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Sample records for exchangeable cations sugarcane

  1. Advancements in Anion Exchange Membrane Cations

    Energy Technology Data Exchange (ETDEWEB)

    Sturgeon, Matthew R. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Long, Hai [National Renewable Energy Lab. (NREL), Golden, CO (United States); Park, Andrew M. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Pivovar, Bryan S. [National Renewable Energy Lab. (NREL), Golden, CO (United States)

    2015-10-15

    Anion-exchange membrane fuel cells (AME-FCs) are of increasingly popular interest as they enable the use of non-Pt fuel cell catalysts, the primary cost limitation of proton exchange membrane fuel cells. Benzyltrimethyl ammonium (BTMA) is the standard cation that has historically been utilized as the hydroxide conductor in AEMs. Herein we approach AEMs from two directions. First and foremost we study the stability of several different cations in a hydroxide solution at elevated temperatures. We specifically targeted BTMA and methoxy and nitro substituted BTMA. We've also studied the effects of adding an akyl spacer units between the ammonium cation and the phenyl group. In the second approach we use computational studies to predict stable ammonium cations, which are then synthesized and tested for stability. Our unique method to study cation stability in caustic conditions at elevated temperatures utilizes Teflon Parr reactors suitable for use under various temperatures and cation concentrations. NMR analysis was used to determine remaining cation concentrations at specific time points with GCMS analysis verifying product distribution. We then compare the experimental results with calculated modeling stabilities. Our studies show that the electron donating methoxy groups slightly increase stability (compared to that of BTMA), while the electron withdrawing nitro groups greatly decrease stability in base. These results give insight into possible linking strategies to be employed when tethering a BTMA like ammonium cation to a polymeric backbone; thus synthesizing an anion exchange membrane.

  2. Forging Colloidal Nanostructures via Cation Exchange Reactions

    Science.gov (United States)

    2016-01-01

    Among the various postsynthesis treatments of colloidal nanocrystals that have been developed to date, transformations by cation exchange have recently emerged as an extremely versatile tool that has given access to a wide variety of materials and nanostructures. One notable example in this direction is represented by partial cation exchange, by which preformed nanocrystals can be either transformed to alloy nanocrystals or to various types of nanoheterostructures possessing core/shell, segmented, or striped architectures. In this review, we provide an up to date overview of the complex colloidal nanostructures that could be prepared so far by cation exchange. At the same time, the review gives an account of the fundamental thermodynamic and kinetic parameters governing these types of reactions, as they are currently understood, and outlines the main open issues and possible future developments in the field. PMID:26891471

  3. Transport of divalent cations: cation exchange capacity of intact xylem vessels.

    Science.gov (United States)

    Van de Geijn, S C; Petit, C M

    1979-12-01

    The cation exchange capacity of the intact xylem vessels in cut shoots of papyrus (Cyperus papyrus spec.) has been determined. The cation exchange capacity is independent of the cation concentration in the transpiration stream, and is equal for Ca and Co. The high value of the cation exchange capacity (0.6 to 1 x 10(-7) equivalents per square centimeter vessel wall surface) leads to the hypothesis that the porous structure of the vessel wall, and not only the inner vessel wall surface, acts as a cation exchanger.Differences between anion ([(32)P]phosphate, [(45)Ca]EDTA(2-), [(115)Cd(m)]-EDTA(2-)), and cation ([(45)Ca](2+), [(115)Cd(m)](2+)) movement are explained in terms of transport with the transpiration flux or by exchange reactions. The competition between exchange sites and natural or synthetic ligands for the divalent cations is discussed.

  4. Cation exchange properties of zeolites in hyper alkaline aqueous media.

    Science.gov (United States)

    Van Tendeloo, Leen; de Blochouse, Benny; Dom, Dirk; Vancluysen, Jacqueline; Snellings, Ruben; Martens, Johan A; Kirschhock, Christine E A; Maes, André; Breynaert, Eric

    2015-02-03

    Construction of multibarrier concrete based waste disposal sites and management of alkaline mine drainage water requires cation exchangers combining excellent sorption properties with a high stability and predictable performance in hyper alkaline media. Though highly selective organic cation exchange resins have been developed for most pollutants, they can serve as a growth medium for bacterial proliferation, impairing their long-term stability and introducing unpredictable parameters into the evolution of the system. Zeolites represent a family of inorganic cation exchangers, which naturally occur in hyper alkaline conditions and cannot serve as an electron donor or carbon source for microbial proliferation. Despite their successful application as industrial cation exchangers under near neutral conditions, their performance in hyper alkaline, saline water remains highly undocumented. Using Cs(+) as a benchmark element, this study aims to assess the long-term cation exchange performance of zeolites in concrete derived aqueous solutions. Comparison of their exchange properties in alkaline media with data obtained in near neutral solutions demonstrated that the cation exchange selectivity remains unaffected by the increased hydroxyl concentration; the cation exchange capacity did however show an unexpected increase in hyper alkaline media.

  5. Fabrication of Cationic Exchange Polystyrene Nanofibers for Drug ...

    African Journals Online (AJOL)

    Purpose: To prepare polystyrene nanofiber ion exchangers (PSNIE) with surface cation exchange functionality using a new method based on electrospinning and also to optimize crosslinking and sulfonation reactions to obtain PSNIE with maximum ion exchange capacity (IEC). Method: The nanofibers were prepared from ...

  6. A Scale Model of Cation Exchange for Classroom Demonstration.

    Science.gov (United States)

    Guertal, E. A.; Hattey, J. A.

    1996-01-01

    Describes a project that developed a scale model of cation exchange that can be used for a classroom demonstration. The model uses kaolinite clay, nails, plywood, and foam balls to enable students to gain a better understanding of the exchange complex of soil clays. (DDR)

  7. High-speed simultaneous ion-exclusion/cation-exchange chromatography of anions and cations on a weakly acidic cation-exchange resin column.

    Science.gov (United States)

    Mori, Masanobu; Tanaka, Kazuhiko; Helaleh, Murad I H; Xu, Qun; Ikedo, Mikaru; Ogura, Yutaka; Sato, Shinji; Hu, Wenzhi; Hasebe, Kiyoshi; Haddad, Paul R

    2003-05-16

    The simultaneous ion-exclusion/cation-exchange separation column packed with a polymethacrylate-based weakly acidic cation-exchange resin of 3 microm particle size was used to achieve the simultaneous high-speed separation of anions and cations (Cl(-), NO3(-), SO4(2-), Na(+), K(+), NH4(+), Ca(2+) and Mg(2+)) commonly found in environmental samples. The high-speed simultaneous separation is based on a combination of the ion-exclusion mechanism for the anions and the cation-exchange mechanism for cations. The complete separation of the anions and cations was achieved in 5 min by elution with 15 mM tartaric acid-2.5 mM 18-crown-6 at a flow-rate of 1.5 ml/min. Detection limits at S/N=3 ranged from 0.36 to 0.68 microM for anions and 0.63-0.99 microM for cations. This method has been applied to the simultaneous determination of anions and cations in several environmental waters with satisfactory results.

  8. Esterification of maleic acid and butanol using cationic exchange ...

    Indian Academy of Sciences (India)

    Dibutyl maleate is a perfumery ester used as an intermediate in the production of paints, adhesives, and copolymers. Esterification of maleic acid and butanol was studied in presence of acidic cation exchange resin as a catalyst. The objective of this work was to test the suitability and efficacy of heterogeneous catalystssuch ...

  9. Esterification of maleic acid and butanol using cationic exchange ...

    Indian Academy of Sciences (India)

    AARTI MULAY

    2017-11-15

    Nov 15, 2017 ... Abstract. Dibutyl maleate is a perfumery ester used as an intermediate in the production of paints, adhesives, and copolymers. Esterification of maleic acid and butanol was studied in presence of acidic cation exchange resin as a catalyst. The objective of this work was to test the suitability and efficacy of ...

  10. Selective oxidation of propane over cation exchanged zeolites

    NARCIS (Netherlands)

    Xu, J.

    2005-01-01

    This thesis focuses on investigation of the fundamental knowledge on a new method for selective oxidation of propane with O2 at low temperature (< 100°C). The relation between propane catalytic selective oxidation and physicochemical properties of cation exchanged Y zeolite has been studied. An

  11. Alloyed copper chalcogenide nanoplatelets via partial cation exchange reactions.

    Science.gov (United States)

    Lesnyak, Vladimir; George, Chandramohan; Genovese, Alessandro; Prato, Mirko; Casu, Alberto; Ayyappan, S; Scarpellini, Alice; Manna, Liberato

    2014-08-26

    We report the synthesis of alloyed quaternary and quinary nanocrystals based on copper chalcogenides, namely, copper zinc selenide-sulfide (CZSeS), copper tin selenide-sulfide (CTSeS), and copper zinc tin selenide-sulfide (CZTSeS) nanoplatelets (NPLs) (∼20 nm wide) with tunable chemical composition. Our synthesis scheme consisted of two facile steps: i.e., the preparation of copper selenide-sulfide (Cu2-xSeyS1-y) platelet shaped nanocrystals via the colloidal route, followed by an in situ cation exchange reaction. During the latter step, the cation exchange proceeded through a partial replacement of copper ions by zinc or/and tin cations, yielding homogeneously alloyed nanocrystals with platelet shape. Overall, the chemical composition of the alloyed nanocrystals can easily be controlled by the amount of precursors that contain cations of interest (e.g., Zn, Sn) to be incorporated/alloyed. We have also optimized the reaction conditions that allow a complete preservation of the size, morphology, and crystal structure as that of the starting Cu2-xSeyS1-y NPLs. The alloyed NPLs were characterized by optical spectroscopy (UV-vis-NIR) and cyclic voltammetry (CV), which demonstrated tunability of their light absorption characteristics as well as their electrochemical band gaps.

  12. Exchangeable cations in some soils of Mt. Stara planina

    Directory of Open Access Journals (Sweden)

    Belanović Snežana

    2005-01-01

    Full Text Available Land use in forest and pasture ecosystems requires the respecting of ecological and economic interactions between the individual components of these ecosystems. The content of nutrition elements in the soil solution depends on soil types, climate conditions and vegetation species, i.e., it is conditioned by their cycling in the ecosystem. This paper studies the cation exchange capacity in pasture and forest soils of Mt. Stara Planina.

  13. Simultaneous separation of inorganic anions and cations by using anion-exchange and cation-exchange columns connected in tandem in ion chromatography.

    Science.gov (United States)

    Karim, Khairil Juhanni Binti Abd; Jin, Ji-Ye; Takeuchi, Toyohide

    2003-05-02

    Inorganic anions and cations in environmental waters were determined by ion chromatography. Stationary and mobile phases were examined for the simultaneous separation of both anions and cations. Cations detection by UV detection requires a mobile phase with a UV absorbing additive, which indirectly visualizes cations as negative peaks. Simultaneous separation of anions and cations were achieved when using an eluent that consists of inorganic acid with weak basic amino acid as additives. It was convenient to separate both anions and cations by coupling anion-exchange and cation-exchange columns in tandem. The order of the separation columns connected affected the elution profiles. When the eluent comprises of multiple anions and a single cation, the anion-exchange column should be connected in the upper stream, whereas when the eluent comprises multiple cations and a single anion, the cation-exchange column should be connected in the upper stream. Use of switching valves also allowed simultaneous separation of anions and cations in a single chromatographic run. In the present work, operating conditions were optimized for the simultaneous separation of anions and cations.

  14. Analysis of Adsorption, Ion Exchange, Thermodynamic Behaviour of Some Organic Cations on Dowex 50WX4-50/H+ Cation Exchanger in Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Ehteram A. Noor

    2011-01-01

    Full Text Available The equilibrium adsorption, ion exchange characteristics of various concentrations of some organic cations from aqueous solutions onto dowex 50WEX/H+ cation exchanger were studied at different temperatures in the range of 30-50 °C. The studied cations showed good adsorptive properties onto dowex 50WX4-5/H+ at different concentrations and temperatures. Main adsorption behaviour was ion exchange between hydrogen ions and the organic cations as indicated from the linear relation between the initial concentration of the organic cations and the released hydrogen ions. It was found that the adsorption affinity of dowex 50WX4-50/H+ towards the studied organic cations depends on the substituent type of the organic cations giving the following increasing order: 1-H < 2-OH < 3-OCH3. Thermodynamic parameters for the adsorption of the studied organic cations were evaluated and discussed. It was found that the adsorption 1-H organic cation was spontaneous, ordered, exothermic and favored with decreasing temperature. On the other hand the adsorption of both 2-OH and 3-OCH3 organic cations was found to be spontaneous and disordered with enthalpy change varies significantly with increasing organic cation concentration, suggesting dipole-dipole adsorption forces as new active sites for adsorption under conditions of relatively high concentrations. Freundlich and Dubinin-Radushkevich adsorption isotherm models reasonably describe the adsorption of the studied organic cations onto dowex 50WX4-50/H+ by segmented straight lines depending on the studied range of concentration, indicating the existence of two different sets of adsorption sites with substantial difference in energy of adsorption. According to Dubinin-Radushkevich adsorption isotherm model, physical-ion exchange mechanism was suggested for the adsorption of 1-H organic cation and both physical and chemical-ion exchange mechanisms were suggested for the adsorption of 2-OH and 3-OCH3 organic cations

  15. Selective organic synthesis over metal cation-exchanged clay catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Tateiwa, J.; Uemura, S. [Kyoto University, Kyoto (Japan)

    1997-09-01

    Results of recent studies conducted by the authors are reviewed on the use, as catalysts, of metal cation-exchanged montmorillonite (M{sup n+}-mont), a modified natural clay with a layer structure, and metal cation-exchanged fluor-tetrasilicic mica (M{sup n+}-TSM), a synthetic clay with a layer structure, for the following organic synthesis: (1) Friedel-Crafts alkylation of phenol with 4-hydroxybutan-2-one to produce 4-(4-hydroxyphenyl)butan-2-one (raspberry ketone), (2) rearrangement of alkyl phenyl ethers to corresponding alkylphenols, (3) aromatic alkylation of phenol with aldehydes and ketones to produce corresponding gem-bis(hydroxyphenyl)alkanes (bisphenols) and alkylphenols, respectively, (4) a facile and an almost quantitative substrate-selective acetalization, (5) alkane oxidation with aqueous tert-butyl hydroperoxide, (6) Prins reaction of styrenes with aldehydes using clay as a Bronsted acid, and (7) inter-and intra-molecular carbonyl-ene reaction using clay as a Lewis acid in condition similar to that of Prins reaction. In almost all cases, the clay catalysts could be regenerated and reused several times, after filtration, washing and drying. 42 refs., 20 figs., 3 tabs.

  16. Computer simulation of methanol exchange dynamics around cations and anions

    Energy Technology Data Exchange (ETDEWEB)

    Roy, Santanu; Dang, Liem X.

    2016-03-03

    In this paper, we present the first computer simulation of methanol exchange dynamics between the first and second solvation shells around different cations and anions. After water, methanol is the most frequently used solvent for ions. Methanol has different structural and dynamical properties than water, so its ion solvation process is different. To this end, we performed molecular dynamics simulations using polarizable potential models to describe methanol-methanol and ion-methanol interactions. In particular, we computed methanol exchange rates by employing the transition state theory, the Impey-Madden-McDonald method, the reactive flux approach, and the Grote-Hynes theory. We observed that methanol exchange occurs at a nanosecond time scale for Na+ and at a picosecond time scale for other ions. We also observed a trend in which, for like charges, the exchange rate is slower for smaller ions because they are more strongly bound to methanol. This work was supported by the US Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences. The calculations were carried out using computer resources provided by the Office of Basic Energy Sciences.

  17. [Study on the defluoridation of drinking water with model-La cation exchange resin].

    Science.gov (United States)

    Huang, Mingyuan; Lü, Changyin

    2003-11-01

    Model-La cation exchange resin was transformed from strong acid cation exchange resin, which was used for the defluoridation of drinking water. The 001 x 7 strong acid cation exchange resin was transformed into model-La cation exchange by soaking in the La(NO3)3 solution. The F- in the water was removed by model-La cation exchange resin under the optimum condition because it was combined into fluoride with the La3+ in the model-La cation exchange resin. The used resin was regenerated with the La(NO3)3 solution and was used to defluoridate many times. The optimum conditions of transform and defluoridation and regeneration were d(rasin) = 0.315-0.600 mm, V(rasin):V(regeneration) = 1:6, t(transform) = 48 h, T = 298.16 K(25 degrees C). The defluoridation capacity was 5.60 mg/g in column test, and 4.08 mg/g in batch test. The model-La cation exchange resin could be used for defluoridation for 8 times. The results suggest that the model-La cation exchange resin is a novel material of defluoridation. This method is easy to master and the pH value of the solution doesn't need to be regenerated that the cost of defluoridation can be reduced significantly and it can be used for a long time.

  18. Exciton dynamics in cation-exchanged CdSe/PbSe nanorods: The role of defects

    Science.gov (United States)

    Lee, Sooho; Wang, Yimeng; Liu, Yawei; Lee, Dongkyu; Lee, Kangha; Lee, Doh C.; Lian, Tianquan

    2017-09-01

    Cation exchange occurs via defect initiated solid-state diffusion, a process that can lead to defect formations. The effect of such inherent defect formation on carrier dynamics of cation-exchanged heterostructures remains poorly understood. Herein, we report exciton dynamics in type II CdSe/PbSe heterostructure nanorods formed via cation exchange. The majority of electrons in CdSe domains decays in 5 ps due to ultrafast carrier trapping. The defect generated by cation exchange can be healed by annealing the as-synthesized CdSe/PbSe heterostructure nanorods. This study suggests a strategy for improving properties of heteronanostructures prepared by cation exchange for applications in photovoltaics and photocatalysis.

  19. Cation Exchange Capacity of Biochar: An urgent method modification

    Science.gov (United States)

    Munera, Jose; Martinsen, Vegard; Mulder, Jan; Tau Strand, Line; Cornelissen, Gerard

    2017-04-01

    A better understanding of the cation exchange capacity (CEC) values of biochar and its acid neutralizing capacity (ANC) is crucial when tailoring a single biochar for a particular soil and crop. Literature values for the CEC of biochar are surprisingly variable, commonly ranging from 5 to 50 cmol+/Kg even as high as 69 to 204 cmol+/Kg and often poorly reproducible, suggesting methodological problems. Ashes and very fine pores in biochar may complicate the analysis and thus compromise the results. Here, we modify and critically assess different steps in a common method for CEC determination in biochar and investigate how the measured CEC may be affected by slow cation diffusion from micro-pores. We modified the existing ammonium acetate (NH4-OAc) method (buffered at pH 7), based on displaced ammonium (NH4+) in potassium chloride (KCl) extracts after removing excess NH4-OAc with alcohol in batch mode. We used pigeon pea biochar (produced at 350 ˚C; particle size 0.5mm to 2mm) to develop the method and we tested its reproducibility in biochars with different ANC. The biochar sample (1.00g) was pH-adjusted to 7 after 2 days of equilibration, using hydrochloric acid (HCl), and washed with water until the conductivity of the water was replacing cations (NH4+ and K+) in micro-pores, we equilibrated the biochar with NH4-OAc for 1 and 7 days, and after washing with alcohol, for 1, 3 and 7 days with KCl. The effects of the washing volume of alcohol (15, 30 and 45 ml) and of the biochar to NH4OAc solution ratio (1:15, 1:30 and 1:45) were also tested. The CEC values were corrected for dry matter content and mass losses during the process. Results indicate that the measured CEC values of the modified method were highly reproducible and that 1 day shaking with NH4OAc and KCl is enough to saturate the exchange sites with NH4+ and subsequently with K+. The biochar to NH4OAc solution ratio did not affect the measured CEC. Three washings with at least 15 ml alcohol are required to

  20. Cation immobilization in pyrolyzed simulated spent ion exchange resins

    Energy Technology Data Exchange (ETDEWEB)

    Luca, Vittorio, E-mail: vluca@cnea.gov.ar [Programa Nacional de Gestion de Residuos Radiactivos, Centro Atomico Constituyentes, Comision Nacional de Energia Atomica, Av. General, Paz 1499, 1650 San Martin, Provincia de Buenos Aires (Argentina); Bianchi, Hugo L. [Gerencia de Quimica, Centro Atomico Constituyentes, Comision Nacional de Energia Atomica, Av. General, Paz 1499, 1650 San Martin, Provincia de Buenos Aires (Argentina); ECyT, Universidad Nacional de General San Martin, Campus Miguelete, Ed. Tornavias, Martin de Irigoyen 3100, 1650 San Martin (Argentina); Conicet, Av. Rivadavia 1917, 1033 Buenos Aires (Argentina); Manzini, Alberto C. [Programa Nacional de Gestion de Residuos Radiactivos, Comision Nacional de Energia Atomica, Av. Del Libertador 8250, CP 1429, Ciudad Autonoma de Buenos Aires (Argentina)

    2012-05-15

    Significant quantities of spent ion exchange resins that are contaminated by an assortment of radioactive elements are produced by the nuclear industry each year. The baseline technology for the conditioning of these spent resins is encapsulation in ordinary Portland cement which has various shortcomings none the least of which is the relatively low loading of resin in the cement and the poor immobilization of highly mobile elements such as cesium. The present study was conducted with cationic resin samples (Lewatit S100) loaded with Cs{sup +}, Sr{sup 2+}, Co{sup 2+}, Ni{sup 2+} in roughly equimolar proportions at levels at or below 30% of the total cation exchange capacity. Low temperature thermal treatment of the resins was conducted in inert (Ar), or reducing (CH{sub 4}) gas atmospheres, or supercritical ethanol to convert the hydrated polymeric resin beads into carbonaceous materials that contained no water. This pyrolytic treatment resulted in at least a 50% volume reduction to give mechanically robust spherical materials. Scanning electron microscope investigations of cross-sections of the beads combined with energy dispersive analysis showed that initially all elements were uniformly distributed through the resin matrix but that at higher temperatures the distribution of Cs became inhomogeneous. Although Cs was found in the entire cross-section, a significant proportion of the Cs occurred within internal rings while a proportion migrated toward the outer surfaces to form a crustal deposit. Leaching experiments conducted in water at 25 Degree-Sign C showed that the divalent contaminant elements were very difficult to leach from the beads heated in inert atmospheres in the range 200-600 Degree-Sign C. Cumulative fractional loses of the order of 0.001 were observed for these divalent elements for temperatures below 500 Degree-Sign C. Regardless of the processing temperature, the cumulative fractional loss of Cs in water at 25 Degree-Sign C reached a plateau or

  1. Exploring backbone-cation alkyl spacers for multi-cation side chain anion exchange membranes

    Science.gov (United States)

    Zhu, Liang; Yu, Xuedi; Hickner, Michael A.

    2018-01-01

    In order to systematically study how the arrangement of cations on the side chain and length of alkyl spacers between cations impact the performance of multi-cation AEMs for alkaline fuel cells, a series of polyphenylene oxide (PPO)-based AEMs with different cationic side chains were synthesized. This work resulted in samples with two or three cations in a side chain pendant to the PPO backbone. More importantly, the length of the spacer between cations varied from 3 methylene (-CH2-) (C3) groups to 8 methylene (C8) groups. The highest conductivity, up to 99 mS/cm in liquid water at room temperature, was observed for the triple-cation side chain AEM with pentyl (C5) or hexyl (C6) spacers. The multi-cation AEMs were found to have decreased water uptake and ionic conductivity when the spacer chains between cations were lengthened from pentyl (C5) or hexyl (C6) to octyl (C8) linking groups. The triple-cation membranes with pentyl (C5) or hexyl (C6) groups between cations showed greatest stability after immersion in 1 M NaOH at 80 °C for 500 h.

  2. Full automation of {sup 68}Ga labelling of DOTA-peptides including cation exchange prepurification

    Energy Technology Data Exchange (ETDEWEB)

    Ocak, M. [Clinical Department of Nuclear Medicine, Medical University Innsbruck, Anichstrasse 35, A-6020 Innsbruck (Austria); Department of Pharmaceutical Technology, Pharmacy Faculty, Istanbul University, Istanbul (Turkey); Antretter, M. [Clinical Department of Nuclear Medicine, Medical University Innsbruck, Anichstrasse 35, A-6020 Innsbruck (Austria); Knopp, R.; Kunkel, F. [Eckert and Ziegler Eurotope GmbH, Berlin (Germany); Petrik, M. [Clinical Department of Nuclear Medicine, Medical University Innsbruck, Anichstrasse 35, A-6020 Innsbruck (Austria); Bergisadi, N. [Department of Pharmaceutical Technology, Pharmacy Faculty, Istanbul University, Istanbul (Turkey); Decristoforo, C. [Clinical Department of Nuclear Medicine, Medical University Innsbruck, Anichstrasse 35, A-6020 Innsbruck (Austria)], E-mail: Clemens.Decristoforo@uki.at

    2010-02-15

    Here we describe a fully automated approach for the synthesis of {sup 68}Ga-labelled DOTA-peptides based on pre-concentration and purification of the generator eluate by using a cation exchange-cartridge and its comparison with fully automated direct labelling applying fractionated elution. Pre-concentration of the eluate on a cation exchange cartridge both using a resin-based and a disposable cation-exchange cartridge efficiently removed {sup 68}Ge as well as major metal contaminations with Fe and Zn. This resulted in a high labelling efficiency of DOTA-peptides at high specific activity (SA) with short synthesis times.

  3. Preparation of Cd/Pb Chalcogenide Heterostructured Janus Particles via Controllable Cation Exchange

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Jianbing; Chernomordik, Boris D.; Crisp, Ryan W.; Kroupa, Daniel M.; Luther, Joseph M.; Miller, Elisa M.; Gao, Jianbo; Beard, Matthew C.

    2015-07-28

    We developed a strategy for producing quasi-spherical nanocrystals of anisotropic heterostructures of Cd/Pb chalcogenides. The nanostructures are fabricated via a controlled cation exchange reaction where the Cd2+ cation is exchanged for the Pb2+ cation. The cation exchange reaction is thermally activated and can be controlled by adjusting the reaction temperature or time. We characterized the particles using TEM, XPS, PL, and absorption spectroscopy. With complete exchange, high quality Pb-chalcogenide quantum dots are produced. In addition to Cd2+, we also find suitable conditions for the exchange of Zn2+ cations for Pb2+ cations. The cation exchange is anisotropic starting at one edge of the nanocrystals and proceeds along the <111> direction producing a sharp interface at a (111) crystallographic plane. Instead of spherical core/shell structures, we produced and studied quasi-spherical CdS/PbS and CdSe/PbSe Janus-type heterostructures. Nontrivial PL behavior was observed from the CdS(e)/PbS(e) heterostructures as the Pb:Cd ratio is increased.

  4. Atomistic understanding of cation exchange in PbS nanocrystals using simulations with pseudoligands

    NARCIS (Netherlands)

    Fan, Z.; Lin, L.; Buijs, W.; Vlugt, T.J.H.; van Huis, MA

    2016-01-01

    Cation exchange is a powerful tool for the synthesis of nanostructures such as core–shell nanocrystals, however, the underlying mechanism is poorly understood. Interactions of cations with ligands and solvent molecules are systematically ignored in simulations. Here, we introduce the concept of

  5. Cation exchange assisted binding-elution strategy for enzymatic synthesis of human milk oligosaccharides (HMOs).

    Science.gov (United States)

    Zhu, Hailiang; Wu, Zhigang; Gadi, Madhusudhan Reddy; Wang, Shuaishuai; Guo, Yuxi; Edmunds, Garrett; Guan, Wanyi; Fang, Junqiang

    2017-09-15

    A cation exchange assisted binding-elution (BE) strategy for enzymatic synthesis of human milk oligosaccharides (HMOs) was developed. An amino linker was used to provide the cation ion under acidic condition which can be readily bound to cation exchange resin and then eluted off by saturated ammonium bicarbonate. Ammonium bicarbonate in the collections was easily removed by vacuum evaporation. This strategy circumvented the incompatible issue between glycosyltransferases and solid support or large polymers, and no purification was needed for intermediate products. With current approach, polyLacNAc backbones of HMOs and fucosylated HMOs were synthesized smoothly. Copyright © 2017 Elsevier Ltd. All rights reserved.

  6. Monovalent and bivalent cations exchange isotherms for faujasites X and Y.

    Science.gov (United States)

    Khabzina, Y; Laroche, C; Pagis, C; Farrusseng, D

    2017-07-05

    This study addresses the modeling of exchange isotherms for faujasite-type zeolites X and Y with K(+), Cs(+), Ca(2+) and Ba(2+) cations based on a large experimental dataset obtained under operating conditions of 0.5 N total normality and an exchange temperature of 80 °C. The isotherm models are based on the mass action law. Ideal solution phase is assumed. Heterogeneity of the solid phase is taken into account by using Barrer and Klinowski's approach to multi-site exchange. Three types of exchange sites are identified on these zeolites. To each exchange site j corresponds a fitted selectivity coefficient Kj. These parameters, estimated by least square method, evaluate the affinity of the studied cations for the identified exchange site. Globally, these fitted coefficients show that the cations considered present better affinity than Na(+), especially for type III sites in faujasite X and type II sites in faujasite Y. For bivalent cations, an exchange with Ba(2+) is always more favorable than with Ca(2+). On faujasite X, type II sites are more strongly preferred by monovalent cations (with the exception of Cs(+)) than by bivalent ones. The opposite trend is observed on faujasite Y, even for Cs(+). These conclusions have been confirmed and are supported by bibliographic data.

  7. Ion Exchange Chromatography-Indirect Ultraviolet Detection for Separation and Determination of Morpholinium Ionic Liquid Cations.

    Science.gov (United States)

    Zhang, Yu; Ma, Yajie; Yu, Hong; Liu, Yongqiang

    2017-01-01

    A rapid analytical method of ion exchange chromatography with indirect ultraviolet detection was developed to determine morpholinium ionic liquid (IL) cations, i.e. N-methyl-N-ethyl morpholinium cation ([MEMo]+) and N-methyl-N-propyl morpholinium cation ([MPMo]+). Chromatographic separation of morpholinium cations was performed on a sulfonic acid base cation exchange column using imidazolium ionic liquid-organic solvent as mobile phase. The effects of chromatographic columns, ultraviolet absorption reagents, imidazolium ILs, detection wavelength, organic solvents, pH values of the mobile phase and column temperature on the retention of morpholinium cations were investigated. The retention times of the cations were clearly decreased by the increase of the alkyl substituent length on imidazolium cation or with the increase of the concentration of 1-ethyl-3-methyl imidazolium tetrafluoroborate. The molecular structure of the anion of imidazolium IL which has UV absorption has influence on determination of the analytes. Under the optimal conditions, the detection limits (signal-to-noise ratio, S/N = 3) were 0.29 and 0.44 mg L-1 The method has been successfully applied to the determination of two ILs synthesized by chemistry laboratory. The method uses the liquid chromatography system, which is widely available in general laboratories, and the simple composition of mobile phase, thus make the quantitative analysis of no UV absorption morpholinium cations possible. © The Author 2016. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

  8. Soil exchangeable cations, sugarcane production and nutrient uptake after wastewater irrigation Cátions trocáveis do solo, produção e extração de nutrientes pela cana-de-açúcar após irrigação com água residuária

    Directory of Open Access Journals (Sweden)

    Rafael Marques Pereira Leal

    2009-04-01

    Full Text Available Wastewater irrigation may benefit agricultural crops with water and essential nutrients (mainly nitrogen, also affecting soil chemistry. The effects of effluent irrigation on yield, stalk nutrient uptake and on soil chemistry over 16 months were studied in a sugarcane (Saccharum spp. crop growing on an Oxisol in Lins, State of São Paulo, Brazil. Irrigated plots received 50% of the recommended mineral-N fertilization and 100, 125, 150 or 200% of the crop water demand, while control plots received neither additional N nor water. The high sodium content of effluent resulted in Na inputs as high as 6.2 t ha-1, along with 1497 kg N ha-1 and 628 kg K ha-1. All the effluent plots except the T125 treatment had higher yields (up to 247 t ha-1 than the control (153 t ha-1. Significant amounts of N (up to 597 kg ha-1 and K (up to 546 kg ha-1 were exported by the plant harvest. Additions of nutrients and Na via irrigation were not compensated by stalk growth, causing a low recovery of N, P, Ca, Na, and showing the relative over N fertilization of the crop. Changes in soil pH, H + Al, Ca, Mg and K were small, whereas Na accumulated over time with irrigation. The treated wastewater irrigation is expected to gain increased importance, requiring careful considerations involving the adequate balance between nutritional inputs via irrigation and optimal plant productivity requirements.A irrigação com águas residuárias pode beneficiar as culturas agrícolas com água e nutrientes essenciais (especialmente nitrogênio, afetando também a química do solo. Os efeitos da irrigação por 16 meses com efluente de esgoto na produtividade, extração de nutrientes pelo colmo, e nos atributos químicos do solo, foram estudados em um Latossolo cultivado com cana-de-açúcar (Saccharum spp., situado em Lins, São Paulo. As parcelas irrigadas receberam 50% do N mineral recomendado e 100, 125, 150 ou 200% da demanda hídrica da cultura, enquanto o controle não recebeu N

  9. Ion transport resistance in Microbial Electrolysis Cells with anion and cation exchange membranes

    NARCIS (Netherlands)

    Sleutels, T.H.J.A.; Hamelers, H.V.M.; Rozendal, R.A.; Buisman, C.J.N.

    2009-01-01

    Previous studies have shown that Microbial Electrolysis Cells (MECs) perform better when an anion exchange membrane (AEM) than when a cation exchange membrane (CEM) separates the electrode chambers. Here, we have further studied this phenomenon by comparing two analysis methods for

  10. Performance analysis of cation and anion exchangers in water treatment plant: an industrial case study

    National Research Council Canada - National Science Library

    Ramzan, Naveed; Feroze, Nadeem; Kazmi, Mohsin; Ashraf, Muhammad Arsalan; Hasan, Sajid

    2012-01-01

    ...% for cation, primary and secondary anion exchangers respectively. The operating time of the water treatment train was significantly increased by achieving adequate capacity utilization of secondary anion exchanger. The low capacity utilization of secondary anion resin due to early silica slippage, has been discussed in the paper.

  11. Characterization and cation exchange capacity of seeds of Ziziphus spina-christi

    Directory of Open Access Journals (Sweden)

    Shadia M. Sirry

    2014-09-01

    Full Text Available There are several naturally existing materials have ability to utilize as ion-exchangers. Most of these materials are by-products of waste material from industry or agriculture. Agriculture ion exchange materials include: lemon orange, grapefruit, apple, peas, broad bean, and meddler peels, kernel core, and grape skins. This research deals with the utilization of agriculture waste biomass of napak seed as natural cation exchanger for removal of cationic pollutant from aqueous solution. Methylene blue dye method was used to determine the cation exchange capacity of the stone and it was characterized by IR and TGA methods. The results showed that the highest dye sorption capacity was found at pH 7, the equilibrium time was 60 min, sorbent dose = 0.1g, particle size 177μm and methylene blue concentration range 10-50 ppm. The equilibrium sorption data were analyzed by Langmuir and Freundlich isotherm models.

  12. Measurement of cation exchange capacity (CEC) on natural zeolite by percolation method

    Science.gov (United States)

    Wiyantoko, Bayu; Rahmah, Nafisa

    2017-12-01

    The cation exchange capacity (CEC)measurement has been carried out in natural zeolite by percolation method. The natural zeolite samples used for cation exchange capacity measurement were activated beforehand with physical activation and chemical activation. The physically activated zeolite was done by calcination process at 600 °C for 4 hours. The natural zeolite was activated chemically by using sodium hydroxide by refluxing process at 60-80 °C for 3 hours. In summary, cation exchange capacity (CEC) determination was performed by percolation, distillation and titration processes. Based on the measurement that has been done, the exchange rate results from physical activated and chemical activated of natural zeolite were 181.90cmol (+)/kg and 901.49cmol (+)/kg respectively.

  13. Cation exchange applications of synthetic tobermorite for the ...

    Indian Academy of Sciences (India)

    Immobilization and solidification of hazardous cations like Cs137 and Sr90 are required while handling the radioactive waste of nuclear power plants. Efforts are on to find a fail proof method of safe disposal of nuclear wastes. In this context, various materials like borosilicate glass, zeolites, cements and synthetic rocks have ...

  14. Tree species affect cation exchange capacity (CEC) and cation binding properties of organic matter in acid forest soils.

    Science.gov (United States)

    Gruba, Piotr; Mulder, Jan

    2015-04-01

    Soil organic matter (SOM) in forest soil is of major importance for cation binding and acid buffering, but its characteristics may differ among soils under different tree species. We investigated acidity, cation exchange properties and Al bonding to SOM in stands of Scots pine, pedunculate oak, Norway spruce, European beech and common hornbeam in southern Poland. The content of total carbon (Ct) was by far the major contributor to total cation exchange capacity (CECt) even in loamy soils and a strong relationship between Ct and CECt was found. The slope of the regression of CECt to Ct increased in the order hornbeam≈oakvalue in the acid pH range was smallest for hornbeam and oak, and largest for spruce and pine soils. This was supported by the apparent dissociation constant (pKapp) values of SOM, which were largest in soils under oak. The maximum values of Al saturation were similar between the stands. However, maximum Al bonding to SOM occurred at higher pH values in soils under pine and spruce than under oak. Therefore, at any value in the acid pH range, the SOM in pine soil has less Al complexed and more adsorbed H+ than SOM from oak soils. Such differences in Al and H bonding are not only important for pH buffering and metal solubility controls, but also for stabilization of SOM via saturation of functional groups by Al and H. Copyright © 2015 Elsevier B.V. All rights reserved.

  15. Sulfonated hydrocarbon graft architectures for cation exchange membranes

    DEFF Research Database (Denmark)

    Nielsen, Mads Møller; Jankova Atanasova, Katja; Hvilsted, Søren

    2013-01-01

    A synthetic strategy to hydrocarbon graft architectures prepared from a commercial polysulfone and aimed as ion exchange membrane material is proposed. Polystyrene is grafted from a polysulfone macroinitiator by atom transfer radical polymerization, and subsequently sulfonated with acetyl sulfate...

  16. Sulfonation Process and Desalination Effect of Polystyrene/PVDF Semi-Interpenetrating Polymer Network Cation Exchange Membrane

    OpenAIRE

    Yin-lin Lei; Yun-jie Luo; Fei Chen; Le-he Mei

    2014-01-01

    With the classical sulfonation method of polystyrene-based strongly acidic cation exchange resins, polystyrene/polyvinylidene fluoride (PVDF) alloy particles were sulfonated to obtain a cation exchange resin, which was then directly thermoformed to prepare a semi-interpenetrating polymer network (semi-IPN) cation exchange membrane. The effects of the swelling agent, sulfonation time and temperature and the relative contents of polystyrene and divinylbenzene (DVB) in the alloy particles on the...

  17. Synthesis and adsorption properties of the cation exchange forms of OFF-type zeolite

    Science.gov (United States)

    Gorshunova, K. K.; Travkina, O. S.; Kustov, L. M.; Kutepov, B. I.

    2016-03-01

    The possibility of the ion-exchange of Na+ and K+ cations contained in OFF-type zeolite for H+, Ni2+, Cu2+, Co2+, and La3+ cations is investigated. Chemical and phase compositions, the morphology of crystals, and the adsorption properties of synthesized samples are studied via X-ray fluorescence and X-ray diffraction analysis, IR spectroscopy, scanning electron microscopy, and adsorption measurements.

  18. Thermochemical Stability Study of Alkyl-Tethered Quaternary Ammonium Cations for Anion Exchange Membrane Fuel Cells

    Energy Technology Data Exchange (ETDEWEB)

    Mohanty, Angela D.; Tignor, Steven E.; Sturgeon, Matthew R.; Long, Hai; Pivovar, Bryan S.; Bae, Chulsung

    2017-01-01

    The increased interest in the use of anion exchange membranes (AEMs) for applications in electrochemical devices has prompted significant efforts in designing materials with robust stability in alkaline media. Most reported AEMs suffer from polymer backbone degradation as well as cation functional group degradation. In this report, we provide comprehensive experimental investigations for the analysis of cation functional group stability under alkaline media. A silver oxide-mediated ion exchange method and an accelerated stability test in aqueous KOH solutions at elevated temperatures using a Parr reactor were used to evaluate a broad scope of quaternary ammonium (QA) cationic model compound structures, particularly focusing on alkyl-tethered cations. Additionally, byproduct analysis was employed to gain better understanding of degradation pathways and trends of alkaline stability. Experimental results under different conditions gave consistent trends in the order of cation stability of various QA small molecule model compounds. Overall, cations that are benzyl-substituted or that are near to electronegative atoms (such as oxygen) degrade faster in alkaline media in comparison to alkyl-tethered QAs. These comprehensive model compound stability studies provide valuable information regarding the relative stability of various cation structures and can help guide researchers towards designing new and promising candidates for AEM materials.

  19. Evaluation of Soil Reaction, Exchangeable Acidity and Cation ...

    African Journals Online (AJOL)

    Adequate application of both organic and inorganic fertilizers will improve the organic matter content which will increase the level of CEC of the soils and also liming was recommended to rise the pH of the soils for enhanced production capacity in the study area. Keywords: Exchangeable Acidity, Soil, Pedons and Fertility ...

  20. Sulfonation Process and Desalination Effect of Polystyrene/PVDF Semi-Interpenetrating Polymer Network Cation Exchange Membrane

    Directory of Open Access Journals (Sweden)

    Yin-lin Lei

    2014-07-01

    Full Text Available With the classical sulfonation method of polystyrene-based strongly acidic cation exchange resins, polystyrene/polyvinylidene fluoride (PVDF alloy particles were sulfonated to obtain a cation exchange resin, which was then directly thermoformed to prepare a semi-interpenetrating polymer network (semi-IPN cation exchange membrane. The effects of the swelling agent, sulfonation time and temperature and the relative contents of polystyrene and divinylbenzene (DVB in the alloy particles on the feasibility of the membrane formation are discussed. The results indicate that a favorable sulfonation degree above 80% and a suitable ion exchange capacity of 1.5–2.4 mmol/g can be gained, with concentrated sulfuric acid as the sulfonation agent and 1,2-dichloroethane as the swelling agent. The running electrical resistance and desalination effect of the prepared cation exchange membrane were measured in a pilot-scale electrodialyser and not only obviously exceeded a commercial heterogeneous cation exchange membrane, but was also very close to a commercial homogenous membrane. In this way, the authors have combined the classical sulfonation method of polystyrene-based cation exchange resins with the traditional thermoforming manufacturing process of heterogeneous cation exchange membranes, to successfully develop a novel, low-price, but relatively high-performance polystyrene/PVDF cation exchange membrane with the semi-IPN structure.

  1. [Determination of soil exchangeable base cations by using atomic absorption spectrophotometer and extraction with ammonium acetate].

    Science.gov (United States)

    Zhang, Yu-ge; Xiao, Min; Dong, Yi-hua; Jiang, Yong

    2012-08-01

    A method to determine soil exchangeable calcium (Ca), magnesium (Mg), potassium (K), and sodium (Na) by using atomic absorption spectrophotometer (AAS) and extraction with ammonium acetate was developed. Results showed that the accuracy of exchangeable base cation data with AAS method fits well with the national standard referential soil data. The relative errors for parallel samples of exchangeable Ca and Mg with 66 pair samples ranged from 0.02%-3.14% and 0.06%-4.06%, and averaged to be 1.22% and 1.25%, respectively. The relative errors for exchangeable K and Na with AAS and flame photometer (FP) ranged from 0.06%-8.39% and 0.06-1.54, and averaged to be 3.72% and 0.56%, respectively. A case study showed that the determination method for exchangeable base cations by using AAS was proven to be reliable and trustable, which could reflect the real situation of soil cation exchange properties in farmlands.

  2. Plant diseases caused by heavy metals and their phytiatry with cation exchangers

    Directory of Open Access Journals (Sweden)

    C. Van Assche

    2015-06-01

    Full Text Available The noxious influence of heavy metals as lead, zinc, copper and lead on higher plants and soil fungi was described. Addition to the soil of Levatit cation exchangers consisting of polystyrene porous resins, charged with calcium or manganese in granulated or powdered form, restored normal plant growth and inhibited the uptake of heavy metals ions.

  3. Enhanced desorption of Cs from clays by a polymeric cation-exchange agent.

    Science.gov (United States)

    Park, Chan Woo; Kim, Bo Hyun; Yang, Hee-Man; Seo, Bum-Kyoung; Lee, Kune-Woo

    2017-04-05

    We report on a new approach to increase the removal of cesium from contaminated clays based on the intercalation of a cationic polyelectrolyte into the clay interlayers. A highly charged cationic polyelectrolyte, polyethyleneimine (PEI), was shown to intercalate into the negatively charged interlayers and readily replaced Cs ions adsorbed on the interlayers of montmorillonite. The polycation desorbed significantly more Cs strongly bound to the clay than did single cations. Moreover, additional NH 4 + treatment following the PEI treatment enhanced desorption of Cs ions that were less accessible by the bulky polyelectrolyte. This synergistic effect of PEI with NH 4 + yielded efficient desorption (95%) of an extremely low concentration of radioactive 137 Cs in the clay, which is very difficult to remove by simple cation-exchange methods due to the increased stability of the binding of Cs to the clay at low Cs concentrations. Copyright © 2016 Elsevier B.V. All rights reserved.

  4. Conventional resin cation exchangers versus EDI for CACE measurement in power plants. Feasibility and practical field results

    Energy Technology Data Exchange (ETDEWEB)

    Sigrist, Manuel [Swan Systeme AG, Hinwil (Switzerland)

    2017-10-15

    The conductivity measurement after a cation exchanger in power plants with steam turbines was introduced soon after 1950 by Larson and Lane. Due to the simple measuring principle, the sensitivity to ionic contaminations and to its high reliability, the conductivity measurement after a cation exchanger (CACE) has become the most commonly used online analytical method in power plants with steam generators. Swan has investigated electro deionisation (EDI) as substitution of the conventional cation exchange resin and has developed a new conductivity instrument using this principle. This paper provides a description of the conventional method for cation conductivity measurements as well as of the new AMI CACE using EDI method.

  5. Influence of acidic eluent for retention behaviors of common anions and cations by ion-exclusion/cation-exchange chromatography on a weakly acidic cation-exchange resin in the H+ -form.

    Science.gov (United States)

    Mori, Masanobu; Tanaka, Kazuhiko; Satori, Tatsuya; Ikedo, Mikaru; Hu, Wenzhi; Itabashi, Hideyuki

    2006-06-16

    Influence of acidic eluent on retention behaviors of common anions and cations by ion-exclusion/cation-exchange chromatography (ion-exclusion/CEC) were investigated on a weakly acidic cation-exchange resin in the H(+)-form with conductivity. Sensitivities of analyte ions, especially weak acid anions (F(-) and HCOO(-)), were affected with degree of background conductivity level with pK(a1) (first dissociation constant) of acid in eluent. The retention behaviors of anions and cations were related to that of elution dip induced after eluting acid to separation column and injecting analyte sample. These results were largely dependent on the natures of acid as eluent. Through this study, succinic acid as the eluent was suitable for simultaneous separation of strong acid anions (SO(4)(2-), Cl(-), NO(3)(-) and I(-)), weak acid anions (F(-), HCOO(-) and CH(3)COO(-)), and cations (Na(+), K(+), NH(4)(+), Mg(2+) and Ca(2+)). The separation was achieved in 20 min under the optimum eluent condition, 20 mM succinic acid/2 mM 18-crown-6. Detection limits at S/N=3 ranged from 0.10 to 0.51 microM for strong acid anions, 0.20 to 5.04 microM for weak acid anions and 0.75 to 1.72 microM for cations. The relative standard deviations of peak areas in the repeated chromatographic runs (n=10) were in the range of 1.1-2.9% for anions and 1.8-4.5% for cations. This method was successfully applied to hot spring water containing strong acid anions, weak acid anions and cations, with satisfactory results.

  6. Mobile phase modifier effects in multimodal cation exchange chromatography.

    Science.gov (United States)

    Holstein, Melissa A; Parimal, Siddharth; McCallum, Scott A; Cramer, Steven M

    2012-01-01

    This study examines protein adsorption behavior and the effects of mobile phase modifiers in multimodal chromatographic systems. Chromatography results with a diverse protein library indicate that multimodal and ion exchange resins have markedly different protein binding behavior and selectivity. NMR results corroborate the stronger binding observed for the multimodal system and provide insight into the structural basis for the observed binding behavior. Protein-binding affinity and selectivity in multimodal and ion exchange systems are then examined using a variety of mobile phase modifiers. Arginine and guanidine are found to have dramatic effects on protein adsorption, yielding changes in selectivity in both chromatographic systems. While sodium caprylate leads to slightly weaker chromatographic retention for most proteins, certain proteins exhibit significant losses in retention in both systems. The presence of a competitive binding mechanism between the multimodal ligand and sodium caprylate for binding to ubiquitin is confirmed using STD NMR. Polyol mobile phase modifiers are shown to result in increased retention for weakly bound proteins and decreased retention for strongly bound proteins, indicating that the overall retention behavior is determined by a balance between changes in electrostatic and hydrophobic interactions. This work provides an improved understanding of protein adsorption and mobile phase modifier effects in multimodal chromatographic systems and sets the stage for future work to develop more selective protein separation systems. Copyright © 2011 Wiley Periodicals, Inc.

  7. First principles derived, transferable force fields for CO2 adsorption in Na-exchanged cationic zeolites.

    Science.gov (United States)

    Fang, Hanjun; Kamakoti, Preeti; Ravikovitch, Peter I; Aronson, Matthew; Paur, Charanjit; Sholl, David S

    2013-08-21

    The development of accurate force fields is vital for predicting adsorption in porous materials. Previously, we introduced a first principles-based transferable force field for CO2 adsorption in siliceous zeolites (Fang et al., J. Phys. Chem. C, 2012, 116, 10692). In this study, we extend our approach to CO2 adsorption in cationic zeolites which possess more complex structures. Na-exchanged zeolites are chosen for demonstrating the approach. These methods account for several structural complexities including Al distribution, cation positions and cation mobility, all of which are important for predicting adsorption. The simulation results are validated with high-resolution experimental measurements of isotherms and microcalorimetric heats of adsorption on well-characterized materials. The choice of first-principles method has a significant influence on the ability of force fields to accurately describe CO2-zeolite interactions. The PBE-D2 derived force field, which performed well for CO2 adsorption in siliceous zeolites, does not do so for Na-exchanged zeolites; the PBE-D2 method overestimates CO2 adsorption energies on multi-cation sites that are common in cationic zeolites with low Si/Al ratios. In contrast, a force field derived from the DFT/CC method performed well. Agreement was obtained between simulation and experiment not only for LTA-4A on which the force field fitting is based, but for other two common adsorbents, NaX and NaY.

  8. Influence of the Ion Coordination Number on Cation Exchange Reactions with Copper Telluride Nanocrystals

    CERN Document Server

    Tu, Renyong; Bertoni, Giovanni; Lak, Aidin; Gaspari, Roberto; Rapallo, Arnaldo; Cavalli, Andrea; De Trizio, Luca; Manna, Liberato

    2016-01-01

    Cu2-xTe nanocubes were used as starting seeds to access metal telluride nanocrystals by cation exchanges at room temperature. The coordination number of the entering cations was found to play an important role in dictating the reaction pathways. The exchanges with tetrahedrally coordinated cations (i.e. with coordination number 4), such as Cd2+ or Hg2+, yielded monocrystalline CdTe or HgTe nanocrystals with Cu2-xTe/CdTe or Cu2-xTe/HgTe Janus-like heterostructures as intermediates. The formation of Janus-like architectures was attributed to the high diffusion rate of the relatively small tetrahedrally coordinated cations, which could rapidly diffuse in the Cu2-xTe NCs and nucleate the CdTe (or HgTe) phase in a preferred region of the host structure. Also, with both Cd2+ and Hg2+ ions the exchange led to wurtzite CdTe and HgTe phases rather than the more stable zinc-blende ones, indicating that the anion framework of the starting Cu2- xTe particles could be more easily deformed to match the anion framework of t...

  9. Fast cation-exchange separation of proteins in a plastic microcapillary disc.

    Science.gov (United States)

    Darton, N J; Reis, N M; Mackley, M R; Slater, N K H

    2011-03-11

    A novel disposable adsorbent material for fast cation-exchange separation of proteins was developed based on plastic microcapillary films (MCFs). A MCF containing 19 parallel microcapillaries, each with a mean internal diameter of 142 μm, was prepared using a melt extrusion process from an ethylene-vinyl alcohol copolymer (EVOH). The MCF was surface functionalized to produce a cation-exchange adsorbent (herein referred as MCF-EVOH-SP). The dynamic binding capacity of the new MCF-EVOH-SP material was experimentally determined by frontal analysis using pure protein solutions in a standard liquid chromatography instrument for a range of superficial flow velocities, u(LS)=5.5-27.7 cm s⁻¹. The mean dynamic binding capacity for hen-egg lysozyme was found to be approximately 100 μg for a 5 m length film, giving a ligand binding density of 413 ng cm⁻². The dynamic binding capacity did not vary significantly over the range of u(LS) tested. The application of this novel material to subtractive chromatography was demonstrated for anionic BSA and cationic lysozyme at pH 7.2. The chromatographic separation of two cationic proteins, lysozyme and cytochrome-c, was also performed with a view to applying this technology to the analysis or purification of proteins. Future applications might include separation based on anion exchange and other modes of adsorption. Copyright © 2011 Elsevier B.V. All rights reserved.

  10. In vivo cation exchange in quantum dots for tumor-specific imaging.

    Science.gov (United States)

    Liu, Xiangyou; Braun, Gary B; Qin, Mingde; Ruoslahti, Erkki; Sugahara, Kazuki N

    2017-08-24

    In vivo tumor imaging with nanoprobes suffers from poor tumor specificity. Here, we introduce a nanosystem, which allows selective background quenching to gain exceptionally tumor-specific signals. The system uses near-infrared quantum dots and a membrane-impermeable etchant, which serves as a cation donor. The etchant rapidly quenches the quantum dots through cation exchange (ionic etching), and facilitates renal clearance of metal ions released from the quantum dots. The quantum dots are intravenously delivered into orthotopic breast and pancreas tumors in mice by using the tumor-penetrating iRGD peptide. Subsequent etching quenches excess quantum dots, leaving a highly tumor-specific signal provided by the intact quantum dots remaining in the extravascular tumor cells and fibroblasts. No toxicity is noted. The system also facilitates the detection of peritoneal tumors with high specificity upon intraperitoneal tumor targeting and selective etching of excess untargeted quantum dots. In vivo cation exchange may be a promising strategy to enhance specificity of tumor imaging.The imaging of tumors in vivo using nanoprobes has been challenging due to the lack of sufficient tumor specificity. Here, the authors develop a tumor-specific quantum dot system that permits in vivo cation exchange to achieve selective background quenching and high tumor-specific imaging.

  11. The colloid fraction and cation-exchange capacity in the soils of Vojvodina, Serbia

    Directory of Open Access Journals (Sweden)

    Nešić Ljiljana

    2015-01-01

    Full Text Available The colloidal complex of soil consists of humus and clay, the most important acidoids which are able to create the bonds between oppositely charged ions (cations through the forces strong enough to provide protection from leaching, and also weak enough to enable absorption through the plant root. This ability becomes more pronounced if the degree of dispersity is higher, i.e. if particles have smaller diameters. Total of 435 soil samples were collected from the surface horizon in 2011, for the purpose of soil fertility control in Vojvodina and prevention of its possible degradation in broader terms. This paper presents a part of study through selected representative soil samples, related to the research results of mechanical composition, basic chemical properties, and cation-exchange capacity in the most frequent types of soils in North Bačka and Banat (chernozem, fluvisol, semiglay, humoglay, solonchak, solonetz, due to the fact that soil fertility and its ecological function in environment protection largely depend on the studied properties. The average content of clay was 25.26%, ranging from 5.76 to 49.44%, the average content of humus was 3.10%, ranging between 1.02 and 4.30%, while the average value of CEC was 27.30 cmol/kg, ranging between 12.03 and 46.06 cmol/kg. Soils with higher content of clay and humus have greater cation-exchange capacity. According to the established average values of CEC in cmol/kg, the order of soil types is as follows: solonetz (40.06, semiglay (31.98, humoglay (30.98, solonchak (26.62, chernozem (22.72, and fluvisol (22.40. Research results have shown that cation-exchange capacity depends on clay fraction and humus content. Higher correlation coefficient between CEC and clay, compared to CEC and humus, indicates that clay content compared to humus content has greater effect on cation-exchange capacity.

  12. Mathematical Modeling of Cation Contamination in a Proton-exchange Membrane

    Energy Technology Data Exchange (ETDEWEB)

    Weber, Adam; Delacourt, Charles

    2008-09-11

    Transport phenomena in an ion-exchange membrane containing both H+ and K+ are described using multicomponent diffusion equations (Stefan-Maxwell). A model is developed for transport through a Nafion 112 membrane in a hydrogen-pump setup. The model results are analyzed to quantify the impact of cation contamination on cell potential. It is shown that limiting current densities can result due to a decrease in proton concentration caused by the build-up of contaminant ions. An average cation concentration of 30 to 40 percent is required for appreciable effects to be noticed under typical steady-state operating conditions.

  13. Enhanced desorption of Cs from clays by a polymeric cation-exchange agent

    Energy Technology Data Exchange (ETDEWEB)

    Park, Chan Woo, E-mail: park85@gmail.com [Decontamination & Decommissioning Research Division, Korea Atomic Energy Research Institute, Daedeok-daero 989-111, Yuseong-gu, Daejeon (Korea, Republic of); Kim, Bo Hyun [Decontamination & Decommissioning Research Division, Korea Atomic Energy Research Institute, Daedeok-daero 989-111, Yuseong-gu, Daejeon (Korea, Republic of); Department of Chemical Engineering, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon (Korea, Republic of); Yang, Hee-Man; Seo, Bum-Kyoung [Decontamination & Decommissioning Research Division, Korea Atomic Energy Research Institute, Daedeok-daero 989-111, Yuseong-gu, Daejeon (Korea, Republic of); Lee, Kune-Woo, E-mail: nkwlee@kaeri.re.kr [Decontamination & Decommissioning Research Division, Korea Atomic Energy Research Institute, Daedeok-daero 989-111, Yuseong-gu, Daejeon (Korea, Republic of)

    2017-04-05

    Highlights: • A cationic polyelectrolyte has excellent ability to desorb Cs bound strongly to clay. • The polycation desorbed significantly more Cs from the clay than did single cations. • Additional NH{sub 4}{sup +} treatment following the polycation treatment enhanced desorption of Cs. • The reaction yielded efficient desorption (95%) of an extremely low concentration of Cs-137 in the clay. - Abstract: We report on a new approach to increase the removal of cesium from contaminated clays based on the intercalation of a cationic polyelectrolyte into the clay interlayers. A highly charged cationic polyelectrolyte, polyethyleneimine (PEI), was shown to intercalate into the negatively charged interlayers and readily replaced Cs ions adsorbed on the interlayers of montmorillonite. The polycation desorbed significantly more Cs strongly bound to the clay than did single cations. Moreover, additional NH{sub 4}{sup +} treatment following the PEI treatment enhanced desorption of Cs ions that were less accessible by the bulky polyelectrolyte. This synergistic effect of PEI with NH{sub 4}{sup +} yielded efficient desorption (95%) of an extremely low concentration of radioactive {sup 137}Cs in the clay, which is very difficult to remove by simple cation-exchange methods due to the increased stability of the binding of Cs to the clay at low Cs concentrations.

  14. Strong cation-exchange chromatography of proteins on a sulfoalkylated monolithic cryogel.

    Science.gov (United States)

    Perçin, Işık; Khalaf, Rushd; Brand, Bastian; Morbidelli, Massimo; Gezici, Orhan

    2015-03-20

    A new strong cation exchanger (SCX) monolithic column was synthesized by at-line surface modification of a cryogel prepared by copolymerization of 2-hydroxyethylmethacrylate (HEMA) and glycidylmethacrylate (GMA). Sodium salt of 3-Mercaptopropane sulfonic acid (3-MPS) was used as the ligand to transform the surface of the monolith into a strong cation exchanger. The obtained material was characterized in terms of elemental analysis, infrared spectroscopy (FTIR), Scanning Electron Microscopy (SEM), Brunauer-Emmett-Teller (BET) N2 adsorption, and used as a stationary phase for strong-cation exchange chromatography of some proteins, such as α-chymotrypsinogen, cytochrome c and lysozyme. Water permeability of the column was calculated according to Darcy's law (2.66×10(-13)m(2)). The performance of the monolithic cryogel column was evaluated on the basis of Height Equivalent to a Theoretical Plate (HETP). Retention behavior of the studied proteins was modeled on the basis of Yamamoto model to understand the role of the ion-exchange mechanism in retention behaviors. The considered proteins were successfully separated, and the obtained chromatogram was compared with that obtained with a non-functionalized cryogel column. Copyright © 2015 Elsevier B.V. All rights reserved.

  15. Radial variations in cation exchange capacity and base saturation rate in the wood of pedunculate oak and European beech

    Energy Technology Data Exchange (ETDEWEB)

    Herbauts, J.; Penninckx, V.; Gruber, W.; Meerts, P. [Universite Libre de Bruxelles, Laboratoire de genetique et d' ecologie vegetales, Brussels (Belgium)

    2002-10-01

    Visual observation of pedunculate oak trees and European beech trees in a mixed forest stand in the Belgian Ardennes revealed decreasing cation concentration profiles in wood. In order to determine whether these profiles are attributable to endogenous factors or to decreased availability of cations in the soil, radial profiles of water-soluble, exchangeable and total cations were investigated. Cation exchange capacity of wood was also determined. Results showed wood cation exchange capacity to decrease from pith to bark in European beech and from pith to outer heartwood in pedunculate oak. Decreasing profiles of exchangeable calcium and magnesium in peduncular oak and exchangeable calcium in European beech were found to be strongly constrained by cation exchange capacity, and thus not related to environmental change. Base cation saturation rate showed no consistent radial change in either species. It was concluded that the results did not provide convincing evidence to attribute the decrease in divalent cation concentration in pedunculate oak and European beech in this location to be due to atmospheric pollution. 42 refs., 1 tab., 4 figs.

  16. Dehydration enthalpy of alkali-cations-exchanged montmorillonite from thermogravimetric analysis.

    Science.gov (United States)

    Kharroubi, M; Balme, S; Henn, F; Giuntini, J C; Belarbi, H; Haouzi, A

    2009-01-15

    Dehydration of a series of homoionic alkali-exchanged montmorillonites is studied at different treatment temperatures by means of thermogravimetric analysis. More specifically, we investigate the last stages of dehydration when the number of adsorbed water molecules corresponds, at maximum, to a monolayer. Weight losses are measured at several constant temperatures as a function of time. Application of Van't Hoff's law yields the dehydration enthalpy. Trends and data similar to those reported from other experimental conditions are found. Comparison with X-ray data and with the dissociation enthalpy of alkali cation/water complexes shows that dehydration of weakly hydrated homoionic alkali montmorillonites results from the competition between opposite energy contributions due to (i) the cation solvation, (ii) the hydration of the silicate interlayer surface, and (iii) the structural swelling. So, depending on the balance between these various energy contributions, different behaviors are observed according to the nature of the alkali cations.

  17. Recent progress and applications of ion-exclusion/ion-exchange chromatography for simultaneous determination of inorganic anions and cations.

    Science.gov (United States)

    Nakatani, Nobutake; Kozaki, Daisuke; Mori, Masanobu; Tanaka, Kazuhiko

    2012-01-01

    One of the ultimate goals of ion chromatography is to determine both anions and cations found in samples with a single chromatographic run. In the present article, recent progress in ion-exclusion/ion-exchange chromatography for the simultaneous determinations of inorganic anions and cations are reviewed. Firstly, the principle and the control for the simultaneous separation and detection of analyte ions using ion-exclusion/cation-exchange chromatography with a weakly acidic cation-exchange column are outlined. Then, advanced chromatographic techniques in terms of analytical time, selectively and sensitivity are summarized. As a related method, ion-exclusion/anion-exchange chromatography with an anion-exchange column could be used for the simultaneous determination of inorganic nitrogen species, such as ammonium, nitrite and nitrate ions. Their usefulness and applications to water-quality monitoring and related techniques are also described.

  18. Concentration of ions Co(II), Ni(II) at the Tokem-250 carboxylic cation exchange for catalysts development

    Science.gov (United States)

    Zharkova, Valentina; Bobkova, Ludmila; Brichkov, Anton; Kozik, Vladimir

    2017-11-01

    Sorption and catalytic properties of the cation exchanger are investigated. It was found that the Tokem-250 has a wide operating range of pH. The value of the effective ionization constant of the functional groups of the cation exchanger (pKa) is 6.59. The Tokem-250 cation exchanger exhibits selectivity to Ni2+ ions to Co2+ (D˜103). This is probably due to the stability of ion-exchange complexes detected by the method of diffuse reflectance electron spectroscopy (ESDD). According to these data, for Co2+ ions, in contrast to Ni2+, tetragonal distortion of octahedral coordination is characteristic, which has a positive effect on the stability of complexes with Co2+. To obtain spherical catalysts on the basis of Tokem-250, cobalt-containing samples of cation exchanger were used. The developed spherical materials have catalytic activity in the reactions of deep and partial oxidation of n-heptane.

  19. Isolation of polybutenylsuccinimide-type dispersants from multigrade lubricating oils by classical cation exchange chromatography

    Energy Technology Data Exchange (ETDEWEB)

    Hui, F.; Machtalere, G.; Xie, J.; Kolodziejczyk, H.; Rosset, R. [Laboratoire de Chimie Analytique, URA CNRS 437, Ecole Superieure de Physique et Chimie Industrielles de la Ville de Paris, Paris (France)

    1997-02-28

    A macroporous cation exchanger is used for the efficient separation of ashless dispersants (polybutenylsuccinimide type) from base oil and additives (viscosity improver (VI), detergent, inhibitors, etc.) of multigrade lubricating oils. Due to the basic character of residual amine groups present in its polyamine chain, the dispersant is retained on the macroporous cation exchanger (H{sup +} form) while base oil and additives are eluted with appropriate solvents. The highly purified dispersant is then recovered through elution with a strong and basic eluent constituted of chloroform-isopropanol-ammonia (35:60:5, v/v). The quality of the isolation is checked all along the separation by Fourier transform infrared (FTIR) spectrometry and size-exclusion chromatography (SEC)

  20. Multicolour synthesis in lanthanide-doped nanocrystals through cation exchange in water

    KAUST Repository

    Han, Sanyang

    2016-10-04

    Meeting the high demand for lanthanide-doped luminescent nanocrystals across a broad range of fields hinges upon the development of a robust synthetic protocol that provides rapid, just-in-time nanocrystal preparation. However, to date, almost all lanthanide-doped luminescent nanomaterials have relied on direct synthesis requiring stringent controls over crystal nucleation and growth at elevated temperatures. Here we demonstrate the use of a cation exchange strategy for expeditiously accessing large classes of such nanocrystals. By combining the process of cation exchange with energy migration, the luminescence properties of the nanocrystals can be easily tuned while preserving the size, morphology and crystal phase of the initial nanocrystal template. This post-synthesis strategy enables us to achieve upconversion luminescence in Ce3+ and Mn2+-activated hexagonal-phased nanocrystals, opening a gateway towards applications ranging from chemical sensing to anti-counterfeiting.

  1. Effects of Cationic Pendant Groups on Ionic Conductivity for Anion Exchange Membranes: Structure Conductivity Relationships

    Science.gov (United States)

    Kim, Sojeong; Choi, Soo-Hyung; Lee, Won Bo

    Anion exchange membranes(AEMs) have been widely studied due to their various applications, especially for Fuel cells. Previous proton exchange membranes(PEMs), such as Nafions® have better conductivity than AEMs so far. However, technical limitations such as slow electrode kinetics, carbon monoxide (CO) poisoning of metal catalysts, high methanol crossover and high cost of Pt-based catalyst detered further usages. AEMs have advantages to supplement its drawbacks. AEMs are environmentally friendly and cost-efficient. Based on the well-defined block copolymer, self-assembled morphology is expected to have some relationship with its ionic conductivity. Recently AEMs based on various cations, including ammonium, phosphonium, guanidinium, imidazolium, metal cation, and benzimidazolium cations have been developed and extensively studied with the aim to prepare high- performance AEMs. But more fundamental approach, such as relationships between nanostructure and conductivity is needed. We use well-defined block copolymer Poly(styrene-block-isoprene) as a backbone which is synthesized by anionic polymerization. Then we graft various cationic functional groups and analysis the relation between morphology and conductivity. Theoretical and computational soft matter lab.

  2. Simultaneous Isolation of Lactoferrin and Lactoperoxidase from Bovine Colostrum by SPEC 70 SLS Cation Exchange Resin

    OpenAIRE

    Liang, Yafei; Wang, Xuewan; Wu, Mianbin; Zhu, Wanping

    2011-01-01

    In this work, simultaneous isolation of lactoferrin (Lf) and lactoperoxidase (Lp) from defatted bovine colostrum by one-step cation exchange chromatography with SPEC 70 SLS ion-exchange resin was investigated. A RP-HPLC method for Lf and Lp determination was developed and optimized as the following conditions: detection wavelength of 220 nm, flow rate of 1 mL/min and acetonitrile concentration from 25% to 75% within 20 min. The adsorption process of Lf on SPEC 70 SLS resin was optimized using...

  3. The Role of Cation/Proton Exchanger NHE9 in Synaptic Transmission & Autism

    OpenAIRE

    Ullman, Julia Collier

    2015-01-01

    Autism spectrum disorders (ASD) are neurodevelopmental syndromes that affect an estimated 1.5 million people in the United States alone. While ASDs arising from single gene mutations are rare, the study of these conditions provides a powerful and effective approach toward understanding the molecular basis for ASD as well as normal social behaviors. Recently, the cation/hydrogen exchanger Nhe9 has surfaced as a locus for inherited autism, with mutations confirmed to abolish expression. In addi...

  4. Evaluation of the field-scale cation exchange capacity of Hanford sediments

    Energy Technology Data Exchange (ETDEWEB)

    Steefel, C.I.

    2003-02-01

    Three-dimensional simulations of unsaturated flow, transport, and multi-component, multi-site cation exchange in the vadose zone were used to analyze the migration of a plume resulting from a leak of the SX-115 tank at the Hanford site, USA. The match within about 0.5 meters of the positions of retarded sodium and potassium fronts suggests that the laboratory-derived parameters may be used in field-scale simulations of radionuclide migration at the Hanford site.

  5. Preparative separation of monoclonal antibody aggregates by cation-exchange laterally-fed membrane chromatography.

    Science.gov (United States)

    Madadkar, Pedram; Sadavarte, Rahul; Butler, Michael; Durocher, Yves; Ghosh, Raja

    2017-06-15

    Cation exchange (CEX) chromatography is widely used for large-scale separation of monoclonal antibody (mAb) aggregates. The aggregates bind more strongly to CEX media and hence elute after the monomeric mAb in a salt gradient. However, monomer-aggregate resolution that is typically obtained is poor, which results in low product recovery. In the current study we address this challenge through the use of cation-exchange laterally-fed membrane chromatography (LFMC). Three different LFMC devices, each containing a bed of strong cation-exchange (S) membranes were used for preparative-scale removal of mAb aggregates. Trastuzumab (IgG1) biosimilar derived from human embryonic kidney 293 (293) cells was used as the primary model mAb in our study. The other mAbs investigated were Chinese hamster ovary (CHO) cell line derived Alemtuzumab (Campath-1H) and a heavy chain chimeric mAb EG2-hFc. In each of these case-studies, aggregates were well-resolved from the respective monomer. The separated and collected monomer and aggregate fractions were analyzed using techniques such as hydrophobic interaction membrane chromatography (HIMC), native polyacrylamide gel electrophoresis (or PAGE), and size-exclusion high-performance liquid chromatography (SE-HPLC). The high efficiency of separation obtained in each case was due to a combination of the small membrane pore size (3-5μm), and the use of LFMC technology, which has been shown to be suitable for high-resolution, multi-component protein separations. Also, the LFMC based separation processes reported in this study were more than an order of magnitude faster than equivalent resin-based, cation exchange chromatography. Copyright © 2017 Elsevier B.V. All rights reserved.

  6. Solubility and cation exchange in phosphate rock and saturated clinoptilolite mixtures

    Science.gov (United States)

    Allen, E. R.; Hossner, L. R.; Ming, D. W.; Henninger, D. L.

    1993-01-01

    Mixtures of zeolite and phosphate rock (PR) have the potential to provide slow-release fertilization of plants in synthetic soils by dissolution and ion-exchange reactions. This study was conducted to examine solubility and cation-exchange relationships in mixtures of PR and NH4- and K-saturated clinoptilolite (Cp). Batch-equilibration experiments were designed to investigate the effect of PR source, the proportion of exchangeable K and NH4, and the Cp to PR ratio on solution N, P, K, and Ca concentrations. The dissolution and cation-exchange reactions that occurred after mixing NH4- and K-saturated Cp with PR increased the solubility of the PR and simultaneously released NH4 and K into solution. The more reactive North Carolina (NC) PR rendered higher solution concentrations of NH4 and K when mixed with Cp than did Tennessee (TN) PR. Solution P concentrations for the Cp-NC PR mixture and the Cp-TN PR mixture were similar. Solution concentrations of N, P, K, and Ca and the ratios of these nutrients in solution varied predictably with the type of PR, the Cp/PR ratio, and the proportions of exchangeable K and NH4 on the Cp. Our research indicated that slow-release fertilization using Cp/PR media may provide adequate levels of N, P, and K to support plant growth. Solution Ca concentrations were lower than optimum for plant growth.

  7. Proton Adsorption Selectivity of Zeolites in Aqueous Media: Effect of Exchangeable Cation Species of Zeolites

    Directory of Open Access Journals (Sweden)

    Moses Wazingwa Munthali

    2015-03-01

    Full Text Available The saturation of negative charges of zeolites by specific cations to modify their physicochemical and catalytic properties has broadened the applications of zeolites. The adsorption behavior of H+ to Li+, Na+, K+, Rb+ and Cs+-saturated Linde-type A, Na-P1, mordenite, X type and Y type zeolites was evaluated at different pH-pM, where pH-pM is equal to log {(M+/(H+} and M+ represents either Li+, Na+, K+, Rb+, or Cs+. In all cases, with decreasing pH-pM, the amounts of alkali metal retention decreased due to the adsorption of H+ via cation exchange reaction. The adsorption selectivity of H+ into the zeolites had a negative correlation with the Si/Al ratio of the zeolites. In each zeolite species, Cs+-saturated zeolite showed the lowest H+ selectivity, and this suggested that Cs+ had the strongest adsorption energy in the alkali metal cations. The adsorption of H+ was strongly affected by diameter and hydration energy of the alkali metal cations, and was also affected by the framework type and Si/Al ratio of the zeolites. The adsorption of H+ into zeolites decreases the amount of cation retention other than with H+ and may cause the elution of Si and Al into aqueous solutions.

  8. Tuning light emission of PbS nanocrystals from infrared to visible range by cation exchange

    Science.gov (United States)

    Binetti, Enrico; Striccoli, Marinella; Sibillano, Teresa; Giannini, Cinzia; Brescia, Rosaria; Falqui, Andrea; Comparelli, Roberto; Corricelli, Michela; Tommasi, Raffaele; Agostiano, Angela; Curri, M. Lucia

    2015-10-01

    Colloidal semiconductor nanocrystals, with intense and sharp-line emission between red and near-infrared spectral regions, are of great interest for optoelectronic and bio-imaging applications. The growth of an inorganic passivation layer on nanocrystal surfaces is a common strategy to improve their chemical and optical stability and their photoluminescence quantum yield. In particular, cation exchange is a suitable approach for shell growth at the expense of the nanocrystal core size. Here, the cation exchange process is used to promote the formation of a CdS passivation layer on the surface of very small PbS nanocrystals (2.3 nm in diameter), blue shifting their optical spectra and yielding luminescent and stable nanostructures emitting in the range of 700-850 nm. Structural, morphological and compositional investigation confirms the nanocrystal size contraction after the cation-exchange process, while the PbS rock-salt crystalline phase is retained. Absorption and photoluminescence spectroscopy demonstrate the growth of a passivation layer with a decrease of the PbS core size, as inferred by the blue-shift of the excitonic peaks. The surface passivation strongly increases the photoluminescence intensity and the excited state lifetime. In addition, the nanocrystals reveal increased stability against oxidation over time. Thanks to their absorption and emission spectral range and the slow recombination dynamics, such highly luminescent nano-objects can find interesting applications in sensitized photovoltaic cells and light-emitting devices.

  9. Tuning light emission of PbS nanocrystals from infrared to visible range by cation exchange

    KAUST Repository

    Binetti, Enrico

    2015-10-27

    Colloidal semiconductor nanocrystals, with intense and sharp-line emission between red and near-infrared spectral regions, are of great interest for optoelectronic and bio-imaging applications. The growth of an inorganic passivation layer on nanocrystal surfaces is a common strategy to improve their chemical and optical stability and their photoluminescence quantum yield. In particular, cation exchange is a suitable approach for shell growth at the expense of the nanocrystal core size. Here, the cation exchange process is used to promote the formation of a CdS passivation layer on the surface of very small PbS nanocrystals (2.3 nm in diameter), blue shifting their optical spectra and yielding luminescent and stable nanostructures emitting in the range of 700–850 nm. Structural, morphological and compositional investigation confirms the nanocrystal size contraction after the cation-exchange process, while the PbS rock-salt crystalline phase is retained. Absorption and photoluminescence spectroscopy demonstrate the growth of a passivation layer with a decrease of the PbS core size, as inferred by the blue-shift of the excitonic peaks. The surface passivation strongly increases the photoluminescence intensity and the excited state lifetime. In addition, the nanocrystals reveal increased stability against oxidation over time. Thanks to their absorption and emission spectral range and the slow recombination dynamics, such highly luminescent nano-objects can find interesting applications in sensitized photovoltaic cells and light-emitting devices.

  10. Study of cation-exchange capacity of soil near fluorspar mining with special reference to Kadipani mine (Gujarat, India).

    Science.gov (United States)

    Pradhan, Alka; Deshmukh, Jitendra P

    2011-10-01

    One of the important functions of soil is exchange of cations, whereby essential trace metals are made available to plants as nutrients. Both minerals and organics fractions of soil exchange the cations. Clay minerals exchange cation because of the presence of negatively charged sites on the mineral while organic materials exchange cations by means of their carboxylate groups and other basic functional groups. Cation exchange in soil provides trace metal nutrients to plant. The metal ions are taken up by the roots while H+ is exchanged for the metal ions. Therefore, the measurement of Cation Exchange Capacity (CEC) of soil is important and this becomes more significant when the mining activity is carried out in the surrounding environment as mining activity may adversely impact the soil texture and organic matter content and sometimes changes the pH which is the main regulator of CEC in soil. The studies related to the assessment of CEC of soil were carried out. 14 soil samples, including one sample of mine site, were collected during summer season from different villages within 10 km radius from the mine site. These samples were then analyzed. The efforts were made to establish the CEC of soil quality of Kadipani, Distt. Vadodara, Gujarat, India. This study is useful for making the decisions regarding the environmental measures required for mining activity.

  11. Analyzing freely dissolved concentrations of cationic surfactant utilizing ion-exchange capability of polyacrylate coated solid-phase microextraction fibers

    NARCIS (Netherlands)

    Chen, Y.|info:eu-repo/dai/nl/322994179; Droge, S.T.J.|info:eu-repo/dai/nl/304834017; Hermens, J.L.M.|info:eu-repo/dai/nl/069681384

    2012-01-01

    A 7-μm polyacrylate (PA) coated fiber was successfully employed to determine freely dissolved concentrations of cationic surfactants by solid-phase microextraction (SPME) and utilizing the capability of the PA-coating to sorb organic cations via ion-exchange at carboxylic groups. Measured

  12. A solid-state cation exchange reaction to form multiple metal oxide heterostructure nanowires.

    Science.gov (United States)

    Chen, Y H; Huang, C W; Yeh, P H; Chen, J Y; Lin, T Y; Chang, C F; Wu, W W

    2016-09-29

    Metal oxide nanostructures have been investigated extensively due to their wide range of physical properties; zinc oxide is one of the most promising materials. It exhibits fascinating functional properties and various types of morphologies. In particular, ZnO heterostructures have attracted great attention because their performance can be modified and further improved by the addition of other materials. In this study, we successfully transformed ZnO nanowires (NWs) into multiple ZnO/Al 2 O 3 heterostructure NWs via a solid-state cation exchange reaction. The experiment was carried out in situ via an ultrahigh vacuum transmission electron microscope (UHV-TEM), which was equipped with a video recorder. Moreover, we analyzed the structure and composition of the heterostructure NWs by Cs-corrected STEM equipped with EDS. Based on these experimental results, we inferred a cation exchange reaction ion path model. Additionally, we investigated the defects that appeared after the cation reaction, which resulted from the remaining zinc ions. These multiple heterostructure ZnO/Al 2 O 3 NWs exhibited excellent UV sensing sensitivity and efficiency.

  13. CATION EXCHANGE CAPACITY OF DOMINANT SOIL TYPES IN THE REPUBLIC OF CROATIA

    Directory of Open Access Journals (Sweden)

    Marija Tomasic

    2013-09-01

    Full Text Available The study was conducted on 18 locations and 11 dominant soil types in the Republic of Croatia including their evolution-genetic horizons. In total, 51 soil samples were examined. Analysis of soil was done by saturating patterns using barium chloride solution in three replications. Descriptive statistics of the analyzed data was conducted. Basic statistical parameters were calculated, and functional dependence between the base saturation (V% of analyzed soil samples and their pH was observed. The correlation coefficient (r between base saturation (V% and pH for all examined soils was r=0.79 (n=51; very strong correlation. For acid soils it was r=0.82 (n=17; very strong correlation, for neutral soils r=0.75 (n=8; very strong correlation, and finally for alkaline soils r=0.15 (n=26; very weak correlation. Cation exchange capacity values ranged from 2.39 cmol+*kg-1 to 33.8 cmol+*kg-1 depending on soil type, pH, organic content and other soil parameters. The content of exchangeable cations in the sum of basic cations ranged from: Ca2+ (16% - 94%, Mg2+ (2% - 41%, K+ (1% - 68% and Na+ (<0.01% also depending on soil type, depth, location and other physical and chemical soil parameters.

  14. Comparison of reversed-phase/cation-exchange/anion-exchange trimodal stationary phases and their use in active pharmaceutical ingredient and counterion determinations.

    Science.gov (United States)

    Liu, Xiaodong; Pohl, Christopher A

    2012-04-06

    This study involved three commercial reversed-phase (RP)/anion-exchange (AEX)/cation-exchange (CEX) trimodal columns, namely Acclaim Trinity P1 (Thermo Fisher Scientific), Obelisc R (SIELC Technologies) and Scherzo SM-C18 (Imtakt). Their chromatographic properties were compared in details with respect to hydrophobicity, anion-exchange capacity, cation-exchange capacity, and selectivity, by studying retention behavior dependency on organic solvent, buffer concentration and pH. It was found that their remarkably different column chemistries resulted in distinctive chromatography properties. Trinity P1 exhibited strong anion-exchange and cation-exchange interactions but low RP retention while Scherzo SM-C18 showed strong reversed-phase retention with little cation-exchange and anion-exchange capacities. For Obelisc R, its reversed-phase capacity was weaker than Scherzo SM-C18 but slightly higher than Trinity P1, and its ion-exchange retentions were between Trinity P1 and Scherzo SM-C18. In addition, their difference in selectivity was demonstrated by examples of determining the active pharmaceutical ingredient (API) and counterion of drug products. Copyright © 2011 Elsevier B.V. All rights reserved.

  15. Synthesis, characterization and applications of a new cation exchanger tamarind sulphonic acid (TSA) resin.

    Science.gov (United States)

    Singh, A V; Sharma, Naresh Kumar; Rathore, Abhay S

    2012-01-01

    A new composite cation exchanger, tamarind sulphonic acid (TSA) resin has been synthesized. The chemically modified TSA ion exchange resin has been used for the removal and preconcentration of Zn2+, Cd2+, Fe2+, Co2+ and Cu2+ ions in aqueous solution and effluent from the Laxmi steel plant in Jodhpur, India. This type of composite represents a new class of hybrid ion exchangers with good ion exchange capacity, stability, reproducibility and selectivity for toxic metal ions found in effluent from the steel industry. The characterization of the resin was carried out by determining the ion-exchange capacity, elemental analysis, pH titration, Fourier transform infrared spectra and thermal analysis. The distribution coefficients (K(d)) of toxic metal ions were determined in a reference aqueous solution and the steel plant effluent at different pH values; the absorbency of different metal ions on the TSA resin was studied for up to 10 cycles. The adsorption of different metal ions on TSA resin follows the order: Co2+ > Cu2+ > Zn2+ > Fe2+ > Cd2+. The ion exchange capacity of TSA resin is 2.87%.

  16. Multidimensional separation of tryptic peptides from human serum proteins using reversed-phase, strong cation exchange, weak anion exchange, and fused-core fluorinated stationary phases

    NARCIS (Netherlands)

    Boichenko, Alexander P.; Govorukhina, Natalia; van der Zee, Ate G. J.; Bischoff, Rainer

    2013-01-01

    Proteome profiling of crude serum is a challenging task due to the wide dynamic range of protein concentrations and the presence of high-abundance proteins, which cover >90% of the total protein mass in serum. Peptide fractionation on strong cation exchange, weak anion exchange in the electrostatic

  17. Activity of some disiloxanes toward the cation exchange resin-catalyst in the siloxane equilibration reaction

    Directory of Open Access Journals (Sweden)

    M. N. GOVEDARICA

    2000-09-01

    Full Text Available The relative activities of four disiloxanes toward the cation exchange resin, which was used as an equilibration catalyst, were determined in such a way that the equilibrium initially present in an arbitrary chosen equilibrate was disturbed by adding the respective disiloxanes to it, and then by recording the viscosity of the equilibrating mixtures as a function of reaction time. As a result, a set of different viscosity-reaction time relationships was obtained, which implies different activities of disiloxanes toward the catalyst. In this way the following decreasing order of acitivites was established: 1,3-tetramethyldisiloxane > 1,3-divinyltetramethyldisiloxane > hexamethyldisiloxane > 1,3-bis(3-carboxypropyltetramethyldisiloxane.

  18. Kinetics of transesterification of methyl acetate and n-octanol catalyzed by cation exchange resins

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Yong; Gao, Li; Li, Xiying; Mao, Liqun [Henan University, Kaifeng (China); Wei, Min [Henan University of Technology, Zhengzhou (China)

    2013-05-15

    The transesterification kinetics of methyl acetate with n-octanol to octyl acetate and methanol were studied using Amberlyst 15 as catalyst in a batch stirred reactor. The influence of the agitation speed, particle size, temperature, catalyst loading, and initial reactants molar ratio was investigated in detail. A pseudo-homogeneous (PH) kinetic model was applied to correlate the experimental data in the temperature range of 313.15 K to 328.15 K. The estimated kinetic parameters made the calculated results in good agreement with the experimental data. A kinetic model describing the transesterification reaction catalyzed by cation exchange resins was developed.

  19. Dual transport properties of anion exchanger 1: the same transmembrane segment is involved in anion exchange and in a cation leak.

    Science.gov (United States)

    Barneaud-Rocca, Damien; Borgese, Franck; Guizouarn, Hélène

    2011-03-18

    Previous results suggested that specific point mutations in human anion exchanger 1 (AE1) convert the electroneutral anion exchanger into a monovalent cation conductance. In the present study, the transport site for anion exchange and for the cation leak has been studied by cysteine scanning mutagenesis and sulfhydryl reagent chemistry. Moreover, the role of some highly conserved amino acids within members of the SLC4 family to which AE1 belongs has been assessed in AE1 transport properties. The results suggest that the same transport site within the AE1 spanning domain is involved in anion exchange or in cation transport. A functioning mechanism for this transport site is proposed according to transport properties of the different studied point mutations of AE1.

  20. Model Simulations of a Field Experiment on Cation Exchange-affected Multicomponent Solute Transport in a Sandy Aquifer

    DEFF Research Database (Denmark)

    Bjerg, Poul Løgstrup; Ammentorp, Hans Christian; Christensen, Thomas Højlund

    1993-01-01

    A large-scale and long-term field experiment on cation exchange in a sandy aquifer has been modelled by a three-dimensional geochemical transport model. The geochemical model includes cation-exchange processes using a Gaines-Thomas expression, the closed carbonate system and the effects of ionic...... of 800 days due to a substantially attenuation in the aquifer. The observed and the predicted breakthrough curves showed a reasonable accordance taking the duration of the experiment into account. However, some discrepancies were observed probably caused by the revealed non-ideal exchange behaviour of K+....

  1. A simple method for estimating cation exchange capacity from water vapor sorption

    DEFF Research Database (Denmark)

    Arthur, Emmanuel; Tuller, Markus

    2016-01-01

    Knowledge of soil cation exchange capacity (CEC) is crucial for soil fertility considerations, sorption and release of polar and non-polar compounds, engineering applications, and other biogeochemical processes. Standard procedures such as the ammonium acetate or the BaCl2 compulsive exchange...... (PTFs) for estimating CEC from soil water content considering hysteresis have been developed based on 203 differently-textured soils. Furthermore, we compared the performance of the new PTFs with existing PTFs that predict CEC from clay content, organic carbon, soil pH and specific surface area. The new...... of the new PTFs, thus a simple measure of soil water content at an arbitrary relative humidity can provide reasonably accurate CEC estimates for large scale studies....

  2. Extraction and derivatization of chemical weapons convention relevant aminoalcohols on magnetic cation-exchange resins.

    Science.gov (United States)

    Singh, Varoon; Garg, Prabhat; Chinthakindi, Sridhar; Tak, Vijay; Dubey, Devendra Kumar

    2014-02-14

    Analysis and identification of nitrogen containing aminoalcohols is an integral part of the verification analysis of chemical weapons convention (CWC). This study was aimed to develop extraction and derivatization of aminoalcohols of CWC relevance by using magnetic dispersive solid-phase extraction (MDSPE) in combination with on-resin derivatization (ORD). For this purpose, sulfonated magnetic cation-exchange resins (SMRs) were prepared using magnetite nanoparticles as core, styrene and divinylbenzene as polymer coat and sulfonic acid as acidic cation exchanger. SMRs were successfully employed as extractant for targeted basic analytes. Adsorbed analytes were derivatized with hexamethyldisilazane (HMDS) on the surface of extractant. Derivatized (silylated) compounds were analyzed by GC-MS in SIM and full scan mode. The linearity of the method ranged from 5 to 200ngmL(-1). The LOD and LOQ ranged from 2 to 6ngmL(-1) and 5 to 19ngmL(-1) respectively. The relative standard deviation for intra-day repeatability and inter-day intermediate precision ranged from 5.1% to 6.6% and 0.2% to 7.6% respectively. Recoveries of analytes from spiked water samples from different sources varied from 28.4% to 89.3%. Copyright © 2014 Elsevier B.V. All rights reserved.

  3. Esterification of palm fatty acid distillate with epychlorohydrin using cation exchange resin catalyst

    Science.gov (United States)

    Budhijanto, Budhijanto; Subagyo, Albertus F. P. H.

    2017-05-01

    Palm Fatty Acid Distillate (PFAD) is one of the wastes from the conversion of crude palm oil (CPO) into cooking oil. The PFAD is currently only utilized as the raw material for low grade soap and biofuel. To improve the economic value of PFAD, it was converted into monoglyceride by esterification process. Furthermore, the monoglyceride could be polymerized to form alkyd resin, which is a commodity of increasing importance. This study aimed to propose a kinetics model for esterification of PFAD with epichlorohydrin using cation exchange resin catalyst. The reaction was the first step from a series of reactions to produce the monoglyceride. In this study, the reaction between PFAD and epichlorohydirne was run in a stirred batch reactor. The stirrer was operated at a constant speed of 400 RPM. The reaction was carried out for 180 minutes on varied temperatures of 60°C, 70°C, 80°C, dan 90°C. Cation exchange resin was applied as solid catalysts. Analysis was conducted periodically by measuring the acid number of the samples, which was further used to calculate PFAD conversion. The data were used to determine the rate constants and the equilibrium constants of the kinetics model. The kinetics constants implied that the reaction was reversible and controlled by the intrinsic surface reaction. Despite the complication of the heterogeneous nature of the reaction, the kinetics data well fitted the elementary rate law. The effect of temperature on the equilibrium constants indicated that the reaction is exothermic.

  4. Morphologically Aligned Cation-Exchange Membranes by a Pulsed Electric Field for Reverse Electrodialysis.

    Science.gov (United States)

    Lee, Ju-Young; Kim, Jae-Hun; Lee, Ju-Hyuk; Kim, Seok; Moon, Seung-Hyeon

    2015-07-21

    A low-resistance ion-exchange membrane is essential to achieve the high-performance energy conversion or storage systems. The formation methods for low-resistance membranes are various; one of the methods is the ion channel alignment of an ion-exchange membrane under a direct current (DC) electric field. In this study, we suggest a more effective alignment method than the process with the DC electric field. First, an ion-exchange membrane was prepared under a pulsed electric field [alternating current (AC) mode] to enhance the effectiveness of the alignment. The membrane properties and the performance in reverse electrodialysis (RED) were then examined to assess the membrane resistance and ion selectivity. The results show that the membrane electrical resistance (MER) had a lower value of 0.86 Ω cm(2) for the AC membrane than 2.13 Ω cm(2) observed for the DC membrane and 4.30 Ω cm(2) observed for the pristine membrane. Furthermore, RED achieved 1.34 W/m(2) of maximum power density for the AC membrane, whereas that for the DC membrane was found to be 1.14 W/m(2) [a RED stack assembled with CMX, used as a commercial cation-exchange membrane (CEM), showed 1.07 W/m(2)]. Thereby, the novel preparation process for a remarkable low-resistance membrane with high ion selectivity was demonstrated.

  5. Effect of ionophores on the rate of intramolecular cation exchange in durosemiquinone ion pairs

    Science.gov (United States)

    Eastman, M. P.; Bruno, G. V.; Mcguyer, C. A.; Gutierrez, A. R.; Shannon, J. M.

    1979-01-01

    The effects of the ionophores 15-crown-5 (15C5), 18-crown-6 (18C6), dibenzo-18-crown-6 (DBC) and cryptand 222 (C222) on intramolecular cation exchange in ion pairs of the sodium salt of the durosemiquinone anion in benzene solution are investigated. Electron paramagnetic resonance spectra of the 18C6 and 15C5 complexes with durosemiquinone reduced by contact with a sodium mirror show an alternating line width which indicates that the sodium ion is being exchanged between equivalent sites near the oxygens of the semiquinone with activation energies of 8.7 and 6.0 kcal/mole and Arrhenius preexponential factors of 9 x 10 to the 12th/sec and 10 to the 12th/sec, respectively. Spectra obtained for the DBC complexes show no evidence of exchange, while those of C222 indicate rapid exchange. It is also noted that the hyperfine splitting constants measured do not change over the 50-K temperature interval studied.

  6. Use of Ionic liquids as additives in ion exchange chromatography for the analysis of cations.

    Science.gov (United States)

    Di, Huawei; Zhu, Xiashi

    2017-11-01

    The behavior of acids (citric acid, nitric acid, oxalic acid, tartaric acid) as a mobile phase and imidazolium ionic liquids (the bromides, tetrafluoroborates and hexafluorophosphates of 1-ethyl, 1-butyl, and 1-hexyl-3-methylimidazolium) as additives in ion exchange chromatography for cations (Na+ , K+ , Mg2+ , Ca2+ ) separation were studied. The results showed that nitric acid and 1-hexyl-3-methyl-imidazolium hexafluorophosphate offered the most interesting features in the separation of cations, such as lower retention time and better resolution. The selected optimal conditions were achieved by adding 0.10 mM 1-hexyl-3-methyl-imidazolium hexafluorophosphate in 4.0 mM HNO3 mobile phase for the separation of four cations with the flow rate of 0.9 mL/min at room temperature (25°C). The linear regression equations of Na+ , K+ , Mg2+ , Ca2+ were S = 4.4763c + 0.0209, S = 3.8903c - 0.0087, S = 6.3974c - 0.0173, and S = 7.601c - 0.0339 and the limits of detection of Na+ , K+ , Mg2+ , Ca2+ were 0.296, 4.98, 0.0970, and 1.22 μg/L, respectively. In this work, four cations in samples were successfully detected. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Cu2Se and Cu Nanocrystals as Local Sources of Copper in Thermally Activated In Situ Cation Exchange

    KAUST Repository

    Casu, Alberto

    2016-01-27

    Among the different synthesis approaches to colloidal nanocrystals a recently developed toolkit is represented by cation exchange reactions, where the use of template nanocrystals gives access to materials that would be hardly attainable via direct synthesis. Besides, post-synthetic treatments, such as thermally activated solid state reactions, represent a further flourishing route to promote finely controlled cation exchange. Here, we report that, upon in situ heating in a transmission electron microscope, Cu2Se nanocrystals deposited on an amorphous solid substrate undergo partial loss of Cu atoms, which are then engaged in local cation exchange reactions with Cu “acceptors” phases represented by rod- and wire- shaped CdSe nanocrystals. This thermal treatment slowly transforms the initial CdSe nanocrystals into Cu2-xSe nanocrystals, through the complete sublimation of Cd and the partial sublimation of Se atoms. Both Cu “donor” and “acceptor” particles were not always in direct contact with each other, hence the gradual transfer of Cu species from Cu2Se or metallic Cu to CdSe nanocrystals was mediated by the substrate and depended on the distance between the donor and acceptor nanostructures. Differently from what happens in the comparably faster cation exchange reactions performed in liquid solution, this study shows that slow cation exchange reactions can be performed at the solid state, and helps to shed light on the intermediate steps involved in such reactions.

  8. CO 2 adsorption in mono-, di- and trivalent cation-exchanged metal-organic frameworks: A molecular simulation study

    KAUST Repository

    Chen, Yifei

    2012-02-28

    A molecular simulation study is reported for CO 2 adsorption in rho zeolite-like metal-organic framework (rho-ZMOF) exchanged with a series of cations (Na +, K +, Rb +, Cs +, Mg 2+, Ca 2+, and Al 3+). The isosteric heat and Henry\\'s constant at infinite dilution increase monotonically with increasing charge-to-diameter ratio of cation (Cs + < Rb + < K + < Na + < Ca 2+ < Mg 2+ < Al 3+). At low pressures, cations act as preferential adsorption sites for CO 2 and the capacity follows the charge-to-diameter ratio. However, the free volume of framework becomes predominant with increasing pressure and Mg-rho-ZMOF appears to possess the highest saturation capacity. The equilibrium locations of cations are observed to shift slightly upon CO 2 adsorption. Furthermore, the adsorption selectivity of CO 2/H 2 mixture increases as Cs + < Rb + < K + < Na + < Ca 2+ < Mg 2+ ≈ Al 3+. At ambient conditions, the selectivity is in the range of 800-3000 and significantly higher than in other nanoporous materials. In the presence of 0.1% H 2O, the selectivity decreases drastically because of the competitive adsorption between H 2O and CO 2, and shows a similar value in all of the cation-exchanged rho-ZMOFs. This simulation study provides microscopic insight into the important role of cations in governing gas adsorption and separation, and suggests that the performance of ionic rho-ZMOF can be tailored by cations. © 2012 American Chemical Society.

  9. Effect of blastfurnace slag addition to Portland cement for cationic exchange resins encapsulation

    Directory of Open Access Journals (Sweden)

    Stefan L.

    2013-07-01

    Full Text Available In the nuclear industry, cement-based materials are extensively used to encapsulate spent ion exchange resins (IERs before their final disposal in a repository. It is well known that the cement has to be carefully selected to prevent any deleterious expansion of the solidified waste form, but the reasons for this possible expansion are not clearly established. This work aims at filling the gap. The swelling pressure of IERs is first investigated as a function of ions exchange and ionic strength. It is shown that pressures of a few tenths of MPa can be produced by decreases in the ionic strength of the bulk solution, or by ion exchanges (2Na+ instead of Ca2+, Na+ instead of K+. Then, the chemical evolution of cationic resins initially in the Na+ form is characterized in CEM I (Portland cement and CEM III (Portland cement + blastfurnace slag cements at early age and an explanation is proposed for the better stability of CEM III material.

  10. Mechanism of improved antibody aggregate separation in polyethylene glycol-modulated cation exchange chromatography.

    Science.gov (United States)

    Kluters, Simon; Neumann, Sebastian; von Hirschheydt, Thomas; Grossmann, Adelbert; Schaubmar, Andreas; Frech, Christian

    2012-11-01

    Ion-exchange chromatography is used in biopharmaceutical downstream processes to reduce product-related impurity levels. Because protein aggregate levels can be considered as a critical quality attribute, the removal of aggregated protein species is of primary importance. The addition of polyethylene glycol (PEG) to the mobile phase in ion-exchange chromatography was found to significantly improve the chromatographic separation of monomers from aggregates. In this work, linear gradient elution experiments with monomeric and aggregated samples of a monoclonal antibody were performed on a strong cation exchange resin at different PEG concentrations to investigate the underlying effects responsible for the observed selectivity improvement. PEG is well known to be excluded from a surface layer volume around the protein and the stationary phase; thus, enhancing adsorption of the preferentially hydrated protein to the hydrated stationary phase. The exclusion volume depends on the accessible surface area of the protein leading to a stronger influence of PEG on larger protein species and thus an improved separation of monomer and aggregates. This hypothesis could be consolidated comparing the distribution equilibrium in PEG solution to that in water by calculating equilibrium constants and transfer free energies using the chromatographic data from the linear gradient elution experiments performed at different pH values. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. pH Transitions in ion-exchange systems: role in the development of a cation-exchange process for a recombinant protein.

    Science.gov (United States)

    Ghose, Sanchayita; McNerney, Thomas M; Hubbard, Brian

    2002-01-01

    Unexpected transient changes in effluent pH can occur during ion-exchange chromatography. Such changes can occur even if a column that is equilibrated with a buffer receives another solution in the same buffer and of the same pH but of a different salt concentration. An attempt is made to understand the basis for this phenomenon and apply it to the process purification of a recombinant protein on a strong cation-exchange resin. Incomplete column equilibration was eliminated as a possible cause of these effects. Various buffering species and various salt ions were studied at different solution concentrations to investigate pH transitions on strong cation-exchange resins. A further comparison was made between cation-exchange resins with different backbone chemistries. On the basis of these studies, a mechanism is proposed for these phenomena based on competitive equilibria between ions from the buffer salts and H(+)/OH(-) ions. In addition to the equilibria between these ions and the functional groups on the resins, charged groups on the resin backbone were also found to contribute to transient pH changes. The results from this study were applied to the cation-exchange step for a recombinant protein that was sensitive to pH excursions to help maintain activity of the protein during the purification process.

  12. Strong Cation Exchange Chromatography in Analysis of Posttranslational Modifications: Innovations and Perspectives

    Science.gov (United States)

    Edelmann, Mariola J.

    2011-01-01

    Strong cation exchange (SCX) chromatography has been utilized as an excellent separation technique that can be combined with reversed-phase (RP) chromatography, which is frequently used in peptide mass spectrometry. Although SCX is valuable as the second component of such two-dimensional separation methods, its application goes far beyond efficient fractionation of complex peptide mixtures. Here I describe how SCX facilitates mapping of the protein posttranslational modifications (PTMs), specifically phosphorylation and N-terminal acetylation. The SCX chromatography has been mainly used for enrichment of these two PTMs, but it might also be beneficial for high-throughput analysis of other modifications that alter the net charge of a peptide. PMID:22174558

  13. Effect of cation exchange on the subsequent reactivity of lignite chars to steam. [108 references

    Energy Technology Data Exchange (ETDEWEB)

    Hippo, E. J.; Walker, Jr., P. L.

    1977-03-01

    The purpose of this investigation is to determine the role which cations in coal play in the subsequent reactivity of chars. It is hoped that this investigation will aid in an understanding of the catalytic nature of inorganic constituents in coal during its gasification. It was found that increased heat treatment temperature decreased reactivity. The decrease in reactivity was shown to be due, at least in part, to the changes in the nature of the cation with increased heat treatment temperature. Reactivity was found to be a linear function of the amount of Ca(++) exchange on the demineralized coal. The constant utilization factor over the wide range of loadings employed indicated that below 800/sup 0/C the calcium did not markedly sinter. Potassium, sodium, and calcium-containing chars were found to be much more reactive than the iron and magnesium-containing chars. However, the iron and magnesium containing chars were more reactive than chars produced from the demineralized coal. The iron char was highly active at first but the iron phase was quickly oxidized to a comparatively unreactive ..gamma..Fe/sub 2/O/sub 3/-Fe/sub 3/O/sub 4/ phase. The state of magnesium was found to be MgO. Sodium and calcium were equally active as catalysts but not as active as potassium.

  14. Reach-scale cation exchange controls on major ion chemistry of an Antarctic glacial meltwater stream

    Science.gov (United States)

    Gooseff, Michael N.; McKnight, Diane M.; Runkel, Robert L.

    2004-01-01

    McMurdo dry valleys of Antarctica represent the largest of the ice-free areas on the Antarctic continent, containing glaciers, meltwater streams, and closed basin lakes. Previous geochemical studies of dry valley streams and lakes have addressed chemical weathering reactions of hyporheic substrate and geochemical evolution of dry valley surface waters. We examine cation transport and exchange reactions during a stream tracer experiment in a dry valley glacial meltwater stream. The injection solution was composed of dissolved Li+, Na+, K+, and Cl-. Chloride behaved conservatively in this stream, but Li+, Na+, and K+ were reactive to varying degrees. Mass balance analysis indicates that relative to Cl-, Li+ and K+ were taken up in downstream transport and Na+ was released. Simulations of conservative and reactive (first-order uptake or generation) solute transport were made with the OTIS (one-dimensional solute transport with inflow and storage) model. Among the four experimental reaches of Green Creek, solute transport simulations reveal that Li+ was removed from stream water in all four reaches, K+ was released in two reaches, taken up in one reach, and Na+ was released in all four reaches. Hyporheic sediments appear to be variable with uptake of Li+ in two reaches, uptake of K+ in one reach, release of K+ in two reaches, and uptake of Na+ in one reach. Mass balances of the conservative and reactive simulations show that from 1.05 to 2.19 moles of Li+ was adsorbed per reach, but less than 0.3 moles of K+ and less than 0.9 moles of Na+ were released per reach. This suggests that either (1) exchange of another ion which was not analyzed in this experiment or (2) that both ion exchange and sorption control inorganic solute transport. The elevated cation concentrations introduced during the experiment are typical of initial flows in each flow season, which flush accumulated dry salts from the streambed. We propose that the bed sediments (which compose the hyporheic

  15. Quantification of unsaturated-zone alteration and cation exchange in zeolitized tuffs at Yucca Mountain, Nevada, USA

    Science.gov (United States)

    Vaniman, David T.; Chipera, Steve J.; Bish, David L.; Carey, J. William; Levy, Schön S.

    2001-10-01

    Zeolitized horizons in the unsaturated zone (UZ) at Yucca Mountain, Nevada, USA, are an important component in concepts for a high-level nuclear waste repository at this site. The use of combined quantitative X-ray diffraction and geochemical analysis allows measurement of the chemical changes that accompanied open-system zeolitization at Yucca Mountain. This approach also provides measures of the extent of chemical migration that has occurred in these horizons as a result of subsequent cation exchange. Mass-balance analysis of zeolitized horizons with extensive cation exchange (drill hole UZ-16) and with only minimal cation exchange (drill hole SD-9) shows that Al is essentially immobile. Although zeolitization occurred in an open system, the mass transfer of constituents other than water is relatively small in initial zeolitization, in contrast to the larger scales of cation exchange that can occur after zeolites have formed. Cation exchange in the clinoptilolite ± mordenite zeolitized horizons is seen in downward-diminishing concentration gradients of Ca, Mg, and Sr exchanged for Na and (to lesser extent) K. Comparison with data from drill hole SD-7, which has multiple zeolitized horizons above the water table, shows that the upper horizons accumulate Ca, Mg, and Sr to such an extent that transport of these elements to the deepest UZ zeolitized horizon can be blocked. Quantitative analysis of zeolite formation yields insight into processes that are implied from laboratory studies and modeling efforts but are otherwise unverified at the site. Such analysis also yields information not provided by or contradicted by some models of flow and transport. The results include the following: (1) evidence of effective downward flow through zeolitic horizons despite the low permeability of these horizons, (2) evidence that alkaline-earth elements accumulated by zeolites are mostly derived from eolian materials in surface soils, (3) validation of the very effective

  16. Anion- or Cation-Exchange Membranes for NaBH4/H2O2 Fuel Cells?

    Science.gov (United States)

    Sljukić, Biljana; Morais, Ana L; Santos, Diogo M F; Sequeira, César A C

    2012-07-19

    Direct borohydride fuel cells (DBFC), which operate on sodium borohydride (NaBH4) as the fuel, and hydrogen peroxide (H2O2) as the oxidant, are receiving increasing attention. This is due to their promising use as power sources for space and underwater applications, where air is not available and gas storage poses obvious problems. One key factor to improve the performance of DBFCs concerns the type of separator used. Both anion- and cation-exchange membranes may be considered as potential separators for DBFC. In the present paper, the effect of the membrane type on the performance of laboratory NaBH4/H2O2 fuel cells using Pt electrodes is studied at room temperature. Two commercial ion-exchange membranes from Membranes International Inc., an anion-exchange membrane (AMI-7001S) and a cation-exchange membrane (CMI-7000S), are tested as ionic separators for the DBFC. The membranes are compared directly by the observation and analysis of the corresponding DBFC's performance. Cell polarization, power density, stability, and durability tests are used in the membranes' evaluation. Energy densities and specific capacities are estimated. Most tests conducted, clearly indicate a superior performance of the cation-exchange membranes over the anion-exchange membrane. The two membranes are also compared with several other previously tested commercial membranes. For long term cell operation, these membranes seem to outperform the stability of the benchmark Nafion membranes but further studies are still required to improve their instantaneous power load.

  17. Pectin–Tin(IV molybdosilicate: An ecofriendly cationic exchanger and its potential for sorption of heavy metals from aqueous solutions

    Directory of Open Access Journals (Sweden)

    Nimisha K. V

    2016-12-01

    Full Text Available A novel composite cation exchanger of biopolymer Pectin and Tin(IV molybdosilicate heteropoly acid salt were prepared by co-precipitation technique. Physico-chemical characterization of Pectin–Tin(IV molybdosilicate was performed using instrumental techniques such as FTIR, TG, XRD and SEM–EDS. Studies were carried out to investigate ion exchange capacity. pH titration carried out shows cationic nature and polyfunctionality of the exchanger. Distribution coefficients of various metal ions were done to explore the ion exchange behavior of cation exchanger. Distribution studies show that the material is highly selective for toxic heavy metal ions such as Cd2+, Cu2+, Al3+ etc. To investigate the environmental applicability of the exchanger some analytically important binary separations and selective separation of metal ions from industrial effluents were achieved. Kinetic and isotherm parameters were evaluated to predict the mechanism of sorption of heavy metal ions. Mass transfer analysis shows that internal particle diffusion and some degree of boundary layer control the sorption process.

  18. High-throughput protein purification under denaturating conditions by the use of cation exchange chromatography.

    Science.gov (United States)

    Alm, Tove; Steen, Johanna; Ottosson, Jenny; Hober, Sophia

    2007-06-01

    A high-throughput protein purification strategy using the polycationic Z(basic) tag has been developed. In order for the strategy to be useful both for soluble and less soluble proteins, a denaturating agent, urea, was used in all purification steps. First, four target proteins were genetically fused to the purification tag, Z(basic). These protein constructs were purified by cation exchange chromatography and eluted using a salt gradient. From the data achieved, a purification strategy was planned including stepwise elution to enable parallel protein purification using a laboratory robot. A protocol that includes all steps, equilibration of the chromatography resin, load of sample, wash, and elution, all without any manual handling steps, was handled by the laboratory robot. The program allows automated purification giving milligram amounts of pure recombinant protein of up to 60 cell lysates. In this study 22 different protein constructs, with different characteristics regarding pI and solubility, were successfully purified by the laboratory robot. The data show that Z(basic) can be used as a general purification tag also under denaturating conditions. Moreover, the strategy enables purification of proteins with different pI and solubility using ion exchange chromatography (IEXC). The procedure is highly reproducible and allows for high protein yield and purity and is therefore a good complement to the commonly used His(6)-tag.

  19. Ion transport resistance in Microbial Electrolysis Cells with anion and cation exchange membranes

    Energy Technology Data Exchange (ETDEWEB)

    Sleutels, Tom H.J.A.; Buisman, Cees J.N. [Sub-Department of Environmental Technology, Wageningen University, Bomenweg 2, P.O. Box 8129, 6700 EV Wageningen (Netherlands); Wetsus, Centre of Excellence for Sustainable Water Technology, Agora 1, P.O. Box 1113, 8900 CC Leeuwarden (Netherlands); Hamelers, Hubertus V.M. [Sub-Department of Environmental Technology, Wageningen University, Bomenweg 2, P.O. Box 8129, 6700 EV Wageningen (Netherlands); Rozendal, Rene A. [Advanced Water Management Centre (AWMC), The University of Queensland, Qld 4072 (Australia)

    2009-05-15

    Previous studies have shown that Microbial Electrolysis Cells (MECs) perform better when an anion exchange membrane (AEM) than when a cation exchange membrane (CEM) separates the electrode chambers. Here, we have further studied this phenomenon by comparing two analysis methods for bio-electrochemical systems, based on potential losses and partial system resistances. Our study reconfirmed the large difference in performance between the AEM configuration (2.1 m{sup 3} H{sub 2} m{sup -3} d{sup -1}) and CEM configuration (0.4 m{sup 3} H{sub 2} m{sup -3} d{sup -1}) at 1 V. This better performance was caused mainly by the much lower internal resistance of the AEM configuration (192 m{omega} m{sup 2}) compared to the CEM configuration (435 m{omega} m{sup 2}). This lower internal resistance could be attributed to the lower transport resistance of ions through the AEM compared to the CEM caused by the properties of both membranes. By analyzing the changes in resistances the limitations in an MEC can be identified which can lead to improved cell design and higher hydrogen production rates. (author)

  20. Estimating Soil Cation Exchange Capacity from Soil Physical and Chemical Properties

    Science.gov (United States)

    Bateni, S. M.; Emamgholizadeh, S.; Shahsavani, D.

    2014-12-01

    The soil Cation Exchange Capacity (CEC) is an important soil characteristic that has many applications in soil science and environmental studies. For example, CEC influences soil fertility by controlling the exchange of ions in the soil. Measurement of CEC is costly and difficult. Consequently, several studies attempted to obtain CEC from readily measurable soil physical and chemical properties such as soil pH, organic matter, soil texture, bulk density, and particle size distribution. These studies have often used multiple regression or artificial neural network models. Regression-based models cannot capture the intricate relationship between CEC and soil physical and chemical attributes and provide inaccurate CEC estimates. Although neural network models perform better than regression methods, they act like a black-box and cannot generate an explicit expression for retrieval of CEC from soil properties. In a departure with regression and neural network models, this study uses Genetic Expression Programming (GEP) and Multivariate Adaptive Regression Splines (MARS) to estimate CEC from easily measurable soil variables such as clay, pH, and OM. CEC estimates from GEP and MARS are compared with measurements at two field sites in Iran. Results show that GEP and MARS can estimate CEC accurately. Also, the MARS model performs slightly better than GEP. Finally, a sensitivity test indicates that organic matter and pH have respectively the least and the most significant impact on CEC.

  1. Surface modification of cation exchange membranes by graft polymerization of PAA-co-PANI/MWCNTs nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Nemati, Mahsa; Hosseini, Sayed Mohsen; Bagheripour, Ehsan [Faculty of Engineering, Arak University, Arak (Iran, Islamic Republic of); Madaeni, Sayed Siavash [Faculty of Engineering, Razi University, Kermanshah (Iran, Islamic Republic of)

    2016-03-15

    Surface modification of polyvinylchloride based heterogeneous cation exchange membrane was performed by graft polymerization of PAA and PAA-co-PANI/MWCNTs nanoparticles. The ion exchange membranes were prepared by solution casting technique. Spectra analysis confirmed graft polymerization clearly. SEM images illustrated that graft polymerization covers the membranes by simple gel network entanglement. The membrane water content was decreased by graft polymerization of PAA-co-PANI/MWCNTs nanoparticles on membrane surface. Membrane transport number and selectivity declined initially by PAA graft polymerization and then began to increase by utilizing of composite nanoparticles in modifier solution. The sodium and barium flux was improved sharply by PAA and PAAco- 0.01%wt PANI/MWCNTs graft polymerization on membrane surface and then decreased again by more increase of PANI/MWCNTs nanoparticles content ratio in modifier solution. The electrodialysis experiment results in laboratory scale showed higher dialytic rate in heavy metals removal for grafted-PAA and grafted-PAA-co-PANI/MWCNTs modified membrane compared to pristine one. Membrane areal electrical resistance was also decreased by introducing graft polymerization of PAA and PAA-co-PANI/MWCNTs NPs on membrane surface.

  2. Synthesis of granular zeolitic materials with high cation exchange capacity from agglomerated coal fly ash

    Energy Technology Data Exchange (ETDEWEB)

    Roberto Juan; Susana Hernandez; Jose Manuel Andres; Carmen Ruiz [Instituto de Carboquimica (CSIC), Zaragoza (Spain)

    2007-08-15

    Fly ash from coal combustion is a potential source of pollution and there is continuous interest in its recycling by converting it into products such as zeolitic materials for use in retaining pollutants. In this paper, production of granular zeolitic material from a commercially-unusable fine-fraction of a lightweight aggregate (LA) building material made from coal fly ash agglomerated with lime, by conventional alkaline activation is described. NaP1 zeolite, K-F zeolite, K-Phillipsite and K-Chabazite were synthesised. The process was optimised by combining four reaction parameters (temperature, alkali concentration, solution/fly ash ratio and reaction time). Zeolitic materials with the highest zeolite yields and cation exchange capacities were selected for future application in environmental processes. End-product zeolitic materials maintain its granular form and this could favour their use in some particular applications for environmental waste treatment (e.g. ionic exchange in column) without any further transformation stages. 21 refs., 6 figs., 6 tabs.

  3. Ultrathin Sicopion Composite Cation-Exchange Membranes: Characteristics and Electrodialytic Performance following a Conditioning Procedure

    Directory of Open Access Journals (Sweden)

    Erik Ayala-Bribiesca

    2012-01-01

    Full Text Available The aim of this work was to investigate the properties of Sicopion membranes: an ultrathin (≈20 μm composite cation-exchange membrane (CEM made from sulphonated poly(ether-ether-ketone (SPEEK containing different levels of sulphonic-functionalized silica particles (SFSPs. Sicopion membranes were conditioned according to the French Normalization Association procedure, consisting in a series of acid and alkaline washes, and their electrodialytic characteristics were compared to an existent commercial food-grade membrane (CMX-SB. Electrical conductivity of Sicopion membranes was higher than that of CMX-SB membranes (9.92 versus 6.98 mS/cm, as well as their water content (34.0 versus 27.6%. As the SFSP level was reduced, the ion-exchange capacity (IEC of Sicopion membranes increased. Concerning their electrodialytic performances, Sicopion membranes presented a lower demineralization rate than CMX-SB membranes (35.9 versus 45.5%, due to an OH− leakage through the pores created by dislodging the SFSP particles during the conditioning procedure.

  4. Simultaneous isolation of lactoferrin and lactoperoxidase from bovine colostrum by SPEC 70 SLS cation exchange resin.

    Science.gov (United States)

    Liang, Yafei; Wang, Xuewan; Wu, Mianbin; Zhu, Wanping

    2011-09-01

    In this work, simultaneous isolation of lactoferrin (Lf) and lactoperoxidase (Lp) from defatted bovine colostrum by one-step cation exchange chromatography with SPEC 70 SLS ion-exchange resin was investigated. A RP-HPLC method for Lf and Lp determination was developed and optimized as the following conditions: detection wavelength of 220 nm, flow rate of 1 mL/min and acetonitrile concentration from 25% to 75% within 20 min. The adsorption process of Lf on SPEC 70 SLS resin was optimized using Lf standard as substrate. The maximum static binding capacity of SPEC 70 SLS resin was of 22.0 mg/g resin at 15 °C, pH 7.0 and adsorption time 3 h. The Lf adsorption process could be well described by the Langmuir adsorption isotherm model, with a maximum adsorption capacity of 21.73 mg/g resin at 15 °C. In batch fractionation of defatted colostrum, the binding capacities of SPEC 70 SLS resin for adsorbing Lf and Lp simultaneously under the abovementioned conditions were 7.60 and 6.89 mg/g resin, respectively, both of which were superior to those of CM Sepharose F.F. or SP Sepharose F.F. resins under the same conditions. As a result, SPEC 70 SLS resin was considered as a successful candidate for direct and economic purification of Lf and Lp from defatted colostrum.

  5. Simultaneous Isolation of Lactoferrin and Lactoperoxidase from Bovine Colostrum by SPEC 70 SLS Cation Exchange Resin

    Directory of Open Access Journals (Sweden)

    Mianbin Wu

    2011-09-01

    Full Text Available In this work, simultaneous isolation of lactoferrin (Lf and lactoperoxidase (Lp from defatted bovine colostrum by one-step cation exchange chromatography with SPEC 70 SLS ion-exchange resin was investigated. A RP-HPLC method for Lf and Lp determination was developed and optimized as the following conditions: detection wavelength of 220 nm, flow rate of 1 mL/min and acetonitrile concentration from 25% to 75% within 20 min. The adsorption process of Lf on SPEC 70 SLS resin was optimized using Lf standard as substrate. The maximum static binding capacity of SPEC 70 SLS resin was of 22.0 mg/g resin at 15 °С, pH 7.0 and adsorption time 3 h. The Lf adsorption process could be well described by the Langmuir adsorption isotherm model, with a maximum adsorption capacity of 21.73 mg/g resin at 15 °С. In batch fractionation of defatted colostrum, the binding capacities of SPEC 70 SLS resin for adsorbing Lf and Lp simultaneously under the abovementioned conditions were 7.60 and 6.89 mg/g resin, respectively, both of which were superior to those of CM Sepharose F.F. or SP Sepharose F.F. resins under the same conditions. As a result, SPEC 70 SLS resin was considered as a successful candidate for direct and economic purification of Lf and Lp from defatted colostrum.

  6. Effects of Acetate on Cation Exchange Capacity of a Zn-Containing Montmorillonite : Physicochemical Significance and Metal Uptake

    NARCIS (Netherlands)

    Stathi, P.; Papadas, I. T.; Enotiadis, A.; Gengler, R. Y. N.; Gournis, D.; Rudolf, P.; Deligiannakis, Y.

    2009-01-01

    Fundamental properties such as cation exchange capacity (CEC), permanent charge, pH(PZC), and metal uptake of a Zn-containing montmorillonite are modified, in a predictable manner, by a mild chemical treatment using acetate. Acetate treatment allows a controllable increase of the CEC of

  7. Cation-exchange high-performance liquid chromatography: Separation of highly basic proteins using volatile acidic solvents

    NARCIS (Netherlands)

    Eijnden-van Raaij, A.J.M. van den; Koornneef, I.; Oostwaard, Th.M.J.; Laat, S.W. de; Zoelen, E.J.J. van

    1987-01-01

    The chromatographic behavior of a number of globular proteins was studied on a Bio-Sil TSK CM-2-SW weak cation exchange HPLC column under acidic conditions. A linear gradient of O-I M NH₄Ac in I M HOAc, inducing a convex pH gradient from 2.4-4.8, resulted in an excellent separation of highly

  8. Preparation and characterization of monovalent ion selective cation exchange membranes based on sulphonated poly(ether ether ketone)

    NARCIS (Netherlands)

    Balster, J.H.; Krupenko, O.; Krupenko, O.; Punt, Ineke G.M.; Stamatialis, Dimitrios; Wessling, Matthias

    2005-01-01

    This paper analyses the separation properties of various commercial cation exchange membranes (CEMs) and tailor made membranes based on sulphonated poly(ether ether ketone) and poly(ether sulphone) for binary electrolyte solutions containing protons and calcium ions. All membranes are thoroughly

  9. Luminescent CuInS2 quantum dots by partial cation exchange in Cu2- xS nanocrystals

    NARCIS (Netherlands)

    Van Der Stam, Ward; Berends, Anne C.; Rabouw, Freddy T.; Willhammar, Tom; Ke, Xiaoxing; Meeldijk, Johannes D.; Bals, Sara; De Mello Donega, Celso

    2015-01-01

    Here, we show successful partial cation exchange reactions in Cu2-xS nanocrystals (NCs) yielding luminescent CuInS2 (CIS) NCs. Our approach of mild reaction conditions ensures slow Cu extraction rates, which results in a balance with the slow In incorporation rate. With this method, we obtain CIS

  10. Improving pH gradient cation-exchange chromatography of monoclonal antibodies by controlling ionic strength.

    Science.gov (United States)

    Zhang, Liangyi; Patapoff, Thomas; Farnan, Dell; Zhang, Boyan

    2013-01-11

    Analytical ion exchange chromatography (IEC) is widely used to profile the charge heterogeneity of therapeutic monoclonal antibodies (mAbs). Since conventional salt gradient IEC methods are product-specific and time-consuming to develop, a previously reported alternative pH gradient IEC (pH-IEC) method using a cation-exchange column has been shown to be a multiproduct charge sensitive separation method for mAbs with isoelectric points between 7.3 and 9.0. In the work presented here, we have extended the application of that pH-IEC method to also profile the charge heterogeneity of mAbs with extreme pI values (e.g. acidic with pI9). A key observation of our work is that for the buffer systems used by Farnan and Moreno, the ionic strength of the mobile phase containing multiple polyamine buffers is pH and concentration dependent, and the ionic strength decreases when the pH increases. For the mobile phase with high buffer concentration the ionic strength is high at low pH values, leading to the flow through of acidic mAbs on the cation-exchange column. The basic mAbs may not have an optimal elution profile as the relatively low ionic strength of the mobile phase reduces the resolution of pH-IEC. To modulate the ionic strength, we introduced a salt gradient in addition to the pH gradient. Studies were performed to optimize the buffer and salt concentrations simultaneously to improve the retention of low pI mAbs and the resolution of high pI mAbs. The optimized salt-mediated pH-IEC method was not only applicable to mAbs over a broader pI range from 6.2 to 9.4, but also offered better resolution for mAbs with pI values between 7.3 and 9.0 than the previously reported pH-IEC method. This salt-mediated pH-IEC method was demonstrated to be robust at various chromatography conditions and capable of assessing manufacturing consistency and monitoring degradation of mAbs. Copyright © 2012 Elsevier B.V. All rights reserved.

  11. Concentration dependence of cation-induced electrohydrodynamic flow passing through an anion exchange membrane

    Science.gov (United States)

    Yano, Ayako; Shirai, Hiroki; Imoto, Moino; Doi, Kentaro; Kawano, Satoyuki

    2017-09-01

    Electrohydrodynamic (EHD) flow is a type of liquid flow driven by an external electric force. In electrolyte solutions, anions and cations usually interact with each other to maintain electroneutrality. Under such a condition, it is difficult to drive a liquid flow by applying electric potentials on the order of 1 V; at least a few tens of volts is required to generate EHD flows, which may not be preferable for aqueous solutions. In this study, we propose a novel method of generating a liquid flow through a channel with cross-sectional dimensions of 1 × 1 mm2, which is placed in an ion exchange membrane to separate the cation and anion transport pathways. When the optimized design of the experimental apparatus was used, EHD flows were successfully generated in aqueous solutions by applying a relatively low electric potential of 2.2 V, and the flow velocity was measured over a wide range of electrolyte concentrations by particle image velocimetry. It was found that high concentration gradients caused the rapid discharge of ions passing through the channel and contributed to achieving a flow speed on the order of 1 mm/s. EHD flows were also theoretically explained using the Navier-Stokes equations to model an ion-drag flow driven by nonequilibrium ion transport in external electric fields. This flow generation method is practical only when ion transport pathways are well controlled and effectively rectified. The present findings will lead to the development of a promising technology to control liquid flows in multiscale fluidic channels.

  12. Influence of Sulfonated-Kaolin On Cationic Exchange Capacity Swelling Degree and Morphology of Chitosan/Kaolin Composites

    Directory of Open Access Journals (Sweden)

    Ozi Adi Saputra

    2016-06-01

    Full Text Available Preparation of sulfonated-kaolin (sKao has been conducted and used as filler on chitosan matrix via solution casting method, namely chitosan/sKao (Cs/sKao. Swelling degree, cationic exchange capacity and thermal stability were evaluated to determine chitosan/sKao membranes performance as proton exchange membrane in fuel cell. Functional group analysis of chitosan, sKao and synthesized products were studied using Fourier Transform Infra-Red (FTIR spectroscopy. In this study, swelling degree and swelling area of Cs/sKao are also studied to determine of membrane ability to swelling which compare to unmodified chitosan/kaolin (Cs/Kao. The presence of sKao in chitosan matrix was able to improve cationic exchange capacity (CEC which proved by morphological study of membrane surface after CEC test. Moreover, Thermal stability of Cs/sKao showed the membrane has meet requirement for PEM application.

  13. On the Structure-Property Relationships of Cation-Exchanged ZK-5 Zeolites for CO2 Adsorption.

    Science.gov (United States)

    Pham, Trong D; Hudson, Matthew R; Brown, Craig M; Lobo, Raul F

    2017-03-09

    The CO2 adsorption properties of cation-exchanged Li-, Na-, K-, and Mg-ZK-5 zeolites were correlated to the molecular structures determined by Rietveld refinements of synchrotron powder X-ray diffraction patterns. Li-, K-, and Na-ZK-5 all exhibited high isosteric heats of adsorption (Qst ) at low CO2 coverage, with Na-ZK-5 having the highest Qst (ca. 49 kJ mol(-1) ). Mg(2+) was located at the center of the zeolite hexagonal prism with the cation inaccessible to CO2 , leading to a much lower Qst (ca. 30 kJ mol(-1) ) and lower overall uptake capacity. Multiple CO2 adsorption sites were identified at a given CO2 loading amount for all four cation-exchanged ZK-5 adsorbents. Site A at the flat eight-membered ring windows and site B/B* in the γ-cages were the primary adsorption sites in Li- and Na-ZK-5 zeolites. Relatively strong dual-cation adsorption sites contributed significantly to an enhanced electrostatic interaction for CO2 in all ZK-5 samples. This interaction gives rise to a migration of Li(+) and Mg(2+) cations from their original locations at the center of the hexagonal prisms toward the α-cages, in which they interact more strongly with the adsorbed CO2 . © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. Cation-exchanged SAPO-34 for adsorption-based hydrocarbon separations: predictions from dispersion-corrected DFT calculations.

    Science.gov (United States)

    Fischer, Michael; Bell, Robert G

    2014-10-21

    The influence of the nature of the cation on the interaction of the silicoaluminophosphate SAPO-34 with small hydrocarbons (ethane, ethylene, acetylene, propane, propylene) is investigated using periodic density-functional theory calculations including a semi-empirical dispersion correction (DFT-D). Initial calculations are used to evaluate which of the guest-accessible cation sites in the chabazite-type structure is energetically preferred for a set of ten cations, which comprises four alkali metals (Li(+), Na(+), K(+), Rb(+)), three alkaline earth metals (Mg(2+), Ca(2+), Sr(2+)), and three transition metals (Cu(+), Ag(+), Fe(2+)). All eight cations that are likely to be found at the SII site (centre of a six-ring) are then included in the following investigation, which studies the interaction with the hydrocarbon guest molecules. In addition to the interaction energies, some trends and peculiarities regarding the adsorption geometries are analysed, and electron density difference plots obtained from the calculations are used to gain insights into the dominant interaction types. In addition to dispersion interactions, electrostatic and polarisation effects dominate for the main group cations, whereas significant orbital interactions are observed for unsaturated hydrocarbons interacting with transition metal (TM) cations. The differences between the interaction energies obtained for pairs of hydrocarbons of interest (such as ethylene-ethane and propylene-propane) deliver some qualitative insights: if this energy difference is large, it can be expected that the material will exhibit a high selectivity in the adsorption-based separation of alkene-alkane mixtures, which constitutes a problem of considerable industrial relevance. While the calculations show that TM-exchanged SAPO-34 materials are likely to exhibit a very high preference for alkenes over alkanes, the strong interaction may render an application in industrial processes impractical due to the large amount

  15. A new semi-empirical kinetic method for the determination of ion exchange constants for the counterions of cationic micelles.

    Science.gov (United States)

    Khan, M Niyaz

    2010-09-15

    A new method, based upon semi-empirical kinetic approach, for the determination of ion exchange constant for ion exchange processes occurring between counterions at the cationic micellar surface is described in this review article. Basically, the method involves a reaction kinetic probe which gives observed pseudo-first-order rate constants (k(obs)) for a nucleophilic substitution reaction between the nonionic and anionic reactants (R and S) in the presence of a constant concentration of both reactants as well as cationic micelles and varying concentrations of an inert inorganic or organic salt (MX). The observed data (k(obs), versus [MX]) fit satisfactorily (in terms of residual errors) to an empirical equation which could be derived from an equation explaining the mechanism of the reaction of the kinetic probe in terms of pseudophase micellar (PM) model coupled with another empirical equation. This (another) empirical equation explains the effect of [MX] on cationic micellar binding constant (K(S)) of the anionic reactant (say S) and gives an empirical constant, K(X/S). The magnitude of K(X/S) is the measure of the ability of X(-) to expel S(-) from a cationic micellar pseudophase to the bulk aqueous phase through ion exchange X(-)/S(-). The values of K(X/S) and K(Y/S) (where Y(-) is another inert counterion) give the ion exchange constant, K(X)(Y) (=K(X)/K(Y) where K(X) and K(Y) represent cationic micellar binding constants of X(-) and Y(-), respectively). The suitability of this method is demonstrated by the use of three different reaction kinetic probes and various MX. Copyright 2010 Elsevier B.V. All rights reserved.

  16. Cationic Polymerization of 1,2-Epoxypropane by an Acid Exchanged Montmorillonite Clay in the Presence of Ethylene Glycol

    Directory of Open Access Journals (Sweden)

    Aïcha Hachemaoui

    2003-10-01

    Full Text Available Abstract: The polymerization of propylene oxide (PO catalysed by maghnite-H+ (mag-H+ in the presence of ethylene glycol was investigated. Mag-H+ is a montmorillonite silicate sheet clay was prepared through a straight forward proton exchange process. It was found that the cationic polymerization of PO was initiated by mag-H+ at 20 °C both in bulk and in solution. The effect of the amount of mag-H+ and solvent was studied. These results indicated the cationic nature of the polymerization A possible initiation pathway, via the transfer of protons from mag-H+ to the monomer, is proposed.

  17. Nitrogen removal from wastewater through microbial electrolysis cells and cation exchange membrane

    Science.gov (United States)

    2014-01-01

    Vulnerability of water resources to nutrients led to progressively stricter standards for wastewater effluents. Modification of the conventional procedures to meet the new standards is inevitable. New technologies should give a priority to nitrogen removal. In this paper, ammonium chloride and urine as nitrogen sources were used to investigate the capacity of a microbial electrolysis cell (MEC) configured by cation exchange membrane (CEM) for electrochemical removal of nitrogen over open-and closed-circuit potentials (OCP and CCP) during biodegradation of organic matter. Results obtained from this study indicated that CEM was permeable to both organic and ammonium nitrogen over OCP. Power substantially mediated ammonium migration from anodic wastewater to the cathode, as well. With a urine rich wastewater in the anode, the maximum rate of ammonium intake into the cathode varied from 34.2 to 40.6 mg/L.h over CCP compared to 10.5-14.9 mg/L.h over OCP. Ammonium separation over CCP was directly related to current. For 1.46-2.12 mmol electron produced, 20.5-29.7 mg-N ammonium was removed. Current also increased cathodic pH up to 12, a desirable pH for changing ammonium ion to ammonia gas. Results emphasized the potential for MEC in control of ammonium through ammonium separation and ammonia volatilization provided that membrane characteristic is considered in their development. PMID:24533446

  18. Mineral carbonation of gaseous carbon dioxide using a clay-hosted cation exchange reaction.

    Science.gov (United States)

    Kang, Il-Mo; Roh, Ki-Min

    2013-01-01

    The mineral carbonation method is still a challenge in practical application owing to: (1) slow reaction kinetics, (2) high reaction temperature, and (3) continuous mineral consumption. These constraints stem from the mode of supplying alkaline earth metals through mineral acidification and dissolution. Here, we attempt to mineralize gaseous carbon dioxide into calcium carbonate, using a cation exchange reaction of vermiculite (a species of expandable clay minerals). The mineralization is operated by draining NaCI solution through vermiculite powders and continuously dropping into the pool of NaOH solution with CO2 gas injected. The mineralization temperature is regulated here at 293 and 333 K for 15 min. As a result of characterization, using an X-ray powder diffractometer and a scanning electron microscopy, two types of pure CaCO3 polymorphs (vaterite and calcite) are identified as main reaction products. Their abundance and morphology are heavily dependent on the mineralization temperature. Noticeably, spindle-shaped vaterite, which is quite different from a typical vaterite morphology (polycrystalline spherulite), forms predominantly at 333 K (approximately 98 wt%).

  19. Facile and green fabrication of cation exchange membrane adsorber with unprecedented adsorption capacity for protein purification.

    Science.gov (United States)

    Khan, M Kamran; Luo, Jianquan; Khan, Rashid; Fan, Jinxin; Wan, Yinhua

    2017-10-27

    Fabricating membrane adsorbers with high adsorption capacity and appreciable throughput for the separation and purification of protein products is challenging in biomedical and pharmaceutical industries. Herein, we report the synthesis of a novel membrane adsorber by functionalizing a nylon microfiltration membrane with alginate dialdehyde (ADA) followed by sulphonic addition, without any solvent usage, and its successful application in the purification of lysozyme. Taking advantage of abundant dual cation exchange (CEX) groups on sulphonic-ADA (S-ADA) ligands, this novel S-ADA-nylon membrane adsorber showed an unprecedented static binding capicity of 286mg/mL for lysozyme adsorption. Meanwhile, the prepared membrane adsorber could be easily regenerated (complete protein elution) under mild conditions and be reused at least for five times. Featured with a unique selectivity, the S-ADA-nylon membrane also captured lysozyme from chicken egg white solution with a high purity (100%) and a high recovery of 98%. The purified lysozyme showed similar specific activity as commercial product. The present work provides a facile, green and low-cost approach for the preparation of high-performance membrane adsorbers, which has a great potential in protein production. Copyright © 2017 Elsevier B.V. All rights reserved.

  20. Design of a strong cation exchange methodology for the evaluation of charge heterogeneity in glatiramer acetate.

    Science.gov (United States)

    Campos-García, Víctor R; López-Morales, Carlos A; Benites-Zaragoza, Eleuterio; Jiménez-Miranda, Armando; Espinosa-de la Garza, Carlos E; Herrera-Fernández, Daniel; Padilla-Calderón, Jesús; Pérez, Néstor O; Flores-Ortiz, Luis F; Medina-Rivero, E

    2017-01-05

    Complex pharmaceuticals are in demand of competent analytical methods able to analyze charge heterogeneity as a critical quality attribute (CQA), in compliance with current regulatory expectations. A notorious example is glatiramer acetate (GA), a complex polypeptide mixture useful for the treatment of relapsing-remitting multiple sclerosis. This pharmaceutical challenges the current state of analytical technology in terms of the capacity to study their constituent species. Thus, a strong cation exchange methodology was designed under the lifecycle approach to support the establishment of GA identity, trough the evaluation of its chromatographic profile, which acts as a charge heterogeneity fingerprint. In this regard, a maximum relative margin of error of 5% for relative retention time and symmetry factor were proposed for the analytical target profile. The methodology met the proposed requirements after precision and specificity tests results, the former comprised of sensitivity and selectivity. Subsequently, method validation was conducted and showed that the method is able to differentiate between intact GA and heterogeneity profiles coming from stressed, fractioned or process-modified samples. In summary, these results provide evidence that the method is adequate to assess charge heterogeneity as a CQA of this complex pharmaceutical. Copyright © 2016 Elsevier B.V. All rights reserved.

  1. Effect of temperature on quantifying glycated (glycosylated) hemoglobin by cation-exchange chromatography.

    Science.gov (United States)

    Flückiger, R; Woodtli, T

    1985-01-01

    As a consequence of nonideal chromatographic conditions, values for stable glycated hemoglobin (HbA1c) determined by cation-exchange chromatography in a commercial minicolumn system (y) or by "high-performance" liquid chromatography (x) differ markedly, yielding the regression line y = 0.82x + 0.6. With use of the protocol specified by the manufacturer, 20% of the HbA1c peak is not collected in the HbA1c fraction. Increasing the ionic strength of the eluting buffer by increasing the operating temperature to 28 degrees C increases the rate of elution from the minicolumn, making results of the two methods more closely comparable (y = 0.98x - 0.22). Because at a given pH the elution volume is determined primarily by the ionic strength, close limits on the composition of the eluting buffer are set by the temperature-dependence of its ionic strength. At a specified temperature and pH the position of a peak can be judged to within a volume of 1 mL if the conductivity of the eluent does not vary by more than +/- 0.05 mS.

  2. Modeling cation exchange capacity and soil water holding capacity from basic soil properties

    Directory of Open Access Journals (Sweden)

    Idowu Olorunfemi

    2016-10-01

    Full Text Available Cation exchange capacity (CEC is a good indicator of soil productivity and is useful for making recommendations of phosphorus, potassium, and magnesium for soils of different textures. Soil water holding capacity (SWHC defines the ability of a soil to hold water at a particular time of the season. This research predicted CEC and SWHC of soils using pedotransfer models developed (using Minitab 17 statistical software from basic soil properties (Sand(S, Clay(C, soil pH, soil organic carbon (SOC and verify the model by comparing the relationship between measured and estimated (obtained by PTFs CEC and SWHC in the Forest Vegetative Zone of Nigeria. For this study, a total of 105 sampling points in 35 different locations were sampled in the study areas. Three sampling points were randomly selected per location and three undisturbed samples were collected at each sampling point. The results showed success in predicting CEC and SWHC from basic soil properties. In this study, five linear regression models for predicting soil CEC and seven linear regression models for predicting SWHC from some soil physical and chemical properties were suggested. Model 5 [CEC = -13.93+2.645 pH +0.0446 C (%+2.267 SOC (%] was best for predicting CEC while model 12 [SWHC (%=36.0- 0.215 S (%+0.113 C (%+10.36 SOC (%] is the most acceptable model for predicting SWHC.

  3. Predicting cation exchange capacity from hygroscopic moisture in agricultural soils of Western Europe

    Energy Technology Data Exchange (ETDEWEB)

    Torrent, J.; Campillo, M.C. del; Barrón, V.

    2015-07-01

    Soil cation exchange capacity (CEC) depends on the extent and negative charge density of surfaces of soil mineral and organic components. Soil water sorption also depends on the extent of such surfaces, giving thus way to significant relationships between CEC and hygroscopic moisture (HM) in many soils. In this work, we explored whether CEC could be accurately predicted from HM in agricultural soils of Mediterranean and humid temperate areas in Western Europe. For this purpose, we examined 243 soils across a wide variation range of their intrinsic properties. Soil CEC was determined using 1 M ammonium acetate at pH 7 and HM at an equilibrium air relative humidity (RH) of 43% (HM43). Most of the variation of soil CEC was explained by HM43 through a linear function (CEC = 1.4 + 0.78HM43; R2 = 0.962; standard deviation = 2.30 cmolc/kg). Coefficients of the regression equation were similar for subgroups of soils differing in moisture regime, clay mineralogy, carbonate content and organic carbon content. Therefore, soil hygroscopic moisture measurements at a fixed RH level provided a simple, robust, inexpensive method for predicting soil CEC. (Author)

  4. Short communication: Predicting cation exchange capacity from hygroscopic moisture in agricultural soils of Western Europe

    Directory of Open Access Journals (Sweden)

    José Torrent

    2015-12-01

    Full Text Available Soil cation exchange capacity (CEC depends on the extent and negative charge density of surfaces of soil mineral and organic components. Soil water sorption also depends on the extent of such surfaces, giving thus way to significant relationships between CEC and hygroscopic moisture (HM in many soils. In this work, we explored whether CEC could be accurately predicted from HM in agricultural soils of Mediterranean and humid temperate areas in Western Europe. For this purpose, we examined 243 soils across a wide variation range of their intrinsic properties. Soil CEC was determined using 1 M ammonium acetate at pH 7 and HM at an equilibrium air relative humidity (RH of 43% (HM43. Most of the variation of soil CEC was explained by HM43 through a linear function (CEC = 1.4 + 0.78HM43; R2 = 0.962; standard deviation = 2.30 cmolc/kg. Coefficients of the regression equation were similar for subgroups of soils differing in moisture regime, clay mineralogy, carbonate content and organic carbon content. Therefore, soil hygroscopic moisture measurements at a fixed RH level provided a simple, robust, inexpensive method for predicting soil CEC.

  5. Isolation of lactoperoxidase using different cation exchange resins by batch and column procedures.

    Science.gov (United States)

    Fweja, Leonard Wt; Lewis, Michael J; Grandison, Alistair S

    2010-08-01

    Lactoperoxidase (LP) was isolated from whey protein by cation-exchange using Carboxymethyl resin (CM-25C) and Sulphopropyl Toyopearl resin (SP-650C). Both batch and column procedures were employed and the adsorption capacities and extraction efficiencies were compared. The resin bed volume to whey volume ratios were 0.96:1.0 for CM-25C and 0.64:1.0 for SP-650 indicating higher adsorption capacity of SP-650 compared with CM-25C. The effluent LP activity depended on both the enzyme activity in the whey and the amount of whey loaded on the column within the saturation limits of the resin. The percentage recovery was high below the saturation point and fell off rapidly with over-saturation. While effective recovery was achieved with column extraction procedures, the recovery was poor in batch procedures. The whey-resin contact time had little impact on the enzyme adsorption. SDS PAGE and HPLC analyses were also carried out, the purity was examined and the proteins characterised in terms of molecular weights. Reversed phase HPLC provided clear distinction of the LP and lactoferrin (LF) peaks. The enzyme purity was higher in column effluents compared with batch effluents, judged on the basis of the clarity of the gel bands and the resolved peaks in HPLC chromatograms.

  6. Kinetics and Thermodynamics of Reserpine Adsorption onto Strong Acidic Cationic Exchange Fiber

    Science.gov (United States)

    Guo, Zhanjing; Liu, Xiongmin; Huang, Hongmiao

    2015-01-01

    The kinetics and thermodynamics of the adsorption process of reserpine adsorbed onto the strong acidic cationic exchange fiber (SACEF) were studied by batch adsorption experiments. The adsorption capacity strongly depended on pH values, and the optimum reserpine adsorption onto the SACEF occurred at pH = 5 of reserpine solution. With the increase of temperature and initial concentration, the adsorption capacity increased. The equilibrium was attained within 20 mins. The adsorption process could be better described by the pseudo-second-order model and the Freundlich isotherm model. The calculated activation energy Ea was 4.35 kJ/mol. And the thermodynamic parameters were: 4.97thermodynamic parameters demonstrated that the adsorption was an endothermic, spontaneous and feasible process of physisorption within the temperature range between 283 K and 323 K and the initial concentration range between 100 mg/L and 300 mg/L. All the results showed that the SACEF had a good adsorption performance for the adsorption of reserpine from alcoholic solution. PMID:26422265

  7. Ionic polymer-metal composite actuators obtained from radiation-grafted cation- and anion-exchange membranes.

    Science.gov (United States)

    Park, Jong Hyuk; Han, Man Jae; Song, Dae Seock; Jho, Jae Young

    2014-12-24

    Two series of ionic polymer-metal composites (IPMCs), one cationic and one anionic, are designed and prepared from radiation-grafted ion-exchange membranes. Through examination of the properties of the membranes synthesized from the two grafting monomers and the two base polymers, acrylic acid-grafted poly(vinylidene fluoride-co-hexafluoropropylene) and quarternized 4-vinylpyridine-grafted poly(ethylene-co-tetrafluoroethylene) with the appropriate amount of ionic groups are employed for the fabrication of cation and anion IPMCs, respectively. The bending displacement of the cation IPMC is comparable to Nafion-based IPMC under direct- and alternating-current voltage, but back-relaxation is not observed. The actuation performance of the anion IPMC is highly improved over those reported earlier in the literature for the other anion IPMCs.

  8. Anion- or Cation-Exchange Membranes for NaBH4/H2O2 Fuel Cells?

    Science.gov (United States)

    Šljukić, Biljana; Morais, Ana L.; Santos, Diogo M. F.; Sequeira, César A. C.

    2012-01-01

    Direct borohydride fuel cells (DBFC), which operate on sodium borohydride (NaBH4) as the fuel, and hydrogen peroxide (H2O2) as the oxidant, are receiving increasing attention. This is due to their promising use as power sources for space and underwater applications, where air is not available and gas storage poses obvious problems. One key factor to improve the performance of DBFCs concerns the type of separator used. Both anion- and cation-exchange membranes may be considered as potential separators for DBFC. In the present paper, the effect of the membrane type on the performance of laboratory NaBH4/H2O2 fuel cells using Pt electrodes is studied at room temperature. Two commercial ion-exchange membranes from Membranes International Inc., an anion-exchange membrane (AMI-7001S) and a cation-exchange membrane (CMI-7000S), are tested as ionic separators for the DBFC. The membranes are compared directly by the observation and analysis of the corresponding DBFC’s performance. Cell polarization, power density, stability, and durability tests are used in the membranes’ evaluation. Energy densities and specific capacities are estimated. Most tests conducted, clearly indicate a superior performance of the cation-exchange membranes over the anion-exchange membrane. The two membranes are also compared with several other previously tested commercial membranes. For long term cell operation, these membranes seem to outperform the stability of the benchmark Nafion membranes but further studies are still required to improve their instantaneous power load. PMID:24958292

  9. Superparamagnetic cation-exchange adsorbents for bioproduct recovery from crude process liquors by high-gradient magnetic fishing

    DEFF Research Database (Denmark)

    Heebøll-Nielsen, Anders; Justesen, S.F.L; Hobley, Timothy John

    2004-01-01

    Different routes were screened for the preparation of superparamagnetic cation-exchange adsorbents for the capture of proteins using high-gradient magnetic fishing. Starting from a polyglutaraldehyde-coated base particle, the most successful of these involved attachment of sulphite to oligomers...... from sweet bovine whey. Subsequently, a high-gradient magnetic fishing process was constructed for the fractionation of whey, in which lactoperoxidase was purified 36-fold and concentrated 4.7-fold...

  10. Ga for Zn Cation Exchange Allows for Highly Luminescent and Photostable InZnP-Based Quantum Dots

    Science.gov (United States)

    2017-01-01

    In this work, we demonstrate that a preferential Ga-for-Zn cation exchange is responsible for the increase in photoluminescence that is observed when gallium oleate is added to InZnP alloy QDs. By exposing InZnP QDs with varying Zn/In ratios to gallium oleate and monitoring their optical properties, composition, and size, we conclude that Ga3+ preferentially replaces Zn2+, leading to the formation of InZnP/InGaP core/graded-shell QDs. This cation exchange reaction results in a large increase of the QD photoluminescence, but only for InZnP QDs with Zn/In ≥ 0.5. For InP QDs that do not contain zinc, Ga is most likely incorporated only on the quantum dot surface, and a PL enhancement is not observed. After further growth of a GaP shell and a lattice-matched ZnSeS outer shell, the cation-exchanged InZnP/InGaP QDs continue to exhibit superior PL QY (over 70%) and stability under long-term illumination (840 h, 5 weeks) compared to InZnP cores with the same shells. These results provide important mechanistic insights into recent improvements in InP-based QDs for luminescent applications. PMID:28706347

  11. Sorption of chlorimuron-ethyl on montmorillonite clays: effects of exchangeable cations, pH, and ionic strength.

    Science.gov (United States)

    Ren, Wenjie; Teng, Ying; Zhou, Qixing; Paschke, Albrecht; Schüürmann, Gerrit

    2014-10-01

    Sorption interaction of chlorimuron-ethyl with montmorillonite clays was investigated under varied types of exchangeable cation, pH, and ionic strength conditions. Chlorimuron-ethyl sorption on bentonites exhibited pronounced cation dependency, and the sorption ability increased as the sequence Ca(2+)- clay type and much weaker for montmorillonites. The decrease of pH at the range of 4.0-6.0 prominently increased sorption of chlorimuron-ethyl on all cation-exchanged montmorillonite clays, and nearly a neglected sorption (about 2 %) can be observed at pH over 7.0. In the presence of CaCl2, sorption of chlorimuron-ethyl on Fe(3+)-bentonite was promoted because of complexion of Ca(2+) and the surface of Fe(3+)-bentonite. However, as the concentration of CaCl2 increased, chlorimuron-ethyl sorption on Ca(2+)- and Fe(3+)-exchanged bentonite decreased, suggesting that Ca bridging was not the prevailing mechanism for sorption of chlorimuron-ethyl on these clays. Furthermore, chlorimuron-ethyl sorption was relatively sensitive to pH, and the change of pH may obscure effect of other factors on the sorption, so it was quite necessary to control pH at a constant value when the effect of other factor was being studied.

  12. Modelling of geochemical reactions and experimental cation exchange in MX 80 bentonite.

    Science.gov (United States)

    Montes-H, G; Fritz, B; Clement, A; Michau, N

    2005-10-01

    Bentonites are widely used for waste repository systems because of their hydrodynamic, surface and chemical-retention properties. MX 80 bentonite (bentonite of Wyoming) contains approximately 85% Na/Ca-montmorillonite and 15% accessory minerals. The dominant presence of Na/Ca-montmorillonite in this clay mineral could cause it to perform exceptionally well as an engineered barrier for a radioactive waste repository because this buffer material is expected to fill up by swelling the void between canisters containing waste and the surrounding ground. However, the Na/Ca-montmorillonite could be transformed to other clay minerals as a function of time under repository conditions. Previous modelling studies based on the hydrolysis reactions have shown that the Na/Ca-montmorillonite-to-Ca-montmorillonite conversion is the most significant chemical transformation. In fact, this chemical process appears to be a simple cation exchange into the engineered barrier. The purpose of the present study was two-fold. Firstly, it was hoped to predict the newly formed products of bentonite-fluid reactions under repository conditions by applying a thermokinetic hydrochemical code (KIRMAT: Kinetic Reactions and Mass Transport). The system modelled herein was considered to consist of a 1-m thick zone of water-saturated engineered barrier. This non-equilibrated system was placed in contact with a geological fluid on one side, which was then allowed to diffuse into the barrier, while the other side was kept in contact with iron-charged water. Reducing initial conditions ( [P(O)2 approximately equals 0] ; Eh=-200 mV) and a constant reaction temperature (100 degrees C) were considered. Secondly, it was hoped to estimate the influence of inter-layer cations (Ca and Na) on the swelling behaviour of the MX 80 bentonite by using an isothermal system of water vapour adsorption and an environmental scanning electron microscope (ESEM) coupled with a digital image analysis (DIA) program. Here, the

  13. Cation Exchange Resins and colonic perforation. What surgeons need to know

    Science.gov (United States)

    Rodríguez-Luna, María Rita; Fernández-Rivera, Enrique; Guarneros-Zárate, Joaquín E.; Tueme-Izaguirre, Jorge; Hernández-Méndez, José Roberto

    2015-01-01

    Introduction Since 1961 the use of Cation Exchange Resins has been the mainstream treatment for chronic hyperkalemia. For the past 25 years different kind of complications derived from its clinical use have been recognized, being the colonic necrosis the most feared and lethal of all. Presentation of case We report a case of a 72-year-old patient with chronic kidney disease, treated with calcium polystyrene sulfonate for hyperkalemia treatment who presented in the emergency department with constipation treated with hypertonic cathartics. With clinical deterioration 48 h later progressed with colonic necrosis requiring urgent laparotomy, sigmoidectomy and open abdomen management with subsequent rectal stump perforation and dead. The histopathology finding: calcium polystyrene sulfonate embedded in the mucosa, consistent with the cause of perforation. Discussion Lillemoe reported the first case series of five uremic patients with colonic perforation associated with the use of SPS in sorbitol in 1987 and in 2009 the FDA removed from the market the SPS containing 70% of sorbitol. The pathophysiologic change of CER goes from mucosal edema, ulcers, pseudomembranes, and the most severe case transmural necrosis. Up to present day, some authors have questioned the use of CER in the setting of lowering serum potassium. Despite its worldwide use in hyperkalemia settings, multiple studies have not demonstrated a significant potassium excretion by CER. Conclusion Despite the low incidence of colonic complication and lethal colonic necrosis associated with the CER clinical use, the general surgeon needs a high index of suspicion when dealing with patients treated with CER and abdominal pain. PMID:26439420

  14. Microcalorimetric study of adsorption of human monoclonal antibodies on cation exchange chromatographic materials.

    Science.gov (United States)

    Dieterle, Michael; Blaschke, Tim; Hasse, Hans

    2008-09-26

    Adsorption of two human monoclonal antibodies on two different strong cation exchange resins is studied by isothermal titration microcalorimetry and independent adsorption isotherm measurements. The pH value is varied between 4.5 and 7.0, using different buffer systems, the temperature is always 25 degrees C. The adsorption isotherm data is fitted using two different Langmuir type models. Combining the calorimetric and the adsorption data, the specific enthalpy of adsorption of the protein Deltah(p)(ads) is determined. At pH values near 7.0, where the antibodies are only weakly charged, the adsorption is exothermal. At small loadings the absolute number of Deltah(p)(ads) is then large and almost constant but it significantly decreases at higher loadings. This shows that the arrangement of antibody molecules on the absorber material depends on the loading and is less favourable at higher loadings. Despite the high positive charge of the antibody at pH values of about 5 the value of Deltah(p)(ads) is almost zero along the entire isotherm. Furthermore, at pH 4.5 even endothermal effects are observed, although high binding capacities are found. At these conditions the adsorption process seems to be strongly influenced by the ions bound to the antibody. Their release upon absorption explains the endothermal caloric effect. The adsorption equilibrium constant K(eq) is calculated from the isotherms. From Deltag(p)(ads) and the calorimetric results for Deltah(p)(ads), Deltas(p)(ads), the entropy change upon adsorption of the protein is found for the different studied conditions.

  15. Molecular Dynamics Study of Hydrogen on Alkali-Earth Metal Cations Exchanged X Zeolites

    Directory of Open Access Journals (Sweden)

    Du Xiaoming

    2014-01-01

    Full Text Available The self-diffusion of hydrogen in Ca2+-, Mg2+- and Ba2+-exchanged X zeolites (Mg46X, Ca46X, and Ba46X has been studied by molecular dynamics (MD simulations for various temperatures and loadings. The results indicate that in the temperature range of 77–298 K and the loading range of 1–80 molecules/cell, the self-diffusion coefficients are found to range from 1.2×10-9 m2·s−1 to 2.3×10-7 m2·s−1 which are in good agreement with the experimental values from the quasielastic neutron scattering (QENS and pulse field gradients nuclear magnetic resonance (PFG NMR measurements. The self-diffusion coefficients decrease with loading due to packing of sorbate-sorbate molecules which causes frequent collusion among hydrogen molecules in pores and increases with increasing temperature because increasing the kinetic energy of the gas molecules enlarges the mean free path of gas molecule. The mechanism of diffusion of hydrogen molecules in these zeolites is transition diffusion. Knudsen diffusion occurs at low loading and the molecular bulk diffusion occurs at higher loading. For given temperature and loading, the self-diffusion coefficients decrease in the order Ba46Xcations. Moreover, the effect of concentration of molecular hydrogen on self-diffusion coefficient also is analyzed using radial distribution function (RDF.

  16. Ambient soil cation exchange capacity inversely associates with infectious and parasitic disease risk in regional Australia.

    Science.gov (United States)

    Liddicoat, Craig; Bi, Peng; Waycott, Michelle; Glover, John; Breed, Martin; Weinstein, Philip

    2018-01-12

    Human contact with soil may be important for building and maintaining normal healthy immune defence mechanisms, however this idea remains untested at the population-level. In this continent-wide, cross-sectional study we examine the possible public health benefit of ambient exposures to soil of high cation exchange capacity (CEC), a surrogate for potential immunomodulatory soil microbial diversity. We compare distributions of normalized mean 2011/12-2012/13 age-standardized public hospital admission rates (cumulative incidence) for infectious and parasitic diseases across regional Australia (representing an average of 29,516 patients/year in 228 local government areas), within tertiles of socioeconomic status and soil exposure. To test the significance of soil CEC, we use probabilistic individual-level environmental exposure data (with or without soil), and group-level variables, in robust non-parametric multilevel modelling to predict disease rates in unseen groups. Our results show that in socioeconomically-deprived areas with high CEC soils, rates of infectious and parasitic disease are significantly lower than areas with low CEC soils. Also, health inequality (relative risk) due to socioeconomic status is significantly lower in areas with high CEC soils compared to low CEC soils (Δ relative risk = 0.47; 95% CI: 0.13, 0.82). Including soil exposure when modelling rates of infectious and parasitic disease significantly improves prediction performance, explaining an additional 7.5% (Δ r 2  = 0.075; 95% CI: 0.05, 0.10) of variation in disease risk, in local government areas that were not used for model building. Our findings suggest that exposure to high CEC soils (typically high soil biodiversity) associates with reduced risk of infectious and parasitic diseases, particularly in lower socioeconomic areas. Copyright © 2018 Elsevier B.V. All rights reserved.

  17. On the Structure-Property Relationships of Cation-Exchanged ZK-5 Zeolites for CO 2 Adsorption

    Energy Technology Data Exchange (ETDEWEB)

    Pham, Trong D. [Department of Chemical and Biomolecular Engineering, University of Delaware, Newark Delaware 19716 USA; Hudson, Matthew R. [Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg Maryland 20899 USA; Brown, Craig M. [Department of Chemical and Biomolecular Engineering, University of Delaware, Newark Delaware 19716 USA; Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg Maryland 20899 USA; Lobo, Raul F. [Department of Chemical and Biomolecular Engineering, University of Delaware, Newark Delaware 19716 USA

    2017-02-16

    The CO2 adsorption properties of cation-exchanged Li-, Na-, K-, and Mg-ZK-5 zeolites were correlated to the molecular structures determined by Rietveld refinements of synchrotron powder X-ray diffraction patterns. Li-, K-, and Na-ZK-5 all exhibited high isosteric heats of adsorption (Qst) at low CO2 coverage, with Na-ZK-5 having the highest Qst (ca. 49 kJ mol-1). Mg2+ was located at the center of the zeolite hexagonal prism with the cation inaccessible to CO2, leading to a much lower Qst (ca. 30 kJ mol-1) and lower overall uptake capacity. Multiple CO2 adsorption sites were identified at a given CO2 loading amount for all four cation-exchanged ZK-5 adsorbents. Site A at the flat eight-membered ring windows and site B/B* in the γ-cages were the primary adsorption sites in Li- and Na-ZK-5 zeolites. Relatively strong dual-cation adsorption sites contributed significantly to an enhanced electrostatic interaction for CO2 in all ZK-5 samples. This interaction gives rise to a migration of Li+ and Mg2+ cations from their original locations at the center of the hexagonal prisms toward the α-cages, in which they interact more strongly with the adsorbed CO2.

  18. Effect of cation exchange resin treatment and addition on sugar as anti-caking agent on retention of nutritional and sensory quality of lemon juice powder during storage

    National Research Council Canada - National Science Library

    Sharma, Satish K; Kaushal, B B. L; Sharma, P C

    2011-01-01

    Lemon juices clarified with enzymatic treatment with and without cation exchange resin treatment were concentrated to 60o Brix in a vacuum evaporator and converted into powders by foam mat drying technique...

  19. Preparation of poly(glycidylmethacrylate-divinylbenzene) weak acid cation exchange stationary phases with succinic anhydride, phthalic anhydride, and maleic anhydride for ion chromatography.

    Science.gov (United States)

    Liu, Junwei; Wang, Yong; Wu, Shuchao; Zhang, Peimin; Zhu, Yan

    2016-08-01

    In this work, poly(glycidylmethacrylate-divinylbenzene) microspheres were prepared and applied for the preparation of weak acid cation exchange stationary phases. Succinic anhydride, phthalic anhydride, and maleic anhydride were selected as carboxylation reagents to prepare three weak acid cation exchangers by direct chemical derivatization reaction without solvent or catalyst. The diameters and dispersity of the microspheres were characterized by scanning electron microscopy; the amount of accessible epoxy groups and mechanical stability were also measured. The weak acid cation exchangers were characterized by Fourier transform infrared spectroscopy; the content of carboxyl groups was measured by traditional acid base titration method. The chromatographic properties were characterized and compared by separating alkali, alkaline earth metal ions and ammonium and polar amines. The separation properties enhanced in the order of succinic anhydride, phthalic anhydride, and maleic anhydride modified poly(glycidylmethacrylate-divinylbenzene) cation exchangers. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. The load and release characteristics on a strong cationic ion-exchange fiber: kinetics, thermodynamics, and influences

    Directory of Open Access Journals (Sweden)

    Yuan J

    2014-07-01

    Full Text Available Jing Yuan, Yanan Gao, Xinyu Wang, Hongzhuo Liu, Xin Che, Lu Xu, Yang Yang, Qifang Wang, Yan Wang, Sanming LiSchool of Pharmacy, Shenyang Pharmaceutical University, Shenyang, People’s Republic of China Abstract: Ion-exchange fibers were different from conventional ion-exchange resins in their non-cross-linked structure. The exchange was located on the surface of the framework, and the transport resistance reduced significantly, which might mean that the exchange is controlled by an ionic reaction instead of diffusion. Therefore, this work aimed to investigate the load and release characteristics of five model drugs with the strong cationic ion-exchange fiber ZB-1. Drugs were loaded using a batch process and released in United States Pharmacopoeia (USP dissolution apparatus 2. Opposing exchange kinetics, suitable for the special structure of the fiber, were developed for describing the exchange process with the help of thermodynamics, which illustrated that the load was controlled by an ionic reaction. The molecular weight was the most important factor to influence the drug load and release rate. Strong alkalinity and rings in the molecular structures made the affinity between the drug and fiber strong, while logP did not cause any profound differences. The drug–fiber complexes exhibited sustained release. Different kinds and concentrations of counter ions or different amounts of drug–fiber complexes in the release medium affected the release behavior, while the pH value was independent of it. The groundwork for in-depth exploration and further application of ion-exchange fibers has been laid. Keywords: ion-exchange fibers, ionic reaction, drug load and release, opposing exchange kinetics, thermodynamics, influences

  1. Indirect UV detection-ion-exclusion/cation-exchange chromatography of common inorganic ions with sulfosalicylic acid eluent.

    Science.gov (United States)

    Kozaki, Daisuke; Mori, Masanobu; Nakatani, Nobutake; Arai, Kaori; Masuno, Tomoe; Koseki, Masakazu; Itabashi, Hideyuki; Tanaka, Kazuhiko

    2013-01-01

    Herein, we describe indirect UV detection-ion-exclusion/cation-exchange chromatography (IEC/CEC) on a weakly acidic cation-exchange resin in the H(+)-form (TSKgel Super IC-A/C) using sulfosalicylic acid as the eluent. The goal of the study was to characterize the peaks detected by UV detector. The peak directions of analyte ions in UV at 315 nm were negative because the molar absorbance coefficients of analyte anions and cations were lower than that of the sulfosalicylic acid eluent. Good chromatographic resolution and high signal-to-noise ratios of analyte ions were obtained for the separations performed using 1.1 mM sulfosalicylic acid and 1.5 mM 18-crown-6 as the eluent. The relative standard deviations (RSDs) of the peak areas ranged from 0.6 to 4.9%. Lower detection limits of the analytes were achieved using indirect UV detection at 315 nm (0.23 - 0.98 μM) than those obtained with conductometric detection (CD) (0.61 - 2.1 μM) under the optimized elution conditions. The calibration curves were linear in the range from 0.01 to 1.0 mM except for Cl(-), which was from 0.02 to 2.0 mM. The present method was successfully applied to determine common inorganic ions in a pond water sample.

  2. An Investigation into the Effect of Cation-exchange on the Adsorption Performance of Indium-based Sodalite-ZMOF

    KAUST Repository

    Samin, Umer A.

    2016-04-13

    There is a pressing need for advanced solid-state materials that can be implemented in industrial gas separation processes to achieve separations with a significantly reduced energy input compared to what is typically required from current technologies. Although certain porous materials like zeolites bear some commercial significance for gas separation; their inherent lack of tunability limits the extent to which these materials may be exploited in industry. Zeolite-like Metal-Organic Frameworks (ZMOFs) are a sub-class of Metal-Organic Framework materials (MOFs) that show a structural semblance to zeolites while possessing the tunability advantages of MOF materials. ZMOFs which are topologically similar to certain zeolites can be functionalised and tuned in numerous ways to improve their gas separation properties. In this work, indium-based sod-ZMOF was tuned by cation-exchange and then characterised by different experimental tools such as single-crystal x-ray diffraction, elemental analysis and gas adsorption. It was found that various parameters like the choice of cation, the concentration of salt solution and the choice of solvent had a significant bearing on the cation-exchange of sod-ZMOF and its subsequent adsorption properties.

  3. Comparison between methods using copper, lanthanum, and colorimetry for the determination of the cation exchange capacity of plant cell walls.

    Science.gov (United States)

    Wehr, J Bernhard; Blamey, F Pax C; Menzies, Neal W

    2010-04-28

    The determination of the cation exchange capacity (CEC) of plant cell walls is important for many physiological studies. We describe the determination of cell wall CEC by cation binding, using either copper (Cu) or lanthanum (La) ions, and by colorimetry. Both cations are strongly bound by cell walls, permitting fast and reproducible determinations of the CEC of small samples. However, the dye binding methods using two cationic dyes, Methylene Blue and Toluidine Blue, overestimated the CEC several-fold. Column and centrifugation methods are proposed for CEC determination by Cu or La binding; both provide similar results. The column method involves packing plant material (2-10 mg dry mass) in a chromatography column (10 mL) and percolating with 20 bed volumes of 1 mM La or Cu solution, followed by washing with deionized water. The centrifugation method uses a suspension of plant material (1-2 mL) that is centrifuged, and the pellet is mixed three times with 10 pellet volumes of 1 mM La or Cu solution followed by centrifugation and final washing with deionized water. In both methods the amount of La or Cu bound to the material was determined by spectroscopic methods.

  4. Mapping cation exchange capacity using a Veris-3100 instrument and invVERIS modelling software.

    Science.gov (United States)

    Koganti, T; Moral, F J; Rebollo, F J; Huang, J; Triantafilis, J

    2017-12-01

    The cation exchange capacity (CEC) is one of the most important soil properties as it influences soil's ability to hold essential nutrients. It also acts as an index of structural resilience. In this study, we demonstrate a method for 3-dimensional mapping of CEC across a study field in south-west Spain. We do this by establishing a linear regression (LR) between the calculated true electrical conductivity (σ - mS/m) and measured CEC (cmol(+)/kg) at various depths. We estimate σ by inverting Veris-3100 data (ECa - mS/m) collected along 47 parallel transects spaced 12m apart. We invert the ECa data acquired from both shallow (0-0.3m) and deep (0-0.9m) array configurations, using a quasi-three-dimensional inversion algorithm (invVeris V1.1). The CEC data was acquired at 40 locations and from the topsoil (0-0.3m), subsurface (0.3-0.6m) and subsoil (0.6-0.9m). The best LR between σ and CEC was achieved using S2 inversion algorithm using a damping factor (λ)=18. The LR (CEC=1.77+0.33×σ) had a large coefficient of determination (R(2)=0.89). To determine the predictive capability of the LR, we validated the model using a cross-validation. Given the high accuracy (root-mean-square-error [RMSE]=1.69 cmol(+)/kg), small bias (mean-error [ME]=-0.00cmol(+)/kg) and large coefficient of determination (R(2)=0.88) and Lin's concordance (0.94), between measured and predicted CEC and at various depths, we conclude we were well able to predict the CEC distribution in topsoil and the subsurface. However, the predictions made in the subsoil were poor due to limited data availability in areas where ECa changed rapidly from small to large values. In this regard, improvements in prediction accuracy can be achieved by collection of ECa in more closely spaced transects, particularly in areas where ECa varies over short spatial scales. Copyright © 2017 Elsevier B.V. All rights reserved.

  5. Ion exchange equilibrium constants

    CERN Document Server

    Marcus, Y

    2013-01-01

    Ion Exchange Equilibrium Constants focuses on the test-compilation of equilibrium constants for ion exchange reactions. The book first underscores the scope of the compilation, equilibrium constants, symbols used, and arrangement of the table. The manuscript then presents the table of equilibrium constants, including polystyrene sulfonate cation exchanger, polyacrylate cation exchanger, polymethacrylate cation exchanger, polysterene phosphate cation exchanger, and zirconium phosphate cation exchanger. The text highlights zirconium oxide anion exchanger, zeolite type 13Y cation exchanger, and

  6. Layered assemblies of a dialuminum-substituted silicotungstate trimer and the reversible interlayer cation-exchange properties.

    Science.gov (United States)

    Kikukawa, Yuji; Yamaguchi, Kazuya; Hibino, Mitsuhiro; Mizuno, Noritaka

    2011-12-19

    Two polyoxometalate assemblies, TBA(9)[{γ-H(2)SiW(10)O(36)Al(2)(μ-OH)(2)(μ-OH)}(3)] (1; TBA = tetra-n-butylammonium) and TBA(6)Li(3)[{γ-H(2)SiW(10)O(36)Al(2)(μ-OH)(2)(μ-OH)}(3)]·18H(2)O (2), were synthesized by trimerization of a dialuminum-substituted silicotungstate monomer. Both 1 and 2 possessed a layered structure composed of a basal sheet unit [TBA(3){γ-H(2)SiW(10)O(36)Al(2)(μ-OH)(2)(μ-OH)}(3)](6-) and interlayer cations. The interconversion between 1 and 2 reversibly took place through interlayer cation exchange. © 2011 American Chemical Society

  7. The investigation on cationic exchange capacity of zeolites: the use as selective ion trappers in the electrokinetic soil technique.

    Science.gov (United States)

    Ursini, Ornella; Lilla, Edo; Montanari, Roberta

    2006-09-21

    The cation exchange capacity (CEC) of porous zeolites allows to adsorb in the framework cavities the cations as pollutant heavy metal ions. We investigate the CEC behaviour of different zeolites in different experimental conditions; in solution where the ion's mobility is spontaneous and free and in the electrokinetic system where the ion's mobility is driven by the electric field. The aim of this study is to investigate if the CEC is an useful property to create a special interface region of zeolites, that if placed in the electrokinetic cell, just before the cathode, could allow to capture and concentrate the heavy metallic ions, during their migrating process. The zeolite 13X investigated in the electrokinetic proofs, retains a good high ions adsorption, even if quite smaller than the relevant free solution condition and well acts as confined trap for the heavy metal ions. In fact no trace of metallic deposition are present on the electrode's surface.

  8. Swelling and electro-osmotic properties of cation-exchange membranes with different structures in methanol-water media

    Science.gov (United States)

    Barragán, V. M.; Villaluenga, J. P. G.; Godino, M. P.; Izquierdo-Gil, M. A.; Ruiz-Bauzá, C.; Seoane, B.

    Electro-osmosis experiments through three cation-exchange membranes with different morphology and similar electric properties have been performed using methanol-water solutions under different experimental conditions. The influence on the electro-osmotic transport of the percentage of methanol on solvent with two different electrolytes, NaCl and LiCl, has been studied. The experimental results show that the presence of methanol in the solutions affects strongly the electro-osmotic flow, and this influence is different depending on the membrane morphology. Correlations among electro-osmotic permeability, swelling behavior, and cell resistance are studied for these membrane systems at different percentages of methanol in solvent.

  9. Three-dimensional lanthanide anionic metal-organic frameworks with tunable luminescent properties induced by cation exchange.

    Science.gov (United States)

    Lu, Wen-Guan; Jiang, Long; Feng, Xiao-Long; Lu, Tong-Bu

    2009-08-03

    Three 3D lanthanide anionic metal-organic frameworks {K(5)[Ln(5)(IDC)(4)(ox)(4)]}(n) x (20H(2)O)(n) with 1D channels were synthesized under hydrothermal conditions [Ln = Gd (1), Tb (2), and Dy (3)]. The K(+) ions within the 1D channel are easily exchanged with various cations. The emission intensities of Tb(III) in 2 increased significantly upon the addition of Ca(2+) ions, while the introduction of other metal ions caused the intensities to be either unchanged or weakened.

  10. Synthesis and characterization of a novel hybrid material as amphoteric ion exchanger for simultaneous removal of cations and anions.

    Science.gov (United States)

    Shah, Brijesh; Chudasama, Uma

    2014-07-15

    A new hybrid chelating ion exchanger zirconium diethylene triamine (ZrD) has been synthesized by a simple sol-gel route using inexpensive and easily available chemicals. ZrD has been characterized for elemental analysis (ICP-AES, CHN analysis), TGA, FTIR, X-ray diffraction, SEM and EDX. Physical and ion exchange characteristics as well as chemical stability of the material in various media have been studied. Structural determination reveals that ZrD exhibits amphoteric character. Anion exchange capacity (AEC) for Cl(-), Br(-), Cr2O7(2-), F(-) and AsO4(3-) has been determined. Cations are exchanged through chelation where coordinating sites are offered by nitrogen atoms present in the amine groups of ZrD. Distribution coefficient Kd for Co(2+), Ni(2+), Cu(2+), Zn(2+) (transition metal ions) and Hg(2+), Cd(2+), Pb(2+) (heavy metal ions) has been evaluated by batch equilibration techniques in aqueous and various electrolyte media/concentrations. Based on α the separation factor, a few binary separations have been performed on a chromatographic column packed with ZrD. The amphoteric behaviour of ZrD has been demonstrated by simultaneous exchange of Cu(2+) and Cl(-) in CuCl2. A study on the regeneration and reuse of ZrD indicates that it is effective upto four cycles without much decline in performance. Copyright © 2014 Elsevier B.V. All rights reserved.

  11. Modification of Nafion Membranes by IL-Cation Exchange: Chemical Surface, Electrical and Interfacial Study

    Directory of Open Access Journals (Sweden)

    V. Romero

    2012-01-01

    A study of time evolution of the impedance curves measured in the system “IL aqueous solution/Nafion-112 membrane/IL aqueous solution” was also performed. This study allows us monitoring the electrical changes associated to the IL-cation incorporation in both the membrane and the membrane/IL solution interface, and it provides supplementary information on the characteristic of the Nafion/DTA+ hybrid material. Moreover, the results also show the significant effect of water on the electrical resistance of the Nafion-112/IL-cation-modified membrane.

  12. Determination of organoarsenic species in marine samples using gradient elution cation exchange HPLC-ICP-MS

    DEFF Research Database (Denmark)

    Sloth, Jens Jørgen; Larsen, Erik Huusfeldt; Julshamn, Kåre

    2003-01-01

    and dimethylarsinoylacetic acid, whereas the cationic arsenocholine ion and tetramethylarsonium ion were not affected. The accuracy of the method for DMA, AsB and TMAs was validated with the CRMs DORM-2 and BCR626 Tuna. The concentrations found for arsenobetaine, dimethylarsinic acid and tetramethylarsonium ion were within...

  13. Simultaneous separation and detection of anions and thiophilic cations using capillary-size anion exchange chromatography with suppressed conductivity detection.

    Science.gov (United States)

    Sötz, Veronika Anna; Kochmann, Sven

    2015-05-01

    In this fundamental study, the simultaneous separation and detection of anions and thiophilic cations in anion exchange chromatography with suppressed conductivity detection is investigated. Mercury(II) and cadmium(II) served as model analytes. Separation and detection was performed by introducing 2-mercaptoethanesulfonate, which forms complexes with both mercury and cadmium with a strong metal-sulfur bond, into the KOH eluent. Additional to the separation on the column, these complexes were able to pass the suppressor. Subsequently, they could be detected as negative peaks. A simple model for the separation mechanism was developed based on these results. Furthermore, the effect of the eluent concentration on the retention factors of both cation complexes and standard anions was examined and quantified. It revealed that the concentration of 2-mercaptoethanesulfonate has more influence on the cations than the KOH concentration. Also, 2.0 mM of 2-mercaptoethanesulfonate had about the same effect on the anion separation as 60 mM KOH. Finally, selectivity and detection limits were investigated. The detection limits were 4.9 μM for mercury and 2.2 μM for cadmium. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. Suppressing Shuttle Effect Using Janus Cation Exchange Membrane for High-Performance Lithium-Sulfur Battery Separator.

    Science.gov (United States)

    Li, Zhen; Han, Yu; Wei, Junhua; Wang, Wenqiang; Cao, Tiantian; Xu, Shengming; Xu, Zhenghe

    2017-12-27

    Suppressing the shuttle effect of polysulfide ions to obtain high durability and good electrochemical performance is of great concern in the field of lithium-sulfur batteries. To address this issue, a Janus membrane consisting of an ultrathin dense layer and a robust microporous layer is fabricated using cation exchange resin. Different from the composite membranes made from polyolefin membranes, the multiple layers of the Janus membrane in this study are synchronously generated by one step, getting rid of the additional complex coating processes. Excellent overall performance is obtained by the cooperation of multiple factors. The excellent ionic selectivity of cation exchange resin renders a great suppression of the shuttle effect, endowing the lithium-sulfur battery with high Coulombic efficiency of 92.0-99.0% (LiNO3-free electrolyte). The ultrathin property of a dense layer renders a low ionic resistance, resulting in 60% higher discharge capacity over the entire C-rates (versus the control sample with Celgard 2400 membrane). The robust macroporous layer supports the ultrathin layer to achieve a free-standing property, ensuring the usability of the Janus membrane.

  15. Assessment of plasma amino acid profile in autism using cation-exchange chromatography with postcolumn derivatization by ninhydrin.

    Science.gov (United States)

    Zaki, Mona Mohamed; Abdel-Al, Hala; Al-Sawi, Mohamed

    2017-02-27

    Autism is a heterogeneous neurodevelopmental disorder. This study aimed to assess the clinical significance of amino acid profile assay in autism using cation-exchange chromatography with ninhydrin postcolumn derivatization. This study included 42 autistic children and 26 apparently healthy children. All participants were subjected to the assay of plasma amino acids (essential, nonessential, and nonstandard) using cation-exchange chromatography with postcolumn derivatization by ninhydrin. The levels of most of the essential amino acids were significantly lower in autistic children than controls. As regards nonessential amino acids, significantly lower levels for plasma cysteine, tyrosine, and serine and significantly higher levels for plasma glutamic acid were recorded in autistic children than controls. Finally, the autistic group demonstrated significantly lower levels of α-aminoadipic acid, carnosine, and β-alanine and significantly higher levels of hydroxyproline, phosphoserine, β-amino-isobutyric acid, and ammonia as compared to controls. The study revealed that autistic children exhibit distinct alterations in the plasma levels of some amino acids, which can in turn participate in the disease etiology and can be applied as a diagnostic tool for early detection of autism.

  16. Comparison of gaseous oxidized Hg measured by KCl-coated denuders, and nylon and cation exchange membranes.

    Science.gov (United States)

    Huang, Jiaoyan; Miller, Matthieu B; Weiss-Penzias, Peter; Gustin, Mae Sexauer

    2013-07-02

    The chemical compounds that make up gaseous oxidized mercury (GOM) in the atmosphere, and the reactions responsible for their formation, are not well understood. The limitations and uncertainties associated with the current method applied to measure these compounds, the KCl-coated denuder, are not known due to lack of calibration and testing. This study systematically compared the uptake of specific GOM compounds by KCl-coated denuders with that collected using nylon and cation exchange membranes in the laboratory and field. In addition, a new method for identifying different GOM compounds using thermal desorption is presented. Different GOM compounds (HgCl2, HgBr2, and HgO) were found to have different affinities for the denuder surface and the denuder underestimated each of these compounds. Membranes measured 1.3 to 3.7 times higher GOM than denuders in laboratory and field experiments. Cation exchange membranes had the highest collection efficiency. Thermodesorption profiles for the release of GOM compounds from the nylon membrane were different for HgO versus HgBr2 and HgCl2. Application of the new field method for collection and identification of GOM compounds demonstrated these vary as a function of location and time of year. Understanding the chemistry of GOM across space and time has important implications for those developing policy regarding this environmental contaminant.

  17. Uncertainties of Gaseous Oxidized Mercury Measurements Using KCl-Coated Denuders, Cation-Exchange Membranes, and Nylon Membranes: Humidity Influences.

    Science.gov (United States)

    Huang, Jiaoyan; Gustin, Mae Sexauer

    2015-05-19

    Quantifying the concentration of gaseous oxidized mercury (GOM) and identifying the chemical compounds in the atmosphere are important for developing accurate local, regional, and global biogeochemical cycles. The major hypothesis driving this work was that relative humidity affects collection of GOM on KCl-coated denuders and nylon membranes, both currently being applied to measure GOM. Using a laboratory manifold system and ambient air, GOM capture efficiency on 3 different collection surfaces, including KCl-coated denuders, nylon membranes, and cation-exchange membranes, was investigated at relative humidity ranging from 25 to 75%. Recovery of permeated HgBr2 on KCl-coated denuders declined by 4-60% during spikes of relative humidity (25 to 75%). When spikes were turned off GOM recoveries returned to 60 ± 19% of permeated levels. In some cases, KCl-coated denuders were gradually passivated over time after additional humidity was applied. In this study, GOM recovery on nylon membranes decreased with high humidity and ozone concentrations. However, additional humidity enhanced GOM recovery on cation-exchange membranes. In addition, reduction and oxidation of elemental mercury during experiments was observed. The findings in this study can help to explain field observations in previous studies.

  18. Room Temperature Cation Exchange Reaction in Nanocrystals for Ultrasensitive Speciation Analysis of Silver Ions and Silver Nanoparticles.

    Science.gov (United States)

    Huang, Ke; Xu, Kailai; Tang, Jie; Yang, Lu; Zhou, Jingrong; Hou, Xiandeng; Zheng, Chengbin

    2015-07-07

    To evaluate the toxicity of silver nanoparticles (AgNPs) and Ag(+) and gain deep insight into the transformation of AgNPs in the environment or organisms, ultrasensitive analytical methods are needed for their speciation analysis. About 40-fold of Cd(2+) in CdTe ionic nanocrystals can be "bombarded-and-exploded" (exchanged) in less than 1 min simply by mixing the nanocrystals with Ag(+) solution at room temperature, while this cation exchange reaction did not occur when only silver nanoparticles were present. On the basis of this striking difference, an ultrasensitive method was developed for speciation analysis of Ag(+) and AgNPs in complex matrices. The released Cd(2+) was reduced to its volatile species by sodium tetrahydroborate, which was separated and swept to an inductively coupled plasma mass spectrometer (ICPMS) or an atomic fluorescence spectrometer (AFS) for the indirect but ultrasensitive detection of Ag(+). Owing to the remarkable signal amplification via the cation exchange reaction and the advantages of chemical vapor generation for sampling, the limit of detection was 0.0003 μg L(-1) for Ag(+) by ICPMS, which was improved by 100-fold compared to the conventional method. Relative standard deviations are better than 2.5% at a concentration of 0.5 μg L(-1) Ag(+) or AgNPs regardless of the detector. The proposed method retains several unique advantages, including ultrahigh sensitivity, speciation analysis, simplicity and being organic reagent-free, and has been successfully utilized for speciation analysis of Ag(+) and AgNPs in environmental water samples and paramecium cells.

  19. Water quality monitoring system for determination of ionic nutrients by ion-exclusion chromatography with spectrophotometric detection on cation- and anion-exchange resin columns using water eluent.

    Science.gov (United States)

    Kozaki, Daisuke; Nakatani, Nobutake; Mori, Masanobu; Nakagoshi, Nobukazu; Tanaka, Kazuhiko

    2012-07-01

    A unified ion-exclusion chromatography (IEC) system for monitoring anionic and cationic nutrients like NH4+, NO2-, NO3-, phosphate ion, silicate ion and HCO3- was developed and applied to several environmental waters. The IEC system consisted of four IEC methodologies, including the IEC with ultraviolet (UV) form connected with detection at 210 nm for determining NH4+ on anion-exchange separation column in OH anion-exchange UV-conversion column in I- form in tandem, the IEC with UV-detection at 210 nm for determining simultaneously NO3- and NO3- on cation-exchange separation column in H+ form, the IEC with UV-detection at 210 nm for determining HCO3- on cation-exchange separation column in H+ form connected with anion-exchange UV-conversion column in I- form in tandem, and the IEC with visible-detection based on molybdenum-blue reaction for determining simultaneously silicate and phosphate ions on cation-exchange separation column in H+ form. These IEC systems were combined through three manually-driven 6-port column selection valves to select each separation column to determine selectively the ionic nutrients. Using this sequential water quality monitoring system, the analytical performances such as calibration linearity, reproducibility, detection limit and recovery were also tested under the optimized chromatographic conditions. This novel water quality monitoring system has been applied successfully for the determination of the ionic eutrophication components in sub-urban river waters.

  20. [Preparation and retention mechanism of a mixed-mode reversed-phase/strong-cationic-exchange chromatographic packing].

    Science.gov (United States)

    Peng, Xitian; Wang, Jue; Feng, Yuqi

    2013-04-01

    A simple and efficient method has been proposed for the preparation of octyl-sulfonic co-bonded silica (OSS) packing by the method of "mixed ligand". The resulting OSS packing was characterized by elemental analysis and ion-exchange capacity to prove the successful immobilization of octyl and sulfonic groups on the surface of silica gel. Then the retention mechanism of several basic analytes on the developed OSS phases was evaluated under the conditions of reversed-phase liquid chromatography (RPLC) mobile phase. The results indicated that the OSS stationary phases demonstrated a mixed-mode reversed-phase/strong-cationic-exchange (RP/SCX) retention mechanism and ion-exchange interaction maybe dominate the retention of the basic analytes. By changing the salt concentration of mobile phase, the one-site and two-site mixed-mode retention models of the several basic analytes on the OSS phases were obtained by investigating the logarithm and reciprocal relationships of retention factor and salt concentration. On the basis of the linear fitting of the two mathematical equations of the retention models, the experimental results demonstrated that the two-site model was more suitable for the description of the retention mechanism of the basic analytes on the OSS phases. Furthermore, the individual RP or SCX contribution to total retention was obtained according to the mathematical equations of the two-site retention mechanism, which can provide some valuable guidance for the separation of complex samples.

  1. Proton Adsorption Selectivity of Zeolites in Aqueous Media: Effect of Exchangeable Cation Species of Zeolites

    OpenAIRE

    Moses Wazingwa Munthali; Erni Johan; Naoto Matsue

    2015-01-01

    The saturation of negative charges of zeolites by specific cations to modify their physicochemical and catalytic properties has broadened the applications of zeolites. The adsorption behavior of H+ to Li+, Na+, K+, Rb+ and Cs+-saturated Linde-type A, Na-P1, mordenite, X type and Y type zeolites was evaluated at different pH-pM, where pH-pM is equal to log {(M+)/(H+)} and M+ represents either Li+, Na+, K+, Rb+, or Cs+. In all cases, with decreasing pH-pM, the amounts of alkali metal retention ...

  2. Design of a fixed-bed ion-exchange process for the treatment of rinse waters generated in the galvanization process using Laminaria hyperborea as natural cation exchanger.

    Science.gov (United States)

    Mazur, Luciana P; Pozdniakova, Tatiana A; Mayer, Diego A; Boaventura, Rui A R; Vilar, Vítor J P

    2016-03-01

    In this study, the removal of zinc from galvanization wastewaters was performed in a fixed bed column packed with brown macro-algae Laminaria hyperborea, acting as a natural cation exchanger (resin). The rinse wastewater presents a zinc concentration between 9 and 22 mg/L, a high concentration of light metals (mainly Na and Ca), a high conductivity (0.5-1.5 mS/cm) and a low organic content (DOC = 7-15 mg C/L). The zinc speciation diagram showed that approximately 80% of zinc is in the form of Zn(2+) and ≅20% as ZnSO4, considering the effluent matrix. From all operational conditions tested for zinc uptake (17 treatment of 2.4 m(3)/day of galvanization wastewater, resulting in an estimated reactants cost of 2.44 €/m(3). Copyright © 2015 Elsevier Ltd. All rights reserved.

  3. Transport of Divalent Cations

    Science.gov (United States)

    Van de Geijn, Siebe C.; Petit, Charles M.

    1979-01-01

    The cation exchange capacity of the intact xylem vessels in cut shoots of papyrus (Cyperus papyrus spec.) has been determined. The cation exchange capacity is independent of the cation concentration in the transpiration stream, and is equal for Ca and Co. The high value of the cation exchange capacity (0.6 to 1 × 10−7 equivalents per square centimeter vessel wall surface) leads to the hypothesis that the porous structure of the vessel wall, and not only the inner vessel wall surface, acts as a cation exchanger. Differences between anion ([32P]phosphate, [45Ca]EDTA2−, [115Cdm]-EDTA2−), and cation ([45Ca]2+, [115Cdm]2+) movement are explained in terms of transport with the transpiration flux or by exchange reactions. The competition between exchange sites and natural or synthetic ligands for the divalent cations is discussed. Images PMID:16661112

  4. Ion-exclusion chromatography with the direct UV detection of non-absorbing inorganic cations using an anion-exchange conversion column in the iodide-form.

    Science.gov (United States)

    Mori, Masanobu; Itabashi, Hideyuki; Ikedo, Mikaru; Tanaka, Kazuhiko

    2006-08-15

    An ion-exclusion chromatographic method for the direct UV detection of non-absorbing inorganic cations such as sodium (Na(+)), ammonium (NH(4)(+)) and hydrazine (N(2)H(5)(+)) ions was developed by connecting an anion-exchange column in the I(-)-form after the separation column. For example, NH(4)(+) is converted to a UV-absorbing molecule, NH(4)I, by the anion-exchange column in the I(-)-form after the ion-exclusion separation on anion-exchange column in the OH(-)-form with water eluent. As a result, the direct UV detection of Na(+), NH(4)(+) and N(2)H(5)(+) could be successfully obtained as well as the well-resolved separation. The calibration graphs of the analyte cations detected with UV at 230nm were linear in the range of 0.001-5.0mM. The detection limits at S/N=3 of the cations were below 0.1muM. This method was applied to real water analysis, the determination of NH(4)(+) in river and rain waters, or that of N(2)H(5)(+) in boiler water, with the satisfactory results. This could be applied also to low- or non-absorbing anions such as fluoride or hydrogencarbonate ions by the combination of a weakly acidic cation-exchange resin in the H(+)-form as the separation column and the anion-exchange conversion column.

  5. Modeling data of copper(II) sorption onto the composite sorbent based on cation exchanger and tin(IV) hydroxide

    Science.gov (United States)

    Ikanina, Elena V.; Kalyaeva, Mariya I.; Markov, Vyacheslav F.

    2017-09-01

    The methodology of stepwise synthesis of the composite sorbent based on cation exchanger and tin(IV) hydroxide was demonstrated. The results of copper(II) sorption onto the composite sorbent are presented. Langmuir, Freundlich and Temkin adsorption isotherms were used in mathematical modeling of the sorption data. The Langmuir model most accurately describes the sorption process. The constants of the Langmuir model and the specific surface area of the composite sorbent were defined. Granules of the composite sorbent were studied by scanning electron microscopy (SEM) and energy-dispersive X-ray microanalysis (EDXMA). The distribution coefficients of copper(II) in the composite sorbent and the sorption degree from CuSO4 aqueous solutions of various concentrations were computed.

  6. Dispersive micro solid phase extraction of amantadine, rimantadine and memantine in chicken muscle with magnetic cation exchange polymer.

    Science.gov (United States)

    Chen, Dawei; Miao, Hong; Zhao, Yunfeng; Wu, Yongning

    2017-04-15

    This study demonstrated a novel dispersive micro solid phase extraction (DMSPE) method for extraction of adamantane drugs (amantadine, rimantadine and memantine) in chicken muscle. The adamantane drugs were extracted from chicken muscle using 1% acidic acetonitrile as extraction solvent. The cleanup of fatty matrices from analytes was achieved by the DMSPE technique using magnetic cation exchange polymer as adsorbent. In this procedure, the experimental parameters and conditions were optimized in detail for the improvement of extraction efficiency. The method showed low limit of detection of 0.03μg/kg and recoveries of the analytes ranged from 87.2% to 109.3% for adamantane drugs. The proposed DMSPE method proved to be simple, effective and suitable for the treatment of adamantane drugs in chicken muscle with a relatively shorter extraction time. Copyright © 2017. Published by Elsevier B.V.

  7. Membrane resistance : The effect of salinity gradients over a cation exchange membrane

    NARCIS (Netherlands)

    Galama, A. H.; Vermaas, D. A.; Veerman, J.; Saakes, M.; Rijnaarts, H. H. M.; Post, J. W.; Nijmeijer, K.

    2014-01-01

    Ion exchange membranes (IEMs) are used for selective transport of ions between two solutions. These solutions are often different in concentration or composition. The membrane resistance (R-M) is an important parameter affecting power consumption or power production in electrodialytic processes. In

  8. Common Ion Effects In Zeoponic Substrates: Dissolution And Cation Exchange Variations Due to Additions of Calcite, Dolomite and Wollastonite

    Science.gov (United States)

    Beiersdorfer, R. E.; Ming, D. W.; Galindo, C., Jr.

    2003-01-01

    c1inoptilolite-rich tuff-hydroxyapatite mixture (zeoponic substrate) has the potential to serve as a synthetic soil-additive for plant growth. Essential plant macro-nutrients such as calcium, phosphorous, magnesium, ammonium and potassium are released into solution via dissolution of the hydroxyapatite and cation exchange on zeolite charged sites. Plant growth experiments resulting in low yield for wheat have been attributed to a Ca deficiency caused by a high degree of cation exchange by the zeolite. Batch-equilibration experiments were performed in order to determine if the Ca deficiency can be remedied by the addition of a second Ca-bearing, soluble, mineral such as calcite, dolomite or wollastonite. Variations in the amount of calcite, dolomite or wollastonite resulted in systematic changes in the concentrations of Ca and P. The addition of calcite, dolomite or wollastonite to the zeoponic substrate resulted in an exponential decrease in the phosphorous concentration in solution. The exponential rate of decay was greatest for calcite (5.60 wt. % -I), intermediate for wollastonite (2.85 wt.% -I) and least for dolomite (1.58 wt.% -I). Additions of the three minerals resulted in linear increases in the calcium concentration in solution. The rate of increase was greatest for calcite (3.64), intermediate for wollastonite (2.41) and least for dolomite (0.61). The observed changes in P and Ca concentration are consistent with the solubilities of calcite, dolomite and wollastonite and with changes expected from a common ion effect with Ca. Keywords: zeolite, zeoponics, common-ion effect, clinoptilolite, hydroxyapatite

  9. Enhanced photocatalytic activity of chromium(VI) reduction and EDTA oxidization by photoelectrocatalysis combining cationic exchange membrane processes

    Energy Technology Data Exchange (ETDEWEB)

    Hsu, Hung-Te, E-mail: der11065@hotmail.com [Institute of Environmental Engineering and Management, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao E. Rd., Taipei 106, Taiwan (China); Chen, Shiao-Shing, E-mail: f10919@ntut.edu.tw [Institute of Environmental Engineering and Management, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao E. Rd., Taipei 106, Taiwan (China); Tang, Yi-Fang, E-mail: sweet39005@hotmail.com [Institute of Environmental Engineering and Management, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao E. Rd., Taipei 106, Taiwan (China); Hsi, Hsing-Cheng, E-mail: hchsi@ntut.edu.tw [Institute of Environmental Engineering and Management, National Taipei University of Technology, No. 1, Sec. 3, Chung-Hsiao E. Rd., Taipei 106, Taiwan (China)

    2013-03-15

    Highlights: ► Chromium(VI) reduction and EDTA oxidization were conducted by photoelectrocatalysis. ► Apply the concept of cationic exchange membrane to enhance the conversion efficiency. ► The optimum TiO{sub 2} loading of 1 g/L was observed at acidic pH with current density 4 mA/cm{sup 2}. ► Transformation pathway of EDTA was determined from analyzed byproducts and molecular orbital package analysis. -- Abstract: A novel technology of photoelectrocatalysis (PEC) combining with cationic exchange membrane (CEM) was proposed for simultaneous reduction of chromium(VI) and oxidization of EDTA. The application of CEM was used to enhance the efficiency for prevention of the re-oxidation of reduced chromium with the electron–hole pairs. In this study, effects of current density, pH, TiO{sub 2} dosage, hydraulic retention time (HRT), light intensity and EDTA/Cr(VI) molar ratio were all investigated. The results showed that the optimum conversion efficiency occurred at 4 mA/cm{sup 2} with the presence of CEM. Higher conversion efficiencies were observed at lower pH due to the electrostatic attractions between positive charged Ti-OH{sub 2}{sup +}, and negatively charged Cr(VI) and EDTA. The optimum TiO{sub 2} loading of 1 g/L was depended mainly on the acidic pH range, especially at higher HRT and irradiation intensity. In addition, higher EDTA/Cr(VI) molar ratio enhanced the reduction efficiency of Cr(VI), indicating EDTA plays the role of hole scavenger in this system. Moreover, incomplete EDTA decomposition contributes to the occurrence of intermediates, including nitrilotriacetic acid, iminodiacetic acid, glycine, oxamic acid, lyoxylic acid, oxalic acid, acetic acid and formic acid, as identified by GC/MS. Consequently, transformation pathway was determined from these analyzed byproducts and molecular orbital package analysis.

  10. Electrochemical characterization of mixed matrix heterogeneous cation exchange membranes modified by simultaneous using ilmenite-co-iron oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Hosseini, Sayed Mohsen; Hamidi, Alireza; Moghadassi, Abdolreza [Faculty of Engineering, Arak University, Arak (Iran, Islamic Republic of); Madaeni, Sayed Siavash [Razi University, Kermanshah (Iran, Islamic Republic of)

    2015-03-15

    Mixed matrix heterogeneous cation exchange membranes were prepared by solution casting technique. Ilmenite-co-iron oxide nanoparticle was also employed as inorganic filler additive in membrane fabrication. The effect of the used additives on membrane electrochemical properties was studied. Membrane ion exchange capacity, membrane potential, transport number and selectivity all were improved by use of FeTiO{sub 3}/Fe{sub 3}O{sub 4} nanoparticles in membrane matrix. Utilizing FeTiO{sub 3}-co-Fe{sub 3}O{sub 4} nanoparticles in the casting solution also led to increase in ionic flux obviously. The modified membranes containing FeTiO{sub 3}-co-Fe{sub 3}O{sub 4} nanoparticles showed higher transport number, selectivity and ionic flux compared to modified membrane containing ilmenite. Electrodialysis experiment in laboratory scale also showed higher cation removal for modified membrane containing FeTiO{sub 3}-co-Fe{sub 3}O{sub 4} nanoparticles compared to other modified membranes and pristine ones. Results showed that membrane areal electrical resistance declined sharply by use of FeTiO{sub 3}-co-Fe{sub 3}O{sub 4} nanoparticles in membrane matrix. Moreover, modified membrane containing ilmenite showed lower electrical resistance compared to others. Results showed that oxidative stability of membranes was decreased slightly by use of FeTiO{sub 3}/Fe{sub 3}O{sub 4} nanoparticles in membrane matrix. The results revealed that modified membranes in this study are comparable with that of other commercial ones.

  11. Advance chromatin extraction enhances performance and productivity of cation exchange chromatography-based capture of Immunoglobulin G monoclonal antibodies.

    Science.gov (United States)

    Nian, Rui; Gagnon, Pete

    2016-07-01

    The impact of host cell-derived chromatin was investigated on the performance and productivity of cation exchange chromatography as a method for capture-purification of an IgG monoclonal antibody. Cell culture supernatant was prepared for loading by titration to pH 6.0, dilution with water to a conductivity of 4mS/cm, then microfiltration to remove solids. DNA content was reduced 99% to 30ppm, histone host cell protein content by 76% to 6300ppm, non-histone host cell protein content by 15% to 321,000ppm, and aggregates from 33% to 15%. IgG recovery was 83%. An alternative preparation was performed, adding octanoic acid, allantoin, and electropositive particles to the harvest at pH 5.3, then removing solids. DNA content was reduced toaggregates were reduced to 2.4%. IgG recovery was 95%. This treatment increased dynamic capacity (DBC) of cation exchange capture to 173g/L and enabled the column to reduce non-histone host proteins to 671ppm. Step recovery was 99%. A single multimodal polishing step further reduced them to 15ppm and aggregates to <0.1%. Overall process recovery was 89%. Productivity at feed stream IgG concentrations of 5-10g/L was roughly double the productivity of a same-size protein A column with a DBC of 55g/L. Copyright © 2016 The Author(s). Published by Elsevier B.V. All rights reserved.

  12. The use of laboratory-determined ion exchange parameters in the predictive modelling of field-scale major cation migration in groundwater over a 40-year period.

    Science.gov (United States)

    Carlyle, Harriet F; Tellam, John H; Parker, Karen E

    2004-01-01

    An attempt has been made to estimate quantitatively cation concentration changes as estuary water invades a Triassic Sandstone aquifer in northwest England. Cation exchange capacities and selectivity coefficients for Na(+), K(+), Ca(2+), and Mg(2+) were measured in the laboratory using standard techniques. Selectivity coefficients were also determined using a method involving optimized back-calculation from flushing experiments, thus permitting better representation of field conditions; in all cases, the Gaines-Thomas/constant cation exchange capacity (CEC) model was found to be a reasonable, though not perfect, first description. The exchange parameters interpreted from the laboratory experiments were used in a one-dimensional reactive transport mixing cell model, and predictions compared with field pumping well data (Cl and hardness spanning a period of around 40 years, and full major ion analyses in approximately 1980). The concentration patterns predicted using Gaines-Thomas exchange with calcite equilibrium were similar to the observed patterns, but the concentrations of the divalent ions were significantly overestimated, as were 1980 sulphate concentrations, and 1980 alkalinity concentrations were underestimated. Including representation of sulphate reduction in the estuarine alluvium failed to replicate 1980 HCO(3) and pH values. However, by including partial CO(2) degassing following sulphate reduction, a process for which there is 34S and 18O evidence from a previous study, a good match for SO(4), HCO(3), and pH was attained. Using this modified estuary water and averaged values from the laboratory ion exchange parameter determinations, good predictions for the field cation data were obtained. It is concluded that the Gaines-Thomas/constant exchange capacity model with averaged parameter values can be used successfully in ion exchange predictions in this aquifer at a regional scale and over extended time scales, despite the numerous assumptions inherent in

  13. Preparation and Cation Exchange Properties of Zeolitic Adsorbents Using Fused Coal Fly Ash and Seawater

    Science.gov (United States)

    Hirai, Takashi; Wajima, Takaaki; Yoshizuka, Kazuharu

    For the development of functional material using coal fly ash discharged from thermal power plants, we have prepared zeolitic adsorbents derived from alkaline fused coal fly ash in several aqueous saline media to obtain the optimized preparation condition. The NH4+ exchange capacity of the product prepared at 80°C for 12 hours in diluted seawater using the precursor fused at 500°C was 4.6 mmol⁄g which is equivalent that of product prepared in deionized water. Zeolite-X and zeolite-A were produced in all aqueous media, in addition hydroxysodalite was produced over 12 hours. It was suggested that zeolite-A transform into hydroxysodalite in the products. The zeolitic adsorbents having high ion exchange capacity could be prepared in twice diluted seawater at 6-12 hours in 80°C using a precursor fused at 500°C.

  14. CATION-EXCHANGE MEMBRANES WITH POLYANILINE SURFACE LAYER FOR WATER TREATMENT

    OpenAIRE

    Dinar Dilshatovich Fazullin; Gennady Vitalevich Mavrin; Michael Pavlovich Sokolov

    2014-01-01

    Ion-exchange membranes are widely used in modern technologies, particularly in the field of water treatment and make it possible to considerably reduce expenses for wastewater treatment and ensure high degree of purification. Currently, perfluorinated sulfated proton-conducting membranes are often used, such as NAFION and its Russian analogue, MF-4SK based on co-polymerization product of a perfluorinated vinyl ether with tetrafluoroethylene. However, with development of the industry, material...

  15. Modification of the quality of water injected into Louisiana gulf coast sands: Effects of cation exchange

    Science.gov (United States)

    Hanor, Jeffrey S.

    1982-06-01

    Interest in artificially recharging selected shallow sands in South Louisiana with fresh water has been stimulated by the desire to retard contamination of municipal groundwater supplies by brackish water, to retard ground subsidence and decrease pumping lifts, and to develop emergency subsurface supplies of potable water for communities dependent on surface waters susceptible to contamination. Results of field experiments, laboratory work, and model calculations demonstrate that ion exchange reactions involving clays dispersed in aquifer sands can be expected to modify significantly the composition of waters injected into Gulf Coast sediments. As little as 0.1 weight percent smectite (montmorillonite) can remove, by exchange with absorbed Na, a significant fraction of the dissolved Ca and Mg present in the injected water. The hardness of the water is thus reduced, which may be a desirable modification in water quality. Exchange occurs as fast as the fluids can be pumped into or out of the aquifer, and the water-softening capacity of the aquifer can be restored by allowing sodium-rich native pore waters to sweep back over the dispersed clays. Each acre of an aquifer 50 feet thick and containing 0.1 wt % smectite could soften half a million gallons of injected Mississippi River water. Many individual Gulf Coast aquifers underlie tens of thousands of acres, and their potential softening capacity is thus enormous. Additional exchange processes involving adjacent aquitard shales presumably will operate over long-term periods. It is possible that Gulf Coast aquifers will be used at some point in the future as processing plants to treat injected water to improve its quality for a variety of municipal and industrial purposes.

  16. Comparing the short and long term stability of biodegradable, ceramic and cation exchange membranes in microbial fuel cells.

    Science.gov (United States)

    Winfield, Jonathan; Chambers, Lily D; Rossiter, Jonathan; Ieropoulos, Ioannis

    2013-11-01

    The long and short-term stability of two porous dependent ion exchange materials; starch-based compostable bags (BioBag) and ceramic, were compared to commercially available cation exchange membrane (CEM) in microbial fuel cells. Using bi-directional polarisation methods, CEM exhibited power overshoot during the forward sweep followed by significant power decline over the reverse sweep (38%). The porous membranes displayed no power overshoot with comparably smaller drops in power during the reverse sweep (ceramic 8%, BioBag 5.5%). The total internal resistance at maximum power increased by 64% for CEM compared to 4% (ceramic) and 6% (BioBag). Under fixed external resistive loads, CEM exhibited steeper pH reductions than the porous membranes. Despite its limited lifetime, the BioBag proved an efficient material for a stable microbial environment until failing after 8 months, due to natural degradation. These findings highlight porous separators as ideal candidates for advancing MFC technology in terms of cost and operation stability. Copyright © 2013 Elsevier Ltd. All rights reserved.

  17. Effect of cation exchange resin treatment and addition on sugar as anti-caking agent on retention of nutritional and sensory quality of lemon juice powder during storage.

    Science.gov (United States)

    Sharma, Satish K; Kaushal, B B L; Sharma, P C

    2011-06-01

    Lemon juices clarified with enzymatic treatment with and without cation exchange resin treatment were concentrated to 60(o) Brix in a vacuum evaporator and converted into powders by foam mat drying technique. Powders obtained from cation exchange resin treated juice were better in quality with respect to acidity, glucose, fructose, sugars, and ascorbic acid contents as compared to those prepared form non treated juice. Further, during 9 months storage, the powders suffered slight loss of acidity, and increase in reducing sugars i.e. glucose and fructose and considerable loss (31-55%) in vitamin C contents. Storage conditions did not bring about any significant change in the ash and hesperidin content of the product. But some losses were registered in the total phenols (23.69%) and sensory quality (from 7.72 to 7.26) of the powders. Further, the powders prepared from cation exchange resin treated juice and those pulverized with cane sugar suffered overall lesser changes in most of the quality parameters during 9 months of storage, thus indicating that, the treatment of lemon juice with cation exchange resin is beneficial for better initial product quality and pulverization of prepared powder with cane sugar is beneficial in reducing the hygroscopicity and retention of quality in a better way.

  18. Development of an on-line weak-cation exchange liquid chromatography-tandem mass spectrometric method for screening aldehyde products in biological matrices

    NARCIS (Netherlands)

    Eggink, M.; Charret, S.; Wijtmans, M.; Lingeman, H.; Kool, J.; Niessen, W.M.; Irth, H.

    2009-01-01

    This paper focuses on the development and optimization of an on-line weak-cation exchange SPE (WCXE) coupled to gradient HPLC with tandem MS detection. The system enables the selective purification and re-concentration of the in-vial derivatized aldehydes from plasma and urine samples. Aldehydes are

  19. Ergot alkaloids in rye flour determined by solid-phase cation-exchange and high-pressure liquid chromatography with fluorescence detection

    DEFF Research Database (Denmark)

    Storm, Ida Marie Lindhardt Drejer; Rasmussen, Peter Have; Strobel, B.W.

    2008-01-01

    Ergot alkaloids are mycotoxins that are undesirable contaminants of cereal products, particularly rye. A method was developed employing clean-up by cation-exchange solid-phase extraction, separation by high-performance liquid chromatography under alkaline conditions and fluorescence detection...

  20. Effect of vapors of water and organic solvents on the luminescence of cation-exchange membranes immobilized with cyclometalated Pt(II) complexes

    Science.gov (United States)

    Khakhalina, M. S.; Tikhomirova, I. Yu.; Puzyk, M. V.

    2010-05-01

    The luminescence quenching of cation-exchange membranes immobilized with cyclometalated Pt(II) complexes by vapors of water and some organic solvents (methanol, ethanol, isopropanol, n-butanol, acetonitrile, and acetone) is studied. The mechanism of the luminescence quenching of complexes is discussed.

  1. Evaluation of strong cation-exchange polymers for the determination of drugs by solid-phase extraction-liquid chromatography-tandem mass spectrometry.

    Science.gov (United States)

    Fontanals, Núria; Miralles, Núria; Abdullah, Norhayati; Davies, Arlene; Gilart, Núria; Cormack, P A G

    2014-05-23

    This paper presents eight distinct strong cation-exchange resins, all of which were derived from precursor resins that had been synthesised using either precipitation polymerisation or non-aqueous dispersion polymerisation. The precursor resins were transformed into the corresponding strong cation-exchange resins by hypercrosslinking followed by polymer analogous reactions, to yield materials with high specific surface areas and strong cation-exchange character. These novel resins were then evaluated as strong cation-exchange (SCX) sorbents in the solid-phase extraction (SPE) of a group of drugs from aqueous samples. Following preliminary experiments, the two best-performing resins were then evaluated in solid-phase extraction-liquid chromatography-tandem mass spectrometry (SPE/LC-MS/MS) to determine a group of drugs from sewage samples. In general, use of these sorbents led to excellent recovery values (75-100%) for most of the target drugs and negligible matrix effects (ME) (<20% ion suppression/enhancement of the analyte signal), when 50mL and 25mL of effluent and influent sewage water samples, respectively, were percolated through the resins. Finally, a validated method based on SPE/LC-MS/MS was used to quantify the target drugs present in different sewage samples. Copyright © 2014 Elsevier B.V. All rights reserved.

  2. Removal of lead compounds from polyvinylchloride in electric wires and cables using cation-exchange resin.

    Science.gov (United States)

    Tsunekawa, Masami; Ito, Mayumi; Yuta, Sasaki; Tomoo, Sakai; Hiroyoshi, Naoki

    2011-07-15

    Recycling treatment of cable insulation resin generated from electric wires and cables was investigated. Conventional insulation PVC contains a lead component, tribase, as a thermal stabilizer and lead removal is necessary to recycle this PVC as insulation resin. This paper describes a solid surface adsorption method using ion exchange resin to remove the fine lead containing particles from PVC dissolved solution. Low lead concentration in the recovered PVC, complying with the requirements of RoHS, was achieved. Copyright © 2011 Elsevier B.V. All rights reserved.

  3. 3D Digital Mapping of Soil Cation Exchange Capacity in Dorud, Lorestan Province

    Directory of Open Access Journals (Sweden)

    R. Taghizadeh Mehrjerdi

    2015-06-01

    Full Text Available There is an increasing demand for reliable large-scale soil datato meet the requirements of models for planning of land-usesystems, characterization of soil pollution, and prediction ofland degradation. Cation exchangecapacity (CEC is among the most important soil propertiesthat are required in soil databases. This paper applied a novel method for whole-soil profile predictions of CEC (to 1 m across Dorudlocated in LorestanProvince. At present research, we combined equal-area spline depth functions with digital soil mapping techniques to predict the vertical and lateral variations of CEC across the study area where limited soil information exists (103 soil profiles. To model the relationship between CEC and environmental factors (i.e. Representative soil forming factors, derived from a digital elevation model and Landsat imagery, a regression tree was applied. Results indicated that some auxiliary data had more influence on the prediction model (i.e. B3 and modified catchment area. Our results also confirmed the regression tree model predicted target variable at the five specific depths with coefficient of determination of 0.84, 0.84, 0.84, 0.66, 0.27 and root mean square of 1.75, 1.84, 1.84, 2.11, and 2.16, respectively. Results showed a reasonable R2 in first four depths ranged from 0.66 to 0.84; while, it decreases to 0.27 in the last depth. Our results also confirmed that the regression tree as a predictive model, digital soil mappingtechniqueand equal area splinesare powerful tools to predict lateral and vertical variation of CEC.

  4. Ionic liquids with amino acids as cations: novel chiral ligands in chiral ligand-exchange capillary electrophoresis.

    Science.gov (United States)

    Mu, Xiaoyu; Qi, Li; Zhang, Haizhi; Shen, Ying; Qiao, Juan; Ma, Huimin

    2012-08-15

    Ionic liquids (ILs) with L-proline (L-Pro) as cations have been developed for the novel chiral ligands coordinated with Cu(II) in chiral ligand exchange capillary electrophoresis (CLE-CE). Four kinds of amino acid ionic liquids (AAILs), including [L-Pro][CF(3)COO], [L-Pro][NO(3)], [L-Pro][BF(4)] and [L-Pro(2)][SO(4)], were successfully synthesized. Among them, [L-Pro][CF(3)COO] was selected as the model ligand to optimize the separation conditions. The influences of AAIL concentration, pH, and methanol concentration on efficiency of chiral separation were investigated. Then it has been testified that the optimal buffer solution consisted of 25.0mM Cu(Ac)(2), 50.0 mM AAIL and 20% (v/v) methanol at pH 4.0. The interesting thing is well enantioresolution could be observed with [L-Pro][CF(3)COO] as the new chiral ligand and nine pairs of labeled D,L-AAs were successfully separated with the resolution ranging from 0.93 to 6.72. Meanwhile, the baseline separation of labeled D,L-AAs could be achieved with the other three kinds of AAILs as ligands. The results have demonstrated the good applicability of AAILs with AAs as cations for chiral separation in CLE-CE system. In addition, comparative study was also conducted for exploring the mechanism of the AAILs as new ligands in CLE-CE. Copyright © 2012 Elsevier B.V. All rights reserved.

  5. A Characterization of Laponite Nanoclays by Dynamic Light Scattering, Scanning Electron Microscopy, and Cation Exchange Capacity by UV-Visible Spectroscopy

    Science.gov (United States)

    Arnold, Randall

    Four different Laponite clays were characterized by dynamic light scattering (DLS), scanning electron microscopy (SEM), and UV-Visible spectroscopy to determine the cation exchange capacity (CEC) to provide a methodology of analysis for other clays. DLS and SEM were utilized to observe the sizes, shape, and inter-particle interactions for the different clays. UV-Visible spectroscopy was implemented to characterize the CEC of each clay via a complexometric reaction with calcium. DLS provided limitedly consistent results due to a disparity in the translational diffusion of particles in suspension due to high aspect ratios and electroviscious forces; however, SEM provided high-resolution images of various particles and agglomerates with unique insight into the intra-particle edge-face, edge-edge, and face-face interactions driven by various electrochemical forces. The experimentally determined CECs, while consistently elevated above reported values, provide accurate first-pass estimations by a direct cation exchange methodology. Advancement of this work might include Mie scattering of angular dependence for DLS, as well as a correction for the electric double layer of the platelets; field emission SEM for microanalysis of single platelets and agglomerates; and using zeta potential to develop a methodology of observing stability and CEC of cation-loaded uncharacterized clays. Establishing a methodology for determining the CEC and cation loading provides the most valuable advancement towards characterizing other clays and linking cation loading to the zeta potential and colloidal stability.

  6. Simultaneous quantitative analysis of uremic toxins by LC-MS/MS with a reversed-phase/cation-exchange/anion-exchange tri-modal mixed-mode column.

    Science.gov (United States)

    Kanemitsu, Yoshitomi; Asaji, Kei; Matsumoto, Yotaro; Tsukamoto, Hiroki; Saigusa, Daisuke; Mukawa, Chikahisa; Tachikawa, Tatsuki; Abe, Takaaki; Tomioka, Yoshihisa

    2017-11-15

    Column choice is crucial to the development of liquid chromatography/tandem mass spectrometry (LC-MS/MS) methods because analyte selectivity is dependent on the nature of the stationary phase. Recently, mixed-mode chromatography, which employs a combination of two or more stationary phases and solvent systems, has emerged as an alternative to multiple, complementary, single-column systems. This report describes the development and validation of a novel analytical method based on LC-MS/MS employing a reversed-phase/cation-exchange/anion-exchange tri-modal column (Scherzo SS-C18; Imtakt) for the simultaneous quantification of various uremic toxins (UTx), including creatinine, 1-methyladenosine, trimethylamine-N-oxide, indoxyl sulfate, p-cresyl sulfate, phenyl sulfate and 4-ethylphenyl sulfate. Stable isotope-labeled compounds were prepared as internal standards (ISs) for each analyte. Mobile phase optimization and appropriate gradient conditions resulted in satisfactory retention and peak resolution that could not have been attained with a single stationary phase LC system. The essential validation parameters, including intra- and inter-assay precision and accuracy, were adequate. The validated method was applied to measure serum levels of the aforementioned compounds in 19 patients with chronic kidney disease. This is the first report detailing the simultaneous quantification of these analytes using stable isotopes as ISs. Our results suggest that Scherzo SS-C18 columns will be considered breakthrough tools in the development of analytical methods for compounds that are difficult to quantify simultaneously in traditional LC systems. Copyright © 2017 Elsevier B.V. All rights reserved.

  7. Acute Hypocalcemia and Metabolic Alkalosis in Children on Cation-Exchange Resin Therapy

    Directory of Open Access Journals (Sweden)

    Aadil Kakajiwala

    2017-01-01

    Full Text Available Background. Sodium polystyrene sulfonate (SPS is a chelating agent used for the treatment of hyperkalemia. SPS has a wide range of exchange capacity requiring close monitoring of serum electrolytes. We observed two patients who developed acute hypocalcemia and increased metabolic alkalosis after initiating SPS therapy. We report these cases to draw attention to the potential risk of this medication in pediatric patients. Case Diagnosis/Treatment. Two children with chronic kidney disease on dialysis were started on SPS for hyperkalemia. Within a week after initiation of the medication, both patients developed hypocalcemia on routine labs without overt clinical manifestations. The hypocalcemia was rapidly corrected with oral supplementation and discontinuation of SPS. Conclusions. Severe hypocalcemia can develop after SPS therapy. The metabolic alkalosis in these patients associated with the hypocalcemia put them at increased risk for complications. Hence, careful attention must be paid to the state of calcium metabolism in all patients receiving SPS. Often calcium supplementation is required to maintain normal calcium levels.

  8. Modification of polyamide-CdS-CdSe composite material films with Ag using a cation–cation exchange reaction

    Energy Technology Data Exchange (ETDEWEB)

    Krylova, V.; Žalenkienė, S.; Dukstienė, N. [Department of Physical and Inorganic Chemistry, Kaunas University of Technology, Radvilenu st. 19, LT-50254, Kaunas (Lithuania); Baltrusaitis, J., E-mail: job314@lehigh.edu [Department of Chemical and Biomolecular Engineering, Lehigh University, B336 Iacocca Hall, 111 Research Drive, Bethlehem, PA 18015 (United States)

    2015-10-01

    Highlights: • We investigated deposition of a mixed CdSe-CdS-Ag{sub 2}Se-Ag{sub 2}S on polyamide. • A single chalcogen precursor – K{sub 2}SeS{sub 2}O{sub 6} – was used. • AAS showed five- to ten-fold excess of chalcogens diffused into PA. • Addition of AgNO{sub 3} resulted in subsurface Ag{sub 2}Se–Ag{sub 2}S formation. - Abstract: Thin mixed CdSe-CdS-Ag{sub 2}Se-Ag{sub 2}S films were deposited on a polyamide 6 (PA) surface by successfully using a cation-exchange reaction between Cd{sup 2+} and Ag{sup +} to convert CdSe-CdS into Ag{sub 2}Se-Ag{sub 2}S. These were deposited using a K{sub 2}SeS{sub 2}O{sub 6} precursor solution at 60 °C followed by cadmium acetate (Cd(CH{sub 3}COO){sub 2}). An aqueous AgNO{sub 3} solution was used as the Ag source. XRD patterns showed a complex PA-Cd-S-Se-Ag film crystalline composition with CdS, CdSe, Ag{sub 2}S and Ag{sub 2}Se peaks. Calculated dislocation density ranged within 5–15 × 10{sup 13} lines·m{sup −2} indicating high quality atomic layers. Atomic Absorption Spectroscopy (AAS) showed five- to ten-fold excess of chalcogens to metals in the thin films formed. No chalcogenides were observed on the sample surface during XPS analysis after Ag exchange due to the desorption of CdS and CdSe layers, not diffused into the bulk of the polymer suggesting that silver chalcogenides were located subsurface, as opposed to the outermost layer, likely comprised of Ag{sub 2}O.

  9. Formation of environmentally persistent free radical (EPFR) in iron(III) cation-exchanged smectite clay.

    Science.gov (United States)

    Nwosu, Ugwumsinachi G; Roy, Amitava; dela Cruz, Albert Leo N; Dellinger, Barry; Cook, Robert

    2016-01-01

    Environmentally persistent free radicals (EPFRs) have been found at a number of Superfund sites, with EPFRs being formed via a proposed redox process at ambient environmental conditions. The possibility of such a redox process taking place at ambient environmental conditions is studied utilizing a surrogate soil system of phenol and iron(III)-exchanged calcium montmorillonite clay, Fe(III)CaM. Sorption of phenol by the Fe(III)CaM is demonstrated by Fourier-transformed infra-red (FT-IR) spectroscopy, as evidenced by the peaks between 1345 cm(-1) and 1595 cm(-1), and at lower frequencies between 694 cm(-1) and 806 cm(-1), as well as X-ray diffraction (XRD) spectroscopy, as shown by an increase in interlayer spacing within Fe(III)CaM. The formation and characterization of the EPFRs is determined by electron paramagnetic resonance (EPR) spectroscopy, showing phenoxyl-type radical with a g-factor of 2.0034 and ΔHP-P of 6.1 G at an average concentration of 7.5 × 10(17) spins per g. EPFRs lifetime data are indicative of oxygen and water molecules being responsible for EPFR decay. The change in the oxidation state of the iron redox center is studied by X-ray absorption near-edge structure (XANES) spectroscopy, showing that 23% of the Fe(III) is reduced to Fe(II). X-ray photoemission spectroscopy (XPS) results confirm the XANES results. These findings, when combined with the EPFR concentration data, demonstrate that the stoichiometry of the EPFR formation under the conditions of this study is 1.5 × 10(-2) spins per Fe(II) atom.

  10. High sensitive detection method for protein by combining the magnetic separation with cation exchange based signal amplification.

    Science.gov (United States)

    Xu, Jin; Zhang, Qian-Mei; Zhao, Dong-Xu; Liu, Ya-Ru; Chen, Ping; Lu, Gui-Hong; Xie, Hai-Yan

    2017-06-01

    PSA is a member of low abundance proteins and serves as a critical indicator of the development and therapy efficacy for prostate cancer. In this study, a facile and high sensitive method was developed for serum PSA detection by integrating the immunomagnetic separation and cation exchange based signal amplification. On the basis of nanoparticle preparation and immunoprobe construction, PSA in serum was captured, separated by the immunomagnetic probe and then interacted with the quantum dots (QDs) based immunofluorescence probe; Zn2+ inside QDs was replaced by Ag+ within seconds, after which fluorescence signal was amplified by Fluozin-3, the Zn2+ responsive dye. Under optimized conditions, low detection limit (1.56pg/mL), wide linear range (1.56-25ng/mL) and good repeatability (intra-coefficient variation=3.18%) were achieved, which is superior to commercialized ELISA kit. These results demonstrated the potential of our high sensitive method for PSA detection in clinical. Copyright © 2017 Elsevier B.V. All rights reserved.

  11. Esterification of oleic acid in a three-phase, fixed-bed reactor packed with a cation exchange resin catalyst.

    Science.gov (United States)

    Son, Sung Mo; Kimura, Hiroko; Kusakabe, Katsuki

    2011-01-01

    Esterification of oleic acid was performed in a three-phase fixed-bed reactor with a cation exchange resin catalyst (Amberlyst-15) at high temperature, which was varied from 80 to 120 °C. The fatty acid methyl ester (FAME) yields in the fixed-bed reactor were increased with increases in the reaction temperature, methanol flow rate and bed height. Moreover, the FAME yields were higher than those obtained using a batch reactor due to an equilibrium shift toward the product that resulted from continuous evaporation of the produced water. In addition, there was no catalyst deactivation during the esterification of oleic acid. However, addition of sunflower oil to the oleic acid reduced the FAME yield obtained from simultaneous esterification and transesterification. The FAME yield was 97.5% at a reaction temperature of 100 °C in the fixed-bed with a height of 5 cm when the methanol and oleic acid feed rates were 8.6 and 9.0 mL/h, respectively. Copyright © 2010 Elsevier Ltd. All rights reserved.

  12. Cation exchange capacity (Qv) estimation in shaly sand reservoirs: case studies in the Junggar Basin, northwest China

    Science.gov (United States)

    Wang, Liang; Mao, Zhi-Qiang; Sun, Zhong-Chun; Luo, Xing-Ping; Deng, Ren-Shuang; Zhang, Ya-Hui; Ren, Bing

    2015-10-01

    Cation exchange capacity (Qv) is a key parameter in resistivity-based water saturation models of shaly sand reservoirs, and the accuracy of Qv calculation is crucial to the prediction of saturations of oil and gas. In this study, a theoretical expression of Qv in terms of shaly sand permeability (Kshaly-sand), total porosity (ϕt), and salinity of formation water (S) is deduced based on the capillary tube model and the physics volume model. Meanwhile, the classical Schlumberger-Doll research (SDR) model has been introduced to estimate Kshaly-sand. On this basis, a novel technique to estimate Qv from nuclear magnetic resonance (NMR) logs is proposed, and the corresponding model is also established, whose model parameters are calibrated by laboratory Qv and NMR measurements of 15 core samples from the Toutunhe formation of the Junggar Basin, northwest China. Based on the experimental data sets, this technique can be extended to reservoir conditions to estimate continuous Qv along the intervals. The processing results of field examples illustrate that the Qv calculated from field NMR logs are consistent with the analyzed results, with the absolute errors within the scope of  ±0.1 mmol cm-3 for the majority of core samples.

  13. Gamma-aminobutyric acid production using immobilized glutamate decarboxylase followed by downstream processing with cation exchange chromatography.

    Science.gov (United States)

    Lee, Seungwoon; Ahn, Jungoh; Kim, Yeon-Gu; Jung, Joon-Ki; Lee, Hongweon; Lee, Eun Gyo

    2013-01-15

    We have developed a gamma-aminobutyric acid (GABA) production technique using his-tag mediated immobilization of Escherichia coli-derived glutamate decarboxylase (GAD), an enzyme that catalyzes the conversion of glutamate to GABA. The GAD was obtained at 1.43 g/L from GAD-overexpressed E. coli fermentation and consisted of 59.7% monomer, 29.2% dimer and 2.3% tetramer with a 97.6% soluble form of the total GAD. The harvested GAD was immobilized to metal affinity gel with an immobilization yield of 92%. Based on an investigation of specific enzyme activity and reaction characteristics, glutamic acid (GA) was chosen over monosodium glutamate (MSG) as a substrate for immobilized GAD, resulting in conversion of 2.17 M GABA in a 1 L reactor within 100 min. The immobilized enzymes retained 58.1% of their initial activities after ten consecutive uses. By using cation exchange chromatography followed by enzymatic conversion, GABA was separated from the residual substrate and leached GAD. As a consequence, the glutamic acid was mostly removed with no detectable GAD, while 91.2% of GABA was yielded in the purification step.

  14. Gamma-Aminobutyric Acid Production Using Immobilized Glutamate Decarboxylase Followed by Downstream Processing with Cation Exchange Chromatography

    Directory of Open Access Journals (Sweden)

    Hongweon Lee

    2013-01-01

    Full Text Available We have developed a gamma-aminobutyric acid (GABA production technique using his-tag mediated immobilization of Escherichia coli-derived glutamate decarboxylase (GAD, an enzyme that catalyzes the conversion of glutamate to GABA. The GAD was obtained at 1.43 g/L from GAD-overexpressed E. coli fermentation and consisted of 59.7% monomer, 29.2% dimer and 2.3% tetramer with a 97.6% soluble form of the total GAD. The harvested GAD was immobilized to metal affinity gel with an immobilization yield of 92%. Based on an investigation of specific enzyme activity and reaction characteristics, glutamic acid (GA was chosen over monosodium glutamate (MSG as a substrate for immobilized GAD, resulting in conversion of 2.17 M GABA in a 1 L reactor within 100 min. The immobilized enzymes retained 58.1% of their initial activities after ten consecutive uses. By using cation exchange chromatography followed by enzymatic conversion, GABA was separated from the residual substrate and leached GAD. As a consequence, the glutamic acid was mostly removed with no detectable GAD, while 91.2% of GABA was yielded in the purification step.

  15. Simplified in vitro refolding and purification of recombinant human granulocyte colony stimulating factor using protein folding cation exchange chromatography.

    Science.gov (United States)

    Vemula, Sandeep; Dedaniya, Akshay; Thunuguntla, Rahul; Mallu, Maheswara Reddy; Parupudi, Pavani; Ronda, Srinivasa Reddy

    2015-01-30

    Protein folding-strong cation exchange chromatography (PF-SCX) has been employed for efficient refolding with simultaneous purification of recombinant human granulocyte colony stimulating factor (rhG-CSF). To acquire a soluble form of renatured and purified rhG-CSF, various chromatographic conditions, including the mobile phase composition and pH was evaluated. Additionally, the effects of additives such as urea, amino acids, polyols, sugars, oxidizing agents and their amalgamations were also investigated. Under the optimal conditions, rhG-CSF was efficaciously solubilized, refolded and simultaneously purified by SCX in a single step. The experimental results using ribose (2.0M) and arginine (0.6M) combination were found to be satisfactory with mass yield, purity and specific activity of 71%, ≥99% and 2.6×10(8)IU/mg respectively. Through this investigation, we concluded that the SCX refolding method was more efficient than conventional methods which has immense potential for the large-scale production of purified rhG-CSF. Copyright © 2014 Elsevier B.V. All rights reserved.

  16. Purification of Monoclonal Antibodies Using a Fiber Based Cation-Exchange Stationary Phase: Parameter Determination and Modeling

    Directory of Open Access Journals (Sweden)

    Jan Schwellenbach

    2016-10-01

    Full Text Available Monoclonal antibodies (mAb currently dominate the market for protein therapeutics. Because chromatography unit operations are critical for the purification of therapeutic proteins, the process integration of novel chromatographic stationary phases, driven by the demand for more economic process schemes, is a field of ongoing research. Within this study it was demonstrated that the description and prediction of mAb purification on a novel fiber based cation-exchange stationary phase can be achieved using a physico-chemical model. All relevant mass-transport phenomena during a bind and elute chromatographic cycle, namely convection, axial dispersion, boundary layer mass-transfer, and the salt dependent binding behavior in the fiber bed were described. This work highlights the combination of model adaption, simulation, and experimental parameter determination through separate measurements, correlations, or geometric considerations, independent from the chromatographic cycle. The salt dependent binding behavior of a purified mAb was determined by the measurement of adsorption isotherms using batch adsorption experiments. Utilizing a combination of size exclusion and protein A chromatography as analytic techniques, this approach can be extended to a cell culture broth, describing the salt dependent binding behavior of multiple components. Model testing and validation was performed with experimental bind and elute cycles using purified mAb as well as a clarified cell culture broth. A comparison between model calculations and experimental data showed a good agreement. The influence of the model parameters is discussed in detail.

  17. Nitrogen and chemical oxygen demand removal from septic tank wastewater in subsurface flow constructed wetlands: substrate (cation exchange capacity) effects.

    Science.gov (United States)

    Collison, Robert S; Grismer, Mark E

    2014-04-01

    The current article focuses on chemical oxygen demand (COD) and nitrogen (ammonium and nitrate) removal performance from synthetic human wastewater as affected by different substrate rocks having a range of porosities and cation exchange capacities (CECs). The aggregates included lava rock, lightweight expanded shale, meta-basalt (control), and zeolite. The first three had CECs of 1 to 4 mequiv/100 gm, whereas the zeolite CEC was much greater (-80 mequiv/100 gm). Synthetic wastewater was gravity fed to each constructed wetland system, resulting in a 4-day retention time. Effluent samples were collected, and COD and nitrogen species concentrations measured regularly during four time periods from November 2008 through June 2009. Chemical oxygen demand and nitrogen removal fractions were not significantly different between the field and laboratory constructed wetland systems when corrected for temperature. Similarly, overall COD and nitrogen removal fractions were practically the same for the aggregate substrates. The important difference between aggregate effects was the zeolite's ammonia removal process, which was primarily by adsorption. The resulting single-stage nitrogen removal process may be an alternative to nitrification and denitrification that may realize significant cost savings in practice.

  18. A universal design of field-effect-tunable microfluidic ion diode based on a gating cation-exchange nanoporous membrane

    Science.gov (United States)

    Liu, Weiyu; Ren, Yukun; Tao, Ye; Yao, Bobin; Liu, Ni; Wu, Qisheng

    2017-11-01

    Based on the continuum mechanics theory, we propose herein a universal design of microfluidic ionic diode based on external concentration polarization of a gating ion-selective medium embedded in the microfluidic network with four power terminals. This micro/nanofluidic hybrid chip employs a cation-exchange nanoporous membrane (CEM) coupled with both a control and output microfluidic channel. Under the action of a vertical electric field throughout the CEM, nanoscale surface conduction of excessive counterions within the charged nanopores is converted to the propagation of either enriched or depleted boundary toward the opposing electrode-terminal in phase with the electroconvective flow, thereby making an adjustment in the electrical conductance of output microchannel for achieving high-flux field-effect current control and diode functionality. Three basic working states, including the "on," "transition," and "off" statuses, are distinguished in different ranges of source voltage magnitude. The rectification factor of the proposed ionic circuit platform can attain one hundred-fold even at small source and gate voltages. The presented field-effect-tunable microfluidic ion diode is easily scalable, permits appreciable fluid flow due to an intrinsically small hydrodynamic resistance, and holds promise for producing high-flux ion current rectification in next-generation integrated circuits.

  19. Evaluation of strong cation exchange versus isoelectric focusing of peptides for multidimensional liquid chromatography-tandem mass spectrometry.

    Science.gov (United States)

    Slebos, Robbert J C; Brock, Jonathan W C; Winters, Nancy F; Stuart, Sarah R; Martinez, Misti A; Li, Ming; Chambers, Mathew C; Zimmerman, Lisa J; Ham, Amy J; Tabb, David L; Liebler, Daniel C

    2008-12-01

    Shotgun proteome analysis platforms based on multidimensional liquid chromatography-tandem mass spectrometry (LC-MS/MS) provide a powerful means to discover biomarker candidates in tissue specimens. Analysis platforms must balance sensitivity for peptide detection, reproducibility of detected peptide inventories and analytical throughput for protein amounts commonly present in tissue biospecimens (cation exchange (SCX) and isoelectric focusing (IEF) separations of peptides prior to LC-MS/MS analysis on a LTQ-Orbitrap hybrid instrument. IEF separations provided superior reproducibility and resolution for peptide fractionation from samples corresponding to both large (100 microg) and small (10 microg) protein inputs. SCX generated more peptide and protein identifications than did IEF with small (10 microg) samples, whereas the two platforms yielded similar numbers of identifications with large (100 microg) samples. In nine replicate analyses of tryptic peptides from 50 microg colon adenocarcinoma protein, overlap in protein detection by the two platforms was 77% of all proteins detected by both methods combined. IEF more quickly approached maximal detection, with 90% of IEF-detectable medium abundance proteins (those detected with a total of 3-4 peptides) detected within three replicate analyses. In contrast, the SCX platform required six replicates to detect 90% of SCX-detectable medium abundance proteins. High reproducibility and efficient resolution of IEF peptide separations make the IEF platform superior to the SCX platform for biomarker discovery via shotgun proteomic analyses of tissue specimens.

  20. Anion- or Cation-Exchange Membranes for NaBH4/H2O2 Fuel Cells?

    Directory of Open Access Journals (Sweden)

    César A. C. Sequeira

    2012-07-01

    Full Text Available Direct borohydride fuel cells (DBFC, which operate on sodium borohydride (NaBH4 as the fuel, and hydrogen peroxide (H2O2 as the oxidant, are receiving increasing attention. This is due to their promising use as power sources for space and underwater applications, where air is not available and gas storage poses obvious problems. One key factor to improve the performance of DBFCs concerns the type of separator used. Both anion- and cation-exchange membranes may be considered as potential separators for DBFC. In the present paper, the effect of the membrane type on the performance of laboratory NaBH4/H2O2 fuel cells using Pt electrodes is studied at room temperature. Two commercial ion-exchange membranes from Membranes International Inc., an anion-exchange membrane (AMI-7001S and a cation-exchange membrane (CMI-7000S, are tested as ionic separators for the DBFC. The membranes are compared directly by the observation and analysis of the corresponding DBFC’s performance. Cell polarization, power density, stability, and durability tests are used in the membranes’ evaluation. Energy densities and specific capacities are estimated. Most tests conducted, clearly indicate a superior performance of the cation-exchange membranes over the anion-exchange membrane. The two membranes are also compared with several other previously tested commercial membranes. For long term cell operation, these membranes seem to outperform the stability of the benchmark Nafion membranes but further studies are still required to improve their instantaneous power load.

  1. Application of mixed-mode, solid-phase extraction in environmental and clinical chemistry. Combining hydrogen-bonding, cation-exchange and Van der Waals interactions

    Science.gov (United States)

    Mills, M.S.; Thurman, E.M.; Pedersen, M.J.

    1993-01-01

    Silica- and styrene-divinylbenzene-based mixed-mode resins that contain C8, C18 and sulphonated cation-exchange groups were compared for their efficiency in isolation of neutral triazine compounds from water and of the basic drug, benzoylecgonine, from urine. The triazine compounds were isolated by a combination of Van der Waals and hydrogen-bonding interactions, and benzoylecgonine was isolated by Van der Waals interactions and cation exchange. All analytes were eluted with a polar organic solvent contaning 2% ammonium hydroxide. Larger recoveries (95%) were achieved on copolymerized mixed-mode resins where C18 and sulfonic acid are in closer proximity than on 'blended' mixed-mode resins (60-70% recovery).

  2. High pH reversed-phase chromatography with fraction concatenation as an alternative to strong-cation exchange chromatography for two-dimensional proteomic analysis

    OpenAIRE

    Yang, Feng; Shen, Yufeng; Camp, David G.; Smith, Richard D.

    2012-01-01

    Orthogonal high-resolution separations are critical for attaining improved analytical dynamic range and protein coverage in proteomic measurements. High pH reversed-phase liquid chromatography (RPLC) followed by fraction concatenation affords better peptide analysis than conventional strong-cation exchange (SCX) chromatography applied for the two-dimensional proteomic analysis. For example, concatenated high pH reversed-phase liquid chromatography increased identification for peptides (1.8-fo...

  3. Rational methods for predicting human monoclonal antibodies retention in protein A affinity chromatography and cation exchange chromatography. Structure-based chromatography design for monoclonal antibodies.

    Science.gov (United States)

    Ishihara, Takashi; Kadoya, Toshihiko; Yoshida, Hideaki; Tamada, Taro; Yamamoto, Shuichi

    2005-11-04

    Rational methods for predicting the chromatographic behavior of human monoclonal antibodies (hMabs) in protein A affinity chromatography and cation exchange chromatography from the amino acid sequences information were proposed. We investigated the relation between the structures of 28 hMabs and their chromatographic behavior in protein A affinity chromatography and cation exchange chromatography using linear gradient elution experiments. In protein A affinity chromatography, the elution pH of the hMabs was correlated with not only the structure of the Fc region (subclass), but also that of the variable region. The elution pH of hMabs that have LYLQMNSL sequences in between the CDR2 and CDR3 regions of the heavy chain became lower among the same subclass of hMabs. In cation exchange chromatography, the peak salt concentrations IR of hMabs that have the same sequences of variable regions (or that have a structural difference in their Fc region, which puts them into a subclass) were similar. The IR values of hMabs were well correlated with the equilibrium association constant Ke, and also with the surface positive charge distribution of the variable region of the heavy chain (corrected surface net positive charge (cN) of the VH region). Based on these findings, we developed rational methods for predicting the retention behavior, which were also tested with eight additional hMabs. By considering the information on the number of binding sites associated with protein adsorption as determined experimentally, and the surface positive charge distribution from the three-dimensional structure of Mab A, we hypothesized that hMabs is separated by cation exchange chromatography as the surface positive charge distribution of the VH region is recognized.

  4. Sugarcane ripener update

    Science.gov (United States)

    The chemical sugarcane ripeners glyphosate and trinexapac-ethyl play an important role in the Louisiana sugarcane industry. Their use allows for earlier starts to the sugarcane harvest season, increase recoverable sucrose (TRS) at the mill, and increases harvest efficiency. Response to ripeners oft...

  5. Effect of the intercalated cation-exchanged on the properties of nanocomposites prepared by 2-aminobenzene sulfonic acid with aniline and montmorillonite

    Energy Technology Data Exchange (ETDEWEB)

    Toumi, I. [Laboratoire de Chimie Organique, Macromoleculaire et des Materiaux, Universite de Mascara, Bp 763 Mascara 29000 (Algeria); Benyoucef, A., E-mail: ghani29000@yahoo.fr [Laboratoire de Chimie Organique, Macromoleculaire et des Materiaux, Universite de Mascara, Bp 763 Mascara 29000 (Algeria); Yahiaoui, A. [Laboratoire de Chimie Organique, Macromoleculaire et des Materiaux, Universite de Mascara, Bp 763 Mascara 29000 (Algeria); Quijada, C. [Departamento de Ingenieria Textil y Papelera, Universidad Politecnica de Valencia, Pza Ferrandiz i Carbonel, E-03801 Alcoy, Alicante (Spain); Morallon, E. [Departamento de Quimica Fisica e Instituto Universitario de Materiales, Universidad de Alicante, Apartado 99, E-03080 Alicante (Spain)

    2013-02-25

    Polymer/montmorillonite nanocomposites were prepared. Intercalation of 2-aminobenzene sulfonic acid with aniline monomers into montmorillonite modified by cation was followed by subsequent oxidative polymerization of monomers in the interlayer spacing. The clay was prepared by cation exchange process between sodium cation in (M-Na) and copper cation (M-Cu). XRD analyses show the manifestation of a basal spacing (d-spacing) for M-Cu changes depending on the inorganic cation and the polymer intercalated in the M-Cu structure. TGA analyses reveal that polymer/M-Cu composites is less stable than M-Cu. The conductivity of the composites is found to be 10{sup 3} times higher than that for M-Cu. The microscopic examinations including TEM picture of the nanocomposite demonstrated an entirely different and more compatible morphology. Remarkable differences in the properties of the polymers have also been observed by UV-Vis and FTIR, suggesting that the polymer produced with presence of aniline has a higher degree of branching. The electrochemical behavior of the polymers extracted from the nanocomposites has been studied by cyclic voltammetry which indicates the electroactive effect of nanocomposite gradually increased with aniline in the polymer chain.

  6. Preparation of a monolithic cation-exchange material with hydrophilic external layers by two-step reversible addition-fragmentation chain transfer polymerization.

    Science.gov (United States)

    Lin, Shen; Zhang, Yingying; Huang, Wei; Dong, Xiangchao

    2017-04-01

    In recent years, the efficient analysis of biological samples has become more important due to the advances of life science and pharmaceutical research and practice. Because biological sample pretreatment is the bottleneck for fast process, material development for efficient sample process in the high-performance liquid chromatography analysis is highly desirable. In this research, a cation-exchange restricted access monolithic column was synthesized by a reversible addition-fragmentation chain transfer polymerization method. Utilizing the controlled/living property of the reversible addition-fragmentation chain transfer method, a monolithic column of cross-linked poly(sulfopropyl methacrylate) was prepared first and then linear poly(glycerol mono-methacrylate) was immobilized covalently on the surface of the polymer. The monolithic material has both functionalities of cation-exchange and protein exclusion. Protein recovery of 94.6% was obtained after grafting of poly(glycerol mono-methacrylate) while the cation-exchange property of the column is still retained. In the study, the relation between the synthetic conditions and properties of the materials was studied. The synthesis conditions including the porogen, monomer concentration, and ratio of monomers/initiator/reversible addition-fragmentation chain transfer agent were optimized. The study provided a method for the preparation of restricted access monolithic columns: a bifunctional material by reversible addition-fragmentation chain transfer polymerization method. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Influence of lime, peat and cation exchanger on the heavy-metal-uptake of vine (Vitis vinifera L. ) from contaminated soils

    Energy Technology Data Exchange (ETDEWEB)

    Mohr, H.D.

    1980-10-01

    In pot experiments with heavy-metal-contaminated soils, the influence of different soil admixtures on growth and heavy-metal-uptake of vine cuttings was investigated. The following results were obtained: 1. The heavy metal uptake of vines from mixtures of soil and garbage-sewage-compost was strongly reduced by a cation exchanger. The heavy metal content of the roots decreased as follows: Cu68-77%; Zn36-74%; Cd29-81%; Mn20-45%; Pb13-52%; Cr7-58%. The Mn-, Zn- and Cu-content of wood, tendrils and leaves also decreased considerably. 2. Vine cuttings, which were cultivated on an acid, artificially Cd-contaminated soil, showed heavy damages and high Cd-contents. Admixtures of lime, cation exchanger or garbage-sewage-sludge-compost strongly reduced the injury of vines and their Cd-content. A combined addition of lime and cation exchanger was most effectful. On the contrary, the toxic effect of Cd was intensified by the acid reaction of peat.

  8. The effect of geometrical presentation of multimodal cation-exchange ligands on selective recognition of hydrophobic regions on protein surfaces.

    Science.gov (United States)

    Woo, James; Parimal, Siddharth; Brown, Matthew R; Heden, Ryan; Cramer, Steven M

    2015-09-18

    The effects of spatial organization of hydrophobic and charged moieties on multimodal (MM) cation-exchange ligands were examined by studying protein retention behavior on two commercial chromatographic media, Capto™ MMC and Nuvia™ cPrime™. Proteins with extended regions of surface-exposed aliphatic residues were found to have enhanced retention on the Capto MMC system as compared to the Nuvia cPrime resin. The results further indicated that while the Nuvia cPrime ligand had a strong preference for interactions with aromatic groups, the Capto MMC ligand appeared to interact with both aliphatic and aromatic clusters on the protein surfaces. These observations were formalized into a new set of protein surface property descriptors, which quantified the local distribution of electrostatic and hydrophobic potentials as well as distinguishing between aromatic and aliphatic properties. Using these descriptors, high-performing quantitative structure-activity relationship (QSAR) models (R(2)>0.88) were generated for both the Capto MMC and Nuvia cPrime datasets at pH 5 and pH 6. Descriptors of electrostatic properties were generally common across the four models; however both Capto MMC models included descriptors that quantified regions of aliphatic-based hydrophobicity in addition to aromatic descriptors. Retention was generally reduced by lowering the ligand densities on both MM resins. Notably, elution order was largely unaffected by the change in surface density, but smaller and more aliphatic proteins tended to be more affected by this drop in ligand density. This suggests that modulating the exposure, shape and density of the hydrophobic moieties in multimodal chromatographic systems can alter the preference for surface exposed aliphatic or aromatic residues, thus providing an additional dimension for modulating the selectivity of MM protein separation systems. Copyright © 2015 Elsevier B.V. All rights reserved.

  9. The grapevine VvCAX3 is a cation/H+ exchanger involved in vacuolar Ca2+ homeostasis.

    Science.gov (United States)

    Martins, Viviana; Carneiro, Filipa; Conde, Carlos; Sottomayor, Mariana; Gerós, Hernâni

    2017-12-01

    The grapevine VvCAX3 mediates calcium transport in the vacuole and is mostly expressed in green grape berries and upregulated by Ca 2+ , Na + and methyl jasmonate. Calcium is an essential plant nutrient with important regulatory and structural roles in the berries of grapevine (Vitis vinifera L.). On the other hand, the proton-cation exchanger CAX proteins have been shown to impact Ca2+ homeostasis with important consequences for fruit integrity and resistance to biotic/abiotic stress. Here, the CAX gene found in transcriptomic databases as having one of the highest expressions in grapevine tissues, VvCAX3, was cloned and functionally characterized. Heterologous expression in yeast showed that a truncated version of VvCAX3 lacking its NNR autoinhibitory domain (sCAX3) restored the ability of the yeast strain to grow in 100-200 mM Ca2+, demonstrating a role in Ca2+ transport. The truncated VvCAX3 was further shown to be involved in the transport of Na+, Li+, Mn2+ and Cu2+ in yeast cells. Subcellular localization studies using fluorescently tagged proteins confirmed VvCAX3 as a tonoplast transporter. VvCAX3 is expressed in grapevine stems, leaves, roots, and berries, especially at pea size, decreasing gradually throughout development, in parallel with the pattern of calcium accumulation in the fruit. The transcript abundance of VvCAX3 was shown to be regulated by methyl jasmonate (MeJA), Ca2+, and Na+ in grape cell suspensions, and the VvCAX3 promotor contains several predicted cis-acting elements related to developmental and stress response processes. As a whole, the results obtained add new insights on the mechanisms involved in calcium homeostasis and intracellular compartmentation in grapevine, and indicate that VvCAX3 may be an interesting target towards the development of strategies for enhancement of grape berry properties.

  10. Micron-sized polymer particles from tanzanian cashew nut shell liquid. Part I: Preparation, functionalization with chloroacetic acid and utilization as cation exchange resin

    Directory of Open Access Journals (Sweden)

    O.O. Ilomo

    2004-06-01

    Full Text Available Micron-sized polymer particles (MSPP were prepared by formaldehyde condensation polymerization of cashew nut shell liquid (CNSL previously emulsified with sodium lauryl sulphate. The sizes of the MSPP were found to range from 0.1 to 4.4 μm. Increasing the emulsifier concentration had the effect of increasing the average particle size as well as the rate of polymerization. On the other hand, the polymerization rate decreased as the amount of the catalyst (sodium hydroxide increased. The MSPP were also found to be insoluble and stable in many organic solvents and in some inorganic reagents. The average number of surface OH groups was found to be 2.29 x 1018 per milligram of polymer particles. Micron-sized carboxylated cation exchange resins (MCCER were obtained by treating MSPP with monochloroacetic acid in an alkaline medium. The MCCER were found to exchange up to about 86 mg of calcium ion per gram of polymer at 30 ºC while the MSPP could exchange up to only about 6 mg of calcium ion per gram of polymer, at the same temperature. Compared to MSPP, the MCCER showed more than a thirteen-fold improvement in cation exchange capacity.

  11. Ion-exclusion/cation-exchange chromatography with dual detection of the conductivity and spectrophotometry for the simultaneous determination of common inorganic anionic species and cations in river and wastewater.

    Science.gov (United States)

    Nakatani, Nobutake; Kozaki, Daisuke; Mori, Masanobu; Hasebe, Kiyoshi; Nakagoshi, Nobukazu; Tanaka, Kazuhiko

    2011-01-01

    Simultaneous determinations of common inorganic anionic species (SO(4)(2-), Cl(-), NO(3)(-), phosphate and silicate) and cations (Na(+), NH(4)(+), K(+), Mg(2+) and Ca(2+)) were conducted using an ion-chromatography system with dual detection of conductivity and spectrophotometry in tandem. The separation of ionic species on a weakly acidic cation-exchange resin was accomplished using a mixture of 100 mM ascorbic acid and 4 mM 18-crown-6 as an acidic eluent (pH 2.6), after which the ions were detected using a conductivity detector. Subsequently, phosphate and silicate were analyzed based on derivatization with molybdate and spectrophotometry at 700 nm. The detection limits at S/N = 3 ranged from 0.11 to 2.9 µM for analyte ionic species. This method was applied to practical river water and wastewater with acceptable criteria for the anion-cation balance and comparisons of the measured and calculated electrical conductivity, demonstrating the usefulness of the present method for water quality monitoring.

  12. Near-Infrared Emitting CuInSe2/CuInS2 Dot Core/Rod Shell Heteronanorods by Sequential Cation Exchange

    Science.gov (United States)

    2015-01-01

    The direct synthesis of heteronanocrystals (HNCs) combining different ternary semiconductors is challenging and has not yet been successful. Here, we report a sequential topotactic cation exchange (CE) pathway that yields CuInSe2/CuInS2 dot core/rod shell nanorods with near-infrared luminescence. In our approach, the Cu+ extraction rate is coupled to the In3+ incorporation rate by the use of a stoichiometric trioctylphosphine-InCl3 complex, which fulfills the roles of both In-source and Cu-extracting agent. In this way, Cu+ ions can be extracted by trioctylphosphine ligands only when the In–P bond is broken. This results in readily available In3+ ions at the same surface site from which the Cu+ is extracted, making the process a direct place exchange reaction and shifting the overall energy balance in favor of the CE. Consequently, controlled cation exchange can occur even in large and anisotropic heterostructured nanocrystals with preservation of the size, shape, and heterostructuring of the template NCs into the product NCs. The cation exchange is self-limited, stopping when the ternary core/shell CuInSe2/CuInS2 composition is reached. The method is very versatile, successfully yielding a variety of luminescent CuInX2 (X = S, Se, and Te) quantum dots, nanorods, and HNCs, by using Cd-chalcogenide NCs and HNCs as templates. The approach reported here thus opens up routes toward materials with unprecedented properties, which would otherwise remain inaccessible. PMID:26449673

  13. Integrated SDS removal and peptide separation by strong-cation exchange liquid chromatography for SDS-assisted shotgun proteome analysis.

    Science.gov (United States)

    Sun, Difei; Wang, Nan; Li, Liang

    2012-02-03

    We report an improved shotgun method for analyzing proteomic samples containing sodium dodecyl sulfate (SDS). This method is based on the use of strong-cation exchange (SCX) liquid chromatography (LC) for SDS removal that can be integrated with peptide separation as the first dimension of the two-dimensional LC tandem mass spectrometry workflow. To optimize the performance of SDS removal, various experimental conditions, including the concentrations of chemical reagents and salts in the sample, the SDS concentration, and the SCX mobile phase composition, were investigated. It was found that a peptide recovery rate of about 90% could be achieved while removing SDS efficiently. One key finding was that, by increasing the SDS concentration to a certain level (0.5%) in the digested peptide sample, the sample recovery rate could be increased. The peptide recovery rate of BSA digests was found to be 90.6 ± 1.0% (n = 3), and SDS in the SCX fractions collected was not detectable by pyrolysis GC-MS, i.e., below the detection limit of 0.00006% for the undesalted SCX fractions. The peptide recovery rates were found to be 90.9% ± 2.7 (n = 3) and 89.5% ± 0.5% (n = 3) for the digests of the membrane-protein-enriched fractions of E. coli cell lysates and the MCF-7 breast cancer cell line, respectively. Compared to the methods that use acid-labile surfactants, such as RapiGest and PPS, for the MCF-7 membrane fraction sample, the SDS method identified, on average (n = 3), more peptides (∼5%) and proteins (∼16%) than the RapiGest method, while the RapiGest method identified more peptides (∼21%) and proteins (∼7%) from the E. coli membrane fraction than the SDS method. In both cases, the two methods identified more peptides and proteins than the PPS method. Since SCX is widely used as the first dimension of 2D-LC MS/MS, integration of SDS removal with peptide separation in SCX does not add any extra steps to the sample handling process. We demonstrated the application of

  14. Insights in understanding aggregate formation and dissociation in cation exchange chromatography for a structurally unstable Fc-fusion protein.

    Science.gov (United States)

    Chen, Zhiqiang; Huang, Chao; Chennamsetty, Naresh; Xu, Xuankuo; Li, Zheng Jian

    2016-08-19

    Cation-exchange chromatography (CEX) of a structurally unstable Fc-fusion protein exhibited multi-peak elution profile upon a salt-step elution due to protein aggregation during intra-column buffer transition where low pH and high salt coexisted. The protein exhibited a single-peak elution behavior during a pH-step elution; nevertheless, the levels of soluble aggregates (i.e. high molecular weight species, HMW) in the CEX eluate were still found up to 12-fold higher than that for the load material. The amount of the aggregates formed upon the pH-step elution was dependent on column loading with maximum HMW achieved at intermediate loading levels, supporting the hypothesis that the aggregation was the result of both the conformational changes of the bound protein and the solution concentration of the aggregation-susceptible proteins during elution. Factors such as high load pH, short protein/resin contact time, hydrophilic resin surface, and weak ionizable ligand were effective, to some extent, to reduce aggregate formation by improving the structural integrity of the bound protein. An orthogonal technique, differential scanning fluorimetry (DSF) using Sypro Orange dye confirmed that the bound protein exposed more hydrophobic area than the native molecule in free solution, especially in the pH 4-5 range. The Sypro Orange dye study of resin surface property also demonstrated that the poly[styrene-divinylbenzene]-based Poros XS with polyhydroxyl surface coating is more hydrophobic compared to the agarose-based CM Sepharose FF and SP Sepharose FF. The hydrophobic property of Poros XS contributed to stronger interactions with the partially unfolded bound protein and consequently to the higher aggregate levels seen in Poros XS eluate. This work also investigates the aggregation reversibility in CEX eluate where up to 66% of the aggregates were observed to dissociate into native monomers over a period of 120h, and links the aggregate stability to such conditions as resin

  15. Obtention of the cation exchange capacity of a natural kaolinite with radioactive tracers; Obtencion de la capacidad de intercambio cationico de una kaolinita natural con trazadores radioactivos

    Energy Technology Data Exchange (ETDEWEB)

    Uribe I, A.; Badillo A, V.E. [Universidad Autonoma de Zacatecas, 98000 Zacatecas (Mexico); Monroy G, F. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico)]. e-mail: Adrya81@hotmail.com

    2005-07-01

    One of the more used techniques for the elimination of the heavy metals present in water systems is to use adsorbent mineral phases like zeolites and clays, among others. The clays are able to exchange easily the fixed ions in the external surface of its crystals or well the ions present in the interlaminar spaces of the structures, for other existent ones in the encircling aqueous solutions for that the Cation exchange capacity (CIC) is defined as the sum of all the cations exchange that a mineral can possess independent to the physicochemical conditions. The CIC is equal to the measure of the total of negative charges of the mineral by mass of the solid (meq/g). In this investigation work, the value of the CIC equal to 2.5 meq/100 g is obtained, of a natural kaolinite from the State of Hidalgo studying the retention of the sodium in the kaolinite with the aid of the radioactive isotope {sup 24} Na and of the selective electrodes technique, making vary the pH value. So is experimentally demonstrated that the CIC is an intrinsic property of the mineral independent of the pH value of the solution and of the charges origin. (Author)

  16. Enrichment and low-level determination of glyphosate, aminomethylphosphonic acid and glufosinate in drinking water after cleanup by cation exchange resin.

    Science.gov (United States)

    Küsters, Markus; Gerhartz, Michael

    2010-04-01

    For the determination of glyphosate, aminomethylphosphonic acid and glufosinate in drinking water, different procedures of enrichment and cleanup were examined using anion exchange or SPE. In many cases interactions of, e.g. alkaline earth metal ions especially calcium could be observed during enrichment and cleanup resulting in loss of analytes. For that reason, a novel cleanup and enrichment procedure for the determination of these phosphonic acid herbicides has been developed in drinking water using cation-exchange resin. In summary, the cleanup procedure with cation-exchange resin developed in this study avoids interactions as described above and is applicable to calcium-rich drinking water samples. After derivatization with 9-fluorenylmethylchloroformate followed by LC with fluorescence detection, LOD of 12, 14 and 12 ng/L and mean recoveries from real-world drinking water samples of 98+/-9, 100+/-16 and 101+/-11% were obtained for glyphosate, aminomethylphosphonic acid and glufosinate, respectively. The low LODs and the high precision permit the analysis of these phosphonic acid herbicides according to the guidelines of the European Commission.

  17. Hybrid organic-inorganic silica monolith with hydrophobic/strong cation-exchange functional groups as a sorbent for micro-solid phase extraction.

    Science.gov (United States)

    Zheng, Ming-Ming; Ruan, Ge-Deng; Feng, Yu-Qi

    2009-11-06

    A hybrid organic-inorganic silica monolith with hydrophobic and strong cation-exchange functional groups was prepared and used as a sorbent for micro-solid phase extraction (micro-SPE). The hybrid silica monolith functionalized with octyl and thiol groups was conveniently synthesized by hydrolysis and polycondensation of a mixture of tetraethoxysilane (TEOS), n-octyltriethoxysilane (C8-TEOS) and 3-mercaptopropyltrimethoxysilane (MPTMS) via a two-step catalytic sol-gel process. Due to the favorable chemical reactivity of mercapto pendant moieties, the obtained hybrid monolith was oxidized using hydrogen peroxide (30%, w/w) to yield sulfonic acid groups, which provided strong cation-exchange sites. The obtained hybrid monolith was characterized by diffused infrared spectroscopy, elemental analysis, scanning electron microscopy and mercury intrusion porosimetry. The results show that the resulting monolith contains much higher carbon (31.6%) and sulfur (4.8%) contents than traditionally bonded silica materials. The extraction performance of the hybrid monolith was evaluated using sulfonamides as testing analytes by micro-SPE on-line coupled to HPLC. The results show that the hybrid monolith with hydrophobic and strong cation-exchange functional groups exhibits high extraction efficiency towards the testing analytes. The column-to-column RSD values were 1.3-9.8% for the extraction of SAs investigated. The extraction performance of the hybrid silica monolith remained practically unchanged after treated with acid (pH 1.0) and basic solutions (pH 10.5). Finally, the application of the hybrid monolith was demonstrated by micro-SPE of sulfonamide residues from milk followed by HPLC-UV analysis. The limits of detection (S/N=3) for eight SAs were found to be 1.0-3.0ng/mL in milk. The recoveries of eight SAs spiked in milk sample ranged from 80.2% to 115.6%, with relative standard deviations less than 11.8%.

  18. Variation in whole DNA methylation in red maple (Acer rubrum) populations from a mining region: association with metal contamination and cation exchange capacity (CEC) in podzolic soils.

    Science.gov (United States)

    Kalubi, K N; Mehes-Smith, M; Spiers, G; Omri, A

    2017-04-01

    Although a number of publications have provided convincing evidence that abiotic stresses such as drought and high salinity are involved in DNA methylation reports on the effects of metal contamination, pH, and cation exchange on DNA modifications are limited. The main objective of the present study is to determine the relationship between metal contamination and Cation exchange capacity (CEC) on whole DNA modifications. Metal analysis confirms that nickel and copper are the main contaminants in sampled sites within the Greater Sudbury Region (Ontario, Canada) and liming has increased soil pH significantly even after 30 years following dolomitic limestone applications. The estimated CEC values varied significantly among sites, ranging between 1.8 and 10.5 cmol(+) kg -1 , with a strong relationship being observed between CEC and pH (r = 0.96**). Cation exchange capacity, significantly lower in highly metal contaminated sites compared to both reference and less contaminated sites, was higher in the higher organic matter limed compared to unlimed sites. There was a significant variation in the level of cytosine methylation among the metal-contaminated sites. Significant and strong negative correlations between [5mdC]/[dG] and bioavailable nickel (r = -0.71**) or copper (r = -0.72**) contents were observed. The analysis of genomic DNA for adenine methylation in this study showed a very low level of [6N-mdA]/dT] in Acer rubrum plants analyzed ranging from 0 to 0.08%. Significant and very strong positive correlation was observed between [6N-mdA]/dT] and soil bioavailable nickel (r = 0.78**) and copper (r = 0.88**) content. This suggests that the increased bioavailable metal levels associated with contamination by nickel and copper particulates are associated with cytosine and adenine methylation.

  19. The role of nonmagnetic d{sup 0} vs. d{sup 10}B-type cations on the magnetic exchange interactions in osmium double perovskites

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Hai L., E-mail: Hai.Feng@cpfs.mpg.de [Max Planck Institute for Chemical Physics of Solids, Dresden 01187 (Germany); Yamaura, Kazunari [Research Center for Functional Materials, National Institute for Materials Science, Tsukuba, Ibaraki 305-0044 (Japan); Tjeng, Liu Hao [Max Planck Institute for Chemical Physics of Solids, Dresden 01187 (Germany); Jansen, Martin, E-mail: M.Jansen@fkf.mpg.de [Max Planck Institute for Chemical Physics of Solids, Dresden 01187 (Germany); Max Planck Institute for Solid State Research, Stuttgart 70569 (Germany)

    2016-11-15

    Polycrystalline samples of double perovskites Ba{sub 2}BOsO{sub 6} (B=Sc, Y, In) were synthesized by solid state reactions. They adopt the cubic double perovskite structures (space group, Fm-3m) with ordered B and Os arrangements. Ba{sub 2}BOsO{sub 6} (B=Sc, Y, In) show antiferromagnetic transitions at 93 K, 69 K, and 28 K, respectively. The Weiss-temperatures are −590 K for Ba{sub 2}ScOsO{sub 6}, −571 K for Ba{sub 2}YOsO{sub 6}, and −155 K for Ba{sub 2}InOsO{sub 6}. Sc{sup 3+} and Y{sup 3+} have the open-shell d{sup 0} electronic configuration, while In{sup 3+} has the closed-shell d{sup 10}. This indicates that a d{sup 0} B-type cation induces stronger overall magnetic exchange interactions in comparison to a d{sup 10}. Comparison of Ba{sub 2}BOsO{sub 6} (B=Sc, Y, In) to their Sr and Ca analogues shows that the structural distortions weaken the overall magnetic exchange interactions. - Graphical abstract: Magnetic properties of osmium double perovskites Ba{sub 2}BOsO{sub 6} (B=Sc, Y, In) were studied. Comparison of Ba{sub 2}BOsO{sub 6}indicates that a d{sup 0} B-type cation induces stronger overall magnetic exchange interactions in comparison to a d{sup 10}. - Highlights: • Magnetic properties of double perovskites Ba{sub 2}BOsO{sub 6} (B=Sc, Y, In) were studied. • A d{sup 0}B-type cation induces stronger magnetic interactions than a d{sup 10}. • Structural distortions weaken the overall Os{sup 5+}-Os{sup 5+} magnetic interactions.

  20. Evaluation of high-capacity cation exchange chromatography for direct capture of monoclonal antibodies from high-titer cell culture processes.

    Science.gov (United States)

    Tao, Yinying; Ibraheem, Aladein; Conley, Lynn; Cecchini, Douglas; Ghose, Sanchayita

    2014-07-01

    Advances in molecular biology and cell culture technology have led to monoclonal antibody titers in excess of 10 g/L. Such an increase can pose concern to traditional antibody purification processes due to limitations in column hardware and binding capacity of Protein A resins. Recent development of high capacity cation exchangers can make cation exchange chromatography (CEX) a promising and economic alternative to Protein A capture. This work investigates the feasibility of using CEX for direct capture of monoclonal antibodies from high titer cell culture fluids. Two resin candidates were selected from seven newer generation cation exchangers for their higher binding capacity and selectivity. Two monoclonal antibodies with widely differing pI values were used to evaluate the capability of CEX as a platform capture step. Screening of loading pH and conductivity showed both resins to be capable of directly capturing both antibodies from undiluted cell culture fluid. At appropriate acidic pH range, product loading of over 65 g/L resin was achieved for both antibodies. A systematic design of experiment (DOE) approach was used to optimize the elution conditions for the CEX step. Elution pH showed the most significant impact on clearance of host cell proteins (HCPs). Under optimal conditions, HCP reduction factors in the range of 9-44 were achieved on the CEX step based on the pI of the antibody. Apart from comparing CEX directly to Protein A as the capture method, material from either modality was also processed through the subsequent polishing steps to compare product quality at the drug substance level. Process performance and product quality was found to be acceptable using the non-affinity based process scheme. The results shown here present a cheaper and higher capacity generic capture method for high-titer antibody processes. © 2014 Wiley Periodicals, Inc.

  1. Separation of aliphatic carboxylic acids and benzenecarboxylic acids by ion-exclusion chromatography with various cation-exchange resin columns and sulfuric acid as eluent.

    Science.gov (United States)

    Ohta, Kazutoku; Ohashi, Masayoshi; Jin, Ji-Ye; Takeuchi, Toyohide; Fujimoto, Chuzo; Choi, Seong-Ho; Ryoo, Jae-Jeong; Lee, Kwang-Pill

    2003-05-16

    The application of various hydrophilic cation-exchange resins for high-performance liquid chromatography (sulfonated silica gel: TSKgel SP-2SW, carboxylated silica gel: TSKgel CM-2SW, sulfonated polymethacrylate resin: TSKgel SP-5PW, carboxylated polymethacrylate resins: TSKgel CM-5PW and TSKgel OA-Pak A) as stationary phases in ion-exclusion chromatography for C1-C7 aliphatic carboxylic acids (formic, acetic, propionic, butyric, isovaleric, valeric, isocaproic, caproic, 2-methylhexanoic and heptanoic acids) and benzenecarboxylic acids (pyromellitic, trimellitic, hemimellitic, o-phthalic, m-phthalic, p-phthalic, benzoic, salicylic acids and phenol) was carried out using diluted sulfuric acid as the eluent. Silica-based cation-exchange resins (TSKgel SP-2SW and TSKgel CM-2SW) were very suitable for the ion-exclusion chromatographic separation of these benzenecarboxylic acids. Excellent simultaneous separation of these benzenecarboxylic acids was achieved on a TSKgel SP-2SW column (150 x 6 mm I.D.) in 17 min using a 2.5 mM sulfuric acid at pH 2.4 as the eluent. Polymethacrylate-based cation-exchange resins (TSKgel SP-5PW, TSKgel CM-5PW and TSKgel OA-Pak A) acted as advanced stationary phases for the ion-exclusion chromatographic separation of these C1-C7 aliphatic carboxylic acids. Excellent simultaneous separation of these C1-C7 acids was achieved on a TSKgel CM-5PW column (150 x 6 mm I.D.) in 32 min using a 0.05 mM sulfuric acid at pH 4.0 as the eluent.

  2. Cation Exchange Combined with Kirkendall Effect in the Preparation of SnTe/CdTe and CdTe/SnTe Core/Shell Nanocrystals.

    Science.gov (United States)

    Jang, Youngjin; Yanover, Diana; Čapek, Richard Karel; Shapiro, Arthur; Grumbach, Nathan; Kauffmann, Yaron; Sashchiuk, Aldona; Lifshitz, Efrat

    2016-07-07

    Controlling the synthesis of narrow band gap semiconductor nanocrystals (NCs) with a high-quality surface is of prime importance for scientific and technological interests. This Letter presents facile solution-phase syntheses of SnTe NCs and their corresponding core/shell heterostructures. Here, we synthesized monodisperse and highly crystalline SnTe NCs by employing an inexpensive, nontoxic precursor, SnCl2, the reactivity of which was enhanced by adding a reducing agent, 1,2-hexadecanediol. Moreover, we developed a synthesis procedure for the formation of SnTe-based core/shell NCs by combining the cation exchange and the Kirkendall effect. The cation exchange of Sn(2+) by Cd(2+) at the surface allowed primarily the formation of SnTe/CdTe core/shell NCs. Further continuation of the reaction promoted an intensive diffusion of the Cd(2+) ions, which via the Kirkendall effect led to the formation of the inverted CdTe/SnTe core/shell NCs.

  3. Effect of Zeolite Modification via Cationic Exchange Method on Mechanical, Thermal, and Morphological Properties of Ethylene Vinyl Acetate/Zeolite Composites

    Directory of Open Access Journals (Sweden)

    N. D. Zaharri

    2013-01-01

    Full Text Available In this research, organozeolite filled ethylene vinyl acetate (EVA composites were prepared in a melt-mixing process and followed by compression molding using hot press machine according to standard test specimen. Prior to mixing process, zeolite was modified via cationic exchange of alkylammonium ions. The effect of zeolite or organozeolite loading from 5 up to 25 volume percentages on the properties of EVA/zeolite composites was evaluated. A combination of Fourier Transform Infrared Radiation (FTIR and scanning electron microscopy (SEM coupled with energy dispersive X-ray (EDX analysis were done to characterize the resultant organoclay. Tensile test was performed in order to study the mechanical properties of the composites. EVA filled with organozeolite showed better tensile properties compared to EVA filled with unmodified zeolite, which might be an indication of enhanced dispersion of organophilic clay in the composites. Meanwhile, morphological study using SEM revealed the fibrillation effect of organozeolite. Besides, thermal properties of the composites were also characterized by using thermogravimetric analysis (TGA and differential scanning calorimetry (DSC. The results showed that the application of the cation exchange treatment increases both decomposition and melting temperature of EVA/zeolite composites.

  4. Improved plasma free metadrenaline analysis requires mixed mode cation exchange solid-phase extraction prior to liquid chromatography tandem mass spectrometry detection.

    Science.gov (United States)

    Clarke, Michael W; Cooke, Brian; Hoad, Kirsten; Glendenning, Paul

    2011-07-01

    The investigation and effective management of phaeochromocytoma involves biochemical measurement of either conjugated total urine or plasma free metadrenalines. Current analytical methods include enzyme-linked immunosorbent assays, high-performance liquid chromatography (HPLC) with electrochemical detection (ECD) or liquid chromatography tandem mass spectrometry (LCMS/MS). Since the first two methods are either extremely laborious, necessitate low sample run numbers, result in slow turnaround times or are subject to analytical interference, a robust, routine clinical method is not achievable. We established a novel sample preparation method to measure plasma free metadrenalines using LCMS/MS. Three different solid-phase extraction (SPE) methods were compared: hydrophilic-lipophilic balance sorbent (HLB), weak cation exchange (WCX) and mixed mode cation exchange (MCX) and their ability to remove interfering compounds prior to LCMS/MS analysis. Maximum recovery of plasma free metadrenaline and plasma free normetadrenaline were achieved by positively charging compounds prior to SPE application. Compared with HLB and WCX cartridges, MCX extraction resulted in chromatography without co-eluting interference with superior assay precision and accuracy. Additionally, samples that could not be quantified because of interference using HPLC/ECD could be readily assayed using this new method. The use of the MCX SPE method with LCMS/MS detection provides an improved assay to measure plasma free metadrenalines in comparison to many available alternative methods.

  5. Application of cation-exchange solid-phase extraction for the analysis of amino alcohols from water and human plasma for verification of Chemical Weapons Convention.

    Science.gov (United States)

    Kanaujia, Pankaj K; Tak, Vijay; Pardasani, Deepak; Gupta, A K; Dubey, D K

    2008-03-28

    The analysis of nitrogen containing amino alcohols, which are the precursors and degradation products of nitrogen mustards and nerve agent VX, constitutes an important aspect for verifying the compliance to the CWC (Chemical Weapons Convention). This work devotes on the development of solid-phase extraction method using silica- and polymer-based SCX (strong cation-exchange) and MCX (mixed-mode strong cation-exchange) cartridges for N,N-dialkylaminoethane-2-ols and alkyl N,N-diethanolamines, from water. The extracted analytes were analyzed by GC-MS (gas chromatography-mass spectrometry) in the full scan and selected ion monitoring modes. The extraction efficiencies of SCX and MCX cartridges were compared, and results revealed that SCX performed better. Extraction parameters, such as loading capacity, extraction solvent, its volume, and washing solvent were optimized. Best recoveries were obtained using 2 mL methanol containing 10% NH(4)OH and limits of detection could be achieved up to 5 x 10(-3) microg mL(-1) in the selected ion monitoring mode and 0.01 microg mL(-1) in full scan mode. The method was successfully employed for the detection and identification of amino alcohol present in water sample sent by Organization for Prohibition of Chemical Weapons (OPCW) in the official proficiency tests. The method was also applied to extract the analytes from human plasma. The SCX cartridge showed good recoveries of amino alcohols from human plasma after protein precipitation.

  6. Fabrication, characterization and photocatalytic properties of Ag/AgI/BiOI heteronanostructures supported on rectorite via a cation-exchange method

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Yunfang [School of Chemistry and Environment, South China Normal University, Guangzhou 510006, Guangdong (China); Fang, Jianzhang, E-mail: fangjzh@scnu.edu.cn [School of Chemistry and Environment, South China Normal University, Guangzhou 510006, Guangdong (China); Guangdong Technology Research Center for Ecological Management and Remediation of Urban Water System, Guangzhou 510006 (China); Lu, Shaoyou [Shenzhen Center for Disease Control and Prevention, Shenzhen 518055 (China); Wu, Yan; Chen, Dazhi; Huang, Liyan [Institute of Engineering Technology of Guangdong Province, Key Laboratory of Water Environmental Pollution Control of Guangdong Province, Guangzhou 510440 (China); Xu, Weicheng; Zhu, Ximiao [School of Chemistry and Environment, South China Normal University, Guangzhou 510006, Guangdong (China); Fang, Zhanqiang [School of Chemistry and Environment, South China Normal University, Guangzhou 510006, Guangdong (China); Guangdong Technology Research Center for Ecological Management and Remediation of Urban Water System, Guangzhou 510006 (China)

    2015-04-15

    Highlights: • Ag/AgI/BiOI-rectorite was prepared by twice cation-exchange process. • Ag/AgI/BiOI-rectorite photocatalyst possessed SPR and adsorption capacity. • Ag/AgI/BiOI-rectorite exhibited highly photocatalytic activity. • Trapped holes and ·O{sub 2}{sup −} were formed active species in the photocatalytic system. - Abstract: In this work, a new plasmonic photocatalyst Ag/AgI/BiOI-rectorite was prepared via a cation exchange process. The photocatalyst had been characterized by X-ray powder diffraction (XRD), Raman spectra, nitrogen sorption (BET), field-emission scanning electron microscope (FE-SEM), X-ray photoelectron spectroscopy (XPS) and UV–vis diffuse reflectance spectroscopy (DRS). The photocatalytic activity, which was evaluated by degradation of rhodamine B (RhB) and bisphenol A (BPA) under visible light irradiation, was enhanced significantly by loading Ag/AgI/BiOI nanoparticles onto rectorite. The photogenerated holes and superoxide radical (·O{sub 2}{sup −}) were both formed as active species for the photocatalytic reactions under visible light irradiation. The existence of metallic Ag particles, which possess the surface plasmon resonance effect, acted as an indispensable role in the photocatalytic reaction.

  7. Selectivity control in synergistic liquid-liquid anion exchange of univalent anions via structure-specific cooperativity between quaternary ammonium cations and anion receptors.

    Science.gov (United States)

    Borman, Christopher J; Bonnesen, Peter V; Moyer, Bruce A

    2012-10-02

    Two anion receptors enhance liquid-liquid anion exchange when added to quaternary alkylammonium chloride anion exchangers, but with a striking dependence on the structure of the alkylammonium cation that suggests a supramolecular cooperative effect. Two anion receptors were investigated, meso-octamethylcalix[4]pyrrole (C4P) and the bisthiourea tweezer 1,1'-(propane-1,3-diyl)bis(3-(4-sec-butylphenyl)thiourea (BTU). Whereas synergism is comparatively weak when either methyltri(C(8,10))alkylammonium chloride (Aliquat 336) or tetraheptylammonium chloride is used with the BTU receptor, synergism between C4P and Aliquat 336 is so pronounced that anion exchange prefers chloride over more extractable nitrate and trifluoroacetate, effectively overcoming the ubiquitous Hofmeister bias. A thermochemical analysis of synergistic anion exchange has been provided for the first time, resulting in the estimation of binding constants for C4P with the ion pairs of A336(+) with Cl(-), Br(-), OAc(F3)(-), NO(3)(-), and I(-).

  8. Microwave-assisted, grafting polymerization preparation of strong cation exchange nylon 6 capillary-channeled polymer fibers and their chromatographic properties.

    Science.gov (United States)

    Jiang, Liuwei; Marcus, R Kenneth

    2017-07-18

    Native nylon 6 C-CP fibers were modified with 2-acrylamido-2-methylpropanesulfonic acid (AMPS) via the microwave-assisted grafting polymerization to affect a strong cation exchange stationary phase. Various concentrations of AMPS and the initiator potassium persulfate (KPS) were used in the modifications. The resultant nylon-SO3H fibers were characterized by Attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), scanning electron microscopy (SEM) and acid-base titrations. The chromatographic properties, including column permeability, protein separation quality, and protein binding capacity, of the nylon-SO3H fiber columns were also studied. The cation exchange ligand densities on the modified fibers (SO3H) were determined to be 50-317 μmol g(-1), in comparison to the cation (COOH) density of 28 μmol g(-1) of native nylon 6 fibers. The modified fiber phase showed increased lysozyme dynamic loading capacities (up to ∼13 mg mL(-1) bed volume) at a linear velocity of ∼90 cm min(-1), while native nylon 6 showed only ∼1 mg mL(-1) lysozyme loading capacity. Fast (30 s-3 min) gradient separations of myoglobin, α-chymotrypsinogen A, and lysozyme were achieved on nylon-SO3H columns, with the separation resolution and peak capacity characterized. The efficiency of surface re-equilibration was probed with an eye toward using the phase as the second dimension in comprehensive two-dimensional liquid chromatography (2D-LC). The results indicate that this nylon-SO3H fiber phase has a good deal of potential for use in high-throughput analytical and preparative protein separations. Copyright © 2017 Elsevier B.V. All rights reserved.

  9. Sugarcane outgrowers in Ethiopia

    DEFF Research Database (Denmark)

    Wendimu, Mengistu Assefa; Henningsen, Arne; Gibbon, Peter

    2016-01-01

    -users. Using data from the oldest and some more recently established sugarcane outgrower schemes in Ethiopia, this paper examines the effects of compulsory participation in sugarcane outgrower production on total household income and asset stocks. Because outgrowers and non-outgrowers may have some differences...

  10. The effect of Sinabung volcanic ash and rock phosphate nanoparticle on CEC (cation exchange capacity) base saturation exchange (K, Na, Ca, Mg) and base saturation at Andisol soils Ciater, West Java

    Science.gov (United States)

    Yuniarti, Anni; Arifin, Mahfud; Sofyan, Emma Trinurasi; Natalie, Betty; Sudirja, Rija; Dahliani, Dewi

    2018-02-01

    Andisol, soil orders which covers an upland area dominantly. The aim of this research is to know the effect between the ameliorant of Sinabung volcanic ashes with the ameliorant of rock phosphatenanoparticle towards CEC and base saturation exchange (K, Na, Ca, Mg) and the base saturation on Ciater's Andisols, West Java. A randomized complete block design (RCBD) factorial with two factors was used in this research. The first factor is the volcanic ash and the second factor is rock phosphate which consists of four levels each amount of 0%, 2.5%, 5%, 7.5% with three replications. The result showed that there was no interaction between volcanic ash and rock phosphate nanoparticle formed in first month and fourth month towards the improvement of CEC and saturation base exchange rate unless magnesium cation exchange increased in fourth month. There was independent effect of volcanic ash formed nanoparticles towards base saturation exchange increased for 5% dose. There was independent effect of rock phosphate formed nanoparticles towards base saturation exchange and increased for 5% dose. The dose combination of volcanic ashes 7.5% with phosphate rock, 5% increased the base saturation in the first month incubation.

  11. Dynamic equilibria in solvent-mediated anion, cation and ligand exchange in transition-metal coordination polymers: solid-state transfer or recrystallisation?

    Science.gov (United States)

    Cui, Xianjin; Khlobystov, Andrei N; Chen, Xinyong; Marsh, Dan H; Blake, Alexander J; Lewis, William; Champness, Neil R; Roberts, Clive J; Schröder, Martin

    2009-09-07

    The solution properties of a series of transition-metal-ligand coordination polymers [ML(X)(n)](infinity) [M=Ag(I), Zn(II), Hg(II) and Cd(II); L=4,4'-bipyridine (4,4'-bipy), pyrazine (pyz), 3,4'-bipyridine (3,4'-bipy), 4-(10-(pyridin-4-yl)anthracen-9-yl)pyridine (anbp); X=NO(3) (-), CH(3)COO(-), CF(3)SO(3) (-), Cl(-), BF(4) (-); n=1 or 2] in the presence of competing anions, metal cations and ligands have been investigated systematically. Providing that the solubility of the starting complex is sufficiently high, all the components of the coordination polymer, namely the anion, the cation and the ligand, can be exchanged on contact with a solution phase of a competing component. The solubility of coordination polymers is a key factor in the analysis of their reactivity and this solubility depends strongly on the physical properties of the solvent and on its ability to bind metal cations constituting the backbone of the coordination polymer. The degree of reversibility of these solvent-induced anion-exchange transformations is determined by the ratio of the solubility product constants for the starting and resultant complexes, which in turn depend upon the choice of solvent and the temperature. The extent of anion exchange is controlled effectively by the ratio of the concentrations of incoming ions to outgoing ions in the liquid phase and the solvation of various constituent components comprising the coordination polymer. These observations can be rationalised in terms of a dynamic equilibrium of ion exchange reactions coupled with Ostwald ripening of crystalline products. The single-crystal X-ray structures of [Ag(pyz)ClO(4)](infinity) (1), {[Ag(4,4'-bipy)(CF(3)SO(3))]CH(3)CN}(infinity) (2), {[Ag(4,4'-bipy)(CH(3)CN)]ClO(4) 0.5 CH(3)CN}(infinity) (3), metal-free anbp (4), [Ag(anbp)NO(3)(H(2)O)](infinity) (5), {[Cd(4,4'-bipy)(2)(H(2)O)(2)](NO(3))(2)4 H(2)O}(infinity) (6) and {[Zn(4,4'-bipy)SO(4)(H(2)O)(3)] 2 H(2)O}(infinity) (7) are reported.

  12. Anion-directed assemblies of cationic metal-organic frameworks based on 4,4'-bis(1,2,4-triazole): syntheses, structures, luminescent and anion exchange properties.

    Science.gov (United States)

    Li, Xinxiong; Gong, Yaqiong; Zhao, Huaixia; Wang, Ruihu

    2014-11-17

    Three cationic metal-organic frameworks (MOFs), Ag(btr)·PF6·0.5CH3CN (1), Ag2(btr)2(H2O)·2CF3SO3·H2O (2), and Ag2(btr)2(NO3)·NO3 (3), were prepared from reaction of 4,4'-bis(1,2,4-triazole) (btr) with silver salts containing different anions. Complex 1 is a three-dimensional (3-D) framework constructed from tetrahedral-shaped nanoscale coordination cages with PF6(-) as counteranions. 2 and 3 are 3-D architectures containing 1-D channels, in which charge-balancing CF3SO3(-) and NO3(-) are located in their respective channels. Luminescent emission of 1-3 shows an obvious red shift compared with the btr ligand. Anion exchange studies show that 1 is able to selectively exchange MnO4(-) in aqueous solution with a modest capacity of 0.56 mol mol(-1); the luminescent emission of 1 is quickly quenched upon MnO4(-) exchange.

  13. Sequential Determination of Total Arsenic and Cadmium in Concentrated Cadmium Sulphate Solutions by Flow-Through Stripping Chronopotentiometry after Online Cation Exchanger Separation

    Directory of Open Access Journals (Sweden)

    Frantisek Cacho

    2012-01-01

    Full Text Available Flow-through stripping chronopotentiometry with a gold wire electrode was used for the determination of total arsenic and cadmium in cadmium sulphate solutions for cadmium production. The analysis is based on the online separation of arsenic as arsenate anion from cadmium cations by means of a cation exchanger. On measuring arsenate in the effluent, the trapped cadmium is eluted by sodium chloride solution and determined in a small segment of the effluent by making use of the same electrode. The elaborated protocol enables a full automatic measurement of both species in the same sample solution. The accuracy of the results was confirmed by atomic absorption spectrometry. The LOD and LOQ for Arsenic were found to be 0.9 μg dm-3 and 2.7 μg dm-3, respectively. A linear response range was observed in the concentration range of 1 to 300 μg dm-3 for sample volumes of 4 mL. The repeatability and reproducibility were found to be 2.9% and 5.2%, respectively. The linear response range for cadmium was found to be 0.5 to 60 g/L. The method was tested on samples from a cadmium production plant.

  14. Synthesis of poly(arylene ether ketone)s bearing skeletal crown ether units for cation exchange membranes

    NARCIS (Netherlands)

    Zoetebier, Bram; Tas, Sinem; Vancso, Gyula J.; Nijmeijer, Dorothea C.; Hempenius, Mark A.

    2015-01-01

    Poly(arylene ether ketone)s (PAEKs) are the most commonly known high-performance materials used for ion exchange and fuel cell membranes. Described here is the design of novel sulfonated PAEKs (SPAEKs) and nonsulfonated PAEKs containing crown ether units in the main chain, which can be used in

  15. Competitiveness of Brazilian sugarcane ethanol compared to US corn ethanol

    Energy Technology Data Exchange (ETDEWEB)

    Crago, Christine L. [Energy Biosciences Institute, 1115 IGB Bldg., 1206 W Gregory Drive, Urbana, IL (United States); Khanna, Madhu [Department of Agricultural and Consumer Economics, 301A Mumford Hall, 1301 W Gregory Drive, Urbana, IL (United States); Barton, Jason [Faculty of Land and Food Systems, University of British Columbia, 2357 Main Mall, Vancouver, BC (Canada); Giuliani, Eduardo [Venture Partners do Brasil, Rua Iguatemi 354 82, Sao Paulo, SP (Brazil); Amaral, Weber [Av. Padua Dias 11 - CP 9, Forest Sciences Departament - ESALQ, University of Sao Paulo, 13148-900, Piracicaba, SP (Brazil)

    2010-11-15

    Corn ethanol produced in the US and sugarcane ethanol produced in Brazil are the world's leading sources of biofuel. Current US biofuel policies create both incentives and constraints for the import of ethanol from Brazil and together with the cost competitiveness and greenhouse gas intensity of sugarcane ethanol compared to corn ethanol will determine the extent of these imports. This study analyzes the supply-side determinants of cost competitiveness and compares the greenhouse gas intensity of corn ethanol and sugarcane ethanol delivered to US ports. We find that while the cost of sugarcane ethanol production in Brazil is lower than that of corn ethanol in the US, the inclusion of transportation costs for the former and co-product credits for the latter changes their relative competitiveness. We also find that the relative cost of ethanol in the US and Brazil is highly sensitive to the prevailing exchange rate and prices of feedstocks. At an exchange rate of US1=R2.15 the cost of corn ethanol is 15% lower than the delivered cost of sugarcane ethanol at a US port. Sugarcane ethanol has lower GHG emissions than corn ethanol but a price of over $113 per ton of CO{sub 2} is needed to affect competitiveness. (author)

  16. A two-layer ONIOM study of thiophene cracking catalyzed by proton- and cation-exchanged FAU zeolite.

    Science.gov (United States)

    Sun, Yingxin; Mao, Xinfeng; Pei, Supeng

    2016-02-01

    A two-layer ONIOM study on the hydrodesulfurization mechanism of thiophene in H-FAU and M-FAU (M = Li(+), Na(+), and K(+)) has been carried out. The calculated results reveal that in H-FAU, for a unimolecular mechanism, the rate-determining step is hydrogenation of alkoxide intermediate. The assistance of H2O and H2S molecules does not reduce the difficulty of the C-S bond cracking step more effectively. A bimolecular hydrodesulfurization mechanism is more favorable due to the lower activation barriers. The rate-determining step is the formation of 2-methylthiophene, not the C-S bond cracking of thiophene. Moreover, the ring opening of thiophene is much easier to occur than the desulfurization step. A careful analysis of energetics indicates that H2S, propene, and methyl thiophene are the major products for the hydrodesulfurization process of thiophene over H-FAU zeolite, in good agreement with experimental findings. In M-FAU zeolites, both unimolecular and bimolecular cracking processes are difficult to occur because of the high energy barriers. Compared to the case on H-FAU, the metal cations on M-FAU increase the difficulty of occurrence of bimolecular polymerization and subsequent C-S bond cracking steps. Graphical abstract Hydrodesulfurization process of thiophene can take place in H-FAU zeolite. Two different mechanisms, unimolecular and bimolecular ones, have been proposed and evaluated in detail. The bimolecular mechanism is more favorable due to lower activation barrier as described in the picture above. Our calculated data indicate that H2S, propene, and methylthiophene are the major products, in good agreement with experimental observations. The effect of metal cations on the reaction mechanism is also investigated in this work.

  17. Preparation and characterization of electrically conducting polypyrrole Sn(IV phosphate cation-exchanger and its application as Mn(II ion selective membrane electrode

    Directory of Open Access Journals (Sweden)

    A.A. Khan

    2011-10-01

    Full Text Available Polypyrrole Sn(IV phosphate, an organic–inorganic composite cation-exchanger was synthesized via sol-gel mixing of an organic polymer, polypyrrole, into the matrices of the inorganic precipitate of Sn(IV phosphate. The physico-chemical properties of the material were determined using Atomic Absorption Spectrometry (AAS, CHN elemental analysis (inductively coupled plasma mass spectrometry, ICP-MS, UV–VIS spectrophotometry, FTIR (Fourier Transform Infra-Red, SEM (Scanning Electron Microscopy, TGA–DTA (Thermogravimetric Analysis–Differential Thermal Analysis, and XRD (X-ray diffraction. Ion-exchange behavior was observed to characterize the material. On the basis of distribution studies, the material was found to be highly selective for toxic heavy metal ion Mn2+. Due to its selective nature, the material was used as an electroactive component for the construction of an ion-selective membrane electrode. The proposed electrode shows fairly good discrimination of mercury ion over several other inorganic ions. The analytical utility of this electrode was established by employing it as an indicator electrode in electrometric titrations for Mn(II in water.

  18. Selective sorption of lead, cadmium and zinc ions by a polymeric cation exchanger containing nano-Zr(HPO3S)2.

    Science.gov (United States)

    Zhang, Qingrui; Pan, Bingcai; Pan, Bingjun; Zhang, Weiming; Jia, Kun; Zhang, Quanxing

    2008-06-01

    A novel polymeric hybrid sorbent, namely ZrPS-001, was fabricated for enhanced sorption of heavy metal ions by impregnating Zr(HPO3S)2 (i.e., ZrPS) nanoparticles within a porous polymeric cation exchanger D-001. The immobilized negatively charged groups bound to the polymeric matrix D-001 would result in preconcentration and permeation enhancement of target metal ions prior to sequestration, and ZrPS nanoparticles are expected to sequester heavy metals selectively through an ion-exchange process. Highly effective sequestration of lead, cadmium, and zinc ions from aqueous solution can be achieved by ZrPS-001 even in the presence of competing calcium ion at concentration several orders of magnitude greater than the target species. The exhausted ZrPS-001 beads are amenable to regeneration with 6 M HCI solution for repeated use without any significant capacity loss. Fixed-bed column treatment of simulated waters containing heavy metals at high or trace levels was also performed. The content of heavy metals in treated effluent approached or met the WHO drinking water standard.

  19. Dowex anion exchanger-loaded-baker's yeast as bi-functionalized biosorbents for selective extraction of anionic and cationic mercury(II) species.

    Science.gov (United States)

    Mahmoud, Mohamed E; Yakout, Amr A; Osman, Maher M

    2009-05-30

    Dowex anion exchanger-immobilized-baker's yeast [Dae-yeast] were synthesized and potentially applied as environmental friendly biosorbents to evaluate the up-take process of anionic and cationic mercury(II) species as well as other metal ions. Optimization of mass ratio of Dowex anion exchanger versus yeast (1:1-1:10) in presence of various interacting buffer solutions (pH 4.0-9.0) was performed and evaluated. Surface modification of [Dae-yeast] was characterized by scanning electron microscopy (SEM) and infrared spectroscopy. The maximum metal biosorption capacity values of [Dae-yeast] towards mercury(II) were found in the range of 0.800-0.960, 0.840-0.950 and 0.730-0.900 mmol g(-1) in presence of buffer solutions pH 2.0, 4.0 and 7.0, respectively. Three possible and different mechanisms are proposed to account for the biosorption of mercury and mercuric species under these three buffering conditions based on ion exchange, ion pair and chelation interaction processes. Factors affecting biosorption of mercury from aqueous medium including the pH effect of aqueous solutions (1.0-7.0), shaking time (1-30 min) and interfering ions were se arched. The potential applications of modified biosorbents for selective biosorption and extraction of mercury from different real matrices including dental filling waste materials, industrial waste water samples and mercury lamp waste materials were also explored. The results denote to excellent percentage extraction values, from nitric acid as the dissolution solvent with a pH 2.0, as determined in the range of 90.77-97.91+/-3.00-5.00%, 90.00-93.40+/-4.00-5.00% and 92.31-100.00+/-3.00-4.00% for the three tested samples, respectively.

  20. The critical relation between chemical stability of cations and water in anion exchange membrane fuel cells environment

    Science.gov (United States)

    Dekel, Dario R.; Willdorf, Sapir; Ash, Uri; Amar, Michal; Pusara, Srdjan; Dhara, Shubhendu; Srebnik, Simcha; Diesendruck, Charles E.

    2018-01-01

    Anion exchange membrane fuel cells can potentially revolutionize energy storage and delivery; however, their commercial development is hampered by a significant technological impedance: the chemical decomposition of the anion exchange membranes during operation. The hydroxide anions, while transported from the cathode to the anode, attack the positively charged functional groups in the polymer membrane, neutralizing it and suppressing its anion-conducting capability. In recent years, several new quaternary ammonium salts have been proposed to address this challenge, but while they perform well in ex-situ chemical studies, their performance is very limited in real fuel cell studies. Here, we use experimental work, corroborated by molecular dynamics modeling to show that water concentration in the environment of the hydroxide anion, as well as temperature, significantly impact its reactivity. We compare different quaternary ammonium salts that have been previously studied and test their stabilities in the presence of relatively low hydroxide concentration in the presence of different amounts of solvating water molecules, as well as different temperatures. Remarkably, with the right amount of water and at low enough temperatures, even quaternary ammonium salts which are considered "unstable", present significantly improved lifetime.

  1. Understanding the reactivity and basicity of zeolites: a periodic DFT study of the disproportionation of N(2)O(4) on alkali-cation-exchanged zeolite Y.

    Science.gov (United States)

    Mignon, Pierre; Pidko, Evgeny A; Van Santen, Rutger A; Geerlings, Paul; Schoonheydt, Robert A

    2008-01-01

    The disproportionation of N(2)O(4) into NO(3)(-) and NO(+) on Y zeolites has been studied through periodic DFT calculations to unravel 1) the role of metal cations and the framework oxygen atoms and 2) the relationship between the NO(+) stretching frequency and the basicity of zeolites. We have considered three situations: adsorption on site II cations with and without a cation at site III and adsorption on a site III cation. We observed that cations at sites II and III cooperate to stabilize N(2)O(4) and that the presence of a cation at site III is necessary to allow the disproportionation reaction. The strength of the stabilization is due to the number of stabilizing interactions increasing with the size of the cation and to the Lewis acidity of the alkali cations, which increases as the size of the cations decreases. In the product, NO(3)(-) interacts mainly with the cations and NO(+) with the basic oxygen atoms of the tetrahedral aluminium through its nitrogen atom. As the cation size increases, the NO(3)(-)...cation interaction increases. As a result, the negative charge of the framework is less well screened by the larger cations and the interaction between NO(+) and the basic oxygen atoms becomes stronger. NO(+) appears to be a good probe of zeolite basicity, in agreement with experimental observations.

  2. Influence of cation substitution and activator site exchange on the photoluminescence properties of Eu3+-doped quaternary pyrochlore oxides.

    Science.gov (United States)

    Mahesh, S K; Rao, P Prabhakar; Thomas, Mariyam; Francis, T Linda; Koshy, Peter

    2013-12-02

    Stannate-based pyrochlore-type red phosphors CaGd(1-x)SnNbO7:xEu(3+), Ca(1-y)Sr(y)Gd(1-x)SnNbO7:xEu(3+), and Ca(0.8-x)Sr0.2GdSnNbO(7+δ): xEu(3+) were prepared via conventional solid-state method. Influence of cation substitution and activator site control on the photoluminescence properties of these phosphors are elucidated using powder X-ray diffraction, Rietveld analysis, Raman spectrum analysis, and photoluminescence excitation and emission spectra. The Eu(3+) luminescence in quaternary pyrochlore lattice exemplifies as a very good structural probe for the detection of short-range disorder in the lattice, which otherwise is not detected by normal powder X-ray diffraction technique. The Eu(3+) emission due to magnetic dipole transition ((5)D0-(7)F1 MD) is modified with the increase in europium concentration in the quaternary pyrochlore red phosphors. (5)D0-(7)F1 MD transition splitting is not observable for low Eu(3+) doping because of the short-range disorder in the pyrochlore lattice. Appearance of narrow peaks in Raman spectra confirms that short-range disorder in the crystal lattice disappears with progressive europium doping. By using Sr as a network modifier ion in place of Ca we were able to increase the f-f transition intensities and europium quenching concentration. The influence of effective positive charge of the central Eu(3+) ions when it replaces a metal ion having lower oxidation state such as Ca(2+) was also investigated. The relative intensities of A1g (∼500 cm(-1)) and F2g (∼330 cm(-1)) Raman vibrational modes get inverted when Eu(3+) ions replaces Ca(2+) ions instead of Gd(3+) as trivalent europium ions can attract the electron cloud of oxygen ions strongly in comparison with divalent calcium ions. The influence of positive charge effect of Eu(3+) in Ca0.7Sr0.2GdSnNbO7+δ:0.1Eu(3+) phosphor is greatly strengthened the charge transfer band and (7)F0-(5)L6 transition intensities than that of the Ca0.8Sr0.2Gd0.9SnNbO7:0.1Eu(3+) phosphor. Our

  3. Microwave-assisted grafting polymerization modification of nylon 6 capillary-channeled polymer fibers for enhanced weak cation exchange protein separations

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Liuwei; Marcus, R. Kenneth, E-mail: marcusr@clemson.edu

    2017-02-15

    A weak cation exchange liquid chromatography stationary phase (nylon-COOH) was prepared by grafting polyacrylic acid on to native nylon 6 capillary-channeled polymer (C-CP) fibers via a microwave-assisted radical polymerization. To the best of our knowledge, this is the first study of applying microwave-assisted grafting polymerization to affect nylon material for protein separation. The C-CP fiber surfaces were characterized by attenuated total reflection (ATR) infrared spectroscopy and scanning electron microscope (SEM). The anticipated carbonyl peak at 1722.9 cm{sup −1} was found on the nylon-COOH fibers, but was not found on the native fiber, indicating the presence of the polyacrylic acid on nylon fibers after grafting. The nylon-COOH phase showed a ∼12× increase in lysozyme dynamic binding capacity (∼12 mg mL{sup −1}) when compared to the native fiber phase (∼1 mg mL{sup −1}). The loading capacity of the nylon-COOH phase is nearly independent of the lysozyme loading concentration (0.05–1 mg mL{sup −1}) and the mobile phase linear velocity (7.3–73 mm s{sup −1}). The reproducibility of the lysozyme recovery from the nylon-COOH (RSD = 0.3%, n = 10) and the batch-to-batch variability in the functionalization (RSD = 3%, n = 5) were also investigated, revealing very high levels of consistency. Fast baseline separations of myoglobin, α-chymotrypsinogen A, cytochrome c and lysozyme were achieved using the nylon-COOH column. It was found that a 5× increase in the mobile phase linear velocity (7.3-to-36.5 mm s{sup −1}) had little effect on the separation resolution. The microwave-assisted grafting polymerization has great potential as a generalized surface modification methodology across the applications of C-CP fibers. - Highlights: • A microwave-assisted grafting method to attach acrylic acid is described for the first time for chromatographic phases. • A high-density, weak cation exchange surface is created on a nylon

  4. Sugarcane-Biorefinery.

    Science.gov (United States)

    Vaz, Sílvio

    2017-03-17

    Concepts such as biorefinery and green chemistry focus on the usage of biomass, as with the oil value chain. However, it can cause less negative impact on the environment. A biorefinery based on sugarcane (Saccharum spp.) as feedstock is an example, because it can integrate into the same physical space, of processes for obtaining biofuels (ethanol), chemicals (from sugars or ethanol), electricity, and heat.The use of sugarcane as feedstock for biorefineries is dictated by its potential to supply sugars, ethanol, natural polymers or macromolecules, organic matter, and other compounds and materials. By means of conversion processes (chemical, biochemical, and thermochemical), sugarcane biomass can be transformed into high-value bioproducts to replace petrochemicals, as a bioeconomy model.

  5. Rapid comprehensive amino acid analysis by liquid chromatography/tandem mass spectrometry: comparison to cation exchange with post-column ninhydrin detection.

    Science.gov (United States)

    Dietzen, Dennis J; Weindel, Annette L; Carayannopoulos, Mary O; Landt, Michael; Normansell, Ellen T; Reimschisel, Tyler E; Smith, Carl H

    2008-11-01

    Ion-exchange chromatography with ninhydrin detection remains the gold standard for detecting inborn errors of amino acid catabolism and transport. Disadvantages of such analysis include long chromatography times and interference from other ninhydrin-positive compounds. The aim of this project was to develop a more rapid and specific technique using liquid chromatography/tandem mass spectrometry (LC/MS/MS). Optimal fragmentation patterns for 32 amino acids were determined on a triple quadrupole mass spectrometer following butylation. Chromatographic characteristics of each of the amino acids were determined using C8 reversed-phase chromatography with 20% acetonitrile/0.1% formic acid as isocratic mobile phase. Quantitation using eleven deuterated internal standards was compared to cation exchange and ninhydrin detection on a Beckman 7300 system. Following methanol extraction and butylation, determination of 32 amino acids required 20 min. The dynamic range of each amino acid was generally 1-1000 micromol/L. Imprecision ranged from 7 to 23% (CV) over 6 months and recovery ranged from 88-125%. Deming regression with the Beckman 7300 yielded slopes from 0.4-1.2, intercepts from -21 to 65 micromol/L, correlation coefficients from 0.84-0.99 and Syx from 2-125 micromol/L. Isobaric amino acids were separated by chromatography (e.g. leucine, isoleucine) or by unique fragmentation (e.g., alanine, beta-alanine). LC/MS/MS is comparable to traditional LC-ninhydrin detection. Mass spectral detection shortens analysis times and reduces potential for interference in detecting inborn metabolic errors.

  6. A three-factor Doehlert matrix design in optimising the determination of octadecyltrimethylammonium bromide by cation-exchange chromatography with suppressed conductivity detection.

    Science.gov (United States)

    Cataldi, Tommaso R I; Orlando, Donatella; Nardiello, Donatella; Rubino, Alessandra; Bianco, Giuliana; Abate, Salvatore; Ciriello, Rosanna; Guerrieri, Antonio

    2007-07-30

    A simple and effective chromatographic method with suppressed conductivity detection was developed and validated to determine dissolved samples of octadecyltrimethylammonium bromide (C18H37N+ Me3Br-, ODTAB) for purity testing. A response surface methodology generated with a Doehlert matrix design was applied to optimize the chromatographic and detection conditions in ion-exchange chromatography (IEC) with conductivity detection in the chemical suppression mode. A three-factor Doehlert design was performed to fit a second-order model and jointly optimize the peak intensity and shorten analysis time through a global desirability function. Regenerant flow rate, volume fraction of acetonitrile in the acidic eluent and its flow rate were studied at seven, five and three levels, respectively. The optimized separation and detection conditions were accomplished by using a cation-exchange column eluted at 0.5 mL min(-1) with an isocratic mobile phase composed of CH3CN and 25 mN H2SO4, 82/18 (v/v). Chemical suppression of ionic conductivity was performed by 100 mN tetrabutylammonium hydroxide (TBAOH) as a regenerant at a flow-rate of 4.0 mL min(-1). Remarkably good agreement was found between predicted and experimental values of signal intensity and chromatographic retention. With the developed method, a linear calibration curve of ODTA+ as bromide salt from 5 to 1000 ppm was obtained using hexadecyltrimethylammonium bromide as internal standard. The estimated limit of detection was 0.3 ppm (S/N=3). The effectiveness of electrochemically suppressed conductivity detection of ODTA+ was also demonstrated, thus making easier the whole detection operation and instrumental needs as well.

  7. Cation-exchange induced high power electrochemical properties of core-shell Ni(OH){sub 2} rate at CoOOH

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Weihua [College of Chemistry and Molecular Science, Wuhan University, 430072 Wuhan (China); Department of Chemistry, Zhengzhou University, 450001 Zhengzhou (China); Yang, Yifu; Shao, Huixia [College of Chemistry and Molecular Science, Wuhan University, 430072 Wuhan (China)

    2011-01-01

    New applications such as hybrid electric vehicles and power backup require rechargeable batteries to combine high energy density with high charge and discharge rate capability. In this study, the core-shell Ni(OH){sub 2} rate at CoOOH composite is constructed via a simple cation-exchange route at moderate conditions. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) with energy dispersive X-ray (EDX), and inductively coupled plasma (ICP) are used to characterize the resulting Ni(OH){sub 2} rate at CoOOH composites. The Ni(OH){sub 2} rate at CoOOH electrode exhibits high power, higher capacity and longer life cycle when it is chosen as an positive electrode material for rechargeable alkaline MH-Ni battery. The enhanced electrochemical performance is attributed to the seamless combination of the CoOOH shell and the Ni(OH){sub 2} core, avoiding the contact resistance between them at a large current density. It is believed that our methodology provides a simple and environment friendly route to a variety of core-shell materials with different composition and novel function. (author)

  8. Analysis of amphetamine and methamphetamine in municipal wastewater influent and effluent using weak cation-exchange SPE and LC-MS/MS.

    Science.gov (United States)

    Boles, Tammy H; Wells, Martha J M

    2016-12-01

    Amphetamine and methamphetamine are emerging contaminants-those for which no regulations currently require monitoring or public reporting of their presence in our water supply. In this research, a protocol for weak cation-exchange (WCX) SPE coupled with LC-MS/MS was developed for determination of emerging contaminants amphetamine and methamphetamine in a complex wastewater matrix. Gradient LC parameters were adjusted to yield baseline separation of methamphetamine from other contaminants. Methamphetamine-D5 was used as the internal standard (IS) to compensate for sample loss during SPE and for signal loss during MS (matrix effects). Recoveries were 102.1 ± 7.9% and 99.4 ± 4.0% for amphetamine and methamphetamine, respectively, using WCX sorbent. Notably, methamphetamine was determined to be present in wastewater influent at each sampling date tested. Amphetamine was present in wastewater influent on two of four sampling dates. Amphetamine concentrations ranged from undetectable to 86.4 ng/L in influent, but it was undetectable in wastewater effluent. Methamphetamine was detected in influent at concentrations ranging from 27.0-60.3 ng/L. Methamphetamine concentration was reduced but incompletely removed at this facility. Although absent in one post-UV effluent sample, concentrations of methamphetamine ranged from 10.8-14.8 ng/L. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  9. Cation-exchange solid-phase and liquid-liquid extraction for the determination of khat alkaloids by reversed phase HPLC-DAD

    Directory of Open Access Journals (Sweden)

    M. Atlabachew

    2015-10-01

    Full Text Available Leaves of khat (Catha edulis are masticated to elicit their psycho-stimulating properties, resulting from the presence of the phenylpropylamino alkaloids. The determination of these alkaloids is important in pharmacological, phytochemical, forensic and law enforcement environments. In this study, the use of strong cation exchange-solid phase extraction (SCX-SPE was investigated as an alternative means of sample purification prior to the determination of cathinone, cathine and norephedrine by reversed phase (C18 high performance liquid chromatography (HPLC. Extraction parameters for SCX, including loading capacity and washing solvents, were established. An existing liquid-liquid extraction (LLE method was improved in terms of recoveries obtained, by using ethyl acetate as extractant. For pure standards of the khat alkaloids, recoveries ranged from 83 to 97%. Preconcentration, using a Genevac evaporator after the addition of acidified water to the sample, restricted analyte losses when compared to concentration under nitrogen. Although comparable recoveries were obtained when preconcentration was achieved in the presence of acidified water by rotary evaporation, this method is not suitable for large sample numbers. Best recoveries, ranging from 94 to 102%, were obtained by SCX from spiked samples. Although the extraction efficiencies of LLE were lower (87-90%, LLE yielded less complex chromatograms, indicating a purer extract.DOI: http://dx.doi.org/10.4314/bcse.v29i3.1

  10. Modeling and robust pooling design of a preparative cation-exchange chromatography step for purification of monoclonal antibody monomer from aggregates.

    Science.gov (United States)

    Borg, Niklas; Brodsky, Yan; Moscariello, John; Vunnum, Suresh; Vedantham, Ganesh; Westerberg, Karin; Nilsson, Bernt

    2014-09-12

    This study has implemented and calibrated a model that describes the separation of the monomer of monoclonal antibodies from the dimer and larger oligomers on preparative-scale using cation-exchange chromatography. A general rate model with temperature dependent diffusion was coupled to a pH- and temperature-dependent steric mass action model. The model was shown to predict the retention of the monomer, dimer, and oligomer at low loadings for different pH levels and temperatures. Additionally, the model was shown to adequately predict the elution behavior of the monomer and soluble aggregates at high loadings within the same ranges with some limitations. The model was not able to accurately describe the shape of the product break-through curves or the slight levels of co-elution of the dimer and oligomer with the monomer at higher pH. The model was used to predict how 12 process variations impact the separation. The model is used to establish an elution end collection criterion such that the step can robustly provide the target purity of monomers. Copyright © 2014 Elsevier B.V. All rights reserved.

  11. Fast analysis of quaternary ammonium pesticides in food and beverages using cation-exchange chromatography coupled with isotope-dilution high-resolution mass spectrometry.

    Science.gov (United States)

    Nardin, Tiziana; Barnaba, Chiara; Abballe, Franco; Trenti, Gianmaria; Malacarne, Mario; Larcher, Roberto

    2017-10-01

    A fast separation based on cation-exchange liquid chromatography coupled with high-resolution mass spectrometry is proposed for simultaneous determination of chlormequat, difenzoquat, diquat, mepiquat and paraquat in several food and beverage commodities. Solid samples were extracted using a mixture of water/methanol/formic acid (69.6:30:0.4, v/v/v), while liquid samples were ten times diluted with the same solution. Separation was carried out on an experimental length-modified IonPac CS17 column (2 × 15 mm(2) ) that allowed the use of formic acid and acetonitrile as mobile phase. Detection limits for food and beverage matrices were established at 1.5 μg/L for chlormequat, difenzoquat and mepiquat, and 3 μg/L for diquat and paraquat, while for drinking water a pre-analytical sample concentration allowed detection limits of 9 and 20 ng/L, respectively. Precision, as repeatability (RSD%), ranged from 0.2 to 24%, with a median value of 6%, and trueness, as recovery, ranged from 64 to 118%, with a median value of 96%. The method developed was successfully applied to investigate the presence of herbicide residues in commercial commodities (mineral water, orange juice, beer, tea, green coffee bean, toasted coffee powder, cocoa bean, white corn flour, rice and sugar samples). © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Quantitative determination of 22 primary aromatic amines by cation-exchange solid-phase extraction and liquid chromatography-mass spectrometry.

    Science.gov (United States)

    Aznar, Margarita; Canellas, Elena; Nerín, Cristina

    2009-07-03

    Primary aromatic amines (PAAs) have been broadly studied due to their high toxicity. In this work a method for the analysis of 22 PAAs in aqueous simulants has been developed. The method is based on a solid-phase extraction step using cation-exchange cartridges and the subsequent analysis of the extracts by ultra-high-performance liquid chromatography with mass spectrometric detection. The recoveries obtained for all the amines analyzed ranged between 81 and 109%, linear range was between 0.03 and 75 microg L(-1), with the RSD values between 4.5 and 13.4% and an average value of 7.5% and limits of detection at microg L(-1) level. The method has been applied to two real samples obtained from migration experiments of polyurethane based laminates to simulant B (water with 3% (w/v) acetic acid) which represents the worst case for the migration of aromatic amines. The main amines found in both samples were methylenedianiline isomers, obtained from the corresponding residual diisocyanates used during polyurethane adhesive polymerization. The total amine concentration found was 26 and 6.3 microg of aniline equivalents per kg of food simulant.

  13. Water-Chemistry Evolution and Modeling of Radionuclide Sorption and Cation Exchange during Inundation of Frenchman Flat Playa

    Energy Technology Data Exchange (ETDEWEB)

    Hershey, Ronald; Cablk, Mary; LeFebre, Karen; Fenstermaker, Lynn; Decker, David

    2013-08-01

    dioxide and calcite; dissolution of sodium chloride, gypsum, and composite volcanic glass; and precipitation of composite clay and quartz represented changes in water as it disappeared from the playa. This modeling provided an understanding of the water-soil geochemical environment, which was then used to evaluate the potential mobility of residual radionuclides into the playa soils by water. Because there is no information on the chemical forms of anthropogenic radionuclides in Frenchman Flat playa soil, it was assumed that soil radionuclides go into solution when the playa is inundated. In mobility modeling, a select group of radionuclides were allowed to sorb onto, or exchange with, playa soil minerals to evaluate the likelihood that the radionuclides would be removed from water during playa inundation. Radionuclide mobility modeling suggested that there would be minimal sorption or exchange of several important radionuclides (uranium, cesium, and technetium) with playa minerals such that they may be mobile in water when the playa is inundated and could infiltrate into the subsurface. Mobility modeling also showed that plutonium may be much less mobile because of sorption onto calcite, but the amount of reactive surface area of playa soil calcite is highly uncertain. Plutonium is also known to sorb onto colloidal particles suspended in water, suspended colloidal particles will move with the water, providing a mechanism to redistribute plutonium when Frenchman Flat playa is inundated. Water chemistry, stable isotopes, and geochemical modeling showed that residual radionuclides in Frenchman Flat playa soils could be mobilized in water when the playa is inundated with precipitation. Also, there is potential for these radionuclides to infiltrate into the subsurface with water. As a result of the information obtained both during this study and the conclusions drawn from it, additional data collection, investigation, and modeling are recommended. Specifically: sampling the

  14. Sugarcane outgrowers in Ethiopia

    DEFF Research Database (Denmark)

    Assefa Wendimu, Mengistu; Henningsen, Arne; Gibbon, Peter

    smallholders. We apply matching methods to analyze the effects of a public sugarcane outgrower scheme in Ethiopia. Participation in the outgrower scheme significantly reduces the income and asset stocks of outgrowers who contributed irrigated land to the outgrower scheme, while the effect was insignificant...

  15. Preparation of a novel weak cation exchange/hydrophobic interaction chromatography dual-function polymer-based stationary phase for protein separation using "thiol-ene click chemistry".

    Science.gov (United States)

    Yang, Fan; Bai, Quan; Zhao, Kailou; Gao, Dong; Tian, Lei

    2015-02-01

    A novel dual-function mixed-mode stationary phase based on poly(glycidyl methacrylate-co-ethylene dimethacrylate) microspheres was synthesized by thiol-ene click chemistry and characterized by infrared spectroscopy and elemental analysis. The new system displays both hydrophobic interaction chromatography (HIC) character in a high salt concentration mobile phase, and weak cation exchange (WCX) chromatography character in a low salt concentration mobile phase. It can be used to separate proteins in both ion-exchange chromatography (IEC) mode and HIC mode. The resolution and selectivity of the stationary phase were evaluated in both HIC mode and IEC mode using protein standards. In comparison with the conventional WCX and HIC columns, the results were satisfactory and acceptable. Protein mass and bioactivity recoveries of more than 96% can be achieved in both HIC mode and IEC mode using this column. The results indicate that the novel dual-function mixed-mode column in many cases can replace the use of two individual WCX and HIC columns. In addition, the effects on protein separation of different ligand structures in the dual-function stationary phase and the pH of the mobile phase used were also investigated in detail. The results show that electrostatic interaction of the ligand with proteins must match the hydrophobicity of the ligand, which is an important factor to prepare the dual-function stationary phase. On the basis of this dual-function mixed-mode chromatography column, a new two-dimensional liquid chromatography technology with a single column system was also developed in this study, and was used to renature and purify recombinant human interferon-γ from inclusion bodies. The mass recovery, purity, and specific bioactivity obtained for the purified recombinant human interferon-γ were 87.2%, 92.4%, and 2.8 × 10(7) IU/mg, respectively, in IEC mode, and 83.4%, 95.2%, and 4.3 × 10(7) IU/mg, respectively, in HIC mode. The results indicate that the

  16. Ternary water in oil microemulsions made of cationic surfactants, water, and aromatic solvents. 2. Droplet sizes and interactions and exchange of material between droplets

    Energy Technology Data Exchange (ETDEWEB)

    Jada, A.; Lang, J.; Zana, R. (CNRS-ULP, Strasbourg (France)); Makhloufi, R.; Hirsch, E.; Candau, S.J. (Laboratoire de Spectrometrie et d' Imagerie Ultrasonores, Strasbourg (France))

    1990-01-11

    Ternary water in oil microemulsions made of cationic surfactants, water, and aromatic solvents have been investigated by means of time-resolved fluorescence quenching, quasi-elastic light scattering, and electrical conductivity in order to determine the surfactant aggregation number N per water droplet, the rate constant k{sub e} for the exchange of material between droplets through collisions with temporary merging, the droplet diffusion coefficient D, and the coefficient of interaction between droplets {alpha} and to study the occurrence of electrical percolation as a function of the surfactant chain length, head-group size, and water content of system (expressed as the molar concentration ratio {omega} = (water)/(surfactant)). Most measurements were performed with chlorobenzene as solvent. In one instance, chlorobenzene was substituted by benzene in order to investigate the effect of the nature of the solvent. For a given surfactant, N and k{sub e} increased with {omega} and upon substituting chlorobenzene by benzene. Also, at a given {omega}, N and k{sub e} increased when the surfactant chain length was decreased. The increases of k{sub e} were always extremely large. The droplet hydrodynamic radii from quasi-elastic light scattering were found to agree with the droplet sizes calculated with the N values from fluorescence quenching. The droplet interaction coefficient {alpha} became more negative as the surfactant chain length decreased, indicating increasingly attractive interdroplet interactions. Finally, electrical percolation was found to occur in all systems where interdroplet interactions were sufficiently attractive. The percolation threshold {omega}-values increased with surfactant chain length.

  17. Organic analysis by ion chromatography. 1. Determination of aromatic amines and aromatic diisocyanates by cation-exchange chromatography with amperometric detection.

    Science.gov (United States)

    Zhu, Yan; Wang, Muhua; Du, Huangyong; Wang, Fang; Mou, Shifen; Haddad, Paul R

    2002-05-17

    A method has been developed for the simultaneous determination of a range of aromatic amines using cation-exchange chromatography performed on a standard ion chromatography column using d.c. amperometric detection. The analytes separated were 2,4- and 2,6-toluenediamine (2,4- and 2,6-TDA), aniline, o-toluidine, benzidine, p-chloroaniline, 4,4'-diaminodiphenyl (4,4'-DDP), m-nitroaniline and 1-naphthylamine. A Dionex CS12 column was used with gradient elution from an initial eluent of 5% CH3CN+35 mM H2SO4 to 27% CH3CN+35 mM H2SO4 (at 35 min). Detection limits in the range 2.6-22.6 microg/l were observed for all analytes except m-nitroaniline, for which the detection limit was 201 microg/l. Linear calibrations and good precision were observed and the method was applied to the determination of benzidine, p-chloroaniline and 1-naphthylamine in wastewater samples. Further, the separation was also used (after some modification of the eluent conditions) for the determination of 2,4- and 2,6-toluene diisocyanate (2,4- and 2,6-TDI) and 4,4'-methylenediphenyl diisocyanate (4,4'-MDI) after their hydrolysis to 2,4-TDA, 2,6-TDA and 4,4'-DDP. Detection limits for 2,6- and 2,4-TDI and 4,4'-MDI were 3.8, 8.2, and 11.2 microg/l, respectively. The method was applied to the determination of diisocyanates in air.

  18. Integrated strong cation-exchange hybrid monolith coupled with capillary zone electrophoresis and simultaneous dynamic pH junction for large-volume proteomic analysis by mass spectrometry.

    Science.gov (United States)

    Zhang, Zhenbin; Sun, Liangliang; Zhu, Guijie; Yan, Xiaojing; Dovichi, Norman J

    2015-06-01

    A sulfonate-silica hybrid strong cation-exchange (SCX) monolith was synthesized at the proximal end of a capillary zone electrophoresis column and used for on-line solid-phase extraction (SPE) sample preconcentration. Sample was prepared in an acidic buffer and deposited onto the SCX-SPE monolith and eluted using a basic buffer. Electrophoresis was performed in an acidic buffer. This combination of buffers results in formation of a dynamic pH junction, which allows use of relatively large elution buffer volume while maintaining peak efficiency and resolution. All experiments were performed with a 50 µm ID capillary, a 1cm long SCX-SPE monolith, a 60cm long separation capillary, and a electrokinetically pumped nanospray interface. The volume of the capillary is 1.1 µL. By loading 21 µL of a 1×10(-7) M angiotensin II solution, an enrichment factor of 3000 compared to standard electrokinetic injection was achieved on this platform while retaining efficient electrophoretic performance (N=44,000 plates). The loading capacity of the sulfonate SCX hybrid monolith was determined to be ~15 pmol by frontal analysis with 10(-5) M angiotensin II. The system was also applied to the analysis of a 10(-4) mg/mL bovine serum albumin tryptic digest; the protein coverage was 12% and 11 peptides were identified. Finally, by loading 5.5 µL of a 10(-3) mg/mL E. coli digest, 109 proteins and 271 peptides were identified in a 20 min separation; the median separation efficiency generated by these peptides was 25,000 theoretical plates. Copyright © 2015 Elsevier B.V. All rights reserved.

  19. LC-MS/MS analysis of pramipexole in mouse plasma and tissues: elimination of lipid matrix effects using weak cation exchange mode based solid-phase extraction.

    Science.gov (United States)

    Guo, Weilin; Li, Gao; Yang, Yanxia; Yang, Conglian; Si, Luqin; Huang, Jiangeng

    2015-04-15

    Intranasal delivery is emerging as a promising alternative for oral or intravenous administration of central nervous system (CNS) drugs, such as pramipexole which is widely used for the treatment of Parkinson's disease. To evaluate the effectiveness of intranasal delivery of pramipexole, preclinical pharmacokinetic and tissue distribution studies following intranasal administration need to be investigated. In this paper, we developed and validated a robust and sensitive LC-MS/MS assay without matrix effect for accurate measurements of pramipexole in mouse plasma and tissue samples. Pramipexole and its stable isotope labeled internal standard (d3-pramipexole) were extracted from biological samples by protein precipitation (PPT) coupled with solid phase extraction (SPE) using weak cation exchange SPE cartridges. Matrix effects were studied using post-column infusion and post-extraction addition experiments by direct monitoring of typical phospholipids including glycerophosphocholines (GPChos) and lysoglycerophosphocholines (Lyso-GPChos). Chromatographic separation was achieved on a Welch Ultimate(®) XB-CN column using isocratic elution with a run time of 3.0 min. The assay was linear in the concentration range of 0.05-100 ng/mL and the intra- and inter-day precision and accuracy met the acceptance criteria. Compared with previous reported assays, the current sample preparation approach exhibited significant reduction of matrix effects due to the dramatically decreased levels of residual matrix components such as GPChos and Lyso-GPChos. This method has been successfully applied to pharmacokinetic and tissue distribution studies of pramipexole in mice following a single intravenous or intranasal dose of 50 μg/kg. Copyright © 2015 Elsevier B.V. All rights reserved.

  20. Online coupling of hydrophilic interaction/strong cation exchange/reversed-phase liquid chromatography with porous graphitic carbon liquid chromatography for simultaneous proteomics and N-glycomics analysis.

    Science.gov (United States)

    Zhao, Yun; Law, Henry C H; Zhang, Zaijun; Lam, Herman C; Quan, Quan; Li, Guohui; Chu, Ivan K

    2015-10-09

    In this study we developed a fully automated three-dimensional (3D) liquid chromatography methodology-comprising hydrophilic interaction separation as the first dimension, strong cation exchange fractionation as the second dimension, and low-pH reversed-phase (RP) separation as the third dimension-in conjunction downstream with additional complementary porous graphitic carbon separation, to capture non-retained hydrophilic analytes, for both shotgun proteomics and N-glycomics analyses. The performance of the 3D system alone was benchmarked through the analysis of the total lysate of Saccharomyces cerevisiae, leading to improved hydrophilic peptide coverage, from which we identified 19% and 24% more proteins and peptides, respectively, relative to those identified from a two-dimensional hydrophilic interaction liquid chromatography and low-pH RP chromatography (HILIC-RP) system over the same mass spectrometric acquisition time; consequently, the 3D platform also provided enhanced proteome and protein coverage. When we applied the integrated technology to analyses of the total lysate of primary cerebellar granule neurons, we characterized a total of 2201 proteins and 16,937 unique peptides for this primary cell line, providing one of its most comprehensive datasets. Our new integrated technology also exhibited excellent performance in the first N-glycomics analysis of cynomolgus monkey plasma; we successfully identified 122 proposed N-glycans and 135 N-glycosylation sites from 122 N-glycoproteins, and confirmed the presence of 38 N-glycolylneuraminic acid-containing N-glycans, a rare occurrence in human plasma, through tandem mass spectrometry for the first time. Copyright © 2015 Elsevier B.V. All rights reserved.

  1. P retention and cation exchange as affected by nanoparticle of volcanic ash and application of phosphate solubilizing bacteria on Andisol Ciater, West Java, Indonesia

    Science.gov (United States)

    Fitriatin, Betty Natalie; Arifin, Mahfud; Devnita, Rina; Yuniarti, Anni; Haryanto, Rachmat; Setiabudi, Mariska Amalia

    2018-02-01

    Andisols is a soil with high retention of phosphate and cannot be absorbed by plants. Some of soil bacteria have the ability to solubilize P and make it available to growing plants are known phosphate solubilizing bacteria (PSB). The research aims to study the effect of nanoparticle volcanic ash and phosphate solubilising bacteria (PSB) on P retention and cation exchangeable (CEC) in Andisol Ciater, West Java. This research was conducted from October 2016 to March 2017. The design of the analysis used was a complete randomized factorial design with two factors. The first factor was nanoparticle volcanic ash (a) consists of four dosages based on weight percentage (0%, 2.5%, 5.0% and 7.5%) and the second factor was PSB (h) consists of two dosages (without biofertilizer and with biofertilizer 1 g/Kg soil). The combination treatments replicated three times were incubated for 4 months. Soil samples were analyzed at first month and fourth month after incubation. The results showed that all dosages of nanoparticle volcanic ash and application of PSB decreased P retention by 75-77% at the first month after incubation. Nanoparticle volcanic ash dosage decreased to 7.5% the P retention reaches 90.36% in the fourth month after incubation. The nanoparticle of volcanic ash dosage 7.5% increased with CEC (24.787 cmol.kg-1 and 16.555 cmol.kg-1) at the first and fourth months after incubation. The application of PSB increased the CEC (28.606 cmol.kg-1) in the first month after incubation.

  2. Actinide cation-cation complexes

    Energy Technology Data Exchange (ETDEWEB)

    Stoyer, Nancy Jane [Univ. of California, Berkeley, CA (United States)

    1994-12-01

    The +5 oxidation state of U, Np, Pu, and Am is a linear dioxo cation (AnO2+) with a formal charge of +1. These cations form complexes with a variety of other cations, including actinide cations. Other oxidation states of actinides do not form these cation-cation complexes with any cation other than AnO2+; therefore, cation-cation complexes indicate something unique about AnO2+ cations compared to actinide cations in general. The first cation-cation complex, NpO2+•UO22+, was reported by Sullivan, Hindman, and Zielen in 1961. Of the four actinides that form AnO2+ species, the cation-cation complexes of NpO2+ have been studied most extensively while the other actinides have not. The only PuO2+ cation-cation complexes that have been studied are with Fe3+ and Cr3+ and neither one has had its equilibrium constant measured. Actinides have small molar absorptivities and cation-cation complexes have small equilibrium constants; therefore, to overcome these obstacles a sensitive technique is required. Spectroscopic techniques are used most often to study cation-cation complexes. Laser-Induced Photacoustic Spectroscopy equilibrium constants for the complexes NpO2+•UO22+, NpO2+•Th4+, PuO2+•UO22+, and PuO2+•Th4+ at an ionic strength of 6 M using LIPAS are 2.4 ± 0.2, 1.8 ± 0.9, 2.2 ± 1.5, and ~0.8 M-1.

  3. Cation dependencies and turnover rates of the human K⁺-dependent Na⁺-Ca²⁺ exchangers NCKX1, NCKX2, NCKX3 and NCKX4.

    Science.gov (United States)

    Jalloul, Ali H; Szerencsei, Robert T; Schnetkamp, Paul P M

    2016-01-01

    The Solute Carrier Family 24 (SLC24) belongs to the CaCA super family of Ca(2+)/cation antiporters and codes for five different K(+)- dependent Na(+)- Ca(2+) exchangers (NCKX1-5). NCKX proteins play a critical role in Ca(2+) homeostasis in a wide variety of biological processes such as vision, olfaction, enamel formation, Melanocortin-4-receptor-dependent satiety and skin pigmentation. NCKX transcripts are widely found throughout the brain. In this study we examine the differences between NCKX1-4 in terms of cation dependencies. We measured changes to Ca(2+) influx via the reverse exchange mode while manipulating external Ca(2+) or K(+) or internal Na(+) concentrations (External Ca(2+) Dependence, External K(+) Dependence and Internal Na(+) Dependence respectively); we also looked at the effect of external Na(+)/Ca(2+) competition and 3' 4'-Dichlorobenzamil on the transport of ions in HEK 293 cell lines. A fluorescence based assay was used to determine differences in transport kinetics of the four membrane spanning exchangers using the Michaelis-Menten constant (Km). Our results show that there are no significant differences between the NCKX isoforms to explain the variation in the specific expression pattern of these exchangers. Copyright © 2015 Elsevier Ltd. All rights reserved.

  4. Unique cover crops for Louisiana sugarcane

    Science.gov (United States)

    Louisiana sugarcane production practices provide a tremendous opportunity for the use of cover crops following the final sugarcane harvest in the fall of one year and prior to replanting sugarcane during the summer of the next year. A Louisiana sugarcane field is typically replanted every four years...

  5. Registration of "CPSG-3481 sugarcane

    Science.gov (United States)

    ‘CPSG-3481’ (Reg. No. , PI 676023) sugarcane (a complex hybrid of Saccharum spp.) was a new cultivar developed through cooperative research conducted by the Shakarganj Sugar Research Institute in Pakistan and the USDA-ARS Sugarcane Field Station in USA, and released to growers for loam soils...

  6. Quantification of sugarcane yellow leaf virus in sugarcane following transmission through aphid vector, Melanaphis sacchari

    National Research Council Canada - National Science Library

    Chinnaraja, C; Viswanathan, R

    2015-01-01

    .... Studies were conducted on the virus transmission by sugarcane aphid Melanaphis sacchari in sugarcane by inoculating virus-free meristem derived from micro- propagated plants of sugarcane cv Co 86032...

  7. Microwave-assisted grafting polymerization modification of nylon 6 capillary-channeled polymer fibers for enhanced weak cation exchange protein separations.

    Science.gov (United States)

    Jiang, Liuwei; Marcus, R Kenneth

    2017-02-15

    A weak cation exchange liquid chromatography stationary phase (nylon-COOH) was prepared by grafting polyacrylic acid on to native nylon 6 capillary-channeled polymer (C-CP) fibers via a microwave-assisted radical polymerization. To the best of our knowledge, this is the first study of applying microwave-assisted grafting polymerization to affect nylon material for protein separation. The C-CP fiber surfaces were characterized by attenuated total reflection (ATR) infrared spectroscopy and scanning electron microscope (SEM). The anticipated carbonyl peak at 1722.9 cm(-1) was found on the nylon-COOH fibers, but was not found on the native fiber, indicating the presence of the polyacrylic acid on nylon fibers after grafting. The nylon-COOH phase showed a ∼12× increase in lysozyme dynamic binding capacity (∼12 mg mL(-1)) when compared to the native fiber phase (∼1 mg mL(-1)). The loading capacity of the nylon-COOH phase is nearly independent of the lysozyme loading concentration (0.05-1 mg mL(-1)) and the mobile phase linear velocity (7.3-73 mm s(-1)). The reproducibility of the lysozyme recovery from the nylon-COOH (RSD = 0.3%, n = 10) and the batch-to-batch variability in the functionalization (RSD = 3%, n = 5) were also investigated, revealing very high levels of consistency. Fast baseline separations of myoglobin, α-chymotrypsinogen A, cytochrome c and lysozyme were achieved using the nylon-COOH column. It was found that a 5× increase in the mobile phase linear velocity (7.3-to-36.5 mm s(-1)) had little effect on the separation resolution. The microwave-assisted grafting polymerization has great potential as a generalized surface modification methodology across the applications of C-CP fibers. Copyright © 2016 Elsevier B.V. All rights reserved.

  8. Redox speciation of iron, manganese, and copper in cerebrospinal fluid by strong cation exchange chromatography - sector field inductively coupled plasma mass spectrometry.

    Science.gov (United States)

    Solovyev, Nikolay; Vinceti, Marco; Grill, Peter; Mandrioli, Jessica; Michalke, Bernhard

    2017-06-22

    A new method of simultaneous redox speciation of iron (II/III), manganese (II/III), and copper (I/II) in cerebrospinal fluid (CSF) has been designed. For the separation of redox species strong cation exchange chromatography (SCX) with isocratic elution was employed. Species were detected using inductively coupled plasma sector field mass spectrometry (ICP-sf-MS), operating at medium resolution. The following parameters were optimized: analytical column, eluent composition and pH, CSF injection volume and dilution factor. Analytical column Dionex IonPac CS5A RFIC 4*250 mm was found to retain and separate species of interest the most effectively under the isocratic elution with a buffer, containing 50 mM ammonium citrate, 7.0 mM pyridine-2,6-dicarboxylic acid at pH = 4.2 and flow rate of 0.8 L min-1. Injection volume of 50 μL with CSF sample dilution of 1/3 (v/v) with the eluent was shown to result in minimal matrix suppression. For species identification, retention time matching with standards was used. The stability of metalloproteins (ferritin, transferrin, and ceruloplasmin) under elution conditions was evaluated. For the quantification of redox species, external calibration was employed. To avoid column contamination, a blank was run after measurement and all quantification values were blank subtracted. For recovery checks, species quantification data was verified against total content of an element, measured by dynamic reaction cell ICP-MS. Recoveries (sum of quantified species vs. total element determinations) were 82.5 ± 22% (Mn), 92 ± 11% (Fe), and 88.7 ± 12% (Cu). The method was tested using 38 real CSF samples. Limits of detection (3σ) for the CSF samples were 0.5 μg L-1, 0.6 μg L-1, and 0.8 μg L-1 for Fe, Mn, and Cu species, respectively. Retention time precision was 1-7.5% (as RSD), whereas peak area RSDs were in the range 5-11%, both depending on the species. Copyright © 2017 Elsevier B.V. All rights reserved.

  9. Development of separation technology for the removal of radium-223 from targeted thorium conjugate formulations. Part II: purification of targeted thorium conjugates on cation exchange columns.

    Science.gov (United States)

    Frenvik, Janne Olsen; Dyrstad, Knut; Kristensen, Solveig; Ryan, Olav B

    2017-09-01

    Tumor targeting pharmaceuticals will play a crucial role in future pharma pipelines. The targeted thorium conjugate (TTC) therapeutic platform could provide real benefit to patients, whereby targeting moieties like monoclonal antibodies are radiolabelled with the alpha-emitting radionuclide thorium-227 ((227)Th, t1/2 = 18.7 days). A potential problem could be the accumulation of the long-lived daughter nuclide radium-223 ((223)Ra, t1/2 = 11.4 days) in the drug product during manufacturing and distribution. Therefore, the level of (223)Ra must be standardized before administration to the patient. The focus in this study has been the removal of (223)Ra, as the other progenies will have a very limited stay in the formulation. In this study, the purification of TTCs labeled with decayed (227)Th has been explored. Columns packed with a strong cation exchange resin have been used to sequester (223)Ra. The separation of TTC from (223)Ra has been evaluated as influenced by both formulation and process parameters with a design of experiments (DOE) study; including citrate or acetate buffer, pH, buffer concentration, presence or absence of pABA + EDTA, resin amount and sodium chloride concentration. The aim was to achieve a separation with high sorption of (223)Ra and accompanying low TTC sorption. The results were analyzed by multivariate analysis. Four regression models of TTC and (223)Ra sorption from citrate and acetate buffered formulations were developed. The predictive accuracy of sorption in the four statistical models was given by standard deviations and confidence intervals. The TTC sorption in citrate and acetate buffered formulations was affected by the identical variables and the variation in TTC sorption was comparable for the two models. However, the DOE variables had a significantly stronger impact on the (223)Ra sorption in citrate buffered formulations than the (223)Ra sorption in acetate buffer. An optimal separation with a TTC sorption

  10. The elution of erbium from a cation exchanger bed by means of the N-hydroxyethyl-ethylene-diamine triacetic acid; Mecanismo de la elucion del erbio en un cambiador cationico con el acido n-hidroxietil-etilen-diamono-triacetico

    Energy Technology Data Exchange (ETDEWEB)

    Amer Amezaga, S.

    1963-07-01

    A physicochemical study of the phenomena resulting when erbium is eluted from a cation-exchanger bed at a steady by means of the N-hydroxyethyl-ethylene-diamine-triacetic acid (HEDTA) is made. Two different retaining beds are used, a hydrogen bed, in which no ammonium passes through, and a zinc bed, which leaks ammonium ion. Good agreement between experimental and calculated values by using the equations deduced for the concentrations of the main species has been achieved, with errors around 1-2% in most of the experiments. (Author) 69 refs.

  11. Cation exchange capacity of an oxisol amended with an effluent from domestic sewage treatment Capacidade de troca catiônica de um latossolo tratado com efluente de tratamento de esgoto doméstico

    Directory of Open Access Journals (Sweden)

    Adriel Ferreira da Fonseca

    2005-12-01

    Full Text Available The addition of Na-rich anthropogenic residues to tropical soils has stimulated the scientific community to study the role of sodium in both the soil solution and the exchange complex. In this study, several different methods were used to calculate the concentration of exchangeable and soluble cations and this data was then used to establish correlations between the level of these cations and both the accumulation of various elements and the dry weight of maize grown in a greenhouse under different conditions. In the closed environments of the pots, the most suitable method for calculating the effective cation exchange capacity (ECEC was the cation exchange capacity calculated by cations removed with barium chloride solution (CEC S. Then again, the actual cation exchange capacity (CEC A should be measured by using Mg adsorption to prevent ionic force from influencing electric charges. A strong positive correlation was obtained between the concentrations of Na in the 1:2 soil:water extracts and the accumulation of Na in the maize plants, indicating saline or double acid extractors are not needed when monitoring the Na concentration only.A disposição de resíduos antropogênicos ricos em sódio nos solos tropicais tem despertado o interesse da comunidade científica em estudar a participação deste elemento no complexo de troca, bem como na solução no solo. Objetivou-se neste trabalho estabelecer correlações entre as concentrações de cátions trocáveis e de cátions solúveis, obtidos por diferentes métodos, com o acúmulo de elementos e com a massa seca no milho. O experimento foi conduzido em casa de vegetação, sob diferentes condições. Para experimentos em ambiente fechado (vasos, o método mais indicado para o cálculo da capacidade de troca catiônica efetiva (CTCe é a capacidade de troca catiônica calculada a partir dos cátions removidos com solução de cloreto de bário. Ainda, a capacidade de troca catiônica atual deve

  12. Development of separation technology for the removal of radium-223 from targeted thorium conjugate formulations. Part I: purification of decayed thorium-227 on cation exchange columns.

    Science.gov (United States)

    Frenvik, Janne Olsen; Dyrstad, Knut; Kristensen, Solveig; Ryan, Olav B

    2017-02-01

    Targeted thorium conjugates (TTCs) are being explored as a potential future platform for specific tumor targeting pharmaceuticals. In TTCs, the alpha emitting radionuclide thorium-227 ((227)Th) with a half-life of 18.697 d is labeled to targeting moieties, such as monoclonal antibodies (mAbs). The amount of daughter nuclide radium-223 ((223)Ra, t1/2 = 11.435 d) will increase during manufacture and distribution, and so a technology for purification is required to assure an acceptable level of (223)Ra is administrated to the patient. Since (223)Ra is the only progeny of (227)Th with a long half-life (days), the progenies of (223)Ra will have a very limited stay in the formulation once (223)Ra is removed. The focus in this study has, therefore, been on the removal of (223)Ra. In this study, the sorption and separation of (223)Ra (radium(II)) and (227)Th (thorium(IV)) on cation exchange columns has been evaluated as a purification method of decayed (227)Th (i.e. prior to radiolabelling of a mAb and formation of TTC). The goal is to minimize the sorption of (227)Th and maximize the sorption of (223)Ra. Statistical experimental design with formulation and process parameters, including buffered formulations comprising citrate and acetate, at various concentrations and pH, presence of free radical scavenger and chelator, and resin amount have been evaluated for impact on the purification process. The studies have been interpreted by the aid of multivariate data analysis. The correlations between design of experimental variables and sorption are summarized by regression models. The predictive accuracy of radionuclide sorption was given by standard deviation and 95% confidence intervals originating from statistical cross validation. Experimental results and statistical models for citrate-buffered formulations verified reproducible and acceptable sorption levels of (223)Ra and (227)Th under selected conditions. For acetate-buffered formulations, prediction of (227)Th

  13. A new type of polyhedron-based metal-organic frameworks with interpenetrating cationic and anionic nets demonstrating ion exchange, adsorption and luminescent properties.

    Science.gov (United States)

    Zhang, Zheng-Jie; Shi, Wei; Niu, Zheng; Li, Huan-Huan; Zhao, Bin; Cheng, Peng; Liao, Dai-Zheng; Yan, Shi-Ping

    2011-06-14

    An interesting new MOF, built with interpenetrating cationic (MOF-A(+)) and anionic (MOF-B(-)) nets that do not require counter ions to balance charge, together with an architectural strategy focused on the use of MOPs as nodes and MOCs as spacers for the generation of 3D frameworks, is reported. This journal is © The Royal Society of Chemistry 2011

  14. Simultaneous determination of N-oxides and free bases of pyrrolizidine alkaloids by cation-exchange solid-phase extraction and ion-pair high-performance liquid chromatography.

    Science.gov (United States)

    Mroczek, Tomasz; Glowniak, Kazimierz; Wlaszczyk, Anna

    2002-03-08

    Cation-exchange solid-phase extraction using LiChrolut SCX (Merck, Darmstadt) cartridges filled with polymeric strong cation-exchanger enabled efficient isolation of both N-oxides and free bases of pyrrolizidine alkaloids (PAs). The recoveries were about 80% for retrorsine-N-oxide, 90% for retrorsine and 100% for senkirkine and were assessed both by TLC-densitometry and ion-pair high-performance liquid chromatography (HPIPC) on Hypersil BDS C8 stationary phase and hexane-l-sulfonic acid as ion-pairing agent. The applied HPIPC gradient procedure was suitable for separation of PAs with various types of structures (N-oxides, free bases, otonecine-PAs). The method limits of detection and quantitation, respectively, ranged from 0.06 ng/microl (senecionine) and 0.2 ng/microl (senkirkine) to 0.1 and 0.35 ng/microl for retrorsine-N-oxide. For each component calibrated by linear regression method, correlation coefficients were higher than 0.9995 (six-point calibration from 4 to 100 microg/ml). The elaborated procedure was used in searching for PAs in plant derived samples from Symphytum sp. (comfrey), Petasites hybridus and Petasites albus (butterbur), Tussilago farfara (coltsfoot), Emilia coccinea (tassel flower) and Doronicum columnae (leopard's bane). For the last three samples macrocyclic PAs (senecionine, senecionine-N-oxide. senkirkine) have been detected for the first time. Details of precision of the analyses are also included.

  15. [Predicting the cadmium bioavailability in the soil of sugarcane field based on the diffusive gradients in thin films with binding phase of sodium polyacrylate].

    Science.gov (United States)

    Wang, Fang-Li; Song, Ning-Ning; Zhao, Yu-Jie; Zhang, Chang-Bo; Shen, Yue; Liu, Zhong-Qi

    2012-10-01

    The diffusive gradients in thin films (DGT) technique with solid-state binding phases has been widely used for in situ collection and measurement of available heavy metals in waters, soils or sediments, whereas DGT with liquid binding phase is primarily used in the in situ analysis of heavy metals in waters. In this paper, rhizosphere soils of sugarcane were collected in Guangxi and the concentrations of cadmium (Cd) were determined by DGT with a solid-state binding phase of chelex100 (chelex100-DGT) and modified DGT with a liquid binding phase of sodium polyacrylate (CDM-PAAS-DGT). The result showed that the Cd contents in soils measured by DGT with both binding phases and Cd in the roots, leaves and unpolished stems of sugarcane had significant positive correlation. The extraction ability of the CDM-PAAAS-DGT was much higher than that of the chelex100-DGT. In addition, multivariate analyses were used to assess the impact of pH, cation exchange capacity (CEC), soil organic matter (OM) and texture. Two principal components were extracted and the linear regression models were established. The Cd bioavailability in soils could be accurately predicted by the CDM-PAAAS-DGT technique, which expanded its applicable area.

  16. Quantification of sugarcane yellow leaf virus in sugarcane following transmission through aphid vector, Melanaphis sacchari

    OpenAIRE

    Chinnaraja, C.; Viswanathan, R.

    2015-01-01

    Yellow leaf caused by Sugarcane yellow leaf virus (SCYLV) is a serious constraint to sugarcane production in India and currently the disease epidemics occur on many of the susceptible varieties under field conditions. Studies were conducted on the virus transmission by sugarcane aphid Melanaphis sacchari in sugarcane by inoculating virus-free meristem derived from micro- propagated plants of sugarcane cv Co 86032 with viruliferous aphids. Virus transmission was confirmed through RT-PCR assays...

  17. Sugarcane for Bioethanol: Soil and Environmental Issues

    NARCIS (Netherlands)

    Hartemink, A.E.

    2008-01-01

    Cultivation of sugarcane for bioethanol is increasing and the area under sugarcane is expanding. Much of the sugar for bioethanol comes from large plantations where it is grown with relatively high inputs. Sugarcane puts a high demands on the soil because of the use of heavy machinery and because

  18. Kenaf and cowpea as sugarcane cover crops

    Science.gov (United States)

    The use of cover crops during the fallow period prior to planting sugarcane has the potential to influence not only the following sugarcane crop, but the economics of the production system as a whole. Typically, a Louisiana sugarcane field is replanted every four years due to declining yields, and,...

  19. Managing damaging freeze events in Louisiana sugarcane

    Science.gov (United States)

    Exposure of sugarcane to damaging frosts occurs in approximately 25% of the sugarcane producing countries of the world, but is most frequent on the mainland of the United States, especially in the state of Louisiana. The frequent winter freezes that occur in the sugarcane areas of Louisiana have fo...

  20. Cátions trocáveis, capacidade de troca de cátions e saturação por bases em solos brasileiros adubados com composto de lixo urbano Exchangeable cations, cation exchange capacity and base saturation in Brazilian soils amended with urban waste compost

    Directory of Open Access Journals (Sweden)

    Cassio Hamilton Abreu Jr.

    2001-12-01

    Full Text Available O uso agrícola do composto de lixo, como fertilizante orgânico, além de melhorar as propriedades do solo, representa uma alternativa importante para gestão de resíduos sólidos domiciliares. Foram estudados os efeitos da aplicação do composto de lixo, proveniente da cidade de São Paulo (Usina de compostagem São Matheus, na dose de 30 g dm-3 (60 t ha-1, na presença e ausência de calcário dolomítico e adubos minerais, sobre os teores de cátions trocáveis (K+, Ca2+, Mg2+ e Na+; a capacidade de troca de cátions (CTC e a saturação por bases (V% de 21 solos ácidos e 5 solos alcalinos. Nos solos alcalinos o calcário foi substituído por gesso. O experimento foi conduzido em condições de casa de vegetação em delineamento em blocos ao acaso, com parcelas em faixas e três repetições. Nos solos ácidos, a aplicação do composto de lixo promoveu aumentos nos teores trocáveis de potássio, cálcio, magnésio e sódio, em média, de 195%, 200%, 86% e 1200%, e elevação da CTC em 42%, refletindo na V%, com aumento médio de 39%. Nos solos alcalinos, esses efeitos foram menos pronunciados, refletindo porém, em média, em aumentos da CTC em 8,4% e da V% em 2%. Os maiores efeitos sobre as propriedades químicas avaliadas foram conseqüências das aplicações do composto + adubo + calcário, nos solos ácidos, e do composto + adubo + gesso, nos solos alcalinos. A aplicação agrícola do composto de lixo urbano é viável, porém seus efeitos sobres as propriedades químicas do solo devem ser monitorados.The use of urban organic solid waste compost as organic fertilizer is an important alternative to solid waste management. This waste has been applied to agricultural lands because of the benefits in relation to soil chemical properties. A greenhouse experiment was conducted to investigate the effects of the application of urban waste compost, at the rate of 30 g dm-3 (60 t ha-1, on the contents of exchangeable cations (K+, Ca2+, Mg2

  1. Categorizing sugarcane cultivar resistance to the sugarcane aphid and yellow sugarcane aphid (Hemiptera: Aphididae).

    Science.gov (United States)

    Akbar, W; Showler, A T; Reagan, T E; White, W H

    2010-08-01

    Sugarcane (Saccharum spp.) in Louisiana is colonized by two aphid species, the sugarcane aphid, Melanaphis sacchari (Zehntner), and the yellow sugarcane aphid, Sipha flava (Forbes) (Hemiptera: Aphididae). The main problem associated with M. sacchari is transmission of sugarcane yellow leaf virus, a casual agent of yellow leaf disease whose absence has been added to certification standards for micropropagated sugarcane in Louisiana. Greenhouse studies were conducted to categorize dominant commercial sugarcane cultivars for their ability to tolerate aphid injury and to express antixenotic or antibiotic effects on both aphid species. Antixenosis tests showed no preference among cultivars by either aphid species. Loss of chlorophyll content in tolerance tests also did not show differences among cultivars for both aphid species. However, antibiosis tests revealed that life history parameters such as the duration of the reproductive period and fecundity of both aphid species were negatively affected on 'HoCP 91-555' compared with 'L 97-128'. Estimation of demographic statistics indicated that both aphid species exhibited a significantly lower intrinsic rate of increase (1.8-2.8-fold) and longer doubling time (1.7-3.1-fold) on HoCP 91-555 relative to L 97-128. From these tests, cultivars in the current study can be ranked from most to the least susceptible as L 97-128 > 'LCP 85-384' > 'HoCP 96-540' > 'Ho 95-988' > HoCP 91-555 for M. sacchari and L 97-128 > LCP 85-384 > HoCP 91-555 for S. flava. Therefore, antibiosis is an important category of resistance in sugarcane to both aphid species, and HoCP 91-555 might provide useful germplasm for developing aphid resistant cultivars.

  2. Anion exchange membranes composed of a poly(2,6-dimethyl-1,4-phenylene oxide) random copolymer functionalized with a bulky phosphonium cation

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Ye; Zhang, Bingzi; Kinsinger, Corey L.; Yang, Yuan; Seifert, Soenke; Yan, Yushan; Mark Maupin, C.; Liberatore, Matthew W.; Herring, Andrew M.

    2016-05-01

    A random copolymer, tris(2,4,6-trimethoxyphenyl) phosphonium functionalized poly(2,6-dimethyl-1,4-phenylene oxide) (PPO-TPQP) was cast from three different solvents: dimethyl sulfoxide (DMSO), ethyl lactate, or a 41:59 vol% mixture of DMSO and ethyl lactate. Solvents were selected via analysis of the Hansen solubility parameters to vary the phase separation of the polymer in the films. An optimized mixture of DMSO and ethyl lactate chosen for film fabrication and this film was contrasted with films cast from the neat constituent solvents. Atomic force microscopy identified domains from nanometer to tens of nanometer sizes, while the light microscopy showed features on the order of micron. SAXS revealed a cation scattering peak with a d-spacing from 7 to 15 A. Trends in conductivity and water diffusion for the membranes vary depending on the solvent from which they are cast. The mixed solvent cast membrane shows a linear Arrhenius behavior indicating fully dissociated cationic/anionic groups, and has the highest bromide conductivity of 3 mS/cm at 95% RH, 90 degrees C. The ethyl lactate cast membrane shows a linear Arrhenius relation in conductivity, but a Vogel-Tamman-Fulcher behavior in its water self-diffusion. While water increases bromide dissociation, water and bromide transport in these films seems to be decoupled. This is particularly true for the film cast from ethyl lactate.

  3. Exchange of lyotropic series cations by micaceous vermiculite and its weathering products determined by electron microscopy and radiochemical analysis. Final technical report, June 1, 1965-October 31, 1978

    Energy Technology Data Exchange (ETDEWEB)

    Jackson, M L

    1978-01-01

    Micaceous vermiculite was found to be ubiquitous in soils, sediments, and aerosol mineral dusts and to adsorb fission product ions, particularly /sup 137/Cs/sup +/ and /sup 90/Sr/sup 2 +/. Crystallographic wedge zones (imaged by ultramicrotomy and electron microscopy) in micaceous vermiculite effected tight fixation of Cs/sup +/. Lowering of mica layer charge occurred in local areas, electronoscopically imaged by use of blister-swelling cations. Nuclear fission particle tracks of U enhanced translayer diffusion of elements, measured mica layer charge and age. Iron-aluminum hydrous oxide coatings adsorbed divalent cations of the alkaline earth, transition, and heavy metal elements from trace concentrations in the presence of 1 M NaNO/sub 3/. Global deposition of dust by rainfall accounted for the wide distribution of Cs-fixing micaceous vermiculite in soils. Origin of the dust was traced through a method developed for isolation of fine quartz silt (1 to 10 ..mu..m diameter). Mass spectrometry of its /sup 18/O//sup 16/O isotopic ratios showed distinctly higher (delta/sup 18/O = 17 to 22%/sub 0/) and lower (delta/sup 18/O = 9 to 15%/sub 0/) ranges in the Northern and Southern Hemispheres, respectively. This difference was traced to the relative proportions of quartz from low-temperature authigenic (chert) vs igneous-metamorphic origin in the respective latitudes, hinging on trans-equatorial continental drift.

  4. An unusual copper(I) halide-based metal-organic framework with a cationic framework exhibiting the release/adsorption of iodine, ion-exchange and luminescent properties.

    Science.gov (United States)

    Xin, Bingjing; Zeng, Guang; Gao, Lu; Li, Yun; Xing, Shanghua; Hua, Jia; Li, Guanghua; Shi, Zhan; Feng, Shouhua

    2013-06-07

    A copper(I) halide-based compound with a formula of [Cu4I3(DABCO)2]I3 (DABCO = N,N'-dimethyl-1,4-diazabicyclo[2.2.2]octane) has been prepared by solvothermal reactions. This compound has been characterized by single-crystal X-ray diffraction, elemental analysis, IR, TG, XPS and powder X-ray diffractions. Structure analyses reveal that this compound is constructed by unprecedented cationic cluster [Cu8I6](2+) and organic ligand DABCO and the channels of this compound are occupied by I2 and I(-). The guest I2 and I(-) can move freely in and out of the host-framework. UV/vis spectra confirm that the I2 molecules in the channels can release into some organic solvents and IR spectra confirm the I(-) was exchanged by SCN(-). In addition, the luminescent properties of this compound in the solid state have also been investigated.

  5. An approach to speed up the isolation of hydrophilic metabolites from natural sources at semipreparative level by using a hydrophilic-lipophilic balance/mixed-mode strong cation exchange-high-performance liquid chromatography/mass spectrometry system.

    Science.gov (United States)

    Espada, Alfonso; Anta, Cristina; Bragado, Aroa; Rodríguez, Jaime; Jiménez, Carlos

    2011-04-01

    An approach to speed up the isolation of hydrophilic metabolites in complex natural matrixes by using a HLB/MCX-HPLC/MS system based on the retention properties of hydrophilic-lipophilic and cation exchange polymeric cartridges was developed. This methodology was successfully applied to the re-isolation of small water soluble compounds with completely different structures from two different natural extracts such as a dipeptide (vanchrobactin) from a bacterium culture broth and a pyrrolidine bearing a carboxylic acid moiety (clionapyrrolidine A) from a sponge. This method improved not only the efficiency of the isolation methodology but also the isolation time in relation to the existing methods. Copyright © 2011 Elsevier B.V. All rights reserved.

  6. Chemical attributes, total organic carbon stock and humified fractions of organic matter soil submitted to different systems of sugarcane management

    Directory of Open Access Journals (Sweden)

    Jean Sérgio Rosset

    2014-10-01

    Full Text Available Mechanized harvesting maintenance of trash from cane sugar and soil application of waste as vinasse and filter cake can improve the system of crop yield. Thus, this study aimed to evaluate the changes in the chemical, the stock of total organic carbon and humified organic matter fractions in an Oxisol cultivated with cane sugar with the following management systems: with sugarcane vinasse application (CCV, without application of burnt cane waste (CQS, with burnt cane vinasse application (CQV, with application of burnt cane filter cake (CQTF and burnt cane with joint application of vinasse and filter cake (CQVTF. For reference we used an area of natural vegetation (NV, Cerrado sensu stricto. Treatment CQVTF showed improvement in soil chemical properties, increased inventory levels of total organic carbon – TOC (values ranging from 21.28 to 40.02 Mg ha-1 and humified fractions of soil organic matter in relation to other treatments. The CQS area at a depth of 0-0.05 m, showed the greatest losses of soil TOC stocks (56.3% compared to NV. The adoption of management presented CCV and chemical attributes of the soil TOC stocks equivalent to those observed in areas with CQV CQTF and despite the short period of adoption (3 years. The TOC correlated with the sum of bases (r = 0.76 **, cation exchange capacity (r = 0.59 ** and base saturation (r = 0.63 **, while the humic acids (r = 0.40 ** fulvic acids (r = 0.49 ** and humin (r = 0.59 ** correlated with the cation exchange capacity of the soil. These results indicate that the preservation of trash in the management of cane sugar added to the application of vinasse and filter cake increases the TOC stocks promoting improvement in soil chemical properties.

  7. Anion exchange membrane

    Science.gov (United States)

    Verkade, John G; Wadhwa, Kuldeep; Kong, Xueqian; Schmidt-Rohr, Klaus

    2013-05-07

    An anion exchange membrane and fuel cell incorporating the anion exchange membrane are detailed in which proazaphosphatrane and azaphosphatrane cations are covalently bonded to a sulfonated fluoropolymer support along with anionic counterions. A positive charge is dispersed in the aforementioned cations which are buried in the support to reduce the cation-anion interactions and increase the mobility of hydroxide ions, for example, across the membrane. The anion exchange membrane has the ability to operate at high temperatures and in highly alkaline environments with high conductivity and low resistance.

  8. Measurement of yield of residues produced in {sup 12}C+{sup nat}Y reaction and subsequent separation of {sup 97}Ru from Y target using cation exchange resin

    Energy Technology Data Exchange (ETDEWEB)

    Maiti, Moumita [Indian Institute of Technology Roorkee, Uttarakhand (India). Dept. of Physics; Lahiri, Susanta [Saha Institute of Nuclear Physics, Kolkata (India). Chemical Sciences Div.

    2015-05-01

    This paper reports the yield of no-carrier-added (NCA) radionuclides produced in {sup 12}C{sup 6+} induced reaction on natural yttrium target at 10 different incident energies in the range of 40 to 75 MeV by the stacked-foil technique, followed by off-line γ-ray spectroscopy. It also reports the radiochemical separation of NCA {sup 97}Ru from the bulk yttrium target. {sup 97}Ru was produced in the yttrium matrix through {sup 89}Y({sup 12}C,4n){sup 97,97m}Rh(EC){sup 97}Ru and {sup 89}Y({sup 12}C,p3n){sup 97}Ru reactions along with the radioisotopes {sup 98}Rh, {sup 97}Rh, {sup 97m}Rh, {sup 93}Tc, {sup 94}Tc, {sup 95}Tc and {sup 93m}Mo. Irradiated target was allowed to cool for the complete decay of short-lived residues and {sup 97}Ru was then separated from the bulk yttrium using the cation exchanger DOWEX-50WX4 in an ion exchange column as well as via solid-liquid extraction (SLX). A total of ∝ 88% NCA {sup 97}Ru was separated in column chromatography without any contamination of bulk, whereas quantitative separation of NCA Ru was achieved in SLX.

  9. Cation (K{sup +}, Mg{sup 2+}, Ca{sup 2+}) exchange in Pb{sup 2+} accumulation by Saccharomyces cerevisiae

    Energy Technology Data Exchange (ETDEWEB)

    Suh, Jung Ho [Dept. of Industrial Chemistry, Ulsan College, Ulsan (Korea); Yun, Jong Won [Dept. of Biotechnology, Taegu University, Kyungbuk (Korea); Kim, Dong Seog [Dept. of Environmental Science, Catholic University of Taegu-Hyosung, Kyungbuk 712-702 (Korea)

    1999-11-01

    The relationship between Pb{sup 2+} accumulation and cation (K{sup +}, Mg{sup 2+}, Ca{sup 2+}) release in Saccharomyces cerevisiae was extensively investigated. As Pb{sup 2+} accumulation proceeded, the release of cellular metal ions such as K{sup +}, Mg{sup 2+} and Ca{sup 2+} was concomitantly released within 24 h, thereafter Pb{sup 2+} penetrated into the inner cellular parts and consequently plasmolysis of the cell was observed by TEM analysis. Pb{sup 2+} accumulation process in S. cerevisiae after 24 h was metabolism-independent because of the absence of cell viability. As the cell storage time was prolonged, the released amount of K{sup +} was markedly increased, while the amount of accumulated Pb{sup 2+} was nearly constant regardless of cell storage time and the time required to reach an equilibrium state was shortened. The autoclaved cells had less Pb{sup 2+} accumulation capacity than the untreated cells, and the amounts of released K{sup +} and Mg{sup 2+} were very low due to the denaturation of cell surface and cell membrane. (orig.)

  10. USE OF STRONG ACID RESIN PUROLITE C100E FOR REMOVING PERMANENT HARDNESS OF WATER – FACTORS AFFECTING CATIONIC EXCHANGE CAPACITY

    Directory of Open Access Journals (Sweden)

    BOGDAN BANDRABUR

    2013-12-01

    Full Text Available This paper experimentally investigates the performance and capacity of Purolite C100E commercial resin recommended for water softening applications in the food industry. The practical ion exchange capacity and the softening process efficiency are studied in batch mode as a function of the sorption specific process factors. Optimum operation conditions were determined as initial pH 7.1, resin dose 8 g dry resin•L-1, temperature 25 oC, contact time of 360 min, and in those conditions the retention capacity for the Ca2+ ions is 17.18 mg•g-1 that corresponds to a removal efficiency equal to 85.7%.

  11. Cation-Exchange Porosity Tuning in a Dynamic 4d-4f-3d Framework for Ni(II) Ion-Selective Luminescent Probe.

    Science.gov (United States)

    Wang, Ying; Wang, Xiu-Guang; Yuan, Bin; Shao, Cheng-Yuan; Chen, Yuan-Yuan; Zhou, Bing-Bing; Li, Ming-Shu; An, Xiao-Mai; Cheng, Peng; Zhao, Xiao-Jun

    2015-05-04

    A heterometallic complex {[Yb2(L)6Cd2][Cd(H2O)6]·6H2O}n (Yb-Cd) (H2L = oxidiacetic acid) was synthesized under hydrothermal conditions. In Yb-Cd, each L chelates to one Yb(3+) center and bonds to two Cd(2+) ions in an anti-anti configuration. Yb and Cd atoms are arrayed alternatively and connected by O-C-O bridges to form a cubic octahedral cage as the secondary building unit. Consequently, topological NaCl nets with high symmetry in the cubic space group Fd-3c have been constructed. The [Cd(H2O)6](2+) moieties lying in the porosity of anionic metal-organic framework (MOF) act as the thermodynamically stable species, required to balance the two negative charges of [Yb2(L)6Cd2](2-) in Yb-Cd. Interestingly, when Yb-Cd was employed as a precursor and emerged in the aqueous solution of Mn(ClO4)2·6H2O or Zn(ClO4)2·6H2O, a reversible single-crystal-to-single-crystal transformation process driven by [Cd(H2O)6](2+) cations has been exhibited to generate the heterotrimetallic coordination polymer {[Yb2(L)6Cd2][Mn(H2O)6]·6H2O}n (Yb-Cd-Mn) or {[Yb2(L)6Cd2][Zn(H2O)6]·6H2O}n (Yb-Cd-Zn). To the best of out knowledge, Yb-Cd-Mn and Yb-Cd-Zn are the first examples representing 4d-4f-3d polymers based on multicarboxylic acid. Luminescent studies reveal that Yb-Cd-Zn may serve as a good candidate of Ni(2+) a luminescent probe. To our knowledge, Yb-Cd-Zn represent the fist example of the 4d-4f-3d framework to exhibit luminescent selectivity for Ni(2+).

  12. Emergy efficiency analysis of sugarcane as a raw material for ethanol production

    Directory of Open Access Journals (Sweden)

    Edney Leandro da Vitória

    2016-12-01

    Full Text Available ABSTRACT In recent years, the expansion of sugarcane cultivation in Brazil and its growing importance in the Brazilian economy have been driven by a sharp increase in fuel alcohol production. This increase in fuel alcohol production was accompanied by increasing interest regarding the impacts of fuel crops in Brazil. In this study, regions of sugarcane expansion into deforested areas in the Atlantic Forest were studied by applying the emergy theory and indices. Environmental and economic inputs and the sustainability of the sugarcane production system were evaluated with the emergy method. The transformity (TR was equal to 1.78E+11 seJ kg-1, the yield rate (EYR was equal to 1.30, the investment rate was equal to 3.29, the environmental load rate was equal to 4.33, the renewability rate was equal to 18.77, and the exchange rate was equal to 1.09. The emergy indices of corn, cassava, wheat, and sugarcane (as raw materials for ethanol production were used. In Brazil, sugarcane production for ethanol production was more emergetically sustainable based on the analysed emergy indices.

  13. Effect of Clay Mineralogy and Exchangeable Cations on Permeability of Saudi Sandstone Reservoirs Effet de la minéralogie des argiles et des cations échangeables sur la perméabilité des réservoirs gréseux d'Arabie Saoudite

    Directory of Open Access Journals (Sweden)

    Dahab A. S.

    2006-11-01

    Full Text Available Reservoir rocks are susceptible to formation damage during secondary recovery operations due to the particular mineralogical, textural and electrochemical properties of the clay minerals they contain. This damage can be explained by the swelling of indigeneous clays present, resulting in the constricting of pores, or by the dispersion of indigeneous nonswelling particle rearrangements during fluid flow, resulting in the plugging of the pore system, or by a combination of the two. This article describes a laboratory study showing the effect of clay mineralogy on the permeability of actual Saudi sandstone reservoirs during water flooding operations. The study shows that the permeability damage of Saudi sandstone reservoirs depends upon the amount of swelling clays and exchangeable ions as well as on the nature of these ions. Monovalent cations cause more damage than multivalent ones but within the same group of metals, those with smaller atomic mass cause more damage. Les roches réservoirs peuvent être endommagées pendant les opérations de récupération secondaire à cause des propriétés minéralogiques, texturales et électrochimiques particulières des minéraux argileux qu'elles contiennent. Cet endommagement peut s'expliquer, soit par le gonflement des argiles qui conduit à un rétrécissement des pores, soit par la migration de particules non gonflantes pendant l'écoulement des fluides qui entraîne le colmatage des milieux poreux, soit par une combinaison des deux mécanismes. Cet article présente une étude de laboratoire montrant l'effet de la minéralogie des argiles sur la perméabilité des roches réservoirs réelles d'Arabie Saoudite pendant des opérations d'injection d'eau. L'étude montre que l'endommagement de la perméabilité des roches réservoirs d'Arabie Saoudite dépend de la quantité d'argiles gonflantes et d'ions échangeables, ainsi que de la nature de ces ions. Les cations monovalents provoquent plus d

  14. Sugarcane rice residue biochars and their applications

    Science.gov (United States)

    Wang, J. J.

    2014-12-01

    Sugarcane production in U.S. involves either pre-harvest burning or after-harvest burning of the residue. Approximately 70-90% of the dry matter of harvested sugarcane trash is lost through open field burning. This practice has caused considerable concerns over air quality and soil sustainability. We propose an alternative conservation approach to convert the sugarcane residue to biochar and used as soil amendment to conserve carbon and potentially improve soil fertility. In this study, fundamental properties of biochars made from sugarcane residue along with rice residues were tested for agronomic and environmental benefits. Sugarcane and rice harvest residues and milling processing byproducts bagasse and rice husk were converted to biochars at different pyrolysis temperatures and characterized. In general, sugarcane leave biochar contained more P, K, Ca and Mg than sugarcane bagasse biochar. Rice straw biochar had more S, K Ca but less P than rice husk biochar. Both biochars had higher available fraction of total P than that of total K. Sugarcane leave biochar converted at 450oC was dominated with various lignin derived phenols as well as non-specific aromatic compounds whereas bagasse biochar was with both lignin derived phenol and poly aromatic hydrocarbon (PAH). Rice straw char was dominated with non-specific aromatic compounds. At 750oC, charred material was dominated with aromatic ethers while losing the aromatic C=C structures. These molecular and surface property differences likely contributed to the difference in water holding capacities observed with these biochars. On the other hand, rice straw biochars produced at different pyrolysis temperatures had no significant effect on rice germination. Soils treated with sugarcane leave/trash biochar significantly enhanced sugarcane growth especially the root length. Treating soil with either sugarcane leave or bagasse char also enhanced soil adsorption capacity of atrazine; a common herbicide used in sugarcane

  15. Biomass of cocoa and sugarcane

    Science.gov (United States)

    Siswanto; Sumanto; Hartati, R. S.; Prastowo, B.

    2017-05-01

    The role of the agricultural sector is very important as the upstream addressing downstream sectors and national energy needs. The agricultural sector itself is also highly dependent on the availability of energy. Evolving from it then it must be policies and strategies for agricultural development Indonesia to forward particularly agriculture as producers as well as users of biomass energy or bioenergy for national development including agriculture balance with agriculture and food production. Exports of biomass unbridled currently include preceded by ignorance, indifference and the lack of scientific data and potential tree industry in the country. This requires adequate scientific supporting data. This study is necessary because currently there are insufficient data on the potential of biomass, including tree biomasanya detailing the benefits of bioenergy, feed and food is very necessary as a basis for future policy. Measurement of the main estate plants biomass such as cocoa and sugarcane be done in 2015. Measurements were also conducted on its lignocellulose content. Tree biomass sugarcane potential measured consist of leaves, stems and roots, with the weight mostly located on the stem. Nevertheless, not all the potential of the stem is a good raw material for bioethanol. For cocoa turned out leaves more prospective because of its adequate hemicellulose content. For sugarcane, leaf buds contain a good indicator of digestion of feed making it more suitable for feed.

  16.  Pressure-induced Fe↔Cu cationic valence exchange and its structural consequences: High-pressure studies of delafossite CuFeO2

    Science.gov (United States)

    Xu, W. M.; Rozenberg, G. Kh.; Pasternak, M. P.; Kertzer, M.; Kurnosov, A.; Dubrovinsky, L. S.; Pascarelli, S.; Munoz, M.; Vaccari, M.; Hanfland, M.; Jeanloz, R.

    2010-03-01

    The present high-pressure studies of CuFeO2 to 30 GPa using x-ray diffraction, along with F57e Mössbauer and Fe and CuK -edge x-ray absorption spectroscopy methods, reveal a sequence of intricate structural/electronic-magnetic pressure-induced transitions. The low-pressure R3¯m structure (0-18 GPa) is composed of sheets of FeS=5/23+ ions alternating with layers of O-CuS=01+-O dumbbells, the latter oriented along the c axis. This structure is characterized by an unusual positive d(c/a)/dP . At 18 GPa a structural transition takes place to a more isotropic C2/c structure with the O-CuS=01+-O axis tilted 28° from the c axis and with negative d(c/a)/dP . This transition corroborates with the onset of long-range antiferromagnetic order. Starting at ˜23GPa , with an initial volume reduction in ˜|ΔV/V0|=0.16 , the Cu-Fe bands overlap and this leads to a (CuS=01+FeS=5/23+)→(CuS=1/22+FeS=22+) interionic valence exchange in about 1/3 of the C2/c-CuFeO2 at 27 GPa. As a result: (i) the Cu2+-O becomes fourfold coordinated and is in a new crystallographic structure with space group P3¯m , and (ii) the Néel temperature increases above twofold [TN(CuS=1/22+FeS=22+)≈2.2TN(CuS=01+FeS=5/23+)] . This sequence of transitions is reversible with minimal hysteresis.

  17. Ethanol production using hemicellulosic hydrolyzate and sugarcane ...

    African Journals Online (AJOL)

    The use of vegetable biomass as substrate for ethanol production could reduce the existing usage of fossil fuels, thereby minimizing negative environmental impacts. Due to mechanical harvesting of sugarcane, the amount of pointer and straw has increased in sugarcane fields, becoming inputs of great energy potential.

  18. Vegetable seedling production with sugarcane bagasse ash

    Science.gov (United States)

    The eleven sugarcane mills in Louisiana processed 380,000 ac and 12.8 million tons of harvested sugarcane in 2014, producing 1.5 million tons of raw sugar (brown sugar), and an estimated 3 million tons of the fibrous plant residue called bagasse. Bagasse is the fibrous material remaining after remov...

  19. Correlations and correlated responses in sugarcane ( Saccharum ...

    African Journals Online (AJOL)

    Studies were carried out for two years at two locations to determine the inter character relationships between various quantitative traits of sugarcane, using eight genetically diversified sugarcane clones. The experiments were laid out in randomized complete block design with three replications. Performance data were used ...

  20. Concentration on Callus Induction in Sugarcane

    African Journals Online (AJOL)

    ABSTRACT: Experiment was designed and conducted to determine the most appropriate concentration of 2, 4-Dichlorophenoxy Acetic Acid suitable for callus induction in sugarcane. Explants were obtained from apical meristems of two sugarcane cultivars (SP726180 and CO-. 001) and cultured in a modified MS medium ...

  1. Ethanol production using hemicellulosic hydrolyzate and sugarcane ...

    African Journals Online (AJOL)

    Juliana

    2015-02-11

    Feb 11, 2015 ... The use of vegetable biomass as substrate for ethanol production could reduce the existing usage of fossil fuels, thereby minimizing negative environmental impacts. Due to mechanical harvesting of sugarcane, the amount of pointer and straw has increased in sugarcane fields, becoming inputs of great.

  2. Cation exchange-based facile aqueous synthesis of small, stable, and nontoxic near-infrared Ag₂Te/ZnS core/shell quantum dots emitting in the second biological window.

    Science.gov (United States)

    Chen, Chi; He, Xuewen; Gao, Li; Ma, Nan

    2013-02-01

    Facile aqueous synthesis of near-infrared Ag(2)Te quantum dots (QDs) and Ag(2)Te/ZnS core/shell QDs emitting in the second biological window is reported. The QD synthesis is based on a straightforward cation exchange process between CdTe QDs and Ag(+) ions conducted in aqueous solution. The prepared Ag(2)Te QDs possess near-infrared emission ranging from 900 to 1300 nm and a quantum yield up to 2.1%. A ZnS shell was grown on the Ag(2)Te QD to further enhance the photoluminescence intensity with a quantum yield of 5.6%. These Ag(2)Te/ZnS core/shell QDs possess robust colloidal stability and photostability with minimum photoluminescence fluctuation upon incubation for 72 h in biological buffer or continuous laser excitation for 120 min. Also, These QDs possess small hydrodynamic size (∼7.6 nm) and are non-cytotoxic to human cells, which is ideal for optical bioimaging in the second biological window.

  3. Development and validation of a UHPLC-MS/MS assay for colistin methanesulphonate (CMS) and colistin in human plasma and urine using weak-cation exchange solid-phase extraction.

    Science.gov (United States)

    Zhao, Miao; Wu, Xiao-Jie; Fan, Ya-Xin; Guo, Bei-Ning; Zhang, Jing

    2016-05-30

    A rapid ultra high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) assay method was developed for determination of CMS and formed colistin in human plasma and urine. After extraction on a 96-well SPE Supra-Clean Weak Cation Exchange (WCX) plate, the eluents were mixed and injected into the UHPLC-MS/MS system directly. A Phonomenex Kinetex XB-C18 analytical column was employed with a mobile phase consisting of solution "A" (acetonitrile:methanol, 1:1, v/v) and solution "B" (0.1% formic acid in water, v/v). The flow rate was 0.4 mL/min with gradient elution over 3.5 min. Ions were detected in ESI positive ion mode and the precursor-product ion pairs were m/z 390.7/101.3 for colistin A, m/z 386.0/101.2 for colistin B, and m/z 402.3/101.2 for polymyxin B1 (IS), respectively. The lower limit of quantification (LLOQ) was 0.0130 and 0.0251 mg/L for colistin A and colistin B in both plasma and urine with accuracy (relative error, %) colistin, which offers a highly efficient tool for the analysis of a large number of clinical samples as well as routine therapeutic drug monitoring. Copyright © 2016 Elsevier B.V. All rights reserved.

  4. Fast speciation of mercury in seawater by short-column high-performance liquid chromatography hyphenated to inductively coupled plasma spectrometry after on-line cation exchange column preconcentration.

    Science.gov (United States)

    Jia, Xiao-Yu; Gong, Di-Rong; Han, Yi; Wei, Chao; Duan, Tai-Cheng; Chen, Hang-Ting

    2012-01-15

    A simple and fast method for trace speciation analysis of mercury (Hg(2+)), methylmercury (MeHg(+)) and ethylmercury (EtHg(+)) in seawater has been developed by short-column high-performance liquid chromatography hyphenated to inductively coupled plasma spectrometry (HPLC-ICP-MS) after on-line cation-exchange column (CEC) preconcentration. The analytes were firstly adsorbed on the CEC without any extraneous reagent, and then were eluted rapidly (within seconds) and completely with a very low concentration of l-cysteine solution, which provides the conveniency for the on-line coupling of the preconcentration method and detection technique. To our best knowledge, it is for the first time to employ the CEC preconcentration technique to trap all of the three mercury species simultaneously at their positive charged status for the purpose of speciation analysis. Under the optimized conditions, a very high preconcentration factor up to 1250 has been obtained with 30mL sample solution, which leads to the very low detection limits of 0.042ngL(-1) for Hg(2+), 0.016ngL(-1) for MeHg(+) and 0.008ngL(-1) for EtHg(+) (as Hg), respectively. With the established method, three seawater samples were also analyzed, and all the three mercury species have been found in each sample, albeit at a very low concentration. Crown Copyright © 2011. Published by Elsevier B.V. All rights reserved.

  5. Optimization of elution salt concentration in stepwise elution of protein chromatography using linear gradient elution data. Reducing residual protein A by cation-exchange chromatography in monoclonal antibody purification.

    Science.gov (United States)

    Ishihara, Takashi; Kadoya, Toshihiko; Endo, Naomi; Yamamoto, Shuichi

    2006-05-05

    Our simple method for optimization of the elution salt concentration in stepwise elution was applied to the actual protein separation system, which involves several difficulties such as detection of the target. As a model separation system, reducing residual protein A by cation-exchange chromatography in human monoclonal antibody (hMab) purification was chosen. We carried out linear gradient elution experiments and obtained the data for the peak salt concentration of hMab and residual protein A, respectively. An enzyme-linked immunosorbent assay was applied to the measurement of the residual protein A. From these data, we calculated the distribution coefficient of the hMab and the residual protein A as a function of salt concentration. The optimal salt concentration of stepwise elution to reduce the residual protein A from the hMab was determined based on the relationship between the distribution coefficient and the salt concentration. Using the optimized condition, we successfully performed the separation, resulting in high recovery of hMab and the elimination of residual protein A.

  6. The use of cation exchange matrix separation coupled with ICP-MS to directly determine platinum group element (PGE) and other trace element emissions from passenger cars equipped with diesel particulate filters (DPF)

    Energy Technology Data Exchange (ETDEWEB)

    Cairns, Warren R.L.; Cozzi, Giulio [Institute for the Dynamics of Environmental Processes-CNR, Venice (Italy); De Boni, Antonella; Gabrieli, Jacopo [University of Venice, Department of Environmental Science, Venice (Italy); Asti, Massimo; Merlone Borla, Edoardo; Parussa, Flavio [Centro Ricerche Fiat, Orbassano (Italy); Moretto, Ezio [FIAT Powertrain Technologies S.p.A, Turin (Italy); Cescon, Paolo; Barbante, Carlo [University of Venice, Department of Environmental Science, Venice (Italy); Institute for the Dynamics of Environmental Processes-CNR, Venice (Italy); Boutron, Claude [Laboratoire de Glaciologie et Geophysique de l' Environnement, UMR CNRS 5183, B.P. 96, Saint Martin d' Heres Cedex (France)

    2011-03-15

    Inductively coupled plasma-mass spectrometry coupled with cation exchange matrix separation has been optimised for the direct determination of platinum group element (PGE) and trace element emissions from a diesel engine car. After matrix separation method detection limits of 1.6 ng g{sup -1} for Pd, 0.4 ng g{sup -1} for Rh and 4.3 ng g{sup -1} for Pt were achieved, the method was validated against the certified reference material BCR 723, urban road dust. The test vehicle was fitted with new and aged catalytic converters with and without diesel particulate filters (DPF). Samples were collected after three consecutive New European Driving Cycle (NEDC) of the particulate and ''soluble'' phases using a home-made sampler optimised for trace element analysis. Emission factors for the PGEs ranged from 0.021 ng km{sup -1} for Rh to 70.5 ng km{sup -1} for Pt; when a DPF was fitted, the emission factors for the PGEs actually used in the catalysts dropped by up to 97% (for Pt). Trace element emission factors were found to drop by a maximum of 92% for Ni to a minimum of 18% for Y when a DPF was fitted; a new DPF was also found to cause a reduction of up to 86% in the emission of particulate matter. (orig.)

  7. The use of cation exchange matrix separation coupled with ICP-MS to directly determine platinum group element (PGE) and other trace element emissions from passenger cars equipped with diesel particulate filters (DPF).

    Science.gov (United States)

    Cairns, Warren R L; De Boni, Antonella; Cozzi, Giulio; Asti, Massimo; Borla, Edoardo Merlone; Parussa, Flavio; Moretto, Ezio; Cescon, Paolo; Boutron, Claude; Gabrieli, Jacopo; Barbante, Carlo

    2011-03-01

    Inductively coupled plasma-mass spectrometry coupled with cation exchange matrix separation has been optimised for the direct determination of platinum group element (PGE) and trace element emissions from a diesel engine car. After matrix separation method detection limits of 1.6 ng g(-1) for Pd, 0.4 ng g(-1) for Rh and 4.3 ng g(-1) for Pt were achieved, the method was validated against the certified reference material BCR 723, urban road dust. The test vehicle was fitted with new and aged catalytic converters with and without diesel particulate filters (DPF). Samples were collected after three consecutive New European Driving Cycle (NEDC) of the particulate and "soluble" phases using a home-made sampler optimised for trace element analysis. Emission factors for the PGEs ranged from 0.021 ng km(-1) for Rh to 70.5 ng km(-1) for Pt; when a DPF was fitted, the emission factors for the PGEs actually used in the catalysts dropped by up to 97% (for Pt). Trace element emission factors were found to drop by a maximum of 92% for Ni to a minimum of 18% for Y when a DPF was fitted; a new DPF was also found to cause a reduction of up to 86% in the emission of particulate matter.

  8. Bandgap and Structure Engineering via Cation Exchange: From Binary Ag2S to Ternary AgInS2, Quaternary AgZnInS alloy and AgZnInS/ZnS Core/Shell Fluorescent Nanocrystals for Bioimaging.

    Science.gov (United States)

    Song, Jiangluqi; Ma, Chao; Zhang, Wenzhe; Li, Xiaodong; Zhang, Wenting; Wu, Rongbo; Cheng, Xiangcan; Ali, Asad; Yang, Mingya; Zhu, Lixin; Xia, Ruixiang; Xu, Xiaoliang

    2016-09-21

    Attention on semiconductor nanocrystals have been largely focused because of their unique optical and electrical properties, which can be applied as light absorber and luminophore. However, the band gap and structure engineering of nanomaterials is not so easy because of their finite size. Here we demonstrate an approach for preparing ternary AgInS2 (AIS), quaternary AgZnInS (AZIS), AgInS2/ZnS and AgZnInS/ZnS nanocompounds based on cation exchange. First, pristine Ag2S quantum dots (QDs) with different sizes were synthesized in one-pot, followed by the partial cation exchange between In(3+) and Ag(+). Changing the initial ratio of In(3+) to Ag(+), reaction time and temperature can control the components of the obtained AIS QDs. Under the optimized conditions, AIS QDs were obtained for the first time with a cation disordered cubic phase and high photoluminescence (PL) quantum yield (QY) up to 32% in aqueous solution, demonstrating the great potential of cation exchange in the synthesis for nanocrystals with excellent optical properties. Sequentially, Zn(2+) ions were incorporated in situ through a second exchange of Zn(2+) to Ag(+)/In(3+), leading to distinct results under different reaction temperature. Addition of Zn(2+) precursor at room temperature produced AIS/ZnS core/shell NCs with successively enhancement of QY, while subsequent heating could obtain AZIS homogeneous alloy QDs with a successively blue-shift of PL emission. This allow us to tune the PL emission of the products from 483 to 675 nm and fabricate the chemically stable QDs core/ZnS shell structure. Based on the above results, a mechanism about the cation exchange for the ternary nanocrystals of different structures was proposed that the balance between cation exchange and diffusion is the key factor of controlling the band gap and structure of the final products. Furthermore, photostability and in vitro experiment demonstrated quite low cytotoxicity and remarkably promising applications in the

  9. Bulk derivatization and cation exchange restricted access media-based trap-and-elute liquid chromatography–mass spectrometry method for determination of trace estrogens in serum

    Energy Technology Data Exchange (ETDEWEB)

    Beinhauer, Jana [Department of Biochemistry, Faculty of Science, Palacký University, Šlechtitelů 11, CZ-783 71 Olomouc (Czech Republic); Centre of the Region Haná for Biotechnological and Agricultural Research - Department of Protein Biochemistry and Proteomics, Faculty of Science, Palacký University, Šlechtitelů 11, CZ-783 71 Olomouc (Czech Republic); Bian, Liangqiao [Shimadzu Center for Advanced Analytical Chemistry, The University of Texas at Arlington, Arlington, TX (United States); Shimadzu Institute for Research Technologies, The University of Texas at Arlington, Arlington, TX (United States); Fan, Hui [Department of Chemistry and Biochemistry, The University of Texas at Arlington, Arlington, TX (United States); Šebela, Marek [Department of Biochemistry, Faculty of Science, Palacký University, Šlechtitelů 11, CZ-783 71 Olomouc (Czech Republic); Centre of the Region Haná for Biotechnological and Agricultural Research - Department of Protein Biochemistry and Proteomics, Faculty of Science, Palacký University, Šlechtitelů 11, CZ-783 71 Olomouc (Czech Republic); Kukula, Maciej [Shimadzu Center for Advanced Analytical Chemistry, The University of Texas at Arlington, Arlington, TX (United States); Shimadzu Institute for Research Technologies, The University of Texas at Arlington, Arlington, TX (United States); Barrera, Jose A. [Shimadzu Institute for Research Technologies, The University of Texas at Arlington, Arlington, TX (United States); and others

    2015-02-09

    Highlights: • Analysis of estrogens in small volume samples at low parts-per-trillion concentration. • Charged bulk derivatization facilitates on-line ion exchange sample preparation. • On-line WCX restricted access media traps analytes, but not proteins and lipids. • Complete preparation and LC–MS/MS analysis completed in 30 min/sample. - Abstract: Estrone (E1), estradiols (α/β-E2), and estriol (E3) are four major metabolically active estrogens exerting strong biological activities at very low circulating concentrations. This paper reports a sensitive and efficient method with automated, on-line clean-up and detection to determine trace estrogens in a small volume of serum samples using liquid chromatography–electrospray ionization–tandem mass spectrometry directly, without off-line liquid–liquid or solid-phase extraction pretreatments. Serum aliquots (charcoal stripped fetal bovine serum, 100 μL) were spiked with four estrogen standards and their corresponding isotope-labeled internal standards, then bulk derivatized with 2-fluoro-1-methyl-pyridium p-toluenesulfonate (2-FMP) to establish the calibration curves and perform method validation. Calibration was established in the concentration ranges of 5–1000 pg mL{sup −1}, and demonstrated good linearity of R{sup 2} from 0.9944 to 0.9997 for the four derivatized estrogens. The lower detection limits obtained were 3–7 pg mL{sup −1}. Good accuracy and precision in the range of 86–112% and 2.3–11.9%, respectively, were observed for the quality control (QC) samples at low, medium, and high concentration levels. The stability tests showed that the derivatized serum samples were stable 8 h after derivatization at room temperature and at least to 48 h if stored at −20 °C. The method was applied to measure trace estrogens in real human and bovine serum samples, and three of four estrogen compounds studied were observed and quantified.

  10. EVALUATION OF SUGARCANE BAGASSE ACID HYDROLYZATE TREATMENTS FOR XYLITOL PRODUCTION

    Directory of Open Access Journals (Sweden)

    P.V. GURGEL

    1998-09-01

    Full Text Available Acid sugarcane bagasse hydrolyzate was submitted to pH shifts in order to remove toxic compounds from the medium. The hydrolyzate was treated with bases containing mono-, di- or tri-valent cations and H2SO4, and its performance as a fermentation medium was evaluated by the production of xylitol by Candida guilliermondii FTI 20037. The use of bases containing mono-valent cations was not an efficient method of detoxification, and the use of a tri-valent cation did not show any detectable improvement in detoxification. The treated hydrolyzate recovery (in volume is greatly affected by the utilized base. Treatment using Al(OH3 and NaOH showed the best hydrolyzate recovery (87.5%, while the others presented a recovery of about 45% of the original hydrolyzate volume. Considering the whole process, best results were achieved by treatment using Al(OH3 and NaOH which allowed 0.55 g of xylitol produced from each gram of xylose in the raw hydrolyzate.

  11. Effects of a vinasse-microorganism blend application on a Vertisol with sugarcane

    Directory of Open Access Journals (Sweden)

    Gallego Blanco Jose Miller

    2012-04-01

    Full Text Available

    The effect of a second dose of vinasse on some physical and chemical properties of a Vertisol was evaluated with cut sugarcane in Valle del Cauca, Colombia. We analyzed the expression of any possible toxicity in foliar tissue samples at the end of the cycle. Vinasse treatments added with two different mixtures of microorganisms were established in a randomized complete block with five replicates: soil without vinasse and no microorganisms; soils with a dose of vinasse, soils with two doses of vinasse; soils with a single dose of vinasse separately evaluated with two different mixtures of microorganisms and soils with two doses of vinasse separately evaluated with two different mixtures of microorganisms. The chemical properties evaluated were pH, soil organic matter content, C, N, P, Ca, Mg, Na, and K content, cation exchange capacity CEC and electrical conductivity EC. The physical properties determined were bulk density, particle density and porosity. There were no significant differences in the physical and chemical properties of the soil for the evaluated cultivation cycle with the application of one or two doses of vinasse with and without microorganisms. Leaf tissue analysis did not show a nutritional imbalance due to the second application.

  12. Trocas gasosas e fluorescência da clorofila a em variedades de cana-de-açúcar submetidas à deficiência hídrica Gas exchange and chlorophyll a fluorescence of sugarcane varieties submitted to water stress

    Directory of Open Access Journals (Sweden)

    Eduardo R. Gonçalves

    2010-04-01

    Full Text Available O estresse hídrico afeta grande parte da agricultura mundial, razão por que se propôs, através deste trabalho, avaliar o comportamento, em casa-de-vegetação, de quatro variedades de cana-de-açúcar (SP79-1011, RB72454, RB98710 e RB92579 submetidas a déficit hídrico durante a fase inicial de crescimento vegetativo. As plantas foram cultivadas em vasos plásticos contendo 15 kg de solo. O estudo foi um fatorial (4 variedades x 3 níveis de água disponível no solo, em delineamento inteiramente casualizado, com cinco repetições. Os níveis de água no solo foram baseados na capacidade de água disponível (CAD ficando assim definidos: controle (80 a 100% da CAD, estresse hídrico moderado (40 a 60% da CAD e estresse hídrico severo (0 a 20% da CAD. A deficiência hídrica provocou reduções significativas na condutância estomática (gs, transpiração foliar (E, fotosíntese líquida (A e na eficiênca de uso da água de produção (EUAp, independente da variedade. As variedades SP79-1011 e RB98710 apresentaram maior sensibilidade estomática, reduzindo gs e E aos 71 dias após início do estresse, mesmo sob condições controle; entretanto, em tais condições A foi pouco afetada, indicando que as plantas são capazes de manter a taxa fotossintética, mesmo com os estômatos parcialmente fechados. O estresse hídrico provocou pouca redução na eficiência fotoquímica potencial das variedades estudadas.Water stress affects a great part of the world's agriculture. Thus, this work was conducted to evaluate photosynthetic traits in four varieties of sugarcane (SP79-1011, RB72454, RB98710 and RB92579 submitted to water stress during the early stage of the vegetative period. The plants were cultivated in plastic pots (15 kg of soil. The study was a factorial (4 varieties x 3 levels of soil water content based on available water capacity (AWC, in a completely randomized design with 5 replications. The levels of water content in the soil

  13. Comparative analysis of cation/proton antiporter superfamily in plants

    Energy Technology Data Exchange (ETDEWEB)

    Ye, Chuyu [ORNL; Yang, Xiaohan [ORNL; Xia, Xinli [Beijing Forestry University, China; Yin, Weilun [Beijing Forestry University, China

    2013-01-01

    The cation/proton antiporter superfamily is associated with the transport of monovalent cations across membranes. This superfamily was annotated in the Arabidopsis genome and some members were functionally characterized. In the present study, a systematic analysis of the cation/proton antiporter genes in diverse plant specieswas reported.We identified 240 cation/proton antiporters in alga, moss, and angiosperm. A phylogenetic tree was constructed showing these 240members are separated into three families, i.e., Na+/H+ exchangers, K+ efflux antiporters, and cation/H+ exchangers. Our analysis revealed that tandem and/or segmental duplications contribute to the expansion of cation/H+ exchangers in the examined angiospermspecies. Sliding windowanalysis of the nonsynonymous/synonymous substitution ratios showed some differences in the evolutionary fate of cation/proton antiporter paralogs. Furthermore, we identified over-represented motifs among these 240 proteins and foundmostmotifs are family specific, demonstrating diverse evolution of the cation/proton antiporters among three families. In addition, we investigated the co-expressed genes of the cation/proton antiporters in Arabidopsis thaliana. The results showed some biological processes are enriched in the co-expressed genes, suggesting the cation/proton antiporters may be involved in these biological processes. Taken together, this study furthers our knowledge on cation/proton antiporters in plants.

  14. Factors Affecting Sugarcane Production in Pakistan

    Directory of Open Access Journals (Sweden)

    Adnan Nazir

    2013-05-01

    Full Text Available This study was undertaken to identify the factors affecting sugarcane production in Pakistan. Data were collected from 387 sugarcane growers from Sindh, Punjab and NWFP province. Data were collected during the period 2007-08. The study reveals that the costs of inputs of sugarcane i.e. urea, DAP, FYM, land preparation, seed and its application, weeding and cost of irrigation were the important factors which influenced on the returns of sugarcane growers. The effectiveness was examined by using the Cobb-Douglas production function; MVP and allocative efficiency were calculated. The coefficient of multiple determinations R2 was 0.9249, which indicated that 92% variation in the cost of inputs was explained by all explanatory variables and the adjusted R2 was 92%. The F-value was 666.94 and was highly significant at 5% level of significance, indicating that the regression model was well fitted. The high prices of inputs, low price of output, delay in payments and lack of scientific knowledge were the major problems in sugarcane production. In order to enhance the productivity of sugarcane in the country, government should solve the identified problems to increase the income of sugarcane growers.

  15. Sugarcane starch: quantitative determination and characterization

    Directory of Open Access Journals (Sweden)

    Joelise de Alencar Figueira

    2011-09-01

    Full Text Available Starch is found in sugarcane as a storage polysaccharide. Starch concentrations vary widely depending on the country, variety, developmental stage, and growth conditions. The purpose of this study was to determine the starch content in different varieties of sugarcane, between May and November 2007, and some characteristics of sugarcane starch such as structure and granules size; gelatinization temperature; starch solution filterability; and susceptibility to glucoamylase, pullulanase, and commercial bacterial and fungal α-amylase enzymes. Susceptibility to debranching amylolytic isoamylase enzyme from Flavobacterium sp. was also tested. Sugarcane starch had spherical shape with a diameter of 1-3 µm. Sugarcane starch formed complexes with iodine, which showed greater absorption in the range of 540 to 620 nm. Sugarcane starch showed higher susceptibility to glucoamylase compared to that of waxy maize, cassava, and potato starch. Sugarcane starch also showed susceptibility to debranching amylolytic pullulanases similar to that of waxy rice starch. It also showed susceptibility to α-amylase from Bacillus subtilis, Bacillus licheniformis, and Aspergillus oryzae similar to that of the other tested starches producing glucose, maltose, maltotriose, maltotetraose, maltopentose and limit α- dextrin.

  16. FAST PYROLYSIS TEST WITH WHOLE SUGARCANE

    Directory of Open Access Journals (Sweden)

    Luis A. B. CORTEZ

    2010-11-01

    Full Text Available This paper shows a preliminary study proposing the usage of whole sugarcane in the thermoconversion process. . Tests were made on fast pyrolysis of biomass as whole sugarcane (bagasse, sugar and sugarcane straw crushed and dry. These experiments were performed in order to verify the suitability of this type of biomass for the fast pyrolysis process in a fluidized bed. The pre-treatment was assessed, during which, for the preparation of the whole sugarcane, an ordinary machine for chopping and grinding was employed. The pyrolysis process was conducted without major changes in the plant operating conditions to other biomass such as sugarcane trash. The efficiency of energy conversion of biomass to fine coal and bio-oil was 41%, resulting in a production of 3034 MJ per ton of the whole sugarcane processed, compared to 1900.6 MJ obtained in the production of ethanol via fermentation, where the conversion efficiency was around 26%. With the advances in this pyrolysis, efficiency may increase in the coming years, an interesting route for production of second generation fuels via catalytic synthesis using syngas from gasification of the mixture of bio-oil and fine charcoal. Keywords: Bioenergy, Whole sugarcane, Bio-oil, Fast pyrolysis.

  17. Development and Integration of an SSR-Based Molecular Identity Database into Sugarcane Breeding Program

    Directory of Open Access Journals (Sweden)

    Yong-Bao Pan

    2016-04-01

    Full Text Available Sugarcane breeding is very difficult and it takes 12 to 14 years to develop a new cultivar for commercial production. This is because sugarcane varieties are highly polyploid, inter-specific hybrids with 100 to 130 chromosomes that may vary across geographical areas. Other obstacles/constraints include the small size of flowers that may not synchronize but may self-pollinate, difficulty in distinguishing hybrids from self progenies, extreme (G × E interactive effect, and potential variety mis-identification during vegetative propagation and varietal exchange. To help cane breeders circumvent these constraints, a simple sequence repeats (SSR-based molecular identity database has been developed at the United States Department of Agriculture-Agricultural Research Service, Sugarcane Research Unit in Houma, LA. Since 2005, approximately 2000 molecular identities have been constructed for clones of sugarcane and related Saccharum species that cover geographical areas including Argentina, Australia, Bangladesh, China, Colombia, India, Mexico, Pakistan, South Africa, Thailand, USA (Louisiana, Florida, Texas, and Hawaii, and Venezuela. The molecular identity database is updated annually and has been utilized to: (1 provide molecular descriptors to newly registered cultivars; (2 identify in a timely fashion any mislabeled or unidentifiable clones from cross parents and field evaluation plots; (3 develop de novo clones of energy cane with S. spontaneum cytoplasm; (4 provide clone-specific fingerprint information for assessing cross quality and paternity of polycross; (5 determine genetic relatedness of parental clones; (6 select F1 hybrids from (elite × wild or (wild × elite crosses; and (7 investigate the inheritance of SSR markers in sugarcane. The integration of the molecular identity database into the sugarcane breeding program may improve the overall efficacy of cultivar development and commercialization.

  18. The effect of sugarcane litter compost to soilphysical mechanical properties and ratoon sugarcane performance

    OpenAIRE

    Iqbal

    2013-01-01

    It is expected that the use of sugarcane litter compost as organic fertilizer in the field will contribute in improving soil structure and increased sugarcane production. The objectives of this study were to identify the quality of sugarcane litter compost and to analyze the influence of the compost to soil chemical, physical and mechanical properties, soil fertility, and ratoon crop growth. The results showed that, based on C/N ratio, the quality of compost produced was appropriate with SNI ...

  19. The first use of a HPLC system at a Louisiana Sugarcane Factory: What it can do for you

    Science.gov (United States)

    Alma Plantation sugarcane factory established and operated the first High Performance Liquid Chromatography (HPLC) system in Louisiana in 2015. Although many HPLC systems exist, the factory opted for a ThermoFisherTM ion chromatography (anion exchange) system with integrated pulsed amperometric det...

  20. Greenhouse Gas Emissions from Brazilian Sugarcane Soils

    Science.gov (United States)

    Carmo, J.; Pitombo, L.; Cantarella, H.; Rosseto, R.; Andrade, C.; Martinelli, L.; Gava, G.; Vargas, V.; Sousa-Neto, E.; Zotelli, L.; Filoso, S.; Neto, A. E.

    2012-04-01

    Bioethanol from sugarcane is increasingly seen as a sustainable alternative energy source. Besides having high photosynthetic efficiency, sugarcane is a perennial tropical grass crop that can re-grow up to five or more years after being planted. Brazil is the largest producer of sugarcane in the world and management practices commonly used in the country lead to lower rates of inorganic N fertilizer application than sugarcane grown elsewhere, or in comparison to other feedstocks such as corn. Therefore, Brazilian sugarcane ethanol potentially promotes greenhouse gas savings. For that reason, several recent studies have attempted to assess emissions of greenhouse gases (GHG) during sugarcane production in the tropics. However, estimates have been mainly based on models due to a general lack of field data. In this study, we present data from in situ experiments on emission of three GHG (CO2, N2O, and CH4) in sugarcane fields in Brazil. Emissions are provided for sugarcane in different phases of the crop life cycle and under different management practices. Our results show that the use of nitrogen fertilizer in sugarcane crops resulted in an emission factor for N2O similar to those predicted by IPCC (1%), ranging from 0.59% in ratoon cane to 1.11% in plant cane. However, when vinasse was applied in addition to mineralN fertilizer, emissions of GHG increased in comparison to those from the use of mineral N fertilizer alone. Emissions increased significantly when experiments mimicked the accumulation of cane trash on the soil surface with 14 tons ha-1and 21 tons ha-1, which emission factor were 1.89% and 3.03%, respectively. This study is representative of Brazilian sugarcane systems under specific conditions for key factors affecting GHG emissions from soils. Nevertheless, the data provided will improve estimates of GHG from Brazilian sugarcane, and efforts to assess sugarcane ethanol sustainability and energy balance. Funding provided by the São Paulo Research

  1. Multiple, simultaneous, independent gradients for a versatile multidimensional liquid chromatography. Part II: Application 2: Computer controlled pH gradients in the presence of urea provide improved separation of proteins: Stability influenced anion and cation exchange chromatography.

    Science.gov (United States)

    Hirsh, Allen G; Tsonev, Latchezar I

    2017-04-28

    This paper details the use of a method of creating controlled pH gradients (pISep) to improve the separation of protein isoforms on ion exchange (IEX) stationary phases in the presence of various isocratic levels of urea. The pISep technology enables the development of computer controlled pH gradients on both cationic (CEX) and anionic (AEX) IEX stationary phases over the very wide pH range from 2 to 12. In pISep, titration curves generated by proportional mixing of the acidic and basic pISep working buffers alone, or in the presence of non-buffering solutes such as the neutral salt NaCl (0-1M), polar organics such as urea (0-8M) or acetonitrile (0-80 Vol%), can be fitted with high fidelity using high order polynomials which, in turn allows construction of a mathematical manifold %A (% acidic pISep buffer) vs. pH vs. [non-buffering solute], permitting precise computer control of pH and the non-buffering solute concentration allowing formation of dual uncoupled liquid chromatographic (LC) gradients of arbitrary shape (Hirsh and Tsonev, 2012 [1]). The separation of protein isoforms examined in this paper by use of such pH gradients in the presence of urea demonstrates the fractionation power of a true single step two dimensional liquid chromatography which we denote as Stability-Influenced Ion Exchange Chromatography (SIIEX). We present evidence that SIIEX is capable of increasing the resolution of protein isoforms difficult to separate by ordinary pH gradient IEX, and potentially simplifying the development of laboratory and production purification strategies involving on-column simultaneous pH and urea unfolding or refolding of targeted proteins. We model some of the physics implied by the dynamics of the observed protein fractionations as a function of both urea concentration and pH assuming that urea-induced native state unfolding competes with native state electrostatic interaction binding to an IEX stationary phase. Implications for in vivo protein

  2. N-glycosylation in sugarcane

    Directory of Open Access Journals (Sweden)

    Maia Ivan G.

    2001-01-01

    Full Text Available The N-linked glycosylation of secretory and membrane proteins is the most complex posttranslational modification known to occur in eukaryotic cells. It has been shown to play critical roles in modulating protein function. Although this important biological process has been extensively studied in mammals, much less is known about this biosynthetic pathway in plants. The enzymes involved in plant N-glycan biosynthesis and processing are still not well defined and the mechanism of their genetic regulation is almost completely unknown. In this paper we describe our first attempt to understand the N-linked glycosylation mechanism in a plant species by using the data generated by the Sugarcane Expressed Sequence Tag (SUCEST project. The SUCEST database was mined for sugarcane gene products potentially involved in the N-glycosylation pathway. This approach has led to the identification and functional assignment of 90 expressed sequence tag (EST clusters sharing significant sequence similarity with the enzymes involved in N-glycan biosynthesis and processing. The ESTs identified were also analyzed to establish their relative abundance.

  3. An-Overview on invertase in sugarcane

    OpenAIRE

    Ansari, Mohammad Israil; Yadav, Ashok; Lal, Ramji

    2013-01-01

    Saccharum officinarum is one of the most cultivated hybrid varieties among the sugarcane varieties. In sugarcane plant sucrose is the major carbohydrate which can be stored and transported. Different physiological and biochemical studies on this crop report that invertase activity and sucrose concentration some how are key limiting step in the process of sucrose accumulation. Significant efforts have been made in relation to the sucrose cycle by altering the sucrose phosphate synthetase, sucr...

  4. Isomerization of propargyl cation to cyclopropenyl cation ...

    Indian Academy of Sciences (India)

    step) for isomerization of the linear propargyl cation to the aromatic cyclopropenyl cation, also probing the phenomenon of solvation of this reaction by simple lone pair donors (NH3, H2O, H2S and HF) which bind to the substrate at two sites.

  5. Isomerization of propargyl cation to cyclopropenyl cation ...

    Indian Academy of Sciences (India)

    Abstract. This ab initio study examines two pathways (one concerted and the other two-step) for isomeri- zation of the linear propargyl cation to the aromatic cyclopropenyl cation, also probing the phenomenon of solvation of this reaction by simple lone pair donors (NH3, H2O, H2S and HF) which bind to the substrate at two.

  6. Sugarcane genes related to mitochondrial function

    Directory of Open Access Journals (Sweden)

    Fonseca Ghislaine V.

    2001-01-01

    Full Text Available Mitochondria function as metabolic powerhouses by generating energy through oxidative phosphorylation and have become the focus of renewed interest due to progress in understanding the subtleties of their biogenesis and the discovery of the important roles which these organelles play in senescence, cell death and the assembly of iron-sulfur (Fe/S centers. Using proteins from the yeast Saccharomyces cerevisiae, Homo sapiens and Arabidopsis thaliana we searched the sugarcane expressed sequence tag (SUCEST database for the presence of expressed sequence tags (ESTs with similarity to nuclear genes related to mitochondrial functions. Starting with 869 protein sequences, we searched for sugarcane EST counterparts to these proteins using the basic local alignment search tool TBLASTN similarity searching program run against 260,781 sugarcane ESTs contained in 81,223 clusters. We were able to recover 367 clusters likely to represent sugarcane orthologues of the corresponding genes from S. cerevisiae, H. sapiens and A. thaliana with E-value <= 10-10. Gene products belonging to all functional categories related to mitochondrial functions were found and this allowed us to produce an overview of the nuclear genes required for sugarcane mitochondrial biogenesis and function as well as providing a starting point for detailed analysis of sugarcane gene structure and physiology.

  7. Analysis of Sugarcane Juice Quality Indexes

    Directory of Open Access Journals (Sweden)

    Zeqing Xiao

    2017-01-01

    Full Text Available The analysis of the quality indexes of sugarcane juice plays a vital role in the process of refining sugarcane, breeding, cultivation, and production management. The paper analyzes the dynamic laws of five quality indexes (i.e., brix, purity, polarization, sucrose content, and reducing sugar combined with graphs over time along the course of crushing season (December–March in Guangxi province of China. During this time, the sugarcane is in the mature stage and hypermature stage. At the beginning of December to early January, during which sugarcane is in the later stage of maturity, the nutrients are accumulating, causing brix, purity, polarization, and sucrose content increase. At the beginning of January to mid-February, due to low temperature and insufficient light, it is not conducive to accumulation of nutrients. However, there is the so-called “sugar back” phenomenon and reducing sugar rises gradually in March, leading to deterioration of the quality of sugarcane juice. The results show that timely harvest of sugarcane is beneficial for sugar making. The regression analysis results show that some of quality indexes have strong correlation between them and the regression models are extremely significant, indicating that the prediction results are ideal.

  8. Sugarcane vinasse: environmental implications of its use.

    Science.gov (United States)

    Christofoletti, Cintya Aparecida; Escher, Janaína Pedro; Correia, Jorge Evangelista; Marinho, Julia Fernanda Urbano; Fontanetti, Carmem Silvia

    2013-12-01

    The inadequate and indiscriminate disposal of sugarcane vinasse in soils and water bodies has received much attention since decades ago, due to environmental problems associated to this practice. Vinasse is the final by-product of the biomass distillation, mainly for the production of ethanol, from sugar crops (beet and sugarcane), starch crops (corn, wheat, rice, and cassava), or cellulosic material (harvesting crop residues, sugarcane bagasse, and wood). Because of the large quantities of vinasse produced, alternative treatments and uses have been developed, such as recycling of vinasse in fermentation, fertirrigation, concentration by evaporation, and yeast and energy production. This review was aimed at examining the available data on the subject as a contribution to update the information on sugarcane vinasse, from its characteristics and chemical composition to alternatives uses in Brazil: fertirrigation, concentration by evaporation, energy production; the effects on soil physical, chemical and biological properties; its influence on seed germination, its use as biostimulant and environmental contaminant. The low pH, electric conductivity, and chemical elements present in sugarcane vinasse may cause changes in the chemical and physical-chemical properties of soils, rivers, and lakes with frequent discharges over a long period of time, and also have adverse effects on agricultural soils and biota in general. Thus, new studies and green methods need to be developed aiming at sugarcane vinasse recycling and disposal. Copyright © 2013 Elsevier Ltd. All rights reserved.

  9. Increased sink strength offsets the inhibitory effect of sucrose on sugarcane photosynthesis.

    Science.gov (United States)

    Ribeiro, Rafael V; Machado, Eduardo C; Magalhães Filho, José R; Lobo, Ana Karla M; Martins, Márcio O; Silveira, Joaquim A G; Yin, Xinyou; Struik, Paul C

    2017-01-01

    Spraying sucrose inhibits photosynthesis by impairing Rubisco activity and stomatal conductance (gs), whereas increasing sink demand by partially darkening the plant stimulates sugarcane photosynthesis. We hypothesized that the stimulatory effect of darkness can offset the inhibitory effect of exogenous sucrose on photosynthesis. Source-sink relationship was perturbed in two sugarcane cultivars by imposing partial darkness, spraying a sucrose solution (50mM) and their combination. Five days after the onset of the treatments, the maximum Rubisco carboxylation rate (Vcmax) and the initial slope of A-Ci curve (k) were estimated by measuring leaf gas exchange and chlorophyll fluorescence. Photosynthesis was inhibited by sucrose spraying in both genotypes, through decreases in Vcmax, k, gs and ATP production driven by electron transport (Jatp). Photosynthesis of plants subjected to the combination of partial darkness and sucrose spraying was similar to photosynthesis of reference plants for both genotypes. Significant increases in Vcmax, gs and Jatp and marginal increases in k were noticed when combining partial darkness and sucrose spraying compared with sucrose spraying alone. Our data also revealed that increases in sink strength due to partial darkness offset the inhibition of sugarcane photosynthesis caused by sucrose spraying, enhancing the knowledge on endogenous regulation of sugarcane photosynthesis through the source-sink relationship. Copyright © 2016 Elsevier GmbH. All rights reserved.

  10. Extraction and characterization of wax from sugarcane bagasse and the enzymatic hydrolysis of dewaxed sugarcane bagasse.

    Science.gov (United States)

    Qi, Gaoxiang; Peng, Fen; Xiong, Lian; Lin, Xiaoqing; Huang, Chao; Li, Hailong; Chen, Xuefang; Chen, Xinde

    2017-03-16

    Extraction of high-value products from agricultural wastes is an important component for sustainable bioeconomy development. In this study, wax extraction from sugarcane bagasse was performed and the beneficial effect of dewaxing pretreatment on the enzymatic hydrolysis was investigated. About 1.2% (w/w) of crude sugarcane wax was obtained from the sugarcane bagasse using the mixture of petroleum ether and ethanol (mass ratio of 1:1) as the extraction agent. Results of Fourier-transform infrared characterization and gas chromatography-mass spectrometry qualitative analysis showed that the crude sugarcane wax consisted of fatty fractions (fatty acids, fatty aldehydes, hydrocarbons, and esters) and small amount of lignin derivatives. In addition, the effect of dewaxing pretreatment on the enzymatic hydrolysis of sugarcane bagasse was also investigated. The digestibilities of cellulose and xylan in dewaxed sugarcane bagasse were 18.7 and 10.3%, respectively, compared with those of 13.1 and 8.9% obtained from native sugarcane bagasse. The dewaxed sugarcane bagasse became more accessible to enzyme due to the disruption of the outermost layer of the waxy materials.

  11. Sugarcane stems as larval habitat for the stable fly (Stomoxys calcitrans in sugarcane plantations

    Directory of Open Access Journals (Sweden)

    Paulo H.D. Cançado

    2013-06-01

    Full Text Available Outbreaks of stable fly, Stomoxys calcitrans, cause losses for livestock producers located near sugarcane mills in Brazil, especially in southern Mato Grosso do Sul. The sugarcane mills are often pointed by local farmers as the primary source of these outbreaks; some mills also joined the farmers in combating the flies. Brazilian beef cattle production has great economic importance in similar level to bio-fuel production as ethanol. In this context, the wide-ranging knowledge on the biology and ecology of the stable fly, including larval habitats and their reproduction sites is extremely important for further development of control programs. This paper aims to report the occurrence and development of S. calcitrans larvae inside sugarcane stems in three municipalities of Mato Grosso do Sul. The sugarcane stems give protection against bad weather conditions and insecticide application. In this way, for sustainable sugarcane growth specific research concerning this situation should be conducted.

  12. Predicting Organic Cation Sorption Coefficients: Accounting for Competition from Sorbed Inorganic Cations Using a Simple Probe Molecule.

    Science.gov (United States)

    Jolin, William C; Goyetche, Reaha; Carter, Katherine; Medina, John; Vasudevan, Dharni; MacKay, Allison A

    2017-06-06

    With the increasing number of emerging contaminants that are cationic at environmentally relevant pH values, there is a need for robust predictive models of organic cation sorption coefficients (Kd). Current predictive models fail to account for the differences in the identity, abundance, and affinity of surface-associated inorganic exchange ions naturally present at negatively charged receptor sites on environmental solids. To better understand how organic cation sorption is influenced by surface-associated inorganic exchange ions, sorption coefficients of 10 organic cations (including eight pharmaceuticals and two simple probe organic amines) were determined for six homoionic forms of the aluminosilicate mineral, montmorillonite. Organic cation sorption coefficients exhibited consistent trends for all compounds across the various homoionic clays with sorption coefficients (Kd) decreasing as follows: KdNa+ > KdNH4+ ≥ KdK+ > KdCa2+ ≥ KdMg2+ > KdAl3+. This trend for competition between organic cations and exchangeable inorganic cations is consistent with the inorganic cation selectivity sequence, determined for exchange between inorganic ions. Such consistent trends in competition between organic and inorganic cations suggested that a simple probe cation, such as phenyltrimethylammonium or benzylamine, could capture soil-to-soil variations in native inorganic cation identity and abundance for the prediction of organic cation sorption to soils and soil minerals. Indeed, sorption of two pharmaceutical compounds to 30 soils was better described by phenyltrimethylammonium sorption than by measures of benzylamine sorption, effective cation exchange capacity alone, or a model from the literature (Droge, S., and Goss, K. Environ. Sci. Technol. 2013, 47, 14224). A hybrid approach integrating structural scaling factors derived from this literature model of organic cation sorption, along with phenyltrimethylammonium Kd values, allowed for estimation of Kd values for more

  13. Mineral Separation in a CELSS by Ion-exchange Chromatography

    Science.gov (United States)

    Ballou, E. V.; Spitze, L. A.; Wong, F. W.; Wydeven, T.; Johnson, C. C.

    1982-01-01

    Operational parameters pertinent to ion exchange chromatography separation were identified. The experiments were performed with 9 mm diameter ion exchange columns and conventional column accessories. The cation separation beds were packed with AG 50W-X2 strong acid cation exchange resin in H(+) form and 200-400 dry mesh particle size. The stripper beds used in some experiments were packed with AG 1-XB strong base cation exchange resin in OH(-) form and 200-400 dry mesh particle size.

  14. Étude de la technique d'échange ionique avec compétition. Cas du dépôt de platine sur support solide acide par échange cationique Research on the Ion Exchange Technique with Competition. Case of Platinum Deposit on a Solid Acid Support by Cation Exchange

    Directory of Open Access Journals (Sweden)

    Ribeiro F.

    2006-11-01

    Full Text Available Cet article présente une étude détaillée de la technique de dépôt de platine sur support acide par échange cationique avec compétition. Cette technique permet d'obtenir à la fois une dispersion quasi atomique et une répartition macroscopique homogène du métal sur la surface du solide. En l'absence de limitations diffusionnelles extra-granulaires, les résultats expérimentaux sont en bon accord avec les prévisions théoriques . This article is a detailed examination of the technique of depositing platinum on an acid support by cation exchange with compétition. This technique produces both a quasi-atomic dispersion and a homogeneous macroscopic distribution of the métal onthe surface of the solid. In the absence of extragranular diffusion limitations, experimental findings are in good agreement with theoretical predictions.

  15. Disease resistance in sugarcane – An overview

    Directory of Open Access Journals (Sweden)

    A. Ramesh Sundar

    2015-12-01

    Full Text Available Sugarcane is one of the important commercial crops cultivated world-wide both under tropical and sub-tropical conditions. The crop gains economic importance by virtue of its industrial potential in terms of products like crystal white sugar, bagasse, pressmud, power etc. Among the various production constraints of the crop, diseases are seen as a major threat for sustaining the productivity of sugarcane. Conventional Breeding is a lengthy process and it involves almost more than 10 years for the release of a commercial variety. Many varieties with superior agronomical traits have succumbed to diseases like red rot and smut during the course of cultivation, which hitherto at the time of release were rated to be resistant. The breakdown of disease resistance is attributed to the possible emergence of new virulent pathotypes. This situation has warranted a pertinent need to have a thorough understanding on inheritance pattern and mechanism of disease resistance in sugarcane, which would aid for quick screening of disease resistant clones and successful management of the diseases, respectively. Overall, there is a paradigm shift in the understanding of plant disease resistance, thanks to the advent of robust molecular tools. An integration of the tools of “Omics” namely genomics, proteomics, metabolomics etc. has further strengthened in deciphering plant-pathogen interactions at the molecular level. With the accomplishments in elucidating sugarcane ESTs, which was ably supported by employing the next generation sequencing platforms to unlock the secrets of pathogenomics in sugarcane, it is now made possible to further improve our understanding on disease resistance in sugarcane. Giving the scenario, the future looks evenmore promising, wherein convincing results are in the offing to thoroughly unravel the enigmatic relationship between sugarcane and its important pathogens.

  16. Biosynthesis of secondary metabolites in sugarcane

    Directory of Open Access Journals (Sweden)

    França S.C.

    2001-01-01

    Full Text Available A set of genes related to secondary metabolism was extracted from the sugarcane expressed sequence tag (SUCEST database and was used to investigate both the gene expression pattern of key enzymes regulating the main biosynthetic secondary metabolism pathways and the major classes of metabolites involved in the response of sugarcane to environmental and developmental cues. The SUCEST database was constructed with tissues in different physiological conditions which had been collected under varied situation of environmental stress. This database allows researchers to identify and characterize the expressed genes of a wide range of putative enzymes able to catalyze steps in the phenylpropanoid, isoprenoid and other pathways of the special metabolic mechanisms involved in the response of sugarcane to environmental changes. Our results show that sugarcane cDNAs encoded putative ultra-violet induced sesquiterpene cyclases (SC; chalcone synthase (CHS, the first enzyme in the pathway branch for flavonoid biosynthesis; isoflavone synthase (IFS, involved in plant defense and root nodulation; isoflavone reductase (IFR, a key enzyme in phenylpropanoid phytoalexin biosynthesis; and caffeic acid-O-methyltransferase, a key enzyme in the biosynthesis of lignin cell wall precursors. High levels of CHS transcripts from plantlets infected with Herbaspirillum rubri or Gluconacetobacter diazotroficans suggests that agents of biotic stress can elicit flavonoid biosynthesis in sugarcane. From this data we have predicted the profile of isoprenoid and phenylpropanoid metabolism in sugarcane and pointed the branches of secondary metabolism activated during tissue-specific stages of development and the adaptive response of sugarcane to agents of biotic and abiotic stress, although our assignment of enzyme function should be confirmed by careful biochemical and genetic supporting evidence.

  17. Sugarcane genes associated with sucrose content

    Directory of Open Access Journals (Sweden)

    Vincentz Michel GA

    2009-03-01

    Full Text Available Abstract Background - Sucrose content is a highly desirable trait in sugarcane as the worldwide demand for cost-effective biofuels surges. Sugarcane cultivars differ in their capacity to accumulate sucrose and breeding programs routinely perform crosses to identify genotypes able to produce more sucrose. Sucrose content in the mature internodes reach around 20% of the culms dry weight. Genotypes in the populations reflect their genetic program and may display contrasting growth, development, and physiology, all of which affect carbohydrate metabolism. Few studies have profiled gene expression related to sugarcane's sugar content. The identification of signal transduction components and transcription factors that might regulate sugar accumulation is highly desirable if we are to improve this characteristic of sugarcane plants. Results - We have evaluated thirty genotypes that have different Brix (sugar levels and identified genes differentially expressed in internodes using cDNA microarrays. These genes were compared to existing gene expression data for sugarcane plants subjected to diverse stress and hormone treatments. The comparisons revealed a strong overlap between the drought and sucrose-content datasets and a limited overlap with ABA signaling. Genes associated with sucrose content were extensively validated by qRT-PCR, which highlighted several protein kinases and transcription factors that are likely to be regulators of sucrose accumulation. The data also indicate that aquaporins, as well as lignin biosynthesis and cell wall metabolism genes, are strongly related to sucrose accumulation. Moreover, sucrose-associated genes were shown to be directly responsive to short term sucrose stimuli, confirming their role in sugar-related pathways. Conclusion - Gene expression analysis of sugarcane populations contrasting for sucrose content indicated a possible overlap with drought and cell wall metabolism processes and suggested signaling and

  18. Sugarcane boiler ash as an amendment for soilless growing media

    Science.gov (United States)

    In 2016, research was conducted to investigate the use of sugarcane bagasse ash (SBA) as an amendment to soilless planting media for the production of vegetable seedlings. Typically, the eleven Louisiana sugarcane mills use a portion of the sugarcane bagasse for fuel, producing over 60,000 tons of S...

  19. Identification of virus isolates inducing mosaic of sugarcane in ...

    African Journals Online (AJOL)

    Sugarcane mosaic disease caused by sugarcane mosaic virus (SCMV), Johnsongrass mosaic virus (JGMV), maize dwarf mosaic virus (MDMV) and sorghum mosaic Virus (SrMV) is an economically important viral disease of sugarcane worldwide. Field survey was conducted to assess the presence of the viruses involve in ...

  20. Reduction of Exudates (Browning) in Sugarcane Micro Propagation ...

    African Journals Online (AJOL)

    Ex plant preparation in the course of sugarcane micro propagation is known to release exudates which lead to the death of sugarcane in vitro. An industrial sugarcane variety (NCS008) was used for the study and was observed to die in less than 14 days in vitro. In a study to reduce the death of this variety, ascorbic acid and ...

  1. Importance and status of sugarcane smut ( Ustilago scitaminea ) in ...

    African Journals Online (AJOL)

    Sugarcane smut (Ustilago scitaminea) is considered as the most prevalent and serious disease in sugarcane producing countries of the world. To determine incidence of sugarcane smut, a total of 144 fields were surveyed at Wonji-Shoa, Metahara and Finchaa on plantcane, first and last ratoon crops from August 2008 to ...

  2. Application of sugarcane bagasse ash as a partial cement ...

    African Journals Online (AJOL)

    Sugarcane bagasse ash is a byproduct of sugar factories found after burning sugarcane bagasse which itself is found after the extraction of all economical sugar from sugarcane. The disposal of this material is already causing environmental problems around the sugar factories. On the other hand, the boost in construction ...

  3. Effect of climate variability on sugarcane breeding in Nigeria | Ishaq ...

    African Journals Online (AJOL)

    Effect of climate variability on sugarcane breeding in Nigeria. ... Flowering in sugarcane (Saccharum species) is poor and variable at many tropical locations due to sub-optimal photoperiod. The situation is often compounded by ... sugar production in Nigeria. Keywords: Climate Change, Variability and Sugarcane Breeding ...

  4. Post-processing, energy production use of sugarcane bagasse ash

    Science.gov (United States)

    Sugarcane bagasse ash (SBA) is a multi-process by-product produced from the milling of sugarcane. Bagasse is the fibrous material remaining after removing the sugar, water, and other impurities from the sugarcane delivered to the mill. Louisiana produces an estimated 2.7 mt of bagasse each year. In ...

  5. Hidrólise parcial da superfície do polyethylene terephthalate (PET: transformando um rejeito em um material de troca catiônica para aplicação ambiental Partial hydrolysis of pet surface: transforming a plastic waste into a material with cationic exchange properties for environmental application

    Directory of Open Access Journals (Sweden)

    Marcelo G. Rosmaninho

    2009-01-01

    Full Text Available In this work it is proposed a simple and versatile undergraduate chemical experiment in polymer and environmental technology based on the process of polyethylene terephthalate (PET hydrolysis. Polyethylene terephthalate from post-consume bottles is submitted to a controlled partial hydrolysis which allows the students to follow the reaction by a simple procedure. The students can explore the reaction kinetics, the effect of catalysts and the exposed polyethylene terephthalate surface area on the hydrolysis reaction. The second and innovative part of this experiment is the technological and environmental application of the hydrolyzed polyethylene terephthalate as a material with cation exchange properties. The surface hydrolyzed polyethylene terephthalate can be used as adsorbent for cationic contaminants.

  6. The Impact of the 2008 Credit Crisis on the Sugarcane Sector: A Study Econometric

    Directory of Open Access Journals (Sweden)

    Flávia de Castro Camioto

    2017-11-01

    Full Text Available The sugarcane industry contributes approximately 2% to the Brazilian GDP, and generates more than 600,000 jobs in nearly a thousand cities. This study aims to determine the main variables that affect the growth of the Brazilian sugarcane sector. For this, econometric techniques were used to quantify the impact of each variable studied in the growth of Gross Domestic Product in this sector from 1980 to 2013. A specific analysis of the impact of the 2008 credit crisis on growth this sector was also performed. The results showed that the variables that impact the growth of Brazilian sugarcane industry are: exchange rate, fuel alcohol consumption, and the average price of a barrel of petroleum. Moreover, it was found that the 2008 crisis contributed negatively to the GDP of this sector. It was possible to conclude that the crisis in this sector had its origin in the optimism in this sector, due to the growth of the sector in 2006 and the global factors in 2008, which was reflected in variables such as exchange rate and the consumption of alcohol fuel, that negatively impacted the sector.

  7. Analyzing Solutions High in Total Dissolved Solids for Rare Earth Elements (REEs) Using Cation Exchange and Online Pre-Concentration with the seaFAST2 Unit; NETL-TRS-7-2017; NETL Technical Report Series; U.S. Department of Energy, National Energy Technology Laboratory: Albany, OR, 2017; p 32

    Energy Technology Data Exchange (ETDEWEB)

    Yang, J. [National Energy Technology Lab. (NETL), Albany, OR (United States); Oregon State Univ., Corvallis, OR (United States). College of Earth, Ocean, and Atmospheric Science; Torres, M. [Oregon State Univ., Corvallis, OR (United States). College of Earth, Ocean, and Atmospheric Science; Verba, C. [National Energy Technology Lab. (NETL), Albany, OR (United States); Oregon State Univ., Corvallis, OR (United States); Hakala, A. [National Energy Technology Lab. (NETL), Pittsburgh, PA, (United States)

    2017-08-01

    The accurate quantification of the rare earth element (REE) dissolved concentrations in natural waters are often inhibited by their low abundances in relation to other dissolved constituents such as alkali, alkaline earth elements, and dissolved solids. The high abundance of these constituents can suppress the overall analytical signal as well as create isobaric interferences on the REEs during analysis. Waters associated with natural gas operations on black shale plays are characterized by high salinities and high total dissolved solids (TDS) contents >150,000 mg/L. Methods used to isolate and quantify dissolved REEs in seawater were adapted in order to develop the capability of analyzing REEs in waters that are high in TDS. First, a synthetic fluid based on geochemical modelling of natural brine formation fluids was created within the Marcellus black shale with a TDS loading of 153,000 mg/L. To this solution, 1,000 ng/mL of REE standards was added based on preliminary analyses of experimental fluids reacted at high pressure and temperature with Marcellus black shale. These synthetic fluids were then run at three different dilution levels of 10, 100, and 1,000–fold dilutions through cation exchange columns using AG50-X8 exchange resin from Eichrom Industries. The eluent from the cation columns were then sent through a seaFAST2 unit directly connected to an inductively coupled plasma mass spectrometer (ICP-MS) to analyze the REEs. Percent recoveries of the REEs ranged from 80–110% and fell within error for the external reference standard used and no signal suppression or isobaric interferences on the REEs were observed. These results demonstrate that a combined use of cation exchange columns and seaFAST2 instrumentation are effective in accurately quantifying the dissolved REEs in fluids that are >150,000 mg/L in TDS and have Ba:Eu ratios in excess of 380,000.

  8. Brazil's sugarcane boom could affect regional temperatures

    Science.gov (United States)

    Schultz, Colin

    2013-04-01

    With the world seeking to cut its dependence on fossil fuels, the use of bioethanol and other biofuels is on the rise. In Brazil, the second largest producer and consumer of bioethanol, this has led to a boom in sugarcane production. Based on new laws and trade agreements, researchers expect Brazil's production of sugarcane-derived ethanol to increase tenfold over the next decade, with considerable land being converted for growing sugarcane. Much of this expansion is expected to come at a loss of some of the country's cerrado savannas. So while a major aim of the turn to biofuels is to reduce the transfer of carbon to the atmosphere and mitigate global climate change, the shifting agricultural activity could have direct consequences on Brazil's climate by changing the region's physical and biogeochemical properties.

  9. Cation-alkane interaction.

    Science.gov (United States)

    Premkumar, J Richard; Sastry, G Narahari

    2014-12-04

    Ab initio computations, up to CCSD(T)/CBS on model systems, and MP2/cc-pVTZ and DFT calculations are performed on cation-alkane and cation-alkene complexes, cation = Li(+), Na(+), Be(2+), Mg(2+), Ca(2+), Cu(+) and Zn(2+); alkane = C(n)H2(n+2) (n = 1-10) and C6H12; and alkene = C2H4 and C6H6. Density functional theory-symmetry adapted perturbation theory (DFT-SAPT) calculations reveal that the cation-alkane interactions are predominantly constituted of induction component. The dramatic modulation of the strength of their interaction and the topological features obtained from atoms in molecules (AIM) analysis are consistent with the characteristics of a typical noncovalent interaction. In contrast to many of the conventional noncovalent interactions, cation-alkane interactions are substantially strong and are comparable in strength to the well studied cation-π interactions.

  10. Generation of crystalline silica from sugarcane burning.

    Science.gov (United States)

    Le Blond, Jennifer S; Horwell, Claire J; Williamson, Ben J; Oppenheimer, Clive

    2010-07-08

    Sugarcane leaves contain amorphous silica, which may crystallise to form crystalline silica polymorphs (cristobalite or quartz), during commercial sugarcane harvesting where sugarcane plants are burned. Respirable airborne particulate containing these phases may present an occupational health hazard. Following from an earlier pilot study (J. S. Le Blond, B. J. Williamson, C. J. Horwell, A. K. Monro, C. A. Kirk and C. Oppenheimer, Atmos. Environ., 2008, 42, 5558-5565) in which experimental burning of sugarcane leaves yielded crystalline silica, here we report on actual conditions during sugarcane burning on commercial estates, investigate the physico-chemical properties of the cultivated leaves and ash products, and quantify the presence of crystalline silica. Commercially grown raw sugarcane leaf was found to contain up to 1.8 wt% silica, mostly in the form of amorphous silica bodies (with trace impurities e.g., Al, Na, Mg), with only a small amount of quartz. Thermal images taken during several pre-harvest burns recorded temperatures up to 1056 degrees C, which is sufficient for metastable cristobalite formation. No crystalline silica was detected in airborne particulate from pre-harvest burning, collected using a cascade impactor. The sugarcane trash ash formed after pre-harvest burning contained between 10 and 25 wt% SiO(2), mostly in an amorphous form, but with up to 3.5 wt% quartz. Both quartz and cristobalite were identified in the sugarcane bagasse ash (5-15 wt% and 1-3 wt%, respectively) formed in the processing factory. Electron microprobe analysis showed trace impurities of Mg, Al and Fe in the silica particles in the ash. The absence of crystalline silica in the airborne emissions and lack of cristobalite in trash ash suggest that high temperatures during pre-harvest burning were not sustained long enough for cristobalite to form, which is supported by the presence of low temperature sylvite and calcite in the residual ash. The occurrence of quartz and

  11. Effects of Copper Exchange Levels on Complexation of Ammonia in ...

    African Journals Online (AJOL)

    NJD

    Cation exchange, catalysis, copper, complexation, copper ammines. 1. Introduction. Copper-exchanged zeolites ... characterization of cation-exchanged zeolites is ammonia.7. Ammonia is small enough (ca. 3.70 × 3.99 .... quartz glass sample cuvettes and the diffuse reflectance spec- troscopy measurements obtained from ...

  12. Removal of cesium ions from clays by cationic surfactant intercalation.

    Science.gov (United States)

    Park, Chan Woo; Kim, Bo Hyun; Yang, Hee-Man; Seo, Bum-Kyoung; Moon, Jei-Kwon; Lee, Kune-Woo

    2017-02-01

    We propose a new approach to remediate cesium-contaminated clays based on intercalation of the cationic surfactant dodecyltrimethylammonium bromide (DTAB) into clay interlayers. Intercalation of DTAB was found to occur very rapidly and involved exchanging interlayer cations. The reaction yielded efficient cesium desorption (∼97%), including of a large amount of otherwise non-desorbable cesium ions by cation exchange with ammonium ions. In addition, the intercalation of DTAB afforded an expansion of the interlayers, and an enhanced desorption of Cs by cation exchange with ammonium ions even at low concentrations of DTAB. Finally, the residual intercalated surfactants were easily removed by a decomposition reaction with hydrogen peroxide in the presence of Cu 2+ /Fe 2+ catalysts. Copyright © 2016 Elsevier Ltd. All rights reserved.

  13. Study of sugarcane pieces as yeast supports for ethanol production from sugarcane juice and molasses.

    Science.gov (United States)

    Liang, Lei; Zhang, Yuan-ping; Zhang, Li; Zhu, Ming-jun; Liang, Shi-zhong; Huang, Yu-nan

    2008-12-01

    Due to the environmental concerns and the increasing price of oil, bioethanol was already produced in large amount in Brazil and China from sugarcane juice and molasses. In order to make this process competitive, we have investigated the suitability of immobilized Saccharomyces cerevisiae strain AS2.1190 on sugarcane pieces for production of ethanol. Electron microscopy clearly showed that cell immobilization resulted in firm adsorption of the yeast cells within subsurface cavities, capillary flow through the vessels of the vascular bundle structure, and attachment of the yeast to the surface of the sugarcane pieces. Repeated batch fermentations using sugarcane supported-biocatalyst were successfully carried out for at least ten times without any significant loss in ethanol production from sugarcane juice and molasses. The number of cells attached to the support increased during the fermentation process, and fewer yeast cells leaked into fermentation broth. Ethanol concentrations (about 89.73-77.13 g/l in average value), and ethanol productivities (about 59.53-62.79 g/l d in average value) were high and stable, and residual sugar concentrations were low in all fermentations (0.34-3.60 g/l) with conversions ranging from 97.67-99.80%, showing efficiency (90.11-94.28%) and operational stability of the biocatalyst for ethanol fermentation. The results of this study concerning the use of sugarcane as yeast supports could be promising for industrial fermentations.

  14. Quantification of sugarcane yellow leaf virus in sugarcane following transmission through aphid vector, Melanaphis sacchari.

    Science.gov (United States)

    Chinnaraja, C; Viswanathan, R

    2015-12-01

    Yellow leaf caused by Sugarcane yellow leaf virus (SCYLV) is a serious constraint to sugarcane production in India and currently the disease epidemics occur on many of the susceptible varieties under field conditions. Studies were conducted on the virus transmission by sugarcane aphid Melanaphis sacchari in sugarcane by inoculating virus-free meristem derived from micro- propagated plants of sugarcane cv Co 86032 with viruliferous aphids. Virus transmission was confirmed through RT-PCR assays and subsequently SCYLV population was established through RT-qPCR. A maximum of 22.3 × 10(3), 3.16 × 10(6) and 4.78 × 10(6) copies of SCYLV-RNA targets were recorded in the plants after 7, 180 and 300 days, respectively. This study showed that the aphid species M. sacchari acts as an effective vector of SCYLV. The relative standard curve method in RT-qPCR efficiently detected the increment in SCYLV copy numbers in sugarcane following transmission through M. sacchari.

  15. Microcollinearity between autopolyploid sugarcane and diploid sorghum genomes

    Directory of Open Access Journals (Sweden)

    Rokhsar Daniel S

    2010-04-01

    Full Text Available Abstract Background Sugarcane (Saccharum spp. has become an increasingly important crop for its leading role in biofuel production. The high sugar content species S. officinarum is an octoploid without known diploid or tetraploid progenitors. Commercial sugarcane cultivars are hybrids between S. officinarum and wild species S. spontaneum with ploidy at ~12×. The complex autopolyploid sugarcane genome has not been characterized at the DNA sequence level. Results The microsynteny between sugarcane and sorghum was assessed by comparing 454 pyrosequences of 20 sugarcane bacterial artificial chromosomes (BACs with sorghum sequences. These 20 BACs were selected by hybridization of 1961 single copy sorghum overgo probes to the sugarcane BAC library with one sugarcane BAC corresponding to each of the 20 sorghum chromosome arms. The genic regions of the sugarcane BACs shared an average of 95.2% sequence identity with sorghum, and the sorghum genome was used as a template to order sequence contigs covering 78.2% of the 20 BAC sequences. About 53.1% of the sugarcane BAC sequences are aligned with sorghum sequence. The unaligned regions contain non-coding and repetitive sequences. Within the aligned sequences, 209 genes were annotated in sugarcane and 202 in sorghum. Seventeen genes appeared to be sugarcane-specific and all validated by sugarcane ESTs, while 12 appeared sorghum-specific but only one validated by sorghum ESTs. Twelve of the 17 sugarcane-specific genes have no match in the non-redundant protein database in GenBank, perhaps encoding proteins for sugarcane-specific processes. The sorghum orthologous regions appeared to have expanded relative to sugarcane, mostly by the increase of retrotransposons. Conclusions The sugarcane and sorghum genomes are mostly collinear in the genic regions, and the sorghum genome can be used as a template for assembling much of the genic DNA of the autopolyploid sugarcane genome. The comparable gene density between

  16. Inoculation of sugarcane with diazotrophic bacteria

    Directory of Open Access Journals (Sweden)

    Nivaldo Schultz

    2014-04-01

    Full Text Available The sugarcane industry, a strategic crop in Brazil, requires technological improvements in production efficiency to increase the crop energy balance. Among the various currently studied alternatives, inoculation with diazotrophic bacteria proved to be a technology with great potential. In this context, the efficiency of a mixture of bacterial inoculant was evaluated with regard to the agronomic performance and N nutrition of sugarcane. The experiment was carried out on an experimental field of Embrapa Agrobiologia, in Seropédica, Rio de Janeiro, using a randomized block, 2 × 3 factorial design (two varieties and three treatments with four replications, totaling 24 plots. The varieties RB867515 and RB72454 were tested in treatments consisting of: inoculation with diazotrophic bacteria, N-fertilized control with 120 kg ha-1 N and absolute control (no inoculation and no N fertilizer. The inoculum was composed of five strains of five diazotrophic species. The yield, dry matter accumulation, total N in the shoot dry matter and the contribution of N by biological fixation were evaluated, using the natural 15N abundance in non-inoculated sugarcane as reference. The bacterial inoculant increased the stalk yield of variety RB72454 similarly to fertilization with 120 kg ha-1 N in the harvests of plant-cane and first ratoon crops, however the contribution of biological N fixation was unchanged by inoculation, indicating that the benefits of the inoculant in sugarcane may have resulted from plant growth promotion.

  17. Genome Editing in Sugarcane: Challenges ahead

    Directory of Open Access Journals (Sweden)

    Chakravarthi Mohan

    2016-10-01

    Full Text Available Genome editing opens new and unique opportunities for researchers to enhance crop production. Until 2013, the zinc finger nucleases (ZFNs and transcription activator-like effector nucleases (TALENs were the key tools used for genome editing applications. The advent of RNA-guided engineered nucleases - the type II clustered regularly interspaced short palindromic repeat (CRISPR/Cas9 (CRISPR-associated system from Streptococcus pyogenes holds great potential since it is simple, effective and more versatile than ZFNs and TALENs. CRISPR/Cas9 system has already been successfully employed in several crop plants. Use of these techniques is in its infant stage in sugarcane. Jung and Altpeter (2016 have reported TALEN mediated approach for the first time to reduce lignin content in sugarcane to make it amenable for biofuel production. This is so far the only report describing genome editing in sugarcane. Large genome size, polyploidy, low transformation efficiency, transgene silencing and lack of high throughput screening techniques are certainly great challenges for genome editing in sugarcane which would be discussed in detail in this review.

  18. Assessment of somaclonal variation in sugarcane

    African Journals Online (AJOL)

    admin

    2012-10-30

    Oct 30, 2012 ... A study was conducted from 2006 to 2008 to assess the variability arising from callus regeneration and its vegetative transmission in a subtropical variety of sugarcane, CoJ 64. Qualitative and quantitative characters were evaluated in the field at maturity in each of the 3 years at the same location. The.

  19. Evaluation of sugarcane ( Saccharum officinarum L.) somaclonal ...

    African Journals Online (AJOL)

    Tissue culture technique was used to obtain salt tolerant variants from embryogenic calli of sugarcane (Saccharum sp. Var. CP48-103) that were cultured on a selective medium containing different levels of NaCl (0, 33, 66, 99 and 132 mM). A total of four plants which regenerated from the tolerant calli were selected but the ...

  20. Assessment of somaclonal variation in sugarcane | Sobhakumari ...

    African Journals Online (AJOL)

    A study was conducted from 2006 to 2008 to assess the variability arising from callus regeneration and its vegetative transmission in a subtropical variety of sugarcane, CoJ 64. Qualitative and quantitative characters were evaluated in the field at maturity in each of the 3 years at the same location. The frequencies of variants ...

  1. Rapid micropropagation of three elite Sugarcane (Saccharum ...

    African Journals Online (AJOL)

    STORAGESEVER

    2008-07-04

    Jul 4, 2008 ... culture. Sabaz Ali Khan1, 3*, Hamid Rashid2, M. Fayyaz Chaudhary1, Zubeda Chaudhry2 and Amber. Afroz2. 1Quaid-i-Azam University, Islamabad, Pakistan. ... Key words: Micropropagation, Sugarcane, Shoot tip, Hormone and Meristem culture. .... were dark green in color initially but changed to light ...

  2. Harvest managements and cultural practices in sugarcane

    Directory of Open Access Journals (Sweden)

    Sérgio Gustavo Quassi de Castro

    2014-02-01

    Full Text Available The presence of trash from the mechanical harvest of green cane on sugarcane plantations promotes changes in the agricultural management, for example, in the mechanical cultural practices of ratoon cane in-between the rows and nitrogen (N fertilization. The goal of this study was to evaluate the performance of sugarcane in different harvest systems, associated to the mechanical cultural practices in interrows and N rates. The study was carried out on a sugarcane plantation in Sales Oliveira, São Paulo, Brazil, with the sugarcane variety SP81-3250, on soil classified as Acrudox, in a randomized block design with split-split plots and four replications. The main treatments consisted of harvest systems (harvesting green cane or burnt cane, the secondary treatment consisted of the mechanical cultural practices in the interrows and the tertiary treatments were N rates (0, 30, 60, 90, 120 and 160 kg ha-1, using ammonium nitrate (33 % N as N source. The harvest systems did not differ in sugarcane yield (tons of cane per hectare - TCH, but in burnt cane, the pol percent and total sugar recovery (TSR were higher. This could be explained by the higher quantity of plant impurities in the harvested raw material in the system without burning, which reduces the processing quality. Mechanical cultural practices in the interrows after harvest had no effect on cane yield and sugar quality, indicating that this operation can be omitted in areas with mechanical harvesting. The application of N fertilizer at rates of 88 and 144 kg ha-1 N, respectively, increased stalk height and TCH quadratically to the highest values for these variables. For the sugar yield per hectare (in pol %, N fertilization induced a linear increase.

  3. Performance of herbicides in sugarcane straw

    Directory of Open Access Journals (Sweden)

    Rosilaine Araldi

    2015-12-01

    Full Text Available The process of mechanical harvesting of sugarcane generates a large deposition of straw on the soil surface, providing a coverage that several studies have found important for reducing the weed population. Although such coverage reduces weed infestations, additional management, including chemical control, is still needed. Thus, this study aimed to evaluate the leaching of atrazine, pendimethalin, metribuzin, clomazone, diuron and hexazinone in sugarcane straw. The experiment was conducted at the School of Agronomic Engineering at UNESP (Sao Paulo State University - Botucatu/SP. The sugarcane straw was collected in the field, cut and placed in quantities of 10t ha-1 in the capsules used as experimental units. The experimental design was completely randomized, using six herbicide treatments and four replications. Within 24 hours after the herbicides were applied in capsules with straw, five different rainfalls (5, 10, 20, 50 and 100mm were simulated. The leached water was collected for chromatographic analysis. The herbicide percentages that crossed the straw layer were statistically correlated with the rainfall amount by the Mitscherlich model that compares the facility of herbicide removal from sugarcane straw. In summary, pendimethalin did not present quantified transposition of the product by sugarcane straw even with a rain simulation of 100 mm. Furthermore, two different profiles of facility to transpose the herbicides in straw were found: one for metribuzin and hexazinone that crossed quickly through the straw layer and another for atrazine, diuron and clomazone that required more rainfall to be leached from coverage to the soil according to the maximum removable amount of each herbicide.

  4. ETUDE DE LA DISTRIBUTION DES CATIONS ECHANGEABLES

    African Journals Online (AJOL)

    SEI Joseph

    l'étude de nombreux paramètres (concentration, température, l'ajout de la bentonite), nous avons démontré que les boues ... haute densité (PEHD) et des matériaux argileux spécifiques de type bentonite. A ce jour ..... [4] - K. VERBURG AND P. BAVEYE “Hysteresis in the binary exchange of cations on 2:1 clay minerals : a.

  5. Oxidative stress response in sugarcane

    Directory of Open Access Journals (Sweden)

    Luis Eduardo Soares Netto

    2001-12-01

    Full Text Available Oxidative stress response in plants is still poorly understood in comparison with the correspondent phenomenon in bacteria, yeast and mammals. For instance, nitric oxide is assumed to play various roles in plants although no nitric oxide synthase gene has yet been isolated. This research reports the results of a search of the sugarcane expressed sequence tag (SUCEST database for homologous sequences involved in the oxidative stress response. I have not found any gene similar to nitric oxide synthase in the SUCEST database although an alternative pathway for nitric oxide synthesis was proposed. I have also found several genes involved in antioxidant defense, e.g. metal chelators, low molecular weight compounds, antioxidant enzymes and repair systems. Ascorbate (vitamin C is a key antioxidant in plants because it reaches high concentrations in cells and is a substrate for ascorbate peroxidase, an enzyme that I found in different isoforms in the SUCEST database. I also found many enzymes involved in the biosynthesis of low molecular weight antioxidants, which may be potential targets for genetic manipulation. The engineering of plants for increased vitamin C and E production may lead to improvements in the nutritional value and stress tolerance of sugarcane. The components of the antioxidant defense system interact and their synthesis is probably closely regulated. Transcription factors involved in regulation of the oxidative stress response in bacteria, yeast and mammals differ considerably among themselves and when I used them to search the SUCEST database only genes with weak similarities were found, suggesting that these transcription regulators are not very conserved. The involvement of reactive oxygen species and antioxidants in plant defense against pathogens is also discussed.A resposta ao estresse oxidativo não é bem conhecida em plantas como em bactérias, leveduras e humanos. Por exemplo, assume-se que óxido nítrico tem várias fun

  6. Climate Change and Sugarcane Production: Potential Impact and Mitigation Strategies

    Directory of Open Access Journals (Sweden)

    Duli Zhao

    2015-01-01

    Full Text Available Sugarcane (Saccharum officinarum L. is an important crop for sugar and bioenergy worldwide. The increasing greenhouse gas emission and global warming during climate change result in the increased frequency and intensity of extreme weather events. Climate change is expected to have important consequences for sugarcane production in the world, especially in the developing countries because of relatively low adaptive capacity, high vulnerability to natural hazards, and poor forecasting systems and mitigating strategies. Sugarcane production may have been negatively affected and will continue to be considerably affected by increases in the frequency and intensity of extreme environmental conditions due to climate change. The degree of climate change impact on sugarcane is associated with geographic location and adaptive capacity. In this paper, we briefly reviewed sugarcane response to climate change events, sugarcane production in several different countries, and challenges for sugarcane production in climate change in order for us to better understand effects of climate change on sugarcane production and to propose strategies for mitigating the negative impacts of climate change and improving sugarcane production sustainability and profitability.

  7. Sugarcane Land Classification with Satellite Imagery using Logistic Regression Model

    Science.gov (United States)

    Henry, F.; Herwindiati, D. E.; Mulyono, S.; Hendryli, J.

    2017-03-01

    This paper discusses the classification of sugarcane plantation area from Landsat-8 satellite imagery. The classification process uses binary logistic regression method with time series data of normalized difference vegetation index as input. The process is divided into two steps: training and classification. The purpose of training step is to identify the best parameter of the regression model using gradient descent algorithm. The best fit of the model can be utilized to classify sugarcane and non-sugarcane area. The experiment shows high accuracy and successfully maps the sugarcane plantation area which obtained best result of Cohen’s Kappa value 0.7833 (strong) with 89.167% accuracy.

  8. Separation of cationic aracyl derivatives of betaines and related compounds.

    Science.gov (United States)

    Storer, Malina K; McEntyre, Christopher J; Lever, Michael

    2006-02-03

    Cationic aracyl esters of betaines can be formed by alkylation with aracyl halides or trifluoromethanesulfonates. HPLC on a non-endcapped strong cation exchange (SCX) column gave high retention of these derivatives. Cation exchange HPLC may be carried out on a normal-phase (silica or alumina) column using a polar organic solvent (acetonitrile, propan-2-ol) containing an aqueous buffer with an organic cation and a hydrophilic anion. Selectivity is affected by the choice of organic solvent and buffer, e.g. alcohols decrease the retention times of hydroxybetaines such as carnitine. Retention is reduced by increasing the water content and the buffer concentration. Capillary electrophoresis migration times are affected by the choice of buffer anion, with low pH citrate buffers favoured.

  9. TECHNOLOGICAL SCENARIOS TO THE DEMAND FOR SUGARCANE

    Directory of Open Access Journals (Sweden)

    Ana Paula Franco Paes Leme Barbosa

    2012-06-01

    Full Text Available From the first decade of the 2000s, it is clear that there is an increase in discussions involving sustainability, including the bioenergy issue, to which Brazil has drawn the attention due to advances in the ethanol industry. Advances in engine technology reflected new opportunities for this industry and, according to the Ten-Year Energy Plan for 2019 developed by the Ministry of Mines and Energy, there is an expected increase in demand for ethanol of 90% by 2019 (Brazil, 2010. However, new technologies for the conversion and use of sugarcane and the complex context of this industry add uncertainties to this sector. Aiming to discuss and include the uncertainties on the agenda of this industry, this study proposes to elaborate and discuss prospective scenarios to the demand for sugarcane. Four scenarios with different perspectives of technological advance and market development were elaborated and discussed in the conclusion.

  10. Extraction and Characterization of Sugarcane Peel Wax

    OpenAIRE

    Inarkar, Mangesh B.; Lele, S. S.

    2012-01-01

    Sugarcane peel is an agrowaste product and contains considerable amount of wax. This has a good technoeconomic potential. In view of this, the present study aims at extraction and characterization of wax from sugarcane peel. The yield of crude wax was 0.95% on dry weight basis. During Fourier transform-infrared spectroscopy (FT-IR) prominent peaks obtained at 2921.73 and 2851.64 (–CH), 1463.44 (–CH2), 1376.96 (–CH3), 1108.4 and 1170.16 (–C–O) 3395.60 (–OH), 1710.25 (–CHO), and 1736.63 (–COOH)...

  11. Incidente of microbial contaminants in sugarcane micropropagation

    Directory of Open Access Journals (Sweden)

    Yelenys Alvarado-Capó

    2003-01-01

    Full Text Available The incidence of microbial contaminants in Establishment, Multiplication and Rooting stages of the sugarcane micropropagation was determined by visual observation of the culture vessels. The type of microorganism was confirmed in observations to the optic microscope. The percentage of contamination for microbial group was determined in 731 apexes in the Establishment stage, in each multiplication subculture (up to the seventh in a total of 5 225 in vitro plants and 6 650 in the Rooting stage. In three stages the presence of microbial contaminants was verified (filamentous fungi, bacteria and yeasts with prevalence of the bacteria (13.7-31.6%. In the Multiplication stage the percentages of bacterial contamination were increased with the number of subcultures. The results indicated the high incidence of microbial contaminants in sugarcane micropropagation and the necessity of paying attention to the control of the bacterial contamination. Key words: bacteria, filamentous fungi, in vitro plants, yeast

  12. Enhanced polyhydroxybutyrate production in transgenic sugarcane.

    Science.gov (United States)

    Petrasovits, Lars A; Zhao, Lihan; McQualter, Richard B; Snell, Kristi D; Somleva, Maria N; Patterson, Nii A; Nielsen, Lars K; Brumbley, Stevens M

    2012-06-01

    Polyhydroxybutyrate (PHB) is a bacterial polyester that has properties similar to some petrochemically produced plastics. Plant-based production has the potential to make this biorenewable plastic highly competitive with petrochemical-based plastics. We previously reported that transgenic sugarcane produced PHB at levels as high as 1.8% leaf dry weight without penalty to biomass accumulation, suggesting scope for improving PHB production in this species. In this study, we used different plant and viral promoters, in combination with multigene or single-gene constructs to increase PHB levels. Promoters tested included the maize and rice polyubiquitin promoters, the maize chlorophyll A/B-binding protein promoter and a Cavendish banana streak badnavirus promoter. At the seedling stage, the highest levels of polymer were produced in sugarcane plants when the Cavendish banana streak badnavirus promoter was used. However, in all cases, this promoter underwent silencing as the plants matured. The rice Ubi promoter enabled the production of PHB at levels similar to the maize Ubi promoter. The maize chlorophyll A/B-binding protein promoter enabled the production of PHB to levels as high as 4.8% of the leaf dry weight, which is approximately 2.5 times higher than previously reported levels in sugarcane. This is the first time that this promoter has been tested in sugarcane. The highest PHB-producing lines showed phenotypic differences to the wild-type parent, including reduced biomass and slight chlorosis. © 2012 The Authors. Plant Biotechnology Journal © 2012 Society for Experimental Biology, Association of Applied Biologists and Blackwell Publishing Ltd.

  13. Gas transfer between the atmosphere and irrigated sugarcane plantation sites under different rainfall in Hawai'i

    Science.gov (United States)

    Miyazawa, Y.; Giambelluca, T. W.; Crow, S. E.; Mudd, R. G.; Youkhana, A.; Nullet, M.; Nakahata, M.

    2015-12-01

    Sugarcane plantation land cover is increasing in area in Brazil, South Asia and the Pacific Islands because of the growing demand for sugar and biofuel production. While a large portion of sugarcane cultivated in Brazil is rain-fed and experiences drought influences on gas exchange, sugarcane in Hawai'i is thought to be buffered from drought effects because it is drip irrigated. Knowledge about carbon sequestration and evapotranspiration rates is fundamental both for the prediction of sugar and biofuel production and for water resource management for the large plantations. To understand gas transfer under spatially and temporally heterogeneous environments, we investigated the leaf- soil- and stand-scale gas transfer processes at two irrigated sugarcane plantation study sites in Hawai'i with contrasting rainfall. Gas and energy transfers were monitored using eddy covariance systems for a full- and later half- crop cycle. Leaf ecophysiological traits were measured for stands of different ages to evaluate the effects of stand age on gas transfer. Carbon sequestration rates (Fc) showed a strong relationship with solar radiation with small differences between sites. Latent heat flux expressed as the evapotranspiration rates (ET) also had a strong relationship with solar radiation, but showed seasonality due to variations in biological control (surface conductance) and atmospheric evaporative demand. The difference in ET and its responses to environments was less clear partly buffered by the differences in the stand age and seasons. The stable Fc-solar radiation relationship despite the variation in surface conductance was partly due to the saturation of net photosynthetic rates with intercellular CO2 concentration and the low sensitivity of net photosynthesis to variations in surface conductance in sugarcane with the C4 photosynthesis pathway. The response of gas transfer to periodic irrigation, rainfall and age-related changes in leaf ecophysiological traits will be

  14. Preliminary observations of sugarcane trash degradation for repurposing as mulch

    Science.gov (United States)

    A potential use for sugarcane trash is to convert it to mulch. This study was undertaken to evaluate whether a compost enhancer or nitrogen would accelerate degradation of leaf trash. Trash was obtained from a sugarcane grower, and was treated with water only, a commercial compost starter composed o...

  15. Persistence and metabolism of fipronil in sugarcane leaves and juice.

    Science.gov (United States)

    Mandal, Kousik; Singh, Balwinder

    2014-02-01

    Fipronil gives effective control of early shoot borer and termites in sugarcane. The persistence and metabolism of fipronil in sugarcane leaves and juice were studied following application of fipronil (Regent 0.3 G) at 75 and 300 g a.i. ha(-1). Samples of sugarcane leaves were collected at various time intervals. Samples of sugarcane juice were collected at harvest. Residues of fipronil and its metabolites were quantified by gas liquid chromatograph. The limit of quantification of fipronil and its metabolites was 0.01 mg kg(-1) for sugarcane leaves and juice. Total residues of fipronil and its metabolites in sugarcane leaves after 7 days of its application at 75 and 300 g a.i. ha(-1) were 0.26 and 0.66 mg kg(-1), respectively. Residues could not be detected after 60 and 90 following fipronil application at either concentration. In sugarcane leaves, fipronil was found to be the main constituent, followed by its metabolites amide, desulfinyl, sulfone and sulfide. Samples of sugarcane juice did not reveal the presence of fipronil or its metabolites following its application at both the dosages at harvest.

  16. Sugarcane straw removal effects on plant growth and stalk yield

    Science.gov (United States)

    There is growing interest in sugarcane straw removal from the field to use as raw material for bioenergy production. In contrast, sugarcane straw removal may have negative implications for many soil ecosystem services and subsequent plant growth. A two-year experiment was conducted at Bom Retiro and...

  17. The political organization of sugarcane production in Western Mexico

    NARCIS (Netherlands)

    Guzman - Flores, E.

    1995-01-01

    The strike of CNC sugarcane producers and the immediate response by the refinery administration are a good example of the ongoing political negotiations between the main actors involved in the organization of sugarcane production in the Valley of Autlán-El Grullo. I introduced in Chapter I

  18. Rumen dry matter degradability of fresh and ensiled sugarcane ...

    African Journals Online (AJOL)

    This study aimed to evaluate the chemical composition and in situ ruminal degradability of fresh (FSC) and ensiled (ESC) sugarcane. In situ dry matter degradability (DMD) was determined using the nylon bag technique with four cows equipped ruminal fistulas. Cows were fed with fresh or ensiled sugarcane and ...

  19. Late season sugarcane performance as affected by soil water deficit ...

    African Journals Online (AJOL)

    A field trial was carried out in Ferké 2 Sugar mill located in northern Ivory Coast, in order to study sugarcane growth and yield response to deficit irrigation imposed over the yield formation stage. The crop used was a first ratoon Co 957, a non flowering late season sugarcane variety. The experiment was completely ...

  20. Assessment of genetic diversity analysis in contrasting sugarcane ...

    African Journals Online (AJOL)

    Sugarcane is an important crop in the country economically, politically and sociologically. It is the second largest agro-industry next to textiles. The selection and combination of parents for crossing rely on an understanding of their genetic structures and molecular diversity. In the present study, 28 sugarcane genotypes were ...

  1. Comparative study on early detection of sugarcane smut ...

    African Journals Online (AJOL)

    Sugarcane smut caused by Sporisorium scitamineum has the potential to result in substantial tonnage loss and significant reduction in sucrose recovery. As early and precise diagnosis is an integral component in the successful management of sugarcane smut, the present study was undertaken to accurately determine the ...

  2. Efficacy of modified polycross method in development of sugarcane ...

    African Journals Online (AJOL)

    The results showed that the modified polycross method is as efficient as the Hawaiian polycross technique and more economical in the development of high yielding commercial sugarcane varieties in low technological developed sugarcane breeding programme. Key Words: Crop cycles, Heritability, Rank Summation Index ...

  3. Impact of biotechnology on sugarcane agriculture and industry

    Science.gov (United States)

    There are nine key issues that can influence the productivity and sustainability of the sugarcane industry. These include land, soil fertility, water, variety, planting density, crop protection, cultural practices, harvesting and processing, and information technology. To all sugarcane farmers, it r...

  4. Growing Sugarcane for Bioenergy – Effects on the Soil

    NARCIS (Netherlands)

    Hartemink, A.E.

    2010-01-01

    An increasing area of sugarcane is being growing for the production of bioenergy. Sugarcane puts a high demands on the soil due to the use of heavy machinery and because large amounts of nutrients are removed with the harvest. Biocides and inorganic fertilizers introduces risks of groundwater

  5. Agrobiodiversity endangered by sugarcane farming in Mumias and ...

    African Journals Online (AJOL)

    user

    Sugarcane can be considered as the single most important cash crop extensively grown in the Lake. Victoria basin of Kenya and Uganda. In Kenya sugarcane is commercially grown in Western and Nyanza provinces, primarily by small scale farmers followed by large-scale farmers and company/factory nucleus estates ...

  6. Somaclonal Variation studies in sugarcane somaclones by using ...

    African Journals Online (AJOL)

    sami

    2012-06-14

    Jun 14, 2012 ... 3Agricultural, Food and Nutritional Science Department, University of Alberta, Edmonton, Canada. 4National Institute of Biotechnology and Genetic Engineering, Faisalabad, Pakistan. Accepted 16 May, 2012. Three sugarcane accessions susceptible to sugarcane mosaic virus; HSF-240, S-2000-US-359, ...

  7. Production of Citric Acid from Solid State Fermentation of Sugarcane ...

    African Journals Online (AJOL)

    Aspergillus niger is the leading microorganism of choice for citric acid production. Sugarcane waste was used as substrate under solid state fermentation to comparatively evaluate the citric acid production capacity of Aspergillus niger isolates and the indigenous microflora in the sugarcane waste. Known optimal cultural ...

  8. Effects of sugarcane waste-products on Cd and Zn fractionation and their uptake by sugarcane (Saccharum officinarum L.).

    Science.gov (United States)

    Akkajit, Pensiri; DeSutter, Thomas; Tongcumpou, Chantra

    2014-01-01

    The effects of three sugarcane waste-products from an ethanol production plant on the fractionation of Cd and Zn in high Cd and Zn contaminated soil and metal accumulation in sugarcane (Saccharum officinarum L.) were studied, using the BCR sequential extraction and aqua regia extraction procedures. A pot experiment was performed for 4 months with four treatments: no-amendments (control), boiler ash (3% w/w), filter cake (3% w/w) and a combination of boiler ash and vinasse (1.5% + 1.5%, w/w). The results showed that all treatments reduced the most bioavailable concentrations of Cd and Zn (BCR1 + 2) in soils (4.0-9.6% and 5.5-6.3%, respectively) and metal uptake (μg) in the aboveground part of the sugarcane (up to 62% and 54% for Cd and Zn, respectively) as compared to the control. No visual symptoms of metal toxicity and no positive effect on the biomass production of sugarcane were observed. Both Cd and Zn were accumulated mainly in the underground parts of the sugarcane (root > shoot ≥ underground sett > leaf; and root > underground sett > shoot > leaf, respectively) and the translocation factors were below 1, indicating low metal uptake. The results suggested that even though sugarcane waste-products insignificantly promote sugarcane growth, they can be used in agriculture due to the low metal accumulation in sugarcane and the reduction in metal bioavailability in the soil.

  9. Determination of common inorganic anions and cations by non-suppressed ion chromatography with column switching.

    Science.gov (United States)

    Amin, Muhammad; Lim, Lee Wah; Takeuchi, Toyohide

    2008-02-29

    An ion chromatography (IC) method has been proposed for the determination of seven common inorganic anions (F(-), H(2)PO(4)(-), NO(2)(-), Cl(-), Br(-), NO(3)(-), and SO(4)(2-)) and/or five common inorganic cations (Na(+), NH(4)(+), K(+), Mg(2+), and Ca(2+)) using a single pump, a single eluent and a single detector. The present system used cation-exchange and anion-exchange columns connected in series via a single 10-port switching valve. The 10-port valve was switched for the separation of either cations or anions in a single chromatographic run. When 1.0mM trimellitic acid (pH 2.94) was used as the eluent, the seven anions and the five cations could be separated on the anion-exchange column and the cation-exchange column, respectively. The elution order was found to be F(-)anions and Na(+)cations. Complete separation of the above anions or cations was demonstrated within 35min each. Detection limits calculated at S/N=3 were 0.05-0.58ppm (mg/l) for the anions and 0.05-0.38ppm for the cations, whereas repeatability values were below 2.26, 2.76, and 2.90% for peak height, peak area and retention time, respectively. The method was successfully applied to the determination of inorganic anions and cations in river water samples.

  10. Sulfur balance of sulfur dioxide-ethanol-water fractionation of sugarcane straw.

    Science.gov (United States)

    You, Xiang; van Heiningen, Adriaan; Sixta, Herbert; Iakovlev, Mikhail

    2017-10-01

    The sulfur balance of SO 2 -ethanol-water (AVAP®) fractionation of sugarcane (SC) straw was investigated. Hydrogen sulfite and sulfite anions are nearly absent in the liquors, despite cations present in straw, whose effect is thus limited to neutralization of lignosulfonic acids decreasing the acidity. Higher degree of sulfonation was observed for dissolved straw lignin compared to wood lignin (0.8-0.9 vs. 0.25 S/C9). Sulfur dioxide amounts of 0.9-1.2, 4.1-4.3 and 44-49g per o.d.kg straw were bound to pulp, precipitated lignin and lignosulfonic acid, respectively, while the rest of SO 2 was recovered by distillation from the spent fractionation suspensions. Copyright © 2017 Elsevier Ltd. All rights reserved.

  11. Role of extracellular cations in cell motility, polarity, and chemotaxis

    Directory of Open Access Journals (Sweden)

    Soll D

    2011-04-01

    Full Text Available David R Soll1, Deborah Wessels1, Daniel F Lusche1, Spencer Kuhl1, Amanda Scherer1, Shawna Grimm1,21Monoclonal Antibody Research Institute, Developmental Studies, Hybridoma Bank, Department of Biology, University of Iowa, Iowa City; 2Mercy Medical Center, Surgical Residency Program, Des Moines, Iowa, USAAbstract: The concentration of cations in the aqueous environment of free living organisms and cells within the human body influence motility, shape, and chemotaxis. The role of extracellular cations is usually perceived to be the source for intracellular cations in the process of homeostasis. The role of surface molecules that interact with extracellular cations is believed to be that of channels, transporters, and exchangers. However, the role of Ca2+ as a signal and chemoattractant and the discovery of the Ca2+ receptor have demonstrated that extracellular cations can function as signals at the cell surface, and the plasma membrane molecules they interact with can function as bona fide receptors that activate coupled signal transduction pathways, associated molecules in the plasma membrane, or the cytoskeleton. With this perspective in mind, we have reviewed the cationic composition of aqueous environments of free living cells and cells that move in multicellular organisms, most notably humans, the range of molecules interacting with cations at the cell surface, the concept of a cell surface cation receptor, and the roles extracellular cations and plasma membrane proteins that interact with them play in the regulation of motility, shape, and chemotaxis. Hopefully, the perspective of this review will increase awareness of the roles extracellular cations play and the possibility that many of the plasma membrane proteins that interact with them could also play roles as receptors.Keywords: extracellular cations, chemotaxis, transporters, calcium, receptors

  12. Identifi cation of Sectarianism

    Directory of Open Access Journals (Sweden)

    Martinovich Vladimir

    2016-03-01

    Full Text Available «New religious movements and society» is traditionally one of the most sophisticated topics in the area of new religions studies. Its problem field is so huge that up to now by far not all important research themes where even touched by scientists from all over the world. The problem of the process of the identification of sectarianism by diff erent societal institutions is one of such untouched themes that is taken as the main subject of this article. This process by itself is an inseparable part of the every societal deliberate reaction to the very existence of unconventional religiosity, its unstructured and mainly structured types. The focal point of the article is step-by-step analysis of the general structure elements of the process of the identification of sectarianism without any reference to the specific time and place of its flow. Special attention is paid to the analysis of the subjects of the identification of sectarianism, to the criteria for religious groups to be qualified as new religious movements, and to the specific features of the process of documents filtration. The causes of selective perception of sectarianism are disclosed. Some main consequences and unpredictable outcomes of the process of the identification of sectarianism are described.

  13. Sorption of the organic cation metoprolol on silica gel from its aqueous solution considering the competition of inorganic cations.

    Science.gov (United States)

    Kutzner, Susann; Schaffer, Mario; Börnick, Hilmar; Licha, Tobias; Worch, Eckhard

    2014-05-01

    Systematic batch experiments with the organic monovalent cation metoprolol as sorbate and the synthetic material silica gel as sorbent were conducted with the aim of characterizing the sorption of organic cations onto charged surfaces. Sorption isotherms for metoprolol (>99% protonated in the tested pH of around 6) in competition with mono- and divalent inorganic cations (Na(+), NH4(+), Ca(2+), and Mg(2+)) were determined in order to assess their influence on cation exchange processes and to identify the role of further sorptive interactions. The obtained sorption isotherms could be described well by an exponential function (Freundlich isotherm model) with consistent exponents (about 0.8). In general, a decreasing sorption of metoprolol with increasing concentrations in inorganic cations was observed. Competing ions of the same valence showed similar effects. A significant sorption affinity of metoprolol with ion type dependent Freundlich coefficients KF,0.77 between 234.42 and 426.58 (L/kg)(0.77) could still be observed even at very high concentrations of competing inorganic cations. Additional column experiments confirm this behavior, which suggests the existence of further relevant interactions beside cation exchange. In subsequent batch experiments, the influence of mixtures with more than one competing ion and the effect of a reduced negative surface charge at a pH below the point of zero charge (pHPZC ≈ 2.5) were also investigated. Finally, the study demonstrates that cation exchange is the most relevant but not the sole mechanism for the sorption of metoprolol on silica gel. Copyright © 2014 Elsevier Ltd. All rights reserved.

  14. Ethanol production from sugarcane bagasse hydrolysate using Pichia stipitis.

    Science.gov (United States)

    Canilha, Larissa; Carvalho, Walter; Felipe, Maria das Graças de Almeida; Silva, João Batista de Almeida e; Giulietti, Marco

    2010-05-01

    The objective of this study was to evaluate the ethanol production from the sugars contained in the sugarcane bagasse hemicellulosic hydrolysate with the yeast Pichia stipitis DSM 3651. The fermentations were carried out in 250-mL Erlenmeyers with 100 mL of medium incubated at 200 rpm and 30 degrees C for 120 h. The medium was composed by raw (non-detoxified) hydrolysate or by hydrolysates detoxified by pH alteration followed by active charcoal adsorption or by adsorption into ion-exchange resins, all of them supplemented with yeast extract (3 g/L), malt extract (3 g/L), and peptone (5 g/L). The initial concentration of cells was 3 g/L. According to the results, the detoxification procedures removed inhibitory compounds from the hemicellulosic hydrolysate and, thus, improved the bioconversion of the sugars into ethanol. The fermentation using the non-detoxified hydrolysate led to 4.9 g/L ethanol in 120 h, with a yield of 0.20 g/g and a productivity of 0.04 g L(-1) h(-1). The detoxification by pH alteration and active charcoal adsorption led to 6.1 g/L ethanol in 48 h, with a yield of 0.30 g/g and a productivity of 0.13 g L(-1) h(-1). The detoxification by adsorption into ion-exchange resins, in turn, provided 7.5 g/L ethanol in 48 h, with a yield of 0.30 g/g and a productivity of 0.16 g L(-1) h(-1).

  15. Sugarcane Flood Tolerance: Current Limits and Future Prospects

    Energy Technology Data Exchange (ETDEWEB)

    Glaz, Barry; Gilbert, Robert

    2010-01-08

    Sugarcane flood tolerance is discussed in this presentation. Related issues are looked at from four perspectives – various limits, physiological and morphological changes, future gains speculations and possible ecological and hydrological applications. Sugarcane flood tolerance and yield changes are presented on several field experiments during the crop various growth phases – (1) after planting with furrow open and with furrow closed, (2) during summer growth and (3) prior to harvest. It is documented that flood or shallow water-table depth do not affect photosynthesis, stomatal conductance and transpiration. It is also documented that roots of all 40 sugarcane genotypes tested in Florida had aerenchyma, while stalks form aerenchyma after being flooded. However, only some genotypes form aerenchyma in stalks without exposure to flood; this provides extra flood tolerance. While it is still a theory, it seems that sugarcane root growth is decreased when roots must grow into water. However, sugarcane roots appear to meet the needs of the plant when flooded for up to 2 weeks. It is concluded that most commercial sugarcane cultivars in Florida can tolerate floods for 1 to 2 weeks and that sugarcane has physiological and morphological traits that allow it to respond well to short-duration floods, while continuous shallow water tables are more harmful to sugarcane than periodic flooding. Given these facts, new strategy of storing water on sugarcane fields is proposed - field A could be flooded for 1-2 weeks, then drained to the field B which would be flooded for 1-2 weeks, then drained to the field C, etc. Research should focus on extending this flood period duration, so new strategies for ecological and hydrological application could be pursued further.

  16. Nitrogen fluxes at the root-soil interface show a mismatch of nitrogen fertilizer supply and sugarcane root uptake capacity

    National Research Council Canada - National Science Library

    Brackin, Richard; Näsholm, Torgny; Robinson, Nicole; Guillou, Stéphane; Vinall, Kerry; Lakshmanan, Prakash; Schmidt, Susanne; Inselsbacher, Erich

    2015-01-01

    ... these with N uptake capacities of sugarcane roots. We show that in fertilized sugarcane soils, fluxes of inorganic N exceed the uptake capacities of sugarcane roots by several orders of magnitude...

  17. Sugarcane Elongin C is involved in infection by sugarcane mosaic disease pathogens

    Energy Technology Data Exchange (ETDEWEB)

    Zhai, Yushan; Deng, Yuqing; Cheng, Guangyuan; Peng, Lei; Zheng, Yanru; Yang, Yongqing, E-mail: yyq287346@163.com; Xu, Jingsheng, E-mail: xujingsheng@126.com

    2015-10-23

    Sugarcane (Saccharum sp. hybrid) provides the main source of sugar for humans. Sugarcane mosaic disease (SMD) is a major threat to sugarcane production. Currently, control of SMD is mainly dependent on breeding resistant cultivars through hybridization, which is time-consuming. Understanding the mechanism of viral infection may facilitate novel strategies to breed cultivars resistant to SMD and to control the disease. In this study, a wide interaction was detected between the viral VPg protein and host proteins. Several genes were screened from sugarcane cDNA library that could interact with Sugarcane streak mosaic virus VPg, including SceIF4E1 and ScELC. ScELC was predicted to be a cytoplasmic protein, but subcellular localization analysis showed it was distributed both in cytoplasmic and nuclear, and interactions were also detected between ScELC and VPg of SCMV or SrMV that reveal ScELC was widely used in the SMD pathogen infection process. ScELC and VPgs interacted in the nucleus, and may function to enhance the viral transcription rate. ScELC also interacted with SceIF4E2 both in the cytoplasm and nucleus, but not with SceIF4E1 and SceIF4E3. These results suggest that ScELC may be essential for the function of SceIF4E2, an isomer of eIF4E. - Highlights: • We cloned ScELC, SceIF4E1, SceIF4E2 and SceIF4E3 from sugarcane accession Badila. • We examined interactions among VPg, ScELC, SceIF4E1, SceIF4E2 and SceIF4E3. • We proofed that ScELC interacted with VPgs of SCMV, SrMV and SCSMV. • We proofed that ScELC interacted with SceIF4E2 but not SceIF4E1 or SceIF4E3.

  18. Transgenic sugarcane overexpressing CaneCPI-1 negatively affects the growth and development of the sugarcane weevil Sphenophorus levis.

    Science.gov (United States)

    Schneider, Vanessa Karine; Soares-Costa, Andrea; Chakravarthi, Mohan; Ribeiro, Carolina; Chabregas, Sabrina Moutinho; Falco, Maria Cristina; Henrique-Silva, Flavio

    2017-01-01

    Transgenic sugarcane expressing CaneCPI-1 exhibits resistance to Sphenophorus levis larvae. Transgenic plants have widely been used to improve resistance against insect attack. Sugarcane is an economically important crop; however, great losses are caused by insect attack. Sphenophorus levis is a sugarcane weevil that digs tunnels in the stem base, leading to the destruction of the crop. This insect is controlled inefficiently by chemical insecticides. Transgenic plants expressing peptidase inhibitors represent an important strategy for impairing insect growth and development. Knowledge of the major peptidase group present in the insect gut is critical when choosing the most effective inhibitor. S. levis larvae use cysteine peptidases as their major digestive enzymes, primarily cathepsin L-like activity. In this study, we developed transgenic sugarcane plants that overexpress sugarcane cysteine peptidase inhibitor 1 (CaneCPI-1) and assessed their potential through feeding bioassays with S. levis larvae. Cystatin overexpression in the transgenic plants was evaluated using semi-quantitative RT-PCR, RT-qPCR, and immunoblot assays. A 50% reduction of the average weight was observed in larvae that fed on transgenic plants in comparison to larvae that fed on non-transgenic plants. In addition, transgenic sugarcane exhibited less damage caused by larval attack than the controls. Our results suggest that the overexpression of CaneCPI-1 in sugarcane is a promising strategy for improving resistance against this insect.

  19. Studies on Municipal Solid Wastes Dumping on Soil Anions, Cations ...

    African Journals Online (AJOL)

    Similarly dumpsite soil nitrate level, percentage organic carbon, organic matter, sulphate and phosphate ions were significantly (P<0.05) increased with increased waste dumping. All the exchangeable cations and trace metals concentrations investigated were higher (P<0.05) than control levels. However, while the ...

  20. Atmospheric CO2 enrichment facilitates cation release from soil.

    Science.gov (United States)

    Cheng, L; Zhu, J; Chen, G; Zheng, X; Oh, N-H; Rufty, T W; Richter, D deB; Hu, S

    2010-03-01

    Atmospheric CO(2) enrichment generally stimulates plant photosynthesis and nutrient uptake, modifying the local and global cycling of bioactive elements. Although nutrient cations affect the long-term productivity and carbon balance of terrestrial ecosystems, little is known about the effect of CO(2) enrichment on cation availability in soil. In this study, we present evidence for a novel mechanism of CO(2)-enhancement of cation release from soil in rice agricultural systems. Elevated CO(2) increased organic C allocation belowground and net H(+) excretion from roots, and stimulated root and microbial respiration, reducing soil redox potential and increasing Fe(2+) and Mn(2+) in soil solutions. Increased H(+), Fe(2+), and Mn(2+) promoted Ca(2+) and Mg(2+) release from soil cation exchange sites. These results indicate that over the short term, elevated CO(2) may stimulate cation release from soil and enhance plant growth. Over the long-term, however, CO(2)-induced cation release may facilitate cation losses and soil acidification, negatively feeding back to the productivity of terrestrial ecosystems.

  1. Lifecycle assessment of fuel ethanol from sugarcane in Brazil

    DEFF Research Database (Denmark)

    Ometto, A. R.; Hauschild, Michael Zwicky; Roma, W. N. L.

    2009-01-01

    This paper presents the lifecycle assessment (LCA) of fuel ethanol, as 100% of the vehicle fuel, from sugarcane in Brazil. The functional unit is 10,000 km run in an urban area by a car with a 1,600-cm(3) engine running on fuel hydrated ethanol, and the resulting reference flow is 1,000 kg......, and study cases at sugarcane farms and fuel ethanol industries in the northeast of SA o pound Paulo State, Brazil. The methodological structure for this LCA study is in agreement with the International Standardization Organization, and the method used is the Environmental Design of Industrial Products...... fuel. The recommendations for the ethanol lifecycle are: harvesting the sugarcane without burning; more environmentally benign agricultural practices; renewable fuel rather than diesel; not washing sugarcane and implementing water recycling systems during the industrial processing; and improving...

  2. CO2 emissions from soil incubated with sugarcane straw and ...

    African Journals Online (AJOL)

    CO2 emissions from soil incubated with sugarcane straw and nitrogen fertilizer. RF de Almeida, CH Silveira, JER Mikhael, FO Franco, BT Ribeiro, A de Siqueira Ferreira, E de Sa Mendonca, B Wendling ...

  3. Development of somaclones in sugarcane genotype BF-162 and ...

    African Journals Online (AJOL)

    pris

    2012-02-21

    2007). Saponins Production in Shoot and Callus Cultures of Gypsophila Paniculata. J. Appl. Sci. Res. 3(10): 1045-1049. Hussnain Z, Afghan S (2006). Impact of major cane diseases on sugarcane yield and sugar recovery.

  4. Diversity of plant growth-promoting bacteria associated with sugarcane.

    Science.gov (United States)

    Antunes, J E L; Lyra, M C C P; Ollero, F J; Freitas, A D S; Oliveira, L M S; Araújo, A S F; Figueiredo, M V B

    2017-05-10

    The sugarcane (Saccharum spp) presents economic importance, mainly for tropical regions, being an important Brazilian commodity. However, this crop is strongly dependent on fertilizers, mainly nitrogen (N). This study assessed the plant growth-promoting bacteria (PGPB) associated with sugarcane that could be used as a potential inoculant to the crop. We evaluated the genetic diversity of PGPB in the plant tissue of sugarcane varieties (RB 867515, RB 1011, and RB 92579). The primer BOX-A1R was used to differentiate the similar isolated and further sequencing 16S rRNA ribosomal gene. The 16S rRNA gene showed the presence of seven different genera distributed into four groups, the genus Bacillus, followed by Paenibacillus (20%), Burkholderia (14%), Herbaspirillum (6%), Pseudomonas (6%), Methylobacterium (6%), and Brevibacillus (3%). The molecular characterization of endophytic isolates from sugarcane revealed a diversity of bacteria colonizing this plant, with a possible biotechnological potential to be used as inoculant and biofertilizers.

  5. Development of somaclones in sugarcane genotype BF-162 and ...

    African Journals Online (AJOL)

    Development of somaclones in sugarcane genotype BF-162 and assessment of variability by random amplified polymorphic DNA (RAPD) and simple sequence repeats (SSR) markers in selected red rot resistant somaclones.

  6. Feasibility of cultivation of sugarcane in agroforestry systems

    Directory of Open Access Journals (Sweden)

    Pinto Luís Fernando Guedes

    2003-01-01

    Full Text Available Brazil is the world's main sugarcane producer and the production system has changed abiding to legal and technical recommendation. In Piracicaba many smallholders grow sugarcane in steep areas. Under such situation, mechanization at harvest makes cultivation impossible. This work assess the viability of agroforestry systems on joining crop production and conservation of natural resources. Soils at 12-20% slope class were identified, tree species which could be cultivated along with sugarcane were selected, and the design of the systems to be adopted was evaluated. Identified area occupies 11,556 ha and the most representative soil types are Typic Kandiuldult and Lithic Hapludoll. The exotic species coconut, eucalyptus, pejibaye and rubber, and eight native species have potential to be grown in contourhedgerows with sugarcane. Initial planting of exotic, domesticated trees is recommended, and gradual introduction of native, non-domesticated species, can be set according to their ecological requirements.

  7. Competitiveness of Brazilian Sugarcane Ethanol Compared to US Corn Ethanol

    OpenAIRE

    Crago, Christine Lasco; Khanna, Madhu; Barton, Jason; Giuliani, Eduardo; Amaral, Weber

    2010-01-01

    Corn ethanol produced in the US and sugarcane ethanol produced in Brazil are the world’s leading sources of biofuel. Current US biofuel policies create both incentives and constraints for the import of ethanol from Brazil, and together with the competitiveness and greenhouse gas intensity of sugarcane ethanol compared to corn ethanol will determine the extent of these imports. This study analyzes the supply-side determinants of this competitiveness and compares the greenhouse gas intensity of...

  8. IMAGE PROCESSING METHOD TO MEASURE SUGARCANE LEAF AREA

    OpenAIRE

    Sanjay B Patil; Dr Shrikant K Bodhe

    2011-01-01

    In order to increase the average sugarcane yield per acres with minimum cost farmers are adapting precision farming technique. This paper includes the area measurement of sugarcane leaf based on image processing method which is useful for plants growth monitoring, to analyze fertilizer deficiency and environmental stress,to measure diseases severity. In image processing method leaf area is calculated through pixel number statistic. Unit pixel in the same digital images represent the same size...

  9. RB975242 and RB975201 - Late maturation sugarcane varieties

    Directory of Open Access Journals (Sweden)

    Monalisa Sampaio Carneiro

    2016-11-01

    Full Text Available The sugarcane varieties RB975201 and RB975242 were developed and released for harvest at the end of the season (late maturation in the CentralSouth region of Brazil. In specific environments, these varieties were compared with commercial standards in sugar yield per area. They are resistant to major sugarcane diseases and present the Bru1 gene of resistance to brown rust.

  10. Comparison of genes fragments coding for ribosomal protein in sugarcane

    Directory of Open Access Journals (Sweden)

    María I. Oloriz

    2005-01-01

    Full Text Available Partial sequences of sugarcane genes, obtained by means of a subtractive library were identified by BLAST alignment against all sequences available in the databases. During the homology search, five genes were identified as chloroplast or citosol ribosomal proteins. The biggest homology obtained among the identified sequences as ribosomal proteins of sugarcane was with the corn genome. Key words: consensus domain, Saccharum spp., subtractive library

  11. Nitrogenous fertilization of sugarcane in a soil with hydromorphy

    Directory of Open Access Journals (Sweden)

    Emma Pineda Ruiz

    2014-07-01

    Full Text Available The element that sugarcane responds to more frequently is nitrogen. A deficiency of this element may decrease the agricultural yields, when applied below the rates the crop needs; and an over-abundance of this element causes smaller sucrose content in sugarcane juice. It is necessary to apply nitrogen fertilizers appropriately at the right time and in the right place. In a long-term (18-year experiment on a Vertisol, where doses ranging from 0 until 250 kg of N.ha-1 were applied, the nitrogen fertilization revealed a positive effect on the agricultural yields of the 14 studied crops, during the first 3 cycles. And all the evaluated stumps responded constantly to the nitrogen fertilization. The rate of consumption was of 1.13 kg of N per ton of sugarcane produced, lower than the one accepted by the Cuban sugarcane growers (1.5 kg of N/t of sugarcane. The organic matter content benefitted where the element was applied, although its content increased in the soil over a long period of time. The objective of this research was to evaluate of the response of sugarcane when nitrogen fertilizers were applied to hydromorphic soils.

  12. Transgenic Sugarcane with a cry1Ac Gene Exhibited Better Phenotypic Traits and Enhanced Resistance against Sugarcane Borer.

    Directory of Open Access Journals (Sweden)

    Shiwu Gao

    Full Text Available We developed sugarcane plants with improved resistance to the sugarcane borer, Diatraea saccharalis (F. An expression vector pGcry1Ac0229, harboring the cry1Ac gene and the selectable marker gene, bar, was constructed. This construct was introduced into the sugarcane cultivar FN15 by particle bombardment. Transformed plantlets were identified after selection with Phosphinothricin (PPT and Basta. Plantlets were then screened by PCR based on the presence of cry1Ac and 14 cry1Ac positive plantlets were identified. Real-time quantitative PCR (RT-qPCR revealed that the copy number of cry1Ac gene in the transgenic lines varied from 1 to 148. ELISA analysis showed that Cry1Ac protein levels in 7 transgenic lines ranged from 0.85 μg/FWg to 70.92 μg/FWg in leaves and 0.04 μg/FWg to 7.22 μg/FWg in stems, and negatively correlated to the rate of insect damage that ranged from 36.67% to 13.33%, respectively. Agronomic traits of six transgenic sugarcane lines with medium copy numbers were similar to the non-transgenic parental line. However, phenotype was poor in lines with high or low copy numbers. Compared to the non-transgenic control plants, all transgenic lines with medium copy numbers had relatively equal or lower sucrose yield and significantly improved sugarcane borer resistance, which lowered susceptibility to damage by insects. This suggests that the transgenic sugarcane lines harboring medium copy numbers of the cry1Ac gene may have significantly higher resistance to sugarcane borer but the sugarcane yield in these lines is similar to the non-transgenic control thus making them superior to the control lines.

  13. ACID HYDROLYSIS OF HEMICELLULOSE FROM SUGARCANE BAGASSE

    Directory of Open Access Journals (Sweden)

    A. PESSOA JR.

    1997-09-01

    Full Text Available Hydrolysis of the hemicellulosic fraction of sugarcane bagasse by sulphuric acid was performed in laboratory (25 mL and semi-pilot (25 L reactors under different conditions of temperature, time and acid concentration. On the laboratory scale, the three highest recovery yields were obtained at: 140ºC for 10 min with 100 mgacid/gdm (yield=73.4%; 140ºC for 20 min with 100 mgacid/gdm (yield=73.9% and 150ºC for 20 min with 70 mgacid/gdm (yield=71.8%. These conditions were also used for hydrolysis in a semi-pilot reactor, and the highest xylose recovery yield (83.3% was obtained at 140ºC for 20 min with 100 mgacid/gdm

  14. Soil uses during the sugarcane fallow period: influence on soil chemical and physical properties and on sugarcane productivity

    Directory of Open Access Journals (Sweden)

    Roniram Pereira da Silva

    2014-04-01

    Full Text Available The planting of diversified crops during the sugarcane fallow period can improve the chemical and physical properties and increase the production potential of the soil for the next sugarcane cycle. The primary purpose of this study was to assess the influence of various soil uses during the sugarcane fallow period on soil chemical and physical properties and productivity after the first sugarcane harvest. The experiment was conducted in two areas located in Jaboticabal, São Paulo State, Brazil (21º 14' 05'' S, 48º 17' 09'' W with two different soil types, namely: an eutroferric Red Latosol (RLe with high-clay texture (clay content = 680 g kg-1 and an acric Red Latosol (RLa with clayey texture (clay content = 440 g kg-1. A randomized block design with five replications and four treatments (crop sequences was used. The crop sequences during the sugarcane fallow period were soybean/millet/soybean, soybean/sunn hemp/soybean, soybean/fallow/soybean, and soybean. Soil use was found not to affect chemical properties and sugarcane productivity of RLe or RLa. The soybean/millet/soybean sequence improved aggregation in the acric Latosol.

  15. Life cycle assessment of sugarcane ethanol production in India in comparison to Brazil

    NARCIS (Netherlands)

    Tsiropoulos, Ioannis; Faaij, André P C; Seabra, Joaquim E A; Lundquist, Lars; Schenker, Urs; Briois, Jean François; Patel, Martin K.

    2014-01-01

    Purpose: India's biofuel programme relies on ethanol production from sugarcane molasses. However, there is limited insight on environmental impacts across the Indian ethanol production chain. This study closes this gap by assessing the environmental impacts of ethanol production from sugarcane

  16. Fermented sugarcane and pineapple beverage produced using Saccharomyces cerevisiae and non‐Saccharomyces yeast

    National Research Council Canada - National Science Library

    Ribeiro, Luciana Silva; Duarte, Whasley Ferreira; Dias, Disney Ribeiro; Schwan, Rosane Freitas

    2015-01-01

    ...) to produce a fermented sugarcane and pineapple drink was evaluated. Co‐ and pure cultures using different proportions of sugarcane juice and pineapple pulp (80:20, 70:30 and 60:40) were prepared...

  17. Sugarcane Water Sustainability Assessment Through the Indicators Extracted from Spatial Models: Case Study of Sugarcane Expansion Hotspots in Brazil

    Science.gov (United States)

    Ferraz, R. P.; Simoes, M.; Dubreuil, V.

    2012-12-01

    The CanaSat project data from INPE (2010) has evidenced the trend of sugarcane expansion into savanna areas in the Midwest region of Brazil that has a great potential for the sugarcane development, in terms of topography and suitable soils, according to Sugarcane Agroecological Zoning (EMBRAPA, 2009). However, in this region the climatic water availability has limitations, once the climate is marked by drought season with a strong water deficiency due to reduction of rainfall (SILVA et al. 2008). There may be serious risks to the sugarcane culture conducted in dryland crop system without any support from additional irrigation. Silva et al. (2008) state that, for the expansion of sugarcane cultivation in the Cerrado region will be necessary supplemental irrigation with 80 to 120 mm of water applied after cutting or planting. In the Brazilian Midwest the sugarcane agroindustry expansion is technically viable, but for the sustainable development of this activity it is necessary an adequate planning based on knowledge about water demand and availability. The aim of this study was to conduct an assessment of the potential water sustainability for the sugarcane cultivation in four microregions in Goiás State, Brazil, through the use of indicators proposed in Indicators System of Sugarcane Water Sustainability Assessment (Ferraz, 2012), that was thought to subsidize the public policies proposals and sectoral planning in strategic level by means of indicators that enable to perform diagnostic and prognostic analysis. These indicators are direct and relevant indexes obtained from data extracted through geoprocessing techniques from integration of many spatial models. The used indicators were: (i) Three indexes expressing the land favorability for sugarcane development conducted in dryland or irrigation system through the establishment of the ratio between the sugarcane suitable area for each different system and the total area of territorial unit of analysis (micro

  18. Sugarcane Water Stress Tolerance Mechanisms and Its Implications on Developing Biotechnology Solutions

    OpenAIRE

    Thais H. S. Ferreira; Tsunada, Max S.; Denis Bassi; Pedro Araújo; Lucia Mattiello; Guidelli, Giovanna V.; Righetto, Germanna L.; Gonçalves, Vanessa R.; Prakash Lakshmanan; Marcelo Menossi

    2017-01-01

    Sugarcane is a unique crop with the ability to accumulate high levels of sugar and is a commercially viable source of biomass for bioelectricity and second-generation bioethanol. Water deficit is the single largest abiotic stress affecting sugarcane productivity and the development of water use efficient and drought tolerant cultivars is an imperative for all major sugarcane producing countries. This review summarizes the physiological and molecular studies on water deficit stress in sugarcan...

  19. Spatial variability of soil attributes and sugarcane yield in relation to topographic location Variabilidade espacial de atributos do solo e produtividade da cultura de cana-de-açúcar em relação a localização topográfica

    Directory of Open Access Journals (Sweden)

    Zigomar M. de Souza

    2010-12-01

    Full Text Available Soils submitted to the same management system in places with little variation of landscape, manifest differentiated spatial variability of their attributes and crop yield. The aim of this work was to investigate the correlation between spatial variability of the soil attributes and sugarcane yield as a result of soil topography. To achieve this objective, a test area of 42 ha located at the São João Sugar Mill, in Araras, in the State of São Paulo, Brazil, was selected. Sugarcane yield was measured with a yield monitor fitted in a sugarcane harvester and GPS signal. A total of 170 soil samples were taken at regular 50 m grid, at a depth of 0 - 0.2 m. The area under study was divided into two sites based on topography. The following soil attributes were analysed: organic matter (OM content, exchangeable potassium (K, calcium (Ca and magnesium (Mg, their base saturation percentage (%BS, cation exchange capacity (CEC, pH, clay, silt, total sand and density. The use of landscape and geostatistics enable defining areas with different spatial variability in soil attributes and crop yield, providing the visualization and definition of homogeneous management zones. The largest spatial variability of soil attributes and sugarcane yield was in the lowest part of the field.Solos submetidos ao mesmo sistema de manejo em locais com pequena variação de relevo manifestam variabilidade espacial diferenciada de atributos do solo e das plantas. Objetivou-se com este trabalho estudar a correlação entre a variabilidade espacial de atributos físicos e químicos do solo com a produtividade da cana-de-açúcar em duas posições do relevo, de acordo com a topografia da área. O estudo foi realizado no município de Araras, SP, em uma área de 42 ha, pertencente à Usina São João. Para o mapeamento da produtividade da cultura da cana-de-açúcar utilizou-se um monitor de produtividade acoplado à colhedora e ao sinal de GPS. Coletaram-se 170 amostras do solo

  20. Impact of Cation form on Structure/Function Relationships of Perflurosulfonic Acid Ionomers

    Science.gov (United States)

    Kusoglu, Ahmet; Shi, Shouwen; Tesfaye, Meron; Weber, Adam

    Perfluorosulfonic-acid (PFSA) ionomers are widely used as ion-exchange solid-electrolytes in electrochemical devices, where their behavior are influenced by the interactions among its sulfonate groups, mobile cations, and water. The properties of a PFSA depends on its hydration, which drives its phase-separated morphology and controls the extent of sulfonate-cation interaction. Thus, cation-form and hydration collectively affect the structure/transport relationship, yet their interplay is still not well known. To elucidate this interplay, water uptake and conductivity of cation-exchanged PFSA are studied at various relative humidities (RHs) and in water, which are then correlated with mechanical properties and nanostructure. With increasing cation size and valence, the modulus increases, while swelling and conductivity decreases. The extent to which the cations impact the conductivity depends on hydration; at low RH the controlling factor is the cation (interactions), while with increasing RH, the key factor becomes water (swelling), although it is also controlled by the cations. Changes in conductivity with cations and RH are analyzed to establish a universal conductivity-hydration correlation, by accounting for charge density and water content.

  1. Water sustainability assessment in Brazilian sugarcane expansion area

    Science.gov (United States)

    Scarpare, F. V.; Ruiz-Correa, S. T.; Hernandes, T. A.; Scanlon, B. R.; Picoli, M. C. A.; Bonomi, A.

    2016-12-01

    Due to the increasing demand for ethanol, sugarcane is expanding into Cerrado (Savannahs), where edaphoclimatic characteristics differ significantly from traditional areas in South-eastern Brazil. It is expected that the sugarcane will be irrigated in those areas to increase yields and ensure stable production. The main objective is to assess the sugarcane land occupation and its dynamics relating its occurrence with the potential and actual yields, the irrigation needs, the production costs, and the water footprint in Paranaíba watershed (222,593 km2 drainage area). The Agroecological Zone Model - FAO was used in order to provide essential data for yield and water requirement assessment. For sugarcane stalk yield estimation, several improvements have been made allowing this tool to assess different irrigation scenarios. In this study, full irrigation which aims to replace 100% of the water deficit until senescence period was considered. The sugarcane occupation and expansion was assessed through EVI approach from 2009/2010 to 2012/2013 crop seasons. It was possible to identify that most part of sugarcane occupation is concentrated in the central area, which presents less potential for yield gain through irrigation and significant water availability issues. With regard to the expansion, an increase of 54% of cane occupation (from 616,899 to 946,589 ha) was detected during the assessed period showing that the main dynamic occurred in central part towards west side and at less extent, to southeaster side. The irrigation management were responsible for increase, on average, 108% of yields while decreasing 42% of water footprints. Simulated yields combine with CanaSoft model estimated a 30% decline in production cost. Although several aspects such as land price and infrastructure must to be considered, in conclusion, the expansion dynamic agrees to the areas with greater yield gain potential through irrigation, lower sugarcane production costs and water footprint

  2. Computational identification and analysis of novel sugarcane microRNAs

    Directory of Open Access Journals (Sweden)

    Thiebaut Flávia

    2012-07-01

    Full Text Available Abstract Background MicroRNA-regulation of gene expression plays a key role in the development and response to biotic and abiotic stresses. Deep sequencing analyses accelerate the process of small RNA discovery in many plants and expand our understanding of miRNA-regulated processes. We therefore undertook small RNA sequencing of sugarcane miRNAs in order to understand their complexity and to explore their role in sugarcane biology. Results A bioinformatics search was carried out to discover novel miRNAs that can be regulated in sugarcane plants submitted to drought and salt stresses, and under pathogen infection. By means of the presence of miRNA precursors in the related sorghum genome, we identified 623 candidates of new mature miRNAs in sugarcane. Of these, 44 were classified as high confidence miRNAs. The biological function of the new miRNAs candidates was assessed by analyzing their putative targets. The set of bona fide sugarcane miRNA includes those likely targeting serine/threonine kinases, Myb and zinc finger proteins. Additionally, a MADS-box transcription factor and an RPP2B protein, which act in development and disease resistant processes, could be regulated by cleavage (21-nt-species and DNA methylation (24-nt-species, respectively. Conclusions A large scale investigation of sRNA in sugarcane using a computational approach has identified a substantial number of new miRNAs and provides detailed genotype-tissue-culture miRNA expression profiles. Comparative analysis between monocots was valuable to clarify aspects about conservation of miRNA and their targets in a plant whose genome has not yet been sequenced. Our findings contribute to knowledge of miRNA roles in regulatory pathways in the complex, polyploidy sugarcane genome.

  3. Louisiana sugarcane entomology: A look at the back and a peek at the future

    Science.gov (United States)

    Controlling insect pests is an important consideration for sugarcane farmers seeking to minimize losses and maximize profits. Research in managing insects has been conducted for almost as long as sugarcane has been grown in Louisiana. This presentation reviews Louisiana sugarcane entomology from the...

  4. Genetic variability in coat protein gene of sugarcane mosaic virus in ...

    African Journals Online (AJOL)

    Sugarcane mosaic virus (SCMV) is one of the three causative viruses of mosaic in sugarcane, a sugar crop widely grown under tropical and subtropical conditions worldwide. Although molecular characterization of SCMV strains was reported from many countries, strain occurring in Pakistan, a major sugarcane producer ...

  5. Evaluation of the juice brix of wild sugarcanes (Saccharum spontaneum indigenous to Japan

    Directory of Open Access Journals (Sweden)

    Takeo Sakaigaichi

    2016-04-01

    Full Text Available Modern sugarcane cultivars are derived from the interspecific crossing between Saccharum officinarum and wild sugarcane, Saccharum spontaneum. The introgression of valuable characteristics from wild sugarcane is recognized as extremely important, but this process typically requires long-term effort over multiple generations of backcrosses owing to the low sugar content of the initial interspecific hybrids. In this study, we aimed to identify Japanese wild sugarcanes with high juice brix in order to promote effective interspecific crossing of sugarcane. Sixty-four accessions from the Nansei Islands and 70 accessions from the Honshu were evaluated for juice brix. Wild sugarcanes with high juice brix were demonstrated to exist among wild sugarcanes indigenous to the Honshu. A significant difference was observed between the median juice brix values of wild sugarcanes of the Nansei Islands and those of the Honshu. The relationship between juice brix and stem traits was then examined in 20 wild sugarcanes, 10 each from the Nansei Islands and the Honshu. The reproducibility of juice brix value in both experiments was confirmed. In contrast to juice brix, stem traits, such as length, diameter, and volume, were typically smaller in wild sugarcanes from the Honshu. Moreover, a negative correlation was observed between the index of stem volume and juice brix. In this study, we identified outstanding wild sugarcanes with high juice brix. Using germplasms from the identified wild sugarcanes in interspecific crossing could contribute to the increases in both yield and sugar content.

  6. Impact of sugarcane field residue and mill bagasse on seed germination

    Science.gov (United States)

    Research indicates that sugarcane field residue and sugarcane mill bagasse may be allelopathic. Allelopathy is the chemical interaction between plants, which may result in the inhibition of plant growth and development. Previous research in Louisiana indicated that sugarcane field residue may inhibi...

  7. Using agent-based simulation to explore sugarcane supply chain transport complexities at a mill scale

    CSIR Research Space (South Africa)

    Price, CS

    2014-09-01

    Full Text Available The sugarcane supply chain (from sugarcane grower to mill) have particular challenges. One of these is that the growers have to deliver their cane to the mill before its quality degrades. The sugarcane supply chain typically consists of many growers...

  8. Barter exchanges

    DEFF Research Database (Denmark)

    Sudzina, Frantisek

    Although barter is often perceived as something that proceeded money, barter is still used. The focus of the paper is on barter exchanges. Barter exchanges are used both in developing countries as well as in developed countries (including the U.S.). They are used by both organizations...... and individuals. They usually allow to exchange good but some include also services. Some exchanges allow only for bi-directional barter, i.e. when only two parties are involved in the exchange. But probably most of the barter exchanges use barter money; this makes it easier to exchange goods and services...

  9. Soil Quality Indexing Strategies for Evaluating Sugarcane Expansion in Brazil

    Science.gov (United States)

    Cherubin, Maurício R.; Karlen, Douglas L.; Cerri, Carlos E. P.; Franco, André L. C.; Tormena, Cássio A.; Davies, Christian A.; Cerri, Carlos C.

    2016-01-01

    Increasing demand for biofuel has intensified land-use change (LUC) for sugarcane (Saccharum officinarum) expansion in Brazil. Assessments of soil quality (SQ) response to this LUC are essential for quantifying and monitoring sustainability of sugarcane production over time. Since there is not a universal methodology for assessing SQ, we conducted a field-study at three sites within the largest sugarcane-producing region of Brazil to develop a SQ index (SQI). The most common LUC scenario (i.e., native vegetation to pasture to sugarcane) was evaluated using six SQI strategies with varying complexities. Thirty eight soil indicators were included in the total dataset. Two minimum datasets were selected: one using principal component analysis (7 indicators) and the other based on expert opinion (5 indicators). Non-linear scoring curves were used to interpret the indicator values. Weighted and non-weighted additive methods were used to combine individual indicator scores into an overall SQI. Long-term conversion from native vegetation to extensive pasture significantly decreased overall SQ. In contrast, conversion from pasture to sugarcane had no significant impact on overall SQ at the regional scale, but site-specific responses were found. In general, sugarcane production improved chemical attributes (i.e., higher macronutrient levels and lower soil acidity); however it has negative effects on physical and biological attributes (i.e., higher soil compaction and structural degradation as well as lower soil organic carbon (SOC), abundance and diversity of macrofauna and microbial activity). Overall, we found that simple, user-friendly strategies were as effective as more complex ones for identifying SQ changes. Therefore, as a protocol for SQ assessments in Brazilian sugarcane areas, we recommend using a small number of indicators (e.g., pH, P, K, Visual Evaluation of Soil Structure -VESS scores and SOC concentration) and proportional weighting to reflect chemical

  10. Soil Quality Indexing Strategies for Evaluating Sugarcane Expansion in Brazil.

    Directory of Open Access Journals (Sweden)

    Maurício R Cherubin

    Full Text Available Increasing demand for biofuel has intensified land-use change (LUC for sugarcane (Saccharum officinarum expansion in Brazil. Assessments of soil quality (SQ response to this LUC are essential for quantifying and monitoring sustainability of sugarcane production over time. Since there is not a universal methodology for assessing SQ, we conducted a field-study at three sites within the largest sugarcane-producing region of Brazil to develop a SQ index (SQI. The most common LUC scenario (i.e., native vegetation to pasture to sugarcane was evaluated using six SQI strategies with varying complexities. Thirty eight soil indicators were included in the total dataset. Two minimum datasets were selected: one using principal component analysis (7 indicators and the other based on expert opinion (5 indicators. Non-linear scoring curves were used to interpret the indicator values. Weighted and non-weighted additive methods were used to combine individual indicator scores into an overall SQI. Long-term conversion from native vegetation to extensive pasture significantly decreased overall SQ. In contrast, conversion from pasture to sugarcane had no significant impact on overall SQ at the regional scale, but site-specific responses were found. In general, sugarcane production improved chemical attributes (i.e., higher macronutrient levels and lower soil acidity; however it has negative effects on physical and biological attributes (i.e., higher soil compaction and structural degradation as well as lower soil organic carbon (SOC, abundance and diversity of macrofauna and microbial activity. Overall, we found that simple, user-friendly strategies were as effective as more complex ones for identifying SQ changes. Therefore, as a protocol for SQ assessments in Brazilian sugarcane areas, we recommend using a small number of indicators (e.g., pH, P, K, Visual Evaluation of Soil Structure -VESS scores and SOC concentration and proportional weighting to reflect

  11. Triazines mobility in sugarcane cultivated soils

    Science.gov (United States)

    Portocarrero, Rocio; Aparicio, Virginia; de Gerónimo, Eduardo; Costa, José Luis

    2017-04-01

    Atrazine and ametryn are pre and post-emergence herbicides, widely used in sugarcane crops in Argentina. Both herbicides are characterized by their moderate to high mobility in soil. The mobility increases with higher soil pH and lower organic matter content (OM). Tucuman province has the main sugarcane cultivated area in the country (>65%), which lies over a shallow aquifer and drains to the Salí river. Most of the cultivated soils from the southeast of the province have a pH> 7.3 and OMmobility. The aim of this study was to estimate the leaching potential of atrazine and ametryn in soils from the southeast of Tucuman under sugarcane production. Miscible displacement experiments were carried out using undisturbed topsoil cores from four production fields, by triplicate. Each column was 15 cm length and 8 cm diameter. The dose of atrazine and ametryn that was applied in the columns corresponds to the equivalent dose used in the field of 2 kg ha-1a.i and 1.2 kg ha-1a.i respectively. Br- was used as a tracer molecule and it was applied previous to the herbicides pulse at a concentration of 150 BrK kg ha-1. Displacement was made with CaCl2 (0.01M) at a flow of 0.4 ml min-1, constant temperature (21°C) and unsaturated conditions (-0,5 m). The leached water samples were analyzed by ultra performance liquid chromatography (Waters® ACQUITY® UPLC) coupled to a mass spectrometer (MS/MSQuattro Premier XE Waters).The breakthrough curves (BTCs) for each compound were estimated by the convection-dispersion equation (using CXTFIT 2.0 program) in order to estimate the transport parameters. Results showed that the hydraulic transport was in equilibrium conditions, meaning that all the soil water is involved in solute convective transport. This could be explained by a soil porosity composed mainly by micro and mesopores, due to natural conditions or by tillage and harvest practices. Water velocity and dispersion range were 0.73-1.6 cm h-1 and 0.24-2.3 cm2 h-1 respectively

  12. Identification and characterization of yeasts in sugarcane silages.

    Science.gov (United States)

    Avila, C L S; Bravo Martins, C E C; Schwan, R F

    2010-11-01

    To enumerate the micro-organisms and to identify the yeast species present during the ensilage of different sugarcane (Saccharum spp.) cultivars. Samples of sugarcane silage were collected at 10, 20, 30 and 40 days from the start of fermentation. Population levels of lactic acid bacteria (LAB), mesophilic facultative anaerobic (MFA) bacteria, filamentous fungi and yeasts were determined. Nine species of yeasts were classified according to traditional methods and confirmed using molecular techniques. LAB dominated the ensiling process of sugarcane, although yeasts were present at relatively high population levels throughout the whole fermentation period. The detected species of yeasts varied according to sugarcane cultivar and time of fermentation. Torulaspora delbrueckii was the predominant yeast, followed by Pichia anomala and Saccharomyces cerevisiae. Knowledge of the population of micro-organisms in general, and of yeasts in particular, present during the fermentation of sugarcane is of fundamental importance in the development of more effective ensiling processes. © 2010 The Authors. Journal of Applied Microbiology © 2010 The Society for Applied Microbiology.

  13. Scenarios of suitable areas of sugarcane crops in Brazil regions

    Science.gov (United States)

    Koga-Vicente, A.

    2011-12-01

    The use of ethanol produced from sugarcane presents advantages to face climate changes as adaptation measure (reduce dependency of fossil fuel) and mitigation measure (reduce GHG emissions and captures CO2). Whereas the increasing demand of ethanol production and the importance of the planning in order to meet a future demand, this work aimed to evaluate suitable areas for sugarcane crops in two Brazilian regions in present and in possible climate change conditions. Scenarios were generated considering climatic risk to sugarcane crops (present and based in IPCC projections for changes in temperature and precipitation values); land available and able to cultivation (baseline is actual conditions and the projections consider public policies; urban and protected areas were eliminated; regions that already have sugarcane crops were eliminated) and food security (areas that are used to food production crops were eliminated). Scenarios show areas with potential for expansion of sugarcane crops in the present conditions and the possible changes that could occur in a climate change scenario. The results can be used to drive public policies in ethanol sector.

  14. Simulated hydroclimatic impacts of projected Brazilian sugarcane expansion

    Science.gov (United States)

    Georgescu, M.; Lobell, D. B.; Field, C. B.; Mahalov, A.

    2013-03-01

    Sugarcane area is currently expanding in Brazil, largely in response to domestic and international demand for sugar-based ethanol. To investigate the potential hydroclimatic impacts of future expansion, a regional climate model is used to simulate 5 years of a scenario in which cerrado and cropland areas (~1.1E6 km2) within south-central Brazil are converted to sugarcane. Results indicate a cooling of up to ~1.0°C during the peak of the growing season, mainly as a result of increased albedo of sugarcane relative to the previous landscape. After harvest, warming of similar magnitude occurs from a significant decline in evapotranspiration and a repartitioning toward greater sensible heating. Overall, annual temperature changes from large-scale conversion are expected to be small because of offsetting reductions in net radiation absorption and evapotranspiration. The decline in net water flux from land to the atmosphere implies a reduction in regional precipitation, which is consistent with progressively decreasing simulated average rainfall for the study period, upon conversion to sugarcane. However, rainfall changes were not robust across three ensemble members. The results suggest that sugarcane expansion will not drastically alter the regional energy or water balance, but could result in important local and seasonal effects.

  15. Sugarcane spirit market share simulation: an application of conjoint analysis

    Directory of Open Access Journals (Sweden)

    João de Deus Souza Carneiro

    2012-12-01

    Full Text Available This study evaluated the influence of packaging and labeling attributes of sugarcane spirit on consumers' behavior by applying the results of conjoint analysis in sugarcane spirit market share simulation. Firstly, a conjoint analysis was performed aiming to estimate the part-worths of each consumer for some sugarcane spirit packaging and labeling attributes. These part-worths were used in the market share simulation using the maximum utility model. It was observed that some packaging and labeling attributes affected consumer's purchase intention and that most consumers showed a similar preference pattern regarding these attributes. These consumers showed preference for the Seleta brand, which was bottled in 700 mL clear glass bottles with a metal screw cap that bore a label illustration unrelated to sugarcane spirit production process and had the information "aged 36 months in oak barrels". This study also showed that conjoint analysis and the use of its results in the market share simulation proved important tools to better understand consumer behavior towards intention to purchase sugarcane spirit.

  16. Sugarcane Bagasse: A Potential Medium for Fungal Cultures

    Directory of Open Access Journals (Sweden)

    Arushdeep Sidana

    2014-01-01

    Full Text Available Worldwide, sugarcane industries produce tons of sugarcane bagasse as residual/waste material. This residual material is rich in complex lignocellulosic substances and may be used as a low cost carbon and energy source for the growth of fungal species. The present work was aimed at designing a sugarcane waste-based medium as a substitute for expensive commercial media for growing fungal cultures. Eight species of fungi, namely, Aspergillus niger, Candida albicans, Saccharomyces cerevisiae, Fusarium sp., and four unidentified species F1, F2, F3, and F5, were grown on the sugarcane bagasse medium which produced remarkable results and competed with standard media like potato dextrose agar, Sabouraud dextrose agar, and cornmeal agar. The designed medium was able to provide nourishment to the fungi as well as prevent the growth of any bacterial or fungal contaminant. The production of spores was more in the sugarcane medium as compared with standard media. Hence, this study led to the discovery of a new and efficient medium for fungal cultures as well as decrease in the waste disposal expenses and efforts.

  17. Catalysis using hydrous metal oxide ion exchanges

    Science.gov (United States)

    Dosch, Robert G.; Stephens, Howard P.; Stohl, Frances V.

    1985-01-01

    In a process which is catalyzed by a catalyst comprising an active metal on a carrier, said metal being active as a catalyst for the process, an improvement is provided wherein the catalyst is a hydrous, alkali metal or alkaline earth metal titanate, zirconate, niobate or tantalate wherein alkali or alkaline earth metal cations have been exchanged with a catalytically effective amount of cations of said metal.

  18. Catalysis using hydrous metal oxide ion exchangers

    Science.gov (United States)

    Dosch, R.G.; Stephens, H.P.; Stohl, F.V.

    1983-07-21

    In a process which is catalyzed by a catalyst comprising an active metal on a carrier, said metal being active as a catalyst for the process, an improvement is provided wherein the catalyst is a hydrous, alkali metal or alkaline earth metal titanate, zirconate, niobate or tantalate wherein alkali or alkaline earth metal cations have been exchanged with a catalytically effective amount of cations of said metal.

  19. Sugarcane Serine Peptidase Inhibitors, Serine Peptidases, and Clp Protease System Subunits Associated with Sugarcane Borer (Diatraea saccharalis) Herbivory and Wounding.

    Science.gov (United States)

    Medeiros, Ane H; Mingossi, Fabiana B; Dias, Renata O; Franco, Flávia P; Vicentini, Renato; Mello, Marcia O; Moura, Daniel S; Silva-Filho, Marcio C

    2016-09-01

    Sugarcane's (Saccharum spp.) response to Diatraea saccharalis (F.) (Lepidoptera: (Crambidae) herbivory was investigated using a macroarray spotted with 248 sugarcane Expressed Sequence Tags (ESTs) encoding serine peptidase inhibitors, serine peptidases. and Clp protease system subunits. Our results showed that after nine hours of herbivory, 13 sugarcane genes were upregulated and nine were downregulated. Among the upregulated genes, nine were similar to serine peptidase inhibitors and four were similar to Bowman-Birk Inhibitors (BBIs). Phylogenetic analysis revealed that these sequences belong to a phylogenetic group of sugarcane BBIs that are potentially involved in plant defense against insect predation. The remaining four upregulated genes included serine peptidases and one homolog to the Arabidopsis AAA+ chaperone subunit ClpD, which is a member of the Clp protease system. Among the downregulated genes, five were homologous to serine peptidases and four were homologous to Arabidopsis Clp subunits (three homologous to Clp AAA+ chaperones and one to a ClpP-related ClpR subunit). Although the roles of serine peptidase inhibitors in plant defenses against herbivory have been extensively investigated, the roles of plant serine peptidases and the Clp protease system represent a new and underexplored field of study. The up- and downregulated D. saccharalis genes presented in this study may be candidate genes for the further investigation of the sugarcane response to herbivory.

  20. Screening for Sugarcane Brown Rust in the First Clonal Stage of the Canal Point Sugarcane Breeding Program

    Directory of Open Access Journals (Sweden)

    Duli Zhao

    2015-07-01

    Full Text Available Sugarcane (Saccharum spp. brown rust (caused by Puccinia melanocephala Syd. & P. Syd. was first reported in the United States in 1978 and is still one of the great challenges for sugarcane production. A better understanding of sugarcane genotypic variation in response to brown rust will help optimize breeding and selection strategies for disease resistance. Brown rust ratings were scaled from non-infection (0 to severe infection (4 with intervals of 0.5 and routinely recorded for genotypes in the first clonal selection stage of the Canal Point sugarcane breeding program in Florida. Data were collected from 14,272 and 12,661 genotypes and replicated check cultivars in 2012 and 2013, respectively. Mean rust rating, % infection, and severity in each family and progeny of female parent were determined, and their coefficients of variation (CV within and among families (females were estimated. Considerable variation exists in rust ratings among families or females. The families and female parents with high susceptibility or resistance to brown rust were identified and ranked. The findings of this study can help scientists to evaluate sugarcane crosses and parents for brown rust disease, to use desirable parents for crossing, and to improve genetic resistance to brown rust in breeding programs.

  1. Functional characterization of sugarcane mustang domesticated transposases and comparative diversity in sugarcane, rice, maize and sorghum

    Directory of Open Access Journals (Sweden)

    Daniela Kajihara

    2012-01-01

    Full Text Available Transposable elements (TEs account for a large portion of plant genomes, particularly in grasses, in which they correspond to 50%-80% of the genomic content. TEs have recently been shown to be a source of new genes and new regulatory networks. The most striking contribution of TEs is referred as “molecular domestication”, by which the element coding sequence loses its movement capacity and acquires cellular function. Recently, domesticated transposases known as mustang and derived from the Mutator element have been described in sugarcane. In order to improve our understanding of the function of these proteins, we identified mustang genes from Sorghum bicolor and Zea mays and performed a phenetic analysis to assess the diversity and evolutionary history of this gene family. This analysis identified orthologous groups and showed that mustang genes are highly conserved in grass genomes. We also explored the transcriptional activity of sugarcane mustang genes in heterologous and homologous systems. These genes were found to be ubiquitously transcribed, with shoot apical meristem having the highest expression levels, and were downregulated by phytohormones. Together, these findings suggest the possible involvement of mustang proteins in the maintenance of hormonal homeostasis.

  2. Sugarcane maturity estimation through edaphic-climatic parameters

    Directory of Open Access Journals (Sweden)

    Scarpari Maximiliano Salles

    2004-01-01

    Full Text Available Sugarcane (Saccharum officinarum L. grows under different weather conditions directly affecting crop maturation. Raw material quality predicting models are important tools in sugarcane crop management; the goal of these models is to provide productivity estimates during harvesting, increasing the efficiency of strategical and administrative decisions. The objective of this work was developing a model to predict Total Recoverable Sugars (TRS during harvesting, using data related to production factors such as soil water storage and negative degree-days. The database of a sugar mill for the crop seasons 1999/2000, 2000/2001 and 2001/2002 was analyzed, and statistical models were tested to estimate raw material. The maturity model for a one-year old sugarcane proved to be significant, with a coefficient of determination (R² of 0.7049*. No differences were detected between measured and estimated data in the simulation (P < 0.05.

  3. Isozyme Analysis on Different Varieties of Sugarcane

    Directory of Open Access Journals (Sweden)

    Johnson M.

    2012-05-01

    Full Text Available Isozymic and protein diversity among five sugarcane varieties viz., Co 6304, Co 85019, Co 8371, Co 89003 and Co 91010 were studied to understand the varietal interrelationship and to identify the biochemical marker for the disease resistance and stress tolerance. The standard technique of vertical gel electrophoresis PAGE was employed for size separation of isozymes. The gel was stained with different staining solutions for different isozyme systems viz. peroxidase, esterase, acid phosphatase, alkaline phosphatase and proteins. Rf values of the banding profiles, similarity index and variation between the varieties were analysed. Among the four enzyme systems, peroxidase profile reveals the difference between the disease resistant / susceptible and abiotic stress tolerant / non tolerant varieties. The two isoperoxidase bands with Rf values 0.62 and 0.66 showed their presence in disease resistant and abiotic tolerant varieties. The presence of two marker bands (0.62, 0.66 of resistant and stress tolerant varieties suggest that the variety Co 6304 may also be resistant to smut, wilt and moderately resistant to red rot and tolerant to drought.

  4. Leaching of Co and Cs from spent ion exchange resins in cement ...

    Indian Academy of Sciences (India)

    Unknown

    2003-08-22

    Aug 22, 2003 ... Abstract. The leaching rate of 60Co and 137Cs from the spent cation exchange resins in cement–bentonite matrix has been studied. The solidification matrix was a standard Portland cement mixed with 290–350 (kg/m3) spent cation exchange resins, with or without 2–5% of bentonite clay. The leaching ...

  5. Leaching of 60 Co and 137 Cs from spent ion exchange resins in ...

    Indian Academy of Sciences (India)

    The leaching rate of 60Co and 137Cs from the spent cation exchange resins in cement–bentonite matrix has been studied. The solidification matrix was a standard Portland cement mixed with 290–350 (kg/m3) spent cation exchange resins, with or without 2–5% of bentonite clay. The leaching rates from the ...

  6. Hydrothermal Transformation of Natural Zeolite from Ende-NTT and Its Application as Adsorbent of Cationic Dye

    National Research Council Canada - National Science Library

    Ngapa, Yulius Dala; Sugiarti, Sri; Abidin, Zaenal

    2016-01-01

    .... The natural zeolite produced synthetic NaP1 and synthetic Faujasite. Based on the research results, the synthesis of zeolite by the hydrothermal method can enhance the adsorption capacity and Cation Exchange Capacity (CEC...

  7. Absenteeism due to occupational diseases among sugarcane workers

    OpenAIRE

    Aline Duarte Ferreira Ceccato; Luiz Carlos Soares de Carvalho Junior; Rafaela Campos Cuissi; Mariane Monteschi; Nayara Galvão Oliveira; Carlos Roberto Padovani; Ercy Mara Cipulo Ramos; Dionei Ramos

    2014-01-01

    The aim of this study was to analyze the frequency of work-related sick leave in sugarcane workers. A total of 1,230 medical excuses for 400 sugarcane workers were analyzed according to the International Classification of Diseases, 10th Revision (ICD-10). The following items were analyzed: diagnosis, sex, and length and season of sick leave. In all the seasons, musculoskeletal diseases showed the highest sick leave rate, following by respiratory diseases (p < 0.05). Sick leave due to musculos...

  8. Cationic polymers and porous materials

    KAUST Repository

    Han, Yu

    2017-04-27

    According to one or more embodiments, cationic polymers may be produced which include one or more monomers containing cations. Such cationic polymers may be utilized as structure directing agents to form mesoporous zeolites. The mesoporous zeolites may include micropores as well as mesopores, and may have a surface area of greater than 350 m2/g and a pore volume of greater than 0.3 cm3/g. Also described are core/shell zeolites, where at least the shell portion includes a mesoporous zeolite material.

  9. Synthetic cation-selective nanotube: permeant cations chaperoned by anions.

    Science.gov (United States)

    Hilder, Tamsyn A; Gordon, Dan; Chung, Shin-Ho

    2011-01-28

    The ability to design ion-selective, synthetic nanotubes which mimic biological ion channels may have significant implications for the future treatment of bacteria, diseases, and as ultrasensitive biosensors. We present the design of a synthetic nanotube made from carbon atoms that selectively allows monovalent cations to move across and rejects all anions. The cation-selective nanotube mimics some of the salient properties of biological ion channels. Before practical nanodevices are successfully fabricated it is vital that proof-of-concept computational studies are performed. With this in mind we use molecular and stochastic dynamics simulations to characterize the dynamics of ion permeation across a single-walled (10, 10), 36 Å long, carbon nanotube terminated with carboxylic acid with an effective radius of 5.08 Å. Although cations encounter a high energy barrier of 7 kT, its height is drastically reduced by a chloride ion in the nanotube. The presence of a chloride ion near the pore entrance thus enables a cation to enter the pore and, once in the pore, it is chaperoned by the resident counterion across the narrow pore. The moment the chaperoned cation transits the pore, the counterion moves back to the entrance to ferry another ion. The synthetic nanotube has a high sodium conductance of 124 pS and shows linear current-voltage and current-concentration profiles. The cation-anion selectivity ratio ranges from 8 to 25, depending on the ionic concentrations in the reservoirs.

  10. Cation exchange applications of synthetic tobermorite for the ...

    Indian Academy of Sciences (India)

    Unknown

    Although the ordinary portland cement (OPC) which is often used in waste management operations alone holds negligible amounts of Cs+ and Sr2+, ... Conditioning is the waste management step in which radioactive waste is immobilized ..... Gour University, Sagar for providing laboratory facilities and Dr J P Shrivastava, ...

  11. Fabrication of Cationic Exchange Polystyrene Nanofibers for Drug ...

    African Journals Online (AJOL)

    Method: The nanofibers were prepared from 15% w/v polystyrene solution in dimethylacetamide (DMAc) containing 0.025 %w/v tetrabutylammonium bromide (TBAB) using electrospinning technique, followed by crosslinking with sulfuric acid/formaldehyde in a ratio ranging from 100/0 to 50/50 v/v and sulfonation in sulfuric ...

  12. an assessment of cation-exchange capability of the carboxylated ...

    African Journals Online (AJOL)

    2004-07-01

    Department of Chemistry, University of Dar es Salaam, Box 35061, Dar es Salaam, Tanzania. (Received July 1, 2004; ... Petrochemicals cannot be sustained due to their high cost and depletion rates that lead ... coatings and brake linings [2, 4, 5], CNSL-based spherical polymer particles for adsorption and immobilization [6] ...

  13. CATION-EXCHANGE SOLID-PHASE AND LIQUID-LIQUID ...

    African Journals Online (AJOL)

    B. S. Chandravanshi

    indicating a purer extract. KEY WORDS: Khat alkaloids, Solid phase extraction, Liquid-liquid extraction, HPLC, Genevac. INTRODUCTION. Khat (Catha edulis Vahl. Endl.) is an evergreen shrub or tree belonging to the Celastraceae family. Although the plant originates from Ethiopia, it occurs in Kenya, Malawi, Uganda,.

  14. PHOTOOXIDATION OF TOLUENE IN CATION-EXCHANGED ZEOLITES. (R825304)

    Science.gov (United States)

    The perspectives, information and conclusions conveyed in research project abstracts, progress reports, final reports, journal abstracts and journal publications convey the viewpoints of the principal investigator and may not represent the views and policies of ORD and EPA. Concl...

  15. Exploring Alkaline Stable Organic Cations for Polymer Hydroxide Exchange Membranes

    Science.gov (United States)

    2015-04-29

    Reinholdt, J. Durand , Journal of Physical Chemistry C 2012, 116, 8510-8522. [151] C. Zhang, J. Hu, J. Cong, Y. Zhao, W. Shen, H. Toyoda, M. Nagatsu...Y. Iriyama, T. Abe, M. Matsuoka, K. Kikuchi, Z. Ogumi, Thin Solid Films 2008, 516, 3309-3313. 147 [155] M. Schieda, S. Roualdes, J. Durand , A

  16. Sugarcane White Leaf Disease Incidences and Population Dynamic of Leafhopper Insect Vectors in Sugarcane Plantations in Northeast Thailand.

    Science.gov (United States)

    Rattanabunta, Chiranan; Hanboonsong, Yupa

    2015-04-01

    The work consisted of two experiments, i.e. Experiment 1 was conducted under controlled environments where sugarcane plants were used as hosts. This investigation aimed to monitor the occurrence of the Sugarcane White Leaf disease and the abundance of Leafhopper insect vectors and also the work aimed to provide useful information in understanding some aspects on epidemiology of the Sugarcane White Leaf disease. A Completely Randomized Design with three replications was used to justify growth and development of Leafhopper insects as affected by different temperatures: 20 (T1), 25 (T2), 30 (T3) and 35 degrees C (T4). Experiment 2 was carried out to determine the numbers of Leafhopper insects with the use of light traps in the sugarcane Field 1 (ratoon plants), Field 2 (newly planted), Field 3 (newly planted) and Field 4 (ratoon plants). The results of Experiment 1 showed that growth and development of Leafhopper insects were highly affected by temperatures i.e. the higher the environmental temperature the faster the growth and development of the insects to reach its full adulthood. At 20 degrees C, Leafhopper insects took 12 days to lay eggs whereas at 25 degrees C the insects took only 6 days. Male reached its adulthood approximately 9 days earlier than female when cultured at 25 degrees C and became approximately one week at 30 degrees C or higher. The results of Experiment 2 showed that the majority of Leafhopper insects were found within the months of June and July for both newly planted and ratoon crops. A small amount was found in May and August with an exceptional case of Field 4 where the highest number of Leafhopper insects was found in April followed by June and July. For Sugarcane White Leaf disease, the disease was found in all months of the year except February for Fields 2 and 3. Newly planted sugarcane plants attained much smaller percentages of disease than those of the ratoon plants.

  17. Charge transfer dissociation (CTD) mass spectrometry of peptide cations using kiloelectronvolt helium cations.

    Science.gov (United States)

    Hoffmann, William D; Jackson, Glen P

    2014-11-01

    A kiloelectronvolt beam of helium ions is used to ionize and fragment precursor peptide ions starting in the 1+ charge state. The electron affinity of helium cations (24.6 eV) exceeds the ionization potential of protonated peptides and can therefore be used to abstract an electron from--or charge exchange with--the isolated precursor ions. Kiloelectronvolt energies are used, (1) to overcome the Coulombic repulsion barrier between the cationic reactants, (2) to overcome ion-defocussing effects in the ion trap, and (3) to provide additional activation energy. Charge transfer dissociation (CTD) of the [M+H](+) precursor of Substance P gives product ions such as [M+H](2+•) and a dominant series of a ions in both the 1+ and 2+ charge states. These observations, along with the less-abundant a + 1 ions, are consistent with ultraviolet photodissociation (UVPD) results of others and indicate that C-C(α) cleavages are possible through charge exchange with helium ions. Although the efficiencies and timescale of CTD are not yet suitable for on-line chromatography, this new approach to ion activation provides an additional potential tool for the interrogation of gas phase ions.

  18. THERMODYNAMICS OF ETHANOLAMMONIUM CATIONES DISSOCIATION IN AQUEOUS SOLUTIONS

    Directory of Open Access Journals (Sweden)

    R. E. Khoma

    2017-03-01

    Full Text Available The literature data on the thermodynamics of ethanolamines onium cations dissociation have been systematized and generalized. The correlation between these cations dissociation thermodynamic functions (DH and DS and physicochemical properties (Tmp., Tbp, Pp, lgPow et al. has been revealed. There was a correlation between lipophilicity determined experimentally and calculated by QSAR. For monoethanolammonium, diethanolammonium, and their N-methyl and N-ethyl derivatives it was found dissociation thermodynamic functions to depend on bases lgPow. Acid-base dissociation of TRIS and triethanolamine onium cations does not correspond to said relationship because TRIS (primary amine, TEA (tertiary amine act differently on aqueous solutions of SO2. TEA, unlike MEA, DEA and MMEA, has a salting out effect towards sulfur dioxide because of competing hydration that promotes sulfite «onium» salts hydrolysis. TRIS promotes S(IV → S(VI sulphooxidation, in contrast to another ethanolamines. Enthalpy–enthropy compensation with isothermodynamic temperature 303 K has been recorded. The revealed correlations may be useful in developing of procedures for air sanitary cleaning from acidic gases; chemisorbents immobilized for gas and ion exchange chromatography; potentiometric methods for fluorocomplex acids determinations. The use of monoethanolamine is most promising to obtain chemisorbents because the thermodynamic functions of its onium cation acid-base dissociation are least dependent on temperature compared to other etanolammonium cations.

  19. Effect of Divalent Cations on RED Performance and Cation Exchange Membrane Selection to Enhance Power Densities

    NARCIS (Netherlands)

    Rijnaarts, Timon; Huerta, Elisa; van Baak, Willem; Nijmeijer, Kitty

    2017-01-01

    Reverse electrodialysis (RED) is a membrane-based renewable energy technology that can harvest energy from salinity gradients. The anticipated feed streams are natural river and seawater, both of which contain not only monovalent ions but also divalent ions. However, RED using feed streams

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

    Science.gov (United States)

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

    2014-12-01

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

  1. The sugarcane signal transduction (SUCAST catalogue: prospecting signal transduction in sugarcane

    Directory of Open Access Journals (Sweden)

    Glaucia Mendes Souza

    2001-12-01

    Full Text Available EST sequencing has enabled the discovery of many new genes in a vast array of organisms, and the utility of this approach to the scientific community is greatly increased by the establishment of fully annotated databases. The present study aimed to identify sugarcane ESTs sequenced in the sugarcane expressed sequence tag (SUCEST project (http://sucest.lad.ic.unicamp.br that corresponded to signal transduction components. We also produced a sugarcane signal transduction (SUCAST catalogue (http://sucest.lad.ic.unicamp.br/private/mining-reports/QG/QG-mining.htm that covered the main categories and pathways. Expressed sequence tags (ESTs encoding enzymes for hormone (gibberellins, ethylene, auxins, abscisic acid and jasmonic acid biosynthetic pathways were found and tissue specificity was inferred from their relative frequency of occurrence in the different libraries. Whenever possible, transducers of hormones and plant peptide signaling were catalogued to the respective pathway. Over 100 receptors were found in sugarcane, which contains a large family of Ser/Thr kinase receptors and also photoreceptors, histidine kinase receptors and their response regulators. G-protein and small GTPases were analyzed and compared to known members of these families found in mammalian and plant systems. Major kinase and phosphatase pathways were mapped, with special attention being given to the MAP kinase and the inositol pathway, both of which are well known in plants.O sequenciamento de ESTs (etiquetas de sequencias transcritas tem possibilitado a descoberta de muitos novos genes em uma ampla variedade de organismos. Um aumento do aproveitamento desta informação pela comunidade científica tem sido possível graças ao desenvolvimento de base de dados contendo seqüências completamente anotadas. O trabalho aqui relatado teve como objetivo a identificação de ESTs de cana de açúcar seqüenciadas através do projeto SUCEST (http://sucest.lad.ic. unicamp.br que

  2. Sugarcane production under smallholder farming systems: Farmers preferred traits, constraints and genetic resources

    Directory of Open Access Journals (Sweden)

    Esayas Tena

    2016-05-01

    Full Text Available Smallholder sugarcane production sector is under researched and underdeveloped with limited industrial link and support. The objectives of this study were to assess the current state of sugarcane production, farmers’ perceived production constraints and preferred traits, and to collect germplasm grown by smallholder farmers in southern Ethiopia for strategic breeding and conservation. The study was conducted across 16 administrative zones, 28 districts and 56 peasant associations involving 560 smallholder sugarcane growers in southern Ethiopia using a participatory rural appraisal (PRA approach. Sugarcane genetic resources were collected through structured sampling. Findings from this study indicated that monocropping was identified as the predominant sugarcane farming system. Respondent farmers prioritized drought tolerance (21%, increased cane yield (20%, early maturity (18%, marketability (17%, and high biomass (14% as the top preferred traits of sugarcane. Ninety diverse sugarcane landraces were collected from homesteads of smallholder farmers. Findings from this study would serve as baseline information towards sugarcane research and development emphasising the constraints and preferences of smallholder sugarcane growers in Ethiopia or similar agro-ecologies. This is the first study to report farmers preferred traits and constraints, and genetic resources of sugarcane under smallholder farming systems in Ethiopia.

  3. Performance of growing rabbits fed graded levels of sugarcane peel ...

    African Journals Online (AJOL)

    Twenty five growing rabbits of mixed breeds and average weight of 894g were used in a seven week feeding trial. Five experimental diets were formulated in which sugarcane peels (SCP) was included at 0, 10, 20, 30 and 40% levels to replace maize offal. The rabbits were balanced for weight and allotted to the treatments ...

  4. Evaluating Brazilian sugarcane expansion effects on soil structure using VESS

    Science.gov (United States)

    Increasing global demand for biofuel has accelerated land-use change (LUC) in Brazil, primarily by replacing degraded pasture with sugarcane (Saccharum officinarum). The intensive echanization associated with this LUC has increased concerns regarding soil structural quality (SSQ). Through decades of...

  5. Establishment of in vitro callus in sugarcane (Saccharum officinarum ...

    African Journals Online (AJOL)

    Admin

    2016-07-20

    Jul 20, 2016 ... are used to produce ethanol (blended for motor fuel) and livestock feed. Bagasse (fibrous portion) is burned to provide heat and electricity for sugar mills, and green tops can be used as livestock feed (Mackintosh, 2000). It accounts for around 70% of the world's sugar (Khan et al., 2004). Sugarcane ...

  6. Determinants of Financial Sustainability of Small Holder Sugarcane ...

    African Journals Online (AJOL)

    The study investigated the impact of farming systems on determinants of smallholder sugarcane farmers (SSFs) financial sustainability (FS) between Block Farming (BF) and Traditional Farming (TF) systems. FS was analyzed by assessing profitability of the farming system. Semi structured questionnaires were administered ...

  7. Life cycle impact assssment of biobased plastics from sugarcane ethanol

    NARCIS (Netherlands)

    Tsiropoulos, Ioannis; Faaij, André; Lundquist, Lars; Schenker, Urs; Biois, J.F.; Patel, M.K.

    The increasing production of bio-based plastics calls for thorough environmental assessments. Using life cycle assessment, this study compares European supply of fully bio-based high-density polyethylene and partially bio-based polyethylene terephthalate from Brazilian and Indian sugarcane ethanol

  8. Mendel’s legacy lives through management of sugarcane pests

    Science.gov (United States)

    Entomology and classical Mendelian genetics have had a long association and Mendel’s legacy continues to live through sugarcane pests. In this paper, we discuss examples of that legacy as applied to conventional and molecular approaches to breeding for insect resistance. We also discuss the applicat...

  9. Ensuring and exploiting the genetic diversity of sugarcane

    Science.gov (United States)

    Modern sugarcane cultivars are complex interspecific hybrids primarily involving Saccharum officinarum and S. spontaneum. In the late 1800s, early breeders in Java, Indonesia recognized the value of interspecific hybridization and began to hybridize the two species, resulting in vigorous and diseas...

  10. Transcriptome analysis of Aspergillus niger grown on sugarcane bagasse

    Science.gov (United States)

    2011-01-01

    Background Considering that the costs of cellulases and hemicellulases contribute substantially to the price of bioethanol, new studies aimed at understanding and improving cellulase efficiency and productivity are of paramount importance. Aspergillus niger has been shown to produce a wide spectrum of polysaccharide hydrolytic enzymes. To understand how to improve enzymatic cocktails that can hydrolyze pretreated sugarcane bagasse, we used a genomics approach to investigate which genes and pathways are transcriptionally modulated during growth of A. niger on steam-exploded sugarcane bagasse (SEB). Results Herein we report the main cellulase- and hemicellulase-encoding genes with increased expression during growth on SEB. We also sought to determine whether the mRNA accumulation of several SEB-induced genes encoding putative transporters is induced by xylose and dependent on glucose. We identified 18 (58% of A. niger predicted cellulases) and 21 (58% of A. niger predicted hemicellulases) cellulase- and hemicellulase-encoding genes, respectively, that were highly expressed during growth on SEB. Conclusions Degradation of sugarcane bagasse requires production of many different enzymes which are regulated by the type and complexity of the available substrate. Our presently reported work opens new possibilities for understanding sugarcane biomass saccharification by A. niger hydrolases and for the construction of more efficient enzymatic cocktails for second-generation bioethanol. PMID:22008461

  11. Establishment of in vitro callus in sugarcane ( Saccharum ...

    African Journals Online (AJOL)

    Sugarcane is an important perennial, polyploidy crop. Based on the growing demand, it has now attracted great attention as cash crop. Tissue culture technique, an alternative method for solving production problem and increasing production, was used in this study. The work was carried out at the Nuclear Institute of ...

  12. Converting developing and mature sugarcane carbohydrates into ethanol

    Energy Technology Data Exchange (ETDEWEB)

    Rolz, Carlos; De Leon, Roberto [Biochemical Engineering Center, Research Institute, Universidad del Valle de Guatemala (Guatemala)

    2010-10-15

    Experiments were performed employing cane particles obtained from sugarcane at different growth stages until maturation measuring the amount of ethanol produced and the carbohydrate consumption in order to estimate the sugarcane growth stage where both parameters were optimized. Two non-flowering commercial cane varieties NA56 and PR752002 were cultivated and samples taken at different time intervals. Two Saccharomyces cerevisae strains were also compared in the trials. Sucrose was poorly consumed in young cane, which was an unexpected result. Fructose on the other hand was the hexose that remained in the medium at the end of the fermentations specially when using mature sugarcane. There was an increasing trend in ethanol production as a function of days after planting (DAP) as expected; however, a plateau was reached after 225 DAP and the maximum value obtained was between 300 and 325 DAP. When these figures were compared with the corresponding DAP used for sugar production, only 25 days less were needed in the field for maximum ethanol production. On the other hand, it was clear from the data that cane harvesting for ethanol production should not be done after the recommended DAP for commercial sugar production. If this is done, the excess fructose present will not be completely utilized by yeast. Finally, it was observed that the yeast with more affinity for sugarcane fibers showed better ethanol yields in all samples tested. (Copyright copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  13. RB962962, a sugarcane cultivar for late harvest

    Directory of Open Access Journals (Sweden)

    Luiz José Oliveira Tavares de Melo

    2014-07-01

    Full Text Available In the Northeast of Brazil, sugarcane cultivar RB962962 is harvested at the end of the cycle, between December and February, with a high sugar yield per area. Recommended for sandy soils of medium texture and fertility, it is resistant to the major diseases and fast-growing in plant and ratoon crops.

  14. Effect of various amino acids on shoot regeneration of sugarcane ...

    African Journals Online (AJOL)

    STORAGESEVER

    2009-04-06

    Apr 6, 2009 ... specific climatic requirements for flowering and seed setting coupled with longer life cycle are major ... fertile seeds (Sugarcane encyclopedia, 1994), and due to difficulties in selfing and crossing, the crop is one of ..... bioassays with tobacco tissue cultures. Physiol Plant 15: 473-479. Quatrano RS (1987).

  15. Advances in marker-assisted breeding of sugarcane

    Science.gov (United States)

    Despite the challenges posed by sugarcane, geneticists and breeders have actively sought to use DNA marker technology to enhance breeding efforts. Markers have been used to explore taxonomy, estimate genetic diversity, and to develop unique molecular fingerprints. Numerous studies have been undertak...

  16. Registration of ‘CP 08-1110’ Sugarcane

    Science.gov (United States)

    ‘CP 08-1110’ (Reg. No.CV-171; PI 678579) sugarcane (a complex hybrid of Saccharum spp.) was developed through cooperative research conducted by the USDA-ARS, the University of Florida, and the Florida Sugar Cane League, Inc. and released to growers for mineral (sand) soils in Florida in October 2014...

  17. Transcriptome analysis of Aspergillus niger grown on sugarcane bagasse

    Directory of Open Access Journals (Sweden)

    Goldman Gustavo H

    2011-10-01

    Full Text Available Abstract Background Considering that the costs of cellulases and hemicellulases contribute substantially to the price of bioethanol, new studies aimed at understanding and improving cellulase efficiency and productivity are of paramount importance. Aspergillus niger has been shown to produce a wide spectrum of polysaccharide hydrolytic enzymes. To understand how to improve enzymatic cocktails that can hydrolyze pretreated sugarcane bagasse, we used a genomics approach to investigate which genes and pathways are transcriptionally modulated during growth of A. niger on steam-exploded sugarcane bagasse (SEB. Results Herein we report the main cellulase- and hemicellulase-encoding genes with increased expression during growth on SEB. We also sought to determine whether the mRNA accumulation of several SEB-induced genes encoding putative transporters is induced by xylose and dependent on glucose. We identified 18 (58% of A. niger predicted cellulases and 21 (58% of A. niger predicted hemicellulases cellulase- and hemicellulase-encoding genes, respectively, that were highly expressed during growth on SEB. Conclusions Degradation of sugarcane bagasse requires production of many different enzymes which are regulated by the type and complexity of the available substrate. Our presently reported work opens new possibilities for understanding sugarcane biomass saccharification by A. niger hydrolases and for the construction of more efficient enzymatic cocktails for second-generation bioethanol.

  18. Ensilage Of Sugarcane Tops Using Urea And Broiler Litter Additives ...

    African Journals Online (AJOL)

    Sugarcane tops (SCT) constitute a source of readily available and cheap agroindustrial by-product for ruminant feeding in Mauritius. Its nutritional constraints are its low digestibility, and low crude protein (CP) content. Wilted SCT (50% DM) was ensiled in the laboratory using a SemiMicro technique with PVC silos.

  19. Registration of ‘CP 04-1844’ Sugarcane

    Science.gov (United States)

    ‘CP 04-1844’ sugarcane (a complex hybrid of Saccharum spp.) was developed through cooperative research conducted by the USDA-ARS, the University of Florida, and the Florida Sugar Cane League, Inc., and was released to growers in Florida on 20 Sept. 2011. CP 04-1844 was selected from the cross X01-03...

  20. Preliminary Evaluation of Some Qualitative Traits of Sugarcane ...

    African Journals Online (AJOL)

    Thirty five local sugarcane (Saccharum spp.) accessions were collected in an expedition in North-Western Nigeria, covering Sokoto, Kebbi, Zamfara, Katsina, Kaduna, Kano and Jigawa States in September 2011. The germplasm accessions were maintained at Usmanu Danfodiyo University Sokoto. Data on leaf colour, leaf ...

  1. Reproducible in vitro regeneration system for purifying sugarcane ...

    African Journals Online (AJOL)

    Genome purification of a selected clone of sugarcane is the key to developing homogenous lines. Generally, regenerated plants after transformation are heterogeneous at genome level, and several successive rounds of selection on antibiotic-containing medium and regeneration cycles are required to purify the genome to ...

  2. Assessment of genetic diversity among sugarcane cultivars using ...

    African Journals Online (AJOL)

    Genetic diversity based on the characterization of genetic makeup, using molecular markers is of utmost importance for breeders in crop improvement programme. A total of 26 microsatellite primers were used to determine the genetic diversity among 40 sugarcane genotypes including their parents. The polymerase chain ...

  3. Estimate of ratooning ability in sugarcane (saccharum officinarum L ...

    African Journals Online (AJOL)

    Ratooning ability (RA) is an important criterion in determining varietal suitability for commercial sugarcane cultivation because of the necessity to spread the costs of planting operations over subsequent ratoon crops. Two estimates of RA were computed with the objective to identify a more suitable approach for estimating ...

  4. Nutrient contents of Soyabeans: A Guide for sugarcane growers ...

    African Journals Online (AJOL)

    This research was conducted on sandy clay loams of the lithosol group under the Zimbabwe soil classification system at The Zimbabwe Sugar Association Experiment Station (Z.S.A.E.S) in the South Eastern Lowveld, the leading sugarcane producing region in Zimbabwe. The objectives of this research were to: 1) analyse ...

  5. Sugarcane aphid spatial distribution in grain sorghum fields

    Science.gov (United States)

    Sorghum is an important summer grain crop in the United States. In 2014, the U.S. produced 432 million bushels of sorghum valued at $1.67 billion on more than 6 million acres. The sugarcane aphid, Melanaphis sacchari (Zehntner), was discovered in damaging numbers in grain sorghum, Sorghum bicolor ...

  6. Sugarcane in vitro culture technology: Opportunities for Kenya's ...

    African Journals Online (AJOL)

    Sugarcane (Saccharum officinarum L.) is one of the most important crops in Kenya and has wide range of economic importance. The sugar industry contributes up to 15% to the country's agricultural gross domestic product and an estimated 25% of the population depends on the industry for their livelihood. However, the ...

  7. Productivity of sugarcane plants of ratooning with fertilizing treatment

    Directory of Open Access Journals (Sweden)

    MUHADIONO

    2010-01-01

    Full Text Available Latief AS, Syarief R, Pramudya B, Muhadiono. 2010. Productivity of sugarcane plants of ratooning with various fertilizing treatments. Nusantara Bioscience 2: 43-47. This research aims to determine the sugarcane plants of ratooning productivity with low external input of fertilization treatment towards farmers can increase profits. The method used is the Completely Randomized Block Design (CRBD with four treatments and three repetitions (4x3. Sugarcane varieties R 579 planted in each patch experiment 5x5 m2. Dosage of fertilizer: P0 = 3.6 kg/year plot experiment was 100% dosage usage of chemical fertilizers used by farmers. Further dosages were P1 (75% = 2.7 kg/plot, P2 (50% = 1.8 kg/plot and P3 (0.25% = 0.9 kg/plot, each supplemented with fertilizer 5 mL of liquid organic/patch a year. Sugarcane crops with a variety of treatment showed no significant difference. The highest productivity was achieved at dosages of P2 (50% chemical fertilizers plus organic fertilizer is 21.67 kg per square meter. Chemical fertilizers can be saved 7 quintals per hectare a year or Rp 997,500 per year. Additional costs of liquid organic fertilizer Rp. 100,000 per hectare year and labor Rp 100,000 per hectare, so the additional advantage of saving farmers fertilizer Rp. 797,500 per year.

  8. pesticide residues in water from tpc sugarcane plantations and ...

    African Journals Online (AJOL)

    ABSTRACT. We report herein, the analysis of water samples collected from TPC Sugarcane Plantation and its environs in Kilimanjaro region, which is the earliest intensive user of pesticides in Tanzania. A total of 50 water samples collected from 18 sampling sites between 2000 and 2001 were analyzed for pesticide ...

  9. RNAseq Transcriptional Profiling following Whip Development in Sugarcane Smut Disease.

    Science.gov (United States)

    Schaker, Patricia D C; Palhares, Alessandra C; Taniguti, Lucas M; Peters, Leila P; Creste, Silvana; Aitken, Karen S; Van Sluys, Marie-Anne; Kitajima, João P; Vieira, Maria L C; Monteiro-Vitorello, Claudia B

    2016-01-01

    Sugarcane smut disease is caused by the biotrophic fungus Sporisorium scitamineum. The disease is characterized by the development of a whip-like structure from the primary meristems, where billions of teliospores are produced. Sugarcane smut also causes tillering and low sucrose and high fiber contents, reducing cane productivity. We investigated the biological events contributing to disease symptoms in a smut intermediate-resistant sugarcane genotype by examining the transcriptional profiles (RNAseq) shortly after inoculating the plants and immediately after whip emission. The overall picture of disease progression suggests that premature transcriptional reprogramming of the shoot meristem functions continues until the emergence of the whip. The guidance of this altered pattern is potentially primarily related to auxin mobilization in addition to the involvement of other hormonal imbalances. The consequences associated with whip emission are the modulation of typical meristematic functions toward reproductive organ differentiation, requiring strong changes in carbon partitioning and energy production. These changes include the overexpression of genes coding for invertases and trehalose-6P synthase, as well as other enzymes from key metabolic pathways, such as from lignin biosynthesis. This is the first report describing changes in the transcriptional profiles following whip development, providing a hypothetical model and candidate genes to further study sugarcane smut disease progression.

  10. RNAseq Transcriptional Profiling following Whip Development in Sugarcane Smut Disease

    Science.gov (United States)

    Taniguti, Lucas M.; Peters, Leila P.; Creste, Silvana; Aitken, Karen S.; Van Sluys, Marie-Anne; Kitajima, João P.; Vieira, Maria L. C.; Monteiro-Vitorello, Claudia B.

    2016-01-01

    Sugarcane smut disease is caused by the biotrophic fungus Sporisorium scitamineum. The disease is characterized by the development of a whip-like structure from the primary meristems, where billions of teliospores are produced. Sugarcane smut also causes tillering and low sucrose and high fiber contents, reducing cane productivity. We investigated the biological events contributing to disease symptoms in a smut intermediate-resistant sugarcane genotype by examining the transcriptional profiles (RNAseq) shortly after inoculating the plants and immediately after whip emission. The overall picture of disease progression suggests that premature transcriptional reprogramming of the shoot meristem functions continues until the emergence of the whip. The guidance of this altered pattern is potentially primarily related to auxin mobilization in addition to the involvement of other hormonal imbalances. The consequences associated with whip emission are the modulation of typical meristematic functions toward reproductive organ differentiation, requiring strong changes in carbon partitioning and energy production. These changes include the overexpression of genes coding for invertases and trehalose-6P synthase, as well as other enzymes from key metabolic pathways, such as from lignin biosynthesis. This is the first report describing changes in the transcriptional profiles following whip development, providing a hypothetical model and candidate genes to further study sugarcane smut disease progression. PMID:27583836

  11. Reproducible in vitro regeneration system for purifying sugarcane ...

    African Journals Online (AJOL)

    Tansgenic Lab

    2012-05-24

    May 24, 2012 ... 1970s, genetic manipulation of sugarcane had been attempted for the .... After 5 days of incubation on callus induction media, calli were sub- cultured onto IP, IPC1 ... Graph showing comparison of % age frequency of callus induction on three different media, and the first three basal segments. A, Explant ...

  12. Segregation analysis of microsatellite (SSR) markers in sugarcane polyploids

    Science.gov (United States)

    Although the microsatellite (SSR) DNA markers have been extensively used in sugarcane breeding research, little is known about its inheritance mechanism. To address this problem, a high throughput molecular genotyping experiment was conducted on 964 single pollen grains and a 288-self progeny S1 map...

  13. Protocol optimization for in vitro mass propagation of two sugarcane ...

    African Journals Online (AJOL)

    SAM

    2014-03-19

    Mar 19, 2014 ... The present study was initiated to optimize in vitro protocol for mass propagation of two commercial sugarcane clones (Co 449 and Co 678) grown in Ethiopia through shoot tip culture. Experiments on shoot multiplication and rooting were laid out in a completely randomized design with factorial treatment ...

  14. Yield potential of non-irrigated sugarcane germplasm accessions in ...

    African Journals Online (AJOL)

    ... strict upland condition. Data obtained from a replicated field trial involving 30 exotic and 18 local sugarcane germplasm collections at the University of Ilorin Sugar Research Institute (USRI), were used to assess their yielding potential under non- irrigated condition. The objective was to determine their suitability as parents ...

  15. Sugarcane straw and the populations of pests and nematodes

    Directory of Open Access Journals (Sweden)

    Leila Luci Dinardo-Miranda

    2013-10-01

    Full Text Available The green cane harvesting represented a significant change in sugarcane ecosystem due to the presence of straw left on the soil and to the absence of fire. These two factors may affect the populations of pests and their natural enemies. Among the pests benefit from the green cane harvesting stand out the spittlebug, Mahanarva fimbriolata, the curculionid Sphenophorus levis and sugarcane borer, Diatraea saccharalis. In areas of green cane harvesting, the population of these species grew faster than in areas of burnt cane. On the other hand, there are virtually no records of attacks by lesser cornstalk borers in areas of green cane harvesting. Populations of plant parasitic nematodes and the beetles Migdolus fryanus, very important pests of sugarcane, were apparently not affected by the green cane harvesting. Despite the absence of more consistent information, it appears that populations of ants and the giant borer Telchin licus can increase in green cane areas, due primarily to the difficulty of pest control. The partial or total removal of straw from the field represents an additional change to the ecosystem that could alter the status of pests and nematodes. It is likely that spittlebug, the curculionid S. levis and sugarcane borer populations decrease if a portion of the straw is removed from the field. However, the pest populations in areas where the straw is collected will not return to their original conditions at the time of burnt cane harvesting because the absence of fire will be maintained.

  16. Moringa extracts used in sugarcane juice treatment and effects on ...

    African Journals Online (AJOL)

    The objective of this study was to evaluate the effects of sugarcane juice treatment using Moringa oleifera leaf and seeds extracts on ethanolic fermentation. The experiment was arranged in a split plot statistical design, with four replications. Main treatments were three sedimentation agents (synthetic polyelectrolyte, ...

  17. Protocol optimization for in vitro mass propagation of two sugarcane ...

    African Journals Online (AJOL)

    The present study was initiated to optimize in vitro protocol for mass propagation of two commercial sugarcane clones (Co 449 and Co 678) grown in Ethiopia through shoot tip culture. Experiments on shoot multiplication and rooting were laid out in a completely randomized design with factorial treatment arrangements.

  18. RNAseq Transcriptional Profiling following Whip Development in Sugarcane Smut Disease.

    Directory of Open Access Journals (Sweden)

    Patricia D C Schaker

    Full Text Available Sugarcane smut disease is caused by the biotrophic fungus Sporisorium scitamineum. The disease is characterized by the development of a whip-like structure from the primary meristems, where billions of teliospores are produced. Sugarcane smut also causes tillering and low sucrose and high fiber contents, reducing cane productivity. We investigated the biological events contributing to disease symptoms in a smut intermediate-resistant sugarcane genotype by examining the transcriptional profiles (RNAseq shortly after inoculating the plants and immediately after whip emission. The overall picture of disease progression suggests that premature transcriptional reprogramming of the shoot meristem functions continues until the emergence of the whip. The guidance of this altered pattern is potentially primarily related to auxin mobilization in addition to the involvement of other hormonal imbalances. The consequences associated with whip emission are the modulation of typical meristematic functions toward reproductive organ differentiation, requiring strong changes in carbon partitioning and energy production. These changes include the overexpression of genes coding for invertases and trehalose-6P synthase, as well as other enzymes from key metabolic pathways, such as from lignin biosynthesis. This is the first report describing changes in the transcriptional profiles following whip development, providing a hypothetical model and candidate genes to further study sugarcane smut disease progression.

  19. Identification, phylogeny, and transcript of chitinase family genes in sugarcane.

    Science.gov (United States)

    Su, Yachun; Xu, Liping; Wang, Shanshan; Wang, Zhuqing; Yang, Yuting; Chen, Yun; Que, Youxiong

    2015-06-02

    Chitinases are pathogensis-related proteins, which play an important role in plant defense mechanisms. The role of the sugarcane chitinase family genes remains unclear due to the highly heterozygous and aneuploidy chromosome genetic background of sugarcane. Ten differentially expressed chitinase genes (belonging to class I~VII) were obtained from RNA-seq analysis of both incompatible and compatible sugarcane genotypes during Sporisorium scitamineum challenge. Their structural properties and expression patterns were analyzed. Seven chitinases (ScChiI1, ScChiI2, ScChiI3, ScChiIII1, ScChiIII2, ScChiIV1 and ScChiVI1) showed more positive with early response and maintained increased transcripts in the incompatible interaction than those in the compatible one. Three (ScChiII1, ScChiV1 and ScChiVII1) seemed to have no significant difference in expression patterns between incompatible and compatible interactions. The ten chitinases were expressed differentially in response to hormone treatment as well as having distinct tissue specificity. ScChiI1, ScChiIV1 and ScChiVII1 were induced by various abiotic stresses (NaCl, CuCl2, PEG and 4 °C) and their involvement in plant immunity was demonstrated by over-expression in Nicotiana benthamiana. The results suggest that sugarcane chitinase family exhibit differential responses to biotic and abiotic stress, providing new insights into their function.

  20. Efficacy of selected herbicide formulations on sugarcane field weeds ...

    African Journals Online (AJOL)

    Terbuthylazine 500 SC and 90 WG were applied as pre-emergence herbicides while dicamba 480 SL and dicamba 70 SG as post emergence herbicides. The result shows that application of the above formulations did not significantly affect the emergence of sugarcane. The efficacy of pre-emergence application decreases ...