WorldWideScience

Sample records for acid chelating resin

  1. CATALYTIC HYDROGENATION OF ACRYLATE ASMMETRIC Dd(Ⅱ)—CHELATING RESINS CONTAINING AMINO ACID LIGANDS

    Wangying; WangHongzuo; 等

    1995-01-01

    The catalytic hydrogenation of palladium chelating resins containing chiral amino acid ligands based on lower crosslinked poly(chloroethyl acrylate) and some effects on the rate of hydrogenation were studied.

  2. Diglycolamic acid functionalized PAMAM-SDB chelating resin for removal of Th(IV) from aqueous and nitric acid medium

    Removal of radionuclides based on solid phase extraction (SPE) also known as solid-liquid extraction is developed considerably in the last few decades due to their simplicity, rapidity, easy operation and cost effectiveness. Various types of sorbents such as organic, inorganic, bio-sorbent, composites and carbon based material have been developed for the recovery of radionuclides. Among the solid sorbents, chelating resins are being increasingly used due to their high adsorption capacity and selectivity. The chelating resins are prepared either by impregnating or grafting the chelating agents on solid substrate. Generally, the adsorption efficiency depends on the type of chelating agent and to some extent on the size and physiochemical properties of the resin. Recovery of actinides from aqueous waste using chelating agent containing >P=O, >C=O or other functional groups of desired basicity and stereochemistry have been extensively studied. Removal of thorium from aqueous solution using diglycolamic acid (DGA) functionalized poly(amido)amine (PAMAM) dendron-styrene divinyl benzene (SDB) chelating resin is presented in this paper

  3. Separation of radiostrontium from alkaline reprocessing waste solution using a fixed-bed column of chelating iminodiacetic acid resin

    A fixed-bed ion exchange column filled with a chelating resin containing iminodiacetic acid functional groups has been tested for removal of strontium from simulated alkaline reprocessing waste solution. The breakthrough curve has been established. Column loading performance is correlated with batch equilibration results. The loaded strontium is eluted in a small volume of 0.5 M HNO3. (author)

  4. SYNTHESES AND ADSORPTION PROPERTIES OF PHENOL-FORMALDEHYDE TYPE CHELATING RESINS BEARING THE FUNCTIONAL GROUP OF TARTARIC ACID

    Rong-jun Qu; Chun-nuan Ji; Yan-zhi Sun; Zhong-fang Li; Guo-xiang Cheng; Ren-feng Song

    2004-01-01

    Several kinds of novel chelating resins bearing the functional group of tartaric acid (TTA-FQ-12, TTA-FQ-23, and TTA-FQ-34) were synthesized by reacting epoxy maleic anhydride, which was prepared through the oxidization reaction of maleic anhydride by hydrogen peroxide, with phenol-formaldehyde resin containing polyamine (FQ resins series). The effects of such factors as reaction time, reaction temperature and pH value on the loading capacity of TTA in resins were investigated. The results showed that the optimum reaction conditions are as follows: time 9-12 h; temperature 90-105℃;pH value 6-10. The loading capacities of TTA can reach 0.15, 0.14, and 0.11 mmol/g-1 when the functional group of FQ resin was -OCH2CH2NHC2H4NH2, -O(CH2CH2NH)2C2H4NH2 and -O(CH2CH2NH)3C2H4NH2), respectively. The structures of resins were characterized by FTIR spectra. The primary study on the adsorption properties of the resins for metal ions showed that there are two kinds of adsorption mechanisms i.e. ion exchange and chelate in the adsorption process.TTA-FQ resins have much higher adsorption selectivity for Pb2+and Zn2+ than for Cu2+ and Ni2+. These resins can probably be used for separating Pb2+ or Zn2+ in the mixture of metal ions or for treating wastewater containing heavy metal ions.

  5. A chelating resin containing trihydroxybenzoic acid as the functional group. Synthesis and adsorption behavior for Th(IV) and U(VI) ions

    A novel glycidyl methacrylate chelating resin has been synthesized through copolymerization of glycidyl methacrylate (GMA) in the presence of divinylbenzene (DVB), the resulting resin was immobilized with 3,4,5-trihydroxybenzoic acid (THBA) to give GMA/DVB/THBA chelating resin. The adsorption of Th(IV) and U(VI) on GMA/DVB/THBA adsorbent was studied as a function of initial concentration, pH, shaking time and temperature. The novel chelating resin shows a high capacity for Th(IV) and U(VI), maximum adsorption of Th(IV) and U(VI) were 56 and 83.6 mg/g, respectively. Kinetic studies showed that the adsorption follows the pseudo second order model referring to the influence of the textural properties of the resin on the rate of adsorption. Thermodynamic parameters such as ΔH deg and ΔS deg were studied and indicated an endothermic process. (author)

  6. Selective separation of uranium(VI) on a chelating styrene-DVB based resin containing quinaldinic acid amide group

    A new chelating styrene-DVB based resin containing quinaldinic acid amide functional group, has been synthesised and characterised. The sorption patterns of Na(I), K(I), Be(II), Ca(II), Mg(II), Zn(II), Cd(II), Cu(II), Pb(II), Ni(II), Bi(III), Fe(III), Ti(IV) and U(VI) have been studied as a function of pH. The resin sorbs U(VI) over a wide range of pH (1.0 to 4.0) with a maximum sorption of 0.32 mmol/g at pH 3.5 to 4.0. Zn(II), Cd(II), Cu(II), Na(II), Pb(II), Fe(III) and Ti(IV) are also sorbed to different extents by the resin while Na(I), K(I), Be(II), Ca(II), Mg(II) and Bi(III) are not sorbed. Conditions for separation of U(VI) from these metal ions have been identified. The eluting agent used for U(VI) is 3 N HNO3 and the recovery recorded is about 99.9 per cent (author). 12 refs., 3 tabs

  7. Selective removal of Ag+ ions from nitric acid medium by alginate microcapsules, Lewatite TP 214 chelating resin, and 200 CT strongly acidic ion exchanger

    Alginate microcapsules containing bis (2, 4, 4-trimethylpenthyl) monothiophosphinic acid (Cyanex 302) were prepared for the selective removal of Ag+ ions from the reprocessing effluents of FBR-MOX fuel. The Ag+ ions are added for the adjustment of oxidation state of Plutonium. We compared uptake properties of aforementioned microcapsules with those of 200 CT a strongly acidic resin, and Lewatite TP 214, a very selective chelating resin for the Ag+ ions. Most of the uptake properties of the microcapsules were amid the 200 CT and Lewatite, and rather similar to the later. The order of uptake kinetic and breakthrough capacity were the same as: 200 CT > Microcapsules > Lewatite; and for selectivity: Lewatite > Microcapsules > 200 CT. However, high selectivity of Lewatite is rather disadvantageous because it makes the elution operation complicated. Advantages of microcapsules include simple preparation procedure, relatively high selectivity and ease of elution even with 3M nitric acid. However, their total capacity is low. For enhancing the total capacity only increasing the active component is not enough since it deteriorates the kinetics, and the new preparation techniques are necessary which are under study. (author)

  8. New Regeneration process of heavy metals loaded chelating resin

    Menoud, P.; Cavin, L.; Renken, A.

    2000-01-01

    An alternative to the classical acid-base regeneration of chelating resins loaded with heavy metals is investigated. The new process consists in recovering the heavy metals with recyclable soluble complexing agents. The semiclosed reactor includes a fixed bed and a stirred tank. A three-parameter model, which implies a double equilibrium in series, is introduced. When less than 10 % of the metal is still fixed on the resin at the end of the desorption, a simplified form of the model with two ...

  9. Effect of the Alkyl Chain Length on the Adsorption Properties of Malonamide Chelating Resins

    In order to investigate the effect of the alkyl chain length of malonamide chelating resins on the rate of uptake of U(VI) ions and Ce(III) Ions, lV,N,N',N'-tetraethyl malonamide (TEMA), N,N,N',N'-tetra-n-propyl malonamide (TPrMA), lV,lV,N',N'-tetra-n-butyl malonamide (TBMA) and N,l V,N',N'-tetra-n-pentyl malonamide (Tamp) chelating resins were synthesized by chemically bonding these function groups to CMS-DVB co-polymer beads. N,lV,N',N'-tetraphenyl malonamide (TPhMA) chelating resin was also investigated and the results of these resins were compared with those of N,lY,N',N-tetra methylmalonamide (TMMA) previously reported. The batch technique was used to study the thermodynamic equilibrium, in terms of distribution coefficient, and the kinetics of the adsorption U(VI) and Ce(III) ions from 3 M HNO3, Acid, and 3 M NaNO3 + 0.05 M HNO3, Salt, media. The introduction ratio of the function group into the polymer base and the uptake of U(VI) ions and C(III) ions were found to decrease with the increase in the alkyl chain length. The uptake was found to diminish in case of TPhMA resin due to the decrease of the function group ratio and the steric-hinder effect

  10. Heavy metal ion uptake properties of polystyrene-supported chelating polymer resins

    A Ravikumar Reddy; K Hussain Reddy

    2003-06-01

    Metal ion uptake properties of polystyrene-supported chelating polymer resins functionalized with (i) glycine, (ii) hydroxy benzoic acid, (iii) Schiff base and (iv) diethanol amine have been investigated. The effects of pH, time and initial concentration on the uptake of metal ions have been studied. The uptake of metal ion depends on pH. The resins are more selective at pH 10 for Pb(II) and Hg(II), whereas at pH 6 they are found to be Cd(II) and Cr(VI) selective. Metal ion uptake properties of resins follow Freundlich’s equation. The resins are recyclable and are therefore employed for the removal of heavy metal pollutants from industrial waste water.

  11. Separation and recovery of uranium ore by chlorinating, chelate resin and molten salt treatment

    Taki, Tomohiro [Japan Nuclear Cycle Development Inst., Kamisaibara, Okayama (Japan). Ningyo Toge Environmental Engineering Center

    2000-12-01

    Three fundamental researches of separation and recovery of uranium from uranium ore are reported in this paper. Three methods used the chloride pyrometallurgy, sodium containing molten salts and chelate resin. When uranium ore is mixed with activated carbon and reacted for one hour under the mixed gas of chlorine and oxygen at 950 C, more than 90% uranium volatilized and vaporization of aluminum, silicone and phosphorus were controlled. The best activated carbon was brown coal because it was able to control the large range of oxygen concentration. By blowing oxygen into the molten sodium hydroxide, the elution rate of uranium attained to about 95% and a few percent of uranium was remained in the residue. On the uranium ore of unconformity-related uranium deposits, a separation method of uranium, molybdenum, nickel and phosphorus from the sulfuric acid elusion solution with U, Ni, As, Mo, Fe and Al was developed. Methylene phosphonic acid type chelate resin (RCSP) adsorbed Mo and U, and then 100 % Mo was eluted by sodium acetate solution and about 100% U by sodium carbonate solution. Ni and As in the passing solution were recovered by imino-diacetic acid type chelate resin and iron hydroxide, respectively. (S.Y.)

  12. Separation and recovery of uranium ore by chlorinating, chelate resin and molten salt treatment

    Three fundamental researches of separation and recovery of uranium from uranium ore are reported in this paper. Three methods used the chloride pyrometallurgy, sodium containing molten salts and chelate resin. When uranium ore is mixed with activated carbon and reacted for one hour under the mixed gas of chlorine and oxygen at 950 C, more than 90% uranium volatilized and vaporization of aluminum, silicone and phosphorus were controlled. The best activated carbon was brown coal because it was able to control the large range of oxygen concentration. By blowing oxygen into the molten sodium hydroxide, the elution rate of uranium attained to about 95% and a few percent of uranium was remained in the residue. On the uranium ore of unconformity-related uranium deposits, a separation method of uranium, molybdenum, nickel and phosphorus from the sulfuric acid elusion solution with U, Ni, As, Mo, Fe and Al was developed. Methylene phosphonic acid type chelate resin (RCSP) adsorbed Mo and U, and then 100 % Mo was eluted by sodium acetate solution and about 100% U by sodium carbonate solution. Ni and As in the passing solution were recovered by imino-diacetic acid type chelate resin and iron hydroxide, respectively. (S.Y.)

  13. Preparation and characterization of chitosan-grafted-poly(2-amino-4,5-pentamethylene-thiophene-3-carboxylic acid N'-acryloyl-hydrazide) chelating resin for removal of Cu(II), Co(II) and Ni(II) metal ions from aqueous solutions.

    Bekheit, M M; Nawar, N; Addison, A W; Abdel-Latif, D A; Monier, M

    2011-05-01

    The graft copolymerization of ethylacrylate (EA) onto chitosan initiated by potassium persulphate and Mohr's salt combined redox initiator system in limited aqueous medium was carried out in heterogeneous media. Moreover, modification of the grafted chitosan was carried out by reaction of the ester group (-COOEt) with 2-amino-4,5-pentamethylene-thiophene-3-carboxylic acid hydrazide which eventually produce chitosan-grafted-poly(2-amino-4,5-pentamethylene-thiophene-3-carboxylic acid N'-acryloyl-hydrazide) (chitosan-g-ATAH) chelating resin. The application of the modified resin for metal ion uptake was studied using Cu(2+), Co(2+) and Ni(2+) ions. The modified chelating resins were characterized using FTIR spectroscopy, SEM and X-ray diffraction. PMID:21277322

  14. Preparation and properties of a new chelating resin containing 1-nitroso-2-naphthol as the functional group.

    Ghosh, J P; Das, H R

    1981-04-01

    A macroreticular polystyrene-based chelating ion-exchanger containing 1-nitroso-2-naphthol as the functional group has been synthesized. The exchange-capacity of the resin for a number of metal ions such as copper(II), iron(III), cobalt(II), nickel(II), palladium(II) and uranium(VI) as a function of pH has been determined. The sorption and elution characteristics for palladium(II) and uranium(VI) have been thoroughly examined with a view to utilizing the resin for separation and concentration of uranium and palladium. Uranium(VI) has been separated from a mixture of ten other metal ions by sorption on the chelating resin and selective elution with 0.5M sodium carbonate. Palladium(II) has been separated from various metal ions by selective sorption on the resin in 1M hydrochloric acid medium. PMID:18962916

  15. Resinas quelantes amidoxímicas Amidoxime chelating resins

    Fernanda M. B. Coutinho

    1999-12-01

    Full Text Available Resinas quelantes com grupos amidoxima foram sintetizadas por copolimerização em suspensão de acrilonitrila (AN e divinilbenzeno (DVB e subsequente modificação química dos grupos ciano por reação com hidroxilamina. Na copolimerização, a proporção de divinilbenzeno e o grau de diluição foram variados. Gelatina e carbonato de cálcio foram usados como estabilizadores de suspensão e sulfato de sódio foi adicionado para reduzir a solubilidade da acrilonitrila em água, por meio do efeito salting out. Os copolímeros de AN/DVB e as resinas amidoxímicas obtidos foram caracterizados por meio de densidade aparente, área específica, volume de poros e teor de nitrogênio. As resinas amidoxímicas foram também avaliadas em relação a capacidade de complexação de íons cobre.Chelating resins with amidoxime groups were synthesized by suspension copolymerization of acrylonitrile (AN and divinylbenzene (DVB and subsequent chemical modification of cyano groups by reaction with hydroxylamine. In the copolymerization, the proportion of divinylbenzene and the dilution degree were varied. Gelatin and calcium carbonate were used as suspension stabilizers and sodium sulphate was added in order to reduce acrylonitrile solubility in water, by salting out effect. The AN/DVB copolymers and amidoxime resins obtained were characterized by apparent density, surface area, pore volume and by the content of nitrogen. The amidoxime resins were also evaluated in relation to the complexation capacity of copper ion.

  16. Flame Atomic Absorption Spectrometric Determination of Trace Metal Ions in Environmental and Biological Samples After Preconcentration on a Newly Developed Amberlite XAD-16 Chelating Resin Containing p-Aminobenzene Sulfonic Acid.

    Islam, Aminul; Ahmad, Akil; Laskar, Mohammad Asaduddin

    2015-01-01

    Amberlite® XAD-16 was functionalized with p-aminobenzene sulfonic acid via an azo spacer in order to prepare a new chelating resin, which was then characterized by water regain value, hydrogen ion capacity, elemental analyses, and IR spectral and thermal studies. The maximum uptake of Cu(II), Ni(II), Zn(II), Co(II), Cr(III), Fe(III), and Pb(II) ions was observed in the pH range 4.0-6.0 with the corresponding half-loading times of 6.5, 7.0, 8.0, 9.0, 11.0, 8.5, and 16.5 min. The sorption data followed Langmuir isotherms and a pseudo-second-order model. Thermodynamic quantities, ΔH and ΔS, based on the variation of the distribution coefficient with temperature were also evaluated. High preconcentration factors of 60-100 up to a low preconcentration limit of 4.0-6.6 μg/L have been achieved for the metal ions. The validity of the method was checked by analyzing standard reference materials and recoveries of trace metals after spiking. The analytical applications of the method were explored by analyzing natural water, mango pulp, mint leaves, and fish. PMID:25857893

  17. Evaluation of extractants and chelating resins in polishing actinide-contaminated waste streams

    At the Los Alamos National Laboratory Plutonium Facility, anion exchange is used for recovering plutonium from nitric acid solutions. Although this approach recovers >99%, the trace amounts of plutonium and other actinides remaining in the effluent require additional processing. We are doing research to develop a secondary unit operation that can directly polish the effluent so that actinide levels are reduced to below the maximum allowed for facility discharge. We selected solvent extraction, the only unit operation that can meet the stringent process requirements imposed; several carbonyl and phosphoryl extractants were evaluated and their performance characterized. We also investigated various engineering approaches for solvent extraction; the most promising was a chelating resin loaded with extractant. Our research now focuses on the synthesis of malonamides, and our goal is to bond these extractants to a resin matrix. 7 refs., 12 figs., 1 tab

  18. The synthesis of macroreticular chelating resins containing amidoxime groups and their properties of recovery of uranium

    Macroreticular chelating resins containing amidoxime groups were successfully synthesized with divinyl benzene (DVB) cross-linking acrylonitrile (AN) copolymer beads as skeleton by suspension polymerization. Influence factors of DVB-AN beads' amidoxime reaction, such as reaction medium, reaction ratio, reaction temperature and time etc. were studied in detail. Copolymer and chelating resins with amidoxime groups having different physical properties and monomer composition were prepared successfully. The factors affecting resin chemical adsorption capacity, such as cross-linking agent, reticulating agent and polar monomer etc. were also explored. The resins had chemical adsorption capacity over 4.0 mmol/g (dry), and ideal results of recovered uranium under the conditions as described

  19. Synthesis and Characterization of polyacrylamide Chelating Resin with Thenoyltrifluoroacetone for Separation of Thorium from Uranium

    New effective chelating resin is synthesized by immobilization of Thenoyltrifluoroacetone (HTTA) on cross linked polyacrylamide. The chelating exchanger is used for separation of uranium (UO22+) and thorium(Th4+). The analyzed metal ions were quantitatively measured by ion chromatographic technique coupled with UV/V is detector and derivatization reaction of Arsenazo(III) at wavelength 660 nm. Different factors affecting the metal ions uptake and hence the separation efficient c y of the chelating polyacrylamide resin were investigated. Optimization of conditions showed that maximum uptake of UO22+ and Th4+ are at ph 4.0 and 3.0 respectively. Isothermal capacity shows a relatively high capacity of the chelating resin towards divalent uranium more than that of tetravalent thorium. The capacity of the chelating resin for UO22+ and Th4+ was found to be 0.05 and 0.034 mmol/gm, respectively. Separation of UO22+ and Th4+ was successively performed using column chromatographic technique loaded with the chelating resin. The retained metal ions were sequentially separated by i socratic elution using 0.1 M HNO3

  20. Synthesis and Analytical Study of New Chelating Resin Containing Sulfadiazine Drug

    Madher N. Abdulla

    2010-01-01

    A new chelating resin was prepared by mixing sulfadiazine drug and TMP (trimethylolphenol). It was polymerized by heating to 90 °C then it was post cured to 100 °C after that it was grinded. The chelating behavior was examined against Cu2+, Ni2+ using patch method in deferent conditions like treatment time and pH at room temperature. The resin show a good loading capacity toward Cu2+ (in treatment time = 3 h & pH=4) = 0.2174 mg ion / 100 mg resin and it show good loading capacity toward Ni2+ ...

  1. Adsorption of Iminodiacetic Acid Resin for Lutetium

    熊春华; 姚彩萍; 王惠君

    2004-01-01

    The adsorption behavior and mechanism of a novel chelate resin,iminodiacetic acid resin(IDAAR) for Lu(Ⅲ) were investigated.The statically saturated adsorption capacity is 210.8 mg·g-1 at 298 K in HAc-NaAc medium.The Lu(Ⅲ) adsorbed on IDAAR can be eluted by 0.5 mol·L-1 HCl and the elution percentage reaches 96.5%.The resin can be regenerated and reused without obvious decrease in adsorption capacity.The apparent adsorption rate constant is k298=2.0×10-5 s-1.The adsorption behavior of IDAAR for Lu(Ⅲ) obeys the Freundlich isotherm.The thermodynamic adsorption parameters,enthalpy change ΔH,free energy change ΔG and entropy change ΔS of IDAAR for Lu(Ⅲ) are 13.1 kJ·mol-1,-1.37 kJ·mol-1 and 48.4 J·mol-1·K-1,respectively.The apparent activation energy is Ea=31.3 kJ·mol-1.The molar coordination ratio of the functional group of IDAAR to Lu(Ⅲ) is about 3∶1.The adsorption mechanism of IDAAR for Lu(Ⅲ) was examined by chemical method and IR spectrometry.

  2. Effect of pH on the release of radionuclides and chelating agents from cement-solidified decontamination ion-exchange resins collected from operating nuclear power stations

    Data are presented on the physical stability and leachability of radionuclides and chelating agents from cement-solidified decontamination ion-exchange resin wastes collected from two operating commercial light water reactors. Small-scale waste--form specimens collected during solidifications performed at the Brunswick Steam Electric Plant Unit 1 and at the James A. FitzPatrick Nuclear Power Station were leach-tested and subjected to compressive strength testing in accordance with the Nuclear Regulatory Commission's ''Technical Position on Waste Form'' (Revision 1). Samples of untreated resin waste collected from each solidification vessel before the solidification process were analyzed for concentrations of radionuclides, selected transition metals, and chelating agents to determine the quantities of these chemicals in the waste-form specimens. The chelating agents included oxalic, citric, and picolinic acids. In order to determine the effect of leachant chemical composition and pH on the stability and leachability of the waste forms, waste-form specimens were leached in various leachants. Results of this study indicate that differences in pH do not affect releases from cement-solidified decontamination ion-exchange resin waste forms, but that differences in leachant chemistry and the presence of chelating agents may affect the releases of radionuclides and chelating agents. Also, this study indicates that the cumulative releases of radionuclides and chelating agents are similar for waste- form specimens that decomposed and those that retained their general physical form. 36 refs., 60 figs., 28 tabs

  3. Ion Exchange Study of Some New Copolymer Resins Derived from 8-Hydroxyquinoline-5-sulphonic Acid, Biuret and Formaldehyde

    Dhakite, P. A.; W. B. Gurnule

    2011-01-01

    Copolymer resins (8-HQSABF) were synthesized by the condensation of 8-hydroxyquinoline-5-sulphonic acid and biuret with formaldehyde in the presence of hydrochloric acid as catalyst, proved to be selective chelation ion exchange copolymer resins for certain metals. Chelation ion exchange properties to these polymers were studied for Cu2+, Cd2+, Co2+ and Zn2+ ions. A batch equilibrium method was employed in the study of the selectivity of the distribution of a given metal ions between the poly...

  4. Determination of trace rare earth elements by X-ray fluorescence spectrometry after preconcentration on a new chelating resin loaded with thorin.

    De Vito, I E; Masi, A N; Olsina, R A

    1999-07-12

    A very stable chelating resin was prepared by adsorption of (o-[3,6-disulfo-2-hidroxy-1-naphthylazo]-benzenearsonic acid) (thorin) on a macroporous resin Amberlite XAD-7. The optimal conditions for preparing it were obtained through the study of the adsorption properties of the resin and the thermodynamic quantities of the adsorption processes. Likewise, the behavior of the loaded resin with the rare earth elements (REE) were studied (pH of retention, sorption kinetics, etc). The conditions to prepare a thin film with this system were also evaluated. The loaded resin was successfully used for the separation and preconcentration of Sm(III), Eu(III) and Gd(III) prior to their determination by X-ray fluorescence (XRF) spectrometry. The preconcentration factor obtained was 500 and the concentrations at low detection limit were 13.8, 17 and 15.7 microg l(-1) for Sm, Eu and Gd, respectively. PMID:18967670

  5. The application of chelating resin to the elimination of interferences in the analysis of trace hazardous elements

    In general, digestion with nitric and sulfuric acids are applied in the analysis of trace elements in solid materials like industrial products and soils. This causes the digested solution to contain high concentrations of sulfate ion. In addition, silicate, chloride and other interferences, which are contained in the material itself, can also be included. These interfering matrices are separated generally through solvent extraction. In stead of the solvent extraction method, we applied the solid phase extraction method using chelating resin, which has a functional group of iminodiacetic acid, for the analysis of trace hazardous metals such as Cd and Pb in industrial products, soils, and other materials containing high concentrations of matrix components. In the presence of high concentrations of interfering ions, over 80% of Cd and Pb and Pb were extracted, with one exception that the recovery of Cd from seawater decreased to 60-30% in the presence of 19g/L of chloride ion. On the other hand, Cr, As and Se were extracted at a low recovery rate with this type of chelating resin. (author)

  6. Determination of trace elements in natural water samples by sir-segmented flow-injection/ICP-MS after preconcentration with a chitosan-based chelating resin

    Ultratrace elements in natural water samples were determined simultaneously by air-segmented flow-injection/inductively coupled plasma-mass spectrometry (SFI/ICP-MS). A small volume of the sample solutions (80 μl) was introduced into a nebulizer by an air-segmented flow-injection (SFI) system, and a maximum of fifteen elements were measured during each run. A chitosan-based chelating resin containing functional groups of iminodiacetate was used to separate and enrich analyte metal ions. A 50-fold preconcentration using 50 ml of sample solutions was achieved by the proposed method, where 1 ml of 0.1 M nitric acid was added to residues after drying the chelating column effluent. At pH 6, several heavy metals (Fe, Ni, Co, Cu, Zn, Ag, Cd, Pb and U) and rare earth elements (REEs) were quantitatively retained on the chelating resin column, whereas alkali and alkaline earth metals were eluted from the column by rinsing with 5 ml of a 0.2 M ammonium acetate solution. Metals adsorbed on the chelating resin column were recovered by elution with 10 ml of 1 M nitric acid. The proposed method was applied to the determination of trace elements in several natural water samples, such as river water and mineral drinking water. (author)

  7. Determination of trace elements in natural water samples by sir-segmented flow-injection/ICP-MS after preconcentration with a chitosan-based chelating resin

    Lee, K.H.; Oshima, Mitsuko; Motomizu, Shoji [Department of Chemistry, Faculty of Science, Okayama University, Okayama (Japan)

    2000-07-01

    Ultratrace elements in natural water samples were determined simultaneously by air-segmented flow-injection/inductively coupled plasma-mass spectrometry (SFI/ICP-MS). A small volume of the sample solutions (80 {mu}l) was introduced into a nebulizer by an air-segmented flow-injection (SFI) system, and a maximum of fifteen elements were measured during each run. A chitosan-based chelating resin containing functional groups of iminodiacetate was used to separate and enrich analyte metal ions. A 50-fold preconcentration using 50 ml of sample solutions was achieved by the proposed method, where 1 ml of 0.1 M nitric acid was added to residues after drying the chelating column effluent. At pH 6, several heavy metals (Fe, Ni, Co, Cu, Zn, Ag, Cd, Pb and U) and rare earth elements (REEs) were quantitatively retained on the chelating resin column, whereas alkali and alkaline earth metals were eluted from the column by rinsing with 5 ml of a 0.2 M ammonium acetate solution. Metals adsorbed on the chelating resin column were recovered by elution with 10 ml of 1 M nitric acid. The proposed method was applied to the determination of trace elements in several natural water samples, such as river water and mineral drinking water. (author)

  8. A new synthesis, characterization and application chelating resin for determination of some trace metals in honey samples by FAAS.

    Daşbaşı, Teslima; Saçmacı, Şerife; Çankaya, Nevin; Soykan, Cengiz

    2016-07-15

    In this study, we developed a simple and rapid solid phase extraction (SPE) method for the separation/preconcentration and determination of some trace metals by flame atomic absorption spectrometry (FAAS). A new chelating resin, poly [2-(4-methoxyphenylamino)-2-oxoethyl methacrylate-co-divinylbenzene-co-2-acrylamido-2-methyl-1-propanesulfonic acid] (MPAEMA-co-DVB-co-AMPS), was synthesized and characterized. This chelating resin was used as a new adsorbent material for determination of Cd(II), Co(II), Cr(III), Cu(II), Fe(III), Mn(II), Pb(II), and Zn(II) ions. The parameters influential on the determination of this trace metals were examined. Under the optimum conditions, the detection limits (DL) of the method for trace metals were found to be (3s) in the range of 0.9-2.2 μg L(-1) (n=21), the preconcentration factor was calculated as 200 and the relative standard deviation was obtained achieved as ⩽2% for n=11. The method was performed for the determination of trace metals in some honey samples and standard reference materials. PMID:26948616

  9. Copper, dioxouranium(VI) and lanthanide chelates of carboxymethylthiosuccinic acid

    Carboxymethylthiosuccinic acid (CMTSA) has three dissociable - COOH groups with pK values 2.91, 3.91, 5.03. Assignment of these values to the different carboxylic groups is given. Cu(II) and UO22+ chelates with CMSTA have been studied potentiometrically at 30degC and μ = 0.1M. The effects of dielectric constant of the solvent medium (dioxane-water) and the ionic strength, on these chelates have been examined. The lanthanides form 1:1 and 1:2 chelates with CMTSA. The plots of log K1 and (log K1 + log K2) versus e2/2r show a break at gadolinium. The thermodynamic parameters for these chelates have been determined. Smaller values of DELTAH show the predominance of the entropy effect in the formation of these chelates. (author)

  10. Chelating resin immobilizing carboxymethylated polyethyleneimine for selective solid-phase extraction of trace elements: Effect of the molecular weight of polyethyleneimine and its carboxymethylation rate.

    Kagaya, Shigehiro; Kajiwara, Takehiro; Gemmei-Ide, Makoto; Kamichatani, Waka; Inoue, Yoshinori

    2016-01-15

    The effect of the molecular weight of polyethyleneimine (PEI), defined as a compound having two or more ethyleneamine units, and of its carboxymethylation rate (CM/N), represented by the ratio of ion-exchange capacity to the amount of N on the resin, on the selective solid-phase extraction ability of the chelating resin immobilizing carboxymethylated (CM) PEI was investigated. The chelating resins (24 types) were prepared by immobilization of diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, PEI300 (MW=ca. 300), and PEI600 (MW=ca. 600) on methacrylate resins, followed by carboxymethylation with various amounts of sodium monochloroacetate. When resins with approximately the same CM/N ratio (0.242-0.271) were used, the recovery of Cd, Co, Cu, Fe, Ni, Pb, Ti, Zn, and alkaline earth elements increased with increasing the molecular weight of PEIs under acidic and weakly acidic conditions; however, the extraction behavior of Mo and V was only slightly affected. This was probably due to the increase in N content of the resin, resulting in an increase in carboxylic acid groups; the difference in the molecular weight of PEIs immobilized on the resin exerts an insignificant influence on the selective extraction ability. The CM/N ratio considerably affected the extraction behavior for various elements. Under acidic and neutral conditions, the recovery of Cd, Co, Cu, Fe, Ni, Pb, Ti, and Zn increased with increasing CM/N values. However, under these conditions, the recovery of alkaline earth elements was considerably low when a resin with low CM/N ratio was used. This is presumably attributed to the different stability constants of the complexes of these elements with aminocarboxylic acids and amines, and to the electrostatic repulsion between the elements and the protonated amino groups in the CM-PEI. The recovery of Mo and V decreased or varied with increasing CM/N values, suggesting that the extraction of these elements occurred mainly

  11. Removal of Cd (II) and Hg(II) by chelating resin Chelex-100

    Afaf Amara-Rekkab; Mohamed Amine Didi

    2015-01-01

    A sensitive, simple method for the determination of amounts of mixture of Hg2+and Cd2+ by spectrophotometry was described based on the formation of the Hg2+- Cd2+- PAN complex in water media. Optimal conditions such as reagent amounts, and pH for the Hg2+- Cd2+ determination were reported. It was found that the 2:1 PAN- Hg2+- Cd2+ complex dominate at pH 13.0. In another hand, the sorption of mixture mercury (II) and cadmium (II) from aqueous medium on a chelating resin Chelex 100 was studied...

  12. Adsorption equilibrium of uranium from seawater on chelating resin containing amide oxime group

    Chelating resins containing amide oxime group were synthesized by radiation-induced graft polymerization. The amount of the amide oxime groups was controlled below about 0.1 mol per kg of base polymer. The adsorption equilibrium of uranium from seawater on this resin was investigated. It was suggested that two neighboring amide oxime groups on the grafted chain captured one uranyl ion, and that single amide oxime ligand had little capacity for the adsorption of uranium. The adsorption equilibrium was correlated by a Langmuir-type equation. The content of neighboring amide oxime groups was 0.406 x 10-3 mol per kg of base polymer, which corresponded to 0.39 % of the total amount of amide oxime groups. The apparent stoichiometric stability constant for the complex of uranyl ion with the neighboring amide oxime groups in seawater was calculated to be 10-21.7. (author)

  13. Removal of Cd (II and Hg(II by chelating resin Chelex-100

    Afaf Amara-Rekkab

    2015-03-01

    Full Text Available A sensitive, simple method for the determination of amounts of mixture of Hg2+and Cd2+ by spectrophotometry was described based on the formation of the Hg2+- Cd2+- PAN complex in water media. Optimal conditions such as reagent amounts, and pH for the Hg2+- Cd2+ determination were reported. It was found that the 2:1 PAN- Hg2+- Cd2+ complex dominate at pH 13.0. In another hand, the sorption of mixture mercury (II and cadmium (II from aqueous medium on a chelating resin Chelex 100 was studied in batch mode. Since the extraction kinetic was obtained, with a mixture of 0.1 g of resin and 5 mL of mixture at 1 mmol/L of initial concentration, extraction equilibrium was reached within 20 min of mixing. The influence of some parameters such as initial mixture ions concentrations, initial pH of aqueous solution, ion strength and the amounts of resin have been studied at fixed temperature (20±1°C. The optimum pH value level for quantitative sorption was up to 2.6. The best performance obtained was 97.1% of extraction yield equivalent to 15.65 mg/g of resin. The pseudo-first- order, pseudo-second-order models and the intra-particle diffusion model were used to describe the kinetic data and rate constants were evaluated.

  14. Spectrophotometric determination of trace iron(III in natural water after its preconcentration with a chelating resin

    ELEONORA-ANA NEAGU

    2002-10-01

    Full Text Available A method for the determination of Fe(III at trace levels is described. Thus, prior to the spectrophotometric determination, a preconcentration of the trace amounts of iron(III using a chelate forming resin is proposed. A strong base anion-exchange resin (Dowex 2X4 loaded with Ferron (7-iodo-8-hydroxyquinoline-5-sulphonic acid was used for Fe(III preconcentration, at pH 2.2. After desorption with 5 % ascorbic acid in 0.5 M HCl, the analyte (converted from Fe(III to Fe(II was determined spectrophotometrically at 510 nm as Fe(II-o-phenanthroline complex. The accuracy of the proposed method was verified by comparing the obtained results with those obtained using AAS with the standard addition method. The sensitivity of the spectrophotometric method (after preconcentration was 0.01 mg Fe(III/ml. The recovery for iron(III at the 7 mg/l level was 97 %.

  15. Radiotracer studies on the uptake of strontium by poly(styrene-DVB) resins containing iminodiacetic acid groups

    Samanta, S.K. [Process Development Div., Bhabha Atomic Research Centre, Trombay, Mumbai (India)

    1999-07-01

    The uptake of strontium has been studied using two commercially available chelating resins containing iminodiacetic acid functional groups. The resins have been characterized with respect to moisture content, swelling behaviour, ion exchange and chelating capacities. The effect of pH, sodium and strontium concentrations on the uptake of strontium has been determined by carrying out batch equilibration tests. The suitability of using such a resin for removal of radiostrontium from radioactive waste solutions has also been tested in laboratory-scale column experiments. (orig.)

  16. Radiotracer studies on the uptake of strontium by poly(styrene-DVB) resins containing iminodiacetic acid groups

    The uptake of strontium has been studied using two commercially available chelating resins containing iminodiacetic acid functional groups. The resins have been characterized with respect to moisture content, swelling behaviour, ion exchange and chelating capacities. The effect of pH, sodium and strontium concentrations on the uptake of strontium has been determined by carrying out batch equilibration tests. The suitability of using such a resin for removal of radiostrontium from radioactive waste solutions has also been tested in laboratory-scale column experiments. (orig.)

  17. Uptake of actinides by sulphonated phosphinic acid resin from acid medium

    The removal of uranium and americium from nitric acid solutions by sulphonated phosphinic acid resin has been investigated. The capacity of the sulphonated resin exceeds the capacities of phosphinic acid resin and commercial cation exchange resin. Other advantages of the sulphonated resin for uranium and americium removal include reduced sensitivity to acidity and inert salt concentration. (author)

  18. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Acrylamide-acrylic acid resin. 573.120 Section 573... Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the...

  19. Effects of a chelating resin on metal bioavailability and toxicity to estuarine invertebrates: Divergent results of field and laboratory tests

    Wilkie, Emma M., E-mail: ewilkie@bio.mq.edu.a [Department of Environmental Sciences, University of Technology Sydney, Broadway, NSW 2007 (Australia); Ecotoxicology and Environmental Contaminants Section, Department of Environment and Climate Change, Lidcombe, NSW 1825 (Australia); Roach, Anthony C. [Ecotoxicology and Environmental Contaminants Section, Department of Environment and Climate Change, Lidcombe, NSW 1825 (Australia); Micevska, Tina [Centre for Environmental Contaminants Research, CSIRO Land and Water, Menai, NSW 2234 (Australia); Kelaher, Brendan P.; Bishop, Melanie J. [Department of Environmental Sciences, University of Technology Sydney, Broadway, NSW 2007 (Australia)

    2010-05-15

    Benthic invertebrates can uptake metals through diffusion of free ion solutes, or ingestion of sediment-bound forms. This study investigated the efficacy of the metal chelating resin SIR 300{sup TM} in adsorbing porewater metals and isolating pathways of metal exposure. A field experiment (Botany Bay, Sydney, Australia) and a laboratory toxicity test each manipulated the availability of porewater metals within contaminated and uncontaminated sediments. It was predicted that within contaminated sediments, the resin would adsorb porewater metals and reduce toxicity to invertebrates, but in uncontaminated sediments, the resin would not significantly affect these variables. Whereas in the laboratory, the resin produced the predicted results, in the field the resin increased porewater metal concentrations of contaminated sediments for at least 34 days and decreased abundances of four macroinvertebrate groups, and richness in all sediments. These contrasting findings highlight the limits of extrapolating the results of laboratory experiments to the field environment. - Laboratory experiments do not predict the effects on porewater metals or macroinvertebrates of adding a chelating resin to metal-contaminated field sediments.

  20. Effects of a chelating resin on metal bioavailability and toxicity to estuarine invertebrates: Divergent results of field and laboratory tests

    Benthic invertebrates can uptake metals through diffusion of free ion solutes, or ingestion of sediment-bound forms. This study investigated the efficacy of the metal chelating resin SIR 300TM in adsorbing porewater metals and isolating pathways of metal exposure. A field experiment (Botany Bay, Sydney, Australia) and a laboratory toxicity test each manipulated the availability of porewater metals within contaminated and uncontaminated sediments. It was predicted that within contaminated sediments, the resin would adsorb porewater metals and reduce toxicity to invertebrates, but in uncontaminated sediments, the resin would not significantly affect these variables. Whereas in the laboratory, the resin produced the predicted results, in the field the resin increased porewater metal concentrations of contaminated sediments for at least 34 days and decreased abundances of four macroinvertebrate groups, and richness in all sediments. These contrasting findings highlight the limits of extrapolating the results of laboratory experiments to the field environment. - Laboratory experiments do not predict the effects on porewater metals or macroinvertebrates of adding a chelating resin to metal-contaminated field sediments.

  1. Investigation of the role of chelating ligand in the synthesis of ion-imprinted polymeric resins on the selective enrichment of uranium(VI)

    Uranyl ion-imprinted polymeric (IIP) resins were prepared by dissolving stoichiometric amounts of uranyl nitrate and selected chelating ligands, viz. salicylaldoxime, catechol, succinicacid, 5,7-dichloroquinoline-8-ol and 4-vinyl pyridine in 2-methoxy ethanol (porogen) and copolymerizing thermally in the presence of 2-hydroxyethylmethacrylate (HEMA) and ethyleneglycol-dimethacrylate (EGDMA), using 2,2'-azobisisobutyronitrile (initiator). Again, IIP resins were also prepared on similar lines by utilizing ternary [uranium-non-vinylated ligand-vinylated ligand (4-vinyl pyridine)] complexes. Non-imprinted polymeric resins were identically prepared in both cases without the use of uranyl imprint ion. The percent enrichment and retention capacity studies showed significant imprinting effect in all cases. However, ion-imprinted polymeric resins formed with succinic acid (SA) or 5,7-dichloroquinoline-8-ol (DCQ) and 4-vinylpyridine (VP) alone gave quantitative enrichment and various parameters that influence the enrichment and elution were then optimized. The percent enrichment of uranium from synthetic seawater solutions was found to be 25.0 ± 0.5 and 83.0 ± 0.8 for SA-VP and DCQ-VP systems, respectively. The DCQ-VP-based IIP resins were successfully tested for the recovery of uranium from real seawater samples

  2. Adsorption characteristics of Ni2+ ion onto the diethylenetriaminepentaacetic acid-melamine / polyvinylidene fluoride blended resin

    Xiaodan Zhao, Laizhou Song, Jun He, Tingying Wu, Ying Qin

    2010-01-01

    Full Text Available The polyvinylidene fluoride blended resin (DTPA-MA/PVDF adsorbent prepared by anchoring the chelating agent diethylenetriaminepentaacetic acid (DTPA to the resin via the amide covalent bond reaction between DTPA and melamine(MA, was used to remove nickel from aqueous solutions. The blended resin was prepared using the combination of solution blending technique and phase inversion process. The blended resin was characterized by Fourier transform infrared spectroscopy (FTIR, 13C nuclear magnetic resonance spectroscopy (13C NMR, environmental scanning electron microscopy (ESEM and N2 adsorption/desorption experiments. The sorption data was fit to linearized adsorption isotherms of the Langmuir, Freundlich, and D-R isotherms models. The batch sorption kinetics was evaluated using pseudo-first-order, pseudo-second-order, and intraparticle diffusion kinetic reaction models. ΔH° is less than 0, ΔG° is lower than 0, and ΔS° is greater than 0, which shows that the adsorption of Ni(II by the blended resin is a spontaneous, exothermic process. The adsorption isotherm fits better to the Langmuir isotherm model and the pseudo-second-order kinetics model gives a better fit to the batch sorption kinetics. The adsorption mechanism is assumed to be ion exchange between the nickel ion and the polyamino polycarboxylic acid chelating group of the blended resin.

  3. Chelating resin from functionalization of chitosan with complexing agent 8-hydroxyquinoline: application for metal ions on line preconcentration system

    This study describes the functionalization of biopolymer chitosan, using the complexing agent 8-hydroxyquinoline (oxine) by reaction of diazotization. The chelating resin was characterized by degree of deacetylation, infrared, Raman spectroscopy. The efficiency of the chelating resin and accuracy of the proposed method was evaluated by the metal ion recovery technique in the analysis of potable water, lake water, seawater and a certified sample of oyster tissue. The metal ions Cd(II) and Cu(II) in the samples were previously enriched in a minicolumn and flow injection flame atomic absorption spectrometry (FI-FAAS) determined the concentrations of the analytes. The chelating resin exhibited high selectivity for Cd(II) at pH 7 and for Cu(II) at pH 10. The eluent concentration was tested by the use of HNO3 in concentrations of 0.1-3 mol l-1 maximum response was obtained at 0.5 mol l-1 for Cd(II) and Cu(II), with R.S.D. values of 0.4%. The analytes gave relative standard deviations (R.S.D.) of 1.5 and 0.7% for solutions of Cd(II) and Cu(II), respectively (n = 7) containing 20 μg l-1 of the metal ions, defining a high reproducibility. The limits of detection (LOD) were 0.1 μg l-1 for Cd(II) and 0.4 μg l-1 for Cu(II). The analytical properties of merit were obtained using the parameters previously optimized with preconcentration time of 90 s. The chelating resin showed chemical stability within a wide range of pH and the efficiency was not altered for the preconcentration of the metal ions during all the experiments

  4. Synthesis, characterization and application of a new chelating resin for solid phase extraction, preconcentration and determination of trace metals in some dairy samples by flame atomic absorption spectrometry.

    Daşbaşı, Teslima; Saçmacı, Şerife; Çankaya, Nevin; Soykan, Cengiz

    2016-11-15

    In this study, a simple and rapid solid phase extraction/preconcentration procedure was developed for determination of Cd(II), Co(II), Cr(III), Cu(II), Fe(III), Mn(II), Pb(II), and Zn(II) trace metals by flame atomic absorption spectrometry (FAAS). A new chelating resin, poly(N-cyclohexylacrylamide-co-divinylbenzene-co-2-acrylamido-2-methyl-1-propanesulfonic acid) (NCA-co-DVB-co-AMPS) (hereafter CDAP) was synthesized and characterized. The influences of the analytical parameters such as pH of the sample solution, type and concentration of eluent, flow rates of the sample and eluent, volume of the sample and eluent, amount of chelating resin, and interference of ions were examined. The limit of detection (LOD) of analytes were found (3s) to be in the range of 0.65-1.90μgL(-1). Preconcentration factor (PF) of 200 and the relative standard deviation (RSD) of ⩽2% were achieved (n=11). The developed method was applied for determination of analytes in some dairy samples and certified reference materials. PMID:27283608

  5. The recovery of by-product uranium from wet process phosphoric acid solutions using selective ion exchange resins

    The extraction of uranium from phosphoric acid using two types of ion exchange resin is reported. Levextrel-type resins containing the synergistic mixture di-2-ethyl hexyl phosphoric acid - tri-octyl phosphine oxide readily extract uranium in the presence of impurities, though Fe2+ inhibits sorption. Elution is possible using 3M H3PO4 at 40 deg C in the presence of Fe2+. Duolite ES 467, a commercially available chelating resin containing aminophosphonic acid groups, extracts uranium in the four- and six-valency state. The kinetics of this resin are slow but improve substantially at 60 deg C. Elution is efficient using (NH4)2CO3 at 20 deg C to produce an enriched product. A conceptual flowsheet is given to illustrate a simple process route using Duolite ES 467. (author)

  6. Adsorption performances and mechanisms of the newly synthesized N,N'-di (carboxymethyl) dithiocarbamate chelating resin toward divalent heavy metal ions from aqueous media

    N,N'-di (carboxymethyl) dithiocarbamate chelating resin (PSDC) was synthesized by anchoring the chelating agent of N,N'-di (carboxymethyl) dithiocarbamate to the chloromethylated PS-DVB (Cl-PS-DVB) matrix, as a new adsorbent for removing divalent heavy metal ions from waste-stream. The physicochemical structures of Cl-PS-DVB and PSDC were elaborately characterized using Fourier transform infrared spectroscopy (FT-IR), elemental analysis (EA), and were further morphologically characterized using BET and BJH methods. The adsorption performances of PSDC towards heavy metals such as Cu(II), Pb(II) and Ni(II) were systematically investigated, based upon which the adsorption mechanisms were deeply exploited. For the above target, the classic batch adsorption experiments were conducted to explore the kinetics and isotherms of the removal processes with pH-value, initial concentration, temperature, and contact time as the controlling parameters. The kinetic and isotherm data could be well elucidated with Lagergren-second-order equation and Langmuir model respectively. The strong affinity of PSDC toward these target soft acids could be well demonstrated with the electrostatic attraction and chelating interaction caused by IDA moiety and sulphur which were namely soft bases on the concept of hard and soft acids and bases (HASB). Thermodynamic parameters, involving ΔHo, ΔSo and ΔGo were also calculated from graphical interpretation of the experimental data. The standard heats of adsorption (ΔHo) were found to be endothermic and the entropy change values (ΔSo) were calculated to be positive for the adsorption of Cu(II), Pb(II) and Ni(II) ions onto the tested adsorbents. Negative values of ΔGo indicated that adsorption processes for all tested metal ions onto PSDC were spontaneous.

  7. Mechanisms of oxide dissolution by acid chelating agents

    In this paper, the different possible rate controlling processes in the dissolution of metallic oxides are examined. In particular, the following situations are assessed: mass-transfer control; coupling of mass-transfer and reactions at the interface; interface equilibration with the solution; various interface disruption and reconstruction phenomena. For each of the above mentioned cases, the influence of variables such as reagent concentration, temperature, pH, fluid hydrodynamics and general and specific catalysts is discussed. Depending upon the particular situation it is found that a more rational basis for the development of reagent is given by these considerations. The influence of chelating agents on both the thermodynamics and kinetics of the process is discussed, and the results of experimental studies in batch on magnetite and various ferrites are presented and discussed. For this purpose, several reagents were studied, including some very effective ones like thioglycolic acid, and others commonly used in actual decontamination, like ethylenediaminetetraacetic acid and oxalic acid. The relation to other (reductive) chemical decontamination procedures is discussed. The relevance of these studies to decontamination of metallic surfaces is discussed

  8. Synthesis of magnetic chelating resins functionalized with tetraethylenepentamine for adsorption of molybdate anions from aqueous solutions

    Magnetic resins were synthesized through polymerization of glycidyl methacrylate (GMA) in the presence of divinylbenzene (DVB) or N,N'-methylenebisacrylamide (MBA) as hydrophobic or hydrophilic crosslinker, respectively and in presence of suspended magnetite particles. The resins containing (DVB or MBA) as crosslinker were immobilized with tetraethylenepentamine (TEP) to give the amino resins, GMA/DVB/TEP (R1-en) and GMA/MBA/TEP (R2-en), respectively. The uptake behavior of the two resins was studied towards molybdate anions and uptake capacities of 4.24 and 6.18 mmol/g [as (Mo(VI)] were obtained using (R1-en) and (R2-en). Kinetic studies showed that the adsorption followed the pseudo-second-order model pointing the influence of the textural properties of the resin on the rate of adsorption. Thermodynamic data indicated an endothermic adsorption process. The uptake of Mo(VI) and regeneration of the resins were also studied using the column method. Regeneration efficiency up to 90-96% was reached using ammonia buffer

  9. A new chelating ion-exchanger containing p-bromophenylhydroxamic acid as functional group

    A new chelating resin based on macroreticular acrylonitrile-divinylbenzene copolymer and containing hydroxamic acid functional groups has been synthesized. It is highly-stable in acidic and alkaline solutions. The sorption characteristics of Cu(II), Cd(II), Pb(II), Zn(II), U(VI), Cr(VI), V(V), Co(II), Ni(II), Ca(II) and Mg(II) have been investigated over the pH range 1.0-6.0. The effect of various electrolytes at different ionic strengths on the Ksub(d) values for Cu(II), Cd(II), Pb(II) and Zn(II) has been studied systematically. Chromatographic separations of copper(II) and nickel(II) from cobalt(II), and of uranium(VI) from chromium(VI) by selective sorption at controlled pH, have been developed. The ion-exchanger can be used for purification of inorganic salts, and analysis of brass and bauxite. (author)

  10. Microwave assisted facile one-pot synthesis of 188Re-complex using a tetrahydroborate exchange resin. A bifunctional chelating agent for radiopharmaceuticals

    A facile one-pot synthesis of 188Re-complex as a bifunctional chelating agent for the preparation of therapeutic radiopharmaceuticals was accomplished with good labeling yields and radiochemical purity by using a tetrahydroborate exchange resin as a reducing agent for a disulfide ligand as well as the [188Re] perrhenate ion under microwave irradiation. (author)

  11. Potentiometric studies on mixed-ligand chelates of uranyl ion with carboxylic acid phenolic acids

    Mixed ligand complexes of UO22+ with bidentate carboxylic and phenolic acids have been studied potentiometrically at 30 ± 0.1degC and μ=0.2M (NaClO4). 1:1 and 1:2 complexes of UO22+ with phthalic acid (PTHA), maleic acid (MAE), malonic acid (MAL), quinolinic acid (QA), 5-sulphosalicylic acid (5-SSA), salicylic acid (SA), and only 1:1 complexes in the case of mandelic acid (MAD) have been detected. The formation of 1:1:1 mixed ligand complexes has been inferred from simultaneous equilibria in the present study. The values of ΔlogK, Ksub(DAL), Ksub(2LA) or Ksub(2AL) for the ternary complexes have been calculated. The stabilities of mixed ligand complexes depend on the size of the chelate ring and the stabilities of the binary complexes. (author). 15 refs

  12. Development of a treatment process for the removal of heavy metals from raw water for drinking water supply using chelating ion exchange resins. Subproject 1. Final report; Entwicklung der Verfahrenstechnik zur Eliminierung von Schwermetallen aus Rohwaessern zur Trinkwassergewinnung mit chelatbildenden Kationenaustauscherharzen zur technischen Reife. Teilprojekt 1. Abschlussbericht

    Overath, H.; Stetter, D.; Doerdelmann, O.

    2002-07-01

    Chelating cation exchange resins with iminodiacetic acid group (Lewatit TP 207 and Amberlite IRC 748) were tested for the removal of heavy metals in a drinking water treatment plant. The pilot scale filtration experiments were conducted by varying the operating conditions, such as flow rate and feed concentrations. Heavy metal concentrations (nickel, lead, cadmium, zinc) in the feed were adjusted between 20 and 200 {mu}g/L. Different methods for regeneration and conditioning of the resins were developed and investigated. Finally the ion exchange resins were tested according to German health regulations for ion exchangers in drinking water treatment. (orig.)

  13. Production of large quantities of 90Y by ion-exchange chromatography using an organic resin and a chelating agent

    The performance of a system composed of an organic cation exchanger (Dowex 50Wx8) and a chelating agent (EDTA) previously described for the successful production of 90Y via a 90Sr/90Y generator is assessed under dynamic conditions. In an attempt to overcome the established limitation of ion-exchange resins for the separation of subcurie quantities of activity, 90Y is repeatedly isolated from an 11.8-GBq (320 mCi) 90Sr cow using a three-column tandem arrangement. The high recovery and radionuclidic purity obtained for 90Y and the parameters of the separation (time, eluant concentration, pH and flow rate range) strongly suggest that Ci quantities of 90Y can be handled satisfactorily by the ion-exchange method. No replacement or treatment of the cow, low waste generation and 90Sr losses less than 0.1% after each run were observed during the present study which, in combination with the low cost of this resin, may result in an attractive alternate method for the production of large quantities of 90Y.

  14. Determination of rare-earth elements in environmental water using chelating resin disk separation/ICP-MS

    A pre-concentration method for rare-earth elements in environmental water samples using chelating resin disk was developed. All rare-earth elements plus Th and U in environmental water samples were determined by ICP-MS. The preconcentration of all rare-earth elements, (Th and U) and the removal of major elements in seawater, such as alkali and alkaline- earth elements, could be carried out quickly by adjusting the sample's pH to 3. By this method barium could be removed along with other alkaline-earth elements from the sample. This reduced the interference of BaO when using ICP-MS, which allowed the analysis of europium with good precision. Using this method rare-earth elements in four environmental standard samples (river water standard sample, JAC0031 (Japan Society for Analytical Chemistry), SLRS-3 (NRC Canada), seawater standard sample CASS-3, NASS-4 (NRC Canada)) and five environmental samples in Aomori (seawater 1, sea mingled with brackish water 3, fresh water 1) were measured. (author)

  15. Comparison of anion exchange resins for recovering plutonium from nitric acid waste

    Microreticular and macroreticular anion exchange resins were compared for their capability of recovering plutonium from nitric acid waste streams. Plutonium breakthrough capacity and elution behavior of the resins were determined as a function of resin properties. Small-bead microreticular resins with a polystyrene matrix containing 4% divinylbenzene cross-linkage showed the best performance. Of the 20- to 50-mesh resins, the macroreticular resin, Amberlite IRA-938, gave the highest plutonium breakthrough capacity and eluted plutonium the fastest

  16. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Acrylamide-acrylic acid resins. 176.110 Section 176.110 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: PAPER AND PAPERBOARD COMPONENTS Substances for Use Only as Components of Paper...

  17. 21 CFR 175.260 - Partial phosphoric acid esters of polyester resins.

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Partial phosphoric acid esters of polyester resins... of polyester resins. Partial phosphoric acid esters of polyester resins identified in this section... prescribed conditions: (a) For the purpose of this section, partial phosphoric acid esters of...

  18. Uptake of lanthanides by sulphonated phosphinic acid resin from acid medium

    Management of High Level Radioactive Liquid Waste (HLW) generated during reprocessing of spent nuclear fuel, is a challenging task considering acidic nature of waste as well as presence of long lived radioactive elements. Apart from actinides the Lanthanides comprise 40% of total fission products formed. Presently there is growing interest for the separation of actinides and lanthanides for effective waste management. Ion Exchange is a better separation technique than solvent extraction, while encountering dilute solutions. Literature survey shows ion exchange resins with phosphorus ligands are very effective in separation of actinides from varying concentrations of nitric acid. This study is undertaken to evaluate the performance of phosphinic and sulphonated phosphinic acid resin for the uptake of Europium and Neodymium lanthanides from nitric acid and their performance was compared with commercially available strong cation exchanger Dowex 50W. Phosphinic acid and sulphonated phosphinic acid resins has been synthesized and characterized as indicated in our earlier work. For extraction studies 250 mg of resin was given contact with 5 ml of solution for 24 hours. In all the cases analysis were carried out by ICP-AES. The results obtained are tabulated in Table. As indicated in the paper it is clear that sulphonated phosphinic acid resin shows better performance compared with Dowex 50W and phosphinic acid resin. It is also observed that there is a decrease in percentage of extraction with increase in acidity

  19. Adsorption of Cu(II), Co(II), and Ni(II) ions by modified magnetic chitosan chelating resin

    Cross-linked magnetic chitosan-isatin Schiff's base resin (CSIS) was prepared for adsorption of metal ions. CSIS obtained was investigated by means of FTIR, 1H NMR, wide-angle X-ray diffraction (WAXRD), magnetic properties and thermogravimetric analysis (TGA). The adsorption properties of cross-linked magnetic CSIS resin toward Cu2+, Co2+ and Ni2+ ions were evaluated. Various factors affecting the uptake behavior such as contact time, temperature, pH and initial concentration of the metal ions were investigated. The kinetic parameters were evaluated utilizing the pseudo-first-order and pseudo-second-order. The equilibrium data were analyzed using the Langmuir, Freundlich, and Tempkin isotherm models. The adsorption kinetics followed the mechanism of the pseudo-second-order equation for all systems studied, evidencing chemical sorption as the rate-limiting step of adsorption mechanism and not involving a mass transfer in solution. The best interpretation for the equilibrium data was given by Langmuir isotherm, and the maximum adsorption capacities were 103.16, 53.51, and 40.15 mg/g for Cu2+, Co2+ and Ni2+ ions, respectively. Cross-linked magnetic CSIS displayed higher adsorption capacity for Cu2+ in all pH ranges studied. The adsorption capacity of the metal ions decreased with increasing temperature. The metal ion-loaded cross-linked magnetic CSIS were regenerated with an efficiency of greater than 88% using 0.01-0.1 M ethylendiamine tetraacetic acid (EDTA).

  20. Adsorption of Cu(II), Co(II), and Ni(II) ions by modified magnetic chitosan chelating resin.

    Monier, M; Ayad, D M; Wei, Y; Sarhan, A A

    2010-05-15

    Cross-linked magnetic chitosan-isatin Schiff's base resin (CSIS) was prepared for adsorption of metal ions. CSIS obtained was investigated by means of FTIR, (1)H NMR, wide-angle X-ray diffraction (WAXRD), magnetic properties and thermogravimetric analysis (TGA). The adsorption properties of cross-linked magnetic CSIS resin toward Cu(2+), Co(2+) and Ni(2+) ions were evaluated. Various factors affecting the uptake behavior such as contact time, temperature, pH and initial concentration of the metal ions were investigated. The kinetic parameters were evaluated utilizing the pseudo-first-order and pseudo-second-order. The equilibrium data were analyzed using the Langmuir, Freundlich, and Tempkin isotherm models. The adsorption kinetics followed the mechanism of the pseudo-second-order equation for all systems studied, evidencing chemical sorption as the rate-limiting step of adsorption mechanism and not involving a mass transfer in solution. The best interpretation for the equilibrium data was given by Langmuir isotherm, and the maximum adsorption capacities were 103.16, 53.51, and 40.15mg/g for Cu(2+), Co(2+) and Ni(2+) ions, respectively. Cross-linked magnetic CSIS displayed higher adsorption capacity for Cu(2+) in all pH ranges studied. The adsorption capacity of the metal ions decreased with increasing temperature. The metal ion-loaded cross-linked magnetic CSIS were regenerated with an efficiency of greater than 88% using 0.01-0.1M ethylendiamine tetraacetic acid (EDTA). PMID:20122793

  1. Adsorption of Cu(II), Co(II), and Ni(II) ions by modified magnetic chitosan chelating resin

    Monier, M., E-mail: monierchem@yahoo.com [Department of Chemistry, Drexel University, Philadelphia, PA (United States); Chemistry Department, Faculty of Science, Mansoura University, Mansoura (Egypt); Ayad, D.M. [Chemistry Department, Faculty of Science, Mansoura University, Mansoura (Egypt); Wei, Y., E-mail: weiyen@drexel.edu [Department of Chemistry, Drexel University, Philadelphia, PA (United States); Sarhan, A.A. [Chemistry Department, Faculty of Science, Mansoura University, Mansoura (Egypt)

    2010-05-15

    Cross-linked magnetic chitosan-isatin Schiff's base resin (CSIS) was prepared for adsorption of metal ions. CSIS obtained was investigated by means of FTIR, {sup 1}H NMR, wide-angle X-ray diffraction (WAXRD), magnetic properties and thermogravimetric analysis (TGA). The adsorption properties of cross-linked magnetic CSIS resin toward Cu{sup 2+}, Co{sup 2+} and Ni{sup 2+} ions were evaluated. Various factors affecting the uptake behavior such as contact time, temperature, pH and initial concentration of the metal ions were investigated. The kinetic parameters were evaluated utilizing the pseudo-first-order and pseudo-second-order. The equilibrium data were analyzed using the Langmuir, Freundlich, and Tempkin isotherm models. The adsorption kinetics followed the mechanism of the pseudo-second-order equation for all systems studied, evidencing chemical sorption as the rate-limiting step of adsorption mechanism and not involving a mass transfer in solution. The best interpretation for the equilibrium data was given by Langmuir isotherm, and the maximum adsorption capacities were 103.16, 53.51, and 40.15 mg/g for Cu{sup 2+}, Co{sup 2+} and Ni{sup 2+} ions, respectively. Cross-linked magnetic CSIS displayed higher adsorption capacity for Cu{sup 2+} in all pH ranges studied. The adsorption capacity of the metal ions decreased with increasing temperature. The metal ion-loaded cross-linked magnetic CSIS were regenerated with an efficiency of greater than 88% using 0.01-0.1 M ethylendiamine tetraacetic acid (EDTA).

  2. Chelation in metal intoxication X: influence of different polyaminocarboxylic acids and thiol chelators in the excretion and tissue distribution of 54Mn in rat

    The influence of some selected polyaminocarboxylic acids and thiol metal binding agents on the urinary and faecal excretions of 54Mn and on the tissue distribution of 54Mn in 54MnC12 administered rats was studied to find a suitable chelating drug for Mn poisoning. HEDTA, CDTA, DTPA and TTHA were highly successful in enhancing the excretion of 54Mn and reducing the tissue levels of 54Mn in rats. The thiol chelators viz. D L-penicillamine, N-acetyl D L-penicillamine and DMS could neither influence the excretion nor the tissue distribution of 54Mn suggesting poor affinity of the metal towards sulfhydryl groups

  3. Grafting iminodiacetic acid on silica nanoparticles for facilitated refolding of like-charged protein and its metal-chelate affinity purification.

    Liu, Hu; Dong, Xiaoyan; Sun, Yan

    2016-01-15

    A series of highly charged nanoscale chelators were fabricated by grafting of poly(glycidyl methacrylate-iminodiacetic acid) (pGI) chains with iminodiacetic acid (IDA) chelating group on silica nanoparticles (SNPs) via atom transfer radical polymerization (ATRP). The nanoscale chelators, denoted as SNPs-pGI, possessed a nickel ion chelating capacity as high as 2800 μmol/g, 50 times higher than the IDA-modified Sepharose FF (IDA-Sepharose) resin reported in literature and offered a high affinity binding capacity for hexahistidine-tagged enhanced green fluorescence protein (6 × His-EGFP) after nickel ion loading. More importantly, the anionic SNPs-pGI of high charge densities displayed much better performance than IDA-Sepharose in facilitating the refolding of like-charged 6 × His-EGFP from inclusion bodies (IBs). For example, for 0.2mg/mL 6 × His-EGFP IB refolding, addition of 6.2 μL/mL SNPs-pGI with the highest charge density led to a refolding yield of 90%, over 43% higher than that obtained with 460 μL/mL IDA-Sepharose. It is notable that the much higher efficiency of the nanoscale chelator was obtained with a chelator consumption corresponding to only 1.4% of IDA-Sepharose. Moreover, the highly charged SNPs-pGI could efficiently facilitate the refolding of 6 × His-EGFP at higher IB concentrations (0.4 and 0.8 mg/mL). After refolding, nickel ions addition led to the recovery of the refolded 6 × His-EGFP with high yield (80%), purity (96%) and enrichment ratio (1.8). All the results suggest that the SNPs-pGI of high charge densities were promising for cost-effective recovery of His-tagged proteins expressed as IBs with the integrative like-charge facilitated refolding and metal-chelate affinity purification strategy. PMID:26755413

  4. Esterification of levulinic acid with butanol over ion exchange resins

    Tejero Iborra, M. Àngels; Ramírez Rangel, Eliana; Fité Piquer, Carles; Tejero Salvador, Xavier; Cunill García, Fidel

    2016-01-01

    Alkyl levulinates are biobased chemicals with a great number of applications and great biofuel potential for blending to conventional diesel or gasoline. The present work focuses on the liquid-phase synthesis of butyl levulinate (BL) by esterification of levulinic acid (LA) with 1-butanol (BuOH) using a set of acidic ion-exchange resins. Experiments were performed at 80 °C and 2.5 MPa in a batch reactor by using an initial molar ratio AL/BuOH of 1/3 and a catalyst loading of 0.8%. It has been...

  5. INTERACTION OF AMINO ACID WITH ION EXCHANGE RESIN Ⅲ.FURTHER INVESTIGA TION OF SUPEREQUIVALENT ADSORPTION MECHANISM OF AMINO ACID ON ION EXCHANGE RESIN

    ZHANGHui; SHAOTong; 等

    1994-01-01

    The adsorption isotherms of glycine,alanine and oxidized glutathion on strong acid cation and strong base anion exchange resins from aqueous solutions were measured and the superequivalent adsorptions of glycine and alanine observed.The infrared spectra of glycine adsorbed on the cation and the anion exchange resins,001×7 and 201×7,were measured.From these results,it is concluded that the amino acid adsorption on the ion exchange resin proceeds not only through ion exchange and proton transfer mechanisms,but also through aminecarboxylate interaction between the adsorbed amino acid molecules,and the formation of second layer of amino acid molecules is the mechanism of superequivalent adsorption of amino acid,the carboxylate or amine groups of the first layer of amino acid molecules on the ion exchange resin act as the exchange sites for the second layer of amino acid molecules.

  6. Determination of uranium in environmental matrices by chelation ion chromatography using a high performance substrate dynamically modified with 2,6-pyridinedicarboxylic acid

    Chelation ion chromatography, involving a high efficiency neutral polystyrene-divinylbenzene resin dynamically coated with 2,6-pyridinedicarboxylic acid, has been developed as a novel technique for the quantitative determination of uranium in complex matrices. An isocratic separation method, using an eluent consisting of 1M KNO3, 0.5 M HNO3 and 0.1 mM 2,6-pyridinedicarboxylic acid, allowed the uranyl ion to elute away from matrix interferences in under ten minutes. Detection was achieved using an Arsenazo III post column reaction system. Good recoveries were obtained from spiked mineral water and sea water and the standard addition curves produced good linearity (r2 > 0.997) with a detection limit, calculated as twice baseline noise, of 20 μg L-1. The procedure was applied to the determination of trace uranium in standard reference water and sediment samples. The results obtained compared well with the certified values for uranium. (orig.)

  7. REMOVAL OF ACID-SOLUBLE LIGNIN FROM BIOMASS EXTRACTS USING AMBERLITE XAD-4 RESIN

    Thomas James Schwartz; Martin Lawoko

    2010-01-01

    This paper describes a method for the removal of acid-soluble lignin from acid hydrolyzed hemicelluloses extracted from a mixture of northern hardwood chips, by using Amberlite XAD-4 resin, which was shown to remove 100% of furan derivatives and 90% of acid-soluble lignin. Subsequent fermentation of the resin treated hydrolyzates gave ethanol yields as high as 97% of theoretical and showed a marked increase in fermentation rate. Regeneration of resin performed with 75% acetone was 85% efficie...

  8. Reactive polymers: part I - Novel polystyrene-anchored copper (II), nickel (II), cobalt (II), iron (III), zinc (II), cadmium (II), molybdenum (VI) and uranium (VI) complexes of the chelating resin containing thiosemicarbazone

    A new chelating resin containing thiosemicarbazone has been synthesized by the reaction of aldehydopolystyrene and thiosemicarbazide. The polystyrene bound thiosemicarbazone reacts with salicylaldehyde leading to the formation of a new Schiff base chelating resin which reacts with sodium monochloroacetate and gives the polymer bound S-acetatothiosemicarbazone. The new chelating resin forms complexes of the types PS-LCuX·S, PS-LNiX·3S, PS-LHNi(acac)2, PS-LCoX·3S, PS-LFeX2·2S, PS-LZnX·S, PS-LCdX·S, PS-LMoO2(acac) and PS-LUO2X·S (where PS-LH = polymeranchored ligand; S = DMF or CH3OH; X=Cl or CH3COO- and acacH = acetylacetone). The chelating resins and complexes have been characterized by elemental analysis, IR and electronic spectra and magnetic measurements. The Cu(II), Ni(II), Co(II), and Fe(III) complexes are paramagnetic while the Zn(II), Cd(II), Mo(VI) and U(VI) complexes are diamagnetic. The IR data indicate the thioenolization of the ligand in the complexes (except in PS-LHNi(acac)2 where it behaves as a neutral bidentate ligand). (author). 24 refs., 2 tabs

  9. Diethylentriaminepenta acetic acid glucose conjugates as a cell permeable iron chelator

    Mona Mosayebnia

    2014-01-01

    Full Text Available Objective: To find out whether DTPA-DG complex can enhance clearance of intracellular free iron. Materials and Methods: Diethylenetriaminepentaacetic acid-D-deoxy-glucosamine (DTPA-DG was synthesized and examined for its activity as a cell-permeable iron chelator in human hepatocellular carcinoma (HEPG2 cell line exposed to high concentration of iron sulfate and compared with deferoxamine (DFO, a prototype iron chelator. The effect of DTPA-DG on cell viability was monitored using the 3-(4,5-dimethythiazol-2-yl-2,5-diphenyl tetrazolium bromide MTT assay as well. Results: There was a significant increase of iron level after iron overload induction in HEPG2 cell culture. DTPA-DG presented a remarkable capacity to iron burden reducing with estimated 50% inhibitory concentration value of 65.77 nM. In fact, glycosyl moiety was gained access of DTPA to intracellular iron deposits through glucose transporter systems. Conclusion: DTPA-DG, more potent than DFO to sequester deposits of free iron with no profound toxic effect. The results suggest the potential of DTPA-DG in chelating iron and permitting its excretion from primary organ storage.

  10. Thermoanalytical Study and Kinetics of New 8-Hydroxyquinoline 5-sulphonic Acid-Oxamide-Formaldehyde Terpolymer Resins

    Singru, Rajesh N.; Anil B. Zade; Gurnule, Wasudeo B.

    2009-01-01

    The terpolymer resins (8-HQ5-SAOF) have been synthesized by the condensation of 8-hydroxyquinoline 5-sulphonic acid (8-HQ5-SA) and oxamide (O) with formaldehyde (F) in the presence of acid catalyst and using varied molar proportion of the reacting monomers. The synthesized terpolymer resins have been characterized by different physico-chemical techniques. Thermogravimetric analysis of all terpolymer resins in present study have been carried out by non-isothermal thermogravimetric analysis tec...

  11. High-performance chelation chromatography of metal ions on sorbents with grafted iminodiacetic acid

    Chromatographic behavior of some alkaline earth, transition, heavy (including uranium) and rare earth metal ions on a group of complexing sorbents, containing surface functional groups of imidodiacetic acid, was studied. Conditions, under which metal retention is determined by complexing on the sorbent surface, were defined and main principles of a new variant of liquid chromatography, i.e. high-performance chelating chromatography of metal ions (HPCCI) were formulated. It is shown that under optimal conditions metal retention correlates linearly in bilogarithmic coordinates with stability constants of the relevant metal complexes. Potentialities of HPCCI analytic application to analysis of objects featuring complex composition were considered

  12. Meso-2,3-dimercaptosuccinic acid: from heavy metal chelation to CdS quantum dots

    Sevinç, Esra; Ertaş, F. Sinem ; Ulusoy, Gülen ; Acar, Havva Yağcı; Özen, Can

    2012-01-01

    DMSA (meso-2,3-dimercaptosuccinic acid) a prescription drug and a heavy-metal chelating agent, is shown to act both as a sulfur source and a capping agent in the aqueous synthesis of CdS quantum dots under mild conditions. Release of sulfur from DMSA depends on the solution pH and the reaction temperature. Combination of 70 C and pH 7.5 was determined as the best reaction conditions for a well-controlled reaction. Changing the SH/Cd ratio from 2.5 to 7 provides QDs emitting from ...

  13. Fast removal of heavy metal ions and phytic acids from water using new modified chelating fiber

    Li Xu; Jin Nan Wang; Ying Meng; Ai Min Li

    2012-01-01

    The graft copolymerization of acrylic acid (AA) onto polyethylene glycol terephthalate (PET) fiber initiated by benzoy peroxide (BPO) was carried out in heterogeneous media.Moreover,modification of the grafted PET fiber (PET-AA) was done by changing the carboxyl group into acylamino group through the reaction with dimethylamine.The modified chelating fiber (NDWJN 1) was characterized using elementary analysis,SEM and FT-IR spectroscopy.Adsorption kinetic curves indicated that NDWJN1 could fast remove heavy metal ions and phytic acids from water effectively.Furthermore,batch kinetic studies indicated that heavy metal ions adsorbed to NDWJN1 could be fitted well by both pseudo-first-order and pseudo-second-order adsorption equations,but the intra-particle diffusion plaved a dominant role in the adsorption of phvtic acids.

  14. Direct acid elution of anionic exchange resins for recovery of uranium

    A process as disclosed for recovering uranium values from a carbonate leach solution which comprises directly eluting a column of resin onto which uranium has been sorbed by flowing a concentrated acidic eluant through the column without preconditioning and/or post-conditioning the resin. The concentrated acidic eluant may be flowed upward or, preferably, downward through the column

  15. Bifuncitonal phosphinic acid resins for the complexation of lanthanides and actinides

    Phosphinic acid ion exchange/redox resins are synthesized by the reaction between polystyrene beads and phosphorus trichloride followed by base hydrolysis. The reaction requires a temperature of 730C for full functionalization to occur. The effect of lower functionalization temperatures on resin acid capacity was determined and the concomitant effect on ion exchange investigated. The acid capacity was found to vary from 1.68 mequiv/g to 4.79 mequiv/g in the functionalization temperature range studied (150C to 730C). The present resin sites loaded with zinc ions is independent of the actual capacity. The extracting ability of the phosphinic acid resin for europium, thorium, uranium, americium, and plutonium was examined as a function of acid concentration from acid nitrate solutions both at varying and constant ionic strength. The phosphinic resins show better extraction for these ions than the sulfonic resins, especially from high acid solution (4M HNO3) due to the superior coordination ability of the phosphoryl oxygen. They also show a higher selectivity for the ions tested over sodium. For example, under conditions where sulfonic resins absorb 85% of the plutonium in solution, the phosphinic acid resins absorb 99.7%

  16. Thermochemical comparisons of homogeneous and heterogeneous acids and bases. 1. Sulfonic acid solutions and resins as prototype Broensted acids

    Arnett, E.M.; Haaksma, R.A.; Chawla, B.; Healy, M.H.

    1986-08-06

    Heats of ionization by thermometric titration for a series of bases (or acids) can be used to compare solid acids (or bases) with liquid analogues bearing the same functionalities in homogeneous solutions. The method is demonstrated for Broensted acids by reacting a series of substituted nitrogen bases with solutions of p-toluenesulfonic acid (PTSA) in acetonitrile and with suspensions of the microporous polymeric arylsulfonic acid resin-Dowex 50W-X8 in the same solvent. Under well-controlled anhydrous conditions there is a good correlation (r = 0.992) between the heats of reaction of the bases with the homogeneous and heterogeneous acid systems, but the homogeneous system gives a more exothermic interaction by 3-4 kcal mol/sup -1/ for a series of 29 substituted pyrimidines, anilines, and some other amines. This difference may be attributed to homohydrogen bonding interactions between excess acid and sulfonate anion sites which are more restricted geometrically in the resin than in solution. Other factors which affect the enthalpy change for the acid-base interaction are the acid/base ratio, the water content of the sulfonic acid, the solvent, and the resin structure (e.g., microporous vs. macroporous). Steric hindrance in the base does not differentiate solid from homogeneous acid. In addition to the use of titration calorimetry, heats of immersion are reported for the Dowex-arylsulfonic acid resins and the Nafion-perfluorinated sulfonic acid resin in a series of basic liquids. The results are compared with each other and with those from a previous study of several varieties of coal.

  17. New method for studying the efficiency of chelating agents of the polyamine acid series for internal decontamination

    We followed the biological fate of a complex formed on one side with either a rare earth (cerium-144) or a transuranium element (plutonium-239), and on the other side with a chelating agent of the polyamino acid series (EDTA, BAETA, DTPA, TTHA). This method allowed to study: 1 - the in vivo stability of the various complexes and to compare them; 2 - the stability of the complexes as a function of the isotope - chelating agent weight relationships; 3 - the metabolism of the chelating agents resulting in stable complexes, i. e. DTPA and TTHA mainly. This simple method brought out the higher efficiency, of DTPA in chelating rare earths and plutonium and for therapeutic purposes. (authors)

  18. Protection of live bacteria from bile acid toxicity using bile acid adsorbing resins.

    Edwards, Alexander D; Slater, Nigel K H

    2009-06-12

    We previously demonstrated that a dry, room temperature stable formulation of a live bacterial vaccine was highly susceptible to bile, and suggested that this will lead to significant loss of viability of any live bacterial formulation released into the intestine using an enteric coating or capsule. We found that bile and acid tolerance is very rapidly recovered after rehydration with buffer or water, raising the possibility that rehydration in the absence of bile prior to release into the intestine might solve the problem of bile toxicity to dried cells. We describe here a novel formulation that combines extensively studied bile acid adsorbent resins with the dried bacteria, to temporarily adsorb bile acids and allow rehydration and recovery of bile resistance of bacteria in the intestine before release. Tablets containing the bile acid adsorbent cholestyramine release 250-fold more live bacteria when dissolved in a bile solution, compared to control tablets without cholestyramine or with a control resin that does not bind bile acids. We propose that a simple enteric coated oral dosage form containing bile acid adsorbent resins will allow improved live bacterial delivery to the intestine via the oral route, a major step towards room temperature stable, easily administered and distributed vaccine pills and other bacterial therapeutics. PMID:19490986

  19. Chelation Properties of Modified Humic Acids Toward Some Trivalent Lanthanide Ions

    Three kinds of humic acids, Fluka (I), Fluka (II), and Ega-chemie (III) were modified through condensation with formaldehyde to afford polymers I, II, and III, respectively. The chelation behavior of these modified humic acids polymers towards the trivalent lanthanide metal-ions, La3+, Ce3+, Nd3+, Sm3+, and Gd3+ was studied by a batch equilibration technique at 25 deg. C as a function of contact time, pH, counter ion and counter ion concentration. The highest metal-ion uptake of the three polymers was achieved at pH 7.0 and by using perchlorate as a counter ion. Results of the study have revealed that polymer II has the highest metal-ion uptake capacity, and that the metal-ion uptake falls in the order: Gd3+ > Sm3+ > Nd3+ > La3+ ≅ Ce3+

  20. Binding of Sr from milk by solid phase extraction with cryptand C222 sorbed on silica gel, cation exchange, chelating or adsorbent resins for simplified 90Sr analysis

    Several commercially available resins have been found to bind the bicyclic polyether cryptand C222 from aqueous acetonitrile solutions. The presence of C222 on some of these resins strongly improved their affinity for Sr, so that relatively small amounts of such resins sorbed Sr from milk. The resins investigated were silica gel, polyacrylic acid crosslinked with divinylbenzene (DVB), polystyrene crosslinked with divinylbenzene (PS-DVB) and PS-DVB containing sulphonate, aminomethylphosphonate, iminodiacetate and mercapto groups. The resins for which binding of C222 resulted in the largest improvement in Sr sorption from milk were PS-DVB containing mercapto groups (Chelite S) and silica gel (Si 60). Thus, 2 ml wet volume of either Chelite S containing 133 μmol of C222, or silica gel Si-60 containing 143 μmol of C222 sorbed 90 and 48%, respectively, of the Sr from 100-ml milk samples. As the sorption of Sr from milk by these systems is relatively slow, contact times of 24-36 h are required to attain these results. The Chelite S-C222 system separates Sr effectively from Cs and Ca. Under the conditions described here some 6% of the natural 40K in milk sorbs with Sr to the resin. Ba behaves similarly to Sr. 90Sr/90Y sorbed on the silica gel Si-60-C222 system can be measured directly and efficiently by liquid scintillation counting. If adequate specificity can be attained this system might provide a very simple method of determining 90Sr in milk

  1. Studies on the adsorption of boric acid on anion exchange resins, 8

    Borate-form anion exchange resin (type I) is repeatedly used between the process of boric acid adsorption at a low temperature (5 0C) and its desorption at a high temperature (80 0C), to control the boric acid concentration of the primary coolant in PWRs. The thermal stability of the borate form anion exchange resin is an important index for evaluating operational reliability of the processes in the long term. To determine the thermal stability of the resins, heat cycle tests were carried out using borate, OH-, and Cl- form resins. Average mole values (average n) of boric acid adsorbed per functional group of the ion exchange resin were not changed by heat cycling. Residual ratios of salt spiliting capacity of the borate form resins decreased in the range of 92 to 97 % for 0.00924 to 0.185 M boric acid solution after 1700 heat cycles. The ratios for OH- or Cl- form resins which were tested as a reference, were 70 and 95 % respectively. The thermal stability of the resin decreased with an increase in the pH value in the resin phase. (author)

  2. Simultaneous determination of trace elements in river-water samples by ICP-MS in combination with a discrete microsampling technique after enrichment with a chitosan-based chelating resin

    A new technique for the preconcentration of trace elements and matrix elimination with a chitosan-based chelating resin was proposed as a useful pretreatment prior to a measurement by inductively coupled plasma-mass spectrometry (ICP-MS). A small volume of the sample solution (80 μl) was discretely introduced into a nebulizer of ICP-MS using a segmented flow injection (SFI) system; a maximum of fifteen elements were simultaneously measured by a single injection. A chitosan-based chelating resin containing iminodiacetate (IDA) functional groups was used for matrix elimination and enrichment of analyte metal ions. Several metal ions, such as Al, Fe, Ni, Co, Cu, Zn, Ag, Cd, Pb and U, were quantitatively retained on the IDA chelating resin in a micro-column (resin: 1 ml) at pH 6, whereas Na, K, Mg and Ca were completely eluted from the column by washing with an ammonium acetate solution. The concentrations of 24 and 26 elements in river water certified reference materials, JAC 0031 and JAC 0032, respectively, were determined by the proposed SFI/ICP-MS system after pretreating the samples with the proposed technique, as well as without any pretreatment. The thus-obtained analytical data were evaluated by comparing them with the reference values, as well as with those obtained in other studies. (author)

  3. Simultaneous determination of trace elements in river-water samples by ICP-MS in combination with a discrete microsampling technique after enrichment with a chitosan-based chelating resin

    Lee, K.H.; Oshima, Mitsuko; Takayanagi, Toshio; Motomizu, Shoji [Department of Chemistry, Faculty of Science, Okayama University, Okayama (Japan)

    2000-07-01

    A new technique for the preconcentration of trace elements and matrix elimination with a chitosan-based chelating resin was proposed as a useful pretreatment prior to a measurement by inductively coupled plasma-mass spectrometry (ICP-MS). A small volume of the sample solution (80 {mu}l) was discretely introduced into a nebulizer of ICP-MS using a segmented flow injection (SFI) system; a maximum of fifteen elements were simultaneously measured by a single injection. A chitosan-based chelating resin containing iminodiacetate (IDA) functional groups was used for matrix elimination and enrichment of analyte metal ions. Several metal ions, such as Al, Fe, Ni, Co, Cu, Zn, Ag, Cd, Pb and U, were quantitatively retained on the IDA chelating resin in a micro-column (resin: 1 ml) at pH 6, whereas Na, K, Mg and Ca were completely eluted from the column by washing with an ammonium acetate solution. The concentrations of 24 and 26 elements in river water certified reference materials, JAC 0031 and JAC 0032, respectively, were determined by the proposed SFI/ICP-MS system after pretreating the samples with the proposed technique, as well as without any pretreatment. The thus-obtained analytical data were evaluated by comparing them with the reference values, as well as with those obtained in other studies. (author)

  4. REMOVAL OF ACID-SOLUBLE LIGNIN FROM BIOMASS EXTRACTS USING AMBERLITE XAD-4 RESIN

    Thomas James Schwartz

    2010-09-01

    Full Text Available This paper describes a method for the removal of acid-soluble lignin from acid hydrolyzed hemicelluloses extracted from a mixture of northern hardwood chips, by using Amberlite XAD-4 resin, which was shown to remove 100% of furan derivatives and 90% of acid-soluble lignin. Subsequent fermentation of the resin treated hydrolyzates gave ethanol yields as high as 97% of theoretical and showed a marked increase in fermentation rate. Regeneration of resin performed with 75% acetone was 85% efficient with respect to acid soluble lignin.

  5. Gas Chromatography Analysis of Resin and Fatty Acids from Laboratory Generated Bleach Plant Effluents

    Chhaya Sharma; S. Mohanty; S. Kumar; N.J. Rao

    2007-01-01

    Laboratory generated spent bleached liquor from the chlorination, caustic extraction stage of mixed wood kraft pulp processing has been analyzed both qualitatively and quantitatively for various resin & fatty acids by using GC. A number of resin acids,saturated and unsaturated fatty acids, chloro fatty and resin acid have been detected and their concentrations are estimated. The results are compared with results on different agriculture residue/hardwood pulps, which were reported earlier. The concentrations of various compounds detected have also been compared with their reported LC50 values.

  6. Influence of the Functionalization Degree of Acidic Ion-Exchange Resins on Ethyl Octyl Ether Formation

    Guilera, J.; Hanková, L. (Libuše); Jeřábek, K. (Karel); Ramírez, E.; Tejero, J.

    2014-01-01

    Ethyl octyl ether (EOE) can be obtained by the ethylation of 1-octanol by means of ethanol or diethyl carbonate over acidic ion-exchange resins. However, EOE formation has to compete with the less steric demanding formation of diethyl ether, by-product obtained from ethanol dehydration or diethyl carbonate decomposition. In the present work, the influence of the resin functionalization degree on EOE formation has been evaluated. A series of partially sulfonated resins were prepared by the sul...

  7. Studies concerning the anion ex-change resins catalyzed esterification of epichlorohydrin with organic acids

    E.I. Muresan

    2009-09-01

    Full Text Available The paper studies the esterification of carboxylic acids with epichlorohydrin over two macroporous strong base anion exchange resins with different polymer matrix. For both resins, the influence of reaction parameters (temperature, catalyst loading, molar ratio on the reaction rate and the yields of the two isomeric esters were investigated.

  8. Evaluation of anion exchange resins for plutonium-uranium separations in nitric acid

    Pellicular, macroreticular and microreticular (gel type) anion exchange resins were compared for separation of plutonium from nitric acid solutions of mixed plutonium-uranium. All the macroreticular resins were 20 to 50 mesh beads. Dowex 1-X4 gel resin was 50 to 80 mesh beads. The resins were held in glass columns with coarse glass frits at the bottom of the columns. The top of the columns contained 50 ml reservoirs. The flow rates were controlled at 4 cm3.min-1.cm-2. One-centimeter bore columns with 15-cm resin bed heights were used for the plutonium elution and breakthrough capacity experiments, whereas 1.7 cm bore columns with 20 cm bed heights were used for the uranium washing experiments. As Pellionex SAX (pellicular resin) and Amberlite IRA-93 (weak base macroreticular anion exchange resin) were found to have better uranium washing and plutonium eluating characteristics than any of the resins tested. However, the capacity of the pellicular resin was much lower than that of the other resins. (T.G.)

  9. Microbiology and biodegradation of resin acids in pulp mill effluents: a minireview.

    Liss, S N; Bicho, P A; Saddler, J N

    1997-07-01

    Resin acids, a group of diterpenoid carboxylic acids present mainly in softwood species, are present in many pulp mill effluents and toxic to fish in recipient waters. They are considered to be readily biodegradable. However, their removal across biological treatment systems has been shown to vary. Recent studies indicate that natural resin acids and transformation products may accumulate in sediments and pose acute and chronic toxicity to fish. Several resin acid biotransformation compounds have also been shown to bioaccumulate and to be more resistant to biodegradation than the original material. Until recently, the microbiology of resin-acid degradation has received only scant attention. Although wood-inhabiting fungi have been shown to decrease the level of resin present in wood, there is no conclusive evidence that fungi can completely degrade these compounds. In contrast, a number of bacterial isolates have recently been described which are able to utilize dehydroabietic or isopimaric acids as their sole carbon source. There appears to be an unusually high degree of substrate specificity with respect of the utilization of abietane congeners and the presence of substituents. Pimaranes do not appear to be attacked to the same extent as the abietanes. This paper reviews the occurrence, chemistry, toxicity, and biodegradation of resin acids in relation to the biological treatment of pulp and paper mill effluents. PMID:9246738

  10. Selective separation of uranium using alizarin red S (ARS)-modified anion-exchange resin or by flotation of U-ARS chelate

    An alizarin red S (ARS)-modified anion exchange resin was prepared by a simple reaction of ARS with the anion exchange Doulite A101 and used for the efficient sorption of uranium from aqueous media. The effect of various parameters on the sorption of U(VI) (pH effect, sorption kinetics, resin capacity and breakthrough curves) was investigated. The modified resin sorbs U(VI) over a wide range of pH (2.8--5) with a maximum sorption capacity of 0.68 mmol/g at pH 3.2 to 4.0. Iron(III), Zr(IV), Ti(IV), Cu(II), and Th(IV) ions are also sorbed to different extents, but Be(II), Bi(III), Ca(II), Mg(II), Pb(II), Hg(II), Zn(II), Cd(II), Al(III), Mn(II), Co(II) and Ni(II) are not sorbed; thus, conditions for separating U(VI) from these metal ions have been identified. For eluting U(VI) from the resin, 0.2 mol/L HCl was used and the recovery recorded was as high as 99.9%. The use of ARS is extended to float uranium quantitatively and selectively from aqueous media at pH ∼ 4 by using oleic acid as a surfactant. The different parameters affecting the flotation process have also been investigated. Uranium(VI) has been effectively separated from natural water samples and certified uranium ores using both procedures

  11. A maturation method of uranium content in resins with acid dissolution

    Acid dissolution method is that with intensively oxidation acid to decompose ion exchanging resins and dissolving U and Fe ion in water, then menstruate the U content by titration. Comparing with our current method of filtering wash, acid dissolution menstruation U can get more accurate result and take less time, use more simple device. (authors)

  12. Effects of chelating agents on protein, oil, fatty acid amd seed mineral concentrations in soybean

    Soybean seed is a major source of protein and oil for human diet. Since not much information is available on the effects of chelating agents on soybean seed composition constituents, the current study aimed to investigate the effects of various chelating agents on soybean [(Glycine max (L.) Merr.)] ...

  13. Acid Ionic Liquids as a New Hardener in Urea-Glyoxal Adhesive Resins

    Hamed Younesi-Kordkheili

    2016-02-01

    Full Text Available The effect of acidic ionic liquid (IL as a new catalyst on the properties of wood-based panels bonded with urea-glyoxal (UG resins was investigated. Different levels of N-methyl-2-pyrrolidone hydrogen sulfate ([HNMP] HSO4 (0, 1, 2, 3 wt % were added to prepared UG resin. The resin was then used for preparing laboratory particleboard panels. Then, the properties of the prepared panels were evaluated. The structure of the prepared UG resin was studied by 13C NMR, and thermal curing behavior of the resin before and after the addition of IL was measured by DSC. Additionally, the main oligomers formed in the UG reaction were identified by matrix-assisted laser desorption/ionization time-of-flight (MALDI TOF mass spectroscopy. The results indicated that IL can be used as an efficient catalyst for UG resin. The physicochemical tests indicated that the addition of [HNMP] HSO4 from 0 to 3 wt % decreased the pH value of the glue-mix, and the pH decreased on curing to the same level as urea-formaldehyde resins. The gel accelerated with increasing catalyst content and with the decreasing of the pH in the UG resin. The panels prepared with IL had higher mechanical strength and dimensional stability compared to those made from UG resins containing NH4Cl. Scanning electron microscope (SEM micrographs showed that the panels prepared with ionic liquid presented low porous. DSC analysis showed that the addition of IL to the UG resin decrease the energy of activation of the curing reaction to render possible cross-linking. The MALDI TOF results indicated a preponderant linearity of the oligomers formed, implying a high energy of activation of curing for UG resins.

  14. SYNTESIS OF THE COMPLEXES OF MACROPOROUS SULFONATED RESINS WITH FERRIC CHLORIDE AND THEIR CATALYTIC BEHAVIOR FOR SETERIFICATION OF ACETIC ACID WITH BUTANOL

    HuangWenqiang; HouXin; 等

    1997-01-01

    The complex resins prepared from macroporous sulfonated resin D72(H+ form) with ferric chloride or ferric chloride hexahydrate have both sites of Bronsted acid and Lewis acid.In the catalysis of exterification of acetic acid with butanol the complex resins show to have much higher catalytic activity than that of its matrix.a conventional sulfonated cation exchange resin D72.

  15. Stereoselective analysis of D and L dansyl amino acids as the mixed chelate copper(II) complexes by HPLC.

    Lam, S

    1984-09-01

    This paper reviews the mixed chelation approach to resolution of the optical isomers of D and L dansyl amino acids by high performance liquid chromatography. The use of eluants containing Cu(II) complexes of L-proline, L-arginine, L-histidine, and L-histidine methyl ester effected the separation of many D and L amino acids, including those with aliphatic, polar, and aromatic substituents. The mechanism of separation, which is based on the preferential ternary complex formation of the analyte amino acid and the chiral chelate with Cu(II) in the mobile phase, is discussed. The stereoselectivity depends mainly on the different steric interactions between the alkyl side chains of the amino acid analytes and the chiral ligands coordinating around Cu(II), although such parameters as pH, temperature, organic modifier, and concentration of the chiral additive also affect the chromatographic separation. Among the chiral ligands studied, L-histidine methyl ester is unique in that it possesses both achiral selectivity for the dansyl amino acids and chiral selectivity for the respective D and L enantiomers. With a mobile phase gradient of acetonitrile in a buffer containing Cu(II) L-histidine methyl ester complex, a stereoselective procedure was devised for the analysis of D and L amino acid enantiomers, achieving the separation that the current amino acid analyzer could not perform. Finally, the use of the mixed chelation approach in two biomedical studies is described. In the first application, the histidine methyl ester gradient was adapted for analyzing amino acids in cerebrospinal fluid; in the second, an L-aspartame Cu(II) complex eluant was developed for measuring the urine concentration of D and L pipecolic acid (piperidine-2-carboxylic acid), a metabolite of lysine. PMID:6490790

  16. Studies on radiolytic degradation of anion exchange resin under acidic condition

    With a view to understand the onset of degradation phenomenon of anion exchange resin used in PUREX process for the final purification of Pu, investigation were carried out to trace the chemical signature of radiolytic degradation species soluble in nitric acidic solutions. With this aim Dowex 1x 4 anion exchange resin was subjected to radiolytic degradation in presence of water and nitric acid medium of different strengths ranging from 2M to 7M. The aqueous acidic solutions have been analysed for the presence of aqueous soluble organic fragments arising from resin matrix and change in acidity. The extracted products have also been analysed by Gas chromatography. GLC fingerprint suggest of several degradation products especially at 7M nitric acid and dose of 87 Mrad. (author)

  17. Microbial activity in an acid resin deposit: Biodegradation potential and ecotoxicology in an extremely acidic hydrocarbon contamination

    Acid resins are residues produced in a recycling process for used oils that was in use in the forties and fifties of the last century. The resin-like material is highly contaminated with mineral oil hydrocarbons, extremely acidic and co-contaminated with substituted and aromatic hydrocarbons, and heavy metals. To determine the potential for microbial biodegradation the acid resin deposit and its surroundings were screened for microbial activity by soil respiration measurements. No microbial activity was found in the core deposit. However, biodegradation of hydrocarbons was possible in zones with a lower degree of contamination surrounding the deposit. An extreme acidophilic microbial community was detected close to the core deposit. With a simple ecotoxicological approach it could be shown that the pure acid resin that formed the major part of the core deposit, was toxic to the indigenous microflora due to its extremely low pH of 0-1. - Acidity is the major toxic factor of the extremely hydrophobic and acidic mixed contamination found in an acid resin deposit

  18. Studies on the absorption of boric acid on anion exchange resin, (1)

    Boron Thermal Regeneration (BTR) with an anion exchange resin is a system for the control of boric acid concentration in the primary coolant of a pressurized water reactor. The absorption characteristics of boric acid on strong base anion exchange resin was investigated at 250C. Boric acid absorption was estimated by analysis of solution eluted with sodium chloride solution, from the ion exchange resin column. The average value adsorbed experimentally per ion exchange group was in the range of 1.4 to 4.2 for boric acid solutions in concentrations of 0.00925 to 0.647 mol dm-3. The pH within the borate form resin was pH 8 to 14 for boric acid solutions in concentrations of 0.00925 to 0.462 mol dm-3. The presence of orthoborate ion, tetraborate (mono and divalent) ion and pentaborate (mono and divalent) ion was anticipated in the resin phase. Acid dissociation constants (pK) of these five ion species were estimated to be 8.95 for orthoborate, 5.6 for monovalent tetraborate, 15.2 for divalent tetraborate, 5.6 for monovalent pentaborate and 13.8 for divalent pentaborate. (author)

  19. Correlation of acid-base properties of substituted polystyrene-azo-pyrocatechol and characteristics of their chelates with zirconium

    Acid-base and complexing properties of new synthesized polymeric chelate-forming sorbents (PCS) - substituents of polystyrene-azo-pyrocatechol - are investigated and quantitative correlations between pKOH of functional analytical group (FAG) of sorbent and Hammet constants for para-substituent and ΔpKOH-ΔpK50 correlations of zirconium chelate-forming and pKOH-lgKstb (Kstb - constant of stability of PCS complexes with zirconium) of polychelates to study regularities of effect of peculiarities of structure and acid-base properties of FAG on parameters of zirconium chemical sorption. Established correlations make it possible to predict quantitative physicochemical parameters of sorbents and zirconium chemisorption process with the aim of directed synthesis and application of PCS in concentrating processes

  20. Fatty Acid Methyl Esters as Biosolvents of Epoxy Resins: A Physicochemical Study

    Medina-González, Yaocihuatl; De Caro, Pascale; Thiebaud-Roux, Sophie; Lacaze-Dufaure, Corinne

    2007-01-01

    The C8 to C18 fatty acid methyl esters (FAME) have been compared as solvents for two epoxy resin pre-polymers, bisphenol A diglycidyl ether (DGEBA) and triglycidyl paminophenol ether (TGPA). It was found that the solubilization limits vary according to the ester and that methyl caprylate is the best solvent of both resins. To explain these solubility performances, physical and chemical properties of FAME were studied, such as the Hansen parameters, viscosity, binary diffusion coefficient and ...

  1. Thermally cured coil-coatings utilizing novel resins and fatty acid methyl esters as reactive diluents

    Johansson, Katarina

    2008-01-01

    Solvent-borne thermally cured coil-coating resins contain large amounts of volatile organic solvents in order to obtain suitable flow for film application. This work describes how the expensive and environmental hazardous volatile organic solvent content of a solvent-borne thermally cured polyester/melamine coil-coating system can be reduced by introduction of fatty acid methyl esters (FAMEs) as reactive diluents and modification of the polyester binder resin. The evaluated reactive diluents,...

  2. Fatty Acid Composition of Tobacco Seed Oil and Synthesis of Alkyd Resin

    MUKHTAR,Azam; ULLAH,Habib; MUKHTAR,Hamid

    2007-01-01

    The fatty acid composition of tobacco seed oil revealed that the oil is rich in unsaturated fatty acids, having linoleic acid (71.63%), oleic acid (13.46%) and palmitic acid (8.72%) as the most abundant unsaturated and saturated fatty acids respectively. So the tobacco oil was characterized as semi-drying type on the basis of fatty acid composition. The synthesis of alkyd resin was carried out by alcoholysis or monoglyceride process using an alkali refined tobacco seed oil, pentaerythritol, cis-1,2,3,6-tetrahydrophthalic anhydride along with lithium hydroxide as catalyst.The alkyd resin so prepared was found to be bright and of low color with high gloss. The drying and hardness properties and adhesion of the tobacco seed oil derived alkyd resin were also found a bit superior to those of other alkyd resins of the same oil length. In addition, the water and acid resistance of the said alkyd was also found comparable to the other alkyds.

  3. Macrocyclic bifunctional chelating agents

    Meares, Claude F.; DeNardo, Sally J.; Cole, William C.; Mol, Min K.

    1987-01-01

    A copper chelate conjugate which is stable in human serum. The conjugate includes the copper chelate of a cyclic tetraaza di-, tri-, or tetra-acetic acid, a linker attached at one linker end to a ring carbon of the chelate, and a biomolecule joined at the other end of the linker. The conjugate, or the linker-copper chelate compound used in forming the conjugate, are designed for use in diagnostic and therapeutic applications which involve Cu(II) localization via the systemic route.

  4. Release of cetyl pyridinium chloride from fatty acid chelate temporary dental cement

    Hurt, Andrew; Coleman, Nichola J.; Tüzüner, Tamer; Bagis, Bora; Korkmaz, Fatih Mehmet; Nicholson, John W.

    2016-01-01

    Abstract Objective To determine whether the antimicrobial nature of a fatty acid chelate temporary dental cement can be enhanced by the addition of 5% cetyl pyridinium chloride (CPC). Materials and methods The temporary cement, Cavex Temporary was employed, and additions of CPC were made to either the base or the catalyst paste prior to mixing the cement. Release of CPC from set cement specimens was followed using reverse-phase HPLC for a period of up to 2 weeks following specimen preparation. Potential interactions between Cavex and CPC were examined by Fourier transform infrared spectroscopy (FTIR) and antimicrobial effects were determined using zone of inhibition measurements after 24 h with disc-shaped specimens in cultured Streptococcus mutans. Results FTIR showed no interaction between CPC and the components of the cement. CPC release was found to follow a diffusion mechanism for the first 6 h or so, and to equilibrate after approximately 2 weeks, with no significant differences between release profiles when the additive was incorporated into the base or the catalyst paste. Diffusion was rapid, and had a diffusion coefficient of approximately 1 × 10−9 m2 s−1 in both cases. Total release was in the range 10–12% of the CPC loading. Zones of inhibition around discs containing CPC were significantly larger than those around the control discs of CPC-free cement. Conclusions The antimicrobial character of this temporary cement can be enhanced by the addition of CPC. Such enhancement is of potential clinical value, though further in vivo work is needed to confirm this. PMID:27335898

  5. Nitrogen-doped carbon nanofoam derived from amino acid chelate complex for supercapacitor applications

    Ramakrishnan, Prakash; Shanmugam, Sangaraju

    2016-06-01

    We report a novel strategy to fabricate the nitrogen-doped mesoporous carbon nanofoam structures (N-MCNF), derived from magnesium amino acid chelate complex (Mg-acc-complex) for its application towards high performance supercapacitor (SCs) system. A series of N-MCNF with well-connected carbon nanofoam structure have been developed by varying the synthesis temperature. The fabricated N-MCNF material possesses a high surface area (1564 m2 g-1) and pore volume (1.767 cm3 g-1) with nitrogen content of 3.42 wt%. A prototypical coin cell type symmetric N-MCNF SC device has been assembled with 1-ethyl-3-methylimidazolium tetrafluoroborate [EMIMBF4] ionic liquid electrolyte, and evaluated for SCs studies. The N-MCNF with high textural properties delivers unprecedented SC performance, such as high specific capacitance (204 Fg-1 at 0.25 Ag-1, 25 °C), high energy density (63.4 Wh kg-1), high power density (35.9 kW kg-1) and long-term cycle life (32,500 cycles). Significantly, N-MCNF materials exhibited high power rate performance, at 500 mV-1 (115 Fg-1) and 25 Ag-1 (166 Fg-1) owing to the uniform mesopore size distribution (∼4 nm). The N-MCNF SC device delivered maximum energy densities of 83.4 and 93.3 Wh kg-1 at 60 °C and 90 °C, respectively. Such outstanding N-MCNF SC device is successfully demonstrated in solar energy harvester applications.

  6. Diterpene resin acids: Major active principles in tall oil against Variegated cutworm,Peridroma saucia (Lepidoptera: Noctuidae).

    Xie, Y; Isman, M B; Feng, Y; Wong, A

    1993-06-01

    Tall oil, a by-product of the kraft process for pulping softwood, has been shown to have insecticidal properties. In the present study, the active principles in tall oil against the variegated cutworm,Peridroma saucia Hübner, were investigated. GC-MS analysis showed that abietic, dehydroabietic, and isopimaric acids were major resin acid components of crude tall oil and depitched tall oil. When crude tall oil samples of differing resin acid composition were incorporated into artificial diet at a concentration of 2.0% fresh weight, they suppressed larval growth by 45-60% compared to controls. This suppression was significantly (P≤0.05) correlated with the equivalent contents of abietic, dehydroabietic, isopimaric, and total resin acids. These results were also evident from a diet choice test, showing that the second-instar larvae obviously selected diets with low levels of resin acids when different diets were randomly arranged in a Petri dish. Bioassays with pure resin acids (abietic, dehydroabietic, and isopimaric acids) demonstrated that all individual chemicals have similar bioactivity against this insect. Comparison of the bioactivities of depitched tall oil and an equivalent mixture of pure resin acids in thePeridroma chronic growth bioassay indicated that pure resin acids and depitched tall oil share a common mode of action to this insect. This study confirms that resin acids are major active principles in tall oil against the variegated cutworm, but other chemicals likely also contribute to the bioactivity of tall oil. PMID:24249127

  7. Sorption of Pu(IV) from nitric acid by bifunctional anion-exchange resins

    Anion exchange is attractive for separating plutonium because the Pu(IV) nitrate complex is very strongly sorbed and few other metal ions form competing anionic nitrate complexes. The major disadvantage of this process has been the unusually slow rate at which the Pu(IV) nitrate complex is sorbed by the resin. The paper summarizes the concept of bifunctional anion-exchange resins, proposed mechanism for Pu(IV) sorption, synthesis of the alkylating agent, calculation of Kd values from Pu(IV) sorption results, and conclusions from the study of Pu(IV) sorption from 7M nitric acid by macroporous anion-exchange resins including level of crosslinking, level of alkylation, length of spacer, and bifunctional vs. monofunctional anion-exchange resins

  8. Novel silica-based ion exchange resin

    NONE

    1997-11-01

    Eichrom`s highly successful Diphonixo resin resembles a conventional ion exchange resin in its use of sulfonic acid ligands on a styrene- divinylbenzene matrix. Diphonix resin exhibits rapid exchange kinetics that allow economical operation of ion exchange systems. Unlike conventional resins, Diphonix resin contains chelating ligands that are diphosphonic acid groups that recognize and remove the targeted metals and reject the more common elements such as sodium, calcium and magnesium. This latter property makes Diphonix ideal for many industrial scale applications, including those involving waste treatment. For treatment of low-level, transuranic (TRU) and high- level radioactive wastes, Diphonix`s polystyrene backbone hinders its application due to radiolytic stability of the carbon-hydrogen bonds and lack of compatibility with expected vitrification schemes. Polystyrene-based Diphonix is approximately 60% carbon- hydrogen. In response to an identified need within the Department of Energy for a resin with the positive attributes of Diphonix that also exhibits greater radiolytic stability and final waste form compatibility, Eichrom has successfully developed a new, silica-based resin version of Diphonix. Target application for this new resin is for use in environmental restoration and waste management situations involving the processing of low-level, transuranic and high-level radioactive wastes. The resin can also be used for processing liquid mixed waste (waste that contains low level radioactivity and hazardous constituents) including mixed wastes contaminated with organic compounds. Silica-based Diphonix is only 10% carbon-hydrogen, with the bulk of the matrix silica.

  9. Methylene crosslinked calix[6]arene hexacaarboxylic acid resin: a highly efficient solid phase extractant for decontamination of lead bearing effluents.

    Adhikari, Birendra Babu; Gurung, Manju; Kawakita, Hidetaka; Jumina; Ohto, Keisuke

    2011-10-15

    Calixarene-based cation exchange resin has been developed by methylene crosslinking of calix[6]arene hexacarboxylic acid derivative and the resin has been exploited for solid phase extraction of some toxic heavy metal ions. The selectivity order of the resin towards some metal ions follows the order Pb(II) > Cu(II)> Zn(II), Ni(II), Co(II). The maximum lead ion binding capacity of the resin was found to be 1.30 mmol g(-1) resin. The loaded lead was quantitatively eluted with dilute acid solution regenerating the resin. Mutual separation of Pb(II), Cu(II) and Zn(II) was achieved by using the column packed with the resin. PMID:21835544

  10. Purification of chlorogenic acid in Flos Lonicerae with system of polar ordered resins

    XIANG Zhi-nan; ZHAN Yu; NING Zheng-xiang

    2007-01-01

    A system of polar ordered resins was established for purification of chlorogenic acid in Flos Lonicerae. It was composed of three reversed phase resins, AB-8, DM-130 and NKA-9, representative for their gradually increased polarity and selectivity. A method of RP-HPLC was used for determination of chlorogenic acid. And the performance of adsorption and desorption for chlorogenic acid with the system of polar ordered resins was studied. Furthermore, the effects of concentration, pH and flow rate of the adsorbate on adsorption ability were researched. It is indicated that the optimum parameters for chlorogenic acid are as follows:pH 3.5 with a flow rate of 2.5 BV/h, the concentration of extract solution at 0.50, 0.40, 0.30 g/L respectively for the adsorptive operation twice, and 6.93, 8.66, 10.39 mol/L ethanol used as gradient eluants. The purity of resulted product of chlorogenic acid arrives 70.20% with yield of 89.79%. With simple procedures, low costs and high purity product, the method of system of polar ordered resins followed by sequential reversed phase separations can be used to refine the chlorogenic acid in the extraction of Flos Lonicerae.

  11. Enteric-coated tablet of risedronate sodium in combination with phytic acid, a natural chelating agent, for improved oral bioavailability.

    Kim, Jeong S; Jang, Sun W; Son, Miwon; Kim, Byoung M; Kang, Myung J

    2016-01-20

    The oral bioavailability (BA) of risedronate sodium (RS), an antiresorptive agent, is less than 1% due to its low membrane permeability as well as the formation of non-absorbable complexes with multivalent cations such as calcium ion (Ca(2+)) in the gastrointestinal tract. In the present study, to increase oral BA of the bisphosphonate, a novel enteric-coated tablet (ECT) dosage form of RS in combination with phytic acid (IP6), a natural chelating agent recognized as safe, was formulated. The chelating behavior of IP6 against Ca(2+), including a stability constant for complex formulation was characterized using the continuous variation method. Subsequently, in vitro dissolution profile and in vivo pharmacokinetic profile of the novel ECT were evaluated comparatively with that of the marketed product (Altevia, Sanofi, US), an ECT containing ethylenediaminetetraacetic acid (EDTA) as a chelating agent, in beagle dogs. The logarithm of stability constant for Ca(2+)-IP6 complex, an equilibrium constant approximating the strength of the interaction between two chemicals to form complex, was 19.05, which was 3.9-fold (p<0.05) and 1.7-fold (p<0.05) higher than those of Ca(2+)-RS and Ca(2+)-EDTA complexes. The release profile of RS from both enteric-coated dosage forms was equivalent, regardless of the type of chelating agent. An in vivo absorption study in beagle dogs revealed that the maximum plasma concentration and area under the curve of RS after oral administration of IP6-containing ECT were approximately 7.9- (p<0.05) and 5.0-fold (p<0.05) higher than those of the marketed product at the same dose (35mg as RS). Therefore, our study demonstrates the potential usefulness of the ECT system in combination with IP6 for an oral therapy with the bisphosphonate for improved BA. PMID:26594027

  12. Adsorption characteristics of boric acid on strong-base anion exchange resin

    The Boron Thermal Regeneration System (BTRS) is capable of controlling boron concentration in primary coolant and reducing the amount of liquid waste at the end of fuel cycle in a pressurized water reactor, but the system has not been in effective operation yet because of the lack of detailed information regarding the boron adsorption characteristics of the ion exchange resin packed in the demineralizers of BTRS. In this study, the adsorption characteristics of boric acid on a strong-base anion exchange resin, an Amberlite IRN-78LC resin in OH- form, were investigated at temperature from 10 .deg. C to 60 .deg. C in the concentrations of boron up to 1500 ppm covering the BTRS operational conditions. A computer code was developed to calculate the composition of borate ions in solution as a function of boron concentration, temperature and pH. From the calculated composition of borate ions and experimental data of adsorption equilibrium, the model was proposed for the adsorption isotherm of boric acid on the resin. The diffusion coefficient of the boric acid in the resin was calculated by the particle diffusion model and found that the temperature dependency of the coefficient follows an Arrhenius equation. The results in this study can be applied for the optimum operation of BTRS

  13. Chemically modified polymeric resins for separation of cations, organic acids, and small polar moleculea by high performance liquid chromatography

    Morris, J.B.

    1993-07-01

    This thesis is divided into 4 parts: a review, ion chromatography of metal cations on carboxylic resins, separation of hydrophilic organic acids and small polar compounds on macroporous resin columns, and use of eluent modifiers for liquid chromatographic separation of carboxylic acids using conductivity detection.

  14. Phosphoric acid esters cannot replace polyvinylphosphonic acid as phosphoprotein analogs in biomimetic remineralization of resin-bonded dentin

    Mai, Sui; Kim, Young Kyung; Toledano, Manuel; Breschi, Lorenzo; Ling, Jun Qi; PASHLEY David H.; Franklin R Tay

    2009-01-01

    Polyvinylphosphonic acid (PVPA), a biomimetic analog of phosphoproteins, is crucial for recruiting polyacrylic acid (PAA)-stabilized amorphous calcium phosphate nanoprecursors during biomimetic remineralization of dentin collagen matrices. This study tested the null hypothesis that phosphoric acid esters of methacrylates in dentin adhesives cannot replace PVPA during bimimetic remineralization of resin-dentin interfaces. Human dentin specimens were bonded with: I) XP Bond, an etch-and-rinse a...

  15. Bonding effectiveness of self-adhesive and conventional-type adhesive resin cements to CAD/CAM resin blocks. Part 2: Effect of ultrasonic and acid cleaning.

    Kawaguchi, Asuka; Matsumoto, Mariko; Higashi, Mami; Miura, Jiro; Minamino, Takuya; Kabetani, Tomoshige; Takeshige, Fumio; Mine, Atsushi; Yatani, Hirofumi

    2016-01-01

    The present study assessed the effect of ultrasonic and acid cleaning on resin cement bonding to CAD/CAM resin blocks. One of two resin cements, PANAVIA V5 (PV5) or PANAVIA SA CEMENT HANDMIX (PSA), were bonded to one of 24 CAD/CAM blocks (KATANA AVENCIA BLOCK). Each cement group was divided into four subgroups: no cleaning (Ctl), ultrasonic cleaning (Uc), acid cleaning (Ac) and Uc+Ac. Micro-tensile bond strengths (µTBSs) were measured immediately and 1, 3, and 6 months after water storage. Block surfaces after each treatment were analyzed by scanning electron microscopy. Analysis of variance revealed a statistically significant effect for the parameters 'surface treatment' (psandblasting was effective in removing residual alumina particles, it did not affect the long-term bonding durability with non-contaminated CAD/CAM resin blocks. PMID:26830822

  16. Organic acids rather than histidine predominate in Ni chelation in Alyssum hyperaccumulator xylem exudate

    A better understanding of Ni uptake mechanisms by hyperaccumulator plants is necessary to improve Ni uptake efficiency for phytoremediation technologies i.e. phytomining. It is known that an important aspect of Ni translocation involves Ni chelation with organic ligands. However, it is still not cle...

  17. Esterification of oleic acid with ethanol catalyzed by sulfonated cation exchange resin: Experimental and kinetic studies

    Graphical abstract: - Highlights: • Esterification of oleic acid with ethanol was investigated in the presence of sulfonated cation exchange resin. • We studied kinetic model of the esterification of oleic acid with ethanol according to experimental data. • The proposed kinetic model can well predict oleic acid conversion. - Abstract: This paper investigated the effects of ethanol to oleic acid molar ratio, reaction temperature, catalyst loading, water content and catalyst recycling on sulfonated cation exchange resin in a stirred batch reactor under atmospheric pressure. When the esterification was carried out with an ethanol to oleic acid (42.4 g) molar ratio of 9:1, reflux of ethanol at 82 °C, 20 g of catalyst and 8 h of reaction time, the oleic acid conversion rate reached approximately 93%. A pseudo-homogeneous kinetic model for describing the esterification of oleic acid with ethanol by the sulfonated cation exchange resin was developed on the basis of laboratorial results. The kinetic model can well predict the oleic acid conversion

  18. Chelatization of Metals Ion (Cu2+, Cd2+ and Cr3+) with ProcessYield of Humic Acid from Peat Soil

    The chelation of metals ion (Cu2+, Cd2+ and Cr3+) with processyields of humic acid from peat soil has been done. The chelatizationcalculation was carried out using a mathematical model of the metals ionneutralization to the humic acid functional group. The model has superioritydue to the introduction of the humic acid concentration conditional and theloading capacity. Chelation is expected to obtain the constant experimentthat agrees with environmental conditional were the chelatization to takeplaces. By the tree neck flask of bath reactor, 250 ml volume at thetemperature of 25 oC chelation have been done and the AAS was used toanalyzes the yield. By mathematical calculate was obviously proved that thechelation constants was not influenced by pH, ionic strength and origin peatsoils. As log β, chelation constants of Cu2+, Cd2+ and Cr3+ were4.67 (± 0.02); 5.98 (± 0.02) and 6.09 (± 0.01) for humic acid fromSumatra I (Silaut III) and 4.68 (± 0.01); 5.97 (± 0.02) and 6.09 (±0.02) for Sumatra II (Silaut IV). While chelation constant Cu2+, Cd2+ andCr3+ from Kalimantan were 4.66 (± 0.03); 5.99 (± 0.01); 6.08 (±0.02). (author)

  19. Adsorption behavior and mechanism of cadmium on strong-acid cation exchange resin

    WANG Fei; WANG Lian-jun; LI Jian-sheng; SUN Xiu-yun; HAN Wei-qing

    2009-01-01

    The adsorption behavior of Cd2+ on 001×7 strong-acid cation exchange resin was studied with the static adsorption method. The adsorption process was analyzed from thermodynamics and kinetics aspects. The influences of experimental parameters such as pH, temperature, initial concentration and adsorption rate were investigated. The experimental results show that in the studied concentration range, 001×7 resin has a good sorption ability for Cd2+, and the equilibrium adsorption data fit to Freundlich isotherms. The adsorption is an exothermic process which runs spontaneously. Kinetic analysis shows that the adsorption rate is mainly governed by liquid film diffusion. The best adsorption condition is pH 4-5. The saturated resin can be regenerated by 3 mol/L nitric acid, and the desorption efficiency is over 98%. The maximal static saturated adsorption capacity is 355 mg/g (wet resin) at 293 K. The adsorption mechanism of Cd2+ on 001×7 resin was discussed based on IR spectra.

  20. Some investigations on the radiation stability of a strongly acidic cation exchange resin

    Dessouki, A. M.; Zahran, A. H.; Rabie, A. M.; Amer, S. I.

    The radiation-chemical stability of Merck Cation Exchanger I, a strongly acidic sulphonated cation exchanger of the polymerization type based on styrene-divinylbenze (DVB) copolymers was investigated. The radiation stability of the resin was assessed from the change in exchange capacity, loss in weight, change in swelling behaviour and formation of new exchange groups. The loss in capacity was 44 and 32% for resin specimens in the H +-form irradiated to 1000 Mrad in air and in vacuum, respectively. The Na +-form of the exchanger showed high resistance to radiation and the loss in capacity did not exceed 7% at a dose of 1000 Mrad. The loss in capacity was accompanied by a loss in weight and a decrease in the degree of swelling of the irradiated resin. The formation of new functional groups of the carboxylic and phenolic types was confirmed. The amount of these group increases with the increase in the integral dose. The amount of sulphuric acid formed as a result of irradiating the resin in the dry and moist states was determined. An increase in the moisture content of the resin resulted in a marked decrease in its radiation stability.

  1. A convenient procedure for the solid-phase synthesis of hydroxamic acids on PEGA resins

    Nandurkar, Nitin Subhash; Petersen, Rico; Qvortrup, Katrine;

    2011-01-01

    An efficient method for the solid-phase synthesis of hydroxamic acids is described. The method comprises the nucleophilic displacement of esters immobilized on PEGA resins with hydroxylamine/sodium hydroxide in isopropanol. The hydroxyaminolysis protocol is compatible with a broad range of PEGA...

  2. Influence of the Functionalization Degree of Acidic Ion-Exchange Resins on Ethyl Octyl Ether Formation

    Guilera, J.; Hanková, Libuše; Jeřábek, Karel; Ramírez, E.; Tejero, J.

    2014-01-01

    Roč. 78, MAY (2014), s. 14-22. ISSN 1381-5148 Grant ostatní: SEURDO(ES) CTQ2010-16047 Institutional support: RVO:67985858 Keywords : acidic ion-exchange resin * sulfonation degree * ISEC Subject RIV: CC - Organic Chemistry Impact factor: 2.515, year: 2014

  3. STUDY ON ADSORPTION OF HUMIC AND PHYIC ACIDS USING RESINS

    WANG Jinnan; LI Aimin; ZHOU Youdong; YANG Zhou; LI Xu

    2008-01-01

    @@ 1. INTRODUCTION Humic acid (HA) and Phytic acid (PA) are present in environment as a result of the decomposition of plant biomass, they are the major components of natural dissolved organic matter (DOM) in natural systems[1].

  4. IMPACT OF ACID WASHING AND CHELATION ON Mg(OH2-BASED HYDROGEN PEROXIDE BLEACHING OF MIXED HARDWOODS CMP AT A HIGH CONSISTENCY

    Somayeh Ghasemi

    2010-09-01

    Full Text Available The removal of transition metal ions is crucial for improving the efficiency of subsequent peroxide bleaching. Acid-washing and chelation have been proposed for such a purpose. However, their influences on the Mg(OH2-based peroxide bleaching of hardwood pulps at a high consistency have not been well documented in the literature. In this work, we studied the influence of acid-washing using sulfuric acid or chelation using diethylenetriaminepentaacetic (DTPA on the Mg(OH2- or NaOH-based hydrogen peroxide bleaching efficiency, effluent properties of bleaching filtrates, and paper properties. The results showed that for Mg(OH2-based peroxide bleaching, the pulp yield and water retention value of acid-washed pulp were higher than those of the chelated pulp; the chemical oxygen demand (COD and turbidity of the bleaching filtrates for the acid-washed pulp were lower than those of the chelated pulp. The bleached acid-washed pulp had lower strength properties than bleached chelated pulp did. Additionally, at a high pulp consistency (25%, the Mg(OH2-based process had a higher bleaching efficiency and superior bleaching effluent properties, but a lower strength properties, in comparison with the NaOH-based process.

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

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

  6. Synthesis of hemicellulose-acrylic acid graft copolymer super water absorbent resin by ultrasonic irradiation technology

    Liu, Fangfang; Conghui DU; Linya ZHANG

    2015-01-01

    The hemicellulose super water absorbent resin is prepared by using ultrasonic irradiation technology, with the waste liquid produced during the preparation of viscose fiber which contains a large amount of hemicellulose as raw material, acrylic acid as graft monomer, N,N’-methylene bis acrylamide (NMBA) as cross linking agent, and (NH4)2S2O8-NaHSO3 as the redox initiation system. The synthesis conditions, structure and water absorption ability of resin are discussed. The results indicate that...

  7. Simultaneous extraction of U and Zr using HDEHP impregnated XAD-7 resin in nitric acid medium

    Feasibility of separating U and Zr from U-Zr alloys using HDEHP impregnated XAD-7 resin was explored in the present study with a view to obtain a sample solution free from matrix elements suitable for carrying out ICP-MS analysis of lanthanides at trace concentrations. Initially, the distributions of U, Zr and lanthanides in the impregnated resin were investigated with different nitric acid concentrations. The separated fractions were analyzed by ICP-MS for trace lanthanides whereas ion chromatography was employed for quantifying U and Zr. It was observed that at 4M HNO3 medium U exhibited high distribution whereas lanthanides showed least distribution in the resin. Zirconium showed significant distribution in 4M HNO3. Hence, 4M HNO3 was found to be optimal in order to extract U and Zr simultaneously. However, heavy rare earths such as Tm, Yb and Lu showed significant Kd values leading to their poor recovery. (author)

  8. Simultaneous separation and detection of actinides in acidic solutions using an extractive scintillating resin.

    Roane, J E; DeVol, T A

    2002-11-01

    An extractive scintillating resin was evaluated for the simultaneous separation and detection of actinides in acidic solutions. The transuranic extractive scintillating (TRU-ES) resin is composed of an inert macroporous polystyrene core impregnated with organic fluors (diphenyloxazole and 1,4-bis-(4-methyl-5-phenyl-2-oxazolyl)benzene) and an extractant (octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide in tributyl phosphate). The TRU-ES resin was packed into FEP Teflon tubing to produce a flow cell (0.2-mL free column volume), which is placed into a scintillation detection system to obtain pulse height spectra and time series data during loading and elution of actinides onto/from the resin. The alpha-particle absolute detection efficiencies ranged from 77% to 96.5%, depending on the alpha energy and quench. In addition to the on-line analyses, off-line analyses of the effluent can be conducted using conventional detection methods. The TRU-ES resin was applied to the quantification of a mixed radionuclide solution and two actual waste samples. The on-line characterization of the mixed radionuclide solution was within 10% of the reported activities whereas the agreement with the waste samples was not as good due to sorption onto the sample container walls and the oxidation state of plutonium. Agreement between the on-line and off-line analyses was within 35% of one another for both waste samples. PMID:12433098

  9. Esterification of free fatty acids in waste cooking oils (WCO): Role of ion-exchange resins

    Nalan Ozbay; Nuray Oktar; N. Alper Tapan [Gazi University, Ankara (Turkey). Faculty of Engineering and Architecture, Department of Chemical Engineering

    2008-08-15

    Although WCO plays a crucial role for the economical production of biodiesel, free fatty acid (FFA) level in the nature of WCO cause saponification problems during transesterification. Acidic ion-exchange resins can be used to decrease WCO free fatty acid level. In this study, activities of resins (Amberlyst-15 (A-15), Amberlyst-35 (A-35), Amberlyst-16 (A-16) and Dowex HCR-W2) in direct FFA esterification were examined in the temperature range of 50-60{sup o}C and the effect of catalyst amount (1-2 wt%) on FFA conversion was also analyzed. FFA conversion increased with increasing reaction temperature and catalyst amount. Order of catalytic activities was found as A-15 > A-35 > A-16 > Dowex HCR-W2. This was related to the size of average pore diameters and magnitude of BET surface area. 44 refs., 11 figs., 2 tabs.

  10. Purification of organic acids by chromatography with strong anionic resins: Investigation of uptake mechanisms.

    Lemaire, Julien; Blanc, Claire-Line; Lutin, Florence; Théoleyre, Marc-André; Stambouli, Moncef; Pareau, Dominique

    2016-08-01

    Bio-based organic acids are promising renewable carbon sources for the chemical industry. However energy-consuming purification processes are used, like distillation or crystallization, to reach high purities required in some applications. That is why preparative chromatography was studied as an alternative separation technique. In a previous work dealing with the purification of lactic, succinic and citric acids, the Langmuir model was insufficient to explain the elution profiles obtained with a strong anionic resin. Consequently the Langmuir model was coupled with a usual ion-exchange model to take into account the retention of their conjugate bases (tailing and apparent delay observed with succinic and citric acids can be explained by the high affinity of succinate and citrate for resin cationic sites. The model was implemented in a preparative chromatography simulation program in order to optimize operating parameters of our pilot-scale ISMB unit (Improved Simulated Moving Bed). The comparison with experimental ISMB profiles was conclusive. PMID:27373374

  11. Chelating agents related to ethylenediamine bis(2-hydroxyphenyl)acetic acid (EDDHA): synthesis, characterization, and equilibrium studies of the free ligands and their Mg2+, Ca2+, Cu2+, and Fe3+ chelates.

    Yunta, Felipe; García-Marco, Sonia; Lucena, Juan J; Gómez-Gallego, Mar; Alcázar, Roberto; Sierra, Miguel A

    2003-08-25

    Iron chelates such as ethylenediamine-N,N'-bis(2-hydroxyphenyl)acetic acid (EDDHA) and their analogues are the most efficient soil fertilizers to treat iron chlorosis in plants growing in calcareous soils. EDDHA, EDDH4MA (ethylenediamine-N,N'-bis(2-hydroxy-4-methylphenyl)acetic acid), and EDDCHA (ethylenediamine-N,N'-bis(2-hydroxy-5-carboxyphenyl)acetic acid) are allowed by the European directive, but also EDDHSA (ethylenediamine-N,N'-bis(2-hydroxy-5-sulfonylphenyl)acetic acid) and EDDH5MA (ethylenediamine-N,N'-bis(2-hydroxy-5-methylphenyl)acetic acid) are present in several commercial iron chelates. In this study, these chelating agents as well as p,p-EDDHA (ethylenediamine-N,N'-bis(4-hydroxyphenyl)acetic acid) and EDDMtxA (ethylenediamine-N,N'-bis(2-metoxyphenyl)acetic acid) have been obtained following a new synthetic pathway. Their chemical behavior has been studied to predict the effect of the substituents in the benzene ring on their efficacy as iron fertilizers for soils above pH 7. The purity of the chelating agents has been determined using a novel methodology through spectrophotometric titration at 480 nm with Fe(3+) as titrant to evaluate the inorganic impurities. The protonation constants were determined by both spectrophotometric and potentiometric methods, and Ca(2+) and Mg(2+) stability constants were determined from potentiometric titrations. To establish the Fe(3+) and Cu(2+) stability constants, a new spectrophotometric method has been developed, and the results were compared with those reported in the literature for EDDHA and EDDHMA and their meso- and rac-isomers. pM values have been also determined to provide a comparable basis to establish the relative chelating ability of these ligands. The purity obtained for the ligands is higher than 87% in all cases and is comparable with that obtained by (1)H NMR. No significant differences have been found among ligands when their protonation and stability constants were compared. As expected, no Fe(3

  12. Eichrom's Diphonix reg-sign resin: Production-scale applications in radioactive waste treatment and iron control in copper electrowinning

    Eichrom's Diphonix reg-sign resin has been phased through synthetic scale-up, pilot testing, and production installation in radioactive waste treatment and hydrometallurgical applications. The geminal diphosphonic acid groups of Diphonix resin allow selective retention by cation-exchange and/or chelation. The resin is effective at low pH where sulfonic and carboxylic acid resins are ineffective. Diphonix resin has been used in nuclear facilities to reduce actinide concentrations in radioactive waste effluents and to reduce waste volumes. The high retention of iron(III) by Diphonix resin in acidic sulfate media has led to an installation capable of removing one ton of iron per day from a copper electrowinning stream. This iron control process diminishes cobalt losses in the electrowinning circuit and significantly reduces operating costs. The authors will discuss the development of these Diphonix resin applications

  13. Oxidative degradation of ion-exchange resins in acid medium. Vol. 3

    Volume reduction of spent ion-exchange resins used in nuclear facilities receive increasing importance due to the increase in storage cost, unstable physical and chemical properties and their relatively high specific activity (in some cases up to 1 Ci per liter). The present study is part of research program on the treatment and immobilization of radioactive spent ion-exchange resins simulate; hydrogen peroxide was used for the oxidative degradation of spent ion-exchange resins simulate in sulphuric acid medium. Five liters ring digester developed in Karlsruhe nuclear research center-(KFK)- in germany was the chosen option to perform the oxidation process. The work reported focused on the kinetics and mechanism of the oxidation process. Heating the organic resins in sulphuric acid results in its carbonization and partial oxidation of only 1.7% of the carbon added. Results show that the oxidation reaction is a relatively slow process of first order with K value in the order of 10-4 min-1, and the main oxidation product was carbon dioxide. The production of carbon oxide in the off gas stream increased sharply by the addition of hydrogen peroxide to the hot sulphuric acid-resin mixture. The results obtained show that more than 97% of the carbon added was oxidized to carbon dioxide and carbon monoxide. The rate constant value (K) of this reaction was calculated to be (1.69±0.13) x 10-2 min-1. The results of gas chromatographic analysis indicate that no significant amounts of hazardous organic materials were detected in the off-gas streams. 6 figs., 4 tabs

  14. A dual chelating sol–gel synthesis of BaTiO{sub 3} nanoparticles with effective photocatalytic activity for removing humic acid from water

    Wang, Peigong [College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024 (China); Fan, Caimei, E-mail: fancm@163.com [College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024 (China); Wang, Yawen; Ding, Guangyue; Yuan, Peihong [College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024 (China)

    2013-02-15

    Graphical abstract: The cubic phase BaTiO{sub 3} nanoparticles can be obtained at 600 °C and changed into tetragonal phase at 900 °C by a dual chelating sol–gel method, and the photocatalytic activities of the photocatalysts calcined at different temperatures were investigated by the removal of humic acid (HA) from water under UV light irradiation. Highlights: ► The humic acid in water was firstly degradated by BaTiO{sub 3} photocatalyst. ► The cubic BaTiO{sub 3} was obtained and changed into tetragonal phase at lower temperature. ► The chelating agents had an important influence on the phase formation of BaTiO{sub 3}. ► The tetragonal phase BaTiO{sub 3} calcined at 900 °C exhibited higher photocatalytic activity under UV irradiation. -- Abstract: In this paper, a dual chelating sol–gel method was used to synthesize BaTiO{sub 3} nanoparticles by using acetylacetone and citric acid as chelating agents. The samples calcined at different temperatures were analyzed by thermogravimetric and differential thermal analysis (TG-DTA), X-ray diffraction (XRD), X-ray photoelectron spectra (XPS), scanning electron microscope (SEM) and UV–vis diffuse reflectance spectra (UV–vis). The results indicated that cubic phase BaTiO{sub 3} nanoparticles about 19.6 nm can be obtained at 600 °C and changed into tetragonal phase at 900 °C about 97.1 nm. All the BaTiO{sub 3} nanoparticles showed effective photocatalytic activities on the removal of humic acid (HA) under UV light irradiation. A comparison of single (acetylacetone or citric acid) and dual chelating (acetylacetone and citric acid) synthetic processes was also studied and the results demonstrated that the dual chelating agents indeed reduced phase transformation temperature from cubic to tetragonal BaTiO{sub 3}.

  15. Influence of anionic species on uranium separation from acid mine water using strong base resins

    The presence of uranium and other elements in high concentrations in acid mine drainage at Pocos de Caldas Uranium Mine (Brazil) is a matter of concern. The acid water pH is around 2.7, the uranium concentration is in the range of 6-14 mg L-1, sulfate concentration near 1400 mg L-1, fluoride 140 mg L-1 and iron 180 mg L-1. In this solution, where sulfate is present in elevated concentrations, uranium is basically in the form of UO2(SO4)34-. This study investigated the separation of uranium from the other anions present in the acid water under batch and column mode using ion exchange technique. The pH studied was 2.7 and 3.9. Two strong base anionic resins were tested. The influence of ions, commonly found in acid waters like sulfate and fluoride, on ion exchange process was also assessed. Equilibrium studies were carried out to determine the maximum adsorption capacities of the resins. The resins showed a significant capacity for uranium uptake which varied from 66 to 108 mg g-1 for IRA 910U and 53 to 79 mg g-1 for Dowex A. The results also showed that SO42- is the most interfering ion and it had a deleterious effect on the recovery in the pH range studied. Fluoride did not affect uranium removal

  16. Study on elution ability of salicylic acid on ion exchange resins in supercritical carbon dioxide

    Ping YUAN; Jianguo CAI; Junjie GONG; Xiu DENG

    2009-01-01

    The elution ability of salicylic acid on ion exchange resins in supercritical carbon dioxide has been studied. Some factors influencing elution recovery,including entrainer, temperature, pressure and the flow rate of supercritical fluid CO2 are discussed in this work.The addition of a small amount of entrainer, such as ethanol, triethanolamine and their mixture to supercritical CO2 can cause dramatic effects on the elution ability. The results show that the salicylic acid can be only slightly eluted from the resin with supercritical CO2 alone with temperatures ranging from 307.15 to 323.15K and pressures ranging from 10 to 30MPa. Meanwhile, with the same T, P conditions, 40.58% and 73.08% salicylic acid can be eluted from the ion exchange resin with ethanol and ethanol + triethanolamine as the entrainer, respec-tively. An improved PR equation of state with VDWl mixing rules is used to calculate the elution recovery of salicylic acid in supercritical CO2 and the results agree well with the experimental data.

  17. Benzyl and Methyl Fatty Hydroxamic Acids Based on Palm Kernel Oil as Chelating Agent for Liquid-Liquid Iron(III) Extraction

    Jamileh Amin; Roshanak Rafiee-Moghaddam; Behnam Mahdavi; Mazyar Peyda; Anuar Kassim; Nor Azah Yusof; Md Jelas Haron; Hossein Jahangirian; Yadollah Abdollahi; Sidik Silong

    2012-01-01

    Liquid-liquid iron(III) extraction was investigated using benzyl fatty hydroxamic acids (BFHAs) and methyl fatty hydroxamic acids (MFHAs) as chelating agents through the formation of iron(III) methyl fatty hydroxamate (Fe-MFHs) or iron(III) benzyl fatty hydroxamate (Fe-BFHs) in the organic phase. The results obtained under optimized conditions, showed that the chelating agents in hexane extract iron(III) at pH 1.9 were realized effectively with a high percentage of extraction (97.2% and 98.1%...

  18. ANALYSIS OF RESIN AND FATTY ACIDS ENRICHED IN PAPERMAKING PROCESS WATERS

    Piia Valto

    2010-02-01

    Full Text Available The applicability of a special pilot-scale installation (Short Circulation Device was studied for demonstrating the enrichment of selected resin and fatty acids in process waters when increasing water reuse during the manufacture of paper. The traditional gas chromatography with flame ionization detection (GC-FID, turbidity, and online sample enrichment (solid phase extraction, SPE for atmospheric pressure chemical ionization-mass spectrometry (APCI-MS measurements were used for the analysis of the resin and fatty acids. The data from all the measurements with unbleached thermomechanical pulp (TMP process waters were in a good agreement, and correlation coefficients (R2 > 0.9 were obtained in each case. Rapid information about the levels of wood extractives in papermaking process waters is of great importance, and it offers a suitable way to predict oncoming pitch problems. It was concluded that the routine control of the extractives level in papermaking process waters is possible by all these methods.

  19. Paramagnetic relaxation enhancement of membrane proteins by incorporation of the metal-chelating unnatural amino acid 2-amino-3-(8-hydroxyquinolin-3-yl)propanoic acid (HQA)

    The use of paramagnetic constraints in protein NMR is an active area of research because of the benefits of long-range distance measurements (>10 Å). One of the main issues in successful execution is the incorporation of a paramagnetic metal ion into diamagnetic proteins. The most common metal ion tags are relatively long aliphatic chains attached to the side chain of a selected cysteine residue with a chelating group at the end where it can undergo substantial internal motions, decreasing the accuracy of the method. An attractive alternative approach is to incorporate an unnatural amino acid that binds metal ions at a specific site on the protein using the methods of molecular biology. Here we describe the successful incorporation of the unnatural amino acid 2-amino-3-(8-hydroxyquinolin-3-yl)propanoic acid (HQA) into two different membrane proteins by heterologous expression in E. coli. Fluorescence and NMR experiments demonstrate complete replacement of the natural amino acid with HQA and stable metal chelation by the mutated proteins. Evidence of site-specific intra- and inter-molecular PREs by NMR in micelle solutions sets the stage for the use of HQA incorporation in solid-state NMR structure determinations of membrane proteins in phospholipid bilayers

  20. Paramagnetic relaxation enhancement of membrane proteins by incorporation of the metal-chelating unnatural amino acid 2-amino-3-(8-hydroxyquinolin-3-yl)propanoic acid (HQA)

    Park, Sang Ho; Wang, Vivian S.; Radoicic, Jasmina; Angelis, Anna A. De; Berkamp, Sabrina; Opella, Stanley J., E-mail: sopella@ucsd.edu [University of California, San Diego, Department of Chemistry and Biochemistry (United States)

    2015-04-15

    The use of paramagnetic constraints in protein NMR is an active area of research because of the benefits of long-range distance measurements (>10 Å). One of the main issues in successful execution is the incorporation of a paramagnetic metal ion into diamagnetic proteins. The most common metal ion tags are relatively long aliphatic chains attached to the side chain of a selected cysteine residue with a chelating group at the end where it can undergo substantial internal motions, decreasing the accuracy of the method. An attractive alternative approach is to incorporate an unnatural amino acid that binds metal ions at a specific site on the protein using the methods of molecular biology. Here we describe the successful incorporation of the unnatural amino acid 2-amino-3-(8-hydroxyquinolin-3-yl)propanoic acid (HQA) into two different membrane proteins by heterologous expression in E. coli. Fluorescence and NMR experiments demonstrate complete replacement of the natural amino acid with HQA and stable metal chelation by the mutated proteins. Evidence of site-specific intra- and inter-molecular PREs by NMR in micelle solutions sets the stage for the use of HQA incorporation in solid-state NMR structure determinations of membrane proteins in phospholipid bilayers.

  1. Extraction behaviour of Am(III) and Eu(III) from nitric acid medium in CMPO-HDEHP impregnated resins

    Saipriya, K.; Kumar, T. [Bhabha Atomic Research Centre Facilities (India). Kalpakkam Reproscessing Plants; Kumaresan, R.; Nayak, P.K.; Venkatesan, K.A.; Antony, M.P. [Indira Gandhi Center for Atomic Research, Kalpakkam (India). Fuel Chemistry Div.

    2016-05-01

    Chromatographic resin containing extractants such as octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO) or bis-(2-ethylhexyl)phosphoric acid (HDEHP) or mixture of extractants (CMPO + HDEHP) in an acrylic polymer matrix was prepared and studied for the extraction of Am(III) and Eu(III) over a range of nitric acid concentration. The effect of various parameters such as concentration of nitric acid in aqueous phase and the concentration of CMPO and HDEHP in the resin phase was studied. The distribution coefficient of Am(III) and Eu(III) in the impregnated resin increased with increased in the concentration of nitric acid for CMPO-impregnated resin, whereas a reverse trend was observed in HDEHP impregnated resin. In case of resin containing both the extractants, synergism was observed at low nitric acid concentration and antagonism at high nitric acid concentration. The mechanism of extraction was probed by slope analysis method at 0.01 and 2 M nitric acid concentrations. Citrate-buffered DTPA was used for the selective separation of Am(III), and a separation factor of 3-4 was obtained at pH 3.

  2. Chelation in metal intoxication XXX: α-mercapto-β-aryl acrylic acids as antidotes to cadmium toxicity

    α-Mercapto-β-(2-furyl) acrylic acid (MFA), α-mercapto-β-(2-hydroxyphenyl) acrylic acid (MHA), β-1,2-phenylene di-α-mercaptoacrylic acid (1,2-PDMA) and β-l,4-phenylene di-α-mercapto acrylic acid (1,4-PDMA) were compared to sodium N-benzyl-D-glucamine dithiocarbamate (NBG-DTC) an effective cadmium chelator, for their ability to mobilize Cd and influence the Cd induced tissue metallothionein (MT) in rats administered 109CdCl2, 72 hr earlier. MFA was almost as effective as NBG-DTC but more effective than MHA in enhancing urinary and faecal excretion of Cd, reducing tissue and blood levels of Cd and in lowering Cd induced increase in hepatic and renal MT contents. 1,2-PDMA and l,4-PDMA were effective only in reducing the hepatic burden of Cd. The results do not indicate any direct relationship between the efficacy of α-mercapto-β-aryl acrylic acids to decorporate body Cd and their lipophilic-hydrophilic character or number-arrangement of their sulfhydryl groups. (author)

  3. Aminolysis of resin-bound N-nosylaziridine-2-carboxylic acids

    Olsen, Christian A; Christensen, Caspar; Nielsen, Birgitte; Farah, Mohamed M; Mohamed, Farah M; Witt, Matthias; Clausen, Rasmus P; Kristensen, Jesper L; Franzyk, Henrik; Jaroszewski, Jerzy W

    2006-01-01

    [Structure: see text] Solid-phase synthesis is a rapidly developing area of organic chemistry, of particular importance for medicinal chemistry and chemical biology. Aziridines have previously only rarely been applied in solid-phase synthesis. In the present work, aminolysis of resin-bound, sprin......-loaded N-nitrobenzenesulfonyl-activated aziridine-2-carboxylic acids has been optimized and employed in the synthesis of a number of open-chain and heterocyclic scaffolds, including enantiopure products....

  4. Method of producing weakly acidic cation exchange resin particles charged with uranyl ions

    Abdelmonem, N.; Ringel, H.; Zimmer, E.

    1981-07-21

    Weakly acidic cationic ion exchange resin particles are charged with uranyl ions by contacting the particles step wise with aqueous uranyl nitrate solution at higher uranium concentrations from stage to stage. An alkaline medium is added to the uranyl nitrate solution in each stage to increase the successive pH values of the uranyl nitrate solution contacting the particles in dependence upon the uranium concentration effective for maximum charging of the particles with uranyl ions.

  5. Removing and recovering of uranium from the acid mine waters by using ion exchange resin

    Ion exchange using resins is one of the few processes capable of reducing ionic contaminants in effluents to very low levels. In this study the process was used to remove and recovery uranium from acid mine waters at Pocos de Caldas-MG Uranium Mining and Milling Plant. The local mineralogical features, allied to the biogeochemical phenomena, owing to presence of pyrite in the rock piles, moreover another factors, resulting acid drainage with several pollutants, including uranium ranging from 6 to 14 mg/l, as sulfate complex, that can be removed by anionic exchanger. The iron interference is eliminated by lime pretreatment of water, increasing pH from 2.6 to 3.3-3.8 to precipitate this cation, without changing the uranium amount. Eight anionic resins were tested, based on the uranium loading, in sorption studies. Retention time, and pH influence was verified for the exchanger chose. With breakthrough of 1 mg U/L and 10 mg U/l in the feed solution, the uranium decontamination level was 94%. Typical values of loading resin were 20-30 g U/l and 70-90 g SO4/l. Uranium elution was done with Na Cl solution. Retention time, saline, and acid concentration were the parameters studied. The concentrate, obtained from the eluate by ammonia precipitation, presented uranium (86,8% as U3 O8) and impurities within commercial specifications. (author)

  6. Screening Analyses of Pinosylvin Stilbenes, Resin Acids and Lignans in Norwegian Conifers

    Anne Fiksdahl

    2006-01-01

    Full Text Available The content and distribution of stilbenes and resin acids in Scots pine (Pinus sylvestris and spruce (Picea abies, sampled in central Norway, have been examined. The contents of pinosylvin stilbenes in pine heartwood/living knots were 0.2-2/2-8 % (w/w. No stilbenes could be detected in spruce (Picea abies. The resin acid contents of pine sapwood/heartwood and knots were 1-4 and 5-10 % (w/w, respectively. Minor amounts of resin acids (< 0.2/< 0.04 %w/w were identified in spruce wood/knots. The lignan content in knots of Norwegian spruce was 6.5 % (w/w. Diastereomerically pure hydroxymatairesinol (HMR, 84 % of total lignans was readily isolated from this source since only minor quantities (2.6 % of total lignans of the allo-HMR diastereomer was detected. Insignificant amounts of lignans were present in the sapwood. Lignans could not be detected in the sapwood or knots of Norwegian sallow (Salix caprea, birch (Betula pendula or juniper (Juniperus communis.

  7. Separation of Fe (III) ions from acidic leach liquor of metasummatite Saghand ore by anion exchange resins

    Ferric ions in dilute acidic leach liquor of uranium ore of Saghand were separated by anion exchange resins. In this research, a simulated solution similar to the actual leach liquor of Saghand was prepared. The simulated solution which was containing chloride and ferric ions. rare earth elements, and some other impurities was treated by different types of Dowex anion exchange resins for ferric ions removal. It appeared that hydrochloric acidic concentration, resin types and particle sizes have a great impact on ferric ions adsorption. Dowex 1 X 4 (200-400 mesh) has the best adsorption of 91% in simulated solution and 79% in actual leach liquor of uranium ore of Saghand respectively

  8. Oxidative degradation of low and intermediate level Radioactive organic wastes 2. Acid decomposition on spent Ion-Exchange resins

    The present work provides a simplified, effective and economic method for the chemical decomposition of radioactively contaminated solid organic waste, especially spent ion - exchange resins. The goal is to achieve volume reduction and to avoid technical problems encountered in processes used for similar purposes (incineration, pyrolysis). Factors efficiency and kinetics of the oxidation of the ion exchange resins in acid medium using hydrogen peroxide as oxidant, namely, duration of treatment and the acid to resin ratio were studied systematically on a laboratory scale. Moreover the percent composition of the off-gas evolved during the decomposition process was analysed. 3 figs., 5 tabs

  9. Preservation of glutamic acid-iron chelate into montmorillonite to efficiently degrade Reactive Blue 19 in a Fenton system under sunlight irradiation at neutral pH

    Huang, Zhujian; Wu, Pingxiao; Gong, Beini; Yang, Shanshan; Li, Hailing; Zhu, Ziao; Cui, Lihua

    2016-05-01

    To further enhance the visible light responsive property and the chemical stability of Fe/clay mineral catalysts, glutamic acid-iron chelate intercalated montmorillonite (G-Fe-Mt) was developed. The physiochemical properties of G-Fe-Mt were investigated by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS), etc. The results showed that glutamic acid-iron chelates were successfully intercalated into the gallery of montmorillonite and the intercalated glutamic acid-iron chelate molecules were well preserved. The product G-Fe-Mt displayed excellent catalytic performance in heterogeneous photo-Fenton reaction under sunlight irradiation at acidic and neutral pH values. The chelation and the visible light responsiveness of glutamic acid produce a synergistic effect leading to greatly enhanced sunlight-Fenton reaction catalyzed by the heterogeneous G-Fe-Mt under neutral pH. G-Fe-Mt is a promising catalyst for advanced oxidation processes.

  10. Resin Catalyst Hybrids

    S. Asaoka

    2005-01-01

    @@ 1Introduction: What are resin catalyst hybrids? There are typically two types of resin catalyst. One is acidic resin which representative is polystyrene sulfonic acid. The other is basic resin which is availed as metal complex support. The objective items of this study on resin catalyst are consisting of pellet hybrid, equilibrium hybrid and function hybrid of acid and base,as shown in Fig. 1[1-5].

  11. Chelation in metal intoxication

    Aaseth, Jan; Skaug, Marit Aralt; Cao, yang;

    2015-01-01

    The present review provides an update of the general principles for the investigation and use of chelating agents in the treatment of intoxications by metals. The clinical use of the old chelators EDTA (ethylenediamine tetraacetate) and BAL (2,3-dimercaptopropanol) is now limited due to the...... inconvenience of parenteral administration, their own toxicity and tendency to increase the neurotoxicity of several metals. The hydrophilic dithiol chelators DMSA (meso-2,3-dimercaptosuccinic acid) and DMPS (2,3-dimercapto-propanesulphonate) are less toxic and more efficient than BAL in the clinical treatment...... of heavy metal poisoning, and available as capsules for oral use. In copper overload, DMSA appears to be a potent antidote, although d-penicillamine is still widely used. In the chelation of iron, the thiols are inefficient, since iron has higher affinity for ligands with nitrogen and oxygen, but the...

  12. Chelation of some transitions, lanthanides and uranium elements with nitrilotriacetic acid and radiolysis of their aqueous solutions

    The present thesis contains chelation studies of some transition metal ions (iron fe (III), cobalt Co (II) and nickel Ni (II), trivalent lanthanide ions (praseodymium pr(III) neodymium nd (III), samarium sm(III), europium Eu(III), gadolinium Gd (III), dysprosium dy (III), erbium Er(III) and ytterbium Yb(III) and uranium (U(IV) and U (V I)) with nitrilotriacetic acid (NTA). spectrophotometric techniques are used to investigate the effectiveness of NTA as a decontaminating agent for radioactive nuclides and to evaluate the optimum conditions under which stable and soluble complexes can be formed. these studies include the effect of PH on the formed complexes and determination of stability constants of the formed species. potentiometric analysis are also performed to follow the formation of binary complexes of some sulpha drugs with investigated metal ions and mixed ligand complexes arising to determine their formation constants

  13. L(+-Lactic acid recovery from cassava bagasse based fermented medium using anion exchange resins

    Rojan P. John

    2008-12-01

    Full Text Available The properties of the ion exchange resins, Amberlite IRA 402, a strong anion exchange resin and IRA 67, a weak anion exchange resin were determined to evaluate their comparative suitability for lactic acid recovery from fermented cassava bagasse. Data on binding capacities and recovery proved that weak base resin in chloride form was the most favourable ones for lactic acid recovery from aqueous solutions and fermentation media. Fermented media obtained through simultaneous saccharification and fermentation of cassava bagasse starch hydrolysate based medium were used for lactic acid recovery study using weak base resin column. Amberlite IRA 67 had much more efficiency than Amberlite IRA 402 to recover lactic acid. Like in other reports, due to the presence of nutrients and ions other than lactate, the binding capacity was slightly lesser while using fermented media (~93% instead of aqueous lactic acid solutions (~98%.As propriedades das resinas de troca iônica, da Amberlite IRA 402, uma resina de troca aniônica forte, e da IRA 67, uma resina de troca aniônica fraca, foram determinadas para se avaliar a adequabilidade comparativa delas à obtenção de ácido lático de bagaço de mandioca fermentado. Dados sobre a capacidade de ligação e sobre a obtenção provaram que a resina de base fraca na forma de cloreto era a mais adequada para a obtenção de ácido lático em soluções aquosas e meios de fermentação. Os meios de fermentação obtidos da sacarificação e da fermentação simultâneas de meios baseados hidrolisados de fécula de bagaço de mandioca foram usados para o estudo da obtenção de ácido lático usando uma coluna de resina de base fraca. A Amberlite IRA 67 mostrou-se muito mais eficaz do que a Amberlite IRA 402 para a obtenção de ácido lático. Como em outros relatórios, devido à presença de nutrientes e íons que não lactatos, a capacidade de ligação foi ligeiramente inferior enquanto se utilizavam meios

  14. Regeneration of Three-Way Automobile Catalysts using Biodegradable Metal Chelating Agent – S, S-Ethylenediamine Disuccinic Acid (S, S-EDDS)

    Regeneration of the activity of three-way catalytic converters (TWCs) was tested for the first time using a biodegradable metal chelating agent (S, S. Ethylenediamine disuccinic acid (S, S-EDDS). The efficiency of this novel environmentally friendly solvent in removing various c...

  15. Biodiesel production from acid oils and ethanol using a solid basic resin as catalyst

    In the search of an alternative fuel to substitute diesel fuel, biodiesel appears as one of the most promising sources of energy for diesel engines because of its environmental advantages and also due to the evolution of the petroleum market. Refined oil is the conventional raw material for the production of this biofuel; however, its major disadvantage is the high cost of its production. Therefore, frying oils, waste oils, crude oils and/or acid oils are being tested as alternative raw materials; nevertheless, there will be some problems if a homogeneous basic catalyst (NaOH) is employed due to the high amount of free fatty acid present in the raw oil. In this work, the transesterification reaction of acid oil using solid resin, Dowex monosphere 550 A, was studied as an alternative process. Ethanol was employed to have a natural and sustainable final product. The reaction temperature's effects, the initial amount of free fatty acid, the molar ratio of alcohol/oil and the type of catalyst (homogeneous or heterogeneous) over the main reaction are analyzed and their effects compared. The results obtained show that the solid resin is an alternative catalyst to be used to produce fatty acid ethyl esters (FAEEs) by a transesterification reaction with a final conversion over 90%. On the other hand, the time required to achieve this conversion is bigger than the one required using conventional technology which employs a homogeneous basic catalyst. This reaction time needs to be optimized. (author)

  16. MULTIELEMENT SOLID PHASE PRECONCENTRATION USING A CHELATING RESIN OF STYRENE DIVINYLBENZENE COPOLYMER AND APPLICATION TO ANALYSIS OF SEAWATER AND FISH OTOLITHS BY INDUCTIVELY COUPLED PLASMA MASS SPECTROMETRY (ICP�MS).

    Zereen, Fahmida; Yilmaz, Vedat; Arslan, Zikri

    2014-01-01

    A new chelating resin has been synthesized by immobilizing 4-(2-thiazolylazo) resorcinol (TAR) onto styrene divinlybenzene copolymer and examined for on-line solid phase extraction/preconcentration of Cd, Co, Cu, Ni, Pb and Zn in seawater and fish otoliths for determination by inductively plasma mass spectrometry (ICP-MS). A volume of 5.0 mL sample solution was loaded onto the mini column of TAR immobilized resin at 2.0 mL min(-1) via a sequential injection system. The optimum pH for multielement preconcentration was around pH 5.5. Recoveries were better than 96% in artificial seawater. Elution was achieved with 1.0 mL of 0.75 mol L(-1) HNO3. The resin possesses large sorption capacity ranging from 82.0 µmol g(-1) for Pb to 319 µmol g(-1) for Cu. The detection limits (3s) varied between 0.0016 µg L(-1) (Cd) and to 0.015 µg L(-1) (Zn) for preconcentration of 5.0 mL blank solutions (pH 5.5). Relative standard deviation (RSD)for three replicate runs was between 0.3% (Cd) and 6% (Zn) at 1.0 µg L(-1) level. The procedure was validated by analysis of Nearshore Seawater certified reference material (CASS-4), and then successfully applied to the determination of the trace elements in fish otoliths (CRM 22) and in coastal seawater and estuarine water samples. PMID:24976635

  17. Heavy metal removal from sludge with organic chelators: Comparative study of N, N-bis(carboxymethyl) glutamic acid and citric acid.

    Suanon, Fidèle; Sun, Qian; Dimon, Biaou; Mama, Daouda; Yu, Chang-Ping

    2016-01-15

    The applicability and performance of a new generation of biodegradable chelator, N, N-Bis(carboxymethyl) glutamic acid (GLDA), for extracting heavy metals from sewage sludge was carried out and compared with citric acid (CA). Targeted metals included Cd, Co, Cu, Zn, Ni and Cr, and their contents in the raw sludge were 63.1, 73.4, 1103.2, 2060.3, 483.9 and 604.1 mg kg(-1) (dry sludge basis), respectively. Metals were divided into six fractions including water soluble, exchangeable, carbonates bound, Fe-Mn bound, organic matters bound and residual fraction via chemical fractionation. Washing results showed that in general GLDA exhibited better performance compared with CA, with removal efficiency of 83.9, 87.3, 81.2, 85.6, 89.3 and 90.2% for Cd, Co, Cu, Zn, Ni and Cr, respectively at equilibrium pH = 3.3. Residual metals were better stabilized in the GLAD-washed sludge than in the CA-washed sludge, and were mostly tightly bonded to the residual fraction. Furthermore, CA promoted phosphorus (P) release while GLDA had an opposite effect and tended to retain P within sludge, which could be beneficial for further application in agricultural use. Findings from this study suggested that GLDA could be a potential replacement for refractory and less environmentally-friendly chelators in the extraction of metals from sludge. PMID:26520041

  18. Correlation of acid-base properties of polymeric chelate sorbents and pH50 of gallium and indium sorption

    Complexing properties of synthesized polymeric chelate-forming sorbents - substituents of polystyrene-azo-pyrocatechol - are investigated and quantitative correlations between pKOH of functional analytical group and pH50 of chelate formation are determined to investigate regularities of interactions in element - sorbent system. Correlations obtained make it possible to realize special forecast on choice and usage of chelate sorbents for separation and concentrating of gallium and indium microquantities from objects of different nature

  19. The fabrication and study of metal chelating stationary phases for the high performance separation of metal ions

    The preparation and characterisation of chelating sorbents suitable for the high efficiency separation of trace metals in complex samples, using a single column and isocratic elution, is described. Hydrophobic, neutral polystyrene divinylbenzene resins were either impregnated with chelating dyes or dynamically modified with heterocyclic organic acids, using physical adsorption and chemisorption processes respectively. A hydrophilic silica substrate was covalently bonded with a chelating aminomethylphosphonic acid group, to assess the chelating potential of this molecule. These substrates were characterised in terms of metal retention capability (selectivity coefficients and capacity factors), separation performance, column efficiency and suitability for analytical applications. Chelating molecules with different ligand groups were found to have unique selectivity patterns dependant upon the conditional stability constants of the chelate. Other factors, including mobile phase constituents - complexing agents, ionic strength and pH, column length and column capacity were additionally investigated to examine their effect upon the separation profiles achieved. The promising metal separation abilities illustrated by a number of these chelating columns were exploited for the determination of trace toxic metals in complex sample matrices using High Performance Chelation Ion Chromatography (HPCIC). This included the determination of beryllium in a certified stream sediment, uranium in seawater and a certified stream sediment, and cadmium, lead and copper in a certified rice flour. The results for each analysis fell within the certified limits, and reproducibility was good. The optimisation of post column detection systems using chromogenic ligands additionally gave good detection limits for the metals in each separation system. (author)

  20. Uranium adsorption from the sulphuric acid leach liquor containing more chlorides with cation-exchange resin SL-406

    The feasibility of uranium adsorption was studied from the sulphuric acid leach liquor of a uranium ore containing more chlorides with cation-exchange resin SL-406. The influence of some factors on uranium adsorption was investigated. It was shown that the resin possesses better selectivity, stability and higher capacity. It can be effectively used to recovery uranium from leach liquors of uranium ores containing more chlorides

  1. Studies on beryllium complexes. V. Chelation of Be2+ ions by anthranilic acid

    After having determined the formation constants of anthranilic acid, the anthranilic acid-Be2+ - H2O system (0.5 M NaClO3 and t=25 deg C) has been studied. The complex BeA+ and the hydroxylated species Be2(OH)A2+, Be3(OH)3A2+, Be3(OH)3A2+ have been identified

  2. Studies on the characteristics of ion exchange resins in the purification system of nuclear power plants

    This research was conducted which involved the synthesis of ion exchange resin used for the purification of various water streams in nuclear power plants. Polymerization of styrene-divinyl-benzene solvent mixtures including catalyst yielded 40-100 mesh various types of beads. The copolymer beads were sulfonated with sulfuric acid to make cation exchange resin, were chloro-methylated with chloromethylmethylether and aminated with various amines in order to make anion exchange resin. The physical properties of copolymer beads and ion exchange resins were evaluated in this study. The cation exchange resin which was synthesized by using 8.5% divinylbenzene and diluent such as n-heptane had almost the same 4.6 meq/g, dry ion exchange capacity as 4.7 meq/g, dry of Westing House Specification WCAP-7452. But at higher divinylbenzene contents than 15%, the ion exchange capacity started to decrease. Anion exchange capacity in this experiment was lower than 3.5 meq/g,dry of Westing House Specification WCAP-7452. An anion exchange resin was synthesized from allylamine monomers via radiation induced-polymerization, and a new chelate resin was prepared from this resin by introducing a dithiocarbamate group, and the adsorption characteristics of metal ions was examined toward the chelate resin. (Author)

  3. Uranium recovery and uranium remove from acid mine waters by ion exchange resin

    Ion exchange using resins is one of few processes capable of reducing contaminants in effluents to very low levels according to environmental legislation. In this study the process was used to remove and recovery uranium from acid mine waters at Pocos de Caldas-MG Uranium Mining and Milling Plant. The presence of pyrite in the waste rock piles, resulting acid drainage with several pollutants. Including uranium ranging from 6 to 14 mg/l, as sulfate complex, that can be removed by an anionic exchanger. Studies of uranium sorption without treatment, and with lime pretreatment of water to precipitate the iron and recovery uranium as commercial product, are presented. Uranium elution was done with NaCl solutions. Saline concentration and retention time were the parameters studied. the uranium decontaminations level in the effluents from acid mine water was 94%. (author)

  4. Overview of analytical procedures for fatty and resin acids in the papermaking process

    Piia Valto

    2012-11-01

    Full Text Available This review describes the role of wood extractives, especially fatty and resin acids, in papermaking, as well as the importance of their removal from process waters. One of the main aims is also to illustrate versatile analysis methods for this purpose and highlight recent developments in corresponding applications. Most of the current methods require time-consuming and laborious sample pretreatment procedures prior to gas chromatography coupled either with flame ionization or mass selective detection. However, some faster, even online techniques with minimum sample pretreatment, are also available, mainly including high performance liquid chromatography coupled with mass spectrometry. The advantages and disadvantages of all analytical procedures are briefly discussed.

  5. Fracture Toughness Evaluation of Hybrid and Nano-hybrid Resin Composites after Ageing under Acidic Environment

    Ferooz M

    2015-03-01

    Full Text Available Statement of Problem: Tooth-coloured restorative materials are brittle with the major shortcomings of sensitivity to flaws and defects. Although various mechanical properties of resin composites have been studied, no fracture toughness test data for nano-hybrid composites under acidic condition for a long period of time has been published. Objectives: To compare the fracture toughness (KIc of two types of resin composites under tensile loading and to assess the effect of distilled water and lactic acid on the resistance of the restoratives to fracture after three months of immersion. Materials and Methods: Four resin composites were used: three nanohybrids [EsteliteSigma Quick (Kuraray, Luna (SDI, Paradigm (3M/ESPE] and one hybrid, Rok (SDI. The specimens were prepared using a custom-made polytetrafluorethylene split mould, stored in distilled water (pH 6.8 or 0.01mol/L lactic acid (pH 4 and conditioned at 37°C for 24 hours, 1 or 3 months. They were loaded under tensile stress using a universal testing machine; the maximum load (N to the specimen failure was recorded and the fracture toughness (KIc was calculated. Data were analysed by ANOVA and Tukey’s test using SPSS, version 18. Results: The results of two-way ANOVA did not show a significant combined effect of material, time, and storage medium on fracture toughness (p= 0.056. However, there was a strong interaction between materials and time (p=0.001 when the storage medium were ignored. After 24 h of immersion in distilled water, Paradigm revealed the highest KIc values followed by Rok, Luna and Estelite. Immersion in either distilled water or lactic acid significantly decreased the fracture toughness of almost all materials as time interval increased. Conclusions: Paradigm showed the highest fracture toughness followed by Rok, Luna and Estelite respectively. As time increased, KIc significantly decreased for almost all resin composites except for Luna which showed a slight decrease

  6. Kinetics study on separation of cadmium from tellurium in acidic solution media using ion-exchange resins

    The feasibility of using ion-exchange resins to separate cadmium from tellurium in acidic solutions of the two metals was investigated. We studied the competitive adsorption of cadmium and tellurium in such resins under varying acid strengths and contact time. We found that low sulfuric acid strength (i.e., 0.5 M) was most effective in removing cadmium from solutions. Different ion-exchange resins were tested for their affinity for cadmium and tellurium ions. In the selected systems, the ion-exchange rate of cadmium was rapid in the first 20 min, and reached equilibrium within 2 h. The Lagergren first-order model described the kinetic data with high coefficient of determination and correlation values. At room temperatures the ion-exchange for cadmium onto the resin followed the Freundlich isotherm model. The maximum removal of cadmium obtained from batch studies using resin A was 91%. Column studies with the same resin showed a removal of cadmium of 99.99% or higher

  7. HTGR fuel development: loading of uranium on carboxylic acid cation-exchange resins using solvent extraction of nitrate

    The reference fuel kernel for recycle of 233U to HTGR's (High-Temperature Gas-Cooled Reactors) is prepared by loading carboxylic acid cation-exchange resins with uranium and carbonizing at controlled conditions. The purified 233UO2(NO3)2 solution from a fuel reprocessing plant contains excess HNO3 (NO3-/U ratio of approximately 2.2). The reference flowsheet for a 233U recycle fuel facility at Oak Ridge uses solvent extraction of nitrate by a 0.3 M secondary amine in a hydrocarbon diluent to prepare acid-deficient uranyl nitrate. This nitrate extraction, along with resin loading and amine regeneration steps, was demonstrated in 14 runs. No significant operating difficulties were encountered. The process is controlled via in-line pH measurements for the acid-deficient uranyl nitrate solutions. Information was developed on pH values for uranyl nitrate solution vs NO3-/U mole ratios, resin loading kinetics, resin drying requirements, and other resin loading process parameters. Calculations made to estimate the capacities of equipment that is geometrically safe with respect to control of nuclear criticality indicate 100 kg/day or more of uranium for single nitrate extraction lines with one continuous resin loading contactor or four batch loading contactors. (auth)

  8. Evaluation of 111In-labeled macrocyclic chelator-amino acid derivatives for cancer imaging

    Purpose: We evaluated new 111In-labeled amino acid derivatives, in which the amino acids are conjugated with1,4,7,10-tetra-azacyclododecane-1,4,7,10-tetraacetic acid (DOTA), 1,4,7,10-tetraazacyclododecane-1,7-diacetic acid (DO2A) or 1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid (DO3A). Methods: DOTA-aminoalanine (DOTA-A), DOTA-aminohomoalanine (DOTA-H), DOTA-lysine (DOTA-L), DO2A-alanine (DO2A-A), DO3A-alanine (DO3A-A) and DO3A-homoalanine (DO3A-H) were labeled with 111In. In vitro cell uptake assays were performed usingHep3B (a human hepatoma cell line), CT26 (a mouse colon cancer cell line) and U87MG (a human glioma cell line). In vitro cell uptake inhibition assays were performed using U87MG and 111In-DO3A-H. U87MG bearing xenografted mice were subject to biodistribution, SPECT imaging, autoradiography, and immunohistochemistry studies. Results: Of the amino acid derivatives and cell lines examined, U87MG and 111In-DO3A-H showed highest uptake in vitro. This uptake was blocked by 2-aminobicyclo-[2,2,1] heptane-2-carboxylic acid (BCH) and by tryptophan. 111In-DO3A-HSPECT imaging of U87MG bearing xenografted mice visualized tumors (mean tumor-to-muscle ratio 3.16±0.74). Autoradiography and immunohistochemistry revealed that 111In-DO3A-H uptake matched L-type amino acid transporter 1 expression. Conclusion: Tumor uptake was successfully imaged using 111In-DO3A-H in U87MG bearing xenografted mice. 111In-DO3A-H appears to be useful for imaging tumors expressing L-type amino acid transporter.

  9. SYNTHESIS OF 2—HYDROXYETHYL ACRYLATE BY USING STRONG ACIDIC CATION ION EXCHANGE RESIN AS CATALYST

    GAODabin

    1992-01-01

    2-Hydroxyethyl acrylate is synthesized from acrylic acid and ethylene glycol under a simple and mild condition by using strong acidic cation ion exchange resin as a catalyst,which could be recycled as long as 10 times with high activation.

  10. Preliminary chelation and dissolution effects of oxalic acid and disodium oxalate on polymeric 123-superconductors

    The polymeric 123-superconductor material was selectively etched by exposure to aqueous solutions of oxalic acid and disodium oxalate. Superconductivity decreased with time. XPS, AES, FTIR and ATF show that the amount of copper at the surface is decreased, shows the presence of bound oxalate and shows a decrease in peaks associated with superconductivity for the sample treated with oxalate

  11. Removal of 5-Amino-2-chlorotoluene-4-sulfonic and Chlorhydric Acids From Wastewater by Weakly Basic Resin: Equilibrium and Kinetics

    2007-01-01

    To study the adsorption of 5-Amino-2-chlorotoluene-4-sulfonic (CLT) and chlorhydric (HCl) acids from wastewater by weakly basic resin.Methods The kinetics and isotherm were studied. Thermodynamic parameters for the adsorption of acids were calculated and discussed.Results The adsorption of CLT and HCl acids followed Langmuir isotherm and the first-order kinetics model.Conclusion The adsorptive affinity of the two acids on D301R is in the order of CLT acid > HCl acid. CLT and HCl acids can be separated.

  12. Synthesis, Characterization and Chelating Properties of Benzimidazole-Salicylic Acid Combined Molecule

    Kamlesh V. Patel; Singh, Arun

    2009-01-01

    Aminomethylation (i.e. Mannich reaction) of benzimidazole was carried out by treating benzimidalzole with formaldehyde and 4-aminosalicylic acid. The resultant compound was designated as 1-(4-carboxy-3-hydroxyphenyl aminomethyl) benzimidazole (BI-SA). The transition metal complexes of Cu2+, Co2+, Ni2+, Mn2+, Zn2+ and Fe3+ of BI-SA have been prepared and characterized by elemental analyses, spectral studies, magnetic moment determination, molar conductivity measurement and microbicidal activity.

  13. Surface roughness of flowable resin composites eroded by acidic and alcoholic drinks

    Claudio Poggio

    2012-01-01

    Full Text Available Aim: The aim of this study is to evaluate the surface roughness of four flowable resin composites following exposure to acidic and alcoholic drinks. Materials and Methods: SureFil SDR flow, TetricEvoFlow, Esthet-X Flow and Amaris Flow HT samples were immersed in artificial saliva, Coca Cola and Chivas Regal Whisky. Each specimen was examined using a Leica DCM 3D microscope: Arithmetical mean height of the surface profiles was measured (Sa. Results: Kruskal-Wallis test showed significant differences among various groups (P<0,001. Mann Whitney test was applied and control groups showed significantly lower Sa values than other groups (P=0,008. Coca Cola groups showed highest Sa values (P<0,021. No significant differences (P=0,14 in surface texture were found among the specimens of the different materials. No significant differences were found among TetricEvoFlow, Esthet-X Flow and Amaris Flow under control conditions nor after Coca Cola application. Under control condition and after Coca Cola application SureFil SDR flow showed significantly higher Sa values. Moreover, after whisky application Amaris Flow showed significantly lower Sa values then the other three groups that showed no significant differences among them. Conclusions: Acidic and alcoholic drinks eroded the surface roughness of all evaluated flowable resin composites.

  14. Radiolytic and chemical degradation of strong acidic ion-exchange resins: Study of ligands formed

    The formation of water-soluble organic ligands by radiolytic and chemical degradation of several strong acidic ion-exchange resins was investigated under conditions close to those of the near field of a cementitious repository. The most important degradation products were studied and their complexing properties evaluated. Irradiation of strong acidic cation exchange resins (Powder PCH and Lewatite S-100) resulted in the formation of mainly sulfate and dissolved organic carbon. High-performance liquid chromatography analysis indicated the presence of oxalate, contributing to 10 to 20% of the organic carbon. The identity of the remainder is unknown. The presence of oxalate as a complexant is consistent with results from earlier work. Complexation studies with Cu2+ and Ni2+ showed the presence of two ligands: oxalate and ligand X. Although ligand X could not be identified, it could be characterized by its concentration ([X]T ∼ 10-5 to 10-6 M), a deprotonation constant (pKH approximately 7.4 at I = 0.1 M), and a complexation constant for the NiX complex (log KNiXapproximately 7.0 at I = 0.1 M). In the absence of irradiation, no evidence for the formation of ligands was found

  15. Separation of rare earths in nitric acid medium by a novel silica-based pyridinium anion exchange resin

    To separate rare earths in nitric acid medium by anion exchange process, a novel silica-based macro-reticular anion exchange resin (SiPyR-N4) with pyridinium as functional group has been synthesized. It was found that the SiPyR-N4 resin exhibits a quite strong adsorption for some rare earths especially the light rare earth elements such as La, Ce, Pr, Nd and Pm whose distribution coefficients onto SiPyR-N4 reach 10-25 dm3/kg-resin, which are much higher than the reported values for these elements with conventional anion exchange resins. The results from the column experiments show that the rare earths can be separated into the three groups: light, moderate and heavy rare earths and, a perfect separation between La-Pr group and Sm-Gd group can be achieved

  16. Direct injection analysis of fatty and resin acids in papermaking process waters by HPLC/MS.

    Valto, Piia; Knuutinen, Juha; Alén, Raimo

    2011-04-01

    A novel HPLC-atmospheric pressure chemical ionization/MS (HPLC-APCI/MS) method was developed for the rapid analysis of selected fatty and resin acids typically present in papermaking process waters. A mixture of palmitic, stearic, oleic, linolenic, and dehydroabietic acids was separated by a commercial HPLC column (a modified stationary C(18) phase) using gradient elution with methanol/0.15% formic acid (pH 2.5) as a mobile phase. The internal standard (myristic acid) method was used to calculate the correlation coefficients and in the quantitation of the results. In the thorough quality parameters measurement, a mixture of these model acids in aqueous media as well as in six different paper machine process waters was quantitatively determined. The measured quality parameters, such as selectivity, linearity, precision, and accuracy, clearly indicated that, compared with traditional gas chromatographic techniques, the simple method developed provided a faster chromatographic analysis with almost real-time monitoring of these acids. PMID:21360668

  17. Environmental biogeochemistry of chelating agents and recommendations for the disposal of chelated radioactive wastes

    The environmental chemistry of the three most common aminopolycarboxylic acid chelating agents, NTA (nitrilotriacetic acid), EDTA (ethylenediaminetetraacetic acid), and DTPA (diethylenetriaminepentaacetic acid) is reviewed. This review includes information on their persistence in the environment, as well as their tendency to form complexes with actinides. Data on the sorption of chelated actinides by geologic substrates and on the uptake of chelated actinides by plants are also presented. Three different technical options for disposing chelated low-level radioactive wastes are proposed: bind the solidified chelated waste in some kind of solid matrix that has a slow leach rate and bury the waste in a ''dry'' disposal site; substitute biodegradable chelating agents in the decontamination reagent for the chelating agents that are persistent in the environment; chemically or thermally degrade the chelating agents in the waste prior to disposal. The relative advantages and disadvantages of each of these options are discussed. 81 refs

  18. Estimation of Stability Constants of Copper(II) Chelates with Amino Acids by Overlapping Spheres Method

    Raos, Nenad

    2005-01-01

    The method of overlapping spheres (OS) was applied to the estimation of stability constants of mono- (log β110) and bis-complexes (log β120) of α-amino acids and their N-alkyl and N,Ndialkyl derivatives with copper(II). The central sphere, with a 0.3 or 0.4 nm radius, was placed at the central (Cu), equatorial (N) or apical (X) position of the coordination polyhedron. The overlapping volume of the central sphere and the van der Waals spheres of neighbouring atoms was calculated and correlated...

  19. Ion-exclusion chromatography with conductimetric detection of aliphatic carboxylic acids on a weakly acidic cation-exchange resin by elution with benzoic acid-beta-cyclodextrin.

    Tanaka, Kazuhiko; Mori, Masanobu; Xu, Qun; Helaleh, Murad I H; Ikedo, Mikaru; Taoda, Hiroshi; Hu, Wenzhi; Hasebe, Kiyoshi; Fritz, James S; Haddad, Paul R

    2003-05-16

    In this study, an aqueous solution consisting of benzoic acid with low background conductivity and beta-cyclodextrin (beta-CD) of hydrophilic nature and the inclusion effect to benzoic acid were used as eluent for the ion-exclusion chromatographic separation of aliphatic carboxylic acids with different pKa values and hydrophobicity on a polymethacrylate-based weakly acidic cation-exchange resin in the H+ form. With increasing concentration of beta-cyclodextrin in the eluent, the retention times of the carboxylic acids decreased due to the increased hydrophilicity of the polymethacrylate-based cation-exchange resin surface from the adsorption of OH groups of beta-cyclodextrin. Moreover, the eluent background conductivity decreased with increasing concentration of beta-cyclodextrin in 1 mM benzoic acid, which could result in higher sensitivity for conductimetric detection. The ion-exclusion chromatographic separation of carboxylic acids with high resolution and sensitivity was accomplished successfully by elution with a 1 mM benzoic acid-10 mM cyclodextrin solution without chemical suppression. PMID:12830884

  20. Lipoic acid in combination with a chelator ameliorates lead-induced peroxidative damages in rat kidney

    Sivaprasad, R.; Nagaraj, M.; Varalakshmi, P. [Department of Medical Biochemistry, University of Madras (Taramani), Chennai 600 113 (India)

    2002-08-01

    The deleterious effect of lead has been attributed to lead-induced oxidative stress with the consequence of lipid peroxidation. The present study was designed to investigate the combined effect of DL-{alpha}-lipoic acid (LA) and meso-2,3-dimercaptosuccinic acid (DMSA) on lead-induced peroxidative damages in rat kidney. The increase in peroxidated lipids in lead-poisoned rats was accompanied by alterations in antioxidant defence systems. Lead acetate (Pb, 0.2%) was administered in drinking water for 5 weeks to induce lead toxicity. LA (25 mg/kg body weight per day i.p) and DMSA (20 mg/kg body weight per day i.p) were administered individually and also in combination during the sixth week. Nephrotoxic damage was evident from decreases in the activities of {gamma}-glutamyl transferase and N-acetyl {beta}-D-glucosaminidase, which were reversed upon combined treatment with LA and DMSA. Rats subjected to lead intoxication showed a decline in the thiol capacity of the cell, accompanied by high malondialdehyde levels along with lowered activities of catalase, superoxide dismutase, glutathione peroxidase and glutathione metabolizing enzymes (glutathione reductase, glucose-6-phosphate dehydrogenase, glutathione-S-transferase). Supplementation with LA as a sole agent showed considerable changes over oxidative stress parameters. The study has highlighted the combined effect of both drugs as being more effective in reversing oxidative damage by bringing about an improvement in the reductive status of the cell. (orig.)

  1. Determination of free Gd3+ as a cyclohexanediaminetetraacetic acid complex by reversed-phase HPLC in ionic gadolinium(III) chelates

    A reversed-phase HPLC method to analyze free Gd3+ in ionic Gd chelates, Gd(EDTA)-, Gd(DPTA)2-, and Gd(DOTA)-, was developed. In the method, free Gd3+ was complexed with cyclohexanediaminetetraacetic acid (CDTA). Either the complexation was carried out before analysis or CDTA was added to the buffered mobile phase (pH 7.4, Tris-HCI) to complex the free metal in the chelate sample. The complex Gd(CDTA)- was separated from the ionic chelate by high-performance liquid chromatography on a C18 reversed-phase Nucleosil column. A fluorescence detection method with 280-and 310-nm excitation and emission wavelengths, respectively, was used for monitoring. The recoverability, the linearity, and the limit of detection (LOD) of the method were determined. The method was evaluated in terms of thermodynamic and kinetic properties of Gd(CDTA)-, Gd(EDTA)-, Gd(DTPA)2-, and Gd(DOTA)-. The LOD for Gd3+ in the ionic chelates was 39 ng. 27 refs., 4 figs., 3 tabs

  2. Transmetallation Versus β-Hydride Elimination : The Role of 1,4 Benzoquinone in Chelation-Controlled Arylation Reactions with Arylboronic Acids

    Sköld, Christian; Kleimark, Jonatan; Trejos, Alejandro; Odell, Luke R; Nilsson Lill, Sten O.; Norrby, Per-Ola; Larhed, Mats

    2012-01-01

    AbstractThe formation of an atypical, saturated, diarylated, Heck/Suzuki, domino product produced under oxidative Heck reaction conditions, employing arylboronic acids and a chelating vinyl ether, has been investigated by DFT calculations. The calculations highlight the crucial role of 1,4-benzoquinone (BQ) in the reaction. In addition to its role as an oxidant of palladium, which is necessary to complete the catalytic cycle, this electron-deficient alkene opens up a low-energy reaction pathw...

  3. Roles of manganese and organic acid chelators in regulating lignin degradation and biosynthesis of peroxidases by Phanerochaete chrysosporium.

    Perez, J.; Jeffries, T W

    1992-01-01

    We studied the effect of manganese and various organic chelators on the distribution, depolymerization, and mineralization of synthetic 14C-labeled lignins (DHP) in cultures of Phanerochaete chrysosporium. In the presence of high levels of manganese [Mn(II) or Mn(III)], along with a suitable chelator, lignin peroxidase (LiP) production was repressed and manganese peroxidase (MnP) production was stimulated. Even though partial lignin depolymerization was observed under these conditions, furthe...

  4. The Mechanism of Sol-Gel Synthesis of Normal Spinel LiMn2O4 with Chelation of Citric Acid

    WU Hui; LEI Jia-heng; CHEN Yong-xi; SUN Yu-bin; YUAN Qi-hua

    2002-01-01

    The sol-gel process of citric acid chelating with metal cations for the synthesis of normal spinel LiMn2O4 and the reaction mechanism were investigated by means of XRD, IR, TG-DTA, and SEM. The results show that at the beginning lithium citrate and chelate compound of citric acid with manganese ions formed, and then with heating the esterification and condensation reactions occured between them and glycol. The products obtained are polymers in which metal cations are distributed homogeneously on atomic scale that ensure high reactivity to cations of Li + and Mn2 + . Firing the gel prepared by this process, the lattice diffusions of solid reactant ions caused by non-homogeneity of reactants are eliminated and avoided. At 400℃ phase-pure LiMn2 O4 with nanometer scale crystallization having precise stoichiometry and perfect crystallization can be obtained. The model of chelate coordinate of double-molecule between citric acid and Mn2 + in the gel network is proposed. It is important for explaining the dispersion state of Mn2 + and the formation process of gel by this model.

  5. Influence of ozone and paracetic acid disinfection on adhesion of resilient liners to acrylic resin

    2016-01-01

    PURPOSE The aim of this study was to evaluate the effect of paracetic acid (PAA) and ozone disinfection on the tensile bond strength (TBS) of silicone-based resilient liners to acrylic resins. MATERIALS AND METHODS One hundred and twenty dumbbell shaped heat-polymerized acrylic resins were prepared. From the mid segment of the specimens, 3 mm of acrylic were grinded off and separated parts were reattached by resilient liners. The specimens were divided into 2 control (control1, control7) and 4 test groups of PAA and ozone disinfection (PAA1, PAA7, ozone1 and ozone7; n=10). While control groups were immersed in distilled water for 10 min (control1) and 7 days (control7), test groups were subjected to PAA (16 g/L) or ozone rich water (4 mg/L) for 1 cycle (10 min for PAA and 60 min for ozone) per day for 7 days prior to tensile tests. Measurements of the TBS were analyzed using 3-way ANOVA and Tukey's HSD test. RESULTS Adhesive strength of Mollosil decreased significantly by application of ozone disinfection. PAA disinfection had no negative effect on the TBS values of Mollosil and Molloplast B to acrylic resin. Single application of ozone disinfection did not have any negative effect on TBS values of Molloplast B, but prolonged exposure to ozone decreased its adhesive strength. CONCLUSION The adhesion of resilient liners to acrylic was not adversely affected by PAA disinfection. Immersion in ozonated water significantly decreased TBS of Mollosil. Prolonged exposure to ozone negatively affects adhesion of Molloplast B to denture base materials. PMID:27555898

  6. Purification of Lactic Acid by Heterogeneous Catalytic Distillation Using Ion-exchange Resins

    马利; 张阳; 杨基础

    2005-01-01

    The purification of lactic acid based on the esterification of raw lactic acid from fermentation broth and then the catalytic distillation hydrolysis of methyl lactate simultaneously to achieve pure lactic acid is reported. The esterification kinetics of lactic acid with methanol catalyzed by strong-acid cation-exchange resins (Amberlyst-15,D001, D002, NKC, 002) was studied under the condition that simulates the real catalytic environment. Experimental results were correlated by a Langmuir-Hinselwood model and the nonideality of the solution was taken into account by using activities calculated by the universal quasichemical functional group activity coefficient (UNIFAC) method.A good agreement between the model and the experimental data was achieved. Continuous purification experiments were conducted to find the optimum column configuration and operation condition for the system. The effects of various parameters, e.g. the length of different section of the column, feed rate and ratio of reactants, packing material and catalyst type, were studied. This novel system shows good separation results in lab scale, and is potential for industrial application.

  7. Fluid extraction using carbon dioxide and organophosphorus chelating agents

    Smart, Neil G.; Wai, Chien M.; Lin, Yuehe; Kwang, Yak Hwa

    1998-01-01

    Methods for extracting metalloid and metal species from a solid or liquid material by exposing the material to a fluid solvent, particularly supercritical CO.sub.2, and a chelating agent are described. The chelating agent forms a chelate with the species, the chelate being soluble in the fluid to allow removal of the species from the material. In preferred embodiments the extraction solvent is supercritical CO.sub.2 and the chelating agent comprises an organophosphorous chelating agent, particularly sulfur-containing organophosphorous chelating agents, including mixtures of chelating agents. Examples of chelating agents include monothiophosphinic acid, di-thiophosphinic acid, phosphine sulfite, phosphorothioic acid, and mixtures thereof. The method provides an environmentally benign process for removing metal and metalloids from industrial waste solutions, particularly acidic solutions. Both the chelate and the supercritical fluid can be regenerated and the contaminant species recovered to provide an economic, efficient process.

  8. Ion-exchange Resin Catalyzed Esterification of Lactic Acid with Isopropanol: a Kinetic Study

    Amrit P. Toor

    2011-05-01

    Full Text Available The kinetic behavior of esterification of lactic acid with isopropanol over an acidic cation exchange resin, Amberlyst 15, was studied under isothermal condition. Isopropyl lactate synthesized in this reaction is an important pharmaceutical intermediate. The experiments were carried out in a stirred batch reactor in the temperature range of 323.15 to 353.15 K. The effect of various parameters such as temperature, molar ratio and catalyst loading was studied. Variation in parameters on rate of reaction demonstrated that the reaction was intrinsically controlled. Kinetic modeling was performed using Eley-Rideal model which acceptably fits the experimental data. The activation energy was found to be 22.007 kJ/mol and frequency factor was 0.036809 l2 g-1 mol-1 min-1 for forward reaction. The value of entropy for the forward reaction was found to be 182.317 J K-1 mol-1 . © 2011 BCREC UNDIP. All rights reserved(Received: 19th January 2011, Revised: 16th March 2011; Accepted: 16th March 2011[How to Cite: A.P. Toor, M. Sharma, S. Thakur, and R. K. Wanchoo. (2011. Ion-exchange Resin Catalyzed Esterification of Lactic Acid with Isopropanol: a Kinetic Study. Bulletin of Chemical Reaction Engineering and Catalysis, 6(1: 39-45. doi:10.9767/bcrec.6.1.791.39-45][How to Link / DOI: http://dx.doi.org/10.9767/bcrec.6.1.791.39-45 || or local:  http://ejournal.undip.ac.id/index.php/bcrec/article/view/791 ] | View in  

  9. Novel bioactive polyester scaffolds prepared from unsaturated resins based on isosorbide and succinic acid

    In this study new biodegradable materials obtained by crosslinking poly(3-allyloxy-1,2-propylene succinate) (PSAGE) with oligo(isosorbide maleate) (OMIS) and small amount of methyl methacrylate were investigated. The porous scaffolds were obtained in the presence of a foaming system consisted of calcium carbonate/carboxylic acid mixture, creating in situ porous structure during crosslinking of liquid formulations. The maximum crosslinking temperature and setting time, the cured porous materials morphology as well as the effect of their porosity on mechanical properties and hydrolytic degradation process were evaluated. It was found that the kind of carboxylic acid used in the foaming system influenced compressive strength and compressive modulus of porous scaffolds. The MTS cytotoxicity assay was carried out for OMIS using hFOB1.19 cell line. OMIS resin was found to be non-toxic in wide range of concentrations. On the ground of scanning electron microscopy (SEM) observations and energy X-ray dispersive analysis (EDX) it was found that hydroxyapatite (HA) formation at the scaffolds surfaces within short period of soaking in phosphate buffer solution occurs. After 3 h immersion a compact layer of HA was observed at the surface of the samples. The obtained results suggest potential applicability of resulted new porous crosslinked polymeric materials as temporary bone void fillers. - Highlights: • Isosorbide-based resin was used as a component of biodegradable scaffolds. • CAC/carboxylic acid system was proven as facile method to obtain porous scaffolds. • Porous scaffolds displayed the formation of hydroxyapatite at their surfaces

  10. Novel bioactive polyester scaffolds prepared from unsaturated resins based on isosorbide and succinic acid

    Śmiga-Matuszowicz, Monika, E-mail: monika.smiga-matuszowicz@polsl.pl [Silesian University of Technology, Department of Physical Chemistry and Technology of Polymers, M. Strzody Street 9, 44-100 Gliwice (Poland); Janicki, Bartosz; Jaszcz, Katarzyna; Łukaszczyk, Jan [Silesian University of Technology, Department of Physical Chemistry and Technology of Polymers, M. Strzody Street 9, 44-100 Gliwice (Poland); Kaczmarek, Marcin [Silesian University of Technology, Department of Biomaterials and Medical Devices Engineering, de Gaulle' a Street 66, 41-800 Zabrze (Poland); Lesiak, Marta; Sieroń, Aleksander L. [Medical University of Silesia, Department of General and Molecular Biology and Genetics, Medyków Street 18, 40-752 Katowice (Poland); Simka, Wojciech [Silesian University of Technology, Department of Chemistry, Inorganic Technology and Fuels, B. Krzywoustego Street 6, 44-100 Gliwice (Poland); Mierzwiński, Maciej; Kusz, Damian [Medical University of Silesia, Department of Orthopedics and Traumatology, Ziołowa Street 45, 40-635 Katowice (Poland)

    2014-12-01

    In this study new biodegradable materials obtained by crosslinking poly(3-allyloxy-1,2-propylene succinate) (PSAGE) with oligo(isosorbide maleate) (OMIS) and small amount of methyl methacrylate were investigated. The porous scaffolds were obtained in the presence of a foaming system consisted of calcium carbonate/carboxylic acid mixture, creating in situ porous structure during crosslinking of liquid formulations. The maximum crosslinking temperature and setting time, the cured porous materials morphology as well as the effect of their porosity on mechanical properties and hydrolytic degradation process were evaluated. It was found that the kind of carboxylic acid used in the foaming system influenced compressive strength and compressive modulus of porous scaffolds. The MTS cytotoxicity assay was carried out for OMIS using hFOB1.19 cell line. OMIS resin was found to be non-toxic in wide range of concentrations. On the ground of scanning electron microscopy (SEM) observations and energy X-ray dispersive analysis (EDX) it was found that hydroxyapatite (HA) formation at the scaffolds surfaces within short period of soaking in phosphate buffer solution occurs. After 3 h immersion a compact layer of HA was observed at the surface of the samples. The obtained results suggest potential applicability of resulted new porous crosslinked polymeric materials as temporary bone void fillers. - Highlights: • Isosorbide-based resin was used as a component of biodegradable scaffolds. • CAC/carboxylic acid system was proven as facile method to obtain porous scaffolds. • Porous scaffolds displayed the formation of hydroxyapatite at their surfaces.

  11. A new chelating resin containing indole-methionine composite: synthesis, characterization and determination of lead and silver after preconcentration in biological and environmental samples

    Derivatized L-methionine having indole backbone has been anchored on polystyrene divinylbenzene matrix and has been found to have selective binding ability for Pb(II) and Ag(I) ions at pH 8.0 and 6.5, respectively. Maximum capacity for Pb(II) at pH 8.0 is 0.35 mmol g1 and for Ag(I) at pH 6.5 is 1.5 mmol g-1. The final resin and its precursors are fully characterized by different instrumental techniques. Detection limits (3 x standard deviation of the blank signal) were 30 ng mL-1 for Pb(II) and 38 ng mL-1 for Ag(I). Recoveries were found to be 97.4 +- 2.6% for Pb(II) at 98% confidence level and 98.2 +- 3.4% for Ag(I) at 97% confidence level. The developed procedure has been successfully applied for preconcentration of Pb(II) and Ag(I) in different environmental and biological samples. The concentration of Pb(II) was determined by flame atomic absorption spectrometry (FAAS) and that of Ag(I) ion by using a scintillation counter equipped with a well type NaI (Tl) crystal detector. (author)

  12. A basic study for the operation of boron thermal regeneration system : Adsorption equilibrium of boric acid on ion exchange resin

    The adsorption characteristics of boric acid on a strong-base anion exchange resin, an Amberlite IRN-78LC resin in OH- form, were investigated at temperature from 10 deg C to 60 deg C in the concentrations of boron up to 1500 ppm covering the BTRS operational conditions. A computer code was developed to calculate the composition of borate ions in solution as a function of boron concentration, temperature and pH. From the calculated composition of borate ions and experimental data of adsorption equilibrium, the model was proposed for the adsorption isotherm of boric acid on the resin. The results in this study can be applied for the optimum operation of BTRS. (Author)

  13. Sorption efficiency of a new sorbent towards uranyl. Phosphonic acid grafted Merrifield resin

    A novel sorbent resin consisting of a Phosphonic Acid grafted on Merrifield Resin (PA-MR) for the extraction of uranyl from nitrate media is described. The sorption behaviour of uranyl cation on PA-MR was investigated using batch equilibrium technique. The effects of parameters such as shaking speed, pH levels, contact time, metal concentrations, ionic strength and temperature were reported. The results show that the sorption capacity increases with increasing both initial uranyl ion concentration and temperature and decreases with increasing ionic strength. Therefore, the optimum condition for the present study should be using 6.6 mg adsorbent per 1.0 mg uranyl in solution with pH 3.6 and shaking at 250 rpm for 180 min. The adsorption behavior of the system was also investigated and found to be in line with Langmuir isotherm. The kinetic data was well described by the pseudo second-order. Thermodynamics data leads to endothermic process ΔH = + 31.03 kJ-1 mol-1, ΔS = + 146.64 J mol-1 K-1 and ΔG = -11.96 kJ mol-1 at 20 K. ΔG decreased to negatives values with increasing temperature indicating that the process was more favoured at high temperature. (author)

  14. Kinetic investigation of the immobilization of chromotropic acid derivatives onto anion exchange resin

    Savić Jasmina

    2007-01-01

    Full Text Available The adsorption kinetics of pyrazol- (РАСА and imidazol-azo-chromo-tropic acid (IACA onto Dowex 1-X8 resin, as a function of the dye concentration and temperature were investigated at pH 4.5. The pseudo-first- and second-order kinetic models and intraparticle diffusion model were used to describe the obtained kinetic data. The adsorption rate constants were found to be in the order of magnitude 10-2 min-1 for all of the used kinetics models. The adsorption capacity increases with increasing initial dye concentration. The study of adsorption kinetics at different temperatures (in the range from 5 to 25 °C reveals an increase in the rate of adsorption and adsorption capacity with increasing temperature. The activation energy (in the case of РАСА 16.6 kJ/mol, and for IACA 11.3 kJ/mol was determined using the Arrhenius dependence. Electrostatic interactions between the dye and resin beads were shown to be the adsorption mechanism.

  15. New method for studying the efficiency of chelating agents of the polyamine acid series for internal decontamination; Methode nouvelle d'etude de l'efficacite des chelateurs de la serie des acides polyamines pour la decontamination interne

    Lafuma, J.; Nenot, J.C.; Morin, M. [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1968-07-01

    We followed the biological fate of a complex formed on one side with either a rare earth (cerium-144) or a transuranium element (plutonium-239), and on the other side with a chelating agent of the polyamino acid series (EDTA, BAETA, DTPA, TTHA). This method allowed to study: 1 - the in vivo stability of the various complexes and to compare them; 2 - the stability of the complexes as a function of the isotope - chelating agent weight relationships; 3 - the metabolism of the chelating agents resulting in stable complexes, i. e. DTPA and TTHA mainly. This simple method brought out the higher efficiency, of DTPA in chelating rare earths and plutonium and for therapeutic purposes. (authors) [French] La methode consiste a suivre le devenir biologique d'un complexe forme d'une part avec une terre rare (cerium 144) ou un transuranien (plutonium 239) et d'autre part avec un chelateur de la serie des acides polyamines (EDTA, BAETA, DTPA, TTHA). Elle permet d'etudier: 1 - la stabilite in vivo des differents complexes, de les comparer; 2 - la stabilite des complexes en fonction des rapports ponderaux isotope - chelateurs; 3 - le metabolisme des chelateurs formant des complexes stables, essentiellement DTPA et TTHA. Cette methode simple degage la suprematie du DTPA en ce qui concerne la chelation des terres rares et du plutonium, et son utilisation a des fins therapeutiques. (auteurs)

  16. Measurement of the acidities of several cation-exchange resins using hydrogen-isotope exchange reaction

    The hydrogen-isotope exchange reaction between ethanol (unlabeled) and one of three cation-exchange resins labeled with tritium has been observed at 40-80degC. The acidity (acidity based on kinetic logic) at each temperature has been obtained from a A'-McKay plot based on the respective data obtained. The following results have been obtained on the basis of both the acidities obtained in this work and the acidities (of several materials) obtained previously. (1) The order of the reactivity is (Amberlite IRC-76)>(Dowex A-1)>(PVA2000>(Amberlite IRC-50) at 60degC. (2) The higher the temperature, the larger is the reactivity of each material. (3) The temperature dependence of the reactivity of Dowex A-1 is the largest in the four. (4) The reactivity of the functional group (i.e., COOH group or OH group) bonded to the polymer chain can be clarified using the A'-McKay plot method. (5) It seems that method can be applied to analyze other reactions, e.g., other isotope-exchange reactions, surface reactions, catalytic reactions, etc. (author)

  17. Neuroprotective effect of the natural iron chelator, phytic acid in a cell culture model of Parkinson's disease

    Disrupted iron metabolism and excess iron accumulation has been reported in the brains of Parkinson's disease (PD) patients. Because excessive iron can induce oxidative stress subsequently causing degradation of nigral dopaminergic neurons in PD, we determined the protective effect of a naturally occurring iron chelator, phytic acid (IP6), on 1-methyl-4-phenylpyridinium (MPP+)-induced cell death in immortalized rat mesencephalic/dopaminergic cells. Cell death was induced with MPP+ in normal and iron-excess conditions and cytotoxicity was measured by thiazolyl blue tetrazolium bromide (MTT assay) and trypan blue staining. Apoptotic cell death was also measured with caspase-3 activity, DNA fragmentation, and Hoechst nuclear staining. Compared to MPP+ treatment, IP6 (30 μmol/L) increased cell viability by 19% (P + treatment was decreased by 55% (P < 0.01) and 52% (P < 0.05), respectively with IP6. Cell survival was increased by 18% (P < 0.05) and 42% (P < 0.001) with 30 and 100 μmol/L of IP6, respectively in iron-excess conditions. A 40% and 52% (P < 0.001) protection was observed in caspase-3 activity with 30 and 100 μmol/L IP6, respectively in iron-excess condition. Similarly, a 45% reduction (P < 0.001) in DNA fragmentation was found with 100 μmol/L IP6. In addition, Hoechst nuclear staining results confirmed the protective effect of IP6 against apoptosis. Similar protection was also observed with the differentiated cells. Collectively, our results demonstrate a significant neuroprotective effect of phytate in a cell culture model of PD

  18. Kinetic studies for sorption of some metal ions from aqueous acid solutions onto TDA impregnated resin

    Kinetic studies for sorption of uranium, thorium and cobalt ions from hydrochloric acid solutions using tri-dodecyl amine (TDA) loaded on Amberlite XAD4 (polystyrene resin supplied by Rohm and Haas) using the batch technique, have been evaluated and assessed. Analysis of the respective data in accordance with three kinetic models revealed that the particle diffusion mechanism is the rate determining step, and the sorption for each metal ion on the impregnated sorbent follows the first order reversible kinetics. Values of the first order rate constants, rate constants of intraparticle transport, and the particle diffusion coefficients for the studied ions were determined. Sorption isotherms, which have been evaluated from the distribution coefficients for these ions, were found in good fit with the Langmuir and Freundlich isotherms. (author)

  19. Low pressure process for continuous fiber reinforced polyamic acid resin matrix composite laminates

    Druyun, Darleen A. (Inventor); Hou, Tan-Hung (Inventor); Kidder, Paul W. (Inventor); Reddy, Rakasi M. (Inventor); Baucom, Robert M. (Inventor)

    1994-01-01

    A low pressure processor was developed for preparing a well-consolidated polyimide composite laminate. Prepreg plies were formed from unidirectional fibers and a polyamic acid resin solution. Molding stops were placed at the sides of a matched metal die mold. The prepreg plies were cut shorter than the length of the mold in the in-plane lateral direction and were stacked between the molding stops to a height which was higher than the molding stops. The plies were then compressed to the height of the stops and heated to allow the volatiles to escape and to start the imidization reaction. After removing the stops from the mold, the heat was increased and 0 - 500 psi was applied to complete the imidization reaction. The heat and pressure were further increased to form a consolidated polyimide composite laminate.

  20. Extraction of palladium from nitric acid medium by commercial resins with phosphinic acid, methylene thiol and isothiouronium moieties attached to polystyrene-divinylbenzene

    Commercially available polystyrene-divinylbenzene (PS-DVB) resins functionalized with isothiouronium (Tulsion CH-95), phosphinic acid (Tulsion CH-96) and methylene thiol (Tulsion CH-97) moieties have been used for separating palladium from nitric acid medium. Extraction of palladium has been studied as a function of time, concentration of nitric acid and palladium. The distribution coefficients (Kd, ml/g) of palladium on sulfur based resins (Tulsion CH-95 and Tulsion CH-97) are higher (5000-104 ml/g in 0.1M nitric acid) than on Tulsion CH-96 resin and decrease with increasing concentration of nitric acid. The initial rate of extraction of palladium by Tulsion CH-95 and Tulsion CH-97 resins was very rapid and the time required for the establishment of equilibrium was a function of palladium concentration in the aqueous phase. The rate data could be fitted by a second order rate equation and the magnitude of rate constant for the extraction of palladium by these resins (∼102M-1 x min-1) decreased in the order of: Tulsion CH-95 > Tulsion CH-97 > Tulsion CH-96. The extraction isotherms of Tulsion CH-95 were fitted by Langmuir adsorption model and the coefficients were obtained by regression. The extraction capacity of palladium on Tulsion CH-95 was found to be ∼20 mg/g at 3M nitric acid. Column experiments have been conducted and the data were fitted using Thomas model. A column utilization of 75% was achieved for the extraction of palladium by Tulsion CH-95 resin. (author)

  1. The Scientific Basis for Chelation: Animal Studies and Lead Chelation

    Smith, Donald; Strupp, Barbara J.

    2013-01-01

    This presentation summarizes several of the rodent and non-human studies that we have conducted to help inform the efficacy and clinical utility of succimer (meso-2,3-dimercaptosuccincinic acid) chelation treatment. We address the following questions: (1) What is the extent of body lead, and in particular brain lead reduction with chelation, and do reductions in blood lead accurately reflect reductions in brain lead? (2) Can succimer treatment alleviate the neurobehavioral impacts of lead poi...

  2. Thermogravimetric and Spectroscopic Analysis of 8-Hydroxyquinoline 5-Sulphonic Acid-melamine-formaldehyde Polymer Resin-IV

    Singru, Rajesh N.

    2012-01-01

    The title terpolymer (8-HQ5-SAMF-IV) synthesized by the condensation of 8-hydroxyquinoline 5-sulphonic acid (8-HQ5-SA) and melamine (M) with formaldehyde (F) in the presence of acid catalyst and using varied 3 : 1 : 5 molar proportions of the reacting monomers. The synthesized terpolymer was characterized by different physicochemical techniques. The thermogravimetric analysis of terpolymer resin prepared in the present study has been carried out by nonisothermal thermogravimetric analysis tec...

  3. Synthesis of polystyrene supported chelating resin containing an oxygen-nitrogen donor bidentate Schiff base and its nickel(II), cobalt(II), copper(II), iron(III), zinc(II), molybdenum(VI) and uranium(VI) complexes

    A new bidentate oxygen-nitrogen donor Schiff base supported on polystyrene matrix has been synthesized by the reaction of aminomethylated polystyrene and salicylaldehyde. The chelating resin reacts with metal complex/metal salt and forms metal bound polymers of the formulae: PS-LNi(CH3COO).3DMF, PS-LCo(CH3COO).DMF, PS-LCu(CH3COO).DMF, PS-LCu(CH3COO).CH3OH, PS-LFeCL2.2DMF, PS-LZnCl.CH3OH, PS-LCd(CH3COO).DMF, PS-LCdCl.CH3OH, PS-LMoO2(acetylacetonato) and PS-LUO2(CH3COO).DMF (where PS-L=deprotonated anion of polymer-anchored ligand). The metal bound polymers have been characterized by elemental analysis, IR, electronic spectra and magnetic susceptibility measurements. The complexes PS-LNi(CH3COO).3DMF, PS-LCo(CH3COO).DMF, PS-LCu(CH3COO).DMF, PS-LCu(CH3COO).CH3OH and PS-LFeCl2.2DMF are paramagnetic while the Zn(II), Cd(II), Mo(VI) and U(VI) complexes are diamagnetic. The Co(II) and Cu(II) complexes exhibit a square planar structure, whereas Ni(II), Fe(III), Mo(VI) and U(VI) complexes are octahedral and Zn(II) and Cd(II) complexes are tetrahedral. (author). 29 refs., 1 tab

  4. THERMODYNAMICS ADSORPTION OF MANGANESE ION ON 1-(2-PYRIDYLAZO)-2-NAPHTHOL-6-SULPHONIC ACID IMPREGNATED RESIN

    2008-01-01

    An ion-exchange resin of type 201×7 was impregnated with the reagent 1-(2-Pyridylazo)-2-naphthol-6-sulphonic Acid (PAN-S). The adsorption characteristics of PAN-S resin for manganese ion were studied on the static equilibrium adsorption. Within temperature range of 288K~313K and the concentration range investigated, equilibrium data for the adsorption of manganese ions from aqueous solutions by PAN-S resin were obtained and correlated with Freundlich and Langmuir equation. The results showed that the process of the adsorption of manganese ions from aqueous solution by PAN-S was an exothermic process. Estimations of the isothermic enthalpy change of adsorption,free energy change and entropy of adsorption are reported,and the adsorption behaviors are reasonably interpreted.

  5. Fabrication of micro-dot arrays and micro-walls of acrylic acid/melamine resin on aluminum by AFM probe processing and electrophoretic coating

    Kurokawa, S.; Kikuchi, T.; Sakairi, M. [Graduate School of Engineering, Hokkaido University, N-13, W-8, Kita-Ku, Sapporo 060-8628 (Japan); Takahashi, H. [Graduate School of Engineering, Hokkaido University, N-13, W-8, Kita-Ku, Sapporo 060-8628 (Japan)], E-mail: takahasi@elechem1-mc.eng.hokudai.ac.jp

    2008-11-30

    Micro-dot arrays and micro-walls of acrylic acid/melamine resin were fabricated on aluminum by anodizing, atomic force microscope (AFM) probe processing, and electrophoretic deposition. Barrier type anodic oxide films of 15 nm thickness were formed on aluminum and then the specimen was scratched with an AFM probe in a solution containing acrylic acid/melamine resin nano-particles to remove the anodic oxide film locally. After scratching, the specimen was anodically polarized to deposit acrylic acid/melamine resin electrophoretically at the film-removed area. The resin deposited on the specimen was finally cured by heating. It was found that scratching with the AFM probe on open circuit leads to the contamination of the probe with resin, due to positive shifts in the potential during scratching. Scratching of the specimen under potentiostatic conditions at -1.0 V, however, resulted in successful resin deposition at the film-removed area without probe contamination. The rate of resin deposition increased as the specimen potential becomes more positive during electrophoretic deposition. Arrays of resin dots with a few to several tens {mu}m diameter and 100-1000 nm height, and resin walls with 100-1000 nm height and 1 {mu}m width were obtained on specimens by successive anodizing, probe processing, and electrophoretic deposition.

  6. Fabrication of micro-dot arrays and micro-walls of acrylic acid/melamine resin on aluminum by AFM probe processing and electrophoretic coating

    Micro-dot arrays and micro-walls of acrylic acid/melamine resin were fabricated on aluminum by anodizing, atomic force microscope (AFM) probe processing, and electrophoretic deposition. Barrier type anodic oxide films of 15 nm thickness were formed on aluminum and then the specimen was scratched with an AFM probe in a solution containing acrylic acid/melamine resin nano-particles to remove the anodic oxide film locally. After scratching, the specimen was anodically polarized to deposit acrylic acid/melamine resin electrophoretically at the film-removed area. The resin deposited on the specimen was finally cured by heating. It was found that scratching with the AFM probe on open circuit leads to the contamination of the probe with resin, due to positive shifts in the potential during scratching. Scratching of the specimen under potentiostatic conditions at -1.0 V, however, resulted in successful resin deposition at the film-removed area without probe contamination. The rate of resin deposition increased as the specimen potential becomes more positive during electrophoretic deposition. Arrays of resin dots with a few to several tens μm diameter and 100-1000 nm height, and resin walls with 100-1000 nm height and 1 μm width were obtained on specimens by successive anodizing, probe processing, and electrophoretic deposition

  7. Application of linear alkyl benzenesulfonic acid resin in chloroprene adhesives%烷基苯酸树脂在氯丁型胶粘剂中的应用

    凌辉; 钟锋; 李军; 陈亮; 刘根伸

    2015-01-01

    以烷基苯酸树脂部分取代酚醛树脂,探讨烷基苯酸树脂和酚醛树脂的混合比对氯丁型胶粘剂粘剂性能的影响。结果表明,当混合树脂中烷基苯酸树脂用量为20%~30%时,胶粘剂综合性能较优。%Using the alkyl benzenesulfonic acid resin partly instead of the phenolic resin, the effect of mixing proportion of benzenesulfonic acid resin and phenolic resin on the performance of chloroprene adhesives was discussed. The results showed that when the benzenesulfonic acid resin content was 20%~30%, the comprehensive performance of adhesives was optimal.

  8. Separation of Technetium in Nitric Acid Solution With an Extractant Impregnated Resin

    An extractant impregnated resin (EIR) was prepared by impregnation of Aliquat 336 into Amberlite XAD-4 for separation of technetium from rhodium in nitric acid solution. The prepared EIR showed high preference for rhenium (chemical analogue of technetium) over rhodium. The adsorption isotherms for rhenium were described well by Langmuir equation in both the single and multi-component systems. Maximum adsorption capacities obtained by modelling the isotherms of rhenium were 2.01 meq g-1 and 1.97 meq g-1 for the single and the multi-component systems, respectively. Column tests were also performed to confirm the separation efficiency of rhenium using a jacketed glass column (diam. 11 x L 150). The EIR column showed successful separation of rhenium with the breakthrough volume of about 122 BV for the breakthrough concentration of 0.08. Also the breakthrough data were modelled successfully by assuming a homogeneous diffusion model in the particle phase. The diffusivities obtained from the modelling were in the order of 10-7 cm2 min-1 for a rhenium. The rhenium adsorbed on the bed could be eluted with a high purity by using a nitric acid solution. (authors)

  9. Novel bioactive polyester scaffolds prepared from unsaturated resins based on isosorbide and succinic acid.

    Smiga-Matuszowicz, Monika; Janicki, Bartosz; Jaszcz, Katarzyna; Łukaszczyk, Jan; Kaczmarek, Marcin; Lesiak, Marta; Sieroń, Aleksander L; Simka, Wojciech; Mierzwiński, Maciej; Kusz, Damian

    2014-12-01

    In this study new biodegradable materials obtained by crosslinking poly(3-allyloxy-1,2-propylene succinate) (PSAGE) with oligo(isosorbide maleate) (OMIS) and small amount of methyl methacrylate were investigated. The porous scaffolds were obtained in the presence of a foaming system consisted of calcium carbonate/carboxylic acid mixture, creating in situ porous structure during crosslinking of liquid formulations. The maximum crosslinking temperature and setting time, the cured porous materials morphology as well as the effect of their porosity on mechanical properties and hydrolytic degradation process were evaluated. It was found that the kind of carboxylic acid used in the foaming system influenced compressive strength and compressive modulus of porous scaffolds. The MTS cytotoxicity assay was carried out for OMIS using hFOB1.19 cell line. OMIS resin was found to be non-toxic in wide range of concentrations. On the ground of scanning electron microscopy (SEM) observations and energy X-ray dispersive analysis (EDX) it was found that hydroxyapatite (HA) formation at the scaffolds surfaces within short period of soaking in phosphate buffer solution occurs. After 3h immersion a compact layer of HA was observed at the surface of the samples. The obtained results suggest potential applicability of resulted new porous crosslinked polymeric materials as temporary bone void fillers. PMID:25491802

  10. Development of a method for calculating the equilibrium and kinetics of ion exchange on a weak acid resin in a ternary system H+-Ca2+-Mg2+

    In technical applications ion exchange resins are applied in filters. The breakthrough behaviour of such filters can be calculated using mathematical relationships for equilibrium and kinetics. An according method has been developed for a ternary ion exchage problem on a weak acid resin. Theoretical results are verified by means of experimental data. (orig.)

  11. Benzyl and Methyl Fatty Hydroxamic Acids Based on Palm Kernel Oil as Chelating Agent for Liquid-Liquid Iron(III Extraction

    Jamileh Amin

    2012-02-01

    Full Text Available Liquid-liquid iron(III extraction was investigated using benzyl fatty hydroxamic acids (BFHAs and methyl fatty hydroxamic acids (MFHAs as chelating agents through the formation of iron(III methyl fatty hydroxamate (Fe-MFHs or iron(III benzyl fatty hydroxamate (Fe-BFHs in the organic phase. The results obtained under optimized conditions, showed that the chelating agents in hexane extract iron(III at pH 1.9 were realized effectively with a high percentage of extraction (97.2% and 98.1% for MFHAs and BFHAs, respectively. The presence of a large amount of Mg(II, Ni(II, Al(III, Mn(II and Co(II ions did affect the iron(III extraction. Finally stripping studies for recovering iron(III from organic phase (Fe-MFHs or Fe-BFHs dissolved in hexane were carried out at various concentrations of HCl, HNO3 and H2SO4. The results showed that the desired acid for recovery of iron(III was 5 M HCl and quantitative recovery of iron(III was achieved from Fe(III-MFHs and Fe(III-BFHs solutions in hexane containing 5 mg/L of Fe(III.

  12. Diphonix trademark Resin: A review of its properties and applications

    The recently developed Diphonix trademark resin is a new multifunctional chelating ion exchange resin containing seminally substituted diphosphonic acid ligands chemically bonded to a styrene-based polymeric matrix. Diphonix can be regarded as a dual mechanism polymer, with a sulfonic acid cation exchange group allowing for rapid access, mostly non-specific, of ions into the polymeric network, and the diphosphonic acid group responsible for specificity (recognition) for a number of metal cations. The Diphonix resin exhibits an extraordinarily strong affinity for actinides, especially in the tetra- and hexavalent oxidation states. It has potential applications in TRU and mixed waste treatment and characterization, and in the development of new procedures for rapid actinide preconcentration and separation from environmental samples. Metal uptake studies have been extended to alkaline earth cations, to transition and post transition metal species, and to metal sorption from neutral or near neutral solutions. Also the kinetic behavior of the resin has been investigated in detail. Influence of the most commonly occurring matrix constituents (Na, Ca, Al, Fe, hydrofluoric, sulfuric, oxalic and phosphoric acids) on the uptake of actinide ions has been measured. This review paper summarizes the most important results studies on the Diphonix resin and gives an overview of the applications already in existence or under development in the fields of mixed waste treatment, actinide separation procedures, treatment of radwaste from nuclear power plants, and removal of iron from copper electrowinning solutions

  13. The poisoning of 201 x 7 resin by humic acid (salt) in recovery of uranium from mine water and its mechanism

    The strong-base ion exchange resin 201 x 7 is used to recover uranium from the nearly neutral and weak alkaline mine water of three mines A, B and C. The poisoning of resin is found very serious. The results of investigation by using infrared spectrometry and others show that the poisoning of the resin originates from the humic acid (salt). The decreasing of speed of ion exchange is the main feature, but there is no significant effect on ion exchange capacity of the resin. The mechanism of the poisoning is also explored and the model of poisoning is given as follows: the humic acid (salt) stops up the vacant sites of the resin as a sponge and occupies a lot of them

  14. Binary and ternary chelates of Sc(III), Y(III) and La(III) with ethylenediamine tetraacetic acid as primary ligand and substituted salicylic acids as secondary ligands

    Study of ternary complex formation of several tripositive metal ions viz. Sc(III), Y(III) and La(III) with ethylenediamine tetraacetic acid (EDTA) as a primary ligand and 5-chlorosalicylic acid (CSA) or 3,5-dibromosalicylic acid (DBSA) as secondary ligands by pH-metric titration technique is reported. The stability order of metal chelates with respect to ligands is observed to be DBSA>CSA and with respect to metal ions Sc(III)>Y(III)>La(III). (B.G.W.)

  15. Extremely enhanced photovoltaic properties of dye-sensitized solar cells by sintering mesoporous TiO2 photoanodes with crystalline titania chelated by acetic acid

    Liu, Bo-Tau; Chou, Ya-Hui; Liu, Jin-Yan

    2016-04-01

    The study presents a significant improvement on the performance of dye-sensitized solar cells (DSSCs) through incorporating the crystalline titania chelated by acetic acid (TAc) into the mesoporous TiO2 photoanodes. The effects of TAc on the blocking layer, mesoporous TiO2 layer, and post-treatment have been investigated. The TAc blocking layer displays compact construction, revealing superior response time and resistance to suppress dark current compared to the blocking layer made from titanium(IV) isopropoxide (TTIP). The power conversion efficiency of DSSCs with the TAc treatment can reach as high as 10.49%, which is much higher than that of pristine DSSCs (5.67%) and that of DSSCs treated by TTIP (7.86%). We find that the TAc incorporation can lead to the decrease of charge transfer resistance and the increase of dye adsorption. The result may be attributed to the fact that the TAc possesses high crystallinity, exposed (101) planes, and acid groups chelated on surface, which are favorable for dye attachment and strong bonding at the FTO/TiO2 and the TiO2/TiO2 interfaces, These improvements result in the remarkable increase of photocurrent and thereby that of power conversion efficiency.

  16. Use of potassium-form cation-exchange resin as a conductimetric enhancer in ion-exclusion chromatography of aliphatic carboxylic acids.

    Iwata, Tomotaka; Mori, Masanobu; Itabashi, Hideyuki; Tanaka, Kazuhiko

    2009-09-15

    In this study, a cation-exchange resin (CEX) of the K(+)-form, i.e., an enhancer resin, is used as a postcolumn conductimetric enhancer in the ion-exclusion chromatography of aliphatic carboxylic acids. The enhancer resin is filled in the switching valve of an ion chromatograph; this valve is usually used as a suppressor valve in ion-exchange chromatography. An aliphatic carboxylic acid (e.g., CH(3)COOH) separated by a weakly acidic CEX column of the H(+)-form converts into that of the K(+)-form (e.g., CH(3)COOK) by passing through the enhancer resin. In contrast, the background conductivity decreases because a strong acid (e.g., HNO(3)) with a higher conductimetric response in an eluent converts into a salt (e.g., KNO(3)) with a lower conductimetric response. Since the pH of the eluent containing the resin enhancer increases from 3.27 to 5.85, the enhancer accelerates the dissociations of analyte acids. Consequently, peak heights and peak areas of aliphatic carboxylic acids (e.g., acetic acid, propionic acid, butyric acid, and valeric acid) with the enhancer resin are 6.3-8.0 times higher and 7.2-9.2 times larger, respectively, than those without the enhancer resin. Calibrations of peak areas for injected analytes are linear in the concentration range of 0.01-1.0mM. The detection limits (signal-to-noise ratio=3) range from 0.10 microM to 0.39 microM in this system, as opposed to those in the range of 0.24-7.1 microM in the separation column alone. The developed system is successfully applied to the determination of aliphatic carboxylic acids in a chicken droppings sample. PMID:19615503

  17. Synthesis and evaluation of different thio-modified cellulose resins for the removal of mercury (II) ion from highly acidic aqueous solutions.

    Takagai, Yoshitaka; Shibata, Atsushi; Kiyokawa, Shigemi; Takase, Tsugiko

    2011-01-15

    Seven different types of thio- and/or amine-modified cellulose resin materials were synthesized and their mercury (II) ion adsorption properties determined. All seven resins showed good mercury (II) adsorption capability in the more neutral pH regions. However, the o-benzenedithiol- and o-aminothiophenol-modified cellulosic resins were found to be very effective in removing mercury (II) ions from strongly acidic media. For example, 93.5-100% mercury (II) ion recoveries from very acid aqueous solutions (nitric acid concentration ranged from 0.1 to 2.0 mol/L) were obtained using the o-benzenedithiol-modified resin while recoveries ranged from ca. 50% to 60% for the o-aminothiophenol-modified resin. An adsorption capacity of 23 mg (as Hg atoms) per gram of resin was observed for the o-benzenedithiol-modified cellulose in the presence of 1.0 mol/L nitric acid. This same resin shows very good selectivity for mercury (II) as only ruthenium (II) also somewhat adsorbed onto it out of 14 other metal ions studied (Ag(+), Al(3+), As(3+), Co(2+), Cd(2+), Cr(3+), Cu(2+), Fe(3+), Mn(2+), Ni(2+), Pt(2+), Pb(2+), Ru(2+), and Zn(2+)). PMID:20974469

  18. Pyridine appended L-methionine: A novel chelating resin for pH dependent Cr speciation with scanning electron microscopic evidence and monitoring of yeast mediated green bio-reduction of Cr(VI) to Cr(III) in environmental samples

    Chemical speciation and pH dependent separation of Cr(III) and Cr(VI) species in environmental samples have been achieved by solid phase extraction using a new chelating resin containing pyridine appended L-methionine. Cr(III) is completely sorbed on the resin at pH 8.0 and Cr(VI) at pH 2.0. Hence a pH dependent separation of Cr(III) and Cr(VI) is possible with a limit of detection of 1.6 μg mL-1 and 0.6 μg mL-1 respectively. The sorption capacity of the resin for Cr(III) and Cr(VI) is 2.8 mmol g-1 and 1.3 mmol g-1 respectively. The sorption of chromium on the resin is supported by scanning electron microscopy (SEM). Complete desorption of Cr(III) and Cr(VI) from 1 g of Cr loaded resin was achieved using 10 mL of 2 mol L-1 HNO3 and 6 mL of 3 mol L-1 HNO3 respectively. Quantitative recoveries of Cr(III) (pH 8.0) and Cr(VI) (pH 2.0) were found to be 96.0% and 98.0% respectively. Reduction efficiency of Rhodotornula mucilaginosa yeast from Cr(VI) to Cr(III) was monitored with this new resin. Concentrations of metal ions were measured by flame atomic absorption spectroscopy (FAAS).

  19. Physical characteristics of cold cured anthracite/coke breeze briquettes prepared from a coal tar acid resin

    Thoms, L.J.; Snape, C.E.; Taylor, D. [University of Strathclyde, Glasgow (United Kingdom). Dept. of Pure and Applied Chemistry

    1999-11-01

    Phenolic resins were synthesised using the whole coal tar acid fraction of the oil from a low temperature carbonisation process. A series of briquettes were prepared using a number of coal tar acid concentrations, cured at ambient temperature with various concentrations of sulphuric acid and were subjected to a variety of physical tests. Excellent briquettes, in terms of mechanical strength, water-proofing characteristics and thermal degradation, were produced with both nominally 10 and 9% w/w resole solution and acid concentrations down to 1.8 M, corresponding to sulphur addition in the briquettes of ca. 0.2% w/w. Briquettes bound with 8% w/w resole solution, however, required stronger acid concentrations to satisfy the test conditions. When the briquettes were combusted up to 850{degree}C, they retained their core shape after 70% weight loss. 16 refs., 4 figs., 4 tabs.

  20. Rapid removal of copper with magnetic poly-acrylic weak acid resin: Quantitative role of bead radius on ion exchange

    Highlights: • The equilibrium adsorption amount of Cu2+ onto NDMC was 267.2 mg/g. • Initial adsorption rate of NDMC was 4 and 8 times that of C106 and IRC-748. • External surface area was determined to be the key factor in rate-controlling. • Adsorption amount onto NDMC was not influenced by Na+ concentration. • 0.01 mM HCl solution could effectively desorb Cu2+. - Abstract: A novel magnetic weak acid resin NDMC was self-synthesized for the removal of Cu2+ from aqueous solutions. NDMC showed superior properties on the removal of Cu2+ compared to commercial resins C106 and IRC-748, which was deeply investigated by adsorption isotherms and kinetic tests. The equilibrium adsorption amount of Cu2+ onto NDMC (267.2 mg/g) was almost twice as large as that onto IRC-748 (120.0 mg/g). The adsorption kinetics of Cu2+ onto the three resins fitted well with the pseudo-second-order equation. The initial adsorption rate h of NDMC was about 4 times that of C106 and nearly 8 times that of IRC-748 at the initial concentration of 500 mg/L. External surface area was determined to be the key factor in rate-controlling by further analyzing the adsorption thermodynamics, kinetics parameters and physicochemical properties of the resins. NDMC resin with the smallest bead radius possessed the largest external surface and therefore exhibited the fastest kinetics. The adsorption amount of Cu2+ onto NDMC was not influenced as the concentration of Na+ increased from 1.0 to 10.0 mM/L. Dilute HCl solution could effectively desorb Cu2+. NDMC demonstrated high stability during 10 adsorption/desorption cycles, showing great potential in the rapid removal of Cu2+ from wastewater

  1. Functionalization of Chitosan with 3,4,5-Trihydroxy Benzoic Acid Moiety for The Uptake of Chromium Species

    Akhmad Sabarudin

    2013-03-01

    Full Text Available Chitosan-based chelating resin, the cross-linked chitosan functionalized with 3,4,5-trihydroxy benzoic acid moiety (CCTS-THBA resin, was newly synthesized and its adsorption behavior toward appropriate elements was investigated. At pH 5-9, the CCTS-THBA resin showed quantitative adsorption (87-91% for Cr (VI, while only < 15% for Cr (III. The addition of cyclohexanediamine tetraacetic acid (CyDTA to the samples resulted in a considerably increase of the adsorption of both chromium species. In this condition, Cr (III is chelated with CyDTA to form anionic complexes at pH 3-5, which was then completely adsorbed on the resin by ion exchange mechanism. Similarly, the adsorption of Cr (VI reached almost 100% in pH range of 3-6. The adsorption capacity of CCTS-THBA resin for Cr (VI was 109 mg g-1.

  2. Chelated minerals for poultry

    SL Vieira

    2008-06-01

    Full Text Available Organic minerals have been subject of an increasing number of investigations recently. These compounds can be considered the most significant event regarding commercial forms of minerals targeting animal supplementation in the last decades. Minerals, especially metals, are usually supplemented in poultry feeds using cheap saline sources and have never required a lot of attention in terms of quality. On the other hand, definitions of organic minerals are very broad and frequently lead to confusion when decision-making becomes necessary. Organic minerals include any mineral bound to organic compounds, regardless of the type of existing bond between mineral and organic molecules. Proteins and carbohydrates are the most frequent candidates in organic mineral combinations. Organic fraction size and bond type are not limitations in organic mineral definition; however, essential metals (Cu, Fe, Zn, and Mn can form coordinated bonds, which are stable in intestinal lumen. Metals bound to organic ligands by coordinated bonds can dissociate within animal metabolism whereas real covalent bonds cannot. Chelated minerals are molecules that have a metal bound to an organic ligand through coordinated bonds; but many organic minerals are not chelates or are not even bound through coordinated bonds. Utilization of organic minerals is largely dependent on the ligand; therefore, amino acids and other small molecules with facilitated access to the enterocyte are supposed to be better utilized by animals. Organic minerals with ligands presenting long chains may require digestion prior to absorption. After absorption, organic minerals may present physiological effects, which improve specific metabolic responses, such as the immune response. Many studies have demonstrated the benefits of metal-amino acid chelates on animal metabolism, but the detection positive effects on live performance is less consistent.

  3. Influence of Chelating Agents on Chromium Fate in Sediment

    WANGXIAOCHANG; SUNJINHE; 等

    1996-01-01

    A laboratory investigation on reaction between chelating agents and chromium was conducted to evaluate the effect of chelating agents on the adsorption and desorption of chromium in sediment.The amount of adsorbed chromium(VI) in sediment decreased slightly by 5%-10% because of addition of chelating agents.Chelating agents inhibited the removal of Cr(Ⅲ)by sediment from solutions and the inhibiting effect was in the order:citric acid>tartaric acid>EDTA,Salicylic acid.No effect of chelating agents on desorption of chromium in sediment was observed.

  4. Removal of Some Chelators from Aqueous Solutions Using Polymeric Ingredients

    This work tries to throw a light on the removal of thenoyl trifluoroacetone (TTA) and ethylene diamine tetraacetic acid (EDTA), extractants extensively used in many nuclear facilities, from aqueous solutions under different experimental conditions using Amberlite XAD resins. The applied resins exhibit high retention ability for the studied chelators with a maximum sorption capacity has the values of 23.9 and 38.0 mgg-1 for sorption of TTA and EDTA on Amberlite XAD4 and 18.6 and 21.2 mgg-1 for their sorption of on Amberlite XAD7. Factors affecting the resin retention ability such as ph value of aqueous solution and presence of co solvent have been studied. The kinetics of sorption behavior, in the applied system, indicate the process to be controlled by more than one diffusion mechanism. Therefore, two diffusion models were utilized to understand and verify the mechanism of sorption processes; they are the film mass transfer model and the interparticle diffusion model. The first model, based on film resistance, gave a successful depiction for sorption of TTA onto Amberlite XAD4 and XAD7 and the second one displayed an acceptable prediction for sorption of EDTA onto Amberlite XAD4

  5. Kinetic Study of Esterification of Acetic Acid with n-butanol and isobutanol Catalyzed by Ion Exchange Resin

    Amrit Pal Toor

    2011-05-01

    Full Text Available Esters are an important pharmaceutical intermediates and very useful perfumery agents. In this study the esterification of acetic acid with n-butanol and iso-butanol over an acidic cation exchange resin, Amberlyst 15 were carried out. The effects of certain parameters such as temperature, catalyst loading, initial molar ratio between reactants on the rate of reaction were studied. The experiments were conducted in a stirred batch reactor in the temperature range of 351.15 K to 366.15K.Variation of parameters on rate of reaction demonstrated that the reaction was intrinsically controlled.The activation energy for the esterification of acetic acid with n-butanol and iso butanol is found to be 28.45 k J/mol and 23.29 kJ/mol respectively. ©2011 BCREC UNDIP. All rights reserved.(Received: 16th December 2010, Revised: 19th March 2011; Accepted: 7th April 2011[How to Cite: A.P. Toor, M. Sharma, G. Kumar, and R. K. Wanchoo. (2011. Kinetic Study of Esterification of Acetic Acid with n-butanol and isobutanol Catalyzed by Ion Exchange Resin. Bulletin of Chemical Reaction Engineering and Catalysis, 6(1: 23-30. doi:10.9767/bcrec.6.1.665.23-30][How to Link / DOI: http://dx.doi.org/10.9767/bcrec.6.1.665.23-30 || or local: http://ejournal.undip.ac.id/index.php/bcrec/article/view/665 ] | View in 

  6. Effect of endodontic chelating solutions on the bond strength of endodontic sealers

    Behram TUNCEL

    2015-01-01

    Full Text Available The purpose of this in vitro study was to evaluate the effect of various chelating solutions on the radicular push-out bond strength of calcium silicate-based and resin-based root canal sealers. Root canals of freshly-extracted single-rooted teeth (n = 80 were instrumented by using rotary instruments. The specimens were randomly divided into 4 groups according to the chelating solutions being tested: (1 17% ethylenediaminetetraacetic acid (EDTA; (2 9% etidronic acid; (3 1% peracetic acid (PAA; and (4 distilled water (control. In each group, the roots were further assigned into 2 subgroups according to the sealer used: (1 an epoxy resin-based sealer (AH Plus and (2 a calcium silicate-based sealer (iRoot SP. Four 1 mm-thick sections were obtained from the coronal aspect of each root (n = 40 slices/group. Push-out bond strength test was performed at a crosshead speed of 1 mm/min., and the bond strength data were analyzed statistically with two-way analysis of variance (ANOVA with Bonferroni’s post hoc test (p 0.05. iRoot SP showed higher resistance to dislocation than AH Plus. Final irrigation with 17% EDTA, 9% Etidronic acid, and 1% PAA did not improve the bond strength of AH Plus and iRoot SP to radicular dentin.

  7. Effect of low-molecular-weight carboxylic acids and selected synthetic chelates on zinc uptake and translocation in two wheat genotypes with different zinc-efficiency

    Sh. Haftbaradaran

    2013-10-01

    Full Text Available Zinc (Zn deficiency in human, which results from diets low in bioavailable zinc, could be eliminated by increasing readily plant-available Zn in soil. Root exudates and organic acids released during decomposition of soil organic matter can affect the availability of Zn. Thus, this hydroponic experiment was conducted to investigate the effect of some chelates on Zn uptake and translocation in two wheat genotypes with different zinc-efficiency. Two wheat genotypes (Triticum aestivum L. Back Cross Rowshan as zinc-efficient and Kavir as zinc-inefficient were exposed to two levels of zinc (10 and 100 µM and six different carboxylic acids (citric, tartaric, oxalic, salicylic, ethylenediamin tetraacetic acid and L-methionine. Results showed that uptake capability of free and complexed species of Zn were completely different. Zn2+ activity in nutrient solution had negative correlation with shoot dry weight and positive correlation with shoot zinc concentration in Kavir genotype, while complexed species had opposite results. Back Cross Rowshan genotype showed opposite results in comparison with Kavir genotype. The response of wheat genotypes to different organic acids varied. EDTA treatment caused the lowest shoot zinc concentration in Kavir genotype (18.8 mg/kg, while the Back Cross Rowshan genotype had highest concentration (99.5 mg/kg. Tartaric acid and citric acid caused the lowest root Zn concentration in the Kavir genotype (26.7 and 58.6 mg/kg, respectively, while the highest content was observed in the Back Cross Rowshan genotype (83.2 and 98.1 mg/kg, respectively. Catalase activity had inverse relationship with root Zn concentration in both genotypes. According to the results of this research, different responses of the wheat genotypes to organic acids are related to different mechanisms of zinc-efficiency in genotypes.

  8. Preparation of molecularly imprinted cross-linked chitosan/glutaraldehyde resin for enantioselective separation of L-glutamic acid.

    Monier, M; El-Sokkary, A M A

    2010-08-01

    In the present study, separation of L-glutamic acid from dilute aqueous solution by solid-phase extraction based on molecular imprinting technique using cross-linked chitosan/glutaraldehyde resin was investigated. L-Glutamic acid imprinted cross-linked chitosan (LGIC) was prepared by cross-linking of chitosan by glutaraldehyde cross-linker, in the presence of L-glutamic acid. Non-imprinted cross-linked chitosan (NIC) as control was also prepared by the same procedure in the absence of template molecules. The morphological structures of both LGIC and NIC were examined by scanning electron microscope (SEM). LGIC particles were applied to determine the optimum operational condition for l-glutamic acid separation from dilute aqueous solution. In adsorption step, optimum pH and retention time were 5.5 and 100 min, while corresponding values in extraction step were 2.5 and 60 min, respectively. The adsorption isotherms indicated that the maximum adsorption capacities of L- and D-glutamic acid on LGIC were 42+/-0.8 and 26+/-1.2mg/g, respectively, while in case of NIC, both L- and D-glutamic acid present the same maximum adsorption capacity 7+/-0.6 mg/g, which confirm that the molecular imprinting technique creates an enantioselectivity of LGIC toward L-glutamic acid. In addition, chiral resolution of l-, d-glutamic acid racemic mixture was carried out using column of LGIC. PMID:20441776

  9. Ethyl octyl ether synthesis from 1-octanol and ethanol or diethyl carbonate on acidic ion-exchange resins

    Guilera Sala, Jordi

    2013-01-01

    Ethyl octyl ether is a bioethanol-derived component that has excellent properties as diesel fuel. This work proved that ethyl octyl ether can be produced successfully in liquid-phase at the temperature range of 130-190ºC by using acidic ion-exchange resins, as suitable and economic catalysts. The use of two promising reactants that can be a renewable compound source, ethanol and diethyl carbonate, have been explored. Both reactants are able to ethylate 1-octanol and form the desired product. ...

  10. Pre-concentration studies of 237Np using sulphonic acid based actinide™ resin

    The absorption studies of the standard 237Np have been performed using actinide™ resin to standardise the selective separation. The supernatant solution was checked for alpha activity of 237Np using scintillation counting technique. It was found that more than 95 % of 237Np was absorbed in the actinide™ resin. The absorbed 237Np from the actinide™ resin was leached out using isopropyl alcohol. The leached out activity of 237Np in the isopropyl alcohol was estimated using same alpha scintillation counting technique and was found to be greater than 95 %. The selective absorption of 237Np resin from the other impurities in actinide™ is helpful in the analytical solution during recycle of fuels as well as in the waste management process. This is very much important because 237Np is one of the long-lived minor actinides produced from the 238U(n, 2n) reaction followed by beta decay. Thus it is useful for the conventional reactor based on natU and fast reactor based on U-Pu fuel. (author)

  11. Chelation in Metal Intoxication

    Flora, Swaran J.S.; Vidhu Pachauri

    2010-01-01

    Chelation therapy is the preferred medical treatment for reducing the toxic effects of metals. Chelating agents are capable of binding to toxic metal ions to form complex structures which are easily excreted from the body removing them from intracellular or extracellular spaces. 2,3-Dimercaprol has long been the mainstay of chelation therapy for lead or arsenic poisoning, however its serious side effects have led researchers to develop less toxic analogues. Hydrophilic chelators like meso-2,3...

  12. Determination of some aliphatic carboxylic acids in anaerobic digestion process waters by ion-exclusion chromatography with conductimetric detection on a weakly acidic cation-exchange resin column.

    Ito, Kazuaki; Takayama, Yohichi; Ikedo, Mikaru; Mori, Masanobu; Taoda, Hiroshi; Xu, Qun; Hu, Wenzhi; Sunahara, Hiroshi; Hayashi, Tsuneo; Sato, Shinji; Hirokawa, Takeshi; Tanaka, Kazuhiko

    2004-06-11

    The determination of seven aliphatic carboxylic acids, formic, acetic, propionic, isobutyric, n-butyric, isovaleric and n-valeric acids in anaerobic digestion process waters was examined using ion-exclusion chromatography with conductimetric detection. The analysis of these biologically important carboxylic acids is necessary as a measure for evaluating and controlling the process. The ion-exclusion chromatography system employed consisted of polymethacrylate-based weakly acidic cation-exchange resin columns (TSKgel OApak-A or TSKgel Super IC-A/C). weakly acidic eluent (benzoic acid), and conductimetric detection. Particle size and cation-exchange capacity were 5 microm and 0.1 meq./ml for TSKgel OApak-A and 3 microm and 0.2 meq./ml for TSKgel Super IC-A/C, respectively. A dilute eluent (1.0-2.0 mM) of benzoic acid was effective for the high resolution and highly conductimetric detection of the carboxylic acids. The good separation of isobutyric and n-butyric acids was performed using the TSKgel Super IC-A/C column (150 mm x 6.0 mm i.d. x 2). The simple and good chromatograms were obtained by the optimized ion-exclusion chromatography conditions for real samples from mesophilic anaerobic digestors, thus the aliphatic carboxylic acids were successfully determined without any interferences. PMID:15250416

  13. Zinc-chelation contributes to the anti-angiogenic effect of ellagic acid on inhibiting MMP-2 activity, cell migration and tube formation.

    Sheng-Teng Huang

    Full Text Available BACKGROUND: Ellagic acid (EA, a dietary polyphenolic compound, has been demonstrated to exert anti-angiogenic effect but the detailed mechanism is not yet fully understood. The aim of this study was to investigate whether the zinc chelating activity of EA contributed to its anti-angiogenic effect. METHODS AND PRINCIPAL FINDINGS: The matrix metalloproteinases-2 (MMP-2 activity, a zinc-required reaction, was directly inhibited by EA as examined by gelatin zymography, which was reversed dose-dependently by adding zinc chloride. In addition, EA was demonstrated to inhibit the secretion of MMP-2 from human umbilical vein endothelial cells (HUVECs as analyzed by Western blot method, which was also reversed by the addition of zinc chloride. Reversion-inducing cysteine-rich protein with Kazal motifs (RECK, known to down-regulate the MMP-2 activity, was induced by EA at both the mRNA and protein levels which was correlated well with the inhibition of MMP-2 activity. Interestingly, zinc chloride could also abolish the increase of EA-induced RECK expression. The anti-angiogenic effect of EA was further confirmed to inhibit matrix-induced tube formation of endothelial cells. The migration of endothelial cells as analyzed by transwell filter assay was suppressed markedly by EA dose-dependently as well. Zinc chloride could reverse these two effects of EA also in a dose-dependent manner. Since magnesium chloride or calcium chloride could not reverse the inhibitory effect of EA, zinc was found to be involved in tube formation and migration of vascular endothelial cells. CONCLUSIONS/SIGNIFICANCE: Together these results demonstrated that the zinc chelation of EA is involved in its anti-angiogenic effects by inhibiting MMP-2 activity, tube formation and cell migration of vascular endothelial cells. The role of zinc was confirmed to be important in the process of angiogenesis.

  14. Rapid removal of copper with magnetic poly-acrylic weak acid resin: Quantitative role of bead radius on ion exchange

    Fu, Lichun; Shuang, Chendong; Liu, Fuqiang, E-mail: jogia@163.com; Li, Aimin, E-mail: liaimin@nju.edu.cn; Li, Yan; Zhou, Yang; Song, Haiou

    2014-05-01

    Highlights: • The equilibrium adsorption amount of Cu{sup 2+} onto NDMC was 267.2 mg/g. • Initial adsorption rate of NDMC was 4 and 8 times that of C106 and IRC-748. • External surface area was determined to be the key factor in rate-controlling. • Adsorption amount onto NDMC was not influenced by Na{sup +} concentration. • 0.01 mM HCl solution could effectively desorb Cu{sup 2+}. - Abstract: A novel magnetic weak acid resin NDMC was self-synthesized for the removal of Cu{sup 2+} from aqueous solutions. NDMC showed superior properties on the removal of Cu{sup 2+} compared to commercial resins C106 and IRC-748, which was deeply investigated by adsorption isotherms and kinetic tests. The equilibrium adsorption amount of Cu{sup 2+} onto NDMC (267.2 mg/g) was almost twice as large as that onto IRC-748 (120.0 mg/g). The adsorption kinetics of Cu{sup 2+} onto the three resins fitted well with the pseudo-second-order equation. The initial adsorption rate h of NDMC was about 4 times that of C106 and nearly 8 times that of IRC-748 at the initial concentration of 500 mg/L. External surface area was determined to be the key factor in rate-controlling by further analyzing the adsorption thermodynamics, kinetics parameters and physicochemical properties of the resins. NDMC resin with the smallest bead radius possessed the largest external surface and therefore exhibited the fastest kinetics. The adsorption amount of Cu{sup 2+} onto NDMC was not influenced as the concentration of Na{sup +} increased from 1.0 to 10.0 mM/L. Dilute HCl solution could effectively desorb Cu{sup 2+}. NDMC demonstrated high stability during 10 adsorption/desorption cycles, showing great potential in the rapid removal of Cu{sup 2+} from wastewater.

  15. Evaluation of copper speciation in model solutions of humic acid by mini-columns packed with Chelex-100 and new chelating agents: Application to speciation of selected heavy metals in environmental water samples

    A solid-phase extraction procedure using mini-columns packed with Chelex-100 and two new chelating agents based on poly(vinyl chloride) functionalized with 3-ferrocenyl-3-hydroxydithioacrylic acid and N,N'-[1,1'-dithiobis(ethylene)]-bis(salicylideneimine) (H2sales) loaded on microcrystalline naphthalene, is reported. The columns were used to separate labile copper fractions in model solutions and in real samples with subsequent determination using electrothermal atomic absorption spectrometry (ETAAS). Various model solutions containing 20 μg L-1 of Cu2+ and 0.0, 0.2, 2.0 and 20.0 mg L-1 of humic acid, respectively, and buffered to pH 6.0, 7.0 and 8.0 were considered. Results showed a decrease in labile copper fraction with increase in humic acid concentration. Application of the procedure to speciation of Cu, Ni, Zn and Pb in various environmental water samples yielded labile fractions in the range of 1.67-55.75% against a total dissolved fraction of 44.08-69.77%. Comparison of the three chelating agents showed that H2sales had a weaker metal chelating strength than Chelex-100, but PVC-FSSH had comparable chelating strength to Chelex-100.

  16. A Robust Epoxy Resins @ Stearic Acid-Mg(OH)2 Micronanosheet Superhydrophobic Omnipotent Protective Coating for Real-Life Applications.

    Si, Yifan; Guo, Zhiguang; Liu, Weimin

    2016-06-29

    Superhydrophobic coating has extremely high application value and practicability. However, some difficult problems such as weak mechanical strength, the need for expensive toxic reagents, and a complex preparation process are all hard to avoid, and these problems have impeded the superhydrophobic coating's real-life application for a long time. Here, we demonstrate one kind of omnipotent epoxy resins @ stearic acid-Mg(OH)2 superhydrophobic coating via a simple antideposition route and one-step superhydrophobization process. The whole preparation process is facile, and expensive toxic reagents needed. This omnipotent coating can be applied on any solid substrate with great waterproof ability, excellent mechanical stability, and chemical durability, which can be stored in a realistic environment for more than 1 month. More significantly, this superhydrophobic coating also has four protective abilities, antifouling, anticorrosion, anti-icing, and flame-retardancy, to cope with a variety of possible extreme natural environments. Therefore, this omnipotent epoxy resins @ stearic acid-Mg(OH)2 superhydrophobic coating not only satisfies real-life need but also has great application potential in many respects. PMID:27265834

  17. Production of {sup 61}Cu using natural cobalt target and its separation using ascorbic acid and common anion exchange resin

    Das, Sujata Saha; Chattopadhyay, Sankha; Barua, Luna [Radiopharmaceuticals Laboratory, Board of Radiation and Isotope Technology (BRIT), Variable Energy Cyclotron Centre (VECC), Kolkata 700064 (India); Das, Malay Kanti, E-mail: mkdas@vecc.gov.in [Radiopharmaceuticals Laboratory, Board of Radiation and Isotope Technology (BRIT), Variable Energy Cyclotron Centre (VECC), Kolkata 700064 (India)

    2012-02-15

    {sup 61}Cu was produced by {sup nat}Co({alpha}, xn){sup 61}Cu reaction. {sup 61}Cu production yield was 89.5 MBq/{mu}Ah (2.42 mCi/{mu}Ah) at the end of irradiation (EOI). A simple radiochemical separation method using anion exchange resin and ascorbic acid has been employed to separate the product radionuclide from inactive target material and co-produced non-isotopic impurities. The radiochemical separation yield was about 90%. Radiochemical purity of {sup 61}Cu was >99% 1 h after EOI. Final product was suitable for making complex with N{sub 2}S{sub 2} type of ligands. - Highlights: Black-Right-Pointing-Pointer High purity, no-carrier added {sup 61}Cu produced from natural cobalt target. Black-Right-Pointing-Pointer {sup 61}Cu separated from impurities using anion exchange resin and ascorbic acid. Black-Right-Pointing-Pointer {sup 61}Cu preparation was successfully used to label N{sub 2}S{sub 2}-type of ligand.

  18. Chain extension and branching of poly(L-lactic acid produced by reaction with a DGEBA-based epoxy resin

    2007-11-01

    Full Text Available Dicarboxylated poly(L-lactic acid (PLLA was synthesized by reacting succinic anhydride with L-lactic acid prepolymer prepared by melt polycondensation. PLLA and epoxy resin based on diglycidyl ether of bisphenol A (DGEBA copolymers were prepared by chain extension of dicarboxylated PLLA with DGEBA. Infrared spectra confirmed the formation of dicarboxylated PLLA and PLLA/DGEBA copolymer. Influences of reaction temperature, reaction time, and the amount of DGEBA on the molecular weight and gel content of PLLA/DGEBA copolymer were studied. The viscosity average molecular weight of PLLA/DGEBA copolymer reached 87 900 when reaction temperature, reaction time, and mol ratio of dicarboxylated PLLA to DGEBA is 150°C, 30 min, and 1:1 respectively, while gel content of PLLA/DGEBA copolymer is almost zero.

  19. Calcium isotope fractionation in liquid chromatography with benzo-18-crown-6 resin in aqueous hydrobromic acid medium

    Liquid chromatography operated in a breakthrough mode was employed to study calcium isotope fractionation in the aqueous hydrobromic acid medium. Highly porous silica beads, the inner pores of which were embedded with a benzo-18-crown-6 ether resin, were used as column packing material. Enrichment of heavier isotopes of calcium was observed in the frontal part of respective calcium chromatograms. The values of the isotope fractionation coefficient were on the order of 10-3. The observed isotope fractionation coefficient was dependent on the concentration of hydrobromic acid in the calcium feed solution; a higher HBr concentration resulted in a smaller fractionation coefficient value. The present calcium isotope effects were most probably mass-dependent, indicating that they mostly came from isotope effects based on molecular vibration. Molecular orbital calculations supported the present experimental results in a qualitative fashion. Chromatography operated in aqueous HBr media is a better system of Ca isotope separation than that operated in aqueous HCl media. (author)

  20. Use of an o-aminobenzoic acid-functionalized XAD-4 copolymer resin for the separation and preconcentration of heavy metal(II) ions

    XAD copolymer resins may be functionalized with heavy metal ion-selective ligands either by covalent linkage to the polymer backbone or by impregnation. These resins may be tailored to be specific for certain heavy metals by adjusting the adsorption and elution parameters, thereby enabling simple and cost-effective spectrophotometric and flame atomic absorption spectrometry (FAAS) determinations of these metals without requiring the more sophisticated coupled instrumental techniques. For the synthesis of o-aminobenzoic acid (ABA)-immobilized XAD-4 copolymer resin that is expected to preconcentrate a number of transition and heavy metals, the azo-linkage method was chosen. For this purpose the copolymer was nitrated, reduced to the corresponding amine, converted to the diazonium salt with nitrite, and reacted with o-aminobenzoic acid to produce the XAD-ABA sorbent. This sorbent was capable of preconcentrating Pb(II), Cd(II), Ni(II), Co(II) and Zn(II) from weakly acidic or neutral aqueous solution. The retained metals were eluted with 1.0 M HNO3 from the resin column, and were subsequently determinated with by flame atomic absorption spectrometry. The developed resin preconcentration and determination method was successfully applied to the analysis of a synthetic metal mixture solution, a certified reference material (CRM) of coal sample, and brackish lake water

  1. Potentiometric studies on stepwise mixed ligand chelate formation of La(III), Pr(III) or Nd(III)-N-hydroxy ethylenediamine-N,N',N'-triacetic acid-mercapto acids

    Solution equilibrium studies on the interaction between 1 : 1, Ln(III)-HEDTA binary chelate (where Ln(III) =La(III), Pr(III) or Nd(III); HEDTA = N-hydroxyl-ethyl-ethylenediamine-N,N',N'-triacetic acid) with certain mercapto acids such as thioglycollic(TGA) and thiomalic (TMEA) have been carried out potentiometrically. Formation constants of the resulting mixed ligand chelates, MAL (where M =La(III), Pr(III) or Nd(III); A = HEDTA and L = TGA or TMEA) have been determined at 30 +- 10 and μ=0.1(KNO3). The values of the formation constant Ksub(MAL) have been interpreted in terms of electrostatic repulsion indicating that the contribution due to π-interaction in M-S bond is not significant. The order of stability in terms of metals ions has been found to be La(III)< Pr(III)< Nd(III) and in terms of secondary ligand as TGA< TMEA. (auth.)

  2. COMPARATIVE STUDY OF THE SHEAR BOND STRENGTH OF COMPOSITE RESIN TO DENTAL ENAMEL CONDITIONED WITH PHOSPHORIC ACID OR Nd: YAG LASER

    EDUARDO Carlos de Paula

    1997-01-01

    Full Text Available This study has been focused on a comparison between the shear bond strength of a composite resin attached to dental enamel surface, after a 35% phosphoric acid etching and after a Nd:YAG laser irradiation with 165.8 J/cm2 of energy density per pulse. After etching and attaching resin to these surfaces, the specimens were thermocycled and then underwent the shearing bond strength tests at a speed of 5 mm/min. The results achieved, after statistical analysis with Student's t-test, showed that the adhesion was significantly greater in the 35% phosphoric acid treated group than in the group treated with the Nd:YAG laser, thus demonstrating the need for developing new studies to reach the ideal parameters for an effective enamel surface conditioning as well as specific adhesives and composite resins when Nd:YAG laser is used

  3. Diphonix{trademark} Resin: A review of its properties and applications

    Chiarizia, R.; Horwitz, E.P. [Argonne National Lab., IL (United States); Alexandratos, S.D. [Univ. of Tennessee, Knoxville, TN (United States). Dept. of Chemistry; Gula, M.J. [Eichrom Industies, Inc., Darien, IL (United States)

    1995-12-31

    The recently developed Diphonix{trademark} resin is a new multifunctional chelating ion exchange resin containing seminally substituted diphosphonic acid ligands chemically bonded to a styrene-based polymeric matrix. Diphonix can be regarded as a dual mechanism polymer, with a sulfonic acid cation exchange group allowing for rapid access, mostly non-specific, of ions into the polymeric network, and the diphosphonic acid group responsible for specificity (recognition) for a number of metal cations. The Diphonix resin exhibits an extraordinarily strong affinity for actinides, especially in the tetra- and hexavalent oxidation states. It has potential applications in TRU and mixed waste treatment and characterization, and in the development of new procedures for rapid actinide preconcentration and separation from environmental samples. Metal uptake studies have been extended to alkaline earth cations, to transition and post transition metal species, and to metal sorption from neutral or near neutral solutions. Also the kinetic behavior of the resin has been investigated in detail. Influence of the most commonly occurring matrix constituents (Na, Ca, Al, Fe, hydrofluoric, sulfuric, oxalic and phosphoric acids) on the uptake of actinide ions has been measured. This review paper summarizes the most important results studies on the Diphonix resin and gives an overview of the applications already in existence or under development in the fields of mixed waste treatment, actinide separation procedures, treatment of radwaste from nuclear power plants, and removal of iron from copper electrowinning solutions.

  4. Use of a polystyrene-divinylbenzene-based weakly acidic cation-exchange resin column and propionic acid as an eluent in ion-exclusion/adsorption chromatography of aliphatic carboxylic acids and ethanol in food samples.

    Mori, Masanobu; Hironaga, Takahiro; Kajiwara, Hiroe; Nakatani, Nobutake; Kozaki, Daisuke; Itabashi, Hideyuki; Tanaka, Kazuhiko

    2011-01-01

    We developed an ion-exclusion/adsorption chromatography (IEAC) method employing a polystyrene-divinylbenzene-based weakly acidic cation-exchange resin (PS-WCX) column with propionic acid as the eluent for the simultaneous determination of multivalent aliphatic carboxylic acids and ethanol in food samples. The PS-WCX column well resolved mono-, di-, and trivalent carboxylic acids in the acidic eluent. Propionic acid as the eluent gave a higher signal-to-noise ratio, and enabled sensitive conductimetric detection of analyte acids. We found the optimal separation condition to be the combination of a PS-WCX column and 20-mM propionic acid. Practical applicability of the developed method was confirmed by using a short precolumn with a strongly acidic cation-exchange resin in the H(+)-form connected before the separation column; this was to remove cations from food samples by converting them to hydrogen ions. Consequently, common carboxylic acids and ethanol in beer, wine, and soy sauce were successfully separated by the developed method. PMID:21558657

  5. Characterization of Group V Dubnium Homologs on DGA Extraction Chromatography Resin from Nitric and Hydrofluoric Acid Matrices

    Despotopulos, J D; Sudowe, R

    2012-02-21

    somewhere between Nb and Pa. Much more recent studies have examined the properties of Db from HNO{sub 3}/HF matrices, and suggest Db forms complexes similar to those of Pa. Very little experimental work into the behavior of element 114 has been performed. Thermochromatography experiments of three atoms of element 114 indicate that the element 114 is at least as volatile as Hg, At, and element 112. Lead was shown to deposit on gold at temperatures about 1000 C higher than the atoms of element 114. Results indicate a substantially increased stability of element 114. No liquid phase studies of element 114 or its homologs (Pb, Sn, Ge) or pseudo-homologs (Hg, Cd) have been performed. Theoretical predictions indicate that element 114 is should have a much more stable +2 oxidation state and neutral state than Pb, which would result in element 114 being less reactive and less metallic than Pb. The relativistic effects on the 7p{sub 1/2} electrons are predicted to cause a diagonal relationship to be introduced into the periodic table. Therefore, 114{sup 2+} is expected to behave as if it were somewhere between Hg{sup 2+}, Cd{sup 2+}, and Pb{sup 2+}. In this work two commercially available extraction chromatography resins are evaluated, one for the separation of Db homologs and pseudo?homologs from each other as well as from potential interfering elements such as Group IV Rf homologs and actinides, and the other for separation of element 114 homologs. One resin, Eichrom's DGA resin, contains a N,N,N',N'-tetra-n-octyldiglycolamide extractant, which separates analytes based on both size and charge characteristics of the solvated metal species, coated on an inert support. The DGA resin was examined for Db chemical systems, and shows a high degree of selectivity for tri-, tetra-, and hexavalent metal ions in multiple acid matrices with fast kinetics. The other resin, Eichrom's Pb resin, contains a di-t-butylcyclohexano 18-crown-6 extractant with isodecanol solvent

  6. Basic physical and chemical properties of ReillexTM-HPQ anion exchange resin and its sorption behavior of halides in aqueous nitric acid solution

    The ReillexTM-HPQ anion exchange resin has a good potential toward the pretreatment of liquid nuclear wastes. In this work, a short procedure was devised to convert 99.997% of the resin from its chloride form to the nitrate form as a foundation of all quantitative measurements. It is determined that the resin can be dried to a constant mass at 60 degree C in 28 hours and the electrostatic effect during weighings can hence be eliminated. The weight ratio between resins dried at 110 degree C and 60 degree C is 0.927±0.005 (one standard deviation). The resin has an apparent pKa of 3.36±0.05. The sorption capacity from primarily the weakly basic ionogenic sites (RNH+) is 1.08±0.04 meq/g for resins dried at 60 degree C. In highly basic solutions, the resin became unstable and started to release a substantial amount of methanol. In nitric acid solutions, the selectivity sequence of halide ions versus nitrate and pertechnetate ions is: TcO4- > I- > NO3- > Br- > Cl- > F-. The HPQ resin showed no sorption of fluoride ions. Although the sorption of chloride ions is also low the data can be modeled well by an equation similar to the Freundlich isotherm at a pH range between 2.0 and 3.0. Both bromide and iodide ions showed moderate sorptions when [HNO3] = 1.00 M and the sorption data can be fitted well to an equation closely related to the Temkin isotherm. 25 refs., 6 figs., 5 tabs

  7. Fermentation and recovery of L-glutamic acid from cassava starch hydrolysate by ion-exchange resin column

    Nampoothiri K. Madhavan

    1999-01-01

    Full Text Available Investigations were carried out with the aim of producing L-glutamic acid from Brevibacterium sp. by utilizing a locally available starchy substrate, cassava (Manihot esculenta Crantz. Initial studies were carried out in shake flasks, which showed that even though the yield was high with 85-90 DE (Dextrose Equivalent value, the maximum conversion yield (~34% was obtained by using only partially digested starch hydrolysate, i.e. 45-50 DE. Fermentations were carried out in batch mode in a 5 L fermenter, using suitably diluted cassava starch hydrolysate, using a 85-90 DE value hydrolysate. Media supplemented with nutrients resulted in an accumulation of 21 g/L glutamic acid with a fairly high (66.3% conversation yield of glucose to glutamic acid (based on glucose consumed and on 81.74% theoretical conversion rate. The bioreactor conditions most conducive for maximum production were pH 7.5, temperature 30°C and an agitation of 180 rpm. When fermentation was conducted in fed-batch mode by keeping the residual reducing sugar concentration at 5% w/v, 25.0 g/L of glutamate was obtained after 40 h fermentation (16% more the batch mode. Chromatographic separation by ion-exchange resin was used for the recovery and purification of glutamic acid. It was further crystallized and separated by making use of its low solubility at the isoelectric point (pH 3.2.

  8. Two percent ethylenediaminetetraacetic acid chelation treatment for band-shaped keratopathy, without blunt scratching after removal of the corneal epithelium

    Kobayashi W; Yokokura S; Hariya T; Nakazawa T

    2015-01-01

    Wataru Kobayashi,1 Shunji Yokokura,1 Takehiro Hariya,1 Toru Nakazawa1–3 1Department of Ophthalmology, 2Department of Retinal Disease Control, Ophthalmology, 3Department of Advanced Ophthalmic Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan Background: The purpose of this study was to assess the effectiveness of 2% ethylenediaminetetraacetic acid (EDTA) for the treatment of band-shaped keratopathy.Methods: We studied 24 eyes of 16 patients with band-shaped kerato...

  9. Regeneration of three-way automobile catalysts using biodegradable metal chelating agent-S, S-ethylenediamine disuccinic acid (S, S-EDDS)

    Regeneration of the activity of three-way catalytic converters (TWCs) was tested for the first time using a biodegradable metal chelating agent (S, S-ethylenediamine disuccinic acid (S, S-EDDS). The efficiency of this novel environmentally friendly solvent in removing various contaminants such as P, Zn, Pb, Cu and S from commercial aged three-way catalysts, and improving their catalytic performance towards CO and NO pollutants removal has been investigated. Four samples of catalysts from the front and rear inlets of two different TWCs with different mileages and aged under completely different driving conditions were investigated. The catalysts were characterized using various techniques, such as X-ray diffraction (XRD), Scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) surface area measurements (N2 adsorption at 77 K). Quantitative ICP-MS analyses and SEM-EDS studies show the removal of Zn, P and Pb. SEM-EDS images obtained at low magnification (50 μm) showed considerable differences in the surface morphology and composition after washing with S, S-EDDS. However, XRD studies indicated neither little to no removal of major contaminant compound phases nor major structural changes due to washing. Correspondingly, little or no enhancement in BET surface area was observed between the used and washed samples. Light-off curves show that the regeneration procedure employed can effectively improve the catalytic performance towards NO pollutant.

  10. A novel malonamide grafted polystyrene-divinyl benzene resin for extraction, pre-concentration and separation of actinides

    A new chelating polymeric extraction chromatographic resin was prepared by chemical anchoring of N,N'-dimethyl-N,N'-dibutyl malonamide (DMDBMA) with chloromethylated Merrifield resin. The grafted resin exhibited stronger binding for hexavalent and tetravalent actinides such as U(VI), Th(IV) and Pu(IV) over trivalent actinides, viz. Am(III) and Pu(III). Batch studies on solid phase extraction performed over a wide range of acid solution (0.01-6 M HNO3) revealed that ternary mixer of uranium, americium and plutonium or thorium, americium and plutonium could be separated from each other at 1 M HNO3. Desorption of U(VI), Pu(IV) and Am(III) from the loaded resin was efficiently carried out using 0.1 M α-HIBA, 0.25 M oxalic acid and 0.01 M EDTA, respectively. Quantitative pre-concentration of actinide ions such as Th(IV) and U(VI) was possible from 3 M HNO3 solution. The practical utility of the grafted resin was evaluated by uranium sorption measurements in several successive cycles. The sorption efficiency of the resin with respect to uranyl ion remained unchanged even after 30 days of continuous use. The surface morphology of the resin was monitored with the help of scanning electron microscopy (SEM) technique

  11. Application of aminO acid chelates in infant milk formulation%氨基酸螯合物在婴幼儿配方奶粉中的应用性能研究

    张晓鸣; 张凤; 贾承胜; 夏书芹; 乐琳

    2009-01-01

    Amino acid chelates were used as mineral additives for fortification of infant milk formulation. The retention of VA, VC, VE as well as POV change during storage were evaluated when adding inorganic salts, organic salts and chelates, respectively. The results indicated that the retention of VA,VC,VE was highest in chelate group, followed by mixed organic group, and inorganic group was the lowest. Higher temperature could accelerate the degradation of vitamins mentioned above. The POV of three group of infant milk formulations all increased after storage, but it was lowest in the chelate group, which suggested that amino acid chelate was better than inorganic and other organic salts when adding into infant milk formulation.%研究氨基酸螯合物在婴幼儿配方奶粉中的应用性能.将不同微量元素添加到婴幼儿配方奶粉中研究其对体系过氧化值及VA、VC、VE稳定性的影响,发现无机组维生素降解非常迅速,螯合组最慢,混合组稍次于螯合组;温度升高会加速维生素的降解;婴幼儿配方奶粉储藏一定时间后POV均略有升高,升高幅度为无机组>混合组>螯合组,表明氨基酸螯合物在婴幼儿配方奶粉中的应用性能优于无机盐和有机盐.

  12. Polar modified post-cross-linked resin and its adsorption toward salicylic acid from aqueous solution: Equilibrium, kinetics and breakthrough studies.

    Fu, Zhenyu; He, Chunlian; Huang, Jianhan; Liu, You-Nian

    2015-08-01

    A novel polar modified post-cross-linked resin PDMPA was synthesized, characterized and evaluated for adsorption of salicylic acid from aqueous solution. PDMPA was prepared by a suspension polymerization of methyl acrylate (MA) and divinylbenzene (DVB), a Friedel-Crafts reaction and an amination reaction. After characterization of the chemical and pore structure of PDMPA, the adsorption behaviors of salicylic acid on PDMPA were determined in comparison with the precursor resins. The equilibrium adsorption capacity of salicylic acid on PDMPA was much larger than the precursor resins and the equilibrium data were correlated by both of the Langmuir and Freundlich models. The pseudo-second-order rate equation fitted the kinetic data better than the pseudo-first-order rate equation, and the micropore diffusion model could characterize the kinetic data very well. The dynamic experimental results showed that the breakthrough point and saturated point of salicylic acid on PDMPA were 40.3 and 92.4BV (1BV=10mL) at a feed concentration of 995.8mg/L and a flow rate of 1.4mL/min, and the resin column could be regenerated by 16.0BV of a mixture desorption solvent containing 0.01mol/L of NaOH (w/v) and 50% of ethanol (v/v). PMID:25863446

  13. Catalytic Upgrading of bio-oil using 1-octene and 1-butanol over sulfonic acid resin catalysts

    Zhang, Zhijun; Wang, Qingwen; Tripathi, Prabhat; Pittman, Charles U.

    2011-02-04

    Raw bio-oil from fast pyrolysis of biomass must be refined before it can be used as a transporation fuel, a petroleum refinery feed or for many other fuel uses. Raw bio-oil was upgraded with the neat model olefin, 1-octene, and with 1-octene/1-butanol mixtures over sulfonic acid resin catalysts frin 80 to 150 degrees celisus in order to simultaneously lower water content and acidity and to increase hydrophobicity and heating value. Phase separation and coke formation were key factors limiting the reaction rate during upgrading with neat 1-octene although octanols were formed by 1-octene hydration along with small amounts of octyl acetates and ethers. GC-MS analysis confirmed that olefin hydration, carboxylic acid esterification, acetal formation from aldehydes and ketones and O- and C-alkylations of phenolic compounds occurred simultaneously during upgrading with 1-octene/1-butanol mixtures. Addition of 1-butanol increased olefin conversion dramatically be reducing mass transfer restraints and serving as a cosolvent or emulsifying agent. It also reacted with carboxylic acids and aldehydes/ketones to form esters, and acetals, respectively, while also serving to stabilize bio-oil during heating. 1-Butanol addition also protected the catalysts, increasing catalyst lifetime and reducing or eliminationg coking. Upgrading sharply increased ester content and decreased the amounts of levoglucosan, polyhydric alcohols and organic acids. Upgrading lowered acidity (pH value rise from 2.5 to >3.0), removed the uppleasant ordor and increased hydrocarbon solubility. Water content decreased from 37.2% to < 7.5% dramatically and calorific value increased from 12.6 MJ kg to about 30.0 MJ kg.

  14. Scientific Opinion on the safety and efficacy of copper compounds (E4) as feed additives for all species: cupric chelate of amino acids hydrate, based on a dossier submitted by Zinpro Animal Nutrition Inc.

    EFSA Panel on Additives and Products or Substances used in Animal Feed

    2013-01-01

    Cupric chelate of amino acids hydrate is safe for all animal species/categories up to the authorised maximum of total copper content in complete feed. Consumption surveys include copper from foodstuffs of animal origin. Since the supplementation of animal feed with copper-containing compounds has not essentially changed over the last decade, no change in the contribution of foodstuffs originating from supplemented animals to the overall copper intake of consumers is expected. No concerns for ...

  15. Scientific opinion on the safety and efficacy of iron compounds (E1 as feed additives for all species: iron chelate of amino acids, hydrate, based on a dossier submitted by Zinpro Animal Nutrition Inc.

    EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP

    2013-07-01

    Full Text Available The use of iron chelate of amino acids, hydrate, as source of iron is considered safe for all animal species/categories when used up to the currently authorised maximum content of total iron in complete feed, with the exception of bovines and poultry for which the maximum tolerated level is 450 mg/kg complete feed, and pets, for which the maximum tolerated level is 600 mg/kg complete feed. The FEEDAP Panel is not in the position to derive a maximum safe iron concentration in feed for horses or fish. Consumption surveys include iron-containing foodstuffs of animal origin. Since the supplementation of animal feed with iron-containing compounds has not essentially changed during the last decades, it is reasonable to assume that the iron levels in food of animal origin used in exposure scenarios originated from animals fed iron-supplemented diets. Since iron chelate of amino acids, hydrate, will be used as a substitute for other iron compounds, its use in animal nutrition would not modify consumer exposure to iron. The additive should be considered as a skin, eye and respiratory irritant and, owing to its residual peptide component, as a skin/respiratory sensitiser. Considering the high background concentration of iron in soil and water, the supplementation of feed with iron chelate of amino acids, hydrate, is not expected to pose an environmental risk. Iron chelate of amino acids, hydrate, is an effective source of iron for all animal species and categories. The FEEDAP Panel recommends that the maximum iron contents in complete feed be reduced as follows: bovines and poultry, 450 mg Fe/kg; and pets, 600 mg Fe/kg.

  16. Separation and conductimetric detection of C1-C7 aliphatic monocarboxylic acids and C1-C7 aliphatic monoamines on unfunctionized polymethacrylate resin columns.

    Ohta, Kazutoku; Towata, Atsuya; Ohashi, Masayoshi; Takeuchi, Toyohide

    2004-06-11

    The application of unfunctionized polymethacrylate resin (TSKgel G3000PWXL) as a stationary phase in liquid chromatography with conductimetric detection for C1-C7 aliphatic monocarboxylic acids (formic acid, acetic acid, propionic acid, butyric acid, isovaleric acid, valeric acid, 3,3-dimethylbutyric acid, 4-methylvaleric acid, hexanoic acid, 2-methylhexanoic acid, 5-methylhexanoic acid and heptanoic acid) and C1-C7 aliphatic monoamines (methylamine, ethylamine, propylamine, isobutylamine, butylamine, isoamylamine, amylamine, 1,3-dimethylbutylamine, hexylamine, 2-heptylamine and heptylamine) was attempted with C8 aliphatic monocarboxylic acids (2-propylvaleric acid, 2-ethylhexanoic acid, 2-methylheptanoic acid and octanoic acid) and C8 aliphatic monoamines (1,5-dimethylhexylamine, 2-ethylhexylamine, 1-methylheptylamine and octylamine) as eluents, respectively. Using 1 mM 2-methylheptanoic acid at pH 4.0 as the eluent, excellent separation and relatively high sensitive detection for these C1-C7 carboxylic acids were achieved on a TSKgel G3000PWXL column (150 mm x 6 mm i.d.) in 60 min. Using 2 mM octylamine at pH 11.0 as the eluent, excellent separation and relatively high sensitive detection for these C1-C7 amines were also achieved on the TSKgel G3000PWXL column in 60 min. PMID:15250420

  17. 微量元素氨基酸螯合物及其在动物生产中的应用%Amino Acid Trace Mineral Chelates in Pigs, Chicken Production

    苏从成

    2011-01-01

    Amino acid trace mineral chelates is a new organic mineral additives, known as the third generation of trace element additives. Amino acid trace mineral chelates were applied widely in animal nutrition in the recent years because of its good stability, easy digestion, high utilization, anti-bacterium and so on. This paper summarized the concept, nutritional characteristics and biological functions of amino acid trace mineral chelates and its applications in animal production.%微量元素氨基酸螯合物是一种新型有机矿物元素添加剂,被称为第三代微量元素添加剂。由于其稳定性好、生物效价高、易消化吸收、抗干扰性强等特点,迅速成为动物营养研究的热点,在各种动物生产中广泛应用。本文就微量元素氨基酸螯合物的概念、营养特性、作用机制及在动物生产中的应用进行综述。

  18. The use of modified divinylbenzene-polystyrene resins in the separation of fermentation products. A case study utilizing amino acids and a dipeptide.

    Casillas, J L; Addo-Yobo, F; Kenney, C N; Aracil, J; Martínez, M

    1992-01-01

    The adsorption of phenylalanine, aspartic acid, asparagine and aspartame from phosphate-buffered aqueous solutions with modified divinyl-benzene-polystyrene resins has been investigated using high pressure liquid chromatography (HPLC). The pH studied was 2.8, the temperature range was 293-313 K and the ionic strength was maintained at 1.0 mol dm-3. Over the range of variables investigated, the adsorption isotherms are linear and may be characterized by temperature and pH-dependent apparent adsorption equilibrium constants, characteristic of the resin-adsorbate system. By studying the dependence on temperature of this adsorption constant, heats of adsorption and entropy of adsorption have been estimated. In terms of the heat liberated on adsorption, the amino acids and a dipeptide can be ranked thus: aspartame > phenylalanine > aspartic acid > asparagine. PMID:1368901

  19. Separation of cobalt from uranium (VI), manganese (II), and lithium on AG50W-X8 resin hydrochloric acid-acetone

    Cobalt can be separated from uranium(VI), manganese(II), and lithium, the most difficult elements to separate from cobalt when using the 8% cross-linked AG50W resin and hydrochloric acid-acetone eluting agents, by eluting uranium(VI) with 0,4M-hydrochloric acid-86% acetone, followed by cobalt with 1M-hydrochloric acid-80% acetone, while manganese(II) and lithium are still retained. Excellent separations are obtained, provided that not more than 10 mg of uranium(VI), 0,5 mmol of manganese(II), and 1 mmol of lithium are present together with 1 mmol of cobalt when a 60 ml resin columm is used. Appropriate elution curves and results for the analysis of synthetic mixtures are presented

  20. Kinetics of the Esterification Reaction between Pentanoic Acid and Methanol Catalyzed by Noncorrosive Cation Exchange Resin

    Sharma, M.; Toor, A. P.; R. K. Wanchoo

    2014-01-01

    Methyl pentanoate, commonly known as methyl valerate, is the methyl ester of pentanoic acid (valeric acid) with a fruity odour. Methyl pentanoate is commonly used in fragrances, beauty care, soap, laundry detergents at levels of 0.1 – 1 %. In its very pure form (purity 99.5 %) it is used as a plasticizer in the manufacture of plastics. In the present investigation, kinetics of esterification of pentanoic acid with methanol catalyzed by heterogeneous catalyst in a batch-type reactor is reporte...

  1. Chelation-assisted Pd-catalysed ortho-selective oxidative C-H/C-H cross-coupling of aromatic carboxylic acids with arenes and intramolecular Friedel-Crafts acylation: one-pot formation of fluorenones.

    Sun, Denan; Li, Bijin; Lan, Jingbo; Huang, Quan; You, Jingsong

    2016-03-01

    Pd-Catalysed ortho-selective oxidative C-H/C-H cross-coupling of aromatic carboxylic acids with arenes and subsequent intramolecular Friedel-Crafts acylation has been accomplished for the first time through a chelation-assisted C-H activation strategy. Starting from the readily available substrates, a variety of fluorenone derivatives are obtained in one pot. The direct use of naturally occurring carboxylic acid functionalities as directing groups avoids unnecessary steps for installation and removal of an extra directing group. PMID:26861768

  2. KINETIC OF ESTERIFICATION OF ETHYL ALCOHOL BY ACETIC ACID ON A CATALYTIC RESIN

    Erol İNCE

    2002-01-01

    Full Text Available The conversion kinetics of diluted acetic acid to ethyl acetate by ethanol esterification in a batch reactor in liquid phase with an acidic polymer catalyst (lewatit series was studied. The intrinsic rate constants have been correlated with the reaction temperature, concentration of catalyst, initial ratios of reactants and initial water concentrations. The kinetic analysis was restricted to the system at hand in which a liquid and vapor phase are at equilibrium.

  3. KINETIC OF ESTERIFICATION OF ETHYL ALCOHOL BY ACETIC ACID ON A CATALYTIC RESIN

    Erol İNCE

    2002-01-01

    The conversion kinetics of diluted acetic acid to ethyl acetate by ethanol esterification in a batch reactor in liquid phase with an acidic polymer catalyst (lewatit series) was studied. The intrinsic rate constants have been correlated with the reaction temperature, concentration of catalyst, initial ratios of reactants and initial water concentrations. The kinetic analysis was restricted to the system at hand in which a liquid and vapor phase are at equilibrium.

  4. Preparation and characterization of anion exchange resin decorated with magnetite nanoparticles for removal of p-toluic acid from aqueous solution

    Davarpanah, Morteza, E-mail: Davarpanah.morteza@gmail.com; Ahmadpour, Ali; Rohani Bastami, Tahereh

    2015-02-01

    Polystyrene resin was covalently functionalized with diethanolamine and then decorated with magnetite nanoparticles by a novel and simple co-precipitation method using iron(II) sulfate as precursor. The products were characterized by Fourier transform infrared spectroscopy, elemental analysis, X-ray diffraction, Mössbauer spectroscopy, field-emission scanning electron microscopy and vibrating sample magnetometer. Adsorption of p-toluic acid (p-TA) onto magnetite-decorated polystyrene (MAG-PS) was studied and compared with that of diethanolamine-functionalized polystyrene and a commercial anion exchange resin. Results showed that the magnetite nanoparticles with an average size of 20.4 nm were successfully formed on the surface of polystyrene resin, and MAG-PS was exhibited high affinity for the removal of p-TA. - Highlights: • .Polystyrene resin was covalently functionalized with diethanolamine. • .The functionalized adsorbents were decorated with magnetite nanoparticles (∼20 nm). • .Proposed magnetization procedure was high-efficient and relatively simple. • .Magnetic adsorbent was presented high affinity for removal of p-toluic acid.

  5. Preparation and characterization of anion exchange resin decorated with magnetite nanoparticles for removal of p-toluic acid from aqueous solution

    Polystyrene resin was covalently functionalized with diethanolamine and then decorated with magnetite nanoparticles by a novel and simple co-precipitation method using iron(II) sulfate as precursor. The products were characterized by Fourier transform infrared spectroscopy, elemental analysis, X-ray diffraction, Mössbauer spectroscopy, field-emission scanning electron microscopy and vibrating sample magnetometer. Adsorption of p-toluic acid (p-TA) onto magnetite-decorated polystyrene (MAG-PS) was studied and compared with that of diethanolamine-functionalized polystyrene and a commercial anion exchange resin. Results showed that the magnetite nanoparticles with an average size of 20.4 nm were successfully formed on the surface of polystyrene resin, and MAG-PS was exhibited high affinity for the removal of p-TA. - Highlights: • .Polystyrene resin was covalently functionalized with diethanolamine. • .The functionalized adsorbents were decorated with magnetite nanoparticles (∼20 nm). • .Proposed magnetization procedure was high-efficient and relatively simple. • .Magnetic adsorbent was presented high affinity for removal of p-toluic acid

  6. Quantitative measurement of metal chelation by fourier transform infrared spectroscopy

    Monika E. Miller

    2015-12-01

    Full Text Available Nutritionally important minerals are more readily absorbed by living systems when complexed with organic acids, resulting in higher consumer demand and premium prices for these products. These chelated metals are produced by reaction of metal oxides and acids in aqueous solution. However, unreacted dry blends are sometimes misrepresented as metal chelates, when in reality they are only simple mixtures of the reactants typically used to synthesize them. This practice has increased interest in developing analytical methods that are capable of measuring the extent of metal chelation for quality control and regulatory compliance. We describe a novel method to rapidly measure the percent chelation of citric and malic acids with calcium, magnesium, and zinc. Utilization of attenuated total reflectance (FTIR-ATR provides for the direct, rapid measurement of solid samples. The inclusion of an internal standard allows independent determination of either free or chelated acids from integrated areas in a single spectrum.

  7. Novel double prodrugs of the iron chelator N,N'-bis(2-hydroxybenzyl)ethylenediamine-N,N'-diacetic acid (HBED): Synthesis, characterization, and investigation of activation by chemical hydrolysis and oxidation.

    Thiele, Nikki A; Abboud, Khalil A; Sloan, Kenneth B

    2016-08-01

    The development of iron chelators suitable for the chronic treatment of diseases where iron accumulation and subsequent oxidative stress are implicated in disease pathogenesis is an active area of research. The clinical use of the strong chelator N,N'-bis(2-hydroxybenzyl)ethylenediamine-N,N'-diacetic acid (HBED) and its alkyl ester prodrugs has been hindered by poor oral bioavailability and lack of conversion to the parent chelator, respectively. Here, we present novel double prodrugs of HBED that have the carboxylate and phenolate donors of HBED masked with carboxylate esters and boronic acids/esters, respectively. These double prodrugs were successfully synthesized as free bases (7a-f) or as dimesylate salts (8a-c,e), and were characterized by (1)H, (13)C, and (11)B NMR; MP; MS; and elemental analysis. The crystal structure of 8a was solved. Three of the double prodrugs (8a-c) were selected for further investigation into their abilities to convert to HBED by stepwise hydrolysis and H2O2 oxidation. The serial hydrolysis of the pinacol and methyl esters of N,N'-bis(2-boronic acid pinacol ester benzyl)ethylenediamine-N,N'-diacetic acid methyl ester dimesylate (8a) was verified by LC-MS. The macro half-lives for the hydrolyses of 8a-c, measured by UV, ranged from 3.8 to 26.3 h at 37 °C in pH 7.5 phosphate buffer containing 50% MeOH. 9, the product of hydrolysis of 8a-c and the intermediate in the conversion pathway, showed little-to-no affinity for iron or copper in UV competition experiments. 9 underwent a serial oxidative deboronation by H2O2 in N-methylmorpholine buffer to generate HBED (k = 10.3 M(-1) min(-1)). The requirement of this second step, oxidation, before conversion to the active chelator is complete may confer site specificity when only localized iron chelation is needed. Overall, these results provide proof of principle for the activation of the double prodrugs by chemical hydrolysis and H2O2 oxidation, and merit further investigation into the

  8. ADSORPTION OF TANNIN ACID ONTO AN AMINATED MACROPOROUS RESIN FROM AQUEOUS SOLUTIONS

    2007-01-01

    A macroporous polymeric adsorbent NG-8 was synthesized with divinylbenzene using conventional suspension polymerization technique. Its aminated product NG-9 was prepared by introducing tertiary amino groups into NG-8 for removal of tannin acid from aqueous solutions. NG-9 could be used directly without a wetting process and had higher adsorption capacity than NG-8, which might be attributed to the enhanced adsorbent-adsorbate interaction due to the tertiary amino groups on the polymeric matrix. The Langmuir equation was successfully employed to describe the adsorption process. The adsorption enthalpy change further validated the uptake of tannin acid on NG-9 to be an enhanced physical adsorption because of the Lewis acid-base interaction. In addition, adsorption kinetic studies testified that the tertiary amino groups on the polymer matrix could decrease the adsorption rate maybe for the hindrance of the tertiary amino groups and water clusters built up.

  9. Computer simulation of metal ion equilibria in biofluids. IV. Plutonium speciation in human blood plasma and chelation therapy using polyaminopolycarboxylic acids

    Duffield, J.R.; May, P.M.; Williams, D.R.

    1984-03-01

    An investigation by computer simulation into the nature of Pu(IV) binding to low-molecular ligands in human blood plasma is described. Particular consideration is given to the interactions of various chelating agents which have been or might be used for treating plutonium intoxication. Formation constants of EDTA and DTPA with Cu(II), Mg(II), Mn(II), Zn(II), and Cd(II) have been measured under biologic conditions of temperature and background electrolyte. The relative ability of these and other chelating agents to cause excretion of plutonium and the concomitant loss of certain essential trace metals has thus been assessed.

  10. Ion-exclusion chromatographic behavior of aliphatic carboxylic acids and benzenecarboxylic acids on a sulfonated styrene--divinylbenzene co-polymer resin column with sulfuric acid containing various alcohols as eluent.

    Ohta, Kazutoku; Towata, Atsuya; Ohashi, Masayoshi

    2003-05-16

    The addition of C1-C7 alcohols (methanol, ethanol, propanol, butanol, heptanol, hexanol and heptanol) to dilute sulfuric acid as eluent in ion-exclusion chromatography using a highly sulfonated styrene-divinylbenzene co-polymer resin (TSKgel SCX) in the H+ form as the stationary phase was carried out for the simultaneous separations of both (a) C1-C7 aliphatic carboxylic acids (formic, acetic, propionic, isobutyric, butyric, isovaleric, valeric, 2-methylvaleric, isocaproic, caproic, 2,2-dimethyl-n-valeric, 2-methylhexanoic, 5-methylhexanoic and heptanoic acids) and (b) benzenecarboxylic acids (pyromellitic, hemimellitic, trimellitic, o-phthalic, m-phthalic, p-phthalic, benzoic and salicylic acids and phenol). Heptanol was the most effective modifier in ion-exclusion chromatography for the improvement of peak shapes and a reduction in retention volumes for higher aliphatic carboxylic acids and benzenecarboxylic acids. Excellent simultaneous separation and relatively highly sensitive conductimetric detection for these C1-C7 aliphatic carboxylic acids were achieved on the TSKgel SCX column (150 x 6 mm I.D.) in 30 min using 0.5 mM sulfuric acid containing 0.025% heptanol as eluent. Excellent simultaneous separation and highly sensitive UV detection at 200 nm for these benzenecarboxylic acids were also achieved on the TSKgel SCX column in 30 min using 5 mM sulfuric acid containing 0.075% heptanol as eluent. PMID:12830881

  11. Ferrocene base metal chelates

    Review of the works, devoted to different types of ferrocene metal chelates and to a possibility of ferrocene-containing ligand modification by means of complexing, is presented. Structure, properties and spectral characteristics of transitional metal, rare earth element, Cd2+, UO22+, Th4+ etc. complexes with ferrocene diketones, ferrocene acyl derivatives based on thiosemicarbazones and hydrazones and other heterometal ferrocene-containing metal chelates, are considered. 134 refs., 1 tab

  12. Chelating polymeric membranes

    Peinemann, Klaus-Viktor

    2015-01-22

    The present application offers a solution to the current problems associated with recovery and recycling of precious metals from scrap material, discard articles, and other items comprising one or more precious metals. The solution is premised on a microporous chelating polymeric membrane. Embodiments include, but are not limited to, microporous chelating polymeric membranes, device comprising the membranes, and methods of using and making the same.

  13. Monohydroxamic acids and bridging dihydroxamic acids as chelators to ruthenium(III) and as nitric oxide donors: syntheses, speciation studies and nitric oxide releasing investigations.

    Griffith, Darren; Krot, Krystyna; Comiskey, Jedd; Nolan, Kevin B; Marmion, Celine J

    2008-01-01

    The synthesis and spectroscopic characterisation of novel mononuclear Ru(III)(edta)(hydroxamato) complexes of general formula [Ru(H2edta)(monoha)] (where monoha = 3- or 4-NH2, 2-, 3- or 4-C1 and 3-Me-phenylhydroxamato), as well as the first example of a Ru(III)-N-aryl aromatic hydroxamate, [Ru(H2edta)(N-Me-bha)].H2O (N-Me-bha = N-methylbenzohydroxamato) are reported. Three dinuclear Ru(III) complexes with bridging dihydroxamato ligands of general formula [{Ru(H2edta)}2(mu-diha)] where diha = 2,6-pyridinedihydroxamato and 1,3- or 1,4-benzodihydroxamato, the first of their kind with Ru(III), are also described. The speciation of all of these systems (with the exception of the Ru-1,4-benzodihydroxamic acid and Ru-N-methylbenzohydroxamic systems) in aqueous solution was investigated. We previously proposed that nitrosyl abstraction from hydroxamic acids by Ru(III) involves initial formation of Ru(III)-hydroxamates. Yet, until now, no data on the rate of nitric oxide (NO) release from hydroxamic acids has been published. We now describe a UV-VIS spectroscopic study, where we monitored the decrease in the ligand-to-metal charge-transfer band of a series of Ru(III)-monohydroxamates with time, with a view to gaining an insight into the NO-releasing properties of hydroxamic acids. PMID:18399240

  14. Scientific Opinion on the safety and efficacy of copper compounds (E4 as feed additives for all species: cupric chelate of amino acids hydrate, based on a dossier submitted by Zinpro Animal Nutrition Inc.

    EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP

    2013-02-01

    Full Text Available Cupric chelate of amino acids hydrate is safe for all animal species/categories up to the authorised maximum of total copper content in complete feed. Consumption surveys include copper from foodstuffs of animal origin. Since the supplementation of animal feed with copper-containing compounds has not essentially changed over the last decade, no change in the contribution of foodstuffs originating from supplemented animals to the overall copper intake of consumers is expected. No concerns for consumer safety are expected from the use of cupric chelate of amino acids hydrate in animal nutrition, which would substitute for other copper sources. The additive should be considered as a skin and eye irritant and, owing to its amino acid/peptide component, as a skin/respiratory sensitiser. Potential risks to soil organisms have been identified as a result of the application of piglet manure. Levels of copper in other types of manure are too low to create a potential risk within the timescale considered. There might also be a potential environmental concern related to the contamination of sediment resulting from drainage and the run-off of copper to surface water. In order to draw a final conclusion, further model validation is needed and some further refinement to the assessment of copper-based feed additives in livestock needs to be considered, for which additional data would be required. The use of copper-containing additives in aquaculture up to the authorised maximum of total copper content in complete feeds is not expected to pose an appreciable risk to the environment. The extent to which copper-resistant bacteria contribute to the overall antibiotic resistance situation cannot be quantified at present. Cupric chelate of amino acids hydrate is recognised as an efficacious source of copper to meet animal requirements.

  15. Wear-resistant and electromagnetic absorbing behaviors of oleic acid post-modified ferrite-filled epoxy resin composite coating

    Wang, Wenjie; Zang, Chongguang; Jiao, Qingjie

    2015-03-01

    The post-modified Mn-Zn ferrite was prepared by grafting oleic acid on the surface of Mn-Zn ferrite to inhibit magnetic nanoparticle aggregation. Fourier Transform Infrared (FT-IR) spectroscopy was used to characterize the particle surfaces. The friction and electromagnetic absorbing properties of a thin coating fabricated by dispersing ferrite into epoxy resin (EP) were investigated. The roughness of the coating and water contact angle were measured using the VEECO and water contact angle meter. Friction tests were conducted using a stainless-steel bearing ball and a Rockwell diamond tip, respectively. The complex permittivity and complex permeability of the composite coating were studied in the low frequency (10 MHz-1.5 GHz). Surface modified ferrites are found to improve magnetic particles dispersion in EP resulting in significant compatibility between inorganic and organic materials. Results also indicate that modified ferrite/EP coatings have a lower roughness average value and higher water contact angle than original ferrite/EP coatings. The enhanced tribological properties of the modified ferrite/EP coatings can be seen from the increased coefficient value. The composite coatings with modified ferrite are observed to exhibit better reflection loss compared with the coatings with original ferrite.

  16. PROPERTIES AND MORPHOLOGY OF LIQUID CHLOROPRENE-METHACRYLIC ACID COPOLYMER MODIFIED EPOXY RESIN/POLY (BUTYL METHACRYLATE) SEMI-IPN

    BIAN Xinsheng; HAN Xiaozu; WANG Xinren; ZHANG Qingyu

    1987-01-01

    A series of liquid chloroprene-methacrylic acid copolymer (CP-co-MAA) modified epoxy resin (ER)/poly (butyl methacrylate) (PBMA) semi-IPN were synthesised. Some physical properties were investigated. DSC diagrams showed two indistinct and inward endothermal transitions corresponding to the transitions of two networks in the semi-IPN system. By observing morphology with SEM technique it shows that there is a multiphase structure, in which CP-co-MAA's domain sizes are about 0.10-0.80μ. With increasing C/E ratio, the domain εizes are getting smaller, which is due to effect of mixing network of CP-co-MAA promoting entanglement and interpenetrating of PBMA and CP-co-MAA-ER network. In most of the semi-IPN's compositions, ER phase readily maintains its phase continuity while PBMA phase presents a hand shape structure. Consequently, crosslinking network keeps in its continuous phase more readily than uncrosslinking one, thus it influences dominantly on the physical properties.

  17. The effect of degradation products of strong acidic cation exchange resins on radionuclide speciation: A case study with Ni2+

    Radiolytic degradation experiments with acidic ion-exchange resins revealed oxalate and an unidentified ligand X to be the most strongly complexing ligands of the degradation products. The influence of these ligands on the Ni speciation in groundwater and cement pore water of a repository is assessed. A complete and reliable thermodynamic database is built for this case study. Missing stability constants are estimated by chemical reasoning. Subsequent sensitivity analyses show whether these species are important or not. The backdoor approach used in this study addresses the following question: What concentrations must the ligand have to significantly influence the Ni speciation? In the case of oxalate, the concentration necessary to complex 90% Ni will never be exceeded within the repository or in its environment due to precipitation of Ca-oxalate solids. Thus, a negative effect of oxalate on Ni speciation and sorption need not be considered in safety assessments. In the case of ligand X, calculations demonstrate that Ni speciation is highly dependent on geochemical conditions and is occasionally ambiguous due to uncertainties in estimated stability constants. Hints are given to deal with these ambiguities in future safety assessment, and further experimental investigations are proposed to decrease uncertainties when necessary

  18. Wear-resistant and electromagnetic absorbing behaviors of oleic acid post-modified ferrite-filled epoxy resin composite coating

    Wang, Wenjie; Zang, Chongguang, E-mail: zangchongguang@bit.edu.cn; Jiao, Qingjie

    2015-03-15

    The post-modified Mn–Zn ferrite was prepared by grafting oleic acid on the surface of Mn–Zn ferrite to inhibit magnetic nanoparticle aggregation. Fourier Transform Infrared (FT-IR) spectroscopy was used to characterize the particle surfaces. The friction and electromagnetic absorbing properties of a thin coating fabricated by dispersing ferrite into epoxy resin (EP) were investigated. The roughness of the coating and water contact angle were measured using the VEECO and water contact angle meter. Friction tests were conducted using a stainless-steel bearing ball and a Rockwell diamond tip, respectively. The complex permittivity and complex permeability of the composite coating were studied in the low frequency (10 MHz–1.5 GHz). Surface modified ferrites are found to improve magnetic particles dispersion in EP resulting in significant compatibility between inorganic and organic materials. Results also indicate that modified ferrite/EP coatings have a lower roughness average value and higher water contact angle than original ferrite/EP coatings. The enhanced tribological properties of the modified ferrite/EP coatings can be seen from the increased coefficient value. The composite coatings with modified ferrite are observed to exhibit better reflection loss compared with the coatings with original ferrite. - Highlights: • The post-modified Mn-Zn ferrite was prepared by grafting oleic acid on its surface to inhibit aggregation. • The increasing in hydrophobicity and dispersion of modified coating improved compatibility between illers and polymer. • The modified fillers can decrease the friction COF of the composite coatings resulting in the enhanced resistance to wear. • The modified ferrite coatings are observed to exhibit better reflection loss compared with coatings with original ferrite.

  19. Wear-resistant and electromagnetic absorbing behaviors of oleic acid post-modified ferrite-filled epoxy resin composite coating

    The post-modified Mn–Zn ferrite was prepared by grafting oleic acid on the surface of Mn–Zn ferrite to inhibit magnetic nanoparticle aggregation. Fourier Transform Infrared (FT-IR) spectroscopy was used to characterize the particle surfaces. The friction and electromagnetic absorbing properties of a thin coating fabricated by dispersing ferrite into epoxy resin (EP) were investigated. The roughness of the coating and water contact angle were measured using the VEECO and water contact angle meter. Friction tests were conducted using a stainless-steel bearing ball and a Rockwell diamond tip, respectively. The complex permittivity and complex permeability of the composite coating were studied in the low frequency (10 MHz–1.5 GHz). Surface modified ferrites are found to improve magnetic particles dispersion in EP resulting in significant compatibility between inorganic and organic materials. Results also indicate that modified ferrite/EP coatings have a lower roughness average value and higher water contact angle than original ferrite/EP coatings. The enhanced tribological properties of the modified ferrite/EP coatings can be seen from the increased coefficient value. The composite coatings with modified ferrite are observed to exhibit better reflection loss compared with the coatings with original ferrite. - Highlights: • The post-modified Mn-Zn ferrite was prepared by grafting oleic acid on its surface to inhibit aggregation. • The increasing in hydrophobicity and dispersion of modified coating improved compatibility between illers and polymer. • The modified fillers can decrease the friction COF of the composite coatings resulting in the enhanced resistance to wear. • The modified ferrite coatings are observed to exhibit better reflection loss compared with coatings with original ferrite

  20. Preparation of molecularly imprinted resin based on chitosan for chiral recognition of S-mandelic acid.

    Monier, M; El-Mekabaty, A

    2013-04-01

    An enantioselective S-mandelic acid (S-MA) imprinted chitosan (SMIC) was prepared by cross-linking of chitosan using formaldehyde cross-linker, in the presence of S-MA as an imprint template molecule and 0.5% acetic acid solution as a solvent. Non-imprinted cross-linked chitosan (NIC) as control was also prepared by the same procedure in absence of template molecules. The surface morphology of both SMIC and NIC were examined by scanning electron microscope (SEM). SMIC particles were applied to determine the optimum operational condition for S-MA separation from dilute aqueous solution. In adsorption step, optimum pH and retention time were 3.5 and 60 min, while corresponding values in extraction step were 1 and 40 min, respectively. Also, the adsorption isotherms indicated that the maximum adsorption capacities of S- and R-MA on SMIC were 100 ± 0.5 and 64 ± 0.8 mg/g, respectively, while in the case of NIC, both R- and S-MA present the same maximum adsorption. PMID:23357795

  1. Scientific opinion on the safety and efficacy of iron compounds (E1) as feed additives for all species: iron chelate of amino acids, hydrate, based on a dossier submitted by Zinpro Animal Nutrition Inc.

    EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP)

    2013-01-01

    The use of iron chelate of amino acids, hydrate, as source of iron is considered safe for all animal species/categories when used up to the currently authorised maximum content of total iron in complete feed, with the exception of bovines and poultry for which the maximum tolerated level is 450 mg/kg complete feed, and pets, for which the maximum tolerated level is 600 mg/kg complete feed. The FEEDAP Panel is not in the position to derive a maximum safe iron concentration in feed for horses o...

  2. Evaluation of an extraction chromatographic resin containing CMPO and ionic liquid for actinide ion uptake from acidic feeds. Pt. II. Batch actinide sorption, radiolytic degradation and column studies

    Ansari, Seraj Ahmed; Mohapatra, Prasanta Kumar [Bhabha Atomic Reseach Centre, Mumbai (India). Radiochimistry Div.

    2014-10-01

    Extraction chromatographic resin prepared by impregnating CMPO-RTIL (C{sub 8}mim{sup +} . NTf{sub 2}{sup -}) on Chromosrob-W for the removal of trivalent actinides and lanthanides from aqueous solutions showed a significant improvement over the previously reported CMPO-n-dodecane resin. The resin was characterized by thermal analysis, for surface area by BET and for surface morphology by SEM. The K{sub d} value of Am(III) by CMPO-RTIL resin was found to be 5805 and 3.8 x 10{sup 4} with 3 M and 0.01 M HNO{sub 3}, respectively. The high K{sub d} values at lower acidity suggested metal ion uptake following a cation exchange mechanism usually seen with ionic liquid based solvents and use of 0.01 M EDTA resulted in a K{sub d} value of 0.11 which was subsequently used as the strippant. Uptake of other actinide ions such as UO{sub 2}{sup 2+}, Pu{sup 4+}, Np{sup 4+} and fission product element ions such as Eu{sup 3+}, Sr{sup 2+} and Cs{sup +} was also studied. Column studies using a feed containing 1 g/L Eu(III) in 3 M HNO{sub 3} suggested complete uptake of the metal ion up to passing 7 mL of the feed solution which corresponded to a column capacity of 7 mg of Eu. The loaded Eu(III) from the columns could be efficiently eluted with 0.01 M EDTA. The column capacity for Eu(III) was measured in the successive cycles of loading and elution and was found to be stable up to 60 d. The results suggested the possible application of the resins in the treatment of dilute laboratory radioactive waste. (orig.)

  3. Evaluation of an extraction chromatographic resin containing CMPO and ionic liquid for actinide ion uptake from acidic feeds. Pt. II. Batch actinide sorption, radiolytic degradation and column studies

    Extraction chromatographic resin prepared by impregnating CMPO-RTIL (C8mim+ . NTf2-) on Chromosrob-W for the removal of trivalent actinides and lanthanides from aqueous solutions showed a significant improvement over the previously reported CMPO-n-dodecane resin. The resin was characterized by thermal analysis, for surface area by BET and for surface morphology by SEM. The Kd value of Am(III) by CMPO-RTIL resin was found to be 5805 and 3.8 x 104 with 3 M and 0.01 M HNO3, respectively. The high Kd values at lower acidity suggested metal ion uptake following a cation exchange mechanism usually seen with ionic liquid based solvents and use of 0.01 M EDTA resulted in a Kd value of 0.11 which was subsequently used as the strippant. Uptake of other actinide ions such as UO22+, Pu4+, Np4+ and fission product element ions such as Eu3+, Sr2+ and Cs+ was also studied. Column studies using a feed containing 1 g/L Eu(III) in 3 M HNO3 suggested complete uptake of the metal ion up to passing 7 mL of the feed solution which corresponded to a column capacity of 7 mg of Eu. The loaded Eu(III) from the columns could be efficiently eluted with 0.01 M EDTA. The column capacity for Eu(III) was measured in the successive cycles of loading and elution and was found to be stable up to 60 d. The results suggested the possible application of the resins in the treatment of dilute laboratory radioactive waste. (orig.)

  4. Comments on chelation therapy

    The primary purpose of actinide chelation is to decrease the risk from radiation-induced cancer. While occupational exposures in the past have mainly involved low specific activity 239Pu, future exposures will increasingly involve high specific activity plutonium, americium, and curium - all of which clear more rapidly from the lung. This will tend to shift the cancer risk from lung to bone and liver. Although therapy with Ca- or Zn-DTPA rapidly removes 241Am from the canine, the sub-human primate, and the human liver, improved methods for removal from bone and lung are needed. DTPA can remove 241Am more easily from the growing skeleton of a child than from the mature skeleton of an adult. Investigators at Karlsruhe are developing chelation agents for oral administration and are investigating the reduction in local dose to bone resulting from chelation therapy

  5. Tin-117m-labeled stannic (Sn/sup 4 +/) chelate of diethylenetriamine pentaacetic acid (DTPA) for application in diagnosis and therapy

    Srivastava, S.C.; Meinken, G.E.; Richards, P.

    1983-08-25

    The radiopharmaceutical reagents of this invention and the class of Tin-117m radiopharmaceuticals are therapeutic and diagnostic agents that incorporate gamma-emitting nuclides that localize in bone after intravenous injection in mammals (mice, rats, dogs, and rabbits). Images reflecting bone structure or function can then be obtained by a scintillation camera that detects the distribution of ionizing radiation emitted by the radioactive agent. Tin-117m-labeled chelates of stannic tin localize almost exclusively in cortical bone. Upon intravenous injection of the reagent, the preferred chelates are phosphonate compounds, preferable, PYP, MDP, EHDP, and DTPA. This class of reagents is therapeutically and diagnostically useful in skeletal scintigraphy and for the radiotherapy of bone tumors and other disorders.

  6. The experimental study on protective effects and mechanisms of chelating agents of catechols amino carboxylic acid for radiation injury induced by actimides(Th-234)

    The decorporative efficacy and antioxidative action of prompt and delayed consecutive administration of catecholicpolyaminopolycarboxylate ligands, 7601 and 9501 for radiothorium in mice were investigated. DTPA and Vitamin E were used as positive controls. The competitive abilities of 7601 and 9501 to mobilize the thorium with BSA were studied. Their inhibition effects on superoxide anionas radicals were measured with electron spin resonance. The results showed that 7601 and 9501 are able to effectively prevent the internal radiation injury induced radiothorium, attributing to their double functions of pronounced removal effectiveness and antioxidative action. Their protective effects were better than DTPA and Vitamin E. The mechanisms of protective effects of 7601 and 9501 for internal radiation injury was close related to competitive ability of chelating agent to chelate the thorium with BSA and oxygen free radical scavenging activities

  7. Effect of the Acidic Dental Resin Monomer 10-methacryloyloxydecyl Dihydrogen Phosphate on Odontoblastic Differentiation of Human Dental Pulp Cells.

    Kim, Eun-Cheol; Park, Haejin; Lee, Sang-Im; Kim, Sun-Young

    2015-11-01

    Although 10-methacryloyloxydecyl dihydrogen phosphate (10-MDP) is frequently used as an acidic resin monomer in dental adhesives, its effect on dental pulp cells (DPCs) has been rarely reported. The purpose of this study was to examine the effects of 10-MDP on the inflammatory response and odontoblastic differentiation of DPCs at minimally toxic concentrations. We found that 10-MDP caused the release of inflammatory cytokines including NO, PGE2, iNOS, COX-2, TNF-α, IL-1β, IL-6 and IL-8 in a concentration-dependent manner. In addition, 10-MDP reduced alkaline phosphatase activity, mineralization nodule formation and mRNA expression of odontoblastic differentiation markers such as dentin sialophosphoprotein, dentin matrix protein-1, osterix and Runx2 in a concentration-dependent manner with low toxicity. In addition, 10-MDP induced activation of nuclear factor-E2-related factor 2 (Nrf2) and its target gene, haeme oxygenase-1 (HO-1). We evaluated whether the effect of 10-MDP was related to the induction of HO-1 and found that treatment with a selective inhibitor of HO-1 reversed the production of 10-MDP-mediated pro-inflammatory cytokines and the inhibition of differentiation markers. Pre-treatment with either a GSH synthesis inhibitor or antioxidants blocked 10-MDP-induced mitogen-activated protein kinases (MAPKs), Nrf2 and NF-κB pathways. Taken together, the results of this study showed that minimally toxic concentrations of 10-MDP promoted an inflammatory response and suppressed odontoblastic differentiation of DPCs by activating Nrf2-mediated HO-1 induction through MAPK and NF-κB signalling. PMID:25847254

  8. Optimisation and status of chelation therapy

    The calcium trisodium salt of diethylenetriaminepentaacetic acid (Ca-DTPA) remains the chelating agent of choice for treatment of incorporated actinides. The zinc trisodium salt (Zn-DTPA) represents a less toxic alternative, when Ca-DTPA is contra-indicated as well as for prolonged chelation therapy; in acute incorporation cases it would be less effective than Ca-DTPA. Specific ion binding chelators such as desferrioxamine (DFOA) and linear tetracatechoylamides, e.g., LICAM(C) proved more effective in animals injected with Pu, Th and Np (not with Am!) but only concerning the radioactivity in the bone; that in the kidneys was substantially increased. The combinations of DFOA or LICAM(C) with Ca-DTPA exerted the best overall effects. After incorporation of soluble uranium-compounds, an infusion of sodium bicarbonate seems at present the most reasonable for enhancing the uranium-excretion and prevention of kidney damage. (author)

  9. Lanthanon chelates of monoprotic tridentate schiff base

    3-(N-thiophene-2-aldimino)propanoic acid (HTP), and its lanthanon chelates were synthesised and studied by physico-chemical techniques. Irving-Rossotti method was followed to determine the dissociation constants of the ligand and formation constants of its lanthanon chelates in aqueous medium (ionic strength μ = 0.01, 0.05 and 0.1 M NaClO4) at 25 0C, 35 0C and 45 0C. Solid lanthanon chelates were characterised by molecular mass, elemental analyses, conductance, magnetic, thermal and spectral analyses and were assigned 1 : 3 (metal-ligand) stoichiometry in which the lanthanon shows nine coordination numbers. Covalent nature of metal-ligand bond was found to increase with increase in atomic number of central lanthanide ion. (author)

  10. Determination of boron concentration in oilfield water with a microfluidic ion exchange resin instrument.

    Floquet, Cedric F A; Sieben, Vincent J; MacKay, Bruce A; Mostowfi, Farshid

    2016-07-01

    We developed and validated a microfluidic instrument for interference-free determination of boron in produced water. The instrument uses a boron-specific chelating resin to separate the analyte from its complex matrix. Ten produced water samples were analyzed with the instrument and the results were successfully validated against ICP-MS measurements. Removing interference effects enables precise boron measurement for wastewater even with high total dissolved solid (TDS) levels. 1,4-Piperazinediethanesulfonic acid conditions the resin and maintains the optimum pH for boron adsorption from the sample. Boron is then eluted from the resin using a 10% sulfuric acid solution and its concentration measured with the colorimetric carminic acid assay in 95% sulfuric acid. The use of a microfluidic mixer greatly enhances the sensitivity and kinetics of the carminic acid assay, by factors of 2 and 7.5, respectively, when compared against the same assay performed manually. A maximum sensitivity of 2.5mg(-1)L, a precision of 4.2% over the 0-40.0mgL(-1) measuring range, a 0.3mgL(-1) limit of detection, and a sampling rate of up to four samples per hour were achieved. Automation and microfluidics reduce the operator workload and fluid manipulation errors, translating into safer and higher-quality measurements in the field. PMID:27154679

  11. Cleanup of demineralizer resins

    Radiocesium is being removed from demineralizers A and B (DA and DB) by a process that was developed from laboratory tests on small samples of resin from the demineralizers. The process was designed to elute the radiocesium from the demineralizer resins and then to resorb it onto the zeolite ion exchangers contained in the Submerged Demineralizer System (SDS). It was also required to limit the maximum cesium activities in the resin eluates (SDSD feeds) so that the radiation field surrounding the pipelines would not be excessive. The process consisted of 17 stages of batch elution. In the initial stage, the resin was contacted with 0.18 M boric acid. Subsequent stages subjected the resin to increasing concentrations of sodium in NaH2BO3-H3BO3 solution (total boron= 0.35 M) and then 1 M sodium hydroxide in the final stages. Results on the performance of the process in the cleanup of the demineralizers at TMI-2 are compared with those obtained from laboratory tests with small samples of the DA and DB resins. To date, 15 stages of batch elution have been completed on the demineralizers at TMI-2, which resulted in the removal of about 750 Ci of radiocesium from DA and about 3300 Ci from DB

  12. Mixed-chelate therapy of intratracheally deposited cadmium oxide

    Mixed-chelate treatment with EDTA and salicylic acid was no more effective in accelerating the removal of intratracheally instilled 109CdO, or in protecting against CdO-induced mortality, than was EDTA given alone

  13. Chelation Therapy for Mercury Poisoning

    Rong Guan; Han Dai

    2009-01-01

    Chelation therapy has been the major treatment for heavy metal poisoning. Various chelating agents have been developed and tested for treatment of heavy metal intoxications, including mercury poisoning. It has been clearly shown that chelating agents could rescue the toxicity caused by heavy metal intoxication, but the potential preventive role of chelating agents against heavy metal poisoning has not been explored much. Recent paper by Siddiqi and colleagues has suggested a protective role o...

  14. Adsorption of humic acid by bi-functional resin JN-10 and the effect of alkali-earth metal ions on the adsorption

    This study investigated the adsorption of humic acid (HA) by bi-functional resin JN-10, which removed the HA more effectively than the commercial resins D-301, D-201, XAD-7, and globe active carbon F-400. The difference between the FT-IR spectroscopy and 13C NMR analysis of JN-10 before and after it adsorbing the HA revealed that both hydrophobic interaction and electric attraction were the adsorption force for the HA. The related thermodynamic parameters exhibited that the adsorption of the HA by JN-10 was an endothermic process. The occurring of adsorption was due to the increase of entropy, and the electric attraction was also a main adsorption force. In order to investigate the influence of the molecule weight (MW) of the HA on its removal by JN-10, the HA with the MWs ranging from 2000 to 100,000 Da was divided into six fractions by ultra-filtration. The HA with a medium MW (6000-10,000 Da) was preferentially removed by JN-10 due to the synergistic effect of hydrophilicity, molecular size, and aromaticity of the HA. The adsorption capacity of JN-10 for the HA increased in the presence of low concentration of alkali-earth metal ions Ca2+ and Mg2+, which neutralized the negative charges of the HA, but it decreased as the concentration of these ions increased because the hydrates formed by the alkali-earth metal ions occupied the adsorption sites of the resin.

  15. Resin-loaded papers: sampling and trace analysis using neutron activation and x-ray spectrography

    Resin-loaded papers, composed of approximately 50 weight percent cellulose and 50 weight percent resin, provide an ideal medium for sampling large volumes of solution, then determining the concentrated elements by either fluorescent x-ray spectrography or neutron activation. This combination of chemistry and spectrography offers a versatile quantitative approach to the determination of trace elements in the ppM-ppB range. Standards and unknowns are prepared by either multiple filtration of solutions through two or more papers to measure the collection efficiency or a radiotracer is added to the solution to serve as a collection monitor. Reagent and paper blanks are incorporated into the analytical procedure. Papers containing strong acid or base resins collect a wide range of ions. Specific ions are collected by either chemical processing of the solution prior to filtration through the resin-loaded paper or by the use of papers loaded with chelating resins having high specificity. Advantages of the resin-loaded paper approach prior to spectrography are: improved analytical accuracy as the standards and unknowns are present in similar matrices; sampling errors are reduced and sensitivity significantly increased by concentration of the elements from a large volume of solution; and x-ray and gamma-ray spectral interferences are greatly reduced compared to bulk analysis. Also standard papers can be reused and stored indefinitely for x-ray applications. Examples of published applications to a wide range of industrial, environmental, and health problems are summaized together with applications by the Bureau of Mines to metallurgical and mining problems. Potential applications of new ion exchange resins and reagent-loaded papers are also considered

  16. Syntheses of polystyrene supported chelating resin containing the Schiff base derived from salicylaldehyde and triethylene tetramine and its copper(II), nickel(II), cobalt(II), iron(III), zinc(II), cadmium(II), molybdenum(VI), zirconium(IV) and uranium(VI) complexes

    A new polymer-anchored chelating ligand has been synthesized by the reaction of chloromethylated polystyrene (containing 0.94 mmol of Cl per gram of resin and 1% cross-linked with divinylbenzene) and the Schiff base derived from salicylaldehyde and triethylenetetramine. A new series of polystyrene supported, Cu(II), Ni(II), Co(II), Fe(III), Zn(II), Cd(II), Zr(IV), dioxomolybdenum (VI) and dioxouranium (VI) complexes of the formulae PS-LCu, PS-LNi, PS-LCo, PS-LFeCl.DMF, PS-LZn, PS-LCd, PS-LZr(OH)2. DMF, PSLMoO2 and PS-LUO2 (where PS-LH2 = polymer-anchored Schiff base and DMF dimethyl-formamide) have been synthesized and characterised by elemental analysis, infrared, electronic spectra and magnetic susceptibility measurements. The complexes PS-LCu, PS-LNi and PS-LCo have square planar structure, PS-LFeCl.DMF, PS-LMoO2 and PS-LUO2 have octahedral structure, PSLZn and PS-LCd are tetrahedral and PS-LZr(OH)2.DMF is pentagonal bipyramidal. The polymer-anchored Cu(II), Co(II) and Fe(III) complexes are paramagnetic while Ni(II), Zn(II), Cd(II), Zr(IV), dioxomolybdenum(VI) and dioxouranium(VI) complexes are diamagnetic. The negative shift of the v (C=N) (azomethine) and the positive shift of v (C--O)(phenolic) are indicative of ONNO donor behaviour of the polymer-anchored Schiff base. (author)

  17. Simultaneous Determination of Anions and Cations in Natural Water by Ion-exclusion/Cation-exchange Chromatography with a Weakly Acidic Cation-exchange Resin Column

    The simultaneous determination of anions (SO4 2-, Cl-, and NO3 -) and cations (Na+, NH4+, K+, Mg2+, and Ca2+) in natural water obtained by Nakdong River waters system in Korea were performed by ion-exclusion/cation exchange chromatography with conductimetric detection. The stationary phase was a polymethacrylate-based weakly acidic cation-exchange resin column in the H+-form and a weak-acid eluent. When using only a 1.4 mM sulfosalicylic acid/6 mM 18-crown-6 ether as an eluent, good resolution of both anions and cations, minimum time required for the separation, and satisfactory detection sensitivity were obtained in a reasonable time. The method was successfully applied to the simultaneous determination of anions and cations in natural waters

  18. Simultaneous Determination of Anions and Cations in Natural Water by Ion-exclusion/Cation-exchange Chromatography with a Weakly Acidic Cation-exchange Resin Column

    Lee, Kwang Pill; Choi, Seong Ho; Park, Yu Chul; Bae, Zun Ung; Lee, Mu Sang; Lee, Sang Hak; Chang, Hye Yong [Graduate School, Kyungpook National University, Daegu (Korea, Republic of); Kwon, Se Mok [Ulsan City Health and Environmental Research Institute, Ulsan (Korea, Republic of); Tanaka, Kazuhiko [National Industrial Research Institute of Nagoya, Nagoya (Japan)

    2003-09-15

    The simultaneous determination of anions (SO{sub 4} {sup 2-}, Cl{sup -}, and NO{sub 3} {sup -}) and cations (Na{sup +}, NH{sup 4+}, K{sup +}, Mg{sup 2+}, and Ca{sup 2+}) in natural water obtained by Nakdong River waters system in Korea were performed by ion-exclusion/cation exchange chromatography with conductimetric detection. The stationary phase was a polymethacrylate-based weakly acidic cation-exchange resin column in the H{sup +}-form and a weak-acid eluent. When using only a 1.4 mM sulfosalicylic acid/6 mM 18-crown-6 ether as an eluent, good resolution of both anions and cations, minimum time required for the separation, and satisfactory detection sensitivity were obtained in a reasonable time. The method was successfully applied to the simultaneous determination of anions and cations in natural waters.

  19. Effect of alcohols on separation behavior of rare earth elements using benzimidazole-type anion-exchange resin in nitric acid solutions

    The mutual separation of rare earth elements based on the ion exchange chromatography has been studied. The effect of alcohols on separation behavior of rare earth elements using the benzimidazole-type anion-exchange resin embedded in high-porous silica beads was investigated in nitric acid/alcohol mixed solvent systems. It was confirmed that the mutual separation of rare earth elements is possible by using our proposed methods. It was found that the distribution coefficients of rare earth elements depend on the corresponding alcoholic relative permittivity and on the steric hindrance due to the hydrophobic interaction among each alcoholic molecule. (author)

  20. Adsorptive separation of rare earths by using chelating chitosan

    Two kinds of chelating chitosan were prepared by chemically modifying chitosan with functional groups of EDTA or DTPA, abbreviated as EDTA- and DTPA-chitosan hereafter, respectively, to investigate the adsorption behaviour for rare earths the mutual separation of which is the most difficult among metal ions on these chelating chitosan from dilute hydrochloric or sulfuric acid solution. The plots of the distribution ratio of a series of rare earths against equilibrium pH lay on different straight lines with slope of 3 corresponding to each earth for both of two chelating chitosan, suggesting that 3 hydrogen ions are released for the adsorption of unit ion of each rare earth by chelate formation with the functional group of EDTA or DTPA and that mutual adsorptive separation between adjacent rare earth is possible with these chelating chitosan. Apparent equilibrium constants of the adsorption were evaluated from the intercepts of these straight lines with the ordinate for each rare earth and for both chelating chitosan. It was found that the equilibrium constants of adsorption on EDTA- or DTPA-chitosan are quite analogous to those of chelate formation with EDTA or DTPA themselves, suggesting that chelating characteristics of these complexones is still maintained after their immobilization on polymer matrices of chitosan. (author)

  1. Ion-exclusion chromatographic separations of C1-C6 aliphatic carboxylic acids on a sulfonated styrene-divinylbenzene co-polymer resin column with 5-methylhexanoic acid as eluent.

    Ohta, Kazutoku; Towata, Atsuya; Ohashi, Masayoshi

    2003-05-16

    The application of C7 aliphatic carboxylic acids (heptanoic, 2-methylhexanoic, 5-methylhexanoic and 2,2-dimethyl-n-valeric acids) as eluents in ion-exclusion chromatography with conductimetric detection for C1-C6 aliphatic carboxylic acids (formic, acetic, propionic, isobutyric, butyric, isovaleric, valeric, isocaproic and caproic acids) was carried out using a highly sulfonated styrene-divinylbenzene co-polymer resin (TSKgel SCX) in the H+ form as a stationary phase. When using 0.05 mM sulfuric acid at pH 4.0 as the eluent, peak shapes of hydrophobic carboxylic acids (isovaleric, valeric, isocaproic and caproic acids) were tailed strongly. In contrast, when using 1 mM these C7 carboxylic acids at pH ca. 4 as the eluents, although system peaks (vacant peaks) corresponding to these C7 carboxylic acids appeared, peak shapes of these hydrophobic acids were improved drastically. Excellent simultaneous separation and relatively high sensitive conductimetric detection for these C1-C6 aliphatic carboxylic acids were achieved in 25 min on the TSKgel SCX column (150 x 6 mm I.D.) using 1 mM 5-methylhexanoic acid at pH 4.0 as the eluent. PMID:12830882

  2. Development of a amidoxime resin for gallium recovering from Bayer liqueur

    Chelating resins have been prepared from acrylonitrile-divinylbenzene copolymer beads produced by suspension polymerization in in presence of an inert diluent. The copolymer beads were reacted with hydroxylamine to produce amidoxime groups in the repeating units derived from cyano groups (acrylonitrile), varied reaction conditions were employed. In this study, a set of experiments have been performed to determine the potential of the amidoxime chelating resin for the adsorption of gallium from Bayer liqueur. (author)

  3. Coadsorption behavior of salicylic acid and sulfosalicylic acid on D201 resin%水杨酸和磺基水杨酸在D201树脂上的共吸附行为

    谢祖芳; 陈渊; 晏全; 童张法; 杨凯清

    2011-01-01

    采用静态法和动态法研究了水溶液中水杨酸和磺基水杨酸在D201树脂上的共吸附行为和吸附选择性.同时竞争吸附、预负荷竞争吸附和等温吸附的结果均表明:水杨酸的存在对磺基水杨酸的吸附影响较小,而磺基水杨酸的存在则大大削弱了水杨酸的吸附,2种溶质在吸附位点上的竞争为主要作用机制.在双溶质(质量浓度比为1∶1)吸附体系中,初始质量浓度对吸附选择性的影响明显,初始质量浓度≤500 mg/L时,树脂对水杨酸或磺基水杨酸的吸附选择性均很小;初始浓度为1 000-2 000 mg/L时,树脂对磺基水杨酸有很高的吸附选择性,利于二者的选择吸附分离.对初始质量浓度均为2 000 mg/L的双溶质水溶液的动态吸附与脱附表明,以1.000 g树脂装柱,吸附出水在250 mL泄漏点内几乎只含水杨酸,磺基水杨酸被吸附于树脂上.室温下以质量分数5%NaCl+2%NaOH溶液作为脱附剂,可完全洗脱树脂上吸附的磺基水杨酸和水杨酸,其分离系数为300,磺基水杨酸的回收率为96%.应用D201树脂能有效实现磺基水杨酸与水杨酸的选择性吸附分离.%The coadsorption behavior and selectivity of salicylic acid and sulfosalicylic acid from aqueous solution on D201 resin were studied by using static and dynamic methods.The experimental results of the simultaneously competitive adsorption, preloading competitive adsorption and isotherm adsorption processes indicate that salicylic acid has very little influence on D201 resin adsorption of the sulfosalicylic acid, but the latter significantly depresses the adsorption of the salicylic acid.The predominant mechanism attributes to the competition of salicylic acid and sulfosalicylic acid for adsorption sites.In the binary solution of salicylic acid and sulfosalicylic acid (mass concentration ratio of 1: 1 ), the initial mass concentration can significantly affect the adsorption selectivity of D201 resin.At an initial

  4. Fixation kinetics of chelated and non-chelated zinc in semi-arid alkaline soils: application to zinc management

    Udeigwe, Theophilus K.; Eichmann, Madeleine; Menkiti, Matthew C.

    2016-07-01

    This study was designed to examine the fixation pattern and kinetics of zinc (Zn) in chelated (ethylenediaminetetraacetic acid, EDTA) and non-chelated mixed micronutrient systems of semi-arid alkaline soils from the Southern High Plains, USA. Soils were characterized for a suite of chemical and physical properties and data obtained from extraction experiments fitted to various kinetic models. About 30 % more plant-available Zn was fixed in the non-chelated system within the first 14 days with only about 18 % difference observed between the two systems by day 90, suggesting that the effectiveness of the chelated compounds tended to decrease over time. The strengths of the relationships of change in available Zn with respect to other micronutrients (copper, iron, and manganese) were higher and more significant in the non-chelated system (average R2 of 0.83), compared to the chelated (average R2 of 0.42). Fixation of plant-available Zn was best described by the power-function model (R2 = 0.94, SE = 0.076) in the non-chelated system, and was poorly described by all the models examined in the chelated system. Reaction rate constants and relationships generated from this study can serve as important tools for micronutrient management and for future micronutrient modeling studies on these soils and other semi-arid regions of the world.

  5. Preparation of thin {alpha}-particle sources using poly-pyrrole films functionalized by a chelating agent; Preparation de sources minces d'emetteurs alpha a l'aide de films de polypyrrole fonctionnalises par un ligand chelatant

    Mariet, C. [CEA Saclay, INSTN, Institut National des Sciences et Techniques Nucleaires, 91 - Gif-sur-Yvette (France); Universite Pierre et Marie Curie, 75 - Paris (France)

    2000-07-01

    This work takes place in the scope of analysis of the {alpha}-particle emitting elements U, Pu and Am present in compound environmental matrix like sols and sediments. The samples diversity and above all the {alpha}-ray characteristics require the analyst to implement a sequence of chemical steps in which the more restricting is the actinides concentration in a uniform and thin layer en allowing an accurately measure of alpha activity. On this account, we studied a new technique for radioactive sources preparation based on tow steps: preparation of a thin film as source support; incorporation of radioactive elements by a chelating extraction mechanism. The thin films were obtained through electro-polymerization of pyrrole monomer functionalized by an chelating ligand able to extract actinides from concentrated acidic solutions. Polymerization conditions of this monomer were perfected, then obtained films were characterized from a physico-chemical point of view. We point out their extracting properties were comparable to (retention capacity, distribution coefficient) to those of usual ion-exchange resins. The underscore of uranyl and americium nitrate complexes formed in the thin layer allowed to calculate the extraction constants in case acid extraction is negligible. Thanks to this results, the values of the coefficients distribution D{sub U} and D{sub Am} could be provided for all nitric solutions in which acid extraction is negligible. Optimal actinides retention conditions in the polymer were defined and used to settle a protocol for plutonium analysis in environmental samples. (author)

  6. Preparation of thin α-particle sources using poly-pyrrole films functionalized by a chelating agent

    This work takes place in the scope of analysis of the α-particle emitting elements U, Pu and Am present in compound environmental matrix like sols and sediments. The samples diversity and above all the α-ray characteristics require the analyst to implement a sequence of chemical steps in which the more restricting is the actinides concentration in a uniform and thin layer en allowing an accurately measure of alpha activity. On this account, we studied a new technique for radioactive sources preparation based on tow steps: preparation of a thin film as source support; incorporation of radioactive elements by a chelating extraction mechanism. The thin films were obtained through electro-polymerization of pyrrole monomer functionalized by an chelating ligand able to extract actinides from concentrated acidic solutions. Polymerization conditions of this monomer were perfected, then obtained films were characterized from a physico-chemical point of view. We point out their extracting properties were comparable to (retention capacity, distribution coefficient) to those of usual ion-exchange resins. The underscore of uranyl and americium nitrate complexes formed in the thin layer allowed to calculate the extraction constants in case acid extraction is negligible. Thanks to this results, the values of the coefficients distribution DU and DAm could be provided for all nitric solutions in which acid extraction is negligible. Optimal actinides retention conditions in the polymer were defined and used to settle a protocol for plutonium analysis in environmental samples. (author)

  7. EDTA: the chelating agent under environmental scrutiny

    Claudia Oviedo; Jaime Rodríguez

    2003-01-01

    The chelating agent EDTA (ethylenediaminetetraacetic acid) is a compound of massive use world wide with household and industrial applications, being one of the anthropogenic compounds with highest concentrations in inland European waters. In this review, the applications of EDTA and its behavior once it has been released into the environment are described. At a laboratory scale, degradation of EDTA has been achieved; however, in natural environments studies detect poor biodegradability. It is...

  8. Comparison of shear bond strength of composite resin to enamel surface with laser etching versus acid etching: An in vitro evaluation

    Upendra A Hoshing

    2014-01-01

    Full Text Available Introduction: The aim of the study is in vitro evaluation of the shear bond strength of composite resin bonded to enamel which is pretreated using acid etchant and Er,Cr:Ysgg. Materials and Methods: 40 extracted human teeth were divided in two groups of 20 each (Groups A and B. In Group A, prepared surface of enamel was etched using 37% phosphoric acid (Scotchbond, 3M. In Group B, enamel was surface treated by a an Er, Cr: YSGG laser system (Waterlase MD, Biolase Technology Inc., San Clemente, CA, USA operating at a wavelength of 2,780 nm and having a pulse duration of 140-200 microsecond with a repetition rate of 20 Hz and 40 Hz. Bonding agent ((Scotchbond Multipurpose, 3M was applied over the test areas on 20 samples of Groups A and B each, and light cured. Composite resin (Ceram X duo Nanoceramic restorative, Densply was applied onto the test areas as a 3 × 3 mm diameter bid, and light cured. The samples were tested for shear bond strength. Results: Mean shear bond strength for acid-etched enamel (26.41 ± 0.66MPa, range 25.155 to 27.150 MPa was significantly higher (P < 0.01 than for laser-etched enamel (16.23 ± 0.71MPa, range 15.233 to 17.334 MPa. Conclusions: For enamel surface, mean shear bond strength of bonded composite obtained after laser etching were significantly lower than those obtained after acid etching.

  9. Synthesis and Application of a New Acrylic Ester Resin for Recycling SIPA from its Water Solution

    2005-01-01

    A new acrylic ester polymer YWB-7 resin was prepared and characterized. The properties of YWB-7 resin were compared with those of the commercial Amberlite XAD-7, Diaion HP2MG and hypercrosslinked macroporous polymer NDA-150 resins. Both surface area and micropore area of YWB-7 resin were bigger than those of XAD-7 resin and HP2MG resin. The YWB-7 resin was successfully employed to recycle 5-sodiosulfoisophthalic acids (SIPA) from its solutions with and without methanol.

  10. Examining the fixation kinetics of chelated and non-chelated copper micronutrient and the applications to micronutrient management in semi-arid alkaline soils

    T. K. Udeigwe; M. B. Eichmann; Menkiti, M. C.

    2015-01-01

    The relationship between the deficiency of a nutrient in plants and its total concentration in the soil is complex. This study examined and compared the fixation and fixation kinetics of copper (Cu) in chelated (Ethylene diamine tetraacetic acid, EDTA) and non-chelated mixed systems of micronutrients in the semi-arid soils of the Southern High Plains, US using findings from Cu extraction studies and kinetic models. Approximately, 22 % more Cu was fixed in the non-chelated system with...

  11. Removal of CdTe in acidic media by magnetic ion-exchange resin: A potential recycling methodology for cadmium telluride photovoltaic waste

    Highlights: • Sulfonated magnetic microsphere was prepared as one strong acid cation-exchange resin. • Cd and Te can be removed directly from the highly acidic leaching solution of CdTe. • Good chemical stability, fast adsorbing rate and quick magnetic separation in strong acidic media. • A potential path for recycling CdTe photovoltaic waste. - Abstract: Sulfonated magnetic microspheres (PSt-DVB-SNa MPs) have been successfully prepared as adsorbents via an aqueous suspension polymerization of styrene-divinylbenzene and a sulfonation reaction successively. The resulting adsorbents were confirmed by means of Fourier transform infrared spectra (FT-IR), X-ray diffraction (XRD), transmission electron microscope (TEM), scanning electron microscope equipped with an energy dispersive spectrometer (SEM-EDS) and vibrating sample magnetometer (VSM). The leaching process of CdTe was optimized, and the removal efficiency of Cd and Te from the leaching solution was investigated. The adsorbents could directly remove all cations of Cd and Te from a highly acidic leaching solution of CdTe. The adsorption process for Cd and Te reached equilibrium in a few minutes and this process highly depended on the dosage of adsorbents and the affinity of sulfonate groups with cations. Because of its good adsorption capacity in strong acidic media, high adsorbing rate, and efficient magnetic separation from the solution, PSt-DVB-SNa MPs is expected to be an ideal material for the recycling of CdTe photovoltaic waste

  12. Removal of CdTe in acidic media by magnetic ion-exchange resin: A potential recycling methodology for cadmium telluride photovoltaic waste

    Zhang, Teng, E-mail: zhangteng@mail.iee.ac.cn; Dong, Zebin; Qu, Fei; Ding, Fazhu; Peng, Xingyu; Wang, Hongyan; Gu, Hongwei

    2014-08-30

    Highlights: • Sulfonated magnetic microsphere was prepared as one strong acid cation-exchange resin. • Cd and Te can be removed directly from the highly acidic leaching solution of CdTe. • Good chemical stability, fast adsorbing rate and quick magnetic separation in strong acidic media. • A potential path for recycling CdTe photovoltaic waste. - Abstract: Sulfonated magnetic microspheres (PSt-DVB-SNa MPs) have been successfully prepared as adsorbents via an aqueous suspension polymerization of styrene-divinylbenzene and a sulfonation reaction successively. The resulting adsorbents were confirmed by means of Fourier transform infrared spectra (FT-IR), X-ray diffraction (XRD), transmission electron microscope (TEM), scanning electron microscope equipped with an energy dispersive spectrometer (SEM-EDS) and vibrating sample magnetometer (VSM). The leaching process of CdTe was optimized, and the removal efficiency of Cd and Te from the leaching solution was investigated. The adsorbents could directly remove all cations of Cd and Te from a highly acidic leaching solution of CdTe. The adsorption process for Cd and Te reached equilibrium in a few minutes and this process highly depended on the dosage of adsorbents and the affinity of sulfonate groups with cations. Because of its good adsorption capacity in strong acidic media, high adsorbing rate, and efficient magnetic separation from the solution, PSt-DVB-SNa MPs is expected to be an ideal material for the recycling of CdTe photovoltaic waste.

  13. Resin composites

    Benetti, Ana Raquel; Peutzfeldt, Anne; Lussi, Adrian;

    2014-01-01

    OBJECTIVE: To investigate how the modulus of elasticity of resin composites influences marginal quality in restorations submitted to thermocyclic and mechanical loading. METHODS: Charisma, Filtek Supreme XTE and Grandio were selected as they were found to possess different moduli of elasticity but...... of resin composite (p=0.81) on the quality of dentine margins was observed, before or after loading. Deterioration of all margins was evident after loading (p<0.0001). More paramarginal enamel fractures were observed after loading in teeth restored with Grandio when compared to Charisma (p=0.......008). CONCLUSIONS: The resin composite with the highest modulus of elasticity resulted in the highest number of gap-free enamel margins but with an increased incidence of paramarginal enamel fractures. CLINICAL SIGNIFICANCE: The results from this study suggest that the marginal quality of restorations can be...

  14. Extraction of metals using supercritical fluid and chelate forming ligand

    A method of extracting metalloid and metal species from a solid or liquid material by exposing the material to a supercritical fluid solvent containing a chelating agent is described. The chelating agent forms chelates that are soluble in the supercritical fluid to allow removal of the species from the material. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is a fluorinated β-diketone. In especially preferred embodiments the extraction solvent is supercritical carbon dioxide, and the chelating agent comprises a fluorinated β-diketone and a trialkyl phosphate, or a fluorinated β-diketone and a trialkylphosphine oxide. Although a trialkyl phosphate can extract lanthanides and actinides from acidic solutions, a binary mixture comprising a fluorinated β-diketone and a trialkyl phosphate or a trialkylphosphine oxide tends to enhance the extraction efficiencies for actinides and lanthanides. The method provides an environmentally benign process for removing contaminants from industrial waste without using acids or biologically harmful solvents. The method is particularly useful for extracting actinides and lanthanides from acidic solutions. The chelate and supercritical fluid can be regenerated, and the contaminant species recovered, to provide an economic, efficient process. 7 figs

  15. Exposure of Atlantic salmon parr (Salmo salar) to a combination of resin acids and a water soluble fraction of diesel fuel oil: A model to investigate the chemical causes of pigmented salmon syndrome

    Pigmented salmon syndrome is a pollutant-induced hemolytic anemia and hyperbilirubinemia. As part of an investigation of this condition, S2 Atlantic salmon parr (Salmo salar) were exposed to a diesel fuel oil, water soluble fraction (WSF) in combination with a mixture of three resin acids (isopimaric, dehydroabietic, and abietic acids) in a continuous-flow freshwater system. The total nominal concentrations of resin acids in the exposure tanks were 10, 50, and 100 microg/L; the diesel WSF was generated in situ and provided a mean hydrocarbon concentration of 2.0 ± 0.1 mg/L (n = 12) during the 9-d exposure period. Exposure to the diesel WSF alone depressed liver bilirubin UDP-glucuronosyl transferase (UDPGT) activity and induced phenol UDPGT activity. Exposure to the diesel WSF in the absence or presence of resin acids induced liver cytochrome P4501A and increased the concentrations in the plasma of the enzymes lactate dehydrogenase, alkaline phosphatase, and glutamic oxaloacetic transaminase. The combined exposure to diesel WSF with either 50 or 100 microg/L total resin acid caused significant elevations in the concentrations of bilirubin in the plasma and many of these fish had yellow pigmentation on the ventral surface and around the gill arches. The results demonstrate that exposure to combinations of two groups of contaminants can result in the manifestation of toxic effects not apparent from exposure to either of these chemicals in isolation

  16. Exposure of Atlantic salmon parr (Salmo salar) to a combination of resin acids and a water soluble fraction of diesel fuel oil: A model to investigate the chemical causes of pigmented salmon syndrome

    Croce, B. [Scottish Office Agriculture, Environment, and Fisheries Dept., Aberdeen (United Kingdom). Marine Lab.]|[Scottish Environmental Protection Agency, Aberdeen (United Kingdom). North East River Purification Board; Stagg, R.M. [Scottish Office Agriculture, Environment, and Fisheries Dept., Aberdeen (United Kingdom). Marine Lab.

    1997-09-01

    Pigmented salmon syndrome is a pollutant-induced hemolytic anemia and hyperbilirubinemia. As part of an investigation of this condition, S2 Atlantic salmon parr (Salmo salar) were exposed to a diesel fuel oil, water soluble fraction (WSF) in combination with a mixture of three resin acids (isopimaric, dehydroabietic, and abietic acids) in a continuous-flow freshwater system. The total nominal concentrations of resin acids in the exposure tanks were 10, 50, and 100 {micro}g/L; the diesel WSF was generated in situ and provided a mean hydrocarbon concentration of 2.0 {+-} 0.1 mg/L (n = 12) during the 9-d exposure period. Exposure to the diesel WSF alone depressed liver bilirubin UDP-glucuronosyl transferase (UDPGT) activity and induced phenol UDPGT activity. Exposure to the diesel WSF in the absence or presence of resin acids induced liver cytochrome P4501A and increased the concentrations in the plasma of the enzymes lactate dehydrogenase, alkaline phosphatase, and glutamic oxaloacetic transaminase. The combined exposure to diesel WSF with either 50 or 100 {micro}g/L total resin acid caused significant elevations in the concentrations of bilirubin in the plasma and many of these fish had yellow pigmentation on the ventral surface and around the gill arches. The results demonstrate that exposure to combinations of two groups of contaminants can result in the manifestation of toxic effects not apparent from exposure to either of these chemicals in isolation.

  17. High-temperature resins

    Serafini, T. T.

    1982-01-01

    The basic chemistry, cure processes, properties, and applications of high temperature resins known as polyimides are surveyed. Condensation aromatic polymides are prepared by reacting aromatic diamines with aromatic dianhydrides, aromatic tetracarboxylic acids, or with dialkyl esters of aromatic tetracarboxylic acids, depending on the intended end use. The first is for coatings or films while the latter two are more suitable for polyimide matrix resins. Prepreg solutions are made by dissolving reactants in an aprotic solvent, and advances in the addition of a diamine on the double bond and radical polymerization of the double bond are noted to have yielded a final cure product with void-free characteristics. Attention is given to properties of the Skybond, Pyralin, and NR-150B polyimide prepreg materials and characteristics of aging in the NP-150 polyimides. Finally, features of the NASA-developed PMR polyimides are reviewed.

  18. Kinetic, equilibrium and thermodynamic studies on sorption of uranium and thorium from aqueous solutions by a selective impregnated resin containing carminic acid.

    Rahmani-Sani, Abolfazl; Hosseini-Bandegharaei, Ahmad; Hosseini, Seyyed-Hossein; Kharghani, Keivan; Zarei, Hossein; Rastegar, Ayoob

    2015-04-01

    In this work, the removal of uranium and thorium ions from aqueous solutions was studied by solid-liquid extraction using an advantageous extractant-impregnated resin (EIR) prepared by loading carminic acid (CA) onto Amberlite XAD-16 resin beads. Batch sorption experiments using CA/XAD-16 beads for the removal of U(VI) and Th(IV) ions were carried out as a function of several parameters, like equilibration time, metal ion concentration, etc. The equilibrium data obtained from the sorption experiments were adjusted to the Langmuir isotherm model and the calculated maximum sorption capacities in terms of monolayer sorption were in agreement with those obtained from the experiments. The experimental data on the sorption behavior of both metal ions onto the EIR beads fitted well in both Bangham and intra-particle diffusion kinetic models, indicating that the intra-particle diffusion is the rate-controlling step. The thermodynamic studies at different temperatures revealed the feasibility and the spontaneous nature of the sorption process for both uranium and thorium ions. PMID:25576783

  19. Photocurable bioactive bone cement based on hydroxyethyl methacrylate-poly(acrylic/maleic) acid resin and mesoporous sol gel-derived bioactive glass.

    Hesaraki, S

    2016-06-01

    This paper reports on strong and bioactive bone cement based on ternary bioactive SiO2-CaO-P2O5 glass particles and a photocurable resin comprising hydroxyethyl methacrylate (HEMA) and poly(acrylic/maleic) acid. The as-cured composite represented a compressive strength of about 95 MPa but it weakened during soaking in simulated body fluid, SBF, qua its compressive strength reached to about 20 MPa after immersing for 30 days. Biodegradability of the composite was confirmed by reducing its initial weight (~32%) as well as decreasing the molecular weight of early cured resin during the soaking procedure. The composite exhibited in vitro calcium phosphate precipitation in the form of nanosized carbonated hydroxyapatite, which indicates its bone bonding ability. Proliferation of calvarium-derived newborn rat osteoblasts seeded on top of the composite was observed during incubation at 37 °C, meanwhile, an adequate cell supporting ability was found. Consequently, it seems that the produced composite is an appropriate alternative for bone defect injuries, because of its good cell responses, high compressive strength and ongoing biodegradability, though more in vivo experiments are essential to confirm this assumption. PMID:27040248

  20. Chelation therapy for metal intoxication: comments from a thermodynamic viewpoint.

    Nurchi, Valeria Marina; Alonso, Miriam Crespo; Toso, Leonardo; Lachowicz, Joanna Izabela; Crisponi, Guido

    2013-10-01

    Chelation therapy plays a prominent role in the clinical treatment of metal intoxication. In this paper the principal causes of metal toxicity are exposed, and the chemical and biomedical requisites of a chelating agent are sketched. The chelating agents currently in use for scavenging toxic metal ions from humans belong to few categories: those characterized by coordinating mercapto groups, by oxygen groups, poliaminocarboxylic acids, and dithiocarbamates. Considering that the complex formation equilibria have been studied for less than 50% of chelators in use, some reflections on the utility of stability constants are presented, together with an evaluation of ligands under the stability profile. The competition between endogenous and toxic target metal ions for the same chelating agent is furthermore examined. A thorough examination of stability constant databases has allowed to select, for each toxic metal, the ligands distinguished by the best pMe values. Even though this selection does not consider the biomedical requisites of a chelating agent, it gives a clear picture both of the pMe values that can be attained, and of the most appropriate chelators for each metal ion. PMID:23895193

  1. Syntheses and characterization of copper (II), nickel (II), iron (III), zinc (II), cadmium (II), zirconium (IV), molybdenum (V and VI) and uranium (VI) complexes of polystyrene supported resin containing the Schiff base derived from 3-formylsalicylic acid and O-aminophenol

    A new series of polystyrene supported metal complexes of the formulae PS-LCu.DMF, PS-LNi.3DMF, PS-LFeCl.2DMF, PS-LZn.DMF, Ps-Lcd.DMF, PS-LMoOCl.DMF, PS-LMoO2.DMF,PS-LZr(OH)2.2DMF and PS-LUO2.DMF (where Ps-L deprotonated polymer-anchored Schiff base) have been synthesized by the reaction of metal salt/metal complex with the chelating resin containing the Schiff base derived from 3-formylsalicylic acid and o-aminophenol. The polymer supported metal complexes have been characterized by elemental analysis, IR, electronic and ESR spectra and magnetic susceptibility measurements. The geometry of the complexes are comparable with the corresponding metal complexes of non-anchored ligands. The polymer supported Cu(II) complex is square planar, Zn(II) and Cd(II) complexes are tetrahedral, Ni(II), Fe(III), U(VI) and Mo(V and VI) complexes are octahedral and zirconium(IV) complex is pentagonal bipyramidal. The polymer-anchored Ni(II), Cu(II), Fe(III) and Mo(V) complexes are paramagnetic while the Zn(II), Cd(II), Zr(IV), U(VI) and Mo(VI) complexes are diamagnetic. (author). 33 refs

  2. New resin gel for uranium determination by diffusive gradient in thin films technique.

    Gregusova, Michaela; Docekal, Bohumil

    2011-01-17

    A new resin gel based on Spheron-Oxin(®) chelating ion-exchanger with anchored 8-hydroxyquinoline functional groups was tested for application in diffusive gradient in thin film technique (DGT) for determination of uranium. Selectivity of uranium uptake from model carbonate loaded solutions of natural water was studied under laboratory conditions and compared with selectivity of the conventional Chelex 100 based resin gel. The affinity of Spheron-Oxin(®) functional groups enables determination of the overall uranium concentration in water containing carbonates up to the concentration level of 10(2) mg L(-1). The effect of uranium binding to the polyacrylamide (APA) and agarose diffusive gels (AGE) was also studied. Uranium is probably bound in both gels by a weak interaction with traces of acrylic acid groups in the structure of APA gel and with pyruvic and sulfonic acid groups in the AGE gel. These sorption effects can be eliminated to the negligible level by prolonged deployment of DGT probes or by disassembling probes after the 1-2 days post-sampling period that is sufficient for release of uranium from diffusive gel and its sorption in resin gel. PMID:21167996

  3. New resin gel for uranium determination by diffusive gradient in thin films technique

    Gregusova, Michaela, E-mail: gregusova@iach.cz [Institute of Analytical Chemistry, Academy of Sciences of the Czech Republic v.v.i., Veveri 97, 602 00 Brno (Czech Republic); Docekal, Bohumil [Institute of Analytical Chemistry, Academy of Sciences of the Czech Republic v.v.i., Veveri 97, 602 00 Brno (Czech Republic)

    2011-01-17

    A new resin gel based on Spheron-Oxin chelating ion-exchanger with anchored 8-hydroxyquinoline functional groups was tested for application in diffusive gradient in thin film technique (DGT) for determination of uranium. Selectivity of uranium uptake from model carbonate loaded solutions of natural water was studied under laboratory conditions and compared with selectivity of the conventional Chelex 100 based resin gel. The affinity of Spheron-Oxin functional groups enables determination of the overall uranium concentration in water containing carbonates up to the concentration level of 10{sup 2} mg L{sup -1}. The effect of uranium binding to the polyacrylamide (APA) and agarose diffusive gels (AGE) was also studied. Uranium is probably bound in both gels by a weak interaction with traces of acrylic acid groups in the structure of APA gel and with pyruvic and sulfonic acid groups in the AGE gel. These sorption effects can be eliminated to the negligible level by prolonged deployment of DGT probes or by disassembling probes after the 1-2 days post-sampling period that is sufficient for release of uranium from diffusive gel and its sorption in resin gel.

  4. Sorption behavior of perrhenate ion on ReillexTM-HP anion exchange resin from nitric acid and sodium nitrate/hydroxide solutions

    The distribution coefficients (K'd) are reported for perrhenate on the nitrate form of ReillexTM-HP, a weak base anion exchange resin, as a function of nitric acid concentration form 0.100 to 10.0 M. Perrhenate K'd values were determined in 1.00 M NaNO3 from pH 2 to 13. The K'd values were determined in solutions containing 1.35 M NaNO3 and variable NaOH, 0.155 to 4.66 M, and in solutions containing 0.655 M NaOH and variable NaNO3, 0.46 to 5.35M. Maximum perrhenate loadings were d is defined by the equation presented here. 30 refs., 4 figs., 1 tab

  5. Iron chelating active packaging: Influence of competing ions and pH value on effectiveness of soluble and immobilized hydroxamate chelators.

    Ogiwara, Yoshiko; Roman, Maxine J; Decker, Eric A; Goddard, Julie M

    2016-04-01

    Many packaged foods utilize synthetic chelators (e.g. ethylenediaminetetraacetic acid, EDTA) to inhibit iron-promoted oxidation or microbial growth which would result in quality loss. To address consumer demands for all natural products, we have previously developed a non-migratory iron chelating active packaging material by covalent immobilization of polyhydroxamate and demonstrated its efficacy in delaying lipid oxidation. Herein, we demonstrate the ability of this hydroxamate-functionalized iron chelating active packaging to retain iron chelating capacity; even in the presence of competing ions common in food. Both immobilized and soluble hydroxamate chelators retained iron chelating capacity in the presence of calcium, magnesium, and sodium competing ions, although at pH 5.0 the presence of calcium reduced immobilized hydroxamate iron chelation. A strong correlation was found between colorimetric and mass spectral analysis of iron chelation by the chelating packaging material. Such chelating active packaging may support reducing additive use in product formulations, while retaining quality and shelf life. PMID:26593563

  6. Contribution to the study of beryllium complexes. IX. Chelation of Be2+ ions by 3-hydroxy butanoic and 2-hydroxy 2-methyl propanoic acids, potentiometric study

    In the field of work on complexation of beryllium, complex equilibria in aqueous solution between beryllium (II) and 3-hydroxybutanoic acid (HA) and 2-hydroxy-2-methyl propanoic acid (HA) were studied by potentiometric (alkalimetric) titration (at ionic strength = 0.5 M by NaClO4 and a temperature T = 25.0 +- 0.10C to show the influence of hydroxyl group in carboxylic ligands. For the system 3-hydroxy butanoic acid, the results show the presence of two mononuclear species: BeA+ and BeA2 and one hydrolized complex: Be3(OH)3A2, but for 2-hydroxy-2-methylpropanoic acid an additional species is identified, in what the alcoolic function is dissociated: Be(H-1A). The formation constants are reported

  7. Mechanism of boron sorption by resin ANB-11G

    Interaction between boron (boric acid) and N-methyl glucamine in the ANB-11G sorbent phase has been studied by IR-spectroscopy and mathematical simulation methods. Sorption is established to proceed with formation of chelate borate anion in the alkali medium as well as of the chelate electroneutral compound in neutral and acid media

  8. Lignin pyrolysis products, lignans, and resin acids as specific tracers of plant classes in emissions from biomass combustion

    Simoneit, B.R.T. (Oregon State Univ., Corvaleis, OR (United States)); Rogge, W.F.; Cass, G.R. (California Inst. of Technology, Pasadena, CA (United States)); Mazurek, M.A. (Brookhaven National Lab., Upton, NY (United States)); Standley, L.J. (Academy of Natural Sciences, Avondale, PA (United States)); Hildemann, L.M. (Stanford Univ., CA (United States))

    1993-11-01

    Biomass smoke aerosols contain thermally unaltered and partially altered biomarker compounds from major vegetation taxa. These compounds range from C[sub 8] to C[sub 31] and include phytosterols, lignans, phenolic products from lignin, and diterpenoids from resins. Certain of the higher molecular weight biomarkers are vaporized from the parent plant material and subsequently condense unaltered into the particle phase. Other compounds undergo pyrolytic alteration and possibly dimerization. In both cases it is possible to assign many of these compounds to the plant taxa of the unburned fuel. The diterpenoids are good indicators for smoke from burning of gymnosperm wood. The relative distribution of the OH/OCH[sub 3] substituent patterns on the phenolic products indicates the plant class of the biomass that was burned. Application of these relationships to the interpretation of ambient smoke aerosols may permit further evaluation of the sources that contribute to regional biomass burning. 80 refs., 5 figs., 1 tab.

  9. Inositol hexa-phosphate: a potential chelating agent for uranium

    Cebrian, D.; Tapia, A.; Real, A.; Morcillo, M.A. [Radiobiology Laboratory, Radiation Dosimetry Unit, Department of Environment, CIEMAT, Avda Complutense 22, 28040 Madrid (Spain)

    2007-07-01

    Chelation therapy is an optimal method to reduce the radionuclide-related risks. In the case of uranium incorporation, the treatment of choice is so far i.v infusion of a 1.4% sodium bicarbonate solution, but the efficacy has been proved to be not very high. In this study, we examine the efficacy of some substances: bicarbonate, citrate, diethylenetriamine pentaacetic acid (DTPA), ethidronate (EHBP) and inositol hexa-phosphate (phytic acid) to chelate uranium using a test developed by Braun et al. Different concentrations of phytic acid, an abundant component of plant seeds that is widely distributed in animal cells and tissues in substantial levels, were tested and compared to the same concentrations of sodium citrate, bicarbonate, EHBP and DTPA. The results showed a strong affinity of inositol hexa-phosphate for uranium, suggesting that it could be an effective chelating agent for uranium in vivo. (authors)

  10. Inositol hexa-phosphate: a potential chelating agent for uranium

    Chelation therapy is an optimal method to reduce the radionuclide-related risks. In the case of uranium incorporation, the treatment of choice is so far i.v infusion of a 1.4% sodium bicarbonate solution, but the efficacy has been proved to be not very high. In this study, we examine the efficacy of some substances: bicarbonate, citrate, diethylenetriamine pentaacetic acid (DTPA), ethidronate (EHBP) and inositol hexa-phosphate (phytic acid) to chelate uranium using a test developed by Braun et al. Different concentrations of phytic acid, an abundant component of plant seeds that is widely distributed in animal cells and tissues in substantial levels, were tested and compared to the same concentrations of sodium citrate, bicarbonate, EHBP and DTPA. The results showed a strong affinity of inositol hexa-phosphate for uranium, suggesting that it could be an effective chelating agent for uranium in vivo. (authors)

  11. Spray drying of bead resins: feasibility tests

    Rockwell International has developed a volume reduction system for low-level reactor wastes based on drying the wastes in a heated-air spray dryer. The drying of slurries of sodium sulfate, boric acid, and powdered ion exchange resins was demonstrated in previous tests. The drying of bead ion exchange resins can be especially difficult due to the relatively large size of bead resins (about 500 to 800 microns) and their natural affinity for water. This water becomes part of the pore structure of the resins and normally comprises 50 t 60 wt % of the resin weight. A 76-cm-diameter spray dryer was used for feasibility tests of spray drying of cation and anion bead resins. These resins were fed to the dryer in the as-received form (similar to dewatered resins) and as slurries. A dry, free-flowing product was produced in all the tests. The volume of the spray-dried product was one-half to one-third the volume of the as-received material. An economic analysis was made of the potential cost savings that can be achieved using the Rockwel spray dryer system. In-plant costs, transportation costs, and burial costs of spray-dried resins were compared to similar costs for disposal of dewatered resins. A typical utility producing 170 m3 (6,000 ft3) per year of dewatered resins can save $600,000 to $700,000 per year using this volume reduction system

  12. Method for separating metal chelates from other materials based on solubilities in supercritical fluids

    Wai, Chien M. (Moscow, ID); Smart, Neil G. (Workington, GB); Phelps, Cindy (Moscow, ID)

    2001-01-01

    A method for separating a desired metal or metalloi from impurities using a supercritical extraction process based on solubility differences between the components, as well as the ability to vary the solvent power of the supercritical fluid, is described. The use of adduct-forming agents, such as phosphorous-containing ligands, to separate metal or metalloid chelates in such processes is further disclosed. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is selected from the group consisting of .beta.-diketones; phosphine oxides, such as trialkylphosphine oxides, triarylphosphine oxides and alkylarylphosphine oxides; phosphinic acids; carboxylic acids; phosphates, such as trialkylphosphates, triarylphosphates and alkylarylphosphates; crown ethers; dithiocarbamates; phosphine sulfides; phosphorothioic acids; thiophosphinic acids; halogenated analogs of these chelating agents; and mixtures of these chelating agents. In especially preferred embodiments, at least one of the chelating agents is fluorinated.

  13. Some aspects of chelation chemistry

    The notions used in chelation chemistry are defined and the possibilities of the experimental recognition of complex formation are described. A review of the quantitative aspects of chelation is given, especially under biological conditions. Some rules concerning the general behaviour of the various metal ions and the organic ligands in chelation phenomena are presented and the specificity problem is discussed. The present status of the decontamination of the main fission products, e.g. rare-earth metals and strontium, with the aid of complexing agents is analysed from a chemical point of view. (author)

  14. SORPTION OF Cu(II) BY POLY(HYDROXAMIC ACID) CHELATING EXCHANGER PREPARED FROM POL(YMETHYL ACRYLATE) GRAFTED OIL PALM EMPTY FRUIT BUNCH (OPEFB)

    Md Jelas Haron; Mariati Tiansih; Nor Azowa Ibrahim; Anuar Kassim; W. M. Z. Wan Yunus

    2009-01-01

    This paper describes the preparation of chemically modified oil palm empty fruit bunch (OPEFB) with hydroxamic acid functional group and its use for the sorption of Cu(II) from aqueous solution. OPEFB was grafted with poly(methylacrylate) (PMA), using H2O2/Fe2+ as initiator. The PMA grafted OPEFB (PMA-OPEFB) was treated with hydroxylammonium chloride in alkaline medium to produce hydroxamic acid grafted fiber (PHA-OPEFB). The FTIR spectrum of OPEFB grafted with PMA showed an intense absorpt...

  15. The Increased Promotion in Cobalt-Molybdenum Hydrodesulfurization Catalysts Supported on Alumina, Activated Carbon and Zirkonia by the Chelating Agent Nitrilotriacetic Acid

    Kaluža, Luděk

    2013-01-01

    The most active CoMo/Al2O3, C and ZrO2 catalysts in benzothiophene HDS were prepared by the impregnation of the support from the solution made by dissolution of MoO3, CoCO3 and nitrilotriacetic acid in water followed by sulfidation without previous calcination.

  16. Metal based pharmacologically active agents: Synthesis, structural characterization, molecular modeling, CT-DNA binding studies and in vitro antimicrobial screening of iron(II) bromosalicylidene amino acid chelates

    Abdel-Rahman, Laila H.; El-Khatib, Rafat M.; Nassr, Lobna A. E.; Abu-Dief, Ahmed M.; Ismael, Mohamed; Seleem, Amin Abdou

    2014-01-01

    In recent years, great interest has been focused on Fe(II) Schiff base amino acid complexes as cytotoxic and antitumor drugs. Thus a series of new iron(II) complexes based on Schiff bases amino acids ligands have been designed and synthesized from condensation of 5-bromosalicylaldehyde (bs) and α-amino acids (L-alanine (ala), L-phenylalanine (phala), L-aspartic acid (aspa), L-histidine (his) and L-arginine (arg)). The structure of the investigated iron(II) complexes was elucidated using elemental analyses, infrared, ultraviolet-visible, thermogravimetric analysis, as well as conductivity and magnetic susceptibility measurements. Moreover, the stoichiometry and the stability constants of the prepared complexes have been determined spectrophotometrically. The results suggest that 5-bromosalicylaldehyde amino acid Schiff bases (bs:aa) behave as dibasic tridentate ONO ligands and coordinate to Fe(II) in octahedral geometry according to the general formula [Fe(bs:aa)2]ṡnH2O. The conductivity values between 37 and 64 ohm-1 mol-1 cm2 in ethanol imply the presence of nonelectrolyte species. The structure of the complexes was validated using quantum mechanics calculations based on accurate DFT methods. Geometry optimization of the Fe-Schiff base amino acid complexes showed that all complexes had octahedral coordination. In addition, the interaction of these complexes with (CT-DNA) was investigated at pH = 7.2, by using UV-vis absorption, viscosity and agarose gel electrophoresis measurements. Results indicated that the investigated complexes strongly bind to calf thymus DNA via intercalative mode and showed a different DNA binding according to the sequence: bsari > bshi > bsali > bsasi > bsphali. Moreover, the prepared compounds are screened for their in vitro antibacterial and antifungal activity against three types of bacteria, Escherichia coli, Pseudomonas aeruginosa and Bacillus cereus and three types of anti fungal cultures, Penicillium purpurogenium, Aspergillus

  17. Chelation therapy in intoxications with mercury, lead and copper

    Cao, yang; Skaug, Marit Aralt; Andersen, Ole;

    2015-01-01

    In the present review we provide an update of the appropriate use of chelating agents in the treatment of intoxications with compounds of mercury, lead and copper. The relatively new chelators meso-2,3-dimercaptosuccinic acid (DMSA) and 2,3-dimercapto-propanesulphonate (DMPS) can effectively...... mobilize deposits of mercury as well as of lead into the urine. These drugs can be administered orally and have relatively low toxicity compared to the classical antidote dimercaptopropanol (BAL). d-Penicillamine has been widely used in copper overload, although 2,3-dimercaptosuccinic acid or...

  18. Thermal degradation of cold cured anthracite/coke breeze briquettes prepared from a coal tar acid resin

    Thoms, L.J.; Snape, C.E.; Taylor, D.; Mullens, J.; Mullens, S. [University of Strathclyde, Glasgow (United Kingdom). Department of Pure & Applied Chemistry

    1999-07-01

    Phenolic resoles were synthesised using a coal tar acid fraction of the oil from a low temperature carbonisation process. Anthracite/coke breeze briquettes were prepared using the tar acid resoles. Thermogravimetric analysis-mass spectrometry of products and combustion of briquettes are described. 4 refs., 1 tab.

  19. Kinetic, equilibrium and thermodynamic studies on sorption of uranium and thorium from aqueous solutions by a selective impregnated resin containing carminic acid

    Highlights: • The objective of the study is to investigate the potential application of a selective EIR for sorption of U(VI) and Th(IV) ions. • The effects of several physiochemical parameters were investigated. • The sorption kinetics and sorption isotherms were used to explain the sorption mechanism. • The thermodynamic studies showed the feasibility of sorption process. • The EIR beads showed a great potential for effective removal of U(VI) and Th(IV) ions. - Abstract: In this work, the removal of uranium and thorium ions from aqueous solutions was studied by solid–liquid extraction using an advantageous extractant-impregnated resin (EIR) prepared by loading carminic acid (CA) onto Amberlite XAD-16 resin beads. Batch sorption experiments using CA/XAD-16 beads for the removal of U(VI) and Th(IV) ions were carried out as a function of several parameters, like equilibration time, metal ion concentration, etc. The equilibrium data obtained from the sorption experiments were adjusted to the Langmuir isotherm model and the calculated maximum sorption capacities in terms of monolayer sorption were in agreement with those obtained from the experiments. The experimental data on the sorption behavior of both metal ions onto the EIR beads fitted well in both Bangham and intra-particle diffusion kinetic models, indicating that the intra-particle diffusion is the rate-controlling step. The thermodynamic studies at different temperatures revealed the feasibility and the spontaneous nature of the sorption process for both uranium and thorium ions

  20. Kinetic, equilibrium and thermodynamic studies on sorption of uranium and thorium from aqueous solutions by a selective impregnated resin containing carminic acid

    Rahmani-Sani, Abolfazl [Wastewater Division, Faculty of Health, Sabzevar University of Medical Sciences, PO Box 319, Sabzevar (Iran, Islamic Republic of); Hosseini-Bandegharaei, Ahmad, E-mail: ahoseinib@yahoo.com [Wastewater Division, Faculty of Health, Sabzevar University of Medical Sciences, PO Box 319, Sabzevar (Iran, Islamic Republic of); Department of Engineering, Kashmar Branch, Islamic Azad University, PO Box 161, Kashmar (Iran, Islamic Republic of); Hosseini, Seyyed-Hossein [Department of Engineering, Kashmar Branch, Islamic Azad University, PO Box 161, Kashmar (Iran, Islamic Republic of); Kharghani, Keivan [Water Division, Department of Engineering, Torbat-e-Hydarieh Branch, Islamic Azad University, PO Box 121, Torbat-e-Hydarieh (Iran, Islamic Republic of); Zarei, Hossein [Department of Engineering, Kashmar Branch, Islamic Azad University, PO Box 161, Kashmar (Iran, Islamic Republic of); Rastegar, Ayoob [Wastewater Division, Faculty of Health, Sabzevar University of Medical Sciences, PO Box 319, Sabzevar (Iran, Islamic Republic of); Department of Engineering, Kashmar Branch, Islamic Azad University, PO Box 161, Kashmar (Iran, Islamic Republic of)

    2015-04-09

    Highlights: • The objective of the study is to investigate the potential application of a selective EIR for sorption of U(VI) and Th(IV) ions. • The effects of several physiochemical parameters were investigated. • The sorption kinetics and sorption isotherms were used to explain the sorption mechanism. • The thermodynamic studies showed the feasibility of sorption process. • The EIR beads showed a great potential for effective removal of U(VI) and Th(IV) ions. - Abstract: In this work, the removal of uranium and thorium ions from aqueous solutions was studied by solid–liquid extraction using an advantageous extractant-impregnated resin (EIR) prepared by loading carminic acid (CA) onto Amberlite XAD-16 resin beads. Batch sorption experiments using CA/XAD-16 beads for the removal of U(VI) and Th(IV) ions were carried out as a function of several parameters, like equilibration time, metal ion concentration, etc. The equilibrium data obtained from the sorption experiments were adjusted to the Langmuir isotherm model and the calculated maximum sorption capacities in terms of monolayer sorption were in agreement with those obtained from the experiments. The experimental data on the sorption behavior of both metal ions onto the EIR beads fitted well in both Bangham and intra-particle diffusion kinetic models, indicating that the intra-particle diffusion is the rate-controlling step. The thermodynamic studies at different temperatures revealed the feasibility and the spontaneous nature of the sorption process for both uranium and thorium ions.

  1. Synthesis, structure elucidation, biological screening, molecular modeling and DNA binding of some Cu(II) chelates incorporating imines derived from amino acids

    Abdel-Rahman, Laila H.; Abu-Dief, Ahmed M.; Ismael, Mohammed; Mohamed, Mounir A. A.; Hashem, Nahla Ali

    2016-01-01

    Three tridentate Schiff bases amino acids were prepared by direct condensation of 3-methoxysalicylaldehyde (MS) or 4-diethylaminosalicylaldehyde (DS) with α-amino acid ligands [L-phenylalanine (P), L-histidine (H) and DL-tryptophan (T)]. The prepared Schiff bases amino acids were investigated by melting points, elemental analysis, 1HNMR and 13CNMR, IR, UV-Vis spectra, conductivity and magnetic measurements analyses. Subsequently, copper was introduced and Cu(II) complexes formed. These complexes were analyzed by thermal and elemental analyses and further investigated by FT-IR and UV/Vis spectroscopies. The experimental results indicating that all Cu(II) complexes contain hydrated water molecules (except DSPCu complex) and don't contain coordinated water molecules. The kinetic and thermal parameters were extracted from the thermal data using Coast and Redfern method. The molar conductance values of the Schiff base amino acid ligands and their Cu(II) complexes were relatively low, showing that these compounds have non-electrolytic nature. Magnetic susceptibility measurements showed the diamagnetic nature of the Schiff base amino acid ligands and paramagnetic nature of their complexes. Additionally, a spectrophotometric method was determined to extract their stability constants. It was found that the complexes possess 1:2 (M:L) stoichiometry. The results suggested that 3-methoxysalicylaldehyde and 4-diethylaminosalicylaldehyde amino acid Schiff bases behave as monobasic tridentate ONO ligands and coordinate Cu(II) ions in octahedral geometry according to the general formula [Cu(HL)2]·nH2O. To further understanding the structural and electronic properties of these complexes, Density Functional Theory (DFT) calculations were employed and provided a satisfactory description. The optimized structures of MST Schiff base ligand and its complex were calculated using DFT. The antimicrobial activity of the Schiff base ligands and their complexes were screened against some

  2. Iron chelators ICL670 and 311 inhibit HIV-1 transcription

    HIV-1 replication is induced by an excess of iron and iron chelation by desferrioxamine (DFO) inhibits viral replication by reducing proliferation of infected cells. Treatment of cells with DFO and 2-hydroxy-1-naphthylaldehyde isonicotinoyl hydrazone (311) inhibit expression of proteins that regulate cell-cycle progression, including cycle-dependent kinase 2 (CDK2). Our recent studies showed that CDK2 participates in HIV-1 transcription and viral replication suggesting that inhibition of CDK2 by iron chelators might also affect HIV-1 transcription. Here we evaluated the effect of a clinically approved orally effective iron chelator, 4-[3,5-bis-(hydroxyphenyl)-1,2,4-triazol-1-yl]-benzoic acid (ICL670) and 311 on HIV-1 transcription. Both ICL670 and 311 inhibited Tat-induced HIV-1 transcription in CEM-T cells, 293T and HeLa cells. Neither ICL670 nor 311 induced cytotoxicity at concentrations that inhibited HIV-1 transcription. The chelators decreased cellular activity of CDK2 and reduced HIV-1 Tat phosphorylation by CDK2. Neither ICL670A or 311 decreased CDK9 protein level but significantly reduced association of CDK9 with cyclin T1 and reduced phosphorylation of Ser-2 residues of RNA polymerase II C-terminal domain. In conclusion, our findings add to the evidence that iron chelators can inhibit HIV-1 transcription by deregulating CDK2 and CDK9. Further consideration should be given to the development of iron chelators for future anti-retroviral therapeutics

  3. Overview of current chelation practices

    Aydinok, Y.

    2011-01-01

    Deferoxamine (DFO) is reference standard therapy for transfusional iron overload since the 1980s. Although it is a highly effective iron chelator, the compliance problem to subcutaneous administration of DFO remains as the major problem. The oral chelator Deferiprone (DFP) has no marketing licence in North America, however, it has been licensed in India since 1994 and the European Union (EU) granted marketing approval for DFP in 1999, specifically for patients with thalassemia major when DFO ...

  4. Bifunctional Chelates for Metal Nuclides

    Brechbiel, Martin W.

    2007-01-01

    The use of “non-standard” metallic radionuclides continues to be an expanding field of investigation. Radiolabeling small molecules, peptides, proteins, and up to nano-particles are all areas of active investigation for both diagnostic and therapeutic applications. All require a common variable – the need for appropriate chelation chemistry for adequate sequestration of the metallic radionuclide that is equal to the intended application. A brief overview of the array of the chelation chemistr...

  5. Alarming use of chelation therapy

    Crisponi, Guido; Nurchi, Valeria Marina; Lachowicz, Joanna I.; Crespo-Alonso, Miriam; Zoroddu, Maria Antonietta; Peana, Massimiliano Francesco

    2014-01-01

    Chelation therapy is a consolidated medical procedure used primarily to hinder the effects of toxic metal ions on human tissues. Its application spans a broad spectrum of disorders, ranging from acute metal intoxication to genetic metal-overload. The use of chelating agents is compromised by a number of serious side effects, mainly attributable to perturbed equilibrium of essential metal ion homeostasis and dislocation of complexed metal ions to dangerous body sites. For this reason, chelatio...

  6. Oxidation of calprotectin by hypochlorous acid prevents chelation of essential metal ions and allows bacterial growth: Relevance to infections in cystic fibrosis.

    Magon, Nicholas J; Turner, Rufus; Gearry, Richard B; Hampton, Mark B; Sly, Peter D; Kettle, Anthony J

    2015-09-01

    Calprotectin provides nutritional immunity by sequestering manganese and zinc ions. It is abundant in the lungs of patients with cystic fibrosis but fails to prevent their recurrent infections. Calprotectin is a major protein of neutrophils and composed of two monomers, S100A8 and S100A9. We show that the ability of calprotectin to limit growth of Staphylococcus aureus and Pseudomonas aeruginosa is exquisitely sensitive to oxidation by hypochlorous acid. The N-terminal cysteine residue on S100A9 was highly susceptible to oxidation which resulted in cross-linking of the protein monomers. The N-terminal methionine of S100A8 was also readily oxidized by hypochlorous acid, forming both the methionine sulfoxide and the unique product dehydromethionine. Isolated human neutrophils formed these modifications on calprotectin when their myeloperoxidase generated hypochlorous acid. Up to 90% of the N-terminal amine on S100A8 in bronchoalveolar lavage fluid from young children with cystic fibrosis was oxidized. Oxidized calprotectin was higher in children with cystic fibrosis compared to disease controls, and further elevated in those patients with infections. Our data suggest that oxidative stress associated with inflammation in cystic fibrosis will stop metal sequestration by calprotectin. Consequently, strategies aimed at blocking extracellular myeloperoxidase activity should enable calprotectin to provide nutritional immunity within the airways. PMID:26006104

  7. SORPTION OF Cu(II BY POLY(HYDROXAMIC ACID CHELATING EXCHANGER PREPARED FROM POL(YMETHYL ACRYLATE GRAFTED OIL PALM EMPTY FRUIT BUNCH (OPEFB

    Md Jelas Haron

    2009-11-01

    Full Text Available This paper describes the preparation of chemically modified oil palm empty fruit bunch (OPEFB with hydroxamic acid functional group and its use for the sorption of Cu(II from aqueous solution. OPEFB was grafted with poly(methylacrylate (PMA, using H2O2/Fe2+ as initiator. The PMA grafted OPEFB (PMA-OPEFB was treated with hydroxylammonium chloride in alkaline medium to produce hydroxamic acid grafted fiber (PHA-OPEFB. The FTIR spectrum of OPEFB grafted with PMA showed an intense absorption band at 1734 cm-1 which is attributed to C=O vibration in the grafted ester. After hydroxylamine treatment, the intensity of absorption band at 1734 cm-1 decreased and new bands appeared at the 1640 cm-1 related to C=O vibration in hydroxamic acid and at the 1568 cm-1 related to the N-H amide. Sorption of Cu(II by PHA-OPEFB was effective over a pH range of 4 to 6. The sorption followed the Langmuir model with maximum capacities of 74.1 mg g-1 at 25 °C. The sorption process was exothermic, as shown by the negative value of enthalpy change, H. The free energy change (G for the sorption was negative, showing that the sorption process was spontaneous. A kinetic study showed that the Cu(II sorption followed a second order kinetic model.

  8. Ethylated Urea - Ether - Modified Urea - Formaldehyde Resins,

    Mathew Obichukwu EDOGA

    2006-07-01

    Full Text Available First, phenol - formaldehyde (PF and urea - formaldehyde (UFII resins were separately conventionally prepared in our laboratory. Also, UF resin synthesized from the acid modified synthesis procedure was synthesized in a purely acid medium of pH 1.0, FU molar ratio of 1.0 and at 50oC (one-stage acid modified-synthesis procedure. Subsequently, the UF resin II was modified during synthesis by incorporating ethylated urea-ether (EUER (i.e. UFIII and glycerol (GLYC (i.e. UFV cured with and without acid curing agent. The structural and physicochemical analyses of the various resin samples were carried out.The results showed that the unmodified UF resin (UF II synthesized in acid medium of pH 1.0, F/U molar ratio 1.0, and at 50oC, cured in absence of acid curing catalyst, showed features in their spectra which are consistent with a tri-, and/or tetra-substituted urea in the reaction to give a 3 - dimensional network cured UF resin. Modification of the UF resin(UF II with ethylated urea-ether and glycerol to produce UF resins III and respectively V prominently increased the absorbance of methylene and ether groups in the spectra which are consistent with increased hydrophobicity and improved hydrolytic stability. For the conventional UF resin (UF I, the only clear distinction between spectra for the UF resin II and UF resins (III/V is the presence of diminished peaks for methylene groups at 2.2 ppm. The relationship between the logarithmic viscosity of cured PF resin with time showed continuos dependence of viscosity with time during cure up to 70 minutes. Similar trends were shown by UF resins (III/V, cured in absence of acid catalyst. In contrast, the conventional UF resins I and UF IV (i.e. UF II cured with NH4CL showed abrupt discontinuity in viscosity with time just after about 20 minutes of cure.

  9. Examination of styrene-divinylbenzene ion exchange resins, used in contact with food, for potential migrants

    Sidwell, John Andrew; Willoughby, Bryan

    2006-01-01

    Abstract This study has investigated the nature of extractable substances from five types of styrene-divinylbenzene ion exchange resins used in the preparation of foodstuffs. Resins examined included strong acid cation resins, strong and weak base anion resins and an active carbon replacement resin. These resins are used for a variety of purposes including water softening, decalcification of sugar syrups, demineralisation, removal of nitrate ions from water and decolourisation. The...

  10. Chelating impact assessment of biological ad chemical chelates on metal extraction from contaminated soils

    Soil contamination is the result of uncontrolled waste dumping and poor practices by humans. Of all the pollutants heavy metals are of particular concern due to their atmospheric deposition, leaching capacity and non-biodegradability. Heavy metal containing effluent is discharged into the agricultural fields and water bodies. This results in the accumulation of heavy metals in soil and the crops grown on that soil. Studies have revealed detrimental impacts on soil fertility and the poor health of animals and humans. Phytoextraction is widely researched for remediation of heavy metal contaminated soil. To enhance the effect of phytoextraction heavy metals have to be available to the plants in soluble form. In this study the potential of different chelating agents was assessed in solubilizing the heavy metals making easy for plants to uptake them. For this purpose efficient chemical and biological chelating agent had to be identified. Along with that an optimum dose and application time for chemical chelating agent was determined. Ethylenediamine tetraacetic acid (EDTA), Diethylene triamine pentaacetic acid (DTPA), Nitriloacetic acid (NTA) were applied to the soil, containing Pb, Cr, Cu and Cd, at different concentrations and application time. Aspergillus niger and Aspergillus flavus were incubated in soil for different time periods. In correspondence with findings of the study, Pb and Cr were best solubilized by 5mM EDTA. For Cd and Cu 5mM DTPA carried out efficient chelation. NTA showed relatively inadequate solubilisation, although for Cr it performed equal to EDTA. A. niger and A. flavus instead of solubilizing adsorbed the metals in their biomass. Adsorption was mainly carried out by A. niger. (author)

  11. Examining the fixation kinetics of chelated and non-chelated copper and the applications to micronutrient management in semiarid alkaline soils

    Udeigwe, T. K.; Eichmann, M. B.; Menkiti, M. C.; Kusi, N. Y. O.

    2016-02-01

    This study examined and compared the fixation and fixation kinetics of copper (Cu) in chelated (ethylene diamine tetraacetic acid, EDTA) and non-chelated mixed systems of micronutrients in the semiarid soils of the Southern High Plains, USA, using findings from Cu extraction studies and kinetic models. Approximately, 22 % more Cu was fixed in the non-chelated system compared to the chelated within the first 14 days with only 7 % difference between the two systems by day 90. Findings suggest a decrease in the effectiveness of chelated micronutrients over time, highlighting the significance of timing even when chelated micronutrients are used. The strengths of the relationship of change in available Cu with respect to other micronutrients (iron (Fe), manganese (Mn), and zinc (Zn)) were higher in the non-chelated system (R2: 0.68-0.94), compared to the chelated (R2: 0.42-0.81), with slopes of 0.40 (Cu-Fe), 0.31 (Cu-Mn), and 1.04 (Cu-Zn) in the non-chelated system and 0.26 (Cu-Fe), 0.22 (Cu-Mn), and 0.90 (Cu-Zn) in the chelated system. Reduction in the amount of available Cu was best described by the power function model (R2 = 0.91, SE = 0.081) in the non-chelated system and second-order model (R2 = 0.95, SE = 0.010) in the chelated system. The applications generated from this study could be used as tools for improved micronutrient management and also provide baseline data for future work in other semiarid/arid alkaline soils of the world. Findings are also more applicable to field settings, an improvement over related previous studies.

  12. Absorption Behavior of Anion Exchange Resin to Minimal Plutonium in 3 to 4 mol/L Nitric Acid Medium

    2008-01-01

    <正>The acidity of liquor in the process of plutonium purification using extraction method is 3 to 4 mol/L and liquor contains minimal plutonium of certain concentration, the reclamation of plutonium is usually

  13. New 111In labeling of IgG: 111In-oxine mediated chelation

    Current methods of 111In chelate conjugation labeling of antibodies expose the protein to pH 5-6 during 111In chelation. These conditions could be detrimental if the antibody is acid labile. We have successfully labeled human IgG via the cyclic anhydride of DPTA and 111In-oxyquinoline(oxine). Chelation was achieved at pH 6.9-8.4 and was complete within 1 min at room temperature. The chelation was sensitive to trace metal contamination on labware and in some reagents (including commercial 111In-oxine). (author)

  14. Chelating capture and magnetic removal of non-magnetic heavy metal substances from soil

    Liren Fan; Jiqing Song; Wenbo Bai; Shengping Wang; Ming Zeng; Xiaoming Li; Yang Zhou; Haifeng Li; Haiwei Lu

    2016-01-01

    A soil remediation method based on magnetic beneficiation is reported. A new magnetic solid chelator powder, FS@IDA (core-shell Fe3O4@SiO2 nanoparticles coated with iminodiacetic acid chelators), was used as a reactive magnetic carrier to selectively capture non-magnetic heavy metals in soil by chelation and removal by magnetic separation. FS@IDA was prepared via inorganic-organic and organic synthesis reactions that generated chelating groups on the surface of magnetic, multi-core, core-shel...

  15. Development of radiation-curable resin based on natural rubber

    A new radiation curable resin based on natural rubber has been developed. The resin was based on the reaction between low molecular weight epoxidised natural rubber and acrylic acid. When formulated with reactive monomers and photoinitiator, it solidified upon irradiation with UV light. The resin may find applications in coating for cellulosic-based substrates and pressure-sensitive adhesive

  16. Targeted Cleavage of HIV RRE RNA by Rev-Coupled Transition Metal Chelates

    Joyner, Jeff C.; Cowan, J. A.

    2011-01-01

    A series of compounds that target reactive metal-chelates to the HIV-1 Rev Response Element (RRE) mRNA have been synthesized. Dissociation constants and chemical reactivity toward HIV RRE RNA have been determined and evaluated in terms of reduction potential, coordination unsaturation, and overall charge associated with the metal-chelate-rev complex. Ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), diethylenetriaminepentaacetic acid (DTPA), and 1,4,7,10-tetraazacyclo-dodec...

  17. Epoxidation of linseed oil-Alkyd resins

    Three types of different linseed oil-alkyd resin ( Alk (I), Alk (II), and Alk (III) ) were prepared with the calculated amounts of mono glycerides and adipic acid (1:1, 1:2, and 2:1 Eq.Wt) respectively via monoglyceride method. The obtained alkyd resins were epoxidized via reaction with the calculated quantities of peracetic acid, which was prepared by the reaction of acetic anhydride with H2O2. Epoxidation occurred with the ratio (1: 1, 1 :3, and 1:6 Eq. Wt) of alkyd to peracetic acid. The effect of reaction time on the epoxy group content was measured during the epoxidation process. The prepared alkyd resins were analyzed by IR and H1NMR. The metal coated film properties of epoxidized alkyd resins were compared with those of unmodified alkyd resins. It was observed that the coating films of epoxidized alkyd resins have better in drying properties, hardness, adhesion, impact and flexibility than those of un epoxidized alkyd resins. The flammability properties of the paper coated films for the prepared brominated epoxidized alkyd resins were found to be fire retardant

  18. Sorption of americium(III) and europium(III) from nitric acid solutions by a novel diglycolamide-grafted silica-based resins. Pt. 2. Sorption isotherms, column and radiolytic stability studies

    Two novel diglycolamide-grafted silica-based resins (DGSRs) were used for the sorption of trivalent actinides and lanthanides from 3 M nitric acid solutions. The sorption of Am(III) onto the resin containing one diglycolamide (DGA) moiety (DGSR-I) was less efficient than the resin containing two DGA moieties (DGSR-II) with Lagergren first order rate constants of (1.20 ± 0.03) x 10-3s-1 and (2.01 ± 0.05) x 10-3s-1, respectively. The maximum sorption of Eu(III) (used as a representative of the trivalent lanthanide/actinide ions in radioactive wastes) was 10.4 ± 1.1 mg g-1 and 13.9 ± 1.3 mg g-1 by the DGSR-I and DGSR-II, respectively. The sorption of Eu(III) on the grafted silica resins followed the Langmuir monolayer sorption phenomenon with sorption energies of 16.5 ± 2.05 and 17.8 ± 1.6 kJ mol-1 for DGSR-I and DGSR-II, respectively. Column experiments revealed that the breakthrough capacity of Eu(III) on the DGSR-II column was higher than that on the DGSR-I column. Efficient elution could be achieved with a 0.01 M EDTA solution. The radiolytic stability of the resins was ascertained by exposing the resins to a gamma ray dose up to 1030 kGy resulting in a decrease of the Kd values with about 50%; at doses d values remained unaffected.

  19. Sorption of americium(III) and europium(III) from nitric acid solutions by a novel diglycolamide-grafted silica-based resins. Pt. 2. Sorption isotherms, column and radiolytic stability studies

    Ansari, Seraj A.; Mohapatra, Prasanta K. [Bahabha Atomic Research Centre, Trombay, Mumbai (India). Radiochemistry Div.; Iqbal, Mudassir; Huskens, Jurriaan; Verboom, Willem [Twente Univ. (Netherlands). Lab. of Molecular Nanofabrication

    2014-07-01

    Two novel diglycolamide-grafted silica-based resins (DGSRs) were used for the sorption of trivalent actinides and lanthanides from 3 M nitric acid solutions. The sorption of Am(III) onto the resin containing one diglycolamide (DGA) moiety (DGSR-I) was less efficient than the resin containing two DGA moieties (DGSR-II) with Lagergren first order rate constants of (1.20 ± 0.03) x 10{sup -3}s{sup -1} and (2.01 ± 0.05) x 10{sup -3}s{sup -1}, respectively. The maximum sorption of Eu(III) (used as a representative of the trivalent lanthanide/actinide ions in radioactive wastes) was 10.4 ± 1.1 mg g{sup -1} and 13.9 ± 1.3 mg g{sup -1} by the DGSR-I and DGSR-II, respectively. The sorption of Eu(III) on the grafted silica resins followed the Langmuir monolayer sorption phenomenon with sorption energies of 16.5 ± 2.05 and 17.8 ± 1.6 kJ mol{sup -1} for DGSR-I and DGSR-II, respectively. Column experiments revealed that the breakthrough capacity of Eu(III) on the DGSR-II column was higher than that on the DGSR-I column. Efficient elution could be achieved with a 0.01 M EDTA solution. The radiolytic stability of the resins was ascertained by exposing the resins to a gamma ray dose up to 1030 kGy resulting in a decrease of the K{sub d} values with about 50%; at doses <500 kGy the K{sub d} values remained unaffected.

  20. Adsorption and Desorption Properties of Phytic Acid from Rice Bran on Anion Exchange Resin%阴离子交换树脂对米糠植酸的吸附解吸性能

    王琳; 罗建平; 查学强; 张海林; 潘利华

    2011-01-01

    通过静态和动态试验研究了6种阴离子交换树脂对植酸的吸附与解吸性能.结果表明,D201树脂对植酸的吸附交换作用较好,且在pH值为2.2时吸附能力最强,静态吸附量达到94.54 mg/g,1.5 mol/L的NaOH溶液利于植酸解吸;Freundlich吸附等温方程可以较好地描述D201树脂对植酸的等温吸附,表明吸附在常温下进行即可;D201树脂对植酸的吸附过程符合Lagergren一级速率方程,表观吸附速率常数k与植酸起始植酸浓度呈负相关关系,与温度呈正相关关系.在D201树脂对植酸的动态吸附与解吸过程中,层析柱管径、上样液浓度、上样液流速和洗脱剂流速对吸附与解吸效果影响较大.%The absorption and desorption properties of phytic acid on anion exchange resin were investigated through static and dynamic experiments. The results showed that D201 resin had the best exchange adsorption performance among all tested resins. The static absorption capacity of D201 resin reached 94. 54 mg/g when the pH value of phytic acid solution was adjusted to 2. 2, and sodium hydroxide solution of 1. 5 mol/L was beneficial to desorption. The absorption behavior of D201 resin for phytic acid obeyed the Freundlich adsorption isotherm equation, indicating that the absorption can be performed under normal temperature. The absorption kinetic data complied with Lagergren pseudo-first-order rate equation. The apparent adsorption rate k has a negative correlation with the initial concentration of phytic acid and has a positive correlation with temperature. As far as the dynamic absorption and desorption of phytic acid on D201 resin was concerned, the effects of chromatography column diameter, sample concentration, sample flowing velocity and eluant flowing velocity were notably observed.

  1. Interacting Blends of Novel Unsaturated Polyester Amide Resin with Styrene

    Hasmukh S. Patel; Panchal, Kumar K.

    2004-01-01

    Novel unsaturated poly (ester-amide) resins (UPEAs) were prepared by the reaction between an epoxy resin, namely diglycidyl ether of bisphenol–A (DGEBA) and unsaturated aliphatic bisamic acids using a base catalyst. These UPEAs were then blended with a vinyl monomer namely, Styrene (STY.) to produce a homogeneous resin syrup. The curing of these UPEAs-STY. resin blends was carried out by using benzoyl peroxide (BPO) as a catalyst and was monitored by using a differential scanning calorimeter ...

  2. Synthesis of highly carboxylate acrylic resins for leather impregnation

    Ollé Otero, Lluís; Solé, M.M.; Shendrik, Alexander; Labastida, L.; Bacardit Dalmases, Anna

    2012-01-01

    This work describes the synthesis of new leather finishing acrylic resins. Four resins ware synthesized varying the concentration of ethyl acrylate, and metracrylic acid. Sodium lauryl sulphate was used as emulsifying system. By means of an experimental design, an optimal resin for leather impregnation was defined. The results obtained indicated that the variation of the monomer concentration influences the resin properties, the hardness of the film, and the penetration into the leather. Most...

  3. Characterization of radionuclide-chelating agent complexes found in low-level radioactive decontamination waste. Literature review

    The US Nuclear Regulatory Commission is responsible for regulating the safe land disposal of low-level radioactive wastes that may contain organic chelating agents. Such agents include ethylenediaminetetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTPA), picolinic acid, oxalic acid, and citric acid, and can form radionuclide-chelate complexes that may enhance the migration of radionuclides from disposal sites. Data from the available literature indicate that chelates can leach from solidified decontamination wastes in moderate concentration (1--100 ppm) and can potentially complex certain radionuclides in the leachates. In general it appears that both EDTA and DTPA have the potential to mobilize radionuclides from waste disposal sites because such chelates can leach in moderate concentration, form strong radionuclide-chelate complexes, and can be recalcitrant to biodegradation. It also appears that oxalic acid and citric acid will not greatly enhance the mobility of radionuclides from waste disposal sites because these chelates do not appear to leach in high concentration, tend to form relatively weak radionuclide-chelate complexes, and can be readily biodegraded. In the case of picolinic acid, insufficient data are available on adsorption, complexation of key radionuclides (such as the actinides), and biodegradation to make definitive predictions, although the available data indicate that picolinic acid can chelate certain radionuclides in the leachates

  4. Characterization of radionuclide-chelating agent complexes found in low-level radioactive decontamination waste. Literature review

    Serne, R.J.; Felmy, A.R.; Cantrell, K.J.; Krupka, K.M.; Campbell, J.A.; Bolton, H. Jr.; Fredrickson, J.K. [Pacific Northwest National Lab., Richland, WA (United States)

    1996-03-01

    The US Nuclear Regulatory Commission is responsible for regulating the safe land disposal of low-level radioactive wastes that may contain organic chelating agents. Such agents include ethylenediaminetetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTPA), picolinic acid, oxalic acid, and citric acid, and can form radionuclide-chelate complexes that may enhance the migration of radionuclides from disposal sites. Data from the available literature indicate that chelates can leach from solidified decontamination wastes in moderate concentration (1--100 ppm) and can potentially complex certain radionuclides in the leachates. In general it appears that both EDTA and DTPA have the potential to mobilize radionuclides from waste disposal sites because such chelates can leach in moderate concentration, form strong radionuclide-chelate complexes, and can be recalcitrant to biodegradation. It also appears that oxalic acid and citric acid will not greatly enhance the mobility of radionuclides from waste disposal sites because these chelates do not appear to leach in high concentration, tend to form relatively weak radionuclide-chelate complexes, and can be readily biodegraded. In the case of picolinic acid, insufficient data are available on adsorption, complexation of key radionuclides (such as the actinides), and biodegradation to make definitive predictions, although the available data indicate that picolinic acid can chelate certain radionuclides in the leachates.

  5. White light emission from Mn2+ doped ZnS nanocrystals through the surface chelating of 8-hydroxyquinoline-5-sulfonic acid

    White light emitting semiconductor nanocrystals (NCs) have been successfully synthesized from 8-hydroxyquinoline-5-sulfonic acid (HQS) decorated manganese doped ZnS NCs through fine tuning the surface-coordination emission and dopant emission of the NC host. The HQS functionalized manganese doped ZnS NCs (QS-ZnS:Mn), with a cubic crystal structure, have the same diameter of about 4.0 nm as ZnS:Mn NCs without HQS. The intensity of the surface-coordination emission peak increased with increasing HQS content or augmenting excited wavelength. The emission of white light was achieved by carefully controlling the dosage of HQS in NCs and appropriately tuning the excited wavelength. The color coordinates (0.35, 0.34) for the efficient white light emitting NCs were very close to the ideal Commission Internationale de l'Eclairage (CIE) chromaticity coordinates for pure white light (0.33, 0.33). The photoluminescence (PL) decay study revealed that the white light emitting NCs exhibited maximum lifetime values at different emission peaks for different NC samples. The study results also indicated that the HQS molecules were attached to the surface of ZnS:Mn NCs in a single coordination fashion due to the steric hindrance effect of the special spherical surface of NCs, which made the QS-ZnS:Mn NCs possess stable and high fluorescent properties in different organic solvents as compared with the conventional small molecule complexes.

  6. 微波皂化法制备紫胶桐酸%Microwave-assisted Saponification for the Preparation of Aleuritic Acid from Lac Resin

    刘世平; 张弘; 周梅村; 郑华; 李凯

    2011-01-01

    In order to prepare aleuritic acid, lac resin was saponified under microwave assistance, followed by salting out and crystallization. The effects of three major process conditions including microwave power, NaOH concentration and microwave treatment time on aleuritic acid yield were explored by one-factor-at-a-time experiments. Further, the three conditions were optimized by response surface methodology. The optimal saponification conditions were microwave treatment power of 200 W, NaOH concentration of 25.8% and microwave treatment time of 31 rain. Under the optimal saponification conditions, the highest yield of aleuritic acid was achieved to be 21.90%. The aleudtic acid obtained was characterized by infrared spectroscopy, X-ray diffraction, differential scanning calorimetry and scanning electron microscope (SEM) as even crystals with high purity. In summary, microwave-assisted saponification can provide a simple, time-saving and high-yield method for the preparation of aleuritic acid.%采用常压微波法对天然紫胶树脂皂化,后经盐析、结晶等一系列操作,制备紫胶桐酸。单因素试验考察微波功率、碱液质量分数及微波时间3个主要因素对紫胶桐酸得率的影响,并以紫胶桐酸得率为响应值,采用响应曲面法对皂化工艺进行优化试验。结果表明,在微波功率200W、碱液质量分数25.8%、微波时间31min条件下,紫胶桐酸得率最大,达到2I.90%。由红外光谱、X射线衍射、差示扫描量热、扫描电镜等表征可知,微波皂化法制备的紫胶桐酸结晶均匀、杂质较少。微波皂化法制备紫胶桐酸简单易行,能有效缩短制备时间,且得率较高。

  7. Immobilization of spent resin with epoxy resin

    immobilization of spent resin using epoxy resin has been conducted. The spent resin was mixtured with epoxy resin in variation of concentration, i.e., 30, 40, 50, 60, 70 weight percent of spent resin. The mixture were pour into the plastic tube, with a diameter of 40 mm and height of 40 mm. The density, compressive strength and leaching rate were respectively measured by quanta chrome, paul weber apparatus and gamma spectrometer. The results showed that the increasing of waste concentration would be decreased the compressive strength, and increased density by immobilized waste. The leaching rate of 137Cs from waste product was not detected in experiment (author)

  8. Preparation of omeprazole enteric-coated pellets with homemade polyacrylic acid resin II%采用国产聚丙烯酸树脂Ⅱ制备奥美拉唑肠溶微丸的研究

    刘羽; 刘燕; 孙备; 王贺

    2009-01-01

    目的 考察采用国产的聚丙烯酸树脂Ⅱ作为肠溶包衣材料制备奥美拉唑肠溶丸的可行性.方法 分别的采用国产聚丙烯酸树脂Ⅱ与Eudragit L30D作为肠溶包衣材料制备奥美拉唑肠溶丸.并对包衣质量加以比较.结果 未碱化聚丙烯酸树脂Ⅱ 60%与95%的乙醇溶液均可包出合格的奥美拉唑小丸,质量与用L30D所制小丸相近.结论 采用国产聚丙烯酸树脂Ⅱ可以用于制备奥美拉唑肠溶微丸.%Aim To study the feasibility of using polyacrylic acid resin II as the omeprazole enteric-coated pellets′coating material.Methods The omeprazole enteric-coated pellets were prepared by using polyacrylic acid resin II.They were compared with the same pellets prepared by using Eudragit L30D.Results Unbasified polyacrylic acid resin II 60% and 95% of the ethanol solution can be used to produce qualified Omeprazole pellets.There were no significant differences.Conclusion The domestic polyacrylic acid resin II can be used as the omeprazole enteric-coated pellets′coating material.

  9. A novel star-shaped poly(carboxylic acid) for resin-modified glass-ionomer restoratives.

    Weng, Y; Howard, L; Xie, D

    2014-07-01

    We have developed a novel glass-ionomer cement (GIC) system composed of photo-curable star-shaped poly(acrylic acid-co-itaconic acid)s. These polyacids were synthesized via a chain-transfer radical polymerization using a newly synthesized multi-arm chain-transfer agent. The star-shaped polyacids showed significantly lower viscosities in water as compared to the linear polyacids. Due to the lower viscosities, the molecular weight (MW) of the polyacids can be significantly increased for enhancing the mechanical strengths while keeping the ease of mixing and handling. The effects of MW, GM-tethering ratio, P/L ratio, and aging on the compressive properties of the experimental cements were significant. The light-cured experimental cements showed significantly improved mechanical strengths i.e. 49% in yield strength, 41% in modulus, 25% in CS, 20% in DTS, and 36% in FS, higher than commercial Fuji II LC. After aging in water for 1 month, the compressive strength of the novel light-cured experimental cement reached 343 MPa, which was 34% and 42% higher than Fuji II and Fuji II LC, respectively. This one-month aged experimental cement was also 23% higher than itself after one day aging, indicating that aging in water can significantly enhance salt-bridge formation for this novel star-shaped polyacid-comprised GIC. PMID:24865692

  10. Examining the fixation kinetics of chelated and non-chelated copper micronutrient and the applications to micronutrient management in semi-arid alkaline soils

    Udeigwe, T. K.; Eichmann, M. B.; Menkiti, M. C.

    2015-10-01

    The relationship between the deficiency of a nutrient in plants and its total concentration in the soil is complex. This study examined and compared the fixation and fixation kinetics of copper (Cu) in chelated (Ethylene diamine tetraacetic acid, EDTA) and non-chelated mixed systems of micronutrients in the semi-arid soils of the Southern High Plains, US using findings from Cu extraction studies and kinetic models. Approximately, 22 % more Cu was fixed in the non-chelated system within the first 14 days with only 7 % difference between the two systems by day 90. Findings suggest a decrease in the effectiveness of chelated micronutrient over time, highlighting the significance of timing even when chelated micronutrients are applied. The strengths of the relationship of change in available Cu with respect to other micronutrients [iron (Fe), manganese (Mn), and zinc (Zn)] were higher in the non-chelated system (R2: 0.68-0.94), compared to the chelated (R2: 0.42-0.81) with slopes of 0.40 (Cu-Fe), 0.31 (Cu-Mn), and 1.04 (Cu-Zn) in the non-chelated system and 0.26 (Cu-Fe), 0.22 (Cu-Mn), and 0.90 (Cu-Zn) in the chelated. Reduction in the amount of available Cu was best described by the power function model (R2 = 0.91, SE = 0.081) in the non-chelated system and second order model (R2 = 0.95, SE = 0.010) in the chelated system. The applications generated from this study could be used as tools for improved micronutrient management and also provide baseline data for future work in other semi-arid/arid alkaline soils of the world. Findings are also more applicable to field settings, an improvement over related previous studies.

  11. Sequestering agent for uranyl chelation: new bi-naphtyl ligands

    The synthesis of phosphonate, sulfocatecholamide (CAMS) and hydroxy-pyridinone (HOPO) bi-naphtyl ligands is presented. Their binding abilities for uranyl cation were determined by UV spectrophotometry in aqueous media versus pH. These titrations showed that the efficiency of these chelating agents depends on the nature of the chelating group. Each ligand shows a more or less pronounced affinity towards uranium. While the bis-phosphonate compound did not show any affinity towards the uranyl ion, the BINHOPO derivative exhibits significant affinity at acidic and neutral pH while the BINCAMS is more efficient at basic pH. (authors)

  12. Regularities in aluminium and indium chemisorption on chelating polymeric sorbents

    Complexation properties of synthesized polymer chelate sorbents: substituted of polystyrene-azo-pyrocatechol are investigated and correlations between pK'OH of functional groups of sorbents as well as pH50 values of chelation and constants of stability (lgKstab) are established for studying regularities of effect of structure and acid-base properties of functional groups of sorbents on the parameters of Al3+ and In3+ chemical sorption. Established correlations make it possible to predict the physicochemical parameters of sorbents and sorption of metal ions with the aim of separation and concentration of aluminium and indium micro account from the objects of different origin

  13. Removing and recovering of uranium from the acid mine waters by using ion exchange resin; Remocao e recuperacao de uranio de aguas acidas de mina por resina de troca ionica

    Nascimento, Marcos Roberto Lopes do

    1998-07-01

    Ion exchange using resins is one of the few processes capable of reducing ionic contaminants in effluents to very low levels. In this study the process was used to remove and recovery uranium from acid mine waters at Pocos de Caldas-MG Uranium Mining and Milling Plant. The local mineralogical features, allied to the biogeochemical phenomena, owing to presence of pyrite in the rock piles, moreover another factors, resulting acid drainage with several pollutants, including uranium ranging from 6 to 14 mg/l, as sulfate complex, that can be removed by anionic exchanger. The iron interference is eliminated by lime pretreatment of water, increasing pH from 2.6 to 3.3-3.8 to precipitate this cation, without changing the uranium amount. Eight anionic resins were tested, based on the uranium loading, in sorption studies. Retention time, and pH influence was verified for the exchanger chose. With breakthrough of 1 mg U/L and 10 mg U/l in the feed solution, the uranium decontamination level was 94%. Typical values of loading resin were 20-30 g U/l and 70-90 g SO{sub 4}/l. Uranium elution was done with Na Cl solution. Retention time, saline, and acid concentration were the parameters studied. The concentrate, obtained from the eluate by ammonia precipitation, presented uranium (86,8% as U{sub 3} O{sub 8}) and impurities within commercial specifications. (author)

  14. Selective Adsorption and Separation of Salicylic Acid and Phenol by 717 Anion Exchange Resin%717阴离子交换树脂选择吸附分离水杨酸和苯酚

    谢祖芳; 童张法; 陈渊; 晏全; 李凤; 吴燕平

    2011-01-01

    The anion exchange resin 717 was used to selectively adsorb and separate the salicylic acid and phenol from their binary aqueous solution. The adsorption behavior of 717 resin for each adsorbate was studied via both dynamic and static methods. The effects of pH value, adsorbate concentration and adsorption time on the adsorption process were investigated, and the isotherm adsorption and adsorption kinetics were also studied.The experimental results show that the pH value of the solution plays the most important role in the adsorption and separation process. At pH of 4.5, the existence of phenol in the solution essentially does not affect the salicylic acid adsorption of the 717 resin, while when the pH is 11, the phenol can be adsorbed by 717 resin to substitute the adsorbed salicylic acid on it, which substantially decreases the salicylic acid adsorption capacity of the resin. In the pH range of 4~8, the 717 resin has very high selective adsorption ability and adsorption capacity for the salicylic acid, and its adsorption capacity for salicylic acid is more than an order of magnitude larger than that for the phenol. With such high adsorption selectivity, the 717 resin is favorable to be used for the separation salicylic acid from the binary aqueous solution of salicylic acid and phenol. The static adsorptions show that the adsorptions of salicylic acid and phenol by 717 resin are in accordance with Freundlieh isotherm model, and the adsorption kinetics data fit well with the Lagergren pseudo-first order rate equation. Dynamic adsorption of the mixed binary aqueous solution of salicylic acid and phenol by 717 resin shows that, in a column with resin of 1.5 g, the first 475 mL of the exit water after adsorption contains essentially only the phenol because almost all the salicylic acid are adsorbed by the resin. It was found that the salicylic acid adsorbed on the resin can be easily eluted by the 5%NaCl+2%NaOH solution at room temperature.%用717阴离子交

  15. Processing large-diameter poly(L-lactic acid) microfiber mesh/mesenchymal stromal cell constructs via resin embedding: an efficient histologic method

    In this study, we performed a complete histologic analysis of constructs based on large diameter ( > 100 μm) poly-L-lactic acid (PLLA) microfibers obtained via dry-wet spinning and rat Mesenchymal Stromal Cells (rMSCs) differentiated towards the osteogenic lineage, using acrylic resin embedding. In many synthetic polymer-based microfiber meshes, ex post processability of fiber/cell constructs for histologic analysis may face deterring difficulties, leading to an incomplete investigation of the potential of these scaffolds. Indeed, while polymeric nanofiber (fiber diameter = tens of nanometers)/cell constructs can usually be embedded in common histologic media and easily sectioned, preserving the material structure and the antigenic reactivity, histologic analysis of large polymeric microfiber/cell constructs in the literature is really scant. This affects microfiber scaffolds based on FDA-approved and widely used polymers such as PLLA and its copolymers. Indeed, for such constructs, especially those with fiber diameter and fiber interspace much larger than cell size, standard histologic processing is usually inefficient due to inhomogeneous hardness and lack of cohesion between the synthetic and the biological phases under sectioning. In this study, the microfiber/MSC constructs were embedded in acrylic resin and the staining/reaction procedures were calibrated to demonstrate the possibility of successfully employing histologic methods in tissue engineering studies even in such difficult cases. We histologically investigated the main osteogenic markers and extracellular matrix molecules, such as alkaline phosphatase, osteopontin, osteocalcin, TGF-β1, Runx2, Collagen type I and the presence of amorphous, fibrillar and mineralized matrix. Biochemical tests were employed to confirm our findings. This protocol permitted efficient sectioning of the treated constructs and good penetration of the histologic reagents, thus allowing distribution and expression of

  16. RAPID DETERMINA TION OF L—GLUTAMIC ACID WITH AN ENZYME REACTOR OFL—GLUTAMIC DECARBOXYLASE IMMOBILIZED ON ION EXCHANGE RESIN

    WUGuoqi; LINGDaren; 等

    2001-01-01

    The preparation and characterization of an immobilized L-glutamic decarboxylase(GDC) were studied.This work is to develop a sensitive method for the determination of L-glutamate using a new biosensor,which consists of an enzyme column reactor of GDC immobilized on a novel ion exchange resin(carboxymethyl-copolymer of allyl dextran and N.N'-methylene-bisacrylamide CM-CADB) and ion analyzer coupled with a CO2 electrode.The conditions for the enzyme immobilization were optimized by the parameters:buffer composition and concentration,adsorption equilibration time,amount of enzyme,temperature,ionic strength and pH.The properties of the immobilized enzyme on CM-CADB were studied by investigating the initial ate of the enzyme reaction,the effect of various parameters on the immobilized GDC activity and its stability.An immobilized GDC enzyme column reactor matched with a flow injection system-ion analyzer coupled with CO2 electrode-data collection system made up the original form of the apparatus of biosensor for determining of L-glutamate acid.The limit of detection is 1.0×10-5M.The linearity response is in the range of 5×10-2-5×10-5M.The equation of linear regression of the calibration curve is y=43.3x+181.6(y is the milli-volt of electrical potential response,x is the logarithm of the concentration of the substrate of L-glutamate acid).The correlation coefficient equals 0.99.The coefficient of varioation equals 2.7%.

  17. Chelating regularities in the series of chelating polymer sorbents and their complexes with vanadium, manganese, and chromium

    Physicochemical properties of new synthesized polymer chelation sorbents - substituted polystyrene-azo-salicylic acid are investigated. Correlations between pKCOOH of functional groups of sorbents with chelation pH50 and vanadium, manganese and chromium lgstab are established with the aim of studying interactions in the ion of element - sorbent system. Established correlations suggest physicochemical properties of the sorbents and sorption parameters of cations of metals with the aim of concentration and separation of V(5), Mn(2) and Cr(3) microamounts from natural and technical objects including environmental ones

  18. K Basin Sludge Conditioning Process Testing Project. Results from Test 4, ''Acid Digestion of Mixed-Bed Ion Exchange Resin''

    Approximately 73 m3 of heterogeneous solid material, ''sludge,'' (upper bound estimate, Packer 1997) have accumulated at the bottom of the K Basins in the 100 K Area of the Hanford Site. This sludge is a mixture of spent fuel element corrosion products, ion exchange materials (organic and inorganic), graphite-based gasket materials, iron and aluminum metal corrosion products, sand, and debris (Makenas et al. 1996, 1997). In addition, small amounts of polychlorinated biphenyls (PCBs) have been found. Ultimately, it is planned to transfer the K Basins sludge to the Hanford double shell tanks (DSTs). The Hanford Spent Nuclear Fuel (HSNF) project has conducted a number of evaluations to examine technology and processing alternatives to pretreat K Basin sludge to meet storage and disposal requirements. From these evaluations, chemical pretreatment has been selected to address criticality issues, reactivity, and the destruction or removal of PCBs before the K Basin sludge can be transferred to the DSTs. Chemical pretreatment, referred to as the K Basin sludge conditioning process, includes nitric acid dissolution of the sludge (with removal of acid insoluble solids), neutrons absorber addition, neutralization, and reprecipitation. Laboratory testing is being conducted by the Pacific Northwest National Laboratory (PNNL) to provide data necessary to develop the sludge conditioning process

  19. Overview of current chelation practices

    Y. Aydinok

    2011-12-01

    Full Text Available Deferoxamine (DFO is reference standard therapy for transfusional iron overload since the 1980s. Although it is a highly effective iron chelator, the compliance problem to subcutaneous administration of DFO remains as the major problem. The oral chelator Deferiprone (DFP has no marketing licence in North America, however, it has been licensed in India since 1994 and the European Union (EU granted marketing approval for DFP in 1999, specifically for patients with thalassemia major when DFO is inadequate, intolerable or unacceptable. There are still limited data available on the use of DFP in children between 6 and 10 years of age, and no data on DFP use in children under 6 years of age. Subsequently the oral chelator Deferasirox (DFX was approved by FDA and EMA for the treatment of patients with transfusional iron overload -older than 2 years of age- as first line therapy, in 2005 and 2006 respectively. The primary objective of iron chelation is to maintain body iron at safe levels at all times but once iron is accumulated, the objective of iron chelation is to reduce tissue iron to safe levels which is a slow process. The chelation regimen, dose and frequency of administration, of the chelator(s are mainly determined based on body iron burden, presence of myocardial iron and the transfusional iron loading rate. A proper monitoring of chelation is of importance for measuring the response rate to a particular regimen and providing dose adjustments to enhance chelation efficacy and to avoid toxicity. Efficacy of a chelation regimen may exhibit individual variability resulting from factors such as absorbtion and metabolism of the chelator. Tolerability and compliance are also individual variables effecting the response to chelation. Understanding of advantages and limitations of chelators, accurately determining chelation needs of patients with iron overload and designing individualized chelation regimens with less toxicity but optimum efficacy

  20. BENCH-SCALE RECOVERY OF LEAD USING AN ELECTROMEMBRANE/CHELATION PROCESS

    This report presents the results of a bench-scale treatability test to investigate key process parameters influencing an innovative chelation electrodeposition process for recovery of lead from contaminated sons. thylenediamine tetraacetic acid (EDTA) and diethylenetriamine penta...

  1. BENCH-SCALE RECOVERY OF LEAD USING AND ELECTRO- MEMBRANE/CHELATION PROCESS

    This report presents the results of a bench-scale treatability test to investigate key process parameters influencing an innovative chelation electrodeposition process for recovery of lead from contaminated sons. thylenediamine tetraacetic acid (EDTA) and diethylenetriamine penta...

  2. Kinetics Studies on Esterification Reaction of Acetic acid with Iso-amyl Alcohol over Ion Exchange Resin as Catalysts

    Bhaskar D. Kulkarni

    2014-01-01

    Full Text Available The low molecular weight organic esters have pleasing smell and are found in applications in the food industry for synthetic essence and perfume. Esterification reactions are ubiquitous reactions especially in pharmaceutical, perfumery and polymer industries, wherein; both heterogeneous and homogeneous catalysts have been extensively used. Iso-amyl acetate (or Iso-pentyl acetate is often called as banana oil, since it has the recognizable odor of this fruit. Iso-amyl acetate is synthesized by esterification of acetic acid with iso-amyl alcohol. (Eq.1. Since the equilibrium does not help the formation of the ester, it must be shifted to the right, in favor of the product, by using a surplus of one of the starting materials. Iso-amyl acetate is a kind of flavor reagent with fruit taste. The use of H2SO4 often originates the problems such as corrosion for equipments and pollution for environment.

  3. Development of a amidoxime resin for gallium recovering from Bayer liqueur; Desenvolvimento de resinas amidoximicas para recuperacao de galio do licor de Bayer

    Coutinho, Fernanda M.B.; Magalhaes, Denise M. [Universidade Federal, Rio de Janeiro, RJ (Brazil). Inst. de Macromoleculas]. E-mail: fern@ima.ufrj.br; Avritscher, Waldemar [Sao Paulo Univ., SP (Brazil). Escola Politecnica. Dept. de Engenharia de Minas; Costa, Thais S. [Parana Univ., Curitiba, PR (Brazil). Dept. de Engenharia Mecanica

    2000-07-01

    Chelating resins have been prepared from acrylonitrile-divinylbenzene copolymer beads produced by suspension polymerization in in presence of an inert diluent. The copolymer beads were reacted with hydroxylamine to produce amidoxime groups in the repeating units derived from cyano groups (acrylonitrile), varied reaction conditions were employed. In this study, a set of experiments have been performed to determine the potential of the amidoxime chelating resin for the adsorption of gallium from Bayer liqueur. (author)

  4. Decomposing method for ion exchange resin

    The present invention concerns a method of decomposing ion exchange resins generated in a nuclear power plant to carbon dioxide reliably in a short period of time. (1) The ion exchange resins are mixed with water, and then they are kept for a predetermined period of time in the presence of an inert gas at high temperature and high pressure exceeding the critical point of water to decompose the ion exchange resins. (2) The ion exchange resins is mixed with water, an oxidant is added and they are kept for a predetermined time in the presence of an inert gas at a high temperature and a high pressure exceeding a critical point of water of an inert gas at a high temperature to decompose the ion exchange resins. (3) An alkali or acid is added to ion exchange resins and water to control the hydrogen ion concentration in the solution and the ion exchange resins are decomposed in above-mentioned (1) or (2). Sodium hydroxide is used as the alkali and hydrochloric acid is used as the acid. In addition, oxygen, hydrogen peroxide or ozone is used as an oxidant. (I.S.)

  5. Samarium-153 and lutetium-177 chelation properties of selected macrocyclic and acyclic ligands

    We describe a simple in vitro characterization of chelation that is useful when choosing an appropriate ligand-metal combination for clinical applications. These properties include the effect of concentration on chelation efficiency, time to maximum chelation, and stability in acidic and serum environments. The macrocyclic ligands nitro-DOTA and nitro-PADOTA, the acyclic ligands nitro-CHX-A-DTPA, nitro-MX-DTPA, DTPA, and a novel terpyridine ligand, TMT-amine, were evaluated as chelate complexes of both intermediate energy β-emitting lanthanides lutetium-177 and samarium-153. The data were compared to results obtained in a previously published study with yttrium-90. Acid lability, time to achieve maximum chelation, and stability in human serum are properties unique to each ligand-metal combination and should be evaluated prior to choosing an appropriate combination for therapeutic applications. Concentration dependence and duration of chelation are general properties of lanthanide and yttrium chelation that can be applied to an appropriate ligand-metal combination to achieve optimum chelation efficiencies

  6. Effectiveness of chelation therapy with time after acute uranium intoxication

    The effect of increasing the time interval between acute uranium exposure and chelation therapy was studied in male Swiss mice. Gallic acid, 4,5-dihydroxy-1,3- benzenedisulfonic acid (Tiron), diethylenetriaminepentaacetic acid (DTPA), and 5-aminosalicylic acid (5-AS) were administered ip at 0, 0.25, 1, 4, and 24 hr after sc injection of 10 mg/kg of uranyl acetate dihydrate. Chelating agents were given at doses equal to one-fourth of their respective LD50 values. Daily elimination of uranium into urine and feces was determined for 4 days after which time the mice were killed, and the concentration of uranium was measured in kidney, spleen, and bone. The excretion of uranium was especially rapid in the first 24 hr. Treatment with Tiron or gallic acid at 0, 0.25, or 1 hr after uranium exposure significantly increased the total excretion of the metal. In kidney and bone, only administration of Tiron at 0, 0.25, or 1 hr after uranium injection, or gallic acid at 1 hr after uranium exposure significantly reduced tissue uranium concentrations. Treatment at later times (4 to 24 hr) did not increase the total excretion of the metal and did not decrease the tissue uranium concentrations 4 days after uranyl acetate administration. The results show that the length of time before initiating chelation therapy for acute uranium intoxication greatly influences the effectiveness of this therapy

  7. Targeted Catalytic Inactivation of Angiotensin Converting Enzyme by Lisinopril-Coupled Transition Metal Chelates

    Joyner, Jeff C.; Hocharoen, Lalintip; Cowan, J. A.

    2012-01-01

    A series of compounds that target reactive transition metal chelates to somatic Angiotensin Converting Enzyme (sACE-1) have been synthesized. Half maximal inhibitory concentrations (IC50) and rate constants for both inactivation and cleavage of full length sACE-1 have been determined and evaluated in terms of metal-chelate size, charge, reduction potential, coordination unsaturation, and coreactant selectivity. Ethylenediamine-tetraacetic acid (EDTA), nitrilotriacetic acid (NTA), 1,4,7,10-tet...

  8. Iron chelation and multiple sclerosis

    Kelsey J. Weigel

    2014-01-01

    Full Text Available Histochemical and MRI studies have demonstrated that MS (multiple sclerosis patients have abnormal deposition of iron in both gray and white matter structures. Data is emerging indicating that this iron could partake in pathogenesis by various mechanisms, e.g., promoting the production of reactive oxygen species and enhancing the production of proinflammatory cytokines. Iron chelation therapy could be a viable strategy to block iron-related pathological events or it can confer cellular protection by stabilizing hypoxia inducible factor 1α, a transcription factor that normally responds to hypoxic conditions. Iron chelation has been shown to protect against disease progression and/or limit iron accumulation in some neurological disorders or their experimental models. Data from studies that administered a chelator to animals with experimental autoimmune encephalomyelitis, a model of MS, support the rationale for examining this treatment approach in MS. Preliminary clinical studies have been performed in MS patients using deferoxamine. Although some side effects were observed, the large majority of patients were able to tolerate the arduous administration regimen, i.e., 6–8 h of subcutaneous infusion, and all side effects resolved upon discontinuation of treatment. Importantly, these preliminary studies did not identify a disqualifying event for this experimental approach. More recently developed chelators, deferasirox and deferiprone, are more desirable for possible use in MS given their oral administration, and importantly, deferiprone can cross the blood–brain barrier. However, experiences from other conditions indicate that the potential for adverse events during chelation therapy necessitates close patient monitoring and a carefully considered administration regimen.

  9. Resistant behavior of a novel silica-based octyl(phenyl)- N, N-diisobutyl carbamoylmethylphoshine oxide neutral extraction resin against nitric acid, temperature and γ-radiation

    Zhang, Anyun; Wei, Yuezhou; Kumagai, Mikio; Koma, Yoshikazu; Koyama, Tomozo

    2005-03-01

    The resistant behavior of a novel silica-based octyl(phenyl)- N, N-diisobutylcarbamoyl-methylphoshine oxide (CMPO) extraction resin (CMPO/SiO 2-P) against HNO 3, temperature and γ-radiation had been investigated. The adsorption properties of the treated CMPO/SiO 2-P resin were evaluated by a 3 M HNO 3 solution containing 0.01 M Nd(III). It was found that 3 M or 0.01 M HNO 3 concentration did not decrease the stability of CMPO/SiO 2-P at 25°C. The HNO 3 concentration effect on the leakage of CMPO/SiO 2-P resin at 80°C was obviously higher than that of at 25°C. The adsorbed amount of Nd(III) onto the treated CMPO/SiO 2-P resin was determined in the range of 0.1769-0.1839 mmol/g, which basically approached to 0.1875 mmol/g, the adsorbed quantity of fresh CMPO/SiO 2-P resin for Nd(III). The contents of P and C leaked from CMPO/SiO 2-P resin obviously increased with an increase in the radiation dose ( ID) from 1.0 to 4.1 MGy in terms of the linear equations: [P]=110.05 ID+21.92 and [C]=7683.8 ID-919.8. The adsorbed amount of Nd(III) onto the radiated CMPO/SiO 2-P resin quickly decreased from 0.1499 to 0.0900 mmol/g according to the equation QNd(III)=-0.0222 ID+0.1778, showing a large quantity of CMPO leaked from CMPO/SiO 2-P resin.

  10. Resistant behavior of a novel silica-based octyl(phenyl)-N,N-diisobutyl carbamoylmethylphoshine oxide neutral extraction resin against nitric acid, temperature and γ-radiation

    The resistant behavior of a novel silica-based octyl(phenyl)-N,N-diisobutylcarbamoyl-methylphoshine oxide (CMPO) extraction resin (CMPO/SiO2-P) against HNO3, temperature and γ-radiation had been investigated. The adsorption properties of the treated CMPO/SiO2-P resin were evaluated by a 3 M HNO3 solution containing 0.01 M Nd(III). It was found that 3 M or 0.01 M HNO3 concentration did not decrease the stability of CMPO/SiO2-P at 25 deg. C. The HNO3 concentration effect on the leakage of CMPO/SiO2-P resin at 80 deg. C was obviously higher than that of at 25 deg. C. The adsorbed amount of Nd(III) onto the treated CMPO/SiO2-P resin was determined in the range of 0.1769-0.1839 mmol/g, which basically approached to 0.1875 mmol/g, the adsorbed quantity of fresh CMPO/SiO2-P resin for Nd(III). The contents of P and C leaked from CMPO/SiO2-P resin obviously increased with an increase in the radiation dose (ID) from 1.0 to 4.1 MGy in terms of the linear equations: [P]=110.05ID+21.92 and [C]=7683.8ID-919.8. The adsorbed amount of Nd(III) onto the radiated CMPO/SiO2-P resin quickly decreased from 0.1499 to 0.0900 mmol/g according to the equation QNd(III)=-0.0222ID+0.1778, showing a large quantity of CMPO leaked from CMPO/SiO2-P resin

  11. Preparation, Spectroscopic Investigation and Biological Activity of New Mixed Ligand Chelates

    Preparation and investigation of new Co(II), Ni(II), Zn(II) and Cr(III) chelates with mixed ligands including Schiff base (L1) formed from the condensation of 4-dimethylaminobenzaldehyde with 2-aminophenol and anthranilic acid (L2) were studied. The obtained Schiff base and mixed ligand chelates were subjected to several physiochemical techniques, in terms of CHN elemental analyses, molar conductivity, magnetic moment measurements, infrared, proton nuclear magnetic resonance, electronic and mass spectra. The analytical data showed the formation of the Schiff base compound and the ratio of metal to ligands of the chelates are 1:1:1(M:L1:L2). The infrared spectral data exhibited that the used ligands behaving as bidentate ligands towards the metal ions. The proton nuclear magnetic resonance spectral data showed the signals of the active groups in the ligands which entered in chelation with Zn(II) metal ion. The electronic spectral results showed the existence of pie (phenyl ring) and n = pie (C=N) of the ligands and suggested the geometrical structures of the chelates. Meanwhile, the mass spectral data revealed the fragmentations of the Schiff base, anthranilic acid and their Ni(II) mixed ligand chelate has been preformed the only chelate conducted for justification. All the prepared mixed chelates were non-electrolyte in nature. The antibacterial activity of the Schiff base, anthranilic acid, metal salts and mixed ligand chelates were studied and found to be that mixed ligand chelates have the most biological activity in comparison to the free ligands and salts. (author)

  12. Compositional analysis of metal chelating materials using near-field photothermal Fourier transform infrared microspectroscopy.

    Moffat, Jonathan G; Mayes, Andrew G; Belton, Peter S; Craig, Duncan Q M; Reading, Mike

    2010-01-01

    Photothermal-Fourier transform-infrared (PT-FT-IR) microspectroscopy employs a thermal probe mounted in a scanning probe microscope (SPM). By placement of the tip of the probe on the surface of a solid sample, it can obtain localized IR spectra of a wide range of samples. A second mode of analysis is also available; a sample can be taken from the selected location using a technique called thermally assisted nanosampling (TAN), then a spectrum can be obtained of the nanosample while the probe is remote from the surface. We report a novel method of local compositional analysis that combines both of these types of measurement; a reagent is attached to the tip using TAN, then the reagent is placed in contact with analyte. IR spectroscopy can then be used to analyze any interaction between the reagent and surface it is placed in contact with. All of these modes of analysis were illustrated using a metal chelating agent. In the surface mode, changes to a solid bead of a chelating resin were measured using standard PT-FT-IR. In the nanosampling mode of analysis, a particle of a chelating polymer was attached to the tip of the probe using TAN and this was placed in contact with a concentrated calcium solution. Strong spectral changes were observed that mirrored those found when exposing the surface bound chelating resin bead to a solution of the same ion. A semiquantitative simulation of the PT spectrum for a chelating resin bead was achieved using a thermal diffusion model derived from photoacoustic spectroscopy indicating that semiquantitative or quantitative measurements will be possible in such a system. PMID:19957959

  13. EPICOR-II resin degradation results from first resin samples of PF-8 and PF-20

    The 28 March 1979 accident at Three Mile Island Unit 2 released approximately 560,000 gallons of contaminated water to the Auxiliary and Fuel Handling Buildings. The water was decontaminated using a demineralization system called EPICOR-II developed by Epicor, Inc. The Low-Level Waste Data Base Development - EPICOR-II Resin/Liner Investigation Project is studying the chemical and physical conditions of the synthetic ion exchange resins found in several EPICOR-II prefilters. This report summarizes results and analyses of the first sampling of ion exchange resins from EPICOR-II prefilters PE-8 and -20. Results are compared with baseline data from tests performed on unirradiated Epicor, Inc. resins to determine if degradation has occurred due to the high internal radiation dose received by the EPICOR-II resins. Results also are compared with recent findings on resin degradation by Battelle Columbus Laboratories and Brookhaven National Laboratory. Analyses comparing test results of resins from EPICOR-II prefilters PF-8 and -20 with unirradiated resins obtained from Epicor, Inc. show resin degradation has occurred in some of the EPICOR-II resins examined. The mechanism of degradation is compared with work of other researchers and is consistent with their findings. The strong acid cation resins (divinylbenzene, styrene base structure) are losing effective cross-linking along with scission of functional groups and are experiencing first an increase and eventually a decrease in total exchange capacity as the absorbed radiation dose increases. The phenolic cation resins (phenol-formaldehyde base structure) show a loss of effective cross-linking and oxidation of the polymer chain. Analyses of resins removed from EPICOR-II prefilters PF-8 and -20 over the next several years should show a further increase in degradation

  14. Binary and ternary chelates of scandium (III), Yttrium (III) and lanthanum (III) with ethyleneglycol-bis(β-aminoethylether)-tetraacetic acid as primary and substituted salicylic acids as secondary ligands

    Formation constants of binary and ternary complexes of the systems of the type: M-L and M-egta-L (M = scandium(III), yttrium(III) and lanthanum(III), egta = ethylene glycol-bis(β-aminoethylether)-tetra acetic acid, L = o-cresotic acid (o-ca), m-cresotic acid (m-ca), 5-chlorosalicyclic acid(csa), and 3,5-dibromosalicylic acid (dbsa)) have been determined pH-metrically at 25deg and μ = 0.1M (KNO3) in 50% (v/v) aqueous-ethanol medium. The order of stabilities of ternary complexes has been compared with those of corresponding binary complexes, and results discussed on the basis of coulombic interactions. (auth.)

  15. Irradiation effects on the storage and disposal of radwaste containing organic ion-exchange media. [3 functional forms of resin - sulfonic acid cation exchanger, quarternary ammonium anion exchanger and mixed bed combination of the two

    Swyler, K.J.; Dodge, C.J.; Dayal, R.

    1983-10-01

    Polystyrene-divinylbenzene (PS-DVB) based ion exchangers are commonly used in water demineralization or decontamination operations at nuclear facilities. Self-irradiation from sorbed radionuclides may affect the properties of radwaste containing these ion-exchange media. The effects of external irradiation on anion, cation, and mixed bed PS-DVB ion exchangers have been investigated under conditions relevant to radwaste storage and disposal. Three effects are emphasized in the present report: (1) release of acids, radionuclides or chemically aggressive species through radiolytic attack on the functional group, (2) radiolytic generation/uptake of corrosive or combustible gases, (3) effect of irradiation on solidification of resins in cement. Special consideration was placed on external variables such as radiation dose rate, resin chemical loading and moisture conditions, accessibility to atmospheric oxygen, and interactions in multicomponent systems. Such variables may affect the correspondence between laboratory results and field performance. 40 references, 24 figures, 28 tables.

  16. Review: Resin Composite Filling

    Desmond Ng

    2010-02-01

    Full Text Available The leading cause of oral pain and tooth loss is from caries and their treatment include restoration using amalgam, resin, porcelain and gold, endodontic therapy and extraction. Resin composite restorations have grown popular over the last half a century because it can take shades more similar to enamel. Here, we discuss the history and use of resin, comparison between amalgam and resin, clinical procedures involved and finishing and polishing techniques for resin restoration. Although resin composite has aesthetic advantages over amalgam, one of the major disadvantage include polymerization shrinkage and future research is needed on reaction kinetics and viscoelastic behaviour to minimize shrinkage stress.

  17. Extraction of Heavy Metals from Sludge Using Biodegradable Chelating Agent N,N-bis(carboxymethyl) Glutamic Acid Tetrasodium%生物可降解螯合剂谷氨酸 N,N -二乙酸四钠对污泥中重金属萃取效率的研究

    吴青; 崔延瑞; 汤晓晓; 杨慧娟; 孙剑辉

    2015-01-01

    N, N-bis ( carboxymethyl) glutamic acid tetrasodium ( GLDA), a novel biodegradable and green chelating agent, has excellent metal chelating ability. Batch experiment was conducted to study the extraction process of Cd, Ni, Cu and Zn in industrial sludge using GLDA. The effects of contact time, pH of the system, content of chelating agent were investigated, and the forms of heavy metals in sludge pre- and post-extraction using the modified BCR sequential extraction procedure were studied. The results showed that GLDA was effective for cadmium extraction in sludge. Several heavy metals could be effectively extracted under the condition of pH 4 and molar ratio of chelating agent to total heavy metal 3: 1. Residual fraction took the largest fraction in Zn, which caused the low extraction efficiency of this metal. Chelating properties were related not only to contact time, pH, chelating agent’s concentration, and stability constant but also to species distribution of metals.%谷氨酸 N,N -二乙酸四钠(GLDA)具有较强金属螯合能力,是新一代生物可降解绿色螯合剂。通过分批提取实验对GLDA 去除工业污泥中 Cd、 Ni、 Cu、 Zn 的萃取过程进行研究,考察了萃取时间、萃取体系 pH 值、螯合剂用量等因素对重金属萃取效果的影响,并采用修正的 BCR 连续提取法分析萃取前后污泥中重金属的形态。结果表明, GLDA 对污泥中 Cd 具有良好的去除效果;体系在 pH =4,螯合剂与重金属总量摩尔比为3:1的条件下,多种重金属取得最佳萃取效果; Zn 主要以残渣态存在,导致该金属萃取率低;螯合能力不仅与萃取时间,萃取体系 pH 值,螯合剂用量,螯合常数等因素有关,而且还与金属的形态分布有关。

  18. Improved paramagnetic chelate for molecular imaging with MRI

    Winter, Patrick; Athey, Phillip; Kiefer, Garry; Gulyas, Gyongyi; Frank, Keith; Fuhrhop, Ralph; Robertson, David; Wickline, Samuel; Lanza, Gregory

    2005-05-01

    The relaxivity and transmetallation of two lipophilic paramagnetic chelates incorporated onto perfluorocarbon nanoparticles, i.e., gadolinium-methoxy-tetraazacyclododecane-tetraacetic acid phosphatidylethanolamine (Gd-MeO-DOTA-PE) and gadolinium-methoxy-tetraazacyclododecane-tetraacetic acid triglycine phosphatidylethanolamine (Gd-MeO-DOTA-triglycine-PE (Gd-MeO-DOTA-triglycine-PE)), were compared to a prototypic gadolinium-diethylene-triamine-pentaacetic acid bis-oleate (Gd-DTPA-BOA) paramagnetic formulation. Nanoparticles with MeO-DOTA-based chelates demonstrated higher relaxivity (40% higher for Gd-MeO-DOTA-PE and 55% higher for Gd-MeO-DOTA-triglycine-PE) and less transmetallation than the original Gd-DTPA-BOA-based agent.

  19. Improved paramagnetic chelate for molecular imaging with MRI

    The relaxivity and transmetallation of two lipophilic paramagnetic chelates incorporated onto perfluorocarbon nanoparticles, i.e., gadolinium-methoxy-tetraazacyclododecane-tetraacetic acid phosphatidylethanolamine (Gd-MeO-DOTA-PE) and gadolinium-methoxy-tetraazacyclododecane-tetraacetic acid triglycine phosphatidylethanolamine (Gd-MeO-DOTA-triglycine-PE (Gd-MeO-DOTA-triglycine-PE)), were compared to a prototypic gadolinium-diethylene-triamine-pentaacetic acid bis-oleate (Gd-DTPA-BOA) paramagnetic formulation. Nanoparticles with MeO-DOTA-based chelates demonstrated higher relaxivity (40% higher for Gd-MeO-DOTA-PE and 55% higher for Gd-MeO-DOTA-triglycine-PE) and less transmetallation than the original Gd-DTPA-BOA-based agent

  20. 以弱碱性树脂去除废水中5-氨基-2-氯苯-4-磺酸和盐酸%Removal of 5-Amino-2-chlorotoluene-4-sulfonic and Chlorhydric Acids from Wastewater by Weakly Basic Resin

    李长海; 许振良; 李春平

    2006-01-01

    This research deals with an investigation of the adsorption of two acids, namely, 5-amino-2-chlorotoluene-4-sulfonic and chlorhydric acids from their solution onto weakly basic resin. The screening of resins, kinetics, and isotherm were studied. The results indicate that the D301R is more appropriate for the removal of acids from solution. The adsorption of acids obeys Langmuir isotherm and the first-order kinetics model. Sorptive affinity of the two acids on D301R was found to be in the order of 5-amino-2-chlorotoluene-4-sulfonic acid>chlorhydric acid. Thermodynamic parameters for the adsorption of acids were calculated and discussed. The maximum removal of acids was observed around 97% and 76% at 25℃ for 5-amino-2-chlorotoluene-4-sulfonic acid and chlorhydric acid, respectively.

  1. 复合二元酸改性环氧树脂的制备工艺研究%Study on Preparation Technology of Dibasic Acid Modified Epoxy Resin

    马群锋; 朱蓓蓓; 周生启

    2014-01-01

    用C36二聚酸、癸二酸与1,4-丁二醇二缩水甘油醚和双酚A型环氧树脂进行扩链反应,制备柔韧性环氧树脂预聚体。考察了配方组成、反应温度和催化剂等因素对羧基转化率的影响。结果表明,对于所给配方,当催化剂用量为0.1%,140℃下反应2 h,反应基本完全。另外,以柔韧性环氧树脂预聚体为基体树脂制备的固化物拉伸强度达到12.0 MPa,断裂伸长率为85%。%We process extender chain reaction with C36 dimer acid, sebacic acid, 1,4-butanediol diglycidyl and bisphenol A type epoxy resin, and produce flexible epoxy resin prepolymers. We investigate the influence of carboxyl conversion rate from formula composition, reaction temperature and catalyst and other factors. The results show that, for given formula, when the dosage of catalyst is 0.1%,it reacts 2h under 140 ℃, and the re-action is substantially complete. In addition, the flexibility of a cured epoxy resin prepolymer matrix resin composition prepared by a tensile strength of 12.0 MPa, elongation at break of 85%.

  2. Development of new metal chelates for animal nutrition and of analytical methods for their quantitative determination and quality control

    Beltrami, Diego

    2009-01-01

    The growing interest for mineral integration to increase mineral bioavalability brought researchers to re-examine accurately the impact that complexes and chelates can have for food industry. In fact, the so-called organic or chelate mineral forms, in particular those associated with amino acids, peptides or other organic molecules, afforded encouraging results in different in vivo tests on animals of economic interest fed with fodder containing minerals in the form of chelates. Moreover, it ...

  3. The Influence of the Chelating Agent Nitrilotriacetic Acid on Promotion of Hydrodesulfurization Activity by Co in CoMo Catalysts Prepared on Al2O3, C, and ZrO2 Supports

    Kaluža, L. (Luděk); Zdražil, M. (Miroslav); Gulková, D. (Daniela); Vít, Z. (Zdeněk)

    2013-01-01

    The chelating agent NTA systematically increased the promotion effect of Co in the sulfided catalysts in comparison to samples prepared without NTA from ammonium heptamolybdate and cobalt nitrate. The promotion effect was increased by the factor 1.13-1.58.

  4. Heavy metal displacement in chelate-irrigated soil during phytoremediation

    Madrid, F.; Liphadzi, M. S.; Kirkham, M. B.

    2003-03-01

    Heavy metals in wastewater sewage sludge (biosolids), applied to land, contaminate soils. Phytoremediation, the use of plants to clean up toxic heavy metals, might remove them. Chelating agents are added to soil to solubilize the metals for enhanced phytoextraction. Yet no studies follow the displacement and leaching of heavy metals in soil with and without roots following solubilization with chelates. The objective of this work was to determine the mobility of heavy metals in biosolids applied to the surface of soil columns (76 cm long; 17 cm diam.) with or without plants (barley; Hordeum vulgare L.). Three weeks after barley was planted, all columns were irrigated with the disodium salt of the chelating agent, EDTA (ethylenediamine tetraacetic acid) (0.5 g/kg soil). Drainage water, soil, and plants were analyzed for heavy metals (Cd, Cu, Fe, Mn, Ni, Pb, Zn). Total concentrations of the heavy metals in all columns at the end of the experiment generally were lower in the top 30 cm of soil with EDTA than without EDTA. The chelate increased concentrations of heavy metals in shoots. With or without plants, the EDTA mobilized Cd, Fe, Mn, Ni, Pb, and Zn, which leached to drainage water. Drainage water from columns without EDTA had concentrations of these heavy metals below detection limits. Only Cu did not leach in the presence of EDTA. Even though roots retarded the movement of Cd, Fe, Mn, Ni, Pb, and Zn through the EDTA-treated soil from 1 d (Cd) to 5 d (Fe), the drainage water from columns with EDTA had concentrations of Cd, Fe, Mn, and Pb that exceeded drinking water standards by 1.3, 500, 620, and 8.6 times, respectively. Because the chelate rendered Cd, Fe, Mn, Ni, Pb, and Zn mobile, it is suggested that the theory for leaching of soluble salts, put forward by Nielsen and associates in 1965, could be applied to control movement of the heavy metals for maximum uptake during chelate-assisted phytoremediation.

  5. Luminescent lanthanide chelates and methods of use

    Selvin, Paul R. (Berkeley, CA); Hearst, John (Berkeley, CA)

    1997-01-01

    The invention provides lanthanide chelates capable of intense luminescence. The celates comprise a lanthanide chelator covalently joined to a coumarin-like or quinolone-like sensitizer. Exemplary sensitzers include 2- or 4-quinolones, 2- or 4-coumarins, or derivatives thereof e.g. carbostyril 124 (7-amino-4-methyl-2-quinolone), coumarin 120 (7-amino-4-methyl-2-coumarin), coumarin 124 (7-amino-4-(trifluoromethyl)-2-coumarin), aminomethyltrimethylpsoralen, etc. The chelates form high affinity complexes with lanthanides, such as terbium or europium, through chelator groups, such as DTPA. The chelates may be coupled to a wide variety of compounds to create specific labels, probes, diagnostic and/or therapeutic reagents, etc. The chelates find particular use in resonance energy transfer between chelate-lanthanide complexes and another luminescent agent, often a fluorescent non-metal based resonance energy acceptor. The methods provide useful information about the structure, conformation, relative location and/or interactions of macromolecules.

  6. f-Element Ion Chelation in Highly Basic Media

    A large body of data has been collected over the last fifty years on the chemical behavior of f-element ions. The ions undergo rapid hydrolysis reactions in neutral or basic aqueous solutions that produce poorly understood oxide-hydroxide species; therefore, most of the fundamental f-element solution chemistry has allowed synthetic and separations chemists to rationally design advanced organic chelating ligands useful for highly selective partitioning and separation of f-element ions from complex acidic solution matrices. These ligands and new examples under development allow for the safe use and treatment of solutions containing highly radioactive species. This DOE/EMSP project was undertaken to address the following fundamental objectives: (1) study the chemical speciation of Sr and lanthanide (Ln) ions in basic aqueous media containing classical counter anions found in waste matrices; (2) prepare pyridine N-oxide phosphonates and phosphonic acids that might act as selective chelators for Ln ions in model basic pH waste streams; (3) study the binding of the new chelators toward Ln ions and (4) examine the utility of the chelators as decontamination and dissolution agents under basic solution conditions. The project has been successful in attacking selected aspects of the very difficult problems associated with basic pH solution f-element waste chemistry. In particular, the project has (1) shed additional light on the initial stages of Ln ion sol-gel-precipitate formulation under basic solution conditions; (2) generated new families of pyridine phosphonic acid chelators; (3) characterized the function of the chelators and (4) examined their utility as oxide-hydroxide dissolution agents. These findings have contributed significantly to an improved understanding of the behavior of Ln ions in basic media containing anions found in typical waste sludges as well as to the development of sludge dissolution agents. The new chelating reagents are easily made and could be

  7. Iron chelation and multiple sclerosis

    Kelsey J. Weigel; Sharon G. Lynch; Steven M. LeVine

    2014-01-01

    Histochemical and MRI studies have demonstrated that MS (multiple sclerosis) patients have abnormal deposition of iron in both gray and white matter structures. Data is emerging indicating that this iron could partake in pathogenesis by various mechanisms, e.g., promoting the production of reactive oxygen species and enhancing the production of proinflammatory cytokines. Iron chelation therapy could be a viable strategy to block iron-related pathological events or it can confer cellular prote...

  8. Some Linguistic Detail on Chelation

    Haworth, Daniel T.

    1998-01-01

    The term chelate was first applied by Morgan and Drew in 1920 to describe the heterocyclic rings formed from bidentate ligands bonding to a central atom. The history of the word ch_l_ is traced from its original Greek meaning through the Latin language to its anglicized form, chela. This word has a very rich history and has been cited by both Greek (Aristotle) and Latin (Cicero, Vergil) philosophers and poets.

  9. Chemical Stablilisation of Sand : Part VIII Furan Resins as Dune and Coastal Sand Stabiliser

    Ram Gopal; Jeevan Singh; Ghanshyam Das

    1990-01-01

    Studies on furan resin as dune sand stabiliser are presented. Influence of acid catalysts, viz. phenol disulphonic acid, sulphuric acid, hydrochloric acid and phosphoric acid and other catalysts, viz. trichlorotoluene and benzoyl chloride along with promoters, zinc chloride and ferric chloride, on the strength of stabilised furan resin-sand specimens has been discussed. Optimisation studies on resin content, catalysts and promoters and curing conditions have revealed that maximum stren...

  10. Chelator induced phytoextraction and in situ soil washing of Cu

    In a soil column experiment, we investigated the effect of 5 mmol kg-1 soil addition of citric acid, ethylenediamine tetraacetate (EDTA), diethylenetriamine-pentaacetate (DTPA) and [S,S]-stereoisomer of ethylenediamine-disuccinate (EDDS) on phytoextraction of Cu from a vineyard soil with 162.6 mg kg-1 Cu, into the test plant Brassica rapa var. pekinensis. We also examined the use of a horizontal permeable barrier, composed of layers of nutrient enriched sawdust and apatite, for reduction of chelator induced Cu leaching. The addition of all chelators, except citric acid, enhanced Cu mobility and caused leaching of 19.5-23% of initial total Cu from the soil column. However, Cu plant uptake did not increase accordingly; the most effective was the EDDS treatment, in which plant Cu concentration reached 37.8±1.3 mg kg-1 Cu and increased by 3.3-times over the control treatment. The addition of none of the chelators in the concentration range from 5 to 15 mmol kg-1 exerted any toxic effect on respiratory soil microorganisms. When EDDS was applied into the columns with horizontal permeable barriers, only 0.53±0.32% of the initial total Cu was leached. Cu (36.7%) was washed from the 18 cm soil layer above the barrier and accumulated in the barrier. Our results indicate that rather than for a reduction of Cu leaching during rather ineffective chelate induced Cu phytoextraction, horizontal permeable barriers could be more effective in a new remediation technique of controlled in situ soil washing of Cu with biodegradable chelates

  11. Chelator induced phytoextraction and in situ soil washing of Cu

    Kos, Bostjan; Lestan, Domen

    2004-11-01

    In a soil column experiment, we investigated the effect of 5 mmol kg{sup -1} soil addition of citric acid, ethylenediamine tetraacetate (EDTA), diethylenetriamine-pentaacetate (DTPA) and [S,S]-stereoisomer of ethylenediamine-disuccinate (EDDS) on phytoextraction of Cu from a vineyard soil with 162.6 mg kg{sup -1} Cu, into the test plant Brassica rapa var. pekinensis. We also examined the use of a horizontal permeable barrier, composed of layers of nutrient enriched sawdust and apatite, for reduction of chelator induced Cu leaching. The addition of all chelators, except citric acid, enhanced Cu mobility and caused leaching of 19.5-23% of initial total Cu from the soil column. However, Cu plant uptake did not increase accordingly; the most effective was the EDDS treatment, in which plant Cu concentration reached 37.8{+-}1.3 mg kg{sup -1} Cu and increased by 3.3-times over the control treatment. The addition of none of the chelators in the concentration range from 5 to 15 mmol kg{sup -1} exerted any toxic effect on respiratory soil microorganisms. When EDDS was applied into the columns with horizontal permeable barriers, only 0.53{+-}0.32% of the initial total Cu was leached. Cu (36.7%) was washed from the 18 cm soil layer above the barrier and accumulated in the barrier. Our results indicate that rather than for a reduction of Cu leaching during rather ineffective chelate induced Cu phytoextraction, horizontal permeable barriers could be more effective in a new remediation technique of controlled in situ soil washing of Cu with biodegradable chelates.

  12. Boron sorption characteristics in resins

    The purpose of boron addition in a nuclear power plant is to control the reactivity. In PHWRs, it is injected into the moderator system in the form of boric anhydride solution, while in PHWRs, it is added to the primary heat transport system in the form of boric acid solution. The required boron levels in PHWRs are controlled by valving in strong base anion exchangers having exchangeable species in OD- form while in PHWRs, the same can be achieved by restoring to the use of Boron Thermal Regeneration System (BTRS). This system operates on the principle of existence of different amounts of various polyborate ions at different temperatures, solution pH's and the boric acid concentrations and on the reversible sorption of these polyions on strong base anion exchange resins. This report describes the salient features of boron sorption characteristics on four types of anion exchange resins, based on experimental data generated in the chemical laboratories of Reactor Engineering Division of the Bhabha Atomic Research Centre, Bombay. The report further makes an attempt to calculate the pH of the resin and solution phases and the percentages of different polyborates and undissociated boric acid, under the experimental conditions investigated. (author). 30 refs., 4 figs., 20 tables

  13. Commercial Ion Exchange Resin Vitrification in Borosilicate Glass

    Bench-scale studies were performed to determine the feasibility of vitrification treatment of six resins representative of those used in the commercial nuclear industry. Each resin was successfully immobilized using the same proprietary borosilicate glass formulation. Waste loadings varied from 38 to 70 g of resin/100 g of glass produced depending on the particular resin, with volume reductions of 28 percent to 68 percent. The bench-scale results were used to perform a melter demonstration with one of the resins at the Clemson Environmental Technologies Laboratory (CETL). The resin used was a weakly acidic meth acrylic cation exchange resin. The vitrification process utilized represented a approximately 64 percent volume reduction. Glass characterization, radionuclide retention, offgas analyses, and system compatibility results will be discussed in this paper

  14. Synergistic Activities of an Efflux Pump Inhibitor and Iron Chelators against Pseudomonas aeruginosa Growth and Biofilm Formation

    Liu, Yang; Yang, Liang; Molin, Søren

    2010-01-01

    The efflux pump inhibitor phenyl-arginine-beta-naphthylamide (PA beta N) was paired with iron chelators 2,2'-dipyridyl, acetohydroxamic acid, and EDTA to assess synergistic activities against Pseudomonas aeruginosa growth and biofilm formation. All of the tested iron chelators synergistically...

  15. Resin Longevity Studies

    Radioactive resin waste has been generated at the Savannah River Site as a result of water treatment at F- and H-Areas. Key factors in the risk assessment of disposing of these materials in trenches include resin retention of 129I, a long-lived isotope, and the degradation rate of the organic resin itself. In order to estimate the degradation of resin wastes during underground burial, simulated aging studies were carried out with Dowex 21K, CG-8, and GT-73 ion exchange resins. These resins have a polystyrene-base but bear different functional groups. The specific resins considered in this study include anion (Dowex 21K), cation (CG8), and neutral (GT73) resins with, respectively, quaternary ammonium, sulfonate, and thiol functionalities. The objective of this study is to carry out laboratory experiments to simulate aging of organic resin wastes in order to (1) determine the functional life span of CG8, GT73 and Dowex 21K resins under field (trench) conditions, and (2) determine the expected performance of these resins as they degrade

  16. Studies on the chelation of aluminium for biological application

    Potentiometric determinations of the strength of chelation of aluminium(III) by citrate and 3-carboxy-1,5-pentanedioic acid have been made at 37,0 plus minus 0,1 degree Celsius and I = 150 mmol dm-3 NaCl. From these results, the citrate complex is inferred to be tridentate with coordination through the two terminal carboxyl groups and the central hydroxyl group. This structure is confirmed by 13C nuclear magnetic resonance

  17. Post-irradiation hardness of resin-modified glass ionomer cements and a polyacid-modified composite resin

    This study examined the post-irradiation hardness of resin-modified glass ionomer cements and a polyacid-modified composite resin using a digital microhardness tester. Change in hardness of these materials over a period of 6 months was compared to that of conventional glass ionomer cements and a composite resin. With the exception of the composite resin, all materials showed a significant increase in hardness over 24 h after their initial set. Dual-cure resin-modified glass ionomer cements showed decreased hardness with increased storage time in saline at 37oC. Results suggest that the addition of resins to glass ionomer cements does not improve initial hardness and does not negate the acid-base reaction of conventional cements. Resin addition may, however, lead to increased water sorption and decreased hardness. (author)

  18. Effect of chelating agents on the distribution of monoclonal antibodies in mice

    The potential for altering the biodistribution of radiolabel from gallium- and indium-labeled mouse monoclonal antibodies was investigated in mice using metal chelating agents. The chelating agents used were desferrioxamine (DFO), diethylenetriaminepentaacetic acid (DTPA), ethylenediamine-di (O-hydroxyphenylacetic acid) (EDHPA), and 2,2' dipyridyl (DIPY). The mouse monoclonal antibody LICR-LON-M8 was labeled with 111In after conjugation to DTPA, and with 67Ga after conjugation to DFO. All the chelating agents except DIPY altered the biodistribution of [67Ga]citrate and [111In]citrate but did not affect the 48-hr tissue uptake of label from [111In]DTPA-M8 or [67Ga]DFO-M8, confirming the in vivo stability of the antibody conjugates. Label fixed in the tissues was inaccessible to the chelating agents, indicating that they will not be suitable for reducing the high background liver radioactivity in patients undergoing scanning with indium-labeled antibodies

  19. Effects of alumina air-abrasion and acidic priming agents on bonding between SUS XM27 steel and auto-polymerizing acrylic resin.

    Ishikawa, Yumi; Ohashi, Norihisa; Koizumi, Hiroyasu; Tanoue, Naomi; Nishiyama, Norihiro; Matsumura, Hideo

    2007-09-01

    The purpose of this study was to evaluate the effects of functional monomers contained in the primers, as well as alumina particle abrasion on bonding between stainless steel and acrylic resin. SUS XM27 steel was primed with one of the following materials; Alloy Primer, Estenia Opaque Primer, M. L. Primer, and Super-Bond Liquid. Steel disks were either ground flat or alumina-blasted, primed with one of the four agents, and bonded with an acrylic resin (Unifast Trad). Bond strength was determined both before and after thermocycling (2,000 or 20,000 cycles). Among the four priming agents, the Alloy Primer and Estenia Opaque Primer, both of which contain 10-methacryloyloxydecyl dihydrogen phosphate (MDP), exhibited better bonding performance than the others. Alumina air-borne particle abrasion considerably improved the durability of bonding between the steel and the resin material. It can be concluded that alumina blasting followed by priming with an MDP agent is recommended for bonding the resin and SUS XM27 steel. PMID:17928724

  20. Status of chelation research: a review

    The current status of research on the removal of actinide elements from the body is reviewed. Items occurring prior to 1980 include evidence for fetal toxicity from Ca-DTPA, the FDA approval of Zn-DTPA for human therapy, the mixed ligand fiasco, and the abrupt wipeout of chelation funding. New concepts that should be explored include improvements in removing radioactivity from lung and bone, the effectiveness of DTPA inside cells, simultaneous therapy with mobilizing agents and chelating agents, prolonging the retention of chelating agents within the body, the oral administration of chelating agents, the effectiveness of LICAM and other new chelating agents, the safety of decorporation procedures, and the effectiveness of chelation therapy on reducing the risk from radionuclide-induced cancer. Some physicians give DTPA by intravenous injection, a safe procedure that should be officially sanctioned

  1. Extraction chromatography of neodymium by an organophosphorous extractant supported on various polymeric resins

    Takigawa, D.Y.

    1993-04-01

    Fifteen resins coated with dihexyl-N,N-diethylcarbamoylmethyl phosphonate (CMP) were studied for their extraction of neodymium (Nd) in 4.0 and 7.0 M nitric acid. Resin properties, such as chemical composition and physical morphology, which can influence Nd extraction as well as subsequent resin regeneration (Nd stripping), were identified. Hydrophilic or polar resins coated with CMP efficiently extracted the Nd. Resins initially washed free of residual monomer and solvent before CMP coating outperformed their untreated counterparts. The macroporous styrene-divinylbenzene hydrophobic resins that were high in surface area were less effective supports compared with hydrophilic microporous Aurorez, polybenzimidazole (PBI) and macroporous Amberlite polyacrylic resins. Only one resin, Duolite C-467, showed no measurable improvement in Nd extraction with CMP coating. CMP-coated Aurorez PBI, a microporous and hydrophilic polymeric resin with an average surface area, showed the best overall efficiency for Nd removal and resin regeneration.

  2. Study on the Epoxy Resin Heat Resistance Modified by Polyamide Acid%聚酰胺酸改性环氧树脂耐热性的研究

    周浩然; 孔德忠; 刘达

    2009-01-01

    The epoxy resin heat resistance was prepared with epoxy modified with PAA, and DDS as curing after the pre-reacting and curing. The effects of the amount of PAA, the amount of curing agent, curing condition, reaction time on the heat resistance of epoxy resin were studied. A better formula and appropriate conditions for curing were chosen. The heat resistance of modified epoxy resin was measured with TG in different proportions, pre-reaction time and different curing conditions. Then, the surface morphology and the fracture morphology of the curing epoxy modified were analyzed with SEM. The result has shown that better curing process conditions of modified epoxy resin are as follows: 120 ℃,1 h→150 ℃,1 h→170 ℃,2 h→200 ℃,2 h→250 ℃,2 h,the proportion is 3h. The decomposition temperature of modified epoxy resin is 411 ℃ after the pre-reacting and curing, which is increased by 80 ℃, compared with the decomposition temperature of non-modified epoxy resin. There is no distinct two-phase structure in EP/PAA/DDS system after the pre-reacting and curing, which indicates that the resin has a good compatibility.%用4, 4′-二氨基二苯基砜(DDS)做固化剂,采用聚酰胺酸(PAA)对环氧树脂(EP)进行改性,研究了PAA用量、固化剂用量和反应时间对环氧树脂耐热性的影响,采用TG测定不同配比、预反应时间及不同固化温度下改性EP的耐热性,利用SEM对最佳配比固化后样品的表面和断面形貌进行了分析.结果表明,改性树脂最佳固化工艺条件为:120 ℃,1 h→150 ℃,1 h→170 ℃,2 h→200 ℃,2 h→250 ℃,2 h;改性树脂配比为mEP∶mPAA∶mDDS=1∶0.75∶0.08;预反应时间3 h,改性EP的热分解温度为411 ℃,比未改姓EP提高了近80 ℃以上;EP/PAA/DDS固化后样品无明显的两相结构,树脂的相容性较好.

  3. In vitro test system for evaluating the effectiveness of chelators

    A procedure has been devised to test in vitro the relative effectiveness of chelating agents for the elimination of radiotoxins from specified, in vivo labeled endogenous ligands. The report describes the elimination of 239Pu from liver homogenates by various chelating agents. The effectivity of a homologous series of polyaminocarboxylic acids (PACA's) was compared to that of certain derivatives containing a straight alkyl group. The effectiveness of these lipophilic PACA's appears to depend on the chain length of the substituent. Lipophilic chelons were more effective in chelating 239Pu than unsubstituted PACA's. Combination of EDTA or DTPA with a number of oligodentate complexing agents were also tested. With EDTA, the removal of Pu was enhanced by p-aminosalicylic acid (PAS), Desferioxamine B (DFOA) and strongly enhanced by 4,5-Dihydroxy-m-benzenedisulfonic acid (Tiron). Only DFOA showed enhanced removal with DTPA. The different behavior of the mixed ligand treatments can be explained by either formation of binary complexes or action on different biological Pu-pools

  4. Iron Chelation Therapy in Myelodysplastic Syndromes

    Giuseppe Saglio; Daniela Cilloni; Emanuela Messa

    2010-01-01

    Myelodysplastic syndromes (MDS) are a heterogeneous disorder of the hematopoietic stem cells, frequently characterized by anemia and transfusion dependency. In low-risk patients, transfusion dependency can be long lasting, leading to iron overload. Iron chelation therapy may be a therapeutic option for these patients, especially since the approval of oral iron chelators, which are easier to use and better accepted by the patients. The usefulness of iron chelation in MDS patients is still unde...

  5. Beliefs about chelation among thalassemia patients

    Trachtenberg Felicia L; Mednick Lauren; Kwiatkowski Janet L; Neufeld Ellis J; Haines Dru; Pakbaz Zahra; Thompson Alexis A; Quinn Charles T; Grady Robert; Sobota Amy; Olivieri Nancy; Horne Robert; Yamashita Robert

    2012-01-01

    Abstract Background Understanding patients’ views about medication is crucial to maximize adherence. Thalassemia is a congenital blood disorder requiring chronic blood transfusions and daily iron chelation therapy. Methods The Beliefs in Medicine Questionnaire (BMQ) was used to assess beliefs in chelation in thalassemia patients from North America and London in the Thalassemia Longitudinal Cohort (TLC) of the Thalassemia Clinical Research Network (TCRN). Chelation adherence was based on patie...

  6. Role of chelates in treatment of cancer

    Tripathi Laxmi

    2007-01-01

    Full Text Available Chelates are used in cancer as cytotoxic agent, as radioactive agent in imaging studies and in radioimmunotherapy. Various chelates based on ruthenium, copper, zinc, organocobalt, gold, platinum, palladium, cobalt, nickel and iron are reported as cytotoxic agent. Monoclonal antibodies labeled with radioactive metals such as yttrium-90, indium-111 and iodine-131 are used in radioimmunotherapy. This review is an attempt to compile the use of chelates as cytotoxic drugs and in radioimmunotherapy.

  7. Diagnostic chelation challenge with DMSA: a biomarker of long-term mercury exposure?

    Frumkin, H; Manning, C C; Williams, P. L.; Sanders, A; Taylor, B.B.; Pierce, M; Elon, L; Hertzberg, V S

    2001-01-01

    Chelation challenge testing has been used to assess the body burden of various metals. The best-known example is EDTA challenge in lead-exposed individuals. This study assessed diagnostic chelation challenge with dimercaptosuccinic acid (DMSA) as a measure of mercury body burden among mercury-exposed workers. Former employees at a chloralkali plant, for whom detailed exposure histories were available (n = 119), and unexposed controls (n = 101) completed 24-hr urine collections before and afte...

  8. Oxidation of Petroleum Resin Based on Dicyclopentadiene Fraction

    Bondaletov, Vladimir Grigoryevich; Bondaletova, Lyudmila Ivanovna; Nguen Van Thanh; Baikova, Nataliya

    2015-01-01

    This work represents the results of obtaining modified petroleum resin based on dicyclopentadiene fraction. The modification is carried out by means of resin oxidation by the Prilezhaev's method. The possibility of epoxidation of dicyclopentadiene double bonds during the process in the residual hydrocarbons is experimentally established. Dependences of acid, bromine and epoxy numbers on oxidation process duration at various "oxidative system: resin PR[DF]" component ratio is found. The modifi...

  9. Optimization of chelators to enhance uranium uptake from tailings for phytoremediation.

    Jagetiya, Bhagawatilal; Sharma, Anubha

    2013-04-01

    A greenhouse experiment was set up to investigate the ability of citric acid (CA), oxalic acid (OA), nitrilotriacetic acid (NTA) and EDTA for phytoremediation of uranium tailings by Indian mustard [Brassica juncea (L.) Czern. et Coss]. Uranium tailings were collected from Umra mining region and mixed with 75% of garden soil which yielded a 25:75 mixture. Prepared pots were divided into four sets and treated with following different concentrations - 0.1, 0.5, 2.5 and 12.5 mmol kg(-1) soil additions for each of the four chelators. Control pots which were not treated with chelators. Experiments were conducted in completely randomized block design with triplicates. The optimum concentrations of these chelators were found on the basis of biomass production, tolerance and accumulation potential. The data collected were expressed statistically. EDTA produced maximum growth depression whereas, minimum occurred in the case of NTA. Maximum U uptake (3.5-fold) in the roots occurred at 2.5 mmol of CA, while NTA proved to be the weakest for the same purpose. Severe toxicity in the form of reduced growth and plant death was recorded at 12.5 mmol of each chelator. Minimum growth inhibition produced by chelators occurred in NTA which was followed by OA, moderate in CA and maximum was traced in EDTA applications. Chelator strengthened U uptake in the present study follows the order: CA>EDTA>OA>NTA. PMID:23267730

  10. Thermal evaluation of resorcinol formaldehyde resin used for treatment of intermediate level liquid radioactive waste

    Resorcinol formaldehyde (RF) resin is used for treatment of intermediate level liquid radioactive waste. The resin is having high specificity for Cs ion. This resin is under use in level treatment cell of Waste Immobilisation Plant at Tarapur. After the saturation of resin column with Cs, it needs regeneration. Regeneration with nitric acid gives the waste which is compatible with the vitrification process. However, there is probability of degradation and nitration of RF resin and the same may have explosive nature. To find out the parameters for safe regeneration, resin samples treated with different molarity of nitric acid were evaluated with differential thermal analyser (DTA) in air as well as in argon atmosphere. The study indicated that the nitration of resin does not start up to 1.17M nitric acid concentration and therefore is safe for elution of Cs from the resin. (author). 3 refs., 1 fig., 1 tab

  11. The use of natural rubber-based material for the preparation of radiation-curable resin. I. The reaction of epoxidised natural rubbers of low molecular weight with acrylic acid

    A synthesis method for the preparation of a new radiation-curable resin based on natural rubber has been established. The method was based on the reaction between epoxidised natural rubbers (ENR) of low molecular weight, i.e. Mn 0f 5,800 to 82,000, with acrylic acid in the presence of a catalyst and an inhibitor. Two grades of ENR namely ENR-25 and ENR-50 corresponding to 25 and 50 mole % epoxidation levels, respectively were used. The acrylation was carried out at temperatures between 95-105 degree C and was monitored by the measurements of the acid value of the reaction mixture as the reaction proceeded. It was confirmed by IR spectroscopic technique that the reaction occurred through the ring opening of the epoxide group of ENR. As a result, the new resin contains radiation-curable acrylate groups as well as hydroxyl groups on its main chain. When formulated with benzophenone, it solidified upon with UV light

  12. High Temperature Transfer Molding Resins

    Connell, John W. (Inventor); Smith, Joseph G., Jr. (Inventor); Hergenrother, Paul M. (Inventor)

    2000-01-01

    High temperature resins containing phenylethynyl groups that are processable by transfer molding have been prepared. These phenylethynyl containing oligomers were prepared from aromatic diamines containing phenylethynyl groups and various ratios of phthalic anhydride and 4-phenylethynlphthalic anhydride in glacial acetic acid to form a mixture of imide compounds in one step. This synthetic approach is advantageous since the products are a mixture of compounds and consequently exhibit a relatively low melting temperature. In addition, these materials exhibit low melt viscosities which are stable for several hours at 210-275 C, and since the thermal reaction of the phenylethynyl group does not occur to any appreciable extent at temperatures below 300 C, these materials have a broad processing window. Upon thermal cure at approximately 300-350 C, the phenylethynyl groups react to provide a crosslinked resin system. These new materials exhibit excellent properties and are potentially useful as adhesives, coatings, films, moldings and composite matrices.

  13. Generation, Fractionation, and Characterization of Iron-Chelating Protein Hydrolysate from Palm Kernel Cake Proteins.

    Zarei, Mohammad; Ghanbari, Rahele; Tajabadi, Naser; Abdul-Hamid, Azizah; Bakar, Fatimah Abu; Saari, Nazamid

    2016-02-01

    Palm kernel cake protein was hydrolyzed with different proteases namely papain, bromelain, subtilisin, flavourzyme, trypsin, chymotrypsin, and pepsin to generate different protein hydrolysates. Peptide content and iron-chelating activity of each hydrolysate were evaluated using O-phthaldialdehyde-based spectrophotometric method and ferrozine-based colorimetric assay, respectively. The results revealed a positive correlation between peptide contents and iron-chelating activities of the protein hydrolysates. Protein hydrolysate generated by papain exhibited the highest peptide content of 10.5 mM and highest iron-chelating activity of 64.8% compared with the other hydrolysates. Profiling of the papain-generated hydrolysate by reverse phase high performance liquid chromatography fractionation indicated a direct association between peptide content and iron-chelating activity in most of the fractions. Further fractionation using isoelectric focusing also revealed that protein hydrolysate with basic and neutral isoelectric point (pI) had the highest iron-chelating activity, although a few fractions in the acidic range also exhibited good metal chelating potential. After identification and synthesis of papain-generated peptides, GGIF and YLLLK showed among the highest iron-chelating activities of 56% and 53%, whereas their IC50 were 1.4 and 0.2 μM, respectively. PMID:26720491

  14. Chelating capture and magnetic removal of non-magnetic heavy metal substances from soil

    Fan, Liren; Song, Jiqing; Bai, Wenbo; Wang, Shengping; Zeng, Ming; Li, Xiaoming; Zhou, Yang; Li, Haifeng; Lu, Haiwei

    2016-02-01

    A soil remediation method based on magnetic beneficiation is reported. A new magnetic solid chelator powder, FS@IDA (core-shell Fe3O4@SiO2 nanoparticles coated with iminodiacetic acid chelators), was used as a reactive magnetic carrier to selectively capture non-magnetic heavy metals in soil by chelation and removal by magnetic separation. FS@IDA was prepared via inorganic-organic and organic synthesis reactions that generated chelating groups on the surface of magnetic, multi-core, core-shell Fe3O4@SiO2 (FS) nanoparticles. These reactions used a silane coupling agent and sodium chloroacetate. The results show that FS@IDA could chelate the heavy metal component of Cd, Zn, Pb, Cu and Ni carbonates, lead sulfate and lead chloride in water-insoluble salt systems. The resulting FS@IDA-Cd and FS@IDA-Pb chelates could be magnetically separated, resulting in removal rates of approximately 84.9% and 72.2% for Cd and Pb, respectively. FS@IDA could not remove the residual heavy metals and those bound to organic matter in the soil. FS@IDA did not significantly alter the chemical composition of the soil, and it allowed for fast chelating capture, simple magnetic separation and facilitated heavy metal elution. FS@IDA could also be easily prepared and reprocessed.

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

    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%.

  16. Biocompatibility of composite resins

    Sayed Mostafa Mousavinasab

    2011-01-01

    Dental materials that are used in dentistry should be harmless to oral tissues, so they should not contain any leachable toxic and diffusible substances that can cause some side effects. Reports about probable biologic hazards, in relation to dental resins, have increased interest to this topic in dentists. The present paper reviews the articles published about biocompatibility of resin-restorative materials specially resin composites and monomers which are mainly based on Bis-GMA and concern...

  17. Effect of alcohols on separation behavior of rare earth elements using benzimidazole-type anion-exchange resin in nitric acid solutions

    Chromatographic separation experiments of trivalent rare earth elements were performed using benzimidazole type anion-exchange resin in nitric/alcohol mixed solvent systems at room temperature. As a result, it was found those trivalent rare earth elements are able to be separated mutually in a 20% HNO3 and 80% MeOH mixed solvent. Based on these results, we systematically examined using various alcohols to make clear the role of alcohols in anion-exchange reactions at various temperatures. (author)

  18. Resin performance monitor

    An ion exchange resin filled in a water cleaning device disposed in a nuclear power plant for maintaining water quality is transferred to a resin leaching vessel, to measure a TOC amount and molecular weight distribution of effluents from the resin. An amount of the effluents adsorbed to each of a pair ion exchange resins is evaluated based on the result, to forecast the extent of degradation of performance of the ion exchange resins due to the adsorption of the effluents. Then more realistic usage of the ion exchange resin is enabled by considering the effects of the effluents from the resin on the pair ion exchange resins, which has not been considered so far. Namely, since the desalting performance can be forecast at an initial stage of the cycle, requirement for the exchange of the resin and regeneration thereof can be judged appropriately, thereby enabling to maintain performance, for example, of a condensate desalting tower satisfactorily, which is also effective for cleaning water in a reactor primary system to high purity. (T.M.)

  19. Conformational study of aromatic ketones: chemical shift reagents: uranium chelates

    A series of benzophenones, 2-benzoyl thiophenes and 2-benzoyl pyridines, all substituted at the benzene ring by an amino acid chain, have been synthesised with the object of examining to what extent the site of the aminoacid chain and the site and nature of the other substituents modify the electronic structure of the molecule and the orientation of each ring with respect to the plane of the carbonyl group. In the second part a study of paramagnetic cations, in particular of uranium, which is able to form stable chelates with beta-diketones was carried out to study their complexing power. The chelates studied are the (hexafluoropentanedionate)4U, the (heptafluorodimethyloctanedionate)4U and the (trifluorophenylbutanedionate)4U

  20. Chelation studies involving decontamination of light lanthanides by polyaminopolycarboxylic

    The present thesis constitutes chelation studies involving decontamination of light lanthanides, cobalt , and uranium with 2,2-bis-acryloyliminomethylene- acid (BAETA) using the spectrophotometric method. the work carried out aimed to clear up the effectiveness of BAETA as a decontaminating agent for radioactive nuclides from human body . the thesis includes a general introduction , outlines the aim of work and contains three main chapters . the results of the work are discussed at the end of the thesis. the first chapter deals with a comprehensive survey of the relevant literature. this includes the metabolism and toxicity of cerium, uranium, cobalt and Ln+3 elements, general methodologies of internal decontamination, choice and effectiveness of chelating agents

  1. MULTIDENTATE TEREPHTHALAMIDATE AND HYDROXYPYRIDONATE LIGANDS: TOWARDS NEW ORALLY ACTIVE CHELATORS

    Abergel, Rebecca J.; Raymond, Kenneth N.

    2011-07-13

    The limitations of current therapies for the treatment of iron overload or radioisotope contamination have stimulated efforts to develop new orally bioavailable iron and actinide chelators. Siderophore-inspired tetradentate, hexadentate and octadentate terephthalamidate and hydroxypyridonate ligands were evaluated in vivo as selective and efficacious iron or actinide chelating agents, with several metal loading and ligand assessment procedures, using {sup 59}Fe, {sup 238}Pu, and {sup 241}Am as radioactive tracers. The compounds presented in this study were compared to commercially available therapeutic sequestering agents [deferoxamine (DFO) for iron and diethylenetriaminepentaacetic acid (DPTA) for actinides] and are unrivaled in terms of affinity, selectivity and decorporation efficacy, which attests to the fact that high metal affinity may overcome the low bioavailability properties commonly associated to multidenticity.

  2. Treatment of some radioactive wastes by using new chelating membranes

    The preparation of chelating membranes containing nitrile and carboxylic acid as functional groups was investigated. The modification of such membranes by chemical treatments to produce significant changes in their properties was studied. This modification results in a higher rate of exchange and higher capacity. The applicability of such modified membranes in the removal of Co-60 and Cs-137 from their wastes were tested. The dependence of these radioactive nuclides uptake on the time and degree of grafting for H CI-, NH2OH-and KOH-treated membranes was investigated. It was found that the adsorption rate and capacity were higher for KOH-treated membrane than those for the NH2OH and H CI treated ones. The prepared grafted membranes have a good affinity towards the adsorption or chelation with Co-60 and Cs-137. This result may make such prepared materials acceptable for practicable use in some radioactive waste treatments and recovery

  3. Multidentate Terephthalamidate And Hydroxypyridonate Ligands: Towards New Orally Active Chelators

    The limitations of current therapies for the treatment of iron overload or radioisotope contamination have stimulated efforts to develop new orally bioavailable iron and actinide chelators. Siderophore-inspired tetradentate, hexadentate and octadentate terephthalamidate and hydroxypyridonate ligands were evaluated in vivo as selective and efficacious iron or actinide chelating agents, with several metal loading and ligand assessment procedures, using 59Fe, 238Pu, and 241Am as radioactive tracers. The compounds presented in this study were compared to commercially available therapeutic sequestering agents (deferoxamine (DFO) for iron and diethylenetriaminepentaacetic acid (DPTA) for actinides) and are unrivaled in terms of affinity, selectivity and decorporation efficacy, which attests to the fact that high metal affinity may overcome the low bioavailability properties commonly associated to multidenticity.

  4. Metal ions, Alzheimer's disease and chelation therapy.

    Budimir, Ana

    2011-03-01

    In the last few years, various studies have been providing evidence that metal ions are critically involved in the pathogenesis of major neurological diseases (Alzheimer, Parkinson). Metal ion chelators have been suggested as potential therapies for diseases involving metal ion imbalance. Neurodegeneration is an excellent target for exploiting the metal chelator approach to therapeutics. In contrast to the direct chelation approach in metal ion overload disorders, in neurodegeneration the goal seems to be a better and subtle modulation of metal ion homeostasis, aimed at restoring ionic balance. Thus, moderate chelators able to coordinate deleterious metals without disturbing metal homeostasis are needed. To date, several chelating agents have been investigated for their potential to treat neurodegeneration, and a series of 8-hydroxyquinoline analogues showed the greatest potential for the treatment of neurodegenerative diseases. PMID:21406339

  5. Modified ion exchange resins - synthesis and properties. Pt. 1

    Doescher, F.; Klein, J.; Pohl, F.; Widdecke, H.

    1982-01-22

    Sulfomethylated resins are prepared by polymer analogous reactions, starting from macroporous poly(styrene-co-divinylbenzene) matrices. Different reaction paths are discussed and used in the synthesis. Sulfomethylation can be achieved by reaction of a chloromethylated resin with dimethyl sulfide and sodium sulfonate or alternatively by oxidation of polymer-bound thiol groups. Both methods give high conversions as shown by IR spectra and titration of the sulfonic acid groups. Poly(1-(4-hydroxysulfomethylphenyl)ethylene) (3) is obtained by reaction of poly(1-(4-hydroxyphenyl)ethylene) (2) resin with formaldehyde/sodium sulfonate. The thermal stability, catalytic activity, and ion exchange equilibria of the sulfomethylated resin are investigated.

  6. Importance of iron chelation therapy

    A. Varoğlu

    2011-01-01

    It is necessary to remember that today patients have different options of chelation treatment, as desferrioxamine, deferiprone and deferasirox are available. However, a patient has to be compliant with treatments. They have always to remember that too much iron causes different complications and could be a barrier for a definitive cure from thalassemia. 由于出现了去铁胺、去铁酮和去铁斯若等药物,病人现在可以选择不同的螯合治疗方式。 然而,病人必须适应这几种治疗方式。 他们必须时刻记住太多的铁元素会引发多种并发症,并对地中海贫血的彻底治疗造成阻碍。...

  7. High-performance liquid chromatography method for ferric iron chelators using a post-column reaction with Calcein Blue.

    Ariga, Tomoko; Ito, Kyoko; Imura, Yuki; Yoshimura, Etsuro

    2015-03-15

    Iron (Fe) is an essential element for higher plants, which take it up from the soil at the root surface and transport it to shoots through the xylem. Fe(III) chelators, such as organic acids and phytosiderophores, play important roles in the acquisition and transportation of Fe(III). Therefore, a selective and sensitive method for analyzing Fe(III) chelators is required to study the many Fe-related physiological mechanisms in plants. A novel analytical approach employing a high-performance liquid chromatography post-column method with fluorescence detection was developed to separate and detect Fe(III) chelators. This method takes advantage of the quenching of the fluorescence of Calcein Blue (CB) that occurs with the formation of an Fe(III)-CB complex and the dequenching that occurs with the release of CB as a result of competition for Fe(III) between CB and an Fe(III) chelator. This simple experimental method does not require complicated pretreatments and can selectively detect Fe(III) chelators according to their Fe(III)-chelating ability. The detection limit for citric acid using this method was 72pmol. Furthermore, this method can also detect unknown Fe(III) chelators that exhibit a high affinity for Fe(III). The method was evaluated with xylem sap of barley, which was shown to contain several Fe(III) chelators. PMID:25658515

  8. Comparative Study of Synthesis Procedures for Urea - Formaldehyde Resins (Part I

    Mathew Obichukwu EDOGA

    2006-07-01

    Full Text Available This paper presents initial results from modifying the conventional synthesis procedure of UF resins, that is reacting urea and formaldehyde first in alkaline medium and subsequently in mild acid medium at reflux (conventional two - stage alkaline - acid synthesis, by conducting the reaction only in purely acid medium at 50oC (modified one - stage acid synthesis.In another attempt, the reaction was carried out in a neutral environment and at atmospheric temperature (modified one - stage neutral synthesis. The structural analysis of the various UF resin samples was carried out. The results showed that the UF resins (II synthesized in acidic media, particularly that of pH 1.0, showed features in their spectra which are consistent with a tri -, and/or tetra - substituted urea in the reaction to give a 3 - dimensional network UF resin. A 3 - dimensional network resin is characterized by little or no hydroxyl groups with increased cross-link-density and hydrophobicity and hence improved hydrolytic stability. For the resin (III obtained from the conventional method, the only clear distinction between spectra for the resins (II synthesized in acid media is the presence of diminished peaks for methylene groups at 2.2 ppm. The resins (I synthesized in neutral medium exhibited almost the same structural characteristics as those of the resin samples (III prepared conventionally. The result also showed that UF resin samples (I and III possessed 5 - 17 percent of free formaldehyde; the UF resin sample (II had approximately zero formaldehyde percentage.

  9. The stability of ion exchangers towards nitric acid and radiation. 1

    The behaviour of the chelating ion exchangers Wofatit MC 50, Dowex A 1 and Chelex 100 with aminoacetic acid - and iminodiacetic acid-groups towards nitric in the range of the concentration 1 ... 10.5 mol/l and at temperatures 0C was determined. It is found that the COOH capacity and the N content are rapidly reduced leading to the formation of CO2 and N2. If the exposure to HNO3 continues there is again a rise in the COOH capacity. The i.r.- and mass spectra show that the iminodiacetic acid-groups are destroyed by nitrosative cleavage and CHO groups result, which are then oxidized to COOH groups. The mass spectrum shows that the aminoacetic acid-groups of the resin are nitrosated, which has also been confirmed by the use of nitric acid labelled with 15N. (author)

  10. 反应与催化精馏耦合提纯乳酸新工艺的研究%Purification of Lactic Acid by Heterogeneous Catalytic Distillation Using Ion-exchange Resins

    马利; 张阳; 杨基础

    2005-01-01

    The purification of lactic acid based on the esterification of raw lactic acid from fermentation broth and then the catalytic distillation hydrolysis of methyl lactate simultaneously to achieve pure lactic acid is reported. The esterification kinetics of lactic acid with methanol catalyzed by strong-acid cation-exchange resins (Amberlyst-15,D001, D002, NKC, 002) was studied under the condition that simulates the real catalytic environment. Experimental results were correlated by a Langmuir-Hinselwood model and the nonideality of the solution was taken into account by using activities calculated by the universal quasichemical functional group activity coefficient (UNIFAC) method.A good agreement between the model and the experimental data was achieved. Continuous purification experiments were conducted to find the optimum column configuration and operation condition for the system. The effects of various parameters, e.g. the length of different section of the column, feed rate and ratio of reactants, packing material and catalyst type, were studied. This novel system shows good separation results in lab scale, and is potential for industrial application.

  11. 氨基酸螯合锌在奶山羊肠道消化吸收规律的研究%Digestion and Absorption of Zinc Amino Acid Chelate in the Intestinal Tract of Dairy Goats

    杨改青; 朱河水; 王林枫; 贺翠婷; 张振; 高建伟; 邵其斌; 冯亚强; 孙波

    2011-01-01

    本试验旨在研究氨基酸螯合锌(Zn-AA)在奶山羊体内的消化吸收规律及其在饲粮中的适宜添加水平.试验选取2.5~3.0岁,体重40~45 kg的关中奶山羊母羊6只,安装永久性瘤胃、十二指肠及回肠瘘管,首先从瘤胃灌注40 mg/kg的Zn-AA溶液,分别在灌注后的24、48、72、96、120、144和168 h采集十二指肠食糜、回肠食糜、粪样和血样,测定样品中锌含量,计算锌在小肠和全肠道消化率,检测血清锌水平,确定最佳采样时间.在此基础上,分别灌注0、20、60、80、100和200 mg/kg的Zn-AA溶液,测定不同水平的Zn-AA在小肠和全肠道的消化率及血清锌水平.结果表明,Zn-AA全肠道消化率在48和96 h分别出现吸收高峰,120 h后Zn-AA在小肠、全肠道的消化率和血清锌水平基本平衡并保持稳定;不同时间和水平的Zn-AA在全肠道的消化率均高于小肠,小肠是Zn-AA吸收的主要部位,大肠对Zn-AA也有不同程度地吸收;60 mg/kg时Zn-AA在全肠道消化率和血清中水平均达到最大值.研究得出,成年奶山羊饲粮中Zn-AA的最适宜添加水平为60 mg/kg,小肠是Zn-AA消化的主要部位,大肠对Zn-AA也表现出较强的消化吸收能力.%This trial was conducted to study the digestion and absorption of zinc amino acid chelate (Zn-AA) in intestinal tract of dairy goats and to determine the optimal supplemental level of Zn-AA in the diet. Six Guanzhong daffy goats aged 2. 5 to 3.0 years old with the body weight of 40 to 45 kg were selected and fixed with permanent fistulas in rumen, duodenum and ileum. At the beginning of the trial, 40 mg/kg Zn-AA solution was infused into the rumen, and samples were collected at 24, 48, 96, 120, 144 and 168 h after infusion. Digesta samples from the duodenum and ileum, and feces samples were collected to detect the zinc levels and calculate the digestibility in the small intestine, entire intestine and large intestine. At the same time, blood samples were

  12. Mixed Intramolecular Hydrogen Bonding in Dihydroxythiophene-based Units and Boron and Technetium Chelation

    Three novel potential metal ion chelating units have been synthesized and characterized: 5-hexylcarbamoyl- 3,4-dihydroxythiophene-2-carboxylic acid methyl ester (5), 3-benzyloxy-4-hydroxythiophene-2,5-dicarboxylic acid bis-hexylamide (6), and 3,4-dihydroxythiophene-2,5-dicarboxylic acid bis-hexylamide (7). The crystal structure of 6 was obtained and suggests the presence of three distinct intramolecular hydrogen bonds, namely [Namide-H···O] [O-H···Oamide] and [Namide-H···S]. Boron chelation with 5, 6 and 7 through the use of BF3, B(OH)3 or B(OMe)3 was probed by 1H, 11B, and 13C NMR spectroscopy. Technetium (I) chelation with 5, 6 and 7 was also studied via HPLC elutions using [99mTc(CO)3(OH2)3]+

  13. Targeted cleavage of HIV RRE RNA by Rev-coupled transition metal chelates.

    Joyner, Jeff C; Cowan, J A

    2011-06-29

    A series of compounds that target reactive metal chelates to the HIV-1 Rev response element (RRE) mRNA have been synthesized. Dissociation constants and chemical reactivity toward HIV RRE RNA have been determined and evaluated in terms of reduction potential, coordination unsaturation, and overall charge associated with the metal-chelate-Rev complex. Ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), diethylenetriaminepentaacetic acid (DTPA), and 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA) were linked to a lysine side chain of a Rev-derived peptide by either EDC/NHS or isothiocyanate coupling. The resulting chelate-Rev (EDTA-Rev, DTPA-Rev, NTA-Rev, and DOTA-Rev) conjugates were used to form coordination complexes with Fe(2+), Co(2+), Ni(2+), and Cu(2+) such that the arginine-rich Rev peptide could mediate localization of the metal chelates to the Rev peptide's high-affinity mRNA binding partner, RRE stem loop IIB. Metal complexes of the extended peptides GGH-Rev and KGHK-Rev, which also contain N-terminal peptidic chelators (ATCUN motifs), were studied for comparison. A fluorescence titration assay revealed high-affinity RRE RNA binding by all 22 metal-chelate-Rev species, with K(D) values ranging from ~0.2 to 16 nM, indicating little to no loss of RNA affinity due to the coupling of the metal chelates to the Rev peptide. Dissociation constants for binding at a previously unobserved low-affinity site are also reported. Rates of RNA modification by each metal-chelate-Rev species were determined and varied from ~0.28 to 4.9 nM/min but were optimal for Cu(2+)-NTA-Rev. Metal-chelate reduction potentials were determined and varied from -228 to +1111 mV vs NHE under similar solution conditions, allowing direct comparison of reactivity with redox thermodynamics. Optimal activity was observed when the reduction potential for the metal center was poised between those of the two principal co-reagents for metal-promoted formation of

  14. Properties of Acrylic Acid Resin Coating Materials Modified by Carbon Nanotubes%碳纳米管改性丙烯酸树脂涂饰材料的性能研究

    孙友昌; 马建中; 鲍艳; 刘海腾; 于玉龙

    2011-01-01

    Firstly, carbon nanotubes were modified and purified by the mix acids, then surface properties of carbon nanotubes were analyzed with the help of the infrared detector. Vinyl leather finishing agent was modified by carbon nanotubes using physical blending and in - situ emulsion polymerization. Tensile strength, elongation at break and water resistance of acrylic resin mem- brane nano- composite coating agent were determined. The results show that carbon nanotubes has the obvious enhancement toughening effect to acrylic resin membrane. Acrylic resin modified by carbon nanotubes has better tensile strength and elongation at break with an increase in the amount of carbon nanotubes, but has worse water resistance. Acrylic resin membrane modified by carbon nanotubes using physical blending and in - situ emulsion polymerization, the comprehensive performance is the best when the dosage of CNTs respectively is 0.04% and 0. 03%. Ultrasonic treatment will decrease the tensile strength and elongation at break, but the water resistance of the film will be increased slightly.%采用混酸对碳纳米管(CNTs)进行改性和纯化,并以此为原料,分别采用物理共混与原位乳液聚合法制备碳纳米管改性丙烯酸树脂皮革涂饰剂,将制备的丙烯酸树脂乳液分别成膜,并对所成薄膜的抗张强度、断裂伸长率、耐水性等进行测定。结果表明:碳纳米管对丙烯酸树脂薄膜有明显的增强增韧效果,随着碳纳米管用量的增加,薄膜的抗张强度、断裂伸长率增加,但耐水性略有下降。采用物理共混法与原位乳液聚合法改性丙烯酸树脂乳液,当CNTs的用量分别为0.04%和0.03%时,改性丙烯酸树脂薄膜的综合性能最好。对改性后的乳液进行超声处理,可使

  15. Extraction of High Quality DNA from Seized Moroccan Cannabis Resin (Hashish)

    El Alaoui, Moulay Abdelaziz; Melloul, Marouane; Alaoui Amine, Sanaâ; Stambouli, Hamid; El Bouri, Aziz; Soulaymani, Abdelmajid; El Fahime, Elmostafa

    2013-01-01

    The extraction and purification of nucleic acids is the first step in most molecular biology analysis techniques. The objective of this work is to obtain highly purified nucleic acids derived from Cannabis sativa resin seizure in order to conduct a DNA typing method for the individualization of cannabis resin samples. To obtain highly purified nucleic acids from cannabis resin (Hashish) free from contaminants that cause inhibition of PCR reaction, we have tested two protocols: the CTAB protoc...

  16. Interacting Blends of Novel Unsaturated Polyester Amide Resin with Vinyl Acetate

    Patel, H. S.; Panchal, K. K.; Patel, S. R.; Desai, S N

    2004-01-01

    Novel unsaturated poly (ester- amide) resins (UPEAs) were prepared by the reaction between an epoxy resin, namely diglycidyl ether of bisphenol–A (DGEBA) and unsaturated aliphatic bisamic acids using a base catalyst. These UPEAs were then blended with a vinyl monomer namely, Vinyl acetate (VA) to produce a homogeneous resin syrup. The curing of these UPEAs-VA resin blends was carried out by using benzoyl peroxide (BPO) as an initiator for the radical polymerization and was monitored by using ...

  17. Microporous phenol–formaldehyde resin-based adsorbents for pre-combustion CO2 capture

    Fernández Martín, Claudia; González Plaza, Marta; García López, Susana; Pis Martínez, José Juan; Rubiera González, Fernando; Pevida García, Covadonga

    2011-01-01

    Different types of phenolic resins were used as precursor materials to prepare adsorbents for the separation of CO2 in pre-combustion processes. In order to obtain highly microporous carbons with suitable characteristics for the separation of CO2 and H2 under high pressure conditions, phenol–formaldehyde resins were synthesised under different conditions. Resol resins were obtained by using an alkaline environment while Novolac resins were synthesised in the presence of acid catalysts. In add...

  18. Reillex/trademark/ HPQ: A new, macroporous polyvinylpyridine resin for separating plutonium using nitrate anion exchange

    Anion exchange in nitric acid is the major aqueous process used to recover and purify plutonium from impure scrap materials. Most strong-base anion exchange resins incorporate a styrene-divinylbenzene copolymer. A newly available, macroporous anion exchange resin based on a copolymer of 1-methyl-4-vinylpyridine and divinylbenzene has been evaluated. Comparative data for Pu(IV) sorption kinetics and capacity are presented for this new resin and two other commonly used anion exchange resins. The new resin offers high capacity and rapid sorption kinetics for Pu(IV) from nitric acid, as well as greater stability to chemical and radiolytic degradation. 8 refs., 12 figs

  19. Chelating agents in pharmacology, toxicology and therapeutics

    The proceedings contain 71 abstracts of papers. Fourteen abstracts were inputted in INIS. The topics covered include: the effects of chelating agents on the retention of 63Ni, 109Cd, 203Hg, 144Ce, 95Nb and the excretion of 210Po, 63Ni, 48V, 239Pu, 241Am, 54Mn; the applications of tracer techniques for studies of the efficacy of chelation therapy in patients with heart and brain disorders; and the treatment of metal poisoning with chelating agents. (J.P.)

  20. Tumor targeting of radiolabeled antibodies using HYNIC chelate

    There is an increasing interest in the use of labeled antibodies for diagnosis of cancers as well as for therapy. Various radiolabeling methods have been used in order to obtain better tumor specific targeting for detection and therapy. It was generally used to tumor targeted immunotherapy and immunodetection that lym-1, mouse monoclonal antibody, was specific binding to surface antigen of Raji. The 3E8 antibody was produced from humanized anti-TAG-72 monoclonal antibody (AKA) by amino acid change in 95-99 residues of heavy chain complementary determinant regions (HCDRs) 3 using phage displayed library technology. In this study, we are investigating the usefulness of HYNIC chelate as a bifunctional chelating agent in radioimmunodetecton of tumor. Two types of antibodies, Lym-1 and 3E8, were used for the conjugation with HYNIC chelate. Lym-1 and 3E8 are specific antibodies to surface antigen of Non-Hogkin's lymphoma and TAG-72 antigen of colorectal carcinoma, respectively. We prepare HYNIC-antibody conjugates, determine radiolabeling yield with 99mTc and evaluate tumor targeting in tumor bearing nude mice model

  1. Enhancing Potentially Plant-Available Lead Concentrations in Contaminated Residential Soils Using a Biodegradable Chelating Agent

    Andra, S.; Datta, R.; Sarkar, D.; Saminathan, S.

    2007-12-01

    Chelation of heavy metals is an important factor in enhancing metal solubility and, hence, metal availability to plants to promote phytoremediation. In the present study, we compared the effects of application of a biodegradable chelating agent, namely, ethylenediaminedisuccinic acid (EDDS) on enhancing plant available form of lead (Pb) in Pb-based paint contaminated residential soils compared to that of a more commonly used, but non-biodegradable chelate, i.e., ethylenediaminetetraacetic acid (EDTA). Development of a successful phytoremediation model for metals such as Pb depends on a thorough understanding of the physical and chemical properties of the soil, along with the optimization of a chelate treatment to mobilize Pb from `unavailable' pools to potentially plant available fraction. In this context, we set out to perform batch incubation experiments to investigate the effectiveness of the two aforementioned chelates in enhancing plant available Pb at four different concentrations (0, 5, 10 and 15 mM/kg soil) and three treatment durations (0, 10 and 30 days). We selected 12 contaminated residential soils from two major metropolitan areas (San Antonio, TX and Baltimore, MD) with varying soil physico-chemical properties - the soils from San Antonio were primarily alkaline and those from Baltimore were typically acidic. Total soil Pb concentrations ranged between 256 mg/kg and 4,182 mg/kg. Our results show that both chelates increased the solubility of Pb, otherwise occluded in the complex soil matrix. For both EDTA and EDDS, the exchangeable concentrations of soil Pb also increased with increase in chelate concentration and incubation time. The most effective treatment was 15 mM chelate kg-1 soil incubated for 30 days, which caused many fold increase in potentially plant available Pb (a combination of the soluble and exchangeable fractions) relative to the unamended controls. Step wise multiple linear regression analysis using chelate-extractable Pb and soil

  2. Separation of organic ion exchange resins from sludge - engineering study

    This engineering study evaluates the use of physical separation technologies to separate organic ion exchange resin from KE Basin sludge prior to nitric acid dissolution. This separation is necessitate to prevent nitration of the organics in the acid dissolver. The technologies under consideration are: screening, sedimentation, elutriation. The recommended approach is to first screen the Sludge and resin 300 microns then subject the 300 microns plus material to elutriation

  3. Separation of organic ion exchange resins from sludge -- engineering study

    Duncan, J.B.

    1998-08-25

    This engineering study evaluates the use of physical separation technologies to separate organic ion exchange resin from KE Basin sludge prior to nitric acid dissolution. This separation is necessitate to prevent nitration of the organics in the acid dissolver. The technologies under consideration are: screening, sedimentation, elutriation. The recommended approach is to first screen the Sludge and resin 300 microns then subject the 300 microns plus material to elutriation.

  4. Study and application on lean resin converting in uranium mill

    The field test about sulphuric acid used to convert lean resin was finished. The results indicated sulphuric acid could replace chlorin in lean resin and could be reclaimed to desorption procedure. The consumption of NaCl decreased, the chlorin concentration of tailing decreased too. Both of uranium loss and waste water volume were reduced. The uranium concentration of tailing decreased and energy saving and emission reduction can be achieved. (authors)

  5. Resin and organic transport in PWR secondary cycles

    Analytical techniques for quantifying low concentrations of cation and anion resins and low-molecular-weight organic acids in power station process streams are described. Average resin concentrations at the outlet of condensate polisher systems and individual vessels at three pressurized water reactors generally were much less than 1 ppB. Organic acid concentrations throughout the cycle at the three study plants also were very low

  6. Reduction of polyester resin shrinkage by means of epoxy resin

    The possibility was investigated of reducing the shrinkage of unsaturated polyester resin taking place in radiation-induced curing, by the addition of epoxy resin. In order to combine chemically both resins, the epoxy component was modified by introducing unsaturated bonds via acrylamide and N-hydroxymethyloloacrylamide. A composition of 90% unsaturated polyester resin and 10% acrylamide-modified epoxy resin, filled with silica (1:1.5), showed a volume shrinkage below 2%. (author)

  7. Low temperature plasma incineration of radioactive ion-exchange resin

    The results of the incineration studies of radioactive ion-exchange resin in an oxygen plasma atmosphere at pressures 20...50 mbar are presented. The plasma is generated using a 27.12 MHz radio frequency (RF) generator. The chamber temperature during the incineration varies between 100...140 deg C depending on the oxygen pressure in the chamber. The virtue of the low-temperature incineration is that the radioactive substances remain in the solid ash. The average retention of 60Co and 137Cs in the incineration chamber was about 94 %. The retention of 99mTc was in the average 77 % and of 131I about 70 %. The results indicate that, within the limit of the measurement accuracy, practically all Co and Cs remains in the chamber and can be recovered and further conditioned with the ash. The rest of technetium and iodine can be easily recovered on any cooled surface right after the incineration chamber. The mass reduction achievable with this method is 95 %. The ion-exchange resins in use at the Loviisa NPP were used as test samples. The activity retention and ashing experiments were made with a 1:1 mixture of granular anion and cation resin. The same kind of mixture is used for the primary water purification at the Loviisa NPP. The test resin was labelled with 60Co, 137Cs, 99mTc and 131I. Also spent Loviisa NPP resin was incinerated. The VVER-440 reactors of the Loviisa NPP use boric acid to control the reactivity of the core. The boric acid in the resin presents an extra cumber in the incineration process tending to prevent the oxygen plasma from getting into contact with the resin. The results with the granulated spent Loviisa NPP resin were drastically inferior to the results with the labelled test resin. The average unburnt residual mass was about 20 %. By prior crushing of the resin equal incineration results could be achieved with the test resin and with the spent Loviisa NPP resin. The low-temperature plasma incineration of radioactive ion-exchange resins presents

  8. Mathematical modeling of the effects of aerobic and anaerobic chelate biodegradation on actinide speciation

    Biodegradation of natural and anthropogenic chelating agents directly and indirectly affects the speciation, and, hence, the mobility of actinides in subsurface environments. We combined mathematical modeling with laboratory experimentation to investigate the effects of aerobic and anaerobic chelate biodegradation on actinide [Np(IV/V), Pu(IV)] speciation. Under aerobic conditions, nitrilotriacetic acid (NTA) biodegradation rates were strongly influenced by the actinide concentration. Actinide-chelate complexation reduced the relative abundance of available growth substrate in solution and actinide species present or released during chelate degradation were toxic to the organisms. Aerobic bio-utilization of the chelates as electron-donor substrates directly affected actinide speciation by releasing the radionuclides from complexed form into solution, where their fate was controlled by inorganic ligands in the system. Actinide speciation was also indirectly affected by pH changes caused by organic biodegradation. The two concurrent processes of organic biodegradation and actinide aqueous chemistry were accurately linked and described using CCBATCH, a computer model developed at Northwestern University to investigate the dynamics of coupled biological and chemical reactions in mixed waste subsurface environments. CCBATCH was then used to simulate the fate of Np during anaerobic citrate biodegradation. The modeling studies suggested that, under some conditions, chelate degradation can increase Np(IV) solubility due to carbonate complexation in closed aqueous systems

  9. Mathematical modelling of the effects of aerobic and anaerobic chelate biodegradation on actinide speciation

    Biodegradation of natural and anthropogenic chelating agents directly and indirectly affects the speciation, and hence, the mobility of actinides in subsurface environments. We combined mathematical modelling with laboratory experimentation to investigate the effects of aerobic and anaerobic chelate biodegradation on actinide [Np(IV/V), Pu(IV)] speciation. Under aerobic conditions, nitrilotriacetic acid (NTA) biodegradation rates were strongly influenced by the actinide concentration. Actinide-chelate complexation reduced the relative abundance of available growth substrate in solution and actinide species present or released during chelate degradation were toxic to the organisms. Aerobic bioutilization of the chelates as electron-donor substrates directly affected actinide speciation by releasing the radionuclides from complexed form into solution, where their fate was controlled by inorganic ligands in the system. Actinide speciation was also indirectly affected by pH changes caused by organic biodegradation. The two concurrent processes of organic biodegradation and actinide aqueous chemistry were accurately linked and described using CCBATCH, a computer model developed at Northwestern University to investigate the dynamics of coupled biological and chemical reactions in mixed waste subsurface environments. CCBATCH was then used to simulate the fate of Np during anaerobic citrate biodegradation. The modelling studies suggested that, under some conditions, chelate degradation can increase Np(IV) solubility due to carbonate complexation in closed aqueous systems. (orig.)

  10. Chelating Tendencies of Bioactive Aminophosphonates

    Kiss, Tamas; Lázár, István; Kafarski, Pawel

    1994-01-01

    The metal-binding abilities of a wide variety of bioactive aminophosphonates, from the simple aminoethanephosphonic acids to the rather large macrocyclic polyaza derivatives, are discussed with special emphasis on a comparison of the analogous carboxylic acid and phosphonic acid systems. Examples are given of the biological importance of metal ion – aminophosphonate interactions in living systems, and also of their actual and potential applicability in medicine.

  11. Fully bio-based epoxy resins

    Ertl, Johanna

    2015-01-01

    Epoxy resins are mainly produced by reacting bisphenol A with epichlorohydrin. Growing concerns about the negative health effects of bisphenol A are urging researchers to find alternatives. In this work diphenolic acid is suggested, as it derives from levulinic acid, obtained from renewable resources. Nevertheless, it is also synthesized from phenol, from fossil resources, which, in the current paper has been substituted by plant-based phenols. Two interesting derivatives were identified: dip...

  12. Chelation therapy after the Trial to Assess Chelation Therapy: results of a unique trial

    Maria D. Avila; Escolar, Esteban; Lamas, Gervasio A.

    2014-01-01

    Purpose of review EDTA chelation therapy has been in off-label use for the treatment of atherosclerosis. We review the results of the first large-scale randomized trial of this treatment. Recent findings The trial to assess chelation therapy was a $30 million National Institutes of Health-funded study of the safety and efficacy of EDTA-based chelation infusions in 1708 post-myocardial infarction (MI) patients. The trial to assess chelation therapy demonstrated a significant (P = 0.035) 18% re...

  13. Characterization Of Cycled Spherical Resorcinol-Formaldehyde Ion Exchange Resin

    This report presents characterization data for two spherical resorcinol-formaldehyde (sRF) resin beds that had processed cesium in non-radioactive and radioactive cycles. All column cycle operations for the resin beds including loading, displacements, elution, regeneration, breakthroughs, and solution analyses are reported in Nash and Duignan, 2009a. That report covered four ion exchange (IX) campaigns using the two ∼11 mL beds in columns in a lead-lag arrangement. The first two campaigns used Savannah River Site (SRS) Tank 2F nonradioactive simulant while the latter two were fed with actual dissolved salt in the Savannah River National Laboratory (SRNL) Shielded Cells. Both radioactive cycles ran to cesium breakthrough of the lead column. The resin beds saw in excess of 400 bed volumes of feed in each cycle. Resin disposal plans in tank farm processing depend on characterizations of resin used with actual tank feed. Following a final 30 bed volume (BV) elution with nitric acid, the resin beds were found to contain detectable chromium, barium, boron, aluminum, iron, sodium, sulfur, plutonium, cesium, and mercury. Resin affinity for plutonium is important in criticality safety considerations. Cesium-137 was found to be less than 10E+7 dpm/g of resin, similar to past work with sRF resin. Sulfur levels are reasonably consistent with other work and are expected to represent sulfur chemistry used in the resin manufacture. There were low but detectable levels of technetium, americium, and curium. Toxicity Characteristic Leaching Procedure (TCLP) work on the used (eluted) resin samples showed significant contents of mercury, barium, and chromium. One resin sample exceeded the TCLP level for mercury while the other metals were below TCLP levels. TCLP organics measurements indicated measurable benzene in one case, though the source was unknown. Results of this work were compared with other work on similar sRF resin characterizations in this report. This is the first work

  14. 热酸蚀刻对氧化锆陶瓷初期粘结强度的影响%Effect of hot acid etching on initial bond strength of zirconia to resin

    许少平; 印厚才; 谢海峰

    2012-01-01

    目的:考察两种酸液在加热条件下蚀刻处理对氧化锆陶瓷与树脂初期粘结强度的影响.方法:制作32个氧化锆陶瓷片,分为4组分别进行表面处理.A组:喷砂;B组:喷砂+H2SO4和(NH4)2SO4混合液煮沸下处理30 min+Clearfil Ceramic Primer涂底剂;C组:喷砂+HF和HNO3混合液煮沸下处理30 min+Clearfil Ceramic Primer涂底剂;D组:喷砂+Clearfil Ceramic Primer涂底剂.制备复合树脂柱,以树脂水门汀将其粘固于处理过的氧化锆陶瓷表面.粘结试件水储24 h后,测试剪切粘结强度.扫描电镜观察各处理组的陶瓷表面.结果:A组的粘结强度值最低,D组其次,B、C组的粘结强度值较高且无显著性差异.扫描电镜观察发现两种酸蚀刻后形成了与喷砂不同的粗化表面形态.结论:两种酸液在加热条件下能够对氧化锆陶瓷进行蚀刻粗化,同时可对其初期粘结强度起到增强作用.%Objective:To investigate the initial bond strength of zirconia etched with two kinds of hot acid mixtures to resin. Methods: Total 32 zirconia ceramic blocks were manufactured and divided into 4 groups received different surface treatments. Group A, sandblasting; group B, sandblasting combined with hot H2SO4 and (NH)2SC4 mixture etching 30 min, and applying Clearfil Ceramic Primer; group C, sandblasting combined with HF and HNO3 mixture etching 30 min, and applying Clearfil Ceramic Primer; group D, sandblasting and applying Clearfil Ceramic Primer. Thirty-two composite resin columns were prepared and cemented on the pre-treated zirconia blocks with composite resin cement. Shear bond strength (SBS) test were executed after water storage for 24 hours. The zirconia surfaces treated with different treatments were observed with a scanning electron microscope. Results: The SBS values were lowest in group A, and higher in group B and group C, among 4 groups, and had no significant difference between group B and group C. There were differences in surface

  15. 聚丙烯酸-海藻酸钠吸水树脂的降解研究%Study on the Degradation of Polyacrylic Acid -Sodium Alginate Absorbent Resin

    黄慧珍

    2012-01-01

    通过土壤掩埋法和菌类生长法研究了聚丙烯酸-海藻酸钠高吸水树脂的降解性能。实验结果表明,聚丙烯酸—海藻酸钠高吸水性树脂具有较好的生物降解性能,能够被土壤以及特定菌类降解,聚丙烯酸—海藻酸钠高吸水性树脂在土壤中埋置65天后降解率达43%,通过菌类降解,50天后降解率达60%。%Polyacrylic acid -sodium alginate superabsorbent degradation properties were studied by soil burial meth- od and fungi growth method. Experimental results showed that Polyacrylic acid -sodium alginate high absorbent resin had a good biodegradability to degradation of soil and specific fungi. Polyacrylic acid - sodium alginate superabsorbent 65 days after being embedded in the soil, the degradation rate could reach 43%. Degradation by fungi, 50 days later, the degra- dation rate could reach 60%.

  16. Fluorescence enhancement by chelation of Eu3+ and Tb3+ ions in sol-gels

    Chelation of rare-earth (RE) ions is investigated as a means of enhancing the optical properties of RE-doped silica sol-gels. Two chelating agents--2,6-pyridine-dicarboxylic acid (PDC) and 3-pyridinepropionic acid (PPA) and two different synthesis techniques are studied. Eu(PDC) gels exhibit intense 5D0→7F2 fluorescence in the red under UV excitation and long fluorescence lifetimes compared to Eu(PPA) gels and to gels without a chelating agent. This behavior indicates that the PDC molecule remains associated with the Eu after incorporation into the gel. Similar behavior is seen for 5D4→7F5 green fluorescence in Tb(PDC)

  17. Immobilisation of ion exchange resins in cement

    Over the last seven years, Low Oxidation State Metal Ion reagents (LOMI) have been used to decontaminate the 100 MW(e) Steam Generating Heavy Water Ractor (SGHWR) at Winfrith. The use of these reagents has resulted in a dilute ionic solution containing activation products which are produced by corrosion of metallic components in the reactor. It has been demonstrated that the amount of activity in the solution can be reduced using organic ion exchanger resins. These resins consist of a cross linked polystyrene with sulphonic acid or quaternary ammonium function groups and can be successfully immobilised in blended cement systems. The formulation which has been developed is produced from a 9 to 1 blend of ground granulated blast furnace slag (BFS) and ordinary Portland cement (OPC) containing 28% ion exchange resin in the water saturated form. If 6% Microsilica is added to the blended cement the waste loading can be increased to 36 w/o. (author)

  18. Adsorption of plant phenols by polystyrene resins

    Akiyoshi Fukushima

    2014-02-01

    Full Text Available Adsorption of nine plant phenols by nine polystyrene ion-exchange resins was investigated in an experimental model system. The phenols were adsorbed by Amberlite CG-120 more efficiently than any other acidically charged resins tested in this study. They were also taken up by anion exchangers. Among them Dowex 1-X8 was found to show the strongest effect on the adsorption of the phenolic constituents applied. A comparison of the efficiency of plant phenol adsorption between two different types of the synthetic polymers revealed that the basically charged polystyrenes had more prefarable affinities for phenols than cation exchangers. For example, the ratio of the efficiency between Amberlite CG-120 and Dowex 1-X8 was roughly calculated to be 3:7 under the present experimental conditions. The adsorption rate of the test phenols was raised mostly by increasing the amount of the resins added, if they were mixed with effective polymers in the incubation model system.

  19. Current Use of Chelation in American Health Care

    Wax, Paul M.

    2013-01-01

    The National Center for Health Statistics estimates that more than 100,000 Americans receive chelation each year, although far fewer than 1 % of these cases are managed by medical toxicologists. Unfortunately, fatalities have been reported after inappropriate chelation use. There are currently 11 FDA-approved chelators available by prescription although chelation products may also be obtained through compounding pharmacies and directly over the internet. Promotion of chelation training is pro...

  20. Use of Cation Exchange Resins for Production of U{sub 3}O{sub 8} Suitable for the Al-U{sub 3}O{sub 8} Powder Metallurgy Process

    Mosley, W.C.

    2001-09-17

    This report describes the production of U{sub 3}O{sub 8} powders from three types of cation exchange resins: Dowex 50W, a strong acid, sulfonate resin; AG MP-50, a macroporous form of sulfonate resin; and Bio-Rex 70, a weak acid, carboxylic resin.

  1. Partitioning minor actinides: a hot test with CMPO/SIO2 extraction resin

    PandT (Partitioning and Transmutation) could allow optimizing the future nuclear fuel cycle. Worldwide there is an increasing interest for advanced spent fuel reprocessing techniques whereby not only U and Pu but in addition the minor actinides Np, Am and Cm and preferably also the long-lived fission products are separated from the to-be-disposed waste. In accelerator driven systems and/or fast reactors the recovered elements could then be transmuted into short-lived or stable fission products. SCK-CEN is testing such an advanced aqueous reprocessing technique on contractual order from IRI (Japanese Institute of Research and Innovation). Their ERIX (Electro Reduction and Ion eXchange) process for MOX (Mixed OXide) fuel from fast breeder reactors consists of anion exchange as main separation method, electrolytic reduction for reducing U(VI) to U(IV) and extraction chromatography for the isolation of the minor actinides Am and Cm. In a sufficiently concentrated nitric acid solution, U, Pu and Np form anionic nitrato complexes that are adsorbed on an anion exchanger, while Am, Cm and most FP (Fission Products) exist as cations that do nearly not interact. In the ERIX process further partitioning of Am and Cm from the FP is based on their different affinity for the specific chelating agents of the extraction resin. The first step in the partitioning of the waste is the separation of Am and Cm together with t he chemically very resembling Ln (Lanthanides) from the FP by extraction chromatography on a CMPO/SiO2-P column. Simultaneously, Zr and Mo are also isolated. IRI prepared a novel silica-based extraction resin by impregnating CMPO into a styrene-divinylbenzene copolymer, which was immobilized in 50 micrometer porous silica particles. Compared to conventional polymeric matrix resins, these new type of silica-based extraction resins have rapid adsorption kinetics and a significantly low pressure drop in a packed column. After preliminary evaluation of the separation

  2. A study of intracellular iron metabolism using pyridoxal isonicotinoyl hydrazone and other synthetic chelating agents

    Rabbit reticulocytes with a high level of non-heme radioiron induced by preincubation with isonicotinic acid hydrazide and transferrin-bound 59Fe, were reincubated with various synthetic chelating agents and the amount of radioiron released from the cells was determined. Some substances, especially derivatives of pyridoxal or 2-hydroxybenzaldehyde and isonicotinic acid hydrazide or benzhydrazide, were found to mobilize significantly iron from 59Fe-labelled reticulocytes. Iron mobilizaiton from reticulocytes by pyridoxal isonicotinoyl hydrazone requires ATP to be produced by cells and is completely blocked by low temperatute (40C). Although the effect of desferrioxamine is also prevented by low temperature, modest iron mobilization due to this chelator seems to occur independently of ATP production in reticulocytes. Pyridoxal isonicotinoyl hydrazone mobilized iron mainly from mitochondria and in part also from ferritin. Although 2,2'-bipyridine seems to enter reticulocyte mitochondria and bind iron there, this chelator is not able to relaease iron either from mitochondria or from the cells. Reticulocytes with a high level of non-heme radioiron are envisaged as a useful system for testing biological effectiveness of various iron chelators. Pyridoxal isonicotinoyl hydrazone was shown to be an effective in vivo chelator since its adminstration to mice decreased 59Fe radioactivity in liver, spleen and kidney. (Auth.)

  3. Aminoalkylated Merrifield Resins Reticulated by Tris-(2-chloroethyl Phosphate for Cadmium, Copper, and Iron (II Extraction

    Mokhtar Dardouri

    2015-01-01

    Full Text Available We aimed to synthesize novel substituted polymers bearing functional groups to chelate heavy metals during depollution applications. Three polyamine functionalized Merrifield resins were prepared via ethylenediamine (EDA, diethylenetriamine (DETA, and triethylenetetramine (TETA modifications named, respectively, MR-EDA, MR-DETA, and MR-TETA. The aminoalkylated polymers were subsequently reticulated by tris-(2-chloroethyl phosphate (TCEP to obtain new polymeric resins called, respectively, MR-EDA-TCEP, MR-DETA-TCEP, and MR-TETA-TCEP. The obtained resins were characterized via attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR, elemental analysis (EA, and thermogravimetric (TGA, thermodynamic (DTA, and differential thermogravimetric (DTG analysis. The synthesized resins were then assayed to evaluate their efficiency to extract metallic ions such as Cd2+, Cu2+, and Fe2+ from aqueous solutions.

  4. Speciation analysis of chromium by separation on a 5-palmitoyl oxine-functionalized XAD-2 resin and spectrophotometric determination with diphenylcarbazide.

    Filik, Hayati; Doğutan, Melek; Apak, Reşat

    2003-07-01

    The method developed in this work for the separation and preconcentration of Cr(III) is based on its retention by an Amberlite XAD-2 copolymer resin functionalized with 5-palmitoyl-8-hydroxyquinoline (oxine), abbreviated XAD-POx, with the ligand covalently bound to the copolymer. Cr(III) sorption was quantitative within the pH range 4.5-7.0 and Cr(VI) was not retained. The Cr(III) held by the resin column was eluted with a hot solution of H(2)O(2) in pH>or=9.0 aqueous NH(3)-NH(4)Cl buffer, and Cr oxidized to CrO(4)(2-) was rejected by the chelating cation-exchanger column. Any Cr(VI) originally present with Cr(III) could be reduced with an acidic solution of H(2)O(2), and retained by the column yielding total Cr results, Cr(VI) being determined from the difference. The resin showed a maximal preconcentration factor of 60 for Cr(III), the LOD and LOQ being 9.3 and 30.1 nmol L(-1), respectively. The developed preconcentration-speciation analysis was finished with a diphenylcarbazide (DPC) spectrophotometric procedure suitable for conventional laboratories. The resin showed excellent salt tolerance, enabling Cr analysis in seawater, and was stable over extended use. All the interferents of this procedure that normally occur in an electroplating effluent, a blended coal CRM, and a standard steel sample could be removed by the recommended procedure, by use of partial and total selectivity at the adsorption and desorption stages, respectively, enabling preconcentration and colorimetric determination of chromium in various complex matrices. PMID:12819851

  5. Application of resin system for sand consolidation, mud-loss control, and channel repairing

    Wasnik, A.; Mete, S.; Ghosh, B. [Maharashtra Inst. of Technology (India)

    2005-11-01

    Sand production is one of the major challenges facing oil well operators. A technique for sand consolidation and channel repairing with a resin system was described along with a methodology for placing a chemical casing during or after drilling a shale zone that is prone to caving. The methodology is intended to facilitate drilling with reduced mud weight, without reducing the hole size. The resin comprises a mixture of elastomers UF, MF and a suitable plasticizer to impart flexibility and impact resistance. The resin system includes both the resin and a hardener which is a mixture of 2 mild Lewis acids to control curing time. A special additive can be used to enhance surface bonding between the sand and resin. Experiments were then performed to examine the efficiency of resin (Asmid 603) with 7 different chemicals and resin Furmel 301 with Furmel catalyst as a curing modifier. The best combination for sand consolidation and chemical casing was found to be resin Asmid 603 with 0.6 per cent o-phosphoric acid at 80 degrees C and Furmel 301 with 2.5 per cent Furmel catalyst and CFNL with 0.6 per cent o-phosphoric acid. When this combination was used, the permeability was found to be nearly zero after consolidation of resin. The newly developed resin system costs one-third that of epoxy resins. Since it is water soluble, it is also easy to handle and environmentally sound. 15 refs., 2 tabs., 6 figs.

  6. Improvement of Oxidative and Metabolic Parameters by Cellfood Administration in Patients Affected by Neurodegenerative Diseases on Chelation Treatment

    Alessandro Fulgenzi; Rachele De Giuseppe; Fabrizia Bamonti; Maria Elena Ferrero

    2014-01-01

    Objective. This prospective pilot study aimed at evaluating the effects of therapy with antioxidant compounds (Cellfood, and other antioxidants) on patients affected by neurodegenerative diseases (ND), who displayed toxic metal burden and were subjected to chelation treatment with the chelating agent calcium disodium ethylenediaminetetraacetic acid (CaNa2EDTA or EDTA). Methods. Two groups of subjects were studied: (a) 39 patients affected by ND and (b) 11 subjects unaffected by ND (controls)....

  7. Assessing the Impact of EDTA Chelating Effect on some Macro- and Microminerals in Prussian Carp (Carassius Gibelio) Tissues

    Marioara Nicula; Iosif Gergen; Monica Harmanescu; Ionut Banatean-Dunea; Adela Marcu; Eliza Simiz; Tiberiu Polen; Mihai Lunca

    2011-01-01

    Chelators are used in chemical analysis, in medical aplications, as water softeners, as decontamination agents on radioactive surfaces and they are ingredients in many commercial products such as shampoos and food preservatives. Such a synthetic chelator is EDTA (ethylenediaminetetraacetic acid). It is considered one of the tools that promises to control the heavy metal pollution in aquaculture. EDTA attaches itself to heavy metals and carries the metals from the fish body. EDTA can also slow...

  8. Predictors of DMSA chelatable lead, tibial lead, and blood lead in 802 Korean lead workers

    Todd, A; Lee, B; Lee, G.; Ahn, K; Moshier, E; Schwartz, B.

    2001-01-01

    OBJECTIVES—To examine the interrelations among chelatable lead (by dimercaptosuccinic acid, DMSA), tibial lead, and blood lead concentrations in 802 Korean workers with occupational exposure to lead and 135 employed controls with only environmental exposure to lead.
METHODS—This was a cross sectional study wherein tibial lead, DMSA chelatable lead, and blood lead were measured. Linear regression was used to identify predictors of the three lead biomarkers, evaluating the influence of age, job...

  9. Copper Chelation in Alzheimer's Disease Protein

    Rose, Frisco; Hodak, Miroslav; Bernholc, Jerry

    2013-03-01

    Alzheimer's disease (AD) is a neurodegenerative disorder affecting millions of people in the U.S. AD is primarily characterized at the cellular level by densely tangled fibrils of amyloid- β protein. These protein clusters have been found in association with elevated levels of multiple transition metals, with copper being the most egregious. Interestingly, metal chelation has shown promise in attenuating the symptoms of AD in recent clinical studies. We investigate this process by constructing an atomistic model of the amyloid- β-copper complex and profile the energetic viability in each of its subsequent disassociation stages. Our results indicate that five energetic barriers must be overcome for full metal chelation. The energy barriers are biologically viable in the presence water mediated bond and proton transfer between the metal and the protein. We model the chelation reaction using a consecutive path nudged elastic band method implemented in our ab initio real-space multi-grid code to obtain a viable sequence. This reaction model details a physically consistent explanation of the chelation process that could lead to the discovery of more effective chelation agents in the treatment of AD.

  10. Metal Ions Extraction with Glucose Derivatives as Chelating Reagents in Supercritical Carbon Dioxide

    Guo Chen YANG; Hai Jian YANG

    2006-01-01

    A series of glucose derivatives have been used as chelating reagents to extract metal ions in supercritical carbon dioxide. With perfluoro-1-octanesulfonic acid tetraethylammonium salt as additive, glucose derivatives were selective for Sr2+ and Pb2+ extraction in supercritical carbon dioxide.

  11. Leaching heavy metals in municipal solid waste incinerator fly ash with chelator/biosurfactant mixed solution.

    Xu, Ying; Chen, Yu

    2015-07-01

    The chelator [S,S]-ethylene diamine disuccinic acid, citric acid, and biosurfactant saponin are selected as leaching agents. In this study, the leaching effect of saponin mixed with either ethylene diamine disuccinic acid or citric acid on the levels of copper, zinc, lead, and cadmium in municipal solid waste incinerator fly ash is investigated. Results indicate that saponin separately mixed with ethylene diamine disuccinic acid and citric acid exhibits a synergistic solubilisation effect on copper, zinc, lead, and cadmium leaching from fly ash. However, saponin and ethylene diamine disuccinic acid mixed solution exhibits a synergistic solubilisation effect that is superior to that of a saponin and citric acid mixed solution. The extraction rate of heavy metal in fly ash leached with a saponin and chelator mixed solution is related to the pH of the leaching solution, and the optimal range of the pH is suggested to be approximately neutral. After leaching with a saponin and chelator mixed solution, copper, zinc, lead, and cadmium contents significantly decreased (p leaching concentrations of copper, zinc, lead, and cadmium in treated fly ash are in accordance with Standard for Pollution Control on the Security Landfill Site for Hazardous Wastes GB18598-2001. PMID:26185165

  12. Chelating compounds as potential flash rust inhibitors and melamine & aziridine cure of acrylic colloidal unimolecular polymers (CUPs)

    Mistry, Jigar Kishorkumar

    Waterborne coatings on ferrous substrates usually show flash rusting which decreases the adhesion of the coating and the corrosion products can form a stain. Chelating compounds were investigated as potential flash rust inhibitors. Compounds being evaluated include amine alcohols, diamines and sulfur containing amines. A new corrosion inhibitor 2,5-bis(thioaceticacid)-1,3,4-thiadiazole (H2ADTZ) was synthesized and its performance characteristics were evaluated. It was noted that the observed structure of 1,3,4-thiadiazolidine-2,5-dithione (also known as 2,5-dimercapto-1,3,4-thiadiazole (DMTD or DMcT)) has been previously reported in three different tautomeric forms including -dithiol and -dithione. The relative stability of each form as well as the synthesis and characterization of the structures of mono- and dialkylated forms of 5-mercapto-1,3,4-thiadiazole-2(3H)-thione (MTT) were examined. The methods of X-ray crystallography, NMR spectroscopy and ab-initio electronic structure calculations were combined to understand the reactivity and structure of each compound. Polymers were synthesized with a 1:7 or 1:8 ratio of acrylic acid to acrylate monomers to produce an acid rich resin. The polymers were reduced and solvent stripped to produce Colloidal Unimolecular Polymers (CUPs). These particles are typically 3-9 nanometers in diameter depending upon the molecular weight. They were then formulated into a clear coating with either a melamine (bake) or an aziridine (ambient cure) and then cured. The melamine system was solvent free, a near zero VOC and the aziridine system was very low to near zero VOC. The coatings were evaluated for their MEK resistance, adhesion, hardness, gloss, flexibility, wet adhesion, abrasion and impact resistance properties.

  13. Radiocatalytic degradation of spent organic ion exchange resins using BaF2/TiO2/Ceramic nanocomposite

    A BaF2/TiO2/ceramic nanocomposite has been prepared to investigate the decomposition of spent resin using high energy radiation for volume reduction. It was found that high energy radiation can be converted by BaF2 scintillator to induce TiO2 based photocatalytic degradation of organic resin. The synthesis of nanocomposite was performed using TiCl4 hydrolysis, EDTA chelating method and calcinated at 450 degree C. The composite was further characterized and used to facilitate radiocatalytic degradation of Purolite cationic resin, Preliminary result exhibited that granular resin will be gradually decomposed into small molecules under 1 MBq 60Co irradiation. The hybridization of photocatalytic TiO2 and radiation-sensitive BaF2 are expected to be a promising tool and have to be studied in more detail. The radiocatalytic degradation of resin will further be studied by weight loss, pH effect, and TOC level.

  14. Study on dehydrochlorination of waste poly (vinyl chloride) resins by microwave irradiation

    Moriwaki, Saburo; Qian, Qingrong; Sunohara, Satoshi; Machida, Motoi; Tatsumoto, Hideki

    Waste poly (vinyl chloride: PVC) resins are experimentally dehydrochlorinated by microwave irradiation. The following unique results are obtained: (1) plasticizer in PVC resin absorbs microwave power more effectively than PVC polymer. The higher the plasticizer content in PVC resin, the higher is the dehydrochlorination reaction (2) low PVC polymer content materials such as cushion floor require high microwave irradiation power to secure a high dehydrochlorination yield, (3) calcium carbonate in PVC resin reacts with released hydrochloric acid gas and results calcium chloride during microwave irradiation, (4) additives in PVC resin strongly influence dehydrochlorination yield, (5) it is evidenced that the PVC copolymer is also dehydrochlorinated by microwave irradiation.

  15. Determination of degradation conditions of exchange resins containing technetium

    The quantification of Tc-99 in spent exchange resins, coming from nuclear power plants, is indispensable to define their administration. The Tc-99 is a pure beta emitter of 210000 years of half-life, volatile and of a high mobility in water and soil. For this reason, the objective of this work is to establish a digestion method of ionic exchange resins containing technetium that retains more than 95% of this radioisotope. Mineralization tests were carried out of a resin Amberlite IRN-150 by means of an oxidation heat, in acid medium, varying the resin mass, the medium volume, the media type, the temperature and the digestion time. The digested samples were analyzed by gas chromatography to estimate the grade of their degradation. The 99mTc was used as tracer to determine the technetium percentage recovered after mineralizing the resin. The digestion process depends on the temperature and the resin mass. At higher temperature better mineralization of samples and to greater resin mass to a constant temperature, less degradation of the resin. The spectra beta of the 99mTc and 99Tc are presented. (Author)

  16. Phytoremediation of Cr(VI) by Spirodela polyrrhiza (L.) Schleiden employing reducing and chelating agents.

    Bala, Rajni; Thukral, Ashwani K

    2011-01-01

    Phytoremediation of Cr(VI) by Spirodela polyrrhiza in binary combinations with low molecular weight organic compounds (LMWOCs) with a reducing or chelating potential, viz., ascorbic acid, citric acid, tartaric acid, oxalic acid, lactic acid, and glycerol was studied in Cr(VI) containing hydroponic media. Significant increase in the relative dry weight of plants with respect to Cr(VI) treated controls was observed with ascorbic acid and glycerol. The uptake of chromium by S. polyrrhiza followed Michaelis-Menten kinetics of active ion uptake. Interaction between Cr and ascorbic acid, oxalic acid, and lactic acid decreased Cr uptake, whereas citric acid, glycerol, and tartaric acid increased it. Supplementation of LMWOCs to Cr(VI) containing media decreased the MDA content of the plants. Multiple regression models revealed that LMWOCs decrease lipid peroxidation independently, as well as that induced by Cr(VI). It was found that superoxide dismutase (SOD), guaiacol peroxidase (GPX), and catalase (CAT) activities were increased significantly in plants growing in media containing Cr(VI). The study established that lactic acid, citric acid, ascorbic acid, and glycerol were most effective in increasing the Cr(VI) phytoremediating potential of S. polyrrhiza and LMWOCs with reducing or chelating properties decrease Cr(VI) stress in S. polyrrhiza. PMID:21598777

  17. Trypanotoxic activity of thiosemicarbazone iron chelators.

    Ellis, Samuel; Sexton, Darren W; Steverding, Dietmar

    2015-03-01

    Only a few drugs are available for treating sleeping sickness and nagana disease; parasitic infections caused by protozoans of the genus Trypanosoma in sub-Saharan Africa. There is an urgent need for the development of new medicines for chemotherapy of these devastating diseases. In this study, three newly designed thiosemicarbazone iron chelators, TSC24, Dp44mT and 3-AP, were tested for in vitro activity against bloodstream forms of Trypanosoma brucei and human leukaemia HL-60 cells. In addition to their iron chelating properties, TSC24 and Dp44mT inhibit topoisomerase IIα while 3-AP inactivates ribonucleotide reductase. All three compounds exhibited anti-trypanosomal activity, with minimum inhibitory concentration (MIC) values ranging between 1 and 100 µM and 50% growth inhibition (GI50) values of around 250 nM. Although the compounds did not kill HL-60 cells (MIC values >100 µM), TSC24 and Dp44mT displayed considerable cytotoxicity based on their GI50 values. Iron supplementation partly reversed the trypanotoxic and cytotoxic activity of TSC24 and Dp44mT but not of 3-AP. This finding suggests possible synergy between the iron chelating and topoisomerase IIα inhibiting activity of the compounds. However, further investigation using separate agents, the iron chelator deferoxamine and the topoisomerase II inhibitor epirubicin, did not support any synergy for the interaction of iron chelation and topoisomerase II inhibition. Furthermore, TSC24 was shown to induce DNA degradation in bloodstream forms of T. brucei indicating that the mechanism of trypanotoxic activity of the compound is topoisomerase II independent. In conclusion, the data support further investigation of thiosemicarbazone iron chelators with dual activity as lead compounds for anti-trypanosomal drug development. PMID:25595343

  18. Purification of degraded TBP solvent using macroreticular anion exchange resin

    Tri-n-butyl phosphate (TBP) diluted with a suitable diluent is commonly used for solvent extraction in Purex process for the recovery of uranium and plutonium from irradiated nuclear fuels. This solvent gets degraded due to various factors, the main degradation product being dibutyl phosphoric acid (HDBP). A solvent cleanup step is generally incorporated in the process for removing the degradation products from the used solvent. A liquid-liquid cleanup system using sodium carbonate or sodium hydroxide solution is routinely used. Considering certain advantages, like the possibility of loading the resin almost to saturation capacity and the subsequent disposal of the spent resin by incineration and the feasibility of adopting it to the process, a liquid-solid system has been tried as an alternate method, employing various available macroreticular anion exchange resins in OH- form for the sorption of HDBP from TBP. After standardizing the various conditions for the satisfactory removal of HDBP from TBP using synthetic mixtures, resins were tested with process solvent in batch contacts. The parameters studied were (1) capacity of different resins for HDBP sorption (2) influence of acidity, uranium and HDBP on the sorption behaviour of the latter (3) removal of fission products from the solvent by the resin and (4) regeneration and recycling of the resin. (author). 2 figs., 13 tabs., 17 refs

  19. Chelating Properties of Peptides from Red Seaweed Pyropia columbina and Its Effect on Iron Bio-Accessibility.

    Cian, Raúl E; Garzón, Antonela G; Ancona, David Betancur; Guerrero, Luis Chel; Drago, Silvina R

    2016-03-01

    The aim of this work was to evaluate copper-chelating, iron-chelating and anticariogenic activity of peptides obtained by enzymatic hydrolysis of P. columbina protein concentrate and to study the effects of chelating peptides on iron bio-accessibility. Two hydrolyzates were obtained from P. columbina protein concentrate (PC) using two hydrolysis systems: alkaline protease (A) and alkaline protease + Flavourzyme (AF). FPLC gel filtration profile of PC shows a peak having molecular weight (MW) higher than 7000 Da (proteins). A and AF hydrolyzates had peptides with medium and low MW (1013 and 270 Da), respectively. Additionally, AF presented free amino acids with MW around 82 Da and higher content of His and Ser. Peptides from AF showed the highest chelating properties measured as copper-chelating activity (the lowest β-carotene oxidation rate: R o ; 0.7 min(-1)), iron-chelating activity (33 %), and phosphorous and Ca(2+) release inhibition (87 and 81 %, respectively). These properties could indicate antioxidant properties, promotion of iron absorption and anticariogenic activity, respectively. In fact, hydrolyzates promoted iron dialyzability (≈16 %), values being higher than that found for P. columbina seaweed. Chelating peptides from both hydrolyzates can maintain the iron in a soluble and bio-accessible form after gastrointestinal digestion. PMID:26860526

  20. Effect of surface pretreatments on resin composite bonding to PEEK.

    Silthampitag, Patcharawan; Chaijareenont, Pisaisit; Tattakorn, Kittipong; Banjongprasert, Chaiyasit; Takahashi, Hidekazu; Arksornnukit, Mansuang

    2016-01-01

    This study evaluated the effect of surface pretreatments on resin composite bonding to polyetheretherketone (PEEK). Four groups of surface pretreatment (no pretreatment, etched with 98% sulfuric acid, etched with piranha solution and sandblasting with 50 µm alumina) were performed on PEEK. Surface roughness, Scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) analysis were examined. Shear bond strength (SBS) and interface characteristics were also evaluated after the specimens were bonded with resin materials. Two-way ANOVA analysis revealed significance on two main effects and interactions. Tukey's multiple comparisons test showed that the SBS of resin composite on PEEK were the highest in the group etched with 98% sulfuric acid and bonded with Heliobond(®) (p<0.05). All pretreatments produced similar spectra of FTIR patterns. SEM demonstrated porosities and pitting from chemical etching, which suggested a significant influence on the adhesion between PEEK and resin materials. PMID:27477234