to handle. Films were stored in an environmental chamber at 50 +/- 5% realtive humidity and 23 +/- 2 degrees C. Optical, mechanical, and water vapor permeability properties were monitored at regular intervals for 16 weeks. Films plasticized with GL and TEA had similar mechanical and water vapor barrier properties during the first few days of fabrication. Films plasticized with S were stronger, with better water vapor barrier properties. Mechanical and water vapor permeability properties of films plasticized with GL changed dramatically over time, whereas the properties of films plasticized with TEA and S remained stable during storage. Color properties of films plasticized with GL, TEA, and S did not change within the time period studied.

  10. Water sensitivity, antimicrobial, and physicochemical analyses of edible films based on HPMC and/or chitosan.

    PubMed

    Sebti, Issam; Chollet, Emilie; Degraeve, Pascal; Noel, Claude; Peyrol, Eric

    2007-02-07

    Several properties of chitosan films associated or not with hydroxypropylmethylcellulose polymer (HPMC) and HPMC films incorporating or not nisin and/or milk fat were studied. Nisin addition at a level of 250 microg mL-1 and likewise chitosan at 1% (w/v) concentration were efficient for total inhibiting Aspergillus niger and Kocuria rhizophila food deterioration microorganisms. HPMC and chitosan films were transparent, whereas nisin and/or fat incorporation induced a 2-fold lightness parameter increase and, consequently, involved more white films. Measurements of tensile strength, as well as ultimate elongation, showed that chitosan and HPMC initial films were elastic and flexible. High thermal treatments and additive incorporation induced less elastic and more plastic films. Water vapor transmission as far as total water desorption rates suggested that chitosan films were slightly sensitive to water. Water transfer was decreased by <60% as compared with other biopolymer films. Regarding its hydrophobic property, the capacity of fat to improve film water barrier was very limited.

  11. Aqueous Wetting Films on Fused Quartz.

    PubMed

    Mazzoco; Wayner

    1999-06-15

    Using an image analyzing interferometer, IAI, the interfacial characteristics of an isothermal constrained vapor bubble, CVB, in a quartz cuvette were studied as a precursor to heat transfer research. The effects of pH and electrolyte concentration on the meniscus properties (curvature and adsorbed film thickness) and the stability of the aqueous wetting films were evaluated. The surface potential in the electric double layer was a function of the cleaning and hydroxylation of the quartz surface. The disjoining pressure isotherm for pure water was very close to that predicted by the Langmuir equation. For aqueous solutions of moderate electrolyte concentration, the Gouy-Chapman theory provided a good representation of the electrostatic effects in the film. The effect of temperature on the film properties of aqueous solutions and pure water was also evaluated: The meniscus curvature decreased with increasing temperature, while Marangoni effects, intermolecular forces, and local evaporation and condensation enhanced waves on the adsorbed film layer. Pure water wetting films were mechanically metastable, breaking into droplets and very thin films (less than 10 nm) after a few hours. Aqueous wetting films with pH 12.4 proved to be stable during a test of several months, even when subjected to temperature and mechanical perturbations. The mechanical stability of wetting films can explain the reported differences between the critical heat fluxes of pure water and aqueous solutions. The IAI-CVB technique is a simple and versatile experimental technique for studying the characteristics of interfacial systems. Copyright 1999 Academic Press.

  12. Study of factors governing oil-water separation process using TiO₂ films prepared by spray deposition of nanoparticle dispersions.

    PubMed

    Gondal, Mohammed A; Sadullah, Muhammad S; Dastageer, Mohamed A; McKinley, Gareth H; Panchanathan, Divya; Varanasi, Kripa K

    2014-08-27

    Surfaces which possess extraordinary water attraction or repellency depend on surface energy, surface chemistry, and nano- and microscale surface roughness. Synergistic superhydrophilic-underwater superoleophobic surfaces were fabricated by spray deposition of nanostructured TiO2 on stainless steel mesh substrates. The coated meshes were then used to study gravity driven oil-water separation, where only the water from the oil-water mixture is allowed to permeate through the mesh. Oil-water separation efficiencies of up to 99% could be achieved through the coated mesh of pore sizes 50 and 100 μm, compared to no separation at all, that was observed in the case of uncoated meshes of the same material and pore sizes. An adsorbed water on the TiO2 coated surface, formation of a water-film between the wires that form the mesh and the underwater superoleophobicity of the structured surface are the key factors that contribute to the enhanced efficiency observed in oil-water separation. The nature of the oil-water separation process using this coated mesh (in which the mesh allows water to pass through the porous structure but resists wetting by the oil phase) minimizes the fouling of mesh so that the need for frequent replacement of the separating medium is reduced. The fabrication approach presented here can be applied for coating large surface areas and to develop a large-scale oil-water separation facility for oil-field applications and petroleum industries.

  13. Spectrophotometric determination of basic fuchsin from various water samples after vortex assisted solid phase extraction using reduced graphene oxide as an adsorbent.

    PubMed

    Tokalıoğlu, Şerife; Yavuz, Emre; Aslantaş, Ayşe; Şahan, Halil; Taşkın, Ferhat; Patat, Şaban

    2015-01-01

    In this study, a fast and simple vortex assisted solid phase extraction method was developed for the separation/preconcentration of basic fuchsin in various water samples. The determination of basic fuchsin was carried out at a wavelength of 554 nm by spectrophotometry. Reduced graphene oxide which was used as a solid phase extractor was synthesized and characterized by X-ray diffraction, scanning electron microscopy and the Brunauer, Emmett and Teller. The optimum conditions are as follows: pH 2, contact times for adsorption and elution of 30 s and 90 s, respectively, 10 mg adsorbent, and eluent (ethanol) volume of 1 mL. The effects of some interfering ions and dyes were investigated. The method was linear in the concentration range of 50-250 μg L(-1). The adsorption capacity was 34.1 mg g(-1). The preconcentration factor, limit of detection and precision (RSD, %) of the method were found to be 400, 0.07 μg L(-1) and 1.2%, respectively. The described method was validated by analyzing basic fuchsin spiked certified reference material (SPS-WW1 Batch 114-Wastewater) and spiked real water samples.

  14. Ultrafine nanoporous palladium-aluminum film fabricated by citric acid-assisted hot-water-treatment of aluminum-palladium alloy film

    SciTech Connect

    Harumoto, Takashi; Tamura, Yohei; Ishiguro, Takashi

    2015-01-15

    Hot-water-treatment has been adapted to fabricate ultrafine nanoporous palladium-aluminum film from aluminum-palladium alloy film. Using citric acid as a chelating agent, a precipitation of boehmite (aluminum oxide hydroxide, AlOOH) on the nanoporous palladium-aluminum film was suppressed. According to cross-sectional scanning transmission electron microscopy observations, the ligament/pore sizes of the prepared nanoporous film were considerably small (on the order of 10 nm). Since this fabrication method only requires aluminum alloy film and hot-water with chelating agent, the ultrafine nanoporous film can be prepared simply and environmentally friendly.

  15. Modeling adsorption: Investigating adsorbate and adsorbent properties

    NASA Astrophysics Data System (ADS)

    Webster, Charles Edwin

    1999-12-01

    Surface catalyzed reactions play a major role in current chemical production technology. Currently, 90% of all chemicals are produced by heterogeneously catalyzed reactions. Most of these catalyzed reactions involve adsorption, concentrating the substrate(s) (the adsorbate) on the surface of the solid (the adsorbent). Pore volumes, accessible surface areas, and the thermodynamics of adsorption are essential in the understanding of solid surface characteristics fundamental to catalyst and adsorbent screening and selection. Molecular properties such as molecular volumes and projected molecular areas are needed in order to convert moles adsorbed to surface volumes and areas. Generally, these molecular properties have been estimated from bulk properties, but many assumptions are required. As a result, different literature values are employed for these essential molecular properties. Calculated molar volumes and excluded molecular areas are determined and tabulated for a variety of molecules. Molecular dimensions of molecules are important in the understanding of molecular exclusion as well as size and shape selectivity, diffusion, and adsorbent selection. Molecular dimensions can also be used in the determination of the effective catalytic pore size of a catalyst. Adsorption isotherms, on zeolites, (crystalline mineral oxides) and amorphous solids, can be analyzed with the Multiple Equilibrium Analysis (MEA) description of adsorption. The MEA produces equilibrium constants (Ki), capacities (ni), and thermodynamic parameters (enthalpies, ΔHi, and entropies, ΔSi) of adsorption for each process. Pore volumes and accessible surface areas are calculated from the process capacities. Adsorption isotherms can also be predicted for existing and new adsorbate-adsorbent systems with the MEA. The results show that MEA has the potential of becoming a standard characterization method for microporous solids that will lead to an increased understanding of their behavior in gas

  16. Water Films, 2nd Edition, 1965-1974.

    ERIC Educational Resources Information Center

    Canadian National Committee, Ottawa (Ontario).

    This is an annotated listing of 455 films on hydrology, as well as on many allied fields. This second edition, much more comprehensive than the first, is not intended to serve as a critical evaluation, but should be used solely as a source of information as to what films are available. All films are listed alphabetically according to their titles…

  17. Using nanoscale amorphous solid water films to create and study deeply supercooled liquid water at interfaces

    NASA Astrophysics Data System (ADS)

    Kay, Bruce

    Molecular beam vapor deposition of water on cryogenic substrates is known to produce amorphous solid films. When heated above their glass transition these films transform into deeply supercooled liquid water. These nanoscale liquid films can be used to study kinetic processes such as diffusion, isotope exchange, crystallization, and solvent mediated reactions in unprecedented detail. This talk will highlight our recent advances in this area. My colleagues Yuntao Xu, Chunqing Yuan, Collin Dibble, R. Scott Smith, Nick Petrik, and Greg Kimmel made important contributions to this work.This work was supported by the U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences. The research was performed using EMSL, a national scientific user facility sponsored by DOE's Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory, which is operated by Battelle, operated for the U.S. DOE under Contract DE-AC05-76RL01830.

  18. Doped, porous iron oxide films and their optical functions and anodic photocurrents for solar water splitting

    SciTech Connect

    Kronawitter, Coleman X.; Mao, Samuel S.; Antoun, Bonnie R.

    2011-02-28

    The fabrication and morphological, optical, and photoelectrochemical characterization of doped iron oxide films is presented. The complex index of refraction and absorption coefficient of polycrystalline films are determined through measurement and modeling of spectral transmission and reflection data using appropriate dispersion relations. Photoelectrochemical characterization for water photo-oxidation reveals that the conversion efficiencies of electrodes are strongly influenced by substrate temperature during their oblique-angle physical vapor deposition. These results are discussed in terms of the films' morphological features and the known optoelectronic limitations of iron oxide films for application in solar water splitting devices.

  19. Acetylated rice starches films with different levels of amylose: Mechanical, water vapor barrier, thermal, and biodegradability properties.

    PubMed

    Colussi, Rosana; Pinto, Vânia Zanella; El Halal, Shanise Lisie Mello; Biduski, Bárbara; Prietto, Luciana; Castilhos, Danilo Dufech; Zavareze, Elessandra da Rosa; Dias, Alvaro Renato Guerra

    2017-04-15

    Biodegradable films from native or acetylated starches with different amylose levels were prepared. The films were characterized according to the mechanical, water vapor barrier, thermal, and biodegradability properties. The films from acetylated high amylose starches had higher moisture content and water solubility than the native high amylose starch film. However, the acetylation did not affect acid solubility of the films, regardless of the amylose content. Films made from high and medium amylose rice starches were obtained; however low amylose rice starches, whether native or acetylated, did not form films with desirable characteristics. The acetylation decreased the tensile strength and increased the elongation of the films. The acetylated starch-based films had a lower decomposition temperature and higher thermal stability than native starch films. Acetylated starches films exhibited more rapid degradation as compared with the native starches films.

  20. Porous polymer films templated by marangoni flow-induced water droplet arrays.

    PubMed

    Cai, Yangjun; Zhang Newby, Bi-min

    2009-07-07

    In this article, we report the development of a novel, simple, and cost-effective method for fabricating porous polymer films with controllable interpore distances, pore sizes, and arrangements using water droplets induced by Marangoni flow as templates. First, a spread-thin ethanol film on a partially water-wettable substrate is exposed to a humid airflow, facilitating the evaporation and recession of the ethanol film. Meanwhile, water in the airflow condenses on the ethanol film and accumulates near the receding contact line, which induces the formation of water fingers at the receding contact line and, finally, ordered arrays of water droplets after detachment. The formation of the hexagonal and square arrays of water droplets is due to the pinning and sliding of the water fingers on the silicone oxide (SiOx) and silicon (Si) substrates, respectively. By varying the thickness of the ethanol film spread on the Si substrate, the sliding velocity of water fingers can be tuned, subsequently leading to the fabrication of other arrangements. The interdroplet distance and droplet size can be dependently controlled by tuning the humidity of the airflow. The ordered arrays of water droplets on the substrate are then utilized to fabricate porous polymer films by dip-coating the substrate with a polystyrene solution. Films with hexagonal and square (and other arrangements) arrays of pores are fabricated on the silicon oxide (SiOx) and silicon (Si) substrates, respectively. The pore size can also be independently tuned by further condensation or evaporation of formed water droplets, leading to porous polymer films with both close- and non-close-packed arrays of pores. The ordered porous polymer films can be further used as templates for fabricating metal post patterns.

  1. Prussian blue caged in alginate/calcium beads as adsorbents for removal of cesium ions from contaminated water.

    PubMed

    Vipin, Adavan Kiliyankil; Hu, Baiyang; Fugetsu, Bunshi

    2013-08-15

    Prussian blue encapsulated in alginate beads reinforced with highly dispersed carbon nanotubes were prepared for the safe removal of cesium ions from aqueous solutions. Equilibrium and kinetic studies were conducted using different models and the goodness of mathematical fitting of the experimental data on the adsorption isotherms was in the order Langmuir>Freundlich, and that of the kinetic models were in the order of pseudo second order>pseudo first order. Fixed bed adsorption column analysis indicated that the beads can be used for large scale treatment of cesium contaminated water.

  2. Photochemistry of alkyl bromides trapped in water ice films

    NASA Astrophysics Data System (ADS)

    Schrems, O.; Okaikwei, B.; Bluszcz, Th.

    2012-04-01

    Photochemical reactions of atmospheric trace gases taking place at the surface of atmospheric ice particles and in bulk ice are important in stratospheric and tropospheric chemistry but also in polar and alpine snowpack chemistry. Consequently, the understanding of the uptake und incorporation of atmospheric trace gases in water ice as well as their interactions with water molecules is very important for the understanding of processes which occur in ice particles and at the air/ice interface. Reactive atmospheric trace gases trapped in ice are subject of photochemical reactions when irradiated with solar UV radiation. Among such compounds bromine species are highly interesting due to their potential of depleting ozone both in the stratosphere and troposphere. Organic bromine gases can carry bromine to the stratosphere. Methyl bromide (CH3Br) is the largest bromine carrier to the stratosphere. It has both natural and anthropogenic sources. In this contribution we will present the results of our laboratory studies of alkyl bromides (methyl, bromide (CH3Br), dimethyl bromide (CH2Br2), n-propyl bromide (C3H7Br), 1,2-dibromoethane C2H4Br2)), trapped in water ice. We have simulated the UV photochemistry of these brominated alkanes isolated in ice films kept at 16 K and for comparison in solid argon matrices. The photoproducts formed in the ice have been identified by means of FTIR spectroscopy. Reflection absorption infrared spectroscopy (RAIRS) is especially useful to study nascent ice surfaces, kinetics of adsorption/decomposition, and heterogeneous catalysis. Among the observed photoproducts we could identify carbon monoxide and carbon dioxide for each alkyl bromide studied. The photoproduct HBr is dissociated in the bulk ice. Based on the experimental observations possible reaction mechanisms will be discussed.

  3. Spectral properties of mixtures of montmorillonite and dark grains - Implications for remote sensing minerals containing chemically and physically adsorbed water

    NASA Technical Reports Server (NTRS)

    Clark, R. N.

    1983-01-01

    The spectral properties from 0.4 to 3 microns of montmorillonite plus dark carbon grains (called opaques) of various sizes are studied as a function of the weight fraction of opaques present. The reflectance level and band depths of the 1.4-, 1.9-, 2.2-, and 2.8-micron water and/or OH absorption features are analyzed using derived empirical relationships and scattering theory. It is found that the absorption band depths and reflectance level are a very nonlinear function of the weight fraction of opaques present but can be predicted in many cases by simple scattering theory. The 2.8-micron bound water fundamental band is the most difficult absorption feature to suppress. The overtone absorptions are suppressed a greater amount than the fundamental but are still apparent even when 10-20 wt pct opaques are present. The relationships observed and the simple scattering theory presented show that quantitative compositional remote sensing studies are feasible for surfaces containing complex mineral mixtures.

  4. Development of Water-Triggered Chitosan Film Containing Glucamylase for Sustained Release of Resveratrol.

    PubMed

    Zhang, Dongliang; Cao, Yanfei; Ma, Chengye; Chen, Shanfeng; Li, Hongjun

    2017-03-29

    There is a paradox when incorporating enzyme into an edible chitosan film that chitosan is dissolved in acid solution and enzyme activity is maintained under mild conditions. A method for maintaining the pH of the chitosan solution at 4-6 to prepare a chitosan film containing β-cyclodextrin, resveratrol-β-cyclodextrin inclusion (RCI), was developed, using glucamylase and acetic acid. A considerable amount of resveratrol was released by the glucamylase-incorporated film within 15 days, and the maximum amount released was 46% of the total resveratrol content. The highest resveratrol release ratio (released resveratrol/total resveratrol) was obtained in the film with 6 mL of RCI. Scratches and spores were generated on the surface of the glucamylase-added film immersed in water (GAFW) for 7 days because of β-cyclodextrin hydrolysis during film drying and water immersion. RCI and β-cyclodextrin were extruded from the film surface and formed teardrops, which were erased by water on the GAFW surface but appeared on the glucamylase-added film without water immersion (GAF). The bubbles generated by the reaction of acetic acid and residual sodium bicarbonate were observed in both glucamylase-free films immersed in water (GFFW) for 7 days and without water immersion (GFF). The FT-IR spectra illustrated that the covalent bond was not generated during water immersion and β-cyclodextrin hydrolysis. The crystal structure of chitosan was destroyed by water immersion and β-cyclodextrin hydrolysis, resulting in the lowest chitosan crystallization peak at 22°. The increasing of water holding capacity determined by EDX presented the following order: GAF, GFFW, GFF, and GAFW.

  5. Damping of short gravity-capillary waves due to oil derivatives film on the water surface

    NASA Astrophysics Data System (ADS)

    Sergievskaya, Irina; Ermakov, Stanislav; Lazareva, Tatyana

    2016-10-01

    In this paper new results of laboratory studies of damping of gravity-capillary waves on the water surface covered by kerosene are presented and compared with our previous analysis of characteristics of crude oil and diesel fuel films. Investigations of kerosene films were carried out in a wide range values of film thicknesses (from some hundreds millimetres to a few millimetres) and in a wide range of surface wave frequencies (from 10 to 27 Hz). The selected frequency range corresponds to the operating wavelengths of microwave, X- to Ka-band radars typically used for the ocean remote sensing. The studied range of film thickness covers typical thicknesses of routine spills in the ocean. It is obtained that characteristics of waves, measured in the presence of oil derivatives films differ from those for crude oil films, in particular, because the volume viscosity of oil derivatives and crude oil is strongly different. To retrieve parameters of kerosene films from the experimental data the surface wave damping was analyzed theoretically in the frame of a model of two-layer fluid. The films are assumed to be soluble, so the elasticity on the upper and lower boundaries is considered as a function of wave frequency. Physical parameters of oil derivative films were estimated when tuning the film parameters to fit theory and experiment. Comparison between wave damping due to crude oil, kerosene and diesel fuel films have shown some capabilities of distinguishing of oil films from remote sensing of short surface waves.

  6. Water-soluble nanocrystalline cellulose films with highly transparent and oxygen barrier properties

    NASA Astrophysics Data System (ADS)

    Cheng, Shaoling; Zhang, Yapei; Cha, Ruitao; Yang, Jinliang; Jiang, Xingyu

    2015-12-01

    By mixing a guar gum (GG) solution with a nanocrystalline cellulose (NCC) dispersion using a novel circular casting technology, we manufactured biodegradable films as packaging materials with improved optical and mechanical properties. These films could act as barriers for oxygen and could completely dissolve in water within 5 h. We also compared the effect of nanocomposite films and commercial food packaging materials on the preservation of food.By mixing a guar gum (GG) solution with a nanocrystalline cellulose (NCC) dispersion using a novel circular casting technology, we manufactured biodegradable films as packaging materials with improved optical and mechanical properties. These films could act as barriers for oxygen and could completely dissolve in water within 5 h. We also compared the effect of nanocomposite films and commercial food packaging materials on the preservation of food. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr07647a

  7. [Extraction of triazine herbicides from environmental water samples with magnetic graphene nanoparticles as the adsorbent followed by determination using gas chromatography-mass spectrometry].

    PubMed

    Zhang, Guijiang; Zang, Xiaohuan; Zhou, Xin; Wang, Lu; Wang, Chun; Wang, Zhi

    2013-11-01

    A novel method was developed for the determination of seven triazine herbicides in environmental water samples by magnetic solid-phase extraction with graphene-based magnetic nanoparticles (G-Fe3O4 MNPs) as the adsorbent coupled with gas chromatography-mass spectrometry detection. The main factors influencing the extraction efficiency including the amount of G-Fe3O4, the extraction time, the pH and the ionic strength of sample solution and the desorption conditions were optimized. Under the optimized experimental conditions, the enrichment factors of the method for the analytes were in the range from 574 to 968; the linearities of the method ranged from 0.01 to 10.0 microg/L for simazine, propazine, metribuzin, simetryn and cyanazine, from 0.05 to 10.0 microg/L for atrazine and from 0.01 to 8.0 microg/L for prometryn, with the correlation coefficients (r) ranging from 0.996 8 to 0.999 8. The limits of detection were in the range between 1.0 and 5.0 ng/L. Good reproducibilities were obtained with the relative standard deviations below 10.5%. The developed method was applied to the analysis of the triazine herbicides in different water samples (lake, well and tap). The recoveries of the method were in the range from 79.8% to 118.3% at the spiked levels of 0.5 microg/L and 2.0 microg/L. The results indicated that the developed method can be used as a simple and efficient technique for the determination of the triazine herbicides in environmental water samples.

  8. Fluorescence dynamics of microsphere-adsorbed sunscreens

    NASA Astrophysics Data System (ADS)

    Krishnan, R.

    2005-03-01

    Sunscreens are generally oily substances which are prepared in organic solvents, emulsions or dispersions with micro- or nanoparticles. These molecules adsorb to and integrate into skin cells. In order to understand the photophysical properties of the sunscreen, we compare steady-state and time-resolved fluorescence in organic solvent of varying dielectric constant ɛ and adsorbed to polystyrene microspheres and dispersed in water. Steady-state fluorescence is highest and average fluorescence lifetime longest in toluene, the solvent of lowest ɛ. However, there is no uniform dependence on ɛ. Sunscreens PABA and padimate-O show complex emission spectra. Microsphere-adsorbed sunscreens exhibit highly non-exponential decay, illustrative of multiple environments of the adsorbed molecule. The heterogeneous fluorescence dynamics likely characterizes sunscreen adsorbed to cells.

  9. Cassava root husks powder as green adsorbent for the removal of Cu(II) from natural river water

    NASA Astrophysics Data System (ADS)

    Jorgetto, A. O.; Silva, R. I. V.; Saeki, M. J.; Barbosa, R. C.; Martines, M. A. U.; Jorge, S. M. A.; Silva, A. C. P.; Schneider, J. F.; Castro, G. R.

    2014-01-01

    Through a series of simple processes, cassava root husks were turned into a fine powder of controlled particle size (63-75 μm). FTIR spectrum demonstrated the existence of alcohol, amine and carboxylic groups; and elemental analysis confirmed the presence of elements of interest such as sulphur, nitrogen and oxygen. Cross-polarized {1H}sbnd 13C NMR technique indicated the existence of methionine and thiamine through the signals observed at 55 ppm and 54 ppm, respectively, and the point of zero charge (pHpzc) was achieved at pH 5.2. The material was applied in solid-phase extraction of Cu(II) via batch experiments. Optimum adsorption pH was found to be in range of 3-6 and in the kinetic experiment the equilibrium was attained in 1 min. The highest adsorption capacity was 0.14 mmol g-1. The adsorption data were fit to the modified Langmuir equation, and the maximum amount of metal species extracted from the solution, Ns, was determined to be ∼0.14 mmol g-1, which is an indicative that the main adsorption mechanism is through chemisorption. Under optimized conditions, the material was utilized in preconcentration experiments, which culminated in an enrichment factor of 41.3-fold. With the aid of the enrichment factor, experiments were carried out to determine the Cu(II) content in tap water and natural water. Preconcentration method was also applied to a certified reference material (1643e) and the concentration found was 23.03 ± 0.79 μg L-1, whereas the specified Cu(II) concentration was 22.7 ± 0.31 μg L-1.

  10. Correlating particle deformation with water concentration profiles during latex film formation: reasons that softer latex films take longer to dry.

    PubMed

    Carter, Farai T; Kowalczyk, Radoslaw M; Millichamp, Ian; Chainey, Malcolm; Keddie, Joseph L

    2014-08-19

    During the past two decades, an improved understanding of the operative particle deformation mechanisms during latex film formation has been gained. For a particular colloidal dispersion, the Routh-Russel deformation maps predict the dominant mechanism for particle deformation under a particular set of conditions (evaporation rate, temperature, and initial film thickness). Although qualitative tests of the Routh-Russel model have been reported previously, a systematic study of the relationship between the film-formation conditions and the resulting water concentration profiles is lacking. Here, the water distributions during the film formation of a series of acrylic copolymer latexes with varying glass-transition temperatures, Tg (values of -22, -11, 4, and 19 °C), have been obtained using GARField nuclear magnetic resonance profiling. A significant reduction in the rate of water loss from the latex copolymer with the lowest Tg was found, which is explained by its relatively low polymer viscosity enabling the growth of a coalesced skin layer. The set of processing parameters where the drying first becomes impeded occurs at the boundary between the capillary deformation and the wet sintering regimes of the Routh-Russel model, which provides strong confirmation of the model's validity. An inverse correlation between the model's dimensionless control parameter and the dimensionless drying time is discovered, which is useful for the design of fast-drying waterborne films.

  11. Photocontrollable water permeation on the micro/nanoscale hierarchical structured ZnO mesh films.

    PubMed

    Tian, Dongliang; Zhang, Xiaofang; Zhai, Jin; Jiang, Lei

    2011-04-05

    Most research of responsive surfaces mainly focus on the wettability transition on different solid substrate surfaces, but the dynamic properties of the micro/nanostructure-enhanced responsive wettability on microscale pore arrays are lacking and still remain a challenge. Here we report the photocontrollable water permeation on micro/nanoscale hierarchical structured ZnO-coated stainless steel mesh films. Especially, for aligned ZnO nanorod array-coated stainless steel mesh film, the film shows good water permeability under irradiation, while it is impermeable to water after dark storage. A detailed investigation indicates that the special nanostructure and the appropriate size of the microscale mesh pores play a crucial role in the excellent controllability over water permeation. The excellent controllability of water permeation on this film is promising in various important applications such as filtration, microreactor, and micro/nano fluidic devices. This work may provide interesting insight into the design of novel functional devices that are relevant to surface wettability.

  12. Water-soluble nanocrystalline cellulose films with highly transparent and oxygen barrier properties.

    PubMed

    Cheng, Shaoling; Zhang, Yapei; Cha, Ruitao; Yang, Jinliang; Jiang, Xingyu

    2016-01-14

    By mixing a guar gum (GG) solution with a nanocrystalline cellulose (NCC) dispersion using a novel circular casting technology, we manufactured biodegradable films as packaging materials with improved optical and mechanical properties. These films could act as barriers for oxygen and could completely dissolve in water within 5 h. We also compared the effect of nanocomposite films and commercial food packaging materials on the preservation of food.

  13. Micro/nanoscale hierarchical structured ZnO mesh film for separation of water and oil.

    PubMed

    Tian, Dongliang; Zhang, Xiaofang; Wang, Xiao; Zhai, Jin; Jiang, Lei

    2011-08-28

    Oil contaminated water is a common problem in the world, thus to effectively separate water and oil is an urgent task for us to resolve. By control of surface wettability of a solid substrate, both superhydrophobicity and superoleophilicity on a film can be realized, which is necessary for water and oil separation. Here we report a stable superhydrophobic and superoleophilic ZnO-coated stainless steel mesh film with special hierarchical micro/nanostructures that can be used to separate a water and oil mixture effectively. Namely, the film is superhydrophobic and water cannot penetrate the mesh film because of the large negative capillary effect, while the film is superoleophilic and liquid paraffin oil can spread out quickly and permeate the mesh film spontaneously due to the capillary effect. A detailed investigation indicates that microscale and nanoscale hierarchical structures and the appropriate size of the microscale mesh pores on the mesh films play an important role in obtaining the excellent water and oil separation property. This work provides an alternative to current separation meshes and is promising in various important applications such as separation and filtration, lab-on-a-chip devices and micro/nanofluidic devices.

  14. Influence of organic films on the evaporation and condensation of water in aerosol.

    PubMed

    Davies, James F; Miles, Rachael E H; Haddrell, Allen E; Reid, Jonathan P

    2013-05-28

    Uncertainties in quantifying the kinetics of evaporation and condensation of water from atmospheric aerosol are a significant contributor to the uncertainty in predicting cloud droplet number and the indirect effect of aerosols on climate. The influence of aerosol particle surface composition, particularly the impact of surface active organic films, on the condensation and evaporation coefficients remains ambiguous. Here, we report measurements of the influence of organic films on the evaporation and condensation of water from aerosol particles. Significant reductions in the evaporation coefficient are shown to result when condensed films are formed by monolayers of long-chain alcohols [C(n)H(2n+1)OH], with the value decreasing from 2.4 × 10(-3) to 1.7 × 10(-5) as n increases from 12 to 17. Temperature-dependent measurements confirm that a condensed film of long-range order must be formed to suppress the evaporation coefficient below 0.05. The condensation of water on a droplet coated in a condensed film is shown to be fast, with strong coherence of the long-chain alcohol molecules leading to islanding as the water droplet grows, opening up broad areas of uncoated surface on which water can condense rapidly. We conclude that multicomponent composition of organic films on the surface of atmospheric aerosol particles is likely to preclude the formation of condensed films and that the kinetics of water condensation during the activation of aerosol to form cloud droplets is likely to remain rapid.

  15. Investigations on humic acid removal from water using surfactant-modified zeolite as adsorbent in a fixed-bed reactor

    NASA Astrophysics Data System (ADS)

    Elsheikh, Awad F.; Ahmad, Umi Kalthom; Ramli, Zainab

    2016-12-01

    Natural organic matter (NOM) is ubiquitous in aquatic environments and has recently become an issue of worldwide concern in drinking water treatment. The major component of NOM is humic acids (HA). In this study, a natural zeolite (mordenite) was modified employing hexadecyltrimethylammonium bromide (HDTMA) to enhance greater efficient sites for sorption of HA. The natural zeolite and surfactant-modified zeolite (SMZ) were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectrometer (FT-IR), N2 Adsorption-desorption isotherms and BET-specific surface area, thermographic analysis, derivative thermographic analysis (TGA-DTA) and Field emission scanning electron microscopy (FESEM). A fixed-bed reactor was used for the removal of HA and the effects of different experimental parameters such as HDTMA loading levels, HA solution flow rate, solution pH and eluent concentration were investigated. The results indicated that the SMZ bed with HDTMA loading of 75% of external cation exchange capacity (ECEC) at a flow rate of 2 BV/h and pH of 10 showed the greatest enhanced removal efficiency of HA while ethanol solutions (25%v/v) with feed flow rate of 2 BV/h were sufficient for complete regeneration of SMZ and desorption of HA. Measurements of surface area of SMZ indicated that a monolayer formation of the surfactant at those conditions allowed the optimum removal of HA.

  16. Photophysical studies of a new water soluble indocarbocyanine dye adsorbed onto microcrystalline cellulose and β-cyclodextrin.

    PubMed

    El-Shishtawy, Reda M; Oliveira, Anabela S; Almeida, Paulo; Ferreira, Diana P; Conceição, David S; Ferreira, Luis F Vieira

    2013-05-15

    A water-soluble indocarbocyanine dye was synthesized and its photophysics were studied for the first time on two solid hosts, microcrystalline cellulose and b-cyclodextrin, as well as in homogeneous media. The inclusion of the indocarbocyanine moiety onto microcrystalline cellulose increased the dye aggregation with both H and J aggregates being formed. Adsorption on b-cyclodextrin enhanced aggregation in a similar way. The fluorescence quantum yields were determined for the powdered samples of the cyanine dye on the two hosts and a significant increase was observed relative to homogeneous solution. A remarkable concentration dependence was also detected in both cases. A lifetime distribution analysis has shown that the indocarbocyanine dye mainly occupies the amorphous part of cellulose and is not entrapped in the crystalline part of this host. In the b-CD case, the adsorption occurs outside the host cavity. In both hosts a strong concentration quenching effect is observed and only monomers emit. Both adsorptions may be explained by stereochemical constraints imposed by the two long sulphoethyl tails linked to nitrogen atoms of the indocarbocyanine dye.

  17. Carbon nanotube sponges as a solid-phase extraction adsorbent for the enrichment and determination of polychlorinated biphenyls at trace levels in environmental water samples.

    PubMed

    Wang, Lei; Wang, Xia; Zhou, Jia-Bin; Zhao, Ru-Song

    2016-11-01

    Carbon nanotube (CNT) sponges has recently attracted considerable attention in numerous fields because of its excellent properties, such as high porosity, light weight, and large surface area. The potential of CNT sponges for the solid-phase extraction (SPE) of organic pollutants at trace levels was investigated in this study for the first time. Seven polychlorinated biphenyls (PCBs) were selected as analytes, and gas chromatography-tandem mass spectrometry was employed for the detection. We optimized important parameters that may influence the efficiency of SPE, including the kind and volume of elution solvent, sample pH, and sample flow rate and volume. Under optimized conditions, low limits of detection (0.72-1.98ngL(-1)), wide range of linearity (10-1000ngL(-1)) and good repeatability (2.69-6.85%, n=5) were obtained. CNT sponges exhibited higher extraction performance than other adsorbent materials under the optimized conditions. Real environmental water samples were analyzed, and satisfactory recoveries (81.1-119.1%) were achieved. All these results demonstrated that CNT sponges are suitable SPE material for the enrichment and sensitive determination of PCBs at trace levels.

  18. One pot synthesis of magnetic graphene/carbon nanotube composites as magnetic dispersive solid-phase extraction adsorbent for rapid determination of oxytetracycline in sewage water.

    PubMed

    Sun, Yunyun; Tian, Jing; Wang, Lu; Yan, Hongyuan; Qiao, Fengxia; Qiao, Xiaoqiang

    2015-11-27

    A simple and time-saving one pot synthesis of magnetic graphene/carbon nanotube composites (M-G/CNTs) was developed that could avoid the tedious drying process of graphite oxide, and G/CNTs were modified by Fe3O4 nanoparticles in the reduction procedure. It contributed to a shorten duration of the synthesis process of M-G/CNTs. The obtained M-G/CNTs were characterized and the results indicated that CNTs and Fe3O4 nanoparticles were served as spacer distributing to the layers of graphene, which was beneficial for enlarging surface area and improving extraction efficiency. Moreover, M-G/CNTs showed good magnetic property and outstanding thermal stability. Then M-G/CNTs were applied as adsorbent of magnetic dispersive solid-phase extraction for rapid extraction and determination of oxytetracycline in sewage water. Under the optimum conditions, good linearity was obtained in the range of 20-800ngmL(-1) and the recoveries were ranged from 95.5% to 112.5% with relative standard deviations less than 5.8%.

  19. Influence of Water Vapors and Hydrogen on the Energy Band Bending in the SnO2 Microcrystals of Polycrystalline Tin Dioxide Films

    NASA Astrophysics Data System (ADS)

    Gaman, V. I.; Almaev, A. V.; Sevast'yanov, E. Yu.; Maksimova, N. K.

    2015-06-01

    The results of studying the dependence of the energy band bending at the interface of contacting SnO2 microcrystals in the polycrystalline tin dioxide film on the humidity level of clean air and hydrogen concentration in the gas mixture of clean air + H2 are presented. The experimental results showed that the bending of energy bands in SnO2 is decreased under exposure to the water vapors and molecular hydrogen. The presence of two types of the adsorption centers for water molecules on the surface of SnO2 is found. It is shown that at the absolute humidity of the gas mixture above 12 g/m3, the H2O and H2 molecules are adsorbed on the same centers, whose surface density is of 1012 сm-2 at a concentration of donor impurity in SnO2 equal to 1018 сm-3.

  20. The cis-bis(decanoate)tin phthalocyanine/DPPC film at the air/water interface.

    PubMed

    Ramos, Salvador; Garza, Cristina; Beltran, Hiram I; Campos-Terán, José; Arenas-Alatorre, Jesús; Castillo, Rolando

    2012-03-01

    Films made of cis-bis-decanoate-tin(IV) phthalocyanine (PcSn10) and racemic dipalmitoylphosphatidylcholine (DPPC) are studied with compression isotherms and Brewster angle microscopy (BAM) at the air/water interface. Films enriched in PcSn10 present phase separation elliptical-shaped domains. These domains present optical anisotropy and molecular order. They are enriched in PcSn10, and the film outside these domains is enriched in DPPC, as shown in by high-angle annular dark-field transmission electron microscopy on Langmuir-Blodgett (LB) transferred films. Film collapse area and atomic force microscopy images of LB transferred films on mica indicate that the films are actually multilayers. A computational survey was performed to determine how the PcSn10 molecules prefer to self-assemble, in films basically made of PcSn10. The relative energetic stability for several dimeric assemblies was obtained, and a crystal model of the film was developed through packing and repeating the PcSn10 molecules, along the crystallographic directions of the unit cell. Our results contribute to understanding the strong interaction between PcSn10 and DPPC at the air/water interface, where even small quantities of DPPC (~1-2%) can modify the film in an important way.

  1. Influence of Aloe vera on water absorption and enzymatic in vitro degradation of alginate hydrogel films.

    PubMed

    Pereira, Rúben F; Carvalho, Anabela; Gil, M H; Mendes, Ausenda; Bártolo, Paulo J

    2013-10-15

    This study investigates the influence of Aloe vera on water absorption and the in vitro degradation rate of Aloe vera-Ca-alginate hydrogel films, for wound healing and drug delivery applications. The influence of A. vera content (5%, 15% and 25%, v/v) on water absorption was evaluated by the incubation of the films into a 0.1 M HCl solution (pH 1.0), acetate buffer (pH 5.5) and simulated body fluid solution (pH 7.4) during 24h. Results show that the water absorption is significantly higher for films containing high A. vera contents (15% and 25%), while no significant differences are observed between the alginate neat film and the film with 5% of A. vera. The in vitro enzymatic degradation tests indicate that an increase in the A. vera content significantly enhances the degradation rate of the films. Control films, incubated in a simulated body fluid solution without enzymes, are resistant to the hydrolytic degradation, exhibiting reduced weight loss and maintaining its structural integrity. Results also show that the water absorption and the in vitro degradation rate of the films can be tailored by changing the A. vera content.

  2. Equilibrium water contents of cellulose films determined via solvent exchange and quartz crystal microbalance with dissipation monitoring.

    PubMed

    Kittle, Joshua D; Du, Xiaosong; Jiang, Feng; Qian, Chen; Heinze, Thomas; Roman, Maren; Esker, Alan R

    2011-08-08

    Model cellulose surfaces have attracted increasing attention for studying interactions with cell wall matrix polymers and as substrates for enzymatic degradation studies. Quartz crystal microbalance with dissipation monitoring (QCM-D) solvent exchange studies showed that the water content of regenerated cellulose (RC) films was proportional to the film thickness (d) and was consistent with about five water molecules per anhydroglucose unit. Sulfated nanocrystalline cellulose (SNC) and desulfated nanocrystalline cellulose (DNC) films had comparable water contents and contained about five times more water than RC films. A cellulase mixture served as a probe for studies of substrate accessibility and degradation. Cellulase adsorption onto RC films was independent of d, whereas degradation times increased with d. However, adsorption onto SNC and DNC films increased with d, whereas cellulase degradation times for DNC films were independent of studied d. Enhanced access to guest molecules for SNC and DNC films revealed they are more porous than RC films.

  3. Equilibrium Water Contents of Cellulose Films Determined via Solvent Exchange and Quartz Crystal Microbalance with Dissipation Monitoring

    SciTech Connect

    Kittle, Joshua D.; Du, Xiaosong; Jiang, Feng; Qian, Chen; Heinze, Thomas; Roman, Maren; Esker, Alan R.

    2011-08-08

    Model cellulose surfaces have attracted increasing attention for studying interactions with cell wall matrix polymers and as substrates for enzymatic degradation studies. Quartz crystal microbalance with dissipation monitoring (QCM-D) solvent exchange studies showed that the water content of regenerated cellulose (RC) films was proportional to the film thickness (d) and was consistent with about five water molecules per anhydroglucose unit. Sulfated nanocrystalline cellulose (SNC) and desulfated nanocrystalline cellulose (DNC) films had comparable water contents and contained about five times more water than RC films. A cellulase mixture served as a probe for studies of substrate accessibility and degradation. Cellulase adsorption onto RC films was independent of d, whereas degradation times increased with d. However, adsorption onto SNC and DNC films increased with d, whereas cellulase degradation times for DNC films were independent of studied d. Enhanced access to guest molecules for SNC and DNC films revealed they are more porous than RC films.

  4. Development of Molecularly Imprinted Polymer in Porous Film Format for Binding of Phenol and Alkylphenols from Water

    PubMed Central

    Gryshchenko, Andriy O.; Bottaro, Christina S.

    2014-01-01

    Molecularly imprinted polymers (MIPs) were fabricated on glass slides with a “sandwich” technique giving ~20 μm thick films. Methanol/water as a solvent, and polyethyleneglycol and polyvinylacetate as solvent modifiers, were used to give a porous morphology, which was studied with scanning electron microscopy and gravimetric analysis. Various MIPs were synthesized through non-covalent imprinting with phenol as the template; itaconic acid, 4-vinylpyridine, and styrene as monomers; ethylene glycol dimethacrylate, triethylene glycol dimethacrylate, and pentaerythritol triacrylate (PETA) as cross-linkers. Binding and imprinting properties of the MIPs were evaluated based on phenol adsorption isotherms. Since phenol has only one weakly acidic hydroxyl group and lacks unique structural characteristics necessary for binding specificity, the preparation of selective MIPs was challenging. The recognition of phenol via hydrogen bonding is suppressed in water, while hydrophobic interactions, though promoted, are not specific enough for highly-selective phenol recognition. Nevertheless, the styrene-PETA MIP gave modest imprinting effects, which were higher at lower concentrations (Imprinting Factor (IF) = 1.16 at 0.5 mg·L−1). The isotherm was of a Freundlich type over 0.1–40 mg·L−1 and there was broad cross-reactivity towards other structurally similar phenols. This shows that phenol MIPs or simple adsorbents can be developed based on styrene for hydrophobic binding, and PETA to form a tighter, hydrophilic network. PMID:24447925

  5. Development of an element-selective monitoring system for adsorbable organic halogens (AOX) with plasma emission spectrometric detection for quasi-continuous waste-water analysis.

    PubMed

    Twiehaus, T; Evers, S; Buscher, W; Cammann, K

    2001-11-01

    An automated quasi-continuously-operating monitor has been developed for element-selective analysis of adsorbable organic halogens (AOX) in water. After extensive optimization the automatic method was applied to the analysis of standard solutions and real waste water samples to prove its analytical applicability. The new instrument is based on the element-selective analysis of halogens by means of a spectroscopic detection system consisting of a microwave-induced helium plasma excitation source (TM010-type; developed in this laboratory) and the plasma emission detector (PED) which operates with oscillating narrow-band interference filters. After enriching the organic components on activated charcoal and pyrolysis in an oxygen stream at 950 degrees C, in accordance with DIN/EN 38409,H14/1485, interfering CO2 and H2O gas generated during combustion is removed from the analytes in the so-called ELSA-system (element-selective AOX-analyzer). For focused injection into the plasma excitation source the analytes (hydrogen halides) are trapped in a deactivated fused silica capillary at -180 degrees C; this is followed by identification and quantification on the basis of element-specific emission of radiation in the VIS and NIR-region (chlorine 837.6 nm, fluorine 685.6 nm). Bromine and iodine could not be detected with satisfactory inter-element selectivity, because of spectral interferences caused by matrix elements, and so results from the respective single-element investigations for determination of AOBr and AOI are not presented. The procedure has been validated and the analytical performance has been examined by calibration with p-chlorophenol and p-fluorophenol. The limit of detection was 1.1 microg (absolute) for chlorine and 6.6 microg (absolute) for fluorine.

  6. Evaluation of heavy crude oil from a water-oil model system as starting material for the preparation of adsorbents type NaY zeolite-templated carbon.

    PubMed

    Elles-Pérez, Cindy J; Muñoz-Acevedo, Amner; Guzmán, Andrés; Camargo, Hernando; Henao, José

    2017-03-22

    In this work, NaY zeolite is explored as a possible "template" to obtain porous materials type ZTC from the adsorption of heavy crude oil in a water-oil model system (emulsion). In order to produce the adsorbents, a cationic surfactant is selected to facilitate the adsorption of the crude oil into the pores of the zeolite and to get the composite, which was activated with controlled thermal treatments (T: 700-800 °C and t: 0.5-1 h) in inert conditions (N2 gaseous). The starting materials, composite and porous carbons were characterized using structural/surface analysis techniques (API Gravity, SARA, IR, XRD, XRF, TGA, Langmuir isotherms, BET and SEM). The results showed that four types of mesoporous carbons were produced with specific surface areas between 70 ± 1 m(2)/g and 220 ± 3 m(2)/g, average pore volumes between 0.144 cm(3)/g and 0.40 cm(3)/g and average pore widths between 4.9 nm and 8.3 nm. The activation conditions of 800 °C and 1 h allowed to make the carbonaceous material with the best surface characteristics (220 ± 3 m(2)/g, 0.27 cm(3)/g, and 4.9 nm). Therefore, it is concluded that under assay conditions employed, the heavy crude oil, as a mixed model (water-oil), from an aqueous environment is a starting material suitable for preparation of "mesoporous" carbons.

  7. Rhodamine 6G and 800 J-heteroaggregates with enhanced acceptor luminescence (HEAL) adsorbed in transparent SiO2 GLAD thin films.

    PubMed

    Sánchez-Valencia, Juan R; Aparicio, Francisco J; Espinós, Juan P; Gonzalez-Elipe, Agustín R; Barranco, Angel

    2011-04-21

    An enhanced fluorescent emission in the near infrared is observed when the Rhodamine 800 (Rh800) and 6G (Rh6G) dyes are coadsorbed in porous SiO(2) optical thin films prepared by glancing angle deposition (GLAD). This unusual behavior is not observed in solution and it has been ascribed to the formation of a new type of J-heteroaggregates with enhanced acceptor luminescence (HEAL). This article describes in detail and explains the main features of this new phenomenology previously referred in a short communication [J. R. Sánchez-Valencia, J. Toudert, L. González-García, A. R. González-Elipe and A. Barranco, Chem. Commun., 2010, 46, 4372-4374]. It is found that the efficiency and characteristics of the energy transfer process are dependent on the Rh6G/Rh800 concentration ratio which can be easily controlled by varying the pH of the solutions used for the infiltration of the molecules or by thermal treatments. A simple model has been proposed to account for the observed enhanced acceptor luminescence in which the heteroaggregates order themselves according to a "head to tail" configuration due to the geometrical constrains imposed by the SiO(2) porous matrix thin film. The thermal stability of the dye molecules within the films and basic optical (absorption and fluorescence) principles of the HEAL process are also described.

  8. Sn(II) oxy-hydroxides as potential adsorbents for Cr(VI)-uptake from drinking water: An X-ray absorption study.

    PubMed

    Pinakidou, Fani; Kaprara, Efthimia; Katsikini, Maria; Paloura, Eleni C; Simeonidis, Konstantinos; Mitrakas, Manassis

    2016-05-01

    The feasibility of implementing a Sn(II) oxy-hydroxide (Sn6O4(OH)4) for the reduction and adsorption of Cr(VI) in drinking water treatment was investigated using XAFS spectroscopies at the Cr-K-edge. The analysis of the Cr-K-edge XANES and EXAFS spectra verified the effective use of Sn6O4(OH)4 for successful Cr(VI) removal. Adsorption isotherms, as well as dynamic Rapid Small Scale Test (RSSCT) in NSF water matrix showed that Sn6O4(OH)4 can decrease Cr(VI) concentration below the upcoming regulation limit of 10μg/L for drinking water. Moreover, an uptake capacity of 7.2μg/mg at breakthrough concentration of 10μg/L was estimated from the RSSCT, while the residual Cr(VI) concentration ranged at sub-ppb level for a significant period of the experiment. Furthermore, no evidence for the formation of Cr(OH)3 precipitates was found. On the contrary, Cr(III)-oxyanions were chemisorbed onto SnO2, which was formed after Sn(II)-oxidation during Cr(VI)-reduction. Nevertheless, changes in the type of Cr(III)-inner sphere complexes were observed after increasing surface coverage: Cr(III)-oxyanions preferentially sorb in a geometry which combines both bidentate binuclear ((2)C) and monodentate ((1)V) geometries, at the expense of the present bidentate mononuclear ((2)E) contributions. On the other hand, the pH during sorption does not affect the adsorption mechanism of Cr(III)-species. The implementation of Sn6O4(OH)4 in water treatment technology combines the advantage of rapidly reducing a large amount of Cr(VI) due to donation of two electrons by Sn(II) and also the strong chemisorption of Cr(III) in a combination of the (2)C and (1)V configurations, which enhances the safe disposal of spent adsorbents.

  9. Freestanding Boron Nitride Nanosheet Films for Ultrafast Oil/Water Separation.

    PubMed

    Li, Taotao; Wang, Liangjie; Zhang, Kai; Xu, Yancui; Long, Xiaoyang; Gao, Shoujian; Li, Ru; Yao, Yagang

    2016-09-01

    Freestanding boron nitride nanosheet (BNNS) films with designed structures are first fabricated by chemical vapor deposition (CVD) methods. As-prepared freestanding BNNS films exhibit outstanding hydrophobicity and lipophilicity properties. Such brilliant behaviors make them applicable in oil/water separation with very high fluxes up to 1 200 000 L m(-2) h(-1) bar(-1) and excellent separation efficiencies (ppm level in terms of the water content in the filtrate).

  10. Bio-nanocomposite films reinforced with cellulose nanocrystals: Rheology of film-forming solutions, transparency, water vapor barrier and tensile properties of films.

    PubMed

    El Miri, Nassima; Abdelouahdi, Karima; Barakat, Abdellatif; Zahouily, Mohamed; Fihri, Aziz; Solhy, Abderrahim; El Achaby, Mounir

    2015-09-20

    This study was aimed to develop bio-nanocomposite films of carboxymethyl cellulose (CMC)/starch (ST) polysaccharide matrix reinforced with cellulose nanocrystals (CNC) using the solution casting method. The CNC were extracted at the nanometric scale from sugarcane bagasse via sulfuric acid hydrolysis and used as reinforcing phase to produce CMC/ST-CNC bio-nanocomposite films at different CNC loading levels (0.5-5.0 wt%). Steady shear viscosity and dynamic viscoelastic measurements of film-forming solution (FFS) of neat CMC, CMC/ST blend and CMC/ST-CNC bio-nanocomposites were evaluated. Viscosity measurements revealed that a transition from Newtonian behavior to shear thinning occurred when CNC were added. The dynamic tests confirmed that all FFS have a viscoelastic behavior with an entanglement network structure, induced by the hydrogen bonding. In regard to the cast film quality, the rheological data showed that all FFS were suitable for casting of films at ambient temperature. The effect of CNC addition on the optical transparency, water vapor permeability (WVP) and tensile properties of bio-nanocomposite films was studied. It was found that bio-nanocomposite films remain transparent due to CNC dispersion at the nanoscale. The WVP was significantly reduced and the elastic modulus and tensile strength were increased gradually with the addition of CNC. Herein, the steps to form new eco-friendly bio-nanocomposite films were described by taking advantage of the combination of CMC, ST and CNC. The as-produced films exhibited good optical transparency, reduced WVP and enhanced tensile properties, which are the main properties required for packaging applications.

  11. Influence of water expulsion on structural properties of V2O5nH2O sol-gel films

    NASA Astrophysics Data System (ADS)

    Gökdemir, F. Pınar; Menda, U. Deneb; Kavak, Pelin; Saatci, A. Evrim; Özdemir, Orhan; Kutlu, Kubilay

    2012-09-01

    Vanadium pentoxide (V2O5) thin films were prepared by dip-coating sol-gel technique by dissolving V2O5 powder in hydrogen peroxide (H2O2), the solution, leading V2O5 sol-gel nanocrystalline films. The films under preparation were exposed different hydration states, n, varying from 6 to 2 determined via XRD measurements. Water molecules were adsorbed in layered structure of V2O5 oxide films and hence the adsorption could be described as an intercalation in which the molecules were trapped in some cavities and were not randomly oriented. (00l) pattern of X-ray diffraction analysis not only approved the one dimensional stacking of V2O5 ribbons but also served to determine basal distance from which hydration state was guessed. The basal distance were calculated from the position of 00l peak and varied from 17.2 Å to 10.6 Å that corresponded to n=6 to n=2 respectively. During the water departure upon heating, the basal distance reduced by steps of 2.8 Å (diameter of vander Walls water molecule) towards 8.8 Å value, attributed to n=0.5. Contrary to common belief of three-step mass loss (two of them were ascribed water expulsion), the process took place in two steps in thermo-gravimetric and differential thermal analysis (TG/DTA) measurements. During the first step, decrease in d exhibited huge endothermic negative thermal expansion of V2O5nH2O sol while crystallization into orthorhombic V2O5 occurred at 357°C (exhothermic peak) in TG as last step.

  12. The uranium from seawater program at PNNL: Overview of marine testing, adsorbent characterization, adsorbent durability, adsorbent toxicity, and deployment studies

    DOE PAGES

    Gill, Gary A.; Kuo, Li -Jung; Janke, Christopher James; ...

    2016-02-07

    The Pacific Northwest National Laboratory's (PNNL) Marine Science Laboratory (MSL) located along the coast of Washington State is evaluating the performance of uranium adsorption materials being developed for seawater extraction under realistic marine conditions with natural seawater. Two types of exposure systems were employed in this program: flow-through columns for testing of fixed beds of individual fibers and pellets and a recirculating water flume for testing of braided adsorbent material. Testing consists of measurements of the adsorption of uranium and other elements from seawater as a function of time, typically 42 to 56 day exposures, to determine the adsorbent capacitymore » and adsorption rate (kinetics). Analysis of uranium and other trace elements collected by the adsorbents was conducted following strong acid digestion of the adsorbent with 50% aqua regia using either Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) or Inductively Coupled Plasma Mass Spectrometer (ICP-MS). The ORNL 38H adsorbent had a 56 day adsorption capacity of 3.30 ± 0.68 g U/ kg adsorbent (normalized to a salinity of 35 psu), a saturation adsorption capacity of 4.89 ± 0.83 g U/kg of adsorbent material (normalized to a salinity of 35 psu) and a half-saturation time of 28 10 days. The AF1 adsorbent material had a 56 day adsorption capacity of 3.9 ± 0.2 g U/kg adsorbent material (normalized to a salinity of 35 psu), a saturation capacity of 5.4 ± 0.2 g U/kg adsorbent material (normalized to a salinity of 35 psu) and a half saturation time of 23 2 days. The ORNL amidoxime-based adsorbent materials are not specific for uranium, but also adsorb other elements from seawater. The major doubly charged cations in seawater (Ca and Mg) account for a majority of the cations adsorbed (61% by mass and 74% by molar percent). For the ORNL AF1 adsorbent material, U is the 4th most abundant element adsorbed by mass and 7th most abundant by molar percentage. Marine testing

  13. The uranium from seawater program at PNNL: Overview of marine testing, adsorbent characterization, adsorbent durability, adsorbent toxicity, and deployment studies

    SciTech Connect

    Gill, Gary A.; Kuo, Li -Jung; Janke, Christopher James; Park, Jiyeon; Jeters, Robert T.; Bonheyo, George T.; Pan, Horng -Bin; Wai, Chien; Khangaonkar, Tarang P.; Bianucci, Laura; Wood, Jordana R.; Warner, Marvin G.; Peterson, Sonja; Abrecht, David G.; Mayes, Richard T.; Tsouris, Costas; Oyola, Yatsandra; Strivens, Jonathan E.; Schlafer, Nicholas J.; Addleman, Shane R.; Chouyyok, Wilaiwan; Das, Sadananda; Kim, Jungseung; Buesseler, Ken; Breier, Crystal; D'Alessandro, Evan

    2016-02-07

    The Pacific Northwest National Laboratory's (PNNL) Marine Science Laboratory (MSL) located along the coast of Washington State is evaluating the performance of uranium adsorption materials being developed for seawater extraction under realistic marine conditions with natural seawater. Two types of exposure systems were employed in this program: flow-through columns for testing of fixed beds of individual fibers and pellets and a recirculating water flume for testing of braided adsorbent material. Testing consists of measurements of the adsorption of uranium and other elements from seawater as a function of time, typically 42 to 56 day exposures, to determine the adsorbent capacity and adsorption rate (kinetics). Analysis of uranium and other trace elements collected by the adsorbents was conducted following strong acid digestion of the adsorbent with 50% aqua regia using either Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) or Inductively Coupled Plasma Mass Spectrometer (ICP-MS). The ORNL 38H adsorbent had a 56 day adsorption capacity of 3.30 ± 0.68 g U/ kg adsorbent (normalized to a salinity of 35 psu), a saturation adsorption capacity of 4.89 ± 0.83 g U/kg of adsorbent material (normalized to a salinity of 35 psu) and a half-saturation time of 28 10 days. The AF1 adsorbent material had a 56 day adsorption capacity of 3.9 ± 0.2 g U/kg adsorbent material (normalized to a salinity of 35 psu), a saturation capacity of 5.4 ± 0.2 g U/kg adsorbent material (normalized to a salinity of 35 psu) and a half saturation time of 23 2 days. The ORNL amidoxime-based adsorbent materials are not specific for uranium, but also adsorb other elements from seawater. The major doubly charged cations in seawater (Ca and Mg) account for a majority of the cations adsorbed (61% by mass and 74% by molar percent). For the ORNL AF1 adsorbent material, U is the 4th most abundant element adsorbed by mass and 7th most abundant by molar percentage. Marine testing at Woods

  14. TiO2 and Fe2O3 films for photoelectrochemical water splitting.

    PubMed

    Krysa, Josef; Zlamal, Martin; Kment, Stepan; Brunclikova, Michaela; Hubicka, Zdenek

    2015-01-09

    Titanium oxide (TiO2) and iron oxide (α-Fe2O3) hematite films have potential applications as photoanodes in electrochemical water splitting. In the present work TiO2 and α-Fe2O3 thin films were prepared by two methods, e.g., sol-gel and High Power Impulse Magnetron Sputtering (HiPIMS) and judged on the basis of physical properties such as crystalline structure and surface topography and functional properties such as simulated photoelectrochemical (PEC) water splitting conditions. It was revealed that the HiPIMS method already provides crystalline structures of anatase TiO2 and hematite Fe2O3 during the deposition, whereas to finalize the sol-gel route the as-deposited films must always be annealed to obtain the crystalline phase. Regarding the PEC activity, both TiO2 films show similar photocurrent density, but only when illuminated by UV light. A different situation was observed for hematite films where plasmatic films showed a tenfold enhancement of the stable photocurrent density over the sol-gel hematite films for both UV and visible irradiation. The superior properties of plasmatic film could be explained by ability to address some of the hematite drawbacks by deposition of very thin films (25 nm) consisting of small densely packed particles and by doping with Sn.

  15. Water adsorption, solvation and deliquescence of alkali halide thin films on SiO2 studied by ambient pressure X-ray photoelectron spectroscopy

    SciTech Connect

    Arima, Kenta; Jiang, Peng; Deng, Xingyi; Bluhm, Henrik; Salmeron, Miquel

    2010-03-31

    The adsorption of water on KBr thin films evaporated onto SiO2 was investigated as a function of relative humidity (RH) by ambient pressure X-ray photoelectron spectroscopy. At 30percent RH adsorbed water reaches a coverage of approximately one monolayer. As the humidity continues to increase, the coverage of water remains constant or increases very slowly until 60percent RH, followed by a rapid increase up to 100percent RH. At low RH a significant number of the Br atoms are lost due to irradiation damage. With increasing humidity solvation increases ion mobility and gives rise to a partial recovery of the Br/K ratio. Above 60percent RH the increase of the Br/K ratio accelerates. Above the deliquescence point (85percent RH), the thickness of the water layer continues to increase and reaches more than three layers near saturation. The enhancement of the Br/K ratio at this stage is roughly a factor 2.3 on a 0.5 nm KBr film, indicating a strong preferential segregation of Br ions to the surface of the thin saline solution on SiO2.

  16. Rheological changes and kinetics of water uptake by poly(ionic liquid)-based thin films.

    PubMed

    Benedetti, Tânia M; Torresi, Roberto M

    2013-12-17

    Water uptake by thin films composed of the poly(ionic liquid) poly[diallyldimethylammonium bis(trifluoromethanesulfonyl)imide] (PDDATf2N) and the ionic liquid N,N-butylmethylpyrrolidinium bis(trifluoromethanesulfonyl)imide (Pyr1.4Tf2N) was studied with a quartz crystal microbalance with dissipation. The data obtained for films with different compositions during the passage of dry and wet N2 flow through the films were simulated with the Kevin-Voigt viscoelastic model for assessment of the mass of uptake water as well as the viscoelastic parameters. Our results show that the ionic liquid acts as a plasticizer, reducing the rigidity of the film and decreasing the capacity of water uptake. Introduction to a Li salt (LiTf2N) increases the water uptake capacity and also affects both elastic and viscous parameters due to aggregation among the ions from the ionic liquid and Li(+). However, due to the preferable interaction of Li(+) ions with water molecules, these aggregates are broken when the film is hydrated. In short, the presence of water in such films affects their mechanical properties, which can reflect in their performances as solid state electrolytes and ion-conducting membranes for electrochemical applications.

  17. Water in polymer membranes. 4. Raman scattering from cellulose acetate films

    SciTech Connect

    Scherer, J.R.; Bailey, G.F.; Kint, S.; Young, R.; Malladi, D.P.; Bolton, B.

    1985-01-17

    Raman scattering was observed from thin film optical waveguides of cellulose acetate exposed to water vapor from 0% to 100% relative humidity (RH), and from dilute solutions of water in methyl acetate. Spectra of cellulose acetate (CA398, 39.8% acetyl) at low RH and cellulose triacetate (CTA) at low and high RH are consistent with the presence of water monomers that are weakly hydrogen bonded to acetyl C=O groups. Differences between the spectra of water in CA398 and CTA at low RH are attributed to sequential hydrogen bonding involving OH groups in CA398. At high RH, CA398 and CTA (to a lesser extent) show bands attributed to water/water interactions that are similar to those found in sequentially hydrogen-bonded hydrates. CA398 films that are annealed at high temperatures exhibit decreased water/water interactions at high RH. Exposure of CA398 films to D/sub 2/O converts > 90% of all polymer OH groups to OD groups. This indicates that water is accessible to nearly all regions of the polymer containing OH groups. Annealing does not alter this accessibility but does reduce the total water content by roughly half, at 100% RH. Hydrogen-bonded C=O groups are associated with a band centered at 1731 cm/sup -1/ which increases in intensity with increasing water content in the film but does not shift in frequency. 38 references, 16 figures, 1 table.

  18. Modulation of ZnO film thickness and formation of water-hyacinth nanostructure

    NASA Astrophysics Data System (ADS)

    Gunasekaran, Ezhilarasan; Shankar, Prabakaran; Mani, Ganesh Kumar; Bosco Balaguru Rayappan, John

    2014-08-01

    The influence of precursor medium was investigated on the structural, morphological, optical and electrical properties of spray pyrolysis deposited nanostructured ZnO thin films. Three batches of ZnO thin films were deposited on glass substrates using three different solvents (water, water-ethanol [ratio of 1:1] and ethanol) based precursor solution of zinc nitrate hexahydrate. The substrate temperature was fixed at 523 K. The variation in film thickness from 150 to 875 nm was observed as the effect of changing solvent medium. X-ray diffraction (XRD) data confirmed the formation of polycrystalline ZnO thin films with hexagonal wurtzite crystallite structure and the estimated crystallite size was found to be ranging from 31 to 55 nm. Scanning electron micrographs revealed the formation of water-hyacinth shaped nanostructures when water-ethanol mixture was used as the solvent medium. Interestingly, UV-vis spectrophotometer revealed the formation of ZnO film with twin optical band gap of 3.15 eV and 3.56 eV when ethanol was used as the solvent medium. The modulation of film thickness and grain size by solvent medium has strongly influenced the electrical conductivity of ZnO thin films. The homogenous nano-spherical grains with uniform grain boundaries showed a good response towards 100 ppm of ammonia at room temperature.

  19. Water absorption and moisture permeation properties of chitosan/poly(acrylamide-co-itaconic acid) IPC films.

    PubMed

    Bajpai, M; Bajpai, S K; Jyotishi, Pooja

    2016-03-01

    In this work, aqueous solutions of chitosan (Ch) and [poly(acrylamide(AAm)-co-itaconicacid(IA)] have been mixed to yield Ch/poly(AAm-co-IA) Inter-polyelectrolyte complex (IPC) films. The films were characterized by FTIR, X-ray diffraction (XRD) and thermo gravimetric analysis (TGA). There was remarkable increase in the crystalline nature of IPC films. The films were investigated for their water absorption capacity in the physiological fluid (PF) of pH 7.4 at 37 °C. The amount of IA present in the film forming solutions affected the water absorption behavior of the resulting films. The dynamic water uptake data were interpreted by various kinetic models. The effect of pH on the swelling ratio (SR) indicated that the films showed highest swelling in lower as well as higher pH media. The water vapor transmission rates (WVTR) were obtained in the range of 6000-6645 g/m(2)/day.

  20. Water repellent porous silica films by sol-gel dip coating method.

    PubMed

    Rao, A Venkateswara; Gurav, Annaso B; Latthe, Sanjay S; Vhatkar, Rajiv S; Imai, Hiroaki; Kappenstein, Charles; Wagh, P B; Gupta, Satish C

    2010-12-01

    The wetting of solid surfaces by water droplets is ubiquitous in our daily lives as well as in industrial processes. In the present research work, water repellent porous silica films are prepared on glass substrate at room temperature by sol-gel process. The coating sol was prepared by keeping the molar ratio of methyltriethoxysilane (MTES), methanol (MeOH), water (H(2)O) constant at 1:12.90:4.74, respectively, with 2M NH(4)OH throughout the experiments and the molar ratio (M) of MTES/Ph-TMS was varied from 0 to 0.22. A simple dip coating technique is adopted to coat silica films on the glass substrates. The static water contact angle as high as 164° and water sliding angle as low as 4° was obtained for silica film prepared from M=0.22. The surface morphological studies of the prepared silica film showed the porous structure with pore sizes typically ranging from 200nm to 1.3μm. The superhydrophobic silica films prepared from M=0.22 retained their superhydrophobicity up to a temperature of 285°C and above this temperature the films became superhydrophilic. The porous and water repellent silica films are prepared by proper alteration of the Ph-TMS in the coating solution. The prepared silica films were characterized by surface profilometer, scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier Transform Infrared (FT-IR) spectroscopy, humidity tests, chemical aging tests, static and dynamic water contact angle measurements.

  1. Sense or no-sense of the sum parameter for water soluble "adsorbable organic halogens" (AOX) and "absorbed organic halogens" (AOX-S18) for the assessment of organohalogens in sludges and sediments.

    PubMed

    Müller, German

    2003-07-01

    "AOX" is the abbreviation of the sum parameter for water soluble "adsorbable organic halogens" in which 'A' stands for adsorbable, 'O' for organic and 'X' for the halogens chlorine, bromine and iodine. After the introduction of the AOX in 1976, this parameter has been correctly used for "real" AOX constituents (DDT and its metabolites, PCBs, etc.) but also misused for non-adsorbable adsorbed OX-compounds, mostly high molecular organohalogens in plants and even to inorganic compounds being neither organic nor adsorbable. The question of natural "Adsorbable Organic Halogens" (AOX) formed by living organisms and/or during natural abiogenic processes has been definitively solved by the known existence of already more than 3650 organohalogen compounds, amongst them the highly reactive, cancerogenic vinyl chloride (VC). The extension of the AOX to AOX-S18 for Sludges and Sediments, in which A stands for adsorbed (not for adsorbable) is questionable. It includes the most important water insoluble technical organochlorine product: polyvinyl chloride, PVC. In addition to organic halogens it also includes inorganic, mineralogenic halides, incorporated mainly in the crystal lattice of fine grained phyllosilicates, the typical clay minerals (kaolinite, montmorillonite, illite and chlorite) which are main constituents of sediments and sedimentary rocks representing the major part of the sedimentary cover of the earth. Other phyllosilicates, biotite and muscovite, major constituents of granites and many metamorphic rocks (gneiss and mica schist) will also contribute to the AOX-S18 especially in soils as result of weathering processes. Since chlorine is incorporated into the mineral structure and, as a consequence, not soluble by the nitric acid analytical step (pH 0.5) of the S18 determination, it will account to the AOX-S18 in the final charcoal combustion step at temperatures >950 degrees C. After heavy rainfalls sewage sludge composition is strongly influenced by

  2. Are the reduction and oxidation properties of nitrocompounds dissolved in water different from those produced when adsorbed on a silica surface? A DFT M05-2X computational study.

    PubMed

    Sviatenko, Liudmyla K; Isayev, Olexandr; Gorb, Leonid; Hill, Frances C; Leszczynska, Danuta; Leszczynski, Jerzy

    2015-05-30

    The reduction and oxidation properties of four nitrocompounds (trinitrotoluene [TNT], 2,4-dinitrotoluene, 2,4-dinitroanisole, and 5-nitro-2,4-dihydro-3H-1,2,4-triazol-3-one [NTO]) dissolved in water as compared with the same properties for compounds adsorbed on a silica surface were studied. To consider the influence of adsorption, cluster models were developed at the M05/tzvp level. A hydroxylated silica (001) surface was chosen to represent a key component of soil. The PCM(Pauling) and SMD solvation models were used to model water bulk influence. The following properties were analyzed: electron affinity, ionization potential, reduction Gibbs free energy, oxidation Gibbs free energy, and reduction and oxidation potentials. It was found that adsorption and solvation decrease gas phase electron affinity, ionization potential, and Gibbs free energy of reduction and oxidation, and thus, promote redox transformation of nitrocompounds. However, in case of solvation, the changes are more significant than for adsorption. This means that nitrocompounds dissolved in water are easier to transform by reduction or oxidation than adsorbed ones. Among the considered compounds, TNT was found to be the most reactive in an electron attachment process and the least reactive for an electron detachment transformation. During ionization, a deprotonation of adsorbed NTO was found to occur.

  3. Formation process of a strong water-repellent alumina surface by the sol-gel method

    NASA Astrophysics Data System (ADS)

    Feng, Libang; Li, Hui; Song, Yongfeng; Wang, Yulong

    2010-03-01

    A novel strong water-repellent alumina thin film is fabricated by chemically adsorbing stearic acid (STA) layer onto the porous and roughened aluminum film coated with polyethyleneimine (PEI). The formation process and the structure of the strong water-repellent alumina film are investigated by means of contact angle measurement and atomic force microscope (AFM). Results show that the water contact angles for the alumina films increase with the increase of the immersion time in the boiling water, and meanwhile, the roughness of the alumina films increases with the dissolution of the boehmite in the boiling water. Finally, the strong water-repellent film with a high water contact angle of 139.1° is obtained when the alumina films have distinct roughened morphology with some papillary peaks and porous structure. Moreover, both the roughened structure and the hydrophobic materials of the STA endow the alumina films with the strong water-repellence.

  4. The role of glycerol and water in flexible silk sericin film.

    PubMed

    Yun, Haesung; Kim, Moo Kon; Kwak, Hyo Won; Lee, Jeong Yun; Kim, Min Hwa; Lee, Ki Hoon

    2016-01-01

    Silk sericin (SS) can be obtained as a byproduct during the silk fiber process, but its application has been limited due to the brittleness of the SS film. To enhance the flexibility of the SS film, glycerol (Glc) has been added as a plasticizer. The addition of Glc enhanced the elongation property of the SS film when the Glc content was 50-70 wt% of SS. Glc also induced the structural transition of SS from a random coil structure to a β-sheet structure. The inconsistent increase of elongation and β-sheet structure of the SS/Glc film were explained by the content of moisture in the SS/Glc film. The moisture content of the SS/Glc film increased proportionally when the Glc content was higher than 50 wt% of SS, which was the same Glc content range that exhibited the plasticizing effect. Therefore, the plasticizing effect on the SS film may occur not only because of Glc but also because of water. Furthermore, water also contributed to the increase in the β-sheet structure development. Our results suggest that the moisture content in the plasticized protein film may play an important role when the plasticizer has hygroscopic properties.

  5. Three Short Films about Water: Presenting Basic Concepts to Students and Stakeholders

    NASA Astrophysics Data System (ADS)

    Arrigo, J. S.; Hooper, R. P.; Michel, A.; Wilde, P.; Lilienfeld, L.

    2011-12-01

    Three short form (3 - 5 minute) movies were produced for CUAHSI, to convey basic concepts such as a hydrologic budget, stores and fluxes of water, and the flowpaths and residence time of water. The films were originally intended to be used by scientists to explain the concepts behind potential environmental observatories, but evolved into serving a broader purpose. The films combine still photos, satellite images, animation and video clips, and interviews with CUAHSI members explaining hydrologic concepts in simple, accessible terms. In producing these films, we have found the importance of engaging scientists in conversation first, to develop a script around key accessible concepts and relevant information. Film and communication professionals play a critical role in distilling the scientific explanation and concepts into accessible, engaging film material. The films have been widely distributed through CD and online to educators for use in courses. Additionally, they provide a way to engage stakeholders, particularly land owners, by conveying basic concepts that are necessary to understand the hydrologic and earth science foundation of many of today's political and environmental issues. The films can be viewed online at the CUAHSI website, which also contains links to other film related resources and programs.

  6. Preparation of TiO2 thin films using water-soluble titanium complexes and their photoinduced properties.

    PubMed

    Katsumata, Ken-ichi; Ohno, Yukiaki; Tomita, Koji; Sakai, Munetoshi; Nakajima, Akira; Kakihana, Masato; Fujishima, Akira; Matsushita, Nobuhiro; Okada, Kiyoshi

    2011-01-01

    Titanium dioxide thin films were prepared by using four water-soluble titanium complexes of titanium-lactate, tartalate, malate and salicylate complex solutions. The crystalline phases detected in the films were anatase. The surface microstructures of the four film samples were different in their grain sizes. Photocatalytic decomposition activity of the four films was almost the same, but their photoinduced hydrophilicities were different. The film prepared using titanium-salicylate complex exhibited lower hydrophilic conversion rate than the other films. Grain size and stress yielded to the film are considered to be important factors on the photoinduced hydrophilicity.

  7. Molecular Adsorber Coating

    NASA Technical Reports Server (NTRS)

    Straka, Sharon; Peters, Wanda; Hasegawa, Mark; Hedgeland, Randy; Petro, John; Novo-Gradac, Kevin; Wong, Alfred; Triolo, Jack; Miller, Cory

    2011-01-01

    A document discusses a zeolite-based sprayable molecular adsorber coating that has been developed to alleviate the size and weight issues of current ceramic puck-based technology, while providing a configuration that more projects can use to protect against degradation from outgassed materials within a spacecraft, particularly contamination-sensitive instruments. This coating system demonstrates five times the adsorption capacity of previously developed adsorber coating slurries. The molecular adsorber formulation was developed and refined, and a procedure for spray application was developed. Samples were spray-coated and tested for capacity, thermal optical/radiative properties, coating adhesion, and thermal cycling. Work performed during this study indicates that the molecular adsorber formulation can be applied to aluminum, stainless steel, or other metal substrates that can accept silicate-based coatings. The coating can also function as a thermal- control coating. This adsorber will dramatically reduce the mass and volume restrictions, and is less expensive than the currently used molecular adsorber puck design.

  8. Facile and scalable synthesis of magnetite/carbon adsorbents by recycling discarded fruit peels and their potential usage in water treatment.

    PubMed

    Ma, Ji; Sun, Shuangshuang; Chen, Kezheng

    2017-02-20

    In this study, apple, banana and orange peels were used as precursor compounds for the mass production of magnetite/carbon adsorbents. A so-called "soak-calcination" procedure was employed by firstly soaking these waste fruit peels in FeCl3 aqueous solutions and secondly calcining these precursors in the nitrogen atmosphere to yield final magnetite/carbon composites. This approach is quite simple and effective to synthesize carbon-based adsorbents on an industrial scale. The as-produced adsorbents feature the merits of appropriate ferromagnetism (>4emug(-1)), high adsorption capacity (several hundreds of milligrams per gram for adsorption of methyl blue, Congo red, rhodamine B and Cr(6+) ions), and good regenerability (>85%).

  9. Water Vapor Permeation of Metal Oxide/Polymer Coated Plastic Films

    NASA Astrophysics Data System (ADS)

    Numata, Yukihiro; Oya, Toshiyuki; Kuwahara, Mitsuru; Ito, Katsuya

    Barrier performance to water vapor permeation of ceramic coated layers deposited on flexible polymer films is of great interest to food packaging, medical device packaging and flat panel display industries. In this study, a new type film in which a ceramic layer is deposited on a polymer coated film was proposed for lower water vapor permeation. It is important how to control interfacial properties between each layer and film for good barrier performance. Several kinds of polymer coated materials were prepared for changing surface free energy of the films before and after depositing the ceramic layer. The ceramic layer, which is composed of mixed material of SiO2 and Al2O3, was adopted under the same conditions. The following results were obtained; 1) Water vapor permeation is not related to the surface energy of polymer coated films, 2) After depositing the ceramic layer, however, a strong correlation is observed between the water vapor permeation and surface free energy. 3) The phenomenon is considered that the polarity of the polymer layers plays a key role in changing the structure of ceramic coated layers.

  10. Preparation of self-supporting Au thin films on perforated substrate by releasing from water-soluble sacrificial layer

    NASA Astrophysics Data System (ADS)

    Miyamoto, Yu; Fujii, Yuma; Yamano, Masafumi; Harigai, Toru; Suda, Yoshiyuki; Takikawa, Hirofumi; Kawano, Takeshi; Nishiuchi, Mamiko; Sakaki, Hironao; Kondo, Kiminori

    2016-07-01

    A self-supporting thin film is useful as a target material for laser-driven ion acceleration experiments. In this study, 100-nm-thick sputtered gold (Au) thin films were released from substrates using water-soluble sacrificial layers, and the released films were subsequently scooped up on perforated substrates. Au thin films were deposited by DC plasma sputtering on the sacrificial layers. In the releasing test, sodium chloride (NaCl) was shown to be most suitable as a sacrificial layer for Au thin films. In addition, sputtered Au thin films with thicknesses of 50 and 150 nm were deposited onto NaCl sacrificial layers, released on water, and scooped up on perforated substrates. Self-supporting Au thin films were obtained for all film thicknesses, but wrinkles and cracks appeared in the 50 nm film.

  11. Electrical instability of high-mobility zinc oxynitride thin-film transistors upon water exposure

    NASA Astrophysics Data System (ADS)

    Kim, Dae-Hwan; Jeong, Hwan-Seok; Kwon, Hyuck-In

    2017-03-01

    We investigate the effects of water absorption on the electrical performance and stability in high-mobility zinc oxynitride (ZnON) thin-film transistors (TFTs). The ZnON TFT exhibits a smaller field-effect mobility, lower turn-on voltage, and higher subthreshold slope with a deteriorated electrical stability under positive gate bias stresses after being exposed to water. From the Hall measurements, an increase of the electron concentration and a decrease of the Hall mobility are observed in the ZnON thin film after water absorption. The observed phenomena are mainly attributed to the water molecule-induced increase of the defective ZnXNY bond and the oxygen vacancy inside the ZnON thin film based on the x-ray photoelectron spectroscopy analysis.

  12. Electrical instability of high-mobility zinc oxynitride thin-film transistors upon water exposure.

    PubMed

    Kim, Dae-Hwan; Jeong, Hwan-Seok; Kwon, Hyuck-In

    2017-03-03

    We investigate the effects of water absorption on the electrical performance and stability in high-mobility zinc oxynitride (ZnON) thin-film transistors (TFTs). The ZnON TFT exhibits a smaller field-effect mobility, lower turn-on voltage, and higher subthreshold slope with a deteriorated electrical stability under positive gate bias stresses after being exposed to water. From the Hall measurements, an increase of the electron concentration and a decrease of the Hall mobility are observed in the ZnON thin film after water absorption. The observed phenomena are mainly attributed to the water molecule-induced increase of the defective ZnXNY bond and the oxygen vacancy inside the ZnON thin film based on the x-ray photoelectron spectroscopy analysis.

  13. Nanoscale cellulose films with different crystallinities and mesostructures--their surface properties and interaction with water.

    PubMed

    Aulin, Christian; Ahola, Susanna; Josefsson, Peter; Nishino, Takashi; Hirose, Yasuo; Osterberg, Monika; Wågberg, Lars

    2009-07-07

    A systematic study of the degree of molecular ordering and swelling of different nanocellulose model films has been conducted. Crystalline cellulose II surfaces were prepared by spin-coating of the precursor cellulose solutions onto oxidized silicon wafers before regeneration in water or by using the Langmuir-Schaefer (LS) technique. Amorphous cellulose films were also prepared by spin-coating of a precursor cellulose solution onto oxidized silicon wafers. Crystalline cellulose I surfaces were prepared by spin-coating wafers with aqueous suspensions of sulfate-stabilized cellulose I nanocrystals and low-charged microfibrillated cellulose (LC-MFC). In addition, a dispersion of high-charged MFC was used for the buildup of polyelectrolyte multilayers with polyetheyleneimine on silica with the aid of the layer-by-layer (LbL) technique. These preparation methods produced smooth thin films on the nanometer scale suitable for X-ray diffraction and swelling measurements. The surface morphology and thickness of the cellulose films were characterized in detail by atomic force microscopy (AFM) and ellipsometry measurements, respectively. To determine the surface energy of the cellulose surfaces, that is, their ability to engage in different interactions with different materials, they were characterized through contact angle measurements against water, glycerol, and methylene iodide. Small incidence angle X-ray diffraction revealed that the nanocrystal and MFC films exhibited a cellulose I crystal structure and that the films prepared from N-methylmorpholine-N-oxide (NMMO), LiCl/DMAc solutions, using the LS technique, possessed a cellulose II structure. The degree of crystalline ordering was highest in the nanocrystal films (approximately 87%), whereas the MFC, NMMO, and LS films exhibited a degree of crystallinity of about 60%. The N,N-dimethylacetamide (DMAc)/LiCl film possessed very low crystalline ordering (<15%). It was also established that the films had different

  14. Detection of heavy metals in water using dye nano-complexants and a polymeric film.

    PubMed

    Hadar, Hodayah Abuhatzira; Bulatov, Valery; Dolgin, Bella; Schechter, Israel

    2013-09-15

    An optical analytical method, based on complexation reactions of organic azo-dyes with heavy metals, is proposed. It is based on a specially designed polymeric film that when submerged in water contaminated with heavy metals it changes its color. The azo-dyes are injected into the tested water, resulting in formation of nano-particles of insoluble complexes. The polymeric film embeds and dissolves these nano-particles and thus allows for spectral and/or visual analysis. This film consists of a PVC polymeric skeleton and an organic solvent, bis(2-ethylhexyl)phthalate, which possesses high affinity to the heavy metal nano-complexes. The method was exemplified for Cd, Ni and Co ions. The method is sensitive in the sub-ppm range. The mechanism and kinetics of the film coloration were reported.

  15. Flow field distribution of liquid film of water lubricated bearing-rotor coupling systems

    NASA Astrophysics Data System (ADS)

    Hu, Q. L.; Hu, J. N.; Ye, X. Y.; Zhang, D. S.; Zheng, J. B.

    2016-05-01

    According to the desalination high-pressure pump water lubricated bearing-rotor coupling systems flow field distribution of liquid film in the starting transient process and its power transmission mechanism can lay the foundation of further exploring and judging lubrication state at the boot process. By using the computational fluid dynamics Fluent secondary development platform and calling the relevant DEFINE macro function to achieve the translation and rotation movement of the journal, we will use the dynamic grid technique to realize the automatic calculation and grid update of water lubricated bearings 3d unsteady liquid film flow field, and finally we will dispose the results of numerical simulation and get the pressure. When the eccentricity is large, film thickness was negatively correlated with the pressure, and positive with the velocity. Differential pressure was negatively correlated with velocity. When the eccentricity is small, film thickness is no significant relationship with differential pressure and velocity. Differential pressure has little difference with velocity.

  16. Critical material attributes (CMAs) of strip films loaded with poorly water-soluble drug nanoparticles: I. Impact of plasticizer on film properties and dissolution.

    PubMed

    Krull, Scott M; Patel, Hardik V; Li, Meng; Bilgili, Ecevit; Davé, Rajesh N

    2016-09-20

    Recent studies have demonstrated polymer films to be a promising platform for delivery of poorly water-soluble drug particles. However, the impact of critical material attributes, for example plasticizer, on the properties of and drug release from such films has yet to be investigated. In response, this study focuses on the impact of plasticizer and plasticizer concentration on properties and dissolution rate of polymer films loaded with poorly water-soluble drug nanoparticles. Glycerin, triacetin, and polyethylene glycol were selected as film plasticizers. Griseofulvin was used as a model Biopharmaceutics Classification System class II drug and hydroxypropyl methylcellulose was used as a film-forming polymer. Griseofulvin nanoparticles were prepared via wet stirred media milling in aqueous suspension. A depression in film glass transition temperature was observed with increasing plasticizer concentration, along with a decrease in film tensile strength and an increase in film elongation, as is typical of plasticizers. However, the type and amount of plasticizer necessary to produce strong yet flexible films had no significant impact on the dissolution rate of the films, suggesting that film mechanical properties can be effectively manipulated with minimal impact on drug release. Griseofulvin nanoparticles were successfully recovered upon redispersion in water regardless of plasticizer or content, even after up to 6months' storage at 40°C and 75% relative humidity, which contributed to similar consistency in dissolution rate after 6months' storage for all films. Good content uniformity (<4% R.S.D. for very small film sample size) was also maintained across all film formulations.

  17. Selective electrochemical reduction of CO2 to CO with a cobalt chlorin complex adsorbed on multi-walled carbon nanotubes in water.

    PubMed

    Aoi, Shoko; Mase, Kentaro; Ohkubo, Kei; Fukuzumi, Shunichi

    2015-06-25

    Electrocatalytic reduction of CO2 occurred efficiently using a glassy carbon electrode modified with a cobalt(II) chlorin complex adsorbed on multi-walled carbon nanotubes at an applied potential of -1.1 V vs. NHE to yield CO with a Faradaic efficiency of 89% with hydrogen production accounting for the remaining 11% at pH 4.6.

  18. In situ spectroelectrochemical and theoretical study on the oxidation of a 4H-imidazole-ruthenium dye adsorbed on nanocrystalline TiO2 thin film electrodes.

    PubMed

    Zhang, Ying; Kupfer, Stephan; Zedler, Linda; Schindler, Julian; Bocklitz, Thomas; Guthmuller, Julien; Rau, Sven; Dietzek, Benjamin

    2015-11-28

    Terpyridine 4H-imidazole-ruthenium(II) complexes are considered promising candidates for use as sensitizers in dye sensitized solar cells (DSSCs) by displaying broad absorption in the visible range, where the dominant absorption features are due to metal-to-ligand charge transfer (MLCT) transitions. The ruthenium(III) intermediates resulting from photoinduced MLCT transitions are essential intermediates in the photoredox-cycle of the DSSC. However, their photophysics is much less studied compared to the ruthenium(II) parent systems. To this end, the structural alterations accompanying one-electron oxidation of the RuIm dye series (including a non-carboxylic RuIm precursor, and, carboxylic RuImCOO in solution and anchored to a nanocrystalline TiO2 film) are investigated via in situ experimental and theoretical UV-Vis absorption and resonance Raman (RR) spectroelectrochemistry. The excellent agreement between the experimental and the TDDFT spectra derived in this work allows for an in-depth assignment of UV-Vis and RR spectral features of the dyes. A concordant pronounced wavelength dependence with respect to the charge transfer character has been observed for the model system RuIm, and both RuImCOO in solution and attached on the TiO2 surface. Excitation at long wavelengths leads to the population of ligand-to-metal charge transfer states, i.e. photoreduction of the central ruthenium(III) ion, while high-energy excitation features an intra-ligand charge transfer state localized on the 4H-imidazole moiety. Therefore, these 4H-imidazole ruthenium complexes investigated here are potential multi-photoelectron donors. One electron is donated from MLCT states, and additionally, the 4H-imidazole ligand reveals electron-donating character with a significant contribution to the excited states of the ruthenium(III) complexes upon blue-light irradiation.

  19. Three-dimensional radiochromic film dosimetry for volumetric modulated arc therapy using a spiral water phantom.

    PubMed

    Tanooka, Masao; Doi, Hiroshi; Miura, Hideharu; Inoue, Hiroyuki; Niwa, Yasue; Takada, Yasuhiro; Fujiwara, Masayuki; Sakai, Toshiyuki; Sakamoto, Kiyoshi; Kamikonya, Norihiko; Hirota, Shozo

    2013-11-01

    We validated 3D radiochromic film dosimetry for volumetric modulated arc therapy (VMAT) using a newly developed spiral water phantom. The phantom consists of a main body and an insert box, each of which has an acrylic wall thickness of 3 mm and is filled with water. The insert box includes a spiral film box used for dose-distribution measurement, and a film holder for positioning a radiochromic film. The film holder has two parallel walls whose facing inner surfaces are equipped with spiral grooves in a mirrored configuration. The film is inserted into the spiral grooves by its side edges and runs along them to be positioned on a spiral plane. Dose calculation was performed by applying clinical VMAT plans to the spiral water phantom using a commercial Monte Carlo-based treatment-planning system, Monaco, whereas dose was measured by delivering the VMAT beams to the phantom. The calculated dose distributions were resampled on the spiral plane, and the dose distributions recorded on the film were scanned. Comparisons between the calculated and measured dose distributions yielded an average gamma-index pass rate of 87.0% (range, 91.2-84.6%) in nine prostate VMAT plans under 3 mm/3% criteria with a dose-calculation grid size of 2 mm. The pass rates were increased beyond 90% (average, 91.1%; range, 90.1-92.0%) when the dose-calculation grid size was decreased to 1 mm. We have confirmed that 3D radiochromic film dosimetry using the spiral water phantom is a simple and cost-effective approach to VMAT dose verification.

  20. Water-free titania-bronze thin films with superfast lithium-ion transport.

    PubMed

    Zhang, Kui; Katz, Michael B; Li, Baihai; Kim, Sung Joo; Du, Xianfeng; Hao, Xiaoguang; Jokisaari, Jacob R; Zhang, Shuyi; Graham, George W; Van der Ven, Anton; Bartlett, Bart M; Pan, Xiaoqing

    2014-11-19

    Using pulsed laser deposition, TiO2 (-) B and its recently discovered variant Ca:TiO2 (-) B (CaTi5O11) are synthesized as highly crystalline thin films for the first time by a completely water-free process. Significant enhancement in the Li-ion battery performance is achieved by manipulating the crystal orientation of the films, used as anodes, with a demonstration of extraordinary structural stability under extreme conditions.

  1. Video- Making a Film of Water Aboard the International Space Station (ISS)

    NASA Technical Reports Server (NTRS)

    2002-01-01

    Saturday Morning Science, the science of opportunity series of applied experiments and demonstrations, performed aboard the International Space Station (ISS) by Expedition 6 astronaut Dr. Don Pettit, revealed some remarkable findings. In this video, Dr. Pettit demonstrates how to make films of pure water. Watch the video to see how he does it, see his two-dimensional beaker, and marvel along with him at how tenacious the films are.

  2. Spreading dynamics of a partially wetting water film atop a MHz substrate vibration

    SciTech Connect

    Altshuler, Gennady; Manor, Ofer

    2015-10-15

    A MHz vibration, or an acoustic wave, propagating in a solid substrate may support the convective spreading of a liquid film. Previous studies uncovered this ability for fully wetting silicon oil films under the excitation of a MHz Rayleigh surface acoustic wave (SAW), propagating in a lithium niobate substrate. Partially wetting de-ionized water films, however, appeared immune to this spreading mechanism. Here, we use both theory and experiment to reconsider this situation and show partially wetting water films may spread under the influence of a propagating MHz vibration. We demonstrate distinct capillary and convective (vibrational/acoustic) spreading regimes that are governed by a balance between convective and capillary mechanisms, manifested in the non-dimensional number θ{sup 3}/We, where θ is the three phase contact angle of the liquid with the solid substrate and We ≡ ρU{sup 2}H/γ; ρ, γ, H, and U are the liquid density, liquid/vapour surface tension, characteristic film thickness, and the characteristic velocity amplitude of the propagating vibration on the solid surface, respectively. Our main finding is that the vibration will support a continuous spreading motion of the liquid film out of a large reservoir if the convective mechanism prevails (θ{sup 3}/We < 1); otherwise (θ{sup 3}/We > 1), the dynamics of the film is governed by the capillary mechanism.

  3. Noncontact atomic force microscopy studies of ultrathin films of amorphous solid water deposited on Au(111).

    PubMed

    Donev, J M K; Yu, Q; Long, B R; Bollinger, R K; Fain, S C

    2005-07-22

    Noncontact atomic force microscopy was used to study the morphological changes of an ultrathin amorphous solid water (ASW) film as a function of deposition temperature, annealing temperature, and annealing time. ASW deposited at 80 or 108 K on Au(111) formed truncated hemispherical clusters of increasing size during annealing at 134 K; these clusters were inferred to be crystalline. The number of nuclei present at the outer surface of the film after deposition was greater for higher deposition temperature. For lower cluster densities, depletion of the ASW film around the clusters was observed when the clusters became larger and dendritic growth was observed when the apparent cluster footprint radius exceeded 100 nm.

  4. Photoelectrochemical water splitting on nanoporous GaN thin films for energy conversion under visible light

    NASA Astrophysics Data System (ADS)

    Cao, Dezhong; Xiao, Hongdi; Fang, Jiacheng; Liu, Jianqiang; Gao, Qingxue; Liu, Xiangdong; Ma, Jin

    2017-01-01

    Nanoporous (NP) GaN thin films, which were fabricated by an electrochemical etching method at different voltages, were used as photoelectrodes during photoelectrochemical (PEC) water splitting in 1 M oxalic acid solution. Upon illumination at a power density of 100 mW cm‑2 (AM 1.5), water splitting is observed in NP GaN thin films, presumably resulting from the valence band edge which is more positive than the redox potential of the oxidizing species. In comparison with NP GaN film fabricated at 8 V, NP GaN obtained at 18 V shows nearly twofold enhancement in photocurrent with the maximum photo-to-hydrogen conversion efficiency of 1.05% at ~0 V (versus Ag/AgCl). This enhancement could be explained with (i) the increase of surface area and surface states, and (ii) the decrease of resistances and carrier concentration in the NP GaN thin films. High stability of the NP GaN thin films during the PEC water splitting further confirms that the NP GaN thin film could be applied to the design of efficient solar cells and solar fuel devices.

  5. Films.

    ERIC Educational Resources Information Center

    Philadelphia Board of Education, PA. Div. of Instructional Materials.

    The Affective Curriculum Research Project produced five films and two records during a series of experimental summer programs. The films and records form part of a curriculum designed to teach to the concerns of students. The films were an effort to describe the Philadelphia Cooperative Schools Program, to explain its importance, and to…

  6. Titanium and Magnesium Co-Alloyed Hematite Thin Films for Photoelectrochemical Water Splitting

    SciTech Connect

    Tang, H.; Yin, W. J.; Matin, M. A.; Wang, H.; Deutsch, T.; Al-Jassim, M. M.; Turner, J. A.; Yan, Y.

    2012-04-01

    Using a combination of density functional theory calculation and materials synthesis and characterization we examine the properties of charge-compensated Ti and Mg co-alloyed hematite thin films for the application of photoelectrochemical (PEC) water splitting. We find that the charge-compensated co-alloying results in the following effects: (1) It enhances the solubility of Mg and Ti, which leads to reduced electron effective mass and therefore increased electron mobility; (2) It tunes the carrier density and therefore allows the optimization of electrical conductivity; and (3) It reduces the density of charged defects and therefore reduces carrier recombination. As a result, the Ti and Mg co-alloyed hematite thin films exhibit improved water oxidation photocurrent magnitudes as compared to pure hematite thin films. Our results suggest that charge-compensated co-alloying is a plausible approach for engineering hematite for the application of PEC water splitting.

  7. Formation of hydroxyl and water layers on MgO films studied with ambient pressure XPS

    NASA Astrophysics Data System (ADS)

    Newberg, John T.; Starr, David E.; Yamamoto, Susumu; Kaya, Sarp; Kendelewicz, Tom; Mysak, Erin R.; Porsgaard, Soeren; Salmeron, Miquel B.; Brown, Gordon E., Jr.; Nilsson, Anders; Bluhm, Hendrik

    2011-01-01

    To understand the interaction of water with MgO(100), a detailed quantitative assessment of the interfacial chemistry is necessary. We have used ambient pressure X-ray photoelectron spectroscopy (XPS) to measure molecular (H 2O) and dissociative (OH) water adsorption on a 4 monolayer (ML) thick MgO(100)/Ag(100) film under ambient conditions. Since the entire 4 ML metal oxide (Ox) film is probed by XPS, the reaction of the MgO film with water can be quantitatively studied. Using a multilayer model (Model 1) that measures changes in Ox thickness from O 1s (film) and Ag 3d (substrate) spectra, it is shown that the oxide portion of the MgO film becomes thinner upon hydroxylation. A reaction mechanism is postulated in which the top-most layer of MgO converts to Mg(OH) 2 upon dissociation of water. Based on this mechanism a second model (Model 2) is developed to calculate Ox and OH thickness changes based on OH/Ox intensity ratios from O 1s spectra measured in situ, with the known initial Ox thickness prior to hydroxylation. Models 1 and 2 are applied to a 0.15 Torr isobar experiment, yielding similar results for H 2O, OH and Ox thickness changes as a function of relative humidity.

  8. Formation of Hydroxyl and Water Layers on MgO Films Studied with Ambient Pressure XPS

    SciTech Connect

    Newberg, J.T.; Starr, D.; Yamamoto, S.; Kaya, S.; Kendelewicz, T.; Mysak, E.R.; Porsgaard, S.; Salmeron, M.B.; Brown Jr., G.E.; Nilsson, A.; Bluhm, H.

    2011-01-01

    To understand the interaction of water with MgO(100), a detailed quantitative assessment of the interfacial chemistry is necessary. We have used ambient pressure X-ray photoelectron spectroscopy (XPS) to measure molecular (H{sub 2}O) and dissociative (OH) water adsorption on a 4 monolayer (ML) thick MgO(100)/Ag(100) film under ambient conditions. Since the entire 4 ML metal oxide (Ox) film is probed by XPS, the reaction of the MgO film with water can be quantitatively studied. Using a multilayer model (Model 1) that measures changes in Ox thickness from O 1s (film) and Ag 3d (substrate) spectra, it is shown that the oxide portion of the MgO film becomes thinner upon hydroxylation. A reaction mechanism is postulated in which the top-most layer of MgO converts to Mg(OH)2 upon dissociation of water. Based on this mechanism a second model (Model 2) is developed to calculate Ox and OH thickness changes based on OH/Ox intensity ratios from O 1s spectra measured in situ, with the known initial Ox thickness prior to hydroxylation. Models 1 and 2 are applied to a 0.15 Torr isobar experiment, yielding similar results for H{sub 2}O, OH and Ox thickness changes as a function of relative humidity.

  9. Dynamic analysis of a closed-cycle solar adsorption refrigerator using two adsorbent-adsorbate pairs

    SciTech Connect

    Hajji, A. ); Worek, W. ); Lavan, Z. )

    1991-05-01

    In this paper a dynamic analysis of a closed-cycle, solar adsorption refrigerator is presented. The instantaneous and daily system performance are studied using two adsorbent-adsorbate pairs, Zeolite 13X-Water and Chabazite-Methanol. The effect of design and operating parameters, including inert material thermal capacitance, matrix porosity, and evaporation and condenser temperatures on the solar and cycle coefficients of performance are evaluated.

  10. Elastic Properties of Films of Water and Noble Gases Condensed at Low Temperatures

    NASA Technical Reports Server (NTRS)

    Pohl, Robert O.

    2003-01-01

    We have shown that there are extensive similarities between the quench-condensed noble gas films and those of amorphous water ice. In particular, both can be quite soft upon deposition and can stiffen considerably when annealed. Furthermore, this stiffening follows a logarithmic time dependence for all substances. The temperature dependence of these behaviors scales with the triple point. The results shown here show a strong thickness dependence, which has implications for any study of mechanical properties of films on substrates. The temperature dependence of the stiffening and the stiffening rate have now been characterized for the noble gases, and these observations provide a roadmap for new experiments on amorphous water ice.

  11. Determination of pyrazole and pyrrole pesticides in environmental water samples by solid-phase extraction using multi-walled carbon nanotubes as adsorbent coupled with high-performance liquid chromatography.

    PubMed

    Ma, Jiping; Lu, Xi; Xia, Yan; Yan, Fengli

    2015-02-01

    A solid-phase extraction (SPE) method using multi-walled carbon nanotubes as adsorbent coupled with high-performance liquid chromatography was developed for the determination of four pyrazole and pyrrole pesticides (fenpyroximate, chlorfenapyr, fipronil and flusilazole) in environmental water samples. Several parameters, such as extraction adsorbent, elution solvent and volume and sample loading flow rate were optimized to obtain high SPE recoveries and extraction efficiency. The calibration curves for the pesticides extracted were linear in the range of 0.05-10 μg L(-1) for chlorfenapyr and fenpyroximate and 0.05-20 μg L(-1) for fipronil and flusilazole, with the correlation coefficients (r(2)) between 0.9966 and 0.9990. The method gave good precisions (relative standard deviation %) from 2.9 to 10.1% for real spiked samples from reservoir water and seawater; method recoveries ranged 92.2-105.9 and 98.5-103.9% for real spiked samples from reservoir water and seawater, respectively. Limits of detection (S/N = 3) for the method were determined to be 8-19 ng L(-1). The optimized method was successfully applied to the determination of four pesticides of pyrazoles and pyrroles in real environmental water samples.

  12. Trace determination of chromium(VI) in environmental water samples using innovative thermally reduced graphene (TRG) modified SiO₂ adsorbent for solid phase extraction and UV-vis spectrophotometry.

    PubMed

    Sereshti, Hassan; Farahani, Mina Vasheghani; Baghdadi, Majid

    2016-01-01

    An innovative thermally reduced graphene (TRG) modified silica-supported 3-aminopropyltriethoxysilane (SiO2-APTES) composite was synthesized and characterized using Fourier transform-infrared spectroscopy (FT-IR) and scanning electron microscopy SEM techniques. The adsorbent was then used in the solid phase extraction (SPE) of Cr (VI) as the Cr (VI)-diphenylcarbazide (DPC) complex with the subsequent measurement by UV-vis spectrophotometry. The adsorbent surface was activated by adding sodium dodecyl sulfate (SDS) to the sample solution. The effect of the main experimental parameters such as type and volume of the extraction solvent, pH, dosage of DPC, SDS, the adsorbent, time of the extraction, and salt concentration on the extraction efficiency were investigated and optimized. A linear dynamic range of 1.3-40 ng mL(-1) with a satisfactory determination coefficient (R(2)) of 0.9930 was obtained. A detection limit of 0.4 ng mL(-1) Cr (VI) was attained when a sample volume of 25 mL was used. Intraday and inter-day precisions were obtained equal to 2.3% and 7.9%, respectively. The enrichment factor (EF) was calculated to be equal to 167. The technique was applied successfully to the determination of Cr (VI) at trace levels in tap, river, sewage and ground water samples and the relative recoveries of the added chromium were in the range of 92.6-109.9%.

  13. Comparative study of GeO2/Ge and SiO2/Si structures on anomalous charging of oxide films upon water adsorption revealed by ambient-pressure X-ray photoelectron spectroscopy

    NASA Astrophysics Data System (ADS)

    Mori, Daichi; Oka, Hiroshi; Hosoi, Takuji; Kawai, Kentaro; Morita, Mizuho; Crumlin, Ethan J.; Liu, Zhi; Watanabe, Heiji; Arima, Kenta

    2016-09-01

    The energy difference between the oxide and bulk peaks in X-ray photoelectron spectroscopy (XPS) spectra was investigated for both GeO2/Ge and SiO2/Si structures with thickness-controlled water films. This was achieved by obtaining XPS spectra at various values of relative humidity (RH) of up to ˜15%. The increase in the energy shift is more significant for thermal GeO2 on Ge than for thermal SiO2 on Si above ˜10-4% RH, which is due to the larger amount of water molecules that infiltrate into the GeO2 film to form hydroxyls. Analyzing the origins of this energy shift, we propose that the positive charging of a partially hydroxylated GeO2 film, which is unrelated to X-ray irradiation, causes the larger energy shift for GeO2/Ge than for SiO2/Si. A possible microscopic mechanism of this intrinsic positive charging is the emission of electrons from adsorbed water species in the suboxide layer of the GeO2 film to the Ge bulk, leaving immobile cations or positively charged states in the oxide. This may be related to the reported negative shift of flat band voltages in metal-oxide-semiconductor diodes with an air-exposed GeO2 layer.

  14. Bovine serum albumin-Cu(II) hybrid nanoflowers: An effective adsorbent for solid phase extraction and slurry sampling flame atomic absorption spectrometric analysis of cadmium and lead in water, hair, food and cigarette samples.

    PubMed

    Yilmaz, Erkan; Ocsoy, Ismail; Ozdemir, Nalan; Soylak, Mustafa

    2016-02-04

    Herein, the synthesis of bovine serum albumin-Cu(II) hybrid nanoflowers (BSA-NFs) through the building blocks of bovine serum albumin (BSA) and copper(II) ions in phosphate buffered saline (PBS) and their use as adsorbent for cadmium and lead ions are reported. The BSA-NFs, for the first time, were efficiently utilized as novel adsorbent for solid phase extraction (SPE) of cadmium and lead ions in water, food, cigarette and hair samples. The method is based on the separation and pre-concentration of Cd(II) and Pb(II) by BSA-NFs prior to determination by slurry analysis via flame atomic absorption spectrometry (FAAS). The analytes were adsorbed on BSA-NFs under the vortex mixing and then the ion-loaded slurry was separated and directly introduced into the flame AAS nebulizer by using a hand-made micro sample introduction system to eliminate a number of drawbacks. The effects of analytical key parameters, such as pH, amount of BSA-NFs, vortexing time, sample volume, and matrix effect of foreign ions on adsorbing of Cd(II) and Pb(II) were systematically investigated and optimized. The limits of detection (LODs) for Cd(II) and Pb(II) were calculated as 0.37 μg L(-)(1) and 8.8 μg L(-)(1), respectively. The relative standard deviation percentages (RSDs) (N = 5) for Cd(II) and Pb(II) were 7.2%, and 5.0%, respectively. The accuracy of the developed procedure was validated by the analysis of certified reference materials (TMDA-53.3 Fortified Water, TMDA-70 Fortified Water, SPS-WW2 Waste Water, NCSDC-73349 Bush Branches and Leaves) and by addition/recovery analysis. The quantitative recoveries were obtained for the analysis of certified reference materials and addition/recovery tests. The method was successfully applied to the analysis of cadmium and lead in water, food, cigarette and hair samples.

  15. Selective retardation of perfume oil evaporation from oil-in-water emulsions stabilized by either surfactant or nanoparticles.

    PubMed

    Binks, Bernard P; Fletcher, Paul D I; Holt, Benjamin L; Beaussoubre, Pascal; Wong, Kenneth

    2010-12-07

    We have used dynamic headspace analysis to investigate the evaporation rates of perfume oils from stirred oil-in-water emulsions into a flowing gas stream. We compare the behavior of an oil of low water solubility (limonene) and one of high water solubility (benzyl acetate). It is shown how the evaporation of an oil of low water solubility is selectively retarded and how the retardation effect depends on the oil volume fraction in the emulsion. We compare how the evaporation retardation depends on the nature of the adsorbed film stabilizing the emulsion. Surfactant films are less effective than adsorbed films of nanoparticles, and the retardation can be further enhanced by compression of the adsorbed nanoparticle films by preshrinking the emulsion drops.

  16. Let's Talk About Water: Using Film Screenings to Engage Students and the Public in Water Science and Policy

    NASA Astrophysics Data System (ADS)

    Saleem Arrigo, J. A.; Berry, K.; Hooper, R. P.; Lilienfeld, L.

    2013-12-01

    "Let's Talk about Water" is a film symposium designed to bring together experts and the public to talk about the complex water issues facing society. The format of the event is quite simple: a panel of experts and the audience view a water documentary (such as "FLOW", "Liquid Assets", or "Gasland") together and there is an extended moderated discussion period following the film between the panel and the audience. Over the course of several events, we have developed best practices that make this simple format very effective. A film creates a context of subject and language for the discussion--it gets the audience and the panel on the same page. The moderators must actively manage the discussion, both challenging the panelists with follow up questions, asking questions to simplify the language the expert is using, and passing a question among panelists to bring out different points of view. The panelists are provided with the film in advance to view and, most importantly, meet the day before the event to discuss the film. This makes for a much more convivial discussion at the event. We have found that these discussions can easily be sustained for 90 to 120 minutes with active audience participation. We have found key element of the event is local relevance. Films should be carefully chosen to resonate with the audience, and the local host is critical in defining the audience, goals and identified panel members. Having local experts from universities and representatives from local water authorities and environmental groups bring a sense of community and a confidence in the audience that the panel members have local knowledge that is important for sustaining discussion. The discussion begins with points raised by the movie (are these issues real? Do they apply here? What are the scientific, engineering, and policy solutions to these problems?) and then segues into a discussion about career opportunities in the water sector, volunteer opportunities in the community or

  17. Preparation and characterization of super-water-repellent Al2O3 coating films with high transparency

    NASA Astrophysics Data System (ADS)

    Minami, Tsutomu; Katata, Noriko; Tadanaga, Kiyoharu

    1997-10-01

    Alumina thin films with a roughness of 20 to 50 nm were formed by immersing the porous alumina gel films prepared by the sol- gel method in boiling water. When hydrolyzed fluoroalkyltrimethoxysilane was coated on the alumina films, the films showed super-water-repellency and high transparency; the contact angle for water of the film was 165 degrees and the transmittance for visible light was higher than 92%. When the fluoroalkyltrimethoxysilane-coated thin films were heat- treated at temperatures higher than 500 degrees Celsius, the films became super-hydrophilic; the contact angle for water on the films was less than 5 degrees. It was shown the existence of air in the pores on the surface caused the super-water- repellency and that of water in the pores caused the super- hydrophilic property. The transparent, super water-repellent and super-hydrophilic coating films formed on glasses, metals, and ceramics have practical applications such as optical lenses, eye-glasses, cover glasses for solar cells, windshields of automobiles, and so on.

  18. Liposomal buccal mucoadhesive film for improved delivery and permeation of water-soluble vitamins.

    PubMed

    Abd El Azim, Heba; Nafee, Noha; Ramadan, Alyaa; Khalafallah, Nawal

    2015-07-05

    This study aims at improving the buccal delivery of vitamin B6 (VB6) as a model highly water-soluble, low permeable vitamin. Two main strategies were combined; first VB6 was entrapped in liposomes, which were then formulated as mucoadhesive film. Both plain and VB6-loaded liposomes (LPs) containing Lipoid S100 and propylene glycol (∼ 200 nm) were then incorporated into mucoadhesive film composed of SCMC and HPMC. Results showed prolonged release of VB6 (72.65%, T50% diss 105 min) after 6h from LP-film compared to control film containing free VB6 (96.37%, T50% diss 30 min). Mucoadhesion was assessed both ex vivo on chicken pouch and in vivo in human. Mucoadhesive force of 0.2N and residence time of 4.4h were recorded. Ex vivo permeation of VB6, across chicken pouch mucosa indicated increased permeation from LP-systems compared to corresponding controls. Interestingly, incorporation of the vesicles in mucoadhesive film reduced the flux by 36.89% relative to LP-dispersion. Meanwhile, both films provided faster initial permeation than the liquid forms. Correlating the cumulative percent permeated ex vivo with the cumulative percent released in vitro indicated that LPs retarded VB6 release but improved permeation. These promising results represent a step forward in the field of buccal delivery of water-soluble vitamins.

  19. Tunable surface wettability and water adhesion of Sb2S3 micro-/nanorod films

    NASA Astrophysics Data System (ADS)

    Zhong, Xin; Zhao, Huiping; Yang, Hao; Liu, Yunling; Yan, Guoping; Chen, Rong

    2014-01-01

    Antimony sulfide (Sb2S3) films were successfully prepared by spin coating Sb2S3 micro-/nanorods with different sizes on glass slides, which was synthesized via a facile and rapid microwave irradiation method. The prepared Sb2S3 micro-/nanorods and films were characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM) and water contact angle (CA). The as-prepared Sb2S3 films exhibited different surface wettabilities ranging from superhydrophilicity to superhydrophobicity, which was strongly dependent on the diameter of Sb2S3 micro-/nanorod. Sb2S3 film made by nanorods possessed superhydrophobic surface and high water adhesive property. After surface modification with stearic acid, the superhydrophobic surface exhibited an excellent self-cleaning property owing to its low adhesive force. The clarification of three possible states including Wenzel's state, 'Gecko' state and Cassie's state for Sb2S3 film surfaces was also proposed to provide a better understanding of interesting surface phenomena on Sb2S3 films.

  20. Preparation of magnetic graphene/mesoporous silica composites with phenyl-functionalized pore-walls as the restricted access matrix solid phase extraction adsorbent for the rapid extraction of parabens from water-based skin toners.

    PubMed

    Feng, Jianan; He, Xinying; Liu, Xiaodan; Sun, Xueni; Li, Yan

    2016-09-23

    In this work, phenyl-functionalized magnetic graphene/mesoporous silica composites (MG-mSiO2-Ph) were prepared and applied as restricted access matrix solid phase extraction (RAM-SPE) adsorbents to determine the parabens in commercially available retail cosmetics. MG-mSiO2-Ph composites were synthesized by a surfactant-mediated co-condensation reaction in which mesoporous silica with phenyl-functionalized pore-walls was coated on a magnetic graphene sheet. The obtained nano-composites were proven to be of sufficient quality for an ideal RAM-SPE adsorbent with a large specific surface area of 369m(2)g(-1), uniform mesopores of 2.8nm, and special phenyl-functionalized pore-walls. Parabens, such as methyl paraben, ethyl paraben and propyl paraben, were extracted from water-based skin toners using one step of the RAM-SPE and were then analysed by a HPLC-DAD system. The SPE conditions were optimized by studying the parameters, such as the adsorbent amount, elution solvent type, adsorption time and desorption time, that influence the extraction efficiency. For each analyte, there were good linearities of approximately 0.10-120μgmL(-1) with determination coefficients (R(2))>0.995. The sensitivity was as low as 0.01-0.025μgmL(-1) for the LOD, and the percent recoveries were 98.37-105.84%. The intra-day and inter-day RSDs were 1.44-6.11% (n=6) and 3.12-11.70% (n=6), respectively. The results indicated that this method with novel RAM-SPE adsorbents is sensitive and convenient. The results also offered an attractive alternative for the extraction and determination of paraben preservatives in a complex matrix, such as cosmetics.

  1. Application of novel, low-cost, laterite-based adsorbent for removal of lead from water: Equilibrium, kinetic and thermodynamic studies.

    PubMed

    Chatterjee, Somak; De, Sirshendu

    2016-01-01

    Contamination of groundwater by carcinogenic heavy metal, e.g., lead is an important issue and possibility of using a natural rock, laterite, is explored in this work to mitigate this problem. Treated laterite (TL- prepared using hydrochloric acid and sodium hydroxide) was successfully utilized for this purpose. The adsorbent was characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive X-ray (EDX), and Fourier Transform Infrared Spectroscopy (FTIR) to highlight its physical and chemical properties. Optimized equilibrium conditions were 1 g L(-1) adsorbent concentration, 0.26 mm size and a pH of 7 ± 0.2. Monolayer adsorption capacity of lead on treated laterite was 15 mg/g, 14.5 and 13 mg g(-1) at temperatures of 303 K, 313 K and 323 K, respectively. The adsorption was exothermic and physical in nature. At 303 K, value of effective diffusivity of (De) and mass transfer co-efficient (Kf) of lead onto TL were 6.5 × 10(-10) m(2)/s and 3.3 × 10(-4) m/s, respectively (solved from shrinking core model of adsorption kinetics). Magnesium and sulphate show highest interference effect on the adsorption of lead by TL. Efficacy of the adsorbent has been verified using real-life contaminated groundwater. Thus, this work demonstrates performance of a cost-effective media for lead removal.

  2. Communication: Distinguishing between bulk and interface-enhanced crystallization in nanoscale films of amorphous solid water

    NASA Astrophysics Data System (ADS)

    Yuan, Chunqing; Smith, R. Scott; Kay, Bruce D.

    2017-01-01

    The crystallization of amorphous solid water (ASW) nanoscale films was investigated using reflection absorption infrared spectroscopy. Two ASW film configurations were studied. In one case the ASW film was deposited on top of and capped with a decane layer ("sandwich" configuration). In the other case, the ASW film was deposited on top of a decane layer and not capped ("no cap" configuration). Crystallization of ASW films in the "sandwich" configuration is about eight times slower than in the "no cap." Selective placement of an isotopic layer (5% D2O in H2O) at various positions in an ASW (H2O) film was used to determine the crystallization mechanism. In the "sandwich" configuration, the crystallization kinetics were independent of the isotopic layer placement whereas in the "no cap" configuration the closer the isotopic layer was to the vacuum interface, the earlier the isotopic layer crystallized. These results are consistent with a mechanism whereby the decane overlayer suppresses surface nucleation and provide evidence that the observed ASW crystallization in "sandwich" films is the result of uniform bulk nucleation.

  3. Facile synthesis of high strength hot-water wood extract films with oxygen-barrier performance

    PubMed Central

    Chen, Ge-Gu; Fu, Gen-Que; Wang, Xiao-Jun; Gong, Xiao-Dong; Niu, Ya-Shuai; Peng, Feng; Yao, Chun-Li; Sun, Run-Cang

    2017-01-01

    Biobased nanocomposite films for food packaging with high mechanical strength and good oxygen-barrier performance were developed using a hot-water wood extract (HWE). In this work, a facile approach to produce HWE/montmorillonite (MMT) based nanocomposite films with excellent physical properties is described. The focus of this study was to determine the effects of the MMT content on the structure and mechanical properties of nanocomposites and the effects of carboxymethyl cellulose (CMC) on the physical properties of the HWE-MMT films. The experimental results suggested that the intercalation of HWE and CMC in montmorillonite could produce compact, robust films with a nacre-like structure and multifunctional characteristics. This results of this study showed that the mechanical properties of the film designated FCMC0.05 (91.5 MPa) were dramatically enhanced because the proportion of HWE, MMT and CMC was 1:1.5:0.05. In addition, the optimized films exhibited an oxygen permeability below 2.0 cm3 μm/day·m2·kPa, as well as good thermal stability due to the small amount of CMC. These results provide a comprehensive understanding for further development of high-performance nanocomposites which are based on natural polymers (HWE) and assembled layered clays (MMT). These films offer great potential in the field of sustainable packaging. PMID:28112259

  4. Facile synthesis of high strength hot-water wood extract films with oxygen-barrier performance

    NASA Astrophysics Data System (ADS)

    Chen, Ge-Gu; Fu, Gen-Que; Wang, Xiao-Jun; Gong, Xiao-Dong; Niu, Ya-Shuai; Peng, Feng; Yao, Chun-Li; Sun, Run-Cang

    2017-01-01

    Biobased nanocomposite films for food packaging with high mechanical strength and good oxygen-barrier performance were developed using a hot-water wood extract (HWE). In this work, a facile approach to produce HWE/montmorillonite (MMT) based nanocomposite films with excellent physical properties is described. The focus of this study was to determine the effects of the MMT content on the structure and mechanical properties of nanocomposites and the effects of carboxymethyl cellulose (CMC) on the physical properties of the HWE-MMT films. The experimental results suggested that the intercalation of HWE and CMC in montmorillonite could produce compact, robust films with a nacre-like structure and multifunctional characteristics. This results of this study showed that the mechanical properties of the film designated FCMC0.05 (91.5 MPa) were dramatically enhanced because the proportion of HWE, MMT and CMC was 1:1.5:0.05. In addition, the optimized films exhibited an oxygen permeability below 2.0 cm3 μm/day·m2·kPa, as well as good thermal stability due to the small amount of CMC. These results provide a comprehensive understanding for further development of high-performance nanocomposites which are based on natural polymers (HWE) and assembled layered clays (MMT). These films offer great potential in the field of sustainable packaging.

  5. Proton transport by bacteriorhodopsin in planar membranes assembled from air-water interface films

    PubMed Central

    Korenbrot, J. I.; Hwang, S. B.

    1980-01-01

    Bacteriorhodopsin, in known amounts and controlled orientation, is incorporated into planar membrane films. These films are formed by the sequential transfer of two air-water interface films onto a thin, hydrophilic, electrically conductive support cast from nitrocellulose. The films are easily accessible to electrical measurements and to control of the ionic milieu on either side of the membrane. The area of the assembled membrane films can be varied between 2.3 x 10(-2) cm2 and 0.7 cm2. Illumination of these films produces photocurrents, photovoltages, and changes in the pH of the surrounding medium. The peak amplitude of the photocurrent increases linearly with light intensity for dim lights, and it approaches a saturating value for brighter lights. In the linear range, the stoichiometry of transport is 0.65 +/- 0.06 protons/absorbed photon. The rate of transport is linearly proportional to light at all intensities tested. The amplitude and kinetics of the photovoltage measured are accurately predicted by the photocurrent generated and the passive electrical features of the film. Parallel measurements of pH and photocurrent reveal that the light-induced changes in pH are fully accounted for by the rate and amount of charge transport across the membrane. Preceding the transport of protons, a transient photovoltage is detected that exhibits no detectable latency, reaches peak in about 80 microseconds, and probably arises from light-induced intramolecular charge displacements. PMID:10822498

  6. Nanostructured tungsten trioxide thin films synthesized for photoelectrocatalytic water oxidation: a review.

    PubMed

    Zhu, Tao; Chong, Meng Nan; Chan, Eng Seng

    2014-11-01

    The recent developments of nanostructured WO3 thin films synthesized through the electrochemical route of electrochemical anodization and cathodic electrodeposition for the application in photoelectrochemical (PEC) water splitting are reviewed. The key fundamental reaction mechanisms of electrochemical anodization and cathodic electrodeposition methods for synthesizing nanostructured WO3 thin films are explained. In addition, the effects of metal oxide precursors, electrode substrates, applied potentials and current densities, and annealing temperatures on size, composition, and thickness of the electrochemically synthesized nanostructured WO3 thin films are elucidated in detail. Finally, a summary is given for the general evaluation practices used to calculate the energy conversion efficiency of nanostructured WO3 thin films and a recommendation is provided to standardize the presentation of research results in the field to allow for easy comparison of reported PEC efficiencies in the near future.

  7. Adsorbent and adsorbent bed for materials capture and separation processes

    DOEpatents

    Liu, Wei

    2011-01-25

    A method device and material for performing adsorption wherein a fluid mixture is passed through a channel in a structured adsorbent bed having a solid adsorbent comprised of adsorbent particles having a general diameter less than 100 um, loaded in a porous support matrix defining at least one straight flow channel. The adsorbent bed is configured to allow passage of a fluid through said channel and diffusion of a target material into said adsorbent under a pressure gradient driving force. The targeted molecular species in the fluid mixture diffuses across the porous support retaining layer, contacts the adsorbent, and adsorbs on the adsorbent, while the remaining species in the fluid mixture flows out of the channel.

  8. Reduction of the water wettability of cellulose film through controlled heterogeneous modification.

    PubMed

    Li, Wei; Wu, Yuehan; Liang, Weiwei; Li, Bin; Liu, Shilin

    2014-04-23

    A facile method had been applied to introduce hydrophobic properties to cellulose materials by incorporation of polyurethane acrylate (PUA) prepolymers into the porous structured cellulose matrix through dip-coating; then, PUA prepolymers were cured around interconnected cellulose fibers under UV light, encapsulating a cellulose matrix with a hydrophobic polymer shell. The characterization of the composite films confirmed the success of the heterogeneous modification, and the chemical structure of the cellulose matrix was preserved. The composite films integrated the merits of cellulose and PUA resin, but the highly hydrophilic behavior of cellulose has been reduced. Contact angle measurements with water demonstrated that the composite films had obvious hydrophobic properties and an obvious reduction in the water uptake and the permeability toward water vapor gas at different relative humidity was also observed. The transmittance of the composite films at 550 nm was about 85%. The thermal and mechanical properties of the composite films were improved when compared with that of PUA resin. The obtained composite based on cellulose and UV curing technology was a good choice for the development of biomass materials with modified surface properties.

  9. Excess thermodynamic properties of thin water films confined between hydrophobized gold surfaces.

    PubMed

    Wang, Jialin; Yoon, Roe-Hoan; Eriksson, Jan Christer

    2011-12-01

    Surface forces between gold surfaces were measured in pure water at temperatures in the range of 10-40 °C using an atomic force microscope (AFM). The surfaces were hydrophobized by self-assembly of alkanethiols (C(n)SH) with n=2 and 16 in ethanol solutions. The data were used to determine the changes in excess free energies (ΔG(f)) of the thin water films per unit area by using the Derjaguin approximation [1]. The free energy data were then used to determine the changes in excess film entropy (ΔS(f)) and the excess film enthalpy (ΔH(f)) per unit area. The results show that both ΔS(f) and ΔH(f) decrease with decreasing film thickness, suggesting that the macroscopic hydrophobic interaction involves building some kind of structures in the intervening thin films of water. It was found that |ΔH(f)|>|TΔS(f)|, which is a necessary condition for an attractive force to appear when the enthalpy and entropy changes are both negative. That macroscopic hydrophobic interaction is enthalpically driven is contrary to the hydrophobic interactions at molecular scale. The results obtained in the present work are used to discuss possible origins for the long-range attractions observed between hydrophobic surfaces.

  10. Sensing of contaminants in potable water using TiO2 functional film

    NASA Astrophysics Data System (ADS)

    Akshatha, N.; Poonia, Monika; Gupta, R. K.; Manjuladevi, V.; Shukla, P.; Gupta, Rajiv

    2016-04-01

    The piezoelectric based quartz crystal microbalance is employed for sensing contaminants in potable water. A spin coated thin layer of TiO2 nanoparticles was formed at the sensing area of a 5 MHz AT-cut quartz wafer. The thin film of TiO2 nanoparticles forms a mesoporous functional layer for the trapping of water borne contaminants. The morphology of the thin film of TiO2 nanoparticles was studied using field emission scanning electron microscope (FESEM). The surface morphology of the TiO2 nanoparticles reveals the mesoporous structures indicating large number of defects and porous sites. Such film was employed for the detection of water borne contaminants by detecting the piezoelectric response from a quartz crystal microbalance. We found the film to be very sensitive to the contaminants. The minimum detection limit was found to be 330 ppb. The effect of surface recharging was also studied by altering the physical conditions so that the film can be used for repetitive usage.

  11. [Study on spectrum of oil film in ice-infested waters].

    PubMed

    Li, Ying; Liu, Bing-Xin; Lan, Guo-Xin; Ma, Long; Gao, Chao

    2010-04-01

    Oil spills in ice-infested waters are a subject of great concern to corporations, local residents, and government agencies, which participate in oil exploration, production, and transportation in ice-infested regions recently. For developing a credible and effective response to oil spill in ice-infested waters, a field experiment was performed on the spectrum of oil film in ice-infested waters. In this experiment, four groups of spectrum samples were collected, including clean sea water, brash ice and even ice and sea water/brash ice/even ice contaminated by diesel and crude oil. The experiment results indicated that: the same sort of oil with different background had different reflectance at the same wavelength, and so did the same sort of oil with the same background but different distribution state; nevertheless there were some common characteristics within the same oil. For example, diesel had two apparent characteristics, no matter on the surface of sea water or brash ice or even ice, the first of which was that the reflectance curves of diesel film were first lower and then higher than that of clean sea water, brash ice or even ice according to the wavelength; the second was that the reflectance curves of diesel film were almost equaled to that of the background between 400 and 510 nm in sea water, 410 and 510 nm in brash ice and 490 and 510 nm in even ice. The spectrum curves of crude oil had a representative sphenoid reflectance-peak which appeared between 750 and 770 nm. These characteristics of oil film in terms of ice and oil type could be effectively used to distinct the oil with sea water and sea ice, meanwhile this experiment would improve and facilitate the detecting and monitoring proposal of oil which had been spilled in moving, broken pack ice and fast-ice environment in the ocean.

  12. Nonlinear vibration induced by the water-film whirl and whip in a sliding bearing rotor system

    NASA Astrophysics Data System (ADS)

    Zhai, Liming; Luo, Yongyao; Wang, Zhengwei; Kitauchi, Seishiro; Miyagawa, Kazuyoshi

    2016-03-01

    Many industrial applications and experiments have shown that sliding bearings often experience fluid film whip due to nonlinear fluid film forces which can cause rotor-stator rub-impact failures. The oil-film whips have attracted many studies while the water-film whips in the water lubricated sliding bearing have been little researched with the mechanism still an open problem. The dynamic fluid film forces in a water sliding bearing are investigated numerically with rotational, whirling and squeezing motions of the journal using a nonlinear model to identify the relationships between the three motions. Rotor speed-up and slow-down experiments are then conducted with the rotor system supported by a water lubricated sliding bearing to induce the water-film whirl/whip and verify the relationship. The experimental results show that the vibrations of the journal alternated between increasing and decreasing rather than continuously increasing as the rotational speed increased to twice the first critical speed, which can be explained well by the nonlinear model. The radial growth rate of the whirl motion greatly affects the whirl frequency of the journal and is responsible for the frequency lock in the water-film whip. Further analysis shows that increasing the lubricating water flow rate changes the water-film whirl/whip characteristics, reduces the first critical speed, advances the time when significant water-film whirling motion occurs, and also increases the vibration amplitude at the bearing center which may lead to the rotor-stator rub-impact. The study gives the insight into the water-film whirl and whip in the water lubricated sliding bearing.

  13. Efficiency of macroporous poly(vinylphosphoramidic acid) resin adsorbing of selected elements and determination of trace dysprosium, holmium, erbium, and ytterbium in waste water by inductively coupled plasma optical emission spectrometry

    SciTech Connect

    Zhan Guangyao; Su Zhixing; Lou Xingyin; Chang Xijun )

    1992-03-01

    A macroporous poly(vinylphosphoramidic acid) resin is synthesized through the reaction of macroporous poly(vinylethylenediamine) resin with formaldehyde and phosphorus acid. The adsorption efficiency of the resin to selected elements is determined. An ICP-OES method has been established for the resin enrichment and separation of trace Dy, Ho, Er and Yb ions in waste water. The ability of the Na-form resin to adsorb Dy, Ho, Er, and Yb ions is far better than the H-form resin. The IR spectra of the resin before and after adsorbing Dy are shown. The mechanism of resin adsorption of Dy is explored. The results of resin enriched waste water analysis from a smelter plant are 31.0 ng/ml for dy, 41.1 ng/ml for Hl, 20.6 ng/ml for Er and 20.2 ng/ml for Yb ions. The recovery of standard additions of Dy, Ho, Er, and Yb to the waste water is in the range of 97.0-98.5%.

  14. Thin film composite polyamide membrane parameters estimation for phenol-water system by reverse osmosis

    SciTech Connect

    Murthy, Z.V.P.; Gupta, S.K.

    1998-12-01

    A commercial thin film composite polyamide reverse osmosis membrane is used to separate an aqueous phenol-water binary system. The separation data are analyzed using a combined film theory-solution-diffusion (CFSD) model and a combined film theory-Spiegler-Kedem (CFSK) model. In the present investigation a new phenomenon is observed: there exists a maximum in the rejection when it is plotted against the product flux through the membrane. This behavior is explained for both models. An equation for J{sub v,min}, which is the value of the product flux J{sub v} at which the rejection reaches a maximum, is derived from both models. Although the parameters for both models are consistent over the range of operating conditions, the CFSK model is more accurate for the phenol-water system.

  15. Epitaxial ferroelectric BiFeO3 thin films for unassisted photocatalytic water splitting

    NASA Astrophysics Data System (ADS)

    Ji, Wei; Yao, Kui; Lim, Yee-Fun; Liang, Yung C.; Suwardi, Ady

    2013-08-01

    Considering energy band alignment and polarization effect, ferroelectric BiFeO3 thin films are proposed as the photoanode in a monolithic cell to achieve unassisted photocatalytic water splitting. Significant anodic photocurrent was observed in our epitaxial ferroelectric BiFeO3 films prepared from sputter deposition. Both negative polarization charges and thinner films were found to promote the anodic photocatalytic reaction. Ultraviolet photoelectron spectroscopy proved that the conduction and valence band edges of BiFeO3 straddle the water redox levels. Theoretical analyses show that the large switchable polarization can modify the surface properties to promote the hydrogen and oxygen evolutions on the surfaces with positive and negative polarization charges, respectively.

  16. Epitaxial ferroelectric BiFeO{sub 3} thin films for unassisted photocatalytic water splitting

    SciTech Connect

    Ji, Wei; Yao, Kui; Lim, Yee-Fun; Suwardi, Ady; Liang, Yung C.

    2013-08-05

    Considering energy band alignment and polarization effect, ferroelectric BiFeO{sub 3} thin films are proposed as the photoanode in a monolithic cell to achieve unassisted photocatalytic water splitting. Significant anodic photocurrent was observed in our epitaxial ferroelectric BiFeO{sub 3} films prepared from sputter deposition. Both negative polarization charges and thinner films were found to promote the anodic photocatalytic reaction. Ultraviolet photoelectron spectroscopy proved that the conduction and valence band edges of BiFeO{sub 3} straddle the water redox levels. Theoretical analyses show that the large switchable polarization can modify the surface properties to promote the hydrogen and oxygen evolutions on the surfaces with positive and negative polarization charges, respectively.

  17. Detection of dimethyl methylphosphonate by thin water film confined surface-enhanced Raman scattering method.

    PubMed

    Wang, Jingjing; Duan, Guotao; Liu, Guangqiang; Li, Yue; Chen, Zhengxing; Xu, Lei; Cai, Weiping

    2016-02-13

    It is important and necessary to effectively detect the chemical warfare agents, such as highly toxic never agent sarin. However, based on the surface-enhanced Raman scattering (SERS) effect, detection of nerve agent simulant dimethyl methylphosphonate (DMMP) which is weakly interacted with SERS-active substrate has been the most challenge for the routine SERS detection method. To overcome this challenge, we put forward a thin water film confined SERS strategy. Under the space-confinement of water film, Raman measurements are carried out in the water evaporation process. The subsequent water evaporation induces concentrating of the DMMP molecules, which are thus successfully restricted within the strong electromagnetic field enhanced area above the SERS substrates, leading to the enhancement of their Raman signals. This study provides a new way to achieve the efficient SERS-based detection of the target molecules weakly interacted with the metal substrates.

  18. Oil film thickness measurement using airborne laser-induced water Raman backscatter

    NASA Technical Reports Server (NTRS)

    Hoge, F. E.; Swift, R. N.

    1980-01-01

    The use of laser-induced water Raman backscatter for remote thin oil film detection and thickness measurement is reported here for the first time. A 337.1-nm nitrogen laser was used to excite the 3400-cm-1 OH stretch band of natural ocean water beneath the oil slick from an altitude of 150 m. The signal strength of the 381-nm water Raman backscatter was always observed to depress when the oil was encountered and then return to its original undepressed value after complete aircraft traversal of the floating slick. After removal of background and oil fluorescence contributions, the ratio of the depressed-to-undepressed airborne water Raman signal intensities, together with laboratory measured oil extinction coefficients, is used to calculate the oil film thickness.

  19. Buoyancy of a thin plate pressing a floating oil film on water.

    PubMed

    Ji, Xiang-Ying; Feng, Xi-Qiao

    2013-06-04

    Because of the superhydrophobicity of their legs, water striders and many other aquatic creatures can stand and walk effortlessly on water. Because of pollution, an oil film may exist on water in some practical situations. To date, however, it remains unclear how the presence of an oil film would affect the wetting behavior of an object floating on water. In this work, we investigated, both theoretically and experimentally, the buoyancy of a thin plate pressing the surface of a bilayered liquid system. In particular, the effect of the oil layer on the buoyancy force was examined. The critical depth and the corresponding buoyancy at the penetration of the plate into the liquids were obtained analytically. For a plate vertically pressing the liquid surface, the force-displacement loop during a complete advancing-receding cycle was analyzed. Experiments were also performed to verify the theoretical results.

  20. Effect of porous polymer films (track membranes) on the isothermal evaporation kinetics of water

    NASA Astrophysics Data System (ADS)

    Novikov, S. N.; Ermolaeva, A. I.; Timoshenkov, S. P.; Korobova, N. E.; Goryunova, E. P.

    2016-06-01

    The kinetics of isothermal evaporation of distilled water that was in remote (10-15-mm) contact with porous polymer films (track membranes (TMs)) was studied by microgravimetry (derivatograph). When the H2O-TM system contained a disperse medium, the supramolecular structure of water changed, and the number of clusters (coherent domains) drastically decreased. The extraction of the light phase from liquid water was correlated with the chemisorption of H2O molecules containing the para-isomer of hydrogen, which predominantly form coherent domains of water.

  1. Electrosynthesis of highly transparent cobalt oxide water oxidation catalyst films from cobalt aminopolycarboxylate complexes.

    PubMed

    Bonke, Shannon A; Wiechen, Mathias; Hocking, Rosalie K; Fang, Xi-Ya; Lupton, David W; MacFarlane, Douglas R; Spiccia, Leone

    2015-04-24

    Efficient catalysis of water oxidation represents one of the major challenges en route to efficient sunlight-driven water splitting. Cobalt oxides (CoOx ) have been widely investigated as water oxidation catalysts, although the incorporation of these materials into photoelectrochemical devices has been hindered by a lack of transparency. Herein, the electrosynthesis of transparent CoOx catalyst films is described by utilizing cobalt(II) aminopolycarboxylate complexes as precursors to the oxide. These complexes allow control over the deposition rate and morphology to enable the production of thin, catalytic CoOx films on a conductive substrate, which can be exploited in integrated photoelectrochemical devices. Notably, under a bias of 1.0 V (vs. Ag/AgCl), the film deposited from [Co(NTA)(OH2 )2 ](-) (NTA=nitrilotriacetate) decreased the transmission by only 10 % at λ=500 nm, but still generated >80 % of the water oxidation current produced by a [Co(OH2 )6 ](2+) -derived oxide film whose transmission was only 40 % at λ=500 nm.

  2. Water vapor permeability, mechanical, optical and sensorial properties of plasticized guar gumedible films

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Edible films were prepared by casting method using guar gum and glycerol in different ratios. The concentration of guar gum was 1.0, 1.5 and 2.0% whereas glycerol concentration was 20, 30 and 40% (w/v). The water vapor permeability (WVP), mechanical properties (tensile strength and elongation), thic...

  3. The effect of water diffusion on the adhesion of organosilicate glass film stacks

    NASA Astrophysics Data System (ADS)

    Tsui, Ting Y.; McKerrow, Andrew J.; Vlassak, Joost J.

    2006-05-01

    Organosilicate glass (OSG) is a material that is used as a dielectric in advanced integrated circuits. It has a network structure similar to that of amorphous silica where a fraction of the Si-O bonds have been replaced by organic groups. It is well known from prior work that OSG is sensitive to subcritical crack growth as water molecules in the environment are transported to the crack tip and assist in rupturing Si-O bonds at the crack tip. In this study, we demonstrate that exposure of an OSG containing film stack to water prior to fracture results in degradation of the adhesion of the film stack. This degradation is the result of the diffusion of water into the film stack. We propose a quantitative model to predict adhesion degradation as a function of exposure time by coupling the results of independent subcritical crack growth measurements with diffusion concentration profiles. The model agrees well with experimental data and provides a novel method for measuring the water diffusion coefficient in film stacks that contain OSG. This study has important implications for the reliability of advanced integrated circuits.

  4. Diode laser-based standoff absorption measurement of water film thickness in retro-reflection

    NASA Astrophysics Data System (ADS)

    Pan, R.; Brocksieper, C.; Jeffries, J. B.; Dreier, T.; Schulz, C.

    2016-09-01

    A dual-wavelength diode laser-based absorption sensor for standoff point measurements of water film thickness on an opaque surface is presented. The sensor consists of a diode laser source, a foil as backscattering target, and off-axis paraboloids for collecting the fraction of the laser radiation transmitted through the liquid layer via retro-reflection. Laser wavelengths in the near infrared at 1412 and 1353 nm are used where the temperature dependence of the liquid water absorption cross section is known. The lasers are fiber coupled and the detection of the retro-reflected light was accomplished through a multimode fiber and a single photodiode using time-division multiplexing. The water film thickness at a given temperature was determined from measured transmittance ratios at the two laser wavelengths. The sensor concept was first validated with measurement using a temperature-controlled calibration cell providing liquid layers of variable and known thickness between 100 and 1000 µm. Subsequently, the sensor was demonstrated successfully during recording the time-varying thickness of evaporating water films at fixed temperatures. The film thickness was recorded as a function of time at three temperatures down to 50 µm.

  5. Effects of drip irrigation under plastic film with saline water on cotton growth and yields

    NASA Astrophysics Data System (ADS)

    Wang, B.; Jin, M.; He, Y.; Zhou, J.; Brusseau, M. L.

    2012-12-01

    To study the influence of different irrigation system for drip irrigation under plastic film with saline water on cotton growth and yields, field experiments at key irrigation experiment station of water resources management division in Bayingolin Mongol Autonomous Prefecture, Xinjiang, China were set up consist of different irrigation ratio (5250, 4500, 3750, 3000m3/hm2), different irrigation times (24, 12 and 8 times) and different rotation irrigation modes. The results show that: with the larger irrigation ratio, the cotton growth and yields was also better, and the significant influence on cotton growth and yields for irrigation ratio is between 3750-4500 m3/hm2. When the irrigation ratio is smaller (3000m3/hm2), cotton growth and yields for irrigation times of 8 times are higher, When the irrigation ratio is bigger (4500m3/hm2), cotton growth for irrigation times of 12 times are better and its cotton yields are higher correspondingly. According to the growth of cotton, yields and water productivity, the suitable irrigation system of cotton is the irrigation ratio of 4500-3750 m3/ hm2 and the irrigation times of 18 times for drip irrigation under plastic film with saline water. For different rotation drip irrigation experiments with saline water and fresh water, the cotton yields and irrigation water productivity is higher under the disposal of SF (rotation irrigation in first 6 times with saline water irrigation and then 6 times with fresh water irrigation) compared to FS (rotation irrigation in first 6 times with fresh water and then 6 times with saline water) and SSFA (rotation irrigation with twice saline water and once fresh water) compared to SFA (alternative irrigation with saline water and fresh water). Compared to the different alternate irrigation experiments, the cotton yields and water productivity for pure saline water irrigation is higher. In addition, the trend is the larger the irrigation ratio and the higher the yields. It maybe dues to the low

  6. Photoassisted oxidation of oil films on water. Final performance report, January 1, 1990--March 31, 1993

    SciTech Connect

    Heller, A.

    1994-04-19

    The objective of the project has been the development of a technology for cleaning up oil spills on water through their photocatalytic oxidation. The photocatalyst used was titanium dioxide. Nanocrytalline TiO{sub 2}, of anatase or anatase/rutile phase, was bound to hollow ceramic microspheres of sufficiently low density to be buoyant on water. In the presence of these, under sunlight, oil films were photocatalytically oxidized by dissolved oxygen.

  7. Insight into the adsorption of PPCPs by porous adsorbents: Effect of the properties of adsorbents and adsorbates.

    PubMed

    Zhu, Zengyin; Xie, Jiawen; Zhang, Mancheng; Zhou, Qing; Liu, Fuqiang

    2016-07-01

    Adsorption is an efficient method for removal of pharmaceuticals and personal care products (PPCPs). Magnetic resins are efficient adsorbents for water treatment and exhibit potential for PPCP removal. In this study, the magnetic hypercrosslinked resin Q100 was used for adsorption of PPCPs. The adsorption behavior of this resin was compared with those of two activated carbons, namely, Norit and F400D. Norit exhibited the fastest adsorption kinetics, followed by Q100. Norit featured a honeycomb shape and long-range ordered pore channels, which facilitated the diffusion of PPCPs. Moreover, the large average pore size of Q100 reduced diffusion resistance. The adsorbed amounts of 11 PPCPs on the three adsorbents increased with increasing adsorbate hydrophobicity. For Q100, a significant linear correlation was observed between the adsorption performance for PPCPs and hydrophobicity (logD value) of adsorbates (R(2) = 0.8951); as such, PPCPs with high logD values (>1.69) could be efficiently removed. Compared with those of Norit and F400D, the adsorption performance of Q100 was less affected by humic acid because of the dominant hydrophobic interaction. Furthermore, Q100 showed improved regeneration performance, which renders it promising for PPCP removal in practical applications.

  8. Water-in-model oil emulsions studied by small-angle neutron scattering: interfacial film thickness and composition.

    PubMed

    Verruto, Vincent J; Kilpatrick, Peter K

    2008-11-18

    The ever-increasing worldwide demand for energy has led to the upgrading of heavy crude oil and asphaltene-rich feedstocks becoming viable refining options for the petroleum industry. Traditional problems associated with these feedstocks, particularly stable water-in-petroleum emulsions, are drawing increasing attention. Despite considerable research on the interfacial assembly of asphaltenes, resins, and naphthenic acids, much about the resulting interfacial films is not well understood. Here, we describe the use of small-angle neutron scattering (SANS) to elucidate interfacial film properties from model emulsion systems. Modeling the SANS data with both a polydisperse core/shell form factor as well as a thin sheet approximation, we have deduced the film thickness and the asphaltenic composition within the stabilizing interfacial films of water-in-model oil emulsions prepared in toluene, decalin, and 1-methylnaphthalene. Film thicknesses were found to be 100-110 A with little deviation among the three solvents. By contrast, asphaltene composition in the film varied significantly, with decalin leading to the most asphaltene-rich films (30% by volume of the film), while emulsions made in toluene and methylnaphthalene resulted in lower asphaltenic contents (12-15%). Through centrifugation and dilatational rheology, we found that trends of decreasing water resolution (i.e., increasing emulsion stability) and increasing long-time dilatational elasticity corresponded with increasing asphaltene composition in the film. In addition to the asphaltenic composition of the films, here we also deduce the film solvent and water content. Our analyses indicate that 1:1 (O/W) emulsions prepared with 3% (w/w) asphaltenes in toluene and 1 wt % NaCl aqueous solutions at pH 7 and pH 10 resulted in 80-90 A thick films, interfacial areas around 2600-3100 cm (2)/mL, and films that were roughly 25% (v/v) asphaltenic, 60-70% toluene, and 8-12% water. The increased asphaltene and water film

  9. Photocatalytic property of titanium dioxide thin films deposited by radio frequency magnetron sputtering in argon and water vapour plasma

    NASA Astrophysics Data System (ADS)

    Sirghi, L.; Hatanaka, Y.; Sakaguchi, K.

    2015-10-01

    The present work is investigating the photocatalytic activity of TiO2 thin films deposited by radiofrequency magnetron sputtering of a pure TiO2 target in Ar and Ar/H2O (pressure ratio 40/3) plasmas. Optical absorption, structure, surface morphology and chemical structure of the deposited films were comparatively studied. The films were amorphous and included a large amount of hydroxyl groups (about 5% of oxygen atoms were bounded to hydrogen) irrespective of the intentional content of water in the deposition chamber. Incorporation of hydroxyl groups in the film deposited in pure Ar plasma is explained as contamination of the working gas with water molecules desorbed by plasma from the deposition chamber walls. However, intentional input of water vapour into the discharge chamber decreased the deposition speed and roughness of the deposited films. The good photocatalytic activity of the deposited films could be attributed hydroxyl groups in their structures.

  10. Proton sponge-functionalized silica as high performance adsorbents for solid-phase extraction of trace perfluoroalkyl sulfonates in the environmental water samples and their direct analysis by MALDI-TOF-MS.

    PubMed

    Cao, Dong; Hu, Ming; Han, Chunguang; Yu, Jiyao; Cui, Lin; Liu, Yongxue; Wang, Hailin; Cai, Yaqi; Kang, Yuehui; Zhou, Yiqi

    2012-05-07

    1,8-Bis(dimethylamino)naphthalene (DMAN), a classical 'proton sponge', was functionalized on silica particles as a novel solid-phase extraction (SPE) adsorbent (DMAN@silica) for extracting perfluoroalkyl sulfonates (PFSs). High reproducibility and excellent extraction capability for PFSs were obtained in a wide pH range (3.0~8.5). The adsorbed PFSs on DMAN@silica sorbents could be efficiently eluted by 1,8-bis(tetramethylguanidino)naphthalene (TMGN) solution which is a proton sponge with higher proton affinity than DMAN. The elution could be directly analyzed by MALDI-TOF-MS using TMGN as matrix. Clear mass spectra for the PFSs were obtained due to no matrix ions interference observed. Furthermore, a novel strategy based on the DMAN@silica-SPE enrichment, followed by MALDI-TOF-MS analysis, was proposed and applied for PFSs quantification in environmental water samples. The calibration curves of each of the target analytes showed a wide linear dynamic range of response (0.1-10 ng L(-1) for perfluorooctane sulfonate (PFOS), perfluorohexyl sulfonate (PFHxS) and perfluorobutylsulfonate (PFBS)), which were over 2 orders of magnitude. The detection limits for PFOS, PFHxS, and PFBS were 0.021, 0.016, and 0.013 ng L(-1), respectively (S/N = 3). Recoveries of PFOS, PFHxS, and PFBS are in the ranges of 92-104%, 95-102%, and 98-109% for spiked river water samples. These results indicated that the prepared DMAN@silica adsorbents could efficiently enrich PFSs and that the proposed method is reliable.

  11. Films

    NASA Astrophysics Data System (ADS)

    Li, Ming; Zhang, Yang; Shao, Yayun; Zeng, Min; Zhang, Zhang; Gao, Xingsen; Lu, Xubing; Liu, J.-M.; Ishiwara, Hiroshi

    2014-09-01

    In this paper, we investigated the microstructure and electrical properties of Bi2SiO5 (BSO) doped SrBi2Ta2O9 (SBT) films deposited by chemical solution deposition. X-ray diffraction observation indicated that the crystalline structures of all the BSO-doped SBT films are nearly the same as those of a pure SBT film. Through BSO doping, the 2Pr and 2Ec values of SBT films were changed from 15.3 μC/cm2 and 138 kV/cm of pure SBT to 1.45 μC/cm2 and 74 kV/cm of 10 wt.% BSO-doped SBT. The dielectric constant at 1 MHz for SBT varied from 199 of pure SBT to 96 of 10 wt.% BSO-doped SBT. The doped SBT films exhibited higher leakage current than that of non-doped SBT films. Nevertheless, all the doped SBT films still had small dielectric loss and low leakage current. Our present work will provide useful insights into the BSO doping effects to the SBT films, and it will be helpful for the material design in the future nonvolatile ferroelectric memories.

  12. Spontaneous cracking of amorphous solid water films and the dependence on microporous structure

    NASA Astrophysics Data System (ADS)

    Bu, Caixia; Dukes, Catherine A.; Baragiola, Raúl A.

    2016-11-01

    Vapor-deposited, porous, amorphous, water-ice films, also called amorphous solid water (ASW), crack spontaneously during growth when the film thickness exceeds a critical value (Lc). We measured the Lc during growth of ASW films as a function of growth temperature (Tg = 10 K, 30 K, and 50 K) and deposition angle (θ = 0°, 45°, and 55°) using a quartz crystal microbalance, an optical interferometer, and an infrared spectrometer. The critical thickness, 1-5 μm under our experimental conditions, increases with Tg and θ, an indication of film porosity. We suggest that ASW films undergo tensile stress due to the mismatch between substrate adhesion and contracting forces derived from the incompletely coordinated molecules on the surfaces of the pores. We provide a model to explain the observed dependences of Lc on the Tg and θ in the context of Griffith theory and estimate the tensile strength of low-temperature ASW to be ˜25-40 MPa. Our model can be applied more generally to describe fracture of other solids with microporous structures, such as metallic or ceramic materials with voids.

  13. Strategies to improve the mechanical strength and water resistance of agar films for food packaging applications.

    PubMed

    Sousa, Ana M M; Gonçalves, Maria P

    2015-11-05

    Agar films possess several properties adequate for food packaging applications. However, their high cost-production and quality variations caused by physiological and environmental factors affecting wild seaweeds make them less attractive for industries. In this work, native (NA) and alkali-modified (AA) agars obtained from sustainably grown seaweeds (integrated multi-trophic aquaculture) were mixed with locust bean gum (LBG) to make 'knife-coated' films with fixed final concentration (1 wt%) and variable agar/LBG ratios. Agar films were easier to process upon LBG addition (viscosity increase and gelling character decrease of the film-forming solutions observed by dynamic oscillatory and steady shear measurements). The mechanical properties and water resistance were optimal for films with 50 and/or 75% LBG contents and best in the case of NA (cheaper to extract). These findings can help reduce the cost-production of agar packaging films. Moreover, the controlled cultivation of seaweeds can provide continuous and reliable feedstock for transformation industries.

  14. Surface shear rheology of WPI-monoglyceride mixed films spread at the air-water interface.

    PubMed

    Carrera Sánchez, Cecilio; Rodríguez Patino, Juan M

    2004-07-01

    Surface shear viscosity of food emulsifiers may contribute appreciably to the long-term stability of food dispersions (emulsions and foams). In this work we have analyzed the structural, topographical, and shear characteristics of a whey protein isolate (WPI) and monoglyceride (monopalmitin and monoolein) mixed films spread on the air-water interface at pH 7 and at 20 degrees C. The surface shear viscosity (etas) depend on the surface pressure and on the composition of the mixed film. The surface shear viscosity varies greatly with the surface pressure. In general, the greater the surface pressure, the greater are the values of etas. The values of etas for the mixed WPI-monoolein monolayer were more than one order of magnitude lower than those for a WPI-monopalmitin mixed film, especially at the higher surface pressures. At higher surface pressures, collapsed WPI residues may be displaced from the interface by monoglyceride molecules with important repercussions on the shear characteristics of the mixed films. A shear-induced change in the topography and a segregation between domains of the film forming components were also observed. The displacement of the WPI by the monoglycerides is facilitates under shear conditions, especially for WPI-monoolein mixed films.

  15. Does the reactive surface area of sandstone depend on water saturation?—The role of reactive-transport in water film

    NASA Astrophysics Data System (ADS)

    Nishiyama, Naoki; Yokoyama, Tadashi

    2013-12-01

    To investigate how mineral-water reactive surface area changes depending on water saturation, flow-through dissolution experiments were performed using a sandstone core at various water saturations. Fontainebleau sandstone with an open porosity of 6.3%, consisting of ∼100% quartz, was used. The water saturation of the core was adjusted to 0%, 51%, or 100%, and at each saturation, water was infiltrated into the core at a constant pressure. The experimental results showed that the total amount of dissolved Si did not change with decreasing water saturation. It can be therefore concluded that virtually all of the mineral surfaces were wetted with water film and allowed the progression of dissolution; i.e., the reactive surface area was not affected by water saturation despite the presence of air in the pores. The results also suggested that the flushing rate of dissolved Si from the interior of the water film to the exterior was fast enough to keep the Si concentration in the film sufficiently lower than the equilibrium concentration of quartz. We derived a reactive-transport model describing dissolution and diffusion in water film. The model shows that the solute concentration in a film is a function of the film thickness, diffusion length, dissolution rate of the mineral, equilibrium concentration, and roughness factor. As for the Fontainebleau sandstone, film thicknesses of 7-18 nm and diffusion lengths of 300-600 μm were estimated. The reactive-transport calculation confirmed that the overall dissolution rate of our sandstone sample was almost unaffected by water saturation, owing to the high flushing efficiency of dissolved Si in water film, which agrees with the experimental result. Application of the model allows us to evaluate whether the reactive surface area and the dissolution rate change with water saturation for a given rock of interest.

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

    PubMed

    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

  17. The influence of the surface composition of mixed monolayer films on the evaporation coefficient of water.

    PubMed

    Miles, Rachael E H; Davies, James F; Reid, Jonathan P

    2016-07-20

    We explore the dependence of the evaporation coefficient of water from aqueous droplets on the composition of a surface film, considering in particular the influence of monolayer mixed component films on the evaporative mass flux. Measurements with binary component films formed from long chain alcohols, specifically tridecanol (C13H27OH) and pentadecanol (C15H31OH), and tetradecanol (C14H29OH) and hexadecanol (C16H33OH), show that the evaporation coefficient is dependent on the mole fractions of the two components forming the monolayer film. Immediately at the point of film formation and commensurate reduction in droplet evaporation rate, the evaporation coefficient is equal to a mole fraction weighted average of the evaporation coefficients through the equivalent single component films. As a droplet continues to diminish in surface area with continued loss of water, the more-soluble, shorter alkyl chain component preferentially partitions into the droplet bulk with the evaporation coefficient tending towards that through a single component film formed simply from the less-soluble, longer chain alcohol. We also show that the addition of a long chain alcohol to an aqueous-sucrose droplet can facilitate control over the degree of dehydration achieved during evaporation. After undergoing rapid gas-phase diffusion limited water evaporation, binary aqueous-sucrose droplets show a continued slow evaporative flux that is limited by slow diffusional mass transport within the particle bulk due to the rapidly increasing particle viscosity and strong concentration gradients that are established. The addition of a long chain alcohol to the droplet is shown to slow the initial rate of water loss, leading to a droplet composition that remains more homogeneous for a longer period of time. When the sucrose concentration has achieved a sufficiently high value, and the diffusion constant of water has decreased accordingly so that bulk phase diffusion arrest occurs in the monolayer

  18. Influence of Water on Chemical Vapor Deposition of Ni and Co thin films from ethanol solutions of acetylacetonate precursors

    PubMed Central

    Weiss, Theodor; Zielasek, Volkmar; Bäumer, Marcus

    2015-01-01

    In chemical vapor deposition experiments with pulsed spray evaporation (PSE-CVD) of liquid solutions of Ni and Co acetylacetonate in ethanol as precursors, the influence of water in the feedstock on the composition and growth kinetics of deposited Ni and Co metal films was systematically studied. Varying the water concentration in the precursor solutions, beneficial as well as detrimental effects of water on the metal film growth, strongly depending on the concentration of water and the β-diketonate in the precursor, were identified. For 2.5 mM Ni(acac)2 precursor solutions, addition of 0.5 vol% water improves growth of a metallic Ni film and reduces carbon contamination, while addition of 1.0 vol% water and more leads to significant oxidation of deposited Ni. By tuning the concentration of both, Ni(acac)2 and water in the precursor solution, the fraction of Ni metal and Ni oxide in the film or the film morphology can be adjusted. In the case of Co(acac)2, even smallest amounts of water promote complete oxidation of the deposited film. All deposited films were analyzed with respect to chemical composition quasi in situ by XPS, their morphology was evaluated after deposition by SEM. PMID:26658547

  19. Effect of binding of an oligomeric cationic fluorosurfactant on the dilational rheological properties of gelatin adsorbed at the air-water interface.

    PubMed

    Rao, Ashwin; Kim, Yongsin; Kausch, Charles M; Thomas, Richard R

    2006-09-12

    The effect of binding of an oligomeric cationic fluorooxetane surfactant on the interfacial properties of adsorbed gelatin-fluorooxetane complexes has been studied using dynamic surface tension and dilational rheological measurements. Adsorption kinetics of gelatin-fluorooxetane complexes are reminiscent of a mixed (barrier/diffusion limited) process, while the dilational rheological properties of the interface exhibit a strong dependence on surfactant concentration. At low surfactant concentrations, dilational surface moduli as well as phase angles are relatively insensitive to the presence of the fluorooxetane. However, at the critical aggregation concentration of the polymer-surfactant system, there is a sharp increase in the complex modulus. Further increase in the fluorooxetane concentration does not significantly affect the complex modulus. The phase angle, however, does increase with increasing fluorooxetane concentration due to the transport of bound fluorooxetane from the subsurface to the solution-air interface. These results indicate that, at fluorooxetane concentrations exceeding the critical aggregation concentration, the polymer-surfactant complexes adsorb to form cross-linked multilayers at the solution-air interface.

  20. Water adsorption, desorption, and clustering on FeO(111).

    PubMed

    Daschbach, John L; Dohnalek, Z; Liu, Shu-Rong; Smith, R Scott; Kay, Bruce D

    2005-05-26

    The adsorption of water on FeO(111) is investigated using temperature programmed desorption (TPD) and infrared reflection absorption spectroscopy (IRAS). Well-ordered 2 ML thick FeO(111) films are grown epitaxially on a Pt(111) substrate. Water adsorbs molecularly on FeO(111) and desorbs with a well resolved monolayer peak. IRAS measurements as a function of coverage are performed for water deposited at 30 and 135 K. For all coverages (0.2 ML and greater), the adsorbed water exhibits significant hydrogen bonding. Differences in IRAS spectra for water adsorbed at 30 and 135 K are subtle but suggest that water adsorbed at 135 K is well ordered. Monolayer nitrogen TPD spectra from water covered FeO(111) surfaces are used to investigate the clustering of the water as a function of deposition or annealing temperature. Temperature dependent water overlayer structures result from differences in water diffusion rates on bare FeO(111) and on water adsorbed on FeO(111). Features in the nitrogen TPD spectra allow the monolayer wetting and 2-dimensional (2D) ordering of water on FeO(111) to be followed. Voids in a partially disordered first water layer exist for water deposited below 120 K and ordered 2D islands are found when depositing water above 120 K.

  1. Nano sponge Mn₂O ₃ as a new adsorbent for the preconcentration of Pd(II) and Rh(III) ions in sea water, wastewater, rock, street sediment and catalytic converter samples prior to FAAS determinations.

    PubMed

    Yavuz, Emre; Tokalıoğlu, Serife; Sahan, Halil; Patat, Saban

    2014-10-01

    In this study, a nano sponge Mn2O3 adsorbent was synthesized and was used for the first time. Various parameters affecting the recovery values of Pd(II) and Rh(III) were examined. The tolerance limits (≥ 90 %) for both Pd(II) and Rh(III) ions were found to be 75,000 mg L(-1) Na(I), 75,000 mg L(-1) K(I), 50,000 mg L(-1) Mg(II) and 50,000 mg L(-1) Ca(II). A 30s contact time was enough for both adsorption and elution. A preconcentration factor of 100 was obtained by using 100mg of the nano sponge Mn2O3. The reusability of the adsorbent was 120 times. Adsorption capacities for Pd(II) and Rh(III) were found to be 42 and 6.2 mg g(-1), respectively. The detection limits were 1.0 µg L(-1) for Pd(II) and 0.37 µg L(-1) for Rh(III) and the relative standard deviations (RSD, %) were found to be ≤ 2.5%. The method was validated by analyzing the standard reference material, SRM 2556 (Used Auto Catalyst Pellets) and spiked real samples. The optimized method was applied for the preconcentration of Pd(II) and Rh(III) ions in water (sea water and wastewater), rock, street sediment and catalytic converter samples.

  2. Charging and transmission of low energy particles through Amorphous Solid Water films

    NASA Astrophysics Data System (ADS)

    Horowitz, Yonatan; Asscher, Micha

    2012-02-01

    The interaction of charged particles with condensed water films has drawn significant attention in recent years due to its importance in biological and atmospheric processes. We have studied low energy electrons (3-25 eV) and positive argon ions (55 eV) charging and transmission effects while striking Amorphous Solid Water (ASW) films, 240-1080 ML thick, deposited on ruthenium single crystal substrate, utilizing contact potential difference (CPD) measurements. Charging by both species has shown a plate capacitor-like behaviour. L-defects energetically located just below the conduction band of ice, are likely to stabilize them. The incoming electrons kinetic energy dictates the maximal CPD by retardation of any further electrons from adding up to the already accumulated charges. Electron transmission measurements (0.5-1.5 microamps) have shown that the maximal and stable CPD values were obtained only following a relatively slow change that has developed within the ASW structure. Upon film stabilization, the spontaneous discharge was measured over a period of up to three hours. UV laser photo-emission study of the charged films has suggested that the negative charges tend to reside primarily at the ASW-vacuum interface, in good agreement with a study of charged water nano-clusters.

  3. Modeling the interaction Between Ethylene Diamine and Water Films on the Surface of a Carbon Nanotube

    NASA Technical Reports Server (NTRS)

    Jaffe, Richard L.; Walther, Jens H.; Zimmerli, Urs; Koumoutsakos, Petros

    2004-01-01

    It has been observed that a carbon nanotube (CNT) AFM tip coated with ethylene diamine (EDA) penetrates the liquid water-air interface more easily than an uncoated nanotube tip. The EDA coating remains intact through repeated cycles of dipping and removal. In order to understand the physical basis for this observation, we use ab initio quantum chemistry calculations to study the EDA-CNT-water interaction and to parameterize a force field describing this system. Molecular dynamics (MD) simulations are carried out for EDA-water mixtures and an EDA-coated carbon nanotube immmed in water. These simulations are similar to our earlier MD study that characterized the CNT-water interface. The attractive CNT-EDA and CNT-water interactions arise primarily from van der Waals forces, and the EDA-EDA, EDA-water and water-water interactions are mainly due to hydrogen bond formation. The binding energ of single EDA molecule to the nanotube is nearly three times larger than the corresponding value found for water (4.3 versus 1.5 kcal mol, respectively). The EDA molecules readily stick to and diffuse along the CNT surface. As a resulf mixing of the EDA and water films does not occur on the timescale of the MD simulations. The EDA film reduces the hydrophobicity of the nanotube surface and acts like a prototypical surfactant in stabilizing the suspension of carbon nanotubes in water. For this presentation, we use the MD simulations to determine how the presence of the carbon nanotube surface perturbs the properties of EDA-water mixtures.

  4. Investigation of the Effect of the Tortuous Pore Structure on Water Diffusion through a Polymer Film Using Lattice Boltzmann Simulations.

    PubMed

    Gebäck, Tobias; Marucci, Mariagrazia; Boissier, Catherine; Arnehed, Johan; Heintz, Alexei

    2015-04-23

    Understanding how the pore structure influences the mass transport through a porous material is important in several applications, not the least in the design of polymer film coatings intended to control drug release. In this study, a polymer film made of ethyl cellulose and hydroxypropyl cellulose was investigated. The 3D structure of the films was first experimentally characterized using confocal laser scanning microscopy data and then mathematically reconstructed for the whole film thickness. Lattice Boltzmann simulations were performed to compute the effective diffusion coefficient of water in the film and the results were compared to experimental data. The local porosities and pore sizes were also analyzed to determine how the properties of the internal film structure affect the water effective diffusion coefficient. The results show that the top part of the film has lower porosity, lower pore size, and lower connectivity, which results in a much lower effective diffusion coefficient in this part, largely determining the diffusion rate through the entire film. Furthermore, the local effective diffusion coefficients were not proportional to the local film porosity, indicating that the results cannot be explained by a single tortuosity factor. In summary, the proposed methodology of combining microscopy data, mass transport simulations, and pore space analysis can give valuable insights on how the film structure affects the mass transport through the film.

  5. Demonstration of a plasma mirror based on a laminar flow water film

    SciTech Connect

    Panasenko, Dmitriy; Shu, Anthony; Gonsalves, Anthony; Nakamura, Kei; Matlis, Nicholas; Toth, Csaba; Leemans, Wim

    2011-07-22

    A plasma mirror based on a laminar water film with low flow speed 0.5-2 cm/s has been developed and characterized, for use as an ultrahigh intensity optical reflector. The use of flowing water as atarget surface automatically results in each laser pulse seeing a new interaction surface and avoids the need for mechanical scanning of the target surface. In addition, the breakdown of water does notproduce contaminating debris that can be deleterious to vacuum chamber conditions and optics, such as is the case when using conventional solid targets. The mirror exhibits 70percent reflectivity, whilemaintaining high-quality of the reflected spot.

  6. Modification of polymorphisms in polyvinylidene fluoride thin films via water and hydrated salt.

    PubMed

    Song, Rui; Xia, Guangmei; Xing, Xueqing; He, Linghao; Zhao, Qiaoling; Ma, Zhi

    2013-07-01

    In this study, the effects of solvent and magnesium chloride hexahydrate (MgCl2·6H2O) on the polymorphism of polyvinylidene fluoride (PVDF) thin films were systematically investigated. Wherein, N,N-dimethylformamide (DMF) and water with different volume ratio were used as mixed solvents to obtain the solution casting films, P series. In addition, MgCl2·6H2O was comparatively added to prepare PVDF/MgCl2·6H2O hybrid films, P-M series. Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and differential scanning calorimeter (DSC) were utilized to study the influence of the water content in the mixed solvents and the hydrated salt on crystallization behavior of PVDF. Further, the morphologic images from scanning electronic microscopy (SEM) and polarized optical microscopy (POM), as well as the pizoelectirc d33 test also supplies the corresponding evidences. As indicated, the water in the mixed solvent shows different effect on main crystal forms of PVDF. At low water content, the solvents may favor the polar phase (β- and γ-phase) mainly by hydrogen bonds interactions between PVDF and water, together with dipolar interactions between PVDF and DMF. At high water content, the nonsolvent water will impose confinement effect on polymer chain diffusion and crystal growth which facilitate the formation of α-phase PVDF. Moreover, magnesium chloride hexahydrate mainly functioned as the nucleation sites for PVDF crystallization. The result of small-angle X-ray scattering (SAXS) implies the content of water or MgCl2·6H2O has little impact on the structure of the long period.

  7. An efficient removal of crystal violet dye from waste water by adsorption onto TLAC/Chitosan composite: A novel low cost adsorbent.

    PubMed

    Jayasantha Kumari, H; Krishnamoorthy, P; Arumugam, T K; Radhakrishnan, S; Vasudevan, D

    2017-03-01

    A composite of Typha latifolia activated carbon (TLAC) (a novel, low cost absorbent) and chitosan (TLAC/Chitosan composite) was prepared. The composite was characterised using IR spectra, XRD, FESEM and Pore size studies. Its effectivity was tested for the removal of crystal violet dye from aqueous solutions. The effect of pH, dose rate and initial dye concentration was evaluated. The adsorption isotherm, kinetics and thermodynamic parameters were studied. Langmuir and Freundlich isotherm models were found fit effectively for the dye adsorption data in the present study. The adsorption followed pseudo-second order kinetics. The evaluated thermodynamic parameters show a spontaneous and exothermic reaction. Overall, this study indicates TLAC/Chitosan composite as an effective adsorbent for the removal of crystal violet dye from aqueous solutions.

  8. The Uranium from Seawater Program at the Pacific Northwest National Laboratory: Overview of Marine Testing, Adsorbent Characterization, Adsorbent Durability, Adsorbent Toxicity, and Deployment Studies

    SciTech Connect

    Gill, Gary A.; Kuo, Li-Jung; Janke, Chris J.; Park, Jiyeon; Jeters, Robert T.; Bonheyo, George T.; Pan, Horng-Bin; Wai, Chien; Khangaonkar, Tarang; Bianucci, Laura; Wood, Jordana R.; Warner, Marvin G.; Peterson, Sonja; Abrecht, David G.; Mayes, Richard T.; Tsouris, Costas; Oyola, Yatsandra; Strivens, Jonathan E.; Schlafer, Nicholas J.; Addleman, R. Shane; Chouyyok, Wilaiwan; Das, Sadananda; Kim, Jungseung; Buesseler, Ken; Breier, Crystal; D’Alessandro, Evan

    2016-02-07

    The Pacific Northwest National Laboratory’s (PNNL) Marine Science Laboratory (MSL) located along the coast of Washington State is evaluating the performance of uranium adsorption materials being developed for seawater extraction under realistic marine conditions with natural seawater. Two types of exposure systems were employed in this program: flow-through columns for testing of fixed beds of individual fibers and pellets and a recirculating water flume for testing of braided adsorbent material. Testing consists of measurements of the adsorption of uranium and other elements from seawater as a function of time, typically 42 to 56 day exposures, to determine the adsorbent capacity and adsorption rate (kinetics). Analysis of uranium and other trace elements collected by the adsorbents was conducted following strong acid digestion of the adsorbent with 50% aqua regia using either Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) or Inductively Coupled Plasma Mass Spectrometer (ICP-MS). The ORNL 38H adsorbent had a 56 day adsorption capacity of 3.30 ± 0.68 g U/ kg adsorbent (normalized to a salinity of 35 psu), a saturation adsorption capacity of 4.89 ± 0.83 g U/kg of adsorbent material (normalized to a salinity of 35 psu) and a half-saturation time of 28 ± 10 days. The AF1 adsorbent material had a 56 day adsorption capacity of 3.9 ± 0.2 g U/kg adsorbent material (normalized to a salinity of 35 psu), a saturation capacity of 5.4 ± 0.2 g U/kg adsorbent material (normalized to a salinity of 35 psu) and a half saturation time of 23 ± 2 days. The ORNL amidoxime-based adsorbent materials are not specific for uranium, but also adsorb other elements from seawater. The major doubly charged cations in seawater (Ca and Mg) account for a majority of the cations adsorbed (61% by mass and 74% by molar percent). For the ORNL AF1 adsorbent material, U is the 4th most abundant element adsorbed by mass and 7th most abundant by molar percentage

  9. Chemically immobilized and physically adsorbed PAN/acetylacetone modified mesoporous silica for the recovery of rare earth elements from the waste water-comparative and optimization study.

    PubMed

    Ramasamy, Deepika Lakshmi; Repo, Eveliina; Srivastava, Varsha; Sillanpää, Mika

    2017-05-01

    This study was aimed at the investigation of Rare Earth Element (REE) recovery from aqueous solution by silica gels with 1-(2-Pyridylazo) 2-naphthol (PAN) and acetyl acetone (Acac) modifications. The two different methods of silica gel chelation, such as chemical immobilization with the help of silane coupling agents (3-aminopropyl triethoxysilane (APTES) and 3-aminopropyl trimethoxysilane (APTMS) in this study) and direct physical adsorption onto the silica surface, is compared in terms of their REE removal efficiency. A comparative analysis between adsorption of different REEs for different silica gels is performed and the influence of parameters such as pH, contact time, temperature and initial concentration has been reported. The effect of calcined adsorbents on the adsorption process is also investigated. Characterization studies on silica gels by Fourier transform infrared spectroscopy (FTIR), Scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD) and zeta potential analysis are performed to better understand the relation between physical/chemical attributes of the adsorbents and their impact on the adsorption process. The experimental results are evaluated and optimal conditions for REE adsorption are identified. Chemically immobilized gels demonstrated immense potential for all the REE under study except Sc, for which, physically loaded gels seemed to be more efficient. The removal of REEs could be achieved at lower pHs by chemically immobilized PAN/Acac gels, making it suitable for many practical applications. The amine functionalized gels before chemical immobilization step were compared with PAN/Acac chemically immobilized gels in single as well as multi element system and the significance of chemical immobilization after amine functionalization is also stated.

  10. Improving rice production sustainability by reducing water demand and greenhouse gas emissions with biodegradable films

    NASA Astrophysics Data System (ADS)

    Yao, Zhisheng; Zheng, Xunhua; Liu, Chunyan; Lin, Shan; Zuo, Qiang; Butterbach-Bahl, Klaus

    2017-01-01

    In China, rice production is facing unprecedented challenges, including the increasing demand, looming water crisis and on-going climate change. Thus, producing more rice at lower environmental cost is required for future development, i.e., the use of less water and the production of fewer greenhouse gas (GHG) per unit of rice. Ground cover rice production systems (GCRPSs) could potentially address these concerns, although no studies have systematically and simultaneously evaluated the benefits of GCRPS regarding yields and considering water use and GHG emissions. This study reports the results of a 2-year study comparing conventional paddy and various GCRPS practices. Relative to conventional paddy, GCRPSs had greater rice yields and nitrogen use efficiencies (8.5% and 70%, respectively), required less irrigation (‑64%) and resulted in less total CH4 and N2O emissions (‑54%). On average, annual emission factors of N2O were 1.67% and 2.00% for conventional paddy and GCRPS, respectively. A cost-benefit analysis considering yields, GHG emissions, water demand and labor and mulching costs indicated GCRPSs are an environmentally and economically profitable technology. Furthermore, substituting the polyethylene film with a biodegradable film resulted in comparable benefits of yield and climate. Overall, GCRPSs, particularly with biodegradable films, provide a promising solution for farmers to secure or even increase yields while reducing the environmental footprint.

  11. Micropatterned Surfaces for Atmospheric Water Condensation via Controlled Radical Polymerization and Thin Film Dewetting.

    PubMed

    Wong, Ian; Teo, Guo Hui; Neto, Chiara; Thickett, Stuart C

    2015-09-30

    Inspired by an example found in nature, the design of patterned surfaces with chemical and topographical contrast for the collection of water from the atmosphere has been of intense interest in recent years. Herein we report the synthesis of such materials via a combination of macromolecular design and polymer thin film dewetting to yield surfaces consisting of raised hydrophilic bumps on a hydrophobic background. RAFT polymerization was used to synthesize poly(2-hydroxypropyl methacrylate) (PHPMA) of targeted molecular weight and low dispersity; spin-coating of PHPMA onto polystyrene films produced stable polymer bilayers under appropriate conditions. Thermal annealing of these bilayers above the glass transition temperature of the PHPMA layer led to complete dewetting of the top layer and the formation of isolated PHPMA domains atop the PS film. Due to the vastly different rates of water nucleation on the two phases, preferential dropwise nucleation of water occurred on the PHPMA domains, as demonstrated by optical microscopy. The simplicity of the preparation method and ability to target polymers of specific molecular weight demonstrate the value of these materials wit