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Ion Exchange (ion + exchange)
Terms modified by Ion Exchange Selected AbstractsHighly Stable Nickel Hexacyanoferrate Nanotubes for Electrically Switched Ion Exchange,ADVANCED FUNCTIONAL MATERIALS, Issue 15 2007W. Chen Abstract Nickel hexacyanoferrate (NiHCF) nanotubes are fabricated by an electrokinetic method based on the distinct surface properties of porous anodic alumina. By this method, nanotubes can be formed rapidly with the morphologies faithfully replicating the nanopores in the template. The prepared nanotubes were carefully characterized using SEM and TEM. Results from IR, UV, EDX, and electrochemical measurements show that the NiHCF nanotubes exist only in the form of K2Ni[Fe(CN)6]. Because of this single composition and unique nanostructure, NiHCF nanotubes show excellently stable cesium-selective ion-exchange ability. The capacity for electrodes modified with NiHCF nanotubes after 500,potential cycles retains 95.3,% of its initial value. Even after 1500 and 3000 cycles, the NiHCF nanotubes still retain 92.2,% and 82.9,%, respectively, of their ion-exchange capacity. [source] Cs+ -Selective Ion Exchange and Magnetic Ordering in a Three-Dimensional Framework Uranyl Vanadium(IV) Phosphate.CHEMINFORM, Issue 16 2007Tatiana Y. Shvareva Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source] Significance of processes in the near-stream zone on stream water acidity in a small acidified forested catchmentHYDROLOGICAL PROCESSES, Issue 2 2001Jens Fölster Abstract The near-stream zone has received increasing attention owing to its influence on stream water chemistry in general and acidity in particular. Possible processes in this zone include cation exchange, leaching of organic matter and redox reactions of sulphur compounds. In this study the influences of processes in the near-stream zone on the acidity in runoff from a small, acidified catchment in central southern Sweden were investigated. The study included sampling of groundwater, soil water and stream water along with hydrological measurements. An input,output budget for the catchment was established based on data from the International Co-operative Programme on Integrated Monitoring at this site. The catchment was heavily acidified by deposition of anthropogenic sulphur, with pH in stream water between 4·4 and 4·6. There was also no relationship between stream flow and pH, which is indicative of chronic acidification. Indications of microbial reduction of sulphate were found in some places near the stream, but the near-stream zone did not have a general impact on the sulphate concentration in discharging groundwater. The near-stream zone was a source of dissolved organic carbon (DOC) in the stream, which had a median DOC of 6·8 mg L1. The influence on stream acidity from organic anions was overshadowed by the effect of sulphate, however, except during a spring flow episode, when additional organic matter was flushed out and the sulphate-rich ground water was mixed with more diluted event water. Ion exchange was not an important process in the near-stream zone of the Kindla catchment. Different functions of the near-stream zone relating to discharge acidity are reported in the literature. In this study there was even a variation within the site. There is therefore a need for more case studies to provide a more detailed understanding of the net effects that the near-stream zone can have on stream chemistry under different circumstances. Copyright © 2001 John Wiley & Sons, Ltd. [source] Highly selective single nucleotide polymorphism recogniton by a chiral (5S) PNA beacon,CHIRALITY, Issue 1 2009Filbert Totsingan Abstract A chiral peptide nucleic acid (PNA) beacon containing a C-5 modified monomer based on L-lysine was synthesized. The terminal amino group of the lysine side chain was linked to a spacer for future applications on surfaces. The PNA beacon bears a carboxyfluorescein fluorophore and a dabcyl quencher at opposite ends. The DNA binding properties were compared with those of a homologous PNA beacon containing only achiral monomers. Both beacons underwent a fluorescence increase in the presence of complementary DNA, with higher efficiency and higher selectivity (evaluated using single mismatched DNA sequences) observed for the chiral monomer containing PNA. Ion exchange (IE) HPLC with fluorimetric detection was used in combination with the beacon for the selective detection of complementary DNA. A fluorescent peak corresponding to the PNA beacon:DNA duplex was observed at a very low detection limit (1 nM). The discriminating capacity of the chiral PNA beacon for a single mismatch was found to be superior to those observed with the unmodified one, thus confirming the potency of chirality for increasing the affinity and specificity of DNA recognition. Chirality, 2009. © 2008 Wiley-Liss, Inc. [source] Electroanalytical Applications of Microporous Zeolites and Mesoporous (Organo)Silicas: Recent TrendsELECTROANALYSIS, Issue 7 2008Alain WalcariusArticle first published online: 10 MAR 200 Abstract Microporous zeolites and ordered mesoporous (organo)silicas have been widely used as electrode modifiers because of their attractive properties (ion exchange and size selectivity of zeolites, well ordered nanoreactors containing a high number of widely accessible active centers in mesoporous (organo)silicas). These properties have been intelligently combined to selected redox processes to improve the response of the resulting modified electrodes or to design novel electrochemical detection schemes. This up-to-date review provides the recent advances made in the electroanalytical applications of zeolite modified electrodes and discusses the interest of ordered mesoporous (organo)silica materials in electroanalysis. [source] Electrochemical Investigation of Binding of Heavy Metal Ions to Turkish LignitesELECTROANALYSIS, Issue 16 2004Erol Pehlivan Abstract Adsorption and desorption of Cu2+, Pb2+, Cd2+, Ni2+ and Zn2+ ions on samples of lignites (young brown coal) from three areas in the vicinity of Konya (Anatolia, Turkey) were followed using the polarographic method of analysis. This method enables the determination of free metal ions in suspensions containing both small and colloidal particles of lignite. Effects of pH, nature of the metal ion, and origin of the lignite on its adsorption capacity were followed. Binding is only between 5 and 30% reversible, indicating that ion exchange is not the predominant factor. The role of the size and shape of cavities inside pulverized lignite and of the functional groups inside these cavities was considered. [source] Amperometric Ion Sensing Using Polypyrrole MembranesELECTROANALYSIS, Issue 5-6 2003Agata Michalska Abstract Oxidation/reduction of conducting polymers, coupled with ion exchange between the polymer and electrolyte solution can be utilized for amperometric ion sensing. Electrochemically deposited "model" polypyrrole membranes doped by chloride (PPyCl) and hexacyanoferrate (PPyFeCN) anions were studied from the point of view of their advantages and limits for amperometric determination of electroinactive anions and cations, respectively. Monotonous dependences of the current on electrolyte concentration were obtained for short reading times after potential step application (in the range of ms). The experimental conditions were optimized to obtain linear dependences: log (current) vs. log (KCl concentration) within the range 10,6,1,M. The advantages of the amperometric method over the potentiometric one are highlighted: much lower effect of redox and pH interferences, wider concentration range, elimination of long conditioning procedure. [source] Mercury speciation by CE: An updateELECTROPHORESIS, Issue 1 2009Petr Kubán Abstract This review provides an update on mercury speciation by CE. It includes a brief discussion on physicochemical properties, toxicity and transformation pathways of mercury species (i.e. methyl-, ethyl-, phenyl- and inorganic mercury) and outlines recent trends in Hg speciation by CE. CE is presented as a complementary technique to chromatographic separation techniques, especially in cases when speed, high efficiency and low sample volumes are required. The development of suitable sample preconcentration/isolation (sample stacking, ion exchange, liquid,liquid,liquid extraction, dual-cloud point extraction) to achieve low LODs for analysis of trace concentrations of mercury species in real samples is emphasized. Hyphenation of CE to element specific detectors (i.e. electrothermal atomic absorption spectrometry, atomic fluorescence spectrometry, inductively coupled plasma-optical emission spectrometry, inductively coupled plasma-mass spectrometry) is discussed as well as a potential of CE in interaction studies that may provide useful information on interaction of various Hg species with selected bio-macromolecules. [source] Optimization of an Iron Intercalated Montmorillonite Preparation for the Removal of Arsenic at Low Concentrations,ENGINEERING IN LIFE SCIENCES (ELECTRONIC), Issue 1 2007D. Masih Abstract A series of iron intercalated montmorillonites (Fe-Monts) were prepared using (i) ion exchange of native sodium and calcium ions with iron ions, (ii) base hydrolysis of inserted iron ions in montmorillonite suspension, and (iii) insertion of pre-hydrolyzed iron colloid in montmorillonite. The materials were characterized by X-ray diffraction and gas adsorption-desorption techniques. The basal d(001)-spacing and BET specific surface area increased after the intercalation of iron species in montmorillonite. Local iron structure studied by X-ray absorption fine structure (XAFS) spectroscopy showed an unsaturation of the Fe···Fe coordination number (N 2.5) of the intercalated iron species as compared to the bulk iron oxyhydroxides (N 6). The Fe-Monts were employed for arsenic removal from aqueous solutions at low concentration (0.2,16 mg/L). Among the Fe-Monts, the one prepared by the hydrolysis of inserted iron ions, was the best in performance. The saturation adsorption amount of the optimized iron-montmorillonite was 4 and 28 times higher for the removal of arsenite and arsenate, respectively, as compared to bulk iron oxyhydroxide (goethite). Compared with bulk iron oxyhydroxide, the Fe-Monts were superior for arsenate uptake and comparable for arsenite. In addition, arsenite adsorbed on the Fe-Monts was found to be oxidized to arsenate based on XAFS spectroscopy. [source] Retinol binding protein isolated from acute renal failure patients inhibits polymorphonuclear leucocyte functionsEUROPEAN JOURNAL OF CLINICAL INVESTIGATION, Issue 11 2004G. Cohen Abstract Background, Protein factors accumulating in sera of patients with end-stage renal disease (ESRD) that interfere with the nonspecific immune response by inhibiting essential functions of polymorphonuclear leucocytes (PMNLs) have previously been described. No such factor has been isolated from acute renal failure (ARF) patients to date. Materials and methods, Using a three-step chromatographic procedure involving ion exchange, size exclusion and hydrophobic interaction chromatography we purified the apo- and holo-form of retinol binding protein (RBP) from high-flux dialyser (polyacrylonitrile; AN69) ultrafiltrates of patients with ARF. Their effect on the chemotaxis of PMNLs isolated from healthy donors was determined by the under-agarose method. Whole-blood assays applying flow cytometry were used to assess phagocytosis and the oxidative metabolism of PMNLs. Apoptosis was assessed by determining the DNA content using propidium iodide. Results, Isolated apo- and holo-forms of RBP were truncated on their C-terminus as determined by mass spectrometry. All isolates significantly inhibited the chemotactic movement of PMNLs obtained from healthy donors and the PMNL oxidative metabolism stimulated by E. coli. These effects were concentration dependent. Retinol binding protein had no influence on the PMNL oxidative metabolism stimulated by PMA and on PMNL phagocytosis. Commercially available RBP isolated from urine influenced PMNL functions in the same way. Inhibition of p38 mitogen-activated protein kinase (MAPK) by SB203580 significantly attenuated the phagocytosis-induced respiratory burst and RBP did not lead to a further decrease. Polymorphonuclear leucocyte apoptosis was significantly inhibited by RBP. Conclusions, The apo- and holo-forms of RBP isolated from the ultrafiltrate of ARF patients inhibit PMNL chemotaxis, oxidative metabolism and apoptosis. Therefore, RBP may be considered a uraemic toxin contributing to a disturbed immune defence. [source] Luminescent Polyoxotungstoeuropate Anion-Pillared Layered Double HydroxidesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 4 2006Filipa L. Sousa Abstract Novel luminescent polyoxometalate anion-pillared layered double hydroxides (LDHs) were prepared by aqueous ion exchange of a Zn,Al LDH precursor in nitrate form with the europium-containing polyoxotungstate anions [EuW10O36]9,, [Eu(BW11O39)(H2O)3]6, and [Eu(PW11O39)2]11,. The host,guest interaction has a strong influence on the nature of the final intercalated species, as evidenced by elemental analysis, powder X-ray diffraction (XRD), infra-red (IR) and Raman spectroscopy, solid state magic-angle spinning (MAS) 11B and 31P NMR spectroscopy, and photoluminescence spectroscopy. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source] Deprotonation of Indole Derivatives in Aqueous Cationic SurfactantsEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 5 2004Nicoletta Spreti Abstract Deprotonations of 5-nitroindole, 1a, and its 2-carboxylate ion, 2a, have been monitored in 0.01, 0.1, and 0.5 M NaOH in micellar solutions of cetyl trialkylammonium bromide, alkyl = Me, Et, nPr, nBu, CTABr, CTEABr, CTPABr, CTBABr. Extents of deprotonation (% f) have been fitted using the pseudophase model of micellar effects with interionic competition described by ion exchange or by independent association constants. Both treatments indicate that base dissociation constants in dilute OH, are lower than in water by factors of ca. 3,11, and decrease with increasing bulk of the head groups, and that these factors increase modestly as the OH, concentration increases to 0.5 M. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) [source] Stresses in ion-exchange layers of soda-lime-silicate glassFATIGUE & FRACTURE OF ENGINEERING MATERIALS AND STRUCTURES, Issue 6 2005T. FETT ABSTRACT This paper presents a new method to determine both the magnitude and the sign of the surface stresses that develop as a consequence of sodium/hydrogen ion exchange in soda-lime-silicate glass immersed in water. At 90 °C, very thin layers that develop at the surfaces of polished glass specimens are found to have extremely high compressive stresses, ,2.4 GPa. The negative sign of the stress is consistent with earlier findings that the ion-exchange process involves hydronium ions (H3O+) and not bare protons (H+). [source] A flammability performance comparison between synthetic and natural clays in polystyrene nanocompositesFIRE AND MATERIALS, Issue 4 2005Alexander B. Morgan Abstract Polymer-clay nanocomposites are a newer class of flame retardant materials of interest due to their balance of mechanical, thermal and flammability properties. Much more work has been done with natural clays than with synthetic clays for nanocomposite flammability applications. There are advantages and disadvantages to both natural and synthetic clay use in a nanocomposite, and some of these, both fundamental and practical, will be discussed in this paper. To compare natural and synthetic clays in regards to polymer flammability, two clays were used. The natural clay was a US mined and refined montmorillonite, while the synthetic clay was a fluorinated synthetic mica. These two clays were used as inorganic clays for control experiments in polystyrene, and then converted into an organoclay by ion exchange with an alkyl ammonium salt. The organoclays were used to synthesize polystyrene nanocomposites by melt compounding. Each of the formulations was analysed by X-ray diffraction (XRD), thermogravimetric analysis (TGA) and transmission electron microscopy (TEM). Flammability performance was measured by cone calorimeter. The data from the experiments show that the synthetic clay does slightly better at reducing the heat release rate (HRR) than the natural clay. However, all the samples, including the inorganic clay polystyrene microcomposites, showed a decreased time to ignition, with the actual nanocomposites showing the most marked decrease. The reason for this is postulated to be related to the thermal instability of the organoclay (via the quaternary alkyl ammonium). An additional experiment using a more thermally stable organoclay showed a time to ignition identical to that of the base polymer. Finally, it was shown that while polymer-clay nanocomposites (either synthetic or natural clay based) greatly reduce the HRR of a material, making it more fire safe, they do not provide ignition resistance by themselves, at least, at practical loadings. Specifically, the cone calorimeter HRR curve data appear to support that these nanocomposites continue to burn once ignited, rather than self-extinguish. Copyright © 2004 John Wiley & Sons, Ltd. [source] Magnetic Multi-Functional Nano Composites for Environmental ApplicationsADVANCED FUNCTIONAL MATERIALS, Issue 8 2009Jie Dong Abstract A novel concept is proposed to synthesize a new class of composites featuring magnetic, molecular sieve and metallic nanoparticle properties. These multi-functional materials have potential applications as recyclable catalysts, disinfectants and sorbents. The magnetic property enables effective separation of the spent composites from complex multiphase systems for regeneration and recycle, safe disposal of the waste and/or recovery of loaded valuable species. The zeolite molecular sieve provides a matrix which supports a remarkably new, simple, efficient and economical method to make stable, supported silver nanoparticles by silver ion exchange and controlled thermal reduction. The silver nanoparticles generated in this way have excellent properties such as high reactivity and good thermal stability without aggregation, which act as nano reactors for desired functionality in a wide range of applications. Magnetic component (Fe3O4), molecular sieve matrix (zeolite) and silver nanoparticles generated by ion exchange followed by controlled reduction, together form this unique novel composite with designed functions. It represents a practically operational, economical, sustainable and environmentally friendly new advanced functional material. This paper focuses on the novel synthesis and characterization of the composite, with an example of applications as sorbents for the removal of vapor-phase mercury from the flue gas of coal-fired power plants. [source] Self-Organized Single-Walled Carbon Nanotube Conducting Thin Films with Honeycomb Structures on Flexible Plastic FilmsADVANCED FUNCTIONAL MATERIALS, Issue 2 2009Nobuo Wakamatsu Abstract Complex 1, synthesized from anionic shortened single-walled carbon nanotubes and cationic ammonium lipid dissolved in organic solvents, is cast on pretreated transparent flexible poly(ethylene terephthalate) (PET) films under a higher relative humidity to form thin films with self-organized honeycomb structures. The cell sizes are controllable by changing the experimental conditions. The lipid, which is the cationic part of complex 1, is easily removed by a simple ion-exchange method, while maintaining the basic honeycomb structures. After the ion exchange, the nanotube honeycomb films on PET with thinner skeletons exhibit a dramatic decrease in the surface resistivity from insulating to conducting. Carbon nanotubes with honeycomb structures formed by the self-organization on flexible polymer films are useful in many areas of nanoscience and technology including nanomaterials, nanoelectronics, nanodevices, catalysts, sensors, and so on. [source] Radon (222Rn) in Ground Water of Fractured Rocks: A Diffusion/Ion Exchange ModelGROUND WATER, Issue 4 2004Warren W. Wood Ground waters from fractured igneous and high-grade sialic metamorphic rocks frequently have elevated activity of dissolved radon (222Rn). A chemically based model is proposed whereby radium (226Ra) from the decay of uranium (238U) diffuses through the primary porosity of the rock to the water-transmitting fracture where it is sorbed on weathering products. Sorption of 226Ra on the fracture surface maintains an activity gradient in the rock matrix, ensuring a continuous supply of 226Ra to fracture surfaces. As a result of the relatively long half-life of 226Ra (1601 years), significant activity can accumulate on fracture surfaces. The proximity of this sorbed 226Ra to the active ground water flow system allows its decay progeny 222Rn to enter directly into the water. Laboratory analyses of primary porosity and diffusion coefficients of the rock matrix, radon emanation, and ion exchange at fracture surfaces are consistent with the requirements of a diffusion/ion-exchange model. A dipole-brine injection/withdrawal experiment conducted between bedrock boreholes in the high-grade metamorphic and granite rocks at the Hubbard Brook Experimental Forest, Grafton County, New Hampshire, United States (42°56,N, 71°43,W) shows a large activity of 226Ra exchanged from fracture surfaces by a magnesium brine. The 226Ra activity removed by the exchange process is 34 times greater than that of 238U activity. These observations are consistent with the diffusion/ion-exchange model. Elutriate isotopic ratios of 223Ra/226Ra and 238U/226Ra are also consistent with the proposed chemically based diffusion/ion-exchange model. [source] MODFLOW/MT3DMS-Based Reactive Multicomponent Transport ModelingGROUND WATER, Issue 2 2003H. Prommer This paper presents a three-dimensional, MODFLOW/MT3DMS-based reactive multicomponent transport model for saturated porous media. Based on a split-operator technique, the model, referred to as PHT3D, couples the transport simulator MT3DMS and the geochemical modeling code PHREEQC-2. Through the flexible, generic nature of PHREEQC-2, PHT3D can handle a broad range of equilibrium and kinetically controlled reactive processes, including aqueous complexation, mineral precipitation/dissolution, and ion exchange. The diversity of potential applications is demonstrated through simulation of five existing literature benchmarks and a new three-dimensional sample problem. The model might be applied to simulate the geochemical evolution of pristine and contaminated aquifers as well as their cleanup. The latter problem class includes the natural and enhanced attenuation/remediation schemes of a wide range of organic and inorganic contaminants. Processes/reactions not included in the standard PHREEQC-2 database but typical for this type of application (e.g., NAPL dissolution, microbial growth/decay) can be defined and included via the extensible PHREEQC-2 database file. [source] Paleosols in Central Illinois as Potential Sources of Ammonium in GroundwaterGROUND WATER MONITORING & REMEDIATION, Issue 4 2009Justin J. G. Glessner Glacially buried paleosols of pre-Holocene age were evaluated as potential sources for anomalously large concentrations of ammonium in groundwater in East Central Illinois. Ammonium has been detected at concentrations that are problematic to water treatment facilities (greater than 2.0 mg/L) in this region. Paleosols characterized for this study were of Quaternary age, specifically Robein Silt samples. Paleosol samples displayed significant capacity to both store and release ammonium through experiments measuring processes of sorption, ion exchange, and weathering. Bacteria and fungi within paleosols may significantly facilitate the leaching of ammonium into groundwater by the processes of assimilation and mineralization. Bacterial genetic material (DNA) was successfully extracted from the Robein Silt, purified, and amplified by polymerase chain reaction to produce 16S rRNA terminal restriction fragment length polymorphism (TRFLP) community analyses. The Robein Silt was found to have established diverse and viable bacterial communities. 16S rRNA TRFLP comparisons to well-known bacterial species yielded possible matches with facultative chemolithotrophs, cellulose consumers, nitrate reducers, and actinomycetes. It was concluded that the Robein Silt is both a source and reservoir for groundwater ammonium. Therefore, the occurrence of relatively large concentrations of ammonium in groundwater monitoring data may not necessarily be an indication of only anthropogenic contamination. The results of this study, however, need to be placed in a hydrological context to better understand whether paleosols can be a significant source of ammonium to drinking water supplies. [source] Hydrophilic and Antimicrobial Zeolite Coatings for Gravity-Independent Water Separation,ADVANCED FUNCTIONAL MATERIALS, Issue 2 2005Abstract Condensing heat exchangers onboard manned spacecraft require hydrophilic fin surfaces to facilitate wetting and wicking of condensate to achieve gravity-independent water separation in the zero- or micro-gravity environment of space. In order to prevent the proliferation of microbes, the coating must also be biocidal. Here we show for the first time that zeolite,A and ZSM-5 coatings deposited via in-situ crystallization on stainless steel and aluminum alloys have excellent hydrophilicity, biocidal properties, and adhesion. Water contact angles below 5° were obtained on most substrates tested. When silver-ion exchange is carried out on the zeolite,A coating, it becomes highly antibacterial. This biocidal capability of zeolite,A is regenerative by repeated ion exchange. All coatings exhibit the highest rating of 5B as determined by adhesion test ASTM D-3359-02 (American Society for Testing and Materials). These properties, in addition to zeolite coating's low-temperature crystallization process and demonstrated corrosion resistance, make zeolite coatings advantageous over the current sol,gel coatings and well suited for use in condensing heat exchangers onboard manned spacecraft. [source] An empirical approach to study the occurrence of ion exchange in the ionic micellar-mediated semi-ionic reactions: Kinetics of the rate of reaction of piperidine with ionized phenyl salicylate in the presence of cationic micellesINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 5 2001M. Niyaz Khan Pseudo-first-order rate constants (kobs),obtained for the cleavage of ionized phenyl salicylate (PS,) at constant [NaOH], [MeCN], [CTAZ]T (total concentration of cetyltrimethylammonium chloride and bromide), [Pip]T (total concentration of piperidine), and varying concentrations of sodium cinnamate, acetate, and butanoate ([NaX]),follow the relationship: kobs = (k0 + , K[NaX])/(1 + K[NaX]), where , and K are empirical parameters. The values of , are almost independent of [CTAZ]T, while K values decrease with the increase in [CTAZ]T within its range 0.006,0.020 M. The values of , and K are explained in terms of pseudophase model of micelle coupled with an empirical relationship: KS = KS0/(1 + ,X/S [NaX]), where KS is the CTAZ micellar binding constant of PS, in the presence of NaX. © 2001 John Wiley & Sons, Inc. Int J Chem Kinet 33: 288,294, 2001 [source] Platinum Nanoparticles Supported on Ionic Liquid-Modified Magnetic Nanoparticles: Selective Hydrogenation CatalystsADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 13 2007Raed Abu-Reziq Abstract A method for supporting platinum nanoparticles on magnetite nanoparticles is described. The method requires modification of the surface of the magnetic nanoparticles with ionic liquid groups. Before modification, the magnetic nanoparticles are not stable and easily aggregate and, after modification, the magnetite nanoparticles become highly stable and soluble in polar or non-polar organic solvents depending on the alkyl group of the linked ionic liquids. The supporting of platinum nanoparticles on the modified magnetic nanoparticles was achieved by adsorbing platinum salts (K2PtCl4) on the surface of the magnetite nanoparticles via ion exchange with the linked ionic liquid groups and then reducing them by hydrazine. The supported platinum nanoparticles were applied in the catalytic hydrogenation of alkynes in which cis -alkenes were selectively produced, and in the hydrogenation of ,,,-unsaturated aldehydes where the allyl alcohols were obtained as the exclusive products. The new catalyst can be easily separated from the reaction mixtures by applying an external magnetic field and recycled. [source] Preparation and characterization of silver containing chitosan fibersJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Yimin Qin Abstract Silver containing chitosan fibers were prepared by blending fine particles of a silver sodium hydrogen zirconium phosphate compound into the spinning solution. It was possible to distribute the silver containing particles in the chitosan fiber because of the high viscosity of the spinning solution and the small diameter of the particles. Because the silver ions are imbedded inside the sodium hydrogen zirconium phosphate complex, the chitosan fibers remain white in color without being oxidized by the silver ions. The release of silver ions from the silver containing chitosan fibers were studied by placing the fibers in contact with distilled water, solution A, and aqueous protein solutions. Results showed that the release of silver ions was low in water, while in solution A and protein solutions, the silver ions are activated through ion exchange and chelation. The silver ions can significantly enhance the antimicrobial properties of the chitosan fibers. Experimental results showed that when placed in contact with the silver containing chitosan fibers, the reduction in bacteria count can be more than 98%. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 3622,3627, 2007 [source] Hydrothermal processing of rice husks: effects of severity on product distributionJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 7 2008Rodolfo Vegas Abstract BACKGROUND: Treatment in aqueous media (hydrothermal or autohydrolysis reactions) is an environmentally friendly technology for fractionating lignocellulosic materials. Rice husks were subjected to hydrothermal processing under a variety of operational conditions to cause the selective breakdown of xylan chains, in order to assess the effects of reaction severity on the distribution of reaction products. RESULTS: The effects of severity (measured by the severity factor, R0) on the concentrations of the major autohydrolysis products (monosaccharides, xylo- and glucooligosaccharides, xylooligosaccharide substituents, acetic acid, acid-soluble lignin and elemental nitrogen) were assessed. The interrelationship between the severity of treatment and molecular weight distribution was established by high-performance size-exclusion chromatography. Selected samples were subjected to refining treatments as ethyl acetate extraction and ion exchange for refining purposes, and the concentrates were assayed by high-performance anion-exchange chromatography and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. CONCLUSIONS The protein equivalent of the products present in liquors accounted for 43 to 51% of the protein present in the raw rice husks. The concentrations of glucose (derived from starchy material) and arabinose (split from the xylan backbone) were fairly constant with severity. Even in treatments at low severity, high molecular weight compounds derived from xylan accounted for a limited part of the stoichiometric amount. Operating under harsh conditions, about 50% of the total xylan-derived compounds corresponded to fractions with a degree of polymerization (DP) < 9. After refining, saccharides accounted for more than 90% of the non-volatile components of the sample. The refined products showed a series of xylose oligomers up to about DP 13, and a series of acetylated xylose oligomers up to about DP 15. Copyright © 2008 Society of Chemical Industry [source] Ammonia exchange on clinoptilolite from mineral deposits located in MexicoJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 6 2004Roberto Leyva-Ramos Abstract This work investigated the ion exchange of ammonia on clinoptilolite obtained from mineral deposits located in San Luis Potosi and Sonora, Mexico. Experimental ion exchange isotherm data were obtained in a batch adsorber. The effects of temperature and solution pH on the ion exchange capacity were studied and it was found that the exchange capacity was slightly increased by augmenting the temperature and by decreasing the pH from 6 to 3. The ion exchange capacity was independent of the diameter of the zeolite particles. The reversibility of ion exchange was analyzed by desorbing the ammonia exchanged on the zeolite. The ion exchange was reversible when 1% NaCl solution was used as the desorbing solution, but more ammonia was desorbed using 1% KCl solution in the desorption step. It was concluded that a considerable amount of ammonia was exchanged on the clinoptilolite and that the exchange capacity was slightly dependent on the temperature and pH. Copyright © 2004 Society of Chemical Industry [source] The removal of iron and cobalt from aqueous solutions by ion exchange with Na-Y zeolite: batch, semi-batch and continuous operationJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 6 2002Jong Sung Kim Abstract The removal of single component and binary mixtures of divalent cobalt and iron from water by ion exchange with synthetic Y zeolite has been studied in batch, semi-batch and continuous modes of operation; the initial metal solution concentration did not exceed 2,mmol,dm,3. Binary Co/Na and Fe/Na ion exchange equilibrium isotherms (294,K) are presented wherein exchange site heterogeneity is evident in the case of the iron treatment. Under conditions of stoichiometric ion exchange, removal efficiencies for both cobalt and iron decrease with increasing metal concentration (0.2,2,mmol,dm,3) and the values were similar for both metals. Removal of cobalt under transient conditions was found to be temperature dependent. In the fixed bed operation, break-through behavior was sensitive to changes in both flow rate and inlet concentration. The break-through profiles for both metals under competitive and non-competitive conditions are presented; iron removal is lower in the presence of cobalt and vice versa. An in situ regeneration of the fully loaded zeolite by back exchange with sodium is considered and the exchange capacity of the regenerated zeolite is reported. The feasibility of employing cycles of heavy metal uptake/zeolite regeneration is addressed. © 2002 Society of Chemical Industry [source] Effects on the removal of Pb2+ from aqueous solution by crab shellJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 11 2001Dong Seog Kim Abstract The effects of temperature, pH, chitin and chitosan on Pb2+ removal by crab shell were investigated. Pb2+ removal by crab shell was greater than that of chitin and chitosan, indicating that chitin did not contribute to Pb2+ removal by crab shell. The quantity and rate of Pb2+ removal increased as the pH value increased. The rate of Pb2+ removal increased with increased temperature, but the maximum amount of Pb2+ removal was constant irrespective of temperature. Metal ions (K+, Na+, Mg2+, Ca2+) were released from crab shell concomitant with Pb2+ removal by ion exchange. The amount of Ca2+ released was greater than any for other metal ions in both Pb2+ and Pb2+ -free solutions. The amount of Ca2+ released in Pb2+ solution was greater than that in Pb2+ -free solution, whereas CO32, release in Pb2+ solution was less than in Pb2+ -free solution. Pb2+ removal was mainly a consequence of dissolution of CaCO3(s) with consequence precipitation of Pb3(CO3)2(OH)2(s) and PbCO3(s). Pb2+ accelerated the dissolution of CaCO3(s) by ion exchange and the precipitation occurred both at the surface and in the inner part of the crab shell. © 2001 Society of Chemical Industry [source] Binding and release studies of a cationic drug from a star-shaped four-arm poly(ethylene oxide)- b -poly(methacrylic acid)JOURNAL OF PHARMACEUTICAL SCIENCES, Issue 2 2010E. He Abstract Star-shape polymers possess higher densities of terminal functional groups and three-dimensional tetrahedron structure that induce significantly different association and interactions with drug compared to linear structure of identical molecular weights. Four-arm poly(ethylene oxide)- b -poly(methacrylic acid) block copolymer was synthesized by atom transfer radical polymerization technique, and it self-assembled into core-shell micelles and extended unimers at low and high pH respectively. The negatively charged carboxylate groups on the polymer chains interacted with a cationic drug through electrostatic interaction forming polymer/drug complexes stabilized by biocompatible hydrophilic PEO segments. The hydrodynamic radius (Rh) of the polymeric aggregates and polymer/drug complexes ranged from 46 to 84,nm and 32 to 55,nm at pH of 4.6 and 8.0 respectively, making them suitable for drug delivery applications. The thermodynamic parameters and interactions between polymer and drug were determined by isothermal titration calorimetric technique. The electrostatic force, hydrogen bonding and hydrophobic interactions controlled the characteristics of polymer/drug formation and complexes when the molar ratios of drug and polymer were varied. Drug selective electrode system was used to measure the dynamic release of imipramine hydrochloride (IPH) from multi-arm PEO- b -PMAA star polymer. The release exponent n was greater than 0.5 indicating a non-Fickian type diffusion behavior, where the release behavior was dominated by chain relaxation induced by ion exchange that was dependent on pH. © 2009 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:782,793, 2010 [source] Physicochemical interactions between drugs and superdisintegrantsJOURNAL OF PHARMACY AND PHARMACOLOGY: AN INTERNATI ONAL JOURNAL OF PHARMACEUTICAL SCIENCE, Issue 12 2008Nelly Fransén We have evaluated the interactions between superdisintegrants and drugs with different physicochemical characteristics, which may affect the in-vivo absorption e.g. after mucosal administration. The binding of sodium salicylate, naproxen, methyl hydroxybenzoate (methylparaben), ethyl hydroxybenzoate (ethylparaben), propyl hydroxybenzoate (propylparaben), atenolol, alprenolol, diphenhydramine, verapamil, amitriptyline and cetylpyridinium chloride monohydrate (CPC) to different superdisintegrants (sodium starch glycolate (SSG), croscarmellose sodium (CCS) and crospovidone) and one unsubstituted comparator (starch) was studied spectrophotometrically. An indication of the in-vivo effect was obtained by measuring the interactions at physiological salt concentrations. SSG was investigated more thoroughly to obtain release profiles and correlation between binding and ionic strength. The results showed that the main interactions with the anionic hydrogels formed by SSG and CCS were caused by ion exchange, whereas the neutral crospovidone exhibited lipophilic interactions with the non-ionic substances. The effect of increased ionic strength was most pronounced at low salt concentrations and the ion exchange interactions were almost completely eradicated at physiological conditions. The release profile of diphenhydramine was significantly affected by the addition of salt. It was thus concluded that the choice of buffer was of great importance for in-vitro experiments with ionic drugs. At physiological salt concentrations the interactions did not appear to be strong enough to influence the in-vivo bioavailability of any of the drug molecules. [source] In situ ethylene homopolymerization and copolymerization catalyzed by zirconocene catalysts entrapped inside functionalized montmorilloniteJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 14 2003Chengbin Liu Abstract Ethylene homopolymerizations and copolymerizations were catalyzed by zirconocene catalysts entrapped inside functionalized montmorillonites that had been rendered organophilic via the ion exchange of the interlamellar cations of layered montmorillonite with hydrochlorides of L -amino acids (AAH+Cl,) or their methyl esters (MeAAH+Cl,), with or without the further addition of hexadecyltrimethylammonium bromide (C16H33N+Me3Br,; R4N+Br,). In contrast to the homogeneous Cp2ZrCl2/methylaluminoxane catalyst for ethylene homopolymerizations and copolymerizations with 1-octene, the intercalated Cp2ZrCl2 activated by methylaluminoxane for ethylene homopolymerizations and copolymerizations with 1-octene proved to be more effective in the synthesis of polyethylenes with controlled molecular weights, chemical compositions and structures, and properties, including the bulk density. The effects of the properties of the organic guests on the preparation and catalytic performance of the intercalated zirconocene catalysts were studied. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2187,2196, 2003 [source] | |||||||||||||||||||||||||||||||||||||