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Sample records for strontium ions adsorption

  1. ADSORPTION OF STRONTIUM IONS FROM WATER ON MODIFIED ACTIVATED CARBONS

    Directory of Open Access Journals (Sweden)

    Mihai Ciobanu

    2016-12-01

    Full Text Available Adsorption of strontium ions from aqueous solutions on active carbons CAN-7 and oxidized CAN-8 has been studied. It has been found that allure of the adsorption isotherms for both studied active carbons are practically identical. Studies have shown that the adsorption isotherms for strontium ions from aqueous solutions are well described by the Langmuir and Dubinin-Radushkevich equations, respectively. The surface heterogeneity of activated carbons CAN-7 and oxidized CAN-8 has been assessed by using Freundlich equation.

  2. Adsorption of strontium (II) metal ions using phosphonate ...

    Indian Academy of Sciences (India)

    Chelation is a process wherein metalions and a polymer/matrix are bound together ... waste: evaporation, chemical precipitation/flocculation, solid-phase separation ... sary to remove strontium from the waste streams before it is discharged to ...

  3. Ion exchange of strontium on synthetic hydroxyapatite

    International Nuclear Information System (INIS)

    Lazic, S.; Vukovic, Z.

    1991-01-01

    Adsorption of strontium ions on synthetic hydroxyapatite was examined using both batch and column methods. The apatite was prepared from aqueous solutions and characterized by standard analytical methods. The sample obtained had characteristics of well crystallized stoichiometric hydroxyapatite. The experimental data for sorption of strontium can be very well fitted with Langmuir's adsorption isotherm. It was found that sorption occurs by an ion exchange reaction between strontium ions in solution and calcium ions in apatite. (author) 14 refs.; 5 figs.; 1 tab

  4. Isotope exchange of strontium and molybdate ions in strontium polymolybdates

    International Nuclear Information System (INIS)

    Atun, G.

    2002-01-01

    The heterogeneous isotopic exchange reactions in strontium polymolybdates of Sr 2+ and MoO 4 2- ions in the strontium nitrate and sodium molybdate solutions have been studied using 90 Sr and 99 Mo as tracers. Electrometric methods have been used to study the compositions of strontium molybdates obtained by adding strontium chloride to a progressively acidified solution of sodium molybdate. It has been found that the exchange fraction increases with increasing chain length of strontium polymolybdate. The exchange equilibrium constant (K ex ) has been calculated between 298 and 348 K as well as ΔG deg, ΔH deg and ΔS deg. The results indicate that Sr 2+ cations have a much higher affinity for exchangers than MoO 4 2- anions. By fitting the data to the Dubinin-Radushkevich (D-R) isotherm it has been shown that the exchange capacity (X m ) for both ions is affected by the ion adsorption process at low temperatures and by the ion exchange process at high temperatures. At high concentrations, the recrystallization process contributes to on the cation exchange but is ineffective on the anion exchange mechanism. (author)

  5. Effect of the synthesis temperature of sodium nona-titanate on batch kinetics of strontium-ion adsorption from aqueous solution

    International Nuclear Information System (INIS)

    Merceille, A.; Weinzaepfel, E.; Grandjean, A.; Merceille, A.; Weinzaepfel, E.; Barre, Y.

    2011-01-01

    Sodium titanate materials are promising inorganic ion exchangers for the adsorption of strontium from aqueous solutions. Sodium nona-titanate exhibits a layered structure consisting of titanate layers and exchangeable sodium ions between the layers. The materials used in this study include samples synthesized by a hydrothermal method at temperatures between 60 degrees C and 200 degrees C. Their structure, composition, and morphology were investigated with X-Ray diffraction measurements; thermogravimetric, compositional and surface area analyses, and scanning electron microscopy. The structure, composition, and morphology depended on the synthesis temperature. Batch kinetics experiments for the removal of strontium from aqueous solutions were performed, and the data were fitted by a pseudo-second-order reaction model and a diffusive model. The strontium extraction capacity also depended on the synthesis temperature and exhibited a maximum for samples synthesized at 100 degrees C. The sorption process occurs in one or two diffusion-controlled steps that also depend on the synthesis temperature. These diffusion-limited steps are the boundary-layer diffusion and intra-particle diffusion in the case of pure nona-titanate synthesized at temperatures lower than 170 degrees C, and only intra-particle diffusion in the case of nona-titanate synthesized at 200 degrees C. (authors)

  6. Adsorption of strontium ions on bentonites of slovak provenance - Influence of pH change of medium

    International Nuclear Information System (INIS)

    Galambos, M.; Kufcakova, J.; Rajec, P.; Paucova, V.

    2007-01-01

    Bentonite is a natural clay and one of the most promising candidates for use as a buffer material in the geological disposal systems for spent fuel and high-level nuclear waste. It is intended to isolate metal canisters with highly radioactive waste products from the surrounding rocks because of its ability to retard the movement of radionuclides by sorption. Slovak republic disposes of many significant deposits of bentonites, e.g. Jelsovy potok, Kopernica, Lieskovec, Lastovce, etc. The bentonites present significant group of natural nanomaterials composed of microcrystallic particles of montmorillonite. Bentonite is characterized by a low hydraulic conductivity, low throughput and excellent sorption capacity for cationic fission products of 235 U (e.g. 89 Sr, 90 Sr, 137 Cs). Sorption of strontium on bentonite from various Slovak deposits was studied using batch technique. Distribution coefficients (K d ) were determined for bentonite-strontium solution system as a function of contact time, pH, sorbent and sorbate concentration. The data were interpreted in term of Langmuir isotherm. The uptake of Sr was rapid and equilibrium was reached almost instantaneously. The effect of pH, on the sorption of metal ions on bentonite was studied by varying the pH of the aqueous metal solutions. The sorption of this nuclide increased by increasing pH. The percentage sorption decreased with increasing metal concentrations. These results could be helpful for nuclear waste management, for waste water effluents containing low concentrations of strontium. (authors)

  7. Adsorption of Pb(II) present in aqueous solution on calcium, strontium and barium hydroxy apatites

    International Nuclear Information System (INIS)

    Vilchis G, J.

    2013-01-01

    Calcium, strontium and barium hydroxy apatites were successfully synthesized by chemical precipitation method, the obtained powders were characterized by the techniques of X-ray diffraction (XRD), scanning electron microscopy (Sem), semi-quantitative elemental analysis (EDS), infrared spectroscopy (IR), and N 2 physisorption studies, complementary to these analytical techniques, was determined the surface fractal dimension (Df), and the amount of surface active sites of the materials, in order to know application as ceramic for water remediation. The ability of Pb(II) ion adsorption present in aqueous solution on the hydroxy apatites synthesized by batch type experiments was studied as a function of contact time, concentration of the adsorbate and temperature. The maximum lead adsorption efficiencies obtained were 0.31, 0.32 and 0.26 mg/g for calcium, strontium and barium hydroxy apatites respectively, achieved an equilibrium time of 20 minutes in the three solid-liquid systems studied. Experimental data were adequately adjusted at the adsorption kinetic model pseudo-second order, for the three cases. Moreover, experimental data of the strontium and calcium hydroxy apatites were adjusted to the Langmuir adsorption isotherm, indicating that the adsorption was through a monolayer, whereas barium hydroxyapatite was adjusted to the Freundlich adsorption isotherm, indicating a multilayer adsorption. The thermodynamic parameters obtained during adsorption studies as a function of temperature showed physisorption, exothermic and spontaneous processes respectively. The results showed that the calcium hydroxyapatite, strontium and barium are an alternative for the Pb(II) ion adsorption present in wastewaters. (Author)

  8. Depression Mechanism of Strontium Ions in Bastnaesite Flotation with Salicylhydroxamic Acid as Collector

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    Shiming Cao

    2018-02-01

    Full Text Available Metal ions are widely present in flotation pulp. Metal ions change solution chemistry and mineral surface properties, consequently affecting mineral flotation. In this work, the effect of strontium ions on bastnaesite flotation with salicylhydroxamic acid (SHA was investigated by microflotation tests, contact angle measurements, zeta-potential measurements, and X-ray photoelectron spectroscopy (XPS analysis. Microflotation tests confirmed that the addition of strontium ions decreased bastnaesite floatability, compared with that in the absence of strontium ions. Contact angle measurements suggested that the pretreatment of strontium ions decreased SHA adsorption. Zeta potential measurements confirmed that the bastnaesite was depressed by the adsorption of positively charged strontium species, and the lower adsorption capacity of SHA onto the bastnaesite surfaces was obtained after modifying with strontium ions. XPS analysis demonstrated that strontium ions adsorbed onto the bastnaesite surfaces through the interaction between strontium ions and oxygen atoms of surface ≡ CeOH 0 groups. This occurrence hindered surface Ce sites which chelated with SHA and therefore, decreased bastnaesite floatability.

  9. Strontium adsorption and penetration in kaolinite at low Sr

    NARCIS (Netherlands)

    Ning, Zigong; Ishiguro, Munehide; Koopal, Luuk K.; Sato, Tsutomu; Kashiwagi, Junichi

    2017-01-01

    Behavior of radioactive strontium (Sr2+) in contaminated soils is an important issue in relation to nuclear power plant accidents. The Sr2+ adsorption on kaolinite and its migration in a kaolinite soil were investigated because toxic effects of radioactive Sr2+ have been found to be very severe for

  10. Surface adsorption in strontium chloride ammines

    DEFF Research Database (Denmark)

    Ammitzbøll, Andreas L.; Lysgaard, Steen; Klukowska, Agata

    2013-01-01

    An adsorbed state and its implications on the ab- and desorption kinetics of ammonia in strontium chloride ammine is identified using a combination of ammonia absorption measurements, thermogravimetric analysis, and density functional theory calculations. During thermogravimetric analysis, ammonia...... desorption originating from the adsorbed state is directly observed below the bulk desorption temperature, as confirmed by density functional theory calculations. The desorption enthalpy of the adsorbed state of strontium chloride octa-ammine is determined with both techniques to be around 37-39 k...

  11. Thermodynamic study on the adsorption of strontium on polyantimonic acid exchanger

    International Nuclear Information System (INIS)

    Li Mingyu; Chen Jing; Wang Jianchen; Zhao Jing

    2007-01-01

    The adsorption of strontium on the polyantimonic acid adsorbent was studied. The equilibrium data for the adsorption of strontium on polyantimonic acid exchanger from aqueous solutions were obtained and correlated with Langmuir-type and Freundlich-type isotherm equation within the temperature range of 293-323 K and the experimental concentration range. Freundlich adsorption isotherms and the isosteric enthalpy indicate that the adsorption of strontium on polyantimonic acid is an endothermic process from aqueous solutions. The enthalpy, free energy, and entropy of adsorption were calculated. The results indicate that the adsorption process is a complex interaction of physical and chemical processes. The adsorption behaviors were reasonably explained. (authors)

  12. Optimization of strontium adsorption from aqueous solution using (mn-Zr) oxide-pan composite spheres

    International Nuclear Information System (INIS)

    Inan, S.; Altas, Y.

    2009-01-01

    The processes based on adsorption and ion exchange have a great role for the pre-concentration and separation of toxic, long lived radionuclides from liquid waste. In Nuclear waste management, the removal of long lived, radiotoxic isotopes from radioactive waste such as strontium reduces the storage problems and facilitates the disposal of the waste. Depending on the waste type, a variety of adsorbents and/or ion exchangers are used. Due to the amorphous structure of hydrous oxides and their mixtures, they don't have reproducible properties. Besides, obtained powders are very fine particles and they can cause operational problems such as pressure drop and filtration. Therefore they are not suitable for column applications. These reasons have recently expedited the study on the preparation of organic-inorganic composite adsorbent beads for industrial applications. PAN, as a stable and porous support for fine particles, provides the utilization of ion exchangers in large scale column applications. The utilization of PAN as a support material with many inorganic ion exchangers was firstly achieved by Sebesta in the beginning of 1990's. Later on, PAN based composite ion exchangers were prepared and used for the removal of radionuclides and heavy metal ions from aqueous solution and waste waters. In this study, spherical (Mn-Zr)oxide-PAN composite were prepared for separation of strontium from aqueous solution in a wide pH range. Sr 2 + adsorption of composite adsorbent was optimized by using experimental design 'Central Composite Design' model.

  13. Comparative study of strontium adsorption on dioctahedral and trioctahedral smectites

    International Nuclear Information System (INIS)

    Galambos, M.; Rosskopfova, O.; Krajnak, A.; Rajec, P.; Osacky, M.; Comenius University, Bratislava

    2012-01-01

    Slovak bentonites characterized by good rheological, mineralogical and chemical stability are considered as suitable sealing barriers for construction of Slovak deep geological repository for high-level radioactive waste and spent nuclear fuel. There is several Slovak bentonite deposits, bentonites of which have appropriate adsorption properties meeting the geotechnical requirements for this type of barriers. Study of adsorption properties of bentonites (mainly smectites) is an essential step for developing the migration model long-lived corrosion and activation products, and fission products of uranium. Nuclear wastes contain the most important nuclear fission products, β-emitter 90 Sr with long half-life, biological half-life and high mobility. The present paper investigates and compares the strontium adsorption properties of bentonites of different mineral composition consisted mainly of dioctahedral and trioctahedral smectites. (author)

  14. Study of cesium and strontium adsorption on slovak bentonite

    International Nuclear Information System (INIS)

    Galambos, M.

    2010-01-01

    Bentonite is a natural clay and one of the most promising candidates for use as a buffer material in the geological disposal systems for high-level radioactive waste and spent nuclear fuel. It is intended to isolate metal canisters with highly radioactive waste products from the surrounding rocks because of its ability to retard the movement of radionuclides by adsorption. Slovak Republic avails of many significant deposits of bentonite. Adsorption of Cs and Sr on five Slovak bentonite of deposits (Jelsovy potok, Kopernica, Lieskovec, Lastovce and Dolna Ves) and montmorillonite K10 (Sigma-Aldrich) has been studied with the using batch of radiometric techniques. Natural, irradiated and natrified samples, in three different kinds of grain size: 15, 45 and 250 μm have been used in the experiments. The adsorptions of Cs and Sr on bentonite under various experimental conditions, such as contact time, adsorbent and adsorbate concentrations, pH after adsorption and effect of pH change, chemical modification, competitive ions and organic agents on the adsorption have been studied. The K d have been determined for adsorbent-Cs/Sr solution system as a function of contact time and adsorbate and adsorbent concentration. The data have been interpreted in terms of Langmuir isotherm. The adsorption of Cs and Sr has increased with increasing metal concentrations. Adsorption of Cs and Sr has been suppressed by presence of organic agents; and of bivalent cations more than univalent cations. By adsorption on natrified samples colloidal particles and pH value increase have been formed. Adsorption experiments carried out show that the most suitable materials intended for use as barriers surrounding a canister of spent nuclear fuel are bentonite of the Jelsovy potok and Kopernica deposits. (author)

  15. Programmed gradient descent biosorption of strontium ions by Saccaromyces cerevisiae and ashing analysis: A decrement solution for nuclide and heavy metal disposal

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Mingxue [Life Science and Engineering College, Southwest University of Science and Technology, Mianyang, 621010 (China); Key Laboratory of Solid Waste Treatment and Resource Recycle, Ministry of Education of China, Mianyang, 621010 (China); Dong, Faqin, E-mail: fqdong@swust.edu.cn [Key Laboratory of Solid Waste Treatment and Resource Recycle, Ministry of Education of China, Mianyang, 621010 (China); Zhang, Wei [Key Laboratory of Solid Waste Treatment and Resource Recycle, Ministry of Education of China, Mianyang, 621010 (China); Nie, Xiaoqin [Fundamental Science on Nuclear Wastes and Environmental Safety Laboratory, Mianyang, 621010 (China); Sun, Shiyong [Key Laboratory of Solid Waste Treatment and Resource Recycle, Ministry of Education of China, Mianyang, 621010 (China); Wei, Hongfu; Luo, Lang; Xiang, Sha; Zhang, Gege [Life Science and Engineering College, Southwest University of Science and Technology, Mianyang, 621010 (China)

    2016-08-15

    Highlights: • A programmed gradient descent biosorption process was designed. • The adsorption and bioaccumulation quantity of strontium ions by yeast cell were measured. • The decrement of biosorbents after biosorption by ashing was analyzed. • A technological flow process of decrement solution for waste disposal was proposed. - Abstract: One of the waste disposal principles is decrement. The programmed gradient descent biosorption of strontium ions by Saccaromyces cerevisiae regarding bioremoval and ashing process for decrement were studied in present research. The results indicated that S. cerevisiae cells showed valid biosorption for strontium ions with greater than 90% bioremoval efficiency for high concentration strontium ions under batch culture conditions. The S. cerevisiae cells bioaccumulated approximately 10% of strontium ions in the cytoplasm besides adsorbing 90% strontium ions on cell wall. The programmed gradient descent biosorption presented good performance with a nearly 100% bioremoval ratio for low concentration strontium ions after 3 cycles. The ashing process resulted in a huge volume and weight reduction ratio as well as enrichment for strontium in the ash. XRD results showed that SrSO{sub 4} existed in ash. Simulated experiments proved that sulfate could adjust the precipitation of strontium ions. Finally, we proposed a technological flow process that combined the programmed gradient descent biosorption and ashing, which could yield great decrement and allow the supernatant to meet discharge standard. This technological flow process may be beneficial for nuclides and heavy metal disposal treatment in many fields.

  16. Biosorption of Strontium from Simulated Nuclear Wastewater by Scenedesmus spinosus under Culture Conditions: Adsorption and Bioaccumulation Processes and Models

    Science.gov (United States)

    Liu, Mingxue; Dong, Faqin; Kang, Wu; Sun, Shiyong; Wei, Hongfu; Zhang, Wei; Nie, Xiaoqin; Guo, Yuting; Huang, Ting; Liu, Yuanyuan

    2014-01-01

    Algae biosorption is an ideal wastewater treatment method when coupled with algae growth and biosorption. The adsorption and bioaccumulation of strontium from simulated nuclear wastewater by Scenedesmus spinosus were investigated in this research. One hundred mL of cultured S. spinosus cells with a dry weight of 1.0 mg in simulated nuclear wastewater were used to analyze the effects on S. spinosus cell growth as well as the adsorption and bioaccumulation characters under conditions of 25 ± 1 °C with approximately 3,000 lux illumination. The results showed that S. spinosus had a highly selective biosorption capacity for strontium, with a maximum bioremoval ratio of 76%. The adsorbed strontium ion on cell walls was approximately 90% of the total adsorbed amount; the bioaccumulation in the cytoplasm varied by approximately10%. The adsorption quantity could be described with an equilibrium isotherm. The pseudo-second-order kinetic model suggested that adsorption was the rate-limiting step of the biosorption process. A new bioaccumulation model with three parameters was proposed and could give a good fit with the experiment data. The results suggested that S. spinosus may be a potential biosorbent for the treatment of nuclear wastewater in culture conditions. PMID:24919131

  17. Biosorption of Strontium from Simulated Nuclear Wastewater by Scenedesmus spinosus under Culture Conditions: Adsorption and Bioaccumulation Processes and Models

    Directory of Open Access Journals (Sweden)

    Mingxue Liu

    2014-06-01

    Full Text Available Algae biosorption is an ideal wastewater treatment method when coupled with algae growth and biosorption. The adsorption and bioaccumulation of strontium from simulated nuclear wastewater by Scenedesmus spinosus were investigated in this research. One hundred mL of cultured S. spinosus cells with a dry weight of 1.0 mg in simulated nuclear wastewater were used to analyze the effects on S. spinosus cell growth as well as the adsorption and bioaccumulation characters under conditions of 25 ± 1 °C with approximately 3,000 lux illumination. The results showed that S. spinosus had a highly selective biosorption capacity for strontium, with a maximum bioremoval ratio of 76%. The adsorbed strontium ion on cell walls was approximately 90% of the total adsorbed amount; the bioaccumulation in the cytoplasm varied by approximately10%. The adsorption quantity could be described with an equilibrium isotherm. The pseudo-second-order kinetic model suggested that adsorption was the rate-limiting step of the biosorption process. A new bioaccumulation model with three parameters was proposed and could give a good fit with the experiment data. The results suggested that S. spinosus may be a potential biosorbent for the treatment of nuclear wastewater in culture conditions.

  18. DETERMINATION OF STRONTIUM IONS IN WATERS WITH A HIGH CONTENT OF SODIUM IONS

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    Tatiana Mitina

    2015-06-01

    Full Text Available This paper reports on the influence of sodium ions on experimental determination of strontium ions concentration in waters with a high content of sodium ions by using emission flame photometry and atomic absorption spectroscopy. For the method of emission flame photometry it was shown that at a wavelength of 460.7 nm (spectral emission line of strontium the emission is linearly dependent on the concentration of sodium ions. The greatest impact of high concentrations of sodium ions on the result of determination the strontium ions concentration has been registered at low levels of strontium. The influence of nitric acid on the results is also discussed. In the case of using atomic absorption spectroscopy method no influence of sodium ions and nitric acid on the results of determination the strontium ions concentration was revealed. The metrological characteristics of both methods are evaluated.

  19. Adsorption of Radioactive Strontium and Caesium from Mixtures of Solutions

    International Nuclear Information System (INIS)

    Haznedaroglu, H.N.

    2002-07-01

    In this thesis, the adsorption of the radioactive Cs and Sr on two different types of cement, Sulfate Resistant Cement and Portland Composed Cement, was investigated. The gamma-active Cs-137 and Sr-85 were used as tracers. Four different mixtures of solutions of Cs and Sr were used in experiments; a) The solution containing trace amount of Sr-85 and Cs-137 b) 1.10 - 5 - 1.10 - 1 M *SrCl 2 solutions containing trace amount of Cs-137 c) 1.10 - 5 - 1.10 - 1 M *CsCl solutions containing trace amount of Sr-85 d) The equal amount of mixtures of 1.10 - 5 - 1.10 - 1 M SrCl 2 and 1.10 - 5 - 1.10 - 1 M CsCl solutions. It was shown that the convenient ph values for the comparison of Cs and Sr adsorption on both cement were 2.5 and 11.0. It was observed that the adsorption capacity of Sr on Sulfate Resistant Cement was twice that for the Portland Composed Cement in the solutions containing trace amount of Cs-137 and 1.10 - 5 - 1.10 - 1 *SrCl 2 . The in cease in adsorption capacity is related to the Ca to Sr ion exchange in Sulfate Resistant Cement containing appreciable amount of C 3 S. The adsorption of Cs and Sr on both types of cement in solutions containing equal amount of CsCl and SrCl 2 was greater than that of individual solutions of CsCl and SrCl 2 . This latter behavior is related to the ion charge, the hydration of ions and the interaction of the Cs with the Sr on the surface of adsorbent. It was observed that although Portland Composed Cement adsorbs Cs selectively, Sulfate Resistant Cement has a greater affinity for Sr. Cs adsorption is not affected by ph changes whilst Sr adsorption is highly dependent on ph

  20. 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.

  1. Batch kinetics, isotherm and thermodynamic studies of adsorption of strontium from aqueous solutions onto low cost rice-straw based carbons.

    Directory of Open Access Journals (Sweden)

    S. M. Yakout

    2010-09-01

    Full Text Available Present study explored the feasibility of using waste rice-straw based carbons as adsorbent for the removal of strontium under different experimental conditions. The batch sorption is studied with respect to solute concentration (2.8 - 110 mg/L, contact time, adsorbent dose (2.5 - 20 g/L and solution temperature (25 - 55oC. The Langmuir and Dubinin-Radushkevich adsorption models were applied to experimental equilibrium data and isotherm constants were calculated using linear regression analysis. A comparison of kinetic models applied to the adsorption of strontium on rice-straw carbon was evaluated for the pseudo-second-order, Elovich, intraparticle diffusion and Bangham’s kinetics models. The experimental data fitted very well the pseudosecond-order kinetic model and also followed by intra-particle diffusion model, whereas diffusion is not only the rate-controlling step. The results show that the sorption capacity increases with an increase in solution temperature from 25 to 55 oC. The thermodynamics parameters were evaluated. The positive value of ΔH (40.93 kJ indicated that the adsorption of strontium onto RS1 carbon was endothermic, which result was supported by the increasing adsorption of strontium with temperature. The positive value of ΔS (121.8 kJ/mol reflects good affinity of strontium ions towards the rice-straw based carbons. The results have establishedgood potentiality for the carbons particles to be used as a sorbent for the removal of strontium from wastewater.

  2. Removal of strontium ions from solutions using granulated zeolites

    International Nuclear Information System (INIS)

    Bronic, J.; Subotic, B.

    1992-01-01

    The ion-exchange process on columns filled with granulated zeolites is determined by several physico-chemical parameters. The influence of these parameters (zeolite type, concentration of exchangeable ions in solution, temperature, flow rate, etc.) on the kinetics of ion-exchange process was studied by measuring the Sr 2+ ion concentration in solution before and after passing through a column filled with various granulated zeolites (zeolite 13X, zeolite A and synthetic mordenite). Using the experimental technique of radioactive labeling by 89 Sr, the distribution of Sr 2+ ions in column fillings were also determined. From the results obtained, the optimal conditions for the most efficient removal of strontium ions from solutions using granulated zeolites can be defined. (author) 24 refs.; 9 figs

  3. Adsorption behavior of strontium on kaolinite and montmorillonite and their mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Atun, G. [Istanbul Univ. (Turkey). Engineering Faculty, Chemistry Dept.; Bascetin, E. [Cekmece Nuclear Research and Training Center, Istanbul (Turkey)

    2004-07-01

    {sup 90}Sr, with a long half-life of 28.5 years, is the most dangerous strontium isotope. The adsorption behavior of radionuclides in the environment are closely related to the safe disposal of radioactive wastes. Since various types of minerals may exist in and around the repositories used for ultimate disposal of nuclear waste, the adsorption behavior of certain radionuclides onto and from these minerals and similar adsorbents should be studied in order to estimate the rates of transport of the nuclides in the event of water penetration into and through the repository. Information on the adsorption properties of the purified individual clay minerals may not be sufficient to predict the adsorption properties of a corresponding mixture, because these clay minerals may interact with each other and lead to modification of the adsorption properties of the mixture as compared to the pure minerals. The adsorption behavior of strontium on kaolinite and montmorillonite minerals and their mixtures was studied by means of a batch method and a tracer technique. (orig.)

  4. Adsorption of strontium on different sodium-enriched bentonites

    Directory of Open Access Journals (Sweden)

    Marinović Sanja R.

    2017-01-01

    Full Text Available Bentonites from three different deposits (Wyoming, TX, USA and Bogovina, Serbia with similar cation exchange capacities were sodium enriched and tested as adsorbents for Sr2+ in aqueous solutions. X-Ray diffraction analysis confirmed successful Na-exchange. The textural properties of the bentonite samples were determined using low-temperature the nitrogen physisorption method. Significant differences in the textural properties between the different sodium enriched bentonites were found. Adsorption was investigated with respect to adsorbent dosage, pH, contact time and the initial concentration of Sr2+. The adsorption capacity increased with pH. In the pH range from 4.0–8.5, the amount of adsorbed Sr2+ was almost constant but 2–3 times smaller than at pH ≈11. Further experiments were performed at the unadjusted pH since extreme alkaline conditions are environmentally hostile and inapplicable in real systems. The adsorption capacity of all the investigated adsorbents toward Sr2+ was similar under the investigated conditions, regardless of significant differences in the specific surface areas. It was shown and confirmed by the Dubinin–Radushkevich model that the cation exchange mechanism was the dominant mechanism of Sr2+ adsorption. Their developed microporous structures contributed to the Sr2+ adsorption process. The adsorption kinetics obeyed the pseudo-second-order model. The isotherm data were best fitted with the Langmuir isotherm model. [Project of the Serbian Ministry of Education, Science and Technological Development, Grant no. III 45001

  5. Adsorption behavior of strontium on binary mineral mixtures of Montmorillonite and Kaolinite

    Energy Technology Data Exchange (ETDEWEB)

    Bascetin, Elvan [Cekmece Nuclear Research and Training Center, P.K.1 34149, Atatuerk Airport, Istanbul (Turkey); Atun, Guelten [Engineering Faculty, Chemistry Department, Istanbul University, 34850 Avcilar, Istanbul (Turkey)]. E-mail: gultena@istanbul.edu.tr

    2006-08-15

    The adsorption behavior of kaolinite and montmorillonite minerals and their mixtures in respect of Sr ion were studied by means of a batch method using {sup 90}Sr as a radio tracer. The effect of several parameters such as temperature, pH, Sr concentration and supporting electrolyte were investigated. Experimentally measured distribution coefficients showed a good agreement to within 98.5-99.7% with theoretically calculated values. The values of adsorption capacity of adsorbents and mean adsorption energy of adsorption were calculated by fitting the adsorption data to Dubinin-Radushkevich isotherm. The adsorption capacity of clay mixtures decreased as kaolinite fractions increased. The mean adsorption energy values of 8.0-9.5 kJ mol{sup -1} showed that adsorption was governed by ion exchange. The Freundlich parameters were used to characterize a site distribution function for binary exchange between Sr and Na.

  6. Adsorption behavior of strontium on binary mineral mixtures of Montmorillonite and Kaolinite

    International Nuclear Information System (INIS)

    Bascetin, Elvan; Atun, Guelten

    2006-01-01

    The adsorption behavior of kaolinite and montmorillonite minerals and their mixtures in respect of Sr ion were studied by means of a batch method using 90 Sr as a radio tracer. The effect of several parameters such as temperature, pH, Sr concentration and supporting electrolyte were investigated. Experimentally measured distribution coefficients showed a good agreement to within 98.5-99.7% with theoretically calculated values. The values of adsorption capacity of adsorbents and mean adsorption energy of adsorption were calculated by fitting the adsorption data to Dubinin-Radushkevich isotherm. The adsorption capacity of clay mixtures decreased as kaolinite fractions increased. The mean adsorption energy values of 8.0-9.5 kJ mol -1 showed that adsorption was governed by ion exchange. The Freundlich parameters were used to characterize a site distribution function for binary exchange between Sr and Na

  7. Adsorption of Cesium, Strontium, and Rubidium radionuclides in the Mag-molecular process: The influence of important factors

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    Fatemeh Tangestani

    2017-09-01

    Full Text Available In this study, the adsorption of cesium, strontium, and rubidium radionuclides by ferritin magmolecules in a batch system was investigated under different experimental conditions. The experiments were conducted in a pilot plant that involved the contactor unit and the magnetic separator unit. The impact of the pollutant concentrations, adsorbent concentration, and pH on the efficiency of the process were investigated thoroughly. The maximum recovery of radionuclides in the studied domain were 57.05%, 85.42% and 71.82% for Cs+, Sr2+ and Rb+ ,respectively, in which the pollutant concentration was 363.63 mg/l, the adsorbent concentration was 0.011 g/l, and the pH was 7.5. The results showed that the ferritin adsorbent in the magmolecular process manifested a higher efficiency in adsorbing the bivalent ions of strontium compared to the univalent ions of cesium and rubidium. Furthermore, the results were statistically analyzed and the model and residual plots of each radionuclide were presented. The results also signified  relationships between the independent variables and recovery.

  8. Strontium-90 in ion-exchange resin used in the Australian FIEFS network

    International Nuclear Information System (INIS)

    Wise, K.N.

    1977-10-01

    In order to determine monthly strontium-90 fallout deposited at the eight Australian monitoring stations, account must be taken of the level of strontium-90 contamination of the ion-exchange resin as prepared for use in the FIEFS. This procedure has always been important in monitoring strontium-90 fallout deposit in Australia because the level of strontium-90 contamination of ion-exchange resin, supplied by manufacturers in the Northern Hemisphere, has remained of the same order of magnitude as the monthly fallout deposit in the Southern Hemisphere

  9. Adsorption on mixtures of ion exchangers

    International Nuclear Information System (INIS)

    Triolo, R.; Lietzke, M.H.

    1979-01-01

    A theoretical study has been made of adsorption on mixtures of ion exchangers. The effect of variables such as the concentration of the ion being adsorbed, the concentration of the supporting electrolyte, loading, the values of the capacities and equilibrium constants for the various exchange processes, and the fraction of each adsorber in the mixture on the observed distribution coefficient has been investigated. A computer program has been written to facilitate the calculation of distribution coefficients for the adsorption of an ion on a given mixture of ion exchangers under a specified set of conditions

  10. Adsorption of Pb(II) present in aqueous solution on calcium, strontium and barium hydroxy apatites; Adsorcion de Pb(II) presente en solucion acuosa sobre hidroxiapatitas de calcio, estroncio y bario

    Energy Technology Data Exchange (ETDEWEB)

    Vilchis G, J.

    2013-07-01

    Calcium, strontium and barium hydroxy apatites were successfully synthesized by chemical precipitation method, the obtained powders were characterized by the techniques of X-ray diffraction (XRD), scanning electron microscopy (Sem), semi-quantitative elemental analysis (EDS), infrared spectroscopy (IR), and N{sub 2} physisorption studies, complementary to these analytical techniques, was determined the surface fractal dimension (Df), and the amount of surface active sites of the materials, in order to know application as ceramic for water remediation. The ability of Pb(II) ion adsorption present in aqueous solution on the hydroxy apatites synthesized by batch type experiments was studied as a function of contact time, concentration of the adsorbate and temperature. The maximum lead adsorption efficiencies obtained were 0.31, 0.32 and 0.26 mg/g for calcium, strontium and barium hydroxy apatites respectively, achieved an equilibrium time of 20 minutes in the three solid-liquid systems studied. Experimental data were adequately adjusted at the adsorption kinetic model pseudo-second order, for the three cases. Moreover, experimental data of the strontium and calcium hydroxy apatites were adjusted to the Langmuir adsorption isotherm, indicating that the adsorption was through a monolayer, whereas barium hydroxyapatite was adjusted to the Freundlich adsorption isotherm, indicating a multilayer adsorption. The thermodynamic parameters obtained during adsorption studies as a function of temperature showed physisorption, exothermic and spontaneous processes respectively. The results showed that the calcium hydroxyapatite, strontium and barium are an alternative for the Pb(II) ion adsorption present in wastewaters. (Author)

  11. Kinetics of isotopic exchange between strontium polymolybdate and strontium ions in aqueous solution

    International Nuclear Information System (INIS)

    Atun, Gulten; Bilgin, Binay; Kilislioglu, Ayben

    2002-01-01

    A heterogeneous isotopic exchange reaction of strontium polymolybdate in strontium chloride solution was studied using 90 Sr as a tracer. The effects of low and high strontium chloride concentration on the rate and mechanism of the isotopic exchange reaction were investigated. It was found that, at high concentrations, the rate is independent of strontium concentration, but, at low concentrations, the rate is proportional to the strontium concentration. These results support a hypothesis that, at low concentrations, the rate is controlled by film diffusion, whereas at high concentrations it is controlled by particle diffusion. Experiments were performed at 293, 303 and 313 K. Activation energy of isotopic exchange reaction and thermodynamic parameters ΔH*, ΔS*, and ΔG* were calculated using the Arrhenius and Eyring equations. The results also indicated that recrystallization is a predominant factor in the present exchange reaction

  12. Kinetics of isotopic exchange between strontium polymolybdate and strontium ions in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Atun, Gulten E-mail: gultena@istanbul.edu.tr; Bilgin, Binay; Kilislioglu, Ayben

    2002-06-01

    A heterogeneous isotopic exchange reaction of strontium polymolybdate in strontium chloride solution was studied using {sup 90}Sr as a tracer. The effects of low and high strontium chloride concentration on the rate and mechanism of the isotopic exchange reaction were investigated. It was found that, at high concentrations, the rate is independent of strontium concentration, but, at low concentrations, the rate is proportional to the strontium concentration. These results support a hypothesis that, at low concentrations, the rate is controlled by film diffusion, whereas at high concentrations it is controlled by particle diffusion. Experiments were performed at 293, 303 and 313 K. Activation energy of isotopic exchange reaction and thermodynamic parameters {delta}H*, {delta}S*, and {delta}G* were calculated using the Arrhenius and Eyring equations. The results also indicated that recrystallization is a predominant factor in the present exchange reaction.

  13. Influences of salt concentration, loading and pH on strontium adsorption

    International Nuclear Information System (INIS)

    Atun, G.; Kaplan, Z.

    1996-01-01

    The adsorption of Sr on clay with contains zeolites and montmorillonite mixtures was investigated in solutions of NaCl by means of a batch technique. Sr retention was reduced with increasing NaCl concentration from 5*10 -4 to 5*10 -1 M. Distribution coefficients (K d ) linearly increased with pH in the acidic region but they were almost independent of pH in neutral and alkaline solutions. By fitting the data of the Dubinin-Radushkevich (D-R) isotherm, the mean energies of adsorption and adsorption capacities of Sr at different pH values were calculated. The results showed that the mode of adsorption below pH 4.5 is ion exchange, while above that value a multilayer adsorption occurs. Adsorption data were fitted to the Freundlich isotherm and from empirical Freundlich parameters a site distribution function was calculated. (author)

  14. Adsorption of ferrous ions onto montmorillonites

    Energy Technology Data Exchange (ETDEWEB)

    Qin, Dawei, E-mail: qdw109@163.com [Qilu University of Technology, Jinan, 250353, Shandong (China); Niu, Xia [Qilu University of Technology, Jinan, 250353, Shandong (China); Qiao, Min; Liu, Gang; Li, Hongxin; Meng, Zhenxiao [Shandong SiBang pharmaceutical co., LTD, Jinan, Shandong, 250200 (China)

    2015-04-01

    Highlights: • Adsorption study of ferrous ions on montmorillonites. • Using ascorbic acid as antioxidants in adsorption process. • Fe (II)-MMT had good affinity for phosphate. - Abstract: The adsorption of Fe (II) onto montmorillonites was investigated through initial concentration, contact time, pH and temperature. During the whole adsorption process, the ascorbic acid (Vitamin C) was added as a kind of antioxidant, at the same time, deionized water (after boiling) and nitrogen protection were also used to avoid oxidation. The Fe{sup 2+}/Fe{sub total} ratio of the iron exists in the Fe-montmorillonites was found more than 95%. Two kinetic models, including pseudo-first-order and pseudo-second-order model, were used to analyze the adsorption process of Fe (II) on montmorillonites. The results of our study showed that adsorption process fitted with pseudo-second-order well. Adsorption isotherms showed that Langmuir model was better than Freundlich model. The thermodynamic parameters ΔG{sup 0} and ΔH{sup 0} were 3.696 kJ/mol and 6.689 kJ/mol (we just gave the values at 298 K), respectively. The positive values at different temperatures showed that the adsorption process was non-spontaneous and endothermic. The characteristics of materials were determined by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Surface area and porosity analyzer, Thermogravimetric analysis (TGA), Differential scanning calorimeter (DSC) and Zeta potential distribution.

  15. Ion adsorption properties of molybdenum (II) bromide

    International Nuclear Information System (INIS)

    Ganzerli-Valentini, M.T.; Meloni, S.; Caramella-Crespi, V.; Borroni, P.A.

    1976-01-01

    The adsorption of about 50 ions on molybdenum dibromide, (Mo 6 Br 8 )Br 4 .2H 2 O in nitric acid was investigated. The behaviour of the investigated elements on MDB in nitric acid, in the concentration range 10 -2 -8M is presented, where the distribution coefficients are given against the HNO 3 molarity. In some cases the elements were investigated in different oxidation states. Most of the elements are not adsorbed or poorly adsorbed, among these the stable anions, thus indicating that bromide ions substitution with other anions is not competitive. The preparation of the adsorber and its characterization is presented and discussed. Adsorption mechanism studies were carried out for some noble metals and chromium. Sorption cannot be ascribed to ion exchange mechanism but to formation of insoluble species, and to settlement of few ions into surface sorption sites or into a limited number of cavitites in the cluster crystal structure of the adsorber. (T.G.)

  16. Investigation of the strontium (Sr(II)) adsorption of an alginate microsphere as a low-cost adsorbent for removal and recovery from seawater.

    Science.gov (United States)

    Hong, Hye-Jin; Ryu, Jungho; Park, In-Su; Ryu, Taegong; Chung, Kang-Sup; Kim, Byuong-Gyu

    2016-01-01

    In this paper, we investigated alginate microspheres as a low-cost adsorbent for strontium (Sr(II)) removal and recovery from seawater. Alginate microspheres have demonstrated a superior adsorption capacity for Sr(II) ions (≈110 mg/g). A Freundlich isotherm model fits well with the Sr(II) adsorption of an alginate microsphere. The mechanism of Sr(II) adsorption is inferred as an ion exchange reaction with Ca(II) ions. The effects of the solution pH and co-existing ions in seawater are also investigated. Except for a pH of 1-2, Sr(II) adsorption capacity is not affected by pH. However, increasing the seawater concentration of metal cations seriously decreases Sr(II) uptake. In particular, highly concentrated (15,000 mg/L) Na(I) ions significantly interfere with Sr(II) adsorption. Sr(II) desorption was performed using 0.1 M HCl and CaCl2. Both regenerants show an excellent desorption efficiency, but the FTIR spectrum reveals that the chemical structure of the microsphere is destroyed after repeated use of HCl. Conversely, CaCl2 successfully desorbed Sr(II) without damage, and the Sr(II) adsorption capacity does not decrease after three repeated uses. The alginate microsphere was also applied to the adsorption of Sr(II) in a real seawater medium. Because of inhibition by co-existing ions, the Sr(II) adsorption capacity was decreased and the adsorption rate was retarded compared with D.I. water. Although the Sr(II) adsorption capacity was decreased, the alginate microsphere still exhibited 17.8 mg/g of Sr(II) uptake in the seawater medium. Considering its excellent Sr(II) uptake in seawater and its reusability, an alginate microsphere is an appropriate cost-effective adsorbent for the removal and recovery of Sr(II) from seawater. Copyright © 2015 Elsevier Ltd. All rights reserved.

  17. Adsorption of ions onto treated natural zeolite

    Directory of Open Access Journals (Sweden)

    Cristiane da Rosa Oliveira

    2007-12-01

    Full Text Available This work presents studies of modification of a natural zeolite by activation with Na+ cations and functionalisation with Ba+2 and/or Cu2+ ions (FZ. The zeolite was characterized, modified and applied in adsorption studies of sulphate and isopropilxanthate ions as flocculated and powdered forms. The reuse of SO4Ba-FZ was investigated by adsorption-removal of either Ba2+ or sulphate ions in stages. Equilibrium data showed that the FZ, flocculated or as powder, provide considerable removal of sulphate ions (q mLangmuir: 1.15 and 1.35 meq.g-1, respectively and isopropilxanthate (q mLangmuir: 0.35 and 0.93 meq.g-1, respectively. The reuse of the SO4-FZ, either powdered or flocculated also uptake significant amount of Ba2+ or sulphate ions (q mLangmuir: 1.15 meq.g-1, providing a new alternative for the exhausted adsorbent. Thus the activated and functionalised zeolites create new options on the materials engineering area with applications in environmental applied adsorption processes.

  18. Infrared and Raman spectroscopic study of ion pairing of strontium(II ...

    African Journals Online (AJOL)

    ABSTRACT. Infrared and Raman spectroscopy techniques have been used to study the ionic interactions of strontium(II) and barium(II) with thiocyanate ion in liquid ammonia. A number of bands were observed in both ν(CN) and ν(CS) regions of infrared and Raman spectra and these were assigned to 1:1 contact ion pair, ...

  19. Preparation of highly stable zeolite-alginate foam composite for strontium(90Sr) removal from seawater and evaluation of Sr adsorption performance.

    Science.gov (United States)

    Hong, Hye-Jin; Kim, Byoung-Gyu; Ryu, Jungho; Park, In-Su; Chung, Kang-Sup; Lee, Sang Moon; Lee, Jin-Bae; Jeong, Hyeon Su; Kim, Hyunchul; Ryu, Taegong

    2018-01-01

    Alginate bead is a promising strontium (Sr) adsorbent in seawater, but highly concentrated Na ions caused over-swelling and damaged the hydrogel bead. To improve the mechanical stability of alginate bead, flexible foam-type zeolite-alginate composite was synthesized and Sr adsorption performance was evaluated in seawater; 1-10% zeolite immobilized alginate foams were prepared by freeze-dry technique. Immobilization of zeolite into alginate foam converted macro-pores to meso-pores which lead to more compact structure. It resulted in less swollen composite in seawater medium and exhibited highly improved mechanical stability compared with alginate bead. Besides, Sr adsorption efficiency and selectivity were enhanced by immobilization of zeolite in alginate foam due to the increase of Sr binding sites (zeolite). In particular, Sr selectivity against Na was highly improved. The 10% zeolite-alginate foam exhibited a higher log K d of 3.3, while the pure alginate foam exhibited 2.7 in the presence of 0.1 M Na. Finally, in the real seawater, the 10% zeolite-alginate foam exhibited 1.5 times higher Sr adsorption efficiency than the pure alginate foam. This result reveals that zeolite-alginate foam composite is appropriate material for Sr removal in seawater due to its swelling resistance as well as improved Sr adsorption performance in complex media. Copyright © 2017 Elsevier Ltd. All rights reserved.

  20. Adsorption of palladium ions by modified carbons from rice husks

    International Nuclear Information System (INIS)

    Mostafa, M.R.

    1994-01-01

    Steam activated carbon of high surface area does not show palladium ions adsorption. Treatment of this carbon with HF acid increases to a great extent the gas adsorption capacity expressed as nitrogen surface area as well as the adsorption capacity of palladium ions from aqueous solution. HHB was loaded in different amounts on to these carbons. The acid sites represent the active fraction of the surface on which the adsorption palladium ions proceed. The uptake of palladium ions by HHB treated carbons is related to the total number of HHB molecules loaded on the carbon surface. (author)

  1. Study of algae's adsorption to uranium ion in water solution

    International Nuclear Information System (INIS)

    Du Yang; Qiu Yongmei; Dan Guiping; Zhang Dong; Lei Jiarong

    2007-01-01

    The adsorption efficiencies of the algae to uranium ion were determined at various pH, uranium ion concentrations, adsorption temperatures and the species of coexisted metal ions, and the effect of coexisted metal ion on the adsorption efficiency was researched. The experimental results at pH= 5-8 are as follows. 1) the adsorption capacity is a constant to be about 1.40 μg/g for the Yantai red alga and the sea spinach, and is changeable in the range of 1.03-2.23 μg/g with pH for the sea edible fungus; 2) for the algae the adsorption efficiency and adsorption capacity are related to uranium ion concentration, and the maximum adsorption efficiency and capacity is 95.8% and 65.4 μg/g, respectively; 3) the adsorption process for 24 h is not dependent on the temperature; 4) the effect of the species of coexisted metal ions on the adsorption capacity of uranium ion is various with the time during adsorption process. (authors)

  2. Biosorption of strontium ions from aqueous solution using modified eggshell materials

    Energy Technology Data Exchange (ETDEWEB)

    Metwally, Sayed S.; Rizk, Hoda E.; Gasser, Mona S. [Atomic Energy Authority, Cairo (Egypt). Hot Laboratories Center

    2017-07-01

    Green composites emphasize renewable starting materials for better economy using biomass materials. Therefore, low-cost composite biosorbent was prepared by modification of eggshell material using heteropoly acid for removal of strontium ions from aqueous solution. The resulted composite was characterized and evaluated for the sorption process using the batch technique. Low concentration of strontium ions was used to evaluate the sorption sensitivity of the prepared composite. The obtained experimental results illustrated that the modification process of eggshell material enhanced the percent uptake from 49.9 to 95.7%. From kinetic studies, the sorption of strontium ions follows the pseudo-second-order kinetic model. The isotherm studies indicated that Langmuir is more applicable than Freundlich isotherm. Moreover, Dubinin-Radushkevich isotherm was studied. Thermodynamic studies revealed that the sorption process is spontaneous and has endothermic nature. Strontium ions can be desorbed from the modified eggshell using HNO{sub 3}, desorption percent was found to be 96.4%; the results revealed the reusability of the modified eggshell for further sorption.

  3. Study of mineral ion exchangers for strontium removal from nuclear waste waters

    International Nuclear Information System (INIS)

    Merceille, A.

    2012-01-01

    The problems of chemical pollution of water have become a major concern and a priority for the nuclear industry. The aim of this work is to study some ion exchangers used for the removal of strontium ions because 90 Sr is one of a major pollutant in nuclear liquid wastes. This study allows linking the physical and chemical properties of these materials and their sorption properties. This work presents therefore the synthesis of two materials - sodium nona-titanate and zeolite A - selected for their specific sorption properties of strontium: A second part of this work is dedicated to the study of specific exchange capacities of these materials for the strontium in presence of other elements such as sodium and calcium. Batch experiments were performed and kinetic and ion exchange models have been applied to understand the selectivity of the materials for strontium removal. Sodium nona-titanate and zeolite A are also studied in actual effluents. Monoliths of zeolite A have been also tested in dynamic ion exchange process. This material is promising for the treatment of radioactive effluents in continuous flow because it joins the sorption properties of the zeolite powder with the advantage of a solid with a macroporous network. (author) [fr

  4. Equilibrium and kinetics studies of metal ion adsorption on dyed ...

    African Journals Online (AJOL)

    Batch equilibration studies were conducted to determine the nature of adsorption of Zn (II) and Cu (II) onto dyed coconut pollens. The nature of adsorption of metal ions was explained using the Langmuir equation. The calculated values of equilibrium parameter indicated favourable adsorption by the adsorbents. Also the ...

  5. Interaction of nitrate, barium, strontium and cadmium ions with fused quartz/water interfaces studied by second harmonic generation.

    Science.gov (United States)

    Hayes, Patrick L; Malin, Jessica N; Konek, Christopher T; Geiger, Franz M

    2008-01-31

    Inorganic anions and cations are ubiquitous in environmental chemistry. Here, we use second harmonic generation to track the interaction of the environmentally important metal cations barium, strontium, and cadmium and the nitrate anion with fused quartz/water interfaces at pH 7. Using a dynamic flow system, we assess the extent of reversibility in the binding process and report the absolute number density of adsorbed cations, their charge densities, and their free energies of adsorption. We also present resonantly enhanced second harmonic generation experiments that show that nitrate is surface active and report the free energies and binding constants for the adsorption process. The second harmonic generation spectrum of surface-bound nitrate shows a new adsorption band that cuts further into the solar spectrum than nitrate in the aqueous or solid state. The results that we obtain for all four inorganic ions and the implications for tropospheric and aquatic chemistry as well as geochemistry are discussed in the context of fundamental science as well as pollutant transport models.

  6. Ion-exchange properties of cesium and strontium into zeolites from sodium salt solutions

    International Nuclear Information System (INIS)

    Kanno, Takuji; Hashimoto, Hiroyuki; Ohtani, Tozo.

    1978-01-01

    The ion-exchange properties of cesium and strontium into zeolite from sodium salt solution has been studied in zeolite A, zeolite X, zeolite Y, mordenite and clinoptilolite. The distribution of cesium into mordenite from about 1 -- 2 M sodium chloride and sodium hydroxide solutions is considerably larger than that into zeolite A. The distribution coefficient for 2 M solution of sodium salts was about 300. Therefore, the separation of cesium from sodium salt solution is possible by using mordenite. The distribution of strontium into zeolites form 1 -- 2 M solutions of sodium chloride and sodium nitrate were in the order of zeolite A>zeolite X>zeolite Y asymptoticaly equals mordenite. The distribution coefficient of 230 was obtained for 1 M solutions of sodium salts. The anion in solutions had no effect on the distribution of cesium and strontium into zeolite from sodium salt solution. (author)

  7. Adsorption of uranyl ions in nanoparticles of magnetite

    International Nuclear Information System (INIS)

    Holland, Helber; Yamaura, Mitiko

    2009-01-01

    This work studied the uranium (VI) adsorption, in the form of UO 2 2+ ions, of the nitride solution by the syntetic magnetite. This solution was prepared by precipitation adding a solution of NaOH to the solution containing the ions Fe 2+ . The time of contact and the isothermal of equilibrium of ions UO 2 2+ adsorption was verified. The isothermal of equilibrium presented more concordance with the Freundlich model, which characterized a heterogeneous adsorption surface of the magnetite. The great advantage of this technology is the combination of two separation techniques, by adsorption and magnetic, resulting in a highly efficient and reusable system

  8. Separation of strontium ions from other alkaline earth metal ions using masking reagent

    International Nuclear Information System (INIS)

    Komatsu, Y.

    1996-01-01

    Cs + and Sr 2+ have been well known as serious elements in high level radioactive waste. Separation of Cs + has already been successful when using an ion-exchange method from solution in the presence of other alkali metal ions. The separation of Sr 2+ is, however, not so easy by any known separation method such as solvent-extraction and ion-exchange methods. This is because Sr 2+ is in the middle of the selectivity series, which is Mg 2+ > Ca 2+ > Sr 2+ > Ba 2+ for the solvent-extraction method and Ba 2+ > Sr 2+ > Ca 2+ > Mg 2+ for the ion- exchange method. In the present study, separation of strontium from other alkaline earth metal ions was studied by a combined use of three types of separation methods at 298 K: the solvent-extraction method was applied for the first separation, in which thenoyltrifluoroacetone (TTA, extractant) and trioctylphosphine oxide ( TOPO, adduct forming ligand) were used for the organic phase of the system. The separation factors for each combination of four alkaline earth metal ions were determined by the values of the distribution ratio. The Mg 2+ was well separated from Sr 2+ by the TTA-TOPO system. However, the separation of the combinations of Ca 2+ -Sr 2+ and Sr 2+ -Ba 2+ was not complete by the above solvent-extraction system. The second separation method, an ion-exchange method was applied using dihydrogen tetratitanate hydrate fibers (H 2 Ti 4 O 9 nH 2 O) as an ion exchanger to separate Sr 2+ and Ba 2+ . The separation factors for each combination of four alkaline earth metal ions were calculated by the values of the distribution coefficients. Ba 2+ was well separated from Sr 2+ by the ion-exchange method. To separate Ca 2+ and Sr 2+ , however, a modified solvent-extraction method was finally used in which H 2 Ti 4 O 9 nH 2 O was used as a masking reagent of Sr 2+ . After the dihydrogen tetratitanate hydrate fibers were contacted with the aqueous solution containing Ca 2+ and Sr 2+ , the organic solution containing TTA and TOPO

  9. Adsorption of heavy metal ions on different clays

    International Nuclear Information System (INIS)

    Kruse, K.

    1992-01-01

    The aim of the present dissertation is to study the adsorption of heavy metal ions (Cd 2+ , Cu 2+ , Pb 2+ , Zn 2+ ) and their mixtures on clays. Different clays and bentonites (Ca 2+ -bentonite, activated Na + -bentonite, special heavy metal adsorber bentonite, two organophilic bentonites and a mixed layer clay) were used. The adsorbed metal ions were desorbed by appropriate solutions of HCl, EDTA and dioctadecyl dimethylammonium bromide. High concentrations of the heavy metal ions in the solutions can be reached. The desorption guarantees economical recycling. After desorption the clays were used (up to three times) for purification of contaminated water. The best experimental conditions, i.e. the highest adsorption of heavy metal ions from aqueous solutions was found for the greatest ratio of adsorbent/adsorbate. The adsorption was very fast. Calcium, sodium bentonites and the heavy metal adsorber bentonite attained the highest adsorption and desorption for Cu 2+, Zn 2+ and Pb 2+ ions. Cd 2+ ions were only absorbed by Silitonit, a special heavy metal absorber bentonite. The mixed layer clay (Opalit) ranges in adsorption and desorption properties below the unmodified Ca 2+ -bentonite (Montigel) or the activated Na + -bentonite. Only Tixosorb and Tixogel (organophilic bentonites) reach the lowest value of heavy metal adsorption. Only lead cations which are characterised by good polarizability were adsorbed at higher rates, therefore the organophilic bentonites are not appropriate for adsorption of heavy metal ions from aqueous solutions. Mixing of the metal ions generally decreases the adsorption of Pb 2+ and increases the adsorption of Cd 2+ . From mixtures if heavy metal ions adsorption and desorption of Cu 2+ ions reached a maximum for all clays. (author) figs., tabs., 56 refs

  10. Strontium (Sr) separation from seawater using titanate adsorbents: Effects of seawater matrix ions on Sr sorption behavior

    Science.gov (United States)

    Ryu, Jungho; Hong, Hye-jin; Ryu, Taegong; Park, In-Su

    2017-04-01

    Strontium (Sr) which has many industrial applications such as ferrite magnet, ceramic, and fire works exists in seawater with the concentration of approximately 7 mg/L. In previous report estimating economic potential on recovery of various elements from seawater in terms of their commercial values and concentrations in seawater, Sr locates upper than approximate break-even line, which implies Sr recovery from seawater can be potentially profitable. Recently, Sr separation from seawater has received great attention in the environmental aspect after Fukushima Nuclear Power Plant (NPP) accident which released much amount of radioactive Sr and Cs. Accordingly, the efficient separation of radioactive elements released to seawater has become critical as an important technological need as well as their removal from radioactive wastes. So far, it has been introduced to separate Sr from aqueous media by various methods including solvent extraction, adsorption by solid materials, and ion exchange. Among them, the adsorption technique using solid adsorbents is of great interest for selectively separating Sr from seawater with respect to low concentration level of Sr. In this study, we synthesized titanate nanotube (TiNT) by simple hydrothermal reaction, characterized its physicochemical properties, and systematically evaluated Sr sorption behavior under various reaction conditions corresponding to seawater environment. The synthesized TiNT exhibited the fibril-type nanotube structure with high specific surface area of 260 m2/g. The adsorption of Sr on TiNT rapidly occurred following pseudo-second-order kinetic model, and was in good agreement with Langmuir isotherm model, indicating maximum adsorption capacity of 97 mg/g. Based on Sr uptake and Na release with stoichiometric balance, sorption mechanism of Sr on TiNT was found to be ion-exchange between Na in TiNT lattice and Sr in solution phase, which was also confirmed by XRD and Raman analysis. Among competitive ions, Ca

  11. Adsorption of heavy metal ions by sawdust of deciduous trees

    International Nuclear Information System (INIS)

    Bozic, D.; Stankovic, V.; Gorgievski, M.; Bogdanovic, G.; Kovacevic, R.

    2009-01-01

    The adsorption of heavy metal ions from synthetic solutions was performed using sawdust of beech, linden and poplar trees. The adsorption depends on the process time, pH of the solution, type of ions, initial concentration of metals and the sawdust concentration in suspension. The kinetics of adsorption was relatively fast, reaching equilibrium for less than 20 min. The adsorption equilibrium follows Langmuir adsorption model. The ion exchange mechanism was confirmed assuming that the alkali-earth metals from the adsorbent are substituted by heavy metal ions and protons. On lowering the initial pH, the adsorption capacity decreased, achieving a zero value at a pH close to unity. The maximum adsorption capacity (7-8 mg g -1 of sawdust) was achieved at a pH between 3.5 and 5 for all the studied kinds of sawdust. The initial concentration of the adsorbate and the concentration of sawdust strongly affect the process. No influence of particles size was evidenced. A degree of adsorption higher than 80% can be achieved for Cu 2+ ions but it is very low for Fe 2+ ions, not exceeding 10%.

  12. Human telomeric G-quadruplex formation and highly selective fluorescence detection of toxic strontium ions.

    Science.gov (United States)

    Qu, Konggang; Zhao, Chuanqi; Ren, Jinsong; Qu, Xiaogang

    2012-03-01

    Strontium ions play important roles in biological systems. The inhalation of strontium can cause severe respiratory difficulties, anaphylactic reaction and extreme tachycardia. Strontium can replace calcium in organisms, inhibit normal calcium absorption and induce strontium "rickets" in childhood. Thus, the development of sensitive and selective methods for the determination of trace amounts of Sr(2+) in aqueous media is of considerable importance for environmental and human health protection. A number of methodologies, such as X-ray energy dispersive spectrometry, inductively coupled argon plasma atomic emission spectroscopy (ICP-AES), atomic absorption spectrometry (AAS) and instrumental thermal neutron activation analysis, have been reported. However, these methods are somewhat complex, costly, time consuming and, especially, need special instruments. Thus, the design of convenient and inexpensive approaches for the sensitive and selective detection of Sr(2+) with rapid, easy manipulation is in ever-increasing demand. To the best of our knowledge, using DNA conformational change to detect Sr(2+) has not yet been reported. Herein we utilized thiazole orange (TO) as a signal reporter to devise a simple Sr(2+) detection assay based on Sr(2+) induced human telomeric DNA conformational change in the presence of SWNTs. The limit of detection is 10 nM Sr(2+) (0.87 μg L(-1)), far below 4 mg L(-1), the U.S. Federal threshold in drinking water defined by the U.S. EPA.

  13. Adsorption of ions by colloids in electrolyte solutions

    International Nuclear Information System (INIS)

    Kallay, N.

    1977-01-01

    The adsorption isotherm for ionic adsorption by colloid particles was evaluated. The adsorption process was treated as the reaction between colloid particles and ions. The colloid particle has been here considered as a reaction entity. The possibility of the surface potential determination was presented. The analyses of the experimental data showed, that (at electrolyte concentration higher than the critical coagulation one) the surface potential reaches its zero value

  14. Radioanalysis of RE enrichment of ion adsorption type RE ores

    CERN Document Server

    Zhao Shu Quan; Hu He Ping; Li Fu Sheng; Chen Ying Min; LiuShiMing

    2002-01-01

    Objective: To analyze the radioactivity in Rare Earth (RE) enrichment of ion adsorption type RE ores. Methods: Using HPGe-gamma spectrometer to analyze the activity ratio of gamma radionuclides in kind of samples, using FJ-2603 low background alpha, beta measurement apparatus to measure their total alpha and total beta activities, and using X-ray fluorescence spectrometer to analyze contents of La sub 2 O sub 3 and Y sub 2 O sub 3 , respectively. Results: HPGe gamma spectroscopy and X-ray fluorescence spectroscopy are simple, convenient and non-destructive methods of analyzing radionuclides and La sub 2 O sub 3 , Y sub 2 O sub 3 in RE enrichment of ion adsorption type RE ores, respectively. Conclusion: The basic data were provided for radiation protection and treatment of gas, liquid and solid waste in RE production of ion adsorption type RE ores; method and experience were provided for studying ion adsorption type RE ores

  15. Adsorption of ion pairs onto graphene flakes and impacts of counterions during the adsorption processes

    Science.gov (United States)

    Zhu, Chang; Yun, Jiena; Wang, Qian; Yang, Gang

    2018-03-01

    Although cations and anions are two integral constituents for all electrolytes, adsorption of ion pairs onto carbonaceous materials gains obviously less attention than adsorption of only cations or anions. Here DFT calculations are employed finding that four adsorption configurations emerge for KI onto graphene flakes (GF) instead of three for the other ion pairs. Reservation of ionic bonds is critical to their stabilities, and the bilateral configurations, where GFs couple with both cations and anions, are disfavored due to rupture of ionic bonds. Relative stabilities of two vertical configurations can be regulated and even reversed through edge-functionalization. Surprisingly, the horizontal adsorption configurations, which are global energy minima as long as present, are non-existent for a majority of ion pairs, and their existence or not is determined by the adsorption differences between halide ions and alkali ions (△Ead). Counterions effects for both cations and anions increase with the atomic electronegativities and cations correspond to stronger counterion effects; e.g., Li+ added on the other side of GFs promotes the adsorption of F- more pronouncedly than edge-functionalization. Mechanisms of electron transfers are also discussed, and three alteration patterns by counterions are observed for each type of adsorption configurations. Furthermore, addition of counterions causes band gaps to vary within a wider range that may be useful to design electronic devices.

  16. The determination of radioactive strontium in environmental samples by preferential ion exchange separation from calcium

    International Nuclear Information System (INIS)

    Fukushima, Hiroto; Nonaka, Nobuhiro; Honda, Tetsutaro; Kimura, Toshimasa; Higuchi, Hideo

    1979-01-01

    The determination of radioactive strontium in environmental samples involves a difficulty in the separation and purification of strontium from large amounts of calcium. The principal technique employed in this study is based on a cation exchange separation after preferential chelation of calcium over strontium by EDTA. The alkaline earth fraction separated from samples is dissolved in 1.2 M HCl and an equivalent amount of EDTA is added. The solution is passed through a Dowex 50W-X8 ion exchange column at a flow rate of 20 ml/min after the pH has been adjusted to 5.1. A fraction of calcium retained on the resin is eluted out with 1.8 l of 2 w/v% EDTA solution at pH 5.1. Then the strontium is eluted with 450 ml of 2 M HCl. The strontium carbonate is precipitated, and the chemical yield is determined. After standing for 14 days to reach the radioactive equilibrium of 90 Sr - 90 Y, the activity of 89 Sr + 90 Sr + 90 Y is measured. Then the activity of 90 Sr + 90 Y is measured by milking the 90 Y. The proposed procedure has been applied to sea water, soil and various ash samples of vegetables, seaweeds and daily foods. The results obtained are in good agreement with those by a classical fuming nitric acid precipitation method. The detection limits are 0.1 pCi/l for 10 l of sea water, 10 pCi/kg for 100 g of soil and 1 pCi/kg-fresh for 20 g ash samples, respectively. (author)

  17. Biosorption of strontium ions from aqueous solution using Ca-alginate biopolymer beads

    International Nuclear Information System (INIS)

    Goek, C.; Aytas, S.; Gerstmann, U.

    2009-01-01

    Biosorption of strontium ions from aqueous solution onto calcium alginate biopolymer beads was investigated in a batch system. Ca-alginate biopolymer beads were prepared from Na-alginate via cross-linking with divalent calcium ions according to the egg box model. Optimum biosorption conditions were determined as a function of initial solution pH, initial Sr concentration, contact time, biomass dosage and temperature. Langmuir, Freundlich and Dubinin-Radushkevich (D-R) models were applied to describe the biosorption isotherm of Sr ions by Ca-alginate biopolymer beads. The thermodynamic parameters (ΔH, ΔS, ΔG) for Sr sorption onto biosorbent were also determined from the temperature dependence. The results indicate that this biosorbent has a good potential for removal of Sr ions from dilute aqueous solution.

  18. Novel Pharmaceutical Strontium Malonate Influence on Calcium and Strontium Adsorption by Dog Femur and by Dog Teeth in a Four-Week Toxicity Study

    DEFF Research Database (Denmark)

    Raffalt, Anders Christer; Christgau, Stephan; Andersen, Jens Enevold Thaulov

    of osteoporosis. As part of this development the compound was administered in doses of 0 (placebo), 300, 1000 and 3000 mg/kg/day to beagle dogs for a period of 4 weeks. We measured the incorporation of strontium in bone, marrow and teeth in this study. Analysis by inductively coupled plasma mass spectrometry...... marginally higher incorporation of strontium suggesting that saturation levels were reached with the lowest dose level. There was no gender difference in strontium incorporation. Correlations of strontium levels with Sr/Ca-ratio and other important biological parameters were investigated....

  19. Equilibrium and kinetics studies of metal ion adsorption on dyed ...

    African Journals Online (AJOL)

    GREGO

    2007-04-02

    Apr 2, 2007 ... Initial concentration of Cu(II) ions = 20 mg/l, adsorbent dose = 1.0 g. Table 2 Experiment Data of ... diffusivity of the metal ion would be independent of the extent of sorption .... exchange and adsorption. Equilibrium parameter.

  20. Adsorption of ferrous ions onto montmorillonites

    Science.gov (United States)

    Qin, Dawei; Niu, Xia; Qiao, Min; Liu, Gang; Li, Hongxin; Meng, Zhenxiao

    2015-04-01

    The adsorption of Fe (II) onto montmorillonites was investigated through initial concentration, contact time, pH and temperature. During the whole adsorption process, the ascorbic acid (Vitamin C) was added as a kind of antioxidant, at the same time, deionized water (after boiling) and nitrogen protection were also used to avoid oxidation. The Fe2+/Fetotal ratio of the iron exists in the Fe-montmorillonites was found more than 95%. Two kinetic models, including pseudo-first-order and pseudo-second-order model, were used to analyze the adsorption process of Fe (II) on montmorillonites. The results of our study showed that adsorption process fitted with pseudo-second-order well. Adsorption isotherms showed that Langmuir model was better than Freundlich model. The thermodynamic parameters ΔG0 and ΔH0 were 3.696 kJ/mol and 6.689 kJ/mol (we just gave the values at 298 K), respectively. The positive values at different temperatures showed that the adsorption process was non-spontaneous and endothermic. The characteristics of materials were determined by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Surface area and porosity analyzer, Thermogravimetric analysis (TGA), Differential scanning calorimeter (DSC) and Zeta potential distribution.

  1. Preferential adsorption of uranium ions in aqueous solutions by polymers

    International Nuclear Information System (INIS)

    Sakuragi, Masako; Ichimura, Kunihiro; Fujishige, Shoei; Kato, Masao

    1981-01-01

    Amidoxime fiber and triazine fiber were prepared by chemical modification of commercially available polyacrylonitril fiber. It was found that the Amidoxime fiber is efficient to adsorb uranium ions in the artificial sea water. The efficiency of the preferential adsorption decreases by treatment the material with an acid-or an alkaline-solution. The triazine fiber adsorbs uranium ions only in aqueous solutions of such uranyl acetate, in the absence of other ions. In the artificial sea water, it adsorbs other ions instead of uranium. The preferential adsorption of uranium ions was further investigated with a series of polystyrenesulfonamides. Among the polystyrene derivatives, those having carboxyl groups, derived from imino diacetic acid (PSt-Imi), β-alanine (PSt-Ala), glycine (PSt-Gly), and sarcosine (PSt-Sar) were qualified for further discussion. However, it was found that the amount of adsorption of uranium ions by PSt-Imi decreases with increasing the volume of the artificial sea water and/or the duration of the treatment. Taking into account the facts, the preferential adsorption of uranium ions by PSt-Imi in aqueous solution was discussed in detail. (author)

  2. Adsorption behavior of radionuclide in water containing sea salts

    International Nuclear Information System (INIS)

    Kani, Yuko; Kamoshida, Mamoru; Asano, Takashi; Tamata, Shin

    2012-01-01

    Waste water caused by the Fukushima Dai-ichi Nuclear Reactor accident contains high level radioactive material with impurities of sea water origin, such as chloride, sodium and magnesium. These impurities have the potential to inhibit the adsorption reaction of radioactive cesium and strontium to adsorbents. We have studied adsorption behavior of radioactive cesium and strontium to adsorbents to measure distribution coefficients (Kd) in the condition of different sea water concentrations. For cesium adsorption, the dependence of Kd on the sea water concentration was affected by the adsorption mechanism of adsorbent; the adsorbents which adsorbed cesium by intercalation showed less dependence of Kd on the sea water concentration, while those adsorbed cesium by ion exchange had smaller Kd with increasing the sea water concentration. For strontium adsorption, Kd decreased as the sea water concentration increased for both adsorbents which adsorbed strontium by intercalation and by ion exchange. The inhibition of intercalation and ion exchange reaction of strontium by calcium ion, that exists high concentration in sea water (400 ppm) and similar hydrated ionic radius with strontium, will cause the decrease of Kd for strontium in the sea water with higher concentration. (author)

  3. Adsorption of heavy metal ions on activated carbon, (5)

    International Nuclear Information System (INIS)

    Yoshida, Hisayoshi; Kamegawa, Katsumi; Arita, Seiji

    1978-01-01

    The adsorption effect of heavy metal ions Cd 2+ , Zn 2+ and Hg 2+ on activated carbon by adding EDTA is reported, utilizing the experimental data. The activated carbons used for the experiment are mostly D, and B, C and F partly. As for the experimental procedure, the solutions of 100 ml which are composed of activated carbon, pH adjusting liquid, EDTA solution and solutions of heavy metals Cd, Zn and Hg, are shaken for 24 hours at 20 deg C, and after the activated carbon is centrifuged and separated for 15 minutes at 3000 rpm, the remaining heavy metal concentrations and pH in the supernatant are measured. The experimental results showed the useful effect on the adsorption of heavy metal ions of Cd, Zn and Hg by adding about 1 mol ratio of (EDTA/heavy metals). The individual experimental results are presented in detail. Concerning the adsorption quantity, 83% of Cd ions remained in the supernatant without addition of EDTA, but less than 1% with addition of about 1 to 5 mol ratio of (EDTA/Cd), and this adsorption effect was almost similar to Zn and Hg, i.e. 100% to 1% in Zn and 70% to 2 or 3% in Hg, under the condition written above. As for the influence of pH on Cd adsorption, the remaining Cd ratio is less than 10%, when pH is 7 to 10.5 at the mol ratio of 1 and 5.5 to 9 at the mol ratio of 10. The adsorption effect was different according to the kinds of activated carbon. The influencing factors for adsorption effect are the concentration of coexisting cations in the solution and the mixing time, etc. The effects of pH on Zn and Hg adsorption were almost similar to Cd. (Nakai, Y.)

  4. Adsorption of lithium ion to amorphous hydrous aluminium oxide

    International Nuclear Information System (INIS)

    Wada, Hideo; Kitamura, Takao; Fujii, Ayako; Katoh, Shunsaku

    1982-01-01

    Adsorption process of lithium ion to amorphous hydrous aluminium oxide (a-HAO) was investigated by pH titration method with lithium chloride-lithium hydroxide mixed solution and X-ray diffraction analysis of a-HAO after pH titration. In the pH titration, the addition of hydroxide ion in amount from 0 to 4.0 mmol.g -1 gave no change to the pH of the solution and caused adsorption of lithium ion equivalent in amount to added hydroxide ion. X-ray diffraction analysis showed the formation of lithium hydrogenaluminate LiH (AlO 2 ) 2 .5H 2 O (LHA) in the a-HAO after pH titration. These results showed that adsorption of lithium ion by a-HAO was related to a reaction which consumed hydroxide ion and formed LHA. In order to elucidate detail process of the reaction, changes of pH, aluminium concentration and lithium concentration of the solution, respectively with time, were determined. The pH of the solution decreased in two stages. At the first stage of the pH decrease, the aluminium concentration increased whereas the lithium concentration did not change. At the second stage, the lithium concentration decreased together with the decrease of the aluminium concentration. It was inferred that adsorption of lithium ion proceeded through dissolution of a-HAO and precipitation of LHA. Theoretical adsorption capacity calculated from the above formula for LHA and aluminium content in a-HAO was 4.7 mmol.g -1 and agreed fairly well with observed value 4.0 mmol.g -1 . (author)

  5. A study of an ion-exchange process for separation of strontium and yttrium

    International Nuclear Information System (INIS)

    Mubarek, M.A.

    1980-01-01

    A study has been carried out to determine optimum conditions for the separation of strontium and yttrium by ion-exchange. The parameters of interest for such separation such as the dimensions of the ion-exchange columns, flow rates through the columns and pH values of the solutions, which affect the overall yield in the process, have been investigated. Application of this method for routine quantitative determinations of Sr-90 in environmental samples, particularly the wet-ashed biological materials has also been studied. The method, although a rapid and convenient one has not been found to yield consistent results probably due to the requirement of stringent analytical controls during the process. (author)

  6. Innovative Highly Selective Removal of Cesium and Strontium Utilizing a Newly Developed Class of Inorganic Ion Specific Media - 16221

    International Nuclear Information System (INIS)

    Denton, Mark S.; Kanatzidis, Mercouri G.

    2009-01-01

    Highly selective removal of Cesium and Strontium is critical for waste treatment and environmental remediation. Cesium-137 is a beta-gamma emitter and Strontium-90 is a beta emitter with respective half-lives of 30 and 29 years. Both elements are present at many nuclear sites. Cesium and Strontium can be found in wastewaters at Washington State's Hanford Site, as well as in waste streams of many Magnox reactor sites. Cesium and Strontium are found in the Reactor Coolant System of light water reactors at nuclear power plants. Both elements are also found in spent nuclear fuel and in high-level waste (HLW) at DOE sites. Cesium and Strontium are further major contributors to the activity and the heat load. Therefore, technologies to extract Cesium and Strontium are critical for environmental remediation waste treatment and dose minimization. Radionuclides such as Cesium-137 and Strontium-90 are key drivers of liquid waste classification at light water reactors and within the DOE tank farm complexes. The treatment, storage, and disposal of these wastes represents a major cost for nuclear power plant operators, and comprises one of the most challenging technology-driven projects for the DOE Environmental Management (EM) program. Extraction technologies to remove Cesium and Strontium have been an active field of research. Four notable extraction technologies have been developed so far for HLW: solvent extraction, prussian blue, crystalline silico-titanate (CST) and organic ion-exchangers (e.g., resorcinol formaldehyde and SuperLig). The use of one technology over another depends on the specific application. For example, the waste treatment plant (WTP) at Hanford is planning on using a highly-selective organic ion-exchange resin to remove Cesium and Strontium. Such organic ion-exchangers use molecular recognition to selectively bind to Cesium and Strontium. However, these organic ion-exchangers are synthesized using multi-step organic synthesis. The associated cost to

  7. Strontium 90 in silts of the Dnieper cascade water reservoirs

    International Nuclear Information System (INIS)

    Romanenko, V.D.; Kuz'menko, M.I.; Matvienko, L.P.; Klenus, V.G.; Nasvit, O.I.

    1989-01-01

    The change of strontium-90 content in water and silts of the Dnieper cascade water reservoirs was analyzed. It was shown, that decrease of strontium-90 content in water in time connected basically with ion exchange adsorption of strontium-90 by residues. A high sorption ability of residues made it possible for radioisotopes to reduce sharply their concentration along depth of soils. The highest concentration of radioisotopes was in the upper layers, enriched by silt. It was ascertained, that strontium-90 migration along depth of residues took place rapidly in the Kiev's water reservoir. Down the cascade strontium-90 content reduced in lower layers of residues as well as in upper layers. 4 tabs

  8. Effects of focused ion beam milling on electron backscatter diffraction patterns in strontium titanate and stabilized zirconia

    DEFF Research Database (Denmark)

    Saowadee, Nath; Agersted, Karsten; Bowen, Jacob R.

    2012-01-01

    This study investigates the effect of focused ion beam (FIB) current and accelerating voltage on electron backscatter diffraction pattern quality of yttria‐stabilized zirconia (YSZ) and Nb‐doped strontium titanate (STN) to optimize data quality and acquisition time for 3D‐EBSD experiments by FIB...

  9. Effect of Temperature on the Removal of Cesium and Strontium Ions from Aqueous Solutions Using Zeolite A

    International Nuclear Information System (INIS)

    El-Kamash, A.M.; El-Naggar, M.R.; El-Dessouky, M.I.

    2008-01-01

    Ion exchange experiments between synthetic zeolite A and aqueous solutions of cesium and strontium ions were conducted at constant total ion concentrations of 0.1 N and at different temperatures in the range from 25 to 60 degree C. Thermodynamic equilibrium constants, calculated from the corresponding Kielland's plots, were used for the calculation of . δG degree δH degree and δS degree. The obtained data indicated that zeolite A exhibits higher affinity for Cs + and Sr +2 ions from solution than host Na + ions

  10. Influence of competitive ions on sorption of strontium on Slovak bentonites

    International Nuclear Information System (INIS)

    Galambos, M.; Kufcakova, J.; Rajec, P.

    2009-01-01

    Production of nuclear energy, processing of irradiated fuel, preparation and use of radionuclides are processes connected with radioactive waste. Safe disposal of radioactive waste, especially of liquid high-level waste and spent nuclear fuel is a common problem of today .The most important way of the waste storage are deep geological repositories that are formed by natural and engineered barriers isolating long-lived radionuclides from the biosphere. Clay is the basic component of these barriers in many cases. Bentonite is generally considered as the most appropriate clay material. The Sr-90 (T 1/2 ∼28 years) is eco-toxically significant radioisotope of strontium has a high extraction yield in nuclear fission. From the achieved results of this work it is possible to conclude that bentonites from the localities of Jelsovy potok, Kopernica, Lastovce and Lieskovec have satisfying sorption properties for ions of strontium. The results indicate that sorption of Sr can be heavily influenced by presence of high cation concentrations of various salts, which can be present e.g. waste waters. (authors)

  11. Influence of competitive ions on sorption of strontium on Slovak bentonites

    International Nuclear Information System (INIS)

    Galambos, M.; Kufcakova, J.; Rajec, P.

    2008-01-01

    Production of nuclear energy, processing of irradiated fuel, preparation and use of radionuclides are processes connected with radioactive waste. Safe disposal of radioactive waste, especially of liquid high-level waste and spent nuclear fuel is a common problem of today .The most important way of the waste storage are deep geological repositories that are formed by natural and engineered barriers isolating long-lived radionuclides from the biosphere. Clay is the basic component of these barriers in many cases. Bentonite is generally considered as the most appropriate clay material. The Sr-90 (T 1/2 ∼28 years) is eco-toxically significant radioisotope of strontium has a high extraction yield in nuclear fission. From the achieved results of this work it is possible to conclude that bentonites from the localities of Jelsovy potok, Kopernica, Lastovce and Lieskovec have satisfying sorption properties for ions of strontium. The results indicate that sorption of Sr can be heavily influenced by presence of high cation concentrations of various salts, which can be present e.g. waste waters. (authors)

  12. The influence of a fulvic acid on the adsorption of europium and strontium by alumina and quartz: effects of pH and ionic strength

    International Nuclear Information System (INIS)

    Norden, M.; Ephraim, J.H.; Allard, B.

    1994-01-01

    A batch method has been employed to study the adsorption of trace quantities of Eu and Sr on α-Al 2 O 3 and SiO 2 as a function of pH (3-9), ionic strength (0.10 and 0.01 M NaClO 4 ) and the presence of a well-characterized aquatic fulvic acid (FA). A comparison of Eu and Sr adsorption by alumina showed that FA could both reduce and enhance metal ion adsorption. In the absence of FA the adsorption of the metal ions onto alumina was a function of both pH and ionic strength. In the presence of FA the ionic strength effect on the Eu adsorption vanished, while the Sr adsorption showed a clear dependence on ionic strength. The adsorption of Eu and Sr on quartz was lower than the adsorption of the metals on alumina. Additionally, the adsorption of Eu and Sr on quartz was apparently lower than the adsorption on alumina in the presence of Fa. For both metal ions the adsorption on quartz was higher at 0.10 M than at 0.01 M NaClO 4 - an observation that was reversed in the case of alumina. Increasing concentrations of FA lowered the pH at which Eu adsorption on alumina would be reduced. (orig.)

  13. Adsorption of copper ions of natural montmorillonite clay

    Directory of Open Access Journals (Sweden)

    Pimneva Ludmila

    2017-01-01

    Full Text Available The prospects of montmorillonite clay using for the extraction of copper ions from natural and waste waters were determined. Specified chemical and phase composition of natural forms of the montmorillonite clay are shown in the article. Quantitative characteristics of adsorption process of copper ions, the statistical exchange capacity is 1,21 (298 К, 1,25 (313 К, 1,43 (333 К. The authors have studied the balance of copper ions by the method of constructing the isotherms. The description of the adsorption process was carried out by the Langmuir, Freundlich and Temkin models. The calculations showed that the best data for the sorption described by Langmuir model. The nature of the interaction of copper ions with montmorillonite clay in natural form is presented. The calculated thermodynamic parameters of the adsorption process, the obtained values of the Gibbs energy have a negative sign -11,5 (298 К, -15,6 (313 К, -16,2 (333 К кJ/mol, that corresponds to a sustainable consolidation of copper ions on the surface of the montmorillonite clay.

  14. Adsorption of heavy metal ions by activated charcoal

    International Nuclear Information System (INIS)

    Fujikawa, Mitsuo

    1978-01-01

    The adsorption effect was measured for several kinds of heavy metal ions, Pb 2+ , Cd 2+ , Cu 2+ and Zn 2+ by passing them through activated charcoal beds and changing the pH values of solutions. The test procedure is to keep the pH value of solution more than 10 at first, filter heavy metal hydroxide deposit, measure the remaining ion concentration in filtrate, and also test the influence of the addition of alkali to each kind of ions. The individual test procedure for each kind of ions is explained. As for the Cd ions, after the detailed experimental procedure is explained, the adsorption characteristic line is shown as the relation between the adsorption quantity and the equilibrium concentration of Cd 2+ . The similar test procedure and the adsorption characteristic lines are shown and evaluated about Pb 2+ , Cu 2+ and Zn 2+ . These lines are all linear, but have different adsorption quantity and inclination in relation to heavy metal ion concentration. Concerning the influence of pH to adsorption, the characteristics of pH increase are presented, when alkali is added by various quantities to Zn 2+ , Cu 2+ , Pb 2+ and Cd 2+ . The pH of Pb 2+ increased to about 10 by adding 0.4 cc alkali and saturates, but the pH of the other ions did not saturate by adding less than 1.5 cc alkali. When the water containing heavy metals are treated, Cd 2+ , Pb 2+ , Cu 2+ and Zn 2+ are removed almost satisfactorily by passing them through active charcoal filters and keeping pH at 10. The experimental concentrations are 0.05 ppm at pH 10 in Cd, 0.86 ppm at 10.3 in Pb, 0 ppm at pH 9.6 in Cu, 0.06 ppm at pH 8.8 and 12.4 ppm at pH 9.8 in Zn. (Nakai, Y.)

  15. Luminescence life time and time-resolved spectroscopy of Cr3+ ions in strontium barium niobate

    International Nuclear Information System (INIS)

    Han, T.P.J.; Jaque, F.; Jaque, D.; Garcia-Sole, J.; Ivleva, L.

    2006-01-01

    This paper reports on the photo-luminescence spectroscopic results of congruent strontium-barium-niobate (SBN) crystals doped with Cr 2 O, at cryogenic temperature (20 K). The experimental results reveal the need of re-assignment of the Cr 3+ ions defect centres in this material. For first time, a broad emission band in the near infrared region centred at ca. 950 nm is reported. This emission band has micro-seconds decaytime constant and a band-width full-width at half-maximum (FWHM) larger than 1700 cm -1 and has been ascribed to the vibronically assisted 4 T 2 →4 A 2 transition. A much narrower emission band centred at ca. 764 nm with milli-seconds decaytime constant and a FWHM band-width of ca. 170 cm -1 is correlated to the 2 E →4 A 2 radiative transition (R-line)

  16. Preparation of Diethylenetriamine Modified Polyacrylonitrile Nanofibers for Cadmium Ion Adsorption

    Directory of Open Access Journals (Sweden)

    Zahra Mokhtari- shorijeh

    2016-07-01

    Full Text Available In this study, the electrospinning method was used to manufacture polyacrylonitrile (PAN nanofibers. The procedure involved spinning a solution of 10%wt PAN in dimethyl formamide (DMF in an electric field of 21 kV and with a tip to collector distance of 16 cm. The nanofibers thus obtained had an average diameter of 100 nm. Then, scanning electron microscopy (SEM images were used to investigate the morphology of the nanofibers. In the next step, the nanofiner surface was modified with diethylenetriamine and FTIR was employed to ensure the presence of amines on the nanofiber surface. The functionalized nanofibers were then used for the first time to adsorb ions of cadmium (a heavy metal with industrial applications and its adsorption capacity was evaluated. The chemical charactristics of the nanofibers and the effects of such parameters as pH, temprature, and contact time on adsorption efficiency were investigated. The results showed that maximum adsorption efficiency was achieved within the first 10 minutes of the process at a pH in the range of 5‒7 when about 80% of the cadmium ions were adsorbed.. Moreover, only slight changes were observed with longer contact times or with increasing temperature. Finally, the adsorption data fitted well with the Langmuir isotherm

  17. Adsorption pertechnetate ions on the substituted Sn-hydroxyapatite

    International Nuclear Information System (INIS)

    Hamarova, A.; Rosskopfova, O.; Pivarciova, L.

    2015-01-01

    Hydroxyapatite is suitable adsorbent for heavy metals and radionuclides due to its large surface area, high stability under redox conditions. SnCl 2 for its reducing properties is used in biomedical applications and industrial technologies, for its reducing properties. The adsorption of TcO 4 - to the HA samples, prepared by wet precipitation method, was studied by the d radio-indication method. Radionuclide 99m Tc was used as radioisotope indicator. The effect of contact time on the adsorption of 99m TcO 4 - ions on the Sn-HA was studied. Sn 2+ ions reduced Tc (VII) to Tc (IV) forming TcO 2 , TcO(OH) 2 or more precisely TcO 2 ·2H 2 O, which can be adsorbed on the surface of the HA, or to form complexes on the surface of the hydroxyapatite. (authors)

  18. Alteration of sediments by hyperalkaline K-rich cement leachate: implications for strontium adsorption and incorporation.

    Science.gov (United States)

    Wallace, Sarah H; Shaw, Samuel; Morris, Katherine; Small, Joe S; Burke, Ian T

    2013-04-16

    Results are presented from 1 year batch experiments where K-rich hyperalkaline pH 13.5 young cement water (YCW) was reacted with sediments to investigate the effect of high pH, mineral alteration, and secondary mineral precipitation on (90)Sr sorption. After reaction with YCW, Sr sorption was found to be greater than 75% in all samples up to 365 days and 98% in a sample reacted for 365 days at 70 °C. Scanning electron microscopy analysis of sediment samples reacted at room temperature showed surface alteration and precipitation of a secondary phase, likely a K-rich aluminosilicate gel. The presence of Sr-Si(Al) bond distances in Sr K-edge extended X-ray absorption fine structure (EXAFS) analysis suggested that the Sr was present as an inner-sphere adsorption complex. However, sequential extractions found the majority of this Sr was still exchangeable with Mg(2+) at pH 7. For the sample reacted for 1 year at 70 °C, EXAFS analysis revealed clear evidence for ∼6 Sr-Si(Al) backscatters at 3.45 Å, consistent with Sr incorporation into the neoformed K-chabazite phase that was detected by X-ray diffraction and electron microscopy. Once incorporated into chabazite, (90)Sr was not exchangeable with Mg(2+), and chemical leaching with pH 1.5 HNO3 was required to remobilize 60% of the (90)Sr. These results indicate that, in high pH cementitious leachate, there is significantly enhanced Sr retention in sediments due to changes in the adsorption mechanism and incorporation into secondary silicate minerals. This suggests that Sr retention may be enhanced in this high pH zone and that the incorporation process may lead to irreversible exchange of the contaminant over extended time periods.

  19. Heavy metal ion adsorption onto polypyrrole-impregnated porous carbon.

    Science.gov (United States)

    Choi, Moonjung; Jang, Jyongsik

    2008-09-01

    Polypyrrole-impregnated porous carbon was readily synthesized using vapor infiltration polymerization of pyrrole monomers. The results show that the functionalized polymer layer was successfully coated onto the pore surface of carbon without collapse of mesoporous structure. The modified porous carbon exhibited an improved complexation affinity for heavy metal ions such as mercury, lead, and silver ions due to the amine group of polypyrrole. The introduced polypyrrole layer could provide the surface modification to be applied for heavy metal ion adsorbents. Especially, polymer-impregnated porous carbon has an enhanced heavy metal ion uptake, which is 20 times higher than that of adsorbents with amine functional groups. Furthermore, the relationship between the coated polymer amount and surface area was also investigated in regard to adsorption capacity.

  20. Adsorption of Heavy Metal Ions from Aqueous Solutions by Bentonite Nanocomposites.

    Science.gov (United States)

    Ma, Jing; Su, Guojun; Zhang, Xueping; Huang, Wen

    2016-08-01

    A series of bentonite nanocomposites have been synthesized by modifying bentonite with hexadecyltrimethylammonium bromide (CTMAB) and the common complexing agents, complexone (ethylene diamine tetraacetic acid, EDTA) or mercaptocomplexant (2-Mercaptobenzothiazole, MBT). These adsorbents are used to remove heavy metal ions (Cu(2+), Zn(2+), Mn(2+),Co(2+)). The Bent-CTMAB-MBT adsorbed metal ions are higher than Bent-CTMAB-EDTA under the same ion concentration in AAS. Compared with the single ion system, the adsorption of the mixed ion system of Cu(2+), Zn(2+), Mn(2+), Co(2+) had decreased differently. In the mixed system, the adsorption of Mn(2+) is significantly lower, but the adsorption of Cu(2+) was highest. The adsorption sequence of these four metal ions was Cu(2+) > Zn(2+) > Co(2+) > Mn(2+), and the selective adsorption was closely related to the hydration energy of heavy metal ions. We could remove more metal ions in different stages with the adsorption sequence.

  1. DEVELOPMENT OF PROTOTYPE TITANATE ION EXCHANGE LOADED MEMBRANES FOR STRONTIUM, CESIUM AND ACTINIDE DECONTAMINATION FROM AQUEOUS MEDIA

    Energy Technology Data Exchange (ETDEWEB)

    Oji, L; Keisha Martin, K; David Hobbs, D

    2008-05-30

    We have successfully incorporated high surface area particles of titanate ion exchange materials (monosodium titanate and crystalline silicotitanate) with acceptable particle size distribution into porous and inert support membrane fibrils consisting of polytetrafluoroethylene (Teflon{reg_sign}), polyethylene and cellulose materials. The resulting membrane sheets, under laboratory conditions, were used to evaluate the removal of surrogate radioactive materials for cesium-137 and strontium-90 from high caustic nuclear waste simulants. These membrane supports met the nominal requirement for nonchemical interaction with the embedded ion exchange materials and were porous enough to allow sufficient liquid flow. Some of this 47-mm size stamped out prototype titanium impregnated ion exchange membrane discs was found to remove more than 96% of dissolved cesium-133 and strontium-88 from a caustic nuclear waste salt simulants. Since in traditional ion exchange based column technology monosodium titanate (MST) is known to have great affinity for the sorbing of other actinides like plutonium, neptunium and even uranium, we expect that the MST-based membranes developed here, although not directly evaluated for uptake of these three actinides because of costs associated with working with actinides which do not have 'true' experimental surrogates, would also show significant affinity for these actinides in aqueous media. It was also observed that crystalline silicotitanate impregnated polytetrafluoroethylene or polyethylene membranes became less selective and sorbed both cesium and strontium from the caustic aqueous salt simulants.

  2. The use of natural and industrial aluminosilicates in the process of adsorption of heavy metals ions

    OpenAIRE

    Tsvetkova, A.; Akayev, O.

    2010-01-01

    The analysis of periodic scientific publications and patent literature was made, in which the possibilities of using natural and industrial silicon-containing compounds as adsorbents of ions of heavy metals are generalized. The conditions of adsorption, as well as the numerical values of the adsorption capacity of the studied materials are described Key words: adsorption, natural and industrial aluminosilicates, heavy metals ions.

  3. Use of extraction chromatography, ion chromatography and liquid scintillation spectrometry for rapid determination of strontium-89 and strontium-90 in food in cases of increased release of radionuclides

    International Nuclear Information System (INIS)

    Heilgeist, M.

    2000-01-01

    For rapid determination of 89 Sr and 90 Sr in food, isocratic ion chromatography used for Sr isolation and purification is integrated in a complete analytical system comprising sample preparation, incineration, dissolution, phosphate precipitation for alkali/alkaline earth separation, and Sr specific extraction chromatography on crown ether basis for Ca/Sr separation. Strontium-89 and 90 Sr are determined by liquid scintillation spectrometry after carbonate precipitation. The components of the mixed spectra obtained are calculated by the computerized spectra subtraction method. Two days plus measuring time are required for single, three for double analysis. The limit of detection for 89 Sr and 90 Sr is ca. 0.1 Bq x kg -1 , related to the fresh produce. (author)

  4. Adsorption of radioactive ions on carnauba-wax aerosols

    Energy Technology Data Exchange (ETDEWEB)

    Paul, A.; Keyser, U. [Physikalisch-Technische Bundesanstalt, Braunschweig (Germany)

    1998-08-01

    A new method based on parallel aerosol size spectrometry and {gamma}-spectrometry is introduced for the measurement of short-lived radioactive ions, fission products or super-heavy elements produced at accelerators. Furthermore a new aerosol generator is presented.The possibility of controlling and changing the aerosol size distribution in the helium aerosol jet produced by the aerosol generator allows the process of the adsorption and transport of radioactive ions on aerosols to be examined for the first time. This is due to the fact that the distribution is surveyed on-line using a negligible part of its total volume and parallel to the transporting flow. The radioactivity of the transported ions is measured by a germanium detector in offline position. In principle, both an on- or offline position with narrow multi-detector geometry (e.g. {beta}{gamma}{gamma}) is possible. (orig.) With 8 figs., 14 refs.

  5. Crystalline silicotitanates--new ion exchanger for selective removal of cesium and strontium from radwastes

    International Nuclear Information System (INIS)

    Dosch, R.G.; Klavetter, E.A.; Stephens, H.P.; Brown, N.E.; Anthony, R.G.

    1996-08-01

    A new class of inorganic ion exchange material called crystalline silicotitanates (CST) has been developed for radioactive waste treatment in a collaborative effort between Sandia National Laboratories and Texas A ampersand M University. The Sandia National Laboratories Laboratory Directed Research and Development program provided the initial funding for this effort and this report summarizes the rapid progress that was achieved. A wide range of compositions were synthesized, evaluated for cesium (Cs) removal efficiency, and a composition called TAM-5 was developed that exhibits high selectivity and affinity for Cs and strontium (Sr). Tests show it can remove parts per million concentrations of Cs + from highly alkaline, high-sodium, simulated radioactive waste solutions modeled after those at Hanford, Oak Ridge, and Savannah River. In experiments with solutions that simulate highly alkaline Hanford defense wastes, the crystalline silicotitanates exhibit distribution coefficients for Cs + of greater than 2,000 ml/g, and distribution coefficients greater than 10,000 ml/g for solutions adjusted to a pH between 1 and 10. In addition, the CSTs were found to exhibit distribution coefficients for Sr + greater than 100,000 ml/g and for plutonium of 2,000 ml/g from simulated Hanford waste. The CST crystal structure was determined and positions of individual atoms identified using x-ray and neutron diffraction. The structural information has permitted identification of the ion exchange sites and provided insights into the strong effect of pH on Cs ion exchange. Information on the synthesis, composition, and structure of CST is considered proprietary and is not discussed in this report

  6. Interface chemistry of nanostructured materials: ion adsorption on mesoporous alumina.

    Science.gov (United States)

    Wang, Yifeng; Bryan, Charles; Xu, Huifang; Pohl, Phil; Yang, Yi; Brinker, C Jeffrey

    2002-10-01

    This paper presents a part of our work on understanding the effect of nanoscale pore space confinement on ion sorption by mesoporous materials. Acid-base titration experiments were performed on both mesoporous alumina and alumina particles under various ionic strengths. The point of zero charge (PZC) for mesoporous alumina was measured to be approximately 9.1, similar to that for nonmesoporous alumina materials, indicating that nanoscale pore space confinement does not have a significant effect on the PZC of pore surfaces. However, for a given pH deviation from the PZC, (pH-PZC), the surface charge per mass on mesoporous alumina was as much as 45 times higher than that on alumina particles. This difference cannot be fully explained by the surface area difference between the two materials. Our titration data have demonstrated that nanoscale confinement has a significant effect, most likely via the overlap of the electric double layer (EDL), on ion sorption onto mesopore surfaces. This effect cannot be adequately modeled by existing surface complexation models, which were developed mostly for an unconfined solid-water interface. Our titration data have also indicated that the rate of ion uptake by mesoporous alumina is relatively slow, probably due to diffusion into mesopores, and complete equilibration for sorption could take 4-5 min. A molecular simulation using a density functional theory was performed to calculate ion adsorption coefficients as a function of pore size. The calculation has shown that as pore size is reduced to nanoscales (<10 nm), the adsorption coefficients of ions can vary by more than two orders of magnitude relative to those for unconfined interfaces. The prediction is supported by our experimental data on Zn sorption onto mesoporous alumina. Owing to their unique surface chemistry, mesoporous materials can potentially be used as effective ion adsorbents for separation processes and environmental cleanup.

  7. Effect of adsorbents and chemical treatments on the removal of strontium from aqueous solutions

    International Nuclear Information System (INIS)

    Ahmadpour, A.; Zabihi, M.; Tahmasbi, M.; Bastami, T. Rohani

    2010-01-01

    In the present investigation, three different solid wastes namely almond green hull, eggplant hull, and moss were initially treated and used as adsorbents for the adsorption of strontium ion from aqueous solutions. Adsorbent types and chemical treatments are proved to have effective roles on the adsorption of Sr(II) ion. Among the three adsorbents, almond green hull demonstrated strong affinity toward strontium ion in different solutions. The effectiveness of this new adsorbent was studied in batch adsorption mode under a variety of experimental conditions such as: different chemical treatments, various amounts of adsorbent, and initial metal-ion concentration. The optimum doses of adsorbent for the maximum Sr(II) adsorption were found to be 0.2 and 0.3 g for 45 and 102 mg L -1 solutions, respectively. High Sr(II) adsorption efficiencies were achieved only in the first 3 min of adsorbent's contact time. The kinetics of Sr(II) adsorption on almond green hull was also examined and it was observed that it follows the pseudo second-order behavior. Both Langmuir and Freundlich models well predicted the experimental adsorption isotherm data. The maximum adsorption capacity on almond green hull was found to be 116.3 mg g -1 . The present study also confirmed that these low cost agriculture byproducts could be used as efficient adsorbents for the removal of strontium from wastewater streams.

  8. Adsorption of citrate ions on hydroxyapatite synthesized by various methods

    International Nuclear Information System (INIS)

    Skwarek, E.; Janusz, W.; Sternik, D.

    2014-01-01

    The specific adsorption of citric acid ions at hydroxyapatite interface was investigated by the means of radioisotope method ( 14 C) as a function of citric acid ions concentration, NaCl concentration and pH. Application of the hydroxyapatite has become wide in the biomaterial field as the Ca 10 (OH) 2 (PO 4 ) 6 possess biocompatibility with human hard tissue. Hydroxyapatite was synthesized using three different methods. The physical properties of the resulting powder were characterized by DTA/TG, XRD, AFM and SEM microscopy. Physicochemical qualities characterizing the electrical double layer of the hydroxyapatite/NaCl solution interface were determined. The zeta potential and the adsorption of citric acid molecule were studied as a function of pH. The point of zero charge and the isoelectric point of samples were determined. Electrical double layer parameters of hydroxyapatite/NaCl interface are influenced by a synthesis method. The points pH pzc and pH IEP for sample 1 are pH pzc 7.5 and pH IEP 3; for sample 2 pH pzc 7.05 and pH IEP 3, for sample 3 pH pzc 6.7 and pH IEP 3. Temperature has weak influence both on pure substance and with citric acid adsorbed, as derivatographic analysis has shown, and characterization of hydroxyapatite structure may be carried out by this thermal analysis. Two phenomena are responsible for citric acid adsorption: phosphate group's replacement at hydroxyapatite surface by citric ions parallel to intraspherical complexes formation. (author)

  9. Potassium iron(III)hexacyanoferrate(II) supported on polymethylmethacrylate ion-exchanger for removal of strontium(II)

    International Nuclear Information System (INIS)

    Taj, S.; Ashraf Chaudhry, M.; Mazhar, M.

    2009-01-01

    Potassium iron(III)hexacyanoferrate(II) supported on poly metylmethacrylate has been synthesized and investigated for the strontium(II) removal from HNO 3 and HCl solutions. The ion exchange material characterized by different techniques and found to be stable in 1.0-4.0 M HNO 3 solutions, has been used to elaborate different parameters related to ion exchange and sorption processes involved. The data collected suggested its use to undertake removal of Sr(II) from more acidic active waste solutions. Thus the material synthesized had been adjudged to present better chances of application for Sr(II) removal as compared to other such materials. (author)

  10. Highly Efficient Adsorption of Copper Ions by a PVP-Reduced Graphene Oxide Based On a New Adsorptions Mechanism

    Institute of Scientific and Technical Information of China (English)

    Yongji Zhang; HuiJuan Chi; WenHui Zhang; Youyi Sun; Qing Liang; Yu Gu; Riya Jing

    2014-01-01

    Polyvinylpyrrolidone-reduced graphene oxide was prepared by modified hummers method and was used as adsorbent for removing Cu ions from wastewater. The effects of contact time and ions concentration on adsorption capacity were examined. The maximum adsorption capacity of 1689 mg/g was observed at an initial p H value of 3.5 after agitating for 10 min. It was demonstrated that polyvinylpyrrolidone-reduced graphene oxide had a huge adsorption capacity for Cu ions, which was 10 times higher than maximal value reported in previous works. The adsorption mechanism was also discussed by density functional theory. It demonstrates that Cu ions are attracted to surface of reduced graphene oxide by C atoms in reduced graphene oxide modified by polyvinylpyrrolidone through physisorption processes, which may be responsible for the higher adsorption capacity. Our results suggest that polyvinylpyrrolidone-reduced graphene oxide is an effective adsorbent for removing Cu ions in wastewater. It also provides a new way to improve the adsorption capacity of reduced graphene oxide for dealing with the heavy metal ion in wastewater.

  11. Semi-automated technique for the separation and determination of barium and strontium in surface waters by ion exchange chromatography and atomic emission spectrometry

    International Nuclear Information System (INIS)

    Pierce, F.D.; Brown, H.R.

    1977-01-01

    A semi-automated method for the separation and the analysis of barium and strontium in surface waters by atomic emission spectrometry is described. The method employs a semi-automated separation technique using ion exchange and an automated aspiration-analysis procedure. Forty specimens can be prepared in approximately 90 min and can be analyzed for barium and strontium content in 20 min. The detection limits and sensitivities provided by the described technique are 0.003 mg/l and 0.01 mg/l respectively for barium and 0.00045 mg/l and 0.003 mg/l respectively for strontium

  12. Competition effect of some metal ions on the complexation of strontium with humic acid. Vol. 4

    Energy Technology Data Exchange (ETDEWEB)

    Helal, A A; Aly, H F; Imam, D M; Khalifa, S M [Atomic Energy Authorty, Cairo (Egypt)

    1996-03-01

    Interaction of radioactive strontium with humic acid present in water streams is of main importance to learn about the fate of strontium in case of accidental release. In this work, formation of Sr-humate precipitate was studied radiometrically and colorimetric at different PH`s. The investigations indicated that formation of the precipitated complex increases with increasing strontium concentration till saturation. The competition effect of other cations in solution such as Ca, Mg, Ba, and Ni was investigated. The humate complexes of these cations were studied colorimetric, and the competition behaviour was investigated using the radiotracer of strontium. The results indicated that presence of Ba, Mg and Ni decreases the Sr-humate complex, while increasing Ca concentration enhances precipitation of Sr with humic acid. 10 figs.

  13. Adsorption preference for divalent metal ions by Lactobacillus casei JCM1134.

    Science.gov (United States)

    Endo, Rin; Aoyagi, Hideki

    2018-05-09

    The removal of harmful metals from the intestinal environment can be inhibited by various ions which can interfere with the adsorption of target metal ions. Therefore, it is important to understand the ion selectivity and adsorption mechanism of the adsorbent. In this study, we estimated the adsorption properties of Lactobacillus casei JCM1134 by analyzing the correlation between its maximum adsorption level (q max ) for seven metals and their ion characteristics. Some metal ions showed altered adsorption levels by L. casei JCM1134 as culture growth time increased. Although it was impossible to identify specific adsorption components, adsorption of Sr and Ba may depend on capsular polysaccharide levels. The maximum adsorption of L. casei JCM1134 (9 h of growth in culture) for divalent metal ions was in the following order: Cu 2+  > Ba 2+  > Sr 2+  > Cd 2+  > Co 2+  > Mg 2+  > Ni 2+ . The q max showed a high positive correlation with the ionic radius. Because this tendency is similar to adsorption occurring through an ion exchange mechanism, it was inferred that an ion exchange mechanism contributed greatly to adsorption by L. casei JCM1134. Because the decrease in the amount of adsorption due to prolonged culture time was remarkable for metals with a large ion radius, it is likely that the adsorption components involved in the ion exchange mechanism decomposed over time. These results and analytical concept may be helpful for designing means to remove harmful metals from the intestinal tract.

  14. Ion exchange removal of strontium from simulated and actual N-Springs well water at the Hanford 100-N Area

    International Nuclear Information System (INIS)

    Brown, G.N.; Carson, K.J.; DesChane, J.R.; Elovich, R.J.; Kafka, T.M.; White, L.R.

    1996-06-01

    Experimental ion exchange studies are being conducted by the Pacific Northwest national Laboratory (PNNL) under the Efficient Separations and Processing (ESP) Crosscutting Program to evaluate newly emerging materials and technologies for removing cesium, strontium, technetium, and transuranic elements from simulated and actual wastes at Hanford. Previous work focused on applications to treat high-level alkaline tank wastes, but many of the technologies can also be applied in process and ground-water remediation. Ultimately, each process must be evaluated in terms of life-cycle costs, removal efficiency, process chemical consumption and recycle, stability of materials exposed to chemicals and radiation, compatibility with other process streams, secondary waste generation, process and maintenance costs, and final material disposal. This report assesses the performance of the 3M-designed Process Absorber Development Unit (PADU) and the AlliedSignal-produced sodium nonatitanate (NaTi) material in trace quantities of strontium from simulated and actual Hanford N-Springs ground water. The experimental objective was to determine the strontium-loading breakthrough profile of a proprietary 3M-engineered material in either disk or cartridge forms

  15. Biosorption of the strontium ion by irradiated Saccharomyces cerevisiae under culture conditions.

    Science.gov (United States)

    Qiu, Liang; Feng, Jundong; Dai, Yaodong; Chang, Shuquan

    2017-06-01

    As a new-emerging method for strontium disposal, biosorption has shown advantages such as high sorption capacity; low cost. In this study, we investigated the potential of Saccharomyces cerevisiae (S. cerevisiae) in strontium disposal under culture conditions and the effects of irradiation on their biosorption capabilities. We found that S. cerevisiae can survive irradiation and grow. Pre-exposure to irradiation rendered S. cerevisiae resistant to further irradiation. Surprisingly, the pre-exposure to irradiation can increase the biosorption capability of S. cerevisiae. We further investigated the factors that influenced the biosorption efficiency, which were (strongest to weakest): pH > strontium concentration > time > temperature. In our orthogonal experiment, the optimal conditions for strontium biosorption by irradiated S. cerevisiae were: pH 7, 150 mg L -1 strontium at the temperature of 32 °C with 30 h. The equilibrium of strontium biosorption was analyzed by Langmuir and Freundlich models, from which the formal model is found to provide a better fit for the experimental results. The kinetics of strontium biosorption by living irradiated S. cerevisiae was found to be comprised of three phases: dramatically increased during 0-9 h, decreased during 12-24 h, and increased during 30-50 h. These results provide a systematic understanding of the biosorption capabilities of irradiated S. cerevisiae, which can contribute to the development of remediating nuclear waste water. Copyright © 2017 Elsevier Ltd. All rights reserved.

  16. The adsorption behavior of functional particles modified by polyvinylimidazole for Cu(II) ion

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Ruixin; Men, Jiying; Gao, Baojiao [School of Chemical Engineering and Environment, North University of China, Taiyuan (China)

    2012-03-15

    In this paper, a novel composite material the silica grafted by poly(N-vinyl imidazole) (PVI), i.e., PVI/SiO{sub 2}, was prepared using 3-methacryloxypropyl trimethoxysilane (MPS) as intermedia through the ''grafting from'' method. The adsorption behavior of metal ions by PVI/SiO{sub 2} was researched by both static and dynamic methods. Experimental results showed that PVI/SiO{sub 2} possessed very strong adsorption ability for metal ions. For different metal ions, PVI/SiO{sub 2} exhibited different adsorption abilities with the following order of adsorption capacity: Cu{sup 2+}> Cd{sup 2+}> Zn{sup 2+}. The adsorption material PVI/SiO{sub 2} was especially good at adsorbing Cu(II) ion and the saturated adsorption capacity could reach up to 49.2 mg/g. The empirical Freundlich isotherm was found to describe well the equilibrium adsorption data. Higher temperatures facilitated the adsorption process and thus increased the adsorption capacity. The pH and grafting amount of PVI had great influence on the adsorption amount. In addition, PVI/SiO{sub 2} particles had excellent eluting and regenerating property using diluted hydrochloric acid solution as eluent. The adsorption ability trended to steady during 10 cycles. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  17. Kinetic studies of uranyl ion adsorption on acrylonitrile (AN) / polyethylene glycol (PEG) interpenetrating networks (IPN)

    International Nuclear Information System (INIS)

    Aycik, G.A.; Gurellier, R.

    2004-01-01

    The kinetics of the adsorption of uranyl ions on amidoximated acrylonitrile (AN)/ polyethylene glycol (PEG) interpenetrating network (IPNs) from aqueous solutions was studied as a function of time and temperature. Adsorption analyses were performed for definite uranyl ion concentrations of 1x10 -2 M and at four different temperatures as 290K, 298K, 308K and 318K. Adsorption time was increased from zero to 48 hours. Adsorption capacities of uranyl ions by PEG/AN IPNS were determined by gamma spectrometer. The results indicate that adsorption capacity increases linearly with increasing temperature. The max adsorption capacity was found as 602 mgu/g IPN at 308K. Adsorption rate was evaluated from the curve plotted of adsorption capacity versus time, for each temperature. Rate constants for uranyl ions adsorption on amidoximated ipns were calculated for 290K, 298K, 308K and 318K at the solution concentration of 1x10 -2 M . The results showed that as the temperature increases the rate constant increases exponentially too. The mean activation energy of uranyl ions adsorption was found as 34.6 kJ/mole by using arrhenius equation. (author)

  18. Adsorption of lead and cadmium ions in aqueous solutions onto modified lignin from alkali glycerol delignication

    International Nuclear Information System (INIS)

    Demirbas, Ayhan

    2004-01-01

    Adsorptions of toxic metal ions (Pb(II) and Cd(II)) onto modified lignin from beech and poplar woods by alkali glycerol delignification are presented in this paper. The material exhibits good adsorption capacity and the adsorption data follow the Langmuir model. The maximum adsorption capacities are 8.2-9.0 and 6.7-7.5 mg/g of the modified lignin for Pb(II) and Cd(II), respectively. The maximum adsorption percentage is 95.8 for Pb(II) for 4 h at 330 K and is 95.0 for Cd(II) for 10 h at 290 K. The adsorption of both the metal ions increased with increasing temperature indicating endothermic nature of the adsorption process. The maximum adsorption percentages of Pb(II) and Cd(II) ions decrease with time till 48 and 42 h and then again increase slightly with time. The adsorption of both heavy metal ions increases with pH. The adsorption of Pb(II) ions reached a maximum at a 5.0 value of pH

  19. Mathematical simulation and calculation of continuous countercurrent process of ion-exchange extraction of strontium from strongly mineralized solutions

    International Nuclear Information System (INIS)

    Nikashina, V.A.; Venitsianov, E.V.; Ivanov, V.A.; Gur'yanova, L.N.; Nikolaev, N.P.; Baturova, L.L.; Moskovskij Gosudarstvennyj Univ., Moscow

    1993-01-01

    A program 'Countercurrent' is developed for the simulation of a continuous ion-exchange extraction of strontium from the strongly mineralized solutions containing NaCl and CaCl 2 using carboxylic cation exchanger KB-4 in countercurrent columns. The use of the program allows one to calculate the consitions of Ca and Sr separation depending on the modes of operation at the stage of sorption as well as regeneration, to calculate a residual Sr content on an overloaded sorbent and Sr separation on an incompletely regenerated KB-4, and to find the optimal separation conditions

  20. Adsorption of Cd(II) Metal Ion on Adsorbent beads from Biomass Saccharomycess cereviceae - Chitosan

    Science.gov (United States)

    Hasri; Mudasir

    2018-01-01

    The adsorbent beads that was preparation from Saccharomycess cereviceae culture strain FN CC 3012 and shrimp shells waste and its application for adsorption of Cd (II) metal ion has been studied. The study start with combination of Saccharomycess cereviceae biomass to chitosan (Sc-Chi), contact time, pH of solution and initial concentration of cations. Total Cd(II) metal ion adsorbed was calculated from the difference of metal ion concentration before and after adsorption by AAS. The results showed that optimum condition for adsorption of Cd(II) ions by Sc-Chi beads was achieved with solution pH of 4, contact time of 60 minutes and initial concentration adsorption 100mg/L. The hydroxyl (-OH) and amino (-NH2) functional groups were believed to be responsible for the adsorption of Cd(II) ions.

  1. The Influence of Salt Anions on Heavy Metal Ion Adsorption on the Example of Nickel

    Science.gov (United States)

    Mende, Mandy; Schwarz, Dana; Steinbach, Christine; Schwarz, Simona

    2018-01-01

    The biodegradable polysaccharide chitosan possesses protonated and natural amino groups at medium pH values and has therefore been used as an adsorbing material for nickel salts in water treatment. Nickel is a problematic heavy metal ion which can cause various diseases and disorders in living organisms. Here, we show the influence of oxyanions (e.g., nitrate and sulfate) to the adsorption of nickel ions. Hence, simultaneously we are addressing the increasing global problem of nitrate and sulfate ion pollution in groundwater and surface water. A series of adsorption experiments was carried out in order to determine (i) the adsorption equilibrium, (ii) the adsorption capacity in dependence on the initial nickel ion concentration, and (iii) the influence of the anion presented in solution for the adsorption capacity. Surface morphology of chitosan flakes before and after the adsorption process has been studied with SEM-EDX analysis. The chitosan flakes exhibited promising adsorption capacities of 81.9 mg·g−1 and 21.2 mg·g−1 for nickel (sulfate) and nickel (nitrate), respectively. The calculated values of Gibbs free energy change ΔG0 confirm the higher adsorption of nickel ions in presence of sulfate ions. Hence, higher anion valence leads to a higher adsorption capacity. PMID:29510485

  2. Comparison of inorganic ion exchange materials for removing cesium, strontium, and transuranic elements from K-basin water

    Energy Technology Data Exchange (ETDEWEB)

    Brown, G.N.; Bontha, J.R.; Carson, K.J.; Elovich, R.J.; DesChane, J.R.

    1997-10-01

    The work presented in this report was conducted by the Pacific Northwest National Laboratory (PNNL) under the Efficient Separations and Crosscutting Program (ESP), Office of Science and Technology, U.S. Department of Energy (DOE). The objective of this work was to investigate radionuclide uptake by several newly produced ion exchange materials under actual waste conditions, and to compare the performance of those materials with that of commercially available ion exchangers. The equilibrium uptake data presented in this report are useful for identifying potential materials that are capable of removing cesium and strontium from 105-KE Basin water. The data show the relative selectivities of the ion exchange materials under similar operating conditions. Additional flow studies are needed to predict material capacities and to develop complete ion exchange process flow sheets. The materials investigated in this study include commercially available ion exchangers such as IONSIV{reg_sign} IE-911 (manufactured by UOP), clinoptilolite (a naturally occurring zeolite), and materials produced on an experimental basis by AlliedSignal (biotites and nonatitanates), 3M (hexacyanoferrates), Selion Technologies, Inc. (hexacyanoferrates and titanates), and Texas A&M University (pharmacosiderites, biotites, and nonatitanates). In all, the performance of 14 ion exchange materials was evaluated at two solution-to-exchanger mass ratios (i.e., 10{sup 4} and 10{sup 5}) using actual 105-KE Basin water. Evaluation consisted of determining cesium and strontium batch distribution coefficients, loading, and decontamination factors. Actual 105-KE Basin water was obtained from a sample collected during the sludge dissolution work conducted by PNNL in FY 1996. This sample was taken from the bottom of the basin and contained significantly higher concentrations of the radioactive constituents than do samples taken from the top of the basin.

  3. Comparison of inorganic ion exchange materials for removing cesium, strontium, and transuranic elements from K-basin water

    International Nuclear Information System (INIS)

    Brown, G.N.; Bontha, J.R.; Carson, K.J.; Elovich, R.J.; DesChane, J.R.

    1997-10-01

    The work presented in this report was conducted by the Pacific Northwest National Laboratory (PNNL) under the Efficient Separations and Crosscutting Program (ESP), Office of Science and Technology, U.S. Department of Energy (DOE). The objective of this work was to investigate radionuclide uptake by several newly produced ion exchange materials under actual waste conditions, and to compare the performance of those materials with that of commercially available ion exchangers. The equilibrium uptake data presented in this report are useful for identifying potential materials that are capable of removing cesium and strontium from 105-KE Basin water. The data show the relative selectivities of the ion exchange materials under similar operating conditions. Additional flow studies are needed to predict material capacities and to develop complete ion exchange process flow sheets. The materials investigated in this study include commercially available ion exchangers such as IONSIV reg-sign IE-911 (manufactured by UOP), clinoptilolite (a naturally occurring zeolite), and materials produced on an experimental basis by AlliedSignal (biotites and nonatitanates), 3M (hexacyanoferrates), Selion Technologies, Inc. (hexacyanoferrates and titanates), and Texas A ampersand M University (pharmacosiderites, biotites, and nonatitanates). In all, the performance of 14 ion exchange materials was evaluated at two solution-to-exchanger mass ratios (i.e., 10 4 and 10 5 ) using actual 105-KE Basin water. Evaluation consisted of determining cesium and strontium batch distribution coefficients, loading, and decontamination factors. Actual 105-KE Basin water was obtained from a sample collected during the sludge dissolution work conducted by PNNL in FY 1996. This sample was taken from the bottom of the basin and contained significantly higher concentrations of the radioactive constituents than do samples taken from the top of the basin

  4. Effect of competing ions and causticization on the ammonia adsorption by a novel poly ligand exchanger (PLE) ammonia adsorption reagent.

    Science.gov (United States)

    Chen, Quanzhou; Zhou, Kanggen; Hu, Yuanjuan; Liu, Fang; Wang, Aihe

    2017-03-01

    In this paper, a poly ligand exchanger, Cu(II)-loaded chelating resin named ammonia adsorption reagent (AMAR), bearing the functional group of weak iminodiacetate acid, was prepared to efficiently remove ammonia from solutions. Batch adsorption equilibrium experiments were conducted under a range of conditions. The effects of pH on the removal of ammonia by AMAR were investigated at 25 °C. The copper loaded on the resin forms a complex with NH 3 in solution under alkaline condition. The effect of alkaline dosage (AD) on the ammonia adsorption was investigated. The maximum breakthrough bed volumes were obtained when the AD was set as 0.75 mmol OH - /mL. The higher AD did not guarantee the better ammonia removal efficiency due to the forming of Cu(OH) 2 precipitate between OH - in solutions and Cu(II) on the resin. The effect of competing ions on the adsorption breakthrough curve of virgin AMAR and causticized AMAR was also investigated. The results demonstrated that the existence of competing ions had a negative impact on the adsorption capacity for both virgin AMAR and causticized AMAR. After causticization, the AMAR was more resistant to the competing ions comparing with virgin AMAR. The bivalent Ca 2+ affects the ammonia adsorption more than does the monovalent Na + .

  5. Influence of Chloride-Ion Adsorption Agent on Chloride Ions in Concrete and Mortar

    Directory of Open Access Journals (Sweden)

    Gai-Fei Peng

    2014-04-01

    Full Text Available The influence of a chloride-ion adsorption agent (Cl agent in short, composed of zeolite, calcium aluminate hydrate and calcium nitrite, on the ingress of chloride ions into concrete and mortar has been experimentally studied. The permeability of concrete was measured, and the chloride ion content in mortar was tested. The experimental results reveal that the Cl agent could adsorb chloride ions effectively, which had penetrated into concrete and mortar. When the Cl agent was used at a dosage of 6% by mass of cementitious materials in mortar, the resistance to the penetration of chloride ions could be improved greatly, which was more pronounced when a combination of the Cl agent and fly ash or slag was employed. Such an effect is not the result of the low permeability of the mortar, but might be a result of the interaction between the Cl agent and the chloride ions penetrated into the mortar. There are two possible mechanisms for the interaction between the Cl agent and chloride ion ingress. One is the reaction between calcium aluminate hydrate in the Cl agent and chloride ions to form Friedel’s salt, and the other one is that calcium aluminate hydrate reacts with calcium nitrite to form AFm during the early-age hydration of mortar and later the NO2− in AFm is replaced by chloride ions, which then penetrate into the mortar, also forming Friedel’s salt. More research is needed to confirm the mechanisms.

  6. Kinetics of adsorption of zinc-ions by doped manganese dioxides

    International Nuclear Information System (INIS)

    Rophael, M.W.; Mourad, W.E.; Khalil, L.B.; Malati, M.A.

    1979-01-01

    Using 65 Zn-labelled solutions, the kinetics of the specific adsorption of Zn 2+ -ions by doped manganese dioxides was studied, at pH values corresponding to their isoelectric points (IEP's), by γ-ray scintillation counting. The rate of the fast adsorption of Zn 2+ -ions by doped dioxides increased in the series: Li + -doped 2+ -ions in about 10 minutes exhibited a similar increase. Compared to the undoped sample, the extent and the rate of adsorption were lower for the samples doped with an ion of valence 4. (author)

  7. Comparative study on the change in index of refraction in ion-exchange interdiffusion in alkali-silicate glasses containing calcium, strontium, barium and titanium oxides

    International Nuclear Information System (INIS)

    Livshits, V.Ya.; Marchuk, E.A.

    1993-01-01

    Different ability to ion exchange from the salts of lithium-sodium-silicate glass melt containing calcium (or strontium, or barium) and titanium oxides in addition has been shown. CaO, SrO and BaO have negative effect, but TiO 2 -positive one on the fullness of ion exchange of lithium-sodium and on the rate of interdiffusion in alkali-silicate glass. The value of change in index of refraction of glass with TiO 2 is twice higher than glass with calcium oxide (or strontium, or barium) as the fourth component

  8. [Application of classical isothermal adsorption models in heavy metal ions/ diatomite system and related problems].

    Science.gov (United States)

    Zhu, Jian; Wu, Qing-Ding; Wang, Ping; Li, Ke-Lin; Lei, Ming-Jing; Zhang, Wei-Li

    2013-11-01

    In order to fully understand adsorption nature of Cu2+, Zn2+, Pb2+, Cd2+, Mn2+, Fe3+ onto natural diatomite, and to find problems of classical isothermal adsorption models' application in liquid/solid system, a series of isothermal adsorption tests were conducted. As results indicate, the most suitable isotherm models for describing adsorption of Pb2+, Cd2+, Cu2+, Zn2+, Mn2+, Fe3+ onto natural diatomite are Tenkin, Tenkin, Langmuir, Tenkin, Freundlich and Freundlich, respectively, the adsorption of each ion onto natural diatomite is mainly a physical process, and the adsorption reaction is favorable. It also can be found that, when using classical isothermal adsorption models to fit the experimental data in liquid/solid system, the equilibrium adsorption amount q(e) is not a single function of ion equilibrium concentration c(e), while is a function of two variables, namely c(e) and the adsorbent concentration W0, q(e) only depends on c(e)/W(0). Results also show that the classical isothermal adsorption models have a significant adsorbent effect, and their parameter values are unstable, the simulation values of parameter differ greatly from the measured values, which is unhelpful for practical use. The tests prove that four-adsorption-components model can be used for describing adsorption behavior of single ion in nature diatomite-liquid system, its parameters k and q(m) have constant values, which is favorable for practical quantitative calculation in a given system.

  9. Effect of the impregnation of carbon cloth with ethylenediaminetetraacetic acid on its adsorption capacity for the adsorption of several metal ions

    International Nuclear Information System (INIS)

    Afkhami, Abbas; Madrakian, Tayyebeh; Amini, Azadeh; Karimi, Ziba

    2008-01-01

    Effect of loading of C-cloth with ethylenediaminetetraacetic acid (EDTA) on the adsorption capacity for the adsorption of several metal cations was studied. The concentration of ions in the solution was monitored using atomic absorption spectrometry. The adsorption isotherm data for the cations were derived at 25 deg. C and treated according to Langmuir and Freundlich models and was found that for most of the investigated cations Langmuir model was more successful. Adsorption capacities determined from Langmuir isotherms. Loading of the adsorbent with EDTA increased the adsorption capacity for the adsorption of all of the investigation ions

  10. Comparative study of ZnO nanorods and thin films for chemical and biosensing applications and the development of ZnO nanorods based potentiometric strontium ion sensor

    Science.gov (United States)

    Khun, K.; Ibupoto, Z. H.; Chey, C. O.; Lu, Jun.; Nur, O.; Willander, M.

    2013-03-01

    In this study, the comparative study of ZnO nanorods and ZnO thin films were performed regarding the chemical and biosensing properties and also ZnO nanorods based strontium ion sensor is proposed. ZnO nanorods were grown on gold coated glass substrates by the hydrothermal growth method and the ZnO thin films were deposited by electro deposition technique. ZnO nanorods and thin films were characterised by field emission electron microscopy [FESEM] and X-ray diffraction [XRD] techniques and this study has shown that the grown nanostructures are highly dense, uniform and exhibited good crystal quality. Moreover, transmission electron microscopy [TEM] was used to investigate the quality of ZnO thin film and we observed that ZnO thin film was comprised of nano clusters. ZnO nanorods and thin films were functionalised with selective strontium ionophore salicylaldehyde thiosemicarbazone [ST] membrane, galactose oxidase, and lactate oxidase for the detection of strontium ion, galactose and L-lactic acid, respectively. The electrochemical response of both ZnO nanorods and thin films sensor devices was measured by using the potentiometric method. The strontium ion sensor has exhibited good characteristics with a sensitivity of 28.65 ± 0.52 mV/decade, for a wide range of concentrations from 1.00 × 10-6 to 5.00 × 10-2 M, selectivity, reproducibility, stability and fast response time of 10.00 s. The proposed strontium ion sensor was used as indicator electrode in the potentiometric titration of strontium ion versus ethylenediamine tetra acetic acid [EDTA]. This comparative study has shown that ZnO nanorods possessed better performance with high sensitivity and low limit of detection due to high surface area to volume ratio as compared to the flat surface of ZnO thin films.

  11. Mathematical simulation and calculation of the continuous countercurrent process of ion-exchange extraction of strontium from strongly mineralized solutions

    International Nuclear Information System (INIS)

    Nikashina, V.A.; Guryanova, L.N.; Baturova, L.L.; Venetsianov, E.V.; Ivanov, V.A.; Nikolaev, N.P.

    1993-01-01

    The program open-quotes Countercurrentclose quotes is developed for the simulation of a continuous ion-exchange extraction of strontium from strongly mineralized NaCl and CaCl 2 solutions using a KB-4 carboxylic cation-exchanger in the countercurrent columns. The program allows one to Calculate the conditions of Ca and Sr separation depending on the mode of operation at the sorption and regeneration stages, the residual Sr content on the overloaded sorbent, and the Sr separation on incompletely regenerated KB-4. It also makes it possible to find the optimal separation conditions. The program open-quotes Countercurrentclose quotes can be also used to simulate other ion-exchange processes

  12. Heavy metal ion adsorption behavior in nitrogen-doped magnetic carbon nanoparticles: Isotherms and kinetic study

    International Nuclear Information System (INIS)

    Shin, Keun-Young; Hong, Jin-Yong; Jang, Jyongsik

    2011-01-01

    Graphical abstract: Display Omitted Research highlights: → The monodisperse and multigram-scale N-MCNPs are fabricated by carbonization of polypyrrole as a carbon precursor. → The synthesized N-MCNPs provide an enhanced adsorption uptake for various heavy metal ions. → The N-MCNPs can be applied to the Langmuir model and pseudo-second-order kinetics. → The iron-impregnated N-MCNPs are reused up to 5 times with no loss of removal efficiency. - Abstract: To clarify the heavy metal adsorption mechanism of nitrogen-doped magnetic carbon nanoparticles (N-MCNPs), adsorption capacity was investigated from the adsorption isotherms, kinetics and thermodynamics points of view. The obtained results showed that the equilibrium adsorption behavior of Cr 3+ ion onto the N-MCNPs can be applied to the Langmuir model and pseudo-second-order kinetics. It indicated that the fabricated N-MCNPs had the homogenous surface for adsorption and all adsorption sites had equal adsorption energies. Furthermore, the adsorption onto N-MCNPs taken place through a chemical process involving the valence forces. According to the thermodynamics, the adsorption process is spontaneous and endothermic in nature which means that the adsorption capacity increases with increasing temperature due to the enhanced mobility of adsorbate molecules. The effects of the solution pH and the species of heavy metal ion on the adsorption uptake were also studied. The synthesized N-MCNPs exhibited an enhanced adsorption capacity for the heavy metal ions due to the high surface area and large amount of nitrogen contents.

  13. An Analytical Model for Adsorption and Diffusion of Atoms/Ions on Graphene Surface

    Directory of Open Access Journals (Sweden)

    Yan-Zi Yu

    2015-01-01

    Full Text Available Theoretical investigations are made on adsorption and diffusion of atoms/ions on graphene surface based on an analytical continuous model. An atom/ion interacts with every carbon atom of graphene through a pairwise potential which can be approximated by the Lennard-Jones (L-J potential. Using the Fourier expansion of the interaction potential, the total interaction energy between the adsorption atom/ion and a monolayer graphene is derived. The energy-distance relationships in the normal and lateral directions for varied atoms/ions, including gold atom (Au, platinum atom (Pt, manganese ion (Mn2+, sodium ion (Na1+, and lithium-ion (Li1+, on monolayer graphene surface are analyzed. The equilibrium position and binding energy of the atoms/ions at three particular adsorption sites (hollow, bridge, and top are calculated, and the adsorption stability is discussed. The results show that H-site is the most stable adsorption site, which is in agreement with the results of other literatures. What is more, the periodic interaction energy and interaction forces of lithium-ion diffusing along specific paths on graphene surface are also obtained and analyzed. The minimum energy barrier for diffusion is calculated. The possible applications of present study include drug delivery system (DDS, atomic scale friction, rechargeable lithium-ion graphene battery, and energy storage in carbon materials.

  14. Efficient adsorption of Hg (II) ions in water by activated carbon modified with melamine

    Science.gov (United States)

    Qin, Hangdao; Meng, Jingling; Chen, Jing

    2018-04-01

    Removal of Hg (II) ions from industrial wastewater is important for the water treatment, and adsorption is an efficient treatment process. Activated carbon (AC) was modified with melamine, which introduced nitrogen-containing functional groups onto AC surface. Original AC and melamine modified activated carbon (ACM) were characterized by elemental analysis, N2 adsorption-desorption, determination of the pH of the point of zero charge (pHpzc) and X-ray photoelectron spectroscopy (XPS) and their performance in the adsorption of Hg(II) ions was investigated. Langmuir model fitted the experimental data of equilibrium isotherms well. ACM showed the higher Hg (II) ions adsorption capacity, increasing more than more than 1.8 times compared to the original one. Moreover, ACM showed a wider pH range for the maximum adsorption than the parent AC.

  15. Adsorption affinity and selectivity of 3-ureidopropyltriethoxysilane grafted oil palm empty fruit bunches towards mercury ions.

    Science.gov (United States)

    Kunjirama, Magendran; Saman, Norasikin; Johari, Khairiraihanna; Song, Shiow-Tien; Kong, Helen; Cheu, Siew-Chin; Lye, Jimmy Wei Ping; Mat, Hanapi

    2017-06-01

    This study was conducted to investigate the potential application of oil palm empty fruit branches (OPEFB) as adsorbents to remove organic methylmercurry, MeHg(II), and inorganic Hg(II) from aqueous solution. The OPEFB was functionalized with amine containing ligand namely 3-ureidopropyltriethoxysilane (UPTES) aiming for better adsorption performance towards both mercury ions. The adsorption was found to be dependent on initial pH, initial concentraton, temperatures, and contact time. The maximum adsorption capacities (Q m.exp ) of Hg(II) adsorption onto OPEFB and UPTES-OPEFB were 0.226 and 0.773 mmol/g, respectively. The Q m.exp of MeHg(II) onto OPEFB, however, was higher than UPTES-OPEFB. The adsorption kinetic data obeyed the Elovich model and the adsorption was controlled by the film-diffusion step. The calculated thermodynamic parameters indicate an endothermic adsorption process. Adsorption data analysis indicates that the adsorption mechanism may include ion-exchange, complexation, and physisorption interactions. The potential applications of adsorbents were demonstrated using oilfield produced water and natural gas condensate. The UPTES-OPEFB offered higher selectivity towards both mercury ions than OPEFB. The regenerability studies indicated that the adsorbent could be reused for multiple cycles.

  16. Adsorption of ions on hematite (α-Fe2O3) : a colloid-chemical study

    NARCIS (Netherlands)

    Breeuwsma, A.

    1973-01-01

    This study is primarily intended to provide a better understanding of the adsorption of ions on hematite (α-Fe 2 O 3 ). In addition, due attention is given to the relation between the ionic adsorption and the colloidal stability of hematite sols.

    Chapter 1. is concerned

  17. Adsorption of Pb(II) ions from aqueous solution using lignin from ...

    African Journals Online (AJOL)

    The adsorption of lead(II) ions from aqueous solution onto alkali lignin extracted from Hagenia abyssinica was investigated by electrochemical methods. The effect of solution pH, lignin dosage and contact time were investigated at room temperature in a batch system. Adsorption equilibrium was approached within 80 min.

  18. Novel adsorptive ultrafiltration membranes derived from polyvinyltetrazole-co-polyacrylonitrile for Cu(II) ions removal

    KAUST Repository

    Kumar, Mahendra

    2016-05-04

    Novel adsorptive ultrafiltration membranes were manufactured from synthesized polyvinyltetrazole−co−polyacrylonitrile (PVT−co−PAN) by nonsolvent induced phase separation (NIPS). PVT−co−PAN with various degree of functionalization (DF) was synthesized via a [3+2] cycloaddition reaction at 60°C using a commercial PAN. PVT−co−PAN with varied DF was then explored to prepare adsorptive membranes. The membranes were characterized by surface zeta potential and static water contact angle measurements, scanning electron microscopy as well as atomic force microscopy (AFM) techniques. It was shown that PVT segments contributed to alter the pore size, charge and hydrophilic behavior of the membranes. The membranes became more negatively charged and hydrophilic after addition of PVT segments. The PVT segments in the membranes served as the major binding sites for adsorption of Cu(II) ions from aqueous solution. The maximum adsorption of Cu(II) ions by the membranes in static condition and in a continuous ultrafiltration of 10 ppm solution was attained at pH = 5. The adsorption data suggest that the Freundlich isotherm model describes well Cu(II) ions adsorption on the membranes from aqueous solution. The adsorption capacity obtained from the Freundlich isotherm model was 44.3 mg g−1; this value is higher than other membrane adsorption data reported in the literature. Overall, the membranes fabricated from PVT−co−PAN are attractive for efficient removal of heavy metal ions under the optimized conditions.

  19. Novel adsorptive ultrafiltration membranes derived from polyvinyltetrazole-co-polyacrylonitrile for Cu(II) ions removal

    KAUST Repository

    Kumar, Mahendra; Shevate, Rahul; Hilke, Roland; Peinemann, Klaus-Viktor

    2016-01-01

    Novel adsorptive ultrafiltration membranes were manufactured from synthesized polyvinyltetrazole−co−polyacrylonitrile (PVT−co−PAN) by nonsolvent induced phase separation (NIPS). PVT−co−PAN with various degree of functionalization (DF) was synthesized via a [3+2] cycloaddition reaction at 60°C using a commercial PAN. PVT−co−PAN with varied DF was then explored to prepare adsorptive membranes. The membranes were characterized by surface zeta potential and static water contact angle measurements, scanning electron microscopy as well as atomic force microscopy (AFM) techniques. It was shown that PVT segments contributed to alter the pore size, charge and hydrophilic behavior of the membranes. The membranes became more negatively charged and hydrophilic after addition of PVT segments. The PVT segments in the membranes served as the major binding sites for adsorption of Cu(II) ions from aqueous solution. The maximum adsorption of Cu(II) ions by the membranes in static condition and in a continuous ultrafiltration of 10 ppm solution was attained at pH = 5. The adsorption data suggest that the Freundlich isotherm model describes well Cu(II) ions adsorption on the membranes from aqueous solution. The adsorption capacity obtained from the Freundlich isotherm model was 44.3 mg g−1; this value is higher than other membrane adsorption data reported in the literature. Overall, the membranes fabricated from PVT−co−PAN are attractive for efficient removal of heavy metal ions under the optimized conditions.

  20. Adsorption behavior of carboxylated cellulose nanocrystal—polyethyleneimine composite for removal of Cr(VI) ions

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Chao; Jin, Ru-Na; Ouyang, Xiao-kun, E-mail: xkouyang@zjou.edu.cn; Wang, Yang-Guang

    2017-06-30

    Highlights: • A carboxylated cellulose nanocrystal-polyethyleneimine composite (CCN-PEI) was prepared. • The as-prepared CCN-PEI was characterized by SEM, TEM, FT-IR, and XPS. • Results suggested that the reusable CCN-PEI could remove Cr(VI) from aqueous solutions with a high adsorption capacity. • The adsorption isotherm, thermodynamics, and kinetics of the adsorption process are also discussed. - Abstract: In this study, a composite adsorbent (CCN-PEI) composed of carboxylated cellulose nanocrystals (CCN) and polyethyleneimine (PEI) was prepared through an amidation reaction between the carboxyl groups of the CCN and the amine groups of the PEI. The adsorption performance of the CCN-PEI was tested by removing Cr(VI) ions from aqueous solutions. The physicochemical properties of the CCN and the Cr(VI) ion-loaded CCN-PEI were studied using scanning electron microscopy (SEM), transmission electron microscopy, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy. To investigate the adsorption kinetics of Cr(VI) ions onto this newly developed CCN-PEI, we performed experiments under different adsorption conditions, by varying the contact time, solution pH, initial Cr(VI) ion concentration, and adsorption temperature. The prepared CCN-PEI exhibited an encouraging uptake capacity of 358.42 mg × g{sup −1}. The adsorption process was fast: within the first 100 min, Cr(VI) ion adsorption onto the CCN-PEI was about 65%, and the adsorption equilibrium was reached within 250 min. Kinetics experiments indicated that the adsorption process could be described by a pseudo-second-order kinetic model. Furthermore, our adsorption equilibrium data fit the Langmuir isotherms well. The calculated thermodynamic parameters, such as the free energy change (ΔG = −2.93 kJ × mol{sup −1}), enthalpy change (ΔH = −5.69 kJ × mol{sup −1}), and entropy change (ΔS = −9.14 kJ × mol{sup −1}), indicate that the adsorption of Cr(VI) ions onto CCN

  1. Adsorption characteristics of Pb(II) and Cu(II) ions by domestic clays

    International Nuclear Information System (INIS)

    Kwon, Ee Yol; Noh, Hea Ran

    1990-01-01

    This investigation was carried out to study the adsorption characteristics of Pb(II) and Cu(II) ions in aqueous solution by using clays of Gampo 35, Bentonite (chulwon) and Mangwoon 95 which were dug in the country. As the results, the adsorption of metal ions clays were reached equilibrium by shaking for about 40-60 minutes. In acidic solution, the adsorptivity of clays was increased as pH increased, however, Gampo 35 showed the high adsorptivity over 90% even at pH2-3. Pb(II) ion showed better removal efficiency than Cu(II) ion. The adsorptivities of adsorbents showed following order: Gampo 35>Bentonite> Mangwoon 95. The adsorption isotherms of Pb(II) ion on clays were well fitted in Freundlich's equation. Freundlich constantstion isotherms of Pb(II) ion on clays were well fitted in Freundlich's equation. Freundlich constants (1/n) of Gampo 35, Bentonite and Mangwoon 95 were 0.195, 0.271 and 0.314, respectively.(Author)

  2. Regularities of ions and surfactants adsorption on metal corrosion products and salt deposites

    International Nuclear Information System (INIS)

    Batrakov, V.V.; Gorichev, I.G.; Martynova, T.V.; Gutenev, A.V.

    1994-01-01

    Adsorption of ions on oxide/solution interface is described using the concepts of existence of acid-base equilibria and assumptions of the Graham-Parson theory on the structure of double electric layer. It is shown that adsorption data are in a good agreement with theoretical aspects. The influence of solution pH on adsorption of certain surfactant organic substances on oxide/solution interface was discussed. Data on adsorption of surfactants on salts-silver iodide and calcium carbonate - are dicussed making allowance for the structure of double electric layer

  3. Investigation of hydrolyzed polyacrylonitrile fibers utilization for the removal of strontium from liquid nuclear waste

    International Nuclear Information System (INIS)

    Kaplan, U.; Altas, Y.

    2009-01-01

    In this study polyacrylonitrile fiber (PANF) was hydrolyzed both with sodium and potassium hydroxide solutions using alkali hydrolysing method and hydrolyzed polyacrylonitrile fibers (HPANF) were obtained. These two types of hydrolyzed fibers were compared taking into consideration strontium adsorption capacities and it was decided that the hydrolysis with KOH solution is more convenient. The hydrolyzed polyacrylonitrile fiber was characterized by DTA/TGA, FTIR and SEM analysis. The adsorption behaviors of HPANF towards Sr ions was investigated by batch technique, the parameters affect the strontium adsorption such as the initial pH of the solution, Sr concentration, temperature, shaking time, adsorbent dose (V/m ratio) were determined. The adaptation of the obtained adsorption equilibrium data to Langmuir and Freundlich isotherm models were investigated and some of the thermodynamic values of the system (ΔGo, ΔHo, ΔSo) were calculated.

  4. Preparation and adsorption behavior for metal ions and humic acid of chitosan derivatives crosslinked by irradiation

    International Nuclear Information System (INIS)

    Zhao Long; Wasikiewicz, J.M.; Mitomo, H.; Nagasawa, N.; Yoshii, F.

    2007-01-01

    This article deals with the determination of the adsorption properties of metal ions and humic acid in wa- ter on crosslinked chitosan derivatives (carboxymethylchitosan) which were formed using the irradiation technique without any additives. The solubility test of these crosslinked materials were investigated in acidic, alkaline media, distilled water, and certain organic solvents. Scanning electron microscopic (SEM) images showed that the crosslinked chitosan derivatives possessed a porous morphological structure. Charged characteristic analyses demonstrated typically pH-dependent properties of the crosslinked materials. The adsorption studies were carded out by the batch method at room temperature. Adsorption of heavy metal ions (such as Cu 2+ , Cd 2+ ) and humic acid onto crosslinked samples was found to be strongly pH-dependent. Adsorption kinetic studies indicated the rapid removal of metal ions, and humic acid from the aqueous solutions. Moreover, isothermal adsorption data revealed that Cu 2+ , Cd 2+ , and humic acid were removed by these crosslinked materials with high efficiency. Adsorption isothermal data were interpreted well by the Langmuir equation. These crosslinked carboxymethylated chitosan derivatives indicate favorable adsorption of metal ions and humic acid. (authors)

  5. Adsorption kinetic parameters of Fe3+ and Ni2+ ions by gyrolite

    Directory of Open Access Journals (Sweden)

    Kestutis Baltakys

    2015-03-01

    Full Text Available In this work the adsorption kinetic parameters for Fe3+ and Ni2+ ions by gyrolite are presented. Additionally, the adsoption mechanism was described by using pseudo first order and pseudo second order  equations. It was determined that the adsorption capacity of gyrolite and intrusion of heavy metals ions in its structure depends on reaction time and the pH value of adsorptive. It was observed that the incorporation of Fe3+ ions occurs more intensive than Ni2+ ions. It was found that in the acidic solution the intrusion of Fe3+ ions into gyrolite structure proceeds by two types of chemical reaction mechanisms: substitution and addition. Meanwhile, nickel ions were participated only in substitution reaction: gyrolite-Ca0 + Mex+ ↔ gyrolite-Me0 + Ca2+. It was observed that the pseudo second order model fit well for iron and nickel ions adsorption mechanism. It was estimated that the adsorption reactions are not reversible process and the crystal structure of gyrolite is stable. Moreover, synthetic adsorbent and the products of sorption were characterized by XRD, STA and FT-IR methods.DOI: http://dx.doi.org/10.5755/j01.ms.21.1.5735

  6. Adsorption of ammonium ion by coconut shell-activated carbon from aqueous solution: kinetic, isotherm, and thermodynamic studies.

    Science.gov (United States)

    Boopathy, Ramasamy; Karthikeyan, Sekar; Mandal, Asit Baran; Sekaran, Ganesan

    2013-01-01

    Ammonium ions are one of the most encountered nitrogen species in polluted water bodies. High level of ammonium ion in aqueous solution imparts unpleasant taste and odor problems, which can interfere with the life of aquatics and human population when discharged. Many chemical methods are developed and being used for removal of ammonium ion from aqueous solution. Among various techniques, adsorption was found to be the most feasible and environmentally friendly with the use of natural-activated adsorbents. Hence, in this study, coconut shell-activated carbon (CSAC) was prepared and used for the removal of ammonium ion by adsorption techniques. Ammonium chloride (analytical grade) was purchased from Merck Chemicals for adsorption studies. The CSAC was used to adsorb ammonium ions under stirring at 100 rpm, using orbital shaker in batch experiments. The concentration of ammonium ion was estimated by ammonia distillate, using a Buchi distillation unit. The influence of process parameters such as pH, temperature, and contact time was studied for adsorption of ammonium ion, and kinetic, isotherm models were validated to understand the mechanism of adsorption of ammonium ion by CSAC. Thermodynamic properties such as ∆G, ∆H, and ∆S were determined for the ammonium adsorption, using van't Hoff equation. Further, the adsorption of ammonium ion was confirmed through instrumental analyses such as SEM, XRD, and FTIR. The optimum conditions for the effective adsorption of ammonium ion onto CSAC were found to be pH 9.0, temperature 283 K, and contact time 120 min. The experimental data was best followed by pseudosecond order equation, and the adsorption isotherm model obeyed the Freundlich isotherm. This explains the ammonium ion adsorption onto CSAC which was a multilayer adsorption with intraparticle diffusion. Negative enthalpy confirmed that this adsorption process was exothermic. The instrumental analyses confirmed the adsorption of ammonium ion onto CSAC.

  7. Adsorption of Cu 2+ , As 3+ and Cd 2+ ions from aqueous solution ...

    African Journals Online (AJOL)

    The adsorption of Cu2+, Cd2+ and As3+ ions on eggshell from aqueous solution was studied under batch conditions at 30, 40, 50 and 60oC and concentrations of 10, 20, 30, 60 and 80 mg/l. The partition coefficient for the ions between aqueous solution and chicken eggshell increased with time and with increase in the ...

  8. Adsorption of Copper Ion using Acrylic Acid-g-Polyaniline in Aqueous Solution

    Science.gov (United States)

    Kamarudin, Sabariah; Mohammad, Masita

    2018-04-01

    A conductive polymer, polyaniline (PANI) has unique electrical behaviour, stable in the environment, easy synthesis and have wide application in various fields. Modification of PANI in order to improve its adsorption capacity has been done. In this study, the polyaniline-grafted acrylic acid has been prepared and followed by adsorption of copper ion in aqueous solution. Acrylic acid, PANI and acrylic acid-g-polyaniline (Aag-PANI) were characterized by FTIR and SEM to determine its characteristic. The adsorption capacity was investigated to study the removal capacity of Cu ion from aqueous solution. Two parameters were selected which are pH (2, 4 and 6) and initial metal ion concentration (50 mg/L, 100 mg/L and 200 mg/L). The maximum adsorption capacity for PANI and Aag-PANI are 1.7 mg/g and 64.6 mg/g, respectively, at an initial concentration of 100 mg/L. The Langmuir adsorption isotherm model and Freundlich adsorption isotherm model have been used and showed that it is heterolayer adsorption by follows the Freundlich isotherm model.

  9. Study on the adsorption of heavy metal ions from aqueous solution on modified SBA-15

    Directory of Open Access Journals (Sweden)

    Liliana Giraldo

    2013-01-01

    Full Text Available Amino-functionalized SBA-15 mesoporous silica was prepared, characterized, and used as an adsorbent for heavy metal ions. The organic - inorganic hybrid material was obtained by a grafting procedure using SBA-15 silica with 3-aminopropyl-triethoxysilane and bis(2,4,4-trimethylpentyl phosphinic acid (Cyanex 272, respectively. The structure and physicochemical properties of the materials were characterized by means of elemental analysis, X-ray diffraction (XRD, nitrogen adsorption - desorption, thermogravimetric analysis, FTIR spectroscopy and immersion calorimetry. The organic functional groups were successfully grafted onto the SBA-15 surface and the ordering of the support was not affected by the chemical modification. The behavior of the grafted solids was investigated for the adsorption of heavy metal ions from aqueous solutions. The hybrid materials showed high adsorption capacity and high selectivity for zinc ions. Other ions, such as cooper and cobalt were absorbed by the modified SBA-15 material.

  10. Removal of Strontium Ions by Immobilized Saccharomyces Cerevisiae in Magnetic Chitosan Microspheres

    Directory of Open Access Journals (Sweden)

    Yanan Yin

    2017-02-01

    Full Text Available A novel biosorbent, immobilized Saccharomyces cerevisiae in magnetic chitosan microspheres was prepared, characterized, and used for the removal of Sr2+ from aqueous solution. The structure and morphology of immobilized S. cerevisiae before and after Sr2+adsorption were observed using scanning electron microscopy with energy dispersive X-ray spectroscopy. The experimental results showed that the Langmuir and Freundlich isotherm models could be used to describe the Sr2+ adsorption onto immobilized S. cerevisiae microspheres. The maximal adsorption capacity (qm was calculated to be 81.96 mg/g by the Langmuir model. Immobilized S. cerevisiae was an effective adsorbent for the Sr2+ removal from aqueous solution.

  11. Removal of strontium ions by immobilized saccharomyces cerevisiae in magnetic chitosan microspheres

    Energy Technology Data Exchange (ETDEWEB)

    Yin, Yanan; Wang, Jian Long; Yang, Xiao Yong; Li, Weihua [Collaborative Innovation Center for Advanced Nuclear Energy Technology, Institute of Nuclear and New Energy Technology, Tsinghua University, Beijing (China)

    2017-02-15

    A novel biosorbent, immobilized Saccharomyces cerevisiae in magnetic chitosan microspheres was prepared, characterized, and used for the removal of Sr{sup 2+} from aqueous solution. The structure and morphology of immobilized S. cerevisiae before and after Sr{sup 2+}adsorption were observed using scanning electron microscopy with energy dispersive X-ray spectroscopy. The experimental results showed that the Langmuir and Freundlich isotherm models could be used to describe the Sr{sup 2+} adsorption onto immobilized S. cerevisiae microspheres. The maximal adsorption capacity (q{sub m}) was calculated to be 81.96 mg/g by the Langmuir model. Immobilized S. cerevisiae was an effective adsorbent for the Sr{sup 2+} removal from aqueous solution.

  12. Adsorption of uranium ions by crosslinked polyester resin functionalized with acrylic acid from aqueous solutions

    International Nuclear Information System (INIS)

    Cemal Oezeroglu; Niluefer Metin

    2012-01-01

    In this paper, the crosslinked polyester resin containing acrylic acid functional groups was used for the adsorption of uranium ions from aqueous solutions. For this purpose, the crosslinked polyester resin of unsaturated polyester in styrene monomer (Polipol 353, Poliya) and acrylic acid as weight percentage at 80 and 20%, respectively was synthesized by using methyl ethyl ketone peroxide (MEKp, Butanox M60, Azo Nobel)-cobalt octoate initiator system. The adsorption of uranium ions on the sample (0.05 g copolymer and 5 mL of U(VI) solution were mixed) of the crosslinked polyester resin functionalized with acrylic acid was carried out in a batch reactor. The effects of adsorption parameters of the contact time, temperature, pH of solution and initial uranium(VI) concentration for U(VI) adsorption on the crosslinked polyester resin functionalized with acrylic acid were investigated. The adsorption data obtained from experimental results depending on the initial U(VI) concentration were analyzed by the Freundlich, Langmuir and Dubinin-Radushkevich (D-R) adsorption isotherms. The adsorption capacity and free energy change were determined by using D-R isotherm. The obtained experimental adsorption data depending on temperature were evaluated to calculate the thermodynamic parameters of enthalpy (ΔH o ), entropy (ΔS o ) and free energy change (ΔG o ) for the U(VI) adsorption on the crosslinked polyester resin functionalized with acrylic acid from aqueous solutions. The obtained adsorption data depending on contact time were analyzed by using adsorption models such as the modified Freundlich, Elovich, pseudo-first order and pseudo-second-order kinetic models. (author)

  13. Enhancement of the secondary ion emission from Si by O/sub 2 and H/sub 2/O adsorption

    International Nuclear Information System (INIS)

    Huan, C.H.; Wee, A.T.S.; Tan, K.L.

    1992-01-01

    The positive and negative secondary ion emission of Si are examined as a function of O/sub 2 and H/sub 2/O surface coverage under conditions of simultaneous adsorption and Ar/sup+ ion bombardment. It is found that the ion-molecule mechanism accounts for the adsorbate-induced signals and that yield enhancement by H/sub 2/O adsorption is less effective than O/sub 2 adsorption. (authors)

  14. Platelet adhesion and plasma protein adsorption control of collagen surfaces by He+ ion implantation

    International Nuclear Information System (INIS)

    Kurotobi, K.; Suzuki, Y.; Nakajima, H.; Suzuki, H.; Iwaki, M.

    2003-01-01

    He + ion implanted collagen-coated tubes with a fluence of 1 x 10 14 ions/cm 2 were exhibited antithrombogenicity. To investigate the mechanisms of antithrombogenicity of these samples, plasma protein adsorption assay and platelet adhesion experiments were performed. The adsorption of fibrinogen (Fg) and von Willebrand factor (vWf) was minimum on the He + ion implanted collagen with a fluence of 1 x 10 14 ions/cm 2 . Platelet adhesion (using platelet rich plasma) was inhibited on the He + ion implanted collagen with a fluence of 1 x 10 14 ions/cm 2 and was accelerated on the untreated collagen and ion implanted collagen with fluences of 1 x 10 13 , 1 x 10 15 and 1 x 10 16 ions/cm 2 . Platelet activation with washed platelets was observed on untreated collagen and He + ion implanted collagen with a fluence of 1 x 10 14 ions/cm 2 and was inhibited with fluences of 1 x 10 13 , 1 x 10 15 and 1 x 10 16 ions/cm 2 . Generally, platelets can react with a specific ligand inside the collagen (GFOGER sequence). The results of platelets adhesion experiments using washed platelets indicated that there were no ligands such as GFOGER on the He + ion implanted collagen over a fluence of 1 x 10 13 ions/cm 2 . On the 1 x 10 14 ions/cm 2 implanted collagen, no platelet activation was observed due to the influence of plasma proteins. >From the above, it is concluded that the decrease of adsorbed Fg and vWf caused the antithrombogenicity of He + ion implanted collagen with a fluence of 1 x 10 14 ions/cm 2 and that plasma protein adsorption took an important role repairing the graft surface

  15. Adsorption efficiencies of calcium (II ion and iron (II ion on activated carbon obtained from pericarp of rubber fruit

    Directory of Open Access Journals (Sweden)

    Orawan Sirichote

    2008-03-01

    Full Text Available Determination of adsorption efficiencies of activated carbon from pericarp of rubber fruit for calcium (II ion and iron (II ion has been performed by flowing the solutions of these ions through a column of activated carbon. The weights of activated carbon in 500 mL buret column (diameter 3.2 cm for flowing calcium (II ion and iron (II ion solutions were 15 g and 10 g, respectively. The initial concentration of calcium ion was prepared to be about eight times more diluted than the true concentration found in the groundwater from the lower part of southern Thailand. Calcium (II ion concentrations were analysed by EDTA titration and its initial concentration was found to be 23.55 ppm. With a flow rate of 26 mL/min, the adsorption efficiency was 11.4 % with passed through volume 4.75 L. Iron (II ion concentrations were analysed by spectrophotometric method; its initial concentration was found to be 1.5565 ppm. At a flow rate of 22 mL/min, the adsorption efficiency was 0.42 % with passed through volume of 34.0 L.

  16. Kinetic studies of uranyl ion adsorption on acrylonitrile (AN)/polyethylene glycol (PEG) interpenetrating networks (IPN)

    International Nuclear Information System (INIS)

    Aycik, G.A.; Gurellier, R.

    2004-01-01

    Full text: The kinetics of the adsorption of uranyl ions on amidoximated acrylonitrile (AN)/ polyethylene glycol (PEG) interpenetrating network (IPNs) from aqueous solutions was studied as a function of time and temperature. The IPNs were prepared by irradiation initiated gamma polymerisation using Co-60 gamma source. Adsorption capacities were performed for definite uranyl ion concentrations of 1x10 -2 M and at four different temperatures as 290K, 298K, 308K and 318K by gamma spectrometer. Adsorption time was increased from zero to 48 hours. The results indicate that adsorption capacity increases linearly with increasing temperature. Temperature and agitation hardly influence equilibrium and kinetics and decreasing of temperature results in a slightly greater time to reach equilibrium. The adsorption of uranyl ions has been studied in a multi step mechanism processes thus comparing chemical sorption and diffusion sorption processes. The experimental data was analysed using various kinetic models to determine the best-fit equation for the adsorption mechanisms. However, it was shown that all models, in general according to the reaction time and uranyl ion concentration in the solution, could describe the adsorption of uranyl ion onto amidoximated IPN, the adsorption kinetics was best described by zeroth order and intraparticle diffusion model whereas that of in increasing time by pseudo first and pseudo second order response respectively. External-intraparticle diffusion and zeroth order process in the IPN structure is proposed as a mass transfer mechanism and the results indicate a diffusion-controlled process. The Mean Activation Energy Of Uranyl Ions Adsorption Was Found As 4,1 Kj/Mole By Using Arrhenius Equation. The Rate Constant, The Equilibrium Adsorption Capacity And The Initial Adsorption Rate Were Calculated For All Models At Each Temperature. Kinetic Parameters Of All Models And The Normalized Standard Deviations Between The Measured And Predicted

  17. Mechanism of ion adsorption to aqueous interfaces: Graphene/water vs. air/water.

    Science.gov (United States)

    McCaffrey, Debra L; Nguyen, Son C; Cox, Stephen J; Weller, Horst; Alivisatos, A Paul; Geissler, Phillip L; Saykally, Richard J

    2017-12-19

    The adsorption of ions to aqueous interfaces is a phenomenon that profoundly influences vital processes in many areas of science, including biology, atmospheric chemistry, electrical energy storage, and water process engineering. Although classical electrostatics theory predicts that ions are repelled from water/hydrophobe (e.g., air/water) interfaces, both computer simulations and experiments have shown that chaotropic ions actually exhibit enhanced concentrations at the air/water interface. Although mechanistic pictures have been developed to explain this counterintuitive observation, their general applicability, particularly in the presence of material substrates, remains unclear. Here we investigate ion adsorption to the model interface formed by water and graphene. Deep UV second harmonic generation measurements of the SCN - ion, a prototypical chaotrope, determined a free energy of adsorption within error of that for air/water. Unlike for the air/water interface, wherein repartitioning of the solvent energy drives ion adsorption, our computer simulations reveal that direct ion/graphene interactions dominate the favorable enthalpy change. Moreover, the graphene sheets dampen capillary waves such that rotational anisotropy of the solute, if present, is the dominant entropy contribution, in contrast to the air/water interface.

  18. Thermal properties and surface reactivity in simulated body fluid of new strontium ion-containing phosphate glasses.

    Science.gov (United States)

    Massera, J; Petit, L; Cardinal, T; Videau, J J; Hupa, M; Hupa, L

    2013-06-01

    In this paper, we investigate the effect of SrO substitution for CaO in 50P₂O₅-10Na₂-(40-x)CaO-xSrO glass system (x from 0 to 40) on the thermal and structural properties and also on the glass reactivity in simulated body fluid (SBF) in order to find new glass candidates for biomedical glass fibers. The addition of SrO at the expense of CaO seems to restrain the leaching of phosphate ions in the solution limiting the reduction of the solution pH. We observed the formation of an apatite layer at the surface of the glasses when in contact with SBF. SrO and MgO were found in the apatite layer of the strontium ion-containing glasses, the concentration of which increases with an increase of SrO content. We think that it is the presence of MgO and SrO in the layer which limits the leaching of phosphate in the solution and thus the glass dissolution in SBF.

  19. Adsorption of heavy metal ions on molybdenum and molybdenum trioxide from dilute aqueous solution

    International Nuclear Information System (INIS)

    Utsunomiya, Taizo; Hoshino, Yoshio; Sakabe, Ken-ichi

    1984-01-01

    The adsorption of heavy metal ions such as Co(II), Cu(II) and Pb(II) on molybdenum powder has been investigated by the batch technique as a function of soaking time, concentration of heavy metal ions and coexisting salts, pH etc. Molybdenum trioxide was also used as an adsorbent for a comparison to discuss the adsorption mechanism. The amount of these heavy metal ions adsorbed was highly pH and coexisting salts dependent. These adsorbents have features of selective adsorption for Pb(II) and large adsorption rate. The adsorption of heavy metal ions on these adsorbents proceeds independently or concurrently by following complex mechanism; (1) cation exchange reaction by hydroxyl radical on the surface of Mo and MoO 3 is predominant for most of heavy metal ions except Pb(II) [Co(II), Mn(II), Fe(III), Ni(II), Zn(II), Cd(II) and Sr(II)], (2) reduction (electron exchange reaction) to low ionic or metallic state after cation exchange reaction [Cu(II) and Ag(I) on Mo] and (3) formation of a compound [Pb(II) on both Mo and MoO 3 ]. (author)

  20. Surface modification of glass beads with glutaraldehyde: Characterization and their adsorption property for metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Ozmen, Mustafa; Can, Keziban; Akin, Ilker; Arslan, Gulsin [Department of Chemistry, Selcuk University, 42031, Konya (Turkey); Tor, Ali, E-mail: ali.alitor@gmail.com [Department of Environmental Engineering, Selcuk University, Engineering Faculty, Campus, 42031, Konya (Turkey); Cengeloglu, Yunus; Ersoz, Mustafa [Department of Chemistry, Selcuk University, 42031, Konya (Turkey)

    2009-11-15

    In this study, a new material that adsorbs the metal ions was prepared by modification of the glass beads surfaces with glutaraldehyde. First, the glass beads were etched with 4 M NaOH solution. Then, they were reacted with 3-aminopropyl-triethoxysilane (APTES). Finally, silanized glass beads were treated with 25% of glutaraldehyde solution. The characterization studies by using Fourier Transform Infrared Spectroscopy (FT-IR), Thermal Gravimetric Analysis (TGA), elemental analysis and Scanning Electron Microscopy (SEM) indicated that modification of the glass bead surfaces was successfully performed. The adsorption studies exhibited that the modified glass beads could be efficiently used for the removal of the metal cations and anion (chromate ion) from aqueous solutions via chelation and ion-exchange mechanisms. For both Pb(II) and Cr(VI), selected as model ions, the adsorption equilibrium was achieved in 60 min and adsorption of both ions followed the second-order kinetic model. It was found that the sorption data was better represented by the Freundlich isotherm in comparison to the Langmuir and Redlich-Peterson isotherm models. The maximum adsorption capacities for Pb(II) and Cr(VI) were 9.947 and 11.571 mg/g, respectively. The regeneration studies also showed that modified glass beads could be re-used for the adsorption of Pb(II) and Cr(VI) from aqueous solutions over three cycles.

  1. Comparison or organic and inorganic ion exchange materials for removal of cesium and strontium from Hanford waste

    Energy Technology Data Exchange (ETDEWEB)

    Brown, G.N.; Carson, K.J.; DesChane, J.R.; Elovich, R.J. [Pacific Northwest National Lab., Richland, WA (United States)

    1997-10-01

    This work is part of an ESP-CP task to develop and evaluate high-capacity, selective, solid extractants for the uptake of cesium, strontium, and technetium (Cs, Sr, and Tc) from nuclear wastes. Pacific Northwest National Laboratory (PNNL) staff, in collaboration with researchers from industry, academia, and national laboratories are investigating these and other novel and commercial ion exchangers for use in nuclear waste remediation of groundwater, HLW, and LLW. Since FY 1995, experimental work at PNNL has focused on small-scale batch distribution (K{sub d}) testing of numerous solid sorbents with actual and simulated Hanford wastes, chemical and radiolytic stability of various organic ion exchanger resins, bench-scale column ion exchange testing in actual and simulated Complexant Concentrate (CC) and Neutralized Current Acid Waste (NCAW), and Tc and Sr removal from groundwater and LLW. In addition, PNNL has continued to support various site demonstrations at the Idaho National Engineering Laboratory, Savannah River Site, West Valley Nuclear Services, Hanford N-Springs, and Hanford N-Basin using technologies developed by their industrial partners. This summary will focus on batch distribution results from the actual waste tests. The data collected in these development and testing tasks provide a rational basis for the selection and direct comparison of various ion exchange materials in simulated and actual HLW, LLW, and groundwater. In addition, prediction of large-scale column loading performance for the materials tested is possible using smaller volumes of actual waste solution. The method maximizes information while minimizing experimental expense, time, and laboratory and process wastes.

  2. Enhanced Adsorption and Recovery of Uranyl Ions by NikR Mutant-Displaying Yeast

    Directory of Open Access Journals (Sweden)

    Kouichi Kuroda

    2014-04-01

    Full Text Available Uranium is one of the most important metal resources, and the technology for the recovery of uranyl ions (UO22+ from aqueous solutions is required to ensure a semi-permanent supply of uranium. The NikR protein is a Ni2+-dependent transcriptional repressor of the nickel-ion uptake system in Escherichia coli, but its mutant protein (NikRm is able to selectively bind uranyl ions in the interface of the two monomers. In this study, NikRm protein with ability to adsorb uranyl ions was displayed on the cell surface of Saccharomyces cerevisiae. To perform the binding of metal ions in the interface of the two monomers, two metal-binding domains (MBDs of NikRm were tandemly fused via linker peptides and displayed on the yeast cell surface by fusion with the cell wall-anchoring domain of yeast α-agglutinin. The NikRm-MBD-displaying yeast cells with particular linker lengths showed the enhanced adsorption of uranyl ions in comparison to the control strain. By treating cells with citrate buffer (pH 4.3, the uranyl ions adsorbed on the cell surface were recovered. Our results indicate that the adsorption system by yeast cells displaying tandemly fused MBDs of NikRm is effective for simple and concentrated recovery of uranyl ions, as well as adsorption of uranyl ions.

  3. Adsorption of Pb, Cd, Zn, Cu and Hg ions on Formaldehyde and ...

    African Journals Online (AJOL)

    Adsorption of Pb(II), Cd(II), Zn(II), Cu(II) and Hg(II) ions on formaldehyde and Pyridine modified bean husks were determined. The adsorption capacity of formaldehyde modified bean husks (mg/g) was: Pb2+, 5.01; Cd2+, 3.63; Zn2+, 2.18; Hg2+, 1.82; Cu2+, 1.58 and that of pyridine modified bean husk was: Hg2+, 6.92; Cd2+ ...

  4. Adsorption study on orange peel: Removal of Ni(II) ions from ...

    African Journals Online (AJOL)

    Yomi

    2012-01-16

    Jan 16, 2012 ... The optimal pH value for Ni(II) adsorption onto the orange peel was found to be 5.0. ... Various bio-sorbents have been examined for the removal of diverse type of ... modifications such as alkaline, acid, ethanol and acetone treatment (Pérez et .... To find a suitable pH for the effective adsorption of. Ni(II) ions ...

  5. Adsorption kinetics of ion of Pb2+ using Tricalcium Phosphate particles

    Science.gov (United States)

    Fadli, A.; Yenti, S. R.; Akbar, F.; Maihendra; Mawarni, F.

    2018-04-01

    One of the heavy metals that can pollute water is Pb2+. The concentration of ion Pb2+ can be removed using the adsorption method. The purpose of this research is to determine the adsorption kinetics model of ions Pb2+ using tricalcium phosphate (TCP) particles with variation of the temperature and adsorbent dosage. Five hundred mililiter Pb2+ solution with of 3 mg/L were added 0,5 gr, 1 gr and 1,5 gr of TCP in a glass beaker and stirred with rate of 300 rpm at a temperature of 30 °C, 40 °C and 50 °C. Pb2+ concentration in solution was analyzed by AAS (Atomic Adsorption Spectroscopy). The results showed that the rate of adsorption increased with the increasing of the temperature and adsorbent dosage. Minimum constant value of adsorption kinetic was 1,720 g/mg.min obtained at temperature of 30 °C and adsorbent dosageof 0,5 gr. The maximum value of adsorption kinetic constant was 9,755 g/mg.min obtained at temperature of 50 °C and adsorbent dosage of 1,5 gr. The appropriate model for adsorption kinetics followed the pseudo second order.

  6. Adsorption studies of phosphate ions on alginate- calcium ...

    African Journals Online (AJOL)

    user

    osmosis, electro dialysis, phytoremediation and phyto- extraction, ion-exchange .... occurred between functional groups of alginate and host material, that is, calcium .... metal ions using wheat based biosorbent; a review of the recent literature.

  7. Modification of porous starch for the adsorption of heavy metal ions from aqueous solution.

    Science.gov (United States)

    Ma, Xiaofei; Liu, Xueyuan; Anderson, Debbie P; Chang, Peter R

    2015-08-15

    Porous starch xanthate (PSX) and porous starch citrate (PSC) were prepared in anticipation of the attached xanthate and carboxylate groups respectively forming chelation and electrostatic interactions with heavy metal ions in the subsequent adsorption process. The lead(II) ion was selected as the model metal and its adsorption by PSX and PSC was characterized. The adsorption capacity was highly dependent on the carbon disulfide/starch and citric acid/starch mole ratios used during preparation. The adsorption behaviors of lead(II) ion on PSXs and PSCs fit both the pseudo-second-order kinetic model and the Langmuir isotherm model. The maximum adsorption capacity from the Langmuir isotherm equation reached 109.1 and 57.6 mg/g for PSX and PSC when preparation conditions were optimized, and the adsorption times were just 20 and 60 min, respectively. PSX and PSC may be used as effective adsorbents for removal of heavy metals from contaminated liquid. Crown Copyright © 2015. Published by Elsevier Ltd. All rights reserved.

  8. Preparation of chitosan/amine modified diatomite composites and adsorption properties of Hg(II) ions.

    Science.gov (United States)

    Fu, Yong; Huang, Yue; Hu, Jianshe; Zhang, Zhengjie

    2018-03-01

    A green functional adsorbent (CAD) was prepared by Schiff base reaction of chitosan and amino-modified diatomite. The morphology, structure and adsorption properties of the CAD were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy and Brunauer Emmett Teller measurements. The effect of pH value, contact time and temperature on the adsorption of Hg(II) ions for the CAD is discussed in detail. The experimental results showed that the CAD had a large specific surface area and multifunctional groups such as amino, hydroxyl and Schiff base. The optimum adsorption effect was obtained when the pH value, temperature and contact time were 4, 25 °C and 120 min, respectively, and the corresponding maximum adsorption capacity of Hg(II) ions reached 102 mg/g. Moreover, the adsorption behavior of Hg(II) ions for the CAD followed the pseudo-second-order kinetic model and Langmuir model. The negative ΔG 0 and ΔH 0 suggested that the adsorption was a spontaneous exothermic process.

  9. ADSORPSI POLUTAN ION DIKROMAT MENGGUNAKAN ZEOLIT ALAM TERMODIFIKASI AMINA (Adsorption of Dichromate Ions Pollutant Using Ammine Modified-Natural Zeolites

    Directory of Open Access Journals (Sweden)

    Eko Sri Kunarti

    2015-11-01

    24,66 kJ/mol. ABSTRACT Chromium (VI is a heavy metal pollutant that is harmful to health and the environment, therefore Cr(VI ions in aqueous solution removal is important to overcome the environmental pollution. Adsorption process is one of simple techniques that can be used to take metal ions. Adsorption study of dichromate ions as a wastewater model of Cr(VI has been conducted in this research by using ammine modified natural zeolite as adsorbents. The research was initiated by preparation of adsorbent of ammine-modified natural zeolites. The preparation was started by washing the natural zeolite (Z using distilled water and refluxing by 3M hydrochloric acid. Refluxed zeolites (ZA were modified by a quaternary ammonium salt, N-cethyl-N,N,N-trimethylammonium bromide (CTAB, and a primary amine, propylamine (PA. The natural zeolite (Z, acid activated zeolite (ZA and amine-modified zeolites were then applied for adsorption of dichromate ions. Characterization of zeolite samples was performed by infrared spectroscopy and X-ray diffraction methods to confirm the crystal structure, and atomic absorption spectroscopy method to analyze the adsorbed dichromate ions. Results showed that all zeolite samples contain clinoptilolite, mordernite and quartz minerals. The zeolite structure was not changed by heat and chemical treatments. Modification of zeolites enhanced the adsorption efficiency of natural zeolites. The dichromate ions were better adsorbed on ammine modified-zeolites compared to that of unmodified-zeolite with adsorption ability of CTAB modified zeolite (CTAB-Z was greater than that of propylammine modified zeolite (PA-Z. The adsorption of dichromate on zeolite samples was achieved in the order of CTAB-Z > PA-Z > ZA > Z, with the adsorption efficiency was about 1.96; 1.74; 0.90 and 0.48 mg/g, respectively. The dichromate ions adsorption by CTAB modified zeolite is chemical adsorption (chemisorption with the adsorption energy of 24.66 kJ/mol.

  10. Optimization of lead (ii) ions adsorption on to chemically activated ...

    African Journals Online (AJOL)

    The derivative thermal analysis (DTA) and thermogravimetric analysis (TGA) profile of the activated carbon were employed in the proximate analysis. The BET surface area shows a high microporous surface area and micropore volume of 840.38 m2/g and 0.30 cc/g respectively which aids sorption efficiency. The adsorption ...

  11. The adsorption kinetics of metal ions onto different microalgae and siliceous earth.

    Science.gov (United States)

    Schmitt, D; Müller, A; Csögör, Z; Frimmel, F H; Posten, C

    2001-03-01

    In the present work the adsorption kinetics of the six metal ions aluminum, zinc, mercury, lead, copper, and cadmium onto living microalgae were measured. The freshwater green microalga Scenedesmus subspicatus, the brackish water diatom Cyclotella cryptica, the seawater diatom Phaeodactylum tricornutum, and the seawater red alga Porphyridium purpureum were the subject of investigation. In most cases the adsorption rate of the metals could be well described by using the equation of the Langmuir adsorption rate expression. Inverse parameter estimation allowed the determination of the rate constants of the adsorption process and the maximum metal content of the algae. The highest values for the rate constant were obtained for Porphyridium purpureum followed by Phaeodactylum tricornutum. High values for the maximum content were obtained for Cyclotella cryptica and Scenedesmus subspicatus. The maximum rate constant was 24.21 h-1 for the adsorption of Hg to Porphyridium purpureum whereas the maximum metal content (0.243 g g-1) was obtained for Zn on Cyclotella cryptica. A comparison of these values with those obtained for the mineral siliceous earth exhibiting low maximum content and high adsorption rates reveals that the mechanism of adsorption onto the algae is a mixture of adsorption and accumulation.

  12. STRONTIUM PRECIPITATION

    Science.gov (United States)

    McKenzie, T.R.

    1960-09-13

    A process is given for improving the precipitation of strontium from an aqueous phosphoric-acid-containing solution with nickel or cobalt ferrocyanide by simultaneously precipitating strontium or calcium phosphate. This is accomplished by adding to the ferrocyanide-containing solution calcium or strontium nitrate in a quantity to yield a concentration of from 0.004 to 0.03 and adjusting the pH of the solution to a value of above 8.

  13. Nuclear quantum effects on adsorption of H2 and isotopologues on metal ions

    Science.gov (United States)

    Savchenko, Ievgeniia; Gu, Bing; Heine, Thomas; Jakowski, Jacek; Garashchuk, Sophya

    2017-02-01

    The nuclear quantum effects on the zero-point energy (ZPE), influencing adsorption of H2 and isotopologues on metal ions, are examined using normal mode analysis of ab initio electronic structure results for complexes with 17 metal cations. The lightest metallic nuclei, Li and Be, are found to be the most 'quantum'. The largest selectivity in adsorption is predicted for Cu, Ni and Co ions. Analysis of the nuclear wavepacket dynamics on the ground state electronic potential energy surfaces (PES) performed for complexes of Li+ and Cu+2 with H2/D2/HD shows that the PES anharmonicity changes the ZPE by up to 9%.

  14. Ion beam irradiation effects in strontium zirconium phosphate with NZP-structure type

    International Nuclear Information System (INIS)

    Gregg, Daniel J.; Karatchevtseva, Inna; Thorogood, Gordon J.; Davis, Joel; Bell, Benjamin D.C.; Jackson, Matthew; Dayal, Pranesh; Ionescu, Mihail; Triani, Gerry; Short, Ken; Lumpkin, Gregory R.; Vance, Eric R.

    2014-01-01

    Ceramics with the sodium zirconium phosphate or NZP type structure have potential as nuclear waste form and inert matrix materials. For both applications the material will be subjected to self-radiation damage from α-decay of the incorporated actinides. In this study, ion-beam irradiation using Au- and He-ions has been used to simulate the consequences of α-decay and the effects of irradiation on the structural and macroscopic properties (density and hardness) have been investigated. Irradiation by Au-ions resulted in a significant volume contraction of ∼7%, a reduction in hardness of ∼30% and a loss in long-range order at fluences above 10 14 Au-ions/cm 2 . In contrast, little effect on the material properties was noted for samples irradiated with He-ions up to a fluence of 10 17 ions/cm 2 . Thermal annealing was investigated for the highest fluence Au-ion irradiated sample and significant decomposition was observed

  15. Lithium ion adsorption and diffusion on black phosphorene nanotube: A first-principles study

    Energy Technology Data Exchange (ETDEWEB)

    Cao, Jin; Shi, Jing, E-mail: sjd865@jxnu.edu.cn; Hu, Yinquan; Wu, Musheng; Ouyang, Chuying; Xu, Bo

    2017-01-15

    Highlights: • Li ion storage performance of the single-walled black phosphorene nanotube was studied. • Li ion adsorption and diffusion on inside/outside wall of SWPNT was studied. • In-PNT system has higher adsorption energy and lower diffusion energy barrier. • 1-D tubular phosphorene improve Li storage performances as an anode material of LIBs. - Abstract: Li ion storage performance of the single-walled black phosphorene nanotube (PNT), which is considered as potential anode materials for high-performance Li-ion batteries (LIBs), is studied from first-principles calculations. The Li ion adsorption, diffusion and structural evolution of the one-dimensional armchair type PNT (aPNT) upon Li intercalation on the inside (in-PNT) and outside (out-PNT) surfaces were explored, comparing with that of the two-dimensional phosphorene (Psheet). A maximum Li storage capacity (at the intercalated state of Li{sub 22}P{sub 44}) is evaluated to be 432 mAh/g. It is also shown that the in-PNT system has higher adsorption energy and lower Li diffusion energy barrier compared with that of the Psheet and the out-PNT systems. The reason on why the better Li storage performance of the in-PNT is also studied from charge distribution and transfer analysis. These results suggest that PNT can be served as potential anode material for LIBs.

  16. Preparation of Amidoxime Polyacrylonitrile Chelating Nanofibers and Their Application for Adsorption of Metal Ions

    Directory of Open Access Journals (Sweden)

    You-Lo Hsieh

    2013-03-01

    Full Text Available Polyacrylonitrile (PAN nanofibers were prepared by electrospinning and they were modified with hydroxylamine to synthesize amidoxime polyacrylonitrile (AOPAN chelating nanofibers, which were applied to adsorb copper and iron ions. The conversion of the nitrile group in PAN was calculated by the gravimetric method. The structure and surface morphology of the AOPAN nanofiber were characterized by a Fourier transform infrared spectrometer (FT-IR and a scanning electron microscope (SEM, respectively. The adsorption abilities of Cu2+ and Fe3+ ions onto the AOPAN nanofiber mats were evaluated. FT-IR spectra showed nitrile groups in the PAN were partly converted into amidoxime groups. SEM examination demonstrated that there were no serious cracks or sign of degradation on the surface of the PAN nanofibers after chemical modification. The adsorption capacities of both copper and iron ions onto the AOPAN nanofiber mats were higher than those into the raw PAN nanofiber mats. The adsorption data of Cu2+ and Fe3+ ions fitted particularly well with the Langmuir isotherm. The maximal adsorption capacities of Cu2+ and Fe3+ ions were 215.18 and 221.37 mg/g, respectively.

  17. Lithium ion adsorption and diffusion on black phosphorene nanotube: A first-principles study

    International Nuclear Information System (INIS)

    Cao, Jin; Shi, Jing; Hu, Yinquan; Wu, Musheng; Ouyang, Chuying; Xu, Bo

    2017-01-01

    Highlights: • Li ion storage performance of the single-walled black phosphorene nanotube was studied. • Li ion adsorption and diffusion on inside/outside wall of SWPNT was studied. • In-PNT system has higher adsorption energy and lower diffusion energy barrier. • 1-D tubular phosphorene improve Li storage performances as an anode material of LIBs. - Abstract: Li ion storage performance of the single-walled black phosphorene nanotube (PNT), which is considered as potential anode materials for high-performance Li-ion batteries (LIBs), is studied from first-principles calculations. The Li ion adsorption, diffusion and structural evolution of the one-dimensional armchair type PNT (aPNT) upon Li intercalation on the inside (in-PNT) and outside (out-PNT) surfaces were explored, comparing with that of the two-dimensional phosphorene (Psheet). A maximum Li storage capacity (at the intercalated state of Li_2_2P_4_4) is evaluated to be 432 mAh/g. It is also shown that the in-PNT system has higher adsorption energy and lower Li diffusion energy barrier compared with that of the Psheet and the out-PNT systems. The reason on why the better Li storage performance of the in-PNT is also studied from charge distribution and transfer analysis. These results suggest that PNT can be served as potential anode material for LIBs.

  18. Adsorption behaviour and kinetics of exchange of Zn2+ and Eu3+ ions on a composite ion exchanger

    International Nuclear Information System (INIS)

    Morcos, T.N.

    2007-01-01

    Equilibria and kinetics of exchange of both Zn2+ and Eu3+ ions on a composite ion-exchanger, cobalt hexacyanocobaltate (III) (CoHCC) incorporated in polyacrylonitrile (PAN), has been studied. The apparent capacity of CoHCC-PAN for Zn2+ and Eu3+ was determined and found to be 0.353 and 0.69 meq/g, respectively. The higher capacity for Eu3+ ions than that for Zn2+ ions is due to the higher electrostatic interaction strength of the higher charge ion with the surface. Freundlich and Langmiur adsorption isotherms were used to investigate solute (Zn2+ or Eu3+) exchange phenomenon at the liquid/solid interface. The results indicated that both Langmuir and Freundlich isotherms fit well for both Zn2+ and Eu3+. Sorption data have been also treated with the Dubinin-Radushkevich equation. The kinetics of Zn2+ or Eu3+ sorption on the composite seems to show that the reaction was proceed via two steps. The first one was fast and probably due to adsorption followed by a slow exchange reaction. In view of the data obtained on the effect of particle size and metal ion concentrations on the rate of exchange reaction, it is concluded that the mechanism for both ions was chemical control. Generally, it seems that there are two exchange sites chemically equivalent but present in pores of different sizes which lead to different degrees of dehydration of the ions sorbed on the two sites

  19. The kinetics and thermodynamics of adsorption of heavy metal ions ...

    African Journals Online (AJOL)

    Titanium-Pillared and Un-Pillared bentonite clays were studied in order to evaluate the thermodynamics and kinetics of heavy metal ion removal from aqueous solutions. The results showed that the maximum sorption of Cu, Cd, Hg and Pb ions occurred within 30 minutes. A pseudo-second order kinetic model was used to ...

  20. Adsorption of fluoride ions onto naturally occurring earth materials ...

    African Journals Online (AJOL)

    Batch sorption system using two naturally occurring earth materials (EM) as adsorbents was investigated to remove fluoride ions from aqueous solution. The system variables studied include initial concentration of the sorbate, agitation time, adsorbent dose, pH, co-ions and temperature. The experimental data fitted well to ...

  1. A computational study of adsorption of divalent metal ions on graphene oxide

    Directory of Open Access Journals (Sweden)

    Somphob Thompho

    2017-12-01

    Full Text Available Adsorption of divalent metal ions (Pb2+,Cd2+, Zn2+,Cu2+ on graphene oxide (GO was studied using density functional theory (DFT. Adsorption geometries and energies, as well as the nature of the binding energy, were calculated for the interaction of divalent metal ions with oxygen-containing groups on the surface of GO. The configurations of the complexes were modeled by placing the divalent metal ions above the center and perpendicular to the surface. Binding of Cu2+ to the GO sheet was predicted to be much stronger than that for other divalent metal ions. Calculated results show good agreement with experimental observations and provide useful information for environmental pollution cleanup.

  2. Single and binary adsorption of Cd (Ⅱ) and Zn (Ⅱ) ions from aqueous solutions onto bottom ash

    Energy Technology Data Exchange (ETDEWEB)

    Sukpreabprom, Hatairat; Arqueropanyo, Orn-anong; Naksata, Wimol; Janhom, Sorapong [Chiang Mai University, Chiang Mai (Thailand); Sooksamiti, Ponlayuth [The Office of Primary Industries and Mines Region 3, Chiang Mai (Thailand)

    2015-05-15

    Bottom ash, a waste obtained from coal-burning power plant, was used as a low cost adsorbent for the removal of Cd (Ⅱ) and Zn (Ⅱ) ions from single and binary systems in batch experiments. The results of adsorption capacity showed that bottom ash could be considered as a potential adsorbent. The uptake of Zn (Ⅱ) ion was greater than that of Cd (Ⅱ) ion. For single adsorption, based on the correlation coefficient (R{sup 2}) values, both Langmuir and Freundlich isotherms suitably described the adsorption equilibrium data in the initial metal ion concentration range of 10-50 mg/L. The multicomponent isotherms, including the extended Langmuir and IAST-Freundlich isotherms, were used to predict the binary adsorption of Cd (Ⅱ) and Zn (Ⅱ) ions. Furthermore, the appropriate multicomponent isotherm was investigated by minimizing the average relative error (ARE) function. It should be confirmed that the extended Langmuir isotherm fitted the binary adsorption equilibrium data satisfactorily.

  3. Adsorption of cadmium (II) ions from aqueous solution by a new low-cost adsorbent-Bamboo charcoal

    Energy Technology Data Exchange (ETDEWEB)

    Wang Fayuan [State Key Joint Laboratory of Environment Simulation and Pollution Control, Department of Environmental Science and Engineering, Tsinghua University, Qinghuayuan, Haidian District, Beijing 100084 (China); Wang Hui, E-mail: wanghui@mail.tsinghua.edu.cn [State Key Joint Laboratory of Environment Simulation and Pollution Control, Department of Environmental Science and Engineering, Tsinghua University, Qinghuayuan, Haidian District, Beijing 100084 (China); Ma Jianwei [State Key Joint Laboratory of Environment Simulation and Pollution Control, Department of Environmental Science and Engineering, Tsinghua University, Qinghuayuan, Haidian District, Beijing 100084 (China)

    2010-05-15

    Batch adsorption experiments were conducted for the adsorption of Cd (II) ions from aqueous solution by bamboo charcoal. The results showed that the adsorption of Cd (II) ions was very fast initially and the equilibrium time was 6 h. High pH ({>=}8.0) was favorable for the adsorption and removal of Cd (II) ions. Higher initial Cd concentrations led to lower removal percentages but higher adsorption capacity. As the adsorbent dose increased, the removal of Cd increased, while the adsorption capacity decreased. Adsorption kinetics of Cd (II) ions onto bamboo charcoal could be best described by the pseudo-second-order model. The adsorption behavior of Cd (II) ions fitted Langmuir, Temkin and Freundlich isotherms well, but followed Langmuir isotherm most precisely, with a maximum adsorption capacity of 12.08 mg/g. EDS analysis confirmed that Cd (II) was adsorbed onto bamboo charcoal. This study demonstrated that bamboo charcoal could be used for the removal of Cd (II) ions in water treatment.

  4. Competitive Adsorption between Nanoparticles and Surface Active Ions for the Oil-Water Interface.

    Science.gov (United States)

    Hua, Xiaoqing; Bevan, Michael A; Frechette, Joelle

    2018-04-24

    Nanoparticles (NPs) can add functionality (e.g., catalytic, optical, rheological) to an oil-water interface. Adsorption of ∼10 nm NPs can be reversible; however, the mechanisms for adsorption and its effects on surface pressure remain poorly understood. Here we demonstrate how the competitive reversible adsorption of NPs and surfactants at fluid interfaces can lead to independent control of both the adsorbed amount and surface pressure. In contrast to prior work, both species investigated (NPs and surfactants) interact reversibly with the interface and without the surface active species binding to NPs. Independent measurements of the adsorption and surface pressure isotherms allow determination of the equation of state (EOS) of the interface under conditions where the NPs and surfactants are both in dynamic equilibrium with the bulk phase. The adsorption and surface pressure measurements are performed with gold NPs of two different sizes (5 and 10 nm), at two pH values, and across a wide concentration range of surfactant (tetrapentylammonium, TPeA + ) and NPs. We show that free surface active ions compete with NPs for the interface and give rise to larger surface pressures upon the adsorption of NPs. Through a competitive adsorption model, we decouple the contributions of NPs wetting at the interface and their surface activity on the measured surface pressure. We also demonstrate reversible control of adsorbed amount via changes in the surfactant concentration or the aqueous phase pH.

  5. Facile and green preparation of novel adsorption materials by combining sol-gel with ion imprinting technology for selective removal of Cu(II) ions from aqueous solution

    Science.gov (United States)

    Ren, Zhongqi; Zhu, Xinyan; Du, Jian; Kong, Delong; Wang, Nian; Wang, Zhuo; Wang, Qi; Liu, Wei; Li, Qunsheng; Zhou, Zhiyong

    2018-03-01

    A novel green adsorption polymer was prepared by ion imprinted technology in conjunction with sol-gel process under mild conditions for the selective removal of Cu(II) ions from aqueous solution. Effects of preparation conditions on adsorption performance of prepared polymers were studied. The ion-imprinted polymer was prepared using Cu(II) ion as template, N-[3-(2-aminoethylamino) propyl] trimethoxysilane (AAPTMS) as functional monomer and tetraethyl orthosilicate (TEOS) as cross-linker. Water was used as solvent in the whole preparation process. The imprinted and non-imprinted polymers were characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), atomic force microscope (AFM), Brunauer, Emmett and Teller (BET) and zeta potential. Three-dimensional network structure was formed and functional monomer was successfully cross-linked into the network structure of polymers. Effects of adsorption conditions on adsorption performance of prepared polymers were studied too. The pH value is of great influence on adsorption behavior. Adsorption by ion-imprinted polymer was fast (adsorption equilibrium was reached within 60 min). The adsorption capacity of Cu(II) ion-imprinted polymer was always larger than that of non-imprinted polymer. Pseudo-second-order kinetics model and Freundlich isotherm model fitted well with adsorption data. The maximum adsorption capacity of Cu(II) ion-imprinted polymer was 39.82 mg·g-1. However, the preparation conditions used in this work are much milder than those reported in literatures. The Cu(II) ion-imprinted polymer showed high selectivity and relative selectivity coefficients for Pb(II), Ni(II), Cd(II) and Co(II). In addition, the prepared ion-imprinted polymer could be reused several times without significant loss of adsorption capacity.

  6. Generation of Electricity at Graphene Interface Governed by Underlying Surface Dipole Induced Ion Adsorption

    Science.gov (United States)

    Yang, Shanshan; Su, Yudan; Wu, Qiong; Zhang, Yuanbo; Tian, Chuanshan

    Aqueous droplet moving along graphene surface can produce electricity This interesting phenomenon provided environment-friendly means to harvest energy from graphene interface in contact with sea wave or rain droplets. However, microscopically, the nature of charge adsorption at the graphene interface is still unclear. Here, utilizing sum-frequency spectroscopy in combined with measurement of electrical power generation, the origin of charge adsorption on graphene was investigated. It was found that the direct ion-graphene interaction is negligibly small, contrary to the early speculation, but the ordered surface dipole from the supporting substrate, such as PET, is responsible for ion adsorption at the interface. Graphene serves as a conductive layer with mild screening of Coulomb interaction when aqueous droplet slips over the surface. These results pave the way for optimization of energy harvesting efficiency of graphene-based device.

  7. Cooperative adsorption of critical metal ions using archaeal poly-γ-glutamate.

    Science.gov (United States)

    Hakumai, Yuichi; Oike, Shota; Shibata, Yuka; Ashiuchi, Makoto

    2016-06-01

    Antimony, beryllium, chromium, cobalt (Co), gallium (Ga), germanium, indium (In), lithium, niobium, tantalum, the platinoids, the rare-earth elements (including dysprosium, Dy), and tungsten are generally regarded to be critical (rare) metals, and the ions of some of these metals are stabilized in acidic solutions. We examined the adsorption capacities of three water-soluble functional polymers, namely archaeal poly-γ-glutamate (L-PGA), polyacrylate (PAC), and polyvinyl alcohol (PVA), for six valuable metal ions (Co(2+), Ni(2+), Mn(2+), Ga(3+), In(3+), and Dy(3+)). All three polymers showed apparently little or no capacity for divalent cations, whereas L-PGA and PAC showed the potential to adsorb trivalent cations, implying the beneficial valence-dependent selectivity of anionic polyelectrolytes with multiple carboxylates for metal ions. PVA did not adsorb metal ions, indicating that the crucial role played by carboxyl groups in the adsorption of crucial metal ions cannot be replaced by hydroxyl groups under the conditions. In addition, equilibrium studies using the non-ideal competitive adsorption model indicated that the potential for L-PGA to be used for the removal (or collection) of water-soluble critical metal ions (e.g., Ga(3+), In(3+), and Dy(3+)) was far superior to that of any other industrially-versatile PAC materials.

  8. Adsorption of Cu(II) and Cr(VI) ions by chitosan: kinetics and ...

    African Journals Online (AJOL)

    The ability of chitosan as an adsorbent for Cu (II) and Cr (VI) ions in aqueous solution was studied. The experiments were done as batch processes. Equilibrium studies were done on both cross-linked and non-cross-linked chitosan for both metals. Cr (VI) adsorption behaviour could be described using the Langmuir ...

  9. Adsorption study on orange peel: Removal of Ni(II) ions from ...

    African Journals Online (AJOL)

    orange peel was investigated to evaluate the effects of pH, initial nickel ion concentration and adsorbent dose on the removal of Ni(II) systematically. The optimal pH value for Ni(II) adsorption onto the orange peel was found to be 5.0. Greater ...

  10. A metal ion charged mixed matrix membrane for selective adsorption of hemoglobin

    NARCIS (Netherlands)

    Tetala, K.K.R.; Skrzypek, K.; Levisson, M.; Stamatialis, D.F.

    2013-01-01

    In this work, we developed a mixed matrix membrane by incorporating 20–40 µm size iminodiacetic acid modified immobeads within porous Ethylene vinyl alcohol (EVAL) polymer matrix. The MMM were charged with copper ions for selective adsorption of bovine hemoglobin in presence of bovine serum albumin.

  11. Ion Adsorption at the Rutile-Water Interface: Linking Molecular and Macroscopic Properties

    Czech Academy of Sciences Publication Activity Database

    Zhang, Z.; Fenter, P.; Cheng, L.; Sturchio, N. C.; Bedzyk, M. J.; Předota, Milan; Bandura, A.; Kubicki, J. D.; Lvov, S. N.; Cummings, P. T.; Chialvo, A. A.; Ridley, M. K.

    2004-01-01

    Roč. 20, č. 12 (2004), s. 4954-4969 ISSN 0743-7463 R&D Projects: GA ČR GP203/03/P083 Institutional research plan: CEZ:AV0Z4072921 Keywords : ion adsorption rutile Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.295, year: 2004

  12. Fabrication of interfacial functionalized porous polymer monolith and its adsorption properties of copper ions

    International Nuclear Information System (INIS)

    Han, Jiaxi; Du, Zhongjie; Zou, Wei; Li, Hangquan; Zhang, Chen

    2014-01-01

    Highlights: • Interface functionalized PGMA porous monolith was fabricated. • The adsorption capacity of Cu 2+ was 35.3 mg/g. • The effects of porous structure on the adsorption of Cu 2+ were studied. • The adsorption behaviors of porous monolith were studied. - Abstract: The interfacial functionalized poly (glycidyl methacrylate) (PGMA) porous monolith was fabricated and applied as a novel porous adsorbent for copper ions (Cu 2+ ). PGMA porous material with highly interconnected pore network was prepared by concentrated emulsion polymerization template. Then polyacrylic acid (PAA) was grafted onto the interface of the porous monolith by the reaction between the epoxy group on PGMA and a carboxyl group on PAA. Finally, the porous monolith was interfacial functionalized by rich amount of carboxyl groups and could adsorb copper ions effectively. The chemical structure and porous morphology of the porous monolith were measured by Fourier transform infrared spectroscopy and scanning electron microscopy. Moreover, the effects of pore size distribution, pH value, co-existing ions, contacting time, and initial concentrations of copper ions on the adsorption capacity of the porous adsorbents were studied

  13. Fabrication of interfacial functionalized porous polymer monolith and its adsorption properties of copper ions

    Energy Technology Data Exchange (ETDEWEB)

    Han, Jiaxi; Du, Zhongjie; Zou, Wei; Li, Hangquan; Zhang, Chen, E-mail: zhangch@mail.buct.edu.cn

    2014-07-15

    Highlights: • Interface functionalized PGMA porous monolith was fabricated. • The adsorption capacity of Cu{sup 2+} was 35.3 mg/g. • The effects of porous structure on the adsorption of Cu{sup 2+} were studied. • The adsorption behaviors of porous monolith were studied. - Abstract: The interfacial functionalized poly (glycidyl methacrylate) (PGMA) porous monolith was fabricated and applied as a novel porous adsorbent for copper ions (Cu{sup 2+}). PGMA porous material with highly interconnected pore network was prepared by concentrated emulsion polymerization template. Then polyacrylic acid (PAA) was grafted onto the interface of the porous monolith by the reaction between the epoxy group on PGMA and a carboxyl group on PAA. Finally, the porous monolith was interfacial functionalized by rich amount of carboxyl groups and could adsorb copper ions effectively. The chemical structure and porous morphology of the porous monolith were measured by Fourier transform infrared spectroscopy and scanning electron microscopy. Moreover, the effects of pore size distribution, pH value, co-existing ions, contacting time, and initial concentrations of copper ions on the adsorption capacity of the porous adsorbents were studied.

  14. Ion adsorption on oxides : surface charge formation and cadmium binding on rutile and hematite

    NARCIS (Netherlands)

    Fokkink, L.G.J.

    1987-01-01

    The adsorption of charge-determining (H +and OH -) and cadmium ions on rutile (TiO 2 ) and hematite (α-Fe

  15. Adsorption of Cu 2+ and Ni 2+ ions from their aqueous solutions ...

    African Journals Online (AJOL)

    The adsorption of Cu2+ and Ni2+ions at room temperature (27°C) onto two types of biomass produced from orange mesocarp namely: untreated orange mesocarp (Me) of 250 μm particle size and xanthated orange mesocarp (XMe) produced from Me of 250 μm particle size were studied. The results obtained showed that ...

  16. A metal ion charged mixed matrix membrane for selective adsorption of hemoglobin

    NARCIS (Netherlands)

    Tetala, K.K.R.; Skrzypek, Katarzyna; Levisson, M.; Stamatialis, Dimitrios

    2013-01-01

    In this work, we developed a mixed matrix membrane by incorporating 20–40 μm size iminodiacetic acid modified immobeads within porous Ethylene vinyl alcohol (EVAL) polymer matrix. The MMM were charged with copper ions for selective adsorption of bovine hemoglobin in presence of bovine serum albumin.

  17. Selective adsorption of ions in charged slit-systems

    Directory of Open Access Journals (Sweden)

    M.Valiskó

    2013-01-01

    Full Text Available We study the selective adsorption of various cations into a layered slit system using grand canonical Monte Carlo simulations. The slit system is formed by a series of negatively charged membranes. The electrolyte contains two kinds of cations with different sizes and valences modeled by charged hard spheres immersed in a continuum dielectric solvent. We present results for various cases depending on the combinations of the properties of the competing cations. We concentrate to the case when the divalent cations are larger than the monovalent cations. In this case, size and charge have counterbalancing effects, which results in interesting selectivity phenomena.

  18. Prediction of equilibrium parameters of adsorption of lead (II) ions onto diatomite

    Science.gov (United States)

    Salman, Taylan; Ardalı, Yüksel; Gamze Turan, N.

    2013-04-01

    Heavy metals from industrial wastewaters are one of the most important environmental issues to be solved today. Due to their toxicity and nonbiodegradable nature, heavy metals cause environmental and public health problems. Various techniques have been developed to remove heavy metals from aqueous solutions. These include chemical precipitation, reverse osmosis, ion Exchange and adsorption. Among them, adsorption is considered to be a particularly competitive and effective process for the removal of heavy metals from aqueous solutions. There is growing interest in using low cost, commercially available materials for the adsorption of heavy metals. Diatomite is a siliceous sedimentary rock having an amorphous form of silica (SiO2. nH2O) containing a small amount of microcrystalline material. It has unique combination of physical and chemical properties such as high porosity, high permeability, small particle size, large surface area, and low thermal conductivity. In addition, it is available in Turkey and in various locations around the world. Therefore, diatomite has been successfully used as adsorbent for the removal of heavy metals. The aim of the study is to investigate the adsorption properties of diatomite. The equilibrium adsorption data were applied to the Langmuir, Freundlich and Dubinin-Radushkevic (D-R) isotherm models. Adsorption experiments were performed under batch process, using Pb (II) initial concentration, pH of solution and contact time as variables. The results demonstrated that the adsorption of Pb (II) was strongly dependent on pH of solution. The effect of pH on adsorption of Pb(II) on diatomite was conducted by varying pH from 2 to 12 at 20 oC. In the pH range of 2.0-4.0, the adsorption percentage increases slightly as the pH increasing. At pH>4, the adsorption percentage decreases with increasing pH because hydrolysis product and the precipitation begin to play an important role in the sorption of Pb (II). At pH4, the maximum adsorption

  19. Adsorption performance of nickel and cadmium ions onto brewer's yeast

    Energy Technology Data Exchange (ETDEWEB)

    Cui, L.; Wu, G. [South-Central Univ. for Nationalities, Wuhan (China). College of Chemical and Materials Science, Key Laboratory of Catalysts and Materials Science of Hubei Province; Jeong, T. [Chonbuk National Univ., Chonbuk (Korea, Republic of). Dept. of Environmental Engineering

    2010-02-15

    Heavy metals must be removed from polluted water streams in order to meet increasingly stringent environmental quality standards. Although various techniques have been used to recover metal ions from wastewater, they are either ineffective when heavy metals are present at low concentrations. In this study, brewer's yeast was used as an adsorbent for the removal of Ni(2) and Cd(2) metal ions from aqueous solution. The surface of the brewer's yeast had 3 main functional groups of sulfonate, carboxyl, and amine groups. The pH of solution played a key role on the uptake of metal ions. Optimum adsorption was obtained at pH 6. An acid solution with a pH of 3 was efficient for the desorption of Ni(2) and Cd(2) ions from loaded brewer's yeast. The desorption efficiency was greater than 90 per cent. The rate of metal ions adsorption onto brewer's yeast was rapid with short contact time. The kinetics of the adsorption process followed the pseudo-second-order kinetic model. Langmuir and Freundlich isotherm models were used to fit the experimental data. The Langmuir isotherm model provided a better fit. The maximum uptakes of Ni(2) and Cd(2) by brewer's yeast were estimated to be 5.34 and 10.17 mg/g, respectively. Electrostatic interaction was found to be the main mechanism of metal ions adsorption on the brewer's yeast. It was concluded that brewer's yeast is a promising adsorbent for the removal of metal ions from wastewater. 21 refs., 3 tabs., 6 figs.

  20. Isolation of radioactive strontium from natural samples. Separation of strontium from alkaline and alkaline earth elements by means of mixed solvent anion exchange

    International Nuclear Information System (INIS)

    Grahek, Z.; Kosutic, K.; Lulic, S.; Kvastek, K.; Eskinja, I.

    1999-01-01

    This paper presents the results of studies which led to the procedures for the chromatographic separation of radioactive strontium from alkaline, earth-alkaline and other elements in natural samples, on columns filled with strong base anion exchangers using alcoholic solutions of nitric acid as eluents. It has been shown that potassium, caesium, calcium, barium, yttrium and strontium can be adsorbed on strong base anion exchangers of the Dowex and Amberlite type, which contain the quaternary ammonium group with nitrate as counter-ion, from solutions of nitric acid in alcohol. Adsorption strength increases in the order methanol 3 in methanol, while they are adsorbed from ethanol and propanol. The adsorption strength is influenced by the polarity of alcohol, by the concentration of nitrate and by pH. The strength with which strontium adsorbs on the exchangers increases in the interval from 0 to 0.25M NH 4 NO 3 in methanol, after which it starts to decrease. Strontium adsorbs to the exchangers from the alcoholic solution of ammonium nitrate twice as strongly as from the alcoholic solution of nitric acid, while a fraction of water in pure alcohol exceeding 10% prevents adsorption. In the mixture of alcohol and nitric acid, the adsorption strength for calcium and strontium increases with the increase of the volume fraction of alcohol with a lower dielectric constant. The rate and strength of adsorption of ions on the exchanger also increase in the series 0.25M HNO 3 in methanol 3 in ethanol 3 in 1-propanol for each individual ion, as well as in the Ca 3 in methanol, 0.25M HNO 3 in ethanol and 0.25M HNO 3 in propanol. Separation is also possible from alcohol mixtures. Strontium separation is most difficult from calcium, while the efficiency of separation increases with a decrease of the polarity of the used alcohol or alcohol mixture. The first group elements of the periodic table are not separated from each other in this way, while the elements of the second group are

  1. Adsorption of manganese(II) ions by EDTA-treated activated carbons

    Energy Technology Data Exchange (ETDEWEB)

    Khan, A.Y.; Mazyck, D.W. [Jones Edmunds & Associates, Gainesville, FL (United States)

    2009-07-01

    The adsorption of manganese(II) ions from aqueous solution onto three different granular activated carbons treated with ethylenediamine tetraacetic acid (EDTA) and its sodium salt was investigated. Characterization of the chelate-treated carbons showed that EDTA altered the physical and chemical properties of the sorbents relative to their untreated counterparts. Furthermore, the modified sorbents exhibited a heightened capacity towards the adsorption of Mn(II) ions from aqueous media. Manganese(II) ion removal increased from 0 to 6.5 mg/g for the lignite coal-based sorbent, from 3.5 to 14.7 mg/g for the wood-based sorbent and from 1.3 to 7.9 mg/g for the bituminous coal-based sorbent. The increased removal is attributed, in part, to the creation of Lewis base sites that participate in covalent interactions and hydrolysis reactions.

  2. Superior lithium adsorption and required magnetic separation behavior of iron-doped lithium ion-sieves

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Shulei; Zheng, Shili; Wang, Zheming; Cui, Wenwen; Zhang, Hailin; Yang, Liangrong; Zhang, Yi; Li, Ping

    2018-01-01

    The recent research on adsorption-based lithium recovery from lithium-containing solutions has been centred on adsorption capacity and separation of lithium ion-sieves powder from solutions. Herein, an effective iron-doped lithium titanium oxide (Fe-doped Li2TiO3) was synthesized by Fe-doping via solid state reactions followed by acid treatment to form iron-doped lithium ion-sieves (Fe/Ti-x(H)). The resulting solid powder displays both superior adsorption capacity of lithium and high separation efficiency of the adsorbent from the solutions. SEM imaging and BET surface area measurement results showed that at Fe doping levels x0.15, Fe-doping led to grain shrinkage as compared to Li2TiO3 and at the same time the BET surface area increased. The Fe/Ti-0.15(H) exhibited saturated magnetization values of 13.76 emu g-1, allowing effective separation of the material from solid suspensions through the use of a magnet. Consecutive magnetic separation results suggested that the Fe/Ti-0.15(H) powders could be applied at large-scale and continuously removed from LiOH solutions with separation efficiency of 96% or better. Lithium adsorption studies indicated that the equilibrium adsorption capacity of Fe/Ti-0.15(H) in LiOH 2 solutions (1.8 g L-1 Li, pH 12) reached 53.3 mg g-1 within 24 h, which was higher than that of pristine Li2TiO3 (50.5 mg g-1) without Fe doping. Competitive adsorption and regeneration results indicated that the Fe/Ti-0.15(H) possessed a high selectivity for Li with facile regeneration. Therefore, it could be expected that the iron-doped lithium ion-sieves have practical applicability potential for large scale lithium extraction and recovery from lithium-bearing solutions.

  3. Kinetics of chloride ion adsorption on stainless alloys by in situ contact electric resistance technique

    International Nuclear Information System (INIS)

    Marichev, V.A.

    2008-01-01

    As the primary reason for pitting of stainless alloys, chloride adsorption is not adequately studied, e.g. kinetic investigations of chloride adsorption are actually absent. We discuss and partly reconsider some well-known facts (e.g. halides order: Cl - > Br - > I - ), disputed points (chloride penetration in passive film), and still unknown aspects of chloride adsorption. For the first time, we report kinetic studies of chloride adsorption on stainless alloys by in situ contact electric resistance technique. The peak-like character of kinetic curves has been found for all studied stainless alloys, but not for pure iron and nickel. This has been considered as a sequence of the substantial charge transfer during chloride adsorption. Opposite to typical d metals, stainless materials are alloys of early and late transition metals having unfilled d-bands with increased number of d-electron vacancies. Such electronic structure is favorable for adsorption of electron donating adsorbates like halide ions. Experimental data of this work are more compatible with possibility of chloride penetration into the passive films on stainless alloys that also might involve a transformation of primary oxy-hydroxide films into oxy-chloride films

  4. Biomimetic magnesium–carbonate-apatite nanocrystals endowed with strontium ions as anti-osteoporotic trigger

    Energy Technology Data Exchange (ETDEWEB)

    Iafisco, Michele, E-mail: michele.iafisco@istec.cnr.it; Ruffini, Andrea; Adamiano, Alessio; Sprio, Simone; Tampieri, Anna

    2014-02-01

    The present work investigates the preparation of biomimetic nanocrystalline apatites co-substituted with Mg, CO{sub 3} and Sr to be used as starting materials for the development of nanostructured bio-devices for regeneration of osteoporotic bone. Biological-like amounts of Mg and CO{sub 3} ions were inserted in the apatite structure to mimic the composition of bone apatite, whereas the addition of increasing quantities of Sr ions, from 0 up to 12 wt.%, as anti-osteoporotic agent, was evaluated. The chemical–physical features, the morphology, the degradation rates, the ion release kinetics as well as the in vitro bioactivity of the as-prepared apatites were fully evaluated. The results indicated that the incorporation of 12 wt.% of Sr can be viewed as a threshold for the structural stability of Mg–CO{sub 3}-apatite. Indeed, incorporation of lower quantity of Sr did not induce considerable variations in the chemical structure of Mg–CO{sub 3}-apatite, while when the Sr doping extent reached 12 wt.%, a dramatically destabilizing effect was detected on the crystal structure thus yielding alteration of the symmetry and distortion of the PO{sub 4}. As a consequence, this apatite exhibited the fastest degradation kinetic and the highest amount of Sr ions released when tested in physiological conditions. In this respect, the surface crystallization of new calcium phosphate phase when immersed in physiological-like solution occurred by different mechanisms and extents due to the different structural chemistry of the variously doped apatites. Nevertheless, all the apatites synthesized in this work exhibited in vitro bioactivity demonstrating their potential use to develop biomedical devices with anti-osteoporotic functionality. - Highlights: • Biomimetic nanocrystalline apatites co-substituted with Mg, CO{sub 3} and Sr were prepared. • Biological-like amounts of Mg and CO{sub 3} were inserted to mimic the composition of bone apatite. • The addition of increasing

  5. Biomimetic magnesium–carbonate-apatite nanocrystals endowed with strontium ions as anti-osteoporotic trigger

    International Nuclear Information System (INIS)

    Iafisco, Michele; Ruffini, Andrea; Adamiano, Alessio; Sprio, Simone; Tampieri, Anna

    2014-01-01

    The present work investigates the preparation of biomimetic nanocrystalline apatites co-substituted with Mg, CO 3 and Sr to be used as starting materials for the development of nanostructured bio-devices for regeneration of osteoporotic bone. Biological-like amounts of Mg and CO 3 ions were inserted in the apatite structure to mimic the composition of bone apatite, whereas the addition of increasing quantities of Sr ions, from 0 up to 12 wt.%, as anti-osteoporotic agent, was evaluated. The chemical–physical features, the morphology, the degradation rates, the ion release kinetics as well as the in vitro bioactivity of the as-prepared apatites were fully evaluated. The results indicated that the incorporation of 12 wt.% of Sr can be viewed as a threshold for the structural stability of Mg–CO 3 -apatite. Indeed, incorporation of lower quantity of Sr did not induce considerable variations in the chemical structure of Mg–CO 3 -apatite, while when the Sr doping extent reached 12 wt.%, a dramatically destabilizing effect was detected on the crystal structure thus yielding alteration of the symmetry and distortion of the PO 4 . As a consequence, this apatite exhibited the fastest degradation kinetic and the highest amount of Sr ions released when tested in physiological conditions. In this respect, the surface crystallization of new calcium phosphate phase when immersed in physiological-like solution occurred by different mechanisms and extents due to the different structural chemistry of the variously doped apatites. Nevertheless, all the apatites synthesized in this work exhibited in vitro bioactivity demonstrating their potential use to develop biomedical devices with anti-osteoporotic functionality. - Highlights: • Biomimetic nanocrystalline apatites co-substituted with Mg, CO 3 and Sr were prepared. • Biological-like amounts of Mg and CO 3 were inserted to mimic the composition of bone apatite. • The addition of increasing quantities of Sr (from 0 to 12

  6. FTIR study of carbon monoxide adsorption on ion-exchanged X, Y and mordenite type zeolites

    Directory of Open Access Journals (Sweden)

    R. HERCIGONJA

    2003-05-01

    Full Text Available In this work Fourier transform infrared (FTIR study has been applied to study the adsorption of carbon monoxide on transition metal (Mn+, Co2+, Ni2+ ion-exchanged zeolites type Y, X and mordenites. The adsorption of CO at room temperature produces overlapping IR absorption bands in the 2120–2200 cm-1 region. The frequency of the band around 2200 cm-1 is found to be dependent not only on the charge-balancing transition metal cation, but also on the framework composition. The frequencies of the band near 1600 cm-1 was found to be dependent on the Si/Al ratio of the investigated zeolites.

  7. Impact of a commercial glyphosate formulation on adsorption of Cd(II) and Pb(II) ions on paddy soil.

    Science.gov (United States)

    Divisekara, T; Navaratne, A N; Abeysekara, A S K

    2018-05-01

    Use of glyphosate as a weedicide on rice cultivation has been a controversial issue in Sri Lanka, due to the hypothesis that the metal complexes of commercial glyphosate is one of the causative factors of Chronic Kidney Disease of unknown aetiology (CKDu) prevalent in some parts of Sri Lanka. The effect of commercial glyphosate on the adsorption and desorption of Cd(II) and Pb(II) ions on selective paddy soil studied using batch experiments, over a wide concentration range, indicates that the Langmuir adsorption isotherm model is obeyed at low initial metal ion concentrations while the Freundlich adsorption isotherm model obeys at high metal ion concentrations in the presence and absence of glyphosate. For all cases, adsorption of both Cd(II) and Pb(II) ions obeys pseudo second order kinetics, suggesting that initial adsorption is a chemisorption process. In the presence of glyphosate formulation, the extent of adsorption of Cd(II) and Pb(II) ions on soil is decreased, while their desorption is increased at high concentrations of glyphosate. Low concentrations of glyphosate formulation do not significantly affect the desorption of metal ions from soil. Reduction of adsorption leads to enhance the concentration of Cd(II) and Pb(II) ions in the aqueous phase when in contact with soil. Copyright © 2018 Elsevier Ltd. All rights reserved.

  8. Calorimetric approach of ions adsorption; Approche calorimetrique de l'absorption d'ions

    Energy Technology Data Exchange (ETDEWEB)

    Lantenois, S. [Montpellier-2 Univ., 34 (France)

    2006-07-01

    The aim of this work is to obtain experimentally thermodynamic data of ions adsorption by micro-calorimetry. Different thermal effects can be measured on different silicon oxides (Spherosil or SBA-15) and with different cations (Cd{sup 2+} and Pb{sup 2+}). The solids are studied in the same experimental conditions in a NaNO{sub 3} solution (10{sup -1} M) at pH of 5 or 7 (adjusted by addition of NaOH or HNO{sub 3}) in terms of the hydrolysis pH of the adsorbed cation. The aqueous solution is a NaNO{sub 3} (10{sup -1} M) solution containing Cd(NO{sub 3}){sub 2} (pH 7.0) or Pb(NO{sub 3}){sub 2} (pH 5.0) at different concentrations (between 5*10{sup -4} and 10{sup -2} M). The thermal effect due to the addition of this solution is measured by titration calorimetry and by flux calorimetry. The complementarity of these two techniques is developed during this study where the titration calorimetry has been used for studying the thermal effects at low concentrations in metallic cations. The flux calorimetry has allowed to analyze systems at stronger concentration in metallic cations and to study the desorption of these cations. This study shows that the thermal effect bound to the surfaces reactivity is composed of a combination of factors. Factors such as surface charges density (pH and protonation deprotonation reactions), the samples preparation (previous calcination) or the capacity of cations to hydrolyze can be revealed by micro-calorimetry. (O.M.)

  9. Near-infrared quantum cutting in Yb3+ ion doped strontium vanadate

    Science.gov (United States)

    Sawala, N. S.; Bajaj, N. S.; Omanwar, S. K.

    2016-05-01

    The materials Sr3-x(VO4)2:xYb were successfully synthesized by co-precipitation method varying the concentration of Yb3+ ions from 0 to 0.06 mol. It was characterize by powder X-ray powder diffraction (XRD) and surface morphology was studied by scanning electronic microscope (SEM). The photoluminescence (PL) properties were studied by spectrophotometers in near infra red (NIR) and ultra violet visible (UV-VIS) region. The Yb3+ ion doped tristrontium vanadate (Sr3(VO4)2) phosphors that can convert a photon of UV region (349 nm) into photons of NIR region (978, 996 and 1026 nm). Hence this phosphor could be used as a quantum cutting (QC) luminescent convertor in front of crystalline silicon solar cell (c-Si) panels to reduce thermalization loss due to spectral mismatch of the solar cells. The theoretical value of quantum efficiency (QE) was calculated from steady time decay measurement and the maximum efficiency approached up to 144.43%. The Sr(3-x) (VO4)2:xYb can be potentiality used for betterment of photovoltaic (PV) technology.

  10. 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

  11. Modeling strontium-cesium-calcium-magnesium-sodium ion exchange equilibria on chabazite with the Wilson equation

    International Nuclear Information System (INIS)

    Perona, J.J.

    1992-01-01

    Chabazite zeolites are used at ORNL for decontamination of wastewaters containing 90 Sr and 137 Cs. Treatability studies have shown that chabazite can remove trace amounts of these nuclides from wastewaters containing much higher concentrations of calcium and magnesium. The design of ion exchange columns for multicomponent systems requires a method for predicting multicomponent equilibria from binary or ternary experiments, since the number of experiments required for an empirical equilibrium model is generally not feasible. Binary interaction parameters for the Wilson equation were used to predict solid-phase activity coefficients for the five-component system, and the sum of squares of deviations between experimental and predicted solution concentrations for the data points available was calculated. The average deviation per data point for the five-component system was about the same as for the calcium-magnesium-sodium ternary system

  12. Chloride Ion Adsorption Capacity of Anion Exchange Resin in Cement Mortar

    Directory of Open Access Journals (Sweden)

    Yunsu Lee

    2018-04-01

    Full Text Available This paper presents the effect of anion exchange resin (AER on the adsorption of chloride ions in cement mortar. The kinetic and equilibrium behaviors of AER were investigated in distilled water and Ca(OH2 saturated solutions, and then the adsorption of chloride ions by the AER in the mortar specimen was determined. The AER was used as a partial replacement for sand in the mortar specimen. The mortar specimen was coated with epoxy, except for an exposed surface, and then immersed in a NaCl solution for 140 days. The chloride content in the mortar specimen was characterized by energy dispersive X-ray fluorescence analysis and electron probe microanalysis. The results showed that the AER could adsorb the chloride ions from the solution rapidly but had a relatively low performance when the pH of its surrounding environment increased. When the AER was mixed in the cement mortar, its chloride content was higher than that of the cement matrix around it, which confirms the chloride ion adsorption capacity of the AER.

  13. Adsorption

    Directory of Open Access Journals (Sweden)

    Sushmita Banerjee

    2017-05-01

    Full Text Available Application of saw dust for the removal of an anionic dye, tartrazine, from aqueous solutions has been investigated. The experiments were carried out in batch mode. Effect of the parameters such as pH, initial dye concentration and temperature on the removal of the dye was studied. Equilibrium was achieved in 70 min. Maximum adsorption of dye was achieved at pH 3. Removal percent was found to be dependent on the initial concentration of dye solution, and maximum removal was found to be 97% at 1 mg/L of tartrazine. The removal increases from 71% to 97% when the initial concentration of dye solution decreases from 15 mg/L to 1 mg/L. The equilibrium adsorption data were analyzed by Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherm models. The (Langmuir adsorption capacity of the adsorbent is found to be 4.71 mg/g at 318 K. Kinetic modeling of the process of removal was carried out and the process of removal was found to follow a pseudo second order model and the value of rate constant for adsorption process was calculated as 2.7 × 10−3 g mg−1 min−1 at 318 K. The thermodynamic parameters such as change in free energy (ΔG°, enthalpy (ΔH° and entropy (ΔS° were determined and the negative values of ΔG° indicated that the process of removal was spontaneous at all values of temperatures. Further, the values of ΔH° indicated the endothermic nature of the process of removal.

  14. Adsorption of heavy metals ions on portulaca oleracea plants

    International Nuclear Information System (INIS)

    Naqvi, R.R.

    2005-01-01

    The aim of this study is to report the ability of portulaca oleracea (Fershi in Urdu) biomass grown in uncontaminated soils to adsorb or uptake lead, cadmium, arsenic, cobalt and copper from aqueous solutions. In order to help understand the metal binding mechanism, laboratory experiments performance to determine optimal binding, and binding capacity for each of the above mentioned metals. These experiments were carried out for the mass of crushed portulaca stems. Portulaca is a plant that grows abundantly in temperature climate in the area of Quetta Balochistan. It has reddish stem and thick succulent leaves. This plant has been found to be good adsorbent for heavy metals ions. (author)

  15. Thermal change and ion exchange properties of zeolite L with cesium and strontium

    International Nuclear Information System (INIS)

    Mimura, Hitoshi; Akiba, Kenichi

    1986-01-01

    Thermal change and ion exchange properties of Cs and Sr have been studied for zeolite L. The zeolite structure is stable below 900 deg C and converts to the amorphous phase above 1000 deg C. The cesium form of zeolite L recrystallized to pollucite (CsAlSi 2 O 6 ) by calcination at 1400 deg C for 1 h or under hydrothermal condition (300 deg C, 290 atm, 24 h). Hydrogen-form zeolites were prepared by the acid treatment in 10 -2 ∼ 10 -1 M HNO 3 solutions or thermal decomposition of NH 4 form zeolites at 460 ∼ 500 deg C. The distribution of Cs and Sr was dependent on equilibrium pH and the distribution coefficient (K d ) was about 10 4 (ml/g) at pH 5 ∼ 7. The exchange capacity of Cs and Sr was 0.89 (meq./g zeolite) and exchanging ratio was 68 % at D sites in main channel. These cations in zeolite were completely eluted with 10 -1 M HNO 3 solution. (author)

  16. Sorptive removal of cesium-137 and strontium-90 from water by unconventional sorbents. 2. Usage of coal fly ash

    International Nuclear Information System (INIS)

    Apak, R.; Atun, G.; Gueclue, K.; Tuetem, E.

    1996-01-01

    It has been shown that coal fly ash is a good adsorbent for both radionuclides of 137 Cs and 90 Sr. Radiocesium adsorption is maximal around the neutral region whereas radiostrontium adsorption increases with pH, especially above pH 8. Cesium retention sharply drops with ionic strength while strontium adsorption increases sharply and steadily at low and moderate concentrations of the inert electrolyte, respectively. The suggested mechanisms of radionuclide retention by fly ash is specific adsorption of Cs + and irreversible ion-exchange uptake of Sr 2+ . The isotherm of adsorption is a Langmuir approximation of the B.E.T. multi-layered sorption. Acid pretreatment of fly ash, though not increasing radionuclide sorption capacity, may be useful in preventing the leach-out of other contaminants from the sorbent into water during the adsorption process. (author)

  17. Sorptive removal of cesium-137 and strontium-90 from water by unconventional sorbents. 2. Usage of coal fly ash

    Energy Technology Data Exchange (ETDEWEB)

    Apak, R.; Atun, G.; Gueclue, K.; Tuetem, E. [Istanbul Univ. (Turkey). Faculty of Engineering

    1996-05-01

    It has been shown that coal fly ash is a good adsorbent for both radionuclides of {sup 137}Cs and {sup 90}Sr. Radiocesium adsorption is maximal around the neutral region whereas radiostrontium adsorption increases with pH, especially above pH 8. Cesium retention sharply drops with ionic strength while strontium adsorption increases sharply and steadily at low and moderate concentrations of the inert electrolyte, respectively. The suggested mechanisms of radionuclide retention by fly ash is specific adsorption of Cs{sup +} and irreversible ion-exchange uptake of Sr{sup 2+}. The isotherm of adsorption is a Langmuir approximation of the B.E.T. multi-layered sorption. Acid pretreatment of fly ash, though not increasing radionuclide sorption capacity, may be useful in preventing the leach-out of other contaminants from the sorbent into water during the adsorption process. (author).

  18. Studies of equilibrium and kinetics of adsorption of cesium ions by graphene oxide

    International Nuclear Information System (INIS)

    Oliveira, Fernando M.; Bueno, Vanessa N.; Oshiro, Maurício T.; Potiens Junior, Ademar J.; Hiromoto, Goro; Sakata, Solange K.; Rodrigues, Debora F.

    2017-01-01

    Cesium is one of the fission products of major radiological concern, it is often found in nuclear radioactive waste generated at nuclear power plants. Graphene Oxide (GO) has attracted great attention due to its functionalized surface, which includes hydroxyl, epoxy, carbonyl and carboxyl groups, with great capacity of complexation with metal ions and can be used as adsorbent to remove cations from aqueous solutions. In this work, a treatment of radioactive waste containing 137 Cs was studied. For the batch experiments of Cs + removal, 133 Cs concentrations remained after the adsorption were determined by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) and the results obtained were analyzed according to the Langmuir and Freundlich isotherms models. The kinetics of adsorption and Gibbs free energy were also determined. The Langmuir model was the best fit and defined a favorable adsorption. The cesium adsorption process is the pseudo-second model and the Gibbs free energy calculation indicated that the adsorption process is spontaneous. (author)

  19. Preparation and adsorption properties of nano magnetite chitosan films for heavy metal ions from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Lasheen, M.R., E-mail: ragaei24@link.net [Water Pollution Research Department, Environmental Research Division, National Research Centre, 33-El Buhoth St., Dokki, Cairo, 12311 (Egypt); El-Sherif, Iman Y., E-mail: iman57us@yahoo.com [Water Pollution Research Department, Environmental Research Division, National Research Centre, 33-El Buhoth St., Dokki, Cairo, 12311 (Egypt); Tawfik, Magda E., E-mail: magdaemileta@yahoo.com [Polymers and Pigments Department, National Research Centre, 33-El Buhoth St., Dokki, Cairo, 12311 (Egypt); El-Wakeel, S.T., E-mail: shaimaa_tw@yahoo.com [Water Pollution Research Department, Environmental Research Division, National Research Centre, 33-El Buhoth St., Dokki, Cairo, 12311 (Egypt); El-Shahat, M.F., E-mail: elshahatmf@hotmail.com [Faculty of Science, Ain Shams University, Khalifa El-Maamon St., Abbasiya Sq., 11566, Cairo (Egypt)

    2016-08-15

    Highlights: • Nano magnetite–chitosan films were prepared by casting method. • The efficiency of the prepared films for removing heavy metals was investigated. • The adsorption mechanism was studied using different isotherm and kinetic models. • Films reuse and metals recovery were studied. - Abstract: Nano magnetite chitosan (NMag–CS) film was prepared and characterized with different analytical methods. X-ray diffraction (XRD) patterns confirmed the formation of a pure magnetite structure and NMag–CS nanocomposite. TEM image of the film, revealed the uniform dispersion of magnetite nanoparticles inside chitosan matrix. The adsorption properties of the prepared film for copper, lead, cadmium, chromium and nickel metal ions were evaluated. Different factors affecting the uptake behavior by the composite films such as time, initial pH and film dose were investigated. The adsorption equilibrium attained using 2 g/L of the film after 120 min of reaction. The equilibrium data were analyzed using Langmuir and Freundlich models. The adsorption kinetics followed the mechanism of the pseudo-second-order equation for all metals. The metals regenerated from films with an efficiency greater than 95% using 0.1 M ethylene diamine tetra acetic acid (EDTA) and films were successfully reused for adsorption.

  20. Studies of equilibrium and kinetics of adsorption of cesium ions by graphene oxide

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Fernando M.; Bueno, Vanessa N.; Oshiro, Maurício T.; Potiens Junior, Ademar J.; Hiromoto, Goro; Sakata, Solange K., E-mail: fmoliveira@ipen.br [Instituto de Pesquisas Energéticas e Nucleares (IPEN/CNEN-SP), São Paulo, SP (Brazil); Rodrigues, Debora F., E-mail: dfrigiro@central.uh.edu [Department of Civil and Environmental Engineering, University of Houston, TX (United States)

    2017-07-01

    Cesium is one of the fission products of major radiological concern, it is often found in nuclear radioactive waste generated at nuclear power plants. Graphene Oxide (GO) has attracted great attention due to its functionalized surface, which includes hydroxyl, epoxy, carbonyl and carboxyl groups, with great capacity of complexation with metal ions and can be used as adsorbent to remove cations from aqueous solutions. In this work, a treatment of radioactive waste containing {sup 137}Cs was studied. For the batch experiments of Cs{sup +} removal, {sup 133}Cs concentrations remained after the adsorption were determined by Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) and the results obtained were analyzed according to the Langmuir and Freundlich isotherms models. The kinetics of adsorption and Gibbs free energy were also determined. The Langmuir model was the best fit and defined a favorable adsorption. The cesium adsorption process is the pseudo-second model and the Gibbs free energy calculation indicated that the adsorption process is spontaneous. (author)

  1. Surface modification of spinel λ-MnO2 and its lithium adsorption properties from spent lithium ion batteries

    International Nuclear Information System (INIS)

    Li, Li; Qu, Wenjie; Liu, Fang; Zhao, Taolin; Zhang, Xiaoxiao; Chen, Renjie; Wu, Feng

    2014-01-01

    Highlights: • A method is designed to synthesize a λ-MnO 2 ion-sieve for lithium ions adsorption. • Ultrasonic treatment with acid is highly efficient for lithium ions extraction. • Surface modification by CeO 2 is used to improve the adsorption capacity. • A 0.5 wt.% CeO 2 -coated ion-sieve shows the best adsorption properties. • λ-MnO 2 ion-sieves are promising for recovering scarce lithium resources. - Abstract: Spinel λ-MnO 2 ion-sieves are promising materials because of their high selectivity toward lithium ions, and this can be applied to the recovery of lithium from spent lithium ion batteries. However, manganese dissolution loss during the delithiation of LiMn 2 O 4 causes a decrease in adsorption capacity and poor cycling stability for these ion-sieves. To improve the lithium adsorption properties of λ-MnO 2 ion-sieves, surface modification with a CeO 2 coating was studied using hydrothermal-heterogeneous nucleation. The structure, morphology and composition of the synthesized materials were determined by XRD, SEM, TEM and EDS. The effect of hydrothermal synthesis conditions and the amount of CeO 2 coating on the adsorption performance of λ-MnO 2 were also investigated. A 0.5 wt.% CeO 2 -coated ion-sieve was synthesized by heating at 120 °C for 3 h and it had better adsorption properties than the bare samples. The effect of ultrasonic treatment on the lithium extraction ratio from LiMn 2 O 4 upon acid treatment at various temperatures was studied and the results were compared with conventional mechanical stirring. We found that ultrasonic treatment at lower temperature gave almost the same maximum lithium extraction ratio and was more efficient and economic

  2. Biosorption of the Copper and Cadmium Ions - a Study through Adsorption Isotherms Analysis

    Directory of Open Access Journals (Sweden)

    Marcia T. Veit

    2007-10-01

    Full Text Available In this work, the biosorption process of copper-cadmium ions binary mixture by using marine algae Sargassum filipendula was investigated. A set of experiments was performed to obtain equilibrium data for the given batch operational conditions - T=30°C, pH=5. The interpretation of equilibrium data was based on the binary adsorption isotherms models in the Langmuir and Freundlich forms. To evaluate the models parameters, nonlinear identification procedure was used based on the Least Square statistical method and SIMPLEX local optimizer. An analysis of the obtained results showed that the marine algae biomass has higher affinity to copper ions than to cadmium ones. The biomass maximum adsorption capacity for the binary system was about 1.16 meq/g.

  3. Nuclear quantum effects on adsorption of H_2 and isotopologues on metal ions

    International Nuclear Information System (INIS)

    Savchenko, Ievgeniia; Gu, Bing; Heine, Thomas; Jakowski, Jacek; Garashchuk, Sophya

    2017-01-01

    The nuclear quantum effects on the zero-point energy (ZPE), influencing adsorption of H_2 and isotopologues on metal ions, are examined in this study using normal mode analysis of ab initio electronic structure results for complexes with 17 metal cations. To estimate for the anharmonicity, a nuclear wavepacket dynamics on the ground state electronic potential energy surfaces (PES) have been employed for complexes of Li"+ and Cu"+"2 with H_2, D_2, HD. The dynamics analysis shows that incorporation of the PES anharmonicity changes the ZPE by up to 9%. Finally, the lightest metallic nuclei, Li and Be, are found to be the most 'quantum'. The largest selectivity in adsorption is predicted for Cu, Ni and Co ions.

  4. Selective adsorption behavior of Cd(II) ion imprinted polymers synthesized by microwave-assisted inverse emulsion polymerization: Adsorption performance and mechanism

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Fang, E-mail: zhufang@tyut.edu.cn [College of Environmental Science and Engineering, Taiyuan University of Technology, Taiyuan, Shanxi, 030024 (China); Li, Luwei [College of Environmental Science and Engineering, Taiyuan University of Technology, Taiyuan, Shanxi, 030024 (China); Xing, Junde [College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan, Shanxi, 030024 (China)

    2017-01-05

    Highlights: • Microwave assisted inverse emulsion polymerization was applied to prepare Cd(II) imprinted polymers. • The adsorption capacity was evaluated by static adsorption experiments. • Pseudo-second-order model and Langmuir adsorption isotherm model had the best agreement with the experimental data. • The adsorption was a spontaneous and endothermic process. • Cd(II) imprinted polymers have specific identification for Cd(II). - Abstract: Microwave-assisted inverse emulsion polymerization method was used to prepare Cd(II) imprinted polymer (IIP) by using β-cyclodextrin (β-CD) and acrylamide (AM) as functional monomer, epichlorohydrin (ECH) as crossing-linking agent, ammonium persulfate as initiator. The Cd(II) imprinted polymer was characterized by SEM, FTIR and TGA. The influences of initial concentration of Cd(II), pH values, temperature, time and competitive ions on adsorption capacity and recognition properties are investigated. Under the optimal conditions, the adsorption capacity could reach 107 mg/g. Furthermore, pseudo first order kinetic model, pseudo second order kinetic model and intra-particular diffusion model were used to describe the adsorption kinetic behavior. Results showed that the pseudo-second-order model (R{sup 2} 0.9928–0.9961) had the best agreement with the experimental data. Langmuir adsorption isotherm model described the experimental data well, which indicated that adsorption was mainly monolayer absorption. Moreover, the study of adsorption thermodynamics (ΔG{sup 0} < 0, ΔH{sup 0} > 0, ΔS{sup 0} > 0) suggested that the adsorption process was a spontaneous and endothermic process. Competitive selectivity experiment revealed that imprinted polymer could selectively recognize Cd(II). It provides a new idea for removing Cd(II) from aqueous solution.

  5. Selective adsorption behavior of Cd(II) ion imprinted polymers synthesized by microwave-assisted inverse emulsion polymerization: Adsorption performance and mechanism

    International Nuclear Information System (INIS)

    Zhu, Fang; Li, Luwei; Xing, Junde

    2017-01-01

    Highlights: • Microwave assisted inverse emulsion polymerization was applied to prepare Cd(II) imprinted polymers. • The adsorption capacity was evaluated by static adsorption experiments. • Pseudo-second-order model and Langmuir adsorption isotherm model had the best agreement with the experimental data. • The adsorption was a spontaneous and endothermic process. • Cd(II) imprinted polymers have specific identification for Cd(II). - Abstract: Microwave-assisted inverse emulsion polymerization method was used to prepare Cd(II) imprinted polymer (IIP) by using β-cyclodextrin (β-CD) and acrylamide (AM) as functional monomer, epichlorohydrin (ECH) as crossing-linking agent, ammonium persulfate as initiator. The Cd(II) imprinted polymer was characterized by SEM, FTIR and TGA. The influences of initial concentration of Cd(II), pH values, temperature, time and competitive ions on adsorption capacity and recognition properties are investigated. Under the optimal conditions, the adsorption capacity could reach 107 mg/g. Furthermore, pseudo first order kinetic model, pseudo second order kinetic model and intra-particular diffusion model were used to describe the adsorption kinetic behavior. Results showed that the pseudo-second-order model (R"2 0.9928–0.9961) had the best agreement with the experimental data. Langmuir adsorption isotherm model described the experimental data well, which indicated that adsorption was mainly monolayer absorption. Moreover, the study of adsorption thermodynamics (ΔG"0 0, ΔS"0 > 0) suggested that the adsorption process was a spontaneous and endothermic process. Competitive selectivity experiment revealed that imprinted polymer could selectively recognize Cd(II). It provides a new idea for removing Cd(II) from aqueous solution.

  6. Removal of copper (II from aqueous solutions by adsorption onto granular activated carbon in the presence of competitor ions

    Directory of Open Access Journals (Sweden)

    Saeed Almohammadi

    2016-04-01

    Full Text Available In this work, the removal of copper from an aqueous solution by granular activated carbon (GAC in the presence of competitor ions was studied. A batch adsorption was carried out and different parameters such as pH, contact time, initial copper concentration and competitor ions concentration were changed to determine the optimum conditions for adsorption. The optimum pH required for maximum adsorption was found to be 4.5 for copper. Equilibrium was evaluated at 144 h at room temperature. The removal efficiency of Cu(II was 71.12% at this time. The kinetics of copper adsorption on activated carbon followed the pseudo second-order model. The experimental equilibrium sorption data were tested using the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich (D-R equations and the Langmuir model was found to be well fitted for copper adsorption onto GAC. The maximum adsorption capacity of the adsorbent for Cu(II was calculated from the Langmuir isotherm and found to be 7.03 mg/g. Subsequently, the removal of copper by granular activated carbon in the presence of Ag1+ and Mn2+ as competitor ions was investigated. The removal efficiency of Cu(II ions without the presence of the competitor ions was 46% at 6 h, while the removal efficiency of Cu(II ions in the presence of competitor ions, Ag1+ and Mn2+ , was 34.76% and 31.73%, respectively.

  7. Removal of copper (II) from aqueous solutions by adsorption onto granular activated carbon in the presence of competitor ions

    International Nuclear Information System (INIS)

    Almohammadi, S.; Mirzaei, M.

    2016-01-01

    In this work, the removal of copper from an aqueous solution by granular activated carbon (GAC) in the presence of competitor ions was studied. A batch adsorption was carried out and different parameters such as p H, contact time, initial copper concentration and competitor ions concentration were changed to determine the optimum conditions for adsorption. The optimum p H required for maximum adsorption was found to be 4.5 for copper. Equilibrium was evaluated at 144 h at room temperature. The removal efficiency of Cu(II) was 71.12% at this time. The kinetics of copper adsorption on activated carbon followed the pseudo second-order model. The experimental equilibrium sorption data were tested using the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich (D-R) equations and the Langmuir model was found to be well fitted for copper adsorption onto GAC. The maximum adsorption capacity of the adsorbent for Cu(II) was calculated from the Langmuir isotherm and found to be 7.03 mg/g. Subsequently, the removal of copper by granular activated carbon in the presence of Ag 1 + and Mn 2 + as competitor ions was investigated. The removal efficiency of Cu(II) ions without the presence of the competitor ions was 46% at 6 h, while the removal efficiency of Cu(II) ions in the presence of competitor ions, Ag 1 + and Mn 2 + , was 34.76% and 31.73%, respectevely.

  8. Adsorption of Nitrite and Nitrate Ions from an Aqueous Solution by Fe-Mg-Type Hydrotalcites at Different Molar Ratios.

    Science.gov (United States)

    Ogata, Fumihiko; Nagai, Noriaki; Kariya, Yukine; Nagahashi, Eri; Kobayashi, Yuhei; Nakamura, Takehiro; Kawasaki, Naohito

    2018-01-01

    In this study, we prepared Fe-Mg-type hydrotalcites (Fe-HT3.0 and Fe-HT5.0) with different molar ratios and evaluated their adsorption capability for nitrite and nitrate ions from aqueous solution. Fe-HT is a typical hydrotalcite-like layered double hydroxide. Adsorption isotherms, as well as the effects of contact time and pH were investigated, and it was found that Fe-HT can adsorb larger amounts of nitrite and nitrate ions than Al-HT (normal-type hydrotalcite). Adsorption isotherm data were fitted to both Freundlich (correlation coefficient: 0.970-1.000) and Langmuir (correlation coefficient: 0.974-0.999) equations. Elemental analysis and binding energy of Fe-HT surface before and after adsorption indicated that the adsorption mechanism was related to the interaction between the adsorbent surface and anions. In addition, the ion exchange process is related to the adsorption mechanism. The adsorption amount increased with increasing temperature (7-25°C). The experimental data fit the pseudo-second-order model better than the pseudo-first-order model. The effect of pH on adsorption was not significant, which suggested that Fe-HT could be used over a wide pH range (4-12). These results indicate that Fe-HT is a good adsorbent for the removal of nitrite and nitrate ions from aqueous solution.

  9. Ion Adsorption Parameters Determined from Zeta Potential and Titration Data for a y-Alumina Nanofiltration Membrane

    NARCIS (Netherlands)

    de Lint, W.B.S.; Benes, Nieck Edwin; Lyklema, Johannes; Bouwmeester, Henricus J.M.; van der Linde, Ab J.; Wessling, Matthias

    2003-01-01

    Theoretical models for the prediction of nanofiltration separation performance as a function of, e.g., pH and electrolyte composition require knowledge on the ion-surface adsorption chemistry. Adsorption parameters have been extracted from electrophoretic mobility measurements on a ceramic y-alumina

  10. Ion adsorption parameters determined from zeta potential and titration data for a gamma-alumina nanofiltration membrane

    NARCIS (Netherlands)

    Samuel de Lint, W.B.; Benes, N.E.; Lyklema, J.; Bouwmeester, H.J.M.; Linde, van der A.J.; Wessling, M.

    2003-01-01

    Theoretical models for the prediction of nanofiltration separation performance as a function of, e.g., pH and electrolyte composition require knowledge on the ion-surface adsorption chemistry. Adsorption parameters have been extracted from electrophoretic mobility measurements on a ceramic -alumina

  11. Ion exchange and adsorption in nuclear chemical engineering

    International Nuclear Information System (INIS)

    Schultz, W.W.; Wheelwright, E.J.; Godbee, H.; Mallory, C.W.; Burney, G.A.; Wallace, R.M.

    1983-01-01

    The nuclear industry involves a number of operations. Uranium ore must first be mined and the uranium recovered from the ore, purified, and concentrated. After the uranium has been enriched and fabricated into fuel elements, it is placed in nuclear reactors where it produces energy, fission products, and transmutation products. Finally, if the fuel cycle is completed, the uranium and useful transmutation products are recovered and separated from each other as well as from the fission products. The uranium may be recycled or used elsewhere, while most of the fission products become waste. Ion exchange finds use in nearly every part of the nuclear fuel cycle; these uses are the subject of this paper

  12. Unified superresolution experiments and stochastic theory provide mechanistic insight into protein ion-exchange adsorptive separations.

    Science.gov (United States)

    Kisley, Lydia; Chen, Jixin; Mansur, Andrea P; Shuang, Bo; Kourentzi, Katerina; Poongavanam, Mohan-Vivekanandan; Chen, Wen-Hsiang; Dhamane, Sagar; Willson, Richard C; Landes, Christy F

    2014-02-11

    Chromatographic protein separations, immunoassays, and biosensing all typically involve the adsorption of proteins to surfaces decorated with charged, hydrophobic, or affinity ligands. Despite increasingly widespread use throughout the pharmaceutical industry, mechanistic detail about the interactions of proteins with individual chromatographic adsorbent sites is available only via inference from ensemble measurements such as binding isotherms, calorimetry, and chromatography. In this work, we present the direct superresolution mapping and kinetic characterization of functional sites on ion-exchange ligands based on agarose, a support matrix routinely used in protein chromatography. By quantifying the interactions of single proteins with individual charged ligands, we demonstrate that clusters of charges are necessary to create detectable adsorption sites and that even chemically identical ligands create adsorption sites of varying kinetic properties that depend on steric availability at the interface. Additionally, we relate experimental results to the stochastic theory of chromatography. Simulated elution profiles calculated from the molecular-scale data suggest that, if it were possible to engineer uniform optimal interactions into ion-exchange systems, separation efficiencies could be improved by as much as a factor of five by deliberately exploiting clustered interactions that currently dominate the ion-exchange process only accidentally.

  13. Selective adsorption of thiophene and 1-benzothiophene on metal-ion-exchanged zeolites in organic medium.

    Science.gov (United States)

    Xue, Mei; Chitrakar, Ramesh; Sakane, Kohji; Hirotsu, Takahiro; Ooi, Kenta; Yoshimura, Yuji; Feng, Qi; Sumida, Naoto

    2005-05-15

    Adsorption of the organic sulfur compounds thiophene (TP) and 1-benzothiophene (1-BTP) in an organic model solution of hydrodesulfurizated gasoline (heptane with 1 wt% toluene and 0.156 mM (5 ppmw as sulfur) TP or 1-BTP) was studied by a batch method at 80 degrees C using metal-ion-exchanged Y-zeolites. Although NaY-zeolite or its acid-treated material rarely adsorbed the organic sulfur compounds, NaY-zeolites exchanged with Ag+, Cu2+, and Ce3+ ions and NH(4)Y-zeolites exchanged with Ce3+ ions showed markedly high adsorptive capacities for TP and 1-BTP. The sulfur uptake increased in the order CuY-zeolite(Na)adsorption isotherms for TP and 1-BTP followed the Langmuir's relationship and the saturation capacities by CeY-zeolite(Na) were calculated as 0.022 and 0.033 mmol/g, respectively. The mole ratios of TP/Ce and 1-BTP/Ce were 0.031 and 0.047, respectively. CeY-zeolite(NH4) which was prepared from NH4Y-zeolite showed less uptake of TP and 1-BTP than CeY-zeolite(Na), probably due to its lower cerium content.

  14. Adsorption Efficiency of Iron Modified Carbons for Removal of Pb(II Ions from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Mohammad Hossein Salmani

    2016-06-01

    Full Text Available Abstract Introduction: The Lead causes severe damage to several systems of the body, especially to bony tissues. Until now, several low-cost biosorbents have been studied for removal of heavy metal ions from aqueous solutions. In the present study, carbonized pomegranate peels modified with Fe2+ and Fe3+ ions and then it was investigated for removal of Pb(II ions from aqueous solution. Materials and methods: the washed granola of pomegranate peel was separately socked with FeCl3 and FeCl2 solutions for 24 h. Then, the granules were carbonized at 400 ºC for 3 h in a programmable furnace in the atmosphere of nitrogen. The adsorption experiments were carried out for two types of iron-modified carbons by batch adsorption using one variable at a time procedures. Results: The optimum conditions were found as contact time 90 min, initial concentration 50 mg/l, and adsorbent dose, 1.00 g/100 ml solution. Maximum removal efficiency was calculated as 84% and 89% for Fe3+ and Fe2+ impregnated pomegranate peel carbons respectively. Conclusion: The iron treatment pomegranate peel carbons modified their surfaces for adsorption of heavy metals. The results showed that chemical modification of the low-cost adsorbents originating from agricultural waste has stood out for metal removal capabilities.

  15. Adsorption of Cadmium Ions from Water on Double-walled Carbon Nanotubes/Iron Oxide Composite

    Directory of Open Access Journals (Sweden)

    Karima Seffah

    2017-12-01

    Full Text Available A new material (DWCNT/iron oxide for heavy metals removal was developed by combining the adsorption features of double-walled carbon nanotubes with the magnetic properties of iron oxides. Batch experiments were applied in order to evaluate adsorption capacity of the DWCNT/iron oxide composite for cadmium ions. The influence of operating parameters such as pH value, amount of adsorbent, initial adsorbate concentration and agitation speed was studied. The adsorption capacity of the DWCNT/iron oxide adsorbent for Cd2+ ions was 20.8 mg g-1, which is at the state of the art. The obtained results revealed that DWCNT/iron oxide composite is a very promising adsorbent for removal of Cd2+ ions from water under natural conditions. The advantage of the magnetic composite is that it can be used as adsorbent for contaminants in water and can be subsequently controlled and removed from the medium by a simple magnetic process.

  16. The effects of ion adsorption on the potential of zero charge and the differential capacitance of charged aqueous interfaces

    Science.gov (United States)

    Uematsu, Yuki; Netz, Roland R.; Bonthuis, Douwe Jan

    2018-02-01

    Using a box profile approximation for the non-electrostatic surface adsorption potentials of anions and cations, we calculate the differential capacitance of aqueous electrolyte interfaces from a numerical solution of the Poisson-Boltzmann equation, including steric interactions between the ions and an inhomogeneous dielectric profile. Preferential adsorption of the positive (negative) ion shifts the minimum of the differential capacitance to positive (negative) surface potential values. The trends are similar for the potential of zero charge; however, the potential of zero charge does not correspond to the minimum of the differential capacitance in the case of asymmetric ion adsorption, contrary to the assumption commonly used to determine the potential of zero charge. Our model can be used to obtain more accurate estimates of ion adsorption properties from differential capacitance or electrocapillary measurements. Asymmetric ion adsorption also affects the relative heights of the characteristic maxima in the differential capacitance curves as a function of the surface potential, but even for strong adsorption potentials the effect is small, making it difficult to reliably determine the adsorption properties from the peak heights.

  17. Adsorption of surfactant ions and binding of their counterions at an air/water interface.

    Science.gov (United States)

    Tagashira, Hiroaki; Takata, Youichi; Hyono, Atsushi; Ohshima, Hiroyuki

    2009-01-01

    An expression for the surface tension of an aqueous mixed solution of surfactants and electrolyte ions in the presence of the common ions was derived from the Helmholtz free energy of an air/water surface. By applying the equation to experimental data for the surface tension, the adsorption constant of surfactant ions onto the air/water interface, the binding constant of counterions on the surfactants, and the surface potential and surface charge density of the interface were estimated. The adsorption constant and binding constant were dependent on the species of surfactant ion and counterion, respectively. Taking account of the dependence of surface potential and surface charge density on the concentration of electrolyte, it was suggested that the addition of electrolyte to the aqueous surfactant solution brings about the decrease in the surface potential, the increase in the surface density of surfactant ions, and consequently, the decrease in the surface tension. Furthermore, it was found that the configurational entropy plays a predominant role for the surface tension, compared to the electrical work.

  18. Manipulating Adsorption-Insertion Mechanisms in Nanostructured Carbon Materials for High-Efficiency Sodium Ion Storage

    Energy Technology Data Exchange (ETDEWEB)

    Qiu, Shen [College of Chemistry and Molecular Sciences, Hubei Key Laboratory of Electrochemical Power Sources, Wuhan University, Wuhan 430072 China; Xiao, Lifen [College of Chemistry, Central China Normal University, Wuhan 430079 China; Pacific Northwest National Laboratory, Richland WA 99352 USA; Sushko, Maria L. [Pacific Northwest National Laboratory, Richland WA 99352 USA; Han, Kee Sung [Pacific Northwest National Laboratory, Richland WA 99352 USA; Shao, Yuyan [Pacific Northwest National Laboratory, Richland WA 99352 USA; Yan, Mengyu [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, School of Materials Science and Engineering, Wuhan University of Technology, Wuhan 430070 China; Liang, Xinmiao [State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics, Chinese Academy of Science, Wuhan 430071 China; Mai, Liqiang [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, School of Materials Science and Engineering, Wuhan University of Technology, Wuhan 430070 China; Feng, Jiwen [State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics, Chinese Academy of Science, Wuhan 430071 China; Cao, Yuliang [College of Chemistry and Molecular Sciences, Hubei Key Laboratory of Electrochemical Power Sources, Wuhan University, Wuhan 430072 China; Ai, Xinping [College of Chemistry and Molecular Sciences, Hubei Key Laboratory of Electrochemical Power Sources, Wuhan University, Wuhan 430072 China; Yang, Hanxi [College of Chemistry and Molecular Sciences, Hubei Key Laboratory of Electrochemical Power Sources, Wuhan University, Wuhan 430072 China; Liu, Jun [Pacific Northwest National Laboratory, Richland WA 99352 USA

    2017-05-12

    Hard carbon is one of the most promising anode materials for sodium-ion batteries, but the low coulombic efficiency is still a key barrier. In this paper we synthesized a series of nanostructured hard carbon materials with controlled architectures. Using a combination of in-situ XRD mapping, ex-situ NMR, EPR, electrochemical techniques and simulations, an “adsorption-intercalation” (A-I) mechanism is established for Na ion storage. During the initial stages of Na insertion, Na ions adsorb on the defect sites of hard carbon with a wide adsorption energy distribution, producing a sloping voltage profile. In the second stage, Na ions intercalate into graphitic layers with suitable spacing to form NaCx compounds similar to the Li ion intercalation process in graphite, producing a flat low voltage plateau. The cation intercalation with a flat voltage plateau should be enhanced and the sloping region should be avoided. Guided by this knowledge, non-porous hard carbon material has been developed which has achieved high reversible capacity and coulombic efficiency to fulfill practical application.

  19. Preparation and adsorption behavior for metal ions and humic acid of chitosan derivatives crosslinked by irradiation

    International Nuclear Information System (INIS)

    Zhao Long; Mitomo, H.; Yoshii, F.

    2006-01-01

    Introduction: Removing metal ions and humic acid from water in water treatment has attracted much environment and health interests. Adsorbents, derived from a nature polymer, are desired in the viewpoints of environment-conscious technologies. Recently, some nature materials such as chitin, chitosan and their derivatives have been identified as an attractive option due to their distinctive properties. For an insoluble adsorbent based on these polymers to be obtained over a broad pH range, modification through crosslinking is required. Crosslinking agents such as glutaric dialdehyde and ethylene glycol diglycidyl ether are frequently used for modification. However, these crosslinking agents are not preferred because of their physiological toxicity. Radiation-crosslinking without any additive in the fabrication process results in a high-purity product. In a previous work, we applied ionizing radiation to induce the crosslinking of carboxymethylchitosan under highly concentrated paste-like conditions. The aim of this study is to investigate the adsorption behavior of metal ions, humic acid on irradiation-crosslinked carboxymethylchitosan. Experimental: Irradiation of chitosan samples at paste-like state was done with an electron beam. The solubility test of these crosslinked materials were investigated in acidic, alkaline media, and some organic solvents. Swelling and charged characteristic analyses demonstrated typically pH-sensitive properties of these crosslinked materials. Scanning electron microscopic images showed that the crosslinked samples possessed porous morphological structure. The adsorption studies were carried out by the batch method at room temperature. Adsorption of heavy metal ions (such as Cu 2+ , Cd 2+ ) and humic acid onto crosslinked samples was found to be strongly pH-dependent. Adsorption kinetic studies indicated the rapid removal of metal ions, and humic acid from the aqueous solutions. Also, isothermal adsorption data revealed that Cu 2

  20. Heavy metal ion removal by adsorption on to biological materials

    International Nuclear Information System (INIS)

    Jansson-Charrier, M.; Guibal, E.; Le Cloirec, P.; Surjous, R.

    1994-01-01

    The development of regulations constraints in the industrial waste-waters management leads to the study of new treatment processes, using raw or functionalized biological materials. These processes show competitive performances in metal ion sorption efficiency for the low metal content effluents. Uptake capacities of Uranium as high as 400 mg.g -1 chitosan, equivalent to the double of the uptake capacity of fungal origin biomass, can be reached. The application of these processes to real mine wastewaters gives efficiency coefficient upper to 90%, the residual concentrations are compatible to a direct injection into the environment. The grafting of functional groups onto the chitosan scales up the sorption performances to uptake capacity upper than 600 mg.g -1 polymer. pH, metal concentration are cited as major parameters, particle size influences both uptake kinetics and sorption equilibrium, in the case of the uranium accumulation by chitosan. The desorption of uranium from the sorbent allows the valorization of uranium and the re-use of the sorbent. (authors). 21 refs., 10 figs

  1. Synthesis and characterization of ceramic/carbon nanotubes composite adsorptive membrane for copper ion removal from water

    Energy Technology Data Exchange (ETDEWEB)

    Tofighy, Maryam Ahmadzadeh; Mohammadi, Toraj [Iran University of Science and Technology (IUST), Tehran (Iran, Islamic Republic of)

    2015-02-15

    We prepared a novel adsorptive membrane by implanting carbon nanotubes (CNTs) in pore channels of ceramic (α-alumina) support via chemical vapor deposition (CVD) method using cyclohexanol and ferrocene as carbon precursor and catalyst, respectively. Optimization of CNTs growth conditions resulted in uniform distribution of the CNTs in the pore channels of the support. The optimized CNTs-ceramic membrane was oxidized with concentrated nitric acid, and chitosan was employed for filling intertube-CNT gaps. The modified CNTs-ceramic membrane was used for copper ion removal from water, and the effects of the modification steps (oxidation and filling intertube-CNT gaps with chitosan) and pH on permeation flux and rejection of the prepared adsorptive membrane were investigated. Moreover, static adsorption was also investigated and Langmuir and Freundlich isotherms and two kinetics models were used to describe adsorption behavior of copper ions by the prepared adsorptive membrane.

  2. Growth and characterization of pure and lithium doped strontium ...

    Indian Academy of Sciences (India)

    TECS

    Abstract. The effect of lithium ion as dopant on the size and transparency of strontium tartrate tetrahydrate. (SrC4H4O6⋅4H2O) crystals are presented in this paper. Growth of single crystals of undoped and lithium doped strontium tartrate tetrahydrate by controlled diffusion of strontium nitrate into the gel charged with.

  3. Removal of zinc (II) ion from aqueous solution by adsorption onto activated palm midrib bio-sorbent

    Science.gov (United States)

    Mulana, F.; Mariana; Muslim, A.; Mohibah, M.; Halim, K. H. Ku

    2018-03-01

    In this paper, palm midrib that was activated with mixed citric acid and tartaric acid as biosorbent was used to remove Zn (II) ion from aqueous solution. The aim of this research is to activate palm midrib by using a mixed citric acid and tartaric acid and to determine adsorption capacity of activated palm midrib biosorbent on Zn (II) ion uptake from aqueous solution. The effect of several parameters such as contact time, initial Zn (II) ion concentration and activator concentration on the degree of Zn (II) ion removal was examined. Atomic Absorption Spectroscopy method was performed to determine adsorbed amount of Zn (II) ion into activated biosorbent. The result showed that the adsorption process was relatively not so fast and equilibrium was reached after contact time of 120 min. The adsorption capacity of biosorbent reached a maximum when the concentration of mixed citric acid and tartaric acid was 1.6 M. The optimum adsorption capacity was 5.72 mg/g. The result was obtained on initial Zn (II) ion concentration of 80 ppm for 120-min contact time. Langmuir isotherm was found as the best fit for the equilibrium data indicating homogeneous adsorption of metal ions onto the biosorbent surface.

  4. Biochar-supported reduced graphene oxide composite for adsorption and coadsorption of atrazine and lead ions

    Science.gov (United States)

    Zhang, Ying; Cao, Bo; Zhao, Lulu; Sun, Lili; Gao, Yan; Li, Jiaojiao; Yang, Fan

    2018-01-01

    To explore potential in application for simultaneous removal of atrazine and lead ions (Pd2+), the adsorption and coadsorption of atrazine and Pd2+ is evaluated onto a novel biochar-supported reduced graphene oxide composite (RGO-BC), which has been successfully developed via slow pyrolysis of graphene oxide (GO) pretreated corn straws. Structure and morphology analysis reveal that GO nanosheets are coated on the surface of biochar (BC) mainly through π-π interactions, notably, GO nanosheets after annealing reduction can basically retain the original morphology, meanwhile, the change of physico-chemical properties on the surface endow excellent adsorption capaities of 26.10 mg g-1 for Pb2+ and 67.55 mg g-1 for atrazine. A significant difference is in sorption of Pb2+ and atrazine on RGO-BC sample in both single- and binary-solute systems. The adsorption capacity of RGO-BC still remained above 54.58 mg g-1 after four times regeneration (81% adsorption capacity remained), demonstrating a promising candidate for the application of removal contaminant in the environment.

  5. Performance evaluation of 24 ion exchange materials for removing cesium and strontium from actual and simulated N-Reactor storage basin water

    Energy Technology Data Exchange (ETDEWEB)

    Brown, G.N.; Carson, K.J.; DesChane, J.R.; Elovich, R.J.

    1997-09-01

    This report describes the evaluation of 24 organic and inorganic ion exchange materials for removing cesium and strontium from actual and simulated waters from the 100 Area 105 N-Reactor fuel storage basin. The data described in this report can be applied for developing and evaluating ion exchange pre-treatment process flowsheets. Cesium and strontium batch distribution ratios (K{sub d}`s), decontamination factors (DF), and material loadings (mmol g{sup -1}) are compared as a function of ion exchange material and initial cesium concentration. The actual and simulated N-Basin waters contain relatively low levels of aluminum, barium, calcium, potassium, and magnesium (ranging from 8.33E-04 to 6.40E-05 M), with slightly higher levels of boron (6.63E-03 M) and sodium (1.62E-03 M). The {sup 137}Cs level is 1.74E-06 Ci L-{sup 1} which corresponds to approximately 4.87E-10 M Cs. The initial Na/Cs ratio was 3.33E+06. The concentration of total strontium is 4.45E-06 M, while the {sup 90}Sr radioactive component was measured to be 6.13E-06 Ci L{sup -1}. Simulant tests were conducted by contacting 0.067 g or each ion exchange material with approximately 100 mL of either the actual or simulated N-Basin water. The simulants contained variable initial cesium concentrations ranging from 1.00E-04 to 2.57E- 10 M Cs while all other components were held constant. For all materials, the average cesium K{sub d} was independent of cesium concentration below approximately 1.0E-06 M. Above this level, the average cesium K{sub d} values decreased significantly. Cesium K{sub d} values exceeding 1.0E+07 mL g{sup -1} were measured in the simulated N-Basin water. However, when measured in the actual N-Basin water the values were several orders of magnitude lower, with a maximum of 1.24E+05 mL g{sup -1} observed.

  6. Ions-induced nanostructuration: effect of specific ionic adsorption on hydrophobic polymer surfaces.

    Science.gov (United States)

    Siretanu, Igor; Chapel, Jean-Paul; Bastos-González, Delfi; Drummond, Carlos

    2013-06-06

    The effect of surface charges on the ionic distribution in close proximity to an interface has been extensively studied. On the contrary, the influence of ions (from dissolved salts) on deformable interfaces has been barely investigated. Ions can adsorb from aqueous solutions on hydrophobic surfaces, generating forces that can induce long-lasting deformation of glassy polymer films, a process called ion-induced polymer nanostructuration, IPN. We have found that this process is ion-specific; larger surface modifications are observed in the presence of water ions and hydrophobic and amphiphilic ions. Surface structuration is also observed in the presence of certain salts of lithium. We have used streaming potential and atomic force microscopy to study the effect of dissolved ions on the surface properties of polystyrene films, finding a good correlation between ionic adsorption and IPN. Our results also suggest that the presence of strongly hydrated lithium promotes the interaction of anions with polystyrene surfaces and more generally with hydrophobic polymer surfaces, triggering then the IPN process.

  7. Adsorption and Desorption of Na+ and NO3− Ions on Thermosensitive NIPAM-co-DMAAPS Gel in Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Eva Oktavia Ningrum

    2017-11-01

    Full Text Available Adsorbent gel with the ability to absorb and to desorb Na+ and NO3− ions simultaneously with temperature swing was synthesized by free radical copolymerization reaction of N-isopropylacrylamide (NIPAM and N,N-dimethyl-(acrylamidopropylammonium propane sulfonate (DMAAPS. In this study, NIPAM acts as a thermosensitive agent and DMAAPS as an adsorbent agent. The purpose of this research is to investigate the effect of temperature and solution concentration on the swelling, adsorption, and desorption behaviors of NIPAM-co-DMAAPS gel. The relationship between adsorption and desorption behaviors of the gel was also elucidated. NaNO3 solution was selected as the target solution in swelling, adsorption, and desorption test. It was observed that the swelling degree of the gel increased as temperature and solution concentration raised. The adsorption amount of ions decreased with the increase of temperature. In contrast, the amount of ions desorbed from the gel increased linearly with temperature.

  8. Adsorption of lead and copper ions from aqueous effluents on rice husk ash in a dynamic system

    Directory of Open Access Journals (Sweden)

    M. G. A. Vieira

    2014-06-01

    Full Text Available This study evaluated the kinetic adsorption of Pb and Cu ions using rice husk ash as adsorbent in a fixed bed. The maximum adsorption capacities obtained for lead and copper ions in the fixed bed were 0.0561 and 0.0682 mmol/g (at 20 ºC, respectively. The thermodynamic studies indicated that the lead adsorption process was exothermic and spontaneous, while the copper adsorption process was endothermic and spontaneous. Characterization results indicated the presence of several functional groups, amorphous silica and a fibrous and longitudinal structure of rice husks. Rice husk ash (RHA from northern Brazil can be used as a bioadsorbent for the individual removal of Pb(II and Cu(II ions from metal-containing effluents.

  9. Factors Affecting the Adsorption of Trivalent Chromium Ions by Activated Carbon Prepared from Waste Rubber Tyres

    Directory of Open Access Journals (Sweden)

    Sylvia E. Benjamin

    2017-08-01

    Full Text Available Economic gains are generally the outcome of industrialization and consequently urbanization. However, positive fiscal index generates a negative impact on natural environment sources heaving pollutant burden on soil, air and water. Industries throw tones of contaminated water into soil and water bodies without proper treatment and create a potential threat for both living and non-living species. Chromium in trivalent state (Cr3+ is added in water bodies and soil through waste water from tanneries, cooling water systems, chemical and pulp and paper industries. The present research work aims at the preparation of an inexpensive activated carbon prepared from non- degradable waste scrap rubber tyres. The carbon produced from scrap rubber tyres was activated by 5% solution of BaCl2 and 0.4 N solution of HCl and verified by ethylene blue solution. The adsorption capacity of the Tyre activated carbon (TAC was investigated for different parameters i.e., initial chromium (III ion concentration, activated carbon dosage, contact/ stirring time and pH. The adsorption capacity of TAC depends on the initial metal ion concentration and the TAC dose. pH of the chromium solution effects the adsorption capacity of TAC due to the formation of tetra hydroxochromate(III complexes,. The results show that TAC offers a cost effective reclamation process for the removal of Cr3+ from effluent waters.

  10. Adsorption of sulfide ions on cerussite surfaces and implications for flotation

    International Nuclear Information System (INIS)

    Feng, Qicheng; Wen, Shuming; Zhao, Wenjuan; Deng, Jiushuai; Xian, Yongjun

    2016-01-01

    Highlights: • A new discussion on the lead sulfide species is introduced. • The Na_2S concentration determines cerussite sulfidization. • The activity of lead sulfide species also determines cerussite sulfidization. • Disulfide and polysulfide in lead sulfide species affect its activity. - Abstract: The adsorption of sulfide ions on cerussite surfaces and implications for flotation were studied by X-ray photoelectron spectroscopy (XPS) analysis, micro-flotation tests, and surface adsorption experiments. The XPS analysis results indicated that lead sulfide species formed on the mineral surface after treatment by Na_2S, and the increase in the Na_2S concentration was beneficial for sulfidization. In addition to the content of lead sulfide species, its activity, which was determined by the proportion of sulfide, disulfide and polysulfide, also played an important role in cerussite sulfidization. Micro-flotation tests results demonstrated that insufficient or excessive addition of Na_2S in pulp solutions has detrimental effects on flotation performance, which was attributed to the dosage of Na_2S and the activity of lead sulfide species formed on the mineral surface. Surface adsorption experiments of sulfide ions determined the residual S concentrations in pulp solutions and provided a quantitative illustration for the inhibition of cerussite flotation by excessive sulfide ions. Moreover, it also revealed that sulfide ions in the pulp solution were transformed onto the mineral surface and formed lead sulfide species. These results showed that both of lead sulfide species and its activity acted as an important role in sulfidization flotation process of cerussite.

  11. Adsorption of sulfide ions on cerussite surfaces and implications for flotation

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Qicheng [State Key Laboratory of Complex Nonferrous Metal Resources Clean Utilization, Kunming University of Science and Technology, Kunming 650093 (China); Faculty of Land Resource Engineering, Kunming University of Science and Technology, Kunming 650093 (China); Wen, Shuming, E-mail: fqckmust@126.com [State Key Laboratory of Complex Nonferrous Metal Resources Clean Utilization, Kunming University of Science and Technology, Kunming 650093 (China); Faculty of Land Resource Engineering, Kunming University of Science and Technology, Kunming 650093 (China); Zhao, Wenjuan [Kunming Metallurgical Research Institute, Kunming 650031 (China); Deng, Jiushuai; Xian, Yongjun [State Key Laboratory of Complex Nonferrous Metal Resources Clean Utilization, Kunming University of Science and Technology, Kunming 650093 (China); Faculty of Land Resource Engineering, Kunming University of Science and Technology, Kunming 650093 (China)

    2016-01-01

    Highlights: • A new discussion on the lead sulfide species is introduced. • The Na{sub 2}S concentration determines cerussite sulfidization. • The activity of lead sulfide species also determines cerussite sulfidization. • Disulfide and polysulfide in lead sulfide species affect its activity. - Abstract: The adsorption of sulfide ions on cerussite surfaces and implications for flotation were studied by X-ray photoelectron spectroscopy (XPS) analysis, micro-flotation tests, and surface adsorption experiments. The XPS analysis results indicated that lead sulfide species formed on the mineral surface after treatment by Na{sub 2}S, and the increase in the Na{sub 2}S concentration was beneficial for sulfidization. In addition to the content of lead sulfide species, its activity, which was determined by the proportion of sulfide, disulfide and polysulfide, also played an important role in cerussite sulfidization. Micro-flotation tests results demonstrated that insufficient or excessive addition of Na{sub 2}S in pulp solutions has detrimental effects on flotation performance, which was attributed to the dosage of Na{sub 2}S and the activity of lead sulfide species formed on the mineral surface. Surface adsorption experiments of sulfide ions determined the residual S concentrations in pulp solutions and provided a quantitative illustration for the inhibition of cerussite flotation by excessive sulfide ions. Moreover, it also revealed that sulfide ions in the pulp solution were transformed onto the mineral surface and formed lead sulfide species. These results showed that both of lead sulfide species and its activity acted as an important role in sulfidization flotation process of cerussite.

  12. Adsorption of Uranyl Ions at the Nano-hydroxyapatite and Its Modification.

    Science.gov (United States)

    Skwarek, Ewa; Gładysz-Płaska, Agnieszka; Bolbukh, Yuliia

    2017-12-01

    Nano-hydroxyapatite and its modification, hydroxyapatite with the excess of phosphorus (P-HAP) and hydroxyapatite with the carbon ions built into the structure (C-HAP), were prepared by the wet method. They were studied by means of XRD, accelerated surface area and porosimetry (ASAP), and SEM. The size of crystallites computed using the Scherrer method was nano-hydroxyapatite (HAP) = 20 nm; P-HAP-impossible to determine; C-HAP = 22 nm; nano-HAP/U(VI) = 13.7 nm; P-HAP/U(VI)-impossible to determine, C-HAP/U(VI) = 11 nm. There were determined basic parameters characterizing the double electrical layer at the nano-HAP/electrolyte and P-HAP/electrolyte, C-HAP/electrolyte inter faces: density of the surface charge and zeta potential. The adsorption properties of nano-HAP sorbent in relation to U(VI) ions were studied by the batch technique. The adsorption processes were rapid in the first 60 min and reached the equilibrium within approximately 120 min (for P-HAP) and 300 min (for C-HAP and nano-HAP). The adsorption process fitted well with the pseudo-second-order kinetics. The Freundlich, Langmuir-Freundlich, and Dubinin-Radushkevich models of isotherms were examined for their ability to the equilibrium sorption data. The maximum adsorption capabilities (q m ) were 7.75 g/g for P-HAP, 1.77 g/g for C-HAP, and 0.8 g/g for HAP at 293 K.

  13. Batch adsorption of cadmium ions from aqueous solution by means of olive cake

    International Nuclear Information System (INIS)

    Al-Anber, Zaid Ahmed; Matouq, Mohammed Abu Dayeh

    2008-01-01

    The use of natural adsorbent such as olive cake to replace expensive imported synthetic adsorbent is particularly appropriate for developing countries such as Jordan. In this study, batch adsorption experiments were carried out for the removal of cadmium ions from its aqueous solution using olive cake as adsorbent. Parameters effects such as temperature, pH and adsorbent dose on the adsorption process were studied. The adsorbent used in this study exhibited as good sorption at approximately pH 6 at temperatures 28, 35 and 45 deg. C. The removal efficiency was found to be 66% at pH 6 and temperature 28 deg. C. The equilibrium data were analyzed using Langmuir and Freundlich isotherm models to calculate isotherm constants. The experimental results were in a good agreement with these models. Results show that when an increasing in temperature from 28 to 45 deg. C, the maximum adsorption capacity (q max ) is decreased from 65.4 to 44.4 mg/g and Freundlich constant (K f ) decreased from 19.9 to 15.7. The thermodynamic parameters for the adsorption process data were evaluated using Langmuir isotherm. The free energy change (ΔG o ) and the enthalpy change (ΔH o ) showed that the process was feasible and exothermic, respectively. The dynamic data fitted to the first order, Lagergren-first order and pseudo second-order kinetic models. The experimental results indicated that the pseudo second-order reaction model provided the best description for these data with a correlation coefficient of 0.99. The adsorption rate constant was calculated as 8.4 x 10 -3 g mg -1 min -1 at 28 deg. C

  14. Synthesis and application of ion imprinting polymer coated magnetic multi-walled carbon nanotubes for selective adsorption of nickel ion

    Science.gov (United States)

    He, Junnan; Shang, Hongzhou; Zhang, Xing; Sun, Xiaoran

    2018-01-01

    A novel nickel ion imprinted polymers (IIPs) based on multi-walled carbon nanotubes (MWCNTs) were synthesized inverse emulsion system, using chitosan(CS) and acrylic acid as the functional monomers, Ni (II) as the template, and N' N-methylene bis-acrylamide as the cross-linker. The chemical structure and morphological feature of the IIPs were characterized by scanning electron microscopy (SEM), Thermogravimetry (TG), X-ray diffraction (XRD), and Fourier transform infrared spectrometer (FTIR). The studies indicated that the gel layer was well grafted on the surface of MWCNTs. Studies on the adsorption ability of the IIPs, by atomic absorption spectrophotometry, demonstrated that IIPs possessed excellent adsorption and selective ability towards Ni (II), fitting to pseudo second-order kinetic isotherms and with a maximum capacity of 19.86 mg/g, and selectivity factor of 13.09 and 4.42. The electrochemical performance of ion imprinting carbon paste electrode (CPE/IIPs) was characterized by Cyclic voltammetry (CV). Studies have shown that CPE/IIPs showed excellent electrochemical performance.

  15. Single and binary adsorption of heavy metal ions from aqueous solutions using sugarcane cellulose-based adsorbent.

    Science.gov (United States)

    Wang, Futao; Pan, Yuanfeng; Cai, Pingxiong; Guo, Tianxiang; Xiao, Huining

    2017-10-01

    A high efficient and eco-friendly sugarcane cellulose-based adsorbent was prepared in an attempt to remove Pb 2+ , Cu 2+ and Zn 2+ from aqueous solutions. The effects of initial concentration of heavy metal ions and temperature on the adsorption capacity of the bioadsorbent were investigated. The adsorption isotherms showed that the adsorption of Pb 2+ , Cu 2+ and Zn 2+ followed the Langmuir model and the maximum adsorptions were as high as 558.9, 446.2 and 363.3mg·g -1 , respectively, in single component system. The binary component system was better described with the competitive Langmuir isotherm model. The three dimensional sorption surface of binary component system demonstrated that the presence of Pb 2+ decreased the sorption of Cu 2+ , but the adsorption amount of other metal ions was not affected. The result from SEM-EDAX revealed that the adsorption of metal ions on bioadsorbent was mainly driven by coordination, ion exchange and electrostatic association. Copyright © 2017 Elsevier Ltd. All rights reserved.

  16. Chitosan-rectorite nanospheres immobilized on polystyrene fibrous mats via alternate electrospinning/electrospraying techniques for copper ions adsorption

    Science.gov (United States)

    Tu, Hu; Huang, Mengtian; Yi, Yang; Li, Zhenshun; Zhan, Yingfei; Chen, Jiajia; Wu, Yang; Shi, Xiaowen; Deng, Hongbing; Du, Yumin

    2017-12-01

    Chitosan (CS), as a kind of well characterized biopolymer, has been used for heavy metal adsorption due to its low cost and high efficacy. However, when used directly, chitosan particles had small surface area and weak mechanical strength which is unfavorable to metal adsorption and reused. Besides, it cannot be easily recycled that may cause a secondary pollution. In this paper, CS and layered silicate rectorite (REC) were fully mixed and the mixtures were subsequently electrosprayed nano-sized spheres, which were immobilized on the surface of electrospun polystyrene (PS) mats for metal adsorption. The morphology analysis taken from SEM confirmed that CS-REC nanospheres were loaded on the surface of PS fibrous mats. Small Angle X-ray diffraction patterns showed that the interlayer distance of REC in composite mats was enlarged by the intercalation of CS chains; such structure meant bigger surface area which was helpful for metal adsorption. The data of contact angle implied that PS mats coated with CS-REC nanospheres exhibited better hydrophilicity than PS mats, which was conductive to adsorption rate. Besides, the copper ions adsorption of composite mats was tested at different conditions including the adsorption time, the initial pH and the initial concentration of copper ion. The results demonstrated that PS mats coated with CS-REC nanospheres had the adsorption capacity up to 134 mg/g. In addition, the addition of REC containing Ca2+ could also improve the metal adsorption because of cation exchange. The desorption assay indicated that PS mats immobilized with CS and CS-REC still kept high adsorption ability which retained 74% and 78% after three adsorption-desorption cycles.

  17. Oxygen adsorption on Cu(111) using low energy ion scattering spectroscopy

    International Nuclear Information System (INIS)

    Zhang, F.M.; Yao, J.; Shen, Y.G.; King, B.V.; O'Connor, D.J.

    1993-01-01

    The surface structure and oxygen adsorption of Cu(l 11) have been studied by 2 keV Li + , He + and Ar + ion scattering . Incident and azimuthal dependences were measured for the clean and O-covered surfaces, and the surface geometry was analysed on the basis of the shadowing features. Experimental results under different oxygen exposures at room temperature showed that the Cu(l 11) surface undergoes a roughening transition and results in a reconstruction where Cu atoms are vertically displaced by about 0.23 Angstroms. 4 refs., 4 figs

  18. Oxygen adsorption on Cu(111) using low energy ion scattering spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, F M; Yao, J; Shen, Y G; King, B V; O` Connor, D J [Newcastle Univ., NSW (Australia). Dept. of Physics

    1994-12-31

    The surface structure and oxygen adsorption of Cu(l 11) have been studied by 2 keV Li{sup +}, He{sup +} and Ar{sup +} ion scattering . Incident and azimuthal dependences were measured for the clean and O-covered surfaces, and the surface geometry was analysed on the basis of the shadowing features. Experimental results under different oxygen exposures at room temperature showed that the Cu(l 11) surface undergoes a roughening transition and results in a reconstruction where Cu atoms are vertically displaced by about 0.23 Angstroms. 4 refs., 4 figs.

  19. Oxygen adsorption on Cu(111) using low energy ion scattering spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, F.M.; Yao, J.; Shen, Y.G.; King, B.V.; O`Connor, D.J. [Newcastle Univ., NSW (Australia). Dept. of Physics

    1993-12-31

    The surface structure and oxygen adsorption of Cu(l 11) have been studied by 2 keV Li{sup +}, He{sup +} and Ar{sup +} ion scattering . Incident and azimuthal dependences were measured for the clean and O-covered surfaces, and the surface geometry was analysed on the basis of the shadowing features. Experimental results under different oxygen exposures at room temperature showed that the Cu(l 11) surface undergoes a roughening transition and results in a reconstruction where Cu atoms are vertically displaced by about 0.23 Angstroms. 4 refs., 4 figs.

  20. The Impact of Template Types on Polyeugenol to the Adsorption Selectivity of Ionic Imprinted Polymer (IIP) Fe Metal Ion

    Science.gov (United States)

    Djunaidi, M. C.; Haris, A.; Pardoyo; Rosdiana, K.

    2018-04-01

    The synthesis of IIP was carried out by variation of Fe(III) ion templates from Fe(NO3)3, K3[Fe(CN)6] and NH4Fe(SO4)2 compounds which then tested IIP selectivity to the Fe metal ions through adsorption process. Ionic Imprinted Polymer (IIP) is a method of printing metal ions bound in a polymer, subsequently released from the polymer matrix to produce a suitable imprint for the target ion. The purposes of this study were to produce IIP from Fe(NO3)3, K3[Fe(CN)6] and NH4Fe(SO4)2 templates, to know the effect of templates on adsorption selectivity of IIP involving imprint cavity, and to know the impact of metal competitor on the selectivity adsorption of IIP to the Fe metals. The results obtained showed that IIP synthesized by variations of Fe(NO3)3, K3[Fe(CN)6] and NH4Fe(SO4)2 templates were successfully synthesized. The adsorption selectivity of Fe (III) metal ion in the Fe(NO3)3 template was greater than that of in the K3[Fe(CN)6] and NH4Fe(SO4)2 templates. The adsorption selectivity of Fe was greater on Fe-Cr compared to on Fe-Cd and Fe-Pb.

  1. Influence of activated carbon surface acidity on adsorption of heavy metal ions and aromatics from aqueous solution

    International Nuclear Information System (INIS)

    Sato, Sanae; Yoshihara, Kazuya; Moriyama, Koji; Machida, Motoi; Tatsumoto, Hideki

    2007-01-01

    Adsorption of toxic heavy metal ions and aromatic compounds onto activated carbons of various amount of surface C-O complexes were examined to study the optimum surface conditions for adsorption in aqueous phase. Cadmium(II) and zinc(II) were used as heavy metal ions, and phenol and nitrobenzene as aromatic compounds, respectively. Activated carbon was de-ashed followed by oxidation with nitric acid, and then it was stepwise out-gassed in helium flow up to 1273 K to gradually remove C-O complexes introduced by the oxidation. The oxidized activated carbon exhibited superior adsorption for heavy metal ions but poor performance for aromatic compounds. Both heavy metal ions and aromatics can be removed to much extent by the out-gassed activated carbon at 1273 K. Removing C-O complexes, the adsorption mechanisms would be switched from ion exchange to Cπ-cation interaction for the heavy metals adsorption, and from some kind of oxygen-aromatics interaction to π-π dispersion for the aromatics

  2. Dielectric behaviour of strontium tartrate single crystals

    Indian Academy of Sciences (India)

    Unknown

    dielectric loss (tan δ) as functions of frequency and temperature. Ion core type ... Since the data on dielectric properties of strontium tartrate trihydrate (STT) do not ... through 'AE' make 15-amp dimmerstat, the rate of heating was maintained ...

  3. Effect of Pb2+ ions on ilmenite flotation and adsorption of benzohydroxamic acid as a collector

    Science.gov (United States)

    Xu, Longhua; Tian, Jia; Wu, Houqin; Lu, Zhongyuan; Yang, Yaohui; Sun, Wei; Hu, Yuehua

    2017-12-01

    The effects of Pb2+ ions on ilmenite flotation and adsorption of benzohydroxamic acid (BHA) as a collector were investigated using microflotation tests, zeta potential measurements, adsorption analysis, Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). The microflotation results indicate that the addition of Pb2+ significantly improves the recovery of ilmenite using BHA as a collector. A maximum recovery of 88.46% is obtained at pH 8.12 in the presence of Pb2+; a maximum recovery of 45% is obtained at the same pH using BHA alone. At pHs below 8.0, lead nitrate are mainly present in the solution as Pb2+ and PbOH+, while at pHs above 8.0, the predominant components are Pb(OH)2(s) and Pb(OH)3-. The adsorption of these lead species influences the zeta potential of ilmenite and the number of activated sites on the ilmenite surface. FTIR and XPS analyses reveal that lead species and BHA react with the metal sites on the ilmenite surface. The lead species in solution are either adsorbed onto the ilmenite surface, which increases the surface activity of ilmenite, or react with BHA in solution to form complexes of lead and BHA.

  4. Adsorption of pertechnetate ion on various active carbons from mineral acid solutions

    International Nuclear Information System (INIS)

    Ito, K.

    1991-01-01

    The adsorption behavior of pertechnetate ion (TcO 4 - ) on active carbon has been studied for various acid solutions, taking as indicative value the distribution coefficient K d of Tc between active carbon surface and solution. In a system where the total anion concentration of the acid and its sodium salt was maintained constant, modifying the pH of the solution proved distinctly to influence the Tc adsorption behavior of active carbon: taking the case of active carbon derived from coconut shell, increasing the acidity raised K d ; around neutrality there occurred a level stage; in the alkali region, K d declined. The rise of K d in the acid region, however, was observed only with active carbon derived from coconut shell, from oil pitch or from saw dust; it failed to occur when the active carbon was derived from coal or from bone. With a hydrochloric acid system, the rise of K d started around 1 M (mol dm -1 ) HCl. Beyond 3 M, on the other hand, a breakthrough occurred, and K d declined with increasing acidity. With a nitric acid system, K d rose from 1 M, and the breakthrough occurred at 2 M. When the adsorption was left to equilibrate beyond 4 h, desorption displacement of TcO 4 - by a coexisting other anion was observed in the case of perchloric acid solutions of concentration above 0.1 M and with sulfuric acid solutions above 0.5 M. (author)

  5. Development of an improved ion-exchange process for removing cesium and strontium from high-level radioactive liquid wastes

    International Nuclear Information System (INIS)

    Wallace, R.M.; Ferguson, R.B.

    1980-11-01

    Processes are being developed to solidify and isolate the biologically hazardous radionuclides from approximately 23 million gallons of alkaline high-level waste accumulated at the Savannah River Plant. The waste consists mainly of a liquid supernate, a damp salt cake, and a gelatinous, insoluble sludge. The reference solidification process involves separation of the water soluble fraction (supernate) from the insoluble fraction, removal of cesium and traces of strontium from the supernate, incorporation of the sludge and the radionuclides from the supernate in glass, and incorporation of the residual salt in concrete. A new process, now being developed, involves sorbing cesium on phenolic resins that contain no strongly acidic sulfonate groups. These resins can then be eluted with formic acid which is not possible with Duolite ARC-359. Duolite CS-100, a phenol-carboxylate resin, was chosen for further development because of its greater breakthrough capacity and because it also sorbs strontium to some extent. Strontium sorption by CS-100 was not sufficient to eliminate the need for Amberlite IRC-718. However, the latter resin can also be eluted with formic acid because its functional groups are weakly acidic. Formic acid elution permits several options to be considered. The preferred option consists simply of mixing the eluate with sludge prior to calcination. Sodium formate, which is formed when the resins in the sodium form are eluted, decomposes rapidly between 450 0 C and 500 0 C and will be destroyed in either the calciner or the melter. The resulting sodium oxide would be incorporated into glass. The principal advantage of the new process is the elimination of a number of process steps

  6. Effect of lithium and sodium ion adsorption on the electronic transport properties of Ti3C2 MXene

    International Nuclear Information System (INIS)

    Berdiyorov, G.R.

    2015-01-01

    Highlights: • Effect of Li and Na ion adsorption on the electronic transport in Ti 3 C 2 MXene is studied. • Fluorinated, oxidized and hydroxylated surfaces are considered. • Enhanced charge transport is obtained for fluorinated and hydroxylated samples. • Electronic transmission is reduced in the oxidized sample. • The pristine and oxidized MXene samples are found to be sensitive to the ions adsorption. - Abstract: MXenes are found to be promising electrode materials for energy storage applications. Recent theoretical and experimental studies indicate the possibility of using these novel low dimensional materials for metal-ion batteries. Herein, we use density-functional theory in combination with the nonequilibrium Green's function formalism to study the effect of lithium and sodium ion adsorption on the electronic transport properties of the MXene, Ti 3 C 2 . Oxygen, hydroxyl and fluorine terminated species are considered and the obtained results are compared with the ones for the pristine MXene. We found that the ion adsorption results in reduced electronic transport in the pristine MXene: depending on the type of the ions and the bias voltage, the current in the system can be reduced by more than 30%. On the other hand, transport properties of the oxygen terminated sample can be improved by the ion adsorption: for both types of ions the current in the system can be increased by more than a factor of 4. However, the electronic transport is less affected by the ions in fluorinated and hydroxylated samples. These two samples show enhanced electronic transport as compared to the pristine MXene. The obtained results are explained in terms of electron localization in the system.

  7. Magnetic and microwave absorption properties of rare earth ions (Sm{sup 3+}, Er{sup 3+}) doped strontium ferrite and its nanocomposites with polypyrrole

    Energy Technology Data Exchange (ETDEWEB)

    Luo, Juhua, E-mail: luojuhua@163.com [School of Materials Engineering, Yancheng Institute of Technology, Yancheng 224051 (China); Xu, Yang; Mao, Hongkai [School of Material Science and Engineering, Jiangsu University, Zhenjiang 212013 (China)

    2015-05-01

    M-type strontium ferrite substituted by RE (RE=Sm{sup 3+}, Er{sup 3+}) were prepared via a sol–gel method. Polypyrrole (PPy)/ferrite nanocomposites (with 20 wt% ferrite) were prepared by in situ polymerization method in the presence of ammonium persulfate. Effect of the substituted RE ions on structure, magnetic properties and microwave absorption properties were investigated by X-ray diffraction (XRD), vibrating sample magnetometer (VSM) and vector network analyzer. All XRD patterns show the single phase of strontium hexaferrite without other intermediate phases. The crystallite size of synthesized particle is within the range of 22.2–38.1 nm. The structural in character of the composites were investigated with FT-IR analysis. It shows that the ferrite successfully packed by PPy. TEM photographs show that the particle size had grown up to 50–100 nm after coating with PPy. In the magnetization for the PPy/SrSm{sub 0.3}Fe{sub 11.7}O{sub 19} (SrEr{sub 0.3}Fe{sub 11.7}O{sub 19}) composites, the coercivity (H{sub c}) of the composites both increased compared with the undoped composite while the saturation magnetization (M{sub s}) appeared opposite change with different RE ions. Considering the electromagnetic loss and impedance matching comprehensively, the Er-doped ferrite/PPy composite got the better microwave absorption performance with the maximum RL value of −24.01 dB in 13.8 GHz at 3.0 mm. And its width (<−10 dB) has reached 7.2 GHz which has covered the whole Ku band. - Highlights: • The influence of RE ions on the structure of PPy/SrRE{sub 0.3}Fe{sub 11.7}O{sub 19} is discussed. • The influence of RE ions on the magnetic properties of PPy/SrRE{sub 0.3}Fe{sub 11.7}O{sub 19} is discussed. • The influence of RE ions on electromagnetic losses of PPy/SrRE{sub 0.3}Fe{sub 11.7}O{sub 19} is discussed. • PPy/SrEr{sub 0.3}Fe{sub 11.7}O{sub 19} possessed the excellent absorption property.

  8. Lithium ion adsorptive properties of spinel-type manganese oxide obtained from MnOOH and Li2CO3

    International Nuclear Information System (INIS)

    Ooi, Kenta; Miyai, Yoshitaka; Katoh, Shunsaku; Abe, Mitsuo.

    1991-01-01

    Spinel-type manganese oxides were prepared by heating a mixture of MnOOH and Li 2 CO 3 (Li/Mn = 0.5) at different temperatures followed by an acid treatment with a HCl solution. Their adsorptive properties for alkali metal ions were investigated by measurement of distribution coefficient (Kd) and by pH titration. The adsorptive properties varied depending on the heating temperature. The sample obtained at 400degC showed the highest Li + adsorptivity from seawater. (author)

  9. Adsorption of cadmium ions on nickel surface skeleton catalysts and its effect on reaction of cathodic hydrogen evolution

    International Nuclear Information System (INIS)

    Korovin, N.V.; Udris, E.Ya.; Savel'eva, O.N.

    1986-01-01

    Cadmium adsorption from different concentration CdSO 4 solutions on nickel surface skeleton catalysts (Ni ssc ) is studied by recording of polarization and potentiodynamic curves using electron microscopy and X-ray spectrometry. Main regularities of cadmium adsorption on Ni ssc are shown to be similar to those on smooth and skeleton nickel. A conclusion is drawn that increase of catalytic activity in reaction of cathodic hydrogen evolution from alkali solutions of Ni ssc base electrodes after their treatment in solutions containing Cd 2+ ions is due to irreversible desorption of strongly and averagely bound hydrogen from electrode surface at cadmium adsorption on them

  10. Incorporating water-release and lateral protein interactions in modeling equilibrium adsorption for ion-exchange chromatography.

    Science.gov (United States)

    Thrash, Marvin E; Pinto, Neville G

    2006-09-08

    The equilibrium adsorption of two albumin proteins on a commercial ion exchanger has been studied using a colloidal model. The model accounts for electrostatic and van der Waals forces between proteins and the ion exchanger surface, the energy of interaction between adsorbed proteins, and the contribution of entropy from water-release accompanying protein adsorption. Protein-surface interactions were calculated using methods previously reported in the literature. Lateral interactions between adsorbed proteins were experimentally measured with microcalorimetry. Water-release was estimated by applying the preferential interaction approach to chromatographic retention data. The adsorption of ovalbumin and bovine serum albumin on an anion exchanger at solution pH>pI of protein was measured. The experimental isotherms have been modeled from the linear region to saturation, and the influence of three modulating alkali chlorides on capacity has been evaluated. The heat of adsorption is endothermic for all cases studied, despite the fact that the net charge on the protein is opposite that of the adsorbing surface. Strong repulsive forces between adsorbed proteins underlie the endothermic heat of adsorption, and these forces intensify with protein loading. It was found that the driving force for adsorption is the entropy increase due to the release of water from the protein and adsorbent surfaces. It is shown that the colloidal model predicts protein adsorption capacity in both the linear and non-linear isotherm regions, and can account for the effects of modulating salt.

  11. Adsorption of arsenite and selenite using an inorganic ion exchanger based on Fe–Mn hydrous oxide

    KAUST Repository

    Szlachta, Małgorzata; Gerda, Vasyl; Chubar, Natalia

    2012-01-01

    The adsorption behaviour and mechanism of As(III) and Se(IV) oxyanion uptake using a mixed inorganic adsorbent were studied. The novel adsorbent, based on Fe(III)-Mn(III) hydrous oxides and manganese(II) carbonate, was synthesised using a hydrothermal precipitation approach in the presence of urea. The inorganic ion exchanger exhibited a high selectivity and adsorptive capacity towards As(III) (up to 47.6mg/g) and Se(IV) (up to 29.0mg/g), even at low equilibrium concentration. Although pH effects were typical for anionic species (i.e., the adsorption decreased upon pH increase), Se(IV) was more sensitive to pH changes than As(III). The rates of adsorption of both oxyanions were high. Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) studies showed that the ion exchange adsorption of both anions took place via OH - groups, mainly from Fe(III) but also Mn(III) hydrous oxides. MnCO 3 did not contribute directly to As(III) and Se(IV) removal. A higher adsorptive capacity of the developed material towards As(III) was partly due to partial As(III) oxidation during adsorption. © 2011 Elsevier Inc.

  12. Adsorption Effectivity Test of Andisols Clay-Zeolite (ACZ) Composite as Chromium Hexavalent (Cr(VI)) Ion Adsorbent

    Science.gov (United States)

    Pranoto; Masykur, A.; Nugroho, Y. A.

    2018-03-01

    Adsorption of chromium hexavalent (Cr(VI)) ion in aqueous solution was investigated. This research was purposed to study the influence of the composition of ACZ, temperature activation, and contact time against adsorption capacity of Cr(VI) ion in aqueous solution. Determination of adsorption effectivity using several parameter such as composition variation of ACZ, contact time, pH, activation temperature, and concentration. In this research, andisol clay and zeolite has been activated with NaOH 3 M and 1 M, respectively. Temperature variation used 100, 200, and 400°C. While composition variation ACZ used 0:100, 25:75, 50:50, 75:25, 100:0. The pH variation was used 2 – 6 and concentration variation using 2, 4, 6, 8, 10, and 12 ppm. Characterization in this research used such as UV-Vis, Surface Area Analyzer (SAA) and Acidity Analysis. Result of this research is known that optimum composition of ACZ was 50:50 with calcination temperature 100°C. Optimum adsorption of Cr(VI) at pH 4 with removal percentage 76.10 % with initial concentration 2 ppm and adsorption capacity is 0.16 mg/g. Adsorption isotherm following freundlich isotherm with value Kf = 0.17 mg/g and value n is 0.963. Based on results, ACZ composite can be used as Cr(VI) ion adsorbents in aqueous solutions.

  13. Adsorption of 90Sr and 90Y by bottom-set beds in the Atlantic ocean

    International Nuclear Information System (INIS)

    Gromov, V.V.; Shakhova, N.F.; Emel'yanov, E.M.

    1978-01-01

    The behaviour of 90 Sr and 90 Y has been studied in an adsorption system of sea water-bottom-set beds of the Atlantic ocean (red clay; pelitic silt). It has been shown that strontium is present in the sea water in one form, viz, Sr 2+ . Adsorption of 90 Sr with bottom-set beds follows the ion-exchange mechanism. Yttrium is present in the sea water at least three forms (two absorbable and one non-absorbable). Yttrium-90 adsorption is an irreversible process and only about 10% 90 Y is desorbed by the sea water from red clay and silt

  14. Determination of deuterium adsorption site on palladium(1 0 0) using low energy ion recoil spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Kambali, I. [Department of Physics, University of Newcastle, Callaghan (Australia); O' Connor, D.J. [Department of Physics, University of Newcastle, Callaghan (Australia)], E-mail: john.oconnor@newcastle.edu.au; Gladys, M.J. [Department of Physics, University of Newcastle, Callaghan (Australia); Karolewski, M.A. [Department of Chemistry, University of Brunei Darussalam, Gadong BE1410 (Brunei Darussalam)

    2008-05-15

    Ion beam analysis has been recently applied to study the adsorption phenomena of some adsorbates on metal surfaces. In this paper, surface recoils created by low energy Ne{sup +} ions are employed to study the adsorption site of deuterium (D) atoms on Pd(1 0 0). This technique is extremely surface sensitive with the capacity for atomic layer depth resolution. From azimuthal angle observations of Pd(1 0 0) specimen, it was found that at room temperature, D was adsorbed in the fourfold hollow site of Pd(1 0 0) at a height of 0.25 {+-} 0.05 A above the surface. The adsorbate remains in the hollow site at all temperatures to 383 K though the vertical height above the surface is found to depend on coverage and for the first time evidence is found of a transition to a p(2 x 2) structure for the adsorbate. There is no evidence of D sitting in the Pd(1 0 0) subsurface at room and higher temperatures.

  15. Equilibria model for pH variations and ion adsorption in capacitive deionization electrodes.

    Science.gov (United States)

    Hemmatifar, Ali; Oyarzun, Diego I; Palko, James W; Hawks, Steven A; Stadermann, Michael; Santiago, Juan G

    2017-10-01

    Ion adsorption and equilibrium between electrolyte and microstructure of porous electrodes are at the heart of capacitive deionization (CDI) research. Surface functional groups are among the factors which fundamentally affect adsorption characteristics of the material and hence CDI system performance in general. Current CDI-based models for surface charge are mainly based on a fixed (constant) charge density, and do not treat acid-base equilibria of electrode microstructure including so-called micropores. We here expand current models by coupling the modified Donnan (mD) model with weak electrolyte acid-base equilibria theory. In our model, surface charge density can vary based on equilibrium constants (pK's) of individual surface groups as well as micropore and electrolyte pH environments. In this initial paper, we consider this equilibrium in the absence of Faradaic reactions. The model shows the preferential adsorption of cations versus anions to surfaces with respectively acidic or basic surface functional groups. We introduce a new parameter we term "chemical charge efficiency" to quantify efficiency of salt removal due to surface functional groups. We validate our model using well controlled titration experiments for an activated carbon cloth (ACC), and quantify initial and final pH of solution after adding the ACC sample. We also leverage inductively coupled plasma mass spectrometry (ICP-MS) and ion chromatography (IC) to quantify the final background concentrations of individual ionic species. Our results show a very good agreement between experiments and model. The model is extendable to a wide variety of porous electrode systems and CDI systems with applied potential. Copyright © 2017 Elsevier Ltd. All rights reserved.

  16. Study of polyethyleneimine- and amidoxime-functionalized hybrid biomass of Spirulina (Arthrospira) platensis for adsorption of uranium (VI) ion.

    Science.gov (United States)

    Bayramoglu, Gulay; Akbulut, Aydin; Arica, M Yakup

    2015-11-01

    This study investigates the potential application of the polyethyleneimine- (PEI) and amidoxime-modified Spirulina (Arthrospira) platensis biomasses for the removal of uranium ion in batch mode using the native biomass as a control system. The uranium ion adsorption was also characterized by attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectra, zeta potential analysis, and surface area measurement studies. The effects of pH, biomass amount, contact time, initial uranium ion concentration, and ionic strength were evaluated by using native and modified algal biomass preparations. The uranium ion removal was rapid, with more than 70% of total adsorption taking place in 40 min, and equilibrium was established within 60 min. From the experimental data, it was found that the amount of adsorption uranium ion on the algal preparations decreased in the following series: amidoxime-modified algal biomass > PEI-modified algal biomass > native algal biomass. Maximum adsorption capacities of amidoxime- and PEI-modified, and native algal biomasses were found to be 366.8, 279.5, and 194.6 mg/g, respectively, in batchwise studies. The adsorption rate of U(VI) ion by amidoxime-modified algal biomass was higher than those of the native and PEI-modified counterparts. The adsorption processes on all the algal biomass preparations followed by the Dubinin-Radushkevitch (D-R) and Temkin isotherms and pseudo-second-order kinetic models. The thermodynamic parameters were determined at four different temperatures (i.e., 15, 25, 35, and 45 °C) using the thermodynamics constant of the Temkin isotherm model. The ΔH° and ΔG° values of U(VI) ion adsorption on algal preparations show endothermic heat of adsorption; higher temperatures favor the process. The native and modified algal biomass preparations were regenerated using 10 mM HNO3. These results show that amidoxime-modified algal biomass can be a potential candidate for effective removal of U(VI) ion from

  17. Adsorption of phosphate in hydrocalumite-like layered double hydroxides: a comparison between memory effect and ion exchange processes

    International Nuclear Information System (INIS)

    Bernardo, M.P.; Moreira, F.K.V.; Ribeiro, C.

    2016-01-01

    Phosphorus is an essential element for agriculture, but the excessive use of this element has caused severe damages to the environment. Layered double hydroxide (LDHs) are excellent candidates to remove PO 4 3- anions through adsorption process. In this work, the phosphate adsorption on hydrocalumite-like (Ca-Al) LDHs was evaluated over the ion exchange and memory effect processes. X-ray diffraction measurements revealed formation of analogous crystalline phases from both process as the phosphate concentration was increased. However, the phosphate quantity adsorbed varied according to the process used. The ion exchange route is the most efficient process to remove phosphate from aqueous medium. (author)

  18. Research advances in adsorption treatment of cesium and cobalt in waste liquid of nuclear power plants by ion exchange resin

    International Nuclear Information System (INIS)

    Liu Dan; Wang Xin; Liu Jiean; Zhu Laiye; Chen Bin; Weng Minghui

    2014-01-01

    Liquid radwaste is unavoidably produced during the operation of nuclear power plants (NPP). With the development of China's nuclear power, much more attention will be paid to the impact of NPP construction on water environment. Radionuclides are the main targets for adsorption treatment of NPP liquid radwaste. Thereinto, cesium and cobalt are typical cationic ones. Currently, ion exchange process is widely used in liquid radwaste treatment system (WLS) of NPP, wherein resin plays a key role. The paper reviewed the research progress on adsorption of cesium and cobalt existed in NPP liquid radwaste using ion exchange resin. (authors)

  19. Optical properties and energy transfer behavior from Tb{sup 3+} to Mn{sup 2+} ions in co-doped zinc strontium phosphate glasses

    Energy Technology Data Exchange (ETDEWEB)

    Liang Xiaoluan [Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237 (China); Xing Zhongwen [Department of Materials Science and Engineering, Nanjing University, Nanjing 210093 (China); Liu Yinyao; Xu Weina; Yang Yunxia [Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237 (China); Chen Guorong, E-mail: grchen@ecust.edu.cn [Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237 (China)

    2011-10-17

    Highlights: {yields} We choose Tb{sup 3+} as the sensitizer to enhance the emission of Mn{sup 2+} ions in ZSP glasses. {yields} We make a serious of characterization on the optical properties of the glasses. {yields} Tb{sup 3+} can transfer its energy to the neighbor Mn{sup 2+} during excitation process. {yields} The energy transfer mechanism is dipolar-quadrupole interaction in phosphate glasses. {yields} Meanwhile, this process is taken by two modes: cross-relaxation and resonant transfer. - Abstract: In this paper, we report optical properties and energy transfer behavior between Tb and Mn in zinc strontium phosphate glasses. Electron Paramagnetic Resonance spectra indicate a stronger hyperfine interaction of Mn{sup 2+}-Mn{sup 2+} pairs with higher MnO concentrations. The co-existence of Tb{sup 3+} and Mn{sup 2+} ions in glasses is clearly evident in the transmittance spectra. Emission spectra show an obvious energy transfer from Tb{sup 3+} to Mn{sup 2+} ions in glasses. Based on Dexter's energy transfer formula and Reisfeld's approximation, the energy transfer mechanism was postulated to proceed via a dipolar-quadrupole interaction. The energy transfer carries out with resonant and cross-relaxation transfer modes with the understanding of Tb{sup 3+} and Mn{sup 2+} energy level diagrams. The decreasing in mean-duration time ({tau}{sub mean}) of Tb{sup 3+} ions obtained from the decay curves make a further evidence of energy transfer from Tb{sup 3+} to Mn{sup 2+} ions in glasses.

  20. Adsorption of Pb(II) ions from aqueous solutions by date bead carbon activated with ZnCl{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Danish, Mohammed; Hashim, Rokiah; Rafatullah, Mohd; Sulaiman, Othman [Division of Bioresource, Paper and Coatings Technology, School of Industrial Technology, Universiti Sains Malaysia, Penang (Malaysia); Ahmad, Anees [Division of Environmental Technology, School of Industrial Technology, Universiti Sains Malaysia, Penang (Malaysia); Govind [Surface Physics and Nanostructures Group, National Physical Laboratory, New Delhi (India)

    2011-04-15

    This study reports on the adsorption characteristics of Pb(II) ions from aqueous solutions using ZnCl{sub 2}-activated date (Phoenix dactylifera) bead (ADB) carbon with respect to change in adsorbent dosage, initial pH, contact time, initial concentration, and temperature of the solution. Kinetic studies of the data showed that the adsorption follows the pseudo-second-order kinetic model. Thermodynamic parameters, enthalpy change ({Delta}H = 55.11 kJ/mol), entropy change ({Delta}S = - 0.193 kJ/mol/K), and Gibbs free energy change ({Delta}G ) were also calculated for the uptake of Pb(II) ions. These parameters show that adsorption on the surface of ADB was feasible, spontaneous in nature, and endothermic between temperatures of 298.2 and 318.2 K. The equilibrium data better fitted the Langmuir and Freundlich isotherm models than the D-R adsorption isotherm model for studying the adsorption behavior of Pb(II) onto the ADB carbon. It could be observed that the maximum adsorption capacity of ADB was 76.92 mg/g at 318.2 K and pH 6.5. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  1. Preparation of chitosan/MCM-41-PAA nanocomposites and the adsorption behaviour of Hg(II) ions

    Science.gov (United States)

    Fu, Yong; Huang, Yue; Hu, Jianshe

    2018-03-01

    A novel functional hybrid mesoporous composite material (CMP) based on chitosan and MCM-41-PAA was reported and its application as an excellent adsorbent for Hg(II) ions was also investigated. Innovatively, MCM-41-PAA was prepared by using diatomite and polyacrylic acid (PAA) with integrated polymer-silica hybrid frameworks, and then CMP was fabricated by introducing MCM-41-PAA to chitosan using glutaraldehyde as a cross-linking agent. The structure and morphology of CMP were characterized by X-ray diffraction, Fourier transform infrared spectra, thermogravimetric analysis, scanning electron microscopy and Brunauer-Emmett-Teller measurements. The results showed that the CMP possessed multifunctional groups such as -OH, -COOH and -NH2 with large specific surface area. Adsorption behaviour of Hg(II) ions onto CMP was fitted better by the pseudo-second-order kinetic model and the Langmuir model when the initial Hg(II) concentration, pH, adsorption temperature and time were 200 mg l-1, 4, 298 K and 120 min, respectively, as the optimum conditions. The corresponding maximum adsorption capacity could reach 164 mg g-1. According to the thermodynamic parameters determined such as free energy, enthalpy and entropy, the adsorption process of Hg(II) ions was spontaneous endothermic adsorption.

  2. Preparation of chitosan/MCM-41-PAA nanocomposites and the adsorption behaviour of Hg(II) ions

    Science.gov (United States)

    Fu, Yong; Huang, Yue; Hu, Jianshe

    2018-01-01

    A novel functional hybrid mesoporous composite material (CMP) based on chitosan and MCM-41-PAA was reported and its application as an excellent adsorbent for Hg(II) ions was also investigated. Innovatively, MCM-41-PAA was prepared by using diatomite and polyacrylic acid (PAA) with integrated polymer–silica hybrid frameworks, and then CMP was fabricated by introducing MCM-41-PAA to chitosan using glutaraldehyde as a cross-linking agent. The structure and morphology of CMP were characterized by X-ray diffraction, Fourier transform infrared spectra, thermogravimetric analysis, scanning electron microscopy and Brunauer–Emmett–Teller measurements. The results showed that the CMP possessed multifunctional groups such as –OH, –COOH and –NH2 with large specific surface area. Adsorption behaviour of Hg(II) ions onto CMP was fitted better by the pseudo-second-order kinetic model and the Langmuir model when the initial Hg(II) concentration, pH, adsorption temperature and time were 200 mg l−1, 4, 298 K and 120 min, respectively, as the optimum conditions. The corresponding maximum adsorption capacity could reach 164 mg g−1. According to the thermodynamic parameters determined such as free energy, enthalpy and entropy, the adsorption process of Hg(II) ions was spontaneous endothermic adsorption. PMID:29657793

  3. Mass measurements of neutron-rich strontium and rubidium isotopes in the region $A \\approx 100$ and development of an electrospray ionization ion source

    CERN Document Server

    de Roubin, Antoine

    An extension of the atomic mass surface in the region $A \\approx 100$ is performed via mass measurements of the $^{100−102}$Sr and $^{100−102}$Rb isotopes with the ion-trap mass spectrometer ISOLTRAP at CERN-ISOLDE. The first direct mass measurements of $^{102}$Sr and $^{101,102}$Rb are reported here. These measurements confirm the continuation of the region of nuclear deformation with the increase of neutron number, at least as far as $N = 65$. In order to interpret the deformation in the strontium isotopic chain and to determine whether an onset of deformation is present in heavier krypton isotopes, a comparison is made between experimental values and theoretical calculations available in the literature. To complete this comparison, Hartree-Fock-Bogoliubov calculations for even and odd isotopes are also presented, illustrating the competition of nuclear shapes in the region. The development of an electrospray ionization ion source is presented. This source can deliver a large range of isobaric masses ...

  4. Preparation of highly ordered cubic NaA zeolite from halloysite mineral for adsorption of ammonium ions

    International Nuclear Information System (INIS)

    Zhao Yafei; Zhang Bing; Zhang Xiang; Wang Jinhua; Liu Jindun; Chen Rongfeng

    2010-01-01

    Well-ordered cubic NaA zeolite was first synthesized using natural halloysite mineral with nanotubular structure as source material by hydro-thermal method. SEM and HRTEM images indicate that the synthesized NaA zeolite is cubic-shaped crystal with planar surface, well-defined edges and symmetrical and uniform pore channels. The adsorption behavior of ammonium ions (NH 4 + ) from aqueous solution onto NaA zeolite was investigated as a function of parameters such as equilibrium time, pH, initial NH 4 + concentration, temperature and competitive cations. The Langmuir and Freundlich adsorption models were applied to describe the equilibrium isotherms. A maximum adsorption capacity of 44.3 mg g -1 of NH 4 + was achieved. The regeneration and reusable ability of this adsorbent was evaluated, and the results indicated that the recovered adsorbent could be used again for NH 4 + removal with nearly constant adsorption capacity. Thermodynamic parameters such as change in free energy (ΔG 0 ), enthalpy (ΔH 0 ) and entropy (ΔS 0 ) were also determined, which indicated that the adsorption was a spontaneous and exothermic process at ambient conditions. Compared with other adsorbents, the as-synthesized NaA zeolite displays a faster adsorption rate and higher adsorption capacity, which implies potential application for removing NH 4 + pollutants from wastewaters.

  5. Preparation of highly ordered cubic NaA zeolite from halloysite mineral for adsorption of ammonium ions

    Energy Technology Data Exchange (ETDEWEB)

    Zhao Yafei [School of Chemical Engineering, Zhengzhou University, Zhengzhou 450001 (China); Zhang Bing, E-mail: zhangb@zzu.edu.cn [School of Chemical Engineering, Zhengzhou University, Zhengzhou 450001 (China); Henan Academy of Sciences, Zhengzhou 450002 (China); Zhang Xiang; Wang Jinhua; Liu Jindun [School of Chemical Engineering, Zhengzhou University, Zhengzhou 450001 (China); Chen Rongfeng [Henan Academy of Sciences, Zhengzhou 450002 (China)

    2010-06-15

    Well-ordered cubic NaA zeolite was first synthesized using natural halloysite mineral with nanotubular structure as source material by hydro-thermal method. SEM and HRTEM images indicate that the synthesized NaA zeolite is cubic-shaped crystal with planar surface, well-defined edges and symmetrical and uniform pore channels. The adsorption behavior of ammonium ions (NH{sub 4}{sup +}) from aqueous solution onto NaA zeolite was investigated as a function of parameters such as equilibrium time, pH, initial NH{sub 4}{sup +} concentration, temperature and competitive cations. The Langmuir and Freundlich adsorption models were applied to describe the equilibrium isotherms. A maximum adsorption capacity of 44.3 mg g{sup -1} of NH{sub 4}{sup +} was achieved. The regeneration and reusable ability of this adsorbent was evaluated, and the results indicated that the recovered adsorbent could be used again for NH{sub 4}{sup +} removal with nearly constant adsorption capacity. Thermodynamic parameters such as change in free energy ({Delta}G{sup 0}), enthalpy ({Delta}H{sup 0}) and entropy ({Delta}S{sup 0}) were also determined, which indicated that the adsorption was a spontaneous and exothermic process at ambient conditions. Compared with other adsorbents, the as-synthesized NaA zeolite displays a faster adsorption rate and higher adsorption capacity, which implies potential application for removing NH{sub 4}{sup +} pollutants from wastewaters.

  6. Preparation of highly ordered cubic NaA zeolite from halloysite mineral for adsorption of ammonium ions.

    Science.gov (United States)

    Zhao, Yafei; Zhang, Bing; Zhang, Xiang; Wang, Jinhua; Liu, Jindun; Chen, Rongfeng

    2010-06-15

    Well-ordered cubic NaA zeolite was first synthesized using natural halloysite mineral with nanotubular structure as source material by hydro-thermal method. SEM and HRTEM images indicate that the synthesized NaA zeolite is cubic-shaped crystal with planar surface, well-defined edges and symmetrical and uniform pore channels. The adsorption behavior of ammonium ions (NH(4)(+)) from aqueous solution onto NaA zeolite was investigated as a function of parameters such as equilibrium time, pH, initial NH(4)(+) concentration, temperature and competitive cations. The Langmuir and Freundlich adsorption models were applied to describe the equilibrium isotherms. A maximum adsorption capacity of 44.3 mg g(-1) of NH(4)(+) was achieved. The regeneration and reusable ability of this adsorbent was evaluated, and the results indicated that the recovered adsorbent could be used again for NH(4)(+) removal with nearly constant adsorption capacity. Thermodynamic parameters such as change in free energy (DeltaG(0)), enthalpy (DeltaH(0)) and entropy (DeltaS(0)) were also determined, which indicated that the adsorption was a spontaneous and exothermic process at ambient conditions. Compared with other adsorbents, the as-synthesized NaA zeolite displays a faster adsorption rate and higher adsorption capacity, which implies potential application for removing NH(4)(+) pollutants from wastewaters. Copyright 2010 Elsevier B.V. All rights reserved.

  7. Influence of pH on the adsorption of uranium ions by oxidized activated carbon and chitosan

    International Nuclear Information System (INIS)

    Park, G.I.; Park, H.S.; Woo, S.I.

    1999-01-01

    The adsorption characteristics of uranyl ions on surface-oxidized carbon were compared with those of powdered chitosan over a wide pH range. In particular, an extensive analysis was made on solution pH variation during the adsorption process or after adsorption equilibrium. Uranium adsorption on the two adsorbents was revealed to be strongly dependent on the initial pH of the solution. A quantitative comparison of the adsorption capacities of the two adsorbents was made, based on the isotherm data obtained at initial pH 3, 4, and 5. In order to analyze the adsorption kinetics incorporated with pH effects, batch experiments at various initial pH values were carried out, and solution pH profiles with the adsorption time were also evaluated. The breakthrough behavior in a column packed with oxidized carbon was also characterized with respect to the variation of effluent pH. Based on these experimental results, the practical applicability of oxidized carbon for uranium removal from acidic radioactive liquid waste was suggested

  8. Fabrication of electrospun polyacrylonitrile ion-exchange membranes for application in lysozyme adsorption

    Directory of Open Access Journals (Sweden)

    2011-04-01

    Full Text Available Ion exchange (IEX chromatography is commonly used in separation and purification systems. However, micropore blockage within its resin structure can easily lead to a reduction in the effectiveness of purification. To tackle this problem, we adopted the concept of membrane separation by combining electrospinning techniques with rapid alkaline hydrolysis to prepare a weak acid IEX nanofibrous membrane (AEA-COOH, consisting of polyethyleneterephthalate (PET meltblown fabric as a supporting layer, with upper and lower IEX layers consisting of polyacrylonitrile (PAN nanofibrous membranes. To determine the characteristics of the AEA-COOH membrane, we used the commercial product Sartobind© C IEX membrane as the standard of comparison. Results showed that the base weight and thickness of AEACOOH were 33 and 64%, relative to Sartobind© C membrane. The thermo-degradable temperature of AEA-COOH membrane (320°C was far higher than that of Sartobind© C (115°C, indicating high thermal stability. Finally, comparisons between the lysozyme adsorption rates and capacity of various IEX membranes confirmed that AEA-COOH was lighter, thinner, faster, possessing higher protein adsorption efficiency than Sartobind© C membrane.

  9. Modification of multi-walled carbon nanotubes with tannic acid for the adsorption of La, Tb and Lu ions

    International Nuclear Information System (INIS)

    Tong, S.; Zhao, S.; Zhou, W.; Jia, Q.; Li, R.

    2011-01-01

    We have prepared an environmental friendly sorbent by modifying multi-walled carbon nanotubes with tannic acid. The adsorption of La (III), Tb (III) and Lu (III) as a function of contact time, initial solution pH, and quantity of adsorbent was studied using a batch technique. Both Langmuir and Freundlich isotherms can be used to describe the process. The major adsorption mechanisms were attributed to ion exchange and surface complexation. The kinetics of the adsorption follows a pseudo-second-order model. The thermodynamic functions ΔH, ΔG, and ΔS indicate that the sorption is endothermically driven. The adsorbed ions can be readily desorbed from the surface with 1 M hydrochloric acid. (author)

  10. Adsorption of gold ions from industrial wastewater using activated carbon derived from hard shell of apricot stones - an agricultural waste.

    Science.gov (United States)

    Soleimani, Mansooreh; Kaghazchi, Tahereh

    2008-09-01

    In this study, hard shell of apricot stones was selected from agricultural solid wastes to prepare effective and low cost adsorbent for the gold separation from gold-plating wastewater. Different adsorption parameters like adsorbent dose, particle size of activated carbon, pH and agitation speed of mixing on the gold adsorption were studied. The results showed that under the optimum operating conditions, more than 98% of gold was adsorbed onto activated carbon after only 3h. The equilibrium adsorption data were well described by the Freundlich and Langmuir isotherms. Isotherms have been used to obtain thermodynamic parameters. Gold desorption studies were performed with aqueous solution mixture of sodium hydroxide and organic solvents at ambient temperatures. Quantitative recovery of gold ions is possible by this method. As hard shell of apricot stones is a discarded as waste from agricultural and food industries, the prepared activated carbon is expected to be an economical product for gold ion recovery from wastewater.

  11. Effects of common groundwater ions on chromate removal by magnetite: importance of chromate adsorption.

    Science.gov (United States)

    Meena, Amanda H; Arai, Yuji

    2016-01-01

    Reductive precipitation of hexavalent chromium (Cr(VI)) with magnetite is a well-known Cr(VI) remediation method to improve water quality. The rapid (important as the reductive precipitation of Cr(III) in describing the removal of Cr(VI) by magnetite, and these interfacial adsorption processes could be impacted by common groundwater ions like sulfate and nitrate. The results of this study highlight new information about the large quantity of adsorbed Cr(VI) surface complexes at the magnetite-water interface. It has implications for predicting the long-term stability of Cr at the magnetite-water interface.Graphical abstractEffects of background anions (sulfate and nitrate) on the Cr(VI) surface coverage at the magnetite-water interface at pH 4 and 9.

  12. Calculation of pollutant removal during groundwater restoration with adsorption and ion exchange

    International Nuclear Information System (INIS)

    Charbeneau, R.J.

    1982-01-01

    A technique is presented for calculating pollutant removal rates during groundwater restoration processes. The hydraulic information required by the method is obtained from the conservative tracer breakthrough curve for a flow system. The influence of adsorption and ion exchange chemistry on species transport is included through application of the method of characteristics. The combined result gives the effluent concentration at a production well as a function of time during a restoration project. The method is applicable for any well pattern and its economy is such that a pencil and paper calculation will suffice for yielding quantitative answers for complex flow problems. The method is applied to calculate ammonium removal rates for site restoration by recirculation with chemical sweeps following in situ leach mining of uranium

  13. Higher adsorption capacity of Spirulina platensis alga for Cr(VI) ions removal: parameter optimisation, equilibrium, kinetic and thermodynamic predictions.

    Science.gov (United States)

    Gunasundari, Elumalai; Senthil Kumar, Ponnusamy

    2017-04-01

    This study discusses about the biosorption of Cr(VI) ion from aqueous solution using ultrasonic assisted Spirulina platensis (UASP). The prepared UASP biosorbent was characterised by Fourier transform infrared spectroscopy, X-ray diffraction, Brunauer-Emmet-Teller, scanning electron spectroscopy and energy dispersive X-ray and thermogravimetric analyses. The optimum condition for the maximum removal of Cr(VI) ions for an initial concentration of 50 mg/l by UASP was measured as: adsorbent dose of 1 g/l, pH of 3.0, contact time of 30 min and temperature of 303 K. Adsorption isotherm, kinetics and thermodynamic parameters were calculated. Freundlich model provided the best results for the removal of Cr(VI) ions by UASP. The adsorption kinetics of Cr(VI) ions onto UASP showed that the pseudo-first-order model was well in line with the experimental data. In the thermodynamic study, the parameters like Gibb's free energy, enthalpy and entropy changes were evaluated. This result explains that the adsorption of Cr(VI) ions onto the UASP was exothermic and spontaneous in nature. Desorption of the biosorbent was done using different desorbing agents in which NaOH gave the best result. The prepared material showed higher affinity for the removal of Cr(VI) ions and this may be an alternative material to the existing commercial adsorbents.

  14. K2 Mn4 O8 /Reduced Graphene Oxide Nanocomposites for Excellent Lithium Storage and Adsorption of Lead Ions.

    Science.gov (United States)

    Hao, Shu-Meng; Qu, Jin; Yang, Jing; Gui, Chen-Xi; Wang, Qian-Qian; Li, Qian-Jie; Li, Xiaofeng; Yu, Zhong-Zhen

    2016-03-01

    Ion diffusion efficiency at the solid-liquid interface is an important factor for energy storage and adsorption from aqueous solution. Although K 2 Mn 4 O 8 (KMO) exhibits efficient ion diffusion and ion-exchange capacities, due to its high interlayer space of 0.70 nm, how to enhance its mass transfer performance is still an issue. Herein, novel layered KMO/reduced graphene oxide (RGO) nanocomposites are fabricated through the anchoring of KMO nanoplates on RGO with a mild solution process. The face-to-face structure facilitates fast transfer of lithium and lead ions; thus leading to excellent lithium storage and lead ion adsorption. The anchoring of KMO on RGO not only increases electrical conductivity of the layered nanocomposites, but also effectively prevents aggregation of KMO nanoplates. The KMO/RGO nanocomposite with an optimal RGO content exhibits a first cycle charge capacity of 739 mA h g -1 , which is much higher than that of KMO (326 mA h g -1 ). After 100 charge-discharge cycles, it still retains a charge capacity of 664 mA h g -1 . For the adsorption of lead ions, the KMO/RGO nanocomposite exhibits a capacity of 341 mg g -1 , which is higher than those of KMO (305 mg g -1 ) and RGO (63 mg g -1 ) alone. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  15. Adsorption and ion-pairing interactions of phospholipids in the system of two immiscible electrolyte solutions. Part II: ...

    Czech Academy of Sciences Publication Activity Database

    Jänchenová, Hana; Štulík, K.; Mareček, Vladimír

    2007-01-01

    Roč. 604, č. 2 (2007), s. 109-114 ISSN 0022-0728 R&D Projects: GA MŠk(CZ) LC06063 Institutional research plan: CEZ:AV0Z40400503 Keywords : liquid/liquid interfaces * adsorption of phosphodolipids * DPPC * surface-active amines * ion pairing Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.580, year: 2007

  16. Electric Double Layer at the Rutile (110) Surface. 2. Adsorption of Ions from Molecular Dynamics and X-ray Experiments

    Czech Academy of Sciences Publication Activity Database

    Předota, Milan; Zhang, Z.; Fenter, P.; Wesolowski, D.J.; Cummings, P.T.

    2004-01-01

    Roč. 108, č. 32 (2004), s. 12061-12072 ISSN 1520-6106 R&D Projects: GA ČR GP203/03/P083; GA ČR GA203/02/0805 Institutional research plan: CEZ:AV0Z4072921 Keywords : ion * adsorption * rutile Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.834, year: 2004

  17. Polydopamine-mediated surface functionalization of electrospun nanofibrous membranes: Preparation, characterization and their adsorption properties towards heavy metal ions

    International Nuclear Information System (INIS)

    Wu, Chunlin; Wang, Heyun; Wei, Zhong; Li, Chuan; Luo, Zhidong

    2015-01-01

    Graphical abstract: - Highlights: • A simple and versatile approach to produce PEI-functionalized nanofibers. • Novel PEI-functionalized PVC nanofibrous membrane was prepared. • Adsorption of PVC@PDA and PVC@PDA-PEI nanofibrous membranes for Cu 2+ was tested. • Isotherms, kinetic model and thermodynamic parameters were investigated. • Adsorption mechanism of Cu 2+ on modified membranes was inferred. - Abstract: In this paper, a simple and versatile approach for the fabrication of a polyethyleneimine (PEI)-functionalized nanofibrous membrane utilizing polydopamine (PDA) as a mediator is proposed. The morphology and structure of the PDA-coated and PEI-grafted nanofibrous membranes were confirmed using scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. Due to a large specific surface area and long fibrous morphology, the synthesized membranes were used as novel adsorbents for copper ion (Cu 2+ ) removal from aqueous solutions. The adsorption of Cu 2+ was investigated on the synthesized membranes regarding the membrane dosages, initial solution pH values, initial solution concentrations, contact times and temperatures. In addition, the adsorption equilibrium data of PEI-grafted membranes were well fitted with the Langmuir adsorption isotherm, and a maximum adsorption capacity value of 33.59 mg g −1 was determined (while it was 21.94 mg g −1 for the PDA-coated membranes). The thermodynamic parameters indicated that Cu 2+ absorption was a spontaneous and exothermic adsorption process. In addition, XPS peak differentiation imitating analysis permitted the proposal of a copper-amine coordination adsorption mechanism that can be used to explain changes in the adsorption properties compared to PDA coating nanofibrous membranes

  18. Preparation of new nano magnetic material Fe3O4@g-C3N4 and good adsorption performance on uranium ion

    Science.gov (United States)

    Long, Wei; Liu, Huijun; Yan, Xueming; Fu, Li

    2018-03-01

    A new nano magnetic material Fe3O4@g-C3N4 was prepared by deposition reduction method, which performed good adsorption performance to uranium ion. Characterization results showed that the g-C3N4 particles were wrapped around the nano magnetic Fe3O4 particles, and the textural properties of this material was improved, so the adsorption performance to uranium ion was good. Adsorption experiments of this material demonstrated that the optimum pH value was 10, the optimum mass of adsorbent was 6.5 mg and the optimum adsorption time was 150 min in the initial concentration of 140 mg/L uranium ion solution system, and the maximum adsorption capacity was up to 352.1 mg/g and the maximum adsorption rate was more than 90%.

  19. Adsorption of Some Hazardous Radionuclides on Cerium(IV) Antimonate

    International Nuclear Information System (INIS)

    Aly, H.F.; Zakaria, E.S.; Shady, S.A.; El-Naggar, I.M.

    1999-01-01

    Cerium(IV) antimonate had been prepared by the dropwise addition of 0.6 M antimony pentachloride and 0.6 M cerium ammonium nitrate solutions by a molar radio of Ce/Sb 0.75. Exchange isotherms for H +/ Co 2+ , H +/ Cs +, H +/ Zn 2+ , H +/ Sr 2+ and H +/ Eu 3+ have been determined at 25, 40 and 60 degree. Besides it was proved that europium is physically adsorbed while zinc, strontium, cobalt and cesium are chemically adsorbed. Moreover, the heat of adsorption of zinc, strontium, cobalt and cesium on cerium(IV) antimonate had been calculated and indicated that cerium(IV) antimonate is of endothermic behaviour towards these ions. Also the distribution coefficients of these ions were determined and it was found that the selectivity in the order: Eu 3+ >Sr 2+ > Cs +> Na +

  20. Adsorption Kinetics of Cd(ll and Pb(ll Ions from Aqueous Solutions by Bamboo-Based Activated Charcoal and Bamboo Dust

    Directory of Open Access Journals (Sweden)

    Stevens Azubuike Odoemelam

    2015-01-01

    Full Text Available The use of bamboo dust (BD and bamboo-based activated charcoal for adsorption of Pb(ll and Cd(ll ions from aqueous solutions were assessed in this work. The effect of contact time on the uptake of these metal ions was studied in batch process. The adsorption data were correlated with pseudo first-order, pseudo second-order and diffusivity kinetic models. Results show that pseudo second-order kinetic model gave the best description for the adsorption process. Kinetic studies further showed that the adsorption transport mechanism was particle-diffusion controlled for the adsorption process. Results obtained generally showed that lead(ll ions were better adsorbed onto both adsorbents as compared to cadmium(ll. Comparison of sorption capacity for the two adsorbents shows that bamboo-based activated charcoal exhibited better removal for the metal ions than the bamboo dust.

  1. Selective adsorption of Pb (II) over the zinc-based MOFs in aqueous solution-kinetics, isotherms, and the ion exchange mechanism.

    Science.gov (United States)

    Wang, Lei; Zhao, Xinhua; Zhang, Jinmiao; Xiong, Zhenhu

    2017-06-01

    Two series of metal-organic frameworks (MOFs) with similar formula units but different central metal ions (M) or organic linkers (L), M-BDC (BDC = terephthalate, M = Zn, Zr, Cr, or Fe), or Zn-L (L = imidazolate-2-methyl, BDC, BDC-NH 2 ), were prepared and employed as the receptors for adsorption lead ions. It was found that the Zn-BDC exhibited a much higher adsorption capacity than the other M-BDC series with various metal ions which have very closely low capacities at same conditions. Furthermore, the Zn-L (L = imidazolate-2-methyl, BDC, BDC-NH 2 ) still have highly efficient adsorption capacity of lead ions, although the adsorption capacity varies with different ligand, as well as the adsorption rate and the equilibrium pH of the solution. This significant high adsorption over Zn-L, different from other M-BDC series with various metal ions (Zr, Cr, or Fe), can be explained by ion exchange between the central metal ions of Zn-L and lead ion in solution. Based on the analysis of FT-IR, X-ray diffraction pattern, the nitrogen adsorption isotherms, the zeta potentials, and the results, a plausible adsorption mechanism is proposed. When equivalent Zn-L were added to equal volume of aqueous solution with different concentration of lead ion, the content of zinc ion in the solution increases with the increase of the initial concentration of lead ions. The new findings could provide a potential way to fabricate new metal organic frameworks with high and selective capacities of the heavy metal ions.

  2. Ion bombardment and adsorption studies on ilmenite (FeTiO3) by X-ray photoelectron spectroscopy

    International Nuclear Information System (INIS)

    Schulze, P.D.

    1983-01-01

    The effects of 5 KeV argon and oxygen ion bombardment on FeTiO3 (ilmenite) at low temperatures have been studied using x-ray photoelectron spectroscopy (XPS). Also, using this same technique, the adsorption of O 2 , NO, N 2 O, and CO at 300 K and the adsorption of O 2 and D 2 O at 150K have been studied. Argon and oxygen ion bombardment of ilmenite have confirmed earlier studies on metal oxides that argon ions generally reduce the anion species while oxygen ions generally oxidize the anion species. The two iron states involved were Fe sup +2 and Fe sup O. The reduction of Ti sup +4 was not verified although a significant shift in the Ti(2p1,3) binding energies toward the metallic state was observed after oxygen ion bombardment at low temperatures. At temperatures above 150K, O 2 adsorbs dissociatively on ilmenite while D 2 O adsorbs molecularly below 170K. Above 300 K NO, N 2 O, and CO do not appear to adsorb dissociatively. Low temperature adsorption of D 2 O was found to be inhibited by predosing the ilmenite with O 2

  3. Ion bombardment and adsorption studies on ilmenite (FeTiO3) by X-ray photoelectron spectroscopy

    Science.gov (United States)

    Schulze, P. D.

    1983-01-01

    The effects of 5 KeV argon and oxygen ion bombardment on FeTiO3 (ilmenite) at low temperatures have been studied using X-ray photoelectron spectroscopy (XPS). Also, using this same technique, the adsorption of O2, NO, N2O, and CO at 300 K and the adsorption of O2 and D2O at 150K have been studied. Argon and oxygen ion bombardment of ilmenite have confirmed earlier studies on metal oxides that argon ions generally reduce the anion species while oxygen ions generally oxidize the anion species. The two iron states involved were Fe sup +2 and Fe sup O. The reduction of Ti sup +4 was not verified although a significant shift in the Ti(2p1,3) binding energies toward the metallic state was observed after oxygen ion bombardment at low temperatures. At temperatures above 150K, O2 adsorbs dissociatively on ilmenite while D2O adsorbs molecularly below 170K. Above 300 K No, N2O, and CO do not appear to adsorb dissociatively. Low temperature adsorption of D2O was found to be inhibited by predosing the ilmenite with O2.

  4. Modeling the adsorption of metal ions (Cu 2+, Ni 2+, Pb 2+) onto ACCs using surface complexation models

    Science.gov (United States)

    Faur-Brasquet, Catherine; Reddad, Zacaria; Kadirvelu, Krishna; Le Cloirec, Pierre

    2002-08-01

    Activated carbon cloths (ACCs), whose efficiency has been demonstrated for microorganics adsorption from water, were here studied in the removal of metal ions from aqueous solution. Two ACCs are investigated, they are characterized in terms of porosity parameters (BET specific surface area, percentage of microporosity) and chemical characteristics (acidic surface groups, acidity constants, point of zero charge). A first part consists in the experimental study of three metal ions removal (Cu 2+, Ni 2+ and Pb 2+) in a batch reactor. Isotherms modeling by Freundlich and Brunauer-Emmett-Teller (BET) equations enables the following adsorption order: Cu 2+>Ni 2+>Pb 2+ to be determined for adsorption capacities on a molar basis. It may be related to adsorbates characteristics in terms of electronegativity and ionic radius. The influence of adsorbent's microporosity is also shown. Adsorption experiments carried out for pH values ranging from 2 to 10 demonstrate: (i) an adsorption occurring below the precipitation pH; (ii) the strong influence of pH, with a decrease of electrostatic repulsion due to the formation of less charged hydrolyzed species coupled with a decrease of activated carbon surface charge as pH increases. The second part focuses on the modeling of adsorption versus the pH experimental data by the diffuse layer model (DLM) using Fiteql software. The model is efficient to describe the system behavior in the pH range considered. Regarding complexation constants, they show the following affinity for ACC: Pb 2+>Cu 2+>Ni 2+. They are related to initial concentrations used for the three metal ions.

  5. Selective recovery of Pd(II) from extremely acidic solution using ion-imprinted chitosan fiber: Adsorption performance and mechanisms

    International Nuclear Information System (INIS)

    Lin, Shuo; Wei, Wei; Wu, Xiaohui; Zhou, Tao; Mao, Juan; Yun, Yeoung-Sang

    2015-01-01

    Highlights: • An acid-resisting chitosan fiber was prepared by ion-imprinting technique. • Pd(II) and ECH were as template and two-step crosslinking agent, respectively. • IIF showed a good adsorption and selectivity performance on Pd(II) solutions. • Selectivity was due to the electrostatic attraction between −NH_3"+ and [PdCl_4]"2"−. • Stable sorption/desorption performance shows a potential in further application. - Abstract: A novel, selective and acid-resisting chitosan fiber adsorbent was prepared by the ion-imprinting technique using Pd(II) and epichlorohydrin as the template and two-step crosslinking agent, respectively. The resulting ion-imprinted chitosan fibers (IIF) were used to selectively adsorb Pd(II) under extremely acidic synthetic metal solutions. The adsorption and selectivity performances of IIF including kinetics, isotherms, pH effects, and regeneration were investigated. Pd(II) rapidly adsorbed on the IIF within 100 min, achieving the adsorption equilibrium. The isotherm results showed that the maximum Pd(II) uptake on the IIF was maintained as 324.6–326.4 mg g"−"1 in solutions containing single and multiple metals, whereas the Pd(II) uptake on non-imprinted fibers (NIF) decreased from 313.7 to 235.3 mg g"−"1 in solution containing multiple metals. Higher selectivity coefficients values were obtained from the adsorption on the IIF, indicating a better Pd(II) selectivity. The amine group, supposedly the predominant adsorption site for Pd(II), was confirmed by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The pH value played a significant role on the mechanism of the selective adsorption in the extremely acidic conditions. Furthermore, the stabilized performance for three cycles of sorption/desorption shows a potential for further large-scale applications.

  6. Selective recovery of Pd(II) from extremely acidic solution using ion-imprinted chitosan fiber: Adsorption performance and mechanisms

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Shuo [School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Wei, Wei [School of Chemical Engineering, Chonbuk National University, Jeonbuk 561-756 (Korea, Republic of); Wu, Xiaohui; Zhou, Tao [School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Mao, Juan, E-mail: monicamao45@hust.edu.cn [School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Yun, Yeoung-Sang, E-mail: ysyun@jbnu.ac.kr [School of Chemical Engineering, Chonbuk National University, Jeonbuk 561-756 (Korea, Republic of)

    2015-12-15

    Highlights: • An acid-resisting chitosan fiber was prepared by ion-imprinting technique. • Pd(II) and ECH were as template and two-step crosslinking agent, respectively. • IIF showed a good adsorption and selectivity performance on Pd(II) solutions. • Selectivity was due to the electrostatic attraction between −NH{sub 3}{sup +} and [PdCl{sub 4}]{sup 2−}. • Stable sorption/desorption performance shows a potential in further application. - Abstract: A novel, selective and acid-resisting chitosan fiber adsorbent was prepared by the ion-imprinting technique using Pd(II) and epichlorohydrin as the template and two-step crosslinking agent, respectively. The resulting ion-imprinted chitosan fibers (IIF) were used to selectively adsorb Pd(II) under extremely acidic synthetic metal solutions. The adsorption and selectivity performances of IIF including kinetics, isotherms, pH effects, and regeneration were investigated. Pd(II) rapidly adsorbed on the IIF within 100 min, achieving the adsorption equilibrium. The isotherm results showed that the maximum Pd(II) uptake on the IIF was maintained as 324.6–326.4 mg g{sup −1} in solutions containing single and multiple metals, whereas the Pd(II) uptake on non-imprinted fibers (NIF) decreased from 313.7 to 235.3 mg g{sup −1} in solution containing multiple metals. Higher selectivity coefficients values were obtained from the adsorption on the IIF, indicating a better Pd(II) selectivity. The amine group, supposedly the predominant adsorption site for Pd(II), was confirmed by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The pH value played a significant role on the mechanism of the selective adsorption in the extremely acidic conditions. Furthermore, the stabilized performance for three cycles of sorption/desorption shows a potential for further large-scale applications.

  7. Adsorption of U(VI) ions from aqueous solutions by activated carbon prepared from Antep pistachio (Pistacia vera L.) shells

    International Nuclear Information System (INIS)

    Donat, Ramazan; Erden, Kadriye Esen

    2017-01-01

    Antep pistachio (Pistacia vera L.) shells an abundant and low cost natural resource in Turkey was used to prepare activated carbon by physiochemical activation and carbon dioxide (CO_2) atmosphere as the activating agents at 700 C for 2 h. The adsorption equilibrium of U(VI) from aqueous solutions on such carbon has been studied using a batch system. The parameters that affect the U(VI) adsorption, such as particle size of adsorbent, contact time, of pH of the solution, and temperature, have been investigated and conditions have also been optimized. The equilibrium data for U(VI) ions' adsorption onto activated carbon well fitted to the Langmuir equation, with a maximum monolayer adsorption capacity of 8.68 mg/g, The Freundlich and Dubinin-Radushkevich (D-R) isotherms have been applied and the data correlated well with Freundlich model and that the adsorption is physical in nature (E_a=15.46 kJ/mol). Thermodynamic parameters [ΔH_s=11.33 kJ/mol, ΔS=0.084 kJ/molK, ΔG (293.15 K)=-13.29 kJ/mol] showed the endothermic heat of adsorption and the feasibility of the process.

  8. Adsorption of U(VI) ions from aqueous solutions by activated carbon prepared from Antep pistachio (Pistacia vera L.) shells

    Energy Technology Data Exchange (ETDEWEB)

    Donat, Ramazan [Pamukkale Univ., Denizli (Turkey). Dept. of Chemistry; Erden, Kadriye Esen [Pamukkale Univ., Kinikli-Denizli (Turkey). Denizli Vocational School of Technical Sciences

    2017-08-01

    Antep pistachio (Pistacia vera L.) shells an abundant and low cost natural resource in Turkey was used to prepare activated carbon by physiochemical activation and carbon dioxide (CO{sub 2}) atmosphere as the activating agents at 700 C for 2 h. The adsorption equilibrium of U(VI) from aqueous solutions on such carbon has been studied using a batch system. The parameters that affect the U(VI) adsorption, such as particle size of adsorbent, contact time, of pH of the solution, and temperature, have been investigated and conditions have also been optimized. The equilibrium data for U(VI) ions' adsorption onto activated carbon well fitted to the Langmuir equation, with a maximum monolayer adsorption capacity of 8.68 mg/g, The Freundlich and Dubinin-Radushkevich (D-R) isotherms have been applied and the data correlated well with Freundlich model and that the adsorption is physical in nature (E{sub a}=15.46 kJ/mol). Thermodynamic parameters [ΔH{sub s}=11.33 kJ/mol, ΔS=0.084 kJ/molK, ΔG (293.15 K)=-13.29 kJ/mol] showed the endothermic heat of adsorption and the feasibility of the process.

  9. N-doping effectively enhances the adsorption capacity of biochar for heavy metal ions from aqueous solution.

    Science.gov (United States)

    Yu, Wenchao; Lian, Fei; Cui, Guannan; Liu, Zhongqi

    2018-02-01

    N-doping was successfully employed to improve the adsorption capacity of biochar (BC) for Cu 2+ and Cd 2+ by direct annealing of crop straws in NH 3 . The surface N content of BC increased more than 20 times by N-doping; meanwhile the content of oxidized-N was gradually diminished but graphitic-N was formed and increased with increasing annealing temperature and duration time. After N-doping, a high graphitic-N percentage (46.4%) and S BET (418.7 m 2 /g) can be achieved for BC. As a result, the N-doped BC exhibited an excellent adsorption capacity for Cu 2+ (1.63 mmol g -1 ) and Cd 2+ (1.76 mmol g -1 ), which was up to 4.0 times higher than that of the original BC. Furthermore, the adsorption performance of the N-doped BC remained stable even at acidic conditions. A positive correlation can be found between adsorption capacity with the graphitic N content on BC surface. The surface chemistry of N-doped BC before and after the heavy metal ions adsorption was carefully examined by XPS and FTIR techniques, which indicated that the adsorption mechanisms mainly included cation-π bonding and complexation with graphitic-N and hydroxyl groups of carbon surfaces. Copyright © 2017 Elsevier Ltd. All rights reserved.

  10. Adsorption of heavy metal ions from aqueous solutions by bio-char, a by-product of pyrolysis

    International Nuclear Information System (INIS)

    Kılıç, Murat; Kırbıyık, Çisem; Çepelioğullar, Özge; Pütün, Ayşe E.

    2013-01-01

    Bio-char, a by-product of almond shell pyrolysis, was used as an alternative adsorbent precursor for the removal of heavy metal ions from aqueous solutions. The adsorption potential of almond shell bio-char for Ni(II) and Co(II) removal was investigated. Adsorption experiments were carried out by varying pH, adsorbent dosage, initial metal ion concentrations, contact time and temperature to determine the optimum conditions. To describe the equilibrium isotherms the experimental data were analyzed by the Langmuir, Freundlich, Dubinin–Radushkevich (D–R) and Temkin isotherm models. Pseudo-first order, pseudo-second order, and intraparticle diffusion kinetic models were used to find out the kinetic parameters and mechanism of adsorption process. The thermodynamic parameters such as ΔG°, ΔH° and ΔS° were calculated for predicting the nature of adsorption. The results showed that bio-char derived from pyrolysis of biomass can be used as a low-cost and effective adsorbent for removal of heavy metal ions from aqueous solutions.

  11. Uniform surface modification of diatomaceous earth with amorphous manganese oxide and its adsorption characteristics for lead ions

    Energy Technology Data Exchange (ETDEWEB)

    Li, Song; Li, Duanyang; Su, Fei; Ren, Yuping; Qin, Gaowu, E-mail: lis@atm.neu.edu.cn

    2014-10-30

    Graphical abstract: - Highlights: • A uniform MnO{sub 2} layer was anchored onto diatomite surface. • Kinetics and isotherms over MnO{sub 2} modified diatomite were studied. • The Pb(II) adsorption is based on ion-exchange mechanism. - Abstract: A novel method to produce composite sorbent material compromising porous diatomaceous earth (DE) and surface functionalized amorphous MnO{sub 2} is reported. Via a simple in situ redox reaction over the carbonized DE powders, a uniform layer of amorphous MnO{sub 2} was anchored onto the DE surface. The hybrid adsorbent was characterized by X-ray diffraction, scanning electron microscopy, and infrared spectroscopy. The batch method has been employed to investigate the effects of surface coating on adsorption performance of DE. According to the equilibrium studies, the adsorption capacity of DE for adsorbing lead ions after MnO{sub 2} modification increased more than six times. And the adsorption of Pb{sup 2+} on the MnO{sub 2} surface is based on ion-exchange mechanism. The developed strategy presents a novel opportunity to prepare composite adsorbent materials by integrating nanocrystals with porous matrix.

  12. Column Adsorption Studies for the Removal of Cr(VI Ions by Ethylamine Modified Chitosan Carbonized Rice Husk Composite Beads with Modelling and Optimization

    Directory of Open Access Journals (Sweden)

    S. Sugashini

    2013-01-01

    Full Text Available The objective of this present study is the optimization of process parameters in adsorption of Cr(VI ions by ethylamine modified chitosan carbonized rice husk composite beads (EAM-CCRCBs using response surface methodology (RSM and continuous adsorption studies of Cr(VI ions by ethylamine modified chitosan carbonized rice husk composite beads (EAM-CCRCBs. The effect of process variables such as initial metal ion concentration, adsorbent dosage and pH were optimized using RSM in order to ensure high adsorption capacity at low adsorbent dosage and high initial metal ion concentration of Cr(VI in batch process. The optimum condition suggested by the model for the process variable such as adsorbent dosage, pH and initial metal ion concentration was 0.14 g, 300 mg/L and pH2 with maximum removal of 99.8% and adsorption capacity of 52.7 mg/g respectively. Continuous adsorption studies were conducted under optimized initial metal ion concentration and pH for the removal of Cr(VI ions using EAM-CCRCBs. The breakthrough curve analysis was determined using the experimental data obtained from the continuous adsorption. Continuous adsorption modelling such as bed depth service model and Thomson model were established by fitting it with experimental data.

  13. The Adsorption of n-Octanohydroxamate Collector on Cu and Fe Oxide Minerals Investigated by Static Secondary Ion Mass Spectrometry

    Directory of Open Access Journals (Sweden)

    Alan N. Buckley

    2012-12-01

    Full Text Available The feasibility of investigating the adsorption of n-octanohydroxamate collector on copper and iron oxide minerals with static secondary ion mass spectrometry has been assessed. Secondary ion mass spectra were determined for abraded surfaces of air-exposed copper metal, malachite, pseudomalachite and magnetite that had been conditioned in aqueous potassium hydrogen n-octanohydroxamate solution, as well as for the corresponding bulk CuII and FeIII complexes. In each case, the chemical species present at the solid/vacuum interface of a similarly prepared surface were established by X-ray photoelectron spectroscopy. The most abundant positive and negative metal-containing fragment ions identified for the bulk complexes were also found to be diagnostic secondary ions for the collector adsorbed on the oxide surfaces. The relative abundances of those diagnostic ions varied with, and could be rationalised by, the monolayer or multilayer coverage of the adsorbed collector. However, the precise mass values for the diagnostic ions were not able to corroborate the different bonding in the copper and iron hydroxamate systems that had been deduced from photoelectron and vibrational spectra. Parent secondary ions were able to provide supporting information on the co-adsorption of hydroxamic acid at each conditioned surface.

  14. Adsorption of endotoxins on Ca2+ -iminodiacetic acid by metal ion affinity chromatography.

    Science.gov (United States)

    Lopes, André Moreni; Romeu, Jorge Sánchez; Meireles, Rolando Páez; Perera, Gabriel Marquez; Morales, Rolando Perdomo; Pessoa, Adalberto; Cárdenas, Lourdes Zumalacárregui

    2012-11-01

    Endotoxins (also known as lipopolysaccharides (LPS)) are undesirable by-products of recombinant proteins, purified from Escherichia coli. LPS can be considered stable under a wide range of temperature and pH, making their removal one of the most difficult tasks in downstream processes during protein purification. The inherent toxicity of LPS makes their removal an important step for the application of these proteins in several biological assays and for a safe parenteral administration. Immobilized metal affinity chromatography (IMAC) enables the affinity interactions between the metal ions (immobilized on the support through the chelating compound) and the target molecules, thus enabling high-efficiency separation of the target molecules from other components present in a mixture. Affinity chromatography is applied with Ca2+ -iminodiacetic acid (IDA) to remove most of the LPS contaminants from the end product (more than 90%). In this study, the adsorption of LPS on an IDA-Ca2+ was investigated. The adsorption Freundlich isotherm of LPS-IDA-Ca2+ provides a theoretical basis for LPS removal. It was found that LPS is bound mainly by interactions between the phosphate group in LPS and Ca2+ ligands on the beads. The factors such as pH (4.0 or 5.5) and ionic strength (1.0 mol/L) are essential to obtain effective removal of LPS for contaminant levels between endotoxin' concentration values less than 100 EU/mL and 100 000 EU/mL. This new protocol represents a substantial advantage in time, effort, and production costs.

  15. Recovery of Chromium Ions From Electroplating Wastewater by Flotation, Gamma Irradiation and Adsorption onto Hydrogels

    International Nuclear Information System (INIS)

    Eid, M.; Dessouki, A.M.; Omar, A.M.

    2005-01-01

    At present, the wastewater treatment facilities in many plating plants are approaching their time for replacement. On this occasion there is a strong requirement to re-evaluate the wastewater treatment measures from the point of view of treatment technology. Laboratory investigation was undertaken on the flotation of Cr (VI) from aqueous suspension over whole ph range, aiming at the separation of chromium by flotation. The cationic surfactant (hexadecyl triethyl ammonium bromide) was applied as a collector. Surface properties, in particular the critical micelle concentration, the effectiveness of surface tension reduction, efficiency, surface excess and the minimum surface area were measured at 30 μ C. The electro-flotation was applied with and without the collector at different times for the removal of chromium (VI). The results were discussed in term of surface properties of the collectors at the solution/air interface. Further work took place by irradiating the water samples by gamma- irradiation to reduce the highly toxic Cr(VI) to the much less toxic and less soluble Cr1 in water; therefore, there is a potential for the complete removal of chromium from aqueous solutions. The possibility of using hydrogels for the uptake of irradiated chromium solutions by different hydrogels was investigated. The structure of the hydrogels was estimated by using FT1R and the pore structure of the hydrogels before and after dictating with chromium ions was monitored by SEM. The adsorption studies show that, it is ph dependent. Lowering of the chromium concentration below the maximum permissible value have been achieved after the treatment of chromium solution by flotation, gamma irradiation and adsorption onto hydrogels

  16. Kinetic study of liquid-phase adsorptive removal of heavy metal ions by almond tree (Terminalia catappa L. leaves waste

    Directory of Open Access Journals (Sweden)

    Michael Horsfall Jnr

    2007-04-01

    Full Text Available The kinetic sorption of five metal ions – Al3+, Cr6+, Zn2+, Ag+ and Mn2+- from aqueous solution onto almond tree leaves (ATL waste in single component system has been studied. The experimental data was analyzed in terms of intraparticle diffusion and rate of adsorption, thus comparing transport mechanism and chemical sorption processes. The sorption rates based on the pseudo-second order rate constants for the five metal ions are 0.018 (Al3+, 0.016 (Cr6+, 0.023 (Zn2+, 0.021 (Ag+ and 0.022 (Mn2+ g/mg.min. The adsorption rates are rapid and within 180 min of agitation more than 85 percent of these metal ions has been removed from solution by the ATL waste biomass. The kinetic data suggest that the overall adsorption process is endothermic, and that the rate-limiting step is a surface diffusion controlled process. The results from this study have revealed that the ATL waste, which is hitherto an environmental nuisance, has the ability to adsorb metal ions from solution and the data are relevant for optimal design of wastewater treatment plants. The low cost and easy availability of ATL waste make potential industrial application a strong possibility.

  17. Investigate the ultrasound energy assisted adsorption mechanism of nickel(II) ions onto modified magnetic cobalt ferrite nanoparticles: Multivariate optimization.

    Science.gov (United States)

    Mehrabi, Fatemeh; Alipanahpour Dil, Ebrahim

    2017-07-01

    In present study, magnetic cobalt ferrite nanoparticles modified with (E)-N-(2-nitrobenzylidene)-2-(2-(2-nitrophenyl)imidazolidine-1-yl) ethaneamine (CoFe 2 O 4 -NPs-NBNPIEA) was synthesized and applied as novel adsorbent for ultrasound energy assisted adsorption of nickel(II) ions (Ni 2+ ) from aqueous solution. The prepared adsorbent characterized by Fourier transforms infrared spectroscopy (FT-IR), transmission electron microscope (TEM), vibrating sample magnetometer (VSM) and X-ray diffraction (XRD). The dependency of adsorption percentage to variables such as pH, initial Ni 2+ ions concentration, adsorbent mass and ultrasound time were studied with response surface methodology (RSM) by considering the desirable functions. The quadratic model between the dependent and independent variables was built. The proposed method showed good agreement between the experimental data and predictive value, and it has been successfully employed to adsorption of Ni 2+ ions from aqueous solution. Subsequently, the experimental equilibrium data at different concentration of Ni 2+ ions and 10mg amount of adsorbent mass was fitted to conventional isotherm models like Langmuir, Freundlich, Tempkin, Dubinin-Radushkevich and it was revealed that the Langmuir is best model for explanation of behavior of experimental data. In addition, conventional kinetic models such as pseudo-first and second-order, Elovich and intraparticle diffusion were applied and it was seen that pseudo-second-order equation is suitable to fit the experimental data. Copyright © 2016 Elsevier B.V. All rights reserved.

  18. Adsorption and bio-sorption of nickel ions and reuse for 2-chlorophenol catalytic ozonation oxidation degradation from water

    International Nuclear Information System (INIS)

    Ma, Wei; Zong, Panpan; Cheng, Zihong; Wang, Baodong; Sun, Qi

    2014-01-01

    Highlights: • Biomass and fly ash which were widespread for adsorption of heavy metal ions. • Preparation of catalyst by saturated adsorbents for 2-chlorophenol ozone degradation. • This work demonstrated that the O 3 /catalyst process was an effective pathway. • The use of nickel ions, fly ash and sawdust to achieve the recycling utilization of resources. -- Abstract: This work explored the preparation of an effective and low-cost catalyst and investigated its catalytic capacity for 2-chlorophenol ozonation oxidation degradation in wastewater by using an ozone oxidation batch reactor. The catalyst was directly prepared by the reuse of fly ash and sawdust after saturated adsorption of nickel ions from wastewater, which was proposed as an efficient and economic approach. The obtained catalyst was characterized by TGA, BET, FTIR, XRD, and SEM, the results showed that fly ash as the basic framework has high specific surface area and the addition of sawdust as the porogen agent could improve the pore structure of the catalyst. The adsorption of nickel ions by fly ash and sawdust from aqueous solution was also investigated in this study. The results obtained from the experiments indicated that adsorption of nickel ions by fly ash and biomass sawdust could be well described by Langmuir isotherm model and pseudo second order kinetic model. The catalytic performance of catalyst was studied in terms of the effect of time, liquid–solid ratio and pH on 2-chlorophenol ozonation degradation. It was found that the catalyst could effectively improve the ozonation reaction rate at pH = 7 with a 2:1 liquid–solid ratio. The kinetic study demonstrated that the reaction followed the first order model, and the rate constant increased 267% (0.03–0.1 min −1 ) of 2-chlorophenol ozonation degradation with 5 mmol/L concentration at pH = 7.0 compared with ozonation alone

  19. Adsorption and bio-sorption of nickel ions and reuse for 2-chlorophenol catalytic ozonation oxidation degradation from water

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Wei, E-mail: chmawv@yahoo.com [School of Chemical Engineering, Dalian University of Technology, Dalian 116024 (China); Zong, Panpan; Cheng, Zihong [School of Chemical Engineering, Dalian University of Technology, Dalian 116024 (China); Wang, Baodong; Sun, Qi [National Institute of Clean-and-low Carbon Energy, Beijing 102209 (China)

    2014-02-15

    Highlights: • Biomass and fly ash which were widespread for adsorption of heavy metal ions. • Preparation of catalyst by saturated adsorbents for 2-chlorophenol ozone degradation. • This work demonstrated that the O{sub 3}/catalyst process was an effective pathway. • The use of nickel ions, fly ash and sawdust to achieve the recycling utilization of resources. -- Abstract: This work explored the preparation of an effective and low-cost catalyst and investigated its catalytic capacity for 2-chlorophenol ozonation oxidation degradation in wastewater by using an ozone oxidation batch reactor. The catalyst was directly prepared by the reuse of fly ash and sawdust after saturated adsorption of nickel ions from wastewater, which was proposed as an efficient and economic approach. The obtained catalyst was characterized by TGA, BET, FTIR, XRD, and SEM, the results showed that fly ash as the basic framework has high specific surface area and the addition of sawdust as the porogen agent could improve the pore structure of the catalyst. The adsorption of nickel ions by fly ash and sawdust from aqueous solution was also investigated in this study. The results obtained from the experiments indicated that adsorption of nickel ions by fly ash and biomass sawdust could be well described by Langmuir isotherm model and pseudo second order kinetic model. The catalytic performance of catalyst was studied in terms of the effect of time, liquid–solid ratio and pH on 2-chlorophenol ozonation degradation. It was found that the catalyst could effectively improve the ozonation reaction rate at pH = 7 with a 2:1 liquid–solid ratio. The kinetic study demonstrated that the reaction followed the first order model, and the rate constant increased 267% (0.03–0.1 min{sup −1}) of 2-chlorophenol ozonation degradation with 5 mmol/L concentration at pH = 7.0 compared with ozonation alone.

  20. Characteristics of equilibrium, kinetics studies for adsorption of Hg(II), Cu(II), and Ni(II) ions by thiourea-modified magnetic chitosan microspheres

    International Nuclear Information System (INIS)

    Zhou Limin; Wang Yiping; Liu Zhirong; Huang Qunwu

    2009-01-01

    Magnetic chitosan microspheres were prepared and chemically modified with thiourea (TMCS) for adsorption of metal ions. TMCS obtained were investigated by means of X-ray diffraction (XRD), IR, magnetic properties and thermogravimetric analysis (TGA). The adsorption properties of TMCS toward Hg 2+ , Cu 2+ , and Ni 2+ ions were evaluated. Various factors affecting the uptake behavior such as contact time, temperature, pH and initial concentration of the metal ions were investigated. The kinetics was evaluated utilizing the pseudo-first-order, pseudo-second-order, and the intra-particle diffusion models. The equilibrium data were analyzed using the Langmuir, Freundlich, and Tempkin isotherm models. The adsorption kinetics followed the mechanism of the pseudo-second-order equation for all systems studied, evidencing chemical sorption as the rate-limiting step of adsorption mechanism and not involving a mass transfer in solution. The best interpretation for the equilibrium data was given by Langmuir isotherm, and the maximum adsorption capacities were 625.2, 66.7, and 15.3 mg/g for Hg 2+ , Cu 2+ , and Ni 2+ ions, respectively. TMCS displayed higher adsorption capacity for Hg 2+ in all pH ranges studied. The adsorption capacity of the metal ions decreased with increasing temperature. The metal ion-loaded TMCS with were regenerated with an efficiency of greater than 88% using 0.01-0.1 M ethylendiamine tetraacetic acid (EDTA)

  1. Adsorption and Desorption of Nickel(II) Ions from Aqueous Solution by a Lignocellulose/Montmorillonite Nanocomposite

    Science.gov (United States)

    Zhang, Xiaotao; Wang, Ximing

    2015-01-01

    A new and inexpensive lignocellulose/montmorillonite (LNC/MMT) nanocomposite was prepared by a chemical intercalation of LNC into MMT and was subsequently investigated as an adsorbent in batch systems for the adsorption-desorption of Ni(II) ions in an aqueous solution. The optimum conditions for the Ni(II) ion adsorption capacity of the LNC/MMT nanocomposite were studied in detail by varying parameters such as the initial Ni(II) concentration, the solution pH value, the adsorption temperature and time. The results indicated that the maximum adsorption capacity of Ni(II) reached 94.86 mg/g at an initial Ni(II) concentration of 0.0032 mol/L, a solution pH of 6.8, an adsorption temperature of 70°C, and adsorption time of 40 min. The represented adsorption kinetics model exhibited good agreement between the experimental data and the pseudo-second-order kinetic model. The Langmuir isotherm equation best fit the experimental data. The structure of the LNC/MMT nanocomposite was characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM), whereas the adsorption mechanism was discussed in combination with the results obtained from scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier-transform infrared spectroscopy analyses (FTIR). The desorption capacity of the LNC/MMT nanocomposite depended on parameters such as HNO3 concentration, desorption temperature, and desorption time. The satisfactory desorption capacity of 81.34 mg/g was obtained at a HNO3 concentration, desorption temperature, and desorption time of 0.2 mol/L, 60 ºC, and 30 min, respectively. The regeneration studies showed that the adsorption capacity of the LNC/MMT nanocomposite was consistent for five cycles without any appreciable loss in the batch process and confirmed that the LNC/MMT nanocomposite was reusable. The overall study revealed that the LNC/MMT nanocomposite functioned as an effective adsorbent in the detoxification of Ni

  2. Adsorption of mercury ions from wastewater by a hyperbranched and multi-functionalized dendrimer modified mixed-oxides nanoparticles.

    Science.gov (United States)

    Arshadi, M; Mousavinia, F; Khalafi-Nezhad, A; Firouzabadi, H; Abbaspourrad, A

    2017-11-01

    In this paper, a novel heterogeneous nanodendrimer with generation of G2.0 was prepared by individual grafting of diethylenetriamine, triazine and l-cysteine methyl ester on the modified aluminum-silicate mixed oxides as a potent adsorbent of Hg(II) ions from aqueous media. The prepared nanodendrimer was characterized by nuclear magnetic resonance spectrum ( 1 H NMR and 13 C NMR), Fourier transform infrared spectroscopy (FT-IR), Diffuse reflectance UV-Vis spectroscopy (DR UV-Vis), zeta potential (ζ), inductively coupled plasma atomic emission spectroscopy (ICP-AES), transmission electron microscopy (TEM), scanning electron microscopy (SEM), nitrogen adsorption experiments at -196°C and elemental analysis. Equilibrium and kinetic models for Hg(II) ions removal were used by investigating the effect of the contact time, adsorbent dosage, initial Hg(II) ions concentrations, effect of solution's temperature, interfering ions, and initial pH. The contact time to approach equilibrium for higher removal was 6min (3232mgg -1 ). The removal of Hg(II) ions has been assessed in terms of pseudo-first- and -second-order kinetics, and the Freundlich, Langmuir and Sips isotherms models have also been applied to the equilibrium removal data. The removal kinetics followed the mechanism of the pseudo-second order equation, where the chemical sorption is the rate-limiting step of removal process and not involving mass transfer in solution, which was further proved by several techniques such as zeta potential, FT-IR and DS UV-vis. The thermodynamic parameters (ΔG, ΔH and ΔS) implied that the removal of mercury ions was feasible, spontaneous and chemically exothermic in nature between 15 and 80°C. The nanodendrimer indicated high reusability due to its high removal ability after 15 adsorption-desorption runs. The adsorption mechanisms of Hg(II) ions onto the nanodendrimer was further studied by diverse techniques such as FTIR, EDS, zeta potential, DR UV-Vis spectroscopy and SEM

  3. The synthesis of Ag/polypyrrole coaxial nanocables via ion adsorption method using different oxidants

    Science.gov (United States)

    Qiu, Teng; Xie, Huxiao; Zhang, Jiangru; Zahoor, Amad; Li, Xiaoyu

    2011-03-01

    Ag/polypyrrole (PPy) coaxial nanocables (NCs) were synthesized by an ion adsorption method. In this method, the pre-made Ag nanowires (NWs) were dispersed in the aqueous solution of copper acetate (Cu(Ac)2), and the Cu2+ ions adsorbed onto the surface of Ag NWs can oxidize pyrrole monomers to polymerize into uniform PPy sheath outside Ag NWs after the Cu(Ac)2-treated Ag NWs were re-dispersed in the aqueous solution of pyrrole. The morphology of NCs was characterized by transmission electron microscope (TEM) and scanning electron microscope (SEM). The relationship between the thickness of polymer sheath and the concentration of Cu(Ac)2 was established. As Cu(Ac)2 which served as the oxidant can also be replaced by AgNO3 in this synthesis, the differences on the structure of polymer sheath caused by different oxidants were studied by surface-enhanced Raman scattering (SERS), high-resolution transmission electron microscope (HR-TEM), Fourier transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS). Comparing with the characterization results of Ag/PPy NCs synthesized using AgNO3 as the oxidant which indicates the random arrangement of PPy chains at the interface between polymer sheath and Ag NWs, PPy chain oxidized by Cu2+ tends to show a relatively ordered conformation at the interface with the pyrrole rings identically taking the plane vertical to the surface of Ag NWs. In addition, although the main part of the polymer sheath was composed of PPy whatever kind of oxidant was used, the sheath of the NCs oxidized by Cu2+ is typical for the existence of Cu(I)-pyrrole coordinate structures with strong Cu(I)-N bond signal shown in XPS characterization.

  4. The synthesis of Ag/polypyrrole coaxial nanocables via ion adsorption method using different oxidants

    International Nuclear Information System (INIS)

    Qiu Teng; Xie Huxiao; Zhang Jiangru; Zahoor, Amad; Li Xiaoyu

    2011-01-01

    Ag/polypyrrole (PPy) coaxial nanocables (NCs) were synthesized by an ion adsorption method. In this method, the pre-made Ag nanowires (NWs) were dispersed in the aqueous solution of copper acetate (Cu(Ac) 2 ), and the Cu 2+ ions adsorbed onto the surface of Ag NWs can oxidize pyrrole monomers to polymerize into uniform PPy sheath outside Ag NWs after the Cu(Ac) 2 -treated Ag NWs were re-dispersed in the aqueous solution of pyrrole. The morphology of NCs was characterized by transmission electron microscope (TEM) and scanning electron microscope (SEM). The relationship between the thickness of polymer sheath and the concentration of Cu(Ac) 2 was established. As Cu(Ac) 2 which served as the oxidant can also be replaced by AgNO 3 in this synthesis, the differences on the structure of polymer sheath caused by different oxidants were studied by surface-enhanced Raman scattering (SERS), high-resolution transmission electron microscope (HR-TEM), Fourier transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS). Comparing with the characterization results of Ag/PPy NCs synthesized using AgNO 3 as the oxidant which indicates the random arrangement of PPy chains at the interface between polymer sheath and Ag NWs, PPy chain oxidized by Cu 2+ tends to show a relatively ordered conformation at the interface with the pyrrole rings identically taking the plane vertical to the surface of Ag NWs. In addition, although the main part of the polymer sheath was composed of PPy whatever kind of oxidant was used, the sheath of the NCs oxidized by Cu 2+ is typical for the existence of Cu(I)–pyrrole coordinate structures with strong Cu(I)–N bond signal shown in XPS characterization.

  5. Effective adsorption of oil droplets from oil-in-water emulsion using metal ions encapsulated biopolymers: Role of metal ions and their mechanism in oil removal.

    Science.gov (United States)

    Elanchezhiyan, S Sd; Prabhu, Subbaiah Muthu; Meenakshi, Sankaran

    2018-06-01

    Herein, synthesized and compared the three different kinds of hybrid bio-polymeric composites viz., lanthanum embedded chitosan/gelatin (La@CS-GEL), zirconium embedded chitosan/gelatin (Zr@CS-GEL) and cerium embedded chitosan/gelatin (Ce@CS-GEL) in terms of their oil uptake efficiency. The adsorption efficiency was studied under various optimized parameters like contact time, pH, dose, initial oil concentration and temperature. The oil adsorption capacity was found to be 91, 82 and 45% for La@CS-GEL, Zr@CS-GEL and Ce@CS-GEL composites respectively. The metals were used as a bridging material to connect both CS and GEL using the hydrophilic groups to enhance the oil recovery by hydrophobic interaction. Also, the introduction of metal ions on the surface of biopolymers would modify the oil/water properties which in turn, decrease the interfacial tension between oil and water phases. The mechanism of oil uptake was explained using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscope (SEM), energy dispersive X-ray (EDAX) and heat of combustion. The experimental data confirmed Langmuir isotherm as the best fit for oil adsorption process. Thermodynamic parameters such as standard free energy (ΔG°), standard enthalpy (ΔH°) and standard entropy (ΔS°) indicated that the oil adsorption was spontaneous and endothermic. The oil adsorption mechanism was established based on isotherm and thermodynamic models. Copyright © 2018 Elsevier B.V. All rights reserved.

  6. Preparation and properties of a novel macro porous Ni2+-imprinted chitosan foam adsorbents for adsorption of nickel ions from aqueous solution.

    Science.gov (United States)

    Guo, Na; Su, Shi-Jun; Liao, Bing; Ding, Sang-Lan; Sun, Wei-Yi

    2017-06-01

    In this study, novel macro porous Ni 2+ -imprinted chitosan foam adsorbents (F-IIP) were prepared using sodium bicarbonate and glycerine to obtain a porogen for adsorbing nickel ions from aqueous solutions. The use of the ion-imprinting technique for adsorbents preparation improved the nickel ion selectivity and adsorption capacity. We characterised the imprinted porous foam adsorbents in terms of the effects of the initial pH value, initial metal ion concentration, and contact time on the adsorption of nickel ions. The adsorption process was described best by Langmuir monolayer adsorption models, and the maximum adsorption capacity calculated from the Langmuir equation was 69.93mgg -1 . The kinetic data could be fitted to a pseudo-second-order equation. Our analysis of selective adsorption demonstrated the excellent preference of the F-IIP foams for nickel ions compared with other coexisting metal ions. Furthermore, tests over five cycle runs suggested that the F-IIP foam adsorbents had good durability and efficiency. Copyright © 2017 Elsevier Ltd. All rights reserved.

  7. Finite-element simulations of the influence of pore wall adsorption on cyclic voltammetry of ion transfer across a liquid-liquid interface formed at a micropore.

    Science.gov (United States)

    Ellis, Jonathan S; Strutwolf, Jörg; Arrigan, Damien W M

    2012-02-21

    Adsorption onto the walls of micropores was explored by computational simulations involving cyclic voltammetry of ion transfer across an interface between aqueous and organic phases located at the micropore. Micro-interfaces between two immiscible electrolyte solutions (micro-ITIES) have been of particular research interest in recent years and show promise for biosensor and biomedical applications. The simulation model combines diffusion to and within the micropore, Butler-Volmer kinetics for ion transfer at the liquid-liquid interface, and Langmuir-style adsorption on the pore wall. Effects due to pore radius, adsorption and desorption rates, surface adsorption site density, and scan rates were examined. It was found that the magnitude of the reverse peak current decreased due to adsorption of the transferring ion on the pore wall; this decrease was more marked as the scan rate was increased. There was also a shift in the half-wave potential to lower values following adsorption, consistent with a wall adsorption process which provides a further driving force to transfer ions across the ITIES. Of particular interest was the disappearance of the reverse peak from the cyclic voltammogram at higher scan rates, compared to the increase in the reverse peak size in the absence of wall adsorption. This occurred for scan rates of 50 mV s(-1) and above and may be useful in biosensor applications using micropore-based ITIES.

  8. Equilibrium, kinetics and mechanism of Au3+, Pd2+ and Ag+ ions adsorption from aqueous solutions by graphene oxide functionalized persimmon tannin.

    Science.gov (United States)

    Wang, Zhongmin; Li, Xiaojuan; Liang, Haijun; Ning, Jingliang; Zhou, Zhide; Li, Guiyin

    2017-10-01

    In this study, a novel bio-adsorbent (PT-GO) was prepared by functionalization persimmon tannin (PT) with graphene oxide (GO) and the effective adsorption behaviors of Au 3+ , Pd 2+ and Ag + ions from aqueous solution was investigated. The PT-GO was characterized by Fourier transform infrared spectrometer (FTIR), scanning electronic microscope (SEM), thermogravimetric analysis (TGA) and Zeta potential. Many influence factors such as pH value, bio-adsorbent dosage, initial concentration of metal ions and contact time were optimized. The maximum adsorption capacity for Au 3+ , Pd 2+ and Ag + was 1325.09mg/g, 797.66mg/g and 421.01mg/g, respectively. The equilibrium isotherm for the adsorption of Au 3+ and Ag + on PT-GO were found to obey the Langmuir model, while the Freundlich model fitted better for Pd 2+ . The adsorption process of Au 3+ , Pd 2+ presented relatively fast adsorption kinetics with pseudo-second-order equation as the best fitting model, while the pseudo-first-order kinetic model was suitable for describing the adsorption of Ag + . Combination of ion exchange, electrostatic interaction and physical adsorption was the mechanism for adsorption of Au 3+ , Pd 2+ and Ag + onto PT-GO bio-adsorbent. Therefore, the PT-GO bio-adsorbent would be an ideal adsorbent for removal of precious metal ions and broaden the potential applications of persimmon tannin in environmental research. Copyright © 2017 Elsevier B.V. All rights reserved.

  9. Adsorption Kinetics and intra particulate diffusivities of Hg, As and Pb ions on unmodified and thiolated coconut fiber

    International Nuclear Information System (INIS)

    Igwe, J. C.; Abia, A. A.; Ibeh, C. A.

    2008-01-01

    As, Hg and Pb are examples of heavy metals which are present in different types of industrial effluents responsible for environmental pollution. Their removal is traditionally made by chemical precipitation, ion-exchange and so on. However, this is expensive and not completely feasible to reduce their concentrations to the levels as low as required by the environmental legislation. Bio sorption is a process in which solids of natural origin are employed for binding the heavy metal. It is a promising alternative method to treat industrial effluents, mainly because of its low cost and high metal binding capacity. The kinetics was studied for bio sorption experiments using coconut fiber for As (III), Hg (II) and Pb (II) ions adsorption. The specific surface area and surface charge density of the coconut fiber are 1.186x10 25 (m 2 /g) and 5.39 xI0 24 (meq/m 2 ), respectively. The maximum adsorption capacity was found to be the highest for Pb (II) followed by Hg (II) and As (Ill). The modification of the adsorbent by thiolation affected the adsorption capacity. Equilibrium sorption was reached for the metal ions at about 60 min. The equilibrium constant and free energy of the adsorption at 30 degree were calculated. The mechanism of sorption was found to obey the particle-diffusion model. The kinetic studies showed that the sorption rates could be described by both pseudo first-order and pseudo second-order models. The pseudo second-order model showed a better fit with a rate constant value of 1.16x10 -4 /min. for all three metal ions.Therefore, the results of this study show that coconut fiber, both modified and unmodified, is an efficient adsorbent for the removal of toxic and valuable metals from industrial effluents

  10. Dynamic filtration and static adsorption of lead ions in aqueous solution by use of blended polysulfone membranes with nano size MCM-41 particles coated by polyaniline.

    Science.gov (United States)

    Toosi, Mohammad Reza; Emami, Mohammad Reza Sarmasti; Hajian, Sudeh

    2018-05-11

    MCM-41 mesopore was prepared by hydrothermal method and used for synthesis of polyaniline/MCM-41 nanocomposite via in situ polymerization. The nanocomposite was blended with polysulfone to prepare mixed matrix membrane in different content of nanocomposite by phase inversion method. Structural and surface properties of the samples were characterized by SEM, XRD, FTIR, AFM, TGA, BET, and zeta potential measurements. Effect of the nanocomposite content on the hydrophilicity, porosity, and permeability of the membrane was determined. Membrane performance was evaluated for removal of lead ions in dynamic filtration and static adsorption. The membranes were found as effective adsorptive filters for removal of lead ions via interactions between active sites of nanocomposite in membrane structure and lead ions during filtration. Results of batch experiments proved adsorptive mechanism of membranes for removal of lead ions with the maximum adsorption capacity of 19.6 mg/g.

  11. Separation of fission strontium from nuclear fuels by ammonium molybdatophosphate

    International Nuclear Information System (INIS)

    Hermann, A.

    1984-01-01

    The separation of fission strontium from solutions of prolonged cooled nuclear fuel has been performed using ammoniummolybdatophosphate (AMP) columns. The sorption mechanism of bivalent ions of AMP has been investigated by column and batch experiments. A pure ion exchange of Sr 2+ for two H + or NH 4 + ions has been established. Conditions for the sepasorption and elution of fission strontium and other fission products on AMP columns are described. (author)

  12. Adsorption Isotherms of Cs+, Co2+, Zn2+ and Eu3+ on Zirconium Vanadate Ion-Exchanger

    International Nuclear Information System (INIS)

    Shady, S.A.; El-Ashery, S.M.; El-Naggar, I.M.

    2009-01-01

    Zirconium vanadate had been prepared by the dropwise addition of 0.1 M sodium vanadate and 0.1 M zirconyl chloride by molar ratio of zirconium/vanadium 2. Exchange isotherms for Cs + /H + , Co 2+ /H + ,Zn 2+ /H + and Eu 3+ /H + have been determined at 25, 40 and 60 degree C. Besides, it was proved that cesium, cobalt, zinc and europium are chemically adsorbed. Moreover, the heat of adsorption of these ions on zirconium vanadate had been calculated and indicated that zirconium vanadate is of endothermic behavior towards these ions

  13. Adsorption of heavy metal ions and azo dyes by crosslinked nanochelating resins based on poly(methylmethacrylate-co-maleic anhydride

    Directory of Open Access Journals (Sweden)

    M. Ghaemy

    2014-03-01

    Full Text Available Chelating resins are suitable materials for the removal of heavy metals in water treatments. A copolymer, Poly(MMA-co-MA, was synthesized by radical polymerization of maleic anhydride (MA and methyl methacrylate (MMA, characterized and transformed into multifunctional nanochelating resin beads (80–150 nm via hydrolysis, grafting and crosslink reactions. The resin beads were characterized by swelling studies, field emission scanning electron microscopy (FESEM and Fourier transform infrared spectroscopy (FTIR. The main purpose of this work was to determine the adsorption capacity of the prepared resins (swelling ratio ~55% towards metal ions such as Hg2+, Cd2+, Cu2+ from water at three different pH values (3, 6 and 9. Variations in pH and types of metal ions have not significantly affected the chelation capacity of these resins. The maximum chelation capacity of one of the prepared resin beads (Co-g-AP3 for Hg2+ was 63, 85.8 and 71.14 mg/g at pH 3, 6 and 9, respectively. Approximately 96% of the metal ions could be desorbed from the resin. Adsorption capacity of these resins towards three commercial synthetic azo dyes was also investigated. The maximum adsorption of dye AY42 was 91% for the resin Co-g-AP3 at room temperature. This insures the applicability of the synthesized resins for industrial applications.

  14. Renewable Modified Cellulose Bearing Chelating Schiff Base for Adsorptive Removal of Heavy Metal Ions and Antibacterial Action.

    Science.gov (United States)

    Saravanan, R; Ravikumar, L

    2017-07-01

      A novel approach toward chemically modified cellulose bearing active chelating Schiff base with hydroxyl group (Cell-Hy) was synthesized. The modified cellulose was examined for its heavy metal ion uptake potential from aqueous solution. The chemical and structural features of the adsorbent were characterized by Fourier transform infrared spectroscopy (FT-IR), solid state 13C-NMR, Scanning Electron Microscopy (SEM), and energy dispersive analysis of X-ray (EDAX) observations. The experimental conditions and adsorption parameters, including pH, initial metal ion concentration, adsorbent dosage, temperature, and contact time were optimized for the removal of Cu(II) and Pb(II) ions. Kinetic parameters, equilibrium adsorption capacities, and correlation coefficients for pseudo-first-order, pseudo-second-order, and intraparticle diffusion models were carried out. The data obtained from the adsorption of Cu(II) and Pb(II) onto Cell-Hy were subjected to Langmuir and Freundlich isotherm models. Thermodynamic parameters have also been evaluated. The antibacterial activity of modified cellulose was tested toward specific bacterial species.

  15. Studies on adsorptions of metallic ions in water by zirconium glyphosate (ZrGP): Behaviors and mechanisms

    Energy Technology Data Exchange (ETDEWEB)

    Jia Yunjie; Zhang Yuejuan [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Box. 98, No.15, Beisanhuan donglu, Beijing 100029 (China); Wang Runwei [State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun 130012 (China); Fan Faying [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Box. 98, No.15, Beisanhuan donglu, Beijing 100029 (China); Xu Qinghong, E-mail: xuqh@mail.buct.edu.cn [State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Box. 98, No.15, Beisanhuan donglu, Beijing 100029 (China)

    2012-01-15

    A new adsorbent named zirconium glyphosate [Zr(O{sub 3}PCH{sub 2}NHCH{sub 2}COOH){sub 2}{center_dot}0.5H{sub 2}O, denoted as ZrGP] and its selective adsorptions to Pb{sup 2+}, Cd{sup 2+}, Mg{sup 2+} and Ca{sup 2+} ions in water were reported in this paper. Compared to other zirconium adsorbents, such as zirconium phosphate [Zr(HPO{sub 4}){sub 2}], ZrGP exhibited highly selective adsorption to Pb{sup 2+} in solution which contained Pb{sup 2+}, Cd{sup 2+}, Mg{sup 2+} and Ca{sup 2+} ions. The loaded ZrGP with metallic ions can be efficaciously regenerated by aqueous solution of HCl (1.0 M) without any noticeable capacity loss, and almost all of it can be reused and recycled. The memory effect on structural regeneration of ZrGP was also found when Mg{sup 2+} and Ca{sup 2+} were adsorbed. To be specific, the structure of ZrGP was destroyed due to adsorbing these two ions, but it could be regenerated after the loaded materials were dipped in HCl solution (1.0 M) for several minutes to remove metallic ions.

  16. Studies on adsorptions of metallic ions in water by zirconium glyphosate (ZrGP): Behaviors and mechanisms

    International Nuclear Information System (INIS)

    Jia Yunjie; Zhang Yuejuan; Wang Runwei; Fan Faying; Xu Qinghong

    2012-01-01

    A new adsorbent named zirconium glyphosate [Zr(O 3 PCH 2 NHCH 2 COOH) 2 ·0.5H 2 O, denoted as ZrGP] and its selective adsorptions to Pb 2+ , Cd 2+ , Mg 2+ and Ca 2+ ions in water were reported in this paper. Compared to other zirconium adsorbents, such as zirconium phosphate [Zr(HPO 4 ) 2 ], ZrGP exhibited highly selective adsorption to Pb 2+ in solution which contained Pb 2+ , Cd 2+ , Mg 2+ and Ca 2+ ions. The loaded ZrGP with metallic ions can be efficaciously regenerated by aqueous solution of HCl (1.0 M) without any noticeable capacity loss, and almost all of it can be reused and recycled. The memory effect on structural regeneration of ZrGP was also found when Mg 2+ and Ca 2+ were adsorbed. To be specific, the structure of ZrGP was destroyed due to adsorbing these two ions, but it could be regenerated after the loaded materials were dipped in HCl solution (1.0 M) for several minutes to remove metallic ions.

  17. Removal of Cd(II) and Pb(II) ions, from aqueous solutions, by adsorption onto sawdust of Pinus sylvestris

    International Nuclear Information System (INIS)

    Taty-Costodes, V. Christian; Fauduet, Henri; Porte, Catherine; Delacroix, Alain

    2003-01-01

    Fixation of heavy metal ions (Cd(II) and Pb(II)) onto sawdust of Pinus sylvestris is presented in this paper. Batch experiments were conducted to study the main parameters such as adsorbent concentration, initial adsorbate concentration, contact time, kinetic, pH solution, and stirring velocity on the sorption of Cd(II) and Pb(II) by sawdust of P. sylvestris. Kinetic aspects are studied in order to develop a model which can describe the process of adsorption on sawdust. The equilibrium of a solution between liquid and solid phases is described by Langmuir model. Scanning electronic microscopy (SEM) coupled with energy dispersive X-ray analysis (EDAX) and X-ray photoelectron spectroscopy (XPS) shows that the process is controlled by a porous diffusion with ion-exchange. The capacity of the metal ions to bind onto the biomass was 96% for Cd(II), and 98% for Pb(II). The sorption followed a pseudo-second-order kinetics. The adsorption of these heavy metals ions increased with the pH and reached a maximum at a 5.5 value. From these results, it can be concluded that the sawdust of P. sylvestris could be a good adsorbent for the metal ions coming from aqueous solutions. Moreover, this material could also be used for purification of water before rejection into the natural environment

  18. Comparison of organic and inorganic ion exchangers for removal of cesium and strontium from simulated and actual Hanford 241-AW-101 DSSF tank waste

    International Nuclear Information System (INIS)

    Brown, G.N.; Bray, L.A.; Carlson, C.D.

    1996-04-01

    A number of organic and inorganic exchangers are being developed and evaluated for cesium removal from Hanford tank wastes. The exchangers of interest that are investigated in this work include powdered (IONSIV reg-sign IE-910; referred to as IE-910) and engineered (IONSIV reg-sign IE-911; referred to as IE-911) forms of the crystalline silico-titanate (CST) inorganic sorbent developed by Sandia National Laboratories (SNL)/Texas A and M and prepared by UOP; a phenol-formaldehyde (CS-100) resin developed by Rohm and Haas; a resorcinol-formaldehyde (R-F) polymer developed at the Westinghouse Savannah River Company (WSRC) and produced by Boulder Scientific; an inorganic zeolite exchanger produced by UOP (IONSIV reg-sign TIE-96; referred to as TIE-96); an inorganic sodium titanate produced by Allied Signal/Texas A and M (NaTi); and a macrocyclic organic resin developed and produced by IBC Advanced Technologies (SuperLig reg-sign 644; referred to as SL-644). Several of these materials are still under development and may not be in the optimal form. The work described in this report involves the direct comparison of the ion exchange materials for the pretreatment of actual and simulated Hanford tank waste. Data on the performance of all of the exchangers with simulated and actual double shell slurry feed (DSSF) is included. The DSSF waste is a mixture of the supernate from tanks 101-AW (70%), 106-AP (20%) and 102-AP (10%). The comparative parameters include radionuclide removal efficiency under a variety of conditions and material properties (e.g., bed density and percent removable water). Cesium and strontium distribution (K d ), lambda (λ = K d x ρ b ), and decontamination factors (DF) are compared as a function of exchanger contact duration, solution composition (Na and Cs concentration), exchanger/waste phase ratio, and multiple sequential contacts

  19. Metaldehyde removal from aqueous solution by adsorption and ion exchange mechanisms onto activated carbon and polymeric sorbents

    Energy Technology Data Exchange (ETDEWEB)

    Tao, Bing [Chemical and Process Engineering, Faculty of Engineering, University of Strathclyde, Glasgow G1 1XW (United Kingdom); Fletcher, Ashleigh J., E-mail: ashleigh.fletcher@strath.ac.uk [Chemical and Process Engineering, Faculty of Engineering, University of Strathclyde, Glasgow G1 1XW (United Kingdom)

    2013-01-15

    Highlights: ► First detailed analysis and study on metaldehyde removal by physical adsorbents. ► Adsorption performance of current method studied to probe reasons for failure of removal. ► Sorption performances of proposed alternative materials studied and mechanism proposed. ► Mechanism explains full sorption and degradation of metaldehyde. ► Results are of marked significance to the water treatment industries. -- Abstract: Metaldehyde removal from aqueous solution was evaluated using granular activated carbon (GAC), a non-functionalised hyper-cross-linked polymer Macronet (MN200) and an ion-exchange resin (S957) with sulfonic and phosphonic functional groups. Equilibrium experimental data were successfully described by Freundlich isotherm models. The maximum adsorption capacity of S957 (7.5 g metaldehyde/g S957) exceeded those of MN200 and GAC. Thermodynamic studies showed that sorption of metaldehyde onto all sorbents is endothermic and processes are controlled by entropic rather than enthalpic changes. Kinetic experiments demonstrated that experimental data for MN200 and GAC obey pseudo-second order models with rates limited by particle diffusion. Comparatively, S957 was shown to obey a pseudo-first order model with a rate-limiting step of metaldehyde diffusion through the solid/liquid interface. Results obtained suggest that metaldehyde adsorption onto MN200 and GAC are driven by hydrophobic interactions and hydrogen bonding, as leaching tendencies were high since no degradation of metaldehyde occurred. Conversely, adsorption of metaldehyde onto S957 occurs via ion-exchange processes, where sulfonic and phosphonic functionalities degrade adsorbed metaldehyde molecules and failure to detect metaldehyde in leaching studies for S957 supports this theory. Consequently, the high adsorption capacity and absence of leaching indicate S957 is promising for metaldehyde removal from source water.

  20. In situ ATR FTIR studies of SO4 adsorption on goethite in the presence of copper ions.

    Science.gov (United States)

    Beattie, D A; Chapelet, J K; Gräfe, M; Skinner, W M; Smith, E

    2008-12-15

    Despite the existence of many single ion sorption studies on iron and aluminum oxides, fewer studies have been reported that describe cosorption reactions. In this work, we present an in situ ATR FTIR study of synergistic adsorption of sulfate (SO4) and copper (Cu) on goethite, which is representative of the minerals and ions present in mine wastes, acid sulfate soils, and other industrial and agricultural settings. Sulfate adsorption was studied as a function of varying pH, and as a function of increasing concentration in the absence and presence of Cu. The presence of Cu ions in solution had a complex effect on the ability of SO4 ions to be retained on the goethite surface with increasing pH, with complete desorption occurring near pH 7 and 9 in the absence and presence of Cu, respectively. In addition, Cu ions altered the balance of inner vs outer sphere adsorbed SO4. The solid phase partitioning of SO4 at pH 3 and pH 5 was elevated by the presence of Cu; in both cases Cu increased the affinity of SO4 for the goethite surface. Complementary ex situ sorption edge studies of Cu on goethite in the absence and presence of SO4 revealed that the Cu adsorption edge shifted to lower pH (6.3 --> 5.6) in the presence of SO4, consistent with a decrease of the electrostatic repulsion between the goethite surface and adsorbing Cu. Based on the ATR FTIR and bulk sorption data we surmise that the cosorption products of SO4 and Cu at the goethite-water interface were not in the nature of ternary complexes under the conditions studied here. This information is critical for the evaluation of the onset of surface precipitates of copper-hydroxy sulfates as a function of pH and solution concentration.

  1. Poly(hydroxyethyl methacrylate-co-methacryloylglutamic acid) nanospheres for adsorption of Cd2+ ions from aqueous solutions

    Science.gov (United States)

    Esen, Cem; Şenay, Raziye Hilal; Feyzioğlu, Esra; Akgöl, Sinan

    2014-02-01

    Poly(2-hydroxyethyl methacrylate-co- N-methacryloyl-( l)-glutamic acid) p(HEMA-MAGA) nanospheres have been synthesized, characterized, and used for the adsorption of Cd2+ ions from aqueous solutions. Nanospheres were prepared by surfactant free emulsion polymerization. The p(HEMA-MAGA) nanospheres were characterized by SEM, FTIR, zeta size, and elemental analysis. The specific surface area of nanospheres was found to be 1,779 m2/g. According to zeta size analysis results, average size of nanospheres is 147.3 nm with poly-dispersity index of 0.200. The goal of this study was to evaluate the adsorption performance of p(HEMA-MAGA) nanospheres for Cd2+ ions from aqueous solutions by a series of batch experiments. The Cd2+ concentration was determined by inductively coupled plasma-optical emission spectrometer. Equilibrium sorption experiments indicated a Cd2+ uptake capacity of 44.2 mg g-1 at pH 4.0 at 25 °C. The adsorption of Cd2+ ions increased with increasing pH and reached a plateau value at around pH 4.0. The data were successfully modeled with a Langmuir equation. A series of kinetics experiments was then carried out and a pseudo-second order equation was used to fit the experimental data. Desorption experiments which were carried out with nitric acid showed that the p(HEMA-MAGA) nanospheres could be reused without significant losses of their initial properties in consecutive adsorption and elution operations.

  2. Kinetics and equilibrium adsorption studies of dimethylamine (DMA) onto ion-exchange resin

    International Nuclear Information System (INIS)

    Hu Qinhai; Meng Yuanyuan; Sun Tongxi; Mahmood, Qaisar; Wu Donglei; Zhu Jianhang; Lu, George

    2011-01-01

    The fine grained resin ZGSPC106 was used to adsorb dimethylamine (DMA) from aqueous solution in the present research. Batch experiments were performed to examine the effects of initial pH of solution and agitation time on the adsorption process. The thermodynamics and kinetics of adsorption were also analyzed. The maximum adsorption was found at natural pH of DMA solution and equilibrium could be attained within 12 min. The equilibrium adsorption data were conformed satisfactorily to the Langmuir equation. The evaluation based on Langmuir isotherm gave the maximal static saturated adsorption capacity of 138.89 mg/g at 293 K. Various thermodynamic parameters such as free energy (ΔG o ), enthalpy (ΔH o ) and entropy (ΔS o ) showed that the adsorption was spontaneous, endothermic and feasible. DMA adsorption on ZGSPC106 fitted well to the pseudo-second-order kinetic model. Furthermore, the adsorption mechanism was discussed by Fourier transform infrared spectroscopy (FT-IR) analysis.

  3. Highly efficient ultrasonic-assisted removal of Hg(II) ions on graphene oxide modified with 2-pyridinecarboxaldehyde thiosemicarbazone: Adsorption isotherms and kinetics studies.

    Science.gov (United States)

    Tadjarodi, Azadeh; Moazen Ferdowsi, Somayeh; Zare-Dorabei, Rouholah; Barzin, Ahmad

    2016-11-01

    A novel adsorbent, based on modifying graphene oxide (GO) chemically with 2-pyridinecarboxaldehyde thiosemicarbazone (2-PTSC) as ligand, was designed by facile process for removal of Hg(II) from aqueous solution. Characterization of the adsorbent was performed using various techniques, such as FT-IR, XRD, XPS, SEM and AFM analysis. The adsorption capacity was affected by variables such as adsorbent dosage, pH solution, Hg(2+) initial concentration and sonicating time. These variables were optimized by rotatable central composite design (CCD) under response surface methodology (RSM). The predictive model for Hg(II) adsorption was constructed and applied to find the best conditions at which the responses were maximized. In this conditions, the adsorption capacity of this adsorbent for Hg(2+) ions was calculated to be 309mgg(-1) that was higher than that of GO. Appling the ultrasound power combined with adsorption method was very efficient in shortening the removal time of Hg(2+) ions by enhancing the dispersion of adsorbent and metal ions in solution and effective interactions among them. The adsorption process was well described by second-order kinetic and Langmuir isotherm model in which the maximum adsorption capacity (Qm) was found to be 555mgg(-1) for adsorption of Hg(2+) ions over the obtained adsorbent. The performance of adsorbent was examined on the real wastewaters and confirmed the applicability of adsorbent for practical applications. Copyright © 2016 Elsevier B.V. All rights reserved.

  4. Growth and Properties of Oxygen and Ion Doped BISMUTH(2) STRONTIUM(2) Calcium COPPER(2) Oxygen (8+DELTA) Single Crystals

    Science.gov (United States)

    Mitzi, David Brian

    1990-01-01

    A directional solidification method for growing large single crystals in the Bi_2Sr _2CaCu_2O _{8+delta} system is reported. Ion substitutions, with replacement of La for Sr and Y for Ca, as well as oxygen doping in these crystals has been explored. Ion doping results in little change of the superconducting transition for substitution levels below 20-25% (as a result of simultaneous oxygen intercalation), while beyond this level, the Meissner signal broadens and the low temperature Meissner signal decreases. Microprobe analysis and x-ray diffraction performed on these more highly substituted single crystals, provides evidence for inhomogeneity and phase segregation into regions of distinct composition. Annealing unsubstituted crystals in increasing partial pressures of oxygen reversibly depresses the superconducting transition temperature from 90K (as made) to 77K (oxygen pressure annealed) while the Hall concentrations increase from n = 3.1(3) times 10 ^{21} cm^{ -3} (0.34 holes/Cu site) to 4.6(3) times 10^{21} cm^{-3} (0.50 holes/Cu site). Further suppression of T_{c} to 72K is possible by annealing in oxygen pressures up to 100atm. No degradation of the Meissner transition or other indications of inhomogeneity or phase segregation with doping are noted, suggesting that oxygen doped Bi_2Sr _2CaCu_2O _{8+delta} is a suitable system for pursuing doping studies. The decrease in T _{c} with concentration for 0.34 <=q n <=q 0.50 indicates that a high carrier concentration regime exists where T_{c} decreases with n and suggests that this decrease does not arise from material inhomogeneity or other materials problems. The physical properties of these Bi _2Sr_2CaCu _2O_{8+delta} crystals, in this high carrier concentration regime, will be discussed.

  5. Adsorption of Zn(II) and Cd(II) ions in batch system by using the Eichhornia crassipes.

    Science.gov (United States)

    Módenes, A N; Espinoza-Quiñones, F R; Borba, C E; Trigueros, D E G; Lavarda, F L; Abugderah, M M; Kroumov, A D

    2011-01-01

    In this work, the displacement effects on the sorption capacities of zinc and cadmium ions of the Eichornia crassipes-type biosorbent in batch binary system has been studied. Preliminary single metal sorption experiments were carried out. An improvement on the Zn(II) and Cd(II) ions removal was achieved by working at 30 °C temperature and with non-uniform biosorbent grain sizes. A 60 min equilibrium time was achieved for both Zn(II) and Cd(II) ions. Furthermore, it was found that the overall kinetic data were best described by the pseudo second-order kinetic model. Classical multi-component adsorption isotherms have been tested as well as a modified extended Langmuir isotherm model, showing good agreement with the equilibrium binary data. Around 0.65 mequiv./g maximum metal uptake associated with the E. crassipes biosorbent was attained and the E. crassipes biosorbent has shown higher adsorption affinity for the zinc ions than for the cadmium ones in the binary system.

  6. Adsorption of heavy metal ion from aqueous solution by nickel oxide nano catalyst prepared by different methods

    Directory of Open Access Journals (Sweden)

    Amira M. Mahmoud

    2015-03-01

    Full Text Available Environmental pollution by heavy metal is arising as the most endangering tasks to both water sources and atmosphere quality today. The treatment of heavy metals is of special concern due to their recalcitrance and persistence in the environment. To limit the spread of the heavy metals within water sources, nickel oxide nanoparticles adsorbents were synthesized and characterized with the aim of removal of one of the aggressive heavy elements, namely; lead ions. Nano nickel oxide adsorbents were prepared using NaOH and oxalic acid dissolved in ethanol as precursors. The results indicated that adsorption capacity of Pb(II ion by NiO-org catalyst is favored than that prepared using NaOH as a precipitant. Nickel oxide nanoparticles prepared by the two methods were characterized structurally and chemically through XRD, DTA, TGA, BET and FT-IR. Affinity and efficiency sorption parameters of the solid nano NiO particles, such as; contact time, initial concentration of lead ions and the dosage of NiO nano catalyst and competitive adsorption behaviors were studied. The results showed that the first-order reaction law fit the reduction of lead ion, also showed good linear relationship with a correlation coefficient (R2 larger than 0.9.

  7. Green Synthesis of Zinc Oxide Nanoparticles for Enhanced Adsorption of Lead Ions from Aqueous Solutions: Equilibrium, Kinetic and Thermodynamic Studies

    Directory of Open Access Journals (Sweden)

    Susan Azizi

    2017-06-01

    Full Text Available In the present study, ZnO nanoparticles (NPs were synthesized in zerumbone solution by a green approach and appraised for their ability to absorb Pb(II ions from aqueous solution. The formation of as-synthesized NPs was established by X-ray diffraction (XRD, Transmission Electron Microscopy (TEM, and UV–visible studies. The XRD and TEM analyses revealed high purity and wurtzite hexagonal structure of ZnO NPs with a mean size of 10.01 ± 2.6 nm. Batch experiments were performed to investigate the impact of process parameters viz. Pb(II concentration, pH of solution, adsorbent mass, solution temperature, and contact time variations on the removal efficiency of Pb(II. The adsorption isotherm data provided that the adsorption process was mainly monolayer on ZnO NPs. The adsorption process follows pseudo-second-order reaction kinetic. The maximum removal efficiencies were 93% at pH 5. Thermodynamic parameters such as enthalpy change (ΔH0, free energy change (ΔG0, and entropy change (ΔS0 were calculated; the adsorption process was spontaneous and endothermic. The good efficiency of the as-synthesized NPs makes them attractive for applications in water treatment, for removal of heavy metals from aqueous system.

  8. Preparation of activated carbon from Tunisian olive-waste cakes and its application for adsorption of heavy metal ions

    International Nuclear Information System (INIS)

    Baccar, R.; Bouzid, J.; Feki, M.; Montiel, A.

    2009-01-01

    The present work explored the use of Tunisian olive-waste cakes, a by-product of the manufacture process of olive oil in mills, as a potential feedstock for the preparation of activated carbon. Chemical activation of this precursor, using phosphoric acid as dehydrating agent, was adopted. To optimize the preparation method, the effect of the main process parameters (such as acid concentration, impregnation ratio, temperature of pyrolysis step) on the performances of the obtained activated carbons (expressed in terms of iodine and methylene blue numbers and specific surface area) was studied. The optimal activated carbon was fully characterized considering its adsorption properties as well as its chemical structure and morphology. To enhance the adsorption capacity of this carbon for heavy metals, a modification of the chemical characteristics of the sorbent surface was performed, using KMnO 4 as oxidant. The efficiency of this treatment was evaluated considering the adsorption of Cu 2+ ions as a model for metallic species. Column adsorption tests showed the high capacity of the activated carbon to reduce KMnO 4 into insoluble manganese (IV) oxide (MnO 2 ) which impregnated the sorbent surface. The results indicated also that copper uptake capacity was enhanced by a factor of up to 3 for the permanganate-treated activated carbon

  9. Preparation of activated carbon from Tunisian olive-waste cakes and its application for adsorption of heavy metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Baccar, R. [Laboratoire Eau Energie Environnement, Ecole Nationale d' Ingenieurs de Sfax, BP W 3038 Sfax (Tunisia)], E-mail: rym.baccar@tunet.tn; Bouzid, J. [Laboratoire Eau Energie Environnement, Ecole Nationale d' Ingenieurs de Sfax, BP W 3038 Sfax (Tunisia)], E-mail: jalel.bouzid@tunet.tn; Feki, M. [Unite de Recherche de Chimie Industrielle et Materiaux, Ecole Nationale d' Ingenieurs de Sfax, BP W 3038 Sfax (Tunisia)], E-mail: mongi.feki@yahoo.fr; Montiel, A. [Laboratoire Eau Energie Environnement, Ecole Nationale d' Ingenieurs de Sfax, BP W 3038 Sfax (Tunisia)], E-mail: montiel.antoine@free.fr

    2009-03-15

    The present work explored the use of Tunisian olive-waste cakes, a by-product of the manufacture process of olive oil in mills, as a potential feedstock for the preparation of activated carbon. Chemical activation of this precursor, using phosphoric acid as dehydrating agent, was adopted. To optimize the preparation method, the effect of the main process parameters (such as acid concentration, impregnation ratio, temperature of pyrolysis step) on the performances of the obtained activated carbons (expressed in terms of iodine and methylene blue numbers and specific surface area) was studied. The optimal activated carbon was fully characterized considering its adsorption properties as well as its chemical structure and morphology. To enhance the adsorption capacity of this carbon for heavy metals, a modification of the chemical characteristics of the sorbent surface was performed, using KMnO{sub 4} as oxidant. The efficiency of this treatment was evaluated considering the adsorption of Cu{sup 2+} ions as a model for metallic species. Column adsorption tests showed the high capacity of the activated carbon to reduce KMnO{sub 4} into insoluble manganese (IV) oxide (MnO{sub 2}) which impregnated the sorbent surface. The results indicated also that copper uptake capacity was enhanced by a factor of up to 3 for the permanganate-treated activated carbon.

  10. The corrosive influence of chloride ions preference adsorption on α-Al{sub 2}O{sub 3} (0 0 0 1) surface

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Chuan-Hui, E-mail: zhangch@ustb.edu.cn; Liu, Min; Jin, Ying; Sun, Dong-Bai, E-mail: dbsun@mater.ustb.edu.cn

    2015-08-30

    Graphical abstract: - Highlights: • The preference adsorption and interaction of Cl{sup −} at increasing monolayer coverage on Al{sub 2}O{sub 3} in solution environment are modeling by DFT with COSMO. • A redefinition critical one plane monolayer of Cl{sup −} is 3/7, and the adsorption energy decrease in three steps, each adsorption energy step only relate to the adsorption site and the morphology. • The weaker interaction between Cl{sup −} and Al{sub 2}O{sub 3} surface but stronger interactions between three Cl{sup −} make the electrons uniformly occupy on the energy levels of three ions. - Abstract: Conductor-like screening model (COSMO), Periodic DFT calculations have been performed on a Al{sub 2}O{sub 3} surface to model the influence of preference adsorption and interaction of chloride ions at increasing monolayer coverage on undefective passive film on Aluminum in solution environment. The results evidence that the critical monolayer of Cl{sup −} is 3/7, which is redefined. With increasing Cl{sup −} adsorption, both the first and second Cl{sup −} move from Al(1) atop and bridge10 sites to O(5) sites, suggesting that the weaker interaction between Cl{sup −} and Al{sub 2}O{sub 3} surface but stronger interactions between three ions make the electrons uniformly occupy on the energy levels of them. More calculations shows that the preference adsorption sites of Cl{sup −} are independent of the surface area of oxide, and the adsorption energy decrease in three steps, each adsorption energy step only relate to the adsorption site and the morphology. On undefective oxide film, low coverage Cl{sup −} adsorption would restrain surface breakdown to happen which is consistent with the experiment results.

  11. Modeling the adsorption of hydrogen, sodium, chloride and phthalate on goethite using a strict charge-neutral ion-exchange theory.

    Science.gov (United States)

    Schulthess, Cristian P; Ndu, Udonna

    2017-01-01

    Simultaneous adsorption modeling of four ions was predicted with a strict net charge-neutral ion-exchange theory and its corresponding equilibrium and mass balance equations. An important key to the success of this approach was the proper collection of all the data, particularly the proton adsorption data, and the inclusion of variable concentrations of conjugate ions from the experimental pH adjustments. Using IExFit software, the ion-exchange model used here predicted the competitive retention of several ions on goethite by assuming that the co-adsorption or desorption of all ions occurred in the correct stoichiometries needed to maintain electroneutrality. This approach also revealed that the retention strength of Cl- ions on goethite increases in the presence of phthalate ions. That is, an anion-anion enhancement effect was observed. The retention of Cl- ions was much weaker than phthalate ions, and this also resulted in a higher sensitivity of the Cl- ions toward minor variations in the surface reactivity. The proposed model uses four goethite surface sites. The drop in retention of phthalate ions at low pH was fully described here as resulting from competitive Cl- reactions, which were introduced in increasing concentrations into the matrix as the conjugate base to the acid added to lower the pH.

  12. Pore Structure and Fluoride Ion Adsorption Characteristics of Zr (IV) Surface-Immobilized Resin Prepared Using Polystyrene as a Porogen

    Science.gov (United States)

    Mizuki, Hidenobu; Ito, Yudai; Harada, Hisashi; Uezu, Kazuya

    Zr(IV) surface-immobilized resins for removal of fluoride ion were prepared by surface template polymerization using polystyrene as a porogen. At polymerization, polystyrene was added in order to increase mesopores (2-50 nm) and macropore (>50 nm) with large macropores (around 300 nm) formed with internal aqueous phase of W⁄O emulsion. The pore structure of Zr(IV) surface-immobilized resins was evaluated by measuring specific surface area, pore volume, and pore size distribution with volumetric adsorption measurement instrument and mercury porosimeter. The adsorption isotherms were well fitted by Langmuir equation. The removal of fluoride was also carried out with column method. Zr(IV) surface-immobilized resins, using 10 g⁄L polystyrene in toluene at polymerization, possessed higher volume of not only mesopores and macropores but also large macropores. Furethermore, by adding the polystyrene with smaller molecular size, the pore volume of mesopores, macropores and large macropores was significantly increased, and the fluoride ion adsorption capacity and the column utilization also increased.

  13. Li-adsorption on doped Mo2C monolayer: A novel electrode material for Li-ion batteries

    Science.gov (United States)

    Mehta, Veenu; Tankeshwar, K.; Saini, Hardev S.

    2018-04-01

    A first principle calculation has been used to study the electronic and magnetic properties of pristine and N/Mn-doped Mo2C with and without Li-adsorption. The pseudopotential method implemented in SIESTA code based on density functional theory with generalized gradient approximation (GGA) as exchange-correlation (XC) potential has been employed. Our calculated results revealed that the Li gets favorably adsorbed on the hexagonal centre in pristine Mo2C and at the top of C-atom in case of N/Mn-doped Mo2C. The doping of Mn and N atom increases the adsorption of Li in Mo2C monolayer which may results in enhancement of storage capacity in Li-ion batteries. The metallic nature of Li-adsorbed pristine and N/Mn-doped Mo2C monolayer implies a good electronic conduction which is crucial for anode materials for its applications in rechargeable batteries. Also, the open circuit voltage for single Li-adsorption in doped Mo2C monolayer comes in the range of 0.4-1.0 eV which is the optimal range for any material to be used as an anode material. Our result emphasized the enhanced performance of doped Mo2C as an anode material in Li-ion batteries.

  14. STRONTIUM AND ACTINIDE SORPTION BY MST AND MMST UNDER CONDITIONS REVELANT TO THE SMALL COLUMN ION-EXCHANGE PROCESS

    Energy Technology Data Exchange (ETDEWEB)

    Taylor-Pashow, K.; Hobbs, D.; Poirier, M.

    2011-05-06

    A series of tests were performed to examine the kinetics of Sr and actinide removal by monosodium titanate (MST) and modified monosodium titanate (mMST) under mixing conditions similar to what will be provided in the Small Column Ion Exchange (SCIX) Program. Similar removal kinetics were seen for two different mixing energies, indicating that under these conditions bulk solution transport is not the rate limiting step for Sr and actinide removal. Sr removal was found to be rapid for both MST and mMST, reaching steady-state conditions within six hours. In contrast, at least six weeks is necessary to reach steady-state conditions for Pu with MST. For mMST, steady-state conditions for Pu were achieved within two weeks. The actual contact time required for the SCIX process will depend on starting sorbate concentrations as well as the requirements for the decontaminated salt solution. During testing leaks occurred in both the MST and mMST tests and evidence of potential desorption was observed. The desorption likely occurred as a result of the change in solids to liquid phase ratio that occurred due to the loss of solution. Based on these results, Savannah River National Laboratory (SRNL) recommended additional testing to further study the effect of changing phase ratios on desorption. This testing is currently in progress and results will be documented in a separate report.

  15. Adsorption behaviors of thiophene, benzene, and cyclohexene on FAU zeolites: Comparison of CeY obtained by liquid-, and solid-state ion exchange

    Energy Technology Data Exchange (ETDEWEB)

    Qin, Yucai [College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao 266555, Shandong (China); Key Laboratory of Petrochemical Catalytic Science and Technology, Liaoning Province, Liaoning Shihua University, Fushun 113001, Liaoning (China); Mo, Zhousheng; Yu, Wenguang; Dong, Shiwei; Duan, Linhai [College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao 266555, Shandong (China); Gao, Xionghou, E-mail: gaoxionghou@petrochina.com.cn [Petrochemical Research Institute, PetroChina Company Limited, 9 Dongzhimen North Street, Dongcheng District, Beijing 100007 (China); Song, Lijuan, E-mail: lsong56@263.net [College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao 266555, Shandong (China); Key Laboratory of Petrochemical Catalytic Science and Technology, Liaoning Province, Liaoning Shihua University, Fushun 113001, Liaoning (China)

    2014-02-15

    Cerium containing Y zeolites were prepared by liquid- (L-CeY) and solid- (S-CeY) state ion exchange from NaY and HY, respectively. The structural and textural properties were characterized by XRD and N{sub 2} adsorption, and acidity properties were characterized by NH{sub 3} temperature-programmed desorption (NH{sub 3}-TPD) and in situ FTIR spectrum of chemisorbed pyridine (in situ Py-FTIR). Furthermore, the single component adsorption and multi-component competitive adsorption behavior of thiophene, benzene and cyclohexene on those zeolites have also been studied by using vapor adsorption isotherms, solution adsorption breakthrough curves, thermogravimetry and derivative thermogravimetry (TG/DTG), frequency response (FR) and in situ FTIR techniques. The results indicate that the primary adsorption mode of benzene is simply micropore filling process, but the nature of effect of aromatics on selective adsorption of thiophene is competitive adsorption. The strong chemical adsorptions and protonization reactions of thiophene and cyclohexene occur upon the Brönsted acid sites of the HY and L-CeY zeolites, and the preferable acid catalytic protonization reactions of olefins hinder the further adsorption of sulfur compounds.

  16. Adsorption of Rh(III) complexes from chloride solutions obtained by leaching chlorinated spent automotive catalysts on ion-exchange resin Diaion WA21J

    International Nuclear Information System (INIS)

    Shen Shaobo; Pan Tonglin; Liu Xinqiang; Yuan Lei; Wang Jinchao; Zhang Yongjian; Guo Zhanchen

    2010-01-01

    It was found that Rh, Pd and Pt contained in the spent ceramic automotive catalysts could be effectively extracted by dry chlorination with chlorine. In order to concentrate Rh(III) ions contained in the chloride solutions obtained, thermodynamic and kinetics studies for adsorption of Rh(III) complexes from the chloride solutions on an anionic exchange resin Diaion WA21J were carried out. Rh, Pd, Pt, Al, Fe, Si, Zn and Pb from the chloride solution could be adsorbed on the resin. The distribution coefficients (K d ) of Rh(III) decreased with the increase in initial Rh(III) concentration or in adsorption temperature. The isothermal adsorption of Rh(III) was found to fit Langmuir, Freundlich and Dubinin-Kaganer-Radushkevich models under the adsorption conditions. The maximum monolayer adsorption capacities Q max based on Langmuir adsorption isotherms were 6.39, 6.61 and 5.81 mg/g for temperatures 18, 28 and 40 deg. C, respectively. The apparent adsorption energy of Rh was about -7.6 kJ/mol and thus Rh(III) adsorption was a physical type. The experimental data obtained could be better simulated by pseudo-first-order kinetic model and the activation energy obtained was 6.54 J/mol. The adsorption rate of Rh(III) was controlled by intraparticle diffusion in most of time of adsorption process.

  17. First-Principles Investigation of Adsorption and Diffusion of Ions on Pristine, Defective and B-doped Graphene

    Directory of Open Access Journals (Sweden)

    Wei Wan

    2015-09-01

    Full Text Available We performed first-principles calculations to reveal the possibility of applying pristine, defective, and B-doped graphene in feasible negative electrode materials of ion batteries. It is found that the barriers for ions are too high to diffuse through the original graphene, however the reduced barriers are obtained by introducing defects (single vacancy, double vacancy, Stone–Wales defect in the graphene. Among the three types of defects, the systems with a double vacancy could provide the lowest barriers of 1.49 and 6.08 eV for Li and Na, respectively. Furthermore, for all kinds of B-doped graphene with the vacancy, the systems with a double vacancy could also provide the lowest adsorption energies and diffusion barriers. Therefore, undoped and B-doped graphene with a double vacancy turn out to be the most promising candidates that can replace pristine graphene for anode materials in ion batteries.

  18. Ion-specific weak adsorption of salts and water/octanol transfer free energy of a model amphiphilic hexapeptide.

    Science.gov (United States)

    Déjugnat, Christophe; Dufrêche, Jean-François; Zemb, Thomas

    2011-04-21

    An amphiphilic hexapeptide has been used as a model to quantify how specific ion effects induced by addition of four salts tune the hydrophilic/hydrophobic balance and induce temperature-dependant coacervate formation from aqueous solution. The hexapeptide chosen is present as a dimer with low transfer energy from water to octanol. Taking sodium chloride as the reference state in the Hofmeister scale, we identify water activity effects and therefore measure the free energy of transfer from water to octanol and separately the free energy associated to the adsorption of chaotropic ions or the desorption of kosmotropic ions for the same amphiphilic peptide. These effects have the same order of magnitude: therefore, both energies of solvation as well as transfer into octanol strongly depend on the nature of the electrolytes used to formulate any buffer. Model peptides could be used on separation processes based on criteria linked to "Hofmeister" but different from volume and valency.

  19. Strontium-90 migration in Hanford sediments, USA

    International Nuclear Information System (INIS)

    Steefel, C.I.; Yang, L.; Carroll, S.A.; Roberts, S.; Zachara, J.M.; Yabusaki, S.B.

    2005-01-01

    Full text of publication follows: Strontium-90 is an important risk-driving contaminant at the Hanford site in eastern Washington, USA. Disposal operations at the Hanford 100-N area released millions of liters of reactor cooling water containing high concentrations of strontium-90 into the vadose zone immediately adjacent to the Columbia River. The effectiveness of pump-and-treat methods for remediation have been questioned, largely because the strontium is strongly sorbed on subsurface sediments via ion exchange reactions and co-precipitation in carbonates. In addition, groundwater monitoring wells show a fluctuating seasonal behavior in which high strontium-90 concentrations correlate with high Columbia River stage, even while average concentrations remain approximately constant. A series of fully saturated reactive transport column experiments have been conducted to investigate the important controls on strontium migration in Hanford groundwater [1]. The experiments were designed to investigate the multicomponent cation exchange behavior of strontium in competition with the cations Na + , Ca +2 , and Mg +2 , the concentration of which differs between river water and groundwater. Reactive transport modeling of the experiments indicates that the Sr +2 selectivity coefficient becomes larger with increasing NaNO 3 concentration, a behavior also shown by the divalent cations Ca +2 and Mg +2 . A new set of column experiments investigates the effect of wetting and drying cycles on strontium- 90 sorption and migration by considering episodic flow in Hanford sediments. In addition, the effect of fluctuating aquifer chemistry as a result of changes in the Columbia River stage on Sr +2 sorption is addressed. Modeling of multicomponent reactive transport under variably saturated conditions is used to interpret the results of the episodic flow/chemistry experiments. [1] Experimental and modeling studies of the migration behavior of strontium in Hanford sediments, USA. C

  20. Synthesis, characterization and metal adsorption properties of the new ion exchanger polymer 3-n-propyl(4-methylpyridinium) silsesquioxane chloride.

    Science.gov (United States)

    Magosso, H A; Panteleimonov, A V; Kholin, Y V; Gushikem, Y

    2006-11-01

    The preparation and anion exchange properties of 3-n-propyl(4-methylpyridinium) silsesquioxane chloride polymer are described. This new polymer was prepared by the sol-gel processing method and is designated as SiPic+Cl-. It is insoluble in water and showed an anion exchange capacity of 1.46x10(-3) mol g-1. The adsorption isotherms of ZnCl2, CdCl2 and HgCl2 were determined from aqueous solutions and the adsorption equilibria simulations fit the model of fixed bidentate centers with the absence of lateral interactions and energetic heterogeneity between them. The metal ions diffuse into the solid solution interface and are dominantly present as MCl2-(4) species for Zn(II), MCl(2-)4 and MCl-3 species for Cd(II) and MCl-3 species for Hg(II).

  1. Specifically colorimetric recognition of calcium, strontium, and barium ions using 2-mercaptosuccinic acid-functionalized gold nanoparticles and its use in reliable detection of calcium ion in water.

    Science.gov (United States)

    Zhang, Jia; Wang, Yong; Xu, Xiaowen; Yang, Xiurong

    2011-10-07

    A colorimetric probe based on 2-mercaptosuccinic acid-functionalized gold nanoparticles has been developed to exhibit selectivity towards Ca(2+), Sr(2+), and Ba(2+) ions over other metallic cations under specified conditions and finds its practical application in detecting Ca(2+) levels in water.

  2. A facile strategy for fabrication of nano-ZnO/yeast composites and their adsorption mechanism towards lead (II) ions

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Wei; Meng, Lingyin [College of Science, Sichuan Agricultural University, Yaan 625014 (China); Mu, Guiqin [Maize Research Institute of Sichuan Agricultural University, Wenjiang 611130 (China); Zhao, Maojun; Zou, Ping [College of Science, Sichuan Agricultural University, Yaan 625014 (China); Zhang, Yunsong, E-mail: yaanyunsong@126.com [College of Science, Sichuan Agricultural University, Yaan 625014 (China)

    2016-08-15

    Highlights: • Nano-ZnO/yeast composites were fabricated by alkali hydrothermal method. • Nano-ZnO was in-situ achieved and anchored on the yeast surface. • Alkali and hydrothermal process cause more exposed funcitional groups on yeast. • Nano-ZnO/yeast composites show higher Pb{sup 2+} adsorption ability than pristine yeast. • Nano-ZnO and exposed functional groups synergistically participate in adsorption. - Abstract: Nano-ZnO/yeast composites were successfully fabricated by one-step alkali hydrothermal method, and their adsorption properties for Pb{sup 2+} ions were also evaluated. Various influencing parameters of nano-ZnO/yeast composites, such as initial pH, contact time and initial Pb{sup 2+} concentration were investigated, respectively. The maximum adsorption capacity of nano-ZnO/yeast composites for Pb{sup 2+} (31.72 mg g{sup −1}) is 2.03 times higher than that of pristine yeast (15.63 mg g{sup −1}). The adsorption mechanism of nano-ZnO/yeast composites was studied by a series of techniques. Scanning electron microscopy (SEM) showed that nano-ZnO is evenly deposited on yeast surface. Atomic force microscopy (AFM) analysis exhibited that the yeast surface is rougher than that of pristine yeast. Energy dispersive X-ray detector (EDX) and X-ray diffraction (XRD) indicated the existence of nano-ZnO on yeast surface. Additionally, X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) measurements further illustrated that alkali hydrothermal method causes not only the generation and anchorage of nano-ZnO on yeast surface but also the exposure of more functional groups (such as amino, carboxyl groups etc.) on yeast surface, both of which could adsorb Pb{sup 2+} via synergistic effect.

  3. A facile strategy for fabrication of nano-ZnO/yeast composites and their adsorption mechanism towards lead (II) ions

    International Nuclear Information System (INIS)

    Zhang, Wei; Meng, Lingyin; Mu, Guiqin; Zhao, Maojun; Zou, Ping; Zhang, Yunsong

    2016-01-01

    Highlights: • Nano-ZnO/yeast composites were fabricated by alkali hydrothermal method. • Nano-ZnO was in-situ achieved and anchored on the yeast surface. • Alkali and hydrothermal process cause more exposed funcitional groups on yeast. • Nano-ZnO/yeast composites show higher Pb"2"+ adsorption ability than pristine yeast. • Nano-ZnO and exposed functional groups synergistically participate in adsorption. - Abstract: Nano-ZnO/yeast composites were successfully fabricated by one-step alkali hydrothermal method, and their adsorption properties for Pb"2"+ ions were also evaluated. Various influencing parameters of nano-ZnO/yeast composites, such as initial pH, contact time and initial Pb"2"+ concentration were investigated, respectively. The maximum adsorption capacity of nano-ZnO/yeast composites for Pb"2"+ (31.72 mg g"−"1) is 2.03 times higher than that of pristine yeast (15.63 mg g"−"1). The adsorption mechanism of nano-ZnO/yeast composites was studied by a series of techniques. Scanning electron microscopy (SEM) showed that nano-ZnO is evenly deposited on yeast surface. Atomic force microscopy (AFM) analysis exhibited that the yeast surface is rougher than that of pristine yeast. Energy dispersive X-ray detector (EDX) and X-ray diffraction (XRD) indicated the existence of nano-ZnO on yeast surface. Additionally, X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) measurements further illustrated that alkali hydrothermal method causes not only the generation and anchorage of nano-ZnO on yeast surface but also the exposure of more functional groups (such as amino, carboxyl groups etc.) on yeast surface, both of which could adsorb Pb"2"+ via synergistic effect.

  4. High adsorptive γ-AlOOH(boehmite)@SiO2/Fe3O4 porous magnetic microspheres for detection of toxic metal ions in drinking water.

    Science.gov (United States)

    Wei, Yan; Yang, Ran; Zhang, Yong-Xing; Wang, Lun; Liu, Jin-Huai; Huang, Xing-Jiu

    2011-10-21

    γ-AlOOH(boehmite)@SiO(2)/Fe(3)O(4) porous magnetic microspheres with high adsorption capacity toward heavy metal ions were found to be useful for the simultaneous and selective electrochemical detection of five metal ions, such as ultratrace zinc(II), cadmium(II), lead(II), copper(II), and mercury(II), in drinking water.

  5. Distribution of strontium in milk component

    International Nuclear Information System (INIS)

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

    2011-01-01

    The distribution of strontium between the milk components, i.e., serum, casein micelles, whey and hydroxyapatite was determined. The sorption on hydroxyapatite was investigated using batch method and radiotracer technique. The aqueous phase comprised of either milk or whey. The sorption of strontium on hydroxyapatite depended on the method of its preparation and on the composition of the aqueous phase. The sorption of strontium was increased with an increase of pH. The presence of citrate species resulted in decrease of the sorption of strontium on hydroxyapatite. The sorption of 85 Sr on hydroxyapatite decreased with the increasing concentration of Ca 2+ ions. Addition of Ca 2+ ions to milk resulted in milk pH decrease. The decrease in pH value after calcium addition to milk is related to exchanges between added calcium and micellar H + . The average value of strontium sorption on casein micelles in milk with presence of hydroxyapatite was (47.3 ± 5.6) %. The average value of sorption of 85 Sr on casein micelles in milk without the addition of hydroxyapatite was (68.9 ± 2.2) %. (author)

  6. Synergistic effect of graphene nanosheets and zinc oxide nanoparticles for effective adsorption of Ni (II) ions from aqueous solutions

    Science.gov (United States)

    Hadadian, Mahboubeh; Goharshadi, Elaheh K.; Fard, Mina Matin; Ahmadzadeh, Hossein

    2018-03-01

    The threat of toxic substances such as heavy metals to public health and wildlife has led to an increasing public awareness. Different techniques for neutralizing the toxic effects of heavy metals in wastewater have been used. Here, we prepared a new and efficient type of adsorbent, zinc oxide-graphene nanocomposite (ZnO-Gr), via a green method to remove Ni (II) ions from aqueous solutions. A facile microwave-assisted hydrothermal technique in the presence of an ionic liquid, 1-hexyl-3-methylimidazolium bis (trifluoromethylsulfonyl) imide [C6mim] [NTf2], was used to prepare ZnO-Gr. The synergistic effect between graphene nanosheets and ZnO nanoparticles in this new adsorbent for Ni (II) ions caused a maximum adsorption capacity of 66.7 mg g-1 at room temperature which is much higher than that of graphene nanosheets (3.8 mg g-1) and other carbonaceous nanomaterials used as an adsorbent in the literature. The maximum desorption percentage (90.32%) was achieved at pH 3.6. By thermodynamic study, we found that the adsorption of this heavy metal ion on ZnO-Gr was spontaneous (Δ G° = -6.14 kJ mol-1) and endothermic (Δ H° = 53.31 kJ mol-1) with entropy change of Δ S° = 199.45 J K-1 mol- 1.

  7. Comparison of adsorption of Cd(II and Pb(II ions on pure and chemically modified fly ashes

    Directory of Open Access Journals (Sweden)

    Sočo Eleonora

    2016-06-01

    Full Text Available The study investigates chemical modifications of coal fly ash (FA treated with HCl or NH4HCO3 or NaOH or Na2edta, based on the research conducted to examine the behaviour of Cd(II and Pb(II ions adsorbed from water solution on treated fly ash. In laboratory tests, the equilibrium and kinetics were examined applying various temperatures (293 - 333 K and pH (2 - 11 values. The maximum Cd(II and Pb(II ions adsorption capacity obtained at 293 K, pH 9 and mixing time 2 h from the Langmuir model can be grouped in the following order: FA-NaOH > FA-NH4HCO3 > FA > FA-Na2edta > FA-HCl. The morphology of fly ash grains was examined via small-angle X-ray scattering (SAXS and images of scanning electron microscope (SEM. The adsorption kinetics data were well fitted by a pseudo-second-order rate model but showed a very poor fit for the pseudofirst order model. The intra-particle model also revealed that there are two separate stages in the sorption process, i.e. the external diffusion and the inter-particle diffusion. Thermodynamics parameters such as free energy, enthalpy and entropy were also determined. A laboratory test demonstrated that the modified coal fly ash worked well for the Cd(II and Pb(II ion uptake from polluted waters.

  8. Adsorption of Phosphate Ion in Water with Lithium-Intercalated Gibbsite

    Directory of Open Access Journals (Sweden)

    Riwandi Sihombing

    2015-12-01

    Full Text Available In order to enhance adsorption capacity of gibbsite (Al(OH3 as an adsorbent for the adsorption of phosphate in water, gibbsite was modified through lithium-intercalation. The purification method of Tributh and Lagaly was applied prior to intercalation. The Li-Intercalation was prepared by the dispersion of gibbsite into LiCl solution for 24 hours. This intercalation formed an cationic clay with the structure of [LiAl2(OH6]+ and exchangeable Cl- anions in the gibbsite interlayer. A phosphate adsorption test using Lithium-intercalated gibbsite (LIG resulted in optimum adsorption occurring at pH 4.5 with an adsorption capacity of 11.198 mg phosphate/g LIG which is equivalent with 1.04 wt% LIG. The adsorption capacity decreased with decreasing amounts of H2PO4-/HPO4- species in the solution. This study showed that LIG has potential as an adsorbent for phosphate in an aqueous solution with pH 4.5–9.5.

  9. Adsorption Behaviour of La(III and Eu(III Ions from Aqueous Solutions by Hydroxyapatite: Kinetic, Isotherm, and Thermodynamic Studies

    Directory of Open Access Journals (Sweden)

    F. Granados-Correa

    2013-01-01

    Full Text Available The hydroxyapatite was successfully synthesized, characterized, and used as an alternative low-cost adsorbent material to study the adsorption behavior of La(III and Eu(III ions from nitrate aqueous solutions as a function of contact time, initial metal ion concentration, pH, and temperature by using a bath technique. The kinetic data correspond very well to the pseudo-second-order equation, and in both cases the uptake was affected by intraparticle diffusion. Isotherm adsorption data were well fitted by the Freundlich model equation with 1/n>1, indicating a multilayer and cooperative-type adsorption. Thermodynamic parameters for the adsorption systems were determinated at 293, 303, 313, and 323 K. These parameters show that adsorptions of La(III and Eu(III ions on hydroxyapatite are endothermic and spontaneous processes. The adsorption was found to follow the order Eu(III > La(III and is dependent on ion concentration, pH, and temperature.

  10. Application of Local Adsorbant From Southeast Sulawesi Clay Immobilized Saccharomyces Cerevisiae Bread’s Yeast Biomass for Adsorption Of Mn(Ii) Metal Ion

    Science.gov (United States)

    R, Halimahtussaddiyah; Mashuni; Budiarni

    2017-05-01

    Southeast Sulawesi has a great stock of clay. It is probably to use as a source of adsorbent. The adsorbent capacity of clay can be largered with teratment using bread’s yeast as biomass. At this research, study of analysis adsorption of Mn(II) metal ion on clay immobilized Saccharomyces cerevisiae bread’s yeast biomass adsorbent has been conducted. The aims of this research were to determine the effects of contact time, pH and concentration of Mn(II) metal ion and to determine the adsorption capacity of clay immobilized S. cerevisiae biomass for adsorbtion of Mn(II) metal ion. Activated clay was synthesized by reaction of clay with KMnO4, H2SO4 and HCl. S. cerevisiae biomass was result by bread’s yeast mashed. Immobilization of S. cerevisiae biomass into clay was done by mixing of ratio of S. cerevisiae bread’s yeast biomass and clay equal to 1:3 (mass of biomassa : mass of clay). The adsorption capacity was determined by using Freundlich and Langmuir adsorption isoterms. The results of FTIR spectrums showed that the functional groups of clay immobilized S. cerevisiae biomass were Si-OH (wave number 1643 cm-1), Si-O-Si (wave number 1033 cm-1), N-H (wave number 2337 cm-1), O-H (wave number 3441cm-1), and C-H (wave number 2931 cm-1). The result of adsorption capacity from Mn(II) metal ion of contact time optimum 120 minutes, pH optimun at 7 and concentration optimum 50 mg/L were 1,816 mg/g; 0,509 mg/g and 2,624mg/g respectively. The adsorption capacity of Mn(II) metal ion with ratio 1:3 (biomass : clay) was 0,1045 mg/g. Type of isothermal adsorption followed the Freunlich adsorption.

  11. Adsorption of Pb(II) ions from aqueous solution by native and activated bentonite: Kinetic, equilibrium and thermodynamic study

    Energy Technology Data Exchange (ETDEWEB)

    Kul, Ali Riza [Yuzuncu Yil University, Faculty of Art and Science, Department of Chemistry, 65080 Van (Turkey); Koyuncu, Huelya, E-mail: hkoyuncu@yyu.edu.tr [Forensic Medicine Foundation, Felek Street No. 45, 06300 Kecioren, Ankara (Turkey)

    2010-07-15

    In this study, the adsorption kinetics, equilibrium and thermodynamics of Pb(II) ions on native (NB) and acid activated (AAB) bentonites were examined. The specific surface areas, pore size and pore-size distributions of the samples were fully characterized. The adsorption efficiency of Pb(II) onto the NB and AAB was increased with increasing temperature. The kinetics of adsorption of Pb(II) ions was discussed using three kinetic models, the pseudo-first-order, the pseudo-second-order and the intra-particle diffusion model. The experimental data fitted very well the pseudo-second-order kinetic model. The initial sorption rate and the activation energy were also calculated. The activation energy of the sorption was calculated as 16.51 and 13.66 kJ mol{sup -1} for NB and AAB, respectively. Experimental results were also analysed by the Langmuir, Freundlich and Dubinin-Redushkevich (D-R) isotherm equations at different temperatures. R{sub L} separation factor for Langmuir and the n value for Freundlich isotherm show that Pb(II) ions are favorably adsorbed by NB and AAB. Thermodynamic quantities such as Gibbs free energy ({Delta}G), the enthalpy ({Delta}H) and the entropy change of sorption ({Delta}S) were determined as about -5.06, 10.29 and 0.017 kJ mol{sup -1} K{sup -1}, respectively for AAB. It was shown that the sorption processes were an endothermic reactions, controlled by physical mechanisms and spontaneously.

  12. Ion exchange chromatography on a new form of tin dioxide for the isolation of strontium radioisotopes from fission products: an application to milk samples

    International Nuclear Information System (INIS)

    Stella, R.; Valentini, M.T.G.; Maggi, L.

    1990-01-01

    An amorphous, partially-reduced tin dioxide, having properties of an inorganic exchanger, was tested for application to fission product separations. Due to the good sorption of both strontium and barium the application of the exchanger to radiostrontium isolation from fission product mixtures is subjected to important restrictions. An application to 90 Sr determination in milk is proposed. (author)

  13. Strontium Removal: Full-Scale Ohio Demonstrations

    Science.gov (United States)

    The objectives of this presentation are to present a brief overview of past bench-scale research to evaluate the impact lime softening on strontium removal from drinking water and present full-scale drinking water treatment studies to impact of lime softening and ion exchange sof...

  14. Ion exchange separation of lead from strontium in certified reference samples and spectrophotometric determination of lead as extractable ion-pair of eosin2- and the lead-cryptand (2.2.2)2+ complex

    International Nuclear Information System (INIS)

    Al-Merey, R.; Al-Shayah, O.

    2004-01-01

    A two-step procedure including anion exchange separation of lead from strontium in geological reference samples and a spectrophotometric determination of the separated lead as lead-cryptate (2.2.2) complex is presented. The exchangeable anion Cl - of the ion exchange resin (Dowex 1x4) is changed to Br - in 6M HBr solution. Lead is quantitatively retained in the column from 0.5M HBr medium, while Sr 2+ , Ba 2+ , Ca 2+ , Mg 2+ , Na + , K + , Fe 3+ , Cr 3+ , and Al 3+ are passed through. Subsequently the retained Ph is eluted from the column with 6M HBr. The separation efficiency of the resin is controlled using mixed standard solution of (Pb, Sr, Ca, Mg, Ba, Na, K, Fe, Cr and Al), and radioactive tracer of 85 Sr and 131 Ba. The resin selectivity coefficient (K) of separating Pb from Sr is found to be K S r P b∼10 9 . The Spectrophotometric method of lead determination is based on the formation of lead-crytate (2.2.2) complex at pH 8.3 using borate/HCl as a buffer solution. Then the ion-pair of eosin 2+ and lead-cryptand (2.2.2) complex is extracted with chloroform, finally the absorbance of the extractable legend is measured at 550 nm. The extraction recovery, accuracy, precision, linearity and detection limit of the spectrophotometric method are 99.58%, 1.7%, 0.080μg mL -1 , o-9μg mL -1 , and 0.060μg mL -1 , respectively. (author)

  15. Ligand adsorption on an activated carbon for the removal of chromate ions from aqueous solutions.

    Science.gov (United States)

    García-Martín, J; López-Garzón, R; Godino-Salido, M Luz; Gutiérrez-Valero, M Dolores; Arranz-Mascarós, P; Cuesta, R; Carrasco-Marín, F

    2005-07-19

    The results presented in this work are related to the design of a guideline to develop specific properties at the surface of an activated carbon (AC). For this, two model aromatic compounds have been synthesized and their electrolytic behavior in aqueous solutions was studied by a potentiometric method. The textural characteristics of the activated carbon were determined by porosimetry methods. The nature of oxygen-carrying functions and the acid-base behavior of the AC surface were characterized by TPD and potentiometric titration methods, respectively. The adsorption and desorption equilibria of the aromatic compounds on activated carbon were measured in aqueous solutions, and the hysteresis between adsorption and desorption, which reveals irreversible adsorption, was discussed on the basis of the frontier orbital theory. HOMO and LUMO orbitals of the adsorbent and adsorbates were calculated, and irreversible adsorption was attributed to the small energy difference between HOMO and LUMO of the aromatic adsorbates and the adsorbent. Adsorption equilibria of K2CrO4 in aqueous solution on the AC alone and on the AC-aromatic ligand adsorbents, respectively, prove the efficient development of specific chemical functions at the carbon surface provided by the adsorbed aromatic compounds.

  16. Adsorption of copper, nickel and lead ions from synthetic semiconductor industrial wastewater by palm shell activated carbon

    International Nuclear Information System (INIS)

    Onundi, Y. B.; Mamun, A. A.; Al Khatib, M. F.; Ahmad, Y. M.

    2010-01-01

    Granular activated carbon produced from palm kernel shell was used as adsorbent to remove copper, nickel and lead ions from a synthesized industrial wastewater. Laboratory experimental investigation was carried out to identify the effect of p H and contact time on adsorption of lead, copper and nickel from the mixed metals solution. Equilibrium adsorption experiments at ambient room temperature were carried out and fitted to Langmuir and Freundlich models. Results showed that p H 5 was the most suitable, while the maximum adsorbent capacity was at a dosage of 1 g/L, recording a sorption capacity of 1.337 mg/g for lead, 1.581 mg/g for copper and 0.130 mg/g for nickel. The percentage metal removal approached equilibrium within 30 minutes for lead, 75 minutes for copper and nickel, with lead recording 100 p ercent , copper 97 p ercent a nd nickel 55 p ercent r emoval, having a trend of Pb 2+ > Cu 2+ > Ni 2+ . Langmuir model had higher R 2 values of 0.977, 0.817 and 0.978 for copper, nickel and lead respectively, which fitted the equilibrium adsorption process more than Freundlich model for the three metals.

  17. Magnesium- and strontium-co-substituted hydroxyapatite: the effects of doped-ions on the structure and chemico-physical properties.

    Science.gov (United States)

    Aina, Valentina; Lusvardi, Gigliola; Annaz, Basil; Gibson, Iain R; Imrie, Flora E; Malavasi, Gianluca; Menabue, Ledi; Cerrato, Giuseppina; Martra, Gianmario

    2012-12-01

    The present study is aimed at investigating the contribution of two biologically important cations, Mg(2+) and Sr(2+), when substituted into the structure of hydroxyapatite (Ca(10)(PO(4))(6)(OH)(2),HA). The substituted samples were synthesized by an aqueous precipitation method that involved the addition of Mg(2+)- and Sr(2+)-containing precursors to partially replace Ca(2+) ions in the apatite structure. Eight substituted HA samples with different concentrations of single (only Mg(2+)) or combined (Mg(2+) and Sr(2+)) substitution of cations have been investigated and the results compared with those of pure HA. The obtained materials were characterized by X-ray powder diffraction, specific surface area and porosity measurements (N(2) adsorption at 77 K), FT-IR and Raman spectroscopies and scanning electron microscopy. The results indicate that the co-substitution gives rise to the formation of HA and β-TCP structure types, with a variation of their cell parameters and of the crystallinity degree of HA with varying levels of substitution. An evaluation of the amount of substituents allows us to design and prepare BCP composite materials with a desired HA/β-TCP ratio.

  18. utilization of adsorption and/or liquid membranes techniques in treatment of some hazardous substances

    International Nuclear Information System (INIS)

    Hussin, L.M.S.

    2011-01-01

    environmental pollution, as a consequence of the industrialization process, is one of the major problems that has to be solved and controlled. The most important treatment processes for metals and dyes contaminated waste streams include chemical precipitation, membrane, filtration, ion exchange, carbon adsorption and coprecipitation/adsorption. However, all these techniques have their inherent advantages and limitations in applications. These processes usually need expensive facility and high maintenance cost. Therefore, there is a need for more economical alternative technologies for the treatment of metals and dyes contaminated waste streams. The aim of present work is to study the treatment of some hazardous substances such as heavy metals e.g. ( lead, cobalt and strontium) and dyes e.g. ( acid red 73, and acid blue 74 ) using either adsorption or liquid emulsion membrane techniques. The experimental part deals with the application of adsorption and liquid emulsion membrane techniques for removal of some hazardous substances such as metal ions ( lead, cobalt and strontium) and dyes (acid red 73 and acid blue 74). All the apparatus and techniques employed were described.

  19. Functionalized mesoporous silicas with crown ether moieties for selective adsorption of lithium ions in artificial sea water.

    Science.gov (United States)

    Sung, Soo Park; Moorthy, Madhappan Santha; Song, Hyun-Jin; Ha, Chang-Sik

    2014-11-01

    Lithium ion has been increasingly recognized in a wide range of industrial applications. In this work, we studied on the adsorption of Li+ in the artificial seawater with high selectivity using methyl-crown ether (AC-SBA-15) and aza-crown ether (HMC-SBA-15) moieties-functionalized mesoporous silica materials. First, methyl-crown ether and aza-crown ether moieties-functionalized mesoporous silica materials were synthesized via two-step post-synthesis process using a grafting method. The functionalized materials were employed to the metal ion adsorption from aqueous solution (artificial seawater) containing Li+, Co2+, Cr3+ and Hg2+. The prepared hybrid material showed high selectivity for Li+ ion in the artificial seawater at pH 8.0. The absorbed amount of Li+ was 73 times higher than Cr3+ for aza-crown ether containing AC-SBA-15 as an absorbent. The absorbed amount of Co2+ (4.5 x 10(-5) mol/g), Cr3+ (1.5 x 10(-5) mol/g) and Hg2+ (2.25 x 10(-4) mol/g) were remarkably lower than the case of Li+. On the other hand, the absorbed amount of various metal ions of HMC-SBA-15 with amine groups in alky chains and crown ether moieties were 1.1 x 10(-3) mol/g for Li+, 5.0 x 10(-5) mol/g for Co2+, 2.9 x 10(-4) mol/g for Cr3+, 2.8 x 10(-4) mol/g for Hg2+ mol/g, respectively.

  20. Adsorption of Phosphate Ion in Water with Lithium-Intercalated Gibbsite

    OpenAIRE

    Riwandi Sihombing; Yuni Krisyuningsih Krisnandi; Rahma Widya; Siti Zahrotul Luthfiyah; Rika Tri Yunarti

    2015-01-01

    In order to enhance adsorption capacity of gibbsite (Al(OH)3 as an adsorbent for the adsorption of phosphate in water, gibbsite was modified through lithium-intercalation. The purification method of Tributh and Lagaly was applied prior to intercalation. The Li-Intercalation was prepared by the dispersion of gibbsite into LiCl solution for 24 hours. This intercalation formed an cationic clay with the structure of [LiAl2(OH)6]+ and exchangeable Cl- anions in the gibbsite interlayer. A phosphate...

  1. The adsorption of Sr(II) and Cs(I) ions by irradiated Saccharomyces cerevisiae

    International Nuclear Information System (INIS)

    Yiming Tan; Jundong Feng; Liang Qiu; Zhentian Zhao; Xiaohong Zhang; Haiqian Zhang

    2017-01-01

    Adsorption behavior and mechanism of Sr(II) and Cs(I) in single and binary solutions using irradiated Saccharomyces cerevisiae was investigated. The effects of several environmental factors on Sr(II) and Cs(I) adsorption to irradiated Saccharomyces cerevisiae was determined. The equilibrium experimental data were simulated by different kinetic models and isotherm models. The combined effect of Sr(II) and Cs(I) on Saccharomyces cerevisiae is generally antagonistic. SEM and EDS analyses indicate that crystals formed on the cell surface are precipitate of Sr(II) and Cs(I), respectively. (author)

  2. Adsorption of Cu(II) and Cr(VI) ions by chitosan: Kinetics and ...

    African Journals Online (AJOL)

    drinie

    2001-01-01

    Jan 1, 2001 ... dimensional structure of the molecules to chelate and remove ions of a specific ... alginates, carrageenan, lignins, proteins, chitin and chitin derivatives. Another ... formation of a chitosan chelate with Cu ions is shown in Fig.1.

  3. Theory of kinetics and equilibrium of ion exchange-adsorption and mechanism of extracting uranium from sea-water with titanic gel

    International Nuclear Information System (INIS)

    Ai Hongtao

    1989-01-01

    An isothermal equation for ion exchange-adsorption is derived by mass action law. The equation can be used to sum up empirical and semiempirical formulas of the exchange adsorption, such as Gapon Equation, Sips Formula, Langmuir Equation and Freundlich Formula. In this paper, by adopting the ion exchange reaction to act as the determining step of the ion exchange adsorption kinetics, and exchange-adsorption kinetics equation is derived. It is verified by he results of a series of experiments in which uranium is extracted form enriched sea-water and natural sea-water with hydrous titanium oxide (titanic gel). This equation can be used to explain not only the results of test which have been applied to prove fast intraparticle diffusion of liquid film deffusion mechanism, but also test data which can be expalined by the co-controlling fast intraparticle and liquid film diffusion, and the kinetic data which can not be clarified by diffusion mechanism. It is proposed that the mechanism of the exchange adsorption of uranium from sea-water with titanic gel is a cationic exchange reaction. A method for calculating the quantity of exchange-adsorption at equilibrium is also given

  4. The coprecipitation of strontium with hydroxyapatite

    International Nuclear Information System (INIS)

    Fujino, Osamu

    1975-01-01

    The distribution behavior of the strontium ion between hydroxyapatite and the parent solution was investigated. The hydroxyapatite was formed by the extremely slow addition of diammonium hydrogenphosphate to solutions of calcium and strontium nitrate buffered with ethylenediamine at 80 0 C. The precipitate yielded a typical X-ray diffraction pattern of hydroxyapatite and had a composition in which the Ca/P molar ratio was 1.67 at pH 6.80. The strontium ion was coprecipitated in the apatite, obeying the Doerner and Hoskins logarithnmic distribution law. The distribution coefficient was scarcely affected by the strontium concentration on the pH value in the parent solution, and had a value of 0.26+-0.02 at 80 0 C. On the other hand, the apparent distribution coefficient was a little affected by such organic anions as acetate, citrate, lactate, glycinate, and glutamate ions. The lattice constants of the precipitates prepared in the research were measured in order to confirm the formation of the solid solutions. (auth.)

  5. In situ co-adsorption of arsenic and iron/manganese ions on raw clays

    Czech Academy of Sciences Publication Activity Database

    Doušová, B.; Lhotka, M.; Grygar, Tomáš; Machovič, V.; Herzogová, L.

    2011-01-01

    Roč. 54, č. 2 (2011), s. 166-171 ISSN 0169-1317 Institutional research plan: CEZ:AV0Z40320502 Keywords : Arsenic * Groundwater * Co-adsorption * Raw clays * Pre-modified clays * Fe/Mn Subject RIV: DD - Geochemistry Impact factor: 2.474, year: 2011

  6. Ion and electron spectroscopy of strontium in the vicinity of the two-photon-excited 5p2 1S0 state

    Science.gov (United States)

    Dimitriou, A.; Cohen, S.

    2014-07-01

    Two-photon ionization of ground-state strontium is investigated experimentally in the 360-370-nm spectral range with dye laser pulses of long (˜ns) duration and low (˜1010W cm-2) intensity. The Sr+ spectra recorded with linear laser polarization are dominated by the presence of the highly correlated 5p21S0 state and by the even parity [4d6d

  7. Examination of Organic Vapor Adsorption onto Alkali Metal and Halide Atomic Ions by using Ion Mobility Mass Spectrometry.

    Science.gov (United States)

    Maiβer, Anne; Hogan, Christopher J

    2017-11-03

    We utilize ion mobility mass spectrometry with an atmospheric pressure differential mobility analyzer coupled to a time-of-flight mass spectrometer (DMA-MS) to examine the formation of ion-vapor molecule complexes with seed ions of K + , Rb + , Cs + , Br - , and I - exposed to n-butanol and n-nonane vapor under subsaturated conditions. Ion-vapor molecule complex formation is indicated by a shift in the apparent mobility of each ion. Measurement results are compared to predicted mobility shifts based upon the Kelvin-Thomson equation, which is commonly used in predicting rates of ion-induced nucleation. We find that n-butanol at saturation ratios as low as 0.03 readily binds to all seed ions, leading to mobility shifts in excess of 35 %. Conversely, the binding of n-nonane is not detectable for any ion for saturation ratios in the 0-0.27 range. An inverse correlation between the ionic radius of the initial seed and the extent of n-butanol uptake is observed, such that at elevated n-butanol concentrations, the smallest ion (K + ) has the smallest apparent mobility and the largest (I - ) has the largest apparent mobility. Though the differences in behavior of the two vapor molecules types examined and the observed effect of ionic seed radius are not accounted for by the Kelvin-Thomson equation, its predictions are in good agreement with measured mobility shifts for Rb + , Cs + , and Br - in the presence of n-butanol (typically within 10 % of measurements). © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

  8. An unprecedented process of peroxide ion formation and its localization in the crystal structure of strontium peroxy-hydroxyapatite Sr_1_0(PO_4)_6(O_2)_x(OH)_2_-_2_x

    International Nuclear Information System (INIS)

    Kazin, Pavel E.; Zykin, Mikhail A.; Dinnebier, Robert E.; Magdysyuk, Oxana V.; Jansen, Martin; Tretyakov, Yury D.

    2012-01-01

    Formation of strontium peroxy-hydroxyapatite solid solution Sr_1_0(PO_4)_6(O_2)_x(OH)_2_-_2_x was studied on annealing the hydroxyapatite in the temperature range 900-1350 C in oxygen, air, and argon atmosphere. The redox process was found to display unprecedented features: (i) the peroxide content increased with raising temperature, (ii) the peroxide content remained substantial even at a low oxygen pressure of 1.013 Pa, (iii) the peroxide content was extremely persistent, and even at a temperature of 1350 C in oxygen atmosphere the peroxide groups substituted more than two-third of the original hydroxide groups. Chemical processes consistent with these features are suggested. In the UV/Vis spectrum, an absorption peak at 300 nm was recorded, which was attributed to an electronic transition in the peroxide ion, since its intensity depended linearly on the peroxide content. In the Raman spectra, a weak band at 765-770 cm"-"1 was ascribed to symmetric stretching vibrations of O_2"2"-. The structures of the compounds were refined from powder X-ray diffraction data using the Rietveld method supported by a maximum entropy method (MEM) electron density calculation. The peroxide ions are localized in the center of the hexagonal channel. At high concentration they tend to order with the associated vacancies along the channels. As a consequence, the width of the channel sections varies, the PO_4 tetrahedra tilt, and the remote strontium atoms are displaced leading to changes in their coordination. Generally, the peroxide for hydroxide substitution manifests itself in the reduction of the overall channel diameter (and its volume), while the volume occupied by out-of-channel ions remains the same. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  9. A facile method to prepare dual-functional membrane for efficient oil removal and in situ reversible mercury ions adsorption from wastewater

    Science.gov (United States)

    Zhang, Qingdong; Liu, Na; Cao, Yingze; Zhang, Weifeng; Wei, Yen; Feng, Lin; Jiang, Lei

    2018-03-01

    In this work, a novel thiol covered polyamide (nylon 66) microfiltration membrane was fabricated by combining mussel-inspired chemistry and coupling reaction, which owns excellent dual-function that can simultaneously remove oil from water efficiently and adsorb the mercury ions contained in the wastewater reversibly. Such membrane exhibited high oil/water separation efficiency, outstanding mercury adsorption ability, and good stability. Moreover, it can be regenerated in nitric acid solution, and maintain its good adsorption performance. The as-prepared membrane showed great potentials for water purification to reduce the heavy metal ion pollution and complicated industrial oily wastewater and living wastewater.

  10. Adsorption of saponin compound in Carica papaya leaves extract using weakly basic ion exchanger resin

    Science.gov (United States)

    Abidin, Noraziani Zainal; Janam, Anathasia; Zubairi, Saiful Irwan

    2016-11-01

    Adsorption of saponin compound in papaya leaves juice extract using Amberlite® IRA-67 resin was not reported in previous studies. In this research, Amberlite® IRA-67 was used to determine the amount of saponin that can be adsorbed using different weights of dry resin (0.1 g and 0.5 g). Peleg model was used to determine the maximum yield of saponin (43.67 mg) and the exhaustive time (5.7 days) prior to a preliminary resin-saponin adsorption study. After adsorption process, there was no significant difference (p>0.05) in total saponin content (mg) for sample treated with 0.1 g (3.79 ± 0.55 mg) and sample treated with 0.5 g (3.43 ± 0.51 mg) dry weight resin. Long-term kinetic adsorption of resin-saponin method (>24 hours) should be conducted to obtain optimum freed saponin extract. Besides that, sample treated with 0.1 g dry weight resin had high free radical scavenging value of 50.33 ± 2.74% compared to sample treated with 0.5 g dry weight resin that had low free radical scavenging value of 24.54 ± 1.66% dry weights. Total saponin content (mg), total phenolic content (mg GAE) and free radical scavenging activity (%) was investigated to determine the interaction of those compounds with Amberlite® IRA-67. The RP-HPLC analysis using ursolic acid as standard at 203 nm showed no peak even though ursolic acid was one of the saponin components that was ubiquitous in plant kingdom. The absence of peak was due to weak solubility of ursolic acid in water and since it was only soluble in solvent with moderate polarity. The Pearson's correlation coefficient for total saponin content (mg) versus total phenolic content (mg GAE) and radical scavenging activity (%) were +0.959 and +0.807. Positive values showed that whenever there was an increase in saponin content (mg), the phenolic content (mg GAE) and radical scavenging activity (%) would also increase. However, as the resin-saponin adsorption was carried out, there was a significant decrease of radical scavenging activity

  11. Rubidium-strontium method

    International Nuclear Information System (INIS)

    Dubansky, A.

    1980-01-01

    The rubidium-strontium geological dating method is based on the determination of the Rb and Sr isotope ratio in rocks, mainly using mass spectrometry. The method is only practical for silicate minerals and rocks, potassium feldspars and slates. Also described is the rubidium-strontium isochrone method. This, however, requires a significant amount of experimental data and an analysis of large quantities of samples, often of the order of tons. The results are tabulated of rubidium-strontium dating of geological formations in the Czech Socialist Republic. (M.S.)

  12. A study on characteristic of selective membrane for strontium analysis

    Energy Technology Data Exchange (ETDEWEB)

    Moon, Seung Hyun; Choi, Young Woo [Kwang-ju Institute of Science and Technology, Kwangju (Korea)

    1999-04-01

    In this study, supported liquid membranes (SLMs) using crown ether were prepared in order to separate strontium ion selectively from a calcium contained solution However, at the higher than 3 N nitric acid concentration of a strip solution, stability of a SLM was declined remarkably owing to the hasty loss of carrier impregnated in supporter and, on account of this phenomena, facilitated transports were not accomplished. And DC18C6 as a neutral carrier affected remarkably the selectivity of strontium and the factor determining permeabilities of metal ions was as a role of DNNS. Consequently, in order to be a optimal SLM for the high permeability and the stable selectivity of strontium, concentration of DC18C6 and DNNS should be 0.1 M and 25 mM, respectively and, at this condition, the relative removal ratio of strontium to calcium was 93.3%. And the change of calcium concentration in the feed solution affected the permeability of strontium. In particular, when the ratio of strontium to calcium concentration in the feed solution was in the range of 1/5 - 1/50, strontium could be separated selectively at stable permeabilities. (author). 17 refs., 19 figs., 3 tabs.

  13. An isotopic method to distinguish between ion exchange and adsorption of diazonium cations of zeolites

    International Nuclear Information System (INIS)

    Mohl, M.; Fejes, P.; Horvath, G.

    1984-01-01

    The ion exchange isotherms of two different diazonium cations have been determined on synthetic mordenite and faujasite using 22 Na as radiotracer. Under similar conditions (but with no radiotracer) the isotherms were followed spectrophotometrically so that a comparison between the amounts of ion exchanged and adsorbed cations can be made. (author)

  14. Laser-ignited frontal polymerization of shape-controllable poly(VI-co-AM) hydrogels based on 3D templates toward adsorption of heavy metal ions

    Science.gov (United States)

    Fan, Suzhen; Liu, Sisi; Wang, Xiao-Qiao; Wang, Cai-Feng; Chen, Su

    2016-06-01

    Given the increasing heavy metal pollution issue, fast preparation of polymeric hydrogels with excellent adsorption property toward heavy metal ions is very attractive. In this work, a series of poly( N-vinylimidazole-co-acrylamide) (poly(VI-co-AM)) hydrogels were synthesized via laser-ignited frontal polymerization (LIFP) for the first time. The dependence of frontal velocity and temperature on two factors monomer ratios and initiator concentrations was systematically investigated. Poly(VI-co-AM) hydrogels with any self-supporting shapes can be synthesized by a one-step LIFP in seconds through the application of 3D templates. These shape-persistent hydrogels are pH-responsive and exhibit excellent adsorption/desorption characteristics toward Mn(II), Zn(II), Cd(II), Ni(II), Cu(II) and Co(II) ions, and the adsorption conformed to the pseudo-second-order kinetic model. The reusability of the hydrogels toward mental ions adsorption was further researched, which suggested that the hydrogels can be reused without serious decrease in adsorption capacity. This work might open a promising strategy to facilely prepare shape-controllable hydrogels and expand the application of LIFP.

  15. Photostriction of strontium ruthenate

    KAUST Repository

    Wei, Tzu-Chiao; Wang, Hsin-Ping; Liu, Heng-Jui; Tsai, Dung-Sheng; Ke, Jr-Jian; Wu, Chung-Lun; Yin, Yu-Peng; Zhan, Qian; Lin, Gong-Ru; Chu, Ying-Hao; He, Jr-Hau

    2017-01-01

    Transition metal oxides with a perovskite crystal structure exhibit a variety of physical properties associated with the lattice. Among these materials, strontium ruthenate (SrRuO3) displays unusually strong coupling of charge, spin and lattice

  16. Adsorption and Formation of Small Na Clusters on Pristine and Double-Vacancy Graphene for Anodes of Na-Ion Batteries.

    Science.gov (United States)

    Liang, Zhicong; Fan, Xiaofeng; Zheng, Weitao; Singh, David J

    2017-05-24

    Layered carbon is a likely anode material for Na-ion batteries (NIBs). Graphitic carbon has a low capacity of approximately 35 (mA h)/g due to the formation of NaC 64 . Using first-principles methods including van der Waals interactions, we analyze the adsorption of Na ions and clusters on graphene in the context of anodes. The interaction between Na ions and graphene is found to be weak. Small Na clusters are not stable on the surface of pristine graphene in the electrochemical environment of NIBs. However, we find that Na ions and clusters can be stored effectively on defected graphene that has double vacancies. In addition, the adsorption energy of small Na clusters near a double vacancy is found to decrease with increasing cluster size. With high concentrations of vacancies the capacity of Na on defective graphene is found to be as much as 10-30 times higher than that of graphitic carbon.

  17. Chromium (VI) ion adsorption by grafted cross-linked chitosan beads in aqueous solution - a mathematical and statistical modeling study.

    Science.gov (United States)

    Igberase, E; Osifo, P; Ofomaja, A

    2017-12-01

    Chitosan outstanding qualities and efficient way of binding metal ions even to near zero concentration is the major reason for special attention. Modification of chitosan allows the polymer to be applied in numerous field of research. Depending on the modification techniques, chitosan possesses increased adsorption capacity. In this study chitosan beads (CS) were formulated from chitosan flakes, the beads were cross-linked with glutaraldehyde and thereafter grafted with ethyldiaminetetraacetic acid. The stability and amine concentration of the beads were determined. The chemical functionalities of the beads were obtained by Fourier transform infrared spectroscopy, X-ray diffraction and thermogravimetric analysis (TGA). However, in the adsorption studies with Cr(VI), the number of runs in the experiment was obtained by response surface methodology (RSM), and the maximum adsorption capacity (Q m ) from each run was determined from the Langmuir model. The results of the experiment showed that the non-modified beads were soluble at pH 1-4 and insoluble at pH 5, while the modified beads were insoluble at pH 1-6. The amine concentration of CS, CCS and grafted cross-linked chitosan beads (GCCS) were 4.4, 3.8 and 5.0 mmol/g, respectively. The point of zero charge (pH PZC ) of GCCS was found to be 4.4. The quadratic model was significant and adequate in describing the experimental data. The difference between experimental and predicted Q m was negligible. From the design matrix and results, increased Q m was achieved at pH 5, contact time 70 min, temperature 45°C, adsorbent dosage 5 g and initial concentration 70 mg/l. The desorption of the beads loaded with Cr(VI) was successful with 0.5 M HCl eluant and contact time of 180 min, leading to cost minimization.

  18. Carbon dioxide adsorption over zeolite-like metal organic frameworks (ZMOFs) having a sod topology: Structure and ion-exchange effect

    Energy Technology Data Exchange (ETDEWEB)

    Chen, C.; Kim, J.; Yang, D.A.; Ahn, W.S. [Inha University, Inchon (Republic of Korea). Dept. of Chemical Engineering

    2011-04-15

    Zeolite-like metal organic framework (ZMOF) materials having rho and sod topologies were experimentally investigated as CO{sub 2} adsorbents for the first time. As-prepared ZMOF materials showed reasonably high CO{sub 2} adsorption capacities (ca. 51 and 53 mg/g(adsorbent) for rho- and sod-ZMOF, respectively) and high CO{sub 2}/N{sub 2} selectivity (> 20) at 298 K and 1 bar. The latter showed a higher heat of adsorption (27-45 kJ/mol). These ZMOFs exhibited better CO{sub 2} adsorption than ZIF-8, a commonly investigated zeolitic imidazolate framework (ZIF) material having the same sod topology but in a neutral framework. Partially ion-exchanged sod-ZMOFs by alkali-metals resulted in improved CO{sub 2} adsorption performance compared with the as-prepared ZMOF. The highest CO{sub 2} adsorption was obtained with K{sup +}-exchanged sod-ZMOF (61 mg/g(adsorbent)), representing a ca. 15% increase in adsorption capacity. Complete desorption of CO{sub 2} in the K{sup +}-sod-ZMOF was attained at mild conditions (40{sup o}C, He purging), and reversible and sustainable CO{sub 2} adsorption performance was demonstrated in 5 sets of recycling runs.

  19. Preparation of novel oxidized mesoporous carbon with excellent adsorption performance for removal of malachite green and lead ion

    Science.gov (United States)

    Zhang, Xialan; Lin, Qilang; Luo, Shiyuan; Ruan, Kezhao; Peng, Kaiping

    2018-06-01

    An oxidized mesoporous carbon (OMC) with fluffy structure was fabricated from the mixture of petroleum asphalt and aluminum isopropoxide, and its structures were characterized by FESEM, TEM, BET, TG, XPS and FT-IR. In addition, bath absorption experiments for malachite green (MG) and lead ion (Pb2+) were carried out to explore the effects of pH, initial concentration, contact time and temperature on its absorption process. Results show that the OMC prepared has a fluffy ultrathin-wall structure with narrow pore size distribution and rich oxygen-containing groups. It exhibits excellent absorption performance for the removal of MG as well as Pb2+, as indicated by that its maximum adsorption capacity is 963.1 mg g-1 for MG and 198.6 mg g-1 for Pb2+. The absorption experimental data are all fitted well with pseudo-second-order model and Frendlich isotherm, respectively. More importantly, the OMC still maintains relatively high adsorption capacity after five cycles.

  20. The fabrication of highly uniform ZnO/CdS core/shell structures using a spin-coating-based successive ion layer adsorption and reaction method

    International Nuclear Information System (INIS)

    Joo, Jinmyoung; Kim, Darae; Yun, Dong-Jin; Jun, Hwichan; Rhee, Shi-Woo; Lee, Jae Sung; Yong, Kijung; Jeon, Sangmin; Kim, Sungjee

    2010-01-01

    We developed a successive ion layer adsorption and reaction method based on spin-coating (spin-SILAR) and applied the method to the fabrication of highly uniform ZnO/CdS core/shell nanowire arrays. Because the adsorption, reaction, and rinsing steps occur simultaneously during spin-coating, the spin-SILAR method does not require rinsing steps between the alternating ion adsorption steps, making the growth process simpler and faster than conventional SILAR methods based on dip-coating (dip-SILAR). The ZnO/CdS core/shell nanowire arrays prepared by spin-SILAR had a denser and more uniform structure than those prepared by dip-SILAR, resulting in the higher power efficiency for use in photoelectrochemical cells.

  1. The fabrication of highly uniform ZnO/CdS core/shell structures using a spin-coating-based successive ion layer adsorption and reaction method

    Energy Technology Data Exchange (ETDEWEB)

    Joo, Jinmyoung; Kim, Darae; Yun, Dong-Jin; Jun, Hwichan; Rhee, Shi-Woo; Lee, Jae Sung; Yong, Kijung; Jeon, Sangmin [System on Chip Chemical Process Research, Department of Chemical Engineering, Pohang University of Science and Technology (POSTECH), Pohang (Korea, Republic of); Kim, Sungjee, E-mail: jeons@postech.ac.kr [Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang (Korea, Republic of)

    2010-08-13

    We developed a successive ion layer adsorption and reaction method based on spin-coating (spin-SILAR) and applied the method to the fabrication of highly uniform ZnO/CdS core/shell nanowire arrays. Because the adsorption, reaction, and rinsing steps occur simultaneously during spin-coating, the spin-SILAR method does not require rinsing steps between the alternating ion adsorption steps, making the growth process simpler and faster than conventional SILAR methods based on dip-coating (dip-SILAR). The ZnO/CdS core/shell nanowire arrays prepared by spin-SILAR had a denser and more uniform structure than those prepared by dip-SILAR, resulting in the higher power efficiency for use in photoelectrochemical cells.

  2. Batch and column adsorption behaviors of Se(IV) and Te(IV) on organic and inorganic ion exchangers from HCl solutions

    Energy Technology Data Exchange (ETDEWEB)

    El-Sweify, Fatma H.; Abdel-Fattah, Alaa El-Din A.; Aly, Shorouk M.; Ghamry, Mohamed A. [Atomic Energy Authority, Cairo (Egypt). Hot Laboratories Center; El-Sheikh, Ragaa [Zagazig Univ. (Egypt). Chemistry Dept.

    2017-07-01

    Adsorption behaviors of Se(IV) and Te(IV) on the inorganic ion exchanger ceric tungstate (CeW) was studied under static and dynamic conditions and compared with the adsorption on the organic cation and anion exchangers Dowex-50X8 and AG-2X8, respectively. The radioactive isotopes {sup 75}Se and {sup 123m}Te were used to trace the respective elements. Some parameters affecting the adsorption were investigated under static conditions. In the case of batch technique the adsorption was studied from slightly acidic HCl as well as slightly alkaline media, i.e. at two pH-ranges. Se(IV) and Te(IV) were adsorbed on both the inorganic ion exchanger (CeW) and on AG-2X8, from slightly alkaline solutions. From the similarity of adsorption on both ion exchangers it was clear that (CeW) acts as an anion exchanger. Moreover, the obtained K{sub d}-values for the adsorption on (CeW) were much higher than those for the adsorption on the organic anion exchanger AG-2X8. Se(IV) was not adsorbed on Dowex-50X8 all over the studied pH-range whereas Te(IV) was slightly adsorbed. Loading and elution behaviors of Se(IV) and Te(IV) on columns of AG-2X8 and (CeW) were studied using solutions of HCl of different concentrations. Some good separation alternatives of Se(IV) and Te(IV) under certain conditions were achieved.

  3. Adsorption of toxic metal ion Cr(VI) from aqueous state by TiO2-MCM-41: equilibrium and kinetic studies.

    Science.gov (United States)

    Parida, Kulamani; Mishra, Krushna Gopal; Dash, Suresh Kumar

    2012-11-30

    This paper deals with the immobilization of various weight percentage of TiO(2) on mesoporous MCM-41, characterization of the materials by X-ray diffraction (XRD), nitrogen adsorption-desorption, Fourier Transform Infrared (FTIR) analysis, UV-vis diffuse reflectance spectroscopy (DRS) and evaluation of the adsorption capacity toward Cr(VI) removal. It is found that the MCM-41 structure retained after loading of TiO(2) but the surface area and pore diameter decreased due to pore blockage. Adsorption of Cr(VI) from aqueous state was investigated on TiO(2)-MCM-41 by changing various parameters such as pH, metal ion concentration, and the temperature. When TiO(2) loading was more than 20 wt.%, the adsorption activity (25)TiO(2)-MCM-41 reduced significantly due to considerable decrease in the surface area. It is also observed that TiO(2) and neat MCM-41 exhibits very less Cr(VI) adsorption compared to TiO(2)-MCM-41. The adsorption of Cr(VI) onto (20)TiO(2)-MCM-41 at pH~5.5 and temperature 323 K was 91% at 100mg/L Cr(VI) metal ion concentration in 80 min. The experimental data fitted well to Langmuir and Freundlich isotherms. The adsorption of Cr(VI) on TiO(2)-MCM-41 followed a second order kinetics with higher values of intra-particle diffusion rate. Thermodynamic parameters suggested that the adsorption process is endothermic in nature and desorption studies indicated a chemisorption mode. Copyright © 2012 Elsevier B.V. All rights reserved.

  4. Synthesizing new types of ultrathin 2D metal oxide nanosheets via half-successive ion layer adsorption and reaction

    Science.gov (United States)

    Gao, Linjie; Li, Yaguang; Xiao, Mu; Wang, Shufang; Fu, Guangsheng; Wang, Lianzhou

    2017-06-01

    Two-dimensional (2D) metal oxide nanosheets have demonstrated their great potential in a broad range of applications. The existing synthesis strategies are mainly preparing 2D nanosheets from layered and specific transition metal oxides. How to prepare the other types of metal oxides as ultrathin 2D nanosheets remains unsolved, especially for metal oxides containing alkali, alkaline earth metal, and multiple metal elements. Herein, we developed a half-successive ion layer adsorption and reaction (SILAR) method, which could synthesize those types of metal oxides as ultrathin 2D nanosheets. The synthesized 2D metal oxides nanosheets are within 1 nm level thickness and 500 m2 · g-1 level surface area. This method allows us to develop many new types of ultrathin 2D metal oxides nanosheets that have never been prepared before.

  5. Selective adsorption of silver(I) ions over copper(II) ions on a sulfoethyl derivative of chitosan.

    Science.gov (United States)

    Petrova, Yulia S; Pestov, Alexandr V; Usoltseva, Maria K; Neudachina, Ludmila K

    2015-12-15

    This study presents a simple and effective method of preparation of N-(2-sulfoethyl) chitosan (NSE-chitosan) that allows obtaining a product with a degree of modification up to 1.0. The chemical structure of the obtained polymers was confirmed by FT-IR and 1H NMR spectroscopies. Cross-linking of N-(2-sulfoethyl) chitosans by glutaraldehyde allows preparation of sorbents for removal and concentration of metal ions. Capacity of sorbents towards hydroxide ions was determined depending on the degree of sulfoethylation under static and dynamic conditions. Dissociation constants of functional amino groups of the analyzed sorbents were determined by potentiometric titration. It was shown that basicity of the amino groups decreased (wherein pKa decreased from 6.53 to 5.67) with increase in degree of sulfoethylation. It explains the significant influence of sulfo groups on selectivity of sorption of metal ions on N-(2-sulfoethyl) chitosan-based sorbents. The investigated substances selectively remove copper(II) and silver(I) ions from solutions of complex composition. Wherein the selectivity coefficient KAg/Cu increased to 20 (pH 6.5, ammonium acetate buffer solution) with increase in degree of sulfoethylation of the sorbent up to 1.0. Copyright © 2015 Elsevier B.V. All rights reserved.

  6. Sorptive removal of cesium-137 and strontium-90 from water by unconventional sorbents. 1. Usage of bauxite wastes (red muds)

    Energy Technology Data Exchange (ETDEWEB)

    Apak, R.; Atun, G.; Gueclue, K.; Tuetem, E.; Keskin, G. [Istanbul Univ. (Turkey). Faculty of Engineering

    1995-10-01

    Bauxite wastes of alumina manufacture, i.e., red muds, have been tested for radiocesium and strontium removal from water. The red muds were water-washed, acid-, and heat-treated before usage to produce hydrous oxide like sorbents. Surface treatment of the sorbent was beneficial for {sup 137}Cs uptake, while heat-treatment was detrimental to the -SOH surface sites responsible for high {sup 90}Sr affinity. Fractionation of the sorbent with respect to apparent grain size did not produce significant differences in the sorption efficiency. The distribution coefficients vs. equilibrium activity in solution showed a maximum with Cs, and a gradual decrease trend with Sr. The solution activity vs. adsorption data were fitted to B.E.T. (essentially types IV-V) isotherms for Cs and B.E.T.-Langmuir isotherms for Sr. Desorption, temperature-, pH-, and ionic strength-dependence tests revealed that the primary mode of sorption for both cations is specific adsorption while the secondary mode is ion exchange. A rise in pH favours the ion-exchange sorption of Sr while the specific adsorption of Cs is negatively affected. Competitive adsorption of an inert electrolyte, i.e., NaCl, severely hinders Cs sorption, while Sr sorption on water-washed red mud is not significantly affected. (author).

  7. Sorptive removal of cesium-137 and strontium-90 from water by unconventional sorbents. 1. Usage of bauxite wastes (red muds)

    International Nuclear Information System (INIS)

    Apak, R.; Atun, G.; Gueclue, K.; Tuetem, E.; Keskin, G.

    1995-01-01

    Bauxite wastes of alumina manufacture, i.e., red muds, have been tested for radiocesium and strontium removal from water. The red muds were water-washed, acid-, and heat-treated before usage to produce hydrous oxide like sorbents. Surface treatment of the sorbent was beneficial for 137 Cs uptake, while heat-treatment was detrimental to the -SOH surface sites responsible for high 90 Sr affinity. Fractionation of the sorbent with respect to apparent grain size did not produce significant differences in the sorption efficiency. The distribution coefficients vs. equilibrium activity in solution showed a maximum with Cs, and a gradual decrease trend with Sr. The solution activity vs. adsorption data were fitted to B.E.T. (essentially types IV-V) isotherms for Cs and B.E.T.-Langmuir isotherms for Sr. Desorption, temperature-, pH-, and ionic strength-dependence tests revealed that the primary mode of sorption for both cations is specific adsorption while the secondary mode is ion exchange. A rise in pH favours the ion-exchange sorption of Sr while the specific adsorption of Cs is negatively affected. Competitive adsorption of an inert electrolyte, i.e., NaCl, severely hinders Cs sorption, while Sr sorption on water-washed red mud is not significantly affected. (author)

  8. Effects of hydrogen peroxide pretreatment of clay minerals on the adsorption of Sr-85 and Tc-95m under anoxic conditions

    International Nuclear Information System (INIS)

    Relyea, J.F.; Washburne, C.D.

    1979-01-01

    Treatment of three clay minerals with hydrogen peroxide affects the observed adsorption behavior of technetium relative to untreated clay under anoxic conditions. A possible adsorption mechanism of Tc is the reduction of TcO - 4 to a more positively charged or better adsorbed species. Oxidation of the clay by H 2 O 2 would hinder the reduction of TcO - 4 by buffering the clay-water system at a higher Eh value, although a difference in measured Eh value may go undetected. Sorption of strontium by the clays under the same conditions is not affected by a pretreatment with H 2 O 2 . The behavior of strontium follows that expected from ion exchange theory. 13 tables

  9. The effect of multi-component adsorption on selectivity in ion exchange displacement systems.

    Science.gov (United States)

    Tugcu, N; Cramer, S M

    2005-01-21

    This paper examines chemically selective displacement chromatography using affinity ranking plots, batch displacer screening experiments, column displacements, multi-component adsorption isotherms and spectroscopy. The affinity ranking plot indicated that the displacers, sucrose octasulfate (SOS) and tatrazine, should possess sufficient affinity to displace the proteins amyloglucosidase and apoferritin over a wide range of operating conditions. In addition, the plots indicated that the separation of these proteins by displacement chromatography would be extremely difficult. Further, the two proteins were shown to have very similar retention times under shallow linear gradient conditions. When batch displacement experiments were carried out, both tartrazine and SOS exhibited significant selectivity differences with respect to their ability to displace these two proteins, in contrast to the affinity ranking plot results. Column displacement experiments carried out with sucrose octasulfate agreed with the predictions of the affinity ranking plots, with both proteins being displaced but poorly resolved under several column displacement conditions. On the other hand, column displacement with tartrazine as the displacer resulted in the selective displacement and partial purification of apoferritin. Single- and multi-component isotherms of the proteins with or without the presence of displacers were determined and were used to help explain the selectivity reversals observed in the column and batch displacement experiments. In addition, fluorescence and CD spectra suggested that the displacers did not induce any structural changes to either of the proteins. The results in this paper indicate that multi-component adsorption behavior can be exploited for creating chemically selective displacement separations.

  10. Boosting the adsorption performance of BN nanosheet as an anode of Na-ion batteries: DFT studies

    Energy Technology Data Exchange (ETDEWEB)

    Hosseinian, A. [Department of Engineering Science, College of Engineering, University of Tehran, P.O. Box 11365-4563, Tehran (Iran, Islamic Republic of); Soleimani-amiri, S. [Department of Chemistry, Karaj Branch, Islamic Azad University, Karaj (Iran, Islamic Republic of); Arshadi, S., E-mail: chemistry_arshadi@pnu.ac.ir [Department of Chemistry, Payame Noor University, Tehran (Iran, Islamic Republic of); Vessally, E. [Department of Chemistry, Payame Noor University, Tehran (Iran, Islamic Republic of); Edjlali, L. [Department of Chemistry, Tabriz Branch, Islamic Azad University, Tabriz (Iran, Islamic Republic of)

    2017-06-28

    Despite the high advance in the Li-ion battery technology, there exist great concerns about its lifetime, safety, cost, and low-temperature performance. It is expected that the Li-ion batteries may be replaced by Na-ion batteries (NIB) because of the low cost, nontoxicity, and wide availability of sodium. Here, we investigated the potential application of BN nanosheets in anode of NIBs by means of density functional theory calculation and introduced a strategy to increase their performance. It was shown that the Na and Na{sup +} are mainly adsorbed on the center of a hexagonal ring of BN sheet with adsorption energies of −0.08 and −33.7 kcal/mol, respectively. Replacing three N atoms of the hexagonal ring with larger P atoms significantly increases the performance of the sheet as an anode of a NIB but the replacement of B by Al decreases the performance. The initial cell voltage of LIB is increased by about 0.67 V after the P-doping which causes a high storage performance with long discharge time. The results are discussed based on the energetic, structural, orbital, charge transfer and electronic properties and provide guidelines to build better high-capacity anode materials for NIBs. - Highlights: • Potential use of BN sheet as anode in Na-ion batteries (NIB) is studied by DFT. • The replacement of B by Al decreases the performance. • The cell voltage of LIB is increased by about 0.67 V after by P-doping. • The order of performance is P-BN > BN >> Al-BN.

  11. Strontium eluting graphene hybrid nanoparticles augment osteogenesis in a 3D tissue scaffold

    Science.gov (United States)

    Kumar, Sachin; Chatterjee, Kaushik

    2015-01-01

    The objective of this work was to prepare hybrid nanoparticles of graphene sheets decorated with strontium metallic nanoparticles and demonstrate their advantages in bone tissue engineering. Strontium-decorated reduced graphene oxide (RGO_Sr) hybrid nanoparticles were synthesized by the facile reduction of graphene oxide and strontium nitrate. X-ray diffraction, transmission electron microscopy, and atomic force microscopy revealed that the hybrid particles were composed of RGO sheets decorated with 200-300 nm metallic strontium particles. Thermal gravimetric analysis further confirmed the composition of the hybrid particles as 22 wt% of strontium. Macroporous tissue scaffolds were prepared by incorporating RGO_Sr particles in poly(ε-caprolactone) (PCL). The PCL/RGO_Sr scaffolds were found to elute strontium ions in aqueous medium. Osteoblast proliferation and differentiation was significantly higher in the PCL scaffolds containing the RGO_Sr particles in contrast to neat PCL and PCL/RGO scaffolds. The increased biological activity can be attributed to the release of strontium ions from the hybrid nanoparticles. This study demonstrates that composites prepared using hybrid nanoparticles that elute strontium ions can be used to prepare multifunctional scaffolds with good mechanical and osteoinductive properties. These findings have important implications for designing the next generation of biomaterials for use in tissue regeneration.The objective of this work was to prepare hybrid nanoparticles of graphene sheets decorated with strontium metallic nanoparticles and demonstrate their advantages in bone tissue engineering. Strontium-decorated reduced graphene oxide (RGO_Sr) hybrid nanoparticles were synthesized by the facile reduction of graphene oxide and strontium nitrate. X-ray diffraction, transmission electron microscopy, and atomic force microscopy revealed that the hybrid particles were composed of RGO sheets decorated with 200-300 nm metallic strontium

  12. Competitive adsorption of Pb(II), Cu(II), and Zn(II) ions onto hydroxyapatite-biochar nanocomposite in aqueous solutions

    Science.gov (United States)

    Wang, Yu-Ying; Liu, Yu-Xue; Lu, Hao-Hao; Yang, Rui-Qin; Yang, Sheng-Mao

    2018-05-01

    A hydroxyapatite-biochar nanocomposite (HAP-BC) was successfully fabricated and its physicochemical properties characterized. The analyses showed that HAP nanoparticles were successfully loaded on the biochar surface. The adsorption of Pb(II), Cu(II), and Zn(II) by HAP-BC was systematically studied in single and ternary metal systems. The results demonstrated that pH affects the adsorption of heavy metals onto HAP-BC. Regarding the adsorption kinetics, the pseudo-second-order model showed the best fit for all three heavy metal ions on HAP-BC. In both single and ternary metal ion systems, the adsorption isotherm of Pb(II) by HAP-BC followed Langmuir model, while those of Cu(II) and Zn(II) fitted well with Freundlich model. The maximum adsorption capacity for each tested metal by HAP-BC was higher than that of pristine rice straw biochar (especially for Pb(II)) or those of other reported adsorbents. Therefore, HAP-BC could explore as a new material for future application in heavy metal removal.

  13. Adsorption of fluids in slitlike pores containing a small amount of mobile ions.

    Science.gov (United States)

    Borówko, M; Bucior, K; Sokołowski, S; Staszewski, T

    2005-11-01

    We apply density functional theory to investigate changes in the phase behavior of a fluid caused by the presence of mobile ions inside the pore. The approach has been based on the fundamental measure density functional theory and on the theory of nonuniform electrolytes developed recently by O. Pizio, A. Patrykiejew, S. Sokołowski [J. Chem. Phys. 121 (2005) 11,957]. We have evaluated capillary condensation phase diagrams for pores of different widths and for different concentrations of confined ions. The calculations have demonstrated that the presence of ions leads to lowering the critical temperature and to an increase of the value of the chemical potential at the capillary condensation point.

  14. Interaction of metal ions and amino acids - Possible mechanisms for the adsorption of amino acids on homoionic smectite clays

    Science.gov (United States)

    Gupta, A.; Loew, G. H.; Lawless, J.

    1983-01-01

    A semiempirical molecular orbital method is used to characterize the binding of amino acids to hexahydrated Cu(2+) and Ni(2+), a process presumed to occur when they are adsorbed in the interlamellar space of homoionic smectite clays. Five alpha-amino acids, beta-alanine, and gamma-aminobutyric acid were used to investigate the metal ion and amino acid specificity in binding. It was assumed that the alpha, beta, and gamma-amino acids would bind as bidentate anionic ligands, forming either 1:1 or 1:2 six-coordinated five, six, and seven-membered-ring chelate complexes, respectively. Energies of complex formation, optimized geometries, and electron and spin distribution were determined; and steric constraints of binding of the amino acids to the ion-exchanged cations in the interlamellar spacing of a clay were examined. Results indicate that hexahydrated Cu(2+) forms more stable complexes than hexahydrated Ni(2+) with all the amino acids studied. However, among these amino acids, complex formation does not favor the adsorption of the biological subset. Calculated energetics of complex formation and steric constraints are shown to predict that 1:1 rather than 1:2 metal-amino acid complexes are generally favored in the clay.

  15. Adsorption and desorption of hydrolyzed metal ions. 3. Scandium and chromium

    International Nuclear Information System (INIS)

    Gray, B.; Matijevic, E.; Clarkson Univ., Potsdam, NY

    1987-01-01

    Adsorption of scandium(III) and chromium(III) species on a PVC latex was measured using radioactive isotopes; the uptake increased with increasing pH. The data were interpreted by combining aspects of the models of James and Healy and also of Anderson and Bockris. The experimental and calculated results agree quite well for scandium, but not for chromium. The deviation in the latter case is believed to be due to polymerization of the hydrolyzed chromium cations and to the interaction of chromium with the anionic surface groups of the latex. Neither of these interactions occur with scandium. Hydrolyzed scandium species adsorbed on the latex were removed by acidifying the dispersion, while chromium complexes were not, substantiating the proposed difference in the chemical nature of chromium and scandium species at the solid/solution interface. 32 refs.; 8 figs.; 8 tabs

  16. Adsorption performances and mechanisms of the newly synthesized N,N'-di (carboxymethyl) dithiocarbamate chelating resin toward divalent heavy metal ions from aqueous media

    International Nuclear Information System (INIS)

    Jing Xiaosheng; Liu Fuqiang; Yang Xin; Ling Panpan; Li Lanjuan; Long Chao; Li Aimin

    2009-01-01

    N,N'-di (carboxymethyl) dithiocarbamate chelating resin (PSDC) was synthesized by anchoring the chelating agent of N,N'-di (carboxymethyl) dithiocarbamate to the chloromethylated PS-DVB (Cl-PS-DVB) matrix, as a new adsorbent for removing divalent heavy metal ions from waste-stream. The physicochemical structures of Cl-PS-DVB and PSDC were elaborately characterized using Fourier transform infrared spectroscopy (FT-IR), elemental analysis (EA), and were further morphologically characterized using BET and BJH methods. The adsorption performances of PSDC towards heavy metals such as Cu(II), Pb(II) and Ni(II) were systematically investigated, based upon which the adsorption mechanisms were deeply exploited. For the above target, the classic batch adsorption experiments were conducted to explore the kinetics and isotherms of the removal processes with pH-value, initial concentration, temperature, and contact time as the controlling parameters. The kinetic and isotherm data could be well elucidated with Lagergren-second-order equation and Langmuir model respectively. The strong affinity of PSDC toward these target soft acids could be well demonstrated with the electrostatic attraction and chelating interaction caused by IDA moiety and sulphur which were namely soft bases on the concept of hard and soft acids and bases (HASB). Thermodynamic parameters, involving ΔH o , ΔS o and ΔG o were also calculated from graphical interpretation of the experimental data. The standard heats of adsorption (ΔH o ) were found to be endothermic and the entropy change values (ΔS o ) were calculated to be positive for the adsorption of Cu(II), Pb(II) and Ni(II) ions onto the tested adsorbents. Negative values of ΔG o indicated that adsorption processes for all tested metal ions onto PSDC were spontaneous.

  17. Adsorption and diffusion of lithium on layered silicon for Li-ion storage.

    Science.gov (United States)

    Tritsaris, Georgios A; Kaxiras, Efthimios; Meng, Sheng; Wang, Enge

    2013-05-08

    The energy density of Li-ion batteries depends critically on the specific charge capacity of the constituent electrodes. Silicene, the silicon analogue to graphene, being of atomic thickness could serve as high-capacity host of Li in Li-ion secondary batteries. In this work, we employ first-principles calculations to investigate the interaction of Li with Si in model electrodes of free-standing single-layer and double-layer silicene. More specifically, we identify strong binding sites for Li, calculate the energy barriers accompanying Li diffusion, and present our findings in the context of previous theoretical work related to Li-ion storage in other structural forms of silicon: the bulk and nanowires. The binding energy of Li is ~2.2 eV per Li atom and shows small variation with respect to Li content and silicene thickness (one or two layers) while the barriers for Li diffusion are relatively low, typically less than 0.6 eV. We use our theoretical findings to assess the suitability of two-dimensional silicon in the form of silicene layers for Li-ion storage.

  18. Evaluation of an ion adsorption method to estimate intragravel flow velocity in salmonid spawning gravels

    Science.gov (United States)

    James L. Clayton; John G. King; Russell F. Thurow

    1996-01-01

    Intragravel water exchange provides oxygenated water, removes metabolic waste, and is an essential factor in salmonid embryo survival. Measurements of intragravel flow velocity have been suggested as an index of gravel quality and also as a useful predictor of fry emergence; however, proposed methods for measuring velocity in gravel are problematic. We evaluate an ion...

  19. Strontium-82/rubidium-82 generator

    International Nuclear Information System (INIS)

    Gennaro, G.P.; Haney, P.S.

    1986-01-01

    Hydroxylapatite, a compound having the formula: M 10 (PO 4 ) 6 (OH) 2 wherein M is calcium, strontium, barium, lead, iron, sodium, potassium, zinc, cadmium, magnesium, aluminium or a rare earth metal, is provided as a support medium for strontium-82 in a strontium-82/rubidium-82 parent-daughter radionuclide generator

  20. Leaching of strontium sulfide from produced clinker in conversion furnace

    International Nuclear Information System (INIS)

    Ghorbanian, S. A.; Salehpour, A. R.; Radpour, S. R.

    2009-01-01

    Iran is rich in mineral resources one of which is mineral Celestine. Basing on current estimations, the capacity of mineral Celestine is over two million tons, 75-95% of which is strontium sulfate. However; in industries such as Color cathode Ray Tubes, pyrochemical processes, ceramics, paint production, zinc purification processes; strontium sulfate is not a direct feed, rather it is largely consumed in the form of strontium carbonate. Two conventional methods are used to produce strontium carbonate from the sulfate; that is direct reaction and black ash methods. Strontium sulfide, as an intermediate component has a key role in black ash process including strontium sulfate reduction by coke, hence producing and leaching the strontium sulfide by hot water. Finally the reaction of strontium sulfate with sodium carbonate lead to strontium carbonate. In this paper, a system was designed to analyze and optimize the process parameters of strontium sulfide production which is less expensive and available solvent in water. Fundamentally, when strontium sulfide becomes in contact with strontium sulfate; Sr(SH) 2 , and Sr(OH) 2 , are produced. The solubility of strontium sulfide depends on water temperature and the maximum solubility achieved at 90 d egree C . The results showed that in the experimental scale, at water to SrS ratio of 6; they sediment for 45 minutes at 95 d egree C in five operational stages; the separation of 95 and 97.1 percent of imported SrS is possible in effluent of fourth and fifth stages, respectively. Thus; four leaching stages could be recommended for pilot scale plants. Also, the results show that at water to SrS ratio of 8, 40 minutes sedimentation at 85-95 d egree C in one operational stage, the separation of 95 percent separation of inputted SrS, is possible. Solvent leaching process is continued till no smell of sulfur components is felt. It could be used as a key role to determine the number of leaching stages in experiments. Finally, the

  1. Superb adsorption capacity of hierarchical calcined Ni/Mg/Al layered double hydroxides for Congo red and Cr(VI) ions

    Energy Technology Data Exchange (ETDEWEB)

    Lei, Chunsheng [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); College of Environmental & Safety Engineering, Changzhou University, Changzhou 213164 (China); Zhu, Xiaofeng [College of Environmental & Safety Engineering, Changzhou University, Changzhou 213164 (China); Zhu, Bicheng; Jiang, Chuanjia; Le, Yao [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Yu, Jiaguo, E-mail: jiaguoyu@yahoo.com [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Department of Physics, Faculty of Science, King Abdulaziz University, Jeddah 21589 (Saudi Arabia)

    2017-01-05

    Highlights: • Ni/Mg/Al layered double hydroxides (NMA-LDHs) synthesized. • NMA-LDHs with hierarchically hollow microsphere structure. • Calcined NMA-LDHs have large adsorption capacities for CR and Cr(VI) ions. - Abstract: The preparation of hierarchical porous materials as catalysts and sorbents has attracted much attention in the field of environmental pollution control. Herein, Ni/Mg/Al layered double hydroxides (NMA-LDHs) hierarchical flower-like hollow microspheres were synthesized by a hydrothermal method. After the NMA-LDHs was calcined at 600 °C, NMA-LDHs transformed into Ni/Mg/Al layered double oxides (NMA-LDOs), which maintained the hierarchical flower-like hollow structure. The crystal phase, morphology, and microstructure of the as-prepared samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy elemental mapping, Fourier transform infrared spectroscopy, and nitrogen adsorption−desorption methods. Both the calcined and non-calcined NMA-LDHs were examined for their performance to remove Congo red (CR) and hexavalent chromium (Cr(VI)) ions in aqueous solution. The maximum monolayer adsorption capacities of CR and Cr(VI) ions over the NMA-LDOs sample were 1250 and 103.4 mg/g at 30 °C, respectively. Thermodynamic studies indicated that the adsorption process was endothermic in nature. In addition, the addition of coexisting anions negatively influenced the adsorption capacity of Cr(VI) ions, in the following order: CO{sub 3}{sup 2−} > SO{sub 4}{sup 2−} > H{sub 2}PO{sub 4}{sup −} > Cl{sup −}. This work will provide new insight into the design and fabrication of advanced adsorption materials for water pollutant removal.

  2. Microstructure and nanomechanical properties of single stalks from diatom Didymosphenia geminata and their change due to adsorption of selected metal ions.

    Science.gov (United States)

    Zgłobicka, Izabela; Chlanda, Adrian; Woźniak, Michał; Łojkowski, Maciej; Szoszkiewicz, Robert; Mazurkiewicz-Pawlicka, Marta; Święszkowski, Wojciech; Wyroba, Elżbieta; Kurzydłowski, Krzysztof J

    2017-08-01

    We present topographical and nanomechanical characterization of single Didymosphenia geminata stalk. We compared the samples before and after adsorption of metal ions from freshwater samples. Transmission electron microscopy studies of single stalk cross-sections have shown three distinct layers and an additional thin extra coat on the external layer (called "EL"). Using scanning electron microscopy and atomic force microscopy (AFM), we found that topography of single stalks after ionic adsorption differed significantly from topography of pristine stalks. AFM nanoindentation studies in ambient conditions yielded elastic moduli of 214 ± 170 MPa for pristine stalks and 294 ± 108 MPa for stalks after ionic adsorption. Statistical tests showed that those results were significantly different. We conducted only preliminary comparisons between ionic adsorption of several stalks in air and in water. While the stalks with ions were on average stiffer than the pristine stalks in air, they became more compliant than the pristine stalks in water. We also heated the stalks and detected EL softening at 50°C ± 15°C. AFM nanoindentation in air on the softened samples yielded elastic moduli of 26 ± 9 MPa for pristine samples and 43 ± 22 MPa for stalks with absorbed metal ions. Substantial decrease of the EL elastic moduli after heating was expected. Significantly different elastic moduli for the samples after ionic adsorption in both cases (i.e., for heated and nonheated samples), as well as behavior of the stalks immersed in water, point to permanent structural EL changes due to ions. © 2017 Phycological Society of America.

  3. Adsorption of metal ions and acid dyes on brewer's refuse and its crosslinked products; Biru shikomikasu oyobi sono kashikaketai ni taisuru kinzoku ion oyobi sansei senryo no kyuchaku

    Energy Technology Data Exchange (ETDEWEB)

    Shimizu, Y.; Kubota, Y.; Higashimura, T. [The University of Shiga Prefecture, Shiga (Japan). Department of Materials Sceince; Kawaguchi, M. [Seisui Kogyo Ltd., Osaka (Japan)

    2000-01-10

    To use brewer's refuse as adsorbent adsorption of metal ions and acid dyes on them and their reaction products with 1,3,5-triacryloylhexahydro-1,3,5-triazine(TAF) were examined. The refuse samples used in the present study are protein rich fraction(Pr) and cellulosics rich fraction(Hr) obtained by sifting brewer's refuse. Adsorptive experiments were conducted by a batchwise method at 303 K. Pr adsorbed more metal ions such as Cr{sup 6+}, Ni{sup 2+}, Co{sup 2+}, especially Fe{sup 3+}, Hg{sup 2+} and Cu{sup 2+} than Hr. But both refuses hardly adsorbed Ca{sup 2+}. Also Pr adsorbed more acid dyes, especially more hydrophobic C. I. Acid Red 88 than C. I. Acid Orange 7- than Hr at pH 5. By crosslinking Pr and Hr using TAF adsorption of acid dyes increased markedly, but adsorption of metal ions decreased. Therefore Pr can be used as adsorbent for acid dyes and metal ions as it is. Moreover the crosslinked products are excellent adsorbents for acid dyes. (author)

  4. Facile synthesis of soluble functional graphene by reduction of graphene oxide via acetylacetone and its adsorption of heavy metal ions

    International Nuclear Information System (INIS)

    Xu, Minghan; Chai, Jing; Hu, Nantao; Huang, Da; Wang, Yuxi; Huang, Xiaolu; Wei, Hao; Yang, Zhi; Zhang, Yafei

    2014-01-01

    The synthesis of graphene (GR) from graphene oxide (GO) typically involves harmful chemical reducing agents that are undesirable for most practical applications. Here we report a green and facile synthesis method for the synthesis of GR that is soluble in water and organic solvents and that includes the additional benefit of adsorption of heavy metal ions. Acetylacetone, as both a reducing agent and a stabilizer, was used to prepare soluble GR from GO. Transmission electron microscopy and atomic force microscopy provide clear evidence for the formation of few-layer GR. The results from Fourier transform infrared spectroscopy and ultraviolet-visible spectroscopy show that reduction of GO to GR has occurred. Raman spectroscopy and X-ray photoelectron spectroscopy also indicate the removal of oxygen-containing functional groups from GO, resulting in the formation of GR. The results of dispersion experiments show that GR can be highly dispersed in water and N,N-Dimethylformamide. The reaction mechanism for acetylacetone reduction of exfoliated GO was also proposed. This method is a facile and environmentally friendly approach to the synthesis of GR and opens up new possibilities for preparing GR and GR-based nanomaterials for large-scale applications. Of even greater interest is that inductively coupled plasma atomic emission spectroscopy suggests that synthesized GR may be applied in the absorption of Cd 2+ and Co 2+ due to the strong coordination capacity of acetylacetone on the surfaces and edges of GR and the large surface area of GR in aqueous solutions. The maximum adsorptions are 49.28 mg g −1 for Cd 2+ , which is 4.5 times higher than that of carbon nanotubes, and 27.78 mg g −1 for Co 2+ , which is 3.6 times higher than that of titania beans. (paper)

  5. Adsorption of amyloglucosidase from Aspergillus niger NRRL 3122 using ion exchange resin

    Directory of Open Access Journals (Sweden)

    Ana Paula Manera

    2008-10-01

    Full Text Available Amyloglucosidase enzyme was produced by Aspergillus niger NRRL 3122 from solid-state fermentation, using deffated rice bran as substrate. The effects of process parameters (pH, temperature in the equilibrium partition coefficient for the system amyloglucosidase - resin DEAE-cellulose were investigated, aiming at obtaining the optimum conditions for a subsequent purification process. The highest partition coefficients were obtained using 0.025M Tris-HCl buffer, pH 8.0 and 25ºC. The conditions that supplied the highest partition coefficient were specified, the isotherm that better described the amyloglucosidase process of adsorption obtained. It was observed that the adsorption could be well described by Langmuir equation and the values of Qm and Kd estimated at 133.0 U mL-1 and 15.4 U mL-1, respectively. From the adjustment of the kinetic curves using the fourth-order Runge-Kutta algorithm, the adsorption (k1 and desorption (k2 constants were obtained through optimization by the least square procedure, and the values calculated were 2.4x10-3 mL U-1 min-1 for k1 and 0.037 min-1 for k2 .A enzima amiloglicosidase foi produzida por Aspergillus niger NRRL 3122 através de fermentação em estado sólido, tendo como substrato farelo de arroz desengordurado. Os efeitos dos parâmetros de processo (pH e temperatura no coeficiente de partição no equilíbrio, para o sistema amiloglicosidase - resina DEAE-celulose foram investigados, com o objetivo de se obter as melhores condições para um posterior processo de purificação. Os maiores coeficientes de partição foram obtidos usando tampão Tris-HCl 0,025M pH 8,0 e 25°C. Determinadas as condições que forneceram o maior coeficiente de partição obteve-se a isoterma que melhor descrevia o processo de adsorção de amiloglicosidase. Foi verificado que adsorção pode ser bem descrita pela equação de Langmuir e os valores de Qm e Kd foram estimados em 133,0 U mL-1 e 15,4 U mL-1 respectivamente. A

  6. Removal of Radionuclides from Waste Water at Fukushima Daiichi Nuclear Power Plant: Desalination and Adsorption Methods - 13126

    Energy Technology Data Exchange (ETDEWEB)

    Kani, Yuko; Kamosida, Mamoru; Watanabe, Daisuke [Hitachi Research Laboratory, Hitachi, Ltd., 7-2-1 Omika-cho, Hitachi, Ibaraki, 319-1221 (Japan); Asano, Takashi; Tamata, Shin [Hitachi Works, Hitachi-GE Nuclear Energy, Ltd. (Japan)

    2013-07-01

    Waste water containing high levels of radionuclides due to the Fukushima Daiichi Nuclear Power Plant accident, has been treated by the adsorption removal and reverse-osmosis (RO) desalination to allow water re-use for cooling the reactors. Radionuclides in the waste water are collected in the adsorbent medium and the RO concentrate (RO brine) in the water treatment system currently operated at the Fukushima Daiichi site. In this paper, we have studied the behavior of radionuclides in the presently applied RO desalination system and the removal of radionuclides in possible additional adsorption systems for the Fukushima Daiichi waste water treatment. Regarding the RO desalination system, decontamination factors (DFs) of the elements present in the waste water were obtained by lab-scale testing using an RO unit and simulated waste water with non-radioactive elements. The results of the lab-scale testing using representative elements showed that the DF for each element depended on its hydrated ionic radius: the larger the hydrated ionic radius of the element, the higher its DF is. Thus, the DF of each element in the waste water could be estimated based on its hydrated ionic radius. For the adsorption system to remove radionuclides more effectively, we studied adsorption behavior of typical elements, such as radioactive cesium and strontium, by various kinds of adsorbents using batch and column testing. We used batch testing to measure distribution coefficients (K{sub d}s) for cesium and strontium onto adsorbents under different brine concentrations that simulated waste water conditions at the Fukushima Daiichi site. For cesium adsorbents, K{sub d}s with different dependency on the brine concentration were observed based on the mechanism of cesium adsorption. As for strontium, K{sub d}s decreased as the brine concentration increased for any adsorbents which adsorbed strontium by intercalation and by ion exchange. The adsorbent titanium oxide had higher K{sub d}s and it

  7. Removal of Radionuclides from Waste Water at Fukushima Daiichi Nuclear Power Plant: Desalination and Adsorption Methods - 13126

    International Nuclear Information System (INIS)

    Kani, Yuko; Kamosida, Mamoru; Watanabe, Daisuke; Asano, Takashi; Tamata, Shin

    2013-01-01

    Waste water containing high levels of radionuclides due to the Fukushima Daiichi Nuclear Power Plant accident, has been treated by the adsorption removal and reverse-osmosis (RO) desalination to allow water re-use for cooling the reactors. Radionuclides in the waste water are collected in the adsorbent medium and the RO concentrate (RO brine) in the water treatment system currently operated at the Fukushima Daiichi site. In this paper, we have studied the behavior of radionuclides in the presently applied RO desalination system and the removal of radionuclides in possible additional adsorption systems for the Fukushima Daiichi waste water treatment. Regarding the RO desalination system, decontamination factors (DFs) of the elements present in the waste water were obtained by lab-scale testing using an RO unit and simulated waste water with non-radioactive elements. The results of the lab-scale testing using representative elements showed that the DF for each element depended on its hydrated ionic radius: the larger the hydrated ionic radius of the element, the higher its DF is. Thus, the DF of each element in the waste water could be estimated based on its hydrated ionic radius. For the adsorption system to remove radionuclides more effectively, we studied adsorption behavior of typical elements, such as radioactive cesium and strontium, by various kinds of adsorbents using batch and column testing. We used batch testing to measure distribution coefficients (K d s) for cesium and strontium onto adsorbents under different brine concentrations that simulated waste water conditions at the Fukushima Daiichi site. For cesium adsorbents, K d s with different dependency on the brine concentration were observed based on the mechanism of cesium adsorption. As for strontium, K d s decreased as the brine concentration increased for any adsorbents which adsorbed strontium by intercalation and by ion exchange. The adsorbent titanium oxide had higher K d s and it was used for

  8. Attractive non-DLVO forces induced by adsorption of monovalent organic ions.

    Science.gov (United States)

    Smith, Alexander M; Maroni, Plinio; Borkovec, Michal

    2017-12-20

    Direct force measurements between negatively charged colloidal particles were carried out using an atomic force microscope (AFM) in aqueous solutions containing monovalent organic cations, namely tetraphenylarsonium (Ph 4 As + ), 1-hexyl-3-methylimidazolium (HMIM + ), and 1-octyl-3-methylimidazolium (OMIM + ). These ions adsorb to the particle surface, and induce a charge reversal. The forces become attractive at the charge neutralization point, but they are stronger than van der Waals forces. This additional and unexpected attraction decays exponentially with a decay length of a few nanometers, and is strikingly similar to the one previously observed in the presence of multivalent ions. This attractive force probably originates from coupled spontaneous charge fluctuations on the respective surfaces as initially suggested by Kirkwood and Shumaker.

  9. ADSORPSI ION SIANIDA DALAM LARUTAN MENGGUNAKAN ADSORBEN HIBRIDA AMINOPROPIL SILIKA GEL DARI SEKAM PADI TERIMPREGNASI ALUMINIUM (Adsorption of Cyanide Ions in Solution Using a Hybrid Adsorbent Aminopropyl Silica Gel from Rice Husks of Impregnated With

    Directory of Open Access Journals (Sweden)

    Amaria Amaria

    2012-03-01

    aminopropil silica gel from rice husk that has been impregnated with aluminum (APSG-Al and silica gel impregnated with aluminum (SG-Al of rice husk silica gel as the material for the adsorption of cyanide ions in solution. The interaction between the adsorbent with cyanide ions in solution performed in a batch system. The parameters examined in this study were the influence of medium pH, the effect of interaction time and the effect of initial concentration of cyanide ion adsorption ability of adsorbent hybrid amino silica gel impregnated with aluminum. Quantitative Analysis of cyanide ions left in the filtrate was tested by means of ion selective electrode. The effect of interaction time data were analyzed with kinetic model, the data of the influence of cyanide ion concentration was analyzed by Langmuir adsorption isotherm model and Freundlich. The results showed that the infrared spectroscopic identification results show APSG-Al adsorbent has silanol groups (Si-OH, siloxil (Si-O-Si, primary amine group, NH2. The result of XRD analysis of the price of 2θ at 65.51 indicates that the aluminum impregnated with the silica in the form of alumina Al2O3. The result of adsorption of cyanide by the hybrid silica gel impregnated with aluminum aminopropil (APSG-Al showed maximum adsorption occurred at pH 5 was 67.62%, silica gel impregnated with aluminum was 51,11%. Study the kinetics of the effect of interaction time showed that the adsorbent APSG-Al and SG-Al-Al has the adsorption rate constant k1 is 2.7, 10-3and 1.9,10-3 min-1, respectively. Adsorption equilibrium data showed that the adsorbent APSG-Al and SG-Al tend to follow the adsorption isotherm model Freundlich.

  10. Strontium isotopic stratigraphy utilizing authigenic dolomites in hemipelagic sediments

    Energy Technology Data Exchange (ETDEWEB)

    Baker, P.A. (Duke Univ., Durham, NC (USA)); Kastner, M. (Scripps Institute of Oceanography, La Jolla, CA (USA)); Elderfield, H. (Univ. of Cambridge (England))

    1990-05-01

    Authigenic dolomites commonly occur in organic-rich, continental margin marine sediments. These dolomites play a key role in the age dating of stratigraphic sections. The dolomites often are the only lithology amenable to paleomagnetic stratigraphy; they preserve siliceous microfossils against diagenetic; recrystallization, and provide useful strontium isotopic stratigraphic ages. Several potential sources of error frequently are unique to the use of authigenic dolomites in the strontium isotope methods. (1) The dolomites occur as cements of the host lithology, hence, they are not a pure phase. Potentially important contaminants during analysis include gypsum clay minerals, feldspars, and iron and manganese oxides. Strontium may occur as a structural substituent ion in these minerals or as a surface-adsorbed ion. Various leaching techniques have been tested to isolate dolomitic strontium. Purer dolomites and strontium-enriched dolomites often can be selected to ease these problems. (2) The dolomites form after the deposition of the host sediment, therefore, they record the diagenetic age not the depositional age. The stable isotopic composition of the dolomites can aid in selection of early formed samples. (3) The dolomites record pore-water strontium isotope compositions, not seawater isotopic compositions. This problem is also minimized by choosing dolomites formed near the sediment-water interface. (4) The dolomites formed near the sediment-water interface originated as rotodolomites and undergo subsequent burial diagenesis, creating a potential for later strontium isotope exchange. This problem is minimized by selecting fresh samples from the interior of nearly impermeable beds and nodules. Results from the Miocene Monterey Formation of California and from the Eocene through Pliocene Pisco basin of Peru show that authigenic dolomites can provide useful strontium isotopic age estimates.

  11. Fluoride and metal ions removal from water by adsorption on nanostructured materials

    OpenAIRE

    Gràcia Lanas, Sara Isabel

    2017-01-01

    Bibliografia Actualmente la contaminación ambiental es un gran enemigo global, siendo uno de los problemas que afectan más al mundo. El presente trabajo se centra en la eliminación de contaminantes acuosos, como el fluoruro o distintos iones metálicos. Diversos materiales nanoestructurados han sido utilizados para la adsorción de los contaminantes de agua anteriormente mencionados. Estos materiales han sido elegidos por la elevada area superficial que ofrecen en un volumen muy pequeño, ren...

  12. Reactivity of surface of metal oxide particles: from adsorption of ions to deposition of colloidal particles

    International Nuclear Information System (INIS)

    Lefevre, Gregory

    2010-01-01

    In this Accreditation to supervise research (HDR), the author proposes an overview of his research works in the field of chemistry. These works more particularly addressed the understanding of the surface reactivity of metal oxide particles and its implication on sorption and adherence processes. In a first part, he addresses the study of surface acidity-alkalinity: measurement of surface reactivity by acid-base titration, stability of metal oxides in suspension, effect of morphology on oxide-hydroxide reactivity. The second part addresses the study of sorption: reactivity of iron oxides with selenium species, sorption of sulphate ions on magnetite, attenuated total reflection infrared spectroscopy (ATR-IR). Adherence effects are addressed in the third part: development of an experimental device to study adherence in massive substrates, deposition of particles under turbulent flow. The last part presents a research project on the effect of temperature on ion sorption at solids/solutions interfaces, and on the adherence of metal oxide particles. The author gives his detailed curriculum, and indicates his various publications, teaching activities, research and administrative responsibilities

  13. Thermoluminescence of strontium tetraborate

    International Nuclear Information System (INIS)

    Santiago, M.; Caselli, E.; Lester, M.

    1999-01-01

    The thermoluminescent properties of crystalline strontium tetraborate are reported. Without activators it has an efficiency comparable to that of TLD-700 powder. Its fading after 40 days amount to less than 2%. The isometric plot shows that most of the emitted light is concentrated at wavelengths ranging from 350 to 450 nm, which accounts partially for the high efficiency. (author)

  14. Removal of ammonium ions by laboratory-synthesized zeolite linde type A adsorption from water samples affected by mining activities in Ghana.

    Science.gov (United States)

    Kwakye-Awuah, Bright; Labik, Linus Kweku; Nkrumah, Isaac; Williams, Craig

    2014-03-01

    Ammonium ion adsorption by laboratory-synthesized zeolite (linde type A; LTA) was investigated in batch kinetics experiments. Synthesized zeolite LTA was characterized by X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy, thermogravimetric analysis, Fourier transform infrared spectroscopy and particle size analysis. Water samples were taken from the Nyam and Tano rivers in Ghana, and 0.8 g of zeolite was added to 100 ml portions of each sample. Portions of the samples were withdrawn every 30 min for 150 min and the concentration of ammonia in each sample was determined. The removal efficiency of zeolite LTA was evaluated by retrieving the zeolite from the water samples and adding to a fresh sample to repeat the process. Equilibrium data were fitted by Langmuir and Freundlich isotherms. Maximum adsorption capacities were 72.99 mg g(-1) for samples from the River Nyam and 72.87 mg g(-1) for samples from the River Tano. The equilibrium kinetic data were analysed using adsorption kinetic models: pseudo-first order and pseudo-second order kinetic models. Linear regression was used to estimate the adsorption and kinetic parameters. The results showed that the adsorption followed pseudo-second order kinetics and suggest that zeolite LTA is a good adsorbent for the removal of nitrogen ammonia from water.

  15. Iodine adsorption on ion-exchange resins and activated carbons: batch testing

    Energy Technology Data Exchange (ETDEWEB)

    Parker, Kent E.; Golovich, Elizabeth C.; Wellman, Dawn M.

    2014-09-30

    Iodine sorption onto seven resins and six carbon materials was evaluated using water from well 299-W19-36 on the Hanford Site. These materials were tested using a range of solution-to-solid ratios. The test results are as follows. The efficacy of the resin and granular activated carbon materials was less than predicted based on manufacturers’ performance data. It is hypothesized that this is due to the differences in speciation previously determined for Hanford groundwater. The sorption of iodine is affected by the iodine species in the source water. Iodine loading on resins using source water ranged from 1.47 to 1.70 µg/g with the corresponding Kd values from 189.9 to 227.0 mL/g. The sorption values when the iodine is converted to iodide ranged from 2.75 to 5.90 µg/g with the corresponding Kd values from 536.3 to 2979.6 mL/g. It is recommended that methods to convert iodine to iodide be investigated in fiscal year (FY) 2015. The chemicals used to convert iodine to iodate adversely affected the sorption of iodine onto the carbon materials. Using as-received source water, loading and Kd values ranged from 1.47 to 1.70 µg/g and 189.8 to 226.3 mL/g respectively. After treatment, loading and Kd values could not be calculated because there was little change between the initial and final iodine concentration. It is recommended the cause of the decrease in iodine sorption be investigated in FY15. In direct support of CH2M HILL Plateau Remediation Company, Pacific Northwest National Laboratory has evaluated samples from within the 200W pump and treat bioreactors. As part of this analysis, pictures taken within the bioreactor reveal a precipitate that, based on physical properties and known aqueous chemistry, is hypothesized to be iron pyrite or chalcopyrite, which could affect iodine adsorption. It is recommended these materials be tested at different solution-to-solid ratios in FY15 to determine their effect on iodine

  16. Iodine adsorption on ion-exchange resins and activated carbons: batch testing

    International Nuclear Information System (INIS)

    Parker, Kent E.; Golovich, Elizabeth C.; Wellman, Dawn M.

    2014-01-01

    Iodine sorption onto seven resins and six carbon materials was evaluated using water from well 299-W19-36 on the Hanford Site. These materials were tested using a range of solution-to-solid ratios. The test results are as follows. The efficacy of the resin and granular activated carbon materials was less than predicted based on manufacturers' performance data. It is hypothesized that this is due to the differences in speciation previously determined for Hanford groundwater. The sorption of iodine is affected by the iodine species in the source water. Iodine loading on resins using source water ranged from 1.47 to 1.70 µg/g with the corresponding K d values from 189.9 to 227.0 mL/g. The sorption values when the iodine is converted to iodide ranged from 2.75 to 5.90 µg/g with the corresponding K d values from 536.3 to 2979.6 mL/g. It is recommended that methods to convert iodine to iodide be investigated in fiscal year (FY) 2015. The chemicals used to convert iodine to iodate adversely affected the sorption of iodine onto the carbon materials. Using as-received source water, loading and K d values ranged from 1.47 to 1.70 µg/g and 189.8 to 226.3 mL/g respectively. After treatment, loading and K d values could not be calculated because there was little change between the initial and final iodine concentration. It is recommended the cause of the decrease in iodine sorption be investigated in FY15. In direct support of CH2M HILL Plateau Remediation Company, Pacific Northwest National Laboratory has evaluated samples from within the 200W pump and treat bioreactors. As part of this analysis, pictures taken within the bioreactor reveal a precipitate that, based on physical properties and known aqueous chemistry, is hypothesized to be iron pyrite or chalcopyrite, which could affect iodine adsorption. It is recommended these materials be tested at different solution-to-solid ratios in FY15 to determine their effect on iodine sorption.

  17. Synthesis and characterization of ultrasound assisted “graphene oxide–magnetite” hybrid, and investigation of its adsorption properties for Sr(II) and Co(II) ions

    Energy Technology Data Exchange (ETDEWEB)

    Tayyebi, Ahmad; Outokesh, Mohammad, E-mail: Outokesh@sharif.edu; Moradi, Shahab; Doram, Amir

    2015-10-30

    Graphical abstract: - Highlights: • Narrow size magnetite NPs were synthesized by ultrasound assisted coprecipitaion method. • A formation mechanism for deposition of magnetite NPs on graphene oxide is proposed. • The formation mechanism supported using X-ray photoelectron spectroscopy analysis. • The modified Langevin equation was used for size estimation of magnetite NPs on M–GO. • Adsorption properties of M–GO for Co(II) and Sr(II) were investigated. - Abstract: Magnetite nanoparticles with a size distribution of 15–21 nm were synthesized and decorated onto surface of graphene oxide by ultrasound assisted precipitation. Size and size distribution of the obtained M–GO hybrid were appreciably finer than the hybrids prepared by stirring method. M–GO is a superparamagnetic material with saturation magnetization of 31 emu g{sup −1}. The Langevin equation was successfully applied for estimation of size of Fe{sub 3}O{sub 4} nanoparticles in M–GO hybrid, with maximum error of 17.5%. The study put forward a formation mechanism for M–GO, based on instrumental analyses. Adsorption isotherms of Sr{sup 2+} and Co{sup 2+} ions, which were fitted by Langmuir monolayer model, displayed two-fold higher capacity for Co{sup 2+} ions, presumably due to its similarity to Fe{sup 2+} (of Fe{sub 3}O{sub 4} component). Uptake of both Co{sup 2+} and Sr{sup 2+} ions were endothermic, and spontaneous, however the former proceeded through inner-shell complex formation, while the latter took place via ion exchange mechanism. Rate of adsorption of Co{sup 2+} was faster, but for both ions, chemical reaction was the rate determining step. Sorption of Sr{sup 2+} and Co{sup 2+} ions greatly increased at pHs above 5, where (1) surface zeta potential changed its sign, and (2) deprotonating reactions at the surface became complete.

  18. Separation and preconcentration of Arsenic(III ions from aqueous media by adsorption on MWCNTs

    Directory of Open Access Journals (Sweden)

    Nahid Tavakkoli

    2017-05-01

    Full Text Available A simple and sensitive method using mini-column packed with multi-walled carbon nanotubes (MWCNTs combined with graphite furnace atomic absorption spectrometry (GFAAS for preconcentration and determination of ultra trace amounts of As(III in an aqueous medium is proposed. The procedure is based on the solid phase extraction of the As(III-sodium diethyldithiocarbamate (As-NaDDTC chelate on MWCNTs. Various parameters such as the effect of pH, eluent type and volume, amount of sorbent, and matrix effects on the quantitative recoveries of analyte ions were evaluated. It was found that sorption is quantitative and desorption occurs with 4.0 mL of 3.0 mol L−1 HNO3 in acetone. The limit of detection of the method was 0.008 ng mL−1 for GFAAS with enrichment factor of 125 and the relative standard deviation (RSD 0.97% (n = 8, C = 10 ng mL−1. This method has been applied to the determination of ultra trace As(III in water and rice plant and its ash successfully.

  19. Flame Spectrophotometric Determination of Strontium in Water and Biological Material

    Energy Technology Data Exchange (ETDEWEB)

    Joensson, G

    1964-10-15

    A flame spectrophotometric method has been developed for the determination of strontium in biological material and water samples. Strontium is determined in the presence of calcium at a wavelength of 4607 A. The intensity of the strontium emission from the sample is increased if n-butanol is added to a solution of the sample in water. With a 6 vol% solution of n-butanol in water, an optimum intensity of 3.5 times that obtained with pure water solution is obtained. Anions and alkali metals which might interfere with the flame spectrophotometric determination are separated from the sample by a simple ion exchange operation. The method allows determination of strontium in solutions down to 0.1{mu}g/ml. In this case the standard deviation is 3.1 % and with a strontium concentration of 1 {mu}g/ml the deviation is 0.9 %. This method has been used for the determination of strontium in samples of varying composition such as bone, meat and skin from fishes, samples of human bones, shell-fish, milk, and water, in which case Sr quantities of 5{mu}g were determined with an analytical error of less than 5 % and Sr{sub q}uantities greater than 10 {mu}g with an error of less than 3 %.

  20. Flame Spectrophotometric Determination of Strontium in Water and Biological Material

    International Nuclear Information System (INIS)

    Joensson, G.

    1964-10-01

    A flame spectrophotometric method has been developed for the determination of strontium in biological material and water samples. Strontium is determined in the presence of calcium at a wavelength of 4607 A. The intensity of the strontium emission from the sample is increased if n-butanol is added to a solution of the sample in water. With a 6 vol% solution of n-butanol in water, an optimum intensity of 3.5 times that obtained with pure water solution is obtained. Anions and alkali metals which might interfere with the flame spectrophotometric determination are separated from the sample by a simple ion exchange operation. The method allows determination of strontium in solutions down to 0.1μg/ml. In this case the standard deviation is 3.1 % and with a strontium concentration of 1 μg/ml the deviation is 0.9 %. This method has been used for the determination of strontium in samples of varying composition such as bone, meat and skin from fishes, samples of human bones, shell-fish, milk, and water, in which case Sr quantities of 5μg were determined with an analytical error of less than 5 % and Sr q uantities greater than 10 μg with an error of less than 3 %

  1. Synthesis of 2,4-dinitrophenylhydrazine loaded sodium dodecyl sulfate-coated magnetite nanoparticles for adsorption of Hg(II ions from an aqueous solution

    Directory of Open Access Journals (Sweden)

    Soheil Sobhanardakani

    2016-09-01

    Full Text Available Background: The rapid increase in agricultural and industrial development has made heavy metal pollution a serious environmental problem and public health threat; therefore, removal of heavy metals from water is important. The current study prepared DNPH@SDS@Fe3O4 nanoparticles as a novel and effective adsorbent for removal of Hg(II ions from an aqueous solution. Methods: A selective adsorbent for Hg(II was synthesized by coating Fe3O4 nanoparticles with sodium dodecyl sulfate which was further functionalized with 2,4-dinitrophenylhydrazine (2,4-DNPH. The synthesized nanoparticles were characterized by Fourier transform infrared spectroscopy (FTIR, x-ray diffraction (XRD, scanning electron microscopy (SEM and SEM–EDXSt. The effects of pH, dose of adsorbent and shaking time on adsorption capacity were investigated. The kinetics and equilibrium of adsorption of the metal ions were thoroughly studied. Results: SEM showed that the size of the nanoparticles was 20 to 35 nm. The maximum adsorption capacity for Hg(II was 164.0 mg g-1 for an adsorbent dose of 0.04 g at pH 7.0, 25°C and the initial metal concentration was 25 mg L-1,which was greater than for most adsorbents previously examined for Hg(II adsorption. Adsorption experimental data showed good correlation with the pseudo-secondorder model and Langmuir isotherm model. Conclusion: The results indicated that the DNPH@SDS@Fe3O4 nanoparticles are an efficient adsorbent for removal of heavy metal from wastewater.

  2. Studies of adsorption and desorption of zinc ions on zeolites by means of 65Zn

    International Nuclear Information System (INIS)

    Foeldesova, M.; Dillinger, P.; Lukac, P.

    2001-01-01

    The uptake of different metals by natural and chemically modified ion-exchangers, including zeolites, were studied in order to minimize the contamination of environment with metals in ionic form. In recent years considerable attention has been devoted to the studies of chemically modified zeolites their properties and applications. The used zeolite originated from the deposit Nizny Hrabovec, eastern Slovakia (NH) and from deposit of Ukraine (U). The zeolite from Slovakia is a clinoptilolite /40 -70%/ type, the zeolite from Ukraine is a mixed mordenite /75%/ and clinoptilolite /25%/ type. A fraction of 1.5 -2.5 mm was separated from the grained zeolite by sieving. The sedimentary zeolites, being the siliceous zeolites, should exhibit substantial non-selectivity for the divalent cations having a high hydration enthalpy , including zinc ( -2026 kJ/g). Zinc is an essential trace element in all-living systems from bacteria to humans. The toxicity of zinc and most of zinc compounds is generally low, however, sometimes industrial and household wastes contain zinc in concentrations, which can be harmful to the environment. The zinc-accompanying impurities, such as cadmium and lead, are of much greater danger .The main source of zinc are waste waters and continuous emission from the production and processing of zinc, other nonferrous smelters, from coal power plants and fossil combustion. The static radio-exchange method using model radioactive solutions was utilized for the determination of the sorption of Zn by the mentioned above zeolitic materials. For this purpose the aqueous solution of 5 · 10 -2 mol dm -3 ZnCl 2 labelled with 65 Zn was used. The areas of application of natural zeolites have been well defined. However, their use can become more efficient after chemical modification. The zeolites acquire new valuable properties, while retaining their original ones. The obtained results make these materials excellent candidates for their potential use for waste water

  3. Batch adsorptive removal of Fe(III, Cu(II and Zn(II ions in aqueous and aqueous organic–HCl media by Dowex HYRW2-Na Polisher resin as adsorbents

    Directory of Open Access Journals (Sweden)

    Abdul-Aleem Soliman Aboul-Magd

    2016-09-01

    Full Text Available Of the metal ions in tap, Nile, waste and sea water samples and some ores were carried out. Removal of heavy metal ions such as Fe(III, Cd(II, Zn(II, Cu(II, Mn(II, Mg(II, and Pb(II from water and wastewater is obligatory in order to avoid water pollution. Batch shaking adsorption experiments to evaluate the performance of nitric and hydrochloric acid solutions in the removal of metal ions by cation exchange resin at the same conditions for both, such as the effect of initial metal ion concentration, different proportions of some organic solvents, H+-ion concentrations and reaction temperature on the partition coefficients. The metal adsorption for the cation exchanger was found to be significant in different media for both nitric and hydrochloric acids, i.e., the adsorption up take of metal ions presented in this work is very significant depending on the characteristics of ions and on the external concentrations of solute. The presence of low ionic strength or low concentration of acids does have a significant adsorption of metal ions on ion-exchange resin. The results show that the ion exchanger could be employed for the preconcentration, separation and the determination.

  4. Influence of selected factors on strontium sorption on bentonites

    International Nuclear Information System (INIS)

    Galambos, M.; Kufcakova, J.; Rajec, P.

    2007-01-01

    Sorption on bentonite will play an important role in retarding the migration of radionuclides from a waste repository. Bentonite is a natural clay and one of the most promising candidates for use as a buffer material in the geological disposal systems for high-level nuclear waste. It is intended to isolate metal canisters with highly radioactive waste products from the surrounding rocks because of its ability to retard the movement of radionuclides by sorption. Bentonite is characterized by low permeability, water swelling capability and excellent sorption potential for cationic radionuclides. To correctly assess the sorption potential of radionuclides on bentonite is essential for the development of predictive migration models. The sorption of strontium on bentonite from different Slovak deposits - Jelsovy potok, Kopernica and Lieskovec has been investigated under various experimental conditions, such as contact time, sorbate concentrations, presence of complementary cation. Sorption was studied using the batch technique. The uptake of Sr was rapid and equilibrium was reached almost instantaneously. The instantaneous uptake may be due to adsorption and/or exchange of the metal with some ions on the surface of the adsorbent. The best sorption characteristics distinguish bentonite Kopernica, sorption capacity for Sr of the fraction under 45 mm is 0,48 mmol·g -1 for Sr. The highest values of distribution coefficient were reached for the bentonite Jelsovy potok. Radiation stability has been investigated, the higher sorption parameters were observed for the irradiated bentonites, which can be explained by the increase of specific surface of the bentonite samples. The presence of complementary cations depresses the sorption of Sr on bentonite. Cations Ca 2+ exhibit higher effect on cesium sorption than the Na 2+ ions. Results indicate that the sorption of Sr 2+ on bentonite will be affected by the presence of high concentrations of various salts in the waste water

  5. Analysis of radioactive strontium

    International Nuclear Information System (INIS)

    1977-01-01

    In environmental radiation survey, radioactive strontium has been analyzed in compliance with the manual ''Analyzing methods for radioactive strontium'' published in 1960 by the Science and Technology Agency, Japan, and revised in 1963. However, in a past decade, progress and development in analyzing methods and measuring equipments have been significant, therefore the manual was revised in 1974. Major revisions are as follows. (1) Analysis of 90 Sr with long half life was changed to the main theme and that of 89 Sr with short half life became a subordinate one. (2) Measuring criteria and sampling volume were revised. (3) Sample collection method was unified. (4) Analyzing method for soil was improved to NaOH-HCl method which has good recovery rate. (5) 90 Y separation method of simple operation was added for sea water analysis besides EDTA and fuming nitric acid methods. (6) Flame spectrometry for quantitative analysis of stable strontium was revised to atomic absorption spectrometry. The contents of the manual comprises 11 chapters describing introduction, measuring criteria for 90 Sr ( 89 Sr), rain and dust, land water, sea water, soil, sea bottom and river bottom sediments (changed from human urine and human bones), crops, milk (the previous one chapter was divided into two), marine organisms, and everyday foods, respectively. (Wakatsuki, Y.)

  6. Highly stable and magnetically separable alginate/Fe3O4 composite for the removal of strontium (Sr) from seawater.

    Science.gov (United States)

    Hong, Hye-Jin; Jeong, Hyeon Su; Kim, Byoung-Gyu; Hong, Jeongsik; Park, In-Su; Ryu, Taegong; Chung, Kang-Sup; Kim, Hyuncheol; Ryu, Jungho

    2016-12-01

    In this study, a highly stable alginate/Fe 3 O 4 composite was synthesized, and systematically investigated for the practical application of strontium (Sr) removal in complex media, such as seawater and radioactive wastewater. To overcome the drawbacks of the use of alginate microspheres, high contents of alginic acid and Fe 3 O 4 were used to provide a more rigid structure with little swelling and facile separation, respectively. The synthesized composite was optimized for particle sizes of seawater spiked with 50 mg/L of Sr, the alginate/Fe 3 O 4 composite showed 12.5 mg/g of Sr uptake, despite the highly concentrated ions in seawater. The adsorption experiment for radio-active 90 Sr revealed a removal efficiency of 67% in real seawater, demonstrating the reliability of the alginate/Fe 3 O 4 composite. Copyright © 2016 Elsevier Ltd. All rights reserved.

  7. Co adsorption in kaolinite

    International Nuclear Information System (INIS)

    Souza, Eliel S.; Silva, Paulo S.C.

    2017-01-01

    Adsorption of metal ions in clay minerals has been used as an alternative to water and effluents treatment. Kaolinite is a clay mineral that presents low specific surface area and exchange ion capacity. Nevertheless, structural modifications can be achieved by means of acid or thermal activation. In this paper, it was studied the surface area of kaolinite/bentonite, kaolinite/activated carbon mixtures, thermal activated kaolinite and thermal activated kaolinite/activated carbon mixture. The mixture of kaolinite/activated carbon was tested for pH, contact time, interfering ions and initial concentration effects in the cobalt adsorption. Results showed that the optimized parameters are pH 6 and contact time of 30 min. Chromium acted as a competitive ion, zinc does not appear to have affected adsorption while iron seems to have favored it. Langmuir and Freundlich isotherms indicated that the adsorption of Co in the mixture of kaolinite/activated carbon is a spontaneous process. (author)

  8. Co adsorption in kaolinite

    Energy Technology Data Exchange (ETDEWEB)

    Souza, Eliel S.; Silva, Paulo S.C., E-mail: eliel201019@hotmail.com, E-mail: pscsilva@ipen.br [Instituto de Pesquisas Energética s e Nucleares (IPEN/CNEN-SP), São Paulo, SP (Brazil)

    2017-07-01

    Adsorption of metal ions in clay minerals has been used as an alternative to water and effluents treatment. Kaolinite is a clay mineral that presents low specific surface area and exchange ion capacity. Nevertheless, structural modifications can be achieved by means of acid or thermal activation. In this paper, it was studied the surface area of kaolinite/bentonite, kaolinite/activated carbon mixtures, thermal activated kaolinite and thermal activated kaolinite/activated carbon mixture. The mixture of kaolinite/activated carbon was tested for pH, contact time, interfering ions and initial concentration effects in the cobalt adsorption. Results showed that the optimized parameters are pH 6 and contact time of 30 min. Chromium acted as a competitive ion, zinc does not appear to have affected adsorption while iron seems to have favored it. Langmuir and Freundlich isotherms indicated that the adsorption of Co in the mixture of kaolinite/activated carbon is a spontaneous process. (author)

  9. Substitution of strontium for calcium in glass ionomer cements (Part ...

    African Journals Online (AJOL)

    Objectives: To investigate the effects of substituting strontium for calcium in fluoroaluminosilicate glass on the mechanical and ion-releasing properties of high-viscosity glass ionomer cements. Design: An exploratory, laboratory-based study. Setting: Dental biomaterials research laboratory, Dental Physical Sciences Unit, ...

  10. Ion-specific weak adsorption of salts and water/octanol transfer free energy of a model amphiphilic hexa-peptide

    International Nuclear Information System (INIS)

    Dejugnat, Ch.; Dufreche, J.F.; Zemb, Th.; Dejugnat, Ch.

    2011-01-01

    An amphiphilic hexa-peptide has been used as a model to quantify how specific ion effects induced by addition of four salts tune the hydrophilic/hydrophobic balance and induce temperature-dependant coacervate formation from aqueous solution. The hexa-peptide chosen is present as a dimer with low transfer energy from water to octanol. Taking sodium chloride as the reference state in the Hofmeister scale, we identify water activity effects and therefore measure the free energy of transfer from water to octanol and separately the free energy associated to the adsorption of chaotropic ions or the desorption of kosmotropic ions for the same amphiphilic peptide. These effects have the same order of magnitude: therefore, both energies of solvation as well as transfer into octanol strongly depend on the nature of the electrolytes used to formulate any buffer. Model peptides could be used on separation processes based on criteria linked to 'Hofmeister' but different from volume and valency. (authors)

  11. Luminescent properties of Eu2+ and Ce3+ ions in strontium litho-silicate Li2SrSiO4

    International Nuclear Information System (INIS)

    Dotsenko, V.P.; Levshov, S.M.; Berezovskaya, I.V.; Stryganyuk, G.B.; Voloshinovskii, A.S.; Efryushina, N.P.

    2011-01-01

    The luminescent properties of Eu 2+ and Ce 3+ ions in Li 2 SrSiO 4 have been studied upon excitation in the 2-20 eV region. Based on the results of luminescent measurements, values of the crystal field splitting and the centroid shift of the Ce 3+ 5d configuration in Li 2 SrSiO 4 were found and compared with those of Ce 3+ ions in some other inorganic compounds. The Eu 2+ ions in Li 2 SrSiO 4 exhibit a broad band emission with a maximum at 576 nm, which is due to the 4f 6 5d→4f 7 transition. It was shown that the long-wavelength position of the Eu 2+ emission in Li 2 SrSiO 4 is caused by the large crystal-field splitting of the Eu 2+ 4f 6 5d configuration and relatively high degree of covalency of the Eu-O bond. The stabilization of Eu 2+ ions in Li 2 SrSiO 4 during the synthesis process requires a strong reducing agent. Two phenomenological approaches to explain the low stability of Eu 2+ in Li 2 SrSiO 4 are also discussed.

  12. Highly Productive Synthesis, Characterization, and Fluorescence and Heavy Metal Ion Adsorption Properties of Poly(2,5-dimercapto-1,3,4-thiadiazole Nanosheets

    Directory of Open Access Journals (Sweden)

    Chao Li

    2017-12-01

    Full Text Available Poly(2,5-dimercapto-1,3,4-thiadiazole (PBT nanosheets were synthesized by chemical oxidative synthesis under mild conditions. The media, oxidant species, monomer concentrations, oxidant/monomer molar ratio, and temperature were optimized to achieve higher yields and better performance. The molecular structure, morphology, and properties of the nanosheets were analyzed by Fourier transform infrared (FT-IR, ultraviolet-visible (UV-Vis, and fluorescence spectroscopies, wide-angle X-ray diffraction (WAXD, matrix-assisted laser desorption/ionization/time-of-flight (MALDI-TOF mass spectrometry, X-ray photoelectron spectroscopy (XPS, scanning electronic microscopy (SEM, transmission electron microscopy (TEM, and simultaneous thermogravimetry and differential scanning calorimetry (TG-DSC. It was found that the polymerization of 2,5-dimercapto-1,3,4-thiadiazole occurs via dehydrogenation coupling between two mercapto groups to form the –S–S– bond. PBTs show the highest polymerization yield of up to 98.47% and form uniform nanosheets with a thickness of 89~367 nm. poly(2,5-dimercapto-1,3,4-thiadiazole polymers (PBTs exhibit good chemical resistance, high thermostability, interesting blue-light emitting fluorescence, and wonderful heavy metal ion adsorption properties. Particularly, the PBT nanosheets having a unique synergic combination of three kinds of active –S–, –SH, and =N– groups with a moderate specific area of 15.85 m2 g−1 exhibit an ultra-rapid initial adsorption rate of 10,653 mg g−1 h−1 and an ultrahigh adsorption capacity of up to 680.01 mg g−1 for mercury ion, becoming ultrafast chelate nanosorbents with a high adsorption capacity. With these impressive properties, PBT nanosheets are very promising materials in the fields of water treatment, sensors, and electrodes.

  13. Rapid method for the radioactive strontium determination in natural samples; Brza metoda za odredjivanje radioaktivnog stroncija u prirodnim uzorcima

    Energy Technology Data Exchange (ETDEWEB)

    Grahek, Z; Kosutic, K; Lulic, S [Rudjer Boskovic Institute, Zagreb (Croatia)

    1997-12-31

    Radioactive strontium isotopes belong to the group of isotopes that are very dangerous for human health. Therefore radioactive strontium is regularly determined in natural samples. When determining strontium isotopes in natural samples, it is necessary to isolate strontium from the sample because strontium isotopes are pure {beta}-emitters. As natural samples contain much more calcium and sodium than strontium it is necessary to isolate a small quantity of strontium from large sample with simultaneous separation of calcium and other interfering elements. For this purposes an elegant method based on ion exchange chromatography has been developed. Namely, examinations with model system have shown that strontium may be separated from calcium on the column filled with anion exchanger and the mixture of the methanol and nitric acid as eluent. It was also shown that yttrium does not separate from strontium but elutes almost simultaneously with it. Yttrium may be separated from strontium on the column filled with cation exchanger DOWEX 50X8 and nitric acid as eluent. According to the above examinations, the procedure of isolation of strontium and yttrium from natural sample has been created (on assumption that {sup 90}Sr and {sup 90}Y in secular equilibrium in sample). Strontium and yttrium have been isolated from natural sample (standard IAEA A-7) on the column filled with the exchanger AMBERLITE CG-400 and the mixture of methanol and nitric acid as eluent. Strontium and yttrium have been separated on the column with cation exchanger. {sup 90}Sr has been determined through {sup 90}Y by counting the solid yttrium oxalate immediately upon isolation and separation from strontium. {sup 90}Sr has also been determined by counting {sup 90}Sr-{sup 90}Y in secular equilibrium after 15 days. The obtained results of determination of {sup 90}Sr through {sup 90}Y and through secular equilibrium {sup 90}Sr-{sup 90}Y correspond to the declared values of standard. (author). 2 figs., 1

  14. Morphology and adsorption of chromium ion on uranium 1,2,4,5-benzenetetracarboxylic acid metal organic framework (MOF

    Directory of Open Access Journals (Sweden)

    Vala Remy M.K.

    2016-01-01

    Full Text Available In this paper, we report the synthesis of metal organic framework of uranium 1,2,4,5-benzene tetracarboxylic acid (U-H4btec MOF by solvothermal method. The obtained MOF was characterized by Fourier transform infrared spectroscopy (FTIR, Scanning electron microscopy (SEM, Transmission electron microscopy (TEM, X-ray diffraction spectroscopy (XRD, Energy dispersive spectroscopy (EDS, thermogravimetric and differential thermogravimetric analysis (TGA/DTA. The morphology of the uranium 1,2,4,5-benzene tetracarboxylic acid MOF observed by SEM, revealed the presence of flaky porous structure. Adsorption of Cr3+ from aqueous solution onto the uranium 1,2,4,5-benzene tetracarboxylic acid MOF was systematically studied. Langmuir and Freundlich adsorption isotherms were applied to determine the adsorption capacity of the MOF to form a monolayer. Kinetic determination of the adsorption of Cr3+ suggested both chemisorption and physisorption probably due to the presence of carbonyl groups within the MOF and its porous structure.

  15. Adsorption of zinc ions on bone char using helical coil-packed bed columns and its mass transfer modeling

    DEFF Research Database (Denmark)

    Moreno-Pérez, J.; Bonilla-Petriciolet, A.; Rojas-Mayorga, C. K.

    2016-01-01

    This study reports the assessment of helical coil-packed bed columns for Zn2+ adsorption on bone char. Zn2+ adsorption breakthrough curves have been obtained using helical coil columns with different characteristics and a comparison has been conducted with respect to the results of straight fixed-bed...... columns. Results showed that the helical coil adsorption columns may offer an equivalent removal performance than that obtained for the traditional packed bed columns but using a compact structure. However, the coil diameter, number of turns, and feed flow appear to be crucial parameters for obtaining...... the best performance in this packed-bed geometry. A mass transfer model for a mobile fluid flowing through a porous media was used for fitting and predicting the Zn2+ breakthrough curves in helical coil bed columns. Results of adsorbent physicochemical characterization showed that Zn2+ adsorption on bone...

  16. Extraction of Lanthanide and Actinide Ions from Aqueous Mixtures Using a Carboxylic Acid-Functionalized Porous Aromatic Framework

    Science.gov (United States)

    2016-01-01

    Porous aromatic frameworks (PAFs) incorporating a high concentration of acid functional groups possess characteristics that are promising for use in separating lanthanide and actinide metal ions, as required in the treatment of radioactive waste. These materials have been shown to be indefinitely stable to concentrated acids and bases, potentially allowing for multiple adsorption/stripping cycles. Additionally, the PAFs combine exceptional features from MOFs and inorganic/activated carbons giving rise to tunable pore surfaces and maximum chemical stability. Herein, we present a study of the adsorption of selected metal ions, Sr2+, Fe3+, Nd3+, and Am3+, from aqueous solutions employing a carbon-based porous aromatic framework, BPP-7 (Berkeley Porous Polymer-7). This material displays high metal loading capacities together with excellent adsorption selectivity for neodymium over strontium based on Langmuir adsorption isotherms and ideal adsorbed solution theory (IAST) calculations. Based in part upon X-ray absorption spectroscopy studies, the stronger adsorption of neodymium is attributed to multiple metal ion and binding site interactions resulting from the densely functionalized and highly interpenetrated structure of BPP-7. Recyclability and combustibility experiments demonstrate that multiple adsorption/stripping cycles can be completed with minimal degradation of the polymer adsorption capacity. PMID:27163056

  17. Organic composite-mediated surface coating of human acellular bone matrix with strontium.

    Science.gov (United States)

    Huang, Yi-Zhou; Wang, Jing-Jing; Huang, Yong-Can; Wu, Cheng-Guang; Zhang, Yi; Zhang, Chao-Liang; Bai, Lin; Xie, Hui-Qi; Li, Zhao-Yang; Deng, Li

    2018-03-01

    Acellular bone matrix (ACBM) provides an osteoconductive scaffold for bone repair, but its osteoinductivity is poor. Strontium (Sr) improves the osteoinductivity of bone implants. In this study, we developed an organic composite-mediated strontium coating strategy for ACBM scaffolds by using the ion chelating ability of carboxymethyl cellulose (CMC) and the surface adhesion ability of dopamine (DOPA). The organic coating composite, termed the CMC-DOPA-Sr composite, was synthesized under a mild condition, and its chemical structure and strontium ion chelating ability were then determined. After surface decoration, the physicochemical properties of the strontium-coated ACBM (ACBM-Sr) scaffolds were characterized, and their biocompatibility and osteoinductivity were determined in vitro and in vivo. The results showed that the CMC-DOPA-Sr composite facilitated strontium coating on the surface of ACBM scaffolds. The ACBM-Sr scaffolds possessed a sustained strontium ion release profile, exhibited good cytocompatibility, and enhanced the osteogenic differentiation of mesenchymal stem cells in vitro. Furthermore, the ACBM-Sr scaffolds showed good histocompatibility after subcutaneous implantation in nude mice. Taken together, this study provided a simple and mild strategy to realize strontium coating for ACBM scaffolds, which resulted in good biocompatibility and improved osteoinductivity. Copyright © 2017 Elsevier B.V. All rights reserved.

  18. Optimization, isotherm, kinetic and thermodynamic studies of Pb(II) ions adsorption onto N-maleated chitosan-immobilized TiO2 nanoparticles from aqueous media

    Science.gov (United States)

    Shaker, Medhat A.; Yakout, Amr A.

    2016-02-01

    Chitosan, CS was chemically engineered by maleic anhydride via simple protocol to produce N-maleated chitosan, MCS which immobilized on anatase TiO2 to synthesize novel eco-friendly nanosorbent (51 ± 3.8 nm), MCS@TiO2 for cost-effective and efficient removal of Pb(II) ions from aqueous media. The chemical structure, surface properties and morphology of MCS@TiO2 were recognized by FTIR, 1H NMR, XRD, TEM, DLS and zeta-potential techniques. The relations between %removal of Pb(II) and different analytical parameters such as solution acidity (pH), MCS@TiO2 dosage, time of contact and initial Pb(II) concentration were optimized using response surface methodology (RSM) and Box-Behnken design (BBD) statistical procedures. The fitting of the experimental data to four different isotherm models at optimized conditions was carried out by various statistical treatments including the correlation coefficient (r), coefficient of determination (r2) and non-linear Chi-square (χ2) test analyses which all confirm the suitability of Langmuir model to explain the adsorption isotherm data. Also, statistics predicted that the pseudo-second-order model is the optimum kinetic model among four applied kinetic models to closely describe the rate equation of the adsorption process. Thermodynamics viewed the adsorption as endothermic and feasible physical process. EDTA could release the sorbed Pb(II) ions from MCS@TiO2 with a recovery above 92% after three sorption-desorption cycles. The novel synthesized nanosorbent is evidenced to be an excellent solid phase extractor for Pb(II) ions from wastewaters.

  19. Bio sorption of strontium from aqueous solution by the new strain of bacillus sp. strain GT-83

    International Nuclear Information System (INIS)

    Tajer Mohammad Ghazvini, P.; Ghorbanzadeh Mashkani, S.; Mazaheri, M.

    2009-01-01

    An attempt was made to isolate bacterial strains capable of removing strontium biologically. In this study ten different water samples collected from Neydasht spring in the north of Iran and then the bacterial species were isolated from the water samples. The initial screening of a total of 50 bacterial isolates resulted in selection of one strain.The isolated strain showed a maximum adsorption capacity with 55 milligrams strontium/g dry wt. It was tentatively identified as Bacillus sp. According to the morphological and biochemical properties, and called strain GT-83. Our studies indicated that Bacillus sp. GT-83 is able to grow aerobically in the presence of 50 mM SrCl 2 , but its growth was inhibited at high levels of strontium concentrations. The bio sorption capacity of Bacillus sp. GT-83 depends strongly on the p H solution. Hence the maximum strontium sorption capacity of Bacillus sp. GT-83 was obtained at pah 10, independent of absence or presence of MgCl 2 of different concentrations. Strontium-salt bio sorption studies were also performed at this p H values. The equilibrium bio sorption of strontium was elevated by increasing the strontium concentration, up to 250 milligrams/l for Bacillus sp. GT-83. The maximum bio sorption of strontium was obtained at temperatures in the range of 30-35 d eg C . The Bacillus sp. GT-83 bio sorbed 97 milligrams strontium/g dry wt at 100 milligrams/l initial strontium concentration without MgCl 2 . When MgCl 2 concentration increased to 15%(w/v), these values dropped to 23.6 milligrams strontium/g dry wt at the same conditions. Uptake of strontium within 5 min of incubation was relatively rapid and the absorption continued slowly thereafter

  20. Study of sorption processes of strontium on the synthetic hydroxyapatite

    International Nuclear Information System (INIS)

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

    2011-01-01

    The sorption of strontium on synthetic hydroxyapatite was investigated using batch method and radiotracer technique. The hydroxyapatite samples were prepared by a wet precipitation process followed by calcination of calcium phosphate that precipitated from aqueous solution. Also, commercial hydroxyapatites were used. The sorption of strontium on hydroxyapatite depended on the method of preparation and it was pH independent ranging from 4 to 9 as a result of buffering properties of hydroxyapatite. The distribution coefficient K d was significantly decreased with increasing concentration of Sr 2+ and Ca 2+ ions in solution with concentration above 1 x 10 -3 mol dm -3 . The percentage strontium sorption for commercial and by wet method prepared hydroxyapatite was in the range of 83-96%, while calcined hydroxyapatite was ranging from 10 to 30%. The experimental data for sorption of strontium have been interpreted in the term of Langmuir isotherm. The sorption of Sr 2+ ions was performed by ion-exchange with Ca 2+ cations on the crystal surface of hydroxyapatite. Although calcined hydroxyapatite is successfully used as biomaterial for hard tissues repair, it is not used for the treatment of liquid wastes. (author)

  1. High-resolution stratigraphy with strontium isotopes.

    Science.gov (United States)

    Depaolo, D J; Ingram, B L

    1985-02-22

    The isotopic ratio of strontium-87 to strontium-86 shows no detectable variation in present-day ocean water but changes slowly over millions of years. The strontium contained in carbonate shells of marine organisms records the ratio of strontium-87 to strontium-86 of the oceans at the time that the shells form. Sedimentary rocks composed of accumulated fossil carbonate shells can be dated and correlated with the use of high precision measurements of the ratio of strontium-87 to strontium-86 with a resolution that is similar to that of other techniques used in age correlation. This method may prove valuable for many geological, paleontological, paleooceanographic, and geochemical problems.

  2. Calculation of the acid-base equilibrium constants at the alumina/electrolyte interface from the ph dependence of the adsorption of singly charged ions (Na+, Cl-)

    Science.gov (United States)

    Gololobova, E. G.; Gorichev, I. G.; Lainer, Yu. A.; Skvortsova, I. V.

    2011-05-01

    A procedure was proposed for the calculation of the acid-base equilibrium constants at an alumina/electrolyte interface from experimental data on the adsorption of singly charged ions (Na+, Cl-) at various pH values. The calculated constants (p K {1/0}= 4.1, p K {2/0}= 11.9, p K {3/0}= 8.3, and p K {4/0}= 7.7) are shown to agree with the values obtained from an experimental pH dependence of the electrokinetic potential and the results of potentiometric titration of Al2O3 suspensions.

  3. Adsorption of Pb(II) ions present in aqueous solution on the oxy hydroxides: boehmite (γ-AIOOH), goethite (α-FeOOH) and manganite (γ-MnOOH)

    International Nuclear Information System (INIS)

    Arreola L, J. E.

    2013-01-01

    Boehmite, goethite and manganite were synthesized by different methods and characterized using X-ray diffraction (XRD), infrared spectroscopy (IR), thermogravimetric study , N 2 physisorption measurements, scanning electron microscopy (Sem), semiquantitative elemental analysis (EDS), as well as additional studies were determined the surface active sites concentration and zero point of charge. Furthermore, we studied the Pb(II) ion adsorption capacity present in aqueous solution on these synthesized materials by batch-type experiments at room temperature, as a function of contact time between the phases liquid-solid system (adsorption kinetics), initial concentration of the adsorbate (adsorption isotherms), ph and temperature. The adsorption equilibrium time of adsorption processes in these studied systems was found at 60 minutes for boehmite and 30 minutes for goethite and manganite respectively after contacting the solid-liquid phase systems. The adsorption capacity of the lead ions on these adsorbent materials depended of lead concentration, ph and temperature of the systems. Were evaluated lead adsorption capacities in these materials to different contact times using an initial concentration of 20 mg/L of Pb(II) ions at ph = 4, the results of three systems were adjusted to second pseudo kinetic model order. With respect to the study of the adsorbate concentration effect, boehmite-Pb(II) and goethite-Pb(II) systems were adjusted to Langmuir isotherm model which proposes that the adsorption is carried out in a monolayer, moreover manganite-Pb(II) system was adjusted Temp kin isotherm model, which assumes that the adsorption heat of all the molecules in the layer decreases linearly with coverage due to adsorbent-adsorbate interactions and adsorption is characterized by a uniform distribution of the binding energies. Were studied the ph effect of Pb(II) ions solution on the adsorption capacity of such adsorbents, it was found that as the ph increases lead solution

  4. Effect Of Particle Size Of Zeolite On The Mass Transfer Coefficient Of Strontium In The Radioactive Waste Ion-Exchange Process

    International Nuclear Information System (INIS)

    Dewi-Susilowati; Suyitno

    1998-01-01

    This research is aimed for finding out the volumetric mass transfer coefficient of the zeolite particle, ks. The experiment has been conducted using an ion exchange column. The column diameter and length are 4.2 cm and 28 cm, respectively. The experiments have been conducted by flowing in the feed to the ion-exchange column containing zeolite with the varied particle diameters, I.e. 20, 40, 60, 80 and 100 mesh. The feed concentrations of Sr(NO 3 ) 2 , have been varied, I.e. 100, 250, 450, 550 and 650 ppm, and so have been the flow rates, I.e/ 35, 49, 70, 90 and 105 ml/minute. Samples of the effluents have been taken at certain series of time and subjected to analysis using an Atomic Absorption Spectrophotometer. The analytical data obtained have shown that the mass transfer coefficient of the zeolite particle is predominantly affected by the zeolite structure, in particular is effected by the number of AI atoms that hold the K ions. The analytical result from the above parameters has been presented in the forms of several groups of dimensionless number. The equations obtained are: (k L *dp)/D L 18.902(Re) 0 ,378 (dp/D) 0 ,6972(Co * ) 0 ,2667 with a mean error of 7.26%; k S 2240.268(dp/D) 1 .553; and each of them is valid in range of: Re: 0.182 - 0.856; dp/D: 0.004 - 0.022; Co * : 9.5408x10 - 5 - 6.2827x10 - 4

  5. 'Applications of stable isotopes in life sciences'. Lead and strontium stable isotope measurements by using a high lateral resolution secondary ion mass spectrometer (NanoSIMS)

    International Nuclear Information System (INIS)

    Sano, Yuji

    2008-01-01

    The method of Pb and Sr isotope measurements at about 5 μm resolution was developed by using a high lateral resolution secondary ion mass spectrometer (NanoSIMS NS50). Since the both elements have radiogenic nuclides such as 206 Pb, 207 Pb, and 87 Sr, natural variations of isotopic ratios are large. It is possible to detect a meaningful variation in a terrestrial sample, even though the experimental error is relatively large. In the case of monazite U-Pb dating, a 4 nA O - primary beam was used to sputter the sample and secondary positive ions were extracted for mass analysis using a Mattauch-Herzog geometry. The multi-collector system was modified to detect 140 Ce + , 204 Pb + , 206 Pb + , 238 U 16 O + , and 238 U 16 O 2 + ions simultaneously. Based on the monazite standard from North-Central Madagascar, we have determined the 206 Pb/ 238 U ratios of samples. 207 Pb/ 206 Pb ratios were measured by a magnet scanning with a single collector mode. 44 monazite grains extracted from a sedimentary rock in Taiwan were analyzed. Observed ages were consistent with the U-Th-Pb chemical ages by EPMA. Then NanoSIMS has been used to measure 87 Sr/ 86 Sr ratios in natural calcium carbonate samples. Multi-collector system was adjusted to detect 43 Ca + , 80 Ca 2 + , 86 Sr + , and 87 Sr + ions at the same time. Magnetic field was scanning for the EM no.4 counter to detect 85 Rb + , 86 Sr + and 87 Sr + , while the EM no.4b can measure 86 Sr + , 87 Sr + , and 88 Sr + , respectively. Repeated analyses of a coral skeleton standard (JCp-1) show that 87 Sr/ 86 Sr ratio agrees well with the seawater signature, after the series of corrections such as Ca dimer, 87 Rb, and a mass bias estimated by 88 Sr/ 86 Sr ratio. The method is applied to an otolith from ayu (Pleco-glossus altivelis altivelis) collected from the Yodo river, Japan. The spatial variation of 87 Sr/ 86 Sr ratios was consistent with amphidromous migration of the fish, namely, born in the lake and grown in the coastal sea

  6. Spectroscopy and Laser-SNMS on stable and radioactive strontium

    Energy Technology Data Exchange (ETDEWEB)

    Bosco, Hauke; Walther, Clemens [Institut fuer Radiooekologie und Strahlenschutz, Leibniz Universitaet Hannover (Germany); Franzmann, Michael [Institut fuer Radiooekologie und Strahlenschutz, Leibniz Universitaet Hannover (Germany); Institut fuer Physik, Johannes Gutenberg Universitaet Mainz (Germany); Kron, Tobias; Wendt, Klaus [Institut fuer Physik, Johannes Gutenberg Universitaet Mainz (Germany)

    2016-07-01

    Nuclear accidents as experienced e.g. in Chernobyl or Fukushima and nuclear weapon tests released considerable activity levels and a variety of medium to long-lived radionuclides into the environment. Strontium-90 appears as a significant share of the fission products in spent nuclear fuel and correspondingly in any possible release. Due to its chemical properties it is subject to long range transport through the environment and can cause considerable dose to man when entering the food chain. Correspondingly, the investigation of speciation and migration channels is of major relevance. A radioanalytical approach is severely hampered by the low beta energy of the strontium-90 decay and the need to separate strontium-90 from the secular equilibrated daughter yttrium-90. Hence, application of a mass spectrometric method without chemical separation of the elements is a promising alternative for low-level investigation of strontium-90. Application of the new Laser-SNMS system at IRS Hannover could well suit those needs. It applies three Ti:Sa lasers for resonant ionization of neutral atoms produced by primary ion sputtering in a SIMS together with a time-of-flight mass analysis which provides high spatial resolution. The analytical measurements are preceded by spectroscopic studies on the level structure of strontium to develop a most efficient ionization scheme.

  7. Strontium-90 - ED 4309

    International Nuclear Information System (INIS)

    Ammerich, M.; Frot, P.; Gambini, D.; Gauron, C.; Moureaux, P.; Herbelet, G.; Lahaye, T.; Le Guen, B.; Pihet, P.; Rannou, A.; Vidal, E.

    2012-12-01

    This sheet presents the characteristics of strontium-90, its origin, and its radio-physical and biological properties. It briefly describes its use in nuclear medicine. It indicates its dosimetric parameters for external exposure, cutaneous contamination, and internal exposure due to acute contamination or to chronic contamination. It indicates and comments the various exposure control techniques: ambient dose rate measurement, surface contamination measurement, atmosphere contamination. It addresses the means of protection: premise design, protection against external exposure and against internal exposure. It describes how areas are delimited and controlled within the premises: regulatory areas, controls to be performed. It addresses the personnel classification, training and medical survey. It addresses the issue of wastes and effluents. It briefly recalls the administrative procedures related to the authorization and declaration of possession and use of sealed and unsealed sources. It indicates regulatory aspects related to the transport of strontium-90, describes what is to be done in case of incident or accident (for the different types of contamination or exposure)

  8. Effects of specific adsorption of copper (II) ion on charge transfer reaction at the thin film LiMn2O4 electrode/aqueous electrolyte interface

    International Nuclear Information System (INIS)

    Nakayama, N.; Yamada, I.; Huang, Y.; Nozawa, T.; Iriyama, Y.; Abe, T.; Ogumi, Z.

    2009-01-01

    This study investigated the effect of a specific adsorption ion, copper (II) ion, on the kinetics of the charge transfer reaction at a LiMn 2 O 4 thin film electrode/aqueous solution (1 mol dm -3 LiNO 3 ) interface. The zeta potential of LiMn 2 O 4 particles showed a negative value in 1 x 10 -2 mol dm -3 LiNO 3 aqueous solution, while it was measured as positive in the presence of 1 x 10 -2 mol dm -3 Cu(NO 3 ) 2 in the solution. The presence of copper (II) ions in the solution increased the charge transfer resistance, and CV measurement revealed that the lithium insertion/extraction reaction was retarded by the presence of small amount of copper (II) ions. The activation energy for the charge transfer reaction in the solution with Cu(NO 3 ) 2 was estimated to be 35 kJ mol -1 , which was ca. 10 kJ mol -1 larger than that observed in the solution without Cu(NO 3 ) 2 . These results suggest that the interaction between the lithium ion and electrode surface is a factor in the kinetics of charge transfer reaction

  9. Selective adsorption of Pb (II) ions by amylopectin-g-poly (acrylamide-co-acrylic acid): A bio-degradable graft copolymer.

    Science.gov (United States)

    Sasmal, Dinabandhu; Maity, Jayanta; Kolya, Haradhan; Tripathy, Tridib

    2017-04-01

    Amylopectin-g-poly (acrylamide-co-acrylic acid) [AP-g-poly (AM-co-AA)] was synthesised in water medium by using potassium perdisulphate as an initiator. The graft copolymer was characterized by molecular weight determination by size exclusion chromatography (SEC), fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) spectroscopy, scanning electron microscope (SEM) studies, thermal analysis, measurement of neutralisation equivalent and biodegradation studies. The graft copolymer was used for Pb (II) ion removal from aqueous solution. The Pb (II) ion removal capacity of the graft copolymer was also compared with another laboratory developed graft copolymer Amylopectin-g-poly (acrylamide) (AP-g-PAM). Both the graft copolymers were also used for the competitive metal ions removal with Pb (II)/Cd (II), Pb (II)/Zn (II), Pb (II)/Ni (II), Pb (II)/Cu (II) pairs separately under similar conditions. AP-g-poly (AM-co-AA) showed better Pb (II) ion adsorbing power over AP-g-PAM and also much selective towards Pb (II) ions. The adsorption follows a second order rate equation and Langmuir isotherm model. Copyright © 2017 Elsevier B.V. All rights reserved.

  10. Dynamic adsorption of mixtures of Rhodamine B, Pb (II), Cu (II) and Zn(II) ions on composites chitosan-silica-polyethylene glycol membrane

    Science.gov (United States)

    Mahatmanti, F. W.; Rengga, W. D. P.; Kusumastuti, E.; Nuryono

    2018-04-01

    The adsorption of a solution mixture of Rhodamine B, Pb (II), Cu (II) and Zn(II) was studied using dynamic methods employing chitosan-silica-polyethylene glycol (Ch/Si/P) composite membrane as an adsorptive membrane. The composite Ch/Si/P membrane was prepared by mixing a chitosan-based membrane with silica isolated from rice husk ash (ASP) and polyethylene glycol (PEG) as a plasticizer. The resultant composite membrane was a stronger and more flexible membrane than the original chitosan-based membrane as indicated by the maximum percentage of elongation (20.5 %) and minimum Young’s Modulus (80.5 MPa). The composite membrane also showed increased mechanical and hydrophilic properties compared to the chitosan membranes. The membrane was used as adsorption membrane for Pb (II), Cu (II), Cd (II) ions and Rhodamine B dyes in a dynamic system where the permeation and selectivity were determined. The permeation of the components was observed to be in the following order: Rhodamine B > Cd (II) > Pb (II) > Cu (II) whereas the selectivity was shown to decrease the order of Cu (II) > Pb (II) > Cd (II) > Rhodamine B.

  11. Adsorption of single Li and the formation of small Li clusters on graphene for the anode of lithium-ion batteries.

    Science.gov (United States)

    Fan, Xiaofeng; Zheng, W T; Kuo, Jer-Lai; Singh, David J

    2013-08-28

    We analyzed the adsorption of Li on graphene in the context of anodes for lithium-ion batteries (LIBs) using first-principles methods including van der Waals interactions. We found that although Li can reside on the surface of defect-free graphene under favorable conditions, the binding is much weaker than to graphite and the concentration on a graphene surface is not higher than in graphite. At low concentration, Li ions spread out on graphene because of Coulomb repulsion. With increased Li content, we found that small Li clusters can be formed on graphene. Although this result suggests that graphene nanosheets can conceivably have a higher ultimate Li capacity than graphite, it should be noted that such nanoclusters can potentially nucleate Li dendrites, leading to failure. The implications for nanostructured carbon anodes in batteries are discussed.

  12. Strontium-90 fluoride data sheet

    Energy Technology Data Exchange (ETDEWEB)

    Fullam, H.T.

    1981-06-01

    This report is a compilation of available data and appropriate literature references on the properties of strontium-90 fluoride and nonradioactive strontium fluoride. The objective of the document is to compile in a single source pertinent data to assist potential users in the development, licensing, and use of /sup 90/SrF/sub 2/-fueled radioisotope heat sources for terrestrial power conversion and thermal applications. The report is an update of the Strontium-90 Fluoride Data Sheet (BNWL-2284) originally issued in April 1977.

  13. Simultaneous efficient adsorption of Pb2+ and MnO4− ions by MCM-41 functionalized with amine and nitrilotriacetic acid anhydride

    International Nuclear Information System (INIS)

    Chen, Feiyun; Hong, Mingzhu; You, Weijie; Li, Chong; Yu, Yan

    2015-01-01

    Highlights: • MCM-41 was successfully modified with amine and nitrilotriacetic acid anhydride. • The adsorbent can simultaneously remove Pb 2+ and MnO 4 − by adjusting pH of the system. • The maximum adsorption capacities of Pb 2+ and MnO 4 − are 147 mg/g and 156 mg/g. • The absorbent exhibits good regeneration and reusability for 5 cycles use. - Abstract: A novel adsorbent NH 2 /MCM-41/NTAA, capable of simultaneous adsorption of cations and anions from aqueous solution, was prepared by immobilization of amine and nitrilotriacetic acid anhydride (NTAA) onto MCM-41. The structures and properties before and after surface modification were systematically investigated through X-ray diffraction (XRD), transmission electron microscope (TEM) and scanning electron microscope (SEM), nitrogen adsorption–desorption, and infrared spectroscopy (FTIR), thermogravimetry (TGA) and X-ray photoelectron spectroscopy (XPS). They together confirm that the amine and NTAA group were chemically bonded to the internal surface of the mesoporous. The NH 2 /MCM-41/NTAA were used to adsorb Pb 2+ and MnO 4 − in an aqueous solution in a batch system, and the maximum adsorption efficiency was found to occur at pH 5.0 and 3.0, respectively. NH 2 /MCM-41/NTAA exhibit preferable removal of Pb 2+ through electrostatic interactions and chelation, whereas it captures MnO 4 − by means of electrostatic interactions. The experimental data are fitted the Langmuir isotherm model reasonably well, with the maximum adsorption capacity of 147 mg/g for Pb 2+ and of 156 mg/g for MnO 4 − . The adsorption rates of both Pb 2+ and MnO 4 − are found to follow the pseudo-second order kinetics. Furthermore, the NH 2 /MCM-41/NTAA adsorbent performs good recyclability and reusability for 5 cycles use. This study indicates a potential applicability of NH 2 /MCM-41/NTAA as new absorbents for effective simultaneous adsorption of hazardous metal ions and anions from wastewater.

  14. Investigation of strontium sorption on Kula volcanites treated with HCl

    International Nuclear Information System (INIS)

    Kuetahyali, C.; Cetinkaya, B.; Acar, M. B.; Isik, N. O.; Cireli, I.

    2009-01-01

    In planning the disposal of radioactive waste in a deep geologic repository, consideration must be given to the ways in which radionuclides might leave the repository and migrate through the geosphere. In performance assessment studies the uptake of the radioactive elements by rock formations play an important role in retarding their aqueous phase migration. Sorption studies of radionuclides have been conducted to obtain data on the distribution coefficient (K d ) that is as an input parameter in the performance assessment of the geological disposal of radioactive wastes. In many studies, the sorption experiments employed natural soils and rocks as sorbents. Adsorption experiments were studied in a batch adsorption system using Sr(NO 3 ) 2 (Merck) solution. Strontium sorption on Kula Volcanites treated with HCl was investigated. Central Composite Design Method was used in the experiments. Sr adsorption was studied as a function of pH, contact time, concentration of adsorbate, and temperature.

  15. Continuous Fixed-Bed Column Study and Adsorption Modeling: Removal of Lead Ion from Aqueous Solution by Charcoal Originated from Chemical Carbonization of Rubber Wood Sawdust

    Directory of Open Access Journals (Sweden)

    Swarup Biswas

    2015-01-01

    Full Text Available The efficiency of chemically carbonized rubber wood sawdust for the removal of lead ion from the aqueous stream was investigated by column process. Chemically carbonized rubber wood sawdust was prepared by treating the sawdust with H2SO4 and HNO3. Maximum removal of lead ion in column process was found as 38.56 mg/g. The effects of operating parameters such as flow rate, bed depth, concentration, and pH were studied in column mode. Experimental data confirmed that the adsorption capacity increased with the increasing inlet concentration and bed depth and decreased with increasing flow rate. Thomas, Yoon-Nelson, and Adams-Bohart models were used to analyze the column experimental data and the relationship between operating parameters. Chemically carbonized rubber wood sawdust was characterized by using Fourier transform infrared spectroscopy. Scanning electron microscope was also utilized for morphological analysis of the adsorbent. Furthermore X-ray fluorescence spectrum analysis and energy dispersive X-ray spectroscopy were also used for the confirmation of lead adsorption process.

  16. Physicochemical Properties and Cellular Responses of Strontium-Doped Gypsum Biomaterials

    OpenAIRE

    Pouria, Amir; Bandegani, Hadis; Pourbaghi-Masouleh, Milad; Hesaraki, Saeed; Alizadeh, Masoud

    2012-01-01

    This paper describes some physical, structural, and biological properties of gypsum bioceramics doped with various amounts of strontium ions (0.19–2.23 wt%) and compares these properties with those of a pure gypsum as control. Strontium-doped gypsum (gypsum:Sr) was obtained by mixing calcium sulfate hemihydrate powder and solutions of strontium nitrate followed by washing the specimens with distilled water to remove residual salts. Gypsum was the only phase found in the composition of both pu...

  17. Local structure and speciation of uranium in strontium orthosilicate: TRFS and EXAFS studies

    International Nuclear Information System (INIS)

    Gupta, Santosh K.; Thulasidas, S.K.; Natarajan, V.; Yadav, A.K.; Bhattacharya, D.

    2015-01-01

    TRFS is used to investigate the valence state and coordination behavior of uranium in strontium orthosilicate. From TRFS measurement it was observed that uranium exists as U(VI) in the form of UO 2 2+ in Sr 2 SiO 4 . Based on life time measurement and EXAFS studies it was inferred that uranyl is stabilized on both 9- and 10- coordinated strontium polyhedra. Majority of uranyl ion occupy relatively asymmetric site in strontium silicate most probably 9-coordinated Sr sites. (author)

  18. Simplified method for the determination of strontium-90 in large amounts of bone-ash

    International Nuclear Information System (INIS)

    Patti, F.; Jeanmaire, L.

    1966-06-01

    The principle of the determination is based on a 3-step process: 1) concentrating the strontium by attacking the ash with nitric acid; 2) elimination of residual phosphoric ions by a double precipitation of strontium oxalate; and 3) extraction of yttrium 90, counted in the oxalate form. The advantages of the method: -) using simple techniques it makes it possible to process 50 g of ash; -) the initial concentration of strontium considerably reduces the volume of the solutions as well as the size of precipitates handled. Fuming nitric acid is used in a specially designed burette. (authors) [fr

  19. Review and assessment of technologies for the separation of strontium from alkaline and acidic media

    International Nuclear Information System (INIS)

    Orth, R.J.; Kurath, D.E.

    1994-01-01

    A literature survey has been conducted to identify and evaluate methods for the separation of strontium from acidic and alkaline media as applied to Hanford tank waste. The most promising methods of solvent extraction, precipitation, and ion exchange are described. The following criteria were used for evaluating the separation methods: Appreciable strontium removal must be demonstrated; Strontium selectivity over bulk components must be demonstrated; The method must show promise for evolving into a practical and fairly simple process; The process should be safe to operate; The method must be robust (i.e., capable of separating strontium from various waste types); Secondary waste generation must be minimized; and The method must show resistance to radiation damage. The methods discussed did not necessarily satisfy all of the above criteria; thus, key areas requiring further development are also given for each method. Less promising solvent extraction, precipitation, and ion exchange methods were also identified; areas for potential development are included in this report

  20. First-principles investigation of adsorption and diffusion of Li on doped silicenes: Prospective materials for lithium-ion batteries

    International Nuclear Information System (INIS)

    Momeni, Mohammad Jafar; Mousavi-Khoshdel, Morteza; Targholi, Ehsan

    2017-01-01

    In this report, we investigate the adsorption energies and diffusion characteristics of Li atom on doped silicenes using first principles density functional theory (DFT) calculations. Our results show that the Li adsorption energy on doped silicenes is larger than pristine silicene. Based on our calculations, Al- and B-doped silicenes, due to creating an electron-deficient center in silicene, show a stronger interaction with Li atom compared to P- and N-doped silicenes. The obtained data for surface and perpendicular diffusion of Li atom show the easier mobility of Li on some doped silicenes compared to pristine silicene. According to our results, doping silicene with nitrogen and phosphorus atoms facilitates the Li surface mobility (diffusion barrier of 0.05 and 0.11 eV, respectively versus 0.18 eV for pure silicene) while, doping with aluminum, speed Li perpendicular diffusion (1.47 eV versus 1.67 eV for pristine silicene). The adsorption energy and diffusion barrier values, show the advantage of doped silicenes for use in LIBs with respect to pure silicene. - Highlights: • Calculation of adsorption energy of lithium on pristine and doped silicenes. • Surface and perpendicular diffusion barrier of Li on doped silicenes. • Examination of electronic structure of Li adsorbed doped silicenes.

  1. First-principles investigation of adsorption and diffusion of Li on doped silicenes: Prospective materials for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Momeni, Mohammad Jafar; Mousavi-Khoshdel, Morteza, E-mail: mmousavi@iust.ac.ir; Targholi, Ehsan

    2017-05-01

    In this report, we investigate the adsorption energies and diffusion characteristics of Li atom on doped silicenes using first principles density functional theory (DFT) calculations. Our results show that the Li adsorption energy on doped silicenes is larger than pristine silicene. Based on our calculations, Al- and B-doped silicenes, due to creating an electron-deficient center in silicene, show a stronger interaction with Li atom compared to P- and N-doped silicenes. The obtained data for surface and perpendicular diffusion of Li atom show the easier mobility of Li on some doped silicenes compared to pristine silicene. According to our results, doping silicene with nitrogen and phosphorus atoms facilitates the Li surface mobility (diffusion barrier of 0.05 and 0.11 eV, respectively versus 0.18 eV for pure silicene) while, doping with aluminum, speed Li perpendicular diffusion (1.47 eV versus 1.67 eV for pristine silicene). The adsorption energy and diffusion barrier values, show the advantage of doped silicenes for use in LIBs with respect to pure silicene. - Highlights: • Calculation of adsorption energy of lithium on pristine and doped silicenes. • Surface and perpendicular diffusion barrier of Li on doped silicenes. • Examination of electronic structure of Li adsorbed doped silicenes.

  2. Double photoionization of strontium

    Energy Technology Data Exchange (ETDEWEB)

    Sokell, Emma; Grimm, Michael; Sheridan, Paul, E-mail: emma.sokell@ucd.i [School of Physics, University College Dublin, Belfield, Dublin 4 (Ireland)

    2010-02-01

    Resonant triple-differential cross-section (TDCS) measurements have been used to study the double photoionization process in strontium. Two sets of measurements were made at the photon energy of the 4p {yields} 4d resonance. The coplanar geometry was used and the fixed analyser, positioned at -90{sup 0} to the main axis of polarization of the photons, detected electrons with {approx}65% of the available excess energy. The mutual angle between the two electrons had a range just short of 90 {yields} 270{sup 0}. The TDCS exhibit unexpected lobes at a mutual angle of 180{sup 0}. Comparison with other measurements made with the same geometry but with different sharings of the available energy indicate that these TDCS all show the unexpected lobe. Some possible explanations for the lobe are considered.

  3. A DFT based analysis of adsorption of Hg2+ ion on chitosan monomer and its citralidene and salicylidene derivatives: Prior to the removal of Hg toxicity.

    Science.gov (United States)

    Hassan, Basila; Rajan, Vijisha K; Mujeeb, V M Abdul; K, Muraleedharan

    2017-06-01

    A Density functional theory based study of adsorption of the toxic metal Hg (II) ion by chitosan monomer and two of its derivatives; citralidene and salicylidene chitosan, has been performed. The effect of structural features on the stability of studied complexes has been analyzed by using Gaussian03 software package. All the possible conformations of these adsorbents were studied using the global minimum geometries. All the adsorbing sites were studied by placing the metal ion on the centroid of the atoms and the stable conformer of the adsorbent-metal ion complex was identified. Interaction between Hg (II) and the adsorbents is found to be electrostatic. Metal ion binding with nitrogen atom is stronger than that with oxygen atoms in all the cases as the charge density of nitrogen is enhanced on Schiff base formation. The advantage of derivatives over chitosan monomer is their stability in acidic media. ΔE value of the complexes are in the order SC-Hg (II)>chitosan-Hg (II)>CC-Hg (II) which indicates that the stability of complexes increases with increase in energy gap. The study reveals that aromatic Schiff base derivatives of chitosan is better for Hg(II) intake than aliphatic derivatives. Copyright © 2017 Elsevier B.V. All rights reserved.

  4. Synthesis of novel inorganic-organic hybrid materials for simultaneous adsorption of metal ions and organic molecules in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Jin, Xinliang [State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Institute of Biochemical Engineering and Environmental Technology, Lanzhou University, Lanzhou 730000 (China); Li, Yanfeng, E-mail: liyf@lzu.edu.cn [State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Institute of Biochemical Engineering and Environmental Technology, Lanzhou University, Lanzhou 730000 (China); Yu, Cui; Ma, Yingxia; Yang, Liuqing; Hu, Huaiyuan [State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Institute of Biochemical Engineering and Environmental Technology, Lanzhou University, Lanzhou 730000 (China)

    2011-12-30

    Highlights: Black-Right-Pointing-Pointer Novel hybrid materials were synthesized and employed in the absorption of heavy metal and organic pollutants. Black-Right-Pointing-Pointer A novel method for amphiphilic adsorbent material synthesis was first reported in this paper. Black-Right-Pointing-Pointer The adsorbent material showed excellent adsorption capacity to Pb(II) and phenol. - Abstract: In this paper, atom transfer radical polymerization (ATRP) and radical grafting polymerization were combined to synthesize a novel amphiphilic hybrid material, meanwhile, the amphiphilic hybrid material was employed in the absorption of heavy metal and organic pollutants. After the formation of attapulgite (ATP) ATRP initiator, ATRP block copolymers of styrene (St) and divinylbenzene (DVB) were grafted from it as ATP-P(S-b-DVB). Then radical polymerization of acrylonitrile (AN) was carried out with pendent double bonds in the DVD units successfully, finally we got the inorganic-organic hybrid materials ATP-P(S-b-DVB-g-AN). A novel amphiphilic hybrid material ATP-P(S-b-DVB-g-AO) (ASDO) was obtained after transforming acrylonitrile (AN) units into acrylamide oxime (AO) as hydrophilic segment. The adsorption capacity of ASDO for Pb(II) could achieve 131.6 mg/g, and the maximum removal capacity of ASDO towards phenol was found to be 18.18 mg/g in the case of monolayer adsorption at 30 Degree-Sign C. The optimum pH was 5 for both lead and phenol adsorption. The adsorption kinetic suited pseudo-second-order equation and the equilibrium fitted the Freundlich model very well under optimal conditions. At the same time FT-IR, TEM and TGA were also used to study its structure and property.

  5. Porous allograft bone scaffolds: doping with strontium.

    Directory of Open Access Journals (Sweden)

    Yantao Zhao

    Full Text Available Strontium (Sr can promote the process of bone formation. To improve bioactivity, porous allograft bone scaffolds (ABS were doped with Sr and the mechanical strength and bioactivity of the scaffolds were evaluated. Sr-doped ABS were prepared using the ion exchange method. The density and distribution of Sr in bone scaffolds were investigated by inductively coupled plasma optical emission spectrometry (ICP-OES, X-ray photoelectron spectroscopy (XPS, and energy-dispersive X-ray spectroscopy (EDS. Controlled release of strontium ions was measured and mechanical strength was evaluated by a compressive strength test. The bioactivity of Sr-doped ABS was investigated by a simulated body fluid (SBF assay, cytotoxicity testing, and an in vivo implantation experiment. The Sr molar concentration [Sr/(Sr+Ca] in ABS surpassed 5% and Sr was distributed nearly evenly. XPS analyses suggest that Sr combined with oxygen and carbonate radicals. Released Sr ions were detected in the immersion solution at higher concentration than calcium ions until day 30. The compressive strength of the Sr-doped ABS did not change significantly. The bioactivity of Sr-doped material, as measured by the in vitro SBF immersion method, was superior to that of the Sr-free freeze-dried bone and the Sr-doped material did not show cytotoxicity compared with Sr-free culture medium. The rate of bone mineral deposition for Sr-doped ABS was faster than that of the control at 4 weeks (3.28 ± 0.23 µm/day vs. 2.60 ± 0.20 µm/day; p<0.05. Sr can be evenly doped into porous ABS at relevant concentrations to create highly active bone substitutes.

  6. Determination of mineral radioactive strontium-{sup 90} in urines; Recherche du strontium mineral radioactif {sup 90}Sr dans les urines

    Energy Technology Data Exchange (ETDEWEB)

    Jeanmaire, L; Jammet, H; Bertrand, S [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

    1959-07-01

    An analytical procedure for radioactive strontium in urine is described. As a first step, a precipitation of calcium oxalate performed on the urine, allows to detect the presence of various fission products and particularly of strontium which is carried by the precipitate. Strontium can then be selectively separated on ion exchange resins. By studying the growth curve of {beta} activity, it is possible to determine the activities which may be attributed to {sup 89}Sr and {sup 90}Sr respectively. (author) [French] Cet article decrit une technique de dosage du strontium radioactif dans les urines. Dans un premier stade, une precipitation d'oxalate de calcium effectuee sur l'urine permet de deceler la presence de differents produits de fission et en particulier du strontium qui est entraine sur ce precipite. Il est possible ensuite de separer selectivement le strontium au moyen de resines echangeuses d'ions. L'examen de le courbe de croissance de l'activite {beta} permet de determiner les activites dues respectivement a {sup 89}Sr et {sup 90}Sr. (auteur)

  7. Adsorption of phosphate in hydrocalumite-like layered double hydroxides: a comparison between memory effect and ion exchange processes; Adsorcao de fosfato em [Ca-Al]-HDL: comparacao entre o efeito de memoria e troca ionica

    Energy Technology Data Exchange (ETDEWEB)

    Bernardo, M.P., E-mail: marcelapiassib@gmail.com [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil); Moreira, F.K.V.; Ribeiro, C. [Embrapa Instrumentacao (LNNA), Sao Carlos, SP (Brazil). Laboratorio Nacional de Nanotecnologia para o Agronegocio

    2016-07-01

    Phosphorus is an essential element for agriculture, but the excessive use of this element has caused severe damages to the environment. Layered double hydroxide (LDHs) are excellent candidates to remove PO{sub 4}{sup 3-} anions through adsorption process. In this work, the phosphate adsorption on hydrocalumite-like (Ca-Al) LDHs was evaluated over the ion exchange and memory effect processes. X-ray diffraction measurements revealed formation of analogous crystalline phases from both process as the phosphate concentration was increased. However, the phosphate quantity adsorbed varied according to the process used. The ion exchange route is the most efficient process to remove phosphate from aqueous medium. (author)

  8. Kinetic study on adsorption of Cr(VI), Ni(II), Cd(II) and Pb(II) ions from aqueous solutions using activated carbon prepared from Cucumis melo peel

    Science.gov (United States)

    Manjuladevi, M.; Anitha, R.; Manonmani, S.

    2018-03-01

    The adsorption of Cr(VI), Ni(II), Cd(II) and Pb(II), ions from aqueous solutions by Cucumis melo peel-activated carbon was investigated under laboratory conditions to assess its potential in removing metal ions. The adsorption behavior of metal ions onto CMAC was analyzed with Elovich, intra-particle diffusion rate equations and pseudo-first-order model. The rate constant of Elovich and intra-particle diffusion on CMAC increased in the sequence of Cr(VI) > Ni(II) > Cd(II) > Pb(II). According to the regression coefficients, it was observed that the kinetic adsorption data can fit better by the pseudo-first-order model compared to the second-order Lagergren's model with R 2 > 0.957. The maximum adsorption of metal ions onto the CMAC was found to be 97.95% for Chromium(VI), 98.78% for Ni(II), 98.55% for Pb(II) and 97.96% for Cd(II) at CMAC dose of 250 mg. The adsorption capacities followed the sequence Ni(II) ≈ Pb(II) > Cr(VI) ≈ Cd(II) and Ni(II) > Pb(II) > Cd(II) > Cr(VI). The optimum adsorption conditions selected were adsorbent dosage of 250 mg, pH of 3.0 for Cr(VI) and 6.0 for Ni(II), Cd(II) and Pb(II), adsorption concentration of 250 mg/L and contact time of 180.

  9. Batch and flow-through continuous stirred reactor experiments of Sr2+-adsorption onto smectite: influence of pH, concentration and ionic strength

    International Nuclear Information System (INIS)

    Guimaraes, V.; Azenha, M.; Silva, A.F.; Bobos, I.

    2012-01-01

    Document available in extended abstract form only. Strontium-90 (t 1/2 = 29.1 years) resulting from the nuclear fission process is one of the main constituents connected with nuclear waste fuel. Concerning the physical properties and sorption behaviour one of the suitable buffer materials used as a backfill in the geological disposal systems for high-level radioactive wastes is smectite. The 2 μm clay fractions of di-octahedral smectite were used for adsorption experiments in batch and flow-through experiments. Flow-through experiments were carried out at different pH (4 and 8) and concentrations (8.00x10 -2 mmolSr 2+ /L, 2.0x10 -1 mmolSr 2+ /L, 3.3x10 -1 mmolSr 2+ /L and 4.1 x10 -1 mmol Sr 2+ /L). Batch experiments were carried out at different ionic strength ([KNO 3 ]=10 -2 M and [KNO 3 ]=10 -3 M), pH (4 and 8), whereas the concentration ranged between 0.19 mmolSr 2+ /L and 9.60 mmolSr 2+ /L. The adsorption strontium rate in flow-through experiments was found higher at pH 4 than at pH 8, where less of 20% amount of strontium was adsorbed on clay surface after 34 hours. This is explained by the surface charge of smectite layers with a permanent negative charge on the basal planes due essentially to isomorphic substitution. Also additional polar sites are conditionally charged by direct protonation of outer edge surfaces. Therefore, more negative sites become available for the strontium ions sorption, as the pH increasing. After adsorption, the clays were submitted to a desorption process. The rate of desorption at pH 4 is initially too fast due to the elevated amount of strontium released by smectite. After 255 min, the strontium amount desorbed is very low and the rate of desorption approached to zero. By contrast at pH 8 the rate of desorption is practically constant, and after 255 min there is a significant amount of strontium released by clay. Due to these different behaviors in different pH conditions, after 10 hours of desorption, the amount of strontium

  10. Application of high resolution X-ray emission spectroscopy on the study of Cr ion adsorption by activated carbon

    International Nuclear Information System (INIS)

    Espinoza-Quinones, Fernando R.; Modenes, Aparecido N.; Camera, Adriana S.; Stutz, Guillermo; Tirao, German; Palacio, Soraya M.; Kroumov, Alexander D.; Oliveira, Ana P.; Alflen, Vanessa L.

    2010-01-01

    In this work granular activated carbon has been chosen as an absorbent in order to investigate the Cr(VI) reduced by adsorption experiments. Several batch chromium-sorption experiments were carried out using 0.25 g of granular activated carbon in 50 mL aqueous solution containing approximately 70 and 140 mg L -1 of Cr(VI) and Cr(III), respectively. Cr-Kβ fluorescence spectra of Cr adsorbed in a carbon matrix and Cr reference materials were measured using a high-resolution Johann-type spectrometer. Based on evidence from the Cr-Kb satellite lines, the Cr(VI) reduction process has actually happened during metal adsorption by the activated carbon.

  11. Rational design of SnO2@C nanocomposites for lithium ion batteries by utilizing adsorption properties of MOFs.

    Science.gov (United States)

    Wang, Meihui; Yang, Hao; Zhou, Xianlong; Shi, Wei; Zhou, Zhen; Cheng, Peng

    2016-01-14

    A facile synthetic strategy is developed to prepare mono-dispersed SnO2 particles within three-dimensional porous carbon frameworks by utilizing the adsorption properties of metal-organic frameworks. This composite exhibits a high reversible capacity of 900 mA h g(-1) at 100 mA g(-1) after 50 cycles, with a stable capacity retention of 880 mA h g(-1) at 100 mA g(-1) even after 200 cycles.

  12. Adsorption de l'eau dissoute dans les mélanges supercarburant-alcools en vue de leur stabilisation. Comparaison entre adsorbants classiques et résines échangeuses d'ions Adsorption of Dissolved Water in Premium-Fuel/Alcohol Blends with a View to Their Stabilization. Comparison Between Conventional Adsorbents and Ion-Exchange Resins

    Directory of Open Access Journals (Sweden)

    Bernasconi C.

    2006-11-01

    Full Text Available Une réponse possible au problème de la déstabilisation par démixtion des mélanges supercarburant-alcools est l'abaissement de leur teneur en eau par adsorption physique. La forte affinité pour l'eau des résines échangeuses d'ions de type polystyrène sulfonate permet d'envisager leur utilisation dans ce cas spécifique d'application. Le principal intérêt de ce nouveau matériau adsorbant est de pouvoir se régénérer avec des calories de bas niveau (100-120°C. Nous avons donc étudié, du point de vue capacité d'adsorption et cinétique d'adsorption, le comportement de cet adsorbant et comparé ses performances à celles d'adsorbants plus classiques tels que le silicagel, l'alumine et le tamis moléculaire 3 Å. Les formes ioniques de la résine mises en oeuvre sont les formes : K+, Na+ et Mg2+. Sur le plan de la capacité totale d'adsorption, la résine, quelle que soit sa forme ionique, présente des performances supérieures à celles de l'alumine et du silicagel. Seule la forme Mg2+ adsorbe autant d'eau que le tamis moléculaire. L'efficacité de la résine est sensible à la nature de l'alcool du mélange considéré et augmente selon la séquence méthanol A possible answer to the problem of destabilization by the segregation of premium-fuel/alcohol blends lies in decreasing their water content by physical adsorption. The strong affinity of water for ion-exchange resins of the polystyrene sulfonate type suggests their use for this specific application. The main advantage of this newadsorbent material is that it can be regenerated with low-level heat (100-120°C. We thus investigated the behavior of this adsorbent from the standpoint of its adsorption capacity and adsorption kinetics. Its performances were compared to those of more conventional adsorbents, such as silicagel, alumina and a 3Å molecular sieve. The ionic forms of the resin used are in the form of K+, Na+ and Mg2+. From the standpoint of total adsorption capacity

  13. Graphene nanosheets as novel adsorbents in adsorption, preconcentration and removal of gases, organic compounds and metal ions

    International Nuclear Information System (INIS)

    Yu, Jin-Gang; Yu, Lin-Yan; Yang, Hua; Liu, Qi; Chen, Xiao-Hong; Jiang, Xin-Yu; Chen, Xiao-Qing; Jiao, Fei-Peng

    2015-01-01

    Due to their high adsorption capacities, carbon-based nanomaterials such as carbon nanotubes, activated carbons, fullerene and graphene are widely used as the currently most promising functional materials. Since its discovery in 2004, graphene has exhibited great potential in many technological fields, such as energy storage materials, supercapacitors, resonators, quantum dots, solar cells, electronics, and sensors. The large theoretical specific surface area of graphene nanosheets (2630 m 2 ·g −1 ) makes them excellent candidates for adsorption technologies. Further, graphene nanosheets could be used as substrates for decorating the surfaces of nanoparticles, and the corresponding nanocomposites could be applied as novel adsorbents for the removal of low concentrated contaminants from aqueous solutions. Therefore, graphene nanosheets will challenge the current existing adsorbents, including other types of carbon-based nanomaterials. - Highlights: • The recent progress of application of graphene in adsorption was presented. • The design and practical application of graphene based composites was discussed. • The future trends and prospects of graphene were analyzed and proposed

  14. Graphene nanosheets as novel adsorbents in adsorption, preconcentration and removal of gases, organic compounds and metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Jin-Gang, E-mail: yujg@csu.edu.cn [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan 410082 (China); Yu, Lin-Yan; Yang, Hua; Liu, Qi [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); Chen, Xiao-Hong [Collaborative Innovation Center of Resource-conserving and Environment-friendly Society and Ecological Civilization, Changsha, Hunan 410083 (China); Jiang, Xin-Yu [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); Chen, Xiao-Qing, E-mail: xqchen@csu.edu.cn [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); Jiao, Fei-Peng, E-mail: jiaofp@163.com [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China)

    2015-01-01

    Due to their high adsorption capacities, carbon-based nanomaterials such as carbon nanotubes, activated carbons, fullerene and graphene are widely used as the currently most promising functional materials. Since its discovery in 2004, graphene has exhibited great potential in many technological fields, such as energy storage materials, supercapacitors, resonators, quantum dots, solar cells, electronics, and sensors. The large theoretical specific surface area of graphene nanosheets (2630 m{sup 2}·g{sup −1}) makes them excellent candidates for adsorption technologies. Further, graphene nanosheets could be used as substrates for decorating the surfaces of nanoparticles, and the corresponding nanocomposites could be applied as novel adsorbents for the removal of low concentrated contaminants from aqueous solutions. Therefore, graphene nanosheets will challenge the current existing adsorbents, including other types of carbon-based nanomaterials. - Highlights: • The recent progress of application of graphene in adsorption was presented. • The design and practical application of graphene based composites was discussed. • The future trends and prospects of graphene were analyzed and proposed.

  15. Batch adsorptive removal of Fe(III), Cu(II) and Zn(II) ions in aqueous and aqueous organic–HCl media by Dowex HYRW2-Na Polisher resin as adsorbents

    OpenAIRE

    Aboul-Magd, Abdul-Aleem Soliman; Al-Husain, Salwa Al-Rashed; Al-Zahrani, Salma Ahmed

    2016-01-01

    Of the metal ions in tap, Nile, waste and sea water samples and some ores were carried out. Removal of heavy metal ions such as Fe(III), Cd(II), Zn(II), Cu(II), Mn(II), Mg(II), and Pb(II) from water and wastewater is obligatory in order to avoid water pollution. Batch shaking adsorption experiments to evaluate the performance of nitric and hydrochloric acid solutions in the removal of metal ions by cation exchange resin at the same conditions for both, such as the effect of initial metal ion ...

  16. Preparation and use of polymeric materials containing hydrophobic anions and plasticizers for separation of cesium and strontium

    International Nuclear Information System (INIS)

    Abney, K.D.; Kinkead, S.A.; Mason, C.F.V.; Rais, J.

    1997-01-01

    Preparation and use is described for polymeric materials containing hydrophobic anions and plasticizers for extraction of cesium and strontium. The use of polymeric materials containing plasticizers which are solvents for hydrophobic anions such as derivatives of cobalt dicarbollide or tetraphenylborate which are capable of extracting cesium and strontium ions from aqueous solutions in contact with the polymeric materials, is described. The polymeric material may also include a synergistic agent for a given ion like polyethylene glycol or a crown ether, for removal of radioactive isotopes of cesium and strontium from solutions of diverse composition and, in particular, for solutions containing large excess of sodium nitrate

  17. Progress and prospect of adsorptive removal of heavy metal ions from aqueous solution using metal-organic frameworks: A review of studies from the last decade.

    Science.gov (United States)

    Wen, Jia; Fang, Ying; Zeng, Guangming

    2018-06-01

    The efficient removal of heavy metals (HMs) from the environment has become an important issue from both biological and environmental perspectives. Recently, porous metal-organic frameworks (MOFs), combining central metals and organic ligands, have been proposed as promising materials in the capture of various toxic substances, including HMs, due to their unique characteristics. Here we review recent progress in the field of water remediation from the perspective of primary HMs (including divalent metals and variable-valent metals) in water pollution and the corresponding MOFs (including virgin and modified MOFs, magnetic MOFs composites and so on) that can remove these metals from water. The reported values of various MOFs for adsorption of heavy metal ions were 8.40-313 mg Pb(II) g -1 , 0.65-2173 mg Hg(II) g -1 , 3.63-145 mg Cd(II) g -1 , 14.0-127 mg Cr(III) g -1 , 15.4-145 mg Cr(VI) g -1 , 49.5-123 mg As(III) g -1 , and 12.3-303 mg As(V) g -1 . The main adsorption mechanisms associated with these processes are chemical (including coordination interaction, chemical bonding and acid-base interactions) and physical (including electrostatic interaction, diffusion and van der Waals force) adsorption, which were discussed in detailed. Further efforts should be made towards expanding the repertoire of MOFs that effectively remove multiple targeted HMs, as well as exploring possible applications of MOFs in the removal of HMs from non-aqueous environments. Copyright © 2018 Elsevier Ltd. All rights reserved.

  18. Influence of differences in resin-matrix structure on ion-exchange adsorption of trace amounts of Ag(I), Co(II) and Cr(III)

    International Nuclear Information System (INIS)

    Matsuzuru, Hideo; Wadachi, Yoshiki

    1975-01-01

    The influence of differences in resin-matrix structure on the ion-exchange adsorption of trace amounts of Ag(I), Co(II) and Cr(III) was studied by using both macroreticular and gel-type resins. The results indicate that the rate-determining step of the exchange mechanism of these ions is film diffusion under conditions of finite volume and at an ionic strengh of 1x10 -4 . The diffusion coefficient decreases w