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Sample records for tailoring permeant sorption

  1. A FAMILY OF PEROXO-TITANATE MATERIALS TAILORED FOR OPTIMAL STRONTIUM ANDACTINIDE SORPTION

    Energy Technology Data Exchange (ETDEWEB)

    Hobbs, D

    2006-08-07

    Achieving global optimization of inorganic sorbent efficacy, as well as tailoring sorbent specificity for target sorbates would facilitate increased wide-spread use of these materials in applications such as producing potable water or nuclear waste treatment. Sodium titanates have long been known as sorbents for radionuclides; {sup 90}Sr and transuranic elements in particular. We have developed a related class of materials, which we refer to as peroxo-titanates: these are sodium titanates or hydrous titanates synthesized in the presence of or treated post-synthesis with hydrogen peroxide. Peroxo-titanates show remarkable and universal improved sorption behavior with respect to separation of actinides and strontium from Savannah River Site (SRS) nuclear waste simulants. Enhancement in sorption kinetics can potentially result in as much as an order of magnitude increase in batch processing throughput. Peroxo-titanates have been produced by three different synthetic routes: post-synthesis peroxide-treatment of a commercially produced monosodium titanate, an aqueous-peroxide synthetic route, and an isopropanol-peroxide synthetic route. The peroxo-titanate materials are characteristically yellow to orange, indicating the presence of protonated or hydrated Ti-peroxo species; and the chemical formula can be generally written as H{sub v}Na{sub w}Ti{sub 2}O{sub 5}-(xH{sub 2}O)[yH{sub z}O{sub 2}] where (v+w) = 2, z = 0-2, and total volatile species accounts for 25-50 wt % of the solid. Further enhancement of sorption performance is achieved by processing, storing and utilizing the peroxo-titanate as an aqueous slurry rather than a dry powder, and post-synthesis acidification. All three synthesis modifications; addition of hydrogen peroxide, use of a slurry form and acidification can be applied more broadly to the optimization of other metal oxide sorbents and other ion separations processes.

  2. Ultraselective Carbon Molecular Sieve Membranes with Tailored Synergistic Sorption Selective Properties.

    Science.gov (United States)

    Zhang, Chen; Koros, William J

    2017-09-01

    Membrane-based separations can reduce the energy consumption and the CO 2 footprint of large-scale fluid separations, which are traditionally practiced by energy-intensive thermally driven processes. Here, a new type of membrane structure based on nanoporous carbon is reported, which, according to this study, is best referred to as carbon/carbon mixed-matrix (CCMM) membranes. The CCMM membranes are formed by high-temperature (up to 900 °C) pyrolysis of polyimide precursor hollow-fiber membranes. Unprecedentedly high permselectivities are seen in CCMM membranes for CO 2 /CH 4 , N 2 /CH 4 , He/CH 4 , and H 2 /CH 4 separations. Analysis of permeation data suggests that the ultrahigh selectivities result from substantially increased sorption selectivities, which is hypothetically owing to the formation of ultraselective micropores that selectively exclude the bulkier CH 4 molecules. With tunable sorption selectivities, the CCMM membranes outperform flexible polymer membranes and traditional rigid molecular-sieve membranes. The capability to increase sorption selectivities is a powerful tool to leverage diffusion selectivities, and has opened the door to many challenging and economically important fluid separations that require ultrafine differentiation of closely sized molecules. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. Tailored Synthesis of Core-Shell Mesoporous Silica Particles—Optimization of Dye Sorption Properties

    Directory of Open Access Journals (Sweden)

    Andrzej Baliś

    2018-04-01

    Full Text Available Monodisperse spherical silica particles, with solid cores and mesoporous shells (SCMS, were synthesized at various temperatures using a one-pot method utilizing a cationic surfactant template. The temperature of the synthesis was found to significantly affect the diameters of both the cores (ca. 170–800 nm and shells (ca. 11–80 nm of the particles, which can be tailored for specific applications that require a high specific surface area of the nanocarriers (mesoporous shells and simultaneously their mechanical robustness for, e.g., facile isolation from suspensions (dense cores. The applied method enabled the formation of the relatively thick mesoporous shells at conditions below room temperature. Radially ordered pores with narrow distributions of their sizes in 3–4 nm range were found in the shells. The adsorption ability of the SCMS particles was studied using rhodamine 6G as a model dye. Decolorization of the dye solution in the presence of the SCMS particles was correlated with their structure and specific surface area and reached its maximum for the particles synthesized at 15 °C. The presented strategy may be applied for the fine-tuning of the structure of SCMS particles and the enhancement of their adsorption capabilities.

  4. Quantum calculations on water in the KcsA channel cavity with permeant and non-permeant ions

    International Nuclear Information System (INIS)

    Kariev, Alisher M.; Green, Michael E.

    2009-01-01

    Different ions in the pore of the KcsA channel behave differently, and we relate this to their solvation. We show that the selectivity is dependent, in part, on the solvation in the cavity (sometimes referred to as the vestibule, it is the region containing water molecules between the intracellular gate and the selectivity filter at the extracellular end of the pore). We have shown earlier that potassium is more dependent at the upper end of the cavity region on solvation by the threonines there, while sodium ion has more water molecules as ligands. In addition, sodium ion is placed asymmetrically, while potassium is nearly exactly symmetric with respect to the four-fold symmetry of the channel. We have now extended these calculations to rubidium and cesium ions, and find that rubidium solvation resembles that of potassium (and both are permeant ions), while cesium resembles sodium (and both are non-permeant), in terms of the geometry of up to eight hydrating, and four non-hydrating, water molecules. In each case, a maximum of 12 water molecules are relevant to the calculation. The placement of the water molecules in the two cases is essentially the same as found from the electron density in the X-ray structure of Zhou and MacKinnon. For Na + and K + , we show that energy decreases from bulk to the cavity to the lowest position in the selectivity filter (accurate energy could not be calculated for the heavier ions). A separate calculation shows that fixing the Na + ion at the position of the K + minimum, followed by re-optimization produced a significantly modified system, not something that could be produced by thermal fluctuations. Moving the K + into the Na + position in the upper cavity led to a small increase in energy, ∼ 3 k B T, but was accompanied by large shifts in the positions of hydrating waters, which would create a major kinetic barrier. Therefore, thermal fluctuations could not invalidate the conclusions of the main calculations.

  5. Theoretical description of transdermal transport of hydrophilic permeants: application to low-frequency sonophoresis.

    Science.gov (United States)

    Tang, H; Mitragotri, S; Blankschtein, D; Langer, R

    2001-05-01

    Application of ultrasound enhances transdermal transport of drugs (sonophoresis). The enhancement may result from enhanced diffusion due to ultrasound-induced skin alteration and/or from forced convection. To understand the relative roles played by these two mechanisms in low-frequency sonophoresis (LFS, 20 kHz), a theory describing the transdermal transport of hydrophilic permeants in both the absence and the presence of ultrasound was developed using fundamental equations of membrane transport, hindered-transport theory, and electrochemistry principles. With mannitol as the model permeant, the role of convection in LFS was evaluated experimentally with two commonly used in vitro skin models- human cadaver heat-stripped skin (HSS) and pig full-thickness skin (FTS). Our results suggest that convection plays an important role during LFS of HSS, whereas its effect is negligible when FTS is utilized. The theory developed was utilized to characterize the transport pathways of hydrophilic permeants during both passive diffusion and LFS with mannitol and sucrose as two probe molecules. Our results show that the porous pathway theory can adequately describe the transdermal transport of hydrophilic permeants in both the presence and the absence of ultrasound. Ultrasound alters the skin porous pathways by two mechanisms: (1) enlarging the skin effective pore radii, or (2) creating more pores and/or making the pores less tortuous. During passive diffusion, both HSS and FTS exhibit the same skin effective pore radii (r = 28 +/- 13 A). In contrast, during LFS, r within HSS is greatly enlarged (r > 125 A), whereas r within FTS does not change significantly (23 +/- 10 A). The observed different roles of convection during LFS across HSS and FTS can be attributed to the different degrees of structural alteration that these two types of skin undergo during LFS. Copyright 2001 Wiley-Liss, Inc. and the American Pharmaceutical Association.

  6. Effect of humic acid (HA) on sulfonamide sorption by biochars

    International Nuclear Information System (INIS)

    Lian, Fei; Sun, Binbin; Chen, Xi; Zhu, Lingyan; Liu, Zhongqi; Xing, Baoshan

    2015-01-01

    Effect of quantity and fractionation of loaded humic acid (HA) on biochar sorption for sulfonamides was investigated. The HA was applied in two different modes, i.e. pre-coating and co-introduction with sorbate. In pre-coating mode, the polar fractions of HA tended to interact with low-temperature biochars via H-bonding, while the hydrophobic fractions were likely to be adsorbed by high-temperature biochars through hydrophobic and π-π interactions, leading to different composition and structure of the HA adlayers. The influences of HA fractionation on biochar sorption for sulfonamides varied significantly, depending on the nature of interaction between HA fraction and sorbate. Meanwhile, co-introduction of HA with sulfonamides revealed that the effect of HA on sulfonamide sorption was also dependent on HA concentration. These findings suggest that the amount and fractionation of adsorbed HA are tailored by the surface properties of underlying biochars, which differently affect the sorption for organic contaminants. - Highlights: • Effect of quantity and fractionation of coated HA on sorption of sulfonamides by BC was studied. • Fractionation of coated HA is tailored by surface properties of BC. • Roles of HA in BC sorption depend on interaction between HA adlayer and sorbate. • Roles of HA in sulfonamide sorption by BC also depend on HA aqueous concentration. - The quantity and fractionation of adsorbed HA play a major role in sulfonamide sorption by biochars

  7. Permeant lipophilicity and vehicle composition influence accumulation of dyes in hair follicles of human skin.

    Science.gov (United States)

    Grams, Ylva Y; Alaruikka, Soile; Lashley, Lisa; Caussin, Julia; Whitehead, Lynne; Bouwstra, Joke A

    2003-04-01

    In skin and hair research drug targeting to the hair follicle is of great interest. Therefore the influence of permeant lipophilicity and vehicle composition on local accumulation has been examined using confocal laser scanning microscopy (CLSM). Formulations saturated with either Oregon Green 488, Bodipy FL C(5) or Bodipy 564/570 C(5) were prepared. The dyes were applied in citric acid buffer, 8% (w/v) surfactants in citric acid buffer or 8% (w/v) surfactants/20% (w/v) propylene glycol in citric acid buffer. Flow-through diffusion experiments were performed with fresh human scalp skin, after which the skin was imaged using CLSM. Diffusion studies showed for Oregon Green 488 (low lipophilicity) a higher flux when applied in citric acid buffer compared to surfactants. In contrast the fluxes of the more lipophilic dyes (Bodipy FL C(5) and Bodipy 564/570 C(5)) are highest when applied in surfactants/propylene glycol. CLSM studies revealed that follicular accumulation increased with (i) a lipophilic dye and (ii) application of lipophilic dyes in surfactants-propylene glycol. Therefore we conclude that targeting to the hair follicle can be increased by the use of lipophilic drugs in combination with surfactant solutions and propylene glycol.

  8. Tailored ceramics

    International Nuclear Information System (INIS)

    Harker, A.B.

    1988-01-01

    In polyphase tailored ceramic forms two distinct modes of radionuclide immobilization occur. At high waste loadings the radionuclides are distributed through most of the ceramic phases in dilute solid solution, as indicated schematically in this paper. However, in the case of low waste loadings, or a high loading of a waste with low radionuclide content, the ceramic can be designed with only selected phases containing the radionuclides. The remaining material forms nonradioactive phases which provide a degree of physical microstructural isolation. The research and development work with polyphase ceramic nuclear waste forms over the past ten years is discussed. It has demonstrated the critical attributes which suggest them as a waste form for future HLW disposal. From a safety standpoint, the crystalline phases in the ceramic waste forms offer the potential for demonstrable chemical durability in immobilizing the long-lived radionuclides in a geologic environment. With continued experimental research on pure phases, analysis of mineral analogue behavior in geochemical environments, and the study of radiation effects, realistic predictive models for waste form behavior over geologic time scales are feasible. The ceramic forms extend the degree of freedom for the economic optimization of the waste disposal system

  9. Sorption by cation exchange

    International Nuclear Information System (INIS)

    Bradbury, M.H.; Baeyens, B.

    1994-04-01

    A procedure for introducing exchange into geochemical/surface complexation codes is described. Beginning with selectivity coefficients, K c , defined in terms of equivalent fractional ion occupancies, a general expression for the molar based exchange code input parameters, K ex , is derived. In natural systems the uptake of nuclides onto complex sorbents often occurs by more than one mechanism. The incorporation of cation exchange and surface complexation into a geochemical code therefore enables sorption by both mechanisms to be calculated simultaneously. The code and model concepts are tested against sets of experimental data from widely different sorption studies. A proposal is made to set up a data base of selectivity coefficients. Such a data base would form part of a more general one consisting of sorption mechanism specific parameters to be used in conjunction with geochemical/sorption codes to model and predict sorption. (author) 6 figs., 6 tabs., 26 refs

  10. Sorption properties of wool

    Directory of Open Access Journals (Sweden)

    Radetić Maja M.

    2004-01-01

    Full Text Available Strict ecological legislation, especially in highly developed countries, imposed requirements for the purification of industrial effluents and the need for efficient oil clean up after sea and inland water spills. Although numerous processes have been developed, the application of sorbents is still one of the most efficient methods to remove heavy metal ions, dyes and crude oil from water. Recently, special attention was paid to sorbents based on natural fibres. A review of studies concerning the sorption properties of wool is presented in this paper. The presence of various functional groups on the wool fibre surface contributes to the efficient sorption of heavy metal ions and dyes. A hydrophobic, scaly surface and fibre crimp strongly influence the high sorption capacity of wool for oil. Wool has great sorption potential even as a recycled material. Accordingly, it can be used as a viable substitute to commercially available synthetic sorbents that show poor biodegradab ility.

  11. Sorption of nickel on chitosan

    International Nuclear Information System (INIS)

    Pivarciova, O.; Rosskopfova, O.; Galambos, M.

    2012-01-01

    This work was focused on the study of sorption properties of nickel on chitosan. Sorption of nickel on the selected sorbents was studied by batch method. Radionuclide 63 Ni was used as a tracer. Langmuir isotherm was used for interpretation of the sorption of nickel on chitosan by varying the concentration of Ni 2 + cations in aqueous phase.

  12. Novel insights for permeant lead structures through in vitro skin diffusion assays of Prunus lusitanica L., the Portugal Laurel

    Science.gov (United States)

    Costa, Maria do Céu; Duarte, Patrícia; Neng, Nuno R.; Nogueira, José M. F.; Costa, Filomena; Rosado, Catarina

    2015-01-01

    As a contribution for the generation of libraries in which a natural product (NP) is used as the guiding structure, this work sought to investigate molecular features of triterpenes as deliver leads to cross the stratum corneum at a significant rate. Seeking a bioguided investigation of the dermocosmetic lead-like potential of triterpenes in Prunus lusitanica L., various extracts were obtained by two different methods (Soxhlet extractor and Accelerated Solvent Extraction-ASE) and analyzed by GC-MS and NMR. In vitro assays were conducted to quantify the friedelin 1 and crude plant extract permeation through a membrane of polydimethylsiloxane (PDMS), as well as their skin penetration enhancement capacity using two model molecules, caffeine 19 and ibuprofen 20. Friedelin 1 was identified as the major component (16-77%, GC) with isolated yield of 51% w/w (94%, GC) from Soxhlet residue (1.7% p/p) of the dried aerial parts of the plant harvested when in early flowering stage. Friedelin 1 promoted the penetration of the lipophilic molecule 20, however, it did not influence the permeation of the hydrophilic permeant 20. On the other hand, the crude extract acted as a retardant of the penetration of both substances. Molecular characteristics for the applicability of P. lusitanica L. in the development of dermocosmetics, as well as a new potential use for friedelin 1 in particular, are demonstrated. Probable mechanisms for chemical penetration enhancement using triterpenes as models for transdermal administration are herein discussed.

  13. Tailored ceramics. Chapter 5

    International Nuclear Information System (INIS)

    Haker, A.B.

    1988-01-01

    In the light of the broad variation in US high-level waste (HLW) types and the uncertainties in future waste production, research on the Rockwell International Science Center has focussed on developing a generic technology for the consolidation of high-level wastes into polyphase ceramics. The basic approach has been to 'tailor' wste compositions with chemical additives so that upon consolidation a dense ceramic assemblage is formed that chemically binds the waste species into known phases. This chapter deals with tailored ceramics for current and future high-level waste compositions. Section 2 gives a historical review of the development of tailored ceramics. Section 3 deals with tailored ceramics designed for specific HLW compositions and with microstructure and phase development. Section 4 discusses chemical and physical properties of tailored ceramic waste forms. In section 5 the various processing steps involved in converting HLW to polycrystalline ceramic forms are described. (author). 159 refs.; 20 figs.; 14 tabs

  14. Technetium Sorption Media Review

    International Nuclear Information System (INIS)

    Duncan, J.B.; Kelly, S.E.; Robbins, R.A.; Adams, R.D.; Thorson, M.A.; Haass, C.C.

    2011-01-01

    This report presents information and references to aid in the selection of 99Tc sorption media for feasibility studies regarding the removal of 99Tc from Hanford's low activity waste. The report contains literature search material for sorption media (including ion exchange media) for the most tested media to date, including SuperLig 639, Reillex HPQ, TAM (Kruion), Purolite A520E and A530E, and Dowex 1X8. The U.S. Department of Energy (DOE), Office of River Protection (ORP) is responsible for management and completion of the River Protection Project (RPP) mission, which comprises both the Hanford Site tank farms and the Waste Treatment and Immobilization Plant (WTP). The RPP mission is to store, retrieve and treat Hanford's tank waste; store and dispose of treated wastes; and close the tank farm waste management areas and treatment facilities in a safe, environmentally compliant, cost-effective and energy-effective manner.

  15. TECHNETIUM SORPTION MEDIA REVIEW

    Energy Technology Data Exchange (ETDEWEB)

    DUNCAN JB; KELLY SE; ROBBINS RA; ADAMS RD; THORSON MA; HAASS CC

    2011-08-25

    This report presents information and references to aid in the selection of 99Tc sorption media for feasibility studies regarding the removal of 99Tc from Hanford's low activity waste. The report contains literature search material for sorption media (including ion exchange media) for the most tested media to date, including SuperLig 639, Reillex HPQ, TAM (Kruion), Purolite A520E and A530E, and Dowex 1X8. The U.S. Department of Energy (DOE), Office of River Protection (ORP) is responsible for management and completion of the River Protection Project (RPP) mission, which comprises both the Hanford Site tank farms and the Waste Treatment and Immobilization Plant (WTP). The RPP mission is to store, retrieve and treat Hanford's tank waste; store and dispose of treated wastes; and close the tank farm waste management areas and treatment facilities in a safe, environmentally compliant, cost-effective and energy-effective manner.

  16. Tailored Porous Materials

    Energy Technology Data Exchange (ETDEWEB)

    BARTON,THOMAS J.; BULL,LUCY M.; KLEMPERER,WALTER G.; LOY,DOUGLAS A.; MCENANEY,BRIAN; MISONO,MAKOTO; MONSON,PETER A.; PEZ,GUIDO; SCHERER,GEORGE W.; VARTULI,JAMES C.; YAGHI,OMAR M.

    1999-11-09

    Tailoring of porous materials involves not only chemical synthetic techniques for tailoring microscopic properties such as pore size, pore shape, pore connectivity, and pore surface reactivity, but also materials processing techniques for tailoring the meso- and the macroscopic properties of bulk materials in the form of fibers, thin films and monoliths. These issues are addressed in the context of five specific classes of porous materials: oxide molecular sieves, porous coordination solids, porous carbons, sol-gel derived oxides, and porous heteropolyanion salts. Reviews of these specific areas are preceded by a presentation of background material and review of current theoretical approaches to adsorption phenomena. A concluding section outlines current research needs and opportunities.

  17. Sorption of actinides onto nanodiamonds

    Energy Technology Data Exchange (ETDEWEB)

    Buchatskaya, Yulia; Romanchuk, Anna; Yakovlev, Ruslan; Kulakova, Inna [Lomonosov Moscow State Univ., Moscow (Russian Federation). Dept. of Chemistry; Shiryaev, Andrei [Russian Academy of Sciences, Moscow (Russian Federation). Frumkin Institute of Physical Chemistry and Electrochemistry; Russian Academy of Sciences, Moscow (Russian Federation). Inst. of Geology of Ore Deposits, Petrography, Mineralogy and Geochemistry; Kalmykov, Stepan [Lomonosov Moscow State Univ., Moscow (Russian Federation). Dept. of Chemistry; Russian Academy of Sciences, Moscow (Russian Federation). Frumkin Institute of Physical Chemistry and Electrochemistry; Russian Academy of Sciences, Moscow (Russian Federation). Vernadsky Institute of Geochemistry and Analytical Chemistry

    2015-06-01

    Detonation nanodiamonds (ND) present a significant part of nanocarbons group, which could be produced on commercial scale by detonation of explosives in a closed chamber. Their unique properties of high surface area, low weight and radiation resistance make ND a prospective candidate for applications in sorption processes in radiochemistry. To study the influence of surface chemistry on sorption properties, apristine sample of ND was treated with acids and hydrogen. The surface chemistry of the samples was characterised by infrared spectroscopy, X-ray photoelectron spectroscopy and Boehm titration. The sorption properties of ND were tested fordifferent radionuclides. The sorption capacity of ND was shown to be higher than those of commonly used radionuclide sorbents like activated carbon and compariable to other members of nanocarbon group like graphene oxide and carbon nanotubes. The sorption properties were shown to be influenced by the presence of oxygen-containing groups on the surface of ND. This represents an opportunity to increase the sorption capacity of ND.

  18. Uranium sorption by tannin resins

    International Nuclear Information System (INIS)

    Olivares Rieumont, S.; Martinez Luzardo, J.; Torres Hernandez, J.; Lima Cazorla, D. de la Rosa.

    1998-01-01

    The sorption of uranium by immobilised Eucalyptus Saligna Sm. and Lysiloma latisiliqua L tannins was investigated. Immobilization condition were analyzed. These resins resulted suitable adsorbent for the concentration of uranium from aqueous systems. The sorption of uranium is pH dependent. At pH 5.5 maximum in sorption capacity is registered. The presence of appreciable amount of sodium chloride do not have any effect on uranium removal. Carbonate and calcium ions in concentrations similar to these that could be found in sea water and other natural water do not decrease the uranium uptake. Tannin resins can be used several times without an appreciable decay of their sorption capacity

  19. Effect of light sources and curing mode techniques on sorption, solubility and biaxial flexural strength of a composite resin.

    Science.gov (United States)

    Carvalho, Andreia Assis; Moreira, Francine do Couto Lima; Fonseca, Rodrigo Borges; Soares, Carlos José; Franco, Eduardo Batista; Souza, João Batista de; Lopes, Lawrence Gonzaga

    2012-01-01

    Adequate polymerization plays an important role on the longevity of the composite resin restorations. The aim of this study was to evaluate the effect of light-curing units, curing mode techniques and storage media on sorption, solubility and biaxial flexural strength (BFS) of a composite resin. Two hundred and forty specimens were made of one composite resin (Esthet-X) in a stainless steel mold (2 mm x 8 mm Ø), and divided into 24 groups (n=10) established according to the 4 study factors: light-curing units: quartz tungsten halogen (QTH) lamp and light-emitting diodes (LED); energy densities: 16 J/cm² and 20 J/cm²; curing modes: conventional (CM) and pulse-delay (PD); and permeants: deionized water and 75% ethanol for 28 days. Sorption and solubility tests were performed according to ISO 4049:2000 specifications. All specimens were then tested for BFS according to ASTM F394-78 specification. Data were analyzed by three-way ANOVA followed by Tukey, Kruskal-Wallis and Mann-Whitney tests (α=0.05). In general, no significant differences were found regarding sorption, solubility or BFS means for the light-curing units and curing modes (p>0.05). Only LED unit using 16 J/cm² and PD using 10 s produced higher sorption and solubility values than QTH. Otherwise, using CM (16 J/cm²), LED produced lower values of BFS than QTH (pcuring units using 16 and 20 J/cm² by CM and PD curing modes produced no influence on the sorption, solubility or BFS of the tested resin.

  20. Review of the sorption of actinides on natural minerals

    International Nuclear Information System (INIS)

    Beall, G.W.

    1981-01-01

    Over the past few years, a large body of data concerning sorption of actinides on geologic media has been built in connection with high-level-waste disposal. The primary aim of the work has been to allow predictions of the migration behavior of these radionuclides in the case of a breach of the repository that allowed groundwater flow through the repository. As a result of this work, some new backfill materials specifically tailored for the actinides have also been designed. Several major mechanisms of sorption that appear to dominate the sorption of actinides have emerged from these studies. These mechanisms can be divided into solution reactions dominated by hydrolysis, chemisorption reactions, and oxidation-reduction reactions. Each of these mechanisms will be discussed in detail, with experimental examples. Surprisingly, one mechanism, cation exchange, does not play an important role; why it fails to operate in any significant way in the environmental pH region will be discussed. The implications of the sorption mechanisms for waste forms and backfill materials will be discussed in detail. These discussions will center primarily around the valence state of the actinide in various waste forms and the effect of various anions on leachability from waste forms and backfill materials

  1. Tailored Barium Swallow Study

    Science.gov (United States)

    ... Different textures of food are often given. The barium is a contrast material that makes the food and liquid show ... MRI Intravenous Contrast Information MRI with or without Contrast Small Bowel Follow Through (SBFT) Tailored Barium Swallow Study The Upper GI Study (GI Series) ...

  2. Sorption properties of carbon nanostructures

    International Nuclear Information System (INIS)

    Eletskii, Aleksandr V

    2004-01-01

    The current status of research in sorption properties of carbon nanotubes (CNTs) is reviewed. The structural peculiarities of CNTs, determining their sorption characteristics, are considered. The mechanisms of sorption of gaseous and condensed substances by such structures are analyzed. Special attention is paid to the problem of using CNTs for storing hydrogen and other gaseous substances. Methods for filling CNTs with liquid materials, based on capillary phenomena and wetting the graphite surface of the CNT with liquids of various nature, are considered. Properties of 'peapods' formed as a result of filling single-walled CNTs with fullerene molecules are reviewed. Also considered are perspectives on the applied usage of the sorption properties of CNTs in electrochemical and fuel cells, and material storage devices, as well as for producing superminiature metallic conductors. (reviews of topical problems)

  3. Sorption of Pesticides to Natural and Synthetic Nanoparticles

    Science.gov (United States)

    Guluzada, Leyla; Luo, Leilei; Pattky, Martin; Anwander, Reiner; Huhn, Carolin; Haderlein, Stefan

    2017-04-01

    Many organic pollutants tend to associate with particles in environment. Such interactions with solid surfaces may not only alter the reactivity and bioavailability of pesticides, but also their uptake. This alteration may occur both in the way and in the amount the compound enters the organisms. In its turn this may change the overall effects of these compounds on organisms and ecosystems. The main goal of the work presented here is to provide mechanistic information on the sorbate-sorbent interactions between nanoparticles and a set of pesticides under environmentally relevant and physiological conditions. As such, the work is part of the interdisciplinary graduate research program EXPAND at the University of Tübingen investigating molecular interactions between pesticides and particles to elucidate how such interactions impact the toxicological effects. To this end, natural and synthetic nanoparticles covering a wide range of physicochemical properties and pesticides for different target organisms were used. Sorption experiments were carried out with insecticides (imidacloprid; thiacloprid), fungicides (hexaconazole; propiconazole) and herbicides (glyphosate with its metabolite AMPA; glufosinate). The choice of the pesticides was based on their environmental significance and their mode of action. Both engineered nanoparticles with tailored surface properties and nanoparticles of natural origin were characterized and applied to cover various modes of sorptive interactions with the pesticides. The impact of various geochemical and physiological conditions including pH, temperature, ionic strength, background electrolytes and DOM (dissolved organic matter) on the sorption of the pesticides to nanoparticles was studied. Sorption kinetics and sorption isotherms were determined and the results are discussed in terms of predominant sorption mechanisms and the suitability of certain nanoparticles for toxicological studies in the framework of the EXPAND project.

  4. Sorption of radionuclides on Yucca Mountain tuffs

    International Nuclear Information System (INIS)

    Meijaer, A.; Triay, I.; Knight, S.; Cisneros, M.

    1989-01-01

    A substantial database of sorption coefficients for important radionuclides on Yucca Mountain tuffs has been obtained by Los Alamos National Laboratory over the past ten years. Current sorption studies are focussed on validation questions and augmentation of the existing database. Validation questions concern the effects of the use of crushed instead of solid rock samples in the batch experiments, the use of oversaturated stock solutions, and variations in water/rock ratios. Sorption mechanisms are also being investigated. Database augmentation activities include determination of sorption coefficients for elements with low sorption potential, sorption on psuedocolloids, sorption on fracture lining minerals, and sorption kinetics. Sorption can provide an important barrier to the potential migration of radionuclides from the proposed repository within Yucca Mountain to the accessible environment. In order to quantify this barrier, sorption coefficients appropriate for the Yucca Mountain groundwater system must be obtained for each of the important radionuclides in nuclear waste. Los Alamos National Laboratories has conducted numerous batch (crushed-rock) sorption experiments over the past ten years to develop a sorption coefficient database for the Yucca Mountain site. In the present site characterization phase, the main goals of the sorption test program will be to validate critical sorption coefficients and to augment the existing database where important data are lacking. 11 refs., 1 fig., 3 tabs

  5. Tailored Random Graph Ensembles

    International Nuclear Information System (INIS)

    Roberts, E S; Annibale, A; Coolen, A C C

    2013-01-01

    Tailored graph ensembles are a developing bridge between biological networks and statistical mechanics. The aim is to use this concept to generate a suite of rigorous tools that can be used to quantify and compare the topology of cellular signalling networks, such as protein-protein interaction networks and gene regulation networks. We calculate exact and explicit formulae for the leading orders in the system size of the Shannon entropies of random graph ensembles constrained with degree distribution and degree-degree correlation. We also construct an ergodic detailed balance Markov chain with non-trivial acceptance probabilities which converges to a strictly uniform measure and is based on edge swaps that conserve all degrees. The acceptance probabilities can be generalized to define Markov chains that target any alternative desired measure on the space of directed or undirected graphs, in order to generate graphs with more sophisticated topological features.

  6. Sorption on inactive repository components

    International Nuclear Information System (INIS)

    Gardiner, M.P.; Smith, A.J.; Williams, S.J.

    1990-11-01

    The near-field of an intermediate level/low level radioactive waste repository will contain significant quantities of iron and steel, Magnox and Zircaloy. Their corrosion products may possess significant sorption capacity for radioelements. The sorption of americium and plutonium onto magnesium hydroxide, zirconium hydroxide, colloidal magnetite and colloidal haematite has been studied under conditions typical of the porewater of a cementitious near-field. R D values ≥ 10 5 m g -1 were measured for both actinides on the oxides and hydroxides. These values are at least as great as those measured on crushed 3:1 Blast Furnace Slag/Ordinary Portland cement. Competitive sorption experiments have shown that sorption onto the corrosion products does not take place in preference to that on the cement or the converse. Magnetite and haematite colloids are positively charged in cement-equilibrated water whilst zirconium hydroxide is negatively charged. Crushed cement was found to be positively charged. Simple experiments show that only a small proportion of haematite colloids is potentially mobile through a column of crushed cement. (author)

  7. Sorption on inactive repository components

    International Nuclear Information System (INIS)

    Gardiner, M.P.; Smith, A.J.; Williams, S.J.

    1990-07-01

    The near-field of an intermediate level/low level radioactive waste repository will contain significant quantities of iron and steel, Magnox and Zircaloy. Their corrosion products may possess significant sorption capacity for radioelements. The sorption of americium and plutonium onto magnesium hydroxide, zirconium hydroxide, colloidal magnetite and colloidal haematite has been studied under conditions typical of the porewater of a cementitious near-field. R D values ≥ 10 5 ml g -1 were measured for both actinides on the oxides and hydroxides. These values are at least as great at those measured on crushed 3:1 Blast Furnace Slag/Ordinary Portland Cement. Competitive sorption experiments have shown that sorption onto the corrosion products does not take place in preference to that on the cement or the converse. Magnetite and haematite colloids are positively charged in cement-equilibrated water whilst zirconium hydroxide is negatively charged. Crushed cement was found to be positively charged. Simple experiments show that only a small proportion of haematite colloids is potentially mobile through a column of crushed cement. (author)

  8. Tailored thrombolytic therapy. A perspective

    NARCIS (Netherlands)

    M.L. Simoons (Maarten); A.E.R. Arnold (Alfred)

    1993-01-01

    textabstractBACKGROUND. In contrast with current standard regimens, it seems more appropriate to tailor thrombolytic therapy to individual patient characteristics. A proposed model for such tailored therapy is based on individual assessment of benefits and risks of thrombolytic therapy, taking into

  9. Sorption of perfluoroalkyl substances in sewage sludge.

    Science.gov (United States)

    Milinovic, Jelena; Lacorte, Silvia; Rigol, Anna; Vidal, Miquel

    2016-05-01

    The sorption behaviour of three perfluoroalkyl substances (PFASs) (perfluorooctanesulfonic acid (PFOS), perfluorooctanoic acid (PFOA) and perfluorobutanesulfonic acid (PFBS)) was studied in sewage sludge samples. Sorption isotherms were obtained by varying initial concentrations of PFOS, PFOA and PFBS. The maximum values of the sorption solid-liquid distribution coefficients (Kd,max) varied by almost two orders of magnitude among the target PFASs: 140-281 mL g(-1) for PFOS, 30-54 mL g(-1) for PFOA and 9-18 mL g(-1) for PFBS. Freundlich and linear fittings were appropriate for describing the sorption behaviour of PFASs in the sludge samples, and the derived KF and Kd,linear parameters correlated well. The hydrophobicity of the PFASs was the key parameter that influenced their sorption in sewage sludge. Sorption parameters and log(KOW) were correlated, and for PFOS (the most hydrophobic compound), pH and Ca + Mg status of the sludge controlled the variation in the sorption parameter values. Sorption reversibility was also tested from desorption isotherms, which were also linear. Desorption parameters were systematically higher than the corresponding sorption parameters (up to sixfold higher), thus indicating a significant degree of irreversible sorption, which decreased in the sequence PFOS > PFOA > PFBS.

  10. PHOSPHORUS SORPTION ISOTHERMS AND EXTERNAL ...

    African Journals Online (AJOL)

    ACSS

    both models fitted well with the P sorption data of the soils. The adsorption maxima (Xm) and bonding energy (b) values of the soils derived from Langmuir model were in the ranges of 560-833 mg P kg-1 and 0.16-20 L kg-1, respectively. The Freundlich capacity factor (Kf) ranged from 237 to 1200 mg kg-1.The EPRs of the ...

  11. Sorption Energy Maps of Clay Mineral Surfaces

    International Nuclear Information System (INIS)

    Cygan, Randall T.; Kirkpatrick, R. James

    1999-01-01

    A molecular-level understanding of mineral-water interactions is critical for the evaluation and prediction of the sorption properties of clay minerals that may be used in various chemical and radioactive waste disposal methods. Molecular models of metal sorption incorporate empirical energy force fields, based on molecular orbital calculations and spectroscopic data, that account for Coulombic, van der Waals attractive, and short-range repulsive energies. The summation of the non-bonded energy terms at equally-spaced grid points surrounding a mineral substrate provides a three dimensional potential energy grid. The energy map can be used to determine the optimal sorption sites of metal ions on the exposed surfaces of the mineral. By using this approach, we have evaluated the crystallographic and compositional control of metal sorption on the surfaces of kaolinite and illite. Estimates of the relative sorption energy and most stable sorption sites are derived based on a rigid ion approximation

  12. PCB Congener Sorption To Carbonaceous Sediment Components: Macroscopic Comparison And Characterization Of Sorption Kinetics And Mechanism

    Science.gov (United States)

    Sorption of polychlorinated biphenyls (PCBs) to sediment is a key process in determining their mobility, bioavailability, and chemical decomposition in aquatic environments. In order to examine the validity of currently used interpretation approaches for PCBs sorption, comparati...

  13. Active Control of Tailored Laminates

    Data.gov (United States)

    National Aeronautics and Space Administration — Part of a proposed suite of technologies to enable a fully morphing seamless wing, this effort focuses on tailoring composite materials to enhance structural...

  14. Uranium sorption from sulfate solutions by polyampholytes

    International Nuclear Information System (INIS)

    Rychkov, V.N.

    2003-01-01

    Uranium sorption from sulfate solutions by aminocarboxylic and aminophosphoric acid polyampholytes is studied. Effect of concentration of sulfuric acid, ammonium sulfate, ph value of solution and concentration of metal in solution on uranium absorptivity by ampholytes is studied. It is determined that sorption process is described satisfactorily by K d =KC p Z equation. Basing on calculated data on uranium ion state in sulfate solutions, analysis of results and data of IR spectroscopy conclusions about uranium sorption process mechanism are made [ru

  15. Applicability of microautoradiography to sorption studies

    International Nuclear Information System (INIS)

    Thompson, J.L.; Wolfsberg, K.

    1979-01-01

    The technique of microautoradiography was applied to the study of the sorption of uranium and americium on five rock types which exist at the Nevada Test Site. It was found that autoradiograms could be prepared in a few days which would allow the specific minerals responsible for sorption to be identified. Furthermore, the state of aggregation of the sorbed species was clearly indicated. It was concluded that microautoradiography was a useful adjunct to currently used methods for studying sorption of certain radionuclides

  16. Moisture sorption in naturally coloured cotton fibres

    Science.gov (United States)

    Ceylan, Ö.; De Clerck, K.

    2017-10-01

    Increasing environmental concerns have stimulated an interest in naturally coloured cottons. As many commercial and technical performance aspects of cotton fibres are influenced by their response towards atmospheric humidity, an in-depth research on moisture sorption behaviour of these fibres using dynamic vapour sorption is carried out. Significant differences were observed in sorption capacity and hysteresis behaviour of brown and green cotton fibres. These differences are mainly attributed to the variations in maturity and crystallinity index of the fibres. This study provides valuable insights into the moisture sorption behaviour of naturally coloured cotton fibres.

  17. Strontium sorption on Savannah River Plant soils

    International Nuclear Information System (INIS)

    Hoeffner, S.L.

    1984-12-01

    A laboratory study of strontium-85 sorption was conducted using Savannah River Plant soil and groundwater from the low-level waste burial ground. Systematic variation of soil and water composition indicates that strontium sorption is most strongly a function of pH. Changes in clay content and in K + , Ca 2+ , or Mg 2+ concentrations influence strontium sorption indirectly through the slight pH changes which result. The ions Na + , Cl - , and NO 3 - have no effect. Ferrous ion, added to groundwater to simulate the conditions of water at the bottom of waste trenches, did not account for low strontium sorption observed with some trench waters

  18. Matrix supported tailored polymer for solid phase extraction of fluoride from variety of aqueous streams

    International Nuclear Information System (INIS)

    Thakur, Neha; Kumar, Sanjukta A.; Wagh, D.N.; Das, Sadananda; Pandey, Ashok K.; Kumar, Sangita D.; Reddy, A.V.R.

    2012-01-01

    Highlights: ► Th complexed with poly (bis[2-(methacryloyloxy)-ethyl]phosphate) as tailored polymer membranes. ► Membranes offered high capacity and selectivity for fluoride in aqueous media. ► Quantitative uptake (80 ± 5%) of fluoride. ► Fast sorption kinetics. ► Reusability of polymer membranes. - Abstract: Fluoride related health hazards (fluorosis) are a major environmental problem in many regions of the world. It affects teeth; skeleton and its accumulation over a long period can lead to changes in the DNA structure. It is thus absolutely essential to bring down the fluoride levels to acceptable limits. Here, we present a new inorganic–organic hybrid polymer sorbent having tailored fixed-sites for fluoride sorption. The matrix supported poly (bis[2-(methacryloyloxy)-ethyl]phosphate) was prepared by photo-initiator induced graft-polymerization in fibrous and microporous (sheet) host poly(propylene) substrates. These substrates were conditioned for selective fluoride sorption by forming thorium complex with phosphate groups on bis[2-methacryloyloxy)-ethyl] phosphate (MEP). These tailored sorbents were studied for their selectivity towards fluoride in aqueous media having different chemical conditions. The fibrous sorbent was found to take up fluoride with a faster rate (15 min for ≈76% sorption) than the sheet sorbent. But, the fluoride loading capacity of sheet sorbent (4320 mg kg −1 ), was higher than fibrous and any other sorbent reported in the literature so far. The sorbent developed in the present work was found to be reusable after desorption of fluoride using NaOH solution. It was tested for solid phase extraction of fluoride from natural water samples.

  19. Phosphorus sorption isotherms and external phosphorus ...

    African Journals Online (AJOL)

    Information on P sorption characteristics of soils is important for making profitable P fertiliser recommendations and designing appropriate P management strategies for improving crop productivity. An experiment was conducted to determine the P sorption capacities and external P requirements (EPR) of some soils of ...

  20. New composite materials to metal sorption

    International Nuclear Information System (INIS)

    Annenkov, V.V.; Danilovtseva, E.N.; Filina, E.A.; Trofimov, B.A.

    2002-01-01

    Complexing-active polymers are promising substances for detoxication of radioactive elements from the polluted soils and natural waters. Tis work is devoted to searching of new polymeric compositions for detoxication of soils and waters from heavy metals. Three systems (azole-carboxylic polyampholytes, polymer-polymer complexes of poly(1-vinylimidazole) (PVI), Ai- and Al-based organo/inorganic composites) were discussed. Sorption properties of new composites were studied using Cu 2+ ions as an example. The sorption equilibrium range time is equals to 20-60 min, sorption capacity attains 280 mg/g. The most effective sorbents are composites on the basis of PVI, poly(4-vinylpyridine) decrease sorption capacity due to hydrophobia of this polymer. Thus, composites on the basis of nitrogen-containing polymers are promising systems for heavy materials sorption. Introduction of Si-, Al-hydroxides into composites allows to decrease cost of the materials and increase their nature-compatibility

  1. Sorption of mercury on chemically synthesized polyaniline

    International Nuclear Information System (INIS)

    Remya Devi, P.S.; Verma, R.; Sudersanan, M.

    2006-01-01

    Sorption of inorganic mercury (Hg 2+ ) and methyl mercury, on chemically synthesized polyaniline, in 0.1-10N HCl solutions has been studied. Hg 2+ is strongly sorbed at low acidities and the extent of sorption decreases with increase in acidity. The sorption of methyl mercury is very low in the HCl concentration range studied. Sorption of Hg 2+ on polyaniline in 0.1-10N LiCl and H 2 SO 4 solutions has also been studied. The analysis of the data indicates that the sorption of Hg 2+ depends on the degree of protonation of polyaniline and the nature of mercury(II) chloride complexes in solution. X-ray photoelectron spectroscopy analysis (XPS) of polyaniline sorbed with mercury show that mercury is bound as Hg 2+ . Sorbed mercury is quantitatively eluted from polyaniline with 0.5N HNO 3 . Polyaniline can be used for separation and pre-concentration of inorganic mercury from aqueous samples. (author)

  2. Cobalt sorption onto Savannah River Plant soils

    International Nuclear Information System (INIS)

    Hoeffner, S.L.

    1985-06-01

    A laboratory study of cobalt-60 sorption was conducted using Savannah River Plant soil and groundwater from the low-level waste burial ground. Systematic variation of soil and water composition indicates that cobalt sorption is most strongly a function of pH. Over a pH range of 2 to 9, the distribution coefficient ranged from 2 to more than 10,000 mL/g. Changes in clay content and in K + , Ca 2+ , or Mg 2+ concentrations influence cobalt sorption indirectly through the slight pH changes which result. The ions Na + , Cl - , and NO 3 - have no effect on cobalt sorption. Ferrous ion, added to groundwater to simulate the condition of water at the bottom of the waste trenches, accounts for part of the decrease in cobalt sorption observed with trench waters. 17 refs., 3 figs., 4 tabs

  3. Chemical equilibria in bio sorption

    International Nuclear Information System (INIS)

    Romero, A.; Gonzalez, F.; Ballester, A.; Blazquez, M. L.; Munoz, J.A.

    2007-01-01

    An experimental study of bio sorption was carried out using six different kinds of algae and five different heavy metals (cadmium, copper, nickel, lead and zinc). Experimental data fitted very well to langmuir's model and this allowed to predict the behaviour of the biomass under specific working conditions. Using the equations of the model under different initial assumptions, a series of mathematical calculations were done for mono metallic, bimetallic and tri metallic systems. the most complicated calculation is that in which, knowing the initial metal concentration (C 0 ), it is necessary to calculate the conditions reached at the equilibrium, this is, q e and C e . This assumption is of great interest from the point of view of the actual applicability of the process. However, in this case, it is necessary to solve very complex mathematical equations which, for multi metallic systems, are of degree n+1, where n is the number of ions present in solution. The excellent correlation between experimental and theoretical data demonstrates that the bio sorption process can be modelling. (Author) 18 refs

  4. d-Tubocurarine and Berbamine: Alkaloids That Are Permeant Blockers of the Hair Cell's Mechano-Electrical Transducer Channel and Protect from Aminoglycoside Toxicity

    Directory of Open Access Journals (Sweden)

    Nerissa K. Kirkwood

    2017-09-01

    Full Text Available Aminoglycoside antibiotics are widely used for the treatment of life-threatening bacterial infections, but cause permanent hearing loss in a substantial proportion of treated patients. The sensory hair cells of the inner ear are damaged following entry of these antibiotics via the mechano-electrical transducer (MET channels located at the tips of the hair cell's stereocilia. d-Tubocurarine (dTC is a MET channel blocker that reduces the loading of gentamicin-Texas Red (GTTR into rat cochlear hair cells and protects them from gentamicin treatment. Berbamine is a structurally related alkaloid that reduces GTTR labeling of zebrafish lateral-line hair cells and protects them from aminoglycoside-induced cell death. Both compounds are thought to reduce aminoglycoside entry into hair cells through the MET channels. Here we show that dTC (≥6.25 μM or berbamine (≥1.55 μM protect zebrafish hair cells in vivo from neomycin (6.25 μM, 1 h. Protection of zebrafish hair cells against gentamicin (10 μM, 6 h was provided by ≥25 μM dTC or ≥12.5 μM berbamine. Hair cells in mouse cochlear cultures are protected from longer-term exposure to gentamicin (5 μM, 48 h by 20 μM berbamine or 25 μM dTC. Berbamine is, however, highly toxic to mouse cochlear hair cells at higher concentrations (≥30 μM whilst dTC is not. The absence of toxicity in the zebrafish assays prompts caution in extrapolating results from zebrafish neuromasts to mammalian cochlear hair cells. MET current recordings from mouse outer hair cells (OHCs show that both compounds are permeant open-channel blockers, rapidly and reversibly blocking the MET channel with half-blocking concentrations of 2.2 μM (dTC and 2.8 μM (berbamine in the presence of 1.3 mM Ca2+ at −104 mV. Berbamine, but not dTC, also blocks the hair cell's basolateral K+ current, IK,neo, and modeling studies indicate that berbamine permeates the MET channel more readily than dTC. These studies reveal key properties of

  5. Sorption of radionuclides on mineral surfaces

    International Nuclear Information System (INIS)

    Berry, J.A.; Cowper, M.M.; Green, A.; Jefferies, N.L.; Linklater, C.M.

    1991-01-01

    The sorption of the radioelements uranium, caesium, radium and americium onto rocks and single mineral phases is being investigated in order to improve the understanding of sorption processes. The spatial distribution of uranium onto rock surfaces has been investigated by immersing thin sections of granite and sandstone into 0.8 ppm uranium solutions for periods of up to three months. The sections have been examined by a number of techniques such as RBS, PIXE and dynamic SIMS. In granite thin sections, uranium is preferentially sorbed onto phyllosilicate minerals (10 -8 g cm -2 ). In the sandstone, iron-rich phases dominate sorption. Enhanced levels of uranium sorption (10 -7 g cm -2 ) were observed on surfaces enriched with iron. Even within single mineral phases, inhomogeneities have been detected. Solution chemistry was also an important factor in uranium sorptive behaviour, with sorption from groundwater inhibited by comparison to that on mineralogically similar thin sections immersed in ultra-high purity water. The sorption of caesium from ultra-high purity water and a synthetic groundwater (0.065M NaCl brine) onto quartz, calcite and kaolinite has been studied by the batch sorption technique. Both calcite and quartz are nonsorbing whilst kaolinite is moderately sorbing. R D values from pure water experiments are a factor of 30 higher than those from groundwater, which reflects competition for cation exchange sites on the kaolinite surface between caesium and sodium and potassium in the groundwater. (author)

  6. Sorption behavior of cesium onto bentonite colloid

    International Nuclear Information System (INIS)

    Iijima, Kazuki; Masuda, Tsuguya; Tomura, Tsutomu

    2004-01-01

    It is considered that bentonite colloid might be generated from bentonite which will be used as buffer material in geological disposal system, and can facilitate the migration of radionuclides by means of sorption. In order to examine this characteristic, sorption and desorption experiments of Cs onto bentonite colloid were carried out to obtain its distribution coefficient (Kd) and information on the reversibility of its sorption. In addition, particle size distribution and shape of colloid were investigated and their effect on the sorption behavior was discussed. Kds for Cs were around 20 m 3 /kg for sorption and 30 m 3 /kg for desorption, in which sorbed Cs was desorbed by 8.4x10 -4 mol/l of NaCl solution. These values did not show any dependencies on Cs concentration and duration of sorption and desorption. The first 20% of sorbed Cs was desorbed reversibly at least. Most of colloidal particles were larger than 200 nm and TEM micrographs showed they had only several sheets of the clay crystal. Obtained Kds for colloidal bentonite were larger than those for powdered bentonite. This can be caused by difference of competing ions in the solution, characteristics of contained smectite, or sorption site density. (author)

  7. Heavy metal sorption by microalgae

    Energy Technology Data Exchange (ETDEWEB)

    Sandau, E. [IGV - Inst. fuer Getreideverarbeitung GmbH, Bergholz-Rehbruecke (Germany); Sandau, P. [IGV - Inst. fuer Getreideverarbeitung GmbH, Bergholz-Rehbruecke (Germany); Pulz, O. [IGV - Inst. fuer Getreideverarbeitung GmbH, Bergholz-Rehbruecke (Germany)

    1996-12-31

    Viable microalgae are known to be able to accumulate heavy metals (bioaccumulation). Against a background of the increasing environmental risks caused by heavy metals, the microalgae Chlorella vulgaris and Spirulina platensis and their potential for the biological removal of heavy metals from aqueous solutions were taken as an example for investigation. Small-scale cultivation tests (50 l) with Cd-resistant cells of Chlorella vulgaris have shown that approx. 40% of the added 10 mg Cd/l was removed from the solution within seven days. At this heavy metal concentration sensitive cells died. Non-viable microalgae are able to eliminate heavy metal ions in a short time by biosorption in uncomplicated systems, without any toxicity problems. Compared with original biomasses, the sorption capacity of microalgal by-products changes only insignificantly. Their low price makes them economical. (orig.)

  8. Metal Sorption to Dolomite Surfaces

    International Nuclear Information System (INIS)

    Brady, P.V.; Papenguth, H.W.; Kelly, J.W.

    1999-01-01

    Potential human intrusion into the Waste Isolation Pilot Plant (WIPP) might release actinides into the Culebra Dolomite where sorption reactions will affect of radiotoxicity from the repository. Using a limited residence time reactor the authors have measured Ca, Mg, Nd adsorption/exchange as a function of ionic strength, P CO2 , and pH at 25 C. By the same approach, but using as input radioactive tracers, adsorption/exchange of Am, Pu, U, and Np on dolomite were measured as a function of ionic strength, P CO2 , and pH at 25 C. Metal adsorption is typically favored at high pH. Calcium and Mg adsorb in near-stoichiometric proportions except at high pH. Adsorption of Ca and Mg is diminished at high ionic strengths (e.g., 0.5M NaCl) pointing to association of Na + with the dolomite surface, and the possibility that Ca and Mg sorb as hydrated, outer-sphere complexes. Sulfate amplifies sorption of Ca and Mg, and possibly Nd as well. Exchange of Nd for surface Ca is favored at high pH, and when Ca levels are low. Exchange for Ca appears to control attachment of actinides to dolomite as well, and high levels of Ca 2+ in solution will decrease Kds. At the same time, to the extent that high P CO2 increase Ca 2+ levels, JK d s will decrease with CO 2 levels as well, but only if sorbing actinide-carbonate complexes are not observed to form (Am-carbonate complexes appear to sorb; Pu-complexes might sorb as well; U-carbonate complexation leads to desorption). This indirect CO 2 effect is observed primarily at, and above, neutral pH. High NaCl levels do not appear to affect to actinide K d s

  9. Sorption of methylxanthines by different sorbents

    Science.gov (United States)

    Dmitrienko, S. G.; Andreeva, E. Yu.; Tolmacheva, V. V.; Terent'eva, E. A.

    2013-05-01

    Sorption of caffeine, theophylline, theobromine, diprophylline, and pentoxyphylline on different sorbents (supercross-linked polystyrene, surface-modified copolymer of styrene and divinylbenzene Strata-X, and carbon nanomaterials Taunit and Diasorb-100-C16T) was studied in a static mode in an effort to find new sorbents suitable for sorption isolation and concentration of methylxanthines. The peculiarities of sorption of methylxanthines were explained in relation to the solution acidity, the nature of the sorbates and their concentration, the nature of the solvent, and the structural characteristics of the sorbents.

  10. Sorption isolation of strontium from seawater

    International Nuclear Information System (INIS)

    Avramenko, V.A.; Zheleznov, V.V.; Kaplun, E.V.; Sokol'nitskaya, T.A.; Yukhkam, A.A.

    2001-01-01

    Sorption isolation of strontium from seawater is considered and prospects of use of selective adsorbents for purification of seawater or liquid radioactive wastes mixed with seawater from 90 Sr are discussed. Comparative analysis of sorptive properties of adsorbents of different nature is done. It is shown that sorption-reagent materials developed by authors can to afford effective separation of 90 Sr from seawater. Possible mechanism of strontium sorption by these adsorbents is considered. The prospect of their use for purification of liquid radioactive wastes from strontium is shown [ru

  11. Sorption of beryllium from sulfuric acid solutions by aminocarboxylic polyampholites

    International Nuclear Information System (INIS)

    Pakholkov, V.S.; Tsevin, A.P.; Rychkov, V.N.

    1985-01-01

    Sorption of beryllium ions from BeSo 4 solutions by aminocarboxylic polyampholites at 18 deg C under steady-state conditions is studied. With the pH value growth the sorption of beryllium ions increases, that is characteristic for sorption according the cation exchange mechanism. Co- sorption of beryllium and uranium from BeSO 4 , UO 2 SO 4 , (NH 4 ) 2 SO 4 solution is considered, and possibility of sorption beryllium purification from uranium impurity is shown

  12. Sorption of metaldehyde using granular activated carbon

    Directory of Open Access Journals (Sweden)

    S. Salvestrini

    2017-09-01

    Full Text Available In this work, the ability of granular activated carbon (GAC to sorb metaldehyde was evaluated. The kinetic data could be described by an intra-particle diffusion model, which indicated that the porosity of the sorbent strongly influenced the rate of sorption. The analysis of the equilibrium sorption data revealed that ionic strength and temperature did not play any significant role in the metaldehyde uptake. The sorption isotherms were successfully predicted by the Freundlich model. The GAC used in this paper exhibited a higher affinity and sorption capacity for metaldehyde with respect to other GACs studied in previous works, probably as a result of its higher specific surface area and high point of zero charge.

  13. Radionuclide sorption on granitic drill core material

    International Nuclear Information System (INIS)

    Eriksen, T.E.; Locklund, B.

    1987-11-01

    Distribution ratios were determined for Sr-85, Cs-134 and Eu-152 on crushed granite and fissure coating/filling material from Stripa mines. Measurements were also carried out on intact fissure surfaces. The experimental data for Sr-85, Cs-134 on crushed material can be accomodated by a sorption model based on the assumption that the crushed material consists of porous spheres with outer and inner surfaces available for sorption. In the case of Eu-152 only sorption on the outer surfaces of the crushed material was observed. The absence of sorption on inner surfaces is most probably due to high depletion of the more strongly sorbed Eu-152 in the water phase and very low diffusivity of Eu-152 in the sorbed state. (orig./HP)

  14. Phenanthrene sorption on biochar-amended soils

    DEFF Research Database (Denmark)

    Kahawaththa Gamage, Inoka Damayanthi Kumari; Moldrup, Per; Paradelo Pérez, Marcos

    2014-01-01

    Biochar, a byproduct resulting from the pyrolysis of biomass, is considered to be an anthropogenic carbonaceous sorbent. Despite a worldwide increase in the application of biochar on agricultural fields to improve crop productivity over the past few decades, there have been few studies...... on their influences on the sorption of environmental contaminants. In a field-based study at two experimental sites in Denmark, we investigated the effect of birch wood-derived biochar (Skogans kol) on the sorption of phenanthrene in soils with different properties. The soil sorption coefficient, Kd (L kg-1......), of phenanthrene was measured on sandy loam and loamy sand soils which have received from zero up to 100 t ha-1 of biochar. Results show that birch wood biochar had a higher Kd compared to soils. Furthermore, the application of birch wood biochar enhanced the sorption of phenanthrene in agricultural soils...

  15. Towards tailor-made participation

    DEFF Research Database (Denmark)

    Agger, Annika

    2012-01-01

    Public participation has become an important element of governance in many Western European countries. However, among scholars and practitioners there is a recognition that participatory governance processes tend to produce systematic exclusions. Knowledge about 'who' participates and 'how......' they participate can enhance our understanding of participatory processes. This paper presents some characterisations of citizens based on a review of the literature on participation. In addition, examples of how to tailor participation for different type of citizens are provided based on studies of urban...... regeneration programmes and local environmental initiatives in Denmark. The paper concludes that in order to broaden the inclusion of affected citizens, public authorities need to be tailor participation processes by applying distinct approaches to different types of citizens...

  16. Sorption of organophosphate esters by carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Yan, Wei; Yan, Li [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); Duan, Jinming [School of Environmental and Municipal Engineering, Xi’an University of Architecture and Technology, Xi’an 710055 (China); Jing, Chuanyong, E-mail: cyjing@rcees.ac.cn [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China)

    2014-05-01

    Graphical abstract: The interfacial interactions between the OPE molecules and CNTs. - Highlights: • Oxygen-containing groups on CNTs change the sorption property for OPEs. • Molecular configuration of OPEs has insignificant impact on their sorption. • Hydrophobic, π–π EDA and Brønsted acid–base interaction occurred between the CNTs and OPEs. - Abstract: Insights from the molecular-level mechanism of sorption of organophosphate esters (OPEs) on carbon nanotubes (CNTs) can further our understanding of the fate and transport of OPEs in the environment. The motivation for our study was to explore the sorption process of OPEs on multi-walled CNTs (MWCNTs), single-walled CNTs (SWCNTs) and their oxidized counterparts (O-MWCNTs and O-SWCNTs), and its molecular mechanism over a wide concentration range. The sorption isotherm results revealed that the hydrophobicity of OPEs dominated their affinities on a given CNT and the π–π electron donor–acceptor (EDA) interaction also played an important role in the sorption of aromatic OPEs. This π–π EDA interaction, verified with Raman and FT-IR spectroscopy, could restrict the radial vibration of SWCNTs and affect the deformation vibration γ(CH) bands of OPE molecules. The OPE surface coverage on CNTs, estimated using the nonlinear Dubinin–Ashtakhov model, indicated that the oxygen-containing functional groups on CNTs could interact with water molecules by H-bonding, resulting in a decrease in effective sorption sites. In addition, FTIR analysis also confirmed the occurrence of Brønsted acid–base interactions between OPEs and surface OH groups of SWCNTs. Our results should provide mechanistic insights into the sorption mechanism of OPE contaminants on CNTs.

  17. Sorption of fomesafen in Brazilian soils

    OpenAIRE

    Silva,G.R.; D'Antonino,L.; Faustino,L.A.; Silva,A.A.; Ferreira,F.A.; Texeira,C.C.

    2013-01-01

    The study of the dynamics of a herbicide in the soil focus on the interactions with environmental components to obtain agronomic efficiency, ensuring selectivity to the culture and risk reduction of environmental impact. This study evaluated the sorption process of fomesafen in the Brazilian soils Ultisol, Cambisol, and Organosol. Besides soil, washed sand was used as an inert material for determination of the sorption ratio of fomesafen in the soil. The bioassay method was applied, using Sor...

  18. Tailoring Earned Value Management. General Guidelines

    National Research Council Canada - National Science Library

    2002-01-01

    Partial Contents: General Principles, A Spectrum of Implementation, OMB Guidance, A Special Note about DOD, Risk Factors to Consider, How can EVMS be tailored, Tailor EVMS to Inherent Risk, Application Thresholds-DoD...

  19. Deep drawing simulation of Tailored Blanks

    NARCIS (Netherlands)

    van den Berg, Albert; Meinders, Vincent T.; Stokman, B.

    1998-01-01

    Tailored blanks are increasingly used in the automotive industry. A tailored blank consists of different metal parts, which are joined by a welding process. These metal parts usually have different material properties. Hence, the main advantage of using a tailored blank is to provide the right

  20. Radionuclides sorption in clay soils

    International Nuclear Information System (INIS)

    Siraky, G.; Lewis, C.; Hamlat, S.; Nollmann, C.E.

    1987-01-01

    The sorption behaviour of clay soils is examined through a parametric study of the distribution coefficient (Kd) for the radionuclides of interest, Cs and Sr. This work is a preliminary stage of the migration studies of these nuclides in a porous medium (ground of Ezeiza, Argentina) and the evaluation of radiologic impact of the removal of low and intermediate activity wastes in shallow trenches. The determination of Kd is performed by a static technique or batch. The phases are separated by centrifugation at 20000 g during 1 hour. The activity of supernatant solution of Cs-137 and Sr-85 is measured in a detecting system of I Na(Tl) well-type. Two types of parameters were changed: a) those related to the determination method: phase separation (centrifugation vs. centrifugation plus filtration); equilibrium period, ratio solid/liquid; b) those related to the geochemical system: pH of contact solution, carrier concentration, competitive ions, ionic strength, desorption. It was observed that the modification of parameters in the Kd-measurement does not change the order of magnitude of results. (Author)

  1. Time series with tailored nonlinearities

    Science.gov (United States)

    Räth, C.; Laut, I.

    2015-10-01

    It is demonstrated how to generate time series with tailored nonlinearities by inducing well-defined constraints on the Fourier phases. Correlations between the phase information of adjacent phases and (static and dynamic) measures of nonlinearities are established and their origin is explained. By applying a set of simple constraints on the phases of an originally linear and uncorrelated Gaussian time series, the observed scaling behavior of the intensity distribution of empirical time series can be reproduced. The power law character of the intensity distributions being typical for, e.g., turbulence and financial data can thus be explained in terms of phase correlations.

  2. Recent progress in sorption mechanisms and models

    International Nuclear Information System (INIS)

    Fedoroff, M.; Lefevre, G.

    2005-01-01

    Full text of publication follows: Sorption-desorption phenomena play an important role in the migration of radioactive species in surface and underground waters. In order to predict the transport of these species, we need a good knowledge of sorption processes and data, together with reliable models able to be included in transport calculation. Traditional approaches based on experimentally determined distribution coefficients (Kd) and sorption isotherms have a limited predictive capability, since they are very sensitive to the numerous parameters characterizing the solution and the solid. Models based on thermodynamic equilibria were developed to account for the influence these parameters: the ion exchange model and the surface complexation models (2-pK mono-site, 1-pK multi-site, with several different electrostatic models: CCM, DLM, BSM, TLM,...). Although these models are very useful, studies performed in recent years showed that they have important theoretical and experimental limitations, which result in the fact that we must be very careful when we use them for extrapolating sorption data to long term and to large natural systems. Among all problems which can be found are: the possibility to fit a set of experimental data with different models, sometimes bad adequacy with the real sorption processes, some theoretical limitations such as a rigorous definition of reference and standard states in surface equilibria, slow kinetics which prevent from equilibrium achievement, irreversibility, solubility and evolution of solid phases... Through the increase of the number of sensitive spectroscopic methods, we are now able to know more about sorption processes at the atomic scale. Models such as the 1-pK CD-MUSIC model can account for the influence of orientation of the faces of the solid. More and more examples of the influence of this orientation on the sorption properties are known. Calculations performed by 'ab initio' modeling is also useful to predict the

  3. The NEA sorption data base (SDB)

    International Nuclear Information System (INIS)

    Ruegger, B.; Ticknor, K.

    1992-01-01

    The current NEA Sorption Data Base is developed to replace the former International Sorption Information Retrieval System (ISIRS) initiated at Pacific Northwest Laboratory and contains about 11,000 distribution coefficients with corresponding experimental condition parameters describing sorption of key nuclides for a large variety of solid and liquid phases. The SDB is designed to run on a micro-computer using the commercially available database software dBASE III Plus. For each recorded sorption experiment, the SDB provides a bibliographical reference, the most complete characterization of the solid and liquid phases available, a description of the experimental conditions and the distribution coefficient or retardation factor for each element studied. When available, parameters such as temperature, initial radionuclide concentration, pH, Eh, contact time, solid to solution ratio, sample origin, oxidation state and type of solution are included. The SDB provides information for a wide variety of rocks or geological materials, buffer backfill candidates, concretes/cements, elements (Am, Cs, Co, I, Np, Pu, Ra, Sr, Se, Tc, U and, to a lesser extent, Ag, Ba, C, Ce, Eu, Fe, Mn, Mo, Na, Nb, Ni, Pd, Pm, Ru, Sb, Sn, Y, Zn, and Zr), or radioisotopes. A compilation of sorption data like SDB provide a readily available source of data for radioactive waste repository performance assessments when site specific data are not available or essential, for example, during a site selection phase. 2 appendices

  4. Radionuclide sorption from the safety evaluation perspective

    International Nuclear Information System (INIS)

    1992-01-01

    Research and development directed towards the assessment of the long-term performance of radioactive waste disposal systems has been recognised as a priority area with a strong need for international co-operation and co-ordination. The ultimate aims is to promote the quality and credibility of safety assessment techniques for radioactive waste disposal. Sorption in the geosphere is one of the key processes for retarding the transport of radionuclide from the underground disposal facility to the biosphere. In many cases, sorption in the near field and in the biosphere is also important. A workshop, organised to favor discussion around a small number of invited papers, was held in October 1991: - to evaluate critically the way sorption processes are incorporated in performance assessment models; - to identify open issues of high priority, and; - to propose future activities to resolve these issues. These proceedings reproduce the invited papers and the conclusions and recommendations adopted by the workshop. Eight papers are in the INIS SCOPE. The main subjects studied are: sorption database comparison, sorption database development and three case studies, experimental techniques, adsorption models

  5. Sorption of radionuclides by tertiary clays

    International Nuclear Information System (INIS)

    Wagner, J.F.; Czurda, K.A.

    1990-01-01

    The sorption capacity of different clay types for some metals (Co, Cs, Sr and Zn), occurring as common radionuclides in radioactive waste deposits, had been analysed by a static (batch technique) and a dynamic method (percolation tests, in which the driving force is a hydraulic gradient). Sorption capacity generally increased with an increasing pH of solution. A decrease of sorption capacity had been observed in the order Zn > Cs ≥ Co > Sr for the batch and Cs > Zn > Sr > Co for the percolation tests. Clay marls showed a distinctly higher sorption respectively retention capacity as pure clays. Sorption capacity depends on solution parameters like type and concentration of radionuclide, pH, salt concentration, etc., and on rock parameters like mineral content (e.g. swelling clay minerals and carbonates), organic material, rock pH, micro fabric, etc. A third parameter of great influence is the contact time between clay and solution. The adsorption isotherms reflect two different adsorption mechanisms: a very rapid adsorption (a few minutes) on the external surfaces of clay minerals and a slow adsorption process (weeks and longer), due to the diffusion of metal ions into the interlayer space of clay minerals. 12 refs., 9 figs., 1 tab

  6. Sorption of Organophosphorus Flame Retardants (OPFRs) on ...

    Science.gov (United States)

    Organophosphorus flame retardants (OPFRs) are widely used as additives in industrial and consumer products such as electrical and electronic products, furniture, plastics, textiles, and building/construction materials. Due to human exposure and potential health effects, OPFRs including tris(2-chloroethyl) phosphate (TCEP), tris(1-chloro-2-propyl) phosphate (TCPP), and tris(1,3-dichloro-2-propyl) phosphate (TDCPP) are EPA Action Plan chemicals for chemical assessments under the Toxic Substances Control Act (TSCA). This work investigated the sorption of these three compounds from the air to settled Arizona Test Dust (ATD) and house dust (HD) in a dual small chamber system. The OPFR exposed dust was analyzed to determine the sorption concentration and sorption rate of OPFRs on the dust. The effect of the composition of the dust on OPFR sorption was evaluated. The results showed that ATD and HD have varied sorption capacity for OPFRs from air. This work explores the relationship between OPFR concentrations in settled dust and air. The data can be used to determine partitioning of OPFRs between the gas phase and settled dust indoors and to inform strategies to reduce exposure and risk.

  7. Sorption of tylosin on clay minerals.

    Science.gov (United States)

    Zhang, Qian; Yang, Chen; Huang, Weilin; Dang, Zhi; Shu, Xiaohua

    2013-11-01

    The equilibrium sorption of tylosin (TYL) on kaolinite and montmorillonite was measured at different solution pH using batch reactor systems. The results showed that all the sorption isotherms were nonlinear and that the nonlinearity decreased as the solution pH increased for a given clay. At a specific aqueous concentration, the single-point sorption distribution coefficient (KD) of TYL decreased rapidly as the solution pH increased. A speciation-dependent sorption model that accounted for the contributions of the cationic and neutral forms of TYL fit the data well, suggesting that the sorption may be dominated by both ion exchange and hydrophobic interactions. The isotherm data also fit well to a dual mode model that quantifies the contributions of a site-limiting Langmuir component (ion exchange) and a non-specific linear partitioning component (hydrophobic interactions). X-ray diffraction analyses revealed that the interlayers of montmorillonite were expanded due to the uptake of TYL. TYL molecules likely form a monolayer surface coverage. Copyright © 2013 Elsevier Ltd. All rights reserved.

  8. Tailor-welded blanks and their production

    Science.gov (United States)

    Yan, Qi

    2005-01-01

    Tailor welded blanks had been widely used in the automobile industry. A tailor welded blank consists of several flat sheets that were laser welded together before stamping. A combination of different materials, thickness, and coatings could be welded together to form a blank for stamping car body panels. As for the material for automobile industry, this technology was one of the development trend for automobile industry because of its weight reduction, safety improvement and economical use of materials. In this paper, the characters and production of tailor welded blanks in the market were discussed in detail. There had two major methods to produce tailor welded blanks. Laser welding would replace mesh seam welding for the production of tailor welded blanks in the future. The requirements on the edge preparation of unwelded blanks for tailor welded blanks were higher than the other steel processing technology. In order to produce the laser welded blank, there had the other process before the laser welding in the factory. In the world, there had three kinds of patterns for the large volume production of tailor welded blanks. In China, steel factory played the important role in the promotion of the application of tailor welded blanks. The competition for the supply of tailor welded blanks to the automobile industry would become fierce in the near future. As a result, the demand for the quality control on the production of tailor welded blanks would be the first priority concern for the factory.

  9. Cadmium ion sorption onto lignocellulosic biosorbent modified by sulfonation: the origin of sorption capacity improvement.

    Science.gov (United States)

    Shin, Eun Woo; Rowell, Roger M

    2005-08-01

    Juniper (Juniperus monosperma), a small-diameter underutilized material, has been studied as a lignocellulosic biosorbent for removing heavy metals from water. In this study, juniper wood was modified by sulfonation to enhance sorption capacity for cadmium in water. The origin of the enhancement was investigated by observing the sorption behaviors and the change in surface functional group concentrations. Cadmium sorption by all juniper wood biosorbents studied was fast and the sorption capacity decreased with decreasing pH, similar to results found for other biosorbents. Sulfonated juniper was found to have at least twice the sorption capacity for cadmium removal from water compared to that of untreated juniper, though the sorption capacity increased with increasing pH. A slight increase in carboxylate content after sulfonation was likely responsible for a small portion of the enhancement. Elemental analysis showed an increase in sulfur content after sulfonation. Diffuse reflectance infrared Fourier transform (DRIFT) spectra showed a decrease in the band at 1660 cm(-1) in the range of carbonyl groups as a result of sulfonation. This indicates that coniferaldehyde groups in the lignin of juniper wood corresponding to this band were substituted into sulfonic acid groups after sulfonation. This interpretation was supported by both the color forming reaction with phloroglucinol-hydrochloric acid and the reaction mechanisms from the acid sulfite pulping process. Consequently, the enhancement of cadmium sorption capacity of juniper wood by sulfonation mainly originated from the production of sulfonic acid groups, which are binding sites for heavy metals.

  10. Sorption of Europium in zirconium silicate

    International Nuclear Information System (INIS)

    Garcia R, G.

    2004-01-01

    Some minerals have the property of sipping radioactive metals in solution, that it takes advantage to manufacture contention barriers that are placed in the repositories of nuclear wastes. The more recent investigations are focused in the development of new technologies guided to the sorption of alpha emissors on minerals which avoid their dispersion in the environment. In an effort to contribute to the understanding of this type of properties, some studies of sorption of Europium III are presented like homologous of the americium, on the surface of zirconium silicate (ZrSiO 4 ). In this work the results of sorption experiences are presented as well as the interpretation of the phenomena of the formation of species in the surface of the zirconium silicate. (Author)

  11. Water sorption and transport in dry crispy bread crust

    NARCIS (Netherlands)

    Meinders, M.B.J.; Nieuwenhuijzen, van N.H.; Tromp, R.H.; Hamer, R.J.; Vliet, van T.

    2010-01-01

    Water sorption and dynamical properties of bread crust have been studied using gravimetric sorption experiments. Water uptake and loss were followed while relative humidity (RH) was stepwise in- or decreased (isotherm experiment) or varied between two adjusted values (oscillatory experiment).

  12. Molecular simulation of polycyclic aromatic hydrocarbon sorption to black carbon

    NARCIS (Netherlands)

    Haftka, J.J.H.; Parsons, J.R.; Govers, H.A.J.

    2009-01-01

    Strong sorption of hydrophobic organic contaminants to soot or black carbon (BC) is an important environmental process limiting the bioremediation potential of contaminated soils and sediments. Reliable methods to predict BC sorption coefficients for organic contaminants are therefore required. A

  13. Tritium sorption on protective coatings for concrete

    International Nuclear Information System (INIS)

    Miller, J.M.; Senohrabek, J.A.; Allsop, P.A.

    1992-11-01

    Because of the high sorption level of tritium on unprotected concrete, a program to examine the effectiveness of various concrete coatings and sealants in reducing tritium sorption was undertaken, and various exposure conditions were examined. Coatings of epoxy, polyurethane, bituminous sealant, bituminous sealant covered with polyvinylidene chloride wrap, alkyd paint, and sodium silicate were investigated with tritium (HTO) vapor concentration, humidity and contact time being varied. An exposure to HT was also carried out, and the effect of humidity on the tritium desorption rate was investigated. The relative effectiveness of the coatings was in the order of bituminous sealant + wrap > bituminous sealant > solvent-based epoxy > 100%-solids epoxy > alkyd paint > sodium silicate. The commercially available coatings for concrete resulted in tritium sorption being reduced to less than 7% of unprotected concrete. This was improved to ∼0.1% with the use of the Saran wrap (polyvinylidene chloride). The amount of tritium sorbed was proportional to tritium concentration. The total tritium sorbed decreased with an increase in humidity. A saturation effect was observed with increasing exposure time for both the coated and unprotected samples. Under the test conditions, complete saturation was not achieved within the maximum 8-hour contact time, except for the solvent-based epoxy. The desorption rate increased with a higher-humidity air purge stream. HT desorbed more rapidly than HTO, but the amount sorbed was smaller. The experimental program showed that HTO sorption by concrete can be significantly reduced with the proper choice of coating. However, tritium sorption on concrete and proposed coatings will continue to be a concern until the effects of the various conditions that affect the adsorption and desorption of tritium are firmly established for both chronic and acute tritium release conditions. Material sorption characteristics must also be considered in

  14. On the derivation of a sorption database

    International Nuclear Information System (INIS)

    Ewart, F.T.; Haworth, A.; Wisbey, S.J.

    1992-01-01

    The safety arguments in support of many radioactive waste repository concepts are heavily dependent on the existence of a sorption reaction. Such a reaction will, in the near field, reduce the magnitude of the release of a number of hazardous radionuclides so that their release to the geosphere is dispersed in time. In the geosphere, the sorption reactions provide a mechanism whereby the migration of the elements released from the repository is retarded and the radioisotopes then subsequently decay. The processes involved in sorption cannot in many cases be satisfactorily represented in thermodynamic terms such as are employed in the description of dissolution and precipitation. Experiments that investigate these reactions are not easy to perform. The sorption parameters that are obtained experimentally for the near field relate, in the UK case, to sorption on to a cementitious surface. These surfaces, since they consist substantially of calcium hydroxide or calcium silicate hydrates, control the aqueous chemistry, do not permit pH changes to be made and limit the range of concentrations of sorbate that may be used. In the far field, on the other hand, the surfaces are not in general so active with respect to the solution chemistry and data can be obtained across a wide spectrum of aqueous chemistries. These data, although they may be useful in testing and parameterizing models, may not have validity under field conditions since the minerals will, inevitably, react to the changes in water chemistry, over geological timescales. The uncertainties in the experimental data are, for many elements and solids, balanced by a reasonable agreement between workers in the values of the parameters used to describe sorption. 22 refs., 1 fig., 1 tab

  15. The effect of the thermal reduction temperature on the structure and sorption capacity of reduced graphene oxide materials

    Energy Technology Data Exchange (ETDEWEB)

    Dolbin, Alexandr V., E-mail: dolbin@ilt.kharkov.ua [B. Verkin Institute for Low Temperature Physics and Engineering of the National Academy of Sciences of Ukraine, 47 Lenin Ave., Kharkov 61103 (Ukraine); Khlistyuck, Maria V.; Esel' son, Valentin B.; Gavrilko, Viktor G.; Vinnikov, Nikolay A.; Basnukaeva, Razet M. [B. Verkin Institute for Low Temperature Physics and Engineering of the National Academy of Sciences of Ukraine, 47 Lenin Ave., Kharkov 61103 (Ukraine); Maluenda, Irene; Maser, Wolfgang K.; Benito, Ana M. [Instituto de Carboquímica, ICB-CSIC, Miguel Luesma Castán, 4, E-50018 Zaragoza (Spain)

    2016-01-15

    Graphical abstract: - Abstract: The influence of reduction temperatures on the structure and the sorption capacity of thermally reduced graphene (TRGO) has been investigated systematically. A set of TRGO materials were prepared by thermal treatment of parent graphene oxide (GO) at five temperatures (T = 200, 300, 500, 700, and 900 °C). Investigations of these materials by X-ray diffraction, Raman spectroscopy and X-ray photoemission spectroscopy methods have shown that both the structure and the residual oxygen functional groups on the TRGO surface can be controlled by varying the temperature of the thermal treatment. The data on the sorption and desorption of {sup 4}He, H{sub 2}, N{sub 2}, Ne and Kr gases in the temperature interval T = 2–290 K clearly demonstrate that the sorption capacity of TRGO is closely related to the structural changes induced by the treatment temperatures. It is important that the sorption capacities of TRGOs treated at 300 °C and at 900 °C significantly increase for all the gases used. The prominent increase in the sorption capacity at 300 °C is attributed to the structural disorder and liberation of the pores caused by the removal of intercalated water and labile oxygen functional groups (oFGs) favored at this temperature. At 900 °C the sorption capacity increases due to the generation of new defects on the TRGO surface, which provide additional access to the internal space between the folds and sheets of the TRGO structure. By tailoring the structural properties we emphasize the potential of TRGO as a highly efficient sorbent.

  16. Sorption Properties of Some Romanian Gingerbread

    Directory of Open Access Journals (Sweden)

    Tulbure Anca

    2014-06-01

    Full Text Available Water activity of gingerbread is very important for keeping the product freshness and shelf life. Water activity is influenced by composition, water content and temperature. The water content of gingerbread could vary according with storage condition. i.e. rH. 11 gingerbread samples were analysed. The water content and water activity lies between 7.0 and 12.6% and respectively 0.590 and 0.715. The sorption isotherms were determined at 30°C by gravimetric method. The moisture sorption is influenced by composition, especially sweeteners and humectants. Honey and invert sugar have the same impact on gingerbread higroscopicity.

  17. Attenuation of polychlorinated biphenyl sorption to charcoal by humic acids

    NARCIS (Netherlands)

    Koelmans, A.A.; Meulman, B.; Meijer, T.; Jonker, M.T.O.

    2009-01-01

    Strong sorption to black carbon may limit the environmental risks of organic pollutants, but interactions with cosorbing humic acid (HA) may interfere. We studied the attenuative effect of HA additions on the sorption of polychlorinated biphenyls (PCBs) to a charcoal. "Intrinsic" sorption to

  18. Suitability of Moshi Pumice for Phosphorus Sorption in Constructed ...

    African Journals Online (AJOL)

    The study of Moshi Pumice's phosphorus sorption behaviours and properties was carried out in laboratory scale where by 1-2 mm, 2-4 mm and 4-8 mm grains were tested using batch experiments. The results show that Moshi Pumice has high phosphorus sorption capacity. The sorption capacity for the Moshi Pumice was ...

  19. Phosphorus sorption in relation to soil grain size and geochemical ...

    African Journals Online (AJOL)

    By using stepwise regression, the combination of Al, Fe, clay and Ca predicted more than 94% of the variation in the P sorption capacity of soils samples from Simiyu and Kagera basins. These four soil properties, which are strongly related to P sorption, could therefore be used as quick tests for predicting the P sorption ...

  20. suitability of murram for phosphorus sorption in constructed wetlands

    African Journals Online (AJOL)

    Mimi

    ABSTRACT: The study of Moshi Pumice's phosphorus sorption behaviours and properties was carried out in laboratory scale where by 1-2 mm, 2-4 mm and 4-8 mm grains were tested using batch experiments. The results show that Moshi Pumice has high phosphorus sorption capacity. The sorption capacity for the Moshi ...

  1. Sorption of perfluorooctane sulfonate to carbon nanotubes in aquatic sediments

    NARCIS (Netherlands)

    Kwadijk, C.J.A.F.; Velzeboer, I.; Koelmans, A.A.

    2013-01-01

    To date, sorption of organic compounds to nanomaterials has mainly been studied for the nanomaterial in its pristine state. However, sorption may be different when nanomaterials are buried in sediments. Here, we studied sorption of Perfluorooctane sulfonate (PFOS) to sediment and to sediment with 4%

  2. Attenuation of polychlorinated biphenyl sorption to charcoal by humic acids.

    NARCIS (Netherlands)

    Koelmans, A.A.; Meulman, B.; Meijer, T.; Jonker, M.T.O.

    2009-01-01

    Strong sorption to black carbon may limit the environmental risks of organic pollutants, but interactions with cosorbing humic acid (HA) may interfere. We studied the attenuative effect of HA additions on the sorption of polychlorinated biphenyls (PCBs) to a charcoal. "Intrinsic" sorption to

  3. Sorption mechanisms of perfluorinated compounds on carbon nanotubes

    International Nuclear Information System (INIS)

    Deng Shubo; Zhang Qiaoying; Nie Yao; Wei Haoran; Wang Bin; Huang Jun; Yu Gang; Xing Baoshan

    2012-01-01

    Sorption of perfluorinated compounds (PFCs) on carbon nanotubes (CNTs) is critical for understanding their subsequent transport and fate in aqueous environments, but the sorption mechanisms remain largely unknown. In this study, the sorption of six PFCs on CNTs increased with increasing C-F chain length when they had a same functional group, and the CNTs with hydroxyl and carboxyl groups had much lower adsorbed amount than the pristine CNTs, indicating that hydrophobic interaction dominated the sorption of PFCs on the CNTs. Electrostatic repulsion suppressed the sorption of PFCs on the CNTs, resulting in the lower sorption with increasing pH. Hydrogen bonding interaction was negligible. The hydrophobic C-F chains can be closely adsorbed on the CNTs surface in parallel to the axis or along the curvature, making it impossible to form micelles on the CNT surface, leading to the lower sorption than other adsorbents. Highlights: ► Sorption capacities of PFOA on different CNTs are less than that on activated carbon and resins. ► Hydrophobic interaction is principally involved in the sorption of PFCs on CNTs. ► Electrostatic repulsion suppresses the sorption of PFCs on CNTs. - Hydrophobic interaction dominated the sorption of perfluorinated compounds on carbon nanotubes, while electrostatic repulsion suppressed their sorption.

  4. Phenanthrene sorption to Chinese coal: Importance of coal's geochemical properties

    International Nuclear Information System (INIS)

    Yan Caixia; Yang Yi; Liu Min; Nie Minghua; Zhou, John L.

    2011-01-01

    Highlights: → Phen was chosen as the probe compound for determining the sorption of PAHs to a series of different Chinese coal samples. → The combined partition and adsorption model yielded a better fit than the Freundlich isotherm. → Compared to total carbon, BC might play more important role in the sorption of Phen to coal samples. → Relationships between aromatic and aliphatic carbon contents and sorption parameters indicated the significance of aromatic and aliphatic carbon in the coal sorption behavior. - Abstract: Phenanthrene (Phen) was chosen as the probe compound for determining the sorption of PAHs to a series of different coal samples from China. Based on elemental analysis and nuclear magnetic resonance (NMR) spectra analysis, coal samples were characterized with different metamorphic evolutional degrees. The experimental sorption data were fitted well by the Freundlich model, suggesting enhanced sorption capacity and strong nonlinearity of coal samples. The combined partition and adsorption model yielded a better fit than the Freundlich isotherm, indicating that adsorption dominated the sorption at low aqueous concentrations. Correlations between coal properties and sorption capacity values indicated that C%, H/C and O/C atomic ratios were the key factors controlling the sorption behavior. Compared to total carbon, BC might play more important role in the sorption of Phen to coal samples. Moreover, there existed nonlinear relationships between combined carbon, aromatic and aliphatic carbon contents and log K Fr and n values, respectively, indicating the significance of aromatic and aliphatic carbon in the coal sorption behavior.

  5. Hydration and sorption characteristics of a polyfunctional weak-base anion exchanger after the sorption of vanillin and ethylvanillin

    Science.gov (United States)

    Rodionova, D. O.; Voronyuk, I. V.; Eliseeva, T. V.

    2016-07-01

    Features of the sorption of substituted aromatic aldehydes by a weak-base anion exchanger under equilibrium conditions are investigated using vanillin and ethylvanillin as examples. Analysis of the sorption isotherms of carbonyl compounds at different temperatures allows us to calculate the equilibrium characteristics of their sorption and assess the entropy and enthalpy contributions to the energy of the process. Hydration characteristics of the macroporous weak-base anion exchanger before and after the sorption of aromatic aldehydes are compared.

  6. Sorption of Pharmaceuticals, Heavy Metals, and Herbicides to Biochar in the Presence of Biosolids.

    Science.gov (United States)

    Bair, Daniel A; Mukome, Fungai N D; Popova, Inna E; Ogunyoku, Temitope A; Jefferson, Allie; Wang, Daoyuan; Hafner, Sarah C; Young, Thomas M; Parikh, Sanjai J

    2016-11-01

    Agricultural practices are increasingly incorporating recycled waste materials, such as biosolids, to provide plant nutrients and enhance soil functions. Although biosolids provide benefits to soil, municipal wastewater treatment plants receive pharmaceuticals and heavy metals that can accumulate in biosolids, and land application of biosolids can transfer these contaminants to the soil. Environmental exposure of these contaminants may adversely affect wildlife, disrupt microbial communities, detrimentally affect human health through long-term exposure, and cause the proliferation of antibiotic-resistant bacteria. This study considers the use of biochar co-amendments as sorbents for contaminants from biosolids. The sorption of pharmaceuticals (ciprofloxacin, triclocarban, triclosan), and heavy metals (Cu, Cd, Ni, Pb) to biochars and biochar-biosolids-soil mixtures was examined. Phenylurea herbicide (monuron, diuron, linuron) sorption was also studied to determine the potential effect of biochar on soil-applied herbicides. A softwood (SW) biochar (510°C) and a walnut shell (WN) biochar (900°C) were used as contrasting biochars to highlight potential differences in biochar reactivity. Kaolinite and activated carbon served as mineral and organic controls. Greater sorption for almost all contaminants was observed with WN biochar over SW biochar. The addition of biosolids decreased sorption of herbicides to SW biochar, whereas there was no observable change with WN biochar. The WN biochar showed potential for reducing agrochemical and contaminant transport but may inhibit the efficacy of soil-applied herbicides. This study provides support for minimizing contaminant mobility from biosolids using biochar as a co-amendment and highlights the importance of tailoring biochars for specific characteristics through feedstock selection and pyrolysis-gasification conditions. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science

  7. A suggested approach toward measuring sorption and applying sorption data to repository performance assessment

    International Nuclear Information System (INIS)

    Rundberg, R.S.

    1991-01-01

    The sorption of radioisotopes in relation to geologic disposal of radioactive wastes is discussed. Properties of the radioactive materials, rocks, and minerals, and the chemistry involved are described. 51 refs., 12 figs. CBS

  8. Sorption of fission nuclides on model milk components. II. Sorption of radiostrontium on hydroxyapatite in milk and whey

    International Nuclear Information System (INIS)

    Rosskopfova, O.; Kopunec, R.; Matel, L.; Macasek, F.

    1999-01-01

    In this work the whey was chosen as a model solution of liquid phase for sorption study of strontium on hydroxyapatite. The whey was obtained using two methods - ultracentrifugation and precipitation of casein. The sorption was studied at a different pH and at a different concentration of calcium. The sorption of strontium on hydroxyapatite from milk was studied, too. (authors)

  9. Acquisition of sorption isotherms for modified woods by the use of dynamic vapour sorption instrumentation. Principles and Practice

    DEFF Research Database (Denmark)

    Engelund, Emil Tang; Klamer, Morten; Venås, Thomas Mark

    2010-01-01

    for obtaining sorption isotherms are very time consuming. With new dynamic vapour sorption (DVS) instrumentation, the acquisition of data for constructing sorption isotherms is suddenly dramatically lowered. Where the traditional methods often required months, data can now be obtained in a matter of days...

  10. Development of mechanistic sorption model and treatment of uncertainties for Ni sorption on montmorillonite/bentonite

    International Nuclear Information System (INIS)

    Ochs, Michael; Ganter, Charlotte; Tachi, Yukio; Suyama, Tadahiro; Yui, Mikazu

    2011-02-01

    Sorption and diffusion of radionuclides in buffer materials (bentonite) are the key processes in the safe geological disposal of radioactive waste, because migration of radionuclides in this barrier is expected to be diffusion-controlled and retarded by sorption processes. It is therefore necessary to understand the detailed/coupled processes of sorption and diffusion in compacted bentonite and develop mechanistic /predictive models, so that reliable parameters can be set under a variety of geochemical conditions relevant to performance assessment (PA). For this purpose, JAEA has developed the integrated sorption and diffusion (ISD) model/database in montmorillonite/bentonite systems. The main goal of the mechanistic model/database development is to provide a tool for a consistent explanation, prediction, and uncertainty assessment of K d as well as diffusion parameters needed for the quantification of radionuclide transport. The present report focuses on developing the thermodynamic sorption model (TSM) and on the quantification and handling of model uncertainties in applications, based on illustrating by example of Ni sorption on montmorillonite/bentonite. This includes 1) a summary of the present state of the art of thermodynamic sorption modeling, 2) a discussion of the selection of surface species and model design appropriate for the present purpose, 3) possible sources and representations of TSM uncertainties, and 4) details of modeling, testing and uncertainty evaluation for Ni sorption. Two fundamentally different approaches are presented and compared for representing TSM uncertainties: 1) TSM parameter uncertainties calculated by FITEQL optimization routines and some statistical procedure, 2) overall error estimated by direct comparison of modeled and experimental K d values. The overall error in K d is viewed as the best representation of model uncertainty in ISD model/database development. (author)

  11. Pyrene sorption by natural organic matter

    Energy Technology Data Exchange (ETDEWEB)

    Chefetz, B.; Deshmukh, A.P.; Hatcher, P.G.; Guthrie, E.A. [Ohio State University, Columbus, OH (USA). Dept. of Chemistry

    2000-07-15

    Sorption of pyrene on various types of natural organic matter (NOM) varying in chemical composition (e.g. high aliphaticity or aromaticity) was examined in batch sorption studies. The NOM samples (cuticle, humin, humic acid, degraded lignin, peat and lignite) were characterized by elemental analyses and solid-state {sup 13}C NMR spectra. Previous studies on polycyclic aromatic hydrocarbons (PAHs) sorption on soils and sediments led to the conclusion that aromatic component of the NOM determines the binding of nonionic compounds and that the polarity of the NOM reduces the binding coefficient of the aromatic NOM moieties. In this study the hypothesis that aliphatic moieties of NOM derived from soils or sediments can contribute significantly to the binding of PAHs in aqueous media was tested. Cuticle and a humin sample from an hnalgal deposit exhibited the highest distribution coefficients (K{sub oc}). Both samples were rich in aliphatic structures and had very low aromaticity (4.6 and 8.8% for cuticle and humin samples, respectively). A positive trend was observed between the K{sub oc} level and the aliphaticity of the NOM, calculated from the {sup 13}C NMR spectra. This study demonstrates that aliphatic NOM compounds significantly sorb pyrene in aqueous solution, thus leading to the conclusion that the contribution of these groups to the sorption of aromatic nonionic pollutants in complex NOM matrices can be significant. 32 refs., 4 figs., 3 tabs.

  12. Enhancement of the bentonite sorption properties.

    Science.gov (United States)

    Mockovciaková, Annamária; Orolínová, Zuzana; Skvarla, Jirí

    2010-08-15

    The almost monomineral fraction of bentonite rock-montmorillonite was modified by magnetic particles to enhance its sorption properties. The method of clay modification consists in the precipitation of magnetic nanoparticles, often used in preparing of ferrofluids, on the surface of clay. The influence of the synthesis temperature (20 and 85 degrees C) and the weight ratio of bentonite/iron oxides (1:1 and 5:1) on the composite materials properties were investigated. The obtained materials were characterized by the X-ray diffraction method and Mössbauer spectroscopy. Changes in the surface and pore properties of the magnetic composites were studied by the low nitrogen adsorption method and the electrokinetic measurements. The natural bentonite and magnetic composites were used in sorption experiments. The sorption of toxic metals (zinc, cadmium and nickel) from the model solutions was well described by the linearized Langmuir and Freundlich sorption model. The results show that the magnetic bentonite is better sorbent than the unmodified bentonite if the initial concentration of studied metals is very low. Copyright 2010 Elsevier B.V. All rights reserved.

  13. Development of a microminiature sorption cooler

    NARCIS (Netherlands)

    Burger, Johannes; Holland, Harry; ter Brake, Marcel; Rogalla, Horst; Wade, Larry

    1997-01-01

    The development of a microcooler for operations below 80 K, for low temperature electronic devices requiring small cooling powers of the order of 10 mW is described. A sorption compressor combined with Joule-Thomson (JT) expansion was selected for miniaturization. The advantage of the system is

  14. A Sorption Hysteresis Model For Cellulosic Materials

    DEFF Research Database (Denmark)

    Frandsen, Henrik Lund; Damkilde, Lars

    2006-01-01

    The equilibrium concentration of adsorbed water in cellulosic materials is dependent on the history of the variations of vapor pressure in the ambient air, i.e. sorption hysteresis. Existing models to describe this phenomenon such as the independent domain theory have numerical drawbacks and/or i...

  15. Sorption of methanol in alkali exchange zeolites

    NARCIS (Netherlands)

    Rep, M.; Rep, M.; Corma, Avelino; Palomares, A.E.; Palomares gimeno, A.E.; van Ommen, J.G.; Lefferts, Leonardus; Lercher, J.A.

    2000-01-01

    Metal cation methanol sorption complexes in MFI (ZSM5), MOR and X have been studied by in situ i.r. spectroscopy in order to understand the nature of interactions of methanol in the molecular sieve pores. The results show that (a) a freely vibrating hydroxy and methyl group of methanol exist on

  16. Radionuclide sorption database for Swiss safety assessment

    International Nuclear Information System (INIS)

    McKinley, I.G.; Hadermann, J.

    1984-10-01

    Recommended sorption data for use in transport models for a Swiss High-Level Waste repository are presented. The models used in 'Project Gewaehr 1985' assume linear sorption isotherms and require elemental partition coefficient (Kd) data. On the basis of a literature search 'realistic' Kd data for 22 elements have been selected for weathered crystalline rock and sediments in contact with a reducing groundwater and also sediments with a less reducing groundwater. In an appendix sorption data for 28 elements on bentonite backfill are given. These data are supplemented with 'conservative' estimates taken to represent minimum reasonable values. Available data are discussed for each element clearly exhibiting (i) the large gaps in knowledge, (ii) their unbalanced distribution between different elements and, hence, (iii) the need for further experiments in the laboratory, the field and analogue studies. An overview of the theoretical concepts of sorption, experimental methodology and data interpretation is given in order to put the values into context. General problem areas are identified. (Auth.)

  17. Sorption of organic gases in residential rooms

    Science.gov (United States)

    Singer, Brett C.; Hodgson, Alfred T.; Hotchi, Toshifumi; Ming, Katherine Y.; Sextro, Richard G.; Wood, Emily E.; Brown, Nancy J.

    Experiments were conducted to characterize organic gas sorption in residential rooms studied "as-is" with furnishings and material surfaces unaltered and in a furnished chamber designed to simulate a residential room. Results are presented for 10 rooms (five bedrooms, two bathrooms, a home office, and two multi-function spaces) and the chamber. Exposed materials were characterized and areas quantified. A mixture of volatile organic compounds (VOCs) was rapidly volatilized within each room as it was closed and sealed for a 5-h Adsorb phase; this was followed by 30-min Flush and 2-h closed-room Desorb phases. Included were alkane, aromatic, and oxygenated VOCs representing a range of ambient and indoor air pollutants. Three organophosphorus compounds served as surrogates for Sarin-like nerve agents. Measured gas-phase concentrations were fit to three variations of a mathematical model that considers sorption occurring at a surface sink and potentially a second, embedded sink. The 3-parameter sink-diffusion model provided acceptable fits for most compounds and the 4-parameter two-sink model provided acceptable fits for the others. Initial adsorption rates and sorptive partitioning increased with decreasing vapor pressure for the alkanes, aromatics and oxygenated VOCs. Best-fit sorption parameters obtained from experimental data from the chamber produced best-fit sorption parameters similar to those obtained from the residential rooms.

  18. Sorption and migration of neptunium in porous sedimentary materials

    International Nuclear Information System (INIS)

    Tanaka, Tadao; Mukai, Masayuki; Nakayama, Shinichi

    2005-01-01

    Column migration experiments of neptunium were conducted for porous sedimentary materials: coastal sand, tuffaceous sand, ando soil, reddish soil, yellowish soil and loess, and migration behavior, sorption mechanisms and chemical formation of Np were investigated. The migration behavior of Np in each material was much different each other, due to chemical formation in solution and/or sorption mechanism of Np. Mathematical models of different concepts were applied to the experimental results to interpret the sorption mechanism and the migration behavior. It can be concluded that both of instantaneous equilibrium sorption and sorption-desorption kinetics have to be considered to model the Np migration in sedimentary materials. (author)

  19. Sorption of niobium on boreal forest soil

    Energy Technology Data Exchange (ETDEWEB)

    Soederlund, Mervi; Hakanen, Martti; Lehto, Jukka [Helsinki Univ. (Finland). Lab. of Radiochemistry

    2015-07-01

    The sorption of niobium (Nb) was investigated on humus and mineral soil samples taken from various depths of a four-metre deep forest soil pit on Olkiluoto Island, southwestern Finland. Mass distribution coefficients, K{sub d}, were determined in batch sorption tests. The steady state of Nb sorption was observed in the mineral soil samples already after one week of equilibration, and sorption decreased with depth from a very high value of 185000 mL/g at 0.7 m to 54000 mL/g at 3.4 m. The reason behind this decrease is probably the tenfold reduction in the specific surface area of the soil at the same depth range. Distribution coefficients were clearly lower in the humus layer (1000 mL/g). The K{sub d} values determined in pure water at a pH range of 4.7-6.5 were at a high level (above 55000 mL/g), but decreased dramatically above pH 6.5, corresponding to the change in the major Nb species from the neutral Nb(OH){sub 5} to the low-sorbing anionic Nb(OH){sub 6}{sup -} and Nb(OH){sub 7}{sup 2-}. However, the K{sub d} values in the model soil solution were in the slightly alkaline range an order of magnitude higher than in pure water, which is probably caused by the formation of calcium niobate surface precipitate or electrostatic interaction between surface-sorbed calcium and solute Nb. Among nine soil constituent minerals kaolinite performed best in retaining Nb in both pure water and model soil solution at pH 8, whereas potassium feldspar showed the poorest sorption. The K{sub d} value for kaolinite was above 500000 mL/g in both solutions, while the respective potassium feldspar values were in the range of 120-220 mL/g.

  20. Modeling Fission Product Sorption in Graphite Structures

    International Nuclear Information System (INIS)

    Szlufarska, Izabela; Morgan, Dane; Allen, Todd

    2013-01-01

    The goal of this project is to determine changes in adsorption and desorption of fission products to/from nuclear-grade graphite in response to a changing chemical environment. First, the project team will employ principle calculations and thermodynamic analysis to predict stability of fission products on graphite in the presence of structural defects commonly observed in very high-temperature reactor (VHTR) graphites. Desorption rates will be determined as a function of partial pressure of oxygen and iodine, relative humidity, and temperature. They will then carry out experimental characterization to determine the statistical distribution of structural features. This structural information will yield distributions of binding sites to be used as an input for a sorption model. Sorption isotherms calculated under this project will contribute to understanding of the physical bases of the source terms that are used in higher-level codes that model fission product transport and retention in graphite. The project will include the following tasks: Perform structural characterization of the VHTR graphite to determine crystallographic phases, defect structures and their distribution, volume fraction of coke, and amount of sp2 versus sp3 bonding. This information will be used as guidance for ab initio modeling and as input for sorptivity models; Perform ab initio calculations of binding energies to determine stability of fission products on the different sorption sites present in nuclear graphite microstructures. The project will use density functional theory (DFT) methods to calculate binding energies in vacuum and in oxidizing environments. The team will also calculate stability of iodine complexes with fission products on graphite sorption sites; Model graphite sorption isotherms to quantify concentration of fission products in graphite. The binding energies will be combined with a Langmuir isotherm statistical model to predict the sorbed concentration of fission products

  1. Modeling Fission Product Sorption in Graphite Structures

    Energy Technology Data Exchange (ETDEWEB)

    Szlufarska, Izabela [University of Wisconsin, Madison, WI (United States); Morgan, Dane [University of Wisconsin, Madison, WI (United States); Allen, Todd [University of Wisconsin, Madison, WI (United States)

    2013-04-08

    The goal of this project is to determine changes in adsorption and desorption of fission products to/from nuclear-grade graphite in response to a changing chemical environment. First, the project team will employ principle calculations and thermodynamic analysis to predict stability of fission products on graphite in the presence of structural defects commonly observed in very high- temperature reactor (VHTR) graphites. Desorption rates will be determined as a function of partial pressure of oxygen and iodine, relative humidity, and temperature. They will then carry out experimental characterization to determine the statistical distribution of structural features. This structural information will yield distributions of binding sites to be used as an input for a sorption model. Sorption isotherms calculated under this project will contribute to understanding of the physical bases of the source terms that are used in higher-level codes that model fission product transport and retention in graphite. The project will include the following tasks: Perform structural characterization of the VHTR graphite to determine crystallographic phases, defect structures and their distribution, volume fraction of coke, and amount of sp2 versus sp3 bonding. This information will be used as guidance for ab initio modeling and as input for sorptivity models; Perform ab initio calculations of binding energies to determine stability of fission products on the different sorption sites present in nuclear graphite microstructures. The project will use density functional theory (DFT) methods to calculate binding energies in vacuum and in oxidizing environments. The team will also calculate stability of iodine complexes with fission products on graphite sorption sites; Model graphite sorption isotherms to quantify concentration of fission products in graphite. The binding energies will be combined with a Langmuir isotherm statistical model to predict the sorbed concentration of fission

  2. Sorption behaviour of perfluoroalkyl substances in soils.

    Science.gov (United States)

    Milinovic, Jelena; Lacorte, Silvia; Vidal, Miquel; Rigol, Anna

    2015-04-01

    The sorption behaviour of three perfluoroalkyl substances (PFASs), perfluorooctane sulfonic acid (PFOS), perfluorooctanoic acid (PFOA) and perfluorobutane sulfonic acid (PFBS), was studied in six soils with contrasting characteristics, especially in the organic carbon content. Sorption isotherms were obtained by equilibrating the soil samples with 0.01 mol L(-1) CaCl2 solutions spiked with increasing concentrations of the target PFAS. The sorption reversibility of PFASs was also tested for some of the samples. Liquid chromatography coupled to tandem mass spectrometry was used to quantify the target PFASs in the solutions. Both the Freundlich and linear models were appropriate to describe the sorption behaviour of PFASs in soils, and enabled us to derive solid-liquid distribution coefficients (Kd) for each compound in each soil. Kd values increased from 19 to 295 mL g(-1) for PFOS, from 2.2 to 38 mL g(-1) for PFOA and from 0.4 to 6.8 mL g(-1) for PFBS, and were positively correlated with the organic carbon content of the soil. KOC values obtained from the correlations were 710, 96 and 17 mL g(-1) for PFOS, PFOA and PFBS, respectively. Whereas Kd values decreased in the sequence PFOS>PFOA>PFBS, desorption yields were lower than 13% for PFOS, from 24 to 58% for PFOA, and from 32 to 60% for PFBS. This shows that the physicochemical characteristics of PFASs, basically their hydrophobicity, controlled their sorption behaviour in soils, with PFOS being the most irreversibly sorbed PFAS. Copyright © 2014 Elsevier B.V. All rights reserved.

  3. SORPTION OF Au(III BY Saccharomyces cerevisiae BIOMASS

    Directory of Open Access Journals (Sweden)

    Amaria Amaria

    2010-07-01

    Full Text Available Au(III sorption by S. cerevisiae biomass extracted from beer waste industry was investigated. Experimentally, the sorption was conducted in batch method. This research involved five steps: 1 identification the functional groups present in the S. cerevisiae biomass by infrared spectroscopic technique, 2 determination of optimum pH, 3 determination of the sorption capacity and energy, 4 determination of the sorption type by conducting desorption of sorbed Au(III using specific eluents having different desorption capacity such as H2O (van der Waals, KNO3 (ion exchange, HNO3 (hydrogen bond, and tiourea (coordination bond, 5 determination of effective eluents in Au(III desorption by partial desorption of sorbed Au(III using thiourea, NaCN and KI. The remaining Au(III concentrations in filtrate were analyzed using Atomic Absorption Spectrophotometer. The results showed that: 1 Functional groups of S. cerevisiae biomass that involved in the sorption processes were hydroxyl (-OH, carboxylate (-COO- and amine (-NH2, 2 maximum sorption was occurred at pH 4, equal to 98.19% of total sorption, 3 The sorption capacity of biomass was 133.33 mg/g (6.7682E-04 mol/g and was involved sorption energy 23.03 kJ mol-1, 4 Sorption type was dominated by coordination bond, 5 NaCN was effective eluent to strip Au(III close to 100%.   Keywords: sorption, desorption, S. cerevisiae biomass, Au(III

  4. Formability of stainless steel tailored blanks

    DEFF Research Database (Denmark)

    Bagger, Claus; Gong, Hui; Olsen, Flemming Ove

    2004-01-01

    In a number of systematic tests, the formability of tailored blanks consisting of even and different combinations of AISI304 and AISI316 in thickness of 0.8 mm and 1.5 mm have been investigated. In order to analyse the formability of tailored blanks with different sheet thickness, a method based ...

  5. Development of sorption database (JAEA-SDB). Update of sorption data including soil and cement systems

    International Nuclear Information System (INIS)

    Suyama, Tadahiro; Tachi, Yukio

    2012-03-01

    Sorption of radionuclides in buffer materials (bentonite) and rocks is the key process in the safe geological disposal of radioactive waste, because migration of radionuclides in this barrier is expected to be controlled by sorption processes. Distribution coefficient (K d ) is therefore important parameter in the performance assessment (PA) of geological disposal. The sorption database including extensive compilations of K d data measured by batch sorption experiments plays key roles in PA-related K d setting and predictive model development under a variety of geochemical conditions. For this purpose, Japan Atomic Energy Agency (JAEA) has developed sorption database (JAEA-SDB) as an important basis for the PA of high-level radioactive waste disposal. This sorption database was firstly developed for the H12 PA, and was improved and updated in view of potential future data needs, focusing on assuring the desired quality level and testing the usefulness of the databases for possible applications to PA-related parameter setting. The present report focuses on updating of the sorption database (JAEA-SDB) by adding K d data for various systems including soil and cement systems, to apply JAEA-SDB for the PA-related K d setting for disposal of low level radioactive wastes including TRU wastes and the evaluation of radionuclide transport in surface soil systems. The updated data includes K d data for soil and cement systems extracted from mainly previous published database, and K d data related to our recent activities on the K d setting and mechanistic model development. As a result, 16,000 K d data from 334 references are added, total K d values in the JAEA-SDB are about 46,000. The updated JAEA-SDB is expected to make it possible to obtain quick overview of the available data, and to have suitable access to the respective data for the performance assessment of various types of radioactive waste. (author)

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

    Science.gov (United States)

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

    2012-09-21

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

  7. Testosterone sorption and desorption: Effects of soil particle size

    Energy Technology Data Exchange (ETDEWEB)

    Qi, Yong, E-mail: yqi01@unomaha.edu [Civil Engineering Dept., University of Nebraska-Lincoln at Omaha Campus, Omaha, NE 68182 (United States); Zhang, Tian C. [Civil Engineering Dept., University of Nebraska-Lincoln at Omaha Campus, Omaha, NE 68182 (United States); Ren, Yongzheng [School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China)

    2014-08-30

    Graphical abstract: - Highlights: • Smaller soil particles have higher sorption and lower desorption rates. • The sorption capacity ranks as clay > silt > sand. • Small particles like clays have less potential for desorption. • Colloids (clays) have high potential to facilitate the transport of hormones in soil–water environments. - Abstract: Soils contain a wide range of particles of different diameters with different mobility during rainfall events. Effects of soil particles on sorption and desorption behaviors of steroid hormones have not been investigated. In this study, wet sieve washing and repeated sedimentation methods were used to fractionate the soils into five ranges. The sorption and desorption properties and related mechanisms of testosterone in batch reactors filled with fractionated soil particles were evaluated. Results of sorption and desorption kinetics indicate that small soil particles have higher sorption and lower desorption rates than that of big ones. Thermodynamic results show the sorption processes are spontaneous and exothermal. The sorption capacity ranks as clay > silt > sand, depending mainly on specific surface area and surface functional groups. The urea control test shows that hydrogen bonding contributes to testosterone sorption onto clay and silt but not on sand. Desorption tests indicate sorption is 36–65% irreversible from clay to sand. Clays have highest desorption hysteresis among these five soil fractions, indicating small particles like clays have less potential for desorption. The results provide indirect evidence on the colloid (clay)-facilitated transport of hormones (micro-pollutants) in soil environments.

  8. Isotherm, kinetic, and thermodynamic study of ciprofloxacin sorption on sediments.

    Science.gov (United States)

    Mutavdžić Pavlović, Dragana; Ćurković, Lidija; Grčić, Ivana; Šimić, Iva; Župan, Josip

    2017-04-01

    In this study, equilibrium isotherms, kinetics and thermodynamics of ciprofloxacin on seven sediments in a batch sorption process were examined. The effects of contact time, initial ciprofloxacin concentration, temperature and ionic strength on the sorption process were studied. The K d parameter from linear sorption model was determined by linear regression analysis, while the Freundlich and Dubinin-Radushkevich (D-R) sorption models were applied to describe the equilibrium isotherms by linear and nonlinear methods. The estimated K d values varied from 171 to 37,347 mL/g. The obtained values of E (free energy estimated from D-R isotherm model) were between 3.51 and 8.64 kJ/mol, which indicated a physical nature of ciprofloxacin sorption on studied sediments. According to obtained n values as measure of intensity of sorption estimate from Freundlich isotherm model (from 0.69 to 1.442), ciprofloxacin sorption on sediments can be categorized from poor to moderately difficult sorption characteristics. Kinetics data were best fitted by the pseudo-second-order model (R 2  > 0.999). Thermodynamic parameters including the Gibbs free energy (ΔG°), enthalpy (ΔH°) and entropy (ΔS°) were calculated to estimate the nature of ciprofloxacin sorption. Results suggested that sorption on sediments was a spontaneous exothermic process.

  9. High accuracy calibration of a dynamic vapor sorption instrument and determination of the equilibrium humidities using single salts

    DEFF Research Database (Denmark)

    Rörig-Dalgaard, Inge; Svensson, Staffan

    2016-01-01

    We present a procedure for accurately calibrating a dynamic vapor sorption (DVS) instrument using single salts. The procedure accounts for and tailors distinct calibration tests according to the fundamental properties of each salt. Especially relevant properties influencing the calibration...... are the heat of solution, heat of condensation, and the kinetics connected to the salt phase transition, as these influence the microclimate surrounding the salts during calibration. All these issues were dealt with to obtain precise calibration results. The DVS instrument comprises two control modes......-known equilibrium RH of each salt solution, the presented method’s results are both accurate with significant agreement and precise with small variation....

  10. Effect of natural organic materials on cadmium and neptunium sorption

    International Nuclear Information System (INIS)

    Kung, K.S.; Triay, I.R.

    1994-01-01

    In a batch sorption study of the effect of naturally occurring organic materials on the sorption of cadmium and neptunium on oxides and tuff surfaces, the model sorbents were synthetic goethite, boehmite, amorphous silicon oxides, and a crushed tuff material from Yucca Mountain, Nevada. An amino acid, 3-(3,4-dihydroxypheny)-DL-alanine (DOPA), and an aquatic-originated fulvic material, Nordic aquatic fulvic acid (NAFA), were used as model organic chemicals. Sorption isotherm results showed that DOPA sorption followed the order aluminum oxide > iron oxide > silicon oxide and that the amount of DOAP sorption for a given sorbent increased as the solution pH was raised. The sorption of cadmium and neptunium on the iron oxide was about ten times higher than that on the aluminum oxide. The sorption of cadmium and neptunium on natural tuff material was much lower than that on aluminum and iron oxides. The sorption of cadmium on iron and aluminum oxides was found to be influenced by the presence of DOPA, and increasing the amount of DOPA coating resulted in higher cadmium sorption on aluminum oxide. However, for iron oxide, cadmium sorption decreased with increasing DOPA concentration. The presence of the model organic materials DOPA and NAFA did not affect the sorption of neptunium on tuff material or on the iron and aluminum oxides. Spectroscopic results indicate that cadmium complexes strongly with DOPA. Therefore, the effect of the organic material, DOPA, on the cadmium sorption is readily observed. However, neptunium is possibly complexed weakly with organic material. Thus, DOPA and NAFA have little effect on neptunium sorption on all sorbents selected for study

  11. Effect of natural organic materials on cadmium and neptunium sorption

    International Nuclear Information System (INIS)

    Kung, K.S.; Triay, I.R.

    1995-01-01

    In a batch sorption study of the effect of naturally occurring organic materials on the sorption of cadmium and neptunium on oxides and tuff surfaces, the model sorbents were synthetic goethite, boehmite, amorphous silicon oxides, and a crushed tuff material from Yucca Mountain, Nevada. An amino acid, 3-(3,4-dihydroxypheny)-DL-alanine (DOPA), and an aquatic-originated fulvic material, Nordic aquatic fulvic acid (NAFA), were used as model organic chemicals. Sorption isotherm results showed that DOPA sorption followed the order aluminum oxide > iron oxide > silicon oxide and that the amount of DOPA sorption for a given sorbent increased as the solution pH was raised. The sorption of cadmium and neptunium on the iron oxide was about ten times higher than that on the aluminum oxide. The sorption of cadmium and neptunium on natural tuff material was much lower than that on aluminum and iron oxides. The sorption of cadmium on iron and aluminum oxides was found to be influenced by the presence of DOPA, and increasing the amount of DOPA coating resulted in higher cadmium sorption on aluminum oxide. However, for iron oxide, cadmium sorption decreased with increasing DOPA concentration. The presence of the model organic materials DOPA and NAFA did not affect the sorption of neptunium on tuff material or on the iron and aluminum oxides. Spectroscopic results indicate that cadmium complexes strongly with DOPA. Therefore, the effect of the organic material, DOPA, on the cadmium sorption is readily observed. However, neptunium is possibly complexed weakly with organic material. Thus, DOPA and NAFA have little effect on neptunium sorption on all sorbents selected for study. (authors). 8 refs., 10 figs

  12. Sorption of zinc on human teeth

    International Nuclear Information System (INIS)

    Helal, A.; Amin, H.; Alian, G.

    1997-01-01

    Zinc containing dental amalgams are sometimes used as fillings by dentists. The freshly mixed mass of the amalgam alloy and liquid mercury packed or condensed into a prepared tooth cavity. Zinc has been included in amalgams alloys up to 2% as an aid in manufacturing by helping to produce clean sound castings of the ingots. Although such restorations have a relatively long service life, they are subject to corrosion and galvanic action, thus releasing metallic products into the oral environment. The aim of this paper is to investigate the uptake (sorption) of Zinc ionic species on human teeth using the radioactive tracer technique. For this purpose the isotope Zn-65 produced from pile-irradiation of zinc metal was used. The various liquids studied were drinking water (tap water), tea, coffee, red tea and chicken soup. Sorption was studied through immersion of a single human tooth (extracted) in each of these liquids

  13. Sorption analyses in materials science: selected oxides

    International Nuclear Information System (INIS)

    Fuller, E.L. Jr.; Condon, J.B.; Eager, M.H.; Jones, L.L.

    1981-01-01

    Physical adsorption studies have been shown to be extremely valuable in studying the chemistry and structure of dispersed materials. Many processes rely on the access to the large amount of surface made available by the high degree of dispersion. Conversely, there are many applications where consolidation of the dispersed solids is required. Several systems (silica gel, alumina catalysts, mineralogic alumino-silicates, and yttrium oxide plasters) have been studied to show the type and amount of chemical and structural information that can be obtained. Some review of current theories is given and additional concepts are developed based on statistical and thermodynamic arguments. The results are applied to sorption data to show that detailed sorption analyses are extremely useful and can provide valuable information that is difficult to obtain by any other means. Considerable emphasis has been placed on data analyses and interpretation of a nonclassical nature to show the potential of such studies that is often not recognized nor utilized

  14. Sorption of three synthetic musks by microplastics.

    Science.gov (United States)

    Zhang, Xiaojun; Zheng, Minggang; Wang, Ling; Lou, Yinghua; Shi, Lei; Jiang, Shujun

    2018-01-01

    Microplastics and synthetic musks (SMs) are two typical organic pollutants in the marine environment. In this study, the sorption of three SMs to microplastics in a simulated seawater environment was examined. Tonalide (AHTN), musk xylene (MX), and musk ketone (MK) were the musks investigated, while polypropylene (PP) was used as the microplastic. It was found that the equilibrium sorption time was about 10h and the adsorption kinetics model conformed to a Lagergren adsorption model. The adsorption capacity increased with decreasing particle size. Adsorption reached a peak at 25°C, and the adsorption capacity was not sensitive to the concentration of sodium chloride. There is a need for more research and monitoring of microplastics in the marine environment due to their strong ability to absorb organic pollutants. Copyright © 2017. Published by Elsevier Ltd.

  15. Uranium sorption on tezontle volcanic rock

    International Nuclear Information System (INIS)

    Lopez M, B. E.; Duran B, J. M.; Iturbe G, J. L.; Olguin G, M. T.

    2009-01-01

    It is described a study that demonstrates that hexavalent uranium ions were sorbed by the naturally occurring mineral using a batch technique. This mineral is found in abundant quantities in Mexico. Our study focused on the separation of U Vi from synthetic aqueous systems of both H 2 O-UO 2 (NO 3 ) 2 .6H 2 O (acid) and H 2 O-Na 4 [UO 2 (CO 3 ) 3 ] (basic). The chemical speciation was performed by using high voltage electrophoresis, and the uranium content was determined by UV-Vis spectroscopy. The quantified U(Vi) sorption by tezontle from acidic and basic systems was 2.72 and 1.68 μmol/g, respectively, and the sorption behavior is discussed considering the surface charge of the tezontle at different ph values based on the point of zero charge characteristic of this material. (Author)

  16. Positron Spectroscopy of Nanodiamonds after Hydrogen Sorption

    Directory of Open Access Journals (Sweden)

    Lyudmila Nikitina

    2018-01-01

    Full Text Available The structure and defects of nanodiamonds influence the hydrogen sorption capacity. Positronium can be used as a sensor for detecting places with the most efficient capture of hydrogen atoms. Hydrogenation of carbon materials was performed from gas atmosphere. The concentration of hydrogen absorbed by the sample depends on the temperature and pressure. The concentration 1.2 wt % is achieved at the temperature of 243 K and the pressure of 0.6 MPa. The hydrogen saturation of nanodiamonds changes the positron lifetime. Increase of sorption cycle numbers effects the positron lifetime, as well as the parameters of the Doppler broadening of annihilation line. The electron-positron annihilation being a sensitive method, it allows detecting the electron density fluctuation of the carbon material after hydrogen saturation.

  17. Sorption studies of radioelements on geological materials

    International Nuclear Information System (INIS)

    Berry, John A.; Yui, Mikazu; Kitamura, Akira

    2007-11-01

    Batch sorption experiments have been carried out to study the sorption of uranium, technetium, curium, neptunium, actinium, protactinium, polonium, americium and plutonium onto bentonite, granodiorite and tuff. Mathematical modelling using the HARPHRQ program and the HATCHES database was carried out to predict the speciation of uranium and technetium in the equilibrated seawater, and neptunium, americium and plutonium in the rock equilibrated water. Review of the literature for thermodynamic data for curium, actinium, protactinium and polonium was carried out. Where sufficient data were available, predictions of the speciation and solubility were made. This report is a summary report of the experimental work conducted by AEA Technology during April 1991-March 1998, and the main results have been presented at Material Research Society Symposium Proceedings and published as proceedings of them. (author)

  18. Sorption of Phenanthrene on Agricultural Soils

    DEFF Research Database (Denmark)

    Soares, Antonio Alves; Møldrup, Per; Minh, Luong Nhat

    2013-01-01

    Polyaromatic hydrocarbon (PAH) sorption to soil is a key process deciding the transport and fate of PAH, and potential toxic impacts in the soil and groundwater ecosystems, for example in connection with atmospheric PAH deposition on soils. There are numerous studies on PAH sorption in relatively...... low organic porous media such as urban soils and groundwater sediments, but less attention has been given to cultivated soils. In this study, the phenanthrene partition coefficient, KD (liter per kilogram), was measured on 143 cultivated Danish soils (115 topsoils, 0–0.25-m soil depth and 28 subsoils...... (COC and NCOC, grams per gram). Multiple regression analyses showed that the NCOC-based phenanthrene partition coefficient (KNCOC) could be markedly higher than the COC-based partition coefficient (KCOC) for soils with a clay/OC ratio

  19. Phosphate sorption characteristics of European alpine soils

    Czech Academy of Sciences Publication Activity Database

    Kaňa, Jiří; Kopáček, Jiří; Camarero, L.; Garcia-Pausas, J.

    2011-01-01

    Roč. 75, č. 3 (2011), s. 862-870 ISSN 0361-5995 R&D Projects: GA ČR(CZ) GA526/09/0567; GA AV ČR(CZ) KJB600960907 Grant - others:EU EMERGE(CZ) EVK1-CT-1999-00032 Institutional research plan: CEZ:AV0Z60170517 Keywords : phosphate sorption * alpine soils * acidification Subject RIV: DJ - Water Pollution ; Quality Impact factor: 1.979, year: 2011

  20. Sorption studies of caesium by complex hexacyanoferrates

    International Nuclear Information System (INIS)

    Jacobi, D.

    1992-01-01

    A comprehensive literature review was carried out on the preparation of complex hexacyanoferrates in a granular form suitable for use in a packed column. The preparation of sodium nickel hexacyanoferrate using a freeze-thaw method was studied in detail and a method developed to produce a consistent and reproducible granular product. The equilibrium and sorption kinetics were studied using batch and column tests, and the process modelled to predict performance under various conditions. (author)

  1. Sorption behaviour of herbicides in soils

    International Nuclear Information System (INIS)

    Luchini, L.C.; Wiendl, F.M.; Ruegg, E.F.; Instituto Biologico, Sao Paulo

    1988-01-01

    Environmental contamination by herbicides is related with the sorption phenomenon of these compounds in the soils. The behaviour of paraquat, 2,4-D and diuron was studied in soils with different physico-chemical properties, through the Freundlich adsorption and desorption isotherms, using 14 C-radiolabeled herbicides. Results of the range of the adsorption-desorption of each herbicide was related mainly with the chemical characteristics of these compounds. (author) [pt

  2. Moisture sorption isotherms of dehydrated whey proteins

    Directory of Open Access Journals (Sweden)

    Suzana Rimac Brnčić

    2010-03-01

    Full Text Available Moisture sorption isotherms describe the relation between the moisture content of the dry material (food and relative humidity of the surrounding environment. The data obtained are important in modelling of drying process conditions, packaging and shelf-life stability of food that will provide maximum retaining of aroma, colour and texture as well as nutritive and biological value. The objective of this research was to establish the equilibrium moisture content and water activity, as well as monolayer value of two commercial powdered whey protein isolates before and after tribomechanical micronisation and enzymatic hydrolysis, respectively. At the same time it was necessary to evaluate the best moisture sorption isotherm equation to fit the experimental data. The equilibrium moisture contents in investigated samples were determined using standard gravimetric method at 20 °C. The range of water activities was 0.11 to 0.75. The monolayer moisture content was estimated from sorption data using Brunauer-Emmett-Teller (BET and Guggenheim-Anderson-de Boer (GAB models. The results have shown that tribomechanically treated whey protein isolates as well as protein hydrolizates had lower monolayer moisture content values as well as higher corresponding water activity. Therefore, in spite of the fact that they have lower moisture content, they can be storage at higher relative humidity compared to untreated samples. BET model gave better fit to experimental sorption data for a water activity range from 0.11-0.54, while GAB model gave the closest fit for a water activity to 0.75.

  3. Moisture sorption isotherms of dehydrated whey proteins

    OpenAIRE

    Suzana Rimac Brnčić; Vesna Lelas; Zoran Herceg; Marija Badanjak

    2010-01-01

    Moisture sorption isotherms describe the relation between the moisture content of the dry material (food) and relative humidity of the surrounding environment. The data obtained are important in modelling of drying process conditions, packaging and shelf-life stability of food that will provide maximum retaining of aroma, colour and texture as well as nutritive and biological value. The objective of this research was to establish the equilibrium moisture content and water activity, as well as...

  4. Trans-channel interactions in batrachotoxin-modified skeletal muscle sodium channels: voltage-dependent block by cytoplasmic amines, and the influence of mu-conotoxin GIIIA derivatives and permeant ions.

    Science.gov (United States)

    Pavlov, Evgeny; Britvina, Tatiana; McArthur, Jeff R; Ma, Quanli; Sierralta, Iván; Zamponi, Gerald W; French, Robert J

    2008-11-01

    External mu-conotoxins and internal amine blockers inhibit each other's block of voltage-gated sodium channels. We explore the basis of this interaction by measuring the shifts in voltage-dependence of channel inhibition by internal amines induced by two mu-conotoxin derivatives with different charge distributions and net charges. Charge changes on the toxin were made at residue 13, which is thought to penetrate most deeply into the channel, making it likely to have the strongest individual interaction with an internal charged ligand. When an R13Q or R13E molecule was bound to the channel, the voltage dependence of diethylammonium (DEA)-block shifted toward more depolarized potentials (23 mV for R13Q, and 16 mV for R13E). An electrostatic model of the repulsion between DEA and the toxin simulated these data, with a distance between residue 13 of the mu-conotoxin and the DEA-binding site of approximately 15 A. Surprisingly, for tetrapropylammonium, the shifts were only 9 mV for R13Q, and 7 mV for R13E. The smaller shifts associated with R13E, the toxin with a smaller net charge, are generally consistent with an electrostatic interaction. However, the smaller shifts observed for tetrapropylammonium than for DEA suggest that other factors must be involved. Two observations indicate that the coupling of permeant ion occupancy of the channel to blocker binding may contribute to the overall amine-toxin interaction: 1), R13Q binding decreases the apparent affinity of sodium for the conducting pore by approximately 4-fold; and 2), increasing external [Na(+)] decreases block by DEA at constant voltage. Thus, even though a number of studies suggest that sodium channels are occupied by no more than one ion most of the time, measurable coupling occurs between permeant ions and toxin or amine blockers. Such interactions likely determine, in part, the strength of trans-channel, amine-conotoxin interactions.

  5. Sorption of radon-222 to natural sediments

    International Nuclear Information System (INIS)

    Wong, C.S.; Chin, Y.P.; Gschwend, P.M.

    1992-01-01

    The sorption of radon to sediments was investigated, since this may affect the use of porewater radon profiles for estimating bed irrigation rates. Batch experiments showed that radon has an organic-carbon-normalized sediment-water partition coefficient (K oc , L kg oc -1 ) of 21.1 ± 2.9 for a Boston Harbor sediment, 25.3 ± 2.1 for a Charles River sediment, and 22.4 ± 2.6 for a Buzzards Bay sediment. These values are in close agreement with predictions using radon's octanol-water partition coefficient (K ow ), which was measured to be 32.4 ± 1.5. Temperature and ionic strength effects on K oc were estimated to be small. Given rapid sorption kinetics, the authors suggest that slurry stripping techniques used by many investigators to measure 222 Rn in sediment samples collect both sorbed and dissolved radon. Sorption effects were included in a transport model to obtain revised estimates of irrigation rates from existing literature profiles. Irrigation rates had to be increased over previously reported values in proportion to the sediment organic matter content

  6. Sorption of antimony on human teeth

    International Nuclear Information System (INIS)

    Nofal, M.; Amin, H.; Alian, G.

    1997-01-01

    The study of the uptake of toxic elements on human teeth represents an interesting research area, as the fate of these elements when present in the human food is of health significance. Since antimony is one of the common toxic elements and since, the chemical behaviour of antimony is similar to that of arsenic, one of the most important toxic elements commonly encountered in cases of food poisoning, it has been decided to investigate its uptake on human teeth and on other restoration materials. The radioactive tracer technique was used to evaluate the concentration of antimony sorbed on teeth. This tracer was obtained by irradiation of antimony metal in the reactor, subsequent dissolution in concentrated sulphuric acid, evaporation to dryness and making the solution 6 M in Hydrochloric acid (1). Antimony prepared in this way is in the trivalent state (Sb III). Sorption was studied in water, tea, coffee, red tea and chicken soup. The highest sorption was achieved from water and chicken soup and least sorption was noticed in case of coffee. The results are presented in the form of the depletion of the radioactivity (A) of antimony with time in presence of a tooth in water and other drinks

  7. Sorption of sulfuryl fluoride by food commodities.

    Science.gov (United States)

    Sriranjini, Venkata-rao; Rajendran, Somiahnadar

    2008-08-01

    The use of sulfuryl fluoride, a structural fumigant for termite and woodborer control, has recently been expanded to treating stored food commodities and food facilities. There is, however, a lack of data on the sorption of sulfuryl fluoride by food commodities. Knowledge about sorption is important in the context of effective treatment and residues. When sulfuryl fluoride was applied at a dose of 50 g m(-3) to various food commodities (total 68) with 300 g per replicate in 0.75 L gas wash bottles (fumigation chambers) at 25 +/- 1 degrees C, in most cases (81%) the gas concentrations in the free space of the commodities exceeded 50 g m(-3) (range 51-80 g m(-3)) at the end of 24 h exposure. In chambers without the substrate, an average concentration of 49.7 g m(-3) was recorded. About 54% of the commodities showed low-level ( 50%). The latter include white oats (terminal gas concentration 17.8 g m(-3)), some of the decorticated split pulses (24.0-29.3 g m(-3)), chickpea flour (26.3 g m(-3)), dried ginger (29.0 g m(-3)), refined wheat flour (30.3 g m(-3)) and coriander powder (40.5 g m(-3)). In unfumigated control commodities, owing to interfering volatiles, Fumiscope readings in the range 0-13 were noted. Sulfuryl fluoride has the advantage of a low or moderate level of sorption with the majority of the food commodities.

  8. Mathematical Modeling of Moisture Sorption Isotherms and Determination of Isosteric Heats of Sorption of Ziziphus Leaves

    Directory of Open Access Journals (Sweden)

    Amel Saad

    2014-01-01

    Full Text Available Desorption and adsorption equilibrium moisture isotherms of Ziziphus spina-christi leaves were determined using the gravimetric-static method at 30, 40, and 50°C for water activity (aw ranging from 0.057 to 0.898. At a given aw, the results show that the moisture content decreases with increasing temperature. A hysteresis effect was observed. The experimental data of sorption were fitted by eight models (GAB, BET, Henderson-Thompson, modified-Chung Pfost, Halsey, Oswin, Peleg, and Adam and Shove. After evaluating the models according to several criteria, the Peleg and Oswin models were found to be the most suitable for describing the sorption curves. The net isosteric heats of desorption and adsorption of Ziziphus spina-christi leaves were calculated by applying the Clausius-Clapeyron equation to the sorption isotherms and an expression for predicting these thermodynamic properties was given.

  9. Plutonium sorption onto hematite colloids at femto- and nanomolar concentrations

    Energy Technology Data Exchange (ETDEWEB)

    Romanchuk, A.Yu.; Kalmykov, S.N.; Aliev, R.A. [Lomonosov Moscow State Univ., Moscow (Russian Federation). Radiochemistry Div.

    2011-07-01

    The surface-mediated reduction of Pu(VI) upon sorption onto hematite colloids is addressed in the paper that bring some new light on the mechanisms of interaction of Pu in high valence states with different Fe(III) oxides. We study the sorption of Pu taken at two different total concentrations around 10{sup -9} and 10{sup -14} M using {sup 239}Pu and short-lived {sup 237}Pu tracer. In order to conclude on the mechanisms of Pu sorption onto hematite, the kinetics of sorption of Pu(IV) and Pu(VI) at two concenrations is studied as well as its leaching behavior. The rate limiting step in Pu(VI) sorption is its surface-mediated reduction. The experimental evidence of the polymerization of Pu(IV) on the surface taken at Pu total concentration of {proportional_to} 10{sup -9} M is presented based on the kinetics of sorption and leaching behavior. (orig.)

  10. Implementation of sorption hysteresis in multi-Fickian moisture transport

    DEFF Research Database (Denmark)

    Frandsen, Henrik Lund; Svensson, Staffan

    2007-01-01

    In the cellular structure of wood, bound-water diffusion and water-vapor diffusion interact via sorption in a complex moisture-transportation system. At low relative humidity, moisture transport may be modeled by a Fickian diffusion equation to a good approximation. At higher relative humidity...... this behavior. The multi-Fickian model describes the combined transport of bound water and vapor and their interaction through sorption. The bound-water concentration is also influenced by sorption hysteresis. In the worst case, sorption hysteresis may result in deviations of up to 30-35% in moisture content....... Hence, for a precise moisture content computation, sorption hysteresis must be taken into account. The present paper explains the relation between sorption hysteresis and multi-Fickian moisture transport, and clarifies how models for the two phenomena are coupled. To illustrate the effects, a finite...

  11. Investigation of metal ions sorption of brown peat moss powder

    Science.gov (United States)

    Kelus, Nadezhda; Blokhina, Elena; Novikov, Dmitry; Novikova, Yaroslavna; Chuchalin, Vladimir

    2017-11-01

    For regularities research of sorptive extraction of heavy metal ions by cellulose and its derivates from aquatic solution of electrolytes it is necessary to find possible mechanism of sorption process and to choice a model describing this process. The present article investigates the regularities of aliovalent metals sorption on brown peat moss powder. The results show that sorption isotherm of Al3+ ions is described by Freundlich isotherm and sorption isotherms of Na+ i Ni2+ are described by Langmuir isotherm. To identify the mechanisms of brown peat moss powder sorption the IR-spectra of the initial brown peat moss powder samples and brown peat moss powder samples after Ni (II) sorption were studied. Metal ion binding mechanisms by brown peat moss powder points to ion exchange, physical adsorption, and complex formation with hydroxyl and carboxyl groups.

  12. Continuous tailoring activities in software engineering

    OpenAIRE

    Ribaud , Vincent; Saliou , Philippe

    2004-01-01

    International audience; Software activities belong to different processes. Tailoring software processes aims to relate the operational software processes of an organization to the effective project. With the information technology industry moving ever faster, established positions are undergoing constant evolutionary change. The failure of a complex tailoring process of a management information system is reported. There is a need to adopt software processes that can operate under constant cha...

  13. Comparison of neptunium sorption results using batch and column techniques

    International Nuclear Information System (INIS)

    Triay, I.R.; Furlano, A.C.; Weaver, S.C.; Chipera, S.J.; Bish, D.L.

    1996-08-01

    We used crushed-rock columns to study the sorption retardation of neptunium by zeolitic, devitrified, and vitric tuffs typical of those at the site of the potential high-level nuclear waste repository at Yucca Mountain, Nevada. We used two sodium bicarbonate waters (groundwater from Well J-13 at the site and water prepared to simulate groundwater from Well UE-25p No. 1) under oxidizing conditions. It was found that values of the sorption distribution coefficient, Kd, obtained from these column experiments under flowing conditions, regardless of the water or the water velocity used, agreed well with those obtained earlier from batch sorption experiments under static conditions. The batch sorption distribution coefficient can be used to predict the arrival time for neptunium eluted through the columns. On the other hand, the elution curves showed dispersivity, which implies that neptunium sorption in these tuffs may be nonlinear, irreversible, or noninstantaneous. As a result, use of a batch sorption distribution coefficient to calculate neptunium transport through Yucca Mountain tuffs would yield conservative values for neptunium release from the site. We also noted that neptunium (present as the anionic neptunyl carbonate complex) never eluted prior to tritiated water, which implies that charge exclusion does not appear to exclude neptunium from the tuff pores. The column experiments corroborated the trends observed in batch sorption experiments: neptunium sorption onto devitrified and vitric tuffs is minimal and sorption onto zeolitic tuffs decreases as the amount of sodium and bicarbonate/carbonate in the water increases

  14. Sorption of fibronectin to human root surfaces in vitro

    International Nuclear Information System (INIS)

    Mendieta, C.; Caravana, C.; Fine, D.H.

    1990-01-01

    The purpose of this study was to determine the conditions that favor the sorption and retention of human plasma fibronectin to cementum. Rectangular root segments prepared from teeth extracted for orthodontic reasons were mounted on a capillary pipette and immersed in solutions of 125 I fibronectin for assay of cementum sorption under various conditions. Kinetic studies showed sorption to be rapid, with 77% of the maximum fibronectin sorption occurring within 1 minute. Fibronectin sorption was reduced when added in conjunction with serum and was inhibited by monovalent ions (such as sodium), but enhanced in the presence of divalent cations (such as calcium). Exposure of cementum to serum partially blocked subsequent sorption of fibronectin, while cementum bound fibronectin was eluted by subsequent exposure to serum. Treatment of cementum with citric acid pH 1.1 (4 minutes) followed by 5% sodium hypochlorite (5 minutes) caused a significant increase in fibronectin sorption with maximum retention upon subsequent exposure to serum (P less than 0.05). Fibronectin sorption to cementum was: rapid, electrostatic in nature, competitive, reversible, Ca+(+)-facilitated, and maximized by prior treatment of the root with citric acid and sodium hypochlorite. It is concluded that sorption of fibronectin to cementum can be achieved for clinical gain; however, conditions of application can significantly influence both accumulation and subsequent release of root sorbed material

  15. Experimental study of strontium sorption on fissure filling material

    International Nuclear Information System (INIS)

    Eriksen, T.E.; Cui, Daqing

    1994-12-01

    We have carried out a comparative study of sorption and desorption of strontium in groundwater on separated magnetic and size fractions of fissure filling material taken from natural fissures in granitic rock. Complete reversibility of the sorption process was demonstrated by identical Freundlich isotherms, isotopic exchangeability and pH dependence of the distribution coefficients Rd. The sorption was found to be strongly pH dependent in the range 3-11. The pH effect can be accommodated in the sorption model by considering the surface areas and surface charges of the minerals in the fissure filling material. 20 refs, 9 figs, 3 tabs

  16. Sorption of tebuconazole onto selected soil minerals and humic acids.

    Science.gov (United States)

    Cadková, Eva; Komárek, Michael; Kaliszová, Regina; Koudelková, Věra; Dvořák, Jiří; Vaněk, Aleš

    2012-01-01

    The aim of the present study was to investigate tebuconazole sorption on common soil minerals (birnessite, ferrihydrite, goethite, calcite and illite) and humic acids (representing soil organic matter). Tebuconazole was used (i) in the commercial form Horizon 250 EW and (ii) as an analytical grade pure chemical. In the experiment with the commercially available tebuconazole, a significant pH-dependent sorption onto the oxides was observed (decreasing sorption with increasing pH). The highest sorption was found for ferrihydrite due to its high specific surface area, followed by humic acids, birnessite, goethite and illite. No detectable sorption was found for calcite. The sorption of analytical grade tebuconazole on all selected minerals was significantly lower compared to the commercial product. The sorption was the highest for humic acids, followed by ferrihydrite and illite and almost negligible for goethite and birnessite without any pH dependence. Again, no sorption was observed for calcite. The differences in sorption of the commercially available and analytical grade tebuconazole can be attributed to the additives (e.g., solvents) present in the commercial product. This work proved the importance of soil mineralogy and composition of the commercially available pesticides on the behavior of tebuconazole in soils.

  17. Determination of sorption of seventy five pharmaceuticals in sewage sludge

    DEFF Research Database (Denmark)

    Hörsing, Maritha; Ledin, Anna; Grabic, Roman

    2011-01-01

    Sorption of 75 active pharmaceutical ingredients (APIs) to three different types of sludge (primary sludge, secondary sludge with short and long sludge age respectively) were investigated. To obtain the sorption isotherms batch studies with the APIs mixture were performed in four nominal concentr......Sorption of 75 active pharmaceutical ingredients (APIs) to three different types of sludge (primary sludge, secondary sludge with short and long sludge age respectively) were investigated. To obtain the sorption isotherms batch studies with the APIs mixture were performed in four nominal...

  18. Effects of ultrasound and sodium lauryl sulfate on the transdermal delivery of hydrophilic permeants: Comparative in vitro studies with full-thickness and split-thickness pig and human skin.

    Science.gov (United States)

    Seto, Jennifer E; Polat, Baris E; Lopez, Renata F V; Blankschtein, Daniel; Langer, Robert

    2010-07-01

    The simultaneous application of ultrasound and the surfactant sodium lauryl sulfate (referred to as US/SLS) to skin enhances transdermal drug delivery (TDD) in a synergistic mechanical and chemical manner. Since full-thickness skin (FTS) and split-thickness skin (STS) differ in mechanical strength, US/SLS treatment may have different effects on their transdermal transport pathways. Therefore, we evaluated STS as an alternative to the well-established US/SLS-treated FTS model for TDD studies of hydrophilic permeants. We utilized the aqueous porous pathway model to compare the effects of US/SLS treatment on the skin permeability and the pore radius of pig and human FTS and STS over a range of skin electrical resistivity values. Our findings indicate that the US/SLS-treated pig skin models exhibit similar permeabilities and pore radii, but the human skin models do not. Furthermore, the US/SLS-enhanced delivery of gold nanoparticles and quantum dots (two model hydrophilic macromolecules) is greater through pig STS than through pig FTS, due to the presence of less dermis that acts as an artificial barrier to macromolecules. In spite of greater variability in correlations between STS permeability and resistivity, our findings strongly suggest the use of 700microm-thick pig STS to investigate the in vitro US/SLS-enhanced delivery of hydrophilic macromolecules. 2010 Elsevier B.V. All rights reserved.

  19. Sorption of nitrate onto amine-crosslinked wheat straw: characteristics, column sorption and desorption properties.

    Science.gov (United States)

    Xing, Xu; Gao, Bao-Yu; Zhong, Qian-Qian; Yue, Qin-Yan; Li, Qian

    2011-02-15

    The nitrate removal process was evaluated using a fixed-bed column packed with amine-crosslinked wheat straw (AC-WS). Column sorption and desorption characteristics of nitrate were studied extensively. Solid-state (13)C NMR and zeta potential analysis validated the existence of crosslinked amine groups in AC-WS. Raman shift of the nitrate peaks suggested the electrostatic attraction between the adsorbed ions and positively charged amine sites. The column sorption capacity (q(ed)) of the AC-WS for nitrate was 87.27 mg g(-1) in comparison with the raw WS of 0.57 mg g(-1). Nitrate sorption in column was affected by bed height, influent nitrate concentration, flow rate and pH, and of all these, influent pH demonstrated an essential effect on the performance of the column. In addition, desorption and dynamic elution tests were repeated for several cycles, with high desorption rate and slight losses in its initial column sorption capacity. Copyright © 2010 Elsevier B.V. All rights reserved.

  20. 3.3. Sorption activity of cross-linked polymers of ethynyl-piperidol

    International Nuclear Information System (INIS)

    Khalikov, D.Kh.

    2012-01-01

    The sorption activity of cross-linked polymers of ethynyl-piperidol was studied. The bilirubin sorption was studied as well. The kinetic of bilirubin sorption and human serum albumin at their joint presence in hydrogel solutions was defined. Bilirubin sorption and change of albumin composition was considered. The sorption of middle molecular peptides was considered as well. The sorption of endogenous toxin by means of ethynyl-piperidol polymers was done.

  1. Sorption of Arsenite onto Mackinawite Coated Sand

    Science.gov (United States)

    Gallegos, T. J.; Hayes, K. F.; Abriola, L. M.

    2004-05-01

    Arsenic contamination of groundwater is a widespread problem affecting aquifers in the United States as well as abroad. Recent strengthening of the US EPA MCL for arsenic has prompted the need for technology capable of removing both arsenite and arsenate from solution. Arsenite, the more toxic form of arsenic, is more difficult to remove from anoxic zones in the subsurface. Studies by others have demonstrated the affinity of some types of iron sulfides for arsenite, such as troilite, pyrite, amorphous iron sulfide and mackinawite. However, these studies have not provided a comprehensive investigation of the macroscopic behavior of arsenite in the presence of crystalline mackinawite in a form that can be readily applied to real-world treatment technologies. This study examines the behavior of arsenite in the presence of mackinawite coated sand. PH edge results demonstrate that arsenite sorption onto mackinawite coated sand increases with increasing pH, reaching maximum removal at pH 10. Arsenite removal, albeit slight, occurring below pH 5 is independent of pH indicative of a different removal mechanism. Isotherm studies show that at low concentrations, removal is Langmuirian in nature. Arsenite sorption abruptly converts to linear behavior at high concentrations, possibly attributed to the saturation of the monolayer. Ionic strength effects were assessed by comparing pH edge data developed for three different concentrations of NaCl background electrolyte solution. Increases in ionic strength enhance the removal of arsenite from solution, suggesting possible inner-sphere surface complexation removal mechanisms. Information gathered in this study can be used to further develop surface complexation models to describe and predict reactivity of arsenite in the presence of mackinawite coated sands in anoxic regions. Mackinawite coated sands investigated here may provide a feasible reactive medium for implementation in above-ground sorption reactors or subsurface

  2. Sorption of pesticides to aquifer minerals

    DEFF Research Database (Denmark)

    Clausen, Liselotte; Fabricius, Ida Lykke

    2000-01-01

    This paper summarizes results from a work were the sorption of five pesticides on seven minerals were studied in order to quantify the adsorption to different mineral surfaces. Investigated mineral phases are: quartz, calcite, kaolinite, a-alumina, and three iron oxides (2-line ferrihydrite......, goethite, lepidocrocite). Selected pesticides are: atrazine, isoproturon, mecoprop, 2,4-D, and bentazone. The results demonstrate that pesticides adsorb to pure mineral surfaces. However, the size of the adsorption depends on the type of pesticide and the type of mineral....

  3. Sorption of cesium on Latvian clays

    International Nuclear Information System (INIS)

    Viss, R.; Drille, M.

    2004-01-01

    Cesium is like potassium - good solubility and mobile in a ground, easily assimilate in organism expressly brawn woof. It is a problem if pollutant is a radioactive 137 Cs. We made experiments to sorption a 2M CsF solution on some Latvian clays which mainly contain hydro micas (cesium content after good elute of clays are in table). We establish, that clay treated with 25 % sulfuric acid adsorb cesium two times more that waste clay. Hereto unstuck elute Cs from clays. (author)

  4. Dynamic water vapour sorption in gluten and starch films

    NARCIS (Netherlands)

    Oliver, L.; Meinders, M.B.J.

    2011-01-01

    Water sorption of gluten and wheat starch films as a function of water activity was studied using gravimetric step-change sorption experiments. Films of different thicknesses were used with the aim to vary the characteristic diffusion time and to get insights in the contribution of the polymer-chain

  5. Analysis of ideal sorption compressor cycles operating with gas mixtures

    NARCIS (Netherlands)

    Tzabar, N.; ter Brake, H.J.M.

    2018-01-01

    Sorption-based compressors are thermally driven and because of the absence of moving parts they are vibration free, and have the potential for long life. Sorption-based compressors have been reported to operate Joule–Thomson (JT) cryogenic coolers with pure working fluids. However, using mixed

  6. Status report on SIRS: sorption information retrieval system

    Energy Technology Data Exchange (ETDEWEB)

    Hostetler, D.D.; Serne, R.J.; Baldwin, A.J.; Petrie, G.M.

    1980-11-01

    Two major uses were identified for the Sorption Information Retrieval System: (1) to aid geochemists in the elucidation of sorption mechanisms; and (2) to aid safety assessment modelers in selection of Kds for any given scenerio. Other benefits such as providing an auditable vehicle for the Kd selection were also discussed.

  7. Synthesis of Nano-sized Boehmites for Optimum Phosphate Sorption

    DEFF Research Database (Denmark)

    Watanabe, Yujiro; Kasama, Takeshi; Fukushi, Keisuke

    2011-01-01

    the highest amount of phosphate sorption (1.73 mmol g-1 at pH 3.3) compared with Al-bearing materials. The reaction mechanism during phosphate sorption was described by the anion exchange reaction between phosphate ions in sodium phosphate solution and hydroxide ions on boehmite surfaces. Therefore...

  8. Sorption of malachite green (MG) by cassava stem biochar (CSB ...

    African Journals Online (AJOL)

    Cassava stem biochar (CSB) was produced by pyrolyzing CS at 500°C for 2 hours at nitrogen environment. Proximate and ultimate analyses were conducted on CS and CSB. Batch sorption experiment on synthetic MG wastewater was optimized for the sorbent dosage, MG solution pH and contact time. Sorption data was ...

  9. Sorption and desorption of diuron in Oxisol under biochar application

    Directory of Open Access Journals (Sweden)

    Fabiano André Petter

    Full Text Available ABSTRACT The objective of this study was to verify the kinetics of sorption and desorption of diuron in an Oxisol under application of biochar. The samples were collected in a field experiment conducted in randomized design blocks consisted of 2 base fertilization levels (0 and 400 kg∙ha−1 NPK 00-20-20 fertilizer formula and 3 doses of biochar (0, 8 and 16 Mg∙ha−1. In the evaluation of sorption and desorption, Batch Equilibrium method was used. The kinetics of sorption and desorption of diuron, total organic carbon, fulvic acid, humic acid and humin, pH and partition coefficient to organic carbon were evaluated. The Freundlich isotherm was adjusted appropriately to describe diuron sorption kinetics in all the studied treatments. The application of biochar provided increment in the sorption (Kf and reduction in the desorption of diuron in 64 and 44%, respectively. This effect is attributed to the biochar contribution to the total organic carbon and C-humin and of these to diuron through hydrophobic interactions and hydrogen bonds. The positive correlation between the partition coefficient to organic carbon and Kf confirms the importance of soil organic compartment in the sorption of diuron. There was no competition of NPK fertilizer for the same sorption site of diuron. The increase and reduction in sorption and desorption, respectively, show that the application of biochar is an important alternative for the remediation of soil leaching of diuron, especially in sandy soils.

  10. Status report on SIRS: sorption information retrieval system

    International Nuclear Information System (INIS)

    Hostetler, D.D.; Serne, R.J.; Baldwin, A.J.; Petrie, G.M.

    1980-11-01

    Two major uses were identified for the Sorption Information Retrieval System: (1) to aid geochemists in the elucidation of sorption mechanisms; and (2) to aid safety assessment modelers in selection of Kds for any given scenerio. Other benefits such as providing an auditable vehicle for the Kd selection were also discussed

  11. Sorption Characterization of Radionuclides on Clays in Yucca Mountain Alluvium

    International Nuclear Information System (INIS)

    M. Ding; P.W. Reimus; S. Chipera; C. Scism

    2006-01-01

    Sorption of 237 Np(V) and 233 U(VI) was measured on clays separated from Yucca Mountain alluvium as a function of solution pH and aqueous actinide concentrations. The results indicate that sorption of U and Np on the separated clay fraction depends strongly on solution pH. Np sorption on clays increases slowly with increasing pH from 3 to 7. Above pH 7, Np sorption on clays increases rapidly up to a pH of about 10. On the other hand, U sorption on clays reaches it maximum at a pH of about 6, with sorption decreasing as pH increases from 6 to 8 and then increasing again as pH increases further from 8 to about 10. The results suggest that a Freundlich isotherm can be used to describe U and Np sorption on clays at pH above 5.5. The results of this study indicate that clay minerals play a very important role in the sorption of U and Np on Yucca Mountain alluvium. Indeed, the clay content of the alluvium is probably considerably more important than water chemistry in predicting the ability of the alluvium to attenuate the transport of these radionuclides

  12. Column Chromatography To Obtain Organic Cation Sorption Isotherms.

    Science.gov (United States)

    Jolin, William C; Sullivan, James; Vasudevan, Dharni; MacKay, Allison A

    2016-08-02

    Column chromatography was evaluated as a method to obtain organic cation sorption isotherms for environmental solids while using the peak skewness to identify the linear range of the sorption isotherm. Custom packed HPLC columns and standard batch sorption techniques were used to intercompare sorption isotherms and solid-water sorption coefficients (Kd) for four organic cations (benzylamine, 2,4-dichlorobenzylamine, phenyltrimethylammonium, oxytetracycline) with two aluminosilicate clay minerals and one soil. A comparison of Freundlich isotherm parameters revealed isotherm linearity or nonlinearity was not significantly different between column chromatography and traditional batch experiments. Importantly, skewness (a metric of eluting peak symmetry) analysis of eluting peaks can establish isotherm linearity, thereby enabling a less labor intensive means to generate the extensive data sets of linear Kd values required for the development of predictive sorption models. Our findings clearly show that column chromatography can reproduce sorption measures from conventional batch experiments with the benefit of lower labor-intensity, faster analysis times, and allow for consistent sorption measures across laboratories with distinct chromatography instrumentation.

  13. Kinetics and reversibility of micropollutant sorption in sludge.

    Science.gov (United States)

    Barret, Maialen; Carrère, Hélène; Patau, Mathieu; Patureau, Dominique

    2011-10-01

    The fate of micropollutants throughout wastewater treatment systems is highly dependent on their sorption interactions with sludge matter. In this study, both the sorption and desorption kinetics of polycyclic aromatic hydrocarbons (PAHs) in activated sludge were shown to be very rapid in comparison to biodegradation kinetics. It was concluded that PAH transfer does not limit their biodegradation and that their fate is governed by the sorption/desorption equilibrium state. The effect of contact time between sludge and PAHs was also investigated. It was shown that aging did not influence the sorption/desorption equilibrium although PAH losses during aging suggest that sequestration phenomena had occurred. This implies that for PAH sorption assessment within treatment processes there is no need to include a contact time dimension. As a consequence, thanks to an innovative approach taking into account sorption equilibria and sequestration, this work has demonstrated that studies in the literature which, in main, deal with micropollutant sorption in sewage sludge with only a short contact time can be extrapolated to real systems in which sorption, desorption and aging occur.

  14. The Economy of Persistence: Mario the Tailor

    Directory of Open Access Journals (Sweden)

    Prudence Black

    2016-03-01

    Full Text Available Mario Conte has had a tailor shop in King Street, Newtown since the mid 1960s. Taking an interview with Mario as its point of departure, this article describes the persistence of a skilled worker whose practices and techniques remain the same in a world that has long changed. While inattentive to what rules might be used to decorate a shop window, Mario continues to make and sew in the way that he learnt in post-war Italy. Mario’s persistence could be described as all the skills and other elements that need to be in place to keep him working, in particular the tradition of tailoring techniques he has remained true to over the last fifty years. The hand stitching of his tailoring is like a metronome of that persistence.

  15. Tailored Codes for Small Quantum Memories

    Science.gov (United States)

    Robertson, Alan; Granade, Christopher; Bartlett, Stephen D.; Flammia, Steven T.

    2017-12-01

    We demonstrate that small quantum memories, realized via quantum error correction in multiqubit devices, can benefit substantially by choosing a quantum code that is tailored to the relevant error model of the system. For a biased noise model, with independent bit and phase flips occurring at different rates, we show that a single code greatly outperforms the well-studied Steane code across the full range of parameters of the noise model, including for unbiased noise. In fact, this tailored code performs almost optimally when compared with 10 000 randomly selected stabilizer codes of comparable experimental complexity. Tailored codes can even outperform the Steane code with realistic experimental noise, and without any increase in the experimental complexity, as we demonstrate by comparison in the observed error model in a recent seven-qubit trapped ion experiment.

  16. Uranium sorption on tezontle volcanic rock

    Energy Technology Data Exchange (ETDEWEB)

    Lopez M, B. E.; Duran B, J. M.; Iturbe G, J. L.; Olguin G, M. T., E-mail: beatriz.lopez@inin.gob.m [ININ, Departamento de Quimica, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

    2009-07-01

    It is described a study that demonstrates that hexavalent uranium ions were sorbed by the naturally occurring mineral using a batch technique. This mineral is found in abundant quantities in Mexico. Our study focused on the separation of U Vi from synthetic aqueous systems of both H{sub 2}O-UO{sub 2}(NO{sub 3}){sub 2}.6H{sub 2}O (acid) and H{sub 2}O-Na{sub 4}[UO{sub 2}(CO{sub 3}){sub 3}] (basic). The chemical speciation was performed by using high voltage electrophoresis, and the uranium content was determined by UV-Vis spectroscopy. The quantified U(Vi) sorption by tezontle from acidic and basic systems was 2.72 and 1.68 mumol/g, respectively, and the sorption behavior is discussed considering the surface charge of the tezontle at different ph values based on the point of zero charge characteristic of this material. (Author)

  17. Zn Isotope Fractionation during Sorption onto Kaolinite.

    Science.gov (United States)

    Guinoiseau, Damien; Gélabert, Alexandre; Moureau, Julien; Louvat, Pascale; Benedetti, Marc F

    2016-02-16

    In this study, we quantify zinc isotope fractionation during its sorption onto kaolinite, by performing experiments under various pH, ionic strength, and total Zn concentrations. A systematic enrichment in heavy Zn isotopes on the surface of kaolinite was measured, with Δ(66)Znadsorbed-solution ranging from 0.11‰ at low pH and low ionic strength to 0.49‰ at high pH and high ionic strength. Both the measured Zn concentration and its isotopic ratio are correctly described using a thermodynamic sorption model that considers two binding sites: external basal surfaces and edge sites. Based on this modeling approach, two distinct Zn isotopic fractionation factors were calculated: Δ(66)Znadsorbed-solution = 0.18 ± 0.06‰ for ion exchange onto basal sites, and Δ(66)Znadsorbed-solution = 0.49 ± 0.06‰ for specific complexation onto edge sites. These two distinct factors indicate that Zn isotope fractionation is dominantly controlled by the chemical composition of the solution (pH, ionic strength).

  18. Status of sorption information retrieval system

    International Nuclear Information System (INIS)

    Hostetler, D.D.; Serne, R.J.; Brandstetter, A.

    1979-09-01

    A Sorption Information Retrieval System (SIRS) is being designed to provide an efficient, computerized, data base for information on radionuclide sorption in geologic media. The data bank will include Kd values for a large number of radionuclides occurring in radioactive wastes originating from the commercial nuclear power industry. Kd values determined to date span several groundwater compositions and a wide variety of rock types and minerals. The data system will not only include Kd values, but also background information on the experiments themselves. This will allow the potential user to retrieve not only the Kd values of interest but also sufficient information to evaluate the accuracy and usefulness of the data. During FY-1979, the logic structure of the system was designed, the software programmed, the data categories selected, and the data format specified. About 40% of the approximately 5000 Kd experiments performed by the Waste Isolation Safety Assessment Program (WISAP) and its subcontractors during FY-1977 and FY-1978 have been evaluated, coded and keypunched. Additional software improvements and system testing are needed before the system will be fully operational. A workshop requested by the NEA was held to discuss potential internatioal participation in the data system

  19. Gas Sorption, Diffusion, and Permeation in Nafion

    KAUST Repository

    Mukaddam, Mohsin Ahmed

    2015-12-22

    The gas permeability of dry Nafion films was determined at 2 atm and 35 °C for He, H2, N2, O2, CO2, CH4, C2H6, and C3H8. In addition, gas sorption isotherms were determined by gravimetric and barometric techniques as a function of pressure up to 20 atm. Nafion exhibited linear sorption uptake for low-solubility gases, following Henry’s law, and convex behavior for highly sorbing condensable gases, indicating rubber-like behavior at 35 °C. XRD results demonstrated that Nafion contains bimodal amorphous chain domains with average d-spacing values of 2.3 and 5.3 Å. Only helium and hydrogen showed relatively high gas permeability of 37 and 7 barrers, respectively; all other gases exhibited low permeability that decreased significantly as penetrant size increased. Dry Nafion was characterized by extraordinarily high selectivities: He/H2 = 5.2, He/CH4 = 445, He/C2H6 = 1275, He/C3H8 = 7400, CO2/CH4 = 28, CO2/C2H6 = 79, CO2/C3H8 = 460, H2/CH4 = 84, H2/C2H6 = 241, and H2/C3H8 = 1400. These high selectivities could make Nafion a potential candidate membrane material for dry feeds for helium recovery and carbon dioxide separation from natural gas and removal of higher hydrocarbons from hydrogen-containing refinery gases.

  20. Mercury Sorption onto Malt Spent Rootlets

    Science.gov (United States)

    Manariotis, I. D.; Anagnostopoulos, V.; Karapanagioti, H. K.; Chrysikopoulos, C.

    2011-12-01

    Mercury is a metal of particular concern due to its toxicity even at relatively low concentrations. The maximum permissible level for mercury in drinking water set by the European Union is 0.001 mg/L. Mercury is released into the environment via four principal pathways: (1) natural processes; i.e. a volcanic eruption, (2) incidental to some other activity; i.e. coal burning power plants, (3) accidentally during the manufacture, breakage or disposal of products that have mercury put into them deliberately, and (4) direct use in industrial settings. The present study focuses on the removal of mercury (II) from aqueous solutions via sorption onto Malt Spent Rootlets (MSR). Batch experiments were conducted employing MSR with size ranging from 0.18 to 1 mm. The effects of pH, mercury concentration, contact time, and solid to liquid ratio on mercury sorption onto MSR were investigated. The highest mercury removal from the aqueous phase, of 41%, was observed at pH of 5.

  1. Sorption and diffusion of Cs and I in concrete

    International Nuclear Information System (INIS)

    Andersson, K.; Torstenfelt, B.; Allard, B.

    1983-01-01

    Concrete has been suggested as a possible encapsulation material for long-term storage of low and medium level radioactive waste. At an underground storage of concrete encapsulated waste, a slow release of radioactive elements into the groundwater by diffusion through the concrete must be considered in the safety analysis. The diffusion may be delayed by sorption reactions on the solid. A wide range of long-lived radionuclides may be present in the low and medium level radioactive waste. Here, the sorption and diffusion of iodide and cesium on slag cement paste and concrete has been studied. The influence of four different water phases (pore water, groundwater, Baltic Sea water and sea water) as well as the influence of some added species (carbonate, sulphate and magnesium) has been investigated. A significant sorption of iodide on cement paste in contact with pore water was observed, indicating that the diffusion may be expected to be retarded in this medium. For cesium the highest sorption was found for concrete and groundwater. This means that the sorption increases as the concrete is weathered. Low or insignificant sorption was found for the cement paste, indicating that the ballast is responsible for the Cs-sorption. Carbonatization enhances the Cs-sorption by about a factor of 3. The diffusivity of Cs in concrete and cement paste was determined to between 2x10 - 14 and 8x10 - 14 m 2 /s in pore water (where an insignificant sorption was observed). The choice of ballast as well as addition of suitable getters with high sorption of the long-lived radionuclides might decrease the mass transfer rate through the cement. (Authors)

  2. LIFE-STYLE SEGMENTATION WITH TAILORED INTERVIEWING

    NARCIS (Netherlands)

    KAMAKURA, WA; WEDEL, M

    The authors present a tailored interviewing procedure for life-style segmentation. The procedure assumes that a life-style measurement instrument has been designed. A classification of a sample of consumers into life-style segments is obtained using a latent-class model. With these segments, the

  3. Tinker Tailor Robot Pi -- The Project

    Science.gov (United States)

    Bianchi, Lynne

    2017-01-01

    Tinker Tailor Robot Pi (TTRP) is an innovative curriculum development project, which started in September 2014. It involves in-service primary and secondary teachers, university academic engineers, business partners and pupils at Key Stages 1, 2 and 3 (ages 5-14). The focus of the work has been to explore how a pedagogy for primary engineering…

  4. A suggested approach toward measuring sorption and applying sorption data to repository performance assessment

    International Nuclear Information System (INIS)

    Rundberg, R.S.

    1992-01-01

    The prediction of radionuclide migration for the purpose of assessing the safety of a nuclear waste repository will be based on a collective knowledge of hydrologic and geochemical properties of the surrounding rock and groundwater. This knowledge along with assumption about the interactions of radionuclides with groundwater and minerals form the scientific basis for a model capable of accurately predicting the repository's performance. Because the interaction of radionuclides in geochemical systems is known to be complicated, several fundamental and empirical approaches to measuring the interaction between radionuclides and the geologic barrier have been developed. The approaches applied to the measurement of sorption involve the use of pure minerals, intact, or crushed rock in dynamic and static experiments. Each approach has its advantages and disadvantages. There is no single best method for providing sorption data for performance assessment models which can be applied without invoking information derived from multiple experiments. 53 refs., 12 figs

  5. Lindane sorption and desorption behaviour on sediment organic matter

    Directory of Open Access Journals (Sweden)

    Tričković Jelena S.

    2013-01-01

    Full Text Available The work is concerned with the sorption and desorption behaviour of lindane on four humic acid fractions (HAs and two humin fractions, sequentially extracted from Ludas lake sediment. All sorption isotherms, fitted to a Freundlich model, were nonlinear. The isotherm linearity increased from 0.757 for the first extracted HA to 0.944 for the ninth HA showing a positive correlation with atomic H/C ratio, while a negative correlation between sorption coefficient and aliphaticity of the isolated HAs was observed. It has been shown that the sorption processes may be strongly influenced by the physical conformation of and accessibility to sediment organic matter (SOM, as demonstrated by high Koc and low n values of humin samples. Despite exhibiting the most nonlinear sorption isotherms, humin samples did not show a pronounced sorption-desorption hysteresis, while the most significant hysteresis was observed for three HA samples. These results support the hypothesis that the aromatic domains in SOM influence strongly the sorption and desorption behaviour of lindane. Our findings may be helpful in understanding the distribution, transport and fate of lindane in soils and sediments.

  6. Web-based sorption database (KAERI-SDB)

    International Nuclear Information System (INIS)

    Lee, Jae Kwang; Baik, Min Hoon

    2010-10-01

    Radionuclide sorption data is necessary for the safety assessment of radioactive waste disposal. However the accessibility to the nuclide sorption database is limited. The web-based sorption database (KAERI-SDB) was developed to provide sorption data in a convenient way. The development of the KAERI-SDB was achieved by improving the performance of pre-existing sorption DB programme (SDB-21C) and incorporating the user requirement. The KAERI-SDB was designed that users can access it by using a web browser. Main functions of the KAERI-SDB include (1) log-in/join, (2) search and store of sorption data and (3) scatter plot chart and index chart. It is expected that the KAERI-SDB is widely applied to the safety assessment of radioactive waste disposal by enhancing the accessibility to experts and practitioner related the nuclear industry and governmental administration. It is also expected that reliabilities for the radioactive waste disposal increased by opening the web-based sorption DB to public

  7. Mechanisms of metal sorption by biochars: Biochar characteristics and modifications.

    Science.gov (United States)

    Li, Hongbo; Dong, Xiaoling; da Silva, Evandro B; de Oliveira, Letuzia M; Chen, Yanshan; Ma, Lena Q

    2017-07-01

    Biochar produced by thermal decomposition of biomass under oxygen-limited conditions has received increasing attention as a cost-effective sorbent to treat metal-contaminated waters. However, there is a lack of information on the roles of different sorption mechanisms for different metals and recent development of biochar modification to enhance metal sorption capacity, which is critical for biochar field application. This review summarizes the characteristics of biochar (e.g., surface area, porosity, pH, surface charge, functional groups, and mineral components) and main mechanisms governing sorption of As, Cr, Cd, Pb, and Hg by biochar. Biochar properties vary considerably with feedstock material and pyrolysis temperature, with high temperature producing biochars with higher surface area, porosity, pH, and mineral contents, but less functional groups. Different mechanisms dominate sorption of As (complexation and electrostatic interactions), Cr (electrostatic interactions, reduction, and complexation), Cd and Pb (complexation, cation exchange, and precipitation), and Hg (complexation and reduction). Besides sorption mechanisms, recent advance in modifying biochar by loading with minerals, reductants, organic functional groups, and nanoparticles, and activation with alkali solution to enhance metal sorption capacity is discussed. Future research needs for field application of biochar include competitive sorption mechanisms of co-existing metals, biochar reuse, and cost reduction of biochar production. Published by Elsevier Ltd.

  8. Water vapor sorption thermodynamics of the Nafion ionomer membrane.

    Science.gov (United States)

    Wadsö, Lars; Jannasch, Patric

    2013-07-18

    The water interactions of polymer electrolyte membranes are of significant interest when these materials are used in, for example, fuel cells. We have therefore studied the sorption thermodynamics of Nafion with a sorption calorimeter that simultaneously measures the sorption isotherm and the mixing (sorption) enthalpy. This unique method is suitable for investigating the sorption thermodynamics of ionic polymers. The measurements were made at 25 °C on a series of samples dried at different temperatures from 25 to 120 °C. The sorption isotherms indicate that the samples dried at 120 °C lost about 0.8 more water molecules per sulfonic group during the drying than did the samples dried at 25 °C, and this result was verified gravimetrically. The mixing enthalpies showed several peaks or plateaus for the samples dried at 60-120 °C. This behavior was seen up to about 2 water molecules per sulfonic group. As these peaks were not directly related to any feature in the sorption isotherm, they probably have their origin in a secondary process, such as a reorganization of the polymer.

  9. A mechanistic approach to the generation of sorption databases

    International Nuclear Information System (INIS)

    Bradbury, M.H.; Baeyens, B.

    1992-01-01

    Sorption of radionuclides in the near and far fields of an underground nuclear waste repository is one of the most important processes retarding their release to the environment. In the vast majority of cases sorption data have been presented in terms of empirical parameters such as distribution coefficients and isotherm equations. A consequence of this empirical methodology is that the sorption data are only strictly valid under the experimental conditions at which they were measured. Implicit in this approach is the need to generate large amounts of data and fitting parameters necessary for an empirical description of sorption under all realistically conceivable conditions which may arise in space and time along the migration pathway to Man. An alternative approach to the problem is to try to understand, and develop model descriptions of, underlying retention mechanisms and to identify those systems parameters which essentially determine the extent of sorption. The aim of this work is to see to what extent currently existing mechanistic models, together with their associated data, can be applied to predict sorption data from laboratory experiments on natural systems. This paper describes the current status of this work which is very much in an early stage of development. An example is given whereby model predictions are compared with laboratory results for the sorption of Np at trace concentrations under oxidizing conditions on a series of minerals relevant to granite formations. 31 refs., 11 figs., 5 tabs

  10. Sorption of Pseudomonas putida onto differently structured kaolinite minerals

    Science.gov (United States)

    Vasiliadou, I. A.; Papoulis, D.; Chrysikopoulos, C.; Panagiotaras, D.; Karakosta, E.; Fardis, M.; Papavassiliou, G.

    2010-12-01

    The presence of bio-colloids (e.g. bacteria and viruses) in the subsurface could be attributed to the release of particles from septic tanks, broken sewer lines or from artificial recharge with treated municipal wastewater. Bio-colloid transport in the subsurface is significantly affected by sorption onto the solid matrix. Bio-colloid attachment onto mobile or suspended in the aqueous phase soil particles (e.g. clay or other minerals) also may influence their fate and transport in the subsurface. The present study focuses on the investigation of Pseudomonas (Ps.) putida sorption onto well (KGa-1) and poorly (KGa-2) crystallized kaolinite minerals. Batch experiments were carried out to determine the sorption isotherms of Ps. putida onto both types of kaolinite particles. The sorption process of Ps. putida onto KGa-1 and KGa-2 is adequately described by a Langmuir isotherm. Attenuated Total Reflection Fourier Transform Infrared Spectroscopy as well as Nuclear Magnetic Resonance were employed to study the sorption mechanisms of Ps. putida. Experimental results indicated that KGa-2 presented higher affinity and sorption capacity than KGa-1. It was shown that electrostatic interactions and structural disorders can influence the sorption capacity of clay particles.

  11. Sorption compressor/mechanical expander hybrid refrigeration

    Science.gov (United States)

    Jones, J. A.; Britcliffe, M.

    1987-01-01

    Experience with Deep Space Network (DSN) ground-based cryogenic refrigerators has proved the reliability of the basic two-stage Gifford-McMahon helium refrigerator. A very long life cryogenic refrigeration system appears possible by combining this expansion system or a turbo expansion system with a hydride sorption compressor in place of the usual motor driven piston compressor. To test the feasibility of this system, a commercial Gifford-McMahon refrigerator was tested using hydrogen gas as the working fluid. Although no attempt was made to optimize the system for hydrogen operation, the refrigerator developed 1.3 W at 30 K and 6.6 W at 60 K. The results of the test and of theoretical performances of the hybrid compressor coupled to these expansion systems are presented.

  12. Sorption of aromatic hydrocarbons onto montmorillonite as affected by norfloxacin

    Energy Technology Data Exchange (ETDEWEB)

    Pei, Zhiguo, E-mail: peizg@rcees.ac.cn [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, PO Box 2871, Beijing 100085 (China); Kong, Jingjing [School of Chemistry and Materials, Fujian Normal University, Fuzhou 350007 (China); Shan, Xiao-quan; Wen, Bei [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, PO Box 2871, Beijing 100085 (China)

    2012-02-15

    Graphical abstract: {sup 1}H NMR spectrum provided direct evidence for {pi}-{pi} and cation-{pi} complexation between PAHs and Nor{sup +} by ring-current-induced upfield chemical shifts of the amino group and methylene group of Nor{sup +}. Highlights: Black-Right-Pointing-Pointer Nor decreases 1,3-DNB sorption, and increases NAPH, PHEN and PYR sorption on montmorillonite. Black-Right-Pointing-Pointer Nor{sup {+-}} increased PHEN and PYR sorption more pronounced than Nor{sup +} and Nor{sup -}. Black-Right-Pointing-Pointer The corresponding mechanisms were described by FTIR and {sup 1}H NMR. - Abstract: Effect of norfloxacin (Nor) on the sorption of 1,3-dinitrobenzene (1,3-DNB), and PAHs (naphthalene (NAPH), phenanthrene (PHEN) and pyrene (PYR)) to K{sup +}-montmorillonite was studied. Nor suppressed 1,3-DNB sorption due to their competition for the same sorption sites. 1,3-DNB was sorbed on K{sup +}-montmorillonite surface via cation-polar interaction and n-{pi} electron donor-acceptor interaction. Nor also was sorbed on these sites through cation exchange, cation bridging and/or surface complexation. Nor increased three PAHs sorption on montmorillonite and the enhanced magnitude was positively correlated with the {pi}-donor strength of three PAHs. The enhanced sorption of PAHs by Nor was primarily attributed to {pi}-{pi} interaction between {pi}-electron-depleted quinoline ring of Nor and {pi}-electron-rich PAHs. Compared with cation (Nor{sup +}) and anion (Nor{sup -}), zwitterion (Nor{sup {+-}}) of Nor increased PHEN and PYR sorption more pronounced due to additional cation-{pi} interaction between the sorbed Nor{sup {+-}} and PAHs. {sup 1}H NMR spectrum provided direct evidence for {pi}-{pi} and cation-{pi} complexation between PAHs and Nor{sup +} in solution by ring-current-induced upfield chemical shifts of amino group and methylene group of Nor{sup +}.

  13. Implementation of sorption hysteresis in multi-Fickian moisture transport

    DEFF Research Database (Denmark)

    Frandsen, Henrik Lund; Svensson, Staffan

    2007-01-01

    In the cellular structure of wood, bound-water diffusion and water-vapor diffusion interact via sorption in a complex moisture-transportation system. At low relative humidities, moisture transport may be modeled by a Fickian diffusion equation with a good approximation. At higher relative......-35% in moisture content. Hence, for a precise moisture content computation, sorption hysteresis must be taken into account. The present paper explains the relation between sorption hysteresis and multi-Fickian moisture transport, and clarifies how models for the two phenomena are coupled. To illustrate...

  14. Sorption of Co2+ on modified inorganic materials

    International Nuclear Information System (INIS)

    Hanzel, R.; Rajec, P.

    1999-01-01

    The aim of this study was preparation and characterization of sorbents on the base a silica-gel matrix with immobilized functional group (imidazole or crown-ether). Sorption of cobalt from aqueous solutions on prepared sorbents in static conditions (by 'batch' method) in the dependence of concentration, pH value,, as well as kinetics of sorption were studied. The influence of heavy or toxic metals [Hg(II), Cd(II), Mn(II), Zn(II), Cu(II), Fe(III), Cr(III), Al(III), Na and K] on sorption of cobalt was studied, too

  15. Sorption and desorption of diuron in Oxisol under biochar application

    OpenAIRE

    Petter, Fabiano André; Ferreira, Tamara Santos; Sinhorin, Adilson Paulo; Lima, Larissa Borges de; Morais, Leidimar Alves de; Pacheco, Leandro Pereira

    2016-01-01

    ABSTRACT The objective of this study was to verify the kinetics of sorption and desorption of diuron in an Oxisol under application of biochar. The samples were collected in a field experiment conducted in randomized design blocks consisted of 2 base fertilization levels (0 and 400 kg∙ha−1 NPK 00-20-20 fertilizer formula) and 3 doses of biochar (0, 8 and 16 Mg∙ha−1). In the evaluation of sorption and desorption, Batch Equilibrium method was used. The kinetics of sorption and desorption of diu...

  16. Effect of illite particle shape on cesium sorption

    Science.gov (United States)

    Rajec, Pavol; Šucha, Vladimír; Eberl, Dennis D.; Środoń, Jan; Elsass, Françoise E.

    1999-01-01

    Samples containing illite and illite-smectite, having different crystal shapes (plates, “barrels”, and filaments), were selected for sorption experiments with cesium. There is a positive correlation between total surface area and Cs-sorption capacity, but no correlation between total surface area and the distribution coefficient, Kd. Generally Kd increases with the edge surface area, although “hairy” (filamentous) illite does not fit this pattern, possibly because elongation of crystals along one axis reduces the number of specific sorption sites.

  17. SORPTION OF Cu2+ IONS ONTO DIATOMITE CONSTITUENTS

    Directory of Open Access Journals (Sweden)

    Vasile Rusu

    2009-06-01

    Full Text Available Studies of the sorption capacity towards Cu2+ ions of diatomite from the Ghidirim location of RM, as well as of the extracted clay phase are presented. Separated clay fraction from diatomic material is clean enough, and especially is rich in montmorillonite. Maximum sorption capacity for studied clay fraction is achieved by rising the temperature of calcination treatment up to 200oC. At higher temperatures the lattice of montmorillonite is contracted and its sorption capacity towards Cu2+ ions decreases strongly.

  18. Interim report on modeling sorption with EQ3/6

    International Nuclear Information System (INIS)

    Viani, B.

    1988-01-01

    Reversible, equilibrium models of sorption to be incorporated into the EQ3/6 geochemical modeling package are summarized. Empirical sorption models as formulated in linear, Langmuir, and Freundlich isotherms will be developed as options to EQ3/6. This work will be done at LLNL. Options for modeling sorption using surface- complexation constructs (diffuse, constant capacitance, and triple-layer models) will also be developed. Development of the surface-complexation options will require part of the work be done under contract. 27 refs., 1 fig

  19. Kinetics of sorption of oil products by hydroxide precipitates

    Energy Technology Data Exchange (ETDEWEB)

    Petrova, N.A.; Dubrovskaya, G.E.; Berezyuk, V.G.; Pushkarev, V.V.

    1976-01-01

    Study of the kinetics of sorption of oils (palm and coriander oils, Genrex-26, Emulsol E-2(B)) under static conditions by aluminum and iron hydroxide precipitates (with FeSO/sub 4/, FeCl/sub 3/, and AlCl/sub 3/ as coagulants) showed that an increase of temperature to 40 to 50/sup 0/C raises the sorption rate substantially. The kinetic relations can be represented by equations for first-order reactions. The calculated rate constants and the values of the empirical activation energies are evidence of physical sorption with diffusion as the controlling step.

  20. Study of sorption and swelling on block coals

    Science.gov (United States)

    Qu, Shijie; Chen, Guoqing; Yang, Jianli; Shen, Wenzhong; Li, Yunmei; Niu, Hongxian; Busch, Andreas

    2013-04-01

    Reducing CO2 emission into atmosphere is very important for the mitigation of global climate change. Many processes have been proposed for this purpose, including CO2 sequestration in un-minable coalbeds and enhance coalbed methane production (CO2-ECBM). Several theoretical studies and worldwide demonstration sites have illustrated the potential of the process.Most of these projects experienced permeability reduction of the coalbed with time, leading to operational difficulties because of the loss of injectability. The permeability reduction is generally considered to be caused by the coal swelling that is induced by gas sorption, because it can narrow or close the cleat of the coalbed. As a result, the migration of injected CO2 in coal pore or cleat becomes more difficult. Therefore, sorption and swelling characterizations are important issues for forecasting the performance of aimed coalbed. In this work, CO2/CH4sorption and swelling isotherms of two Chinese block coals (QS and YQ) were measured simultaneously under different temperature and pressure conditions. It was found that the swelling ratio of coal block by CO2 sorption increased with the increase of the gas sorption amount until it approached to a value of ~3 mmol-gas/g-coal and decreased slightly afterwards for both coals; while the swelling ratio of coal block by CH4 sorption increased with the increase of the gas sorption amount in the entire test region for both coals. By correlating the gas sorption amount and the corresponding swelling ratio, it was found that the swelling ratio of coal block is independent of temperature and coal type when the gas sorption amount is less than ~2mmol/g-coal. The differential profile of the swelling ratio with respect to sorption amount is appeared with a maximum value at ~1 mmol/g-coal for CH4 and at ~1.8 mmol/g-coal for CO2. Based on the theories related to gas sorption and solid surface energy, a mathematical model which correlates sorption and swelling behavior

  1. Sorption of molybdenum by cellulose polyphosphate from acid solutions

    International Nuclear Information System (INIS)

    Luneva, N.K.; Oputina, A.G.; Ermolenko, I.N.

    1985-01-01

    The sorption of molybdenum on cellulose polyphosphate from acid solutions of ammonium molybdate depending on the phosphorus content in samples, concentration and pH of the solution, sorption time is studied. It is shown that a maximum molybdenum content on the cellulose samples with different phosphorus content is pointed out at an ammonium molybdate concentration 0.02 M. Saturation of the sorption curve is attained at molar ratio of adsrbed molybdenum to phosphorus 1:4. In case of small fillings the compound with molybdenum to phosphorus ratio 1:10 is formed

  2. Arsenic Sorption on Mechanically Activated Magnetite and Olivine

    Directory of Open Access Journals (Sweden)

    Zdenka Bujňáková

    2012-12-01

    Full Text Available Arsenic sorption on mechanically activated minerals such as magnetite Fe3O4 (Kiruna, Sweden and olivine (Mg,Fe2SiO4 (Ǻheim,Norway has been studied and compared in this work. Experiments were carried out with non-activated and mechanically activatedsamples. The activation of both minerals was performed in a planetary mill at different milling conditions. The specific surface areaand consequent sorption activity were enhanced by mechanical activation. The using of olivine seems to be better than magnetite fromthe point of view of milling time, which is necessary for achievement of the same sorption effect.

  3. Sorption of trace cesium on 21 Hanford Site sediment types

    International Nuclear Information System (INIS)

    Routson, R.C.; Barney, G.S.; Smith, R.M.; Delegard, C.A.

    1980-03-01

    Sorption of trace cesium (Cs) was measured on 21 Hanford Site sediment types. A Box-Behnken statistical design was used to develop empirical-statistical equations predicting 137 Cs sorption as a function of the equilibrium concentrations of macroions Na + , K + , and Ca +2 in solution over the concentration ranges of 3.0 to 0.001M, 0.2 to 0.002M, and 0.2 to 0.002M, respectively. These equations are required to estimate trace Cs transport from Hanford ground disposal sites. Average Cs sorption equations for the 21 sediments will be presented and discussed

  4. Radionuclide sorption-desorption pattern in soils from Spain

    Energy Technology Data Exchange (ETDEWEB)

    Gil-Garcia, C.J.; Rigol, A.; Rauret, G. [Departament de Quimica Analitica, Universitat de Barcelona, Marti i Franques 1-11, 3a Planta, 08028 Barcelona (Spain); Vidal, M. [Departament de Quimica Analitica, Universitat de Barcelona, Marti i Franques 1-11, 3a Planta, 08028 Barcelona (Spain)], E-mail: miquel.vidal@ub.edu

    2008-02-15

    The pattern of radiostrontium and radiocesium sorption-desorption was examined in 30 Spanish soils by the quantification of the distribution coefficients (K{sub d}) with batch tests, the evaluation of sorption reversibility with a single extraction, the estimation of sorption dynamics by the application of drying-wetting cycles, and the calculation of K{sub d}{sup adjusted} values as an input for risk assessment models. The data obtained overlapped with those found in soils from other climatic areas, suggesting identical interaction mechanisms and allowing the extrapolation of parameterisations and prediction models among different scenarios.

  5. Modeling and Prediction of Soil Water Vapor Sorption Isotherms

    DEFF Research Database (Denmark)

    Arthur, Emmanuel; Tuller, Markus; Moldrup, Per

    2015-01-01

    Soil water vapor sorption isotherms describe the relationship between water activity (aw) and moisture content along adsorption and desorption paths. The isotherms are important for modeling numerous soil processes and are also used to estimate several soil (specific surface area, clay content.......93) for a wide range of soils; and (ii) develop and test regression models for estimating the isotherms from clay content. Preliminary results show reasonable fits of the majority of the investigated empirical and theoretical models to the measured data although some models were not capable to fit both sorption...... directions accurately. Evaluation of the developed prediction equations showed good estimation of the sorption/desorption isotherms for tested soils....

  6. Development of a Self-Consistent Model of Plutonium Sorption: Quantification of Sorption Enthalpy and Ligand-Promoted Dissolution

    Energy Technology Data Exchange (ETDEWEB)

    Powell, Brian [Clemson Univ., SC (United States); Kaplan, Daniel I [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Arai, Yuji [Univ. of Illinois, Urbana-Champaign, IL (United States); Becker, Udo [Univ. of Michigan, Ann Arbor, MI (United States); Ewing, Rod [Stanford Univ., CA (United States)

    2016-12-29

    This university lead SBR project is a collaboration lead by Dr. Brian Powell (Clemson University) with co-principal investigators Dan Kaplan (Savannah River National Laboratory), Yuji Arai (presently at the University of Illinois), Udo Becker (U of Michigan) and Rod Ewing (presently at Stanford University). Hypothesis: The underlying hypothesis of this work is that strong interactions of plutonium with mineral surfaces are due to formation of inner sphere complexes with a limited number of high-energy surface sites, which results in sorption hysteresis where Pu(IV) is the predominant sorbed oxidation state. The energetic favorability of the Pu(IV) surface complex is strongly influenced by positive sorption entropies, which are mechanistically driven by displacement of solvating water molecules from the actinide and mineral surface during sorption. Objectives: The overarching objective of this work is to examine Pu(IV) and Pu(V) sorption to pure metal (oxyhydr)oxide minerals and sediments using variable temperature batch sorption, X-ray absorption spectroscopy, electron microscopy, and quantum-mechanical and empirical-potential calculations. The data will be compiled into a self-consistent surface complexation model. The novelty of this effort lies largely in the manner the information from these measurements and calculations will be combined into a model that will be used to evaluate the thermodynamics of plutonium sorption reactions as well as predict sorption of plutonium to sediments from DOE sites using a component additivity approach.

  7. Environmental Conditions Influencing Sorption of Inorganic Anions to Multiwalled Carbon Nanotubes Studied by Column Chromatography.

    Science.gov (United States)

    Metzelder, Florian; Schmidt, Torsten C

    2017-05-02

    Sorption to carbon-based nanomaterials is typically studied in batch experiments. An alternative method offering advantages to study sorption is column chromatography. Sorbent packed columns are used and sorption data are determined by relating sorbate retention to that of a nonretarded tracer. We have now for the first time applied this technique to study the influence of environmental conditions on sorption of inorganic anions (bromide, nitrite, nitrate, and iodide) to multiwalled carbon nanotubes. Deuterium oxide was used as nonretarded tracer. Sorption isotherms were best described by the Freundlich model. Sorption increased in the order bromide 4.5 the surface charge was negative, but sorption was still detectable at pH 6 and 9. Consequently, other forces than electrostatic attraction contributed to sorption. These forces may include H-bonding as indicated by sorption enthalpy determined by variation of column temperature. Overall, column chromatography represents a promising alternative in sorption studies to reveal sorbent properties.

  8. Aeroelastic tailoring of composite aircraft wings

    Science.gov (United States)

    Mihaila-Andres, Mihai; Larco, Ciprian; Rosu, Paul-Virgil; Rotaru, Constantin

    2017-07-01

    The need of a continuously increasing size and performance of aerospace structures has settled the composite materials as the preferred materials in aircraft structures. Apart from the clear capacity to reduce the structural weight and with it the manufacture cost and the fuel consumption while preserving proper airworthiness, the prospect of tailoring a structure using the unique directional stiffness properties of composite materials allows an aerospace engineer to optimize aircraft structures to achieve particular design objectives. This paper presents a brief review of what is known as the aeroelastic tailoring of airframes with the intent of understanding the evolution of this research topic and at the same time providing useful references for further studies.

  9. Tailoring quantum structures for active photonic crystals

    DEFF Research Database (Denmark)

    Kuznetsova, Nadezda

    This work is dedicated to the tailoring of quantum structures, with particular attention to the integration of selective area grown (SAG) active material into photonic crystal (PhC) slabs. The platform based on active PhC is vital to the realization of highly efficient elements with low energy......; in particular, the emission control of SAG QW matched the operating wavelength of photonic crystals. A strong photoluminescence signal in the slow light regime with the group index of 18 was demonstrated....

  10. Sorption-desorption behavior of polybrominated diphenyl ethers in soils.

    Science.gov (United States)

    Olshansky, Yaniv; Polubesova, Tamara; Vetter, Walter; Chefetz, Benny

    2011-10-01

    Polybrominated diphenyl ethers (PBDEs) are flame retardants that are commonly found in commercial and household products. These compounds are considered persistent organic pollutants. In this study, we used 4,4'-dibromodiphenyl ether (BDE-15) as a model compound to elucidate the sorption and desorption behavior of PBDEs in soils. The organic carbon-normalized sorption coefficient (K(OC)) of BDE-15 was more than three times higher for humin than for bulk soils. However, pronounced desorption hysteresis was obtained mainly for bulk soils. For humin, increasing concentration of sorbed BDE-15 resulted in decreased desorption. Our data illustrate that BDE-15 and probably other PBDEs exhibit high sorption affinity to soils. Moreover, sorption is irreversible and thus PBDEs can potentially accumulate in the topsoil layer. We also suggest that although humin is probably a major sorbent for PBDEs in soils, other humic materials are also responsible for their sequestration. Copyright © 2011 Elsevier Ltd. All rights reserved.

  11. Transformation and sorption of illicit drug biomarkers in sewer biofilms

    DEFF Research Database (Denmark)

    Ramin, Pedram; Brock, Andreas Libonati; Causanilles Llanes, Ana

    2017-01-01

    , 16 drug biomarkers were selected, including the major human metabolites of mephedrone, methadone, cocaine, heroin, codeine and tetrahydrocannabinol (THC). Transformation and sorption of these substances were assessed in targeted batch experiments using laboratory-scale biofilm reactors operated under...

  12. Effects of sorption hysteresis on radionuclide releases from waste packages

    International Nuclear Information System (INIS)

    Barney, G.S.; Reed, D.T.

    1985-01-01

    A one-dimensional, numerical transport model was used to calculate radionuclide releases from waste packages emplaced in a nuclear waste repository in basalt. The model incorporates both sorption and desorption isotherm parameters measured previously for sorption of key radionuclides on the packing material component of the waste package. Sorption hysteresis as described by these isotherms lowered releases of some radionuclides by as much as two orders of magnitude. Radionuclides that have low molar inventories (relative to uranium), high solubility, and strongly sorbed, are most affected by sorption hysteresis. In these cases, almost the entire radionuclide inventory is sorbed on the packing material. The model can be used to help optimize the thickness of the packing material layer by comparing release rate versus packing material thickness curves with Nuclear Regulatory Commission (NRC) and Environmental Protection Agency (EPA) release limits

  13. Sorption-cooled continuous miniature dilution refrigeration for astrophysical applications

    Science.gov (United States)

    May, Andrew J.; Calisse, Paolo G.; Coppi, Gabriele; Haynes, Vic; Martinis, Lorenzo; McCulloch, Mark A.; Melhuish, Simon J.; Piccirillo, Lucio

    2016-07-01

    A progress report is provided on the development of a tiltable continuous miniature dilution refrigerator and associated 3He/4He sorption coolers. These systems are currently being developed to provide sub-Kelvin cooling of the bolometer arrays for several ground- and balloon-based experiments which aim to measure the polarization of the Cosmic Microwave Background (QUBIC, LSPE and POLARBEAR-2). The novel tiltable miniaturised system benefits from a lack of external circulation pumps and a mechanically simple design. The condenser of the twin-pumped recirculating diluter is cooled continuously by two 3He/4He sorption coolers. The sorption pumps are operated by convective heat switches. The dilution unit features a thermally separated mixing chamber, still and step heat exchangers. The designs and analyses of both the sorption coolers and the diluter are reported; both systems have been manufactured and are presently under test.

  14. Sorption of radioiodine in organo-clays and -soils

    International Nuclear Information System (INIS)

    Bors, J.

    1990-01-01

    In the framework of investigations on the sorption of radioiodine to natural and artificially altered soil components, a number of clay minerals and natural soils were treated with quaternary alkylammonium ions to replace the exchangeable metal cations. With help of batch experiments the resulting organo-clays were tested with respect to their sorption capability of radioiodine quantified by the distribution ratio (R D -value). Treatment of bentonite, vermiculite and cretaceous clay as well as of samples from natural horizons of chernozem soil with hexadecylpyridinium (HDPY + ) and benzethonium (BE + ) exhibited sorptions rates and amounts, which are several orders of magnitude higher than those of the respective untreated samples. Moderate increases of the R D -values were found after cation exchange with hexadecyltrimethylammonium (HDTMA + ), while the applications of trimethylphenylammonium (TMPA + ) and tetramethylammonium (TMA + ) were ineffective. Considerable sorption of radioiodine was observed with the commercially available Bentone. (orig.)

  15. Sorption of radioiodine in organo-clays and -soils

    Energy Technology Data Exchange (ETDEWEB)

    Bors, J. (Niedersaechsisches Inst. fuer Radiooekologie, Hannover (Germany, F.R.))

    1990-01-01

    In the framework of investigations on the sorption of radioiodine to natural and artificially altered soil components, a number of clay minerals and natural soils were treated with quaternary alkylammonium ions to replace the exchangeable metal cations. With help of batch experiments the resulting organo-clays were tested with respect to their sorption capability of radioiodine quantified by the distribution ratio (R{sub D}-value). Treatment of bentonite, vermiculite and cretaceous clay as well as of samples from natural horizons of chernozem soil with hexadecylpyridinium (HDPY{sup +}) and benzethonium (BE{sup +}) exhibited sorptions rates and amounts, which are several orders of magnitude higher than those of the respective untreated samples. Moderate increases of the R{sub D}-values were found after cation exchange with hexadecyltrimethylammonium (HDTMA{sup +}), while the applications of trimethylphenylammonium (TMPA{sup +}) and tetramethylammonium (TMA{sup +}) were ineffective. Considerable sorption of radioiodine was observed with the commercially available Bentone. (orig.).

  16. Sorption of 237Pu by the diatom Asterionella formosa

    International Nuclear Information System (INIS)

    Conway, H.L.; Wahlgren, M.A.; Peterson, N.; Nelson, D.M.

    1976-01-01

    Knowledge of the behavior of the man-made radionuclide plutonium within aquatic environments is of fundamental importance in assessing its potential hazards and ecological impact. The sorption of plutonium by phytoplankton and other algae is the dominant factor in the biological transport of plutonium in the aquatic environment, and it has been suggested that sorption by phytoplankton may be responsible for the seasonal loss of plutonium from the epilimnion of Lake Michigan. A unialgal diatom culture was spiked with 237 Pu tracer solution in an attempt to simulate the behavior of fallout plutonium observed in field studies. The results were encouraging in that the 237 Pu in the filtered lake water medium exhibited strongly anionic properties similar to fallout plutonium in Lake Michigan, with limited sorption on container walls. The purpose of the present study was to extend the investigations of the sorption of plutonium by phytoplankton in a controlled environment using continuous culture techniques

  17. Sorption and desorption of insecticides in Brazilian soils

    International Nuclear Information System (INIS)

    Luchini, L.C.; Lord, K.A.; Ruegg, E.F.

    1980-01-01

    The sorption from aqueous solution of ten Brazilian soil types of four organochlorine, two organophosphorus and one carbamate insecticide was determined in the laboratory using gas chromatographic and radiometric techniques. Measurements showed that soils richest in organic matter, sorbed all substances except aldrin more strongly than the other soils. DDT was the most and aldrin the least sorbed organochlorine pesticide, being dieldrin sorbed two to four times more strongly than aldrin. Sorption of lindane varied in different soils. The organophosphate insecticides malathion and parathion were strongly sorbed in the soils richest in organic matter and weakly sorbed in the poorest soils heing moderately sorbed by the other soils. Sorption of carbaryl by all soils is small. Lindane was desorbed from the soil richest in organic matter and the extent of desorption was dependent on the sorption time. (Author) [pt

  18. Tailored Trustworthy Spaces: Solutions for the Smart Grid

    Data.gov (United States)

    Networking and Information Technology Research and Development, Executive Office of the President — The NITRD workshop on Tailored Trustworthy Spaces: Solutions for the Smart Grid was conceived by the Federal government to probe deeper into how Tailored Trustworthy...

  19. Tailored information about cancer risk and screening: a systematic review.

    NARCIS (Netherlands)

    Albada, A.; Ausems, M.G.E.M.; Bensing, J.M.; Dulmen, S. van

    2009-01-01

    OBJECTIVE: To study interventions that provide people with information about cancer risk and about screening that is tailored to their personal characteristics. We assess the tailoring characteristics, theory base and effects on risk perception, knowledge and screening behavior of these

  20. Sorption of Groundwater Dissolved Organic Carbon onto Minerals

    Science.gov (United States)

    Rutlidge, H.; Oudone, P.; McDonough, L.; Meredith, K.; Andersen, M. S.; O'Carrol, D. M.; Baker, A.

    2017-12-01

    Our understanding of groundwater organic matter (OM) as a carbon source or sink in the environmental carbon cycle is limited. The dynamics of groundwater OM is mainly governed by biological processing and its sorption to minerals. In saturated groundwaters, dissolved OM (DOM) represents one part of the groundwater organic carbon pool. Without consideration of the DOM sorption, it is not possible to quantify governing groundwater OM processes. This research explores the rate and extent of DOM sorption on different minerals. Groundwater DOM samples, and International Humic Substances Society (IHSS) standard solutions, were analysed. Each was mixed with a range of masses of iron coated quartz, clean quartz, and calcium carbonate, and shaken for 2 hours to reach equilibrium before being filtered through 0.2 μm for total dissolved organic carbon (DOC) and composition analysis by size-exclusion chromatography-organic carbon detection (LC-OCD). Sorption isotherms were constructed and groundwater DOM sorption were compared to the sorption of IHSS standards. Initial results suggest that for the IHSS standards, the operationally-defined humic substances fraction had the strongest sorption compared to the other LC-OCD fractions and total DOC. Some samples exhibited a small increase in the low molecular weight neutral (LMW-N) aqueous concentration with increasing humic substances sorption. This gradual increase observed could be the result of humic substances desorbing or their breakdown during the experiment. Further results comparing these IHSS standards with groundwater samples will be presented. In conjunction with complementary studies, these results can help provide more accurate prediction of whether groundwater OM is a carbon source or sink, which will enable the management of the groundwater resources as part of the carbon economy.

  1. Phenanthrene sorption to sequentially extracted soil humic acids and humins.

    Science.gov (United States)

    Kang, Seunghun; Xing, Baoshan

    2005-01-01

    Humic substances strongly influence the environmental fate of hydrophobic organic chemicals in soils and sediments. In this study, the sorption of phenanthrene by humic acids (HAs) and humins was examined. HAs were obtained from progressively extracting a soil, eight times with 0.1 M Na4P207 and two times with 0.1 M NaOH solution, and then the residue was separated into two humin fractions by their organic carbon contents. The chemical and structural heterogeneity of the HAs and humins were characterized by elemental analysis, ultraviolet-visible spectroscopy, diffuse reflectance infrared Fourier transform spectroscopy, and solid-state 13C NMR. There were significant chemical and structural differences among the HA fractions and humins; the later extracted HAs had relatively high aliphatic carbons content. All sorption data were fitted to a Freundlich equation, S = K(F)C(N), where S and C are the sorbed and solution-phase concentrations, respectively, and K(F) and N are constants. All of the phenanthrene sorptions were nonlinear, and the nonlinearity decreased with further extractions from 0.90 (first extracted HA) to 0.96 (ninth HA) and was the lowest (0.88) for the higher organic carbon content humin. Phenanthrene sorption coefficient by HAs significantly increased with progressive extractions, being the highest for the humins. For HAs isotherms, a positive trend was observed between the sorption coefficient and the aliphaticity, but a negative relation was shown between the nonlinearity and the aliphaticity and between the sorption capacity and polarity of HAs. Phenanthrene sorption was greatly affected by chemical structure and composition of humic substances, even from a same soil. In addition, polarity of humic substances seems to mainly regulate the magnitude of phenanthrene sorption rather than structure.

  2. Further developments of the RES3T sorption database

    International Nuclear Information System (INIS)

    Brendler, V.

    2002-01-01

    RES 3 T - the Rossendorf expert system for surface and sorption thermodynamics currently under development has been expanded towards the provision of comprehensive sorption data sets suitable for complex natural systems of rocks and soils. Also a statistical evaluation of the available SCM (surface complexation model) data is now implemented. Finally, a normalization of SCM parameters to a standard site density has been incorporated. (orig.)

  3. Features of sorption process on fibers filled by inorganic sorbents

    International Nuclear Information System (INIS)

    Mikheeva, M.N.; Novikov, Yu.P.; Komarevskiy, V.M.; Myasoedov, B.F.; Mezhirov, M.S.; Idiatulov, R.K.; Fedorova, A.N.

    1986-01-01

    For the extraction of micro components from sea water the fibrous polyacrylonitrile material filled by fine-grained sorbent was proposed. As a sorbent the material on the basis of titanium dioxde was used. The kinetics and thermodynamics of sorption was studied at temperature range 20-65 deg C. According to obtained data the distribution ratio and limiting volumes of fibers at metal sorption from sea water were evaluated.

  4. Moisture Sorption Characteristics of Corn Stover and Big Bluestem

    OpenAIRE

    Karunanithy, C.; Muthukumarappan, K.; Donepudi, A.

    2013-01-01

    Moisture content is an important feedstock quality in converting it into energy through biochemical or thermochemical platforms. Knowledge of moisture sorption relationship is useful in drying and storage to preserve the quality of feedstocks. Moisture sorption isotherms for potential feedstocks such as corn stover and big bluestem are missing. EMC values of corn stover and big bluestem were determined using static gravimetric technique with saturated salt solutions (ERH 0.12–0.89) at differe...

  5. Sorption and pertechnetate by salts of molybdophosphoric acid

    International Nuclear Information System (INIS)

    Suess, M.; Pfrepper, G.

    1983-01-01

    The sorption of pertechnetate on salts of molybdophosphoric acid from nitric acid and in the presence of electrolytes was investigated. Distribution coefficients from 10 to 100 ml/g were found. The sorption of pertechnetate can be increased by the addition of K + , NH 4 + , Rb + and Cs + salts. A saturation capacity of proportional 0,19 mmol/g ammonium phosphomolybdate was found from the adsorption isotherms. The formation of alkali metal pertechnetate associates in the sorbent phase is supposed. (orig.)

  6. Effect of Mouthwashes on Solubility and Sorption of Restorative Composites

    OpenAIRE

    Leal, Jos? Pereira; da Silva, Jaqueline Damasceno; Leal, Rafaelle Fernanda Mel?o; Oliveira-J?nior, Carlos da Cunha; Prado, Vera L?cia Gomes; Vale, Glauber Campos

    2017-01-01

    Objective Composites sorption and solubility can be precursors of several chemical and physical processes, which lead to deleterious effects on the polymer structure. This study evaluated the effect of mouthwashes on solubility and sorption of composite resins. Materials and Methods Forty-two specimens of each evaluated composite (Filtek Bulk Fill Flow, Opallis Flow, Durafill VS, and Filtek Z350) were prepared and randomized into seven groups for each solution (mouth rinses with and without a...

  7. Kinetics of the sorption of triterpene saponin by hypercrosslinked polystyrene

    Science.gov (United States)

    Mironenko, N. V.; Brezhneva, T. A.; Selemenev, V. F.

    2013-03-01

    The kinetics of sorption of triterpene saponin by the polymer sorbent NM-200 is considered. The influence of the surface activity of glycoside on the rate of formation and structure of the adsorption layer on the sorbent's surface is established. The rate-determining step of sorption is found to be diffusion into the sorbent grain. The value of the activation energy demonstrates the determining role of dispersion forces in the interaction between triterpene saponin and the polymer sorbent MN-200.

  8. Modelling of a diffusion-sorption experiment on sandstone

    International Nuclear Information System (INIS)

    Smith, P.A.

    1989-11-01

    The results of a diffusion-sorption experiment on a sample of Darley Dale sandstone, using simulated groundwater spiked with a mixture of 125 I, 85 Sr and 137 Cs, are modelled by a one-dimensional porous medium approach in which sorption is described by Freundlich isotherms. The governing equations are solved analytically for the special case of a linear isotherm, and numerically using the computer code RANCHDIFF for non-linear isotherms. A set of time-dependent, ordinary differential equations is obtained using the Lagrange interpolation technique and integrated by Gear's variable order predictor-corrector method. It is shown that the sorption behaviour of 85 Sr can be modelled successfully by a linear isotherm, using a sorption parameter consistent with batch-sorption tests. The behaviour of 137 Cs may be modelled by a non-linear isotherm, but the amount of 137 Cs sorbed is less than that anticipated from batch-sorption tests. 125 I is assumed to be non-sorbing and is used to determine the porosity of the sandstone. (author) 10 figs., 4 tabs., 6 refs

  9. Surface complexation modeling of americium sorption onto volcanic tuff.

    Science.gov (United States)

    Ding, M; Kelkar, S; Meijer, A

    2014-10-01

    Results of a surface complexation model (SCM) for americium sorption on volcanic rocks (devitrified and zeolitic tuff) are presented. The model was developed using PHREEQC and based on laboratory data for americium sorption on quartz. Available data for sorption of americium on quartz as a function of pH in dilute groundwater can be modeled with two surface reactions involving an americium sulfate and an americium carbonate complex. It was assumed in applying the model to volcanic rocks from Yucca Mountain, that the surface properties of volcanic rocks can be represented by a quartz surface. Using groundwaters compositionally representative of Yucca Mountain, americium sorption distribution coefficient (Kd, L/Kg) values were calculated as function of pH. These Kd values are close to the experimentally determined Kd values for americium sorption on volcanic rocks, decreasing with increasing pH in the pH range from 7 to 9. The surface complexation constants, derived in this study, allow prediction of sorption of americium in a natural complex system, taking into account the inherent uncertainty associated with geochemical conditions that occur along transport pathways. Published by Elsevier Ltd.

  10. Water sorption and solubility of core build-up materials.

    Science.gov (United States)

    Zankuli, M A; Devlin, H; Silikas, N

    2014-12-01

    To investigate the variation in water sorption and solubility across a range of different core build-up materials. Five materials were tested, four of which are resin-based materials (Grandio Core, Core.X Flow, Bright Flow Core, Speedee) and one resin-modified glass ionomer (Fuji II LC). All specimens (n=10) were immersed in 10ml distilled water in individual glass containers and weighed at one week, 14 and 28 days. After a total immersion time of 28 days, 7 specimens were dried to a constant mass, in a desiccator for 28 days. Three samples of each material were not dried, but were left in distilled water for 1 year, to determine the long-term water sorption properties. Specimens were weighed at monthly intervals until 6 months and then at the 9th and 12th months. Each specimen was measured using a digital electronic caliper (Mitutoyo Corporation, Japan). After 28 days immersion, the change in water sorption and solubility of the materials ranged from 12.9 to 67.1μg/mm(3) (PGrandio Core had the lowest water sorption and solubility among the tested materials. According to the ISO 4049 standards, all the tested materials showed acceptable water sorption and solubility, apart from the water sorption behavior of Fuji II LC. Copyright © 2014 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

  11. Characteristics of and sorption to biochars derived from waste material

    Science.gov (United States)

    Sun, Huichao; Kah, Melanie; Sigmund, Gabriel; Hofmann, Thilo

    2015-04-01

    Biochars can exhibit a high sorption potential towards heavy metals and organic contaminants in various environmental matrices (e.g., water, soil). They have therefore been proposed for environmental remediation purposes to sequester contaminants. To date, most studies have focused on the physicochemical and sorption properties of mineral phases poor biochars, which are typically produced from plant residues. Only little knowledge is available for biochars derived from human and animal waste material, which are typically characterized by high mineral contents (e.g., sewage sludge, manure). Using human and animal waste as source material to produce biochars would support the development of attractive combined strategies for waste management and remediation. The potential impact of mineral phases on the physicochemical and sorption properties of biochars requires further studies so that the potential as sorbent material can be evaluated. With this purpose, different source material biochars were produced at 200°C, 350°C and 500°C, to yield a series of biochars representing a range of mineral content. The derived biochars from wood shavings (heavy metals and polycyclic aromatic hydrocarbons) of all materials were within the guidelines values proposed by the International Biochar Initiative, indicating their suitability for environmental application. Single point sorption coefficients for the model sorbate pyrene were measured to investigate the effect of mineral content, feedstock, pyrolysis temperature, particle size fractions and acid demineralization on sorption behavior. Overall, sorption of pyrene was strong for all materials (4 remediation applications.

  12. Sorption behavior of uranium(VI) on a biotite mineral

    International Nuclear Information System (INIS)

    Idemitsu, K.; Obata, K.; Furuya, H.; Inagaki, Y.

    1995-01-01

    Biotite has the most important role for the sorption of radionuclides in granitic rocks. Experiments on the sorption of uranium(VI) on biotite were conducted to understand the fundamental controls on uranium sorption on biotite mineral, including the effects of pH and uranium concentration in solution. Biotite powder (mesh 32--60) were washed with 1N HCl for a week and were rinsed twice with deionized water for a week. This HCl treatment was necessary to avoid the effects by other minerals. The agreement between surface adsorption coefficient, Ka, of both biotites with and without HCl treatment was within one order of magnitude. The peak Ka value was in the range of 0.1 to 0.01 cm 3 /cm 2 around pH 6. A comparison of aqueous uranium speciations and sorption results indicates that neutral uranyl hydroxide could be an important species sorbed on the biotite. Sequential desorption experiments with KCl and HCl solutions were also carried out after sorption experiments to investigate sorption forms of uranium. Approximately 20% of uranium in solution were sorbed on the biotite as an exchangeable ion. The fraction of exchangeable uranium had a little dependence on pH. The other uranium could not be extracted even by 6N HCl solution. It is possible that most of the uranium could be precipitated as U(IV) via Fe(II) reduction on the biotite surface

  13. Sorption of aromatic organic pollutants to grasses from water

    Science.gov (United States)

    Barbour, J.P.; Smith, J.A.; Chiou, C.T.

    2005-01-01

    The influence of plant lipids on the equilibrium sorption of three aromatic solutes from water was studied. The plant-water sorption isotherms of benzene, 1,2-dichlorobenzene, and phenanthrene were measured over a large range of solute concentrations using sealed vessels containing water, dried plant material, and solute. The plant materials studied include the shoots of annual rye, tall fescue, red fescue, and spinach as well as the roots of annual rye. Seven out of eight sorption isotherms were linear with no evidence of competitive effects between the solutes. For a given plant type, the sorption coefficient increased with decreasing solute water solubility. For a given solute, sorption increased with increasing plant lipid content. The estimated lipid-water partition coefficients of individual solutes were found to be significantly greater than the corresponding octanol-water partition coefficients. This indicates that plant lipids are a more effective partition solvent than octanol for the studied aromatic compounds. As expected, the solute lipid-water partition coefficients were log-linearly related to the respective water solubilities. For the compounds studied, partitioning into the lipids is believed to be the primary sorption mechanism. ?? 2005 American Chemical Society.

  14. Effect of Mouthwashes on Solubility and Sorption of Restorative Composites

    Directory of Open Access Journals (Sweden)

    José Pereira Leal

    2017-01-01

    Full Text Available Objective. Composites sorption and solubility can be precursors of several chemical and physical processes, which lead to deleterious effects on the polymer structure. This study evaluated the effect of mouthwashes on solubility and sorption of composite resins. Materials and Methods. Forty-two specimens of each evaluated composite (Filtek Bulk Fill Flow, Opallis Flow, Durafill VS, and Filtek Z350 were prepared and randomized into seven groups for each solution (mouth rinses with and without alcohol and distilled water and stored for seven days. Solubility and sorption tests were performed according to ISO4049. Data were analyzed using 2-way-ANOVA followed by Tukey’s test for means comparison (α=0.05. In addition, paired t-test was performed to analyze the alcohol effect on the studied composite resin properties. Results. Listerine Cool Mint (containing alcohol in its composition caused the greatest degree of sorption for all composites tested in comparison to other rinses, while for solubility this behavior was observed for Opallis Flow and Durafill VS composite resins (p<0.05. Regarding the composites, Opallis Flow showed the highest sorption and solubility values in general (p<0.05. Conclusion. Overall, the sorption and solubility of composites were higher in mouthwashes containing alcohol in its composition, with Opallis Flow being the most affected composite resin.

  15. Moisture sorption isotherms and thermodynamic properties of bovine leather

    Science.gov (United States)

    Fakhfakh, Rihab; Mihoubi, Daoued; Kechaou, Nabil

    2018-04-01

    This study was aimed at the determination of bovine leather moisture sorption characteristics using a static gravimetric method at 30, 40, 50, 60 and 70 °C. The curves exhibit type II behaviour according to the BET classification. The sorption isotherms fitting by seven equations shows that GAB model is able to reproduce the equilibrium moisture content evolution with water activity for moisture range varying from 0.02 to 0.83 kg/kg d.b (0.9898 thermodynamic properties such as isosteric heat of sorption, sorption entropy, spreading pressure, net integral enthalpy and entropy. Net isosteric heat of sorption and differential entropy were evaluated through direct use of moisture isotherms by applying the Clausius-Clapeyron equation and used to investigate the enthalpy-entropy compensation theory. Both sorption enthalpy and entropy for desorption increase to a maximum with increasing moisture content, and then decrease sharply with rising moisture content. Adsorption enthalpy decreases with increasing moisture content. Whereas, adsorption entropy increases smoothly with increasing moisture content to a maximum of 6.29 J/K.mol. Spreading pressure increases with rising water activity. The net integral enthalpy seemed to decrease and then increase to become asymptotic. The net integral entropy decreased with moisture content increase.

  16. Sorption Coefficients for Iodine, Silver, and Cesium on Dust Particles

    International Nuclear Information System (INIS)

    Stempniewicz, M.M.; Goede, P.

    2014-01-01

    This paper describes the work performed to find relevant experimental data and find the sorption coefficients that represent well the available data for cesium, iodine, and silver on dust particles. The purpose of this work is to generate a set of coefficients that may be recommended for the computer code users. The work was performed using the computer code SPECTRA. Calculations were performed for the following data: • I-131 on AVR dust; • Ag-110m on AVR dust; • Cs-13 and Cs-137 on AVR dust. Available data was matched using the SPECTRA Sorption Model. S = A(T) · C V -B(T) · C d . The results are summarized as follows: • The available data can be correlated. The data scatter is about 4 orders of magnitude. Therefore the coefficients of the Langmuir isotherms vary by 4 orders of magnitude. • Sorption rates are higher at low temperatures and lower at high temperatures. This tendency has been observed in the data compiled at Oak Ridge. It is therefore surmised that the highest value of the sorption coefficients are appropriate for the low temperatures and the lowest value of the sorption coefficients are appropriate for the high temperatures. The recommended sorption coefficients are presented in this paper. • The present set of coefficients is very rough and should be a subject for future verification against experimental data. (author)

  17. Lay Health Influencers: How They Tailor Brief Tobacco Cessation Interventions

    Science.gov (United States)

    Yuan, Nicole P.; Castaneda, Heide; Nichter, Mark; Nichter, Mimi; Wind, Steven; Carruth, Lauren; Muramoto, Myra

    2012-01-01

    Interventions tailored to individual smoker characteristics have increasingly received attention in the tobacco control literature. The majority of tailored interventions are generated by computers and administered with printed materials or web-based programs. The purpose of this study was to examine the tailoring activities of community lay…

  18. Sorption of organic water pollutants on dead vegetable biomass; Sorption organischer Wasserschadstoffe an abgestorbene pflanzliche Biomasse

    Energy Technology Data Exchange (ETDEWEB)

    Kraeuter, A.

    2001-03-01

    Hemp-derived biological sorption agents were produced, and their physical, chemical and sorptive characteristics were tested in batch and filter tests. The experiments were accompanied by model calculations. In the natural state, the sorption agents had a kation exchange capacity of 0.1-0.3 mmol/g, modified sorption agents had about 2 mmol/g. Kationized hemp had values of 0.34 mmol/g and thermally modified hemp absorption agents absorbed more than 1.2 mmol/g of dichlorophenol. In the case of a liquid effluent from a textile dyeing plant, only a discoloration effect was achieved. The absorption agents can be regenerated, combusted or composted after use. [German] Im Rahmen dieser Arbeit wurden naturbelassene und modifizierte Billig-Biosorbentien aus Hanfschaeben zur Entfernung organischer Schadstoffe aus Waessern hergestellt und ihre physikalischen, chemischen und sorptiven Eigenschaften in Batch- und Filterversuchen untersucht. Wegen der Komplexheit des Systems ''Biosorption organischer Wasserschadstoffe'' wurden die ermittelten Sorptionsisothermen mit den Ansaetzen nach Langmuir und Freundlich beschrieben. Die Sorptionskinetik und das Durchbruchsverhalten wurde ebenfalls mit einfachen Ansaetzen modelliert. Naturbelassene Hanfschaeben erreichten Kationenaustauschkapazitaeten von 0,1-0,3 mmol/g, entsprechend modifizierte Hanfschaeben ca. 2 mmol/g. Kationisierte Hanfschaeben dagegen erreichten Anionenaustauschkapazitaeten von 0,34 mmol/g und thermisch modifizierte Hanfschaeben sorbierten bis ueber 1,2 mmol/g Dichlorphenol. Bei der Behandlung eines Abwassers aus einer Textilfaerberei beschraenkte sich die Reinigungsleistung der hergestellten Biosorbentien auf eine Entfaerbung. Nach Schadstoffbeladung koennen die Hanfschaeben regeneriert, thermisch verwertet oder kompostiert werden. (orig.)

  19. Artificial neural network approaches for the sorption isotherms, enthalpy and entropy of heat sorption of two types block rubber products

    OpenAIRE

    Yutthana Tirawanichakul; Jutarut Tasara; Supawan Tirawanichakul

    2013-01-01

    Knowledge of the temperature and relative humidity (or water activity) dependence of moisture sorption phenomenaof agro-industrial products provides valuable information about changes related to the thermodynamics of the system. Thusthe moisture sorption characteristics in terms of equilibrium moisture contents (EMC), enthalpy and entropy of heat sorptionof natural rubber (NR) for producing STR 20 and skim block rubber were investigated. Simulation modeling of water sorptionisotherms was perf...

  20. MEMS tandem ion-sorption micropump

    Science.gov (United States)

    Grzebyk, T.

    2017-12-01

    This paper presents a two-stage MEMS ion-sorption micropump, which works in a wide range of pressures—it allows efficient evacuation of gases from the internal volume of any microsystem starting from atmospheric pressure down to 10‑6 hPa. The miniature pre-vacuum pump is realized as a two-electrode silicon–glass structure with a very close inter-electrode distance. The use of the silicon substrate as a getter material instead of a metallic layer significantly increases the pumping capacity and as a result, the initial pressure can be reduced to a level of 1 hPa. From this point the pumping is continued with the second glow-discharge high vacuum micropump. This pump is a multilayer structure, in which ions are trapped in crossed electric and magnetic fields. It allows further reduction of pressure down to 10‑6 hPa. Both pumps are technologically compatible and together they enable the on-chip generation of avacuum at the desired level in a variety of miniaturized devices.

  1. CO2 sorption to subsingle hydration layer montmorillonite clay studied by excess sorption and neutron diffraction measurements.

    Science.gov (United States)

    Rother, Gernot; Ilton, Eugene S; Wallacher, Dirk; Hauβ, Thomas; Schaef, Herbert T; Qafoku, Odeta; Rosso, Kevin M; Felmy, Andrew R; Krukowski, Elizabeth G; Stack, Andrew G; Grimm, Nico; Bodnar, Robert J

    2013-01-02

    Geologic storage of CO(2) requires that the caprock sealing the storage rock is highly impermeable to CO(2). Swelling clays, which are important components of caprocks, may interact with CO(2) leading to volume change and potentially impacting the seal quality. The interactions of supercritical (sc) CO(2) with Na saturated montmorillonite clay containing a subsingle layer of water in the interlayer region have been studied by sorption and neutron diffraction techniques. The excess sorption isotherms show maxima at bulk CO(2) densities of ≈ 0.15 g/cm(3), followed by an approximately linear decrease of excess sorption to zero and negative values with increasing CO(2) bulk density. Neutron diffraction experiments on the same clay sample measured interlayer spacing and composition. The results show that limited amounts of CO(2) are sorbed into the interlayer region, leading to depression of the interlayer peak intensity and an increase of the d(001) spacing by ca. 0.5 Å. The density of CO(2) in the clay pores is relatively stable over a wide range of CO(2) pressures at a given temperature, indicating the formation of a clay-CO(2) phase. At the excess sorption maximum, increasing CO(2) sorption with decreasing temperature is observed while the high-pressure sorption properties exhibit weak temperature dependence.

  2. Application of simplified desorption method to sorption study. (2) Sorption of neptunium (V) on montmorillonite-based mixtures

    International Nuclear Information System (INIS)

    Kozai, Naofumi; Ohnuki, Toshihiko

    2013-01-01

    To elucidate the sorption behaviors of radionuclides in multi-mineral systems and the mutual effects of minerals on the sorption, this paper carried out the sorption and desorption experiments of neptunium(V) on montmorillonite-based two-mineral mixtures. The Np sorbed on montmorillonite at pH from 4 to 8 was desorbed with 1M KCl solutions, indicating that the sorption was cation exchange. The Np sorbed on apatite and calcite was nondesorbable with 1M KCl solutions, which is in harmony with the knowledge that Np forms strong complexes with the phosphate groups of apatite and the carbonate groups of calcite. This study utilized these clear distinguishes of the desorption behaviors for examining the two-mineral systems. In montmorillonite-apatite mixtures, the sorption on the montmorillonite was decreased and Np was accumulated on the apatite. In montmorillonite-calcite mixtures, the sorption on the montmorillonite was decreased due to the interference by the calcium and carbonate ions dissolved from calcite while no accumulation of Np to calcite was observed. (author)

  3. Forming of an axially tailored automotive channel section through hot stamping of tailor-welded blanks

    Science.gov (United States)

    Peister, C.; George, R.; Omer, K.; Worswick, M. J.; Malcolm, S.; Dykeman, J.; Yau, C.; Soldaat, R.; Bernert, W.

    2017-09-01

    In this work, top-hat cross-section axial crush rail specimens with tailored properties along their length were investigated. These top-hat channels were hot stamped in a fully cooled die set from tailor-welded blanks (TWBs). The blanks were laser-welded and comprised Usibor® 1500-AS joined to Ductibor® 500-AS in 1.2 mm and 1.6 mm thicknesses. Micro-hardness measurements were taken along the length of the formed specimens to map the hardness profile along their length. The effect of gauge thickness on hardness was evaluated. The hardness profile of these TWB parts was compared to that of parts formed using tailored in-die heating (IDH).

  4. Sorption data bases for generic Swiss argillaceous rock systems

    International Nuclear Information System (INIS)

    Bradbury, M. H.; Baeyens, B.; Thoenen, T.

    2010-09-01

    In Switzerland the site selection procedure for both high level waste (HLW) and low and intermediate level waste (L/ILW) repositories is specified by the Swiss Federal Office of Energy in the Sectoral Plan for Deep Geological Repositories. In the forthcoming stage 2 of this plan, potential sites will be identified within regions previously selected based on the presence of suitable host rocks, namely Opalinus Clay, 'Brauner Dogger', Effingen Member and Helvetic Marl. Preliminary safety analyses are an integral part of this procedure, and require, amongst other information, the radionuclide sorption properties of the host rock. This report describes a methodology to develop a Generic Rock Sorption Data Base (GR-SDB) for argillaceous rocks. The method will be used to compile specific SDBs for the above mentioned host rocks. Arguments are presented that the main factor influencing sorption on argillaceous rocks is the phyllosilicate mineral content. These minerals are particularly effective at binding metals to their surfaces by cation exchange and surface complexation. Generally, the magnitude of sorption is directly correlated with the phyllosilicate content (2:1 type clays: illite/smectite/illitesmectite mixed layers), and this parameter best reflects the sorption potential of a given mineral assembly. Consequently, sorption measurements on illite were preferably used as source data for the GR-SDB. The second component influencing radionuclide sorption is the porewater chemistry. In the present report, generic water compositions were extracted from the analytical ranges of deep ground waters in various sedimentary formations in Switzerland. In order to cover the range of ionic strength (I) and pH values of Swiss ground waters in argillaceous rocks, five types of generic water compositions were defined, combining low, intermediate and high values of ionic strength and pH. The GR-SDB for in situ conditions was derived using conversion factors (CF). As the name

  5. Advances in Precision Medicine: Tailoring Individualized Therapies.

    Science.gov (United States)

    Matchett, Kyle B; Lynam-Lennon, Niamh; Watson, R William; Brown, James A L

    2017-10-25

    The traditional bench-to-bedside pipeline involves using model systems and patient samples to provide insights into pathways deregulated in cancer. This discovery reveals new biomarkers and therapeutic targets, ultimately stratifying patients and informing cohort-based treatment options. Precision medicine (molecular profiling of individual tumors combined with established clinical-pathological parameters) reveals, in real-time, individual patient's diagnostic and prognostic risk profile, informing tailored and tumor-specific treatment plans. Here we discuss advances in precision medicine presented at the Irish Association for Cancer Research Annual Meeting, highlighting examples where personalized medicine approaches have led to precision discovery in individual tumors, informing customized treatment programs.

  6. Tailored antireflective biomimetic nanostructures for UV applications

    Energy Technology Data Exchange (ETDEWEB)

    Morhard, Christoph; Pacholski, Claudia; Spatz, Joachim P [Department of New Materials and Biosystems, Max Planck Institute for Metals Research, Heisenbergstrasse 3, D-70569 Stuttgart (Germany); Lehr, Dennis; Brunner, Robert; Helgert, Michael [Carl Zeiss Jena GmbH, Technology Center, Carl-Zeiss-Promenade 10, D-07745 Jena (Germany); Sundermann, Michael, E-mail: Pacholski@mf.mpg.de [Carl Zeiss Jena GmbH, Technology Center, Carl-Zeiss-Strasse 56, D-73447 Oberkochen (Germany)

    2010-10-22

    Antireflective surfaces composed of biomimetic sub-wavelength structures that employ the 'moth eye principle' for reflectance reduction are highly desirable in many optical applications such as solar cells, photodetectors and laser optics. We report an efficient approach for the fabrication of antireflective surfaces based on a two-step process consisting of gold nanoparticle mask generation by micellar block copolymer nanolithography and a multi-step reactive ion etching process. Depending on the RIE process parameters nanostructured surfaces with tailored antireflective properties can easily be fabricated that show optimum performance for specific applications.

  7. Catalytic gasification of biomass (Miscanthus) enhanced by CO2 sorption.

    Science.gov (United States)

    Zamboni, I; Debal, M; Matt, M; Girods, P; Kiennemann, A; Rogaume, Y; Courson, C

    2016-11-01

    The main objective of this work concerns the coupling of biomass gasification reaction and CO 2 sorption. The study shows the feasibility to promote biomass steam gasification in a dense fluidized bed reactor with CO 2 sorption to enhance tar removal and hydrogen production. It also proves the efficiency of CaO-Ca 12 Al 14 O 33 /olivine bi-functional materials to reduce heavy tar production. Experiments have been carried out in a fluidized bed gasifier using steam as the fluidizing medium to improve hydrogen production. Bed materials consisting of CaO-based oxide for CO 2 sorption (CaO-Ca 12 Al 14 O 33 ) deposited on olivine for tar reduction were synthesized, their structural and textural properties were characterized by Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), and temperature-programmed reduction (TPR) methods, and the determination of their sorption capacity and stability analyzed by thermogravimetric analysis (TGA). It appears that this CaO-Ca 12 Al 14 O 33 /olivine sorbent/catalyst presents a good CO 2 sorption stability (for seven cycles of carbonation/decarbonation). Compared to olivine and Fe/olivine in a fixed bed reactor for steam reforming of toluene chosen as tar model compound, it shows a better hydrogen production rate and a lower CO 2 selectivity due to its sorption on the CaO phase. In the biomass steam gasification, the use of CaO-Ca 12 Al 14 O 33 /olivine as bed material at 700 °C leads to a higher H 2 production than olivine at 800 °C thanks to CO 2 sorption. Similar tar concentration and lighter tar production (analyzed by HPLC/UV) are observed. At 700 °C, sorbent addition allows to halve tar content and to eliminate the heaviest tars.

  8. Sorption of tylosin and sulfamethazine on solid humic acid.

    Science.gov (United States)

    Guo, Xuetao; Tu, Bei; Ge, Jianhua; Yang, Chen; Song, Xiaomei; Dang, Zhi

    2016-05-01

    Tylosin (TYL) and sulfamethazine (SMT) are ionizable and polar antimicrobial compounds, which have seeped into the environment in substantial amounts via fertilizing land with manure or sewage. Sorption of TYL and SMT onto humic acid (HA) may affect their environmental fate. In this study, the sorption of TYL and SMT on HA at different conditions (pH, ionic strength) was investigated. All sorption isotherms fitted well to the Henry and Freundlich models and they were highly nonlinear with values of n between 0.5 and 0.8, which suggested that the HA had high heterogeneity. The sorption of TYL and SMT on HA decreased with increasing pH (2.0-7.5), implying that the primary sorption mechanism could be due to cation exchange interactions between TYL(+)/SMT(+) species and the functional groups of HA. Increasing ionic strength resulted in a considerable reduction in the Kd values of TYL and SMT, hinting that interactions between H bonds and π-π EDA might be an important factor in the sorption of TYL and SMT on HA. Results of Fourier transform infrared (FT-IR) and (13)C-nuclear magnetic resonance (NMR) analysis further demonstrated that carboxyl groups and O-alkyl structures in the HA could interact with TYL and SMT via ionic interactions and H bonds, respectively. Overall, this work gives new insights into the mechanisms of sorption of TYL and SMT on HA and hence aids us in assessing the environmental risk of TYL and SMT under diverse conditions. Copyright © 2015. Published by Elsevier B.V.

  9. Sorption of radionuclides from spent fuel in crystalline rocks

    International Nuclear Information System (INIS)

    Nikula, A.

    1982-10-01

    The safe disposal of spent nuclear fuel or reprocessed waste is an essential element in the expansion of the nuclear power industry. Stable rock formations e.g. granite are considered to be potential sites for disposal. A major factor in evaluating the degree of safety of the disposal is the sorption of radionuclides in rock, which affects their retardation. The report considers the chemical forms of the hazardous radionuclides of spent nuclear fuel in groundwater and the effects of the water's properties on them. In the groundwater near the Olkiluoto power plant site cesium, strontium and radium are in cationic form, iodine as I - . Technetium would occur as TcO +2 , but the pertechnetate form is also possible. Uranium most probably would be as U(VI) plutonium and neptunium as Np(IV) or Np(V). The valences for thorium, americium and curium are not changed in this groundwater and would be +4, +3 and +3, respectively. The actinides in groundwater are all in hydrated or complex form. An increase on the ionic stregth of the groundwater in most instances causes a decrease in the sorption of nuclides since the ion exchange capacity of the rock is limited. Anionic ligands also decrease sorption of cations by complex formation. In some case, on the other hand, high salt concentrations may cause formation of radiocolloids of lanthanides and neptunium and thus increase sorption. In all cases the degree of sorption described by the distribution ratio Ksub(d) was influenced by the pH of the groundwater. Sorption of cesium and strontium increased with growing pH. The sorption behaviour of actinides was in positive correlation with formation of hydroxide complexes at different pH values. The Ksub(d) values of Cs, Sr, Co, Ni and Am for Olkiluoto granites were found to agree with Swedish values, also determined at ambient atmospheric conditions

  10. Natural minerals and synthetic materials for sorption of radioactive anions

    Energy Technology Data Exchange (ETDEWEB)

    Kang, Mun Ja; Chun, Kwan Sik; Kim, Seung Soo

    1998-07-01

    Technetium-99 and iodine-129 are fission products with long half-lives, and exist as highly soluble anionic species. Studies on natural and synthetic materials sorbing TcO{sub 4} and/or I have been performed by several researchers. The application of these materials as an additive in the high-level waste disposal has been considered. The iron- or sulfide-containing minerals such as metal iron, iron powder, stibnite and pyrrhotite show a high capacity for TcO{sub 4} sorption. And the small amounts of activated carbon are reported to have high distribution coefficients recently. In the iodine sorption studies, sulfide-, copper-, lead- or mercury-containing minerals can be a candidate. Pyrite, chalcopyrite, galena, Cu{sub 2}S and CuS reveal a high capacity for I sorption. The synthetic materials were found to have high sorption capacity and compensate the defects of natural minerals, which contain hydrous oxides such as zirconium oxide, aluminium oxide and mercarbide. The mercarbide has the high distribution coefficients for the sorption of TcO{sub 4} and I. Recently it was proposed that the synthetic clay, hydrotalcite, could be useful for the fixation of anion. However, to determine the applicability of those natural and synthetic materials as an additive to a buffer or backfill material for sorption of TcO{sub 4} and/or I, the sorption behavior of the anions on those materials under the repository conditions should be identified. (author). 32 refs., 21 tabs., 10 figs

  11. Sericitization of illite decreases sorption capabilities for cesium

    Science.gov (United States)

    Choung, S.; Hwang, J.; Han, W.; Shin, W.

    2017-12-01

    Release of radioactive cesium (137Cs) to environment occurs through nuclear accidents such as Chernobyl and Fukushima. The concern is that 137Cs has long half-life (t1/2 = 30.2 years) with chemical toxicity and γ-radiation. Sorption techniques are mainly applied to remove 137Cs from aquatic environment. In particular, it has been known well that clay minerals (e.g, illite) are effective and economical sorbents for 137Cs. Illite that was formed by hydrothermal alteration exist with sericite through "sericitization" processes. Although sericite has analogous composition and lattice structure with illite, the sorptive characteristics of illite and sericite for radiocesium could be different. This study evaluated the effects of hydrothermal alteration and weathering process on illite cesium sorption properties. Natural illite samples were collected at Yeongdong area in Korea as the world-largest hydrothermal deposits for illite. The samples were analyzed by XRF, XRD and SEM-EDX to determine mineralogy, chemical compositions and morphological characteristics, and used for batch sorption experiments. The Yeongdong illites predominantly consist of illite, sericite, quartz, and albite. The measured cesium sorption distribution coefficients (Kd,Cs) of reference illite and sericite were approximately 6000 and 400 L kg-1 at low aqueous concentration (Cw 10-7 M), respectively. In contrast, Kd,Cs values for the Yeongdong illite samples ranged from 500 to 4000 L kg-1 at identical concentration. The observed narrow and sharp XRD peak of sericite indicated that the sericite has better crystallinity compared to illite. These experimental results suggested that sericitization processes of illite can decline the sorption capabilities of illite for cesium under various hydrothermal conditions. In particular, weathering experiments raised the cesium sorption to illite, which seems to be related to the increase of preferential sorption sites for cesium through crystallinity destruction

  12. Comparing uranyl sorption complexes on soil and reference clays

    International Nuclear Information System (INIS)

    Chisholm-Brause, C.J.; Berg, J.M.; Conradson, S.D.; Morris, D.E.; McKinley, J.P.; Zachara, J.M.

    1993-01-01

    Clay minerals and other components in natural soils may play a key role in limiting the mobility of uranium in the environment through the formation of sorption complexes. Reference clays are frequently used as models to study sorption processes because they have well-known chemical and physical properties, but they may differ chemically and morphologically from clays derived from natural soils. Therefore, inferences based on reference clay data have been questioned. The authors have used luminescence and x-ray absorption spectroscopies to characterize the sorption complexes of aqueous uranyl (UO 2 2+ ) species on two soil smectites from the Kenoma and Ringold formations, and compared these results to those obtained on reference smectite clays. The pH dependence of uptake suggests that the ratio of sorption on amphoteric edge sites is greater for the soil smectites than for reference clays such as Wyoming montmorillonite (SWy-1). The luminescence spectra for uranyl sorbed to the soil clays are very similar to those for uranyl sorbed principally to the edge sites of SWy-1. This observation supports the solution data suggesting that adsorption to amphoteric sites is a more important mechanism for soil clays. However, the spectral data indicate that the sorption complexes on natural and reference clays are quite similar. Furthermore, as with the reference clays, the authors have found that the chemistry of the solution plays a greater role in defining the sorption complex than does the clay matrix. Thus, if differences in surface properties are adequately taken into account, the reference clays may serve as useful analogs for soil clays in investigations of metal-ion sorption

  13. Sorption of technetium-hydroxyapatite composite chitosan from aqueous solution

    International Nuclear Information System (INIS)

    Pivarciova, L.; Rosskopfova, O.; Galambos, M.; Rajec, P.

    2013-01-01

    Biomaterials such as natural polymers (chitosan) and hydroxyapatite have important application in material for bone replacement. Most of chitosan/hydroxyapatite composites are prepared by mixing the hydroxyapatite particles with chitosan matrices. Another method of preparation of chitosan/hydroxyapatite composite is in-situ generation of nano-hydroxyapatite in chitosan matrix. The most common biomaterial used in the past years in hard tissue regeneration was hydroxyapatite, owing to its properties as biocompatibility, bioactivity, non-toxicity, non-immunogenicity etc. Chitosan is polyaminosacharide, partially deacetylated product of chitin. Chitosan can be used in combination with other materials to enhance bone growth such as bone filling paste. Aims of this work were: the influence of the contact time on sorption of pertechnate anions on chitosan/hydroxyapatite composites; the effect of pH on sorption of pertechnate anions on chitosan/hydroxyapatite composites; the effect of foreign ions on sorption of pertechnate anions on chitosan/hydroxyapatite composites. The author concluded: the percentage of technetium sorption after 1 hour of contact time was > 97 %. In the initial pH range of 2.9-10.2, the percentage of technetium sorption on chitosan/hydroxyapatite composites CH/HA(A), CH/HA(B), CH/HA 30:70, ZCH was > 98 % and on CH/HA 50:50 was > 94%. Competition effect of Fe 2+ towards TcO 4 :- sorption is stronger than competition effect of other observed cations for all examined composites with the same weight ratio. The percentage of the technetium sorption was the same for all composites with weight ratio of 30:70. (authors)

  14. Sorption mechanisms of chromate with coprecipitated ferrihydrite in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Mamun, Abdullah Al, E-mail: mamun@toki.waseda.jp [Graduate School of Creative Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo 169-8555 (Japan); Morita, Masao, E-mail: masao.swimer@akane.waseda.jp [Graduate School of Creative Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo 169-8555 (Japan); Matsuoka, Mitsuaki, E-mail: m-matsuoka@aoni.waseda.jp [Faculty of Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo 169-8555 (Japan); Tokoro, Chiharu, E-mail: tokoro@waseda.jp [Faculty of Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo 169-8555 (Japan)

    2017-07-15

    Highlights: • Coprecipitation showed twice the sorption density of simple adsorption at pH 5. • Mechanism shift from outer- to inner-sphere surface complexation at high Cr/Fe. • In coprecipitation the mechanism shift occurs at lower Cr/Fe ratios than adsorption. • Higher-molar-ratio bidentate binuclear Cr−Fe bonds; yielded ferrihydrite expansion. - Abstract: Hexavalent chromium (Cr(VI)) attracted researchers’ interest for its toxicity, natural availability and removal difficulty. Nevertheless, its sorption mechanism is not clearly understood yet. In this work, we elucidated the sorption mechanism of the co-precipitation of chromates with ferrihydrite through quantitative analysis. The influence of Cr/Fe molar ratio on sorption was investigated by zeta potential measurements, X-ray diffraction (XRD) and X-ray adsorption fine-structure analysis (XAFS). Coprecipitation at pH 5 showed almost twice the sorption density of adsorption at pH 5. In co-precipitation, a shift of the XRD peak due to inner-sphere sorption of chromate was observed at Cr/Fe molar ratio 0.5. For adsorption, the same peak shift was confirmed at Cr/Fe molar ratio of 1. Zeta potential at pH 5 suggested that the sorption mechanism changed at Cr/Fe molar ratio 0.25 for coprecipitation and at Cr/Fe molar ratio of 1 for adsorption. Fitting of Cr and Fe K-edge extended X-ray adsorption fine-structure suggested that ferrihydrite immobilized Cr(VI) via outer sphere surface complexation for lower Cr/Fe ratios and via inner-sphere surface complexation for higher molar ratios. At higher molar ratios, bidentate binuclear Cr−Fe bonds were well established, thus resulting in the expansion of the ferrihydrite structure.

  15. Laser cutting of sheets for Tailored Blanks

    DEFF Research Database (Denmark)

    Bagger, Claus; Olsen, Flemming Ove

    1999-01-01

    Over the past few years there has been an enormous increase in the use of tailored blanks, especially in the automotive industry. Often the sheets for tailored blanks are shear cut, but results have been reported that the allowable sheet gap distance should not exceed 0.1 mm in order to obtain...... sound welds. Laser cutting the sheets may therefore be an alternative to shear cutting, if the cut kerf squareness can be kept below 0.05 mm.In a number of systematic laboratory experiments the effects of the major process parameters in laser cutting have been investigated. Each cut was quantified...... by the squareness, the surface roughness and the burr height. Mild steel as well as high strength steel with and with out galvanisation with thickness' of 0.7(5) and 1.25 were used.In the tests the difference in cut quality between a 5" and a 7.5" focusing lens were tested and the effect of using pulsed mode laser...

  16. Sorption of tetracycline on organo-montmorillonites

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Niu; Wang, Ming-xia; Liu, Ming-ming; Liu, Fan [College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070 (China); Weng, Liping [Department of Soil Quality, Wageningen University, P.O. Box 8005, 6700 EC, Wagneningen (Netherlands); Koopal, Luuk K. [Laboratory of Physical Chemistry and Colloid Science, Wageningen University, Dreijenplein 6, 6703 HB Wageningen (Netherlands); Tan, Wen-feng, E-mail: wenfeng.tan@hotmail.com [College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070 (China); State Key Laboratory of Soil Erosion and Dryland Farming on the Loess Plateau, Institute of Soil and Water Conservation, Chinese Academy of Sciences and Ministry of Water Resources, Yangling, Shanxi 712100 (China)

    2012-07-30

    Highlights: Black-Right-Pointing-Pointer The sorption capacity of tetracycline on Mont. modified with QACs was highly promoted. Black-Right-Pointing-Pointer Tetracycline adsorbed on organoclay was affected by the amount and the length of QACs. Black-Right-Pointing-Pointer Tetracycline adsorption on organoclay exhibited high pH-dependence below 5. - Abstract: Tetracycline (TC) is a veterinary antibiotic that is frequently detected as pollutant in the environment. Powerful adsorbents are required for removing TC. The present paper compares the TC adsorption capacity of Na-montmorillonite (Na-mont) with six organo-montmorillonites (organo-monts). Three quaternary ammonium cations (QACs) with different alkyl-chain lengths were used as modifiers. Powder X-ray diffraction indicated that the d{sub 001} values of organo-monts increased with increasing the QACs loading and alkyl-chain length. The CECs of the organo-monts were substantially lower than that of Na-mont and decreased with QACs chain length and increased loading. The modeling of the adsorption kinetics revealed that the processes of TC adsorption on the tested samples could be well fitted by the pseudo-second-order equation. The maximum adsorption capacities of TC on the organo-monts (1000-2000 mmol/kg) were considerably higher than that on Na-mont (769 mmol/kg). Both the Langmuir and Freundlich model could fit the adsorption isotherms. The TC adsorption to the organo-monts increase significantly with decreasing the pH below 5.5 because of the electrostatic interaction, and a high QACs loading performed better than a low loading at around pH 3.

  17. Calcium silicate hydrate: Crystallisation and alkali sorption

    International Nuclear Information System (INIS)

    Hong, S.

    2000-01-01

    Homogeneous single C-S-H gels has been prepared for the investigation of alkali binding potential and crystallisation. A distribution coefficient, R d , was introduced to express the partition of alkali between solid and aqueous phases at 25 deg. C. R d is independent of alkali hydroxide concentration and depends only on Ca:Si ratio over wide ranges of alkali concentration. The trend of numerical values of R d indicates that alkali bonding into the solid improves as its Ca:Si ratio decreases. Reversibility is demonstrated, indicating a possibility of constant R d value of the material. Al has been introduced to form C-A-S-H gels and their alkali sorption properties also determined. Al substituted into C-S-H markedly increases R d , indicating enhancement of alkali binding. However, the dependence of R d on alkali concentration is non-ideal with composition. A two-site model for bonding is presented. Crystallisation both under saturated steam and 1 bar vapour pressure has been investigated. It has been shown that heat treatment by saturated steam causes crystallisation of gels. The principal minerals obtained were (i) C-S-H gel and Ca(OH) 2 at -55 deg. C, (ii) 1.1 nm tobermorite, jennite and afwillite at 85 -130 deg. C, and (iii) xonotlite, foshagite and hillebrandite at 150-180 deg. C. Properties of crystalline C-S-H were also reported for reversible phase transformation, pH conditioning ability, seeding effect and solubility. At 1 bar pressure, crystallisation is slower than in saturated steam due to lower water activity. Tobermorite-like nanodomains develop during reaction at low Ca/Si ratios. In some Ca-rich compositions, Ca(OH) 2 is exsolved and occurs as nano-sized crystallites. (author)

  18. Improved hydrogen sorption kinetics in wet ball milled Mg hydrides

    Energy Technology Data Exchange (ETDEWEB)

    Meng, Li

    2011-05-04

    In this work, wet ball milling method is used in order to improve hydrogen sorption behaviour due to its improved microstructure of solid hydrogen materials. Compared to traditional ball milling method, wet ball milling has benefits on improvement of MgH{sub 2} microstructure and further influences on its hydrogen sorption behavior. With the help of solvent tetrahydrofuran (THF), wet ball milled MgH{sub 2} powder has much smaller particle size and its specific surface area is 7 times as large as that of dry ball milled MgH{sub 2} powder. Although after ball milling the grain size is decreased a lot compared to as-received MgH{sub 2} powder, the grain size of wet ball milled MgH{sub 2} powder is larger than that of dry ball milled MgH{sub 2} powder due to the lubricant effect of solvent THF during wet ball milling. The improved particle size and specific surface area of wet ball milled MgH{sub 2} powder is found to be determining its hydrogen sorption kinetics especially at relatively low temperatures. And it also shows good cycling sorption behavior, which decides on its industrial applicability. With three different catalysts MgH{sub 2} powder shows improved hydrogen sorption behavior as well as the cyclic sorption behavior. Among them, the Nb{sub 2}O{sub 5} catalyst is found to be the most effective one in this work. Compared to the wet ball milled MgH{sub 2} powder, the particle size and specific surface area of the MgH{sub 2} powder with catalysts are similar to the previous ones, while the grain size of the MgH{sub 2} with catalysts is much finer. In this case, two reasons for hydrogen sorption improvement are suggested: one is the reduction of the grain size. The other may be as pointed out in some literatures that formation of new oxidation could enhance the hydrogen sorption kinetics, which is also the reason why its hydrogen capacity is decreased compared to without catalysts. After further ball milling, the specific surface area of wet ball milled Mg

  19. Sorption-desorption behavior of polybrominated diphenyl ethers in soils

    Energy Technology Data Exchange (ETDEWEB)

    Olshansky, Yaniv; Polubesova, Tamara [Department of Soil and Water Sciences, Robert H. Smith Faculty of Agriculture, Food and Environment, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100 (Israel); Vetter, Walter [Institute of Food Chemistry (170b), University of Hohenheim, Garbenstr. 28, D-70599 Stuttgart (Germany); Chefetz, Benny, E-mail: chefetz@agri.huji.ac.il [Department of Soil and Water Sciences, Robert H. Smith Faculty of Agriculture, Food and Environment, The Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100 (Israel)

    2011-10-15

    Polybrominated diphenyl ethers (PBDEs) are flame retardants that are commonly found in commercial and household products. These compounds are considered persistent organic pollutants. In this study, we used 4,4'-dibromodiphenyl ether (BDE-15) as a model compound to elucidate the sorption and desorption behavior of PBDEs in soils. The organic carbon-normalized sorption coefficient (K{sub OC}) of BDE-15 was more than three times higher for humin than for bulk soils. However, pronounced desorption hysteresis was obtained mainly for bulk soils. For humin, increasing concentration of sorbed BDE-15 resulted in decreased desorption. Our data illustrate that BDE-15 and probably other PBDEs exhibit high sorption affinity to soils. Moreover, sorption is irreversible and thus PBDEs can potentially accumulate in the topsoil layer. We also suggest that although humin is probably a major sorbent for PBDEs in soils, other humic materials are also responsible for their sequestration. - Highlights: > BDE-15 exhibited pronounced desorption hysteresis. > BDE-15 sowed higher sorption affinity to humin as compared to the bulk soils. > Sequestration of PBDEs depends on soil organic matter constitutes other than humin. - Pronounced desorption hysteresis was observed for BDE-15 in natural soils.

  20. INFLUENCES OF SOIL PROPERTIES ON CHROMIUM (III SORPTION

    Directory of Open Access Journals (Sweden)

    R. Salmasi, F. Salmasi

    2007-07-01

    Full Text Available Soil adsorbing properties reduce sorption ability of the metal, which in turn may influence decision for remediation at contaminated sites. The objective of this study is presentation of a model based on soil properties to estimate the sorption of Cr(III in chromium contaminated soils. Twenty uncontaminated soil samples, with properties similar to the contaminated soils were selected from around of city of Tabriz and treated with Cr as CrCl3. A multiple regression analysis with statgraph software was used to drive an expression that related Cr sorption to common soil properties. The results showed that four soil properties were important in determining the amount of Cr adsorbed by the soils including pH, cation exchange capacity, total inorganic carbon and clay content with nearly 80% variability in Cr sorption and a reasonable level of confidence by this model. The obtained model suggested that Cr(III sorption was enhanced by higher soil pH, more total inorganic carbon, more clay, and higher cation exchange capacity.

  1. Ethylene oxide removal by sorption on aluminium oxide

    Directory of Open Access Journals (Sweden)

    Arsenijević Zorana Lj.

    2009-01-01

    Full Text Available The dynamics of ethylene oxide sorption and desorption on Al2O3 sorbent were investigated. The investigations of ethylene oxide sorption on Al2O3 show that significant sorption appeared above 125°C. The removal of sorbed ethylene oxide from Al2O3 was achieved by continuous increasing of the temperature up to 450°C in air stream. The analysis of desorbed products show that 90% of adsorbed ethylene oxide is converted to CO2 and the rest consists of the three derivatives of ethylene oxide. The exact composition of desorbed organic products will be determined in further investigation. The desorption temperature profiles point out the presence of two exothermic picks, as was confirmed by detection of CO2 and derivates of ethylene oxide at these temperatures. Investigation of textural characteristics and thermal stability of Al2O3 sorbent show that there are no changes of any characteristics of Al2O3 in sorption/desorption operating temperatures regimes. Only at 700°C the specific surface area of Al2O3 decreases of about 10%. This indicates that the investigated Al2O3 is convenient material for removal of ethylene oxide by sorption.

  2. Phenanthrene sorption to soil humic acid and different humin fractions.

    Science.gov (United States)

    Wen, Bei; Zhang, Jing-Jing; Zhang, Shu-Zhen; Shan, Xiao-Quan; Khan, Shahamat U; Xing, Baoshan

    2007-05-01

    This study was undertaken to provide an insight into the effect of heterogeneous soil organic matter (SOM) on the sorption of phenanthrene. Humic acid (HA) and humin were extracted from a peat soil. Humin was further fractionated into bound-humic acid (BHA), lipid, and insoluble residue (IR) fractions. Heterogeneous natures of these fractions were characterized by elemental analysis, ultraviolet-visible spectroscopy, Fourier transform infrared spectroscopy, and solid-state 13C NMR. Aliphaticity of the fractions followed the order lipid >BHA > HA > IR, while the polarity order was IR > BHA> HA > lipid. Sorption of phenanthrene on these fractions fitted the Freundlich equation, suggesting that phenanthrene sorption isotherms of lipid were almost linear (N = 0.993), while those of HA, BHA, and IR were nonlinear, with N values ranging from 0.723 to 0.910. The N values followed the order lipid > HA > BHA > IR and were significantly correlated inversely with their polarities (p Organic carbon-normalized sorption coefficients (K(FOC)) were independent of aliphatic or aromatic contents of the SOM fractions. The results suggested that SOM, especially for the humin fractions, was highly heterogeneous in terms of elemental composition, structure, and polarity. Such heterogeneity was considered to be responsible forthe nonlinear sorption of phenanthrene.

  3. Sorption of Emerging Organic Wastewater Contaminants to Four Soils

    Directory of Open Access Journals (Sweden)

    Sarah Roberts

    2014-04-01

    Full Text Available Conventional onsite wastewater treatment system design relies on a septic tank and soil treatment unit (STU for treatment of wastewater and integration of the final effluent into the environment. Organic water contaminants (OWCs, chemicals found in pharmaceutical drugs, detergents, surfactants, and other personal care and cleaning products, have been observed in septic tank effluent and the environment. Sorption of OWC mass to soil is a key mechanism in the removal and retardation of many of these chemicals in effluent as it travels through an STU. The primary purpose of this study was to investigate the relationship between the fraction of organic carbon of soil and the equilibrium sorption partitioning coefficient of a selected group of relevant and diverse OWCs. A secondary goal is to evaluate current methods of modeling the sorption of selected OWCs in soil. Five point Freundlich isotherms were constructed from equilibrium sorption batch tests for target OWCs with four different soils. For soils with organic carbon fraction between 0.021 and 0.054, Kd values were calculated between 60 and 185 for 4-nonylphenol, 75 to 260 for triclosan, 115 to 270 for bisphenol-A, 3 to 255 for 17β-estradiol, 40 to 55 for 17α-ethynylestradiol, and 28 to 70 for estrone. An empirically derived, direct relationship between foc and Kd may be a useful approach to estimating sorption for a soil based on organic carbon content.

  4. Sorption and desorption of indaziflam degradates in several agricultural soils

    Directory of Open Access Journals (Sweden)

    Diego Gonçalves Alonso

    2016-04-01

    Full Text Available ABSTRACT Processes regulating pesticide fate in the environment are influenced by the physicochemical properties of pesticides and soils. Sorption and desorption are important processes as they regulate the movement of pesticides in soil. Although sorption-desorption is widely studied for herbicides, studies involving their metabolites in soil are scarce. Sorption and desorption of indaziflam metabolites (indaziflam-triazinediamine (FDAT, indaziflam-triazine-indanone (ITI and indaziflam-carboxilic acid (ICA were investigated in six Brazilian (BRA soils and three United States (USA soils with different physicochemical properties. The Freundlich equation described sorption of the metabolites for all soils (R2 > 0.98; 1/n ~ 1. Sorption order (Kf was ITI > ICA > FDAT. Mean values of Kf,oc were 453, 289, and 81 (BRA and 444, 48, and 48 (USA for metabolites ITI, ICA, and FDAT respectively. Desorption was hysteretic for all metabolites in all soils. These results suggest that these metabolites fall in the classification range of mobile to moderately mobile in soils.

  5. Sorption and predicted mobility of herbicides in Baltic soils.

    Science.gov (United States)

    Sakaliene, Ona; Papiernik, Sharon K; Koskinen, William C; Spokas, Kurt A

    2007-08-01

    This study was undertaken to determine sorption coefficients of eight herbicides (alachlor, amitrole, atrazine, simazine, dicamba, imazamox, imazethapyr, and pendimethalin) to seven agricultural soils from sites throughout Lithuania. The measured sorption coefficients were used to predict the susceptibility of these herbicides to leach to groundwater. Soil-water partitioning coefficients were measured in batch equilibrium studies using radiolabeled herbicides. In most soils, sorption followed the general trend pendimethalin > alachlor > atrazine approximately amitrole approximately simazine > imazethapyr > imazamox > dicamba, consistent with the trends in hydrophobicity (log K(ow)) except in the case of amitrole. For several herbicides, sorption coefficients and calculated retardation factors were lowest (predicted to be most susceptible to leaching) in a soil of intermediate organic carbon content and sand content. Calculated herbicide retardation factors were high for soils with high organic carbon contents. Estimated leaching times under saturated conditions, assuming no herbicide degradation and no preferential water flow, were more strongly affected by soil textural effects on predicted water flow than by herbicide sorption effects. All herbicides were predicted to be slowest to leach in soils with high clay and low sand contents, and fastest to leach in soils with high sand content and low organic matter content. Herbicide management is important to the continued increase in agricultural production and profitability in the Baltic region, and these results will be useful in identifying critical areas requiring improved management practices to reduce water contamination by pesticides.

  6. Effect of Mouthwashes on Solubility and Sorption of Restorative Composites.

    Science.gov (United States)

    Leal, José Pereira; da Silva, Jaqueline Damasceno; Leal, Rafaelle Fernanda Melão; Oliveira-Júnior, Carlos da Cunha; Prado, Vera Lúcia Gomes; Vale, Glauber Campos

    2017-01-01

    Composites s orption and solubility can be precursors of several chemical and physical processes, which lead to deleterious effects on the polymer structure. This study evaluated the effect of mouthwashes on solubility and sorption of composite resins. Forty-two specimens of each evaluated composite (Filtek Bulk Fill Flow, Opallis Flow, Durafill VS, and Filtek Z350) were prepared and randomized into seven groups for each solution (mouth rinses with and without alcohol and distilled water) and stored for seven days. Solubility and sorption tests were performed according to ISO4049. Data were analyzed using 2-way-ANOVA followed by Tukey's test for means comparison ( α = 0.05). In addition, paired t -test was performed to analyze the alcohol effect on the studied composite resin properties. Listerine Cool Mint (containing alcohol in its composition) caused the greatest degree of sorption for all composites tested in comparison to other rinses, while for solubility this behavior was observed for Opallis Flow and Durafill VS composite resins ( p < 0.05). Regarding the composites, Opallis Flow showed the highest sorption and solubility values in general ( p < 0.05). Overall, the sorption and solubility of composites were higher in mouthwashes containing alcohol in its composition, with Opallis Flow being the most affected composite resin.

  7. Deep Drawing of High-Strength Tailored Blanks by Using Tailored Tools

    Directory of Open Access Journals (Sweden)

    Thomas Mennecart

    2016-01-01

    Full Text Available In most forming processes based on tailored blanks, the tool material remains the same as that of sheet metal blanks without tailored properties. A novel concept of lightweight construction for deep drawing tools is presented in this work to improve the forming behavior of tailored blanks. The investigations presented here deal with the forming of tailored blanks of dissimilar strengths using tailored dies made of two different materials. In the area of the steel blank with higher strength, typical tool steel is used. In the area of the low-strength steel, a hybrid tool made out of a polymer and a fiber-reinforced surface replaces the steel half. Cylindrical cups of DP600/HX300LAD are formed and analyzed regarding their formability. The use of two different halves of tool materials shows improved blank thickness distribution, weld-line movement and pressure distribution compared to the use of two steel halves. An improvement in strain distribution is also observed by the inclusion of springs in the polymer side of tools, which is implemented to control the material flow in the die. Furthermore, a reduction in tool weight of approximately 75% can be achieved by using this technique. An accurate finite element modeling strategy is developed to analyze the problem numerically and is verified experimentally for the cylindrical cup. This strategy is then applied to investigate the thickness distribution and weld-line movement for a complex geometry, and its transferability is validated. The inclusion of springs in the hybrid tool leads to better material flow, which results in reduction of weld-line movement by around 60%, leading to more uniform thickness distribution.

  8. Sorption-desorption of radiocesium interception potential in tropical soils

    International Nuclear Information System (INIS)

    Roque, Mario L.; Boaretto, Rodrigo M.; Boaretto, Antonio E.; Smolders, Erik E.T.

    2000-01-01

    A study of sorption of radiocaesium in soils of tropical climate (Brazil) was carried. The values of definitive fixation of the radiocaesium were determined by analytic methodology of sorption-desorption and the availability to plants were calculated by the determination of radiocesium interception potential (RIP). The values of sorption varied from 1,2 to 74,8% and the fixation varied from 3,2% to 32,2%. The results shown that the radiocaesium did remain adsorbed mainly to the frayed edge site. The low values of interception potential and definitive fixation demonstrated high capacity of the tropical soils in disposal the radionuclide for the solution and, consequently, to plants. (author)

  9. Sorption behavior of thorium onto montmorillonite and illite

    International Nuclear Information System (INIS)

    Iida, Yoshihisa; Barr, Logan; Yamaguchi, Tetsuji; Hemmi, Ko

    2016-01-01

    Thorium (Th)-229 is one of the important radionuclides for the performance assessment calculations for high-level radioactive waste repositories. The sorption behavior of Th onto montmorillonite and illite were investigated by batch sorption experiments. Experiments were carried out under variable pH and carbonate concentrations. The sorbability of montmorillonite was higher than that of illite. Distribution coefficients, K d (m 3 kg -1 ), decreased with increased carbonate concentrations and showed the minimal value at around pH 10. The sorption behaviors of Th were analyzed by the non-electrostatic surface complex model with PHREEQC computer program. The model calculations were able to explain the experimental results reasonably well. The decreases of K d was likely due to the stabilization of aqueous species by hydroxo-carbonate complexations in the solutions. (author) [ja

  10. Autoradiographic studies of actinide sorption in groundwater systems

    International Nuclear Information System (INIS)

    O'Kelley, G.D.; Beall, G.W.; Allard, B.

    1980-01-01

    Autoradiography is a convenient and sensitive technique for the study of spacial distributions of alpha radioactive nuclides on slabs of rock or on other planar surfaces. The autoradiographic camera contains an arrangement for placing in firm contact Polaroid sheet film, a plastic scintillator screen, and the radioactive face of the specimen. As an example of the use of the autoradiographic method, a series of sorption experiments were carried out in which synthetic groundwater solutions of americium, neptunium, uranium, and plutonium were contacted with Climax Stock granite under aerated and anoxic conditions at pH 8 to 9. The sorption observed at specific mineral sites was correlated with data on sorption of these actinides on pure minerals

  11. Sorption behaviour of caesium on a bentonite sample

    International Nuclear Information System (INIS)

    Hurel, C.; Marmier, N.; Fromage, F.; Seby, F.; Bourg, A.C.M.; Giffaut, E.

    2002-01-01

    Sorption of elements like Cs on clay is one of the principal processes delaying their release from deep repositories of nuclear wastes into the environment. The sorption processes taking place between non-purified natural clay material (bentonite) and synthetic groundwater (containing Ca, Mg, Na, K and carbonates) were therefore studied experimentally and modelled for Cs to determine whether thermodynamic computer codes capable of predicting the behaviour of this element in natural systems might be developed. The model used, based on the properties of a pure montmorillonite phase, incorporates the surface reactions for natural major ions and sorbing cations but does not have any adjustable parameters. The weight of each parameters used in the model is assessed. Surface reactions are classified as either major or minor, and a simplified model of Cs sorption that considers only the major processes is proposed. This simplified model might correspond to the less sophisticated thermodynamic model included in coupled geochemistry-transport models. (orig.)

  12. Radionuclide and metal sorption on cement and concrete

    CERN Document Server

    Ochs, Michael; Wang, Lian

    2016-01-01

    Cementitious materials are being widely used as solidification/stabilisation and barrier materials for a variety of chemical and radioactive wastes, primarily due to their favourable retention properties for metals, radionuclides and other contaminants. The retention properties result from various mineral phases in hydrated cement that possess a high density and diversity of reactive sites for the fixation of contaminants through a variety of sorption and incorporation reactions. This book presents a state of the art review and critical evaluation of the type and magnitude of the various sorption and incorporation processes in hydrated cement systems for twenty-five elements relevant for a broad range of radioactive and industrial wastes. Effects of cement evolution or ageing on sorption/incorporation processes are explicitly evaluated and quantified. While the immobilisation of contaminants by mixing-in during hydration is not explicitly addressed, the underlying chemical processes are similar. A quantitativ...

  13. MOLECULAR DYNAMICS MODELING OF SORPTION OF PESTICIDES ONTO THE SURFACES OF KAOLINITE

    Science.gov (United States)

    To accurately predict the fate of contaminants in the environment and to make sound decisions about environmental remediation, we must accurately understand sorption mechanisms and surface reactivity of environmental particles. Sorption of selected pesticides on kaolinite surface...

  14. Sorption of 3,3',4,4'-tetrachlorobiphenyl by microplastics: A case study of polypropylene.

    Science.gov (United States)

    Zhan, Zhiwei; Wang, Jundong; Peng, Jinping; Xie, Qilai; Huang, Ying; Gao, Yifan

    2016-09-15

    Though plastics show good chemical inertness, they could sorb polychlorinated biphenyls (PCBs) and other toxic pollutants from the surrounding environment. Thus, ingestion of microplastics by marine organisms potentially enhances the transport and bioavailability of toxic chemicals. However, there is lack of studies on the sorption capacity, mechanism and factors affecting the sorption behavior. Here, sorption of PCBs by microplastics in the simulated seawater was studied using the batch oscillation equilibration technique, in which polypropylene (PP) and 3,3',4,4'-tetrachlorobiphenyl (PCB77) acted as model plastic and PCB, respectively. Factors including particle size, temperature and solution environment were investigated. Results showed that, equilibrium sorption time is about 8h and sorption capacity increase with decreasing particle size and temperature. Different sorption capacity in three solution environments was observed. Equilibrium data in three solution environments fitted very well to the Langmuir sorption model, indicating chemical sorption is the predominant mechanism. Copyright © 2016 Elsevier Ltd. All rights reserved.

  15. Study of the sorption properties of the peat for removal of heavy metals

    International Nuclear Information System (INIS)

    Hayrapetyan, S.S.; Gevorgyan, S.A.; Hayrapetyan, L.S.; Bareghamyan, S.F.; Pirumyan, G.P.

    2016-01-01

    The processes of sorption of several heavy metals on peat samples taken from basin of lake Sevan (near Vardenis Gegharkunik region of Armenia) were investigated. The peat samples were taken from different locations from 1 m depth. The sorption processes have been done in the static mode. The peat samples were used without any modification, i.e. the sorption properties of natural raw peat were studied. The studies were conducted on the basis of synthetic solution containing ions of these following metals - Ni, Co, As, U, Ba. The sorption properties of peat were estimated by ICP-MS. Thus, peat can be a very effective sorption medium for removal of heavy metals from water. Most of them are absorbed in the first minutes of peat exposure to aqueous solution. For the sorption of barium, uranium, arsenic peat exhibits very high sorption efficiency. For comparison, their relative sorption values about 10 times more than those of cobalt, nickel and zinc.

  16. Sorption isotherms: A review on physical bases, modeling and measurement

    Energy Technology Data Exchange (ETDEWEB)

    Limousin, G. [Atomic Energy Commission, Tracers Technology Laboratory, 38054 Grenoble Cedex (France) and Laboratoire d' etude des Transferts en Hydrologie et Environnement (CNRS-INPG-IRD-UJF), BP 53, 38041 Grenoble Cedex (France)]. E-mail: guillaumelimousin@yahoo.fr; Gaudet, J.-P. [Laboratoire d' etude des Transferts en Hydrologie et Environnement (CNRS-INPG-IRD-UJF), BP 53, 38041 Grenoble Cedex (France); Charlet, L. [Laboratoire de Geophysique Interne et Techtonophysique - CNRS-IRD-LCPC-UJF-Universite de Savoie, BP 53, 38041 Grenoble Cedex (France); Szenknect, S. [Atomic Energy Commission, Tracers Technology Laboratory, 38054 Grenoble Cedex (France); Barthes, V. [Atomic Energy Commission, Tracers Technology Laboratory, 38054 Grenoble Cedex (France); Krimissa, M. [Electricite de France, Division Recherche et Developpement, Laboratoire National d' Hydraulique et d' Environnement - P78, 6 quai Watier, 78401 Chatou (France)

    2007-02-15

    The retention (or release) of a liquid compound on a solid controls the mobility of many substances in the environment and has been quantified in terms of the 'sorption isotherm'. This paper does not review the different sorption mechanisms. It presents the physical bases underlying the definition of a sorption isotherm, different empirical or mechanistic models, and details several experimental methods to acquire a sorption isotherm. For appropriate measurements and interpretations of isotherm data, this review emphasizes 4 main points: (i) the adsorption (or desorption) isotherm does not provide automatically any information about the reactions involved in the sorption phenomenon. So, mechanistic interpretations must be carefully verified. (ii) Among studies, the range of reaction times is extremely wide and this can lead to misinterpretations regarding the irreversibility of the reaction: a pseudo-hysteresis of the release compared with the retention is often observed. The comparison between the mean characteristic time of the reaction and the mean residence time of the mobile phase in the natural system allows knowing if the studied retention/release phenomenon should be considered as an instantaneous reversible, almost irreversible phenomenon, or if reaction kinetics must be taken into account. (iii) When the concentration of the retained substance is low enough, the composition of the bulk solution remains constant and a single-species isotherm is often sufficient, although it remains strongly dependent on the background medium. At higher concentrations, sorption may be driven by the competition between several species that affect the composition of the bulk solution. (iv) The measurement method has a great influence. Particularly, the background ionic medium, the solid/solution ratio and the use of flow-through or closed reactor are of major importance. The chosen method should balance easy-to-use features and representativity of the studied

  17. Sorption and desorption of carbamazepine from water by smectite clays.

    Science.gov (United States)

    Zhang, Weihao; Ding, Yunjie; Boyd, Stephen A; Teppen, Brian J; Li, Hui

    2010-11-01

    Carbamazepine is a prescription anticonvulsant and mood stabilizing pharmaceutical administered to humans. Carbamazepine is persistent in the environment and frequently detected in water systems. In this study, sorption and desorption of carbamazepine from water was measured for smectite clays with the surface negative charges compensated with K+, Ca2+, NH4+, tetramethylammonium (TMA), trimethylphenylammonium (TMPA) and hexadecyltrimethylammonium (HDTMA) cations. The magnitude of sorption followed the order: TMPA-smectite≥HDTMA-smectite>NH4-smectite>K-smectite>Ca-smectite⩾TMA-smectite. The greatest sorption of carbamazepine by TMPA-smectite is attributed to the interaction of conjugate aromatic moiety in carbamazepine with the phenyl ring in TMPA through π-π interaction. Partitioning process is the primary mechanism for carbamazepine uptake by HDTMA-smectite. For NH4-smectite the urea moiety in carbamazepine interacts with exchanged cation NH4+ by H-bonding hence demonstrating relatively higher adsorption. Sorption by K-, Ca- and TMA-smectites from water occurs on aluminosilicate mineral surfaces. These results implicate that carbamazepine sorption by soils occurs primarily in soil organic matter, and soil mineral fractions play a secondary role. Desorption of carbamazepine from the sorbents manifested an apparent hysteresis. Increasing irreversibility of desorption vs. sorption was observed for K-, Ca-, TMA-, TMPA- and HDTMA-clays as aqueous carbamazepine concentrations increased. Desorption hysteresis of carbamazepine from K-, Ca-, NH4-smectites was greater than that from TMPA- and HDTMA-clays, suggesting that the sequestrated carbamazepine molecules in smectite interlayers are more resistant to desorption compared to those sorbed by organic phases in smectite clays. Copyright © 2010 Elsevier Ltd. All rights reserved.

  18. Indoor sorption of surrogates for sarin and related nerve agents.

    Science.gov (United States)

    Singer, Brett C; Hodgson, Alfred T; Destaillats, Hugo; Hotchi, Toshifumi; Revzan, Kenneth L; Sextro, Richard G

    2005-05-01

    Sorption rate parameters were determined for three organophosphorus (OP) compounds [dimethyl methylphosphonate (DMMP), diethyl ethylphosphonate (DEEP), and triethyl phosphate (TEP)] as surrogates for the G-type nerve agents sarin (GB), soman (GD), and tabun (GA). OP surrogates were injected and vaporized with additional volatile organic compounds into a 50 m3 chamber finished with painted wallboard. Experiments were conducted at two furnishing levels: (i) chamber containing only hard surfaces including a desk, a bookcase, tables, and chairs and (ii) with the addition of plush materials including carpet with cushion, draperies, and upholstered furniture. Each furnishing level was studied with aged and new painted wallboard. Gas-phase concentrations were measured during sealed chamber adsorb and desorb phases and then fit to three mathematical variations of a previously proposed sorption model having a surface sink and allowing for an embedded sink. A four-parameter model allowing unequal transport rates between surface and embedded sinks provided excellent fits for all conditions. To evaluate the potential effect of sorption, this model was incorporated into an indoor air quality simulation model to predict indoor concentrations of a G-type agent and a nonsorbing agent for hypothetical outdoor releases with shelter-in-place (SIP) response. Sorption was simulated using a range of parameters obtained experimentally. Simulations considered outdoor Gaussian plumes of 1- and 5-h duration and infiltration rates of 0.1, 0.3, and 0.9 h(-1). Indoor toxic loads (TL) for a 10-h SIP were calculated as integral C2 dt for a G-type agent. For the 5-h plume, sheltering reduced TLs for the nonsorbing agent to approximately 10-65% of outdoor levels. Analogous TLs for a G-type agent were 2-31% or 0.3-12% of outdoor levels assuming slow or moderate sorption. The relative effect of sorption was more pronounced for the longer plume and higher infiltration rates.

  19. Advances in Precision Medicine: Tailoring Individualized Therapies

    Directory of Open Access Journals (Sweden)

    Kyle B. Matchett

    2017-10-01

    Full Text Available The traditional bench-to-bedside pipeline involves using model systems and patient samples to provide insights into pathways deregulated in cancer. This discovery reveals new biomarkers and therapeutic targets, ultimately stratifying patients and informing cohort-based treatment options. Precision medicine (molecular profiling of individual tumors combined with established clinical-pathological parameters reveals, in real-time, individual patient’s diagnostic and prognostic risk profile, informing tailored and tumor-specific treatment plans. Here we discuss advances in precision medicine presented at the Irish Association for Cancer Research Annual Meeting, highlighting examples where personalized medicine approaches have led to precision discovery in individual tumors, informing customized treatment programs.

  20. Tailored vacuum chambers for AC magnets

    International Nuclear Information System (INIS)

    Harvey, A.

    1985-01-01

    The proposed LAMPF-II accelerator has a 60-Hz booster synchrotron and a 3-Hz main ring. To provide a vacuum enclosure inside the magnets with low eddycurrent losses and minimal field distortion, yet capable of carrying rf image currents and providing beam stabilization, we propose an innovative combination pipe. Structurally, the enclosure is high-purity alumina ceramic, which is strong, radiation resistant, and has good vacuum properties. Applied to the chamber are thin, spaced, silver conductors using adapted thick-film technology. The conductor design can be tailored to the stabilization requirements, for example, longitudinal conductors for image currents, circumferential for transverse stabilization. The inside of the chamber has a thin, resistive coating to avoid charge build-up. The overall 60-Hz power loss is less than 100 W/m

  1. Tailored vacuum chambers for AC magnets

    International Nuclear Information System (INIS)

    Harvey, A.

    1985-01-01

    The proposed LAMPF-II accelerator has a 60-Hz booster synchrotron and a 3-Hz main ring. To provide a vacuum enclosure inside the magnets with low eddy-current losses and minimal field distortion, yet capable of carrying RF image currents and providing beam stabilization, the authors propose an innovative combination pipe. Structurally, the enclosure is high-purity alumina ceramic, which is strong, radiation resistant, and has good vacuum properties. Applied to the chamber are thin, spaced, silver conductors using adapted thick-film technology. The conductor design can be tailored to the stabilization requirements, for example, longitudinal conductors for image currents, circumferential for transverse stabilization. The inside of the chamber has a thin, resistive coating to avoid charge build-up. The overall 60-Hz power loss is less than 100 W/m

  2. Tailoring Atomic Wavefunctions with Designer Pulses

    Science.gov (United States)

    Reinhold, Carlos O.

    1998-05-01

    Manipulation and control of the electronic states of atoms provides an exciting new area of research in atomic physics with important potential applications. Such control can be achieved using ``designer'' electromagnetic pulses whose strengths are comparable to the Coulomb electric field and whose durations are of the order of the classical orbital period of the atom. Coherent control of the electron dynamics requires complete knowledge of the initial state as well as of the pulses whose shapes can be carefully tailored at will. In this presentation we report on experimental and theoretical control of atomic wavefunctions using very high-n Rydberg atoms and designer half-cycle pulses. We discuss new possibilities in producing and probing coherent atomic wavepackets and the first realization of the periodically kicked atom, a paradigmatic system of non-linear dynamics using a superposition of half-cycle pulses.

  3. Engineering tailored nanoparticles with microbes: quo vadis?

    Science.gov (United States)

    Prasad, Ram; Pandey, Rishikesh; Barman, Ishan

    2016-01-01

    In the quest for less toxic and cleaner methods of nanomaterials production, recent developments in the biosynthesis of nanoparticles have underscored the important role of microorganisms. Their intrinsic ability to withstand variable extremes of temperature, pressure, and pH coupled with the minimal downstream processing requirements provide an attractive route for diverse applications. Yet, controlling the dispersity and facile tuning of the morphology of the nanoparticles of desired chemical compositions remains an ongoing challenge. In this Focus Review, we critically review the advances in nanoparticle synthesis using microbes, ranging from bacteria and fungi to viruses, and discuss new insights into the cellular mechanisms of such formation that may, in the near future, allow complete control over particle morphology and functionalization. In addition to serving as paradigms for cost-effective, biocompatible, and eco-friendly synthesis, microbes hold the promise for a unique template for synthesis of tailored nanoparticles targeted at therapeutic and diagnostic platform technologies. © 2015 Wiley Periodicals, Inc.

  4. Sorption of 60 Co in natural zeolite (clinoptilolite)

    International Nuclear Information System (INIS)

    Hernandez B, E.

    1996-01-01

    A Mexican zeolite (clinoptilolite) from Taxco, Guerrero, was partially stabilized with sodium cations. Radioactive Cobalt ( 60 Co) was used to study the Co 2+ sorption in the stabilized zeolite (Na + ). It was found that sorption in general does not favour the diffusion of cobalt between framework, it explains because of it is a natural zeolite and its composition heterogeneous decrease its exchange capacity by the generated competence to the existence other type of exchange ions. The cobalt retention reached the highest level, around 0.408 m eq Co 2+ /g in the Na-Clinoptilolite. The crystallinity of the aluminosilicates was maintained during experiments, it was verified by XRD patterns. (Author)

  5. Sorption, Diffusion and Solubility Databases for Performance Assessment

    International Nuclear Information System (INIS)

    Garcia Gutierrez, M.

    2000-01-01

    This report presents a deterministic and probabilistic databases for application in Performance Assessment of a high-level radioactive waste disposal. This work includes a theoretical description of sorption, diffusion and solubility phenomena of radionuclides in geological media. The report presents and compares the databases of different nuclear wastes management agencies, describes the materials in the Spanish reference system, and the results of sorption diffusion and solubility in this system, with both the deterministic and probabilistic approximation. The probabilistic approximation is presented in the form of probability density functions (pdf). (Author) 52 refs

  6. Hysteresis and Temperature Dependency of Moisture Sorption – New Measurements

    DEFF Research Database (Denmark)

    Rode, Carsten; Hansen, Kurt Kielsgaard

    2011-01-01

    for combined heat and moisture transport in materials. There is a need for further elaboration of the importance of these issues, and it is the intent of this paper to contribute to such elaboration. The paper seeks to contribute to the knowledge base about such sorption characteristic by presenting some new...... measurements of hysteresis and temperature dependency of the moisture sorption characteristics of three different porous building materials: aerated concrete, cement paste and spruce. Scanning curves are measured for all three materials where periods with adsorption and desorption interrupt each other...

  7. Sorption and desorption of diuron in Oxisol under biochar application

    OpenAIRE

    Petter,Fabiano André; Ferreira,Tamara Santos; Sinhorin,Adilson Paulo; Lima,Larissa Borges de; Morais,Leidimar Alves de; Pacheco,Leandro Pereira

    2016-01-01

    ABSTRACT The objective of this study was to verify the kinetics of sorption and desorption of diuron in an Oxisol under application of biochar. The samples were collected in a field experiment conducted in randomized design blocks consisted of 2 base fertilization levels (0 and 400 kg∙ha−1 NPK 00-20-20 fertilizer formula) and 3 doses of biochar (0, 8 and 16 Mg∙ha−1). In the evaluation of sorption and desorption, Batch Equilibrium method was used. The kinetics of sorpti...

  8. Bio-sorption of Tl-201 radionuclide on olive pomace

    International Nuclear Information System (INIS)

    Yapici, Sinan; Eroglu, Hayrettin; Varoglu, Erhan

    2011-01-01

    This work presents an investigation on the bio-sorption of Tl-201 radionuclide used in nuclear medicine on olive pomace. The experimental parameters were chosen as temperature, the initial pH of the solution, stirring speed, bio-sorbent dose and nominal particle size of bio-sorbent. The initial pH of the solution was found to be the most effective parameter. Thermodynamic analysis gave negative values for ΔG and ΔH. The kinetics of the bio-sorption process fitted very well to the pseudo-second order rate model.

  9. Sorption behaviour of some radioactive isotopes on treated fly ash

    International Nuclear Information System (INIS)

    Abdel-Raouf, M.W.; El-Dessouky, M.I.; Aly, H.F.

    1997-01-01

    The uptake of the radioactive isotopes 134 Cs, 60 Co and 152 , 1 54 Eu from aqueous solutions on treated fly ash has been investigated in terms of the factors affecting the sorption using the batch method at room temperature (20 1 degree C). The selectivity order for the studied radioisotopes on the treated fly ash was found in accordance with their cationic charges, i.e., Eu 3+ > Co 2+ >> Cs + . Pyrolysis residue of domestic waste was investigated as an alternative sorbent and its sorption capability was compared with that of fly ash. The feasibility of using treated fly ash as a sorbent, has been assessed. 3 figs., 7 tabs

  10. Cerium sorption in grounds modified by anti-deflation treatment

    International Nuclear Information System (INIS)

    Firsova, L.P.; Bogatyrev, I.O.

    2001-01-01

    Influence of soils and grounds treatment by anti-deflation compositions on the size of the soil particles was studied. Under static conditions sorption of 144 Ce by turf-podsolic soils prior to an after their modification by the anti-deflation reagents, i.e. bitumens and insoluble in water polyelectrolytic complexes, was considered. Degrees of 144 Ce sorption in the soil-solution systems, depending on solutions pH, presence of alkali metal carbonates and cerium concentration, were determined [ru

  11. Hydrogen peroxide modified sodium titanates with improved sorption capabilities

    Science.gov (United States)

    Nyman, May D [Albuquerque, NM; Hobbs, David T [North Augusta, SC

    2009-02-24

    The sorption capabilities (e.g., kinetics, selectivity, capacity) of the baseline monosodium titanate (MST) sorbent material currently being used to sequester Sr-90 and alpha-emitting radioisotopes at the Savannah River Site are significantly improved when treated with hydrogen peroxide; either during the original synthesis of MST, or, as a post-treatment step after the MST has been synthesized. It is expected that these peroxide-modified MST sorbent materials will have significantly improved sorption capabilities for non-radioactive cations found in industrial processes and waste streams.

  12. Sorption Properties of Steam Treated Wood and Plant Fibres

    DEFF Research Database (Denmark)

    Hoffmeyer, Preben; Jensen, Signe Kamp; Jones, Dennis

    2003-01-01

    Hygrothermal treatment of wood and plant fibres was carried out to improve the dimensional stability of the fibres and products made from these. Fibres of Norway spruce, beech, wheat and hemp were included. The efficiency of the treatment was assessed by studying the moisture sorption properties...... sorption sites. The annual plant fibres proved less susceptible than wood fibres to chemical breakdown from steam treatment. The component most susceptible to chemical breakdown was hemicellulose. Beech, wheat and hemp showed only a modest decrease of cellulose content, even at high temperatures, whereas...

  13. Tailoring the Crystal Structure Toward Optimal Super Conductors

    Science.gov (United States)

    2016-06-23

    AFRL-AFOSR-VA-TR-2016-0210 TAILORING THE CRYSTAL STRUCTURE TOWARD OPTIMAL SUPERCONDUCTORS Emilia Morosan WILLIAM MARSH RICE UNIV HOUSTON TX Final...TAILORING THE CRYSTAL STRUCTURE TOWARD OPTIMAL SUPERCONDUCTORS 5a. CONTRACT NUMBER FA9550-11-1-0023 5b. GRANT NUMBER 5c. PROGRAM ELEMENT NUMBER 6...Form 298 Back (Rev. 8/98) DISTRIBUTION A: Distribution approved for public release. TAILORING THE CRYSTAL STRUCTURE TOWARD OPTIMAL SUPERCONDUCTORS

  14. Artificial neural network approaches for the sorption isotherms, enthalpy and entropy of heat sorption of two types block rubber products

    Directory of Open Access Journals (Sweden)

    Yutthana Tirawanichakul

    2013-02-01

    Full Text Available Knowledge of the temperature and relative humidity (or water activity dependence of moisture sorption phenomenaof agro-industrial products provides valuable information about changes related to the thermodynamics of the system. Thusthe moisture sorption characteristics in terms of equilibrium moisture contents (EMC, enthalpy and entropy of heat sorptionof natural rubber (NR for producing STR 20 and skim block rubber were investigated. Simulation modeling of water sorptionisotherms was performed using the 10 non-linear regression EMC models and the multilayer artificial neural network (ANNapproach. The results showed that the predicted EMC results using the modified Oswin model was the best fitting model forboth NR samples. However, the predicted values of ANN model were more accurate than those predicted results using nonlinear regression method. Finally, enthalpy and entropy of heat sorption for both NR samples were evaluated by applying theClausius-Clapeyron equation showing as the negative exponential function of moisture content.

  15. Influence of soil properties and test conditions on sorption and desorption of testosterone

    Science.gov (United States)

    In this study, batch sorption and desorption experiments were conducted for testosterone using four agricultural soils and five clay minerals. Significant differences in sorption behavior were observed between abiotic and biotic systems. The Freundlich sorption coefficient Kf (µg per g)/(µg per mL) ...

  16. Present status of developments in physical sorption cooling for space applications

    NARCIS (Netherlands)

    Benthem, B.; Doornink, J.; Boom, E.; Holland, Herman J.; Lerou, P.P.P.M.; Burger, Johannes Faas; ter Brake, Hermanus J.M.

    2014-01-01

    A sorption cooler uses the Joule–Thomson effect for cooling a gas by expanding it through a flow restriction. The flow of gas is sustained by a compressor consisting of one or more sorption cells, which cyclically adsorb and desorb gas according to the fully reversible process of physical sorption.

  17. Sorption of lead by settling pond soils after reclamation treatments

    Science.gov (United States)

    Asensio, Verónica; Forján, Rubén; Vega, Flora A.; Andrade, Luisa; Covelo, Emma F.

    2013-04-01

    The reclamation of degraded soils adding waste amendments can add significant concentrations of Pb. Because of this, it is important to know the sorption capacity of Pb by the soils where wastes with high concentrations of this metal are applied. To determine the sorption capacity of Pb by mine soils, before and after reclamation treatments, four different sites were selected at a settling pond mine zone: an untreated one as the control sample (B1), a vegetated one with pines for 21 years (B2v), a vegetated with eucalyptus for 6 years (B3v) and an amended with sewage sludges and paper mill residues for 5 months (B4w). All soils had one horizon except B4w, where twice were sampled (B4Aw and B4Bw). The B4Bw is considered analogous of the control soil. To evaluate the sorption capacity by the soils, sorption isotherms were constructed using single-metal solutions of Pb2+ nitrates (0.03, 0.05, 0.08, 0.1 and 0.5 mmol L-1) containing 0.01 M NaNO3 as background electrolyte (Vega et al., 2009). The overall capacity of the soil to sorb Pb was evaluated as the slope Kr (Vega et al., 2008). The obtained results show that the sorption isotherm of Pb by control soil (B1) and its analogous (B4Bw) are of L-type curve, whereas the sorption isotherms of the treated soils (B2v, B3v and B4Aw) are of H-type curve (Giles et al., 1974). The most of the obtained isotherms do not fit with the models of Langmuir or Freundlich, therefore sorption capacity was evaluated by Kr parameter. According to the obtained Kr parameter, B1 and B4Bw have the lowest Pb sorption capacity (Kr = 0.480 and 0.556, respectively), which increased two times after recently waste amending (B4Aw; Kr = 0.998). The vegetated sites (B2v and B3v) also have higher sorption capacity than B1, but lower than B4Aw (Kr = 0.692 and 0.725, respectively). The highest sorption capacity of Pb by the amended soil is due to its characteristics such as high pH and organic carbon content. This is corroborated by the significantly

  18. Cadmium sorption in solution by a chitin: effect of pH; Sorption du cadmium en solution par une chitine: effet du pH

    Energy Technology Data Exchange (ETDEWEB)

    Benguella, B.; Benaissa, H. [Universtie de Tlemcen, Lab. de Materiaux Sorbants et Traitement des Eaux, Dept. de Chimie, Faculte des Sciences, Tlemcen (Algeria)

    2001-07-01

    The pH is an essential factor to take into consideration in the sorption mechanisms of metals: it acts both on the metal speciation in solution and on the chemical behaviour of the surface of the sorbing material, and thus indirectly on the sorption mechanism. The effect of the initial pH of the solution on the cadmium sorption by raw state chitin has been studied in static conditions. The approach used is the determination of the sorption kinetics and equilibria for different values of initial pH (pH < 7-7.5). An increase of the initial pH value of the solution leads to an increase of the cadmium sorption capacity by chitin at the equilibrium. The Langmuir model has revealed to be convenient for a mathematical description of the sorption isotherms obtained. (J.S.)

  19. Promoting a Culture of Tailoring for Systems Engineering Policy Expectations

    Science.gov (United States)

    Blankenship, Van A.

    2016-01-01

    NASA's Marshall Space Flight Center (MSFC) has developed an integrated systems engineering approach to promote a culture of tailoring for program and project policy requirements. MSFC's culture encourages and supports tailoring, with an emphasis on risk-based decision making, for enhanced affordability and efficiency. MSFC's policy structure integrates the various Agency requirements into a single, streamlined implementation approach which serves as a "one-stop-shop" for our programs and projects to follow. The engineers gain an enhanced understanding of policy and technical expectations, as well as lesson's learned from MSFC's history of spaceflight and science missions, to enable them to make appropriate, risk-based tailoring recommendations. The tailoring approach utilizes a standard methodology to classify projects into predefined levels using selected mission and programmatic scaling factors related to risk tolerance. Policy requirements are then selectively applied and tailored, with appropriate rationale, and approved by the governing authorities, to support risk-informed decisions to achieve the desired cost and schedule efficiencies. The policy is further augmented by implementation tools and lifecycle planning aids which help promote and support the cultural shift toward more tailoring. The MSFC Customization Tool is an integrated spreadsheet that ties together everything that projects need to understand, navigate, and tailor the policy. It helps them classify their project, understand the intent of the requirements, determine their tailoring approach, and document the necessary governance approvals. It also helps them plan for and conduct technical reviews throughout the lifecycle. Policy tailoring is thus established as a normal part of project execution, with the tools provided to facilitate and enable the tailoring process. MSFC's approach to changing the culture emphasizes risk-based tailoring of policy to achieve increased flexibility, efficiency

  20. Sorption of Heavy Metals from Mine Wastewater by Activated ...

    African Journals Online (AJOL)

    A study on sorption of heavy metal ions: Lead (Pb2+), Copper (Cu2+) and Cadmium (Cd2+) from mine wastewater by activated carbons prepared from coconut husk was conducted. The activated carbons were prepared by carbonisation of the husk at 900 ºC pyrolysis temperature, followed by steam activation of the ...

  1. Development of a 15 K hydrogen-based sorption cooler

    NARCIS (Netherlands)

    Burger, Johannes Faas; Holland, Herman J.; Meijer, R.J.; Linder, M.; ter Brake, Hermanus J.M.

    2010-01-01

    At the University of Twente, a 15 K hydrogen-based sorption cooler is under development, which has no moving parts and, therefore, is essentially vibration-free. Moreover, it has the potential of a very long life. Although the cooler may operate standalone, it is designed to precool a helium-based

  2. Sorption phenomena of modification of clinoptilolite tuffs by surfactant cations.

    Science.gov (United States)

    Rozić, M; Ivanec Sipusić, D; Sekovanić, L; Miljanić, S; Curković, L; Hrenović, J

    2009-03-15

    The sorption of cationic surfactant hexadecyltrimethylammonium (HDTMA) onto the solid/liquid interfaces of different clinoptilolite rich tuffs (CT) is examined. Examined were CT from Serbia with 75% clinoptilolite, CT from Turkey with 70% clinoptilolite, and CT from Croatia with 60% clinoptilolite. The sorption of HDTMA cations increased in the following order: CT from Serbia>CT from Turkey>CT from Croatia. The maximum amounts of sorbed HDTMA cations, normalized with regard to external cation exchange capacities of tuffs, were 1.79, 1.70, and 1.14 for Serbian, Turkish, and Croatian CT. FTIR analysis of samples with the maximum amount of sorbed HDTMA cations showed that HDTMA chains on Serbian CT adopt mainly a stretched all-trans conformation, while at the surfaces of CT from Turkey and Croatia the amount of gauche conformations increased. The zeta potentials of CT samples with the maximum amount of sorbed HDTMA cations and the sorption of benzoate anions on these samples increased in the following order: CT from Turkey>CT from Serbia>CT from Croatia. It can be assumed that on the surface of CT from Turkey iron (hydr)oxide clusters or nanoparticles with positive surface sites are present, due to which the isoelectric point is sifted toward lower and the zeta potential toward higher values. Therefore, the sorption of benzoate anions on modified CT from Turkey is also higher.

  3. Sorption and desorption of silver ions by bentonite clays.

    Science.gov (United States)

    Constantino, Leonel Vinicius; Quirino, Juliana Nunes; Monteiro, Alessandra Maffei; Abrão, Taufik; Parreira, Paulo Sérgio; Urbano, Alexandre; Santos, Maria Josefa

    2017-04-01

    Anthropogenic activities have increased the concentration of metal species in the environment. The toxicity of silver ions to aquatic and terrestrial organisms has required monitoring by analytical methods, besides actions to promote its control as pollutant. Sorption and desorption processes are directly related to the mobility and availability of metal ions in the environment. In this context, clay minerals can be used for pre-concentration, removal and recovery of silver ions from aqueous solution. Herein, two bentonite clays (BaVC-1 and SWy-2) were characterised and applied to investigate the sorption and desorption of silver ions. Isotherms were fitted to the dual-mode Langmuir-Freundlich model to qualify and quantify sorption sites and evaluate the mobilisation process. The maximum sorption capacity was 743 and 849 meq kg -1 for BaVC-1 and SWy-2, respectively. Hysteresis index (HI) and mobilisation factor (MF) suggest that the desorption of silver ions in BaVC-1 is about four times more conducive compared to that in SWy-2, although both materials have demonstrated a great potential for Ag + pre-concentration from aqueous solutions.

  4. Evaluation of phosphorus sorption characteristics of soils from the ...

    African Journals Online (AJOL)

    The evaluation of phosphorus sorption characteristics of soils and their relation to soil properties from the Bambouto sequence of Baranka 1, Baranka 2, Femock 1 and Femock 2 has been studied. Phosphorus, an essential plant nutrient, is often not readily available to plants and this deficiency tends to limit plant growth.

  5. phosphorus sorption in relation to soil grain size and geochemical

    African Journals Online (AJOL)

    Mgina

    ABSTRACT. The phosphorus sorption characteristics of eight surface soil samples representative of the land use and landscape in the Simiyu and Kagera River basins were determined using the Langmuir equation. The Langmuir P adsorption maximum (Cmax) ranged from 109 to 802 mg kg-1, while. Langmuir coefficient ...

  6. Sorption of lead from aqueous solution by modified activated carbon ...

    African Journals Online (AJOL)

    They were based on using powdered activated carbon (PACI), which was prepared from olive stones generated, as plant wastes, and modified with aqueous oxidizing agent such as (NH 4)2S2O8. The main parameters (pH, sorbent, lead concentrations, stirring times and temperature) influencing the sorption process in ...

  7. New Composite Sorbents for Caesium and Strontium Ions Sorption

    Directory of Open Access Journals (Sweden)

    Mykola Kartel

    2017-06-01

    Full Text Available Composite lignocellulose-inorganic sorbents derived from plant residues of agriculture and food industry, modified with ferrocyanides of d-metals and hydrated antimony pentoxide were prepared. Caesium and strontium ions removal from water was tested by radiotracer method. Sorption of heavy metal ions, methylene blue, gelatin, vitamin B12 was also studied.

  8. Sorption processes of radiocesium in soil and bedrock

    Energy Technology Data Exchange (ETDEWEB)

    Lehto, Jukka [Helsinki Univ. (Finland). Lab. of Radiochemistry

    2015-06-01

    Three recent studies on cesium sorption in soil and bedrock are reviewed. {sup 137}Cs, originating from fallouts of nuclear weapons tests and the Chernobyl accident was found to decrease in an exponential manner in forest soil, and the highest fraction in soil profiles was found in the organic layer. Also, the mineral layer below the organic layer contained a large fraction of cesium inventory but at depths below 20 cm only a very small fraction was observed. In the bedrock of Olkiluoto, where the final repository for spent nuclear fuel from the Finnish nuclear power plants will be constructed, mica mineral biotite plays the most important role in cesium sorption. The selectivity of biotite decreases in the order Cs > K > Na > Ca and the overall selectivity coefficient for Cs/Ca exchange was approximately five and seven orders of magnitude higher than those for Cs/Na and Cs/K exchange reactions, respectively. Ion exchange isotherms for Cs/Na and Cs/K exchange were modelled by assuming three different ion exchange sites: frayed edge sites (FES), basal plane sites and intermediate sites. The selectivity coefficients derived for these sites were successfully used to predict cesium sorption in a mica gneiss rock. Sorption of cesium in mineral soil layers from the Olkiluoto overburden were studied using three different approaches: model batch experiments, an in-situ method and calculations. All three approaches gave the same trend but the distribution coefficient values varied in range of one order of magnitude.

  9. Effect of Moisture Sorption State on Vibrational Properties of Wood

    Science.gov (United States)

    Jianxiong Lu; Jiali Jiang; Yiqiang Wu; Xianjun Li; Zhiyong Cai

    2012-01-01

    The purpose of this study was to investigate the vibrational properties and corresponding anisotropicity in wood during different states of moisture sorption. Samples of maple (Acer spp.) and red oak (Quercus rubra Michx.f.) were moisture conditioned by the adsorption process from an ovendried state and by the desorption process...

  10. Moisture Sorption in Artificially aged wood-plastic composites

    Science.gov (United States)

    B. Kristoffer Segerholm; Rebecca E. Ibach; Magnus E.P. Wålinder

    2012-01-01

    Moisture sorption in wood-plastic composites (WPCs) affects their durability and dimensional stability. In certain outdoor exposures, the moisture properties of WPCs are altered due to e.g. cracks induced by swelling and shrinkage of the components, as well as UV degradation or biological attack. The aim of this work was to study the effect of different artificial...

  11. Moisture Sorption Characteristics of Dambu-nama – A Nigerian ...

    African Journals Online (AJOL)

    Moisture sorption characteristics of traditional Dambu-nama (control) (TDBN) and laboratory Dambu-nama (LDBN), a cooked, pounded, shredded and dried Nigerian meat product, were determined at four different temperatures (10oC, 20oC, 30oC and 40oC) and relative humidities of 10 – 96% using the standard static, ...

  12. Effect of surfactants on the survival and sorption of viruses.

    Science.gov (United States)

    Chattopadhyay, Devamita; Chattopadhyay, Sandip; Lyon, William G; Wilson, John T

    2002-10-01

    There is an increasing concern about the protection of groundwater from contamination by enteric viruses and the prevention of outbreaks of waterborne diseases. Knowledge of survivability and transport of viruses from their point of origin is necessary to determine their potential effects on the neighboring groundwater systems. The distribution of virus is, in turn, dependent on the physical and chemical compositions of the surrounding soil and subsurface systems. For the present study, we have determined the effects of different surfactants (cationic, anionic, nonionic, and biological) and natural organic matter (NOM) on bacteriophages. Results indicated that surfactants and NOM adversely affect phage survival in binary systems, with surfactants being the most harmful. Studies with ternary systems also showed that the presence of surfactants reduced sorption of phages on sorbents either by occupying available sorption sites on the sorbent material or by displacing the sorbed phages from the sorbent surface. Water contact angles of the selected phages and different sorbent surfaces have been measured. Experimental data demonstrated that the sorption of hydrophobic viruses was favored by hydrophobic sorbents, while the sorption of hydrophilic viruses was favored by hydrophilic sorbents.

  13. Sorption kinetics of diuron on volcanic ash derived soils.

    Science.gov (United States)

    Cáceres-Jensen, Lizethly; Rodríguez-Becerra, Jorge; Parra-Rivero, Joselyn; Escudey, Mauricio; Barrientos, Lorena; Castro-Castillo, Vicente

    2013-10-15

    Diuron sorption kinetic was studied in Andisols, Inceptisol and Ultisols soils in view of their distinctive physical and chemical properties: acidic pH and variable surface charge. Two types of kinetic models were used to fit the experimental dates: those that allow to establish principal kinetic parameters and modeling of sorption process (pseudo-first-order, pseudo-second-order), and some ones frequently used to describe solute transport mechanisms of organic compounds on different sorbents intended for remediation purposes (Elovich equation, intraparticle diffusion, Boyd, and two-site nonequilibrium models). The best fit was obtained with the pseudo-second-order model. The rate constant and the initial rate constant values obtained through this model demonstrated the behavior of Diuron in each soil, in Andisols were observed the highest values for both parameters. The application of the models to describe solute transport mechanisms allowed establishing that in all soils the mass transfer controls the sorption kinetic across the boundary layer and intraparticle diffusion into macropores and micropores. The slowest sorption rate was observed on Ultisols, behavior which must be taken into account when the leaching potential of Diuron is considered. Copyright © 2013 Elsevier B.V. All rights reserved.

  14. The sorption induced glass transition in amorphous glassy polymers

    NARCIS (Netherlands)

    van der Vegt, N.F.A.; Wessling, Matthias; Strathmann, H.; Briels, Willem J.

    1999-01-01

    Sorption of CO2 in both the glassy and the rubbery state of an amorphous polyethylenelike polymer was investigated using molecular dynamics simulations. The temperature was chosen such that the system was in its glassy state at low solute concentrations and its rubbery state at large solute

  15. Modeling polychlorinated biphenyl sorption isotherms for soot and coal

    NARCIS (Netherlands)

    Jantunen, A.P.K.; Koelmans, A.A.; Jonker, M.T.O.

    2010-01-01

    Sorption isotherms (pg-ng/L) were measured for 11 polychlorinated biphenyls (PCBs) of varying molecular planarity from aqueous solution to two carbonaceous geosorbents, anthracite coal and traffic soot. All isotherms were reasonably log-log-linear, but smooth for traffic soot and staircase-shaped

  16. Measurement of in situ monomer sorption in polyu(propylene)

    NARCIS (Netherlands)

    Pater, J.T.M.; Weickert, G.; Fait, Anna; Mei, Gabriele

    2005-01-01

    An experimental method has been developed to compare the amount of monomer absorbed in freshly produced poly(propylene) with the amount of monomer absorbed in the same material after degassing. It has been found that propylene sorption in freshly produced poly(propylene) is significantly higher than

  17. Sorption characteristics of methylene blue onto Nypa fruiticans lignin ...

    African Journals Online (AJOL)

    The sorption characteristics of soda lignin extracted from Nypa fruiticans for the removal of methylene blue dye from aqueous solution was investigated in this study, as an ethically sound way of utilizing this unexploited abundant natural resource. Equilibrium data were fitted to the Langmuir and Freundlich isotherm ...

  18. Sorption of Cs-137 and Co-60 in Natural Zeolites

    International Nuclear Information System (INIS)

    Chales Suarez, G.; Moreno Alvarez, D.; Coutin Correa, D.

    1996-01-01

    The sorption of Cs-137 and Co-60 in natural zeolites under different conditions was studied. The behaviour of samples of mineral and rock from different deposit of the country was obtained and the decontamination of radioactive waters containing both radionuclides was performed; as part of the research to determine its application in the treatment of radioactive wastes in the country

  19. Aminosilane-Functionalized Cellulosic Polymer for Increased Carbon Dioxide Sorption

    KAUST Repository

    Pacheco, Diana M.

    2012-01-11

    Improvement in the efficiency of CO 2 separation from flue gases is a high-priority research area to reduce the total energy cost of carbon capture and sequestration technologies in coal-fired power plants. Efficient CO 2 removal from flue gases by adsorption systems requires the design of novel sorbents capable of capturing, concentrating, and recovering CO 2 on a cost-effective basis. This paper describes the preparation of an aminosilane-functionalized cellulosic polymer sorbent with enhanced CO 2 sorption capacity and promising performance for use in postcombustion carbon capture via rapid temperature-swing adsorption systems. The introduction of aminosilane functionalities onto the backbone of cellulose acetate was achieved by the anhydrous grafting of N-(2-aminoethyl)-3- aminoisobutyldimethylmethoxysilane. The dry sorption capacity of the modified cellulosic polymer reached 27 cc (STP) CO 2/cc sorbent (1.01 mmol/g sorbent) at 1 atm and 39 cc (STP) CO 2/cc sorbent (1.46 mmol/g sorbent) at 5 atm and 308 K. The amine loading achieved was 5.18 mmol amine(nitrogen)/g sorbent. Exposure to water vapor after the first dry sorption cycle increased the dry sorption capacity of the sorbent by 12% at 1 atm, suggesting its potential for rapid cyclic adsorption processes under humid feed conditions. The CO 2 sorbent was characterized in terms of chemical composition, density changes, molecular structure, thermal stability, and surface morphology. © 2011 American Chemical Society.

  20. Sorption of organophosphate and triazine agrochemicals on biochars and soils

    Science.gov (United States)

    Biochars are known to strongly sorb polar and nonpolar organic compounds, and biochar soil amendment can have counteracting impacts on the efficacy of, and runoff contamination by agrochemicals. This study investigated the sorption-desorption isotherms and kinetics of triazine (deisopropylatrazine)...

  1. Effects of soil properties on boron sorption in savanna soils ...

    African Journals Online (AJOL)

    The influence of soil properties on boron (B) sorption and the relationship between B adsorption and extractable forms of Fe and Al oxides were investigated in eight soils from the Nigerian Savanna. The equilibration of B was achieved by adding 20 ml of boric acid solution containing 30 mg B g-1 soil to 4g of the soil ...

  2. Interaction of Dissolution, Sorption and Biodegradation on Transport ...

    Indian Academy of Sciences (India)

    58

    Groundwater flow equation is solved to obtain the hydraulic head distribution at all nodes for a particular time level. Having ... In Eqn. (6), first term on the L.H.S represents the transient term, second term represents the sorption of dissolved BTEX on ...... The following symbols are used in this paper: ∝ . . = Longitudinal ...

  3. Sorption characteristics of technetium on crosslinked chitosan from aqueous solution

    International Nuclear Information System (INIS)

    Pivarciova, L.; Rosskopfova, O.; Galambos, M.; Rajec, P.

    2014-01-01

    Sorption of technetium on crosslinked chitosan was studied using batch techniques in static arrangement of experiment under aerobic conditions at laboratory temperature. The adsorption of technetium was rapid and the percentage of the technetium sorption was > 98 %. In the pH range of 3-11 adsorption of technetium on crosslinked chitosan was > 98 %. The competition effect of Fe 3+ towards TcO 4 - sorption on crosslinked chitosan was stronger than the competition effect of other observed cations. The selectivity of crosslinked chitosan for these cations in solution with the concentration above 1·10 -3 mol·dm -3 was in the order Fe 3+ > Ca 2+ > Na + > Fe 2+ . The competition effect of (ClO 4 ) - towards TcO 4 - sorption was stronger than the competition effect of (SO 4 ) 2 - ions. From these results it can be expected that crosslinked chitosan could be a suitable sorbent for the immobilization of technetium in the liquid radioactive waste. (authors)

  4. Sorption of thallium(I) ions by peat.

    Science.gov (United States)

    Robalds, Artis; Klavins, Maris; Dreijalte, Liga

    2013-01-01

    The increasing industrial use of thallium has raised the need for removal of this highly toxic element from wastewater. Thallium is more toxic than cadmium, copper, zinc, lead and mercury and as it is easily accumulated in humans, animals and plants, it poses a threat to both the environment and human health. Peat has been used as an effective, relatively cheap and easily available sorbent to treat waters containing heavy metals. In this study, peat was characterized and used as sorbent for the removal of Tl(I) ions from aqueous solution. The effect of initial Tl(I) concentration, pH, contact time, temperature and ionic strength was studied in batch mode. The maximum sorption capacity of peat reached 24.14 mg/g at 20 °C and initial Tl(I) concentration of 500 mg/L. Sorption capacity was found to be pH dependent and maximum uptake occurred at pH 10. Kinetic data revealed that sorption was relatively rapid - 82.8% of Tl(I) ions were sorbed in the first 10 min. The kinetics of sorption was analyzed using pseudo-first order and pseudo-second order models. Results show that peat can be used as an effective sorbent to remove Tl(I) ions from aqueous solutions.

  5. Isothermal, kinetic and thermodynamic studies on basic dye sorption ...

    African Journals Online (AJOL)

    PRECIOUS

    2009-12-15

    Dec 15, 2009 ... In this paper, a new cation sorbent, which bore carboxyl and hydroxyl groups of tartaric acid (TA) derived from esterified wheat straw (EWS), was originally prepared by solid phase thermochemistry method. The isotherm, kinetics and thermodynamics of basic dye sorptions from aqueous solution onto.

  6. Isothermal, kinetic and thermodynamic studies on basic dye sorption ...

    African Journals Online (AJOL)

    In this paper, a new cation sorbent, which bore carboxyl and hydroxyl groups of tartaric acid (TA) derived from esterified wheat straw (EWS), was originally prepared by solid phase thermochemistry method. The isotherm, kinetics and thermodynamics of basic dye sorptions from aqueous solution onto EWS were investigated ...

  7. Moisture sorption in mixtures of biopolymer, disaccharides and water

    NARCIS (Netherlands)

    Sman, van der R.G.M.

    2013-01-01

    The moisture sorption of ternary mixtures of biopolymer, sugar and water is investigated by means of the Free-Volume-Flory-Huggins (FVFH) theory. The earlier FVFH theory developed for binary mixtures of biopolymer/water and sugar/water has to be modified to account for two effects: 1) the change in

  8. Sorption of Molecular Oxygen by Metal-Ion Exchanger Nanocomposites

    Science.gov (United States)

    Krysanov, V. A.; Plotnikova, N. V.; Kravchenko, T. A.

    2018-03-01

    Kinetic features are studied of the chemisorption and reduction of molecular oxygen from water by metal-ion exchanger nanocomposites that differ in the nature of the dispersed metal and state of oxidation. In the Pd equilibrium sorption coefficient for oxygen dissolved in water ranges from 20 to 50, depending on the nature and oxidation state of the metal component.

  9. KINETIC STUDIES ON THE SORPTION OF LEAD AND CADMIUM ...

    African Journals Online (AJOL)

    Kinetic investigations are necessary for determining the rate of reaction and mechanism. The kinetics of the sorption of Pb2+ and Cd2+ from aqueous solution on to the biomass of C. bicolor was studied by batch equilibrium technique. The removal of the two metal ions was found to be > 60% depending on the initial metal ...

  10. Meta-analysis of pesticide sorption in subsoils

    Science.gov (United States)

    Jarvis, Nicholas

    2017-04-01

    It has been known for several decades that sorption koc values tend to be larger in soils that are low in organic carbon (i.e. subsoils). Nevertheless, in a regulatory context, the models used to assess leaching of pesticides to groundwater still rely on a constant koc value, which is usually measured on topsoil samples. This is mainly because the general applicability of any improved model approach that is also simple enough to use for regulatory purposes has not been demonstrated. The objective of this study was therefore first to summarize and generalize available literature data in order to assess the magnitude of any systematic increase of koc values in subsoil and to test an alternative model of subsoil sorption that could be useful in pesticide risk assessment and management. To this end, a database containing the results of batch sorption experiments for pesticides was compiled from published studies in the literature, which placed at least as much emphasis on measurements in subsoil horizons as in topsoil. The database includes 967 data entries from 46 studies and for 34 different active substances (15 non-ionic compounds, 13 weak acids, 6 weak bases). In order to minimize pH effects on sorption, data for weak acids and bases were only included if the soil pH was more than two units larger than the compound pKa. A simple empirical model, whereby the sorption constant is given as a power law function of the soil organic carbon content, gave good fits to most data sets. Overall, the apparent koc value, koc(app), for non-ionic compounds and weak bases roughly doubled as the soil organic carbon content decreased by a factor of ten. The typical increase in koc(app) was even larger for weak acids: on average koc(app) increased by a factor of six as soil organic carbon content decreased by a factor of ten. These results suggest the koc concept currently used in leaching models should be replaced by an alternative approach that gives a more realistic

  11. TECHNETIUM SORPTION BY CEMENTITIOUS MATERIALS UNDER REDUCING CONDITIONS

    Energy Technology Data Exchange (ETDEWEB)

    Kaplan, D.; Estes, S.; Arai, Y.; Powell, B.

    2012-01-31

    The objective of this study was to measure Tc sorption to cementitious materials under reducing conditions to simulate Saltstone Disposal Facility conditions. Earlier studies were conducted and the experimental conditions were found not to simulate those of the facility. Through a five month subcontract with Clemson University, sorption of {sup 99}Tc to four cementitious materials was examined within an anaerobic glovebag targeting a 0.1% H2(g)/ 99.9% N{sub 2}(g) atmosphere. Early experiments based on Tc sorption and Eh indicated that 0.1% H{sub 2}(g) (a reductant) was necessary to preclude experimental impacts from O{sub 2}(g) diffusion into the glovebag. Preliminary data to date (up to 56 days) indicates that sorption of {sup 99}Tc to cementitious materials increased with increasing slag content for simulated saltstone samples. This is consistent with the conceptual model that redox active sulfide groups within the reducing slag facilitate reduction of Tc(VII) to Tc(IV). These experiments differ from previous experiments where a 2% H{sub 2}(g) atmosphere was maintained (Kaplan et al., 2011 (SRNL-STI-2010-00668)). The impact of the 2% H{sub 2}(g) reducing atmosphere on this data was examined and determined to cause the reduction of Tc in experimental samples without slag. In the present ongoing study, after 56 days, Tc sorption by the 50-year old cement samples (no slag) was undetectable, whereas Tc sorption in the cementitious materials containing slag continues to increase with contact time (measured after 1, 4, 8, 19 and 56 days). Sorption was not consistent with spike concentrations and steady state has not been demonstrated after 56 days. The average conditional K{sub d} value for the Vault 2 cementitious material was 6,362 mL/g (17% slag), for the TR547 Saltstone (45% slag) the conditional K{sub d} was 1258 mL/g, and for TR545 (90% slag) the conditional K{sub d} was 12,112 mL/g. It is anticipated that additional samples will be collected until steady state

  12. Sorption of organic gases in a furnished room

    Energy Technology Data Exchange (ETDEWEB)

    Singer, Brett C.; Revzan, Kenneth L.; Hotchi, Toshifumi; Hodgson, Alfred T.; Brown, Nancy J.

    2003-11-30

    We present experimental data and semi-empirical models describing the sorption of organic gases in a simulated indoor residential environment. Two replicate experiments were conducted with 20 volatile organic compounds (VOCs) in a 50-m{sup 3} room finished with painted wallboard, carpet and cushion, draperies and furnishings. The VOCs span a wide volatility range and include ten Hazardous Air Pollutants. VOCs were introduced to the static chamber as a pulse and their gas-phase concentrations were measured during a net adsorption period and a subsequent net desorption period. Three sorption models were fit to the measured concentrations for each compound to determine the simplest formulation needed to adequately describe the observed behavior. Sorption parameter values were determined by fitting the models to adsorption period data then checked by comparing measured and predicted behavior during desorption. The adequacy of each model was evaluated using a goodness of fit parameter calculated for each period. Results indicate that sorption usually does not greatly affect indoor concentrations of methyl-tert-butyl ether, 2-butanone, isoprene and benzene. In contrast, sorption appears to be a relevant indoor process for many of the VOCs studied, including C{sub 8}-C{sub 10} aromatic hydrocarbons (HC), terpenes, and pyridine. These compounds sorbed at rates close to typical residential air change rates and exhibited substantial sorptive partitioning at equilibrium. Polycyclic aromatic HCs, aromatic alcohols, ethenylpyridine and nicotine initially adsorbed to surfaces at rates of 1.5 to >6 h{sup -1} and partitioned 95 to >99% in the sorbed phase at equilibrium.

  13. Temperature and curing time affect composite sorption and solubility

    Directory of Open Access Journals (Sweden)

    Fabrício Luscino Alves de Castro

    2013-04-01

    Full Text Available Objective: This study evaluated the effect of temperature and curing time on composite sorption and solubility. Material and Methods: Seventy five specimens (8×2 mm were prepared using a commercial composite resin (ICE, SDI. Three temperatures (10°C, 25°C and 60°C and five curing times (5 s, 10 s, 20 s, 40 s and 60 s were evaluated. The specimens were weighed on an analytical balance three times: A: before storage (M1; B: 7 days after storage (M2; C: 7 days after storage plus 1 day of drying (M3. The storage solution consisted of 75% alcohol/25% water. Sorption and solubility were calculated using these three weights and specimen dimensions. The data were analyzed using the Kruskal-Wallis and Mann-Whitney U Tests (α=5%. Results: The results showed that time, temperature and their interaction influenced the sorption and solubility of the composite (p0.05. The 60°C composite temperature led to lower values of sorption for all curing times when compared with the 10°C temperature (p0.05. Solubility was similar at 40 s and 60 s for all temperatures (p>0.05, but was higher at 10°C than at 60°C for all curing times (p0.05. Conclusions: In conclusion, higher temperatures or longer curing times led to lower sorption and solubility values for the composite tested; however, this trend was only significant in specific combinations of temperature and curing times.

  14. Sorption study of U{sup +6} in Brazilian soils

    Energy Technology Data Exchange (ETDEWEB)

    Junior, Antonio P.; Wasserman, Maria A.V.; Mantovano, Jose L.; Carvalho, Leonel M., E-mail: apjunior@ien.gov.br, E-mail: mwasserman@ien.gov.br, E-mail: mantovan@ien.gov.br, E-mail: leonel@ien.gov.br [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeiro, RJ (Brazil); Perez, Daniel V., E-mail: daniel@cnps.embrapa.br [Empresa Brasileira de Pesquisas Agropecuarias (Embrapa Solos-CNPS), Rio de Janeiro, RJ (Brazil)

    2015-07-01

    The uranium mining is one of the main activities of the nuclear fuel cycle that can contribute to the increased exposure to radioactive materials and is one of the main routes of contamination of soil by natural radionuclides. This study investigated the sorption of uranium in brazilian soils, through sorption isotherms performed in batch. In this study, two types of soils were selected: Ferralsols Red and Nitosol. The adjustment of the experimental data to the kinetic models were evaluated by two approaches: the traditional, based on the coefficient of determination (R{sup 2}); and the theoretical and informative, based on Corrected Akaike Information Criteria (AIC{sub C}). The coefficient of determination (R{sup 2}), revealed that, although empirical, both the kinetic model, Freundlich and Langmuir, describes satisfactorily the experimental data, showing R{sup 2} values higher than 0.9, while the partition constant model was not suitable for describe these sorption data. The AICC model analysis showed that the Langmuir model fit the U sorption curve well for Ferralsols Red, while the Freundlich model fits better to Nitosol. This study has highlighted the role of organic matter on the sorption of uranium in highly weathered soils, rich in oxyhydroxides and low activity clays. The Kd values reported in this study differ from those recommended by the United States Environmental Protection Agency, therefore must be considered as reference values for highly weathered soils, since it refers to Brazilian pedoenvironmental conditions. The low Kd values obtained in this study allowed to evaluate the high vulnerability of highly weathered soils to uranium contamination. (author)

  15. Glyphosate sorption and desorption in soils with distinct phosphorus levels

    Directory of Open Access Journals (Sweden)

    Prata Fábio

    2003-01-01

    Full Text Available The sorption of glyphosate by soils occurs due to the inner sphere complex formation with metals of soil oxides, which are related to the soil phosphate adsorption capacity. The aim of this study was to evaluate the effects of increasing rates of phosphorus on sorption and desorption of glyphosate in three soils with different mineralogical attributes. Soils were a Rhodic Kandiudalf, an Anionic Acrudox and a Typic Humaquept. Soil samples were amended with KH2PO4 at equivalent rates of 0; 1,000; 5,000; 20,000 and 50,000 kg ha-1 of P2O5, which are high from the agricultural point of view, but necessary in order to perform sorption and desorption studies. The experimental design consisted of a completely randomized factorial: 2 soils x 5 phosphorus rates and 3 replicates. For the sorption experiments, five glyphosate solutions were employed (0.42; 0.84; 1.68; 3.36 and 6.72 mg L-1, with a 14C radioactivity of 0.233 kBq mL-1. Four steps of the desorption procedure with CaCl2 0.01 mol L-1 and one extraction with Mehlich 3 were performed only at one concentration (0.84 mol L-1. Soil samples were afterwards biologically oxidized to establish the radioactive balance. Glyphosate competes with phosphorus for specific sorption sites, but this competition becomes important when phosphorus is present at rates higher than 1,000 mg dm-3. Moreover, a small amount of applied glyphosate was extracted (<10%, and the extraction increased with increasing soil phosphorus content.

  16. Transient solute transport with sorption in Poiseuille flow

    Science.gov (United States)

    Hesse, M. A.; Zhang, L.; Wang, M.

    2016-12-01

    Sorption onto the wall has been observed to both increase [Lungu and Moffatt, 1982] and decrease the average solute transport velocity [Golay, 1958], relative to the mean flow velocity. Similarly, opposite conclusion have been reached for the effect of sorption on dispersion. In this work, we study transient solute transport in Poiseuille flow with sorptive boundary and initial transversely uniform distribution (linear release) to reconcile the two different views on solute transport (figure 1) with sorption. Two-dimensional simulations in figure 2 show that there is a transition from fast transport dominated by a fast-moving pulse in the middle of the channel at early times, to slow transport at late times once desorption from the walls becomes important. A set of series solutions for zeroth, first and second longitudinal moment have been derived and we show that the zeroth-order term in the solution corresponds to the slow transport in the late regime, while the first-order term corresponds to the fast transport in the early regime (figure 3). Based on the analytical solution, the time scales for early regime and late regimes of both the velocity and the dispersion coefficient have been determined for an equilibrium sorption model and a kinetic linear sorption model. Furthermore, we give approximated analytical solution when both adsorption and desorption are slow. References M.J.E. Golay. Theory of chromatography in open and coated tubular columns iwth round and rectangular cross-sections. In D.H.Desty, editor, Gas Chromatography, pages 36-53, New York, 1958. Academic Press Inc. E.M. Lungu and H.K. Moffatt. the effect of wall conductance on heat diffusion in duct flow. Journal of Engineering Mathematics, 1692 ;121-136, 1982.

  17. THE SORPTION OF OFLOXACIN BY HYDRATED ALUMINA AND SILICON

    Directory of Open Access Journals (Sweden)

    A. N. Chebotarev

    2016-11-01

    Full Text Available The sorption of ofloxacin (OFL – the antibiotic from class of fluoroquinolones has been studied on alumina (γ-Al2O3 different acid-base modifications – acidic Al2O3(acidic, neutral Al2O3 (Neutral and the basic Al2O3 (core and amorphous silica – silica gel (SG L 5/40 and aerosil A-300. Determination of ofloxacin in solutions has been carried out by spectrophotometry on spectrophotometer SF-46 at λ = 291 nm and acidity 7. To clarify the nature of the sorption surfaces of OFL hydrated on aluminum and silicon oxides were studied according to the degree of extraction (S% from pH, contact time of the phases (min. sample from the sorbent mass (g; sorption isotherms were built and antibiotic desorption was studied. The OFL significant recovery (~ 60% is observed at the pH range of 4 ÷ 8, and reaches its maximum (80-85% at pH 7. The maximum degree of extraction of the antibiotic on aerosil A-300 and L 5/40 silica realized at pH 6 and it was ~ 80%. Comparative analysis of the forms constructed isotherms (L – type indicates a significant affinity investigated hydrated oxides to sorbate. The value of the static exchange capacity and concentration ratios can proof that. Differences in the quantitative characteristics of sorption of aluminum and silicon oxides are associated with nature and the acid-base properties of adsorption sites. In the study of the OFL concentrates desorption in static mode dilute NaOH and HNO3 solutions it was found that growth desorption degree occured with increasing concentration. Desorption was 2-3 times better in the case of aluminum oxide than silicon oxide when there were the same concentrations of acid and alkali. This is another confirmation of the participation in various sorption interactions forces of physical and chemical nature.

  18. Tailored cognitive-behavioral therapy for fibromyalgia: two case studies.

    NARCIS (Netherlands)

    Koulil, S. van; Lankveld, W.G.J.M. van; Kraaimaat, F.W.; Helmond, T. van; Vedder, A.; Hoorn, H. van; Cats, H.; Riel, P.L.C.M. van; Evers, A.W.M.

    2008-01-01

    OBJECTIVE: To illustrate a multidisciplinary group treatment for patients with fibromyalgia (FM) tailored to the patient's cognitive-behavioral pattern. METHOD: In a case-study design the tailored treatment approaches of two FM patients were described. One patient characterized by avoidance behavior

  19. Tailorable software architectures in the accelerator control system environment

    International Nuclear Information System (INIS)

    Mejuev, Igor; Kumagai, Akira; Kadokura, Eiichi

    2001-01-01

    Tailoring is further evolution of an application after deployment in order to adapt it to requirements that were not accounted for in the original design. End-user tailorability has been extensively researched in applied computer science from HCl and software engineering perspectives. Tailorability allows coping with flexibility requirements, decreasing maintenance and development costs of software products. In general, dynamic or diverse software requirements constitute the need for implementing end-user tailorability in computer systems. In accelerator physics research the factor of dynamic requirements is especially important, due to frequent software and hardware modifications resulting in correspondingly high upgrade and maintenance costs. In this work we introduce the results of feasibility study on implementing end-user tailorability in the software for accelerator control system, considering the design and implementation of distributed monitoring application for 12 GeV KEK Proton Synchrotron as an example. The software prototypes used in this work are based on a generic tailoring platform (VEDICI), which allows decoupling of tailoring interfaces and runtime components. While representing a reusable application-independent framework, VEDICI can be potentially applied for tailoring of arbitrary compositional Web-based applications

  20. Understanding the impact of graphene sheet tailoring on the ...

    Indian Academy of Sciences (India)

    channel was tailored into different shapes and found that with the introduction of edge roughness along the border of GNR sheet the bandgap of GNRFET channel increases. Tailoring the channel decreases mobility and transmission probability to a great extent and thus the performance of I–V characteristics of GNRFET ...

  1. Phosphorus sorption-desorption and effects of temperature, pH and salinity on phosphorus sorption in marsh soils from coastal wetlands with different flooding conditions.

    Science.gov (United States)

    Bai, Junhong; Ye, Xiaofei; Jia, Jia; Zhang, Guangliang; Zhao, Qingqing; Cui, Baoshan; Liu, Xinhui

    2017-12-01

    Wetland soils act as a sink or source of phosphorus (P) to the overlaying water due to phosphorus sorption-desorption processes. Litter information is available on sorption and desorption behaviors of phosphorus in coastal wetlands with different flooding conditions. Laboratory experiments were conducted to investigate phosphorus sorption-desorption processes, fractions of adsorbed phosphorus, and the effects of salinity, pH and temperature on phosphorus sorption on soils in tidal-flooding wetlands (TW), freshwater-flooding wetlands (FW) and seasonal-flooding wetlands (SW) in the Yellow River Delta. Our results showed that the freshly adsorbed phosphorus dominantly exists in Occluded-P and Fe/AlP and their percentages increased with increasing phosphorus adsorbed. Phosphorus sorption isotherms could be better described by the modified Langmuir model than by the modified Freundlich model. A binomial equation could be properly used to describe the effects of salinity, pH, and temperature on phosphorus sorption. Phosphorus sorption generally increased with increasing salinity, pH, and temperature at lower ranges, while decreased in excess of some threshold values. The maximum phosphorus sorption capacity (Q max ) was larger for FW soils (256 mg/kg) compared with TW (218 mg/kg) and SW soils (235 mg/kg) (p freshwater restoration can contribute to controlling the eutrophication status of water bodies through increasing P sorption. Copyright © 2017 Elsevier Ltd. All rights reserved.

  2. A study of selenium and tin sorption on granite and goethite

    International Nuclear Information System (INIS)

    Ticknor, K.V.; McMurry, J.

    1996-01-01

    Sensitivity analyses based on an illustrative performance assessment case study of a disposal concept for nuclear fuel waste have shown that radioisotopes of Se and Sn could have a significant effect on cumulative radioactive dose if they were to be transported through the geosphere without retardation. Static batch sorption methods, coupled with 2 n factorial experimental designs, were used to determine the extent to which Se and Sn can be sorbed by granite and goethite as a function of total dissolved solids concentration, (TDS), natural fulvic acid concentration as dissolved organic carbon, [DOC], pH and, for the studies with Se, the Se concentration, [Se]. Aqueous speciation and the saturation indices of solubility-controlling solid phases were estimated using the speciation code HARPHRQ with the HATCHES thermodynamic database. The experimental results indicated that Se sorption on granite was low and not affected by changes in [DOC] or [TDS]. Increased [Se] and increased pH decreased sorption. For Se sorption on goethite, the pH range was narrow but indicated that sorption decreased as pH increased. Increased [TDS] and [Se] lowered sorption on goethite, but changes in (DOC] had no effect on sorption. For Sn, increased pH, [TDS] and [DOC] decreased sorption on granite. For Sn sorption on goethite, increased [DOC] resulted in decreased sorption, but differences in [TDS] and pH had little consistent effect on sorption. (author)

  3. A study of selenium and tin sorption on granite and geothite

    International Nuclear Information System (INIS)

    Ticknor, K.V.; McMurry, J.

    1996-01-01

    Sensitivity analyses based on an illustrative performance assessment case study of a disposal concept for nuclear fuel waste have shown that radioisotopes of Se and Sn could have a significant effect on cumulative radioactive dose if they were to be transported through the geosphere without retardation. Static batch sorption methods, coupled with 2 n factorial experimental designs, were used to determine the extent to which Se and Sn can be sorbed by granite and goethite as a function of total dissolved solids concentration, [TDS], natural fulvic acid concentration as dissolved organic carbon, [DOC], pH and, for the studies with Se, the Se concentration, [Se]. Aqueous speciation and the saturation indices of solubility-controlling solid phases were estimated using the speciation code HARPHRQ with the HATCHES thermodynamic database. The experimental results indicated that Se sorption on granite was, low and not affected by changes in [DOC] or [TDS]. Increased [Se] and increased pH decreased sorption. For Se sorption on goethite, the pH range was narrow but indicated that sorption decreased as pH increased. Increased [TDS] and [Se] lowered sorption on goethite, but changes in [DOC] had no effect on sorption. For Sn, increased pH, [TDS] and [DOC] decreased sorption on granite. For Sn sorption on goethite, increased [DOC] resulted in decreased sorption, but differences in [TDS] and pH had little consistent effect on sorption. (orig.)

  4. Effect of cosolutes on the sorption of phenanthrene onto mineral surface of river sediments and kaolinite.

    Science.gov (United States)

    Wu, Yinghong; Liu, Fang; Zhang, Wen; Wang, Lei

    2014-01-01

    Sorption of phenanthrene onto the natural sediment with low organic carbon content (OC%), organic-free sediment, and kaolinite was investigated through isotherm experiments. Effects of cosolutes (pyrene, 4-n-nonyphenol (NP), and humic acid (HA)) on phenanthrene sorption were also studied by comparing apparent solid-water distribution coefficients (K d (app)) of phenanthrene. Two addition sequences, including "cosolute added prior to phenanthrene" and "cosolute and phenanthrene added simultaneously," were adopted. The Freundlich model fits phenanthrene sorption on all 3 sorbents well. The sorption coefficients on these sorbents were similar, suggesting that mineral surface plays an important role in the sorption of hydrophobic organic contaminants on low OC% sediments. Cosolutes could affect phenanthrene sorption on the sorbents, which depended on their properties, concentrations, and addition sequences. Pyrene inhibited phenanthrene sorption. Sorbed NP inhibited phenanthrene sorption at low levels and promoted sorption at high levels. Similar to NP, effect of HA on phenanthrene sorption onto the natural sediment depended on its concentrations, whereas, for the organic-free sediment and kaolinite, preloading of HA at high levels led to an enhancement in phenanthrene K d (app) while no obvious effect was observed at low HA levels; dissolved HA could inhibit phenanthrene sorption on the two sorbents.

  5. Variation in phenanthrene sorption coefficients with soil organic matter fractionation: the result of structure or conformation?

    Science.gov (United States)

    Bonin, Julia L; Simpson, Myrna J

    2007-01-01

    Sorption of phenanthrene to varying soil types was investigated to better understand sorption processes. Humic acid and humin fractions were isolated from each soil sample, and sorption coefficients were measured by batch equilibration. Samples were characterized by carbon analysis and 13C cross polarization magic angle spinning (CP/ MAS) nuclear magnetic resonance (NMR) spectroscopy. Measured organic carbon-normalized sorption coefficients (Koc) of the fractions were greater in all cases when compared to the soils. The humin fractions exhibited greater Koc values than did source samples, suggesting that fractionation may reorganize organic matter in humin resulting in an increased availability of and/or more favorable sorption domains. Mass balance calculations revealed that the sum of sorption to the fractions is greater than sorption to the whole sample. The greatest difference between sorption values was found to occur with the mineral soils, suggesting that clay minerals influence the physical conformation of soil organic matter (SOM) and availability of sorption domains. The mass balance, sorption data, and a lack of consistent trends between observed Kco values and solid-state 13C NMR data suggest that the physical conformation of SOM and chemical characteristics both play important roles in sorption processes.

  6. Removal of organic compounds from natural underground water in sorption and sono-sorption processes on selected activated carbons

    Directory of Open Access Journals (Sweden)

    Pietrzyk Andżelika

    2017-01-01

    Full Text Available The article rated removal efficiency of organic matter in the processes of sorption and sono-sorption of underground water grasped for municipal purposes. The studies were conducted in laboratory scale and verified in pilot scale at the Water Treatment Plant Tarnobrzeg-Jeziórko. In the research used granular activated carbons, ie. WD-Extra, WG-12, Norit Row 0.8 and Filtrasorb 300. The processes efficiency was evaluated on the basis of changes in the following parameters, ie.: total organic carbon (TOC, permanganate index, UV absorbance, turbidity and colour. The ultrasounds were generated by means of disintegrator Sonics&Materials VCX 130, using the sonication time of 1 and 5 minutes. The results obtained for the batch tests allowed to observe a beneficial effect of ultrasound on the efficiency of the removal of organic material in the sorption process. The combination of sonication and sorption on activated carbon increased the efficiency of the removal of organic matter by 6–37% for TOC, and 18.6–27.9% for permanganate index, depending on the sorbent used. The positive laboratory results were not confirmed in a pilot scale. In the flow conditions the sonication process did not affect the efficiency of removal of organic matter on the filter model with a bed of activated carbon.

  7. Iodine sorption by ion-exchange fiber on the basis of polyacrylonitrile and AV-17 anionite under static conditions

    International Nuclear Information System (INIS)

    Tarchigina, N.I.; Artemov, A.V.; Ksenzenko, V.I.

    1986-01-01

    Iodine sorption from natural waters by a qualitatively new sorbent - ion-exchange fiber on the basis of polyacrylonitrile and AV-17 anionite is investigated. Mechanism of iodine sorption by ion-exchange material is suggested. Iodine sorption kinetics by fibrous sorbent under static conditions is described. Iodine sorption efficient constants are determined by experimental data processing with the use of electronic computer

  8. Sorption of a nonionic surfactant Tween 80 by minerals and soils

    Energy Technology Data Exchange (ETDEWEB)

    Kang, Soyoung, E-mail: soyoung@pusan.ac.kr; Jeong, Hoon Young, E-mail: hjeong@pusan.ac.kr

    2015-03-02

    Highlights: • Tween 80 sorption varies significantly among soil minerals. • Sorption mechanisms and atomic compositions explain to mineral-specific sorption. • Clay minerals and SOM in soils are the key contributors to Tween 80 sorption. • Hysteresis suggests the potential difficulty in removing residual surfactants. - Abstract: Batch experiments were conducted to evaluate Tween 80 sorption by oxides, aluminosilicates, and soils. For oxides, the sorption by silica and alumina follow linear isotherms, and that by hematite follows a Langmuir isotherm. Considering isotherm type and surface coverage, Tween 80 may partition into the silica/alumina–water interface, whereas it may bind to hematite surface sites. Among aluminosilicates, montmorillonite shows the greatest sorption due to the absorption of Tween 80 into interlayers. For other aluminosilicates, it sorbs to surfaces, with the sorption increasing as plagioclase < vermiculite < kaolinite. This results from the relative reactivity among surface sites: ≡NaOH, ≡CaOH << ≡SiOH < ≡AlOH. Experiments using dry- and wet-sieved soils reveal that fine-grained clay minerals, difficult to separate by dry-sieving, contribute significantly to Tween 80 sorption. The greater sorption by untreated soils than H{sub 2}O{sub 2}-treated soils indicates that soil organic matter is a vital sorbent. The sorption hysteresis, contributed to by clay minerals and soil organic matter, is characterized by the greater sorption during the desorption than the sorption stages. This suggests the potential difficulty in removing surfactants from soils. Also, sorption of surfactants can adversely affect surfactant-enhanced remediation by decreasing the aquifer permeability and the availability of surfactants for micellar solubilization.

  9. Ceramic laminates with tailored residual stresses

    Directory of Open Access Journals (Sweden)

    Baudín, C.

    2009-12-01

    Full Text Available Severe environments imposed by new technologies demand new materials with better properties and ensured reliability. The intrinsic brittleness of ceramics has forced scientists to look for new materials and processing routes to improve the mechanical behaviour of ceramics in order to allow their use under severe thermomechanical conditions. The laminate approach has allowed the fabrication of a new family of composite materials with strength and reliability superior to those of monolithic ceramics with microstructures similar to those of the constituent layers. The different ceramic laminates developed since the middle 1970´s can be divided in two large groups depending on whether the development of residual stresses between layers is the main design tool. This paper reviews the developments in the control and tailoring of residual stresses in ceramic laminates. The tailoring of the thickness and location of layers in compression can lead to extremely performing structures in terms of strength values and reliability. External layers in compression lead to the strengthening of the structure. When relatively thin and highly compressed layers are located inside the material, threshold strength, crack bifurcation and crack arrest during fracture occur.

    Las severas condiciones de trabajo de las nuevas aplicaciones tecnológicas exigen el uso de materiales con mejores propiedades y alta fiabilidad. La potencialidad de uso de materiales frágiles, como los cerámicos, en estas aplicaciones exige el desarrollo de nuevos materiales y métodos de procesamiento que mejoren su comportamiento mecánico. El concepto de material laminado ha permitido la fabricación de una nueva familia de materiales con tensiones de fractura y fiabilidad superiores a las de materiales monolíticos con microestructuras similares a las de las láminas que conforman el laminado. Los distintos materiales laminados desarrollados desde mediados de los años 70 se pueden

  10. Tailoring magnetism by light-ion irradiation

    International Nuclear Information System (INIS)

    Fassbender, J; Ravelosona, D; Samson, Y

    2004-01-01

    Owing to their reduced dimensions, the magnetic properties of ultrathin magnetic films and multilayers, e.g. magnetic anisotropies and exchange coupling, often depend strongly on the surface and interface structure. In addition, chemical composition, crystallinity, grain sizes and their distribution govern the magnetic behaviour. All these structural properties can be modified by light-ion irradiation in an energy range of 5-150 keV due to the energy loss of the ions in the solid along their trajectory. Consequently the magnetic properties can be tailored by ion irradiation. Similar effects can also be observed using Ga + ion irradiation, which is the common ion source in focused ion beam lithography. Examples of ion-induced modifications of magnetic anisotropies and exchange coupling are presented. This review is limited to radiation-induced structural changes giving rise to a modification of magnetic parameters. Ion implantation is discussed only in special cases. Due to the local nature of the interaction, magnetic patterning without affecting the surface topography becomes feasible, which may be of interest in applications. The main patterning technique is homogeneous ion irradiation through masks. Focused ion beam and ion projection lithography are usually only relevant for larger ion masses. The creation of magnetic feature sizes below 50 nm is shown. In contrast to topographic nanostructures the surrounding area of these nanostructures can be left ferromagnetic, leading to new phenomena at their mutual interface. Most of the material systems discussed here are important for technological applications. The main areas are magnetic data storage applications, such as hard magnetic media with a large perpendicular magnetic anisotropy or patterned media with an improved signal to noise ratio and magnetic sensor elements. It will be shown that light-ion irradiation has many advantages in the design of new material properties and in the fabrication technology of

  11. Formability Studies on Transverse Tailor Welded Blanks

    International Nuclear Information System (INIS)

    Bhaskar, V. Vijay; Narasimhan, K.

    2005-01-01

    Tailor Welded Blanks (TWB) technology is one of the several approaches that have been used to reduce the weight of the automobile body. TWBs are made up of two or more blanks having different/same properties (geometry, material etc.) prior to forming. The formability of these blanks depends on material and geometric parameters like strength ratio and thickness ratio. The study of these blanks can be classified on the basis of the weld orientation chosen viz. transverse weld or longitudinal weld with respect to the major straining direction.This paper studies the formability issues related to transverse TWB by FE simulation. The formability is assessed by analyzing tensile and Limit Dome Height (LDH) tests. The weld region is assumed to be a line in all the simulations. While modeling the tensile test, ultimate tensile strength (UTS) and elongation are monitored, and in LDH testing, pole height and maximum load (in near plane strain condition) are monitored. LDH testing shows that as thickness ratio increases, the load bearing capacity and the pole height decreases. There is a contribution from both the thicker and the thinner blank to the overall deforming volume. Failure location analysis shows that there is an abrupt change in the location of the failure from punch nose region to weld line region as the thickness ratio reaches a critical magnitude (1.08).The study of material properties shows that as the yield strength ratio (S ratio) and strain hardening exponent ratio (N ratio) between the blanks increases, the maximum load which the blank can sustain without failure (UTS) increases. This becomes constant and comparable to that of single sheet at higher N and S ratios

  12. Formability Studies on Transverse Tailor Welded Blanks

    Science.gov (United States)

    Bhaskar, V. Vijay; Narasimhan, K.

    2005-08-01

    Tailor Welded Blanks (TWB) technology is one of the several approaches that have been used to reduce the weight of the automobile body. TWBs are made up of two or more blanks having different/same properties (geometry, material etc.) prior to forming. The formability of these blanks depends on material and geometric parameters like strength ratio and thickness ratio. The study of these blanks can be classified on the basis of the weld orientation chosen viz. transverse weld or longitudinal weld with respect to the major straining direction. This paper studies the formability issues related to transverse TWB by FE simulation. The formability is assessed by analyzing tensile and Limit Dome Height (LDH) tests. The weld region is assumed to be a line in all the simulations. While modeling the tensile test, ultimate tensile strength (UTS) and elongation are monitored, and in LDH testing, pole height and maximum load (in near plane strain condition) are monitored. LDH testing shows that as thickness ratio increases, the load bearing capacity and the pole height decreases. There is a contribution from both the thicker and the thinner blank to the overall deforming volume. Failure location analysis shows that there is an abrupt change in the location of the failure from punch nose region to weld line region as the thickness ratio reaches a critical magnitude (1.08). The study of material properties shows that as the yield strength ratio (S ratio) and strain hardening exponent ratio (N ratio) between the blanks increases, the maximum load which the blank can sustain without failure (UTS) increases. This becomes constant and comparable to that of single sheet at higher N and S ratios.

  13. Automatically producing tailored web materials for public administration

    Science.gov (United States)

    Colineau, Nathalie; Paris, Cécile; Vander Linden, Keith

    2013-06-01

    Public administration organizations commonly produce citizen-focused, informational materials describing public programs and the conditions under which citizens or citizen groups are eligible for these programs. The organizations write these materials for generic audiences because of the excessive human resource costs that would be required to produce personalized materials for everyone. Unfortunately, generic materials tend to be longer and harder to understand than materials tailored for particular citizens. Our work explores the feasibility and effectiveness of automatically producing tailored materials. We have developed an adaptive hypermedia application system that automatically produces tailored informational materials and have evaluated it in a series of studies. The studies demonstrate that: (1) subjects prefer tailored materials over generic materials, even if the tailoring requires answering a set of demographic questions first; (2) tailored materials are more effective at supporting subjects in their task of learning about public programs; and (3) the time required to specify the demographic information on which the tailoring is based does not significantly slow down the subjects in their information seeking task.

  14. Comparing tailored and untailored text messages for smoking cessation

    DEFF Research Database (Denmark)

    Skov-Ettrup, Lise; Ringgaard, L W; Dalum, Peter

    2014-01-01

    The aim was to compare the effectiveness of untailored text messages for smoking cessation to tailored text messages delivered at a higher frequency. From February 2007 to August 2009, 2030 users of an internet-based smoking cessation program with optional text message support aged 15-25 years were...... consecutively randomized to versions of the program that offered either tailored or untailored text messages. Thirty-day point abstinence from smoking was measured self-reportedly at 12-months follow-up. Response rates were 36.3% and 38.1% in the tailored and untailored group, respectively. We analyzed...

  15. Use of thermodynamic sorption models to derive radionuclide Kd values for performance assessment: Selected results and recommendations of the NEA sorption project

    Science.gov (United States)

    Ochs, M.; Davis, J.A.; Olin, M.; Payne, T.E.; Tweed, C.J.; Askarieh, M.M.; Altmann, S.

    2006-01-01

    For the safe final disposal and/or long-term storage of radioactive wastes, deep or near-surface underground repositories are being considered world-wide. A central safety feature is the prevention, or sufficient retardation, of radionuclide (RN) migration to the biosphere. To this end, radionuclide sorption is one of the most important processes. Decreasing the uncertainty in radionuclide sorption may contribute significantly to reducing the overall uncertainty of a performance assessment (PA). For PA, sorption is typically characterised by distribution coefficients (Kd values). The conditional nature of Kd requires different estimates of this parameter for each set of geochemical conditions of potential relevance in a RN's migration pathway. As it is not feasible to measure sorption for every set of conditions, the derivation of Kd for PA must rely on data derived from representative model systems. As a result, uncertainty in Kd is largely caused by the need to derive values for conditions not explicitly addressed in experiments. The recently concluded NEA Sorption Project [1] showed that thermodynamic sorption models (TSMs) are uniquely suited to derive K d as a function of conditions, because they allow a direct coupling of sorption with variable solution chemistry and mineralogy in a thermodynamic framework. The results of the project enable assessment of the suitability of various TSM approaches for PA-relevant applications as well as of the potential and limitations of TSMs to model RN sorption in complex systems. ?? by Oldenbourg Wissenschaftsverlag.

  16. Sorption mechanism of solvent vapors to coals; Sekitan eno yobai joki no shuchaku kiko no kaiseki

    Energy Technology Data Exchange (ETDEWEB)

    Shimizu, K.; Takanohashi, T.; Iino, M. [Tohoku University, Sendai (Japan). Institute for Chemical Reaction Science

    1996-10-28

    With an objective to clarify the interactions between micropore structure of coal and solvent reagents, a sorption experiment was carried out under solvent saturated vapor pressure. Low-volatile bituminous coal, Pocahontas No. 3 coal, has the aromatic ring structure developed, and makes solvent more difficult to diffuse into coal, hence sorption amount is small. Methanol has permeated since its polarity is high. High-volatile bituminous coal, Illinois No. 6 coal, makes solvent penetrate easily, and the sorption amount was large with both of aromatic and polar solvents. Since brown coal, Beulah Zap coal, contains a large amount of oxygen, and hydrogen bonding is predominant, sorption amount of cyclohexane and benzene having no polarity is small. Methanol diffuses while releasing hydrogen bond due to its polarity, and its sorption amount is large. A double sorption model is available, which expresses the whole sorption amount as a sum of physical sorption amount and amount of permeation into coal. This model was applied when it explained successfully the sorption behavior of the solvents relative to coals, excepting some of the systems. However, also observed were such abnormal behavior as sorption impediment due to interactions between coal surface and solvents, and permeation impediment due to hydroxyl groups inside the coals. 1 ref., 10 figs., 2 tabs.

  17. Water sorption and water permeability properties of edible film made from potato peel waste

    Directory of Open Access Journals (Sweden)

    Siti Hajar OTHMAN

    Full Text Available Abstract The water sorption and permeability properties of edible film produced from potato peel waste was investigated under different levels of relative humidity (23, 33, 43, 57, 75% RH and temperatures (5, 30, 50 °C. The water sorption behaviour and isotherms of the film were investigated by fitting water sorption data to the Peleg model and the Guggenheim, Anderson de Boer model (GAB model. The amount of moisture content, time required for the moisture content of the film to reach equilibrium, water sorption rate, and water sorption capacity increased when the relative humidity increased. The effect of temperature on moisture content, water sorption rate, water sorption capacity, and monolayer moisture content is complex and related to the water activity as well as the moisture content. Based on R2 and RMSE values, the Peleg and GAB models were respectively determined as excellent models to predict the water sorption properties of the films, thus supporting the reliability of water sorption behaviour prediction. The water vapour transmission rate and water vapour permeability increased with an increase in relative humidity and temperature. The sorption and permeability properties of the film are worth investigation since the final application of the film as food packaging is ultimately dependent on these behaviours.

  18. The role of sorption and bacteria in mercury partitioning and bioavailability in artificial sediments

    International Nuclear Information System (INIS)

    Zhong Huan; Wang Wenxiong

    2009-01-01

    This study compared the relative importance of three types of sorption (organic matter-particle, mercury-organic matter and mercury-particle) in controlling the overall mercury partitioning and bioavailability in sediments. We found that all three types of sorption were important for both inorganic mercury (Hg) and methylated mercury (MeHg). Mercury-particle sorption was more important than mercury-fulvic acid (FA) sorption in increasing the mercury concentrations with increasing aging. Bioavailability (quantified by gut juice extraction from sipunculans) was mainly controlled by mercury-particle sorption, while FA-particle and mercury-FA sorption were not as important, especially for MeHg. Bacterial activity also increased the partitioning of Hg or MeHg in the sediments and was further facilitated by the presence of organic matter. The bioavailability of Hg or MeHg from sediments was only slightly influenced by bacterial activity. This study highlights the importance of sorption from various sources (especially mercury-particle sorption) as well as bacteria in controlling the partitioning and bioavailability of Hg or MeHg in sediments. - Mercury-particle sorption was more important than mercury-organic matter and organic matter-particle sorption in controlling the partitioning of Hg or MeHg in sediments

  19. Sorption of Hydrophobic Organic Contaminants to Glacially Deposited Sediments of Central Illinois

    Science.gov (United States)

    Jeong, S.; Werth, C. J.; Wander, M. M.

    2003-04-01

    The nature and distribution of solid phase carbonaceous material strongly affect the sorption of hydrophobic organic contaminants (HOCs) to soils and sediments. High surface area carbonaceous materials (HSCM, e.g. charcoal, soot) and mature organic matter facies (e.g. humin, kerogen) exhibit high sorption capacities, nonlinear sorption isotherms, and sorption-desorption hysteresis. The accurate characterization of carbonaceous material type and distribution are crucial for prediction of the fate of HOCs in soils and sediments. The objectives of this work are to determine the type(s) of carbonaceous material that controls adsorption in central Illinois groundwater sediments, and to determine how oxidative weathering affects sorption capacity. Sediment samples were collected from oxidized and reduced zones of the Chanute Air Force Base in Rantoul (Illinois, USA) and treated to obtain fractions of the sediment samples enriched in different types of carbonaceous materials (e.g., humic acid, kerogen, black carbon). The different fractions were then evaluated for their sorption capacity and mechanism to sorb trichloroethylene (TCE), a common groundwater pollutant. Isotherm results indicate that kerogen primarily controls the sorption of TCE. Isotherm results also show that the Koc (sorption distribution coefficient normalized by the fraction of organic carbon) for the reduced sediment is larger than that for the oxidized sediment. Current experiments are focused on the question of whether kerogen oxidation or kerogen protection by mineral precipitates reduces the sorption capacity in the oxidized sediments, and on whether kerogen controls sorption in groundwater sediments not affected by glaciation.

  20. Impact of coal structural heterogeneity on the nonideal sorption of organic contaminants.

    Science.gov (United States)

    Shi, Xin; Fu, Heyun; Li, Yuan; Mao, Jingdong; Zheng, Shourong; Zhu, Dongqiang

    2011-06-01

    Carbonaceous geosorbents (black carbon, coal, and humin/kerogen) play a primary role in the nonideal sorption (isotherm nonlinearity, hysteresis, and multiphasic kinetics) of hydrophobic organic chemicals by soils and sediments. The present study investigated the impact of coal structural heterogeneity on sorption/desorption of two model monoaromatic compounds (1,3-dichlorobenzene and 1,3-dinitrobenzene). Due to the higher degree of aromaticity and condensation, anthracite showed stronger sorption affinity and nonlinearity and slower sorption kinetics than lignite. Removal of humic substances by alkali extraction and/or mineral fraction by acidification did not much affect organic carbon-normalized sorption coefficient to the coal, suggesting nearly complete accessibility of adsorption sites on the condensed organic carbon. However, the treatments greatly increased sorption kinetics and meanwhile alleviated hysteresis of 1,3-dinitrobenzene, as compared with the original lignite. These observations were attributed to the enhanced exposure of high-energy adsorption sites on the condensed organic carbon after exfoliating the surface coverage by humic substances and minerals. An empirical biphasic pseudo-second-order model consisting of a fast sorption phase and a slow sorption phase adequately quantified the overall sorption kinetics for the coal sorbents. The results indicated that the condensed organic carbon, in combination with other structural components, controls the nonideal sorption of unburned coal. Copyright © 2011 SETAC.

  1. Yucca Mountain Project far-field sorption studies and data needs

    International Nuclear Information System (INIS)

    Meijer, A.

    1990-09-01

    Batch sorption experiments in which radionuclides dissolved in groundwaters from Yucca Mountain were sorbed onto samples of crushed tuff have resulted in a substantial database of sorption coefficients for radionuclides of interest to the repository program. Although this database has been useful in preliminary evaluations of Yucca Mountain as a potential site for a nuclear waste repository, the database has limitations that must be addressed before it can be used for performance assessment calculations in support of a license application for a waste repository. The purpose of this paper is to: review the applicability of simple (constant) sorption coefficients in transport calculations; review and evaluate alternative methods for the derivation of sorption coefficients; summarize and evaluate the present YMP sorption database to identify areas of data sufficiency and significant data gaps; summarize our current understanding of pertinent sorption mechanisms and associated kinetic parameters; evaluate the significance to the YMP of potential problems in the experimental determination and field application of sorption coefficients as enumerated by the NRC (Nuclear Regulatory Commission, 1987) in its technical position paper on sorption; formulate and evaluate strategies for the resolution of NRC concerns regarding experimental problems; and formulate a position on the sorption coefficient database and the level of understanding of sorption mechanisms likely to be required in the licensing application. 75 refs., 1 fig., 2 tabs

  2. Ofloxacin sorption in soils after long-term tillage: The contribution of organic and mineral compositions

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Dandan; Chen, Bingfa; Wu, Min, E-mail: kustless@gmail.com; Liang, Ni; Zhang, Di; Li, Hao; Pan, Bo

    2014-11-01

    Intensive human activities in agricultural areas resulted in significant alteration of soil properties, which consequently change their interactions with various contaminants. This process needs to be incorporated in contaminant behavior prediction and their risk assessment. However, the relevant study is missing. This work was designed to examine the change of soil properties and ofloxacin (OFL) sorption after tillage. Soil samples were collected in Yuanyang, Mengzi, and Dianchi areas with different agricultural activities. Although the mineral compositions of soils from Yuanyang and Dianchi differed greatly, these compositions are similar after tillage, especially for paddy soils. Soil pH decreased generally after OFL sorption, suggesting that ion exchange of OFL with protons in soil organic matter (SOM) was important for OFL sorption. However, a positive relationship between SOM and OFL sorption was not observed. On the contrary, increased SOM decreased OFL sorption when soils from the same geological location were compared. Generally speaking, tillage activities or dense vegetations greatly decreased OFL sorption. The higher OFL sorption in B horizon than A horizon suggested limited leaching of OFL through soil columns. The summed sorption calculated based on the sorption of individual soil components and their percentages in soils was higher than the intact soil. This phenomenon may be understood from the interactions between soil components, such as the coating of SOM on mineral particles. This study emphasizes that soil should be treat as a dynamic environmental matrix when assessing antibiotic behaviors and risks, especially in the area with intense human activities. - Highlights: • Mineral compositions tend to be similar after tillage. • Increased SOM decreases OFL sorption for soils from the same geological location. • Tillage activities or dense vegetations greatly decrease OFL sorption. • The summed sorption of individual soil components is

  3. The application of macroporous copolymers in the sorption of heavy and precious metals from aqueous solutions

    Directory of Open Access Journals (Sweden)

    Nastasović Aleksandra B.

    2006-01-01

    Full Text Available Macroporous crosslinked poly(GMA-co-EGDMA was synthesized by the suspension copolymerisation and functionalized by the ring-opening reaction of the pendant epoxy groups with ethylene diamine. The porosity parameters (specific pore volume, specific surface area, and pore diameter, which corresponds to half of the pore volume for the initial and amino-functionalized copolymer samples were calculated from the cumulative pore volume distribution curves obtained by mercury porosimetry. The selectivity, sorption capacity and sorption rate of amino-functionalized poly(GMA-co-EGDMA-en were determined under static conditions. The sorption of Cu(ll and Ag(l ions on poly(GMA-co-EGDMA-en was very rapid (ti/2 value about 1 min. Slower sorption was observed for Au(lll ions with a ti/2 value of 6.5 minutes. The different rates of Au(lll, Cu(ll and Ag(l sorption could be applied for gold, copper and silver ion separation from mixed solutions. The sorption of Ni(ll and Cu(ll ions from galvanic solution under competitive conditions was also fast, with ti/2 values of 0.5 and 2 min, respectively. However, Zn(ll sorption was considerably slower (a ti/2 of 10 min. Similar results were obtained for galvanic solution under dynamic conditions, i.e., the metal sorption capacities of poly(GMA-co-EGDMA-en decreased in the order: Ni(ll > Cu(ll >> Zn(ll. The reusability of amino-functionalized poly(GMA-co-EGDMA for Cu(ll sorption was tested in four sorption/desorption cycles. Regeneration experiments were performed with 0.1 and 1 M H2SO4 showed a Cu(ll capacity loss of 50 % in the first sorption/desorption cycle. The sorption capacity increased when additional neutralization with 0.1 and 1 M NaOH was performed after each sorption/desorption cycle.

  4. Sorption and Transport of Sildenafil in Natural Soils

    Science.gov (United States)

    Boudinot, F. G.; Vulava, V. M.

    2013-12-01

    Pharmaceutical Chemicals (PCs) mainly enter our ecosystems from discharges of treated wastewater and have direct effects on the ecological health of that area. Sildenafil citrate (Viagra) is one such PC, whose presence has been reported in stream waters. Although one study has shown that sildenafil is not harmful in bacterial and fungal environments, there remains much unknown about its fate elsewhere in ecosystems. Sildenafil is a complex organic molecule with two amino functional groups that result in pKa's of 7.27 and 5.97. It also has a high solubility of 3.5 g/L. Given that sildenafil consumption (and concurrently disposal) is on the rise, it is essential that its behavior in the natural environment be better understood. The goal of this study was to quantify the sorption and transport behavior of sildenafil in differing natural soils with varying compositions. Pristine A- and B- horizon soil samples from several soil series were collected in a managed forest near Charleston, SC and used for these studies. The soils were characterized for physical and chemical properties: soil organic matter content ranged between 0.6-7.6%, clay content between 6-20%, and soil pH between 4-5. These soils were then used to perform kinetic reaction, sorption, and column transport experiments. Batch kinetic experiments showed a fast reaction rate in both clay-rich and organic-rich soils and an equilibration time of less than 24 hours. Batch reactor sorption experiments provided data for sorption isotherms (plot of sildenafil in solution, C vs. sildenafil sorbed in soil, q) which were nonlinear. The isotherms were fit using Freundlich model (q=KfCn, where Kf and n are fitting parameters). Sildenafil sorbed more strongly to clay-rich soils compared with organic-rich soils with less clay. It is hypothesized that permanent negative charge on clay mineral surfaces form ionic bonds with positively charged amines in sildenafil in acidic pHs. Transport experiments were conducted using

  5. Sorption kinetics of selected volatile organic compounds in humin.

    Science.gov (United States)

    Shih, Yang-Hsin; Wu, Shian-Chee

    2002-10-01

    Each component of the chemically heterogeneous soil exhibits a unique sorption behavior toward organic sorbates. The sorption kinetics of some volatile organic compounds (VOCs) in pressed humin disks was investigated by tracking the weight change of the disks with a microbalance. Higher sorbing capacity for more polar VOCs as well as C13 nuclear magnetic resonance data indicates that humin was more hydrophilic than Aldrich humic acid (Milwaukee, WI, USA). The apparent diffusivity of acetone, toluene, and hexane in the disks ranged from 10(-8) to 10(-10) cm2/s. The sorbed toluene in humin does not seem persistent to desorption; however, acetone and hexane, either as polar or linear compounds in humin, show persistence against desorption. On completion of the desorption experiments, there were approximately 35 and 20% sorbate residue for acetone and hexane, respectively.

  6. Sorption of radionuclides from Pb-Bi melt. Report 1

    International Nuclear Information System (INIS)

    Konovalov, Eh.E.; Il'icheva, N.S.; Trifonova, O.E.

    2015-01-01

    Results of laboratory investigations of sorption and interfacial distribution of 54 Mn, 59 Fe, 60 Co, 106 Ru, 125 Sb, 137 Cs, 144 Ce, 154,155 Eu and 235,238 U radionuclides in the system Pb-Bi melt - steel surface are analyzed. It is shown that 106 Ru and 125 Sb are concentrated in Pb-Bi melt and other radionuclides with higher oxygen affinity are sorbed on oxide deposits on structural materials. Temperature dependences of sorption efficiency of radionuclides are studied. It is shown that there is sharp increase of this value for all radionuclides near the temperature range 350-400 deg C. Recommendations are given on the use of 106 Ru and 125 Sb as a reference for fuel element rupture detection system with radiometric monitoring of coolant melt samples and 137 Cs, 134 Cs, 134m Cs with radiometric monitoring of sorbing samples [ru

  7. Uranium (Vi) sorption onto zirconium diphosphate chemically modified

    Energy Technology Data Exchange (ETDEWEB)

    Garcia G, N. [Universidad Autonoma del Estado de Mexico, Facultad de Quimica, Paseo Tollocan esquina Paseo Colon s/n, Toluca 50120, Estado de Mexico (Mexico); Ordonez R, E., E-mail: nidgg@yahoo.com.m [ININ, Carretera Mexico-Toluca s/n, Ocoyoacac 52750, Estado de Mexico (Mexico)

    2010-10-15

    This work deals with the uranium (Vi) speciation after sorption onto zirconium diphosphate (ZrP{sub 2}O{sub 7}) surface, hydrated and in a surface modified with organic acids. Oxalic and citric acids were chosen to modify the ZrP{sub 2}O{sub 7} surface because they have poly carboxylic groups and they mimic the organic matter in nature. Thus the interest of this work is to evaluate the uranium (Vi) sorption edge at different s ph values in natural and modified surfaces. The luminescence technique (fluorescence and phosphorescence, respectively) was used for the quantification and speciation of uranyl sorbed at the zirconium diphosphate interface. The fluorescence experiment, showed that adsorption of uranyl on surface of zirconium diphosphate tends to 100%. The speciation shows that there are different complexes in surface which were formed between zirconium diphosphate and uranyl, since it is produced a displacement of wavelength in fluorescence spectra of each system. (Author)

  8. Thermal and sorption behavior of polyacrylonitrile supported hydrous titanium dioxide

    International Nuclear Information System (INIS)

    Ali, I.M.; El-Zahhar, A.A.; Zakaria, E.S.

    2005-01-01

    Modification of the physico-chemical properties of hydrous titanium dioxide (TiO 2 ) was conducted by using binding polyacrylonitrile (PAN) for the preparation of larger size particles having higher granular strength. The thermal behavior of the obtained composite has been studied by thermogravimetric and differential thermal analysis (TG/DTA). Sorption behavior of the TiO 2 -PAN composite for removal of some hazardous radionuclides has been studied at different conditions such as, pH, contact time, ion concentrations and reaction temperature as well as the drying temperature. The effects of interfering ions as well as some complexing agents on the distribution ratio of the sorption process have been determined. As a result of the obtained data the optimum conditions for the removal of the studied radionuclides were recommended. (author)

  9. Dynamic design of gas sorption J-T refrigerator

    International Nuclear Information System (INIS)

    Chan, C.K.

    1986-01-01

    A long-life Joule-Thomson refrigerator which is heat powered, involves no sealing, and has few mechanical parts and is desirable for longterm sensor cooling in space. In the gas-sorption J-T refrigerator, cooling is achieved by gas sorption (either adsorption or absorption) processes. Currently, a modular, single-stage refrigerator is being designed and built to be operated at 20 K. The design was analyzed using a dynamic model, which is described here. The model includes the kinetics of the compressors and the heat switches, the heat transfer of the pre-coolers and the heat exchangers, the on/off ratio of the check valves, and the impedance of the J-T valve. The cooling power, the cycle time, and the operating conditions were obtained in terms of the power input, the heat sink temperature, and the J-T impedance

  10. Dynamic design of gas sorption J-T refrigerator

    Science.gov (United States)

    Chan, C. K.

    1986-01-01

    A long-life Joule-Thomson refrigerator which is heat powered, involves no sealing, and has few mechanical parts is desirable for long-term sensor cooling in space. In the gas-sorption J-T refrigerator, cooling is achieved by gas sorption (either adsorption or absorption) processes. Currently, a modular, single-stage refrigerator is being designed and built to be operated at 20 K. The design was analyzed using a dynamic model, which is described here. The model includes the kinetics of the compressors and the heat switches, the heat transfer of the pre-coolers and the heat exchangers, the on/off ratio of the check valves, and the impedance of the J-T valve. The cooling power, the cycle time, and the operating conditions were obtained in terms of the power input, the heat sink temperature, and the J-T impedance.

  11. Carbon dioxide sorption in a nanoporous octahedral molecular sieve

    Science.gov (United States)

    Williamson, Izaak; Nelson, Eric B.; Li, Lan

    2015-08-01

    We have performed first-principles density functional theory calculations, incorporated with van der Waals interactions, to study CO2 adsorption and diffusion in nanoporous solid—OMS-2 (Octahedral Molecular Sieve). We found the charge, type, and mobility of a cation, accommodated in a porous OMS-2 material for structural stability, can affect not only the OMS-2 structural features but also CO2 sorption performance. This paper targets K+, Na+, and Ba2+ cations. First-principles energetics and electronic structure calculations indicate that Ba2+ has the strongest interaction with the OMS-2 porous surface due to valence electrons donation to the OMS-2 and molecular orbital hybridization. However, the Ba-doped OMS-2 has the worst CO2 uptake capacity. We also found evidence of sorption hysteresis in the K- and Na-doped OMS-2 materials.

  12. Radionuclide sorption on low-exchange capacity Hanford site soils

    International Nuclear Information System (INIS)

    Routson, R.C.; Barney, G.S.; Smith, R.M.

    1984-01-01

    Trace Distribution Coefficients (Kd values) for 134 Cs, 85 Sr, and 60 Co sorption were found to be a function of sediment type (soil type) and of the solution concentration of macroions including NA + , K + , and Ca +2 over wide macroion concentration ranges. These Kd value functions are required as input sorption parameters to a mass transport model. Four methods were evaluated for measuring the Kd value macroion functional relationships for each sediment type. Precision, bias, and cost effectiveness were compared for choosing a preferred method. The prefered method, an empirical-statistical method (Box-Behnken method), was found to be as precise and unbiased as the other methods and the most cost effective. 12 references, 7 figures, 10 tables

  13. [The sorption of antisense oligodeoxyribonucleotides by Mycoplasma cells].

    Science.gov (United States)

    Egorov, O V; Panchenko, L P; Skripal', I G

    1996-01-01

    The paper deals with kinetics of binding of antisense oligodesoxyribonucleotides, complementary to certain sequences 16 S RNA of mollicutes, by the cells of three representatives of class Mollicutes: Acholeplasma laidlawii PG-8. Mycoplasma pneumoniae FH and M. fermentans PG-18. It is shown that binding of antisense oligonucleotides by the mollicute cells depends on temperature and age of cultures. The highest level of sorption of labelled antisense oligodesoxyribonucleotides by the cells of mycoplasmas corresponded to the phase of logarithmic growth of each of the studied mollicute strains. The lengthening of nucleotide chain from 5 to 15 nucleotide bases did not result in the decrease of sorption of the studied oligodesoxyribonucleotides by the mollicute cells.

  14. Sorption data base for performance assessment of radwaste repository

    International Nuclear Information System (INIS)

    Cho, Y.H.; Jung, J.; Lee, J.K.; Hahn, P.S.

    2001-01-01

    Sorption data base (SDB) provides readily available data for the performance assessment of radwaste repository when site-specific data are not available and/or more reference data are needed. The software developed in the Korea Atomic Energy Research Institute (KAERI), SDB-21C, is a graphic user interface (GUI) program that provides efficient and user friendly tools for evaluating the large amount of sorption data. The data base of distribution coefficients compiled in the program contains about 11,000 Nuclear Energy Agency (NEA) data and 2,000 KAERI data up to now while the addition of new data is under progress. Furthermore, the parametric model and its compiled data sets are also included in SDB-21C. (author)

  15. Semiconductor quantum optics with tailored photonic nanostructures

    Energy Technology Data Exchange (ETDEWEB)

    Laucht, Arne

    2011-06-15

    single photon emission into the waveguide. The results obtained during the course of this thesis contribute significantly to the understanding of coupling phenomena between excitons in self-assembled quantum dots and optical modes of tailored photonic nanostructures realized on the basis of two-dimensional photonic crystals. While we highlight the potential for advanced applications in the direction of quantum optics and quantum computation, we also identify some of the challenges which will need to be overcome on the way. (orig.)

  16. Tailoring aerogel electrodes for electrochemical applications

    Science.gov (United States)

    Sakamoto, Jeffrey Steven

    2001-07-01

    The principal theme of the dissertation research was determining the relation between aerogel electrode morphology and electrochemical performance. Issues such as electrical wiring and mass transport in transition metal oxide, aerogel electrodes were addressed and designs were tailored for electrochemical applications. Single-wall carbon nanotubes were used to form the electronically conducting network in lithium intercalation electrodes that incorporated vanadium oxide aerogel as the active material. The similarities in morphology and dimensional scale for the nanotubes and V2O5 ribbons enabled excellent electrical contact to be made between the two phases without seriously affecting the aerogel nanostructure. The electrodes exhibited specific capacities in excess of 400 mAh/g at high discharge rates and retained this level of capacity on cycling. A second research goal was to improve mass transport within the aerogel electrode by minimizing tortuosity. In this research, hierarchically ordered vanadium oxide aerogel electrodes were designed and fabricated. The electrodes have two discrete and independent levels or porosity. At one level, ordered, interconnected macropores were fabricated using the templating process. At another level, interconnected mesopores were created using sol-gel synthesis and ambient drying. Electrochemical activity towards lithium was demonstrated using cyclic voltammetry and chronopotentiometry. These data are believed to be the first to demonstrate electrochemical activity for the class of materials based on the inverse opal structure. Several Group I cations and multivalent cations were reversibly, and electrochemically reacted with vanadium oxide aerogel. The molar capacities of the Group I elements (Na+ = 3.0 moles and K+ = 2.0) were high and comparable to Li+ (3.6 moles). Interestingly, the electron equivalent capacity for Mg2+ (4.0) was higher than Li+ and agrees well with the chemical titration capacity. Galvanostatic rate

  17. Semiconductor quantum optics with tailored photonic nanostructures

    International Nuclear Information System (INIS)

    Laucht, Arne

    2011-01-01

    the understanding of coupling phenomena between excitons in self-assembled quantum dots and optical modes of tailored photonic nanostructures realized on the basis of two-dimensional photonic crystals. While we highlight the potential for advanced applications in the direction of quantum optics and quantum computation, we also identify some of the challenges which will need to be overcome on the way. (orig.)

  18. Detection of tritium sorption on four soil materials

    International Nuclear Information System (INIS)

    Teng Yanguo; Zuo Rui; Wang Jinsheng; Hu Qinhong; Sun Zongjian; Zeng Ni

    2011-01-01

    In order to measure groundwater age and design nuclear waste disposal sites, it is important to understand the sorption behavior of tritium on soils. In this study, batch tests were carried out using four soils from China: silty clays from An County and Jiangyou County in Sichuan Province, both of which could be considered candidate sites for Very Low Level Waste disposal; silty sand from Beijing; and loess from Yuci County in Shanxi Province, a typical Chinese loess region. The experimental results indicated that in these soil media, the distribution coefficient of tritium is slightly influenced by adsorption time, water/solid ratio, initial tritium specific activity, pH, and the content of humic and fulvic acids. The average distribution coefficient from all of these influencing factors was about 0.1-0.2 mL/g for the four types of soil samples. This relatively modest sorption of tritium in soils needs to be considered in fate and transport studies of tritium in the environment. - Research highlights: → In this study, batch sorption tests validate the adsorption of tritium on all of the four tested soil samples collected in China, and the distribution coefficient is found to be non-zero and less than 0.4 mL/g. The experimental results indicated that in these soil media, the distribution coefficient of tritium is slightly influenced by adsorption time, water/solid ratio, initial tritium specific activity, pH, and the content of humic and fulvic acids. This relatively modest sorption of tritium in soils needs to be considered in fate and transport studies of tritium in the environment.

  19. Selective Sorption of Dissolved Organic Carbon Compounds by Temperate Soils

    Science.gov (United States)

    Jagadamma, Sindhu; Mayes, Melanie A.; Phillips, Jana R.

    2012-01-01

    Background Physico-chemical sorption onto soil minerals is one of the major processes of dissolved organic carbon (OC) stabilization in deeper soils. The interaction of DOC on soil solids is related to the reactivity of soil minerals, the chemistry of sorbate functional groups, and the stability of sorbate to microbial degradation. This study was conducted to examine the sorption of diverse OC compounds (D-glucose, L-alanine, oxalic acid, salicylic acid, and sinapyl alcohol) on temperate climate soil orders (Mollisols, Ultisols and Alfisols). Methodology Equilibrium batch experiments were conducted using 0–100 mg C L−1 at a solid-solution ratio of 1∶60 for 48 hrs on natural soils and on soils sterilized by γ-irradiation. The maximum sorption capacity, Qmax and binding coefficient, k were calculated by fitting to the Langmuir model. Results Ultisols appeared to sorb more glucose, alanine, and salicylic acid than did Alfisols or Mollisols and the isotherms followed a non-linear pattern (higher k). Sterile experiments revealed that glucose and alanine were both readily degraded and/or incorporated into microbial biomass because the observed Qmax under sterile conditions decreased by 22–46% for glucose and 17–77% for alanine as compared to non-sterile conditions. Mollisols, in contrast, more readily reacted with oxalic acid (Qmax of 886 mg kg−1) and sinapyl alcohol (Qmax of 2031 mg kg−1), and no degradation was observed. The reactivity of Alfisols to DOC was intermediate to that of Ultisols and Mollisols, and degradation followed similar patterns as for Ultisols. Conclusion This study demonstrated that three common temperate soil orders experienced differential sorption and degradation of simple OC compounds, indicating that sorbate chemistry plays a significant role in the sorptive stabilization of DOC. PMID:23209742

  20. Effect of competing cations on strontium sorption to surficial sediments

    International Nuclear Information System (INIS)

    Bunde, R.L.; Rosentreter, J.J.

    1995-01-01

    The following study was conducted to determine strontium distribution coefficients (K d 'S) of a surficial sediment at the Idaho National Engineering Laboratory (INEL), Idaho. Batch experimental techniques were used to determine K d 's which describe the partitioning of a solute between the solution and solid phase. A surficial sediment was mixed with synthesized aqueous solutions designed to chemically simulate wastewater disposed to infiltrations ponds near the Idaho Chemical Processing Plant at the INEL with respect to major ionic character and pH. The effects of variable concentrations of competing cations (sodium, potassium, calcium and magnesium) on strontium sorption were investigated at a fixed pH of 8.00. The pH of the natural system shows no appreciable variation, whereas a marked variability in cation concentration has been noted. Strontium sorption was impacted to a greater degree by the concentration of calcium and magnesium in solution than by the presence of sodium or potassium. However, extreme sodium solution concentrations of 1.0 to 5.0 g/L dramatically reduced strontium sorption. In all cases, strontium K d 's decreased as the concentration of calcium and magnesium in solution increased. Linear isotherm model K d 's ranged from 12.0 to 84.7 mL/g. Analysis of data from these experiments indicated that moderate concentrations of calcium and magnesium (less than 40 mg/L) and high concentrations of sodium (1.0 to 5.0 g/L) in wastewater increase strontium mobility by decreasing the sorption of strontium on surficial sediments beneath infiltration ponds at the INEL

  1. Lead and cadmium sorption mechanisms on magnetically modified biochars

    Czech Academy of Sciences Publication Activity Database

    Trakal, L.; Veselská, V.; Šafařík, Ivo; Vítková, M.; Číhalová, S.; Komárek, M.

    2016-01-01

    Roč. 203, MAR (2016), s. 318-324 ISSN 0960-8524 R&D Projects: GA MŠk(CZ) LD14066 Institutional support: RVO:67179843 Keywords : pyrolysis bio-chars * aqueous-solutions * heavy-metals * removal * adsorption * water * contaminants * pb * temperatures * copper * Magnetic biochar * Fe oxide impregnation * Metal sorption * Cation release * Wastewater treatment Subject RIV: EI - Biotechnology ; Bionics Impact factor: 5.651, year: 2016

  2. Heat pipes and solid sorption transformations fundamentals and practical applications

    CERN Document Server

    Vasiliev, LL

    2013-01-01

    Developing clean energy and utilizing waste energy has become increasingly vital. Research targeting the advancement of thermally powered adsorption cooling technologies has progressed in the past few decades, and the awareness of fuel cells and thermally activated (heat pipe heat exchangers) adsorption systems using natural refrigerants and/or alternatives to hydrofluorocarbon-based refrigerants is becoming ever more important. Heat Pipes and Solid Sorption Transformations: Fundamentals and Practical Applications concentrates on state-of-the-art adsorption research and technologies for releva

  3. Pesticide sorption and leaching potential on three Hawaiian soils.

    Science.gov (United States)

    Hall, Kathleen E; Ray, Chittaranjan; Ki, Seo Jin; Spokas, Kurt A; Koskinen, William C

    2015-08-15

    On the Hawaiian Islands, groundwater is the principal source of potable water and contamination of this key resource by pesticides is of great concern. To evaluate the leaching potential of four weak acid herbicides [aminocyclopyrachlor, picloram, metsulfuron-methyl, biologically active diketonitrile degradate of isoxaflutole (DKN)] and two neutral non-ionizable herbicides [oxyfluorfen, alachlor], their sorption coefficients were determined on three prevalent soils from the island of Oahu. Metsulfuron-methyl, aminocylcopyrachlor, picloram, and DKN were relatively low sorbing herbicides (K(oc) = 3-53 mL g(-1)), alachlor was intermediate (K(oc) = 120-150 mL g(-1)), and oxyfluorfen sorbed very strongly to the three soils (K(oc) > 12,000 mL g(-1)). Following determination of K(oc) values, the groundwater ubiquity score (GUS) indices for these compounds were calculated to predicted their behavior with the Comprehensive Leaching Risk Assessment System (CLEARS; Tier-1 methodology for Hawaii). Metsulfuron-methyl, aminocyclopyrachlor, picloram, and DKN would be categorized as likely leachers in all three Hawaiian soils, indicating a high risk of groundwater contamination across the island of Oahu. In contrast, oxyfluorfen, regardless of the degradation rate, would possess a low and acceptable leaching risk due to its high sorption on all three soils. The leaching potential of alachlor was more difficult to classify, with a GUS value between 1.8 and 2.8. In addition, four different biochar amendments to these soils did not significantly alter their sorption capacities for aminocyclopyrachlor, indicating a relatively low impact of black carbon additions from geologic volcanic inputs of black carbon. Due to the fact that pesticide environmental risks are chiefly dependent on local soil characteristics, this work has demonstrated that once soil specific sorption parameters are known one can assess the potential pesticide leaching risks. Published by Elsevier Ltd.

  4. Surface complexation model of uranyl sorption on Georgia kaolinite

    Science.gov (United States)

    Payne, T.E.; Davis, J.A.; Lumpkin, G.R.; Chisari, R.; Waite, T.D.

    2004-01-01

    The adsorption of uranyl on standard Georgia kaolinites (KGa-1 and KGa-1B) was studied as a function of pH (3-10), total U (1 and 10 ??mol/l), and mass loading of clay (4 and 40 g/l). The uptake of uranyl in air-equilibrated systems increased with pH and reached a maximum in the near-neutral pH range. At higher pH values, the sorption decreased due to the presence of aqueous uranyl carbonate complexes. One kaolinite sample was examined after the uranyl uptake experiments by transmission electron microscopy (TEM), using energy dispersive X-ray spectroscopy (EDS) to determine the U content. It was found that uranium was preferentially adsorbed by Ti-rich impurity phases (predominantly anatase), which are present in the kaolinite samples. Uranyl sorption on the Georgia kaolinites was simulated with U sorption reactions on both titanol and aluminol sites, using a simple non-electrostatic surface complexation model (SCM). The relative amounts of U-binding >TiOH and >AlOH sites were estimated from the TEM/EDS results. A ternary uranyl carbonate complex on the titanol site improved the fit to the experimental data in the higher pH range. The final model contained only three optimised log K values, and was able to simulate adsorption data across a wide range of experimental conditions. The >TiOH (anatase) sites appear to play an important role in retaining U at low uranyl concentrations. As kaolinite often contains trace TiO2, its presence may need to be taken into account when modelling the results of sorption experiments with radionuclides or trace metals on kaolinite. ?? 2004 Elsevier B.V. All rights reserved.

  5. An Investigation of Chitosan for Sorption of Radionuclides

    Science.gov (United States)

    2012-06-05

    heavy metals, uranium and other actinides , and the rare earths. Alkali and alkaline earth metals have received little attention due to their low...15]. The importance and role of metal hydrolysis on biomass sorption has also been addressed by Gadd and White, for the case of 14 actinides , which are...biopolymers. Biologi- cal Trace Element Research 2002, 86, 227–36. [35] Ishikawa, S.; Suyama, K Biosorption of actinides from dilute waste actinide so

  6. Research of Oil Product Sorption Processes by Ferromagnetic Sorbents

    OpenAIRE

    Mironovs, Viktors; Treijs, Juris; Teirumnieks, Edmunds

    2015-01-01

    In paper, is given overview of sorbents with ferromagnetic particles. The series of newly designed composite sorbents SOMSOR, are described. Described experiment of oil spill collection from water surface, which comprises of sorbent spreading and collection. Oil sorption by capillary forces, is discussed. Concluded that use of ferromagnetic sorbents a promising direction in the field of water purification from light oil products since it allows expanding the scope of the used powder sorbents,...

  7. Analysis of factors influencing Cu(II sorption by clinoptiolite

    Directory of Open Access Journals (Sweden)

    Šljivić-Ivanović Marija Z.

    2013-01-01

    Full Text Available Experimental design methodology represents a powerful tool for the analysis and optimization of various processes. Immobilization of toxic substances by sorption onto low-cost materials gained a lot of attention in the last decade. Fundamental knowledge about sorption processes and their practical use can be improved by experimental planning and statistical analysis. In this study, the effects of initial metal concentration and pH, as well as the sorbent mass and particle size, on Cu(II sorption by natural clinoptilolite were evaluated and compared. Full factorial experimental design at two levels was applied. Statistically significant factors were determined considering residual Cu(II concentrations as a system response. The Pareto graphs of standardized effects, Main effect plots and Interaction plots were created using statistical software. Initial sorbate concentration, sorbent mass and their interaction were recognized as statistically significant, at 95 % confidence level. Main effect plot approved that sorbent mass increase and initial Cu(II concentration decrease caused reduction of residual Cu(II concentration in solution. On the other hand, the change of initial solution pH and sorbent particle size didn’t provoke significant response changes. Bearing in mind that pH is the factor with large effect on heavy metal sorption, insignificant influence of initial pH detected in this study can be explained by buffering properties of the applied clinoptilolite and relatively narrow pH range chosen in order to prevent sorbent dissolution on one side and sorbate precipitation on the other. By regression analysis, the mathematical model for process description was derived. The correlation between predicted and experimental values was high (R2>0.99. In the investigated ranges of parameters, the obtained empirical equation can be applied for the prediction of system response.

  8. Technetium-99 toxicity to plants and sorption by soils

    International Nuclear Information System (INIS)

    Gast, R.G.; Thorvig, L.H.; Landa, E.R.; Gallagher, K.J.

    1978-01-01

    The potential toxic effects of 99 Tc on germinating seeds and young seedlings of wheat (Triticum aestivum L.), barley (Hordeum vulgare L.), oats (Avena sativa L.), radishes (Raphanus sativus L.), soybeans (Glycine max L.), and corn (Zea mays L.) were studied by germinating and growing seedlings in 50 ml of one-third to one-half strength Hoagland solution containing increasing 99 Tc concentrations. All species showed shoot and root tissue yield reductions at low 99 Tc concentrations, with greatest yield reductions for the three small grains and radishes occurring below 2.5 μCi 99 Tc/50 ml solution or 3.0 μg Tc/ml. The greatest yield reductions for soybeans and corn occurred at higher 99 Tc concentrations in solution but at comparable concentrations in tissue. Significant yield reductions in wheat seedlings occurred after post-germination additions of 99 Tc. This indicates that seedlings are sensitive to 99 Tc toxicity at later stages of growth. Wheat plants grown to maturity in soils to which 99 Tc was added 7, 17, and 33 days after planting showed much greater 99 Tc concentrations in older than in newer leaves; concentrations in seeds were 40 to 80 times less than those in vegetative tissue. Results for 99 Tc sorption on four different samples of Nicollet (Aquic Hapludoll) and Bergland (Aeric Haplaquept) soils showed little sorption by the Nicollet soils. In contrast, all Bergland samples showed significant but variable sorption rates. Although there were some differences in the chemical and physical properties of the Bergland samples, it is difficult to correlate these differences with differences in their 99 Tc sorption properties

  9. Sorption of heavy metals on lignite impregnated with chitosan

    Czech Academy of Sciences Publication Activity Database

    Havelcová, Martina; Mizera, Jiří; Machovič, V.; Borecká, Lenka; Přibyl, Oldřich; Krausová, Ivana

    2013-01-01

    Roč. 10, č. 1 (2013), s. 105-110 ISSN 1214-9705 R&D Projects: GA ČR(CZ) GBP108/12/G108 Institutional support: RVO:67985891 ; RVO:61389005 Keywords : lignite * chitosan * heavy metal s * sorption Subject RIV: DJ - Water Pollution ; Quality Impact factor: 0.667, year: 2013 http://www.irsm.cas.cz/index_en.php?page=acta_detail_doi&id=19

  10. U(VI) sorption on granite: prediction and experiments

    International Nuclear Information System (INIS)

    Nebelung, C.; Brendler, V.

    2010-01-01

    One widely accepted approach - component additivity (CA) - to describe the sorption of contaminants onto complex materials such as rocks or soils is based on the assumption that the surface of a complex mineral assemblage is composed of a mixture of mineral constituents whose surface properties are known from independent studies. An internally consistent SCM (surface complexation model) database can be developed that describes the adsorption reactions of solutes to each phase. Here, the capability of such a methodology was tested, using the code MINTEQA2 including thermodynamic data of the NEA-TDB, and literature data for SCM, namely the DDL model. The sorption characteristics of U(VI) on granite (from Eibenstock, Saxony, Germany, with the main components quartz, albite, orthoclase, and muscovite) was predicted and then compared to batch experiments. Granite plays an important role in the remediation of former uranium ore mining and milling sites, but is also one of the host rocks considered for final disposal of nuclear materials. Safety assessment requires a detailed understanding of this system and its retention potential with regard to hazardous components. Namely the sorption of uranium in this complex rock is not fully understood yet. The experiments thus also provided a better understanding of the far-field behaviour in granitic geological nuclear repositories. The robustness of the prediction was tested by variation of the granite composition and the variation of the specific surface area (SSA) - first all components were predicted with a uniform granite SSA, second with a distinct SSA for each granite component (determined on pure minerals for the same grain size fractions). Changes in compositions yielded only marginal differences in the prediction. Different approaches to SSA showed somewhat larger deviations. In conclusion, the CA methodology is a valid and robust approach to U(VI) sorption onto complex substrates such as granite, provided sufficient

  11. Experience of Implementing Moisture Sorption Control in Historical Archives

    Directory of Open Access Journals (Sweden)

    P. Zítek

    2006-01-01

    Full Text Available This paper deals with a novel approach to inhibiting the harmful impact of moisture sorption in old art works and historical exhibits preserved in remote historic buildings that are in use as depositories or exhibition rooms for cultural heritage collections. It is a sequel to the previous work presented in [2], where the principle of moisture sorption stabilization was explained. Sorption isotherm investigations and EMC control implementation in historical buildings not provided with heating are the main concern in this paper. The proposed microclimate adjustment consists in leaving the interior temperature to run almost its spontaneous yearly cycle, while the air humidity is maintained in a specific relationship to the current interior temperature. The interior air humidity is modestly adjusted to protect historical exhibits and art works from harmful variations in the content of absorbed moisture, which would otherwise arise owing to the interior temperature drifts. Since direct measurements of moisture content are not feasible, the air humidity is controlled via a model-based principle. Two long-term implementations of the proposed microclimate control have already proved that it can permanently maintain a constant moisture content in the preserved exhibits. 

  12. Hollow fiber adsorbents for CO2 capture: Kinetic sorption performance

    KAUST Repository

    Lively, Ryan P.

    2011-07-01

    We describe a CO 2 capture platform based on hollow polymeric fibers with sorbent particles embedded in the porous fiber wall for post-combustion CO 2 capture. These fibers are intended for use in a rapid temperature swing adsorption (RTSA) process. The RTSA system utilizes the hollow fiber morphology by flowing cooling water on the bore-side of the fibers during sorption to prevent temperature rise associated with the sorption enthalpy. Steam or hot water is flowed through the bores during desorption to desorb CO 2 rapidly. To minimize material transfer between the bore and the fiber wall, a dense Neoprene ® lumen layer is cast on the bore-side of the fiber wall. In this paper, the key sorption step and associated kinetic resistances for the uncooled fibers are examined and evaluated for this portion of the RTSA process. Chopped fibers in a packed bed, as well as fibers assembled into a parallel flow module, have been tested in a simulated flue gas stream. Kinetic limitations in the hollow fiber modules are largely overcome by increasing the superficial gas velocity and the fiber packing in the module-indicating that film diffusion is the controlling mass transfer limitation in the fiber system. The un-cooled fiber modules lose apparent capacity as superficial velocities are increased, likely indicating non-isothermal operation, whereas the actively-cooled fibers in the packed bed maintain apparent capacity at all flowrates studied. © 2011 Elsevier B.V.

  13. Sorption and biodegradation of artificial sweeteners in activated sludge processes.

    Science.gov (United States)

    Tran, Ngoc Han; Gan, Jie; Nguyen, Viet Tung; Chen, Huiting; You, Luhua; Duarah, Ankur; Zhang, Lifeng; Gin, Karina Yew-Hoong

    2015-12-01

    There is limited information on the occurrence and removal of artificial sweeteners (ASs) in biological wastewater treatment plants, and in particular, the contribution of sorption and biodegradation to their removal. This study investigated the fate of ASs in both the aqueous and solid phases in a water reclamation plant (WRP). All the four targeted ASs, i.e. acesulfame (ACE), sucralose (SUC), cyclamate (CYC) and saccharine (SAC), were detected in both the aqueous and solid phases of raw influent and primary effluent samples. The concentrations of CYC and SAC in secondary effluent or MBR permeate were below their method detection limits. ACE and SUC were persistent throughout the WRP, whereas CYC and SAC were completely removed in biological treatment (>99%). Experimental results showed that sorption played a minor role in the elimination of the ASs due to the relatively low sorption coefficients (Kd), where Kd<500L/kg. In particular, the poor removal of ACE and SUC in the WRP may be attributed to their physiochemical properties (i.e. logKow<0 or logD<3.2) and chemical structures containing strong withdrawing electron functional groups in heterocyclic rings (i.e. chloride and sulfonate). Copyright © 2015 Elsevier Ltd. All rights reserved.

  14. Experimental and theoretical study of Co sorption in clay montmorillonites

    Science.gov (United States)

    Gil Rebaza, A. V.; Montes, M. L.; Taylor, M. A.; Errico, L. A.; Alonso, R. E.

    2018-03-01

    Montmorillonite (MMT) clays are 2:1 layered structures which in natural state may allocate different hydrated cations such as M-nH2O (M = Na, Ca, Fe, etc) in its interlayer space. Depending on the capability for ion sorption, these materials are interesting for environmental remediation. In this work we experimentally study the Co sorption in a natural Na-MMT using UV-visible spectrometry and XRD on semi-oriented samples, and then analyze the sorption ability of this clay by means of ab initio calculation performed on pristine MMT. The structural properties of Na-MMT and Co-adsorbed MMT, and the hyperfine parameters at different atomic sites were analyzed and compared with the experimental ones for the first, and for the case of the hyperfine parameters, presented for the first time for the last. The theoretical predictions based on total energy considerations confirm that Co incorporation replacing Na is energetically favorable. Also, the basal spacing d001 experimentally obtained is well reproduced.

  15. Sorption of Organophosphorus Flame-Retardants on Settled ...

    Science.gov (United States)

    Dust is an important sink for indoor air pollutants, such as organophosphorus flame-retardants (OPFRs) that are used as additives in industrial and consumer products including electrical and electronic products, furniture, plastics, textile, and building/construction materials. This research investigated the sorption of OPFRs, tris(2-chloroethyl) phosphate (TCEP), tris(1-chlor-2-propyl) phosphate (TCPP), and tris(1,3-dichloro-2-propyl) phosphate (TDCPP) on settled Arizona Test Dust (ATD) using a dual small chamber system. During the test, seven free film release paper dust trays covered with ATD were placed in the sink test chamber. Constant gas phase OPFRs from the source chamber were dosed into the test chamber. The dust evenly spread on each dust tray was removed from the test chamber at different exposure times to determine the amount of OPFRs absorbed by the dust. The ATD has been characterized for a nominal particle size and surface area. The mass of dust on each of seven dust trays was weighed before the dust was placed inside the sink chamber. OPFRs concentrations at the inlet and faceplate of the test chamber were monitored by collecting polyurethane foam (PUF) samples. The OPFR exposed dust and PUF samples were extracted by 1:1 ethyl acetate/methylene chloride and analyzed on GC/MS. The data were used to calculate the OPFR sorption concentration on the dust through dust/air partition. Settled dust can adsorb OPFR from air. The sorption concentration wa

  16. Sorption-desorption dynamics of radiocaesium in organic matter soils

    International Nuclear Information System (INIS)

    Valcke, E.; Cremers, A.

    1994-01-01

    A systematic study has been carried out on the radiocaesium sorption properties of 25 soils (forest, peat) covering organic matter (OM) contents in the range of 10-97%. Predictions are made for radiocaesium partitioning between micaceous Frayed Edge Sites (FES) and regular exchange sites (RES) on the basis of specific radiocaesium interception potentials of the soil and overall exchange capacity. It is shown that for soils with a very high OM content (>80%), significant fractions are present in a readily reversible form in the OM phase. In soils of low-medium OM content (<40%), only a very minor fraction is present in the OM exchange complex. Experimental findings, based on a desorption screening with a variety of desorption agents are in agreement with these predictions. On the basis of a study of sorption kinetics, some additional tools are available for identifying problem soils. In cases of very high OM content, radiocaesium adsorption is completed within hours demonstrating the involvement of the OM sites. In soils for which interception occurs in the FES, sorption continues to proceed for periods of 2-3 weeks. In conclusion, some examples are presented on radiocaesium desorption using ion exchangers as radiocaesium sinks in promoting desorption. For a peaty soil, near quantitative desorption is accomplished. For forest soils with OM contents in a range of 10-40%, fixation levels of 30-50% are demonstrated

  17. A FIXED BED SORPTION SYSTEM FOR DEFLUORIDATION OF GROUND WATER

    Directory of Open Access Journals (Sweden)

    Ayoob Sulaiman

    2009-06-01

    Full Text Available The presence of excess fluoride in ground water has become a global threat with as many as 200 million people affected in more than 35 countries in all the continents. Of late, there have been significant advances in the knowledge base regarding the effects of excess fluoride on human health. As a result, defluoridation of ground water is regarded as one of the key areas of attention among the universal water community triggering global research. This study describes the sorptive responses of a newly developed adsorbent, alumina cement granules (ALC, in its real-life application in fixed beds, for removing fluoride from the ground waters of a rural Indian village. ALC exhibited almost consistent scavenging capacity at various bed depths in column studies with an enhanced adsorption potential of 0.818 mg/g at a flow rate of 4 ml/min. The Thomas model was examined to describe the sorption process. The process design parameters of the column were obtained by linear regression of the model. In all the conditions examined, the Thomas model could consistently predict its characteristic parameters and describe the breakthrough sorption profiles in the whole range of sorption process.

  18. APPLICATION OF MEMBRANE SORPTION REACTOR TECHNOLOGY FOR LRW MANAGEMENT

    International Nuclear Information System (INIS)

    Glagolenko, Yuri; Dzekun, Evgeny; Myasoedovg, Boris; Gelis, Vladimir; Kozlitin, Evgeny; Milyutin, Vitaly; Trusov, Lev; Rengel, Mike; Mackay, Stewart M.; Johnson, Michael E.

    2003-01-01

    A new membrane-sorption technology has been recently developed and industrially implemented in Russia for the treatment of the Liquid (Low-Level) Radioactive Waste (LRW). The first step of the technology is a precipitation of the radionuclides and/or their adsorption onto sorbents of small particle size. The second step is filtration of the precipitate/sorbent through the metal-ceramic membrane, Trumem.. The unique feature of the technology is a Membrane-Sorption Reactor (MSR), in which the precipitation / sorption and the filtration of the radionuclides occur simultaneously, in one stage. This results in high efficiency, high productivity and compactness of the equipment, which are the obvious advantages of the developed technology. Two types of MSR based on Flat Membranes device and Centrifugal Membrane device were developed. The advantages and disadvantages of application of each type of the reactors are discussed. The MSR technology has been extensively tested and efficiently implemented at ''Mayak '' nuclear facility near Chelyabinsk, Russia as well as at other Russian sites. The results of this and other applications of the MSR technology at the different Russian nuclear facilities are discussed. The results of the first industrial applications of the MSR technology for radioactive waste treatment in Russia and analysis of the available information about LRW accumulated in other countries imply that this technology can be successfully used for the Low Level Radioactive Waste treatment in the USA and in other nuclear countries

  19. Kinetic modeling of water sorption by roasted and ground coffee

    Directory of Open Access Journals (Sweden)

    Fernanda Machado Baptestini

    2017-05-01

    Full Text Available The objective of this study was to model the kinetics of water sorption in roasted and ground coffee. Crude Arabica coffee beans with an initial moisture content of 0.1234 kgwkgdm-1 were used. These beans were roasted to a medium roast level (SCCA # 55 and ground at three particle sizes: coarse (1.19 mm, medium (0.84 mm and fine (0.59 mm. To obtain the water sorption isotherms and the isosteric heat, different conditions of temperature and relative humidity were analyzed using the dynamic method at 25ºC (0.50, 0.60, 0.70, and 0.80 of RH and 30°C (0.30, 0.40, 0.50, 0.60, 0.70, and 0.80 of RH and using the static method at 25ºC (0.332 and 0.438 of RH. The GAB model best represented the hygroscopic equilibrium of roasted coffee at every particle size. Isosteric heat of sorption for the fine particle size increased with increments of equilibrium moisture content, indicating a strong bond energy between water molecules and the product components. The Gibbs free energy decreased with the increase in equilibrium moisture content and with temperature.

  20. Molecular tailoring approach for exploring structures, energetics and ...

    Indian Academy of Sciences (India)

    Keywords. Molecular clusters; linear scaling methods; molecular tailoring approach (MTA); Hartree-Fock (HF) method; density functional theory (DFT); Møller-Plesset second order (MP2) method; molecular electron density (MED); molecular electrostatic potential.

  1. Building Tailorable Hypermedia Systems: The embedded-interpreter approach

    DEFF Research Database (Denmark)

    Grønbæk, Kaj; Malhotra, Jawahar

    1994-01-01

    This paper discusses an approach for developing dynamically tailorable hypermedia systems in an object-oriented environment. The approach is aimed at making applications developed in compiled languages like Beta and C++ tailorable at run-time. The approach is based on use of: 1) a hypermedia......-store, a solution for handling persistent interpreted objects is presented. Finally, the approach is compared with other environments supporting tailoring.......-type. The paper describes the framework and illustrates how the interpreter is integrated. It describes steps involved in tailoring a specific hypermedia system with a new drawing media-type, where graphical objects can be endpoints for links. Since the hypermedia framework uses a persistent object...

  2. Past, present, and future of computer-tailored nutrition education

    NARCIS (Netherlands)

    J. Brug (Hans); A. Oenema (Anke); M.K. Campbell (Marci)

    2003-01-01

    textabstractComputer-tailored nutrition education is an innovative and promising tool to motivate people to make healthy dietary changes. It provides respondents with individualized feedback about their dietary behaviors, motivations, attitudes, norms, and skills and mimics the

  3. Can Deterrence Be Tailored? Strategic Forum, Number 225, January 2007

    National Research Council Canada - National Science Library

    Bunn, M. E

    2007-01-01

    .... The Bush administration has outlined a concept for tailored deterrence to address the distinctive challenges posed by advanced military competitors, regional powers armed with weapons of mass destruction (WMD...

  4. CO2 sorption on surface-modified carbonaceous support: Probing the influence of the carbon black microporosity and surface polarity

    International Nuclear Information System (INIS)

    Gargiulo, Valentina; Alfè, Michela; Ammendola, Paola; Raganati, Federica; Chirone, Riccardo

    2016-01-01

    Graphical abstract: - Highlights: • CO 2 -sorbent materials preparation by surface modification of CB. • CB functionalization (amino-groups), CB coating (Fe 3 O 4 ), CB impregnation (ionic liquid). • Sorbents bearing basic functionalities exhibit the higher CO 2 sorption capacity. • Microporous supporting material limits the CO 2 accessibility toward the adsorbing material. - Abstract: The use of solid sorbents is a convenient option in post-combustion CO 2 capture strategies. Sorbents selection is a key point because the materials are required to be both low-cost and versatile in typical post-combustion conditions in order to guarantee an economically advantageous overall process. This work compares strategies to tailor the chemico-physical features of carbon black (CB) by surface-modification and/or coating with a CO 2 -sorbent phase. The influence of the CB microporosity, enhanced by chemical/thermal treatments, is also taken into account. Three CB surface modifications are performed and compared: (i) oxidation and functionalization with amino-groups, (ii) coating with iron oxides and (iii) impregnation with an ionic liquid (IL). The CO 2 capture performance is evaluated on the basis of the breakthrough curves measured at atmospheric pressure and room temperature in a lab-scale fixed bed micro-reactor. Most of tested solids adsorb a CO 2 amount significantly higher than a 13X zeolite and DARCO FGD (Norit) activated carbon (up to 4 times more in the best case). The sorbents bearing basic functionalities (amino-groups and IL) exhibit the highest CO 2 sorption capacity. The use of a microporous carbonaceous support limits the accessibility of CO 2 toward the adsorbing phase (IL or FM) lowering the number of accessible binding sites for CO 2 .

  5. Tailored Health Communication: Crafting the Patient Message for HIV TIPS

    Science.gov (United States)

    Merrill, Jacqueline; Kukafka, Rita; Bakken, Suzanne; Ferat, Rachel; Agopian, Eliz; Messeri, Peter

    2003-01-01

    The HIV TIPS project will pilot and evaluate the use of web-based information technology on prescription errors and quality of care by providing tailored practice guidelines and patient education in ambulatory practice settings of the National AIDS Education and Training Centers (NAETC) network. In the first phase of the project, we tailored messages to guide patient adherence and self-care, using DHHS guidelines. We developed a method based on communication theory to ensure complete and effective messages. PMID:14728437

  6. Low-loss and bendable THz fiber with tailored dispersion

    DEFF Research Database (Denmark)

    Nielsen, Kristian; Rasmussen, Henrik K.; Adam, Aurèle J. L.

    2009-01-01

    A polymer THz fiber made of Topas and having a Photonic Crystal Fiber structure is demonstrated. It has low broadband loss and the dispersion of the fiber can be tailored by adjusting the structural parameters.......A polymer THz fiber made of Topas and having a Photonic Crystal Fiber structure is demonstrated. It has low broadband loss and the dispersion of the fiber can be tailored by adjusting the structural parameters....

  7. Sorption of chromium(VI) and chromium(III) on aluminium hydroxide

    International Nuclear Information System (INIS)

    Music, S.

    1986-01-01

    Factors that influence the sorption of Cr(VI) and Cr(III) on aluminium hydroxide were investigated. The sorption of chromates decreases as the pH of the suspension increases. The mechanism of CrOsub(4)sup(2-) sorption was interpreted in terms of reactions between chromates and -OH and/or Hsub(2)O groups at the hydroxide/liquid interface. It was shown that chromates are more tightly sorbed on aluminium hydroxide compared to other anions, e.g. chlorides. On the other hand, specifically absorbed anions, such as molybdates, compete strongly with chromates for the sorption sites. The sorption of chromium(III) increases with the pH of the suspension. Also, the sorption of chromium(III) is suppressed in the presence of citrate ions. The best conditions for the fixation of Cr(VI) and Cr(III) by aluminium hydroxide are presented. (author)

  8. Effects of mineralogy on the sorption of strontium and cesium onto Calico Hills tuff

    International Nuclear Information System (INIS)

    Meyer, R.E.; Arnold, W.D.; Case, F.I.; O'Kelley, G.D.; Land, J.F.

    1990-01-01

    Sorption and desorption measurements were made of strontium and cesium onto clinoptilolite and Calico Hills Tuff. The object was to see whether there was a correlation between sorption of strontium and cesium onto Calico Hills Tuff and the clinoptilolite based on the content of clinoptilolite in the Calico Hills Tuff. If sorption onto Calico Hills Tuff is solely due to the presence of clinoptilolite, then the ratios of the sorption ratios on tuff to those on clinoptilolite at similar conditions should be the weight fraction of the clinoptilolite in the tuff. The experimental evidence showed that the ratios were generally near 0.5 for both cesium and strontium sorption and that ion-exchange processes were operative for the clinoptilolite and the tuff. However, the ratios differed to a small extent for different conditions, and there were indications that other sorption processes were also involved. 7 refs., 7 figs., 2 tabs

  9. The sorption and mechanical properties of the modified cement matrix used for conditioning of radioactive waste

    International Nuclear Information System (INIS)

    Dogaru, Daniela; Nuculae, Ortenzia; Jinescu, Gheorghita; Duliu, Octavian; Dogaru, Gheorghe

    2008-01-01

    Full text: Radioactive contaminant sorption onto concrete represents one of the most important retardation mechanisms in engineered barriers such as the conditioning matrix itself, concrete walls and concrete floors. During the life of a disposal facility for radioactive waste, the sorption properties as well as the mechanical properties of the cement are affected by both external and internal processes. The most important sorbing material present in concrete is the hydrated cement. The sorption data obtained for specific cement or cement mixes in general may be used to characterize a given cement type. In order to improve the mechanical and sorption properties of the cement matrix, different additives were used in the laboratory tests. The used additives are known to have good sorption properties. The paper describes the influence of the concentration of additives on the mechanical and sorption properties of the cement matrix. As radioactive contaminants 134 Cs, 60 Co, 3 H, 241 Am were used. (authors)

  10. Concurrent Co2+ and Sr2+ sorption from binary mixtures using aluminum industry waste: Kinetic study

    Science.gov (United States)

    Milenković, A.; Smičiklas, I.; Šljivić-Ivanović, M.; Vukelić, N.

    2015-12-01

    Multi-component sorption studies are essential to identify the applicability of red mud as a lowcost sorbent for the simultaneous removal of metal ions from wastewaters. Sorption kinetics of Co2+ and Sr2+ ions was investigated, at different total concentrations of mixtures and different molar ratios of two cations. Kinetics of metal sorption from binary systems was found to be well described by pseudo-second order rate model. Equilibrium sorbed amounts and equilibrium times for Co2+ sorption increased with the increase of its total concentration in the mixture, whereas pseudo-second order rate constants exhibited the opposite trend. Sr2+ sorption was strongly suppressed in the presence of Co2+ ions, and the removal efficiency decreased with increasing concentration and mole fraction of Co2+. Red mud can be used for simultaneous Co2+ and Sr2+ removal from mixtures of lower initial concentration, otherwise Co2+ sorption is dominant.

  11. Technetium Sorption by Cementitious Materials Under Reducing Conditions

    Energy Technology Data Exchange (ETDEWEB)

    Kaplan, Daniel I. [Savannah River Site (SRS), Aiken, SC (United States); Estes, Shanna L. [Environmental Engineering and Earth Sciences, Clemson University, Clemson, SC (United States); Powell, Brian A. [Environmental Engineering and Earth Sciences, Clemson University, Clemson, SC (United States)

    2012-09-28

    The objective of this study was to measure technetium ({sup 99}Tc) sorption to cementitious materials under reducing conditions to simulate Saltstone Disposal Facility conditions. {sup 99}Tc(VII) batch sorption experiments were conducted for 319 days in an inert glovebag with a variety of cementitious materials (aged cement, Vault 2, TR545, and TR547) containing varying amounts of blast furnace slag. Between 154 and 319 days, the {sup 99}Tc aqueous concentrations tended to remain constant and samples amended with different initial {sup 99}Tc concentrations, tended to merge at about 10{sup -9} M for Vault 2 (17% slag) and TR545 (90% slag) and 10{sup -8} M for TR547 (45% slag). This data provided strong evidence that solubility, and not adsorption (K{sub d} values), was controlling aqueous {sup 99}Tc concentrations. Laboratory data superimposed over thermodynamic speciation diagrams further supported the conclusion that solubility, and not adsorption controlled {sup 99}Tc aqueous concentrations. The oxidation state of the aqueous {sup 99}Tc at the end of the sorption experiment was determined by solvent extraction to be almost entirely {sup 99}Tc(VII). The pH of the present system was ~11.8. Previously proposed solubility controlling phases including Tc-sulfides may be present, but do not appear to control solubility. After the 319 day sorption period, the suspensions were removed from the glovebag and a desorption step under oxic conditions was conducted for 20 days by adding oxic, pH-buffered solutions to the suspensions. {sup 99}Tc aqueous concentrations increased by more than an order of magnitude and Eh increased by several hundred millivolts within 24 hours after the introduction of the oxic solutions. These desorption results are consistent with re-oxidation and dissolution/desorption of {sup 99}Tc(IV) phases possibly present in the cementitious materials after the anoxic sorption step of the experiment. Aqueous {sup 99}Tc concentrations continued to increase

  12. Pollution and pollution tolerance as regards the sorption of organic chemicals in urban soils; Sorption organischer Chemikalien

    Energy Technology Data Exchange (ETDEWEB)

    Blume, H.P.; Wu Qinglan; Strehl, M. [Kiel Univ. (Germany). Inst. fuer Pflanzenernaehrung und Bodenkunde; Abend, S. [Kiel Univ. (Germany). Inst. fuer Anorganische Chemie; Rexilius, L. [Pflanzenschutzamt des Landes Schleswig-Holstein, Kiel (Germany); Schleuss, U. [Kiel Univ. (Germany). Oekologie-Zentrum]|[Zentrum fuer Agrarlandschafts- und Landnutzungsforschung Muencheberg (Germany)

    1997-12-31

    The behaviour of pollutants in soils concerning, for example, their immobilisation, transport, biodegradation, or uptake by useful plants is to large degree determined by the sorption properties of the soil in question. The degree of sorption is an all-important parameter in any model description of the behaviour of pollutants in soils. The aim of the present part-project was to estimate by means of simple field methods the binding capacity of anthropogenic urban soils for environmentally consequential organic chemicals and to assess the results with regard to soil and water protection. [Deutsch] Das Verhalten von Schadstoffen in Boeden, wie z.B. Immobilisierung, Transport, biologischer Abbau, Aufnahme durch Kulturpflanzen, wird von den Sorptionseigenschaften im Boden wesentlich beeinflusst. Bei allen Modellbeschreibungen ueber das Verhalten von Schadstoffen in Boeden ist die Staerke der Sorption ein unersetzbarer Parameter. Ziel dieses Teilprojektes war es, das Bindungsvermoegen der anthropogenen Stadtboeden fuer umweltrelevante organische Chemikalien mittels einfacher Feldmethoden abzuschaetzen und im Hinblick auf Boden- und Gewaesserschutz zu bewerten. (orig./SR)

  13. Plutonium-239 sorption and transport on/in unsaturated sediments. Comparison of batch and column experiments for determining sorption coefficients

    International Nuclear Information System (INIS)

    Jinchuan Xie; Jiachun Lu; Xiaohua Zhou; Xuhui Wang; Mei Li; Lili Du; Yueheng Liu; Guoqing Zhou

    2013-01-01

    Sorption (distribution) coefficients of plutonium were most often derived by static batch experiments. However, it is not clear how unsaturated flow conditions including moisture content and pore water velocity change the sorption coefficients. Transport experiments of plutonium through the unsaturated sediments packed into the columns were then performed in order to determine the sorption coefficients (column-K ds ). Static batch experiments were also conducted to obtain batch-K ds and then compare the differences between batch-K ds and column-K ds . The results show that unsaturated flow conditions had no significant effect on column-K ds , and the average column-K d value was 1.74 ± 0.02 m 3 /kg. By comparison, batch-K d values spanned several orders of magnitude, regardless of the specified liquid-solid conditions. Moreover, the batch-K d (22.7 m 3 /kg) at the standard L/S (4 mL/g) recommended by ASTM D 4319 was over an order of magnitude larger than the average column-K d . (author)

  14. Preparation of pure TiO2 sorption material

    International Nuclear Information System (INIS)

    Špendlíková, Irena; Raindl, Jakub; Němec, Mojmír

    2013-01-01

    Among the natural or anthropogenic radionuclides of very low concentrations nowadays measured in environmental samples, the radionuclide of 236 U has been recently included. In these ultra-trace analyses, the purity of sorption materials is very important and the traditional preparation procedures have to be optimized to minimize possible contamination. In the case of the determination of natural concentration of 236 U ( 236 U/ 238 U ∼ 10 -10 - 10 -14 ), the sample treatment procedure has to be modified in order to eliminate possible contamination from anthropogenic 236 U that may result even in more than ten thousand times higher 236 U/ 238 U ratios. Many inorganic and organic materials have been proposed for the extraction of uranium. However, only several of them are suitable for the uranium sorption from the solutions of low uranium concentration, but relatively high salt content, such as fresh water, sea water etc. At the same time they have to meet other limiting parameters such as fast kinetics, chemical stability, and low costs. Among the inorganic sorption materials, titanium dioxide has been studied for years with promising results. Titanium dioxides can be prepared via the hydrolysis of titanium compounds, either inorganic salts or organic derivatives, but their properties strongly depend on the preparation conditions. In classical procedures, titanium dioxides are prepared from commercial inorganic salts, such as sulphates or chlorides, or even from industrial intermediates of the titanium white production. Typically, the resulting titanium dioxides are contaminated with uranium already from the origin. Assuming that most organic compounds do not contain uranium and that it is possible to find 'uranium free' water, titanium dioxide free of uranium contamination could be prepared by the hydrolysis of organic titanium derivatives. The aim of this study was to find a suitable way of pure titanium dioxide preparation and to optimize the preparation

  15. Technetium Sorption By Cementitious Materials Under Reducing Conditions

    Energy Technology Data Exchange (ETDEWEB)

    Kaplan, Daniel I. [Savannah River National Lab., Aiken, SC (United States); Estes, Shanna L. [Clemson Univ., SC (United States). Environmental Engineering and Earth Sciences; Arai, Yuji [Clemson Univ., SC (United States). College of Agriculture, Forestry and Life Sciences; Powell, Brian A. [Clemson Univ., SC (United States). Environmental Engineering and Earth Sciences

    2013-07-18

    The objective of this study was to measure Tc sorption to cementitious materials under reducing conditions to simulate Saltstone Disposal Facility conditions. Earlier studies were conducted and the experimental conditions were found not to simulate those of the facility. Through a five month subcontract with Clemson University, sorption of {sup 99}Tc to four cementitious materials was examined within an anaerobic glovebag targeting a 0.1% H{sub 2}(g)/ 99.9% N{sub 2}(g) atmosphere. Early experiments based on Tc sorption and Eh indicated that 0.1% H{sub 2}(g) (a reductant) was necessary to preclude experimental impacts from O{sub 2}(g) diffusion into the glovebag. Preliminary data to date (up to 56 days) indicates that sorption of {sup 99}Tc to cementitious materials increased with increasing slag content for simulated saltstone samples. This is consistent with the conceptual model that redox active sulfide groups within the reducing slag facilitate reduction of Tc(VII) to Tc(IV). These experiments differ from previous experiments where a 2% H{sub 2}(g) atmosphere was maintained (Kaplan et al., 2011 (SRNL-STI-2010-00668)). The impact of the 2% H{sub 2}(g) reducing atmosphere on this data was examined and determined to cause the reduction of Tc in experimental samples without slag. In the present ongoing study, after 56 days, Tc sorption by the 50-year old cement samples (no slag) was undetectable, whereas Tc sorption in the cementitious materials containing slag continues to increase with contact time (measured after 1, 4, 8, 19 and 56 days). Sorption was not consistent with spike concentrations and steady state has not been demonstrated after 56 days. The average conditional K{sub d} value for the Vault 2 cementitious material was 873 mL/g (17% slag), for the TR547 Saltstone (45% slag) the conditional K{sub d} was 168 mL/g, and for TR545 (90% slag) the conditional K{sub d} was 1,619 mL/g. It is anticipated that additional samples will be collected until steady state

  16. Study of sorption of REE and TPE on sorbents containing ferro- and ferricyanide-ions

    International Nuclear Information System (INIS)

    Gelis, V.M.; Chuveleva, Eh.A.; Firsova, L.A.; Bashlykova, I.B.

    2003-01-01

    Sorptive properties are studied of anionites of different structure containing ferro- and ferricyanide-ions relative to rare earths and transplutonium elements in static and dynamic conditions. It is shown that in the case of rare earths sorption the full anionite capacity via ferrocyanide-ions is used. Influence of solution acidity on rare earths and transplutonium elements sorption is investigated. It is determined that rare earths sorption does not take place on anionites containing ferricyanide-ions, but Am is absorbed [ru

  17. Capacity and mechanisms of ammonium and cadmium sorption on different wetland-plant derived biochars

    International Nuclear Information System (INIS)

    Cui, Xiaoqiang; Hao, Hulin; Zhang, Changkuan; He, Zhenli; Yang, Xiaoe

    2016-01-01

    The objective of this study was to investigate the relationship between Cd 2+ /NH 4 + sorption and physicochemical properties of biochars produced from different wetland plants. Biochars from six species of wetland plants (i.e., Canna indica, Pennisetum purpureum Schum, Thalia dealbata, Zizania caduciflora, Phragmites australis and Vetiveria zizanioides) were obtained at 500 °C and characterized, and their sorption for ammonium and cadmium was determined. There were significant differences in elemental composition, functional groups and specific surface area among the biochars derived from different wetland plant species. Sorption of ammonium and cadmium on the biochars could be described by a pseudo second order kinetic model, and the simple Langmuir model fits the isotherm data better than the Freundlich or Temkin model. The C. indica derived biochar had the largest sorption capacity for NH 4 + and Cd 2+ , with a maximum sorption of 13.35 and 125.8 mg g −1 , respectively. P. purpureum Schum derived biochar had a similar maximum sorption (119.3 mg g −1 ) for Cd 2+ . Ammonium sorption was mainly controlled by cation exchange, surface complexation with oxygen-containing functional groups and the formation of magnesium ammonium phosphate compounds, whereas for Cd 2+ sorption, the formation of cadmium phosphate precipitates, cation exchange and binding to oxygen-containing groups were the major possible mechanisms. In addition, the sorption of ammonium and cadmium was not affected by surface area and microporosity of the biochars. - Highlights: • Biochars varied in physicochemical properties and adsorption capacity. • Canna indica derived biochar has a high sorption capacity for Cd 2+ . • NH 4 + and Cd 2+ sorption on biochars fits a pseudo second order and Langmuir model. • Sorption mechanism is related to complexation, cation exchange and precipitation.

  18. Capacity and mechanisms of ammonium and cadmium sorption on different wetland-plant derived biochars

    Energy Technology Data Exchange (ETDEWEB)

    Cui, Xiaoqiang [Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058 (China); Hao, Hulin [Ningbo Raw Water Resource Research Academy, Ningbo (China); Zhang, Changkuan [Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058 (China); He, Zhenli [Indian River Research and Education Center, Institute of Food and Agricultural Sciences, University of Florida, Fort Pierce, FL 34945 (United States); Yang, Xiaoe, E-mail: xyang571@yahoo.com [Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058 (China)

    2016-01-01

    The objective of this study was to investigate the relationship between Cd{sup 2+}/NH{sub 4}{sup +} sorption and physicochemical properties of biochars produced from different wetland plants. Biochars from six species of wetland plants (i.e., Canna indica, Pennisetum purpureum Schum, Thalia dealbata, Zizania caduciflora, Phragmites australis and Vetiveria zizanioides) were obtained at 500 °C and characterized, and their sorption for ammonium and cadmium was determined. There were significant differences in elemental composition, functional groups and specific surface area among the biochars derived from different wetland plant species. Sorption of ammonium and cadmium on the biochars could be described by a pseudo second order kinetic model, and the simple Langmuir model fits the isotherm data better than the Freundlich or Temkin model. The C. indica derived biochar had the largest sorption capacity for NH{sub 4}{sup +} and Cd{sup 2+}, with a maximum sorption of 13.35 and 125.8 mg g{sup −1}, respectively. P. purpureum Schum derived biochar had a similar maximum sorption (119.3 mg g{sup −1}) for Cd{sup 2+}. Ammonium sorption was mainly controlled by cation exchange, surface complexation with oxygen-containing functional groups and the formation of magnesium ammonium phosphate compounds, whereas for Cd{sup 2+} sorption, the formation of cadmium phosphate precipitates, cation exchange and binding to oxygen-containing groups were the major possible mechanisms. In addition, the sorption of ammonium and cadmium was not affected by surface area and microporosity of the biochars. - Highlights: • Biochars varied in physicochemical properties and adsorption capacity. • Canna indica derived biochar has a high sorption capacity for Cd{sup 2+}. • NH{sub 4}{sup +} and Cd{sup 2+} sorption on biochars fits a pseudo second order and Langmuir model. • Sorption mechanism is related to complexation, cation exchange and precipitation.

  19. Sorption of ions Pb2+ by cryogels on the basis of polyvinyl alcohol and bentonite clay

    Directory of Open Access Journals (Sweden)

    А. Seralin

    2012-03-01

    Full Text Available Cryogels on the basis of polyvinyl alcohol and bentonite clay were synthesized. Influences of factors of environment (pH, temperature on properties of composites and them sorption ability were considered. In given article it is resulted sorption kinetics of lead ions on bentonite clay, and also composite cryogel on the basis of polyvinyl alcohol and bentonite clay. It was established that composite cryogels shows much bigger sorption ability.

  20. Influence of the temperature in the uranium (Vi) sorption in zirconium diphosphate

    International Nuclear Information System (INIS)

    Garcia G, N.; Solis, D.; Ordonez R, E.

    2012-10-01

    In the present work was evaluated the uranium (Vi) sorption at 10, 20, 30, 40 and 60 C on the zirconium diphosphate (ZrP 2 O 7 ). They were carried out kinetic and isotherms using the method by lots, these will allow to fix the sorption time (kinetic) and to explain the behavior of this sorption in different ph conditions and temperature (isotherm). The quantity of retained uranium in the surface was quantified by means of the fluorescence technique. (Author)

  1. Comparative evaluation for the sorption capacity of four carbonaceous sorbents to phenol

    Directory of Open Access Journals (Sweden)

    Ding Feng Jin

    2016-10-01

    Full Text Available Sorption kinetics and isotherms of phenol by four carbonaceous sorbents (activated carbon (AC, mesoporous carbon (MPC, bamboo biochar (BBC and oak wood biochar (OBC were compared in this study. MPC has the fastest sorption rate and initial sorption potential, which were indicated by sorption rate constants and initial sorption rate “h” in a pseudo-second-order kinetic model. The ordered and straight pore structure of MPC facilitated the accessibility of phenol. The AC showed the greatest sorption capacity towards phenol with maximum sorption of 123 mg/g as calculated by the Langmuir model. High surface area, complexity of pore structure, and the strong binding force of the π–π electron-donor-acceptor interaction between phenol molecules and AC were the main mechanisms. The BBC and OBC had much slower sorption and lower sorption capacity (33.04 and 29.86 mg/g, respectively, compared to MPC (73.00 mg/g and AC, indicating an ineffective potential for phenol removal from water.

  2. Characterization of the sorption behavior of trivalent actinides on zirconium(IV) oxide

    Energy Technology Data Exchange (ETDEWEB)

    Eibl, Manuel; Huittinen, Nina [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Surface Processes; Virtanen, S.; Merilaeinen, S.; Lehto, J. [Helsinki Univ. (Finland); Rabung, T. [Karlsruhe Institute of Technology (KIT), Karlsruhe (Germany). Inst. for Nuclear Waste Disposal

    2017-06-01

    The uptake of trivalent Eu and Cm on zirconium(IV) oxide was investigated in batch sorption and TRLFS studies, respectively. Sorption of Eu{sup 3+} was found to start at a pH-value of 4. Based on TRLFS results, sorption of Cm{sup 3+} was assigned to occur through innersphere complex formation at the zirconia surface. A deconvolution of the TRLFS emission spectra gave three different sorption species with strong red-shifts of the peak positions (600.3 nm, 604.3 nm and 608.2 nm) compared to similar systems.

  3. Sorption of microamounts of Cesup(3+), Pmsup(3+), Gdsup(3+) and Ybsup(3+) on aluminium hydroxide

    International Nuclear Information System (INIS)

    Music, S.

    1986-01-01

    The sorption of microamounts of trivalent lanthanides (Lnsup(3+)) on freshly precipitated Al(OH)sub(3) was measured in dependence on pH and on the time of sorption. The influence of organic complexing ligands and inorganic electrolytes on the sorption process was also investigated. The mechanism of sorption is discussed. Freshly precipitated Al(OH)sub(3) could be used for the preconcentration of microamounts of trivalent lanthanides. However, the preconcentration was not quantitative in the presence of high concentrations of complexing ligands (citrate and similar) which formed strong complexes with Lnsup(3+) ions. (author)

  4. Sorption Characteristics of Sediments in the Upper Mississippi River System Above Lake Pepin

    National Research Council Canada - National Science Library

    James, W

    1999-01-01

    This technical note examines equilibrium phosphorus processes and sorption characteristics for sediments collected from the Minnesota River, immediately upstream from its confluence with the Upper Mississippi River (UMR...

  5. An update of the sorption database. Correction and addition of published literature data

    International Nuclear Information System (INIS)

    Saito, Yoshihiko; Suyama, Tadahiro; Kitamura, Akira; Shibata, Masahiro; Sasamoto, Hiroshi; Ochs, Michael

    2007-07-01

    Japan Nuclear Cycle Development Institute (JNC) had developed the sorption database (JNC-SDB) which includes distribution coefficient (K d ) data of important radioactive elements for bentonite and rocks in order to define a dataset to evaluate the safety function of retardation by natural barrier and engineered barrier in the H12 report. Then, JNC added to the database the sorption data from 1998 to 2003 collected by literature survey. In this report, Japan Atomic Energy Agency (JAEA) has updated the sorption database: (1) JAEA has widely collected the sorption data in order to extend the sorption database. The JNC-SDB has been added the published data which are not registered in the sorption database so far. (2) For the convenience of users the JNC-SDB was partially improved such as the automatic graph function. (3) Moreover, errors during data input in the part of the JNC-SDB were corrected on the basis of reviewing data in the database according to the guideline; 'evaluating and categorizing the reliability of distribution coefficient values in the sorption database'. In this updated JNC-SDB, 3,205 sorption data for 23 elements, which are important for performance assessment were included. The frequency of K d for some elements was clearly shown by addition of the sorption data. (author)

  6. Competitive sorption of persistent organic pollutants onto microplastics in the marine environment

    International Nuclear Information System (INIS)

    Bakir, Adil; Rowland, Steven J.; Thompson, Richard C.

    2012-01-01

    Highlights: ► Organic pollutants are present as complex mixtures in the marine environment. ► The competitive sorption of phenanthrene and DDT in a bi-solute system was investigated onto PVC and PE. ► DDT outcompeted phenanthrene for sorption onto plastic. ► DDT also appeared to have a negative effect on the sorption of phenanthrene onto plastic when added at high concentration. - Abstract: Plastics are known to sorb persistent organic pollutants from seawater. However, studies to quantify sorption rates have only considered the affinity of chemicals in isolation, unlike the conditions in the environment where contaminants are present as complex mixtures. Here we examine whether phenanthrene and 4,4′-DDT, in a mixture, compete for sorption sites onto PVC with no added additives (unplasticised PVC or uPVC) and Ultra-High Molecular Weight polyethylene. Interactions were investigated by exposing particles of uPVC and UHMW PE to mixtures of 3H and 14C radiolabelled Phe and DDT. Changes in sorption capacity were modelled by applying a Freundlich binding sorption isotherms. An Extended Langmuir Model and an Interaction Factor Model were also applied to predict equilibrium concentrations of pollutants onto plastic. This study showed that in a bi-solute system, DDT exhibited no significantly different sorption behaviour than in single solute systems. However, DDT did appear to interfere with the sorption of Phe onto plastic, indicating an antagonistic effect.

  7. Evaluation of sorption capacity of modified wood biomass for arsenic five-valent oxyanions

    International Nuclear Information System (INIS)

    Littera, P.; Antoska, R.; Cernansky, S.; Sevc, J.; Kolencik, M.; Budzakova, M.

    2009-01-01

    In the present work is assessed bio-sorption of arsenic oxyanions, which represent one of two most common special arsenic occurring in contaminated waters. A wood biomass was used as sorbent, which was modified by amorphous oxohydroxides of iron to increase sorption capacity, to whom arsenic has high affinity. The work estimated sorption capacity of wood biomass adjusted by oxohydroxides of iron. The Langmuir model as well as the Freundlich model were suitable for evaluation of experimental results. Maximal sorption capacity of investigated sorbent was 9.259 mg/g, what is comparable with values published by other authors.

  8. Reversibility of sorption of plutonium-239 onto hematite and goethite colloids

    International Nuclear Information System (INIS)

    Lu, N.; Cotter, C.R.; Kitten, H.D.; Bentley, J.; Triay, I.R.

    1998-01-01

    Laboratory batch sorption experiments were conducted to evaluate: (1) sorption of plutonium-239 ( 239 Pu) on different iron oxide colloids (hematite and geothite), (2) sorption kinetics of colloidal Pu(IV) and soluble Pu(V) onto these two colloids, and (3) desorption of colloidal Pu(IV) and soluble Pu(V) from 239 Pu-loaded colloids as a function of time. Natural groundwater and carbonate-rich synthetic groundwater were used in this study. To examine the possible influence of bicarbonate on 239 Pu sorption, an additional set of experiments was conducted in sodium nitrate (NaNO 3 ) solutions under carbon dioxide free environments. Our results show that colloidal Pu(IV) as well as soluble Pu(V) was rapidly adsorbed by hematite and goethite colloids in both natural and synthetic groundwater. The amount of 239 Pu adsorbed by both iron oxide colloids in synthetic groundwater was higher than in natural groundwater. The presence of carbonate did not influence the sorption of 239 Pu. While sorption of soluble Pu(V) is a slow process, sorption of colloidal Pu(IV) occurs rapidly. Desorption of Pu from iron oxide colloids is much slower than the sorption processes. Our findings suggest that different sorption and desorption behaviors of 239 Pu by iron oxide colloids in groundwater may facilitate the transport of 239 Pu along potential flowpaths from the areas contaminated by radionuclide and release to the accessible environment. (orig.)

  9. The effect of particle size on sorption of estrogens, androgens and progestagens in aquatic sediment

    International Nuclear Information System (INIS)

    Sangster, Jodi L.; Oke, Hugues; Zhang, Yun; Bartelt-Hunt, Shannon L.

    2015-01-01

    Highlights: • Two sediments were used to evaluate the effects of particle size on steroid sorption. • Sorption capacity did not increase with decreasing particle size for all steroids. • Particle interactions affect the distribution of steroids within the whole sediments. • Preferential sorption to fine particles was observed. - Abstract: There is growing concern about the biologic effects of steroid hormones in impacted waterways. There is increasing evidence of enhanced transport and biological effects stemming from steroid hormones associated with soils or sediments; however, there are limited studies evaluating how steroid hormone distribution between various particle sizes within whole sediments affects steroid fate. In this study, sorption of 17β-estradiol, estrone, progesterone, and testosterone was evaluated to different size fractions of two natural sediments, a silty loam and a sandy sediment, to determine the steroid sorption capacity to each fraction and distribution within the whole sediment. Sorption isotherms for all steroid hormones fit linear sorption models. Sorption capacity was influenced more by organic carbon content than particle size. Interactions between size fractions were found to affect the distribution of steroids within the whole sediments. All four steroids preferentially sorbed to the clay and colloids in the silty loam sediment at the lowest aqueous concentration (1 ng/L) and as aqueous concentration increased, the distribution of sorbed steroid was similar to the distribution by weight of each size fraction within the whole sediment. In the sandy sediment, preferential sorption to fine particles was observed.

  10. Synthesis, characterization and trivalent arsenic sorption potential of Ce-Al nanostructured mixed oxide

    Science.gov (United States)

    Bhattacharya, S.; Gupta, K.; Ghosh, U. C.

    2017-04-01

    Arsenic contamination in the ground water has serious health consequences in many parts of the world. The surface sorption method for arsenic mitigation has been widely investigated due to its simple method, inexpensive operation, highly efficient and low content of by-products. In the present study, nanostructured hydrated cerium aluminum oxide (NHCAO) was synthesized and characterized and its arsenic (III) sorption behavior from the aqueous solution was studied. The material was characterized in SEM, FE-SEM, TEM, AFM, XRD, and FT-IR. Batch method was used for the kinetics of As (III) sorption on nanoparticles at 303 (± 1.6) K and at pH 7.0 (± 0.2). The experiments on isotherm subject were performed individually at 288K, 303K, 318K temperatures at pH 7.0 (± 0.2) using the batch sorption method. In the kinetics study of arsenic (III) sorption, the sorption percentage was observed to remain nearly unchanged up to pH 9.0, thereafter only slight reduction in sorption percentage. The equilibrium sorption results were tested using the models of Langmuir and the Freundlich isotherm. The Langmuir model is the most fitted model for the sorption reaction. NHCAO was highly efficient in As(III) removal out of the water in the extensive range of pH and could be used for arsenic removal from contaminated water.

  11. Sorption of chromium(III) and chromium(VI) on lead sulfide

    International Nuclear Information System (INIS)

    Music, S.

    1985-01-01

    The sorption of chromium(III) and chromium(VI) on lead sulfide was investigated in dependence on pH, time of sorption, and on the concnetrations of sorbate and sorbent. The mechanisms of the sorption of Crsup(3+) and CrOsub(4)sup(2-) traces on lead sulfide are discussed; a difference between CrOsub(4)sup(2-) sorption on PbS and α-Fesub(2)Osub(3) was found. Sulfates and molybdates affect the removal of chromates from aqueous solutions. Lead sulfide carrier prepared in this work was also used for the preconcentration of chromium(III) and chromium(VI) from tap water. (author)

  12. Effects of mineralogy on sorption of strontium and cesium onto Calico Hills Tuff

    International Nuclear Information System (INIS)

    Meyer, R.E.; Arnold, W.D.; Case, F.I.; O'Kelley, G.D.; Land, J.F.

    1990-04-01

    The sorption properties of tuff formations at the proposed site for the high-level nuclear waste repository at Yucca Mountain, Nevada, have been extensively studied. Sorption and desorption measurements were made of strontium and cesium onto clinoptilolite and Calico Hills Tuff. The object was to see whether there was a correlation between sorption of strontium and cesium onto Calico Hills Tuff and the sorption of strontium and cesium onto clinoptilolite based on the content of clinoptilolite in the Calico Hills Tuff. 13 refs., 10 figs., 6 tabs

  13. Cs-137 sorption and desorption in relation to properties of 17 soils

    International Nuclear Information System (INIS)

    Kerpen, W.

    1988-01-01

    For Cs-137 sorption and desorption studies material of Ap and Ah horizons from 17 soils with wide varying soil properties was selected. The soils were: Podsol, Luvisol, Chernozem, Cambisol, Phaeozem, Arenosol, Gleysol and other soils. The Cs-137 sorption and desorption experiments were carried out in aqueous solution (20 g of soil) under standardized conditions for two reasons: (1) to determine the amounts of Cs-137 sorption, desorption and remains as a function of different soils and (2) to evaluate the soil parameters which govern the sorption, desorption processes. Concerning the second point the sorption values, the amount of 137 Cs desorbed within four desorption cycles and the 137 Cs remains after four desorption cycles were correlated with pH, grain size, sorption capacity (CEC), and other soil properties. It will be shown that generally Cs-137 sorption, desorption and remains depend primarily on the pH of the soil. The middle sand proved to be an indicator for the strenght of sorption, and desorption processes. Sorption and desorption studies lead to the same results as found in biotest experiments

  14. Equilibrium sorption of cobalt, cesium, and strontium on Bandelier Tuff: analysis of alternative mathematical modeling

    International Nuclear Information System (INIS)

    Polzer, W.L.; Fuentes, H.R.; Essington, E.H.; Roensch, F.R.

    1985-01-01

    Sorption isotherms are derived from batch equilibrium data for cobalt, cesium and strontium on Bandelier Tuff. Experiments were conducted at an average temperature of 23 0 C and equilibrium was defined at 48 hours. The solute concentrations ranged from 0 to 500 mg/L. The radioactive isotopes 60 Co, 137 Cs, and 85 Sr were used to trace the sorption of the stable solutes. The Linear, Langmuir, Freundlich and a Modified Freundlich isotherm equations are evaluated. The Modified Freundlich isotherm equation is validated as a preferred general mathematical tool for representing the sorption of the three solutes. The empirical constants derived from the Modified Freundlich isotherm equation indicate that under dynamic flow conditions strontium will move most rapidly and cobalt least rapidly. On the other hand, chemical dispersion will be greatest for cesium and least for strontium. Hill Plots of the sorption data suggest that in the region of low saturation sorption of all three solutes is impeded by interactions among sorption sites; cobalt exhibits the greatest effect of interactions and strontium shows only a minimal effect. In the saturation region of 50% or more, sorption of cobalt is enhanced slightly by interactions among sorption sites whereas sorption of cesium and strontium appears to be independent of site interactions. 9 references, 4 figures, 2 tables

  15. Sorption of Arsenic from Desalination Concentrate onto Drinking Water Treatment Solids: Operating Conditions and Kinetics

    Directory of Open Access Journals (Sweden)

    Xuesong Xu

    2018-01-01

    Full Text Available Selective removal of arsenic from aqueous solutions with high salinity is required for safe disposal of the concentrate and protection of the environment. The use of drinking water treatment solids (DWTS to remove arsenic from reverse osmosis (RO concentrate was studied by batch sorption experiments. The impacts of solution chemistry, contact time, sorbent dosage, and arsenic concentration on sorption were investigated, and arsenic sorption kinetics and isotherms were modeled. The results indicated that DWTS were effective in removing arsenic from RO concentrate. The arsenic sorption process followed a pseudo-second-order kinetic model. Multilayer adsorption was simulated by Freundlich equation. The maximum sorption capacities were calculated to be 170 mg arsenic per gram of DWTS. Arsenic sorption was enhanced by surface precipitation onto the DWTS due to the high amount of calcium in the RO concentrate and the formation of ternary complexes between arsenic and natural organic matter (NOM bound by the polyvalent cations in DWTS. The interactions between arsenic and NOM in the solid phase and aqueous phase exhibited two-sided effects on arsenic sorption onto DWTS. NOM in aqueous solution hindered the arsenic sorption onto DWTS, while the high organic matter content in solid DWTS phase enhanced arsenic sorption.

  16. Sorption and cosorption of the nonionic herbicide mefenacet and heavy metals on soil and its components.

    Science.gov (United States)

    Liu, Zhenyu; Guo, Huiqin; He, Huan; Sun, Cheng

    2012-01-01

    Sorption and cosorption of the nonionic herbicide mefenacet and two typical metals (copper and silver) on black soil and its components (kaolinite and humic acid) were investigated. It was found that because of their different valences and properties, Cu2+ and Ag+ presented different effects on the sorption of mefenacet. Due to the competition of Cu2+, along with the shells of dense water formed by its surface complexation, for sorption surface area with mefenacet, the addition of Cu2+ decreased the sorption amount of mefenacet on soil and its components, especially on humic acid. However, the addition of Ag+ significantly enhanced the sorption of mefenacet, which was attributed to the softness of the cation that weakened the hydrophilicity of the local region around Ag(+)-complexed functionalities, and thus mitigated the competitive sorption of water. In addition, the sorption of mefenacet on soil with or without the two metals was generally decreased with increasing pH, which was caused by the hydrolysis of carbonyl and carboxyl groups on the surface of the sorbents, pi-pi interaction between mefenacet and the soil organic matter, and so on. On the other hand, the presence of mefenacet seemed to have little effect on the sorption of Cu2+ and Ag+, indicating that Cu2+ and Ag+ might be sorbed strongly on the tested sorbents and the mefenacet added was too low in concentration to affect the sorption of the metals.

  17. Sorption behaviour of uranium and thorium on cryptomelane-type hydrous manganese dioxide from aqueous solution

    International Nuclear Information System (INIS)

    El-Naggar, I.M.; El-Absy, M.A.; Abdel-Hamid, M.M.; Aly, H.F.

    1993-01-01

    The kinetics of sorption of uranium and thorium from aqueous nitrate solutions on cryptomelane-type hydrous manganese dioxide (CRYMO) was studied. The exchange of uranium is particle diffusion controlled while that of thorium is chemical reaction at the exchange sites. Sorption of uranium and thorium by CRYMO has been also studied as a function of metal concentrations and temperature. The sorption of both cations is found to be an endothermic process and increases markedly with temperature between 30 and 60 degree C. The sorption results have been analysed by the langmuir adsorption isotherm over the entire range of uranium and thorium concentrations investigated. 35 refs., 8 figs., 5 tabs

  18. Prediction of clay content from water vapour sorption isotherms considering hysteresis and soil organic matter content

    DEFF Research Database (Denmark)

    Arthur, E.; Tuller, M.; Møldrup, Per

    2015-01-01

    for estimating clay content from hygroscopic water at different relative humidity (RH) levels while considering hysteresis and organic matter content. Continuous adsorption/desorption vapour sorption isotherm loops were measured for 150 differently textured soils with a state-of-the-art vapour sorption analyser...... vapour sorption, which can be measured within a shorter period of time, have recently been developed. Such models are often based on single-point measurements of water adsorption and do not account for sorption hysteresis or organic matter content. The present study introduces regression relationships...... model encompasses all 150 soils regardless of organic carbon (OC) content, the second model considers only soils with OC

  19. The effect of particle size on sorption of estrogens, androgens and progestagens in aquatic sediment

    Energy Technology Data Exchange (ETDEWEB)

    Sangster, Jodi L.; Oke, Hugues; Zhang, Yun; Bartelt-Hunt, Shannon L., E-mail: sbartelt2@unl.edu

    2015-12-15

    Highlights: • Two sediments were used to evaluate the effects of particle size on steroid sorption. • Sorption capacity did not increase with decreasing particle size for all steroids. • Particle interactions affect the distribution of steroids within the whole sediments. • Preferential sorption to fine particles was observed. - Abstract: There is growing concern about the biologic effects of steroid hormones in impacted waterways. There is increasing evidence of enhanced transport and biological effects stemming from steroid hormones associated with soils or sediments; however, there are limited studies evaluating how steroid hormone distribution between various particle sizes within whole sediments affects steroid fate. In this study, sorption of 17β-estradiol, estrone, progesterone, and testosterone was evaluated to different size fractions of two natural sediments, a silty loam and a sandy sediment, to determine the steroid sorption capacity to each fraction and distribution within the whole sediment. Sorption isotherms for all steroid hormones fit linear sorption models. Sorption capacity was influenced more by organic carbon content than particle size. Interactions between size fractions were found to affect the distribution of steroids within the whole sediments. All four steroids preferentially sorbed to the clay and colloids in the silty loam sediment at the lowest aqueous concentration (1 ng/L) and as aqueous concentration increased, the distribution of sorbed steroid was similar to the distribution by weight of each size fraction within the whole sediment. In the sandy sediment, preferential sorption to fine particles was observed.

  20. Sorption of uranium from carbonate-containing solutions by inorganic sorbents. IX. Kinetics of uranium sorption by fibers packed with finely divided sorbents

    International Nuclear Information System (INIS)

    Mikheeva, M.N.; Myasoedov, B.F.; Novikov, Yu.P.; Komarevskii, V.M.; Mezhirov, M.S.; Idiatulov, R.K.; Fedorova, A.N.

    1988-01-01

    We studied the kinetics at 20-65 degree C of uranium sorption from carbonate-containing seawaters at pH 7.85 ± 0.05 by polyacrylonitrile fibers to which was added, during preparation, 50-80% of Termoksid-5 titanium-containing sorbent ground to 1-3 μm. The sorption kinetics was described by an equation relating the theoretical uranium sorption rate constant to temperature and uranium concentration in the original solution. The constant was independent of the degree to which the fiber was packed with sorbent over the range studied

  1. Sorption of selenate on soils and pure phases: kinetic parameters and stabilisation

    Energy Technology Data Exchange (ETDEWEB)

    Loffredo, N. [Institut de Radioprotection et Surete Nucleaire (IRSN), DEI/SECRE/Laboratoire de Radioecologie et d' Ecotoxicologie, Cadarache, Bat 186, BP3, 13115 Saint-Paul-lez-Durance Cedex (France); Mounier, S. [Laboratoire PROTEE, Universite du Sud Toulon-Var, BP 20132, La Garde 83957 (France); Thiry, Y. [Agence Nationale pour la gestion des Dechets Radioactifs (Andra), Parc de la Croix Blanche, 1/7 rue Jean Monnet, 92298 Chatenay-Malabry Cedex (France); Coppin, F., E-mail: frederic.coppin@irsn.fr [Institut de Radioprotection et Surete Nucleaire (IRSN), DEI/SECRE/Laboratoire de Radioecologie et d' Ecotoxicologie, Cadarache, Bat 186, BP3, 13115 Saint-Paul-lez-Durance Cedex (France)

    2011-09-15

    This study was conducted to identify the principle selenate carrier phases for two selected soils, by comparing their reactivity with selenate to that of pure phases of the solids. Silica, calcium carbonate, aluminium hydroxide, goethite, bentonite and humic acid were selected as the main soil carrier phases. Comparisons were made first on the parameter values obtained with the best fit of a kinetic sorption model which can discriminate instantaneous sorption from kinetically limited sorption. Then comparisons were made of the ability for each solid to stabilise selenate by measuring the ratio of the partition coefficient for sorption (Kd{sub sorption}) over that of the desorption (Kd{sub desorption}). Kinetics and stabilisation were used to help elucidate the nature of interactions with the test solid phases for a large range of selenate concentrations. The experiments were conducted over 165 h in batch reactors, the solid being isolated from the solution by dialysis tubing, at two pH (5.4 and 8) and three selenate concentrations (1 x 10{sup -3}, 1 x 10{sup -6} and 1 x 10{sup -8} mol L{sup -1}). The results obtained showed that only aluminium hydroxide can sorb selenate throughout the studied pH range (pH 5.4 to 8.0). The sorption capacity on this mineral was high (Kd{sub sorption} > 100 to 1 x 10{sup 4} L kg{sup -1}) and the selenate was mainly stabilized by the formation of inner sphere complexes. The sorption on goethite occurred at pH 5.4 (Kd{sub sorption} 52 L kg{sup -1}), mainly as outer sphere complexes, and was null at pH 8. On silica, a weak sorption was observed only at pH 5.4 and at 165 h (Kd{sub sorption} 4 L kg{sup -1}). On bentonite, calcium carbonate and humic acid no significant sorption was observed. Concerning the two soils studied, different behaviours were observed for selenate. For soil Ro (pH 5.4), Kd{sub sorption} was low (8 L kg{sup -1}) compared to soil Bu (pH 8) (70 L kg{sup -1}). The sorption behaviour of selenate on soil Ro was mainly

  2. Sorption/desorption reversibility of polycyclic aromatic hydrocarbons (PAHs) in soils and carbonaceous materials

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Guohui

    2008-07-01

    Understanding sorption/desorption is an important prerequisite for the prediction of fate and transport of pollutants in the environment. During the last two decades, numerous studies have reported hysteresis phenomenon for the interaction of hydrophobic organic contaminants (HOCs) with natural organic matter (NOM). It manifests as nonsingular sorption/desorption isotherms or different rates for sorption and desorption, where during desorption a higher affinity of a compound on a given sorbent and a longer time scale for release than for sorption is observed. Other studies showed that some of the reported sorption/desorption hysteresis phenomena are due to experimental artifacts, mainly resulting from non-attainment of sorption equilibrium before desorption experiments, which result in 'pseudo-hysteresis'. Except for the hypothesis of sorbent reconfiguration, clear experimental evidence for the physical or chemical mechanisms proposed to lead to hysteresis is still lacking. In this study, sorption/desorption equilibrium and kinetics of phenanthrene sorption/desorption from two soils and three carbonaceous samples were investigated using both batch and column techniques. The main objective of this work was to monitor hysteresis phenomenon by carefully recovering the solute mass in the system and to compare sorption/desorption equilibria and kinetics thermodynamically. Nonsingular isotherms and higher desorption enthalpies as well as increased activation energies with proceeding desorption are expected if significant hysteresis exists. Sorption-desorption cycles were carried out to compare equilibrium isotherms and associated sorption/desorption enthalpies (AeH, isosteric heats). Instead of the traditional decant-and-refill batch method, the experiments were conducted using a newly designed batch protocol, which enables the determination of sorption/desorption isotherms at different temperatures using a closed batch system. This method additionally allows

  3. Sorption of short-lived radionuclides in a layer of sorbent with spherical granules

    International Nuclear Information System (INIS)

    Karlin, Yu.V.

    1993-01-01

    Sorption methods have found wide application in the purification of liquid radioactive wastes. The working element in sorption methods for this purpose is usually a sorption column with a fixed layer of sorbent. Continuous-action equipment with a moving layer of sorbent is very seldom used. When a fixed layer of sorbent is used its wear and prolonged mixing in the sorption column are reduced to a minimum, and maximum purification is achieved due to the advantages of the dynamic method of sorption over the static method. The time of protective action of the sorbent layer is determined by the time taken for the radionuclide to pass through the sorption column, and for the majority of radionuclides is determined by numerous parameters, including the type of sorbent and radionuclide, the rate of flow through the sorbent, the size of the sorbent granules, etc. The physical and chemical aspects of this process have been investigated in detail, and numerous methods for modeling it mathematically have been developed and have been used to develop methods of designing sorption column apparatus. The specific nature of the radionuclides as unstable materials enables the hypothetical case of a open-quotes perpetualclose quotes sorption filter to be represented. In fact, to achieve this it is only necessary to assume that the half-life of the radionuclide is so small that the rate of decay of the radionuclide in the sorption column (both in the sorbed state and in the aqueous phase of the sorption layer) is equal to the rate that it is fed into the column in the flow of liquid radioactive waste. In this case the sorption front of the radionuclide in the column wall remains fixed after a certain initial period. In this paper, a mathematical model of such a hypothetical filter for the case of spherical sorbent granules is considered

  4. The influences of pH and ionic strength on the sorption of tylosin on goethite.

    Science.gov (United States)

    Guo, Xuetao; Yang, Chen; Wu, Yinai; Dang, Zhi

    2014-02-01

    As one of the widely used antibiotics in the world, the environmental risks of tylosin (TYL) received more and more attention. In order to assess its environmental fate and ecological effects accurately, it is necessary to understand the sorption properties of TYL on the soils/sediments. The sorption of TYL on goethite at different pH and ionic strength conditions were measured through a series of batch experiments and the sorption data of TYL were fitted by Freundlich and dual-mode sorption models. It was obvious that sorption was strongly dependent on pH and ionic strength. Sorption capacity of TYL increased as the pH increased and ionic strength decreased. The pH and ionic strength-dependent trends might be related with complexation between cationic/neutral TYL species and goethite. The sorption affinity of TYL on goethite decreased as ionic strength increased, which only occurred at higher TYL concentrations, suggested that inner complex might have dominated process at low concentrations and outer complex might occur at higher concentrations of TYL. Spectroscopic evidence indicated that tricarbonylamide and hydroxyl functional groups of TYL might be accounted for the sorption on mineral surfaces. The experimental data of TYL sorption could be fitted by surface complexation model (FITEQL), indicating that ≡FeOH with TYL interaction could be reasonably represented as a complex formation of a monoacid with discrete sites on goethite. The sorption mechanism of TYL might be related with surface complexation, electrostatic repulsion, and H-bounding on goethite. It should be noticed that the heterogeneous of sorption affinity of TYL on goethite at various environment to assess its environment risk.

  5. Sorption of antibiotic sulfamethoxazole varies with biochars produced at different temperatures

    International Nuclear Information System (INIS)

    Zheng, Hao; Wang, Zhenyu; Zhao, Jian; Herbert, Stephen; Xing, Baoshan

    2013-01-01

    Sorption of sulfonamides on biochars is poorly understood, thus sulfamethoxazole (SMX) sorption on biochars produced at 300–600 °C was determined as a function of pH and SMX concentration, as well as the inorganic fractions in the biochars. Neutral SMX molecules (SMX 0 ) were dominant for sorption at pH 1.0–6.0. Above pH 7.0, although biochars surfaces were negatively-charged, anionic SMX species sorption increased with pH and is regulated via charge-assisted H-bonds. SMX 0 sorption at pH 5.0 was nonlinear and adsorption-dominant for all the biochars via hydrophobic interaction, π–π electron donor–acceptor interaction and pore-filling. The removal of inorganic fraction reduced SMX sorption by low-temperature biochars (e.g., 300 °C), but enhanced the sorption by high-temperature biochars (e.g., 600 °C) due to the temperature-dependent inorganic fractions in the biochars. These observations are useful for producing designer biochars as engineered sorbents to reduce the bioavailability of antibiotics and/or predict the fate of sulfonamides in biochar-amended soils. -- Highlights: •Sulfamethoxazole (SMX) sorption on biochars at pH 5.0 was adsorption-dominant. •Removal of inorganic fractions in low-temperature biochars reduced SMX sorption. •Removal of inorganic fractions in high-temperature biochars enhanced SMX sorption. •Anionic SMX was adsorbed on negatively charged biochar via charge-assisted H-bond. -- Solution pH and biochar property control the sorption amount and mechanisms of antibiotic sulfamethoxazole

  6. Sorption of pesticides in tropical and temperate soils from Australia and the Philippines.

    Science.gov (United States)

    Oliver, Danielle P; Kookana, Rai S; Quintana, Belen

    2005-08-10

    The sorption behavior of diuron, imidacloprid, and thiacloprid was investigated using 22 soils collected in triplicate from temperate environments in Australia and tropical environments in Australia and the Philippines. Within the temperate environment in Australia, the soils were selected from a range of land uses. The average KOC values (L/kg) for imidacloprid were 326, 322, and 336; for thiacloprid, the values were 915, 743, and 842; and for diuron, the values were 579, 536, and 618 for the Ord (tropical), Mt. Lofty (temperate), and Philippines (tropical) soils, respectively. For all soils, the sorption coefficients decreased in the following order: thiacloprid > diuron > imidacloprid. There were no significant differences in sorption behavior between the tropical soils from the Philippines and the temperate soils from Australia. Sorption was also not significantly related with soil characteristics, namely, organic carbon (OC) content, clay content, and pH, for any of the three chemicals studied. When the data were sorted into separate land uses, the sorption of all three chemicals was highly correlated (P soils from the Philippines. Sorption coefficients for all three chemicals were highly correlated with OC in temperate, native soils only when one extreme value was removed. The relationships between sorption of all three chemicals and OC in temperate, pasture soils were best described by a polynomial. Sorption coefficients for imidacloprid and thiacloprid determined in the temperate pasture soils remained fairly consistent as the OC content increased from 3.3 to 5.3%, indicating that, although the total OC in the pasture soils was increasing, the component of OC involved with sorption of these two compounds may have been remaining constant. This study demonstrated that the origin of the soils (i.e., temperate vs tropical) had no significant effect on the sorption behavior, but in some cases, land use significantly affected the sorption behavior of the three

  7. Kinetic sorption of contaminants of emerging concern by a palygorskite-montmorillonite filter medium.

    Science.gov (United States)

    Berhane, Tedros M; Levy, Jonathan; Krekeler, Mark P S; Danielson, Neil D

    2017-06-01

    Kinetic sorption of bisphenol A (BPA), carbamazepine (CMZ) and ciprofloxacin (CIP) by three palygorskite-montmorillonite (Pal-Mt) granule sizes was studied. For BPA, CMZ and CIP, apparent sorption equilibrium was reached within about 3, 5 and 16 h, respectively. The highest and the lowest sorption capacities were by the small and the large granule sizes, respectively. Experimental results were compared to various sorption kinetics models to gain insights regarding the sorption processes and achieve a predictive capacity. The pseudo-second order (PSO) and the Elovich models performed the best while the pseudo-first order (PFO) model was only adequate for CMZ. The intraparticle-diffusion (IPD) model showed a two-step linear plot of BPA, CMZ and CIP sorption versus square root of time that was indicative of surface-sorption followed by IPD as a rate-limiting process before equilibrium was reached. Using the pseudo-first order (PFO) and the pseudo-second order (PSO) rate constants combined with previously-established Langmuir equilibrium sorption models, the kinetic sorption (k a ) and desorption (k d ) Langmuir kinetic rate constants were theoretically calculated for BPA and CIP. Kinetic sorption was then simulated using these theoretically calculated k a and k d values, and the simulations were compared to the observed behavior. The simulations fit the observed sorbed concentrations better during the early part of the experiments; the observed sorption during later times occurred more slowly than expected, supporting the hypothesis that IPD becomes a rate-limiting process during the course of the experiment. Copyright © 2017 Elsevier Ltd. All rights reserved.

  8. Shape-Tailored Features and their Application to Texture Segmentation

    KAUST Repository

    Khan, Naeemullah

    2014-04-01

    Texture Segmentation is one of the most challenging areas of computer vision. One reason for this difficulty is the huge variety and variability of textures occurring in real world, making it very difficult to quantitatively study textures. One of the key tools used for texture segmentation is local invariant descriptors. Texture consists of textons, the basic building block of textures, that may vary by small nuisances like illumination variation, deformations, and noise. Local invariant descriptors are robust to these nuisances making them beneficial for texture segmentation. However, grouping dense descriptors directly for segmentation presents a problem: existing descriptors aggregate data from neighborhoods that may contain different textured regions, making descriptors from these neighborhoods difficult to group, leading to significant errors in segmentation. This work addresses this issue by proposing dense local descriptors, called Shape-Tailored Features, which are tailored to an arbitrarily shaped region, aggregating data only within the region of interest. Since the segmentation, i.e., the regions, are not known a-priori, we propose a joint problem for Shape-Tailored Features and the regions. We present a framework based on variational methods. Extensive experiments on a new large texture dataset, which we introduce, show that the joint approach with Shape-Tailored Features leads to better segmentations over the non-joint non Shape-Tailored approach, and the method out-performs existing state-of-the-art.

  9. Mechanisms of nickel sorption by a bacteriogenic birnessite

    Energy Technology Data Exchange (ETDEWEB)

    Pena, J.; Kwon, K.D.; Refson, K.; Bargar, J.R.; Sposito, G.

    2010-04-01

    A synergistic experimental-computational approach was used to study the molecular-scale mechanisms of Ni sorption at varying loadings and at pH 6-8 on the biogenic hexagonal birnessite produced by Pseudomonas putida GB-1. We found that Ni is scavenged effectively by bacterial biomass-birnessite assemblages. At surface excess values below 0.18 mol Ni kg{sup -1} sorbent (0.13 mol Ni mol{sup -1} Mn), the biomass component of the sorbent did not interfere with Ni sorption on mineral sites. Extended X-ray absorption fine structure (EXAFS) spectra showed two dominant coordination environments: Ni bound as a triple-corner-sharing (Ni-TCS) complex at vacancy sites and Ni incorporated (Ni-inc) into the MnO{sub 2} sheet, with the latter form of Ni favored at high sorptive concentrations and decreased proton activity. In parallel to our spectral analysis, first-principles geometry optimizations based on density functional theory (DFT) were performed to investigate the structure of Ni surface complexes at vacancy sites. Excellent agreement was achieved between EXAFS- and DFT-derived structural parameters for Ni-TCS and Ni-inc. Reaction-path calculations revealed a pH-dependent energy barrier associated with the transition from Ni-TCS to Ni-inc. Our results are consistent with the rate-limited incorporation of Ni at vacancy sites in our sorption samples, but near-equilibrium state of Ni in birnessite phases found in nodule samples. This study thus provides direct and quantitative evidence of the factors governing the occurrence of Ni adsorption versus Ni incorporation in biogenic hexagonal birnessite, a key mineral in the terrestrial manganese cycle.

  10. Theory of molecular hydrogen sorption for hydrogen storage

    Science.gov (United States)

    Zhang, Shengbai

    2011-03-01

    Molecular hydrogen (H2) sorption has the advantage of fast kinetics and high reversibility. However, the binding strength is often too weak to be operative at near room temperatures. Research into such hydrogen sorption materials has branched into the study of pure van der Waals (vdW) physisorption and that of weak chemisorption (known to exist in the so-called Kubas complexes). In either case, however, theoretical tools to describe such weak interactions are underdeveloped with error bars that often exceed the strength of the interaction itself. We have used quantum-chemistry (QC) based approaches to benchmark the various available DFT methods for four classes of weak chemisorption systems [Sun et al., Phys. Rev. B 82, 073401 (2010)]. These involve complexes containing Li, Ca, Sc, and Ti with increased strength of H2 binding from predominantly vdW to mostly Kubas-like. The study reveals that most of the DFT functionals within the generalized gradient approximation underestimate the binding energy, oppose to overestimating it. The functionals that are easy to use yet yielding results reasonably close to those of accurate QC are the PBE and PW91. I will also discuss the effort of implementing vdW interaction into the currently available density functional methods [Sun, J. Chem. Phys. 129, 154102 (2008)]. The rationale is that while the true vdW is an electron-electron correlation, a DFT plus classical dispersion approach may be too simple and unnecessary within the DFT. A local pseudopotential approach has been developed to account for the core part of the polarizability of the elements. Applications to a number of benchmark systems yield good agreement with QC calculations. The application of this method and the QC methods to vdW hydrogen binding will also be discussed. Work supported by DOE/BES and DOE/EERE Hydrogen Sorption Center of Excellence under RPI subcontracts No. J30546/J90336.

  11. Radionuclide sorption and migration studies of getters for backfill barriers

    International Nuclear Information System (INIS)

    Nowak, E.J.

    1980-07-01

    Bentonite and hectorite clay minerals were chosen for study and development as potential backfill materials for testing in the proposed Waste Isolation Pilot Plant (WIPP), a radioactive waste repository and test facility in bedded salt. This choice of materials was based on initial screening results which are presented and on the predicted physical properties of these materials. These properties were verified experimentally in concentrated brines specific to the WIPP site. Distribution coefficients, K/sub d/, were calculated from batch sorption measurements on bentonite and hectorite in the nearly saturated brines A and B. The resulting K/sub d/ values were in the range of (1 to 5) x 10 3 ml/g for europium; (2 to 40) x 10 3 ml/g for plutonium(IV); and (4 to 16) x 10 3 ml/g for americium(III). A silica- and calcite-containing sand mixed with bentonite and hectorite acted as a sorber of americium(III) but was merely an inert diluent for plutonium(IV). Pertechnetate anions (TcO 4 - ) sorbed on activated charcoal with K/sub d/ values in the range of (0.2 to 0.4) x 10 3 ml/g. Pertechnetate, cesium, and strontium ions in brine were not sorbed appreciably by bentonite or hectorite. Although experimental evidence is given for a possible role of solubility in the sorption of europium on getters, other data presented here and evidence from the literature are inconsistent with a simple single reaction sorption mechanism. It is concluded that a backfill containing bentonite on hectorite and activated charcoal is potentially an effective barrier to the migration of Eu(III), Pu(IV), and Am(III) cations and, with further development, to the migration of TcO 4 - anions as well

  12. Sorption capacity of plastic debris for hydrophobic organic chemicals.

    Science.gov (United States)

    Lee, Hwang; Shim, Won Joon; Kwon, Jung-Hwan

    2014-02-01

    The occurrence of microplastics (MPs) in the ocean is an emerging world-wide concern. Due to high sorption capacity of plastics for hydrophobic organic chemicals (HOCs), sorption may play an important role in the transport processes of HOCs. However, sorption capacity of various plastic materials is rarely documented except in the case of those used for environmental sampling purposes. In this study, we measured partition coefficients between MPs and seawater (KMPsw) for 8 polycyclic aromatic hydrocarbons (PAHs), 4 hexachlorocyclohexanes (HCHs) and 2 chlorinated benzenes (CBs). Three surrogate polymers - polyethylene, polypropylene, and polystyrene - were used as model plastic debris because they are the major components of microplastic debris found. Due to the limited solubility of HOCs in seawater and their long equilibration time, a third-phase partitioning method was used for the determination of KMPsw. First, partition coefficients between polydimethylsiloxane (PDMS) and seawater (KPDMSsw) were measured. For the determination of KMPsw, the distribution of HOCs between PDMS or plastics and solvent mixture (methanol:water=8:2 (v/v)) was determined after apparent equilibrium up to 12 weeks. Plastic debris was prepared in a laboratory by physical crushing; the median longest dimension was 320-440 μm. Partition coefficients between polyethylene and seawater obtained using the third-phase equilibrium method agreed well with experimental partition coefficients between low-density polyethylene and water in the literature. The values of KMPsw were generally in the order of polystyrene, polyethylene, and polypropylene for most of the chemicals tested. The ranges of log KMPsw were 2.04-7.87, 2.18-7.00, and 2.63-7.52 for polyethylene, polypropylene, and polystyrene, respectively. The partition coefficients of plastic debris can be as high as other frequently used partition coefficients, such as 1-octanol-water partition coefficients (Kow) and log KMPsw showed good linear

  13. Novel compact sorption generators for car air conditioning

    Energy Technology Data Exchange (ETDEWEB)

    Tamainot-Telto, Z.; Metcalf, S.J.; Critoph, R.E. [School of Engineering, University of Warwick, Gibet Hill Road, Coventry CV4 7AL (United Kingdom)

    2009-06-15

    A prototype compact generator using the activated carbon-ammonia pair based on the plate heat exchanger concept has been designed and built at Warwick University. The novel generator has low thermal mass and good heat transfer. The heat exchanger uses nickel-brazed shims and spacers to create adsorbent layers only 4 mm thick between pairs of liquid flow channels of very low thermal mass. The prototype sorption generator manufactured was evaluated under EU car air conditioning test conditions. The prototype sorption generator is described and its experimental performance reported. While driven with waste heat from the engine coolant water (at 90 C), a pair of the current prototype generators (loaded with about 1 kg of activated carbon) operating out of phase has produced an average cooling power 1.6 kW with about 2 kW peaks. The typical average COP obtained is 0.22. (author) [French] Un prototype du generateur compact, base sur le concept des echangeurs de chaleur a plaques et utilisant la paire charbon actif-ammoniac, a ete concu et construit a l'Universite de Warwick. Le nouveau generateur a une faible inertie thermique et un excellent transfert de chaleur. L' echangeur utilise des plaques ayant des micro-canaux et des intercalaires brases au Nickel pour creer des couches d'adsorbant de 4 mm d'epaisseur entre les paires de plaques a l'interieur desquelles circule le fluide liquide. Le prototype du generateur a sorption ainsi fabrique a ete teste suivant des conditions prescrites par la Norme Europeenne de la Climatisation Automobile. Le prototype du generateur a sorption est decrit et ses performances experimentales presentees. Une paire dudit prototype (contenant chacun 1 kg the charbon actif), operant avec dephasage et ulisant des pertes thermiques en provenance de l'eau de refroidissement de moteur (a 90 C), a produit une puissance frigorifique moyenne de 1.6 kW avec une valeur maximum de 2 kW. La valeur typique du COP moyen est de

  14. Sorption-desorption properties of saponite-containing material

    Science.gov (United States)

    Morozova, M. V.; Frolova, M. A.; Makhova, T. A.

    2017-11-01

    The sorption mechanism of the mineral additive showed that self-saturation of the saponite-containing material with water vapors has a long-term nature (12 days). The nature of desorption differs from adsorption isotherm, i.e. the adsorption/desorption hysteresis is observed. Saponite-containing material samples studied after moisture desorption using infrared spectroscopy demonstrated that chemical compounds in the material have the ability to form calcium silicate hydrates when saturated with water. This fact along with the additive capability to control the water-cement ratio during concrete curing contributes to significantly better physical and chemical properties (strength, frost resistance) of the concrete composite.

  15. Uranium sorption by the help of apricot shell

    International Nuclear Information System (INIS)

    Khakimov, N.; Nazarov, Kh.M.; Mirsaidov, I.U.; Akhmedov, M.Z.

    2010-01-01

    increase of doses for population more than 1 mSv/year which is foreseen by radiation safety norms. The samples were taken from these lands for investigation of uranium concentration. Almonds, peach and apricot shells were among taken samples. Chemical analysis showed that there are no observations of uranium tracks in almonds and peach shells. However analysis of apricot shell revealed uranium content. Uranium concentration in apricot shells taken from Taboshar city, 4-5 times exceeds its content in apricot fruits and kernel of a shell. Thus, the apricots become the object of laboratory investigations. We took samples of apricot shell from different regions of Northern Tajikistan - Kayrakum, Isfara, Chkalovsk, Ayni, Gafurov, J.Rasulov and other cities. The average gamma-background on ground surface, where fruits were taken, in samples is 15-30 micro roentgen/hour but in fruits there is no uranium concentration. Here we can use apricot as indicator for uranium detection. There is no uranium in apricot fruits since the trees are growing up on non-contaminated by radionuclides soils. For identification of optimal sorption regime a number of tests were carried out. The sorption characteristics of apricot shell depending on seed size of crushed shell, on temperature, on ph medium and from duration of soaking. Coefficient of shells' swelling capacity is equal to 1,17. The sorption properties of apricot shell at constant regime showed that while increasing solution temperature and decreasing the apricot's shell size, the uranium extraction is increasing. However the influence of ph on sorption percentage has extreme character. Extremum point is equal to 3,65 ph. It is considered that the optimal parameter of crushed shell's size is 1 mm and ph is 3,65. In these conditions, uranium concentration in sorbent reached 1,721 kg/tons, which is in absolute grams is = 0,0344 g. Further, change dynamics of uranium sorption process from mine and drainage waters is studied in

  16. Test of zircon materials for sorption of europium

    International Nuclear Information System (INIS)

    Ordonez R, E.; Fernandez V, S.M.; Garcia R, G.

    2003-01-01

    In previous works it has already been made notice that some phosphates have the property of sipping radioactive metals in solution, what takes advantage to fabricate reactive barriers that are placed in the repositories of nuclear wastes. In our laboratory it has been obtained to the zirconium silicate (ZrSiO 4 ) and the alpha zirconium hydrogen phosphate (Zr(HPO 4 ) 2H 2 0) starting from sea sand in an easy and economic way. With the interest of knowing if these compounds can be used in contention barriers the evaluation of their surface properties it is made and of europium sorption. (Author)

  17. Method of increasing efficiency of uranium sorption from acid pulp

    International Nuclear Information System (INIS)

    Parobek, P.; Hinterholzinger, O.; Baloun, S.; Homolka, V.; Vanek, J.; Vebr, Z.

    1989-01-01

    Acid pulp containing uranium is adjusted to pH 2.5 to 4 with alkaline agents, such as alkaline pulp, lime milk, finely ground limestone or soda, or a combination thereof. The treated pulp is put into contact with an ion exchanger whose pH has been adjuste to a range of 2.5 to 4. Partial pulp neutralization causes the hydrolysis of the iron present and an overall reduction in salt contents and a significant increase in the ion exchanger sorptio capacity and thus the overall sorption efficiency. The quality o the eluate and of the uranium concentrate improves. (B.S.)

  18. Isothermal titration calorimetry of sorption processes. A promising approach

    Energy Technology Data Exchange (ETDEWEB)

    Jordan, Norbert; Foerstendorf, Harald [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Surface Processes; Drobot, B. [Technische Univ. Dresden (Germany); Fahmy, Karim [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Biophysics; Reder, Christian

    2017-06-01

    As a consequence of nuclear waste disintegration heat, elevated temperatures in the near field may influence radionuclide retention significantly. However, there is a nearly complete lack of spectroscopic investigations of sorption processes at elevated temperatures. In addition, experimental data on free Gibbs energy (Δ{sub R}G), enthalpy (Δ{sub R}H) and entropy (Δ{sub R}S) of reactions of most radionuclides including fission products such as {sup 79}Se are sparse. Using the Se(IV)/hematite system, we show that microcalorimetry can provide these thermodynamic parameters with high accuracy and in a manner that allows studying various radionuclides.

  19. Sorption of cobalt on organic and inorganic intercalated clays

    International Nuclear Information System (INIS)

    Nava-Galve, G.; Pacheco, G.; Fetter, G.; Bulbulian, S.

    1996-01-01

    A Mexican montmorillonite clay was intercalated on the one hand with aluminium or zirconium polyhydroxications, and on the other with two organic compounds. Radioactive cobalt was used to study the Co 2+ sorption curves in the original and pillared clays. It was found that pillaring in general in does not favour the diffusion of cobalt between the layers specially the organic pillared clays. In equilibrium, the cobalt retention reached the highest level, around 0.7 meq/g in the Zr pillared clay. (author). 8 refs., 7 figs., 3 tabs

  20. Inhibitory effects of extracellular polymeric substances on ofloxacin sorption by natural biofilms.

    Science.gov (United States)

    Zhang, Liwen; Dong, Deming; Hua, Xiuyi; Guo, Zhiyong

    2018-06-01

    Natural biofilms have strong affinities for organic contaminants, and their extracellular polymeric substances (EPS) have been thought to control the sorption process. However, the role of EPS in the sorption of antibiotics, an emerging concern, is poorly understood. Here, soluble (SEPS) and bound EPS (BEPS) were extracted from intact biofilms incubated at different lengths of time to obtain SEPS- and BEPS-free biofilms. Batch sorption experiments and infrared spectroscopy were used to investigate the role of EPS in the sorption of ofloxacin (OFL) by natural biofilms. The sorption capacities of OFL onto intact biofilms were lower than that those onto SEPS-free and BEPS-free biofilms. Partition and Langmuir adsorption contributed to the sorption of OFL onto these biofilms. SEPS and BEPS suppressed partitioning of OFL into biofilm organic matter. Meanwhile, the formation of hydrogen bonds could affect the Langmuir adsorption of OFL onto BEPS-free biofilms. These sorption mechanisms occurred simultaneously and enhanced the sorption capacities of biofilms after EPS removal. The information obtained in this study is beneficial for understanding the interaction mechanisms between antibiotics and natural biofilms. Copyright © 2017 Elsevier B.V. All rights reserved.

  1. Using mechanisms of hydrolysis and sorption to reduce siloxanes occurrence in biogas of anaerobic sludge digesters

    DEFF Research Database (Denmark)

    Gatidou, Georgia; Arvaniti, Olga S.; Stasinakis, Athanasios S.

    2016-01-01

    Hydrolysis of hexamethylcyclotrisiloxane (D3), octamethylcyclotetrasiloxane (D4), decamethylcyclopentasiloxane (D5), dodecamethylcyclohexasiloxane (D6) and dodecamethylcyclohexasilane (D6_silane) and their sorption to digested sludge was studied in batch experiments. Hydrolysis was affected...... of all siloxanes in biogas, enhancing their removal through hydrolysis and sorption to sludge....

  2. Investigating roles of organic and inorganic soil components in sorption of polar and nonpolar aromatic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Shi Xin; Ji Liangliang [State Key Laboratory of Pollution Control and Resource Reuse/School of the Environment, Nanjing University, Jiangsu 210093 (China); Zhu Dongqiang, E-mail: zhud@nju.edu.c [State Key Laboratory of Pollution Control and Resource Reuse/School of the Environment, Nanjing University, Jiangsu 210093 (China)

    2010-01-15

    The main objective of the present study was to assess the roles of various soil components in sorption of organic compounds differing in polarity. Removal of the whole soil organic matter decreased sorption by approximately 86% for nonpolar 1,3,5-trichlorobenzene (TCB), but only 34-54% for highly polar 1,3,5-trinitrobenzene (TNB); however, removal of the extractable humic/fulvic acids did not much affect sorption of the two sorbates. With normalization of solute hydrophobicity, TNB exhibits several orders of magnitude stronger sorption compared with TCB to maize burn residue (black carbon), extracted humic acid and Na{sup +}-saturated montmorillonite clay, suggesting specific sorptive interactions for TNB with the individual model soil components. It was proposed that sorption of TCB to the bulk soil was dominated by hydrophobic partition to the condensed, non-extractable fraction of organic matters (humin/kerogen and black carbon), while interactions with soil clay minerals were an important additional factor for sorption of TNB. - Soil humin and black carbon play a predominant role in sorption of 1,3,5-trichlorobenzene, while polar interactions with soil clay minerals are an important additional factor for sorption of 1,3,5-trinitrobenzene.

  3. Comparative sorption of benzo[alpha]phrene to different humic acids and humin in sediments.

    Science.gov (United States)

    Zhang, Jinghuan; He, Mengchang; Shi, Yehong

    2009-07-30

    Sediment/soil organic matter (SOM) is the predominant sorbents for hydrophobic organic compounds (HOCs). The identification and comparison of sorption characterization of HOCs by different organic matter fractions are essential to predict the fate and transport of HOCs in soils and sediments. The objectives of this paper are to compare the sorption of benzo[alpha]phrene (BaP) to the humic acid (HA) and humin (HM) extracted from different sediments. The HA and HM were extracted with 0.1M NaOH from five sediments in different areas in China, and their sorption isotherms for BaP were determined. All sorption isotherms were nonlinear and nonlinearity increased in the order HAsorption capacities on the HA fractions were significantly related to their aliphaticity, but negatively correlated to aromatic carbon. However, more aromatic carbon in HM fractions can result in higher K(oc) values of BaP than HA. This implied the importance of both aliphatic and aromatic groups in BaP sorption. HM contributed to 54-92% of the total sorption depending on initial concentrations, clearly indicating the dominance of HM in BaP sorption by the sediments.

  4. Prediction of the glyphosate sorption coefficient across two loamy agricultural fields

    DEFF Research Database (Denmark)

    Paradelo Pérez, Marcos; Norgaard, Trine; Moldrup, Per

    2015-01-01

    and glyphosate sorption coefficients were determined. Multiple linear regression (MLR) analyses were performed using nine geo-referenced soil properties as variables to identify the parameters related with glyphosate sorption. Scenarios considered in the analyses included: (i) each field separately, (ii) both...

  5. The ternary sorption system U(VI)-phosphate-silica explained by spectroscopy and thermodynamic modelling

    Energy Technology Data Exchange (ETDEWEB)

    Foerstendorf, Harald; Stockmann, Madlen; Heim, Karsten; Mueller, Katharina; Brendler, Vinzenz [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Surface Processes; Comarmond, M.J.; Payne, T.E. [Australian Nuclear Science and Technology Organisation, Lucas Heights (Australia); Steudtner, Robin [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Inst. of Resource Ecology

    2017-06-01

    Spectroscopic data of sorption processes potentially provide direct impact on Surface Complexation Modelling (SCM) approaches. Based on spectroscopic data of the ternary sorption system U(VI)/phosphate/silica strongly suggesting the formation of a precipitate as the predominant surface process, SCM calculations accurately reproduced results from classical batch experiments.

  6. β-Zeolite modified by ethylenediamine for sorption of Th(IV)

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Peng; Wu, Hanyu; Yuan, Ni; Yin, Zhuoxin; Pan, Duoqiang; Wu, Wangsuo [Lanzhou Univ. (China). Radiochemistry Lab.; Ministry of Education, Lanzhou (China). Key Lab. of Special Function Materials and Structure Design

    2017-08-01

    β-Zeolite-EDA was modified with ethylenediamine (EDA) after synthesized. The synthesized material was characterized and used for removal of Th(IV) from aqueous solutions. The influences of pH, ionic strength, contact time, temperature and humic acid (HA) on Th(IV) sorption onto synthesized β-zeolite-EDA was studied by batch technique. The dynamic process showed that the sorption of Th(IV) onto β-zeolite-EDA matched the pseudo-second-order kinetics model. The sorption of Th(IV) on β-zeolite-EDA was significantly dependent on pH values, the sorption percentage increased markedly at pH 3.5-4.5, and then maintained a steady state as pH values increased. Through simulating the sorption isotherms by Langmuir, Freundlich and Dubini-Radushkevich (D-R) models, it could be seen respectively that the sorption pattern of Th(IV) on β-zeolite-EDA was mainly controlled by surface complexation, and that the sorption processes was endothermic and spontaneous. The presence of HA increased Th(IV) sorption on β-zeolite-EDA.

  7. Oscillatory water sorption test for determining water uptake behavior in bread crust

    NARCIS (Netherlands)

    Nieuwenhuijzen, N.H. van; Tromp, R.H.; Hamer, R.J.; Vliet, T. van

    2007-01-01

    In this work, water sorption kinetics of bread crust are described using an oscillatory sorption test in combination with a Langmuir type equation. Both kinetic and thermodynamic information could be obtained at the same time. An advantage of applying a Langmuir type equation for a quantitative

  8. Studies on the effect of pH on the sorption of cadmium (ll), nickel (II ...

    African Journals Online (AJOL)

    VI) from aqueous solution by bio-sorption using African white star apple was examined. The adsorption process was found to be highly pH-dependent and the results indicate that the optimum pH for sorption of Cd (ll) and Ni (ll) was 6.0 while Pb ...

  9. Influence of geochemical parameters on the sorption and desorption behaviour of europium and gadolinium onto kaolinite.

    Science.gov (United States)

    Kautenburger, Ralf; Beck, Horst P

    2010-06-01

    In this study we investigated the sorption and desorption behaviour of europium and gadolinium (homologues of the actinides americium and curium) onto the clay mineral kaolinite KGa-1b. In the model system metal/kaolinite, sorption isotherms and pH-edges were determined in different batch experiments. Calcium and magnesium as competing cations were used to simulate the influence of water hardness on the sorption and desorption processes. After centrifugation, the free metal ions in the supernatant solution were analysed by ICP-MS. With increasing lanthanide concentration, especially the relative desorption of these metals from kaolinite rises significantly before the cation exchange capacity (CEC) of 0.94 meq per 100 g is reached. This indicates that low lanthanide concentrations will result in a relatively lower metal migration due to sorption reactions at higher active sites in comparison with higher lanthanide concentrations. The K(d)-values and sorption isotherms of Eu(iii) and Gd(iii) were determined at pH 5.0 (+/-0.02) and analysed with Freundlich and Langmuir sorption models. The experimental data can best be fitted by Langmuir sorption isotherm. The pH-value has only a minor influence on the sorption onto kaolinite. Only at low pH-values (kaolinite to the aquifer.

  10. Equilibrium, kinetics and thermodynamic studies for sorption of chlorobenzenes on CTMAB modified bentonite and kaolinite.

    Science.gov (United States)

    Shu, Yuehong; Li, Laisheng; Zhang, Qiuyun; Wu, Honghai

    2010-01-15

    The sorption of chlorobenzenes (CBs) by cetyltrimethylammonium bromide (CTMAB) modified bentonite and kaolinite was investigated. The sorption isotherms for CBs were nearly linear, suggesting that sorption could be described by a distribution process. The distribution coefficient (K(d)) was primarily affected by the amount of sorbed surfactant. The organic carbon normalized sorption coefficient (K(oc)), however, was particularly dependent on arrangement of the surfactant cations. The K(d) of CBs was larger for CTMAB-bentonites than that for CTMAB-kaolinites, while the case for K(oc) was opposite. Thus, the clay mineral structure and morphology had a considerable influence on the surfactant arrangement, which was responsible for the partitioning of CBs. The sorption of CBs onto both CTMAB-bentonites and CTMAB-kaolinites followed pseudo-second-order kinetics. The intra-particle diffusion model for sorption was also investigated and compared to identify sorption mechanism. The sorption of CBs both on CTMAB-bentonites and CTMAB-kaolinites was exothermic in nature and accompanied by an increase in entropy and a decrease in Gibbs energy in the temperature range of 15-35 degrees C. The results indicated that CBs strongly interacted with CTMAB modified bentonite and kaolinite.

  11. Spatial Moment Equations for a Groundwater Plume with Degradation and Rate-Limited Sorption

    Science.gov (United States)

    In this note, we analytically derive the solution for the spatial moments of groundwater solute concentration distributions simulated by a one-dimensional model that assumes advective-dispersive transport with first-order degradation and rate-limited sorption. Sorption kinetics...

  12. Considering Organic Carbon for Improved Predictions of Clay Content from Water Vapor Sorption

    DEFF Research Database (Denmark)

    Arthur, Emmanuel; Tuller, Markus; Moldrup, Per

    2014-01-01

    to water vapor sorption isotherms that can be rapidly measured with a fully automated vapor sorption analyzer are a viable alternative. In this presentation we evaluate the performance of recently developed regression models based on comparison with standard CF measurements for soils with high organic...

  13. Sorption of radionuclides on geological samples from the Bradwell, Elstow, Fulbeck and Killingholme site investigations

    International Nuclear Information System (INIS)

    Berry, J.A.; Coates, H.A.; Green, A.; Littleboy, A.K.

    1988-06-01

    The sorption of chloride, caesium, calcium, nickel and americium on geological samples collected during the site investigations at Bradwell, Elstow, Fulbeck and Killingholme has been studied. Through-diffusion and batch sorption techniques were used and experiments were designed to give a direct comparison between the sorptive behaviour of material from each site. (author)

  14. Sorption and desorption of naphthalene by soil organic matter: importance of aromatic and aliphatic components.

    Science.gov (United States)

    Gunasekara, Amrith S; Xing, Baoshan

    2003-01-01

    Nonlinear isotherm behavior has been reported for the sorption of hydrophobic organic compounds (HOCs) in soil organic matter (SOM), but the exact mechanisms are unknown. Our objective was to provide insight into the sorption mechanism of HOCs in SOM by studying the sorption-desorption processes of naphthalene in a mineral soil, its humic fractions, and lignin. Additionally, humin and lignin were used for studying the effects of temperature and cosolvent on HOC sorption. All isotherms were nonlinear. The humin and lignin isotherms became more linear at elevated temperatures and with the addition of methanol indicating a condensed to expanded structural phase transition. Isotherm nonlinearity and hysteresis increased in the following order: soil humic acid (HA) soil soil humin. Of the samples, aliphatic-rich humin exhibited the largest degree of nonlinearity and had the highest sorption capacity for naphthalene. High nonlinearity and hysteresis in humin were most likely caused by its condensed structure. A novel aliphatic, amorphous condensed conformation is proposed. This conformation can account for both high sorption capacities and increased nonlinearity observed for aliphatic-rich samples and can explain many sorption disparities discussed in the literature. This study clearly illustrates the importance of both aliphatic and aromatic moieties for HOC sorption in SOM.

  15. Sorption and catalytic oxidation of Fe(II) at the surface of calcite

    NARCIS (Netherlands)

    Mettler, S.; Wolthers, M.; Charlet, L.; Von Gunten, U.

    The effect of sorption and coprecipitation of Fe(II) with calcite on the kinetics of Fe(II) oxidation was investigated. The interaction of Fe(II) with calcite was studied experimentally in the absence and presence of oxygen. The sorption of Fe(II) on calcite occurred in two distinguishable steps:

  16. Isothermes de sorption de la laterite stabilisee au ciment et du ...

    African Journals Online (AJOL)

    Mots clés : Isotherme de sorption, composite ciment-bois, latérite stabilisée, hystérèse de sorption, confort thermique. Buildings construction has as principal objective to protect the occupants from climate excesses (hot, cold) by creating satisfactory microclimate inside them, favourable to the performance of various activities ...

  17. Effect of soil pH on sorption of salinomycin in clay and sandy soils

    African Journals Online (AJOL)

    use

    such as water solubility, soil pH, volatility, and sorption, influence antibiotic transport in soils. Typical manure may also contain high levels of ammonia that would tend to increase the pH of soil solution, thus affecting the. *Corresponding author. E- mail: jayashree.ramaswamy@gmail. com. sorption of certain compounds.

  18. Kinetics and Equilibrium Sorption Models: Fitting Plutonium, Strontium, Uranium and Neptunium Loading on Monosodium Titanate (MST)

    Energy Technology Data Exchange (ETDEWEB)

    Fondeur, F

    2006-03-08

    The Dubinin-Astashov (DA) isotherm parameters for U, Pu, Sr and Np have been updated to include additional data obtained since the original derivation. The DA isotherms were modified to include a kinetic function derived by Rahn to describe sorbate loading from the beginning of sorption up to steady state. The final functions describe both kinetic and thermodynamic sorption.

  19. Kinetic and equilibrium characteristics of sorption of saponin of Quillaja Saponaria Molina on chitosan

    Science.gov (United States)

    Mironenko, N. V.; Smuseva, S. O.; Brezhneva, T. A.; Selemenev, V. F.

    2016-12-01

    The equilibrium and kinetic curves of the sorption of saponin of Quillaja saponaria molina on chitosan were analyzed. The inner diffusion was found to be limiting, and its coefficients were calculated. It was found that the form of the curves of the sorption isotherms of saponin is determined by the competing processes of association in solution and absorption by chitosan.

  20. Influence of non-hydrophobic factors on the sorption of ionizable xenobiotics to solids

    DEFF Research Database (Denmark)

    Lützhøft, Hans-Christian Holten; Franco, Antonio; Trapp, Stefan

    2011-01-01

    the parameters describing the extent of sorption. Realizing that ionizable chemicals like weak acids and bases not always sorb according to their hydrophobicity, a correcting factor has been suggested. Correcting the hydrophobic sorption according to the Henderson-Hasselbalch equation has recently shown...

  1. An insight into the removal of fluoroquinolones in activated sludge process: Sorption and biodegradation characteristics.

    Science.gov (United States)

    Wang, Lu; Qiang, Zhimin; Li, Yangang; Ben, Weiwei

    2017-06-01

    The detailed sorption steps and biodegradation characteristics of fluoroquinolones (FQs) including ciprofloxacin, enrofloxacin, lomefloxacin, norfloxacin, and ofloxacin were investigated through batch experiments. The results indicate that FQs at a total concentration of 500μg/L caused little inhibition of sludge bioactivity. Sorption was the primary removal pathway of FQs in the activated sludge process, followed by biodegradation, while hydrolysis and volatilization were negligible. FQ sorption on activated sludge was a reversible process governed by surface reaction. Henry and Freundlich models could describe the FQ sorption isotherms well in the concentration range of 100-300μg/L. Thermodynamic parameters revealed that FQ sorption on activated sludge is spontaneous, exothermic, and enthalpy-driven. Hydrophobicity-independent mechanisms determined the FQ sorption affinity with activated sludge. The zwitterion of FQs had the strongest sorption affinity, followed by cation and anion, and aerobic condition facilitated FQ sorption. FQs were slowly biodegradable, with long half-lives (>100hr). FQ biodegradation was enhanced with increasing temperature and under aerobic condition, and thus was possibly achieved through co-metabolism during nitrification. This study provides an insight into the removal kinetics and mechanism of FQs in the activated sludge process, but also helps assess the environmental risks of FQs resulting from sludge disposal. Copyright © 2016. Published by Elsevier B.V.

  2. Sorption of benzothiazoles onto sandy aquifer material under equilibrium and nonequlibrium conditions

    Directory of Open Access Journals (Sweden)

    Kragulj Marijana M.

    2014-01-01

    Full Text Available In this study, the sorption behaviour of 1,3-benzothiazole (BT and 2-(methylthiobenzothiazole (MTBT was investigated on Danube geosorbent under equilibrium and nonequilibrium conditions. All sorption isotherms fitted well with the Freundlich model (R2=0.932-0.993. The results showed that organic matter of the Danube geosorbent has a higher sorption affinity for the more hydrophobic MTBT compared to BT. However, sorption-desorption experiments showed that MTBT was more easily desorbed than BT molecules, which indicates the importance of absorption relative to adsorption in the overall sorption mechanism of MTBT. In general, molecules of BT and MTBT were more easily desorbed in the lower concentration range, which resulted in an increase in the hysteresis indices with increasing concentrations. Column experiments revealed that retention of the investigated compounds on the aquifer material followed the compound’s hydrophobicity. BT showed a lower retention, in accordance with its lower sorption affinity obtained in the static experiments, while MTBT showed a greater sorption affinity, and thus had a longer retention time on the column. Thus during transport BT represent greater risk for groundwaters than MTBT. These results have increased our understanding of benzothiazoles sorption and desorption process which represent one of the most important factors which influence the behaviour of organic compounds in the environment.

  3. The ternary sorption system U(VI)-phosphate-silica explained by spectroscopy and thermodynamic modelling

    International Nuclear Information System (INIS)

    Foerstendorf, Harald; Stockmann, Madlen; Heim, Karsten; Mueller, Katharina; Brendler, Vinzenz; Steudtner, Robin

    2017-01-01

    Spectroscopic data of sorption processes potentially provide direct impact on Surface Complexation Modelling (SCM) approaches. Based on spectroscopic data of the ternary sorption system U(VI)/phosphate/silica strongly suggesting the formation of a precipitate as the predominant surface process, SCM calculations accurately reproduced results from classical batch experiments.

  4. Application of HPLC capacity coefficients to characterize the sorption of polycyclic aromatic compounds to humic acid

    DEFF Research Database (Denmark)

    Nielsen, T.; Helweg, C.; Siigur, K.

    1997-01-01

    The sorption coefficients to humic acid of 46 PAC having a wide range in polarity were compared with the capacity coefficients of the PAC to a non-polar HPLC column material (ODS) and a polar one (Diol). It is shown that polar interactions contribute to the sorption of polar PAC in addition...

  5. Sorption of organic compounds to activated carbons. Evaluation of isotherm models

    NARCIS (Netherlands)

    Pikaar, I.; Koelmans, A.A.; Noort, van P.C.M.

    2006-01-01

    Sorption to 'hard carbon' (black carbon, coal, kerogen) in soils and sediments is of major importance for risk assessment of organic pollutants. We argue that activated carbon (AC) may be considered a model sorbent for hard carbon. Here, we evaluate six sorption models on a literature dataset for

  6. Diffusion experiments for estimating radiocesium and radiostrontium sorption in unsaturated soils from Spain: Comparison with batch sorption data

    Energy Technology Data Exchange (ETDEWEB)

    Aldaba, D. [Departament de Quimica Analitica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Rigol, A., E-mail: annarigol@ub.edu [Departament de Quimica Analitica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Vidal, M. [Departament de Quimica Analitica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain)

    2010-09-15

    As sorption data obtained from batch tests are often used to estimate pollutant transport in unsaturated soils, comparison between sorption data obtained in the two conditions is required to ensure a correct risk assessment. With this aim, radiostrontium and radiocesium apparent diffusion coefficients (D{sub a}) were quantified in nine unsaturated soils, and the derived distribution coefficients (K{sub d}) were compared with K{sub d} data from batch experiments. The D{sub a}(Sr) and the D{sub a}(Cs) ranged from 1.8 x 10{sup -11} to 1.5 x 10{sup -10} m{sup 2} s{sup -1}, and from 1.0 x 10{sup -13} to 5.9 x 10{sup -11} m{sup 2} s{sup -1}, respectively. The D{sub a}(Sr) varied according to both soil packing parameters and properties governing Sr interaction. For Cs, the soil sorption properties explained the variation on D{sub a}(Cs). The K{sub d} values derived from D{sub a} (from 0.014 to 1.8 L kg{sup -1} for Sr; from 0.55 to 942 L kg{sup -1} for Cs) were lower than from batch tests (from 1 to 97 L kg{sup -1} for Sr; from 10 to 14,600 L kg{sup -1} for Cs), thus indicating that batch data may not accurately describe radionuclide transport in unsaturated soils. However, the two sets of data correlated well, thus suggesting that radionuclide transport can be estimated from batch tests, which are faster than diffusion experiments.

  7. Aeroelastic Tailoring of Transport Wings Including Transonic Flutter Constraints

    Science.gov (United States)

    Stanford, Bret K.; Wieseman, Carol D.; Jutte, Christine V.

    2015-01-01

    Several minimum-mass optimization problems are solved to evaluate the effectiveness of a variety of novel tailoring schemes for subsonic transport wings. Aeroelastic stress and panel buckling constraints are imposed across several trimmed static maneuver loads, in addition to a transonic flutter margin constraint, captured with aerodynamic influence coefficient-based tools. Tailoring with metallic thickness variations, functionally graded materials, balanced or unbalanced composite laminates, curvilinear tow steering, and distributed trailing edge control effectors are all found to provide reductions in structural wing mass with varying degrees of success. The question as to whether this wing mass reduction will offset the increased manufacturing cost is left unresolved for each case.

  8. Sorption of selected organic compounds from water to a peat soil and its humic-acid and humin fractions: Potential sources of the sorption nonlinearity

    Science.gov (United States)

    Chiou, C.T.; Kile, D.E.; Rutherford, D.W.; Sheng, G.; Boyd, S.A.

    2000-01-01

    The sorption isotherms of ethylene dibromide (EDB), diuron (DUN), and 3,5-dichlorophenol (DCP) from water on the humic acid and humin fractions of a peat soil and on the humic-acid of a muck soil have been measured. The data were compared with those of the solutes with the whole peat from which the humic-acid (HA) and humin (HM) fractions were derived and on which the sorption of the solutes exhibited varying extents of nonlinear capacities at low relative concentrations (C(e)/S(w)). The HA fraction as prepared by the density-fractionated method is relatively pure and presumably free of high- surface-area carbonaceous material (HSACM) that is considered to be responsible for the observed nonlinear sorption for nonpolar solutes (e.g., EDB) on the peat; conversely, the base-insoluble HM fraction as prepared is presumed to be enriched with HSACM, as manifested by the greatly higher BET- (N2) surface area than that of the whole peat. The sorption of EDB on HA exhibits no visible nonlinear effect, whereas the sorption on HM shows an enhanced nonlinearity over that on the whole peat. The sorption of polar DUN and DCP on HA and HM display nonlinear effects comparable with those on the whole peat; the effects are much more significant than those with nonpolar EDB. These results conform to the hypothesis that adsorption onto a small amount of strongly adsorbing HSACM is largely responsible for the nonlinear sorption of nonpolar solutes on soils and that additional specific interactions with the active groups of soil organic matter are responsible for the generally higher nonlinear sorption of the polar solutes.

  9. CO2 sorption on surface-modified carbonaceous support: Probing the influence of the carbon black microporosity and surface polarity

    Science.gov (United States)

    Gargiulo, Valentina; Alfè, Michela; Ammendola, Paola; Raganati, Federica; Chirone, Riccardo

    2016-01-01

    The use of solid sorbents is a convenient option in post-combustion CO2 capture strategies. Sorbents selection is a key point because the materials are required to be both low-cost and versatile in typical post-combustion conditions in order to guarantee an economically advantageous overall process. This work compares strategies to tailor the chemico-physical features of carbon black (CB) by surface-modification and/or coating with a CO2-sorbent phase. The influence of the CB microporosity, enhanced by chemical/thermal treatments, is also taken into account. Three CB surface modifications are performed and compared: (i) oxidation and functionalization with amino-groups, (ii) coating with iron oxides and (iii) impregnation with an ionic liquid (IL). The CO2 capture performance is evaluated on the basis of the breakthrough curves measured at atmospheric pressure and room temperature in a lab-scale fixed bed micro-reactor. Most of tested solids adsorb a CO2 amount significantly higher than a 13X zeolite and DARCO FGD (Norit) activated carbon (up to 4 times more in the best case). The sorbents bearing basic functionalities (amino-groups and IL) exhibit the highest CO2 sorption capacity. The use of a microporous carbonaceous support limits the accessibility of CO2 toward the adsorbing phase (IL or FM) lowering the number of accessible binding sites for CO2.

  10. New ceramics incorporated with industrial by-products as pore formers for sorption of toxic chromium from aqueous media

    Science.gov (United States)

    Domopoulou, Artemi

    2015-04-01

    The incorporation of secondary resources including various industrial wastes as pore-forming agents into clayey raw material mixtures for the development of tailored porous ceramic microstructures is currently of increasing interest. In the present research, sintered ceramic compacts were developed incorporated with industrial solid by-products as pore formers, and then used as new sorbents for chromium removal from aqueous media. The microstructures obtained were characterized through X-ray diffraction (XRD) analysis as well as scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectrometry (EDX). Sorption potential of chromium from synthetic solutions on the porous ceramics was studied by static adsorption experiments as a function of the pore-former percentage in the ceramic matrix as well as the initial heavy metal (chromium) concentration, solution pH and temperature. Kinetic studies were conducted and adsorption isotherms of chromium were determined using the Langmuir equation. Preliminary experimental results concerning the adsorption characteristics of chromium on the ceramic materials produced appear encouraging for their possible beneficial use as new sorbents for the removal of toxic chromium from aqueous media. Keywords: sorbents, ceramics, industrial solid by-products, pore-former, chromium. Acknowledgements: This research has been co-financed by the European Union (European Social Fund - ESF) and Greek national funds through the Operational Program "Education and Lifelong Learning" of the National Strategic Reference Framework (NSRF) - Research Funding Program ARCHIMEDES III: Investing in knowledge society through the European Social Fund.

  11. The Effects of Nanostructure on the Hydrogen Sorption Properties of Magnesium-Based Metallic Compounds: A Review

    Directory of Open Access Journals (Sweden)

    Luca Pasquini

    2018-02-01

    Full Text Available In this review, I examine the influence of nanoscale materials features on the hydrogen-metal interaction. The small system size, the abundance of surfaces/interfaces, and the spatial distribution of phases are the key factors to understand the hydrogen sorption properties of nanomaterials. In order to describe nanoscale-specific thermodynamic changes, I present a quantitative model applicable to every hydride-forming material, independently on its composition and atomic structure. The effects of surface free energy, interface free energy, and elastic constraint, are included in a general expression for the thermodynamical bias. In the frame of this model, I critically survey theoretical and experimental results hinting at possible changes of thermodynamic parameters, and in particular, enthalpy and entropy of hydride formation, in nanostructured Mg-based metallic compounds as compared to their coarse-grained bulk counterparts. I discuss the still open controversies, such as destabilization of ultra-small clusters and enthalpy–entropy compensation. I also highlight the frequently missed points in experiments and data interpretation, such as the importance of recording full hydrogen absorption and desorption isotherms and of measuring the hysteresis. Finally, I try to address the open questions that may inspire future research, with the ambition of tailoring the properties of hydride nanomaterials through a deeper understanding of their thermodynamics.

  12. Kinetic Sorption Studies of Heavy Metal Contamination on Indian Expansive Soil

    Directory of Open Access Journals (Sweden)

    M. K. Gupta

    2009-01-01

    Full Text Available Sorption of metallic cadmium from the pH adjusted aqueous solutions at varying initial concentrations onto an alluvial (clay soil through batch sorption experiments was studied. The pH of the initial concentrations ranging between 50 mg/L to 250 mg/L was varied from 3.0 to 8.0. The sorption experiments were carried out for different durations and up to 16 hours. The cadmium continued to sorb till the last experimental pH=8. The experimental sorption data fitted very well with both Langmuir and Freundlich isotherm models and Freundlich model gave higher correlation coefficients. The pseudo-second order kinetics model was most agreeable with the experimental sorption data, whereas the pseudo-first order model was found to be insufficient.

  13. Factors influencing sorption of ciprofloxacin onto activated sludge: Experimental assessment and modelling implications

    DEFF Research Database (Denmark)

    Polesel, Fabio; Lehnberg, Kai; Dott, Wolfgang

    2015-01-01

    and described, particularly for zwitterionic chemicals. Here we present an assessment of the effects of pH and iron salt dosing on the sorption of ciprofloxacin onto activated sludge using laboratory experiments and full-scale fate modelling. Experimental results were described with Freundlich isotherms...... and showed that non-linear sorption occurred under all the conditions tested. The greatest sorption potential was measured at pH = 7.4, at which ciprofloxacin is speciated mostly as zwitterion. Iron salt dosing increased sorption under aerobic and, to a lesser extent, anoxic conditions, whereas no effect...... was registered under anaerobic conditions. The activated sludge model for xenobiotics (ASM-X) was extended with Freundlich-based sorption kinetics and used to predict the fate of ciprofloxacin in a wastewater treatment plant (WWTP). Scenario simulations, using experimental Freundlich parameters, were used...

  14. Oil sorbents with high sorption capacity, oil/water selectivity and reusability for oil spill cleanup.

    Science.gov (United States)

    Wu, Daxiong; Fang, Linlin; Qin, Yanmin; Wu, Wenjuan; Mao, Changming; Zhu, Haitao

    2014-07-15

    A sorbent for oil spill cleanup was prepared through a novel strategy by treating polyurethane sponges with silica sol and gasoline successively. The oil sorption capacity, oil/water selectivity, reusability and sorption mechanism of prepared sorbent were studied. The results showed that the prepared sorbent exhibited high sorption capacity and excellent oil/water selectivity. 1g of the prepared sorbent could adsorb more than 100 g of motor oil, while it only picks up less than 0.1 g of water from an oil-water interface under both static and dynamic conditions. More than 70% of the sorption capacity remained after 15 successive sorption-squeezing cycles, which suggests an extraordinary high reusability. The prepared sorbent is a better alternative of the commercial polypropylene sorbent which are being used nowadays. Copyright © 2014 Elsevier Ltd. All rights reserved.

  15. Sorption of carrier-free sulfate (35S) by diatomaceous earth pretreated with zirconium ions

    International Nuclear Information System (INIS)

    Friedmann, Ch.; Schoenfeld, T.

    1977-01-01

    By pretreating diatomaceous earth with zirconium ion solutions of pH 1.5-2.0, a good sorbent for carrier-free sulfate ( 35 S) from weakly acid solutions is obtained. In contrast, there is practically no sulfate sorption by untreated diatomaceous earth. As the pH is increased, sulfate sorption by the pretreated sorbent is suppressed. An increase in the concentration of Cl - or NO 3 - ions also reduces sorption. Analysis of the influence of the concentration of these ions on sulfate sorption shows that a 1:1 exchange process takes place, i.e. when one sulfate ion is sorbed it replaces one chloride (or nitrate) ion at a sorption site on the surface. The affinity of the Zr pretreated sorbent for sulfate is much greater than that for chloride or nitrate; an estimate of the mass action exchange constants sulfate-chloride and sulfate-nitrate leads to values between 10 3 and 10 4 . (author)

  16. Kinetic modeling of heavy metal sorption by vinyl pyridine based copolymer

    Directory of Open Access Journals (Sweden)

    Maksin Danijela D.

    2012-01-01

    Full Text Available Commercial macroporous poly(4-vinylpyridine-co-divinylbenzene [P4VPD], known as REILLEX-425 was characterized by mercury porosimetry, nitrogen physisorption, Fourier transformed infrared (FTIR spectroscopy and elemental analysis. Sorption rates of P4VPD for Cu(II, Co(II and Cr(VI ions were determined in static non-competitive experiments, at room temperature (298 K. Rapid sorption was observed, especially for Co(II, with half time, t1/2, of 1.5 min and high experimental maximal capacity, Qmax, of 3.08 mmol g-1. Four kinetic models (pseudo-first and pseudo-second order model, intraparticle diffusion and Boyd model were used for analyzing metal sorption by P4VPD. Metal ions sorption is well represented by the pseudo-second-order model, with definite influence of pore and film diffusion on sorption rates. [Projekat Ministarstva nauke Republike Srbije, br. III43009

  17. Sorption of uranium(VI) by La-Al-carboxymethyl konjac glucomannan microsphere sorbent

    International Nuclear Information System (INIS)

    Siyao Sun; Liping Wu; Xuegang Luo

    2017-01-01

    The microsphere of carboxymethyl konjac glucomannan immobilizing La 3+ and Al 3+ (CMKGM-La-Al) has been explored for sorption of U(VI). The maximum U(VI) sorption capacity of the microsphere is found to be 45.4 mg g -1 at pH 5. Experimental data are fitted well with the linear Langmuir and linear pseudo-first-order kinetic model. The sorption process is endothermic, spontaneous and favorable. The possible mechanism of CMKGM modification and sorption of U(VI) on CMKGM-La-Al involves ion exchange and coordination reaction. The comparison between CMKGM-La-Al and other sorbents suggests that CMKGM-La-Al can be considered as an effective sorbent for U(VI) sorption. (author)

  18. Gas sorption properties of zwitterion-functionalized carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Surapathi, Anil; Chen, Hang-yan; Marand, Eva; Karl Johnson, J.; Sedlakova, Zdenka

    2013-02-01

    We have functionalized carbon nanotubes with carboxylic acid and zwitterion groups. We have evaluated the effect of functionalization by measuring the sorption of CO{sub 2}, CH{sub 4}, and N{sub 2} at 35°C for pressures up to 10 bar. Zwitterion functionalized nanotubes were found to be highly hygroscopic. Thermal gravimetric analysis indicates that water can be desorbed at about 200°C. The adsorption of gases in zwitterion functionalized nanotubes is dramatically reduced compared with nanotubes functionalized with carboxylic acid groups. The presence of water on the zwitterion functionalized nanotube reduces the sorption even further. Molecular simulations show that three or more zwitterion groups per tube entrance are required to significantly reduce the flux of CO{sub 2} into the tubes. Simulations also show that gas phase water is rapidly sorbed into the zwitterion functionalized nanotubes, both increasing the free energy barrier to CO{sub 2} entering the tube and also lowering the equilibrium adsorption through competitive adsorption.

  19. Modeling of Cd(II) sorption on mixed oxide

    International Nuclear Information System (INIS)

    Waseem, M.; Mustafa, S.; Naeem, A.; Shah, K.H.; Hussain, S.Y.; Safdar, M.

    2011-01-01

    Mixed oxide of iron and silicon (0.75 M Fe(OH)3:0.25 M SiO/sub 2/) was synthesized and characterized by various techniques like surface area analysis, point of zero charge (PZC), energy dispersive X-rays (EDX) spectroscopy, Thermogravimetric and differential thermal analysis (TG-DTA), Fourier transform infrared spectroscopy (FTIR) and X-rays diffraction (XRD) analysis. The uptake of Cd/sup 2+/ ions on mixed oxide increased with pH, temperature and metal ion concentration. Sorption data have been interpreted in terms of both Langmuir and Freundlich models. The Xm values at pH 7 are found to be almost twice as compared to pH 5. The values of both DH and DS were found to be positive indicating that the sorption process was endothermic and accompanied by the dehydration of Cd/sup 2+/. Further, the negative value of DG confirms the spontaneity of the reaction. The ion exchange mechanism was suggested to take place for each Cd/sup 2+/ ions at pH 5, whereas ion exchange was found coupled with non specific adsorption of metal cations at pH 7. (author)

  20. Sorption of uranium on rocks in anaerobic groundwater

    International Nuclear Information System (INIS)

    Hakanen, M.

    1992-12-01

    Spent nuclear fuel contains substantial amounts of long lived isotopes of actinoide elements, the most abundant of which is the oxide from uranium in the fuel matrix. The behaviour of uranium, also present in small concentrations in natural rocks and waters, is redox sensitive. The concentration controlling mechanisms in groundwaters of uranium are not well-known. In this work a series of laboratory experiments was made to study the redox and sorption behaviour of uranium under anaerobic conditions. The experiments indicated that a part of uranium(VI) was reduced to uranium(IV). The sorbed uranium was of mixed oxidation states. The redox potential of water was not an appropriate indicator of the U(IV)/U(VI) ratio. Spiking of the water with the U(IV) was followed by very strong sorption. The derived lower limit (conservative) and the realistic mass distribution ratios (R d ) for U(IV) are 0.7 m 3 /kg and 3.5 m 3 /kg. (orig.)

  1. Reversible Ammonia Sorption for the Primary Life Support System (PLSS)

    Science.gov (United States)

    Wojtowicz, Marek A.; Cosgrove, Joseph E.; Serio, Michael A.; Jennings, Mallory A.

    2012-01-01

    Results are presented on the development of regenerable trace-contaminant (TC) sorbent for use in Extravehicular Activities (EVAs), and more specifically in the Primary Life Support System (PLSS). Since ammonia is the most important TC to be captured, data presented in this paper are limited to ammonia sorption, with results relevant to other TCs to be reported at a later time. The currently available TC-control technology involves the use of a packed bed of acid-impregnated granular charcoal. The sorbent is non-regenerable, and its use is associated with appreciable pressure drop, i.e. power consumption. The objective of this work is to demonstrate the feasibility of using vacuum-regenerable sorbents for PLSS application. In this study, several carbon sorbent monoliths were fabricated and tested. Multiple adsorption/vacuum-regeneration cycles were demonstrated at room temperature, as well as carbon surface conditioning that enhances ammonia sorption without impairing sorbent regeneration. Depending on sorbent monolith geometry, the reduction in pressure drop with respect to granular sorbent was found to be between 50% and two orders of magnitude. Resistive heating of the carbon sorbent monolith was demonstrated by applying voltage to the opposite ends of the monolith.

  2. Moisture Sorption Characteristics of Corn Stover and Big Bluestem

    Directory of Open Access Journals (Sweden)

    C. Karunanithy

    2013-01-01

    Full Text Available Moisture content is an important feedstock quality in converting it into energy through biochemical or thermochemical platforms. Knowledge of moisture sorption relationship is useful in drying and storage to preserve the quality of feedstocks. Moisture sorption isotherms for potential feedstocks such as corn stover and big bluestem are missing. EMC values of corn stover and big bluestem were determined using static gravimetric technique with saturated salt solutions (ERH 0.12–0.89 at different temperatures (20, 30, and 40°C. Depending upon the ERH values, EMC values were ranged from 8.0 to 19.6 and 8.8 to 19.2% db for corn stover and big bluestem, respectively, and they followed typical type II isotherm found in food materials. Nonlinear regression was used to fit five commonly used three-parameter isotherm models (i.e., modified Oswin model, modified Halsey model, modified Chung-Pfost model, modified Henderson model, and the modified Guggenheim-Anderson-de Boer (GAB model to the experimental data. Modified Halsey emerged as the best model with high F-statistic and R2 values with low Em and Es and fairly random scattered residual plot for corn stover and big bluestem. These models can be used to predict the equilibrium moisture content of these feedstocks starting from harvesting, drying, preprocessing, transportation, storage, and conversion.

  3. Structure and sorption properties of CNC reinforced PVA films.

    Science.gov (United States)

    Popescu, Maria-Cristina

    2017-08-01

    Bio-nanocomposite films based on cellulose nanocrystals reinforced poly(vinyl alcohol) were obtained by solvent casting method. To assess the structural features of the films, different spectral techniques (FTIR, 2D COS and XRD) have been used. Infrared and 2D correlation spectroscopy evidenced the presence of H-bond interactions between the PVA and CNC, and the variation in the conformational rearrangements, while XRD showed that the crystallite size and the crystallinity degree were affected by the incorporation of CNC. At low content of CNC in the PVA matrix, the crystallinity degree decreased to 29.9%, while at higher CNC content increased to 80.6%, comparing to PVA (35.4%). To evaluate the interaction with water, contact angle measurement, water sorption and NIR spectroscopy were used, respectively. The increase of the CNC content induced a reduction in water sorption ability from 93% for PVA to 75% for PVA/CNC films, indicating the involvement of the hydroxyl groups in new hydrogen bonded interactions. By analyzing the variation of the NIR bands from 1930, 1902 and 1985nm, was observed that the water molecules interact with the polymer matrix through moderate hydrogen bond before diffusing into the free volume of the matrix and form stronger hydrogen bonds. Copyright © 2017 Elsevier B.V. All rights reserved.

  4. Sorption of Antimony from Organic Solutions on Inorganic Sorbents

    International Nuclear Information System (INIS)

    El-Dessouky, S.I.; Zakaria, N.; Alian, A.

    2000-01-01

    Sorption of 124 Sb(III) from its complexes in benzene, toluene, o-xylene and chloroform on an artificial inorganic exchanger (chabazite, a) and on bone charcoal (b.ch) was investigated using the static method. Complexes pf Sb(III) with these non-polar organic liquids were prepared by extraction of its chloride by each liquid from 12 M H 2 SO 4 . For the various liquids the order of the uptake in case of chabazite is o-xylene> toluene > benzene> chloroform and in case of b.ch the order is benzene> toluene > chloroform> o-xylene. This suggests different sorption mechanisms for the two studied sorbents, one of them (chabazite) being purely an inorganic sorbent. In general the uptake of Sb(III) from all solvents studied is much higher by b.ch than by chabazite. The uptake of Sb(III) from these non-aqueous solvents by b.ch is also much higher than its uptake by four previously studied sorbents: ashless filter paper cellulose, pyrolysis residue from domestic waste, bentonite elay from upper Egypt and fly ash from a thermal electricity station. The desorption of Sb(III) from the loaded sorbents by 1M HCI was also studied and found maximum within 30 minutes

  5. Behavior of Samarium III during the sorption process

    International Nuclear Information System (INIS)

    Ordonez R, E.; Garcia G, N.; Garcia R, G.

    2004-01-01

    In this work the results of the behavior of samarium in solution are presented, in front of a fine powder of zirconium silicate (zircon). For that which is necessary to characterize the zircon, studying the crystallinity, the morphology, the surface area and the isoelectric point. The behavior of samarium in solution is studied by means of the elaboration of isotherm of sorption, using the technique by lots. One observes that to pH values of nearer to the isoelectric point (pH = 7.23) the process of sorption of the samarium begins, reaching a maximum to near pH at 9. The technique of luminescence is used to determine the concentration of the sipped samarium (phosphorescence) and also to make the speciation of the species formed in the surface of the zircon (phosphorescence). The results can be extrapolated with the plutonium when making the modeling of the migration of alpha emitting coming from the repositories of radioactive waste since both they have similar chemical properties (they are homologous). (Author)

  6. Sorption and fixation of large cations by shale formations

    International Nuclear Information System (INIS)

    Brindley, G.W.

    1977-01-01

    Large cations such as Cs + are preferentially sorbed and partially fixed by fine-grained 2 : 1 type layer silicates such as micas, vermiculites, smectites and various mixed-layer minerals. Since these minerals are common constituents of many shale formations, these formations may provide suitable location for the burial of radioactive waste containers. However, the usual investigations of cation sorption and fixation must be extended to the conditions likely to develop in the vicinity of buried radioactive waste. Prior to possible leakage from buried containers, elevated temperatures around the burial site will develop leading to hydrothermal modification of the surrounding mineralogy. A range of temperature and of mineralogy must be envisaged. If and when leakage occurs, an outward diffusion of radioactive ions will occur by solvation in the fluids in the shale. The ratio of radioactive ions/normal ions will diminish outwards from the source. At near distances from the source high temperature modifications of the clay minerals and high concentrations of radioactive cations may lead to saturation of the fixation capacity. At greater distances, little or no thermal modification of the clay minerals and lower concentrations of ions will permit maximum sorption and fixation

  7. Effect of the cationic composition of sorption solution on the quantification of sorption-desorption parameters of heavy metals in soils

    International Nuclear Information System (INIS)

    Sastre, J.; Rauret, G.; Vidal, M.

    2006-01-01

    We obtained the sorption isotherms of Cd, Cu, Pb and Zn in clay, clay saline and organic soils. The distribution coefficients (K d ) were determined in 0.02 eq l -1 CaCl 2 and in a solution that simulated the soil solution cationic composition. The K d values greatly varied with the composition of the sorption solution and the initial metal concentration. The sorption experiments were complemented with the quantification of the extractable metal, to estimate the reversibility of metal sorption. The extraction yields depended on the metal-soil combination, and the initial metal concentration, showing no correlation with previous K d values. The effect of the solution composition in mobility predictions was estimated through a Retention Factor, defined as the ratio of the K d versus the extraction yield. Results showed that risk was over- or underestimated using the CaCl 2 medium in soils with a markedly different soil solution composition. - Sorption solution composition modifies metal sorption-desorption pattern in soils

  8. Sorption databases for increasing confidence in performance assessment - 16053

    International Nuclear Information System (INIS)

    Richter, Anke; Brendler, Vinzenz; Nebelung, Cordula; Payne, Timothy E.; Brasser, Thomas

    2009-01-01

    World-wide activities focus on the remediation of radioactively contaminated sites. One common aim is to deliver a more profound chemical base for risk assessment, namely all those physico-chemical phenomena governing the contamination plume development in time and space. Coupled transport codes able to tackle this challenge have to simplify the resulting very complex reaction pattern. To do so in an adequate way requires extending the knowledge about retardation and mobilisation phenomena and the underlying basic processes and interactions (e.g. physisorption, chemisorption, surface precipitation). Interactions at the solid-liquid interface can be described by complementary approaches, the empirical K d concept and the mechanistic Surface Complexation Models (SCM). K d 's are used by most reactive transport and risk assessment codes due to the straightforward numerics involved. In addition, the K d concept is often the only feasible option for complex solid phases. However, the K d concept is a rather simplistic approach. Many very different basic physicochemical phenomena are subsumed in just one conditional parameter. Therefore, extrapolating K d values may yield very large uncertainties. SCM account adsorption of ions on surface sites as complexation reaction comparable to complexation in solution. The electrical charge at the surface is determined by the chemical reactions of the mineral functional groups, including acid-base reactions and formation of ion pairs and coordinative complexes. The required parameters are site-independent and applicable despite large variations in geochemical conditions. This presents a high potential to increase confidence in safety analysis and risk assessment studies (performance assessment). The mechanistic description of sorption processes with SCM allows a thermodynamically consistent calculation of the species distribution between liquid and solid phase combined with more reliable inter- and extrapolations. However, this

  9. Benzene and MTBE Sorption in Fine Grain Sediments

    Science.gov (United States)

    Leal-Bautista, R. M.; Lenczewski, M. E.

    2003-12-01

    The practice of adding methyl tert-butyl ether (MTBE) to gasoline started in the late 1970s and increased dramatically in the 1990s. MTBE first was added as a substitute for tetra-ethyl lead then later as a fuel oxygenate. Although the use of MTBE has resulted in significant reduction in air pollution, it has become a significant groundwater contaminant due to its high solubility in water, high environmental mobility, and low potential for biodegradation. A recent report (1999-2001) by the Metropolitan Water District of Southern California in collaboration with United State Geological Survey and the Oregon Health and Science University found that MTBE was the second most frequent detected volatile organic compound in groundwater. In Illinois, MTBE has been found in 26 of the 1,800 public water supplies. MTBE has also been blended in Mexico into two types of gasoline sold in the country by the state oil company (PEMEX) but is not monitored in groundwater at this time. Early research on MTBE considered it unable to adsorb to soils and sediments, however, by increasing the organic matter and decreasing the size of the grains (silts or clays) this may increase sorption. The objective of this study is to determine if fine grained materials have the potential for sorption of MTBE due to its high specific surface area (10-700 m 2/g) and potentially high organic matter (0.5-3.8%). The experiment consisted of sorption isotherms to glacial tills from DeKalb, Illinois and lacustrine clays from Chalco, Mexico. Experiments were performed with various concentrations of MTBE and benzene (10, 50, 100, 500 and 1000 ug/L) at 10° C and 25° C. Results showed a range of values for the distribution coefficient (Kd, linear model). At 10° C the Kd value for MTBE was 0.187 mL/g for lacustrine clay while the glacial loess had a value of 0.009 mL/g. The highest Kd values with MTBE were 0.2859 mL/g for organic rich lacustrine clays and 0.014 mL/g for glacial loess at 25° C. The highest

  10. Sorption and Release of Organics by Primary, Anaerobic, and Aerobic Activated Sludge Mixed with Raw Municipal Wastewater

    Science.gov (United States)

    Modin, Oskar; Saheb Alam, Soroush; Persson, Frank; Wilén, Britt-Marie

    2015-01-01

    New activated sludge processes that utilize sorption as a major mechanism for organics removal are being developed to maximize energy recovery from wastewater organics, or as enhanced primary treatment technologies. To model and optimize sorption-based activated sludge processes, further knowledge about sorption of organics onto sludge is needed. This study compared primary-, anaerobic-, and aerobic activated sludge as sorbents, determined sorption capacity and kinetics, and investigated some characteristics of the organics being sorbed. Batch sorption assays were carried out without aeration at a mixing velocity of 200 rpm. Only aerobic activated sludge showed net sorption of organics. Sorption of dissolved organics occurred by a near-instantaneous sorption event followed by a slower process that obeyed 1st order kinetics. Sorption of particulates also followed 1st order kinetics but there was no instantaneous sorption event; instead there was a release of particles upon mixing. The 5-min sorption capacity of activated sludge was 6.5±10.8 mg total organic carbon (TOC) per g volatile suspend solids (VSS) for particulate organics and 5.0±4.7 mgTOC/gVSS for dissolved organics. The observed instantaneous sorption appeared to be mainly due to organics larger than 20 kDa in size being sorbed, although molecules with a size of about 200 Da with strong UV absorbance at 215–230 nm were also rapidly removed. PMID:25768429

  11. Governing factors for motor oil removal from water with different sorption materials.

    Science.gov (United States)

    Rajaković-Ognjanović, V; Aleksić, G; Rajaković, Lj

    2008-06-15

    This paper has been focused on the sorbent efficiency for motor oil removal from water. Two types of sorbents were investigated: organic and inorganic. Natural wool fibers (NWFs) and recycled-wool-based nonwoven material (RWNM)) were tested as organic type of sorbents. Sepiolite, bentonite and zeolite have been chosen as representative inorganic sorbents. Sorption was carried out in batch sorption system. Efficiency of oil removal was determined by measuring the oil concentration before and after the sorption process. Extractive-gravimetric method and refractive index determination have been applied as analytical methods for determination of oil concentration in water. Governing factors for sorbent efficiency were proposed, analysed and compared. It was concluded that sorption process is mostly affected by mass of sorbent, sorption time, temperature and pH value of water. NWFs, which were the most efficient sorbent showed maximal efficiency and maximal sorption capacity: 0.1 g of NWFs after 10 min at 20 degrees C and pH 8.00 sorbed 3.3 g of motor oil from 300 mL of water polluted with 4.5 g of motor oil. Maximal efficiency for all sorbents investigated was reached after 30 min of sorption processes, it was 95.0% for NWF, 43.0% for NRWM, 20.7% for sepiolite, 19.6% for bentonite and 21.2% for zeolite. Physical adsorption onto all sorbents is a favorable process (sorption efficiency decrease with increasing temperature) while sorption onto bentonite and zeolite is a result of both physical adsorption and chemisorption (sorption efficiency increase with increasing temperature, up to 80 degrees C).

  12. SORPTION AND SOLUBILITY OF LOW-SHRINKAGE RESIN-BASED DENTAL COMPOSITES

    Directory of Open Access Journals (Sweden)

    Sevda Yantcheva

    2016-04-01

    Full Text Available Background: Resin-based composites are well-established restorative materials. However, these materials may absorb significant amounts of water when exposed to aqueous environments. Sorption and solubility are affecting composite restorations by two different mechanisms; the first is the up taking of water producing an increased weight and the second is the dissolution of materials in water, leading to a weight reduction of the final conditioned samples. Objective: To measure the water sorption and solubility of different low-shrinkage resin-based composites. Six materials were selected: Filtek P60, Filtek Ultimate, SonicFill, Filtek Silorane, Kalore and Venus Diamond. Materials and methods: Five disc specimens were prepared of each material and polymerized with diode light-curing unit. Water sorption and solubility of the different materials were were calculated by means of weighting the samples before and after water immersion and desiccation. Data were statistically analyzed using Shapiro-Wilk One Way Analysis of Variance followed by the Holm-Sidak comparison test . Results: There were significant differences (p<=0.001 between materials regarding sorption and solubility. Regarding sorption F. Silorane showed lowest values, followed by SonicFill, without significant difference between them. Statistical significant differences exist between F. Silorane and F.P60, F. Ultimate, Kalore. Significant differences exist between SonicFill and F. Ultimate. F.Silorane (-0.018 and Kalore (-0.010 showed lowest values of solubility but there were marginal difference among all composites investigated. Conclusions: 1.The material with lowest values of sorption and solubility was F.Silorane. 2. The attained sorption and solubility values for composites are influenced by the differences in resin matrix composition and filler contend. 3. Modifications of dimethacrylate matrix did not minimize significantly sorption and solubility of composites. 4. Besides water

  13. New approach in modeling Cr(VI) sorption onto biomass from metal binary mixtures solutions

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Chang [College of Environmental Science and Engineering, Anhui Normal University, South Jiuhua Road, 189, 241002 Wuhu (China); Chemical Engineering Department, Escola Politècnica Superior, Universitat de Girona, Ma Aurèlia Capmany, 61, 17071 Girona (Spain); Fiol, Núria [Chemical Engineering Department, Escola Politècnica Superior, Universitat de Girona, Ma Aurèlia Capmany, 61, 17071 Girona (Spain); Villaescusa, Isabel, E-mail: Isabel.Villaescusa@udg.edu [Chemical Engineering Department, Escola Politècnica Superior, Universitat de Girona, Ma Aurèlia Capmany, 61, 17071 Girona (Spain); Poch, Jordi [Applied Mathematics Department, Escola Politècnica Superior, Universitat de Girona, Ma Aurèlia Capmany, 61, 17071 Girona (Spain)

    2016-01-15

    In the last decades Cr(VI) sorption equilibrium and kinetic studies have been carried out using several types of biomasses. However there are few researchers that consider all the simultaneous processes that take place during Cr(VI) sorption (i.e., sorption/reduction of Cr(VI) and simultaneous formation and binding of reduced Cr(III)) when formulating a model that describes the overall sorption process. On the other hand Cr(VI) scarcely exists alone in wastewaters, it is usually found in mixtures with divalent metals. Therefore, the simultaneous removal of Cr(VI) and divalent metals in binary mixtures and the interactive mechanism governing Cr(VI) elimination have gained more and more attention. In the present work, kinetics of Cr(VI) sorption onto exhausted coffee from Cr(VI)–Cu(II) binary mixtures has been studied in a stirred batch reactor. A model including Cr(VI) sorption and reduction, Cr(III) sorption and the effect of the presence of Cu(II) in these processes has been developed and validated. This study constitutes an important advance in modeling Cr(VI) sorption kinetics especially when chromium sorption is in part based on the sorbent capacity of reducing hexavalent chromium and a metal cation is present in the binary mixture. - Highlights: • A kinetic model including Cr(VI) reduction, Cr(VI) and Cr(III) sorption/desorption • Synergistic effect of Cu(II) on Cr(VI) elimination included in the model • Model validation by checking it against independent sets of data.

  14. Binary Component Sorption of Cadmium, and Copper Ions onto Yangtze River Sediments with Different Particle Sizes

    Directory of Open Access Journals (Sweden)

    Jianxin Fan

    2017-11-01

    Full Text Available Sorption is a crucial process that influences immobilization and migration of heavy metals in an aqueous environment. Sediments represent one of the ultimate sinks for heavy metals discharged into water body. Moreover, the particle size of sediments plays an extremely important role in the immobilization of heavy metals. In this study, the sorption and desorption of cadmium (Cd and copper (Cu onto sediments with different particle sizes were investigated to predict the rate and capacity of sorption, to understand their environmental behaviors in an aqueous environment. Batch sorption and kinetic experiments were conducted to obtain the retained amount and rate of Cd and Cu in a binary system. Experimental data were simulated using sorption models to ascertain the sorption capacity and the kinetic rate. Results of European Communities Bureau of Reference (BCR sequential extraction showed the highest concentration of Cd (0.344 mg kg−1, and its distribution varied with sediment particle size and site. Furthermore, most of Cu (approximately 57% to 84% existed as a residual fraction. The sorption of Cu onto six sediments followed a pseudo-first order reaction, whereas that of Cd followed a pseudo-second order reaction. Additionally, the competitive Langmuir model fitted the batch sorption experimental data extremely well. The highest sorption capacities of Cd and Cu reach 0.641 mmol kg−1 and 62.3 mmol kg−1, respectively, on the smallest submerged sediment particles. The amounts of Cu and Cd desorbed (mmol kg−1 increased linearly with the initial concentration increasing. Thus, sediment texture is an important factor that influences the sorption of heavy metal onto sediments.

  15. Estimation of soil sorption coefficients of veterinary pharmaceuticals from soil properties.

    Science.gov (United States)

    ter Laak, Thomas L; Gebbink, Wouter A; Tolls, Johannes

    2006-04-01

    Environmental exposure assessment of veterinary pharmaceuticals requires estimating the sorption to soil. Soil sorption coefficients of three common, ionizable, antimicrobial agents (oxytetracycline [OTC], tylosin [TYL], and sulfachloropyridazine [SCP]) were studied in relation to the soil properties of 11 different soils. The soil sorption coefficient at natural pH varied from 950 to 7,200, 10 to 370, and 0.4 to 35 L/kg for OTC, TYL, and SCP, respectively. The variation increased by almost two orders of magnitude for OTC and TYL when pH was artificially adjusted. Separate soil properties (pH, organic carbon content, clay content, cation-exchange capacity, aluminum oxyhydroxide content, and iron oxyhydroxide content) were not able to explain more than half the variation observed in soil sorption coefficients. This reflects the complexity of the sorbent-sorbate interactions. Partial-least-squares (PLS) models, integrating all the soil properties listed above, were able to explain as much as 78% of the variation in sorption coefficients. The PLS model was able to predict the sorption coefficient with an accuracy of a factor of six. Considering the pH-dependent speciation, species-specific PLS models were developed. These models were able to predict species-specific sorption coefficients with an accuracy of a factor of three to four. However, the species-specific sorption models did not improve the estimation of sorption coefficients of species mixtures, because these models were developed with a reduced data set at standardized aqueous concentrations. In conclusion, pragmatic approaches like PLS modeling might be suitable to estimate soil sorption for risk assessment purposes.

  16. Kinetics of neptunium(V) sorption and desorption on goethite: An experimental and modeling study

    Science.gov (United States)

    Tinnacher, Ruth M.; Zavarin, Mavrik; Powell, Brian A.; Kersting, Annie B.

    2011-11-01

    Various sorption phenomena, such as aging, hysteresis and irreversible sorption, can cause differences between contaminant (ad)sorption and desorption behavior and lead to apparent sorption 'asymmetry'. We evaluate the relevance of these characteristics for neptunium(V) (Np(V)) sorption/desorption on goethite using a 34-day flow-cell experiment and kinetic modeling. Based on experimental results, the Np(V) desorption rate is much slower than the (ad)sorption rate, and appears to decrease over the course of the experiment. The best model fit with a minimum number of fitting parameters was achieved with a multi-reaction model including (1) an equilibrium Freundlich site (site 1), (2) a kinetically-controlled, consecutive, first-order site (site 2), and (3) a parameter ψ, which characterizes the desorption rate on site 2 based on a concept related to transition state theory (TST). This approach allows us to link differences in adsorption and desorption kinetics to changes in overall reaction pathways, without assuming different adsorption and desorption affinities (hysteresis) or irreversible sorption behavior a priori. Using modeling as a heuristic tool, we determined that aging processes are relevant. However, hysteresis and irreversible sorption behavior can be neglected within the time-frame (desorption over 32 days) and chemical solution conditions evaluated in the flow-cell experiment. In this system, desorption reactions are very slow, but they are not irreversible. Hence, our data do not justify an assumption of irreversible Np(V) sorption to goethite in transport models, which effectively limits the relevance of colloid-facilitated Np(V) transport to near-field environments. However, slow Np(V) desorption behavior may also lead to a continuous contaminant source term when metals are sorbed to bulk mineral phases. Additional long-term experiments are recommended to definitely rule out irreversible Np(V) sorption behavior at very low surface loadings and

  17. Tailoring training to the need: Reaching all the workers

    International Nuclear Information System (INIS)

    Jones, E.

    1987-01-01

    By developing a comprehensive concept for radiation protection training at Oak Ridge National Laboratory, we are providing a complete program with easy access for additional radiation protection training upon demand. A framework for implementation of a program tailored to reach differing segments of the workforce quickly and effectively is outlined and illustrated with ORNL program experience. 10 refs

  18. Molecular tailoring approach for exploring structures, energetics and ...

    Indian Academy of Sciences (India)

    Administrator

    4,5 proposed a density matrix divide-and-conquer (DC) method for electronic structure calculation of large molecules. The method is based on partitioning the density matrix and is applicable to both HF and DFT level of theories. Subsequently, Gadre et al. 6 formulated the. Molecular Tailoring Approach (MTA) for evaluating.

  19. Design and Testing of Aeroelastically Tailored Wings Under Maneuver Loading

    NARCIS (Netherlands)

    Werter, N.P.M.; Sodja, J.; De Breuker, R.

    2016-01-01

    The goal of the present paper is to provide experimental validation data for the aeroelastic analysis of composite aeroelastically tailored wings with a closed-cell cross-sectional structure. Several rectangular wings with differ- ent skin thicknesses and composite layups are designed in order to

  20. Tailoring the particulate properties of aluminates prepared by ...

    Indian Academy of Sciences (India)

    Administrator

    Tailoring the particulate properties of aluminates prepared by combustion method. T MIMANI and K C PATIL. Department of Inorganic and Physical Chemistry, Indian Institute of Science,. Bangalore 560 012, India. Aluminium based spinels constitute an interesting class of oxide ceramics with technological applications such ...