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Sample records for copper ions

  1. Interactions of catechins with copper ions

    OpenAIRE

    Řihošková, Petra

    2014-01-01

    Charles University in Prague Faculty of Pharmacy in Hradec Králové Department of Pharmaceutical botanic and ecology Candidate: Mgr. Petra Řihošková Supervisor: PharmDr. Jana Karlíčková, Ph.D. Title of Thesis: Interactions of catechins with copper ions Keywords: catechins, chelating activity, copper, bathocuproine, hematoxylin, antioxidants Flavonoids are a class of plant polyphenols with significant antioxidant activity, which positively affects human health. Flavonoids are able to chelate me...

  2. Copper ion liquid-like thermoelectrics

    Science.gov (United States)

    Liu, Huili; Shi, Xun; Xu, Fangfang; Zhang, Linlin; Zhang, Wenqing; Chen, Lidong; Li, Qiang; Uher, Ctirad; Day, Tristan; Snyder, G. Jeffrey

    2012-05-01

    Advanced thermoelectric technology offers a potential for converting waste industrial heat into useful electricity, and an emission-free method for solid state cooling. Worldwide efforts to find materials with thermoelectric figure of merit, zT values significantly above unity, are frequently focused on crystalline semiconductors with low thermal conductivity. Here we report on Cu2-xSe, which reaches a zT of 1.5 at 1,000 K, among the highest values for any bulk materials. Whereas the Se atoms in Cu2-xSe form a rigid face-centred cubic lattice, providing a crystalline pathway for semiconducting electrons (or more precisely holes), the copper ions are highly disordered around the Se sublattice and are superionic with liquid-like mobility. This extraordinary ‘liquid-like’ behaviour of copper ions around a crystalline sublattice of Se in Cu2-xSe results in an intrinsically very low lattice thermal conductivity which enables high zT in this otherwise simple semiconductor. This unusual combination of properties leads to an ideal thermoelectric material. The results indicate a new strategy and direction for high-efficiency thermoelectric materials by exploring systems where there exists a crystalline sublattice for electronic conduction surrounded by liquid-like ions.

  3. Copper Ion as a New Leakage Tracer

    Directory of Open Access Journals (Sweden)

    Modaresi J.

    2013-12-01

    Full Text Available Statement of Problem: Most failures of root canal treatments are caused by bacteria. Studies showed that the most common cause of endodontic failures were the incomplete obturation of the root canal and the lack of adequate apical seal. Some in-vitro methods are used to estimate sealing quality, generally by measuring microleakage that allows the tracer agent to penetrate the filled canal.Purpose: Conventional methods of evaluating the seal of endodontically treated teeth are complicated and have some drawbacks. We used copper ion diffusion method to assess the leakage and the results were compared to dye penetration method.Materials and Method: The crowns of 21 extracted teeth were cut off at the CEJ level. After preparing the canals, the teeth were placed in tubes containing saline. They were divided randomly into 15 experimental cases; 3 positive and 3 negative controls. Positive controls were filled by single cone without sealer while the experimental and the negative control groups were filled by lateral technique. The coronal portion of gutta was removed and 9mm was left. The external surface of each tooth was coated with nail polish. Two millimeters of apical portion was immersed into 9ml of distilled water and 0.3ml of CuSO4 solution was injected into the coronal portion. After 2 days, copper sulfate was measured by an atomic absorption spectrophotometer. The teeth were then immersed in 2% methylene blue for 24 hours, sectioned and the extent of dye penetration was measured by a stereomicroscope.Results: The maximum and minimum recorded copper ion concentrations for the experimental group were 18.37 and 2.87ppm respectively. The maximum and minimum recorded dye penetrations for the experimental group were 8.5 and 3.5mm respectively. The statistical analysis, adopting paired samples test, showed poor correlation between average recorded results of two methods.Conclusion: Based on our results, there was no significant correlation between

  4. Synthesis of copper nanoparticles in polycarbonate by ion implantation

    Indian Academy of Sciences (India)

    Annu Sharma; Suman Bahniwal; Sanjeev Aggarwal; S Chopra; D Kanjilal

    2011-07-01

    Copper nanoparticles have been synthesized in polycarbonate by 75 KeV Cu– ion implantation with various doses ranging from 6.4 × 1015 to 1.6 × 1017 ions/cm2 with a beam current density of 800 nA/cm2. The composites formed were structurally characterized using Ultraviolet-Visible (UV-Visible) absorption spectroscopy. The appearance of particle plasmon resonance peak, characteristic of copper nanoparticles at 603 nm in absorption spectra of polycarbonate implanted to a dose of 1.6 × 1017 ions/cm2, indicates towards the formation of copper nanoparticles in polycarbonate. Transmission electron microscopy further confirms the formation of copper nanoparticles having size ∼ 3.15 nm. The formation of copper nanoparticles in the layers carbonized by Cu– implantation has been discussed. The synthesized copper-polycarbonate nanocomposite has been found to be more conducting than polycarbonate as ascertained using current–voltage characteristics.

  5. Release behavior of copper ion in a novel contraceptive composite.

    Science.gov (United States)

    Li, Juan; Suo, Jinping; Huang, Xunbin; Ye, Chang; Wu, Xiwang

    2007-09-01

    The universally used contraceptive method, the Cu-IUD, an effective contraceptive, is being increasingly used worldwide for family planning. To avoid abnormal bleeding, pain, partial and complete expulsion associated with the burst release of copper during the first few days, a novel cross-linked composite based on poly vinyl alcohol (PVA) that contains copper ions, but not metallic copper, was synthesized. PVA, well known for its good processability, high strength, long-term temperature and pH stability and biocompatibility, was used as the matrix material. The corrosion products and the release rate of copper ions after soaking in simulated body fluid (SBF) for different time spans were studied by environmental scanning electron microscopy, X-ray energy dispersive spectroscopy, X-ray diffraction and atomic absorption spectrophotometer. No significant change on time dependence for the release rate of copper ions in the composite compared with that of metallic copper was found. Moreover, no other new elements, such as P, Cl and Ca, appeared on the surface of the composite and no Cu(2)O formed after immersing in SBF for 90 days. Burst release of copper ions can be avoided by loading copper ions in this polymer material. Release channels would not be obstructed by the deposition of corrosion products and nearly all of the copper loaded in the composites could be an effective contraceptive.

  6. Measurement of Electron-Ion Relaxation in Warm Dense Copper

    Science.gov (United States)

    Cho, B. I.; Ogitsu, T.; Engelhorn, K.; Correa, A. A.; Ping, Y.; Lee, J. W.; Bae, L. J.; Prendergast, D.; Falcone, R. W.; Heimann, P. A.

    2016-01-01

    Experimental investigation of electron-ion coupling and electron heat capacity of copper in warm and dense states are presented. From time-resolved x-ray absorption spectroscopy, the temporal evolution of electron temperature is obtained for non-equilibrium warm dense copper heated by an intense femtosecond laser pulse. Electron heat capacity and electron-ion coupling are inferred from the initial electron temperature and its decrease over 10 ps. Data are compared with various theoretical models.

  7. Metallic copper corrosion rates, moisture content, and growth medium influence survival of copper ion-resistant bacteria

    DEFF Research Database (Denmark)

    Elguindi, J; Moffitt, S; Hasman, Henrik

    2010-01-01

    The rapid killing of various bacteria in contact with metallic copper is thought to be influenced by the influx of copper ions into the cells, but the exact mechanism is not fully understood. This study showed that the kinetics of contact killing of copper surfaces depended greatly on the amount...... of moisture present, copper content of alloys, type of medium used, and type of bacteria. We examined antibiotic- and copper ion-resistant strains of Escherichia coli and Enterococcus faecium isolated from pig farms following the use of copper sulfate as feed supplement. The results showed rapid killing...... of both copper ion-resistant E. coli and E. faecium strains when samples in rich medium were spread in a thin, moist layer on copper alloys with 85% or greater copper content. E. coli strains were rapidly killed under dry conditions, while E. faecium strains were less affected. Electroplated copper...

  8. Simultaneous Platinum and Copper Ion Attachment to a Human Copper Chaperone Protein

    Science.gov (United States)

    Hodak, Miroslav; Cvitkovic, John; Yu, Corey; Dmitriev, Oleg; Kaminski, George; Bernholc, Jerry

    2015-03-01

    Cisplatin is a potent anti-cancer drug based on a platinum ion. However, its effectiveness is decreased by cellular resistance, which involves cisplatin attaching to copper transport proteins. One of such proteins is Atox1, where cisplatin attaches to the copper binding site. Surprisingly, it was shown that both cisplatin and copper can attach to Atox1 at the same time. To study this double metal ion attachment, we use the KS/FD DFT method, which combines Kohn-Sham DFT with frozen-density DFT to achieve efficient quantum-mechanical description of explicit solvent. Calculations have so far investigated copper ion attachment to CXXC motifs present in Atox1. The addition of the platinum ion and the competition between the two metals is currently being studied. These calculations start from a molecular mechanics (MM) structural model, in which glutathione groups provide additional ligands to the Pt ion. Our goals are to identify possible Cu-Pt structures and to determine whether copper/platinum attachment is competitive, independent, or cooperative. Results will be compared to the 1H, N1 5 -HSQC NMR experiments, in which binding of copper and cisplatin to Atox1 produces distinct secondary chemical shift signatures, allowing for kinetic studies of simultaneous metal binding.

  9. [Atomic absorption spectrophotometry study of copper ion release by copper-bearing intrauterine devices].

    Science.gov (United States)

    Berthou, J; Chrétien, F C; Driguez, P A

    1998-11-01

    Copper release from copper-bearing IUD's was studied in vitro and in vivo using atomic absorption spectrophotometry in deionized water, normal saline solution and normal ovulatory cervical mucus. In these media, copper release from a 375 mm2 DIU occurs without latency, showing comparable amounts for identical time intervals. Daily copper release was shown to be respectively 8 and 11 times higher in cervical mucus and normal saline solution than in deionized water. Although copper ions are detectable in ovulatory cervical mucus under physiological conditions, the copper content appears 5 to 6 times higher in women bearing a copper IUD. Obviously, the copper amount is dependent on the copper exposed surface: the daily in vitro release from a 250 mm2 IUD is 18% inferior to that observed from a 375 mm2 model. In vivo, the daily copper release in ovulatory mucus of 380 or 200 mm2 IUD users is respectively 5 and 3.5 times higher than in controls.

  10. Copper(I) electrode function of two types of copper(II) ion-selective electrodes.

    Science.gov (United States)

    Neshkova, M; Sheytanov, H

    1985-08-01

    The response of two types of solid-state copper ion-selective electrodes with homogeneous membranes of CuAgSe and Cu(2-x)Se has been investigated in copper(I) solutions, prepared electrochemically by insitu generation from a copper anode in chloride medium. The selectivity coefficient K(pot)(Cu+, Cu(2+)) both types of electrodes has been determined. It is 10(-5.7) for the copper selenide sensor, and 10(-6.2) for the copper silver selenide one. These values are very close to that calculated for an exchange reaction proceeding on the electrode surface. The similarity in K(pot)(Cu+ ,Cu(2+)) values for different chalcogenidebased sensors suggests a common potential-generating mechanism. High chloride concentration does not interfere with the electrode response towards Cu(I), but distorts the electrode response to Cu(II).

  11. Erosion of Copper Target Irradiated by Ion Beam

    CERN Document Server

    Polosatkin, S V; Grishnyaev, E S; Konstantinov, S G; Shoshin, A A

    2012-01-01

    Erosion of copper target irradiated by deuterium ion beam with ultimate fluence is studied. The target originally destined for neutron generation represents bulk copper substrate covered by 3-\\mum titanium layer. The target was irradiated by deuterium ion beam generated in Bayard-Alpert type ion source with energy of ions 17.5 keV/nuclear. Maximal fluence in the center of the target achieves 2.5x10^23atoms/cm^2. Measurements of the profile of irradiated target and estimation of fluence shows that physical sputtering is a dominating process that determines the target erosion Most interesting feature is growth of \\mum-size tadpole-shaped structures, localized in the cracks of the surface. RFA analysis of these structures showed extremely large (up to 60%at.) carbon content.

  12. Seeding of silicon by copper ion implantation for selective electroless copper plating

    Energy Technology Data Exchange (ETDEWEB)

    Bhansali, S.; Sood, D.K.; Zmood, R.B. [Microelectronic and Materials Technology Centre, Royal Melbourne Institute of Technolgy, Melbourne, VIC (Australia)

    1993-12-31

    We report on the successful use of copper(self) ion implantation into silicon to seed the electroless plating of copper on silicon (100) surfaces. Copper ions have been implanted to doses of 5E14-6.4E16 ions/cm{sup 2} using a MEEVA ion implanter at extraction voltage of 40kV. Dose was varied in fine steps to determine the threshold dose of 2E15 Cu ions/cm{sup 2} for `seed` formation of copper films on silicon using a commercial electroless plating solution. Plated films were studied with Rutherford backscattering spectrometry, scanning electron microscopy, EDX and profilometry . The adhesion of films was measured by `scotch tape test`. The adhesion was found to improve with increasing dose. However thicker films exhibited rather poor adhesion and high internal stress. SEM results show that the films grow first as isolated islands which become larger and eventually impinge into a continuous film as the plating time is increased. (authors). 5 refs., 1 tab., 3 figs.

  13. Visual Observation of Dissolution of Copper Ions from a Copper Electrode

    Science.gov (United States)

    Ikemoto, Isao; Saitou, Kouichi

    2013-01-01

    During electrolysis, to visually observe the conversion of a metal to its cation, either the cation or its complex ion should have a distinct color while the electrolyte solution must be colorless and transparent. A demonstration is described in which copper is used as the electrodes and sodium polyacrylate (a superabsorbent polymer) solution is…

  14. Visual Observation of Dissolution of Copper Ions from a Copper Electrode

    Science.gov (United States)

    Ikemoto, Isao; Saitou, Kouichi

    2013-01-01

    During electrolysis, to visually observe the conversion of a metal to its cation, either the cation or its complex ion should have a distinct color while the electrolyte solution must be colorless and transparent. A demonstration is described in which copper is used as the electrodes and sodium polyacrylate (a superabsorbent polymer) solution is…

  15. Removal of copper ions from electroplating rinse water using electrodeionization

    Institute of Scientific and Technical Information of China (English)

    Xiao FENG; Jun-song GAO; Zu-cheng WU

    2008-01-01

    An improved configuration of the membrane stack was adopted in the electrodeionization (EDI)cell to prevent precipitation of bivalent metal hydroxide during the running.The operational parameters that influenced the removal of copper ions from the dilute solution were optimized.The result showed that a moderate decrease in the inlet pH value and a moderate increase in the applied voltage could achieve a better removaI effect.The steady process of electroplating wastewater treatment could be achieved with a removal efficiency ofmore than 99.5%and an enrichment factor of 5~14.The concentration of copper in purlfled water was less than 0.23 mg/L.This demonstrated the applicability of recovering heavy metal ions and purifled water from electroplating effluent for industrial reuse.

  16. Comparison and distribution of copper oxide nanoparticles and copper ions in activated sludge reactors.

    Science.gov (United States)

    Zhang, Dongqing; Trzcinski, Antoine P; Oh, Hyun-Suk; Chew, Evelyn; Tan, Soon Keat; Ng, Wun Jern; Liu, Yu

    2017-05-12

    Copper oxide nanoparticles (CuO NPs) are being increasingly applied in the industry which results inevitably in the release of these materials into the hydrosphere. In this study, simulated waste-activated sludge experiments were conducted to investigate the effects of Copper Oxide NPs at concentrations of 0.1, 1, 10 and 50 mg/L and to compare it with its ionic counterpart (CuSO4). It was found that 0.1 mg/L of CuO NPs had negligible effects on Chemical Oxygen Demand (COD) and ammonia removal. However, the presence of 1, 10 and 50 mg/L of CuO NPs decreased COD removal from 78.7% to 77%, 52.1% and 39.2%, respectively (P copper ions were more toxic towards microorganisms compared to CuO NPs. CuO NPs were removed effectively (72-93.2%) from wastewater due to a greater biosorption capacity of CuO NPs onto activated sludge, compared to the copper ions (55.1-83.4%). The SEM images clearly showed the accumulation and adsorption of CuO NPs onto activated sludge. The decrease in Live/dead ratio after 5 h of exposure of CuO NPs and Cu(2+) indicated the loss of cell viability in sludge flocs.

  17. Incorporation of copper ions into crystals of T2 copper-depleted laccase from Botrytis aclada

    Energy Technology Data Exchange (ETDEWEB)

    Osipov, E. M., E-mail: e.m.osipov@gmail.com [A. N. Bach Institute of Biochemistry, Leninsky pr. 33, Moscow 119071 (Russian Federation); Polyakov, K. M. [A. N. Bach Institute of Biochemistry, Leninsky pr. 33, Moscow 119071 (Russian Federation); Engelhardt Institute of Molecular Biology, Vavilova str. 32, Moscow 119991 (Russian Federation); Tikhonova, T. V. [A. N. Bach Institute of Biochemistry, Leninsky pr. 33, Moscow 119071 (Russian Federation); Kittl, R. [BOKU – University of Natural Resources and Life Sciences, Muthgasse 18, 1190 Wien (Austria); Dorovatovskii, P.V. [RSC ‘Kurchatov Institute’, Acad. Kurchatov sq. 1, Moscow 123182 (Russian Federation); Shleev, S. V.; Popov, V. O. [A. N. Bach Institute of Biochemistry, Leninsky pr. 33, Moscow 119071 (Russian Federation); RSC ‘Kurchatov Institute’, Acad. Kurchatov sq. 1, Moscow 123182 (Russian Federation); Ludwig, R. [BOKU – University of Natural Resources and Life Sciences, Muthgasse 18, 1190 Wien (Austria)

    2015-11-18

    The restoration of the native form of laccase from B. aclada from the type 2 copper-depleted form of the enzyme was investigated. Copper ions were found to be incorporated into the active site after soaking the depleted enzyme in a Cu{sup +}-containing solution. Laccases belong to the class of multicopper oxidases catalyzing the oxidation of phenols accompanied by the reduction of molecular oxygen to water without the formation of hydrogen peroxide. The activity of laccases depends on the number of Cu atoms per enzyme molecule. The structure of type 2 copper-depleted laccase from Botrytis aclada has been solved previously. With the aim of obtaining the structure of the native form of the enzyme, crystals of the depleted laccase were soaked in Cu{sup +}- and Cu{sup 2+}-containing solutions. Copper ions were found to be incorporated into the active site only when Cu{sup +} was used. A comparative analysis of the native and depleted forms of the enzymes was performed.

  18. Preparation and characterization of microgels sensitive toward copper II ions.

    Science.gov (United States)

    Muratalin, Marat; Luckham, Paul F

    2013-04-15

    An emulsion polymerization technique has been used to prepare chemically crosslinked microgels in aqueous suspension that are sensitive to the presence of copper ions. Poly(N-isopropylacrylamide) (PNIPAM) was copolymerized with different amounts of 1-vinylimidazole (VI), and the resultant microgels exhibited multi-responsive behavior being sensitive to changes in temperature, pH and to the presence of metal ions, particularly copper. These swelling properties of the microgel particles were characterized using dynamic light scattering (DLS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The effect of temperature showed that the microgel particles shrunk continuously as the temperature was raised, up to a temperature of 50°C, and the volume phase transition temperature, VPTT, has been shifted to higher temperatures (in the range of 35-45°C) compared to pure PNIPAM microgels where the VPTT≈30-35°C. The particle size of these microgels was also investigated as a function of pH; the microgel particles became swollen at low pH and collapsed at high pH, due to the ionization of the VI component of the microgels. Most interesting, however, was the effect of the copper ion concentration in solution. The PNIPAM-co-VI microgels were found to swell with increasing concentration of Cu(2+) up to 0.3g/l of Cu(2+) due to adsorption of the cations inside the particle, which leads to charging up the internal phase of the microgel. However, at higher concentrations of added copper (II) ions, the binding forces of complexation lead to conformational changes to the microgel resulting in weaker polymer-solvent interaction and consequential shrinkage again of the polymer. In addition, the copper (II) uptake was calculated, and the uptake was found to be well described by the Langmuir adsorption isotherm, with up to 2g of copper II being taken up by 1g of microgel. Copyright © 2013 Elsevier Inc. All rights reserved.

  19. Fundamental features of copper ion precipitation using sulfide as a precipitant in a wastewater system.

    Science.gov (United States)

    Choi, Jung-Yoon; Kim, Dong-Su; Lim, Joong-Yeon

    2006-01-01

    We have investigated the precipitation features of copper ion using sulfide as a precipitant by varying the mole ratio of sulfide to copper ion, pH, temperature and the kind and concentration of complexing agent. In the precipitation of copper ion by sulfide, sludge is produced as cupric sulfide; thus, there is a possibility for its recycled use in photochemical and ceramic processes. When the ratio of the concentration of copper ion to sulfide was increased to more than 1.0, the extent of precipitation was very high. As the ratio was increased, nucleation time was decreased and crystal growth rate was raised. The higher the pH, the greater the amount of precipitated copper ion due to lowered solubility of cupric sulfide. When temperature changed from 25 degrees C to 55 degrees C, the precipitation of copper ion was increased a little. On the basis of estimated thermodynamic parameters such as Gibbs free energy and enthalpy, the precipitation reaction was spontaneous and endothermic. The precipitation of copper ion was lowered in the presence of complexing agent and it was affected by the stability of the copper complex. The feasibility test for the application of precipitation treatment to actual wastewater containing copper ion showed, although there was a little decrease in the removal of copper, the precipitation extent of copper was higher than 90% compared with that for artificial wastewater.

  20. Copper ions inactivate S-ade-nosylhomocysteine hydrolase

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    S-adenosylhomocysteine (AdoHcy) hydrolase isan enzyme that regulates biomethylation and some otherphysiological processes. Recombinant AdoHcy hydrolase wasoverexpressed in E. coli JM109 and purified with ion ex-change and gel filtration chromatographies. The effects ofcopper ions (Cu2+) on the activity of AdoHcy hydrolase wereinvestigated and the results showed that Cu2+ inhibited theenzyme's activity by a concentration and time-dependentprocess. The inhibition constant (Ki) and the apparent rateconstant (kapp) were calculated to be (14 + 4) nmol @ L-1 and(1.08 + 0.15) min-1, respectively. The existence of the naturalsubstrate Ado could to some extent prevent Cu2+ from inac-tivating the enzyme, suggesting that copper ions possiblycould compete with the natural substrate on enzyme's sub-strate binding site. Further studies on the mechanism of in-hibition are being carried out.

  1. The role of copper ions in pathophysiology and fluorescent sensors for the detection thereof.

    Science.gov (United States)

    Verwilst, Peter; Sunwoo, Kyoung; Kim, Jong Seung

    2015-04-04

    Copper ions are indispensible to life and maintaining tight control over the homeostasis of copper ions in the body is a prerequisite to sustaining health. Aberrations in normal copper levels, both systemic as well as on a tissue or cellular scale, are implicated in a wide range of diseases, such as Menkes disease, Wilson's disease, Alzheimer's disease, Parkinson's disease and transmissible spongiform encephalopathy (prion diseases). The current understanding of how copper influences these diseases is described. The field of fluorescent copper sensors both functioning via a reaction based mechanism as well as by directly binding copper ions has known an inflation in recent years, and the importance of this field to elucidating the role of copper in cell biology is pointed out. Progress in these tightly interwoven fields has resulted in a better understanding of a number of diseases related to copper imbalances and current developments might open the path for novel and innovating therapies to address these diseases.

  2. Removal of adsorbent particles od copper ions by Jet flotation; Remocion de particulas adsorbentes de iones cobre por flotacion Jet

    Energy Technology Data Exchange (ETDEWEB)

    Santander, M.; Tapia, P.; Pavez, O.; Valderrama, L.; Guzman, D.

    2009-07-01

    The present study shows the results obtained on the removal of copper ions from synthetic effluents by using the adsorbent particles flotation technique (APF) in a Jet flotation cell (Jameson type). In a typical experimental run, a mineral with high quartz content was used as adsorbent particles in the adsorption and flotation experiments, to determine optimal pH conditions, adsorbent particles concentration; flotation reagents dosage and air/effluent flow ratio for applying in the Jet cell to maximize the efficiency of copper ions adsorptions and the removal of particles adsorbents containing the absorbed copper ions. The results indicate the at pH>7 and at adsorbent particles concentration of 2 kg.m{sup -}3, 99% of copper ions is adsorbed and, when the air/effluent flow ratio applied in the Jet cell is 0,2, 98% of absorbent particles containing the adsorbed copper ions is removed. (Author) 39 refs.

  3. The Mechanism of the Copper Ion Catalyzed Autoxidation of Cysteine in Alkaline Medium

    NARCIS (Netherlands)

    Koningsberger, D.C.; Zwart, J.; Wolput, J.H.M.C. van

    1981-01-01

    Quantitative e.s.r. measurements carried out during the copper catalysed alkaline autoxidation of cysteine show that the Cu(II)-dicysteine complex represents almost the total amount of copper. Only a small fraction (<2%) of the copper ions might be present in a state which is not detectable by e.s.r

  4. Texture coefficient analysis of ion beam irradiated copper nanowires

    Energy Technology Data Exchange (ETDEWEB)

    Rana, Pallavi, E-mail: prana.phy@gmail.com; Chaudhary, Ritika, E-mail: chauhanrpc@gmail.com; Chauhan, R. P. [Department of Physics, National Institute of Technology, Kurukshetra-136119 (India)

    2016-05-23

    Radiation may deteriorate physical properties of the materials and leave negative as well as positive impacts especially on crystalline materials. The energy deposited by ions to the grains and grain boundaries could also influence other properties of grains like: strain, reflection of charge carriers from grain boundaries, in addition to their grain size and orientation. The intensity of a peak in the XRD spectra is the direct reflection of orientation of a miller plane in the crystal. The increased intensity symbolizes the crystalline behavior due to defects annealing, while decreased intensity portray the defects formation and slender amorphisation. Orientation distribution function is a probability distribution function that quantified the texture of a polycrystalline material. The coefficients of harmonic expansion of orientation distribution function is the measurement of the texture coefficient ‘TC’. This study focused on the investigation of effect of ion beam irradiation on the preffered orientation of the planes of copper nanowires.

  5. SETUP AND PERFORMANCE OF THE RHIC INJECTOR ACCELERATORS FOR THE 2005 RUN WITH COPPER IONS.

    Energy Technology Data Exchange (ETDEWEB)

    AHRENS, L.; ALESSI, J.; GARDNER, C.J.

    2005-05-16

    Copper ions for the 2005 run [1] of the Relativistic Heavy Ion Collider (RHIC) at Brookhaven National Laboratory (BNL) are accelerated in the Tandem, Booster and AGS prior to injection into RHIC. The setup and performance of these accelerators with copper are reviewed in this paper.

  6. Investigation of peptide based surface functionalization for copper ions detection using an ultrasensitive mechanical microresonator

    DEFF Research Database (Denmark)

    Cagliani, Alberto; Fischer, Lee MacKenzie; Rasmussen, Jakob Lyager

    2011-01-01

    In the framework of developing a portable label-free sensor for multi arrayed detection of heavy metals in drinking water, we present a mechanical resonator-based copper ions sensor, which uses a recently synthesized peptide Cysteine–Glycine–Glycine–Histidine (CGGH) and the l-Cysteine (Cys) peptide...... devices to detect a concentration of 10μM of copper in water, we regenerate the surface by removing the copper ions from the functionalization layer using EDTA....

  7. Biosorption of copper (II) ions from synthetic aqueous solutions by drying bed activated sludge

    Energy Technology Data Exchange (ETDEWEB)

    Benaissa, H., E-mail: ho_benaissa@yahoo.fr [Laboratory of Sorbent Materials and Water Treatment, Department of Chemistry, Faculty of Sciences, University of Tlemcen, P.O. Box 119, 13000 Tlemcen (Algeria); Elouchdi, M.A. [Laboratory of Sorbent Materials and Water Treatment, Department of Chemistry, Faculty of Sciences, University of Tlemcen, P.O. Box 119, 13000 Tlemcen (Algeria)

    2011-10-30

    Highlights: {yields} Dried activated sludge has been investigated for the removal of copper ions from aqueous synthetic solutions, in batch conditions. {yields} Copper uptake was time contact, initial copper concentration, initial pH solution and copper salt type dependent. {yields} Maximum copper uptake obtained was q{sub m} = 62.50 mg/g (0.556 mmol/g) under the investigated experimental conditions. - Abstract: In the present work, the usefulness of dried activated sludge has been investigated for the removal of copper ions from synthetic aqueous solutions. Kinetic data and equilibrium sorption isotherm were measured in batch conditions. The influence of some parameters such as: contact time, initial copper concentration, initial pH of solution and copper salt nature on copper biosorption kinetics has been studied. Copper uptake was time contact, initial copper concentration, initial pH solution and copper salt type dependent. Maximum copper sorption was found to occur at initial pH 5. Two simplified kinetic models including a first-order rate equation and a pseudo second-order rate equation were selected to describe the biosorption kinetics. The process followed a pseudo second-order rate kinetics. The process mechanism was found to be complex, consisting of external mass transfer and intraparticle mass transfer diffusion. Copper biosorption process was particle-diffusion-controlled, with some predominance of some external mass transfer at the initial stages for the different experimental parameters studied. Langmuir and Freundlich models were used to describe sorption equilibrium data at natural pH of solution. Results indicated that the Langmuir model gave a better fit to the experimental data than the Freundlich model. Maximum copper uptake obtained was q{sub m} = 62.50 mg/g (0.556 mmol/g) under the investigated experimental conditions. Scanning electron microscopy coupled with X-ray energy dispersed analysis for copper-equilibrated dried activated sludge

  8. Correlation between Copper Ion Concentration in Cervical Mucus and Fllbrinolytic Activity in Menstrual Blood in Copper-releasiag IUD Users

    Institute of Scientific and Technical Information of China (English)

    林建华; 潘家骧; 严隽鸿

    1993-01-01

    In the present study, 44 women using TCu220c-IUD or inert-IUD were asked to make follow-ups before insertion and at the 1st., 3rd., 6th, 9th and 12th month after insertion The mean menstrual blood loss, the fibrinalytic activity including the activation of tissue-plasminogen activator (t-PA) and the amount of plasminogen PIG) and fibrinogen-fibrin degradation products (FDP) in menstrual blood and the copper ion concentration in cervical mucus were determined. The correlation between the copper ion concentration and the fibrinalytic activity was considered. It was found that the change of the copper ion concentration was positively correlated with that of the activition of t-PA and the amount of FDP. On the contrary, the change ofthe copper ion concentration was inversely related to the change of PLG value. It is concluded that the high copper ion level can enhance the activation of fibrinolytic system in human endometrium and induce the increase of menorrhagia.

  9. Efficient electron-induced removal of oxalate ions and formation of copper nanoparticles from copper(II oxalate precursor layers

    Directory of Open Access Journals (Sweden)

    Kai Rückriem

    2016-06-01

    Full Text Available Copper(II oxalate grown on carboxy-terminated self-assembled monolayers (SAM using a step-by-step approach was used as precursor for the electron-induced synthesis of surface-supported copper nanoparticles. The precursor material was deposited by dipping the surfaces alternately in ethanolic solutions of copper(II acetate and oxalic acid with intermediate thorough rinsing steps. The deposition of copper(II oxalate and the efficient electron-induced removal of the oxalate ions was monitored by reflection absorption infrared spectroscopy (RAIRS. Helium ion microscopy (HIM reveals the formation of spherical nanoparticles with well-defined size and X-ray photoelectron spectroscopy (XPS confirms their metallic nature. Continued irradiation after depletion of oxalate does not lead to further particle growth giving evidence that nanoparticle formation is primarily controlled by the available amount of precursor.

  10. Copper ion-exchanged channel waveguides optimization for optical trapping.

    Science.gov (United States)

    Reshak, A H; Khor, K N; Shahimin, M M; Murad, S A Z

    2013-08-01

    Optical trapping of particles has become a powerful non-mechanical and non-destructive technique for precise particle positioning. The manipulation of particles in the evanescent field of a channel waveguide potentially allows for sorting and trapping of several particles and cells simultaneously. Channel waveguide designs can be further optimized to increase evanescent field prior to the fabrication process. This is crucial in order to make sure that the surface intensity is sufficient for optical trapping. Simulation configurations are explained in detail with specific simulation flow. Discussion on parameters optimization; physical geometry, optical polarization and wavelength is included in this paper. The effect of physical, optical parameters and beam spot size on evanescent field has been thoroughly discussed. These studies will continue toward the development of a novel copper ion-exchanged waveguide as a method of particle sorting, with biological cell propulsion studies presently underway.

  11. Morphology of gold and copper ion-plated coatings

    Science.gov (United States)

    Spalvins, T.

    1978-01-01

    Copper and gold films (0.2 to 2 microns thick) were ion plated onto polished 304-stainless-steel, glass, mica surfaces. These coatings were examined by SEM for defects in their morphological growth. Three types of defects were distinguished: nodular growth, abnormal or runaway growth, and spits. The cause for each type of defect was investigated. Nodular growth is due to inherent substrate microdefects, abnormal or runaway growth is due to external surface inclusions, and spits are due to nonuniform evaporation (ejection of droplets). All these defects induce stresses and produce porosity in the coatings and thus weaken their mechanical properties. During surface rubbing, large nodules are pulled out, leaving vacancies in the coatings.

  12. Copper electrodeposition from cuprous chloride solutions containing lead, zinc or iron ions

    Institute of Scientific and Technical Information of China (English)

    M. Tchoumou; M. Roynette Ehics

    2005-01-01

    Cuprous chloride hydrochloric acid solutions were electrolysed in a two compartments cell without agitation for copper extraction. It is found that the current density affects the colour and the size of copper deposits. During electrodeposition of copper from cuprous solution in the presence of various concentrations of lead, zinc or iron ions at different current densities, it is observed that lead is codeposited with copper by increasing current density.In all experiments, the current efficiency for the copper deposition reaction fluctuates between 88.50% and 95.50%.

  13. Als1 and Als3 regulate the intracellular uptake of copper ions when Candida albicans biofilms are exposed to metallic copper surfaces.

    Science.gov (United States)

    Zheng, Sha; Chang, Wenqiang; Li, Chen; Lou, Hongxiang

    2016-05-01

    Copper surfaces possess efficient antimicrobial effect. Here, we reported that copper surfaces could inactivate Candida albicans biofilms within 40 min. The intracellular reactive oxygen species in C. albicans biofilms were immediately stimulated during the contact of copper surfaces, which might be an important factor for killing the mature biofilms. Copper release assay demonstrated that the copper ions automatically released from the surface of 1 mm thick copper coupons with over 99.9% purity are not the key determinant for the copper-mediated killing action. The susceptibility test to copper surfaces by using C. albicans mutant strains, which were involved in efflux pumps, adhesins, biofilms formation or osmotic stress response showed that als1/als1 and als3/als3 displayed higher resistance to the copper surface contact than other mutants did. The intracellular concentration of copper ions was lower in als1/als1 and als3/als3 than that in wild-type strain. Transcriptional analysis revealed that the expression of copper transporter-related gene, CRP1, was significantly increased in als1/als1, als3/als3, suggesting a potential role of ALS1 and ALS3 in absorbing ions by regulating the expression of CRP1 This study provides a potential application in treating pathogenic fungi by using copper surfaces and uncovers the roles of ALS1 and ALS3 in absorbing copper ions for C. albicans.

  14. A new copper containing MALDI matrix that yields high abundances of [peptide + Cu]+ ions.

    Science.gov (United States)

    Wu, Zhaoxiang; Fernandez-Lima, Francisco A; Perez, Lisa M; Russell, David H

    2009-07-01

    The dinuclear copper complex (alpha-cyano-4-hydroxycinnamic acid (CHCA) copper salt (CHCA)(4)Cu(2)), synthesized by reacting CHCA with copper oxide (CuO), yields increased abundances of [M + xCu - (x-1)H](+) (x = 1-6) ions when used as a matrix for matrix-assisted laser desorption ionization (355 nm Nd:YAG laser). The yield of [M + xCu - (x-1)H](+) (x = 1 to approximately 6) ion is much greater than that obtained by mixing peptides with copper salts or directly depositing peptides onto oxidized copper surfaces. The increased ion yields for [M + xCu - (x-1)H](+) facilitate studies of biologically important copper binding peptides. For example, using this matrix we have investigated site-specific copper binding of several peptides using fragmentation chemistry of [M + Cu](+) and [M + 2Cu - H](+) ions. The fragmentation studies reveal interesting insight on Cu binding preferences for basic amino acids. Most notable is the fact that the binding of a single Cu(+) ion and two Cu(+) ions are quite different, and these differences are explained in terms of intramolecular interactions of the peptide-Cu ionic complex.

  15. Effects of Excess Copper Ions on Decidualization of Human Endometrial Stromal Cells.

    Science.gov (United States)

    Li, Ying; Kang, Zhen-Long; Qiao, Na; Hu, Lian-Mei; Ma, Yong-Jiang; Liang, Xiao-Huan; Liu, Ji-Long; Yang, Zeng-Ming

    2017-05-01

    The aim of this study was to investigate the effects of copper ions on decidualization of human endometrial stromal cells (HESCs) cultured in vitro. Firstly, non-toxic concentrations of copper D-gluconate were screened in HESCs based on cell activity. Then, the effects of non-toxic concentrations of copper ions (0~250 μM) were examined on decidualization of human endometrial stromal cells. Our data demonstrated that the mRNA expressions of insulin-like growth factor binding protein (IGFBP-1), prolactin (PRL), Mn-SOD, and FOXO1were down-regulated during decidualization following the treatments with 100 or 250 μM copper ions. Meanwhile, the amount of malonaldehyde (MDA) in the supernatant of HESCs was increased. These results showed that in vitro decidualization of HESCs was impaired by copper treatment.

  16. Kinetics of copper ion absorption by cross-linked calcium polyacrylate membranes

    Science.gov (United States)

    Philipp, W. H.; May, C. E.

    1983-01-01

    The absorption of copper ions from aqueous copper acetate solutions by cross-linked calcium acrylate membranes was found to obey parabolic kinetics similar to that found for oxidation of metals that form protective oxide layers. For pure calcium polyacrylate membranes the rate constant was essentially independent of copper acetate concentration and film thickness. For a cross-linked copolymer film of polyvinyl alcohol and calcium polyacrylate, the rate constant was much greater and dependent on the concentration of copper acetate. The proposed mechanism in each case involves the formation of a copper polyacrylate phase on the surface of the membrane. The diffusion of the copper ion through this phase appears to be the rate controlling step for the copolymer film. The diffusion of the calcium ion is apparently the rate controlling step for the calcium polyacrylate. At low pH, the copper polyacrylate phase consists of the normal copper salt; at higher pH, the phase appears to be the basic copper salt.

  17. Copper diffusivity in boron-doped silicon wafer measured by dynamic secondary ion mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Koh, Songfoo [S.E.H (M) Sdn. Bhd., Lot 2, Lorong Enggang 35, Ulu Klang FTZ, 54200 Selangor (Malaysia); You, Ahheng [Faculty of Engineering and Technology, Multimedia University, Jalan Ayer Keroh Lama, Bukit Beruang, 75450 Melaka (Malaysia); Tou, Teckyong, E-mail: tytou@mmu.edu.my [Faculty of Engineering, Multimedia Univesity, Jalan Multimedia, 63100 Cyberjaya (Malaysia)

    2013-03-20

    Highlights: ► Effective copper diffusivity in boron-doped silicon wafer was measured. ► Dynamic secondary ion mass spectrometry was used. ► Interstitial copper ions were first drifted to surface region and allowed to back-diffuse. ► Boron concentration largely influenced the effect copper diffusivity. -- Abstract: The effective copper diffusivity (D{sub eff}) in boron-doped silicon wafer was measured using a Dynamic Secondary Ion Mass Spectrometry (D-SIMS) that was incorporated with an out-drift technique. By this technique, positive interstitial copper ions (Cu{sub I}{sup +}) migrated to the surface region when a continuous charge of electrons showered on the oxidized silicon wafer, which was also bombarded by primary O{sub 2}{sup +} ions. The Cu{sub I}{sup +} ions at the surface region diffused back to the bulk when the electron showering stopped. The D-SIMS recorded the real-time distribution of Cu{sub I}{sup +} ions, generating depth profiles for in-diffusion of copper for silicon-wafer samples with different boron concentrations. These were curve-fitted using the standard diffusion expressions to obtain different D{sub eff} values, and compared with other measurement techniques.

  18. Studying the Adsorption Behavior of Copper Ions in Industrial Wastewater, Using Modified Electrospun Polymeric Nano Fiber

    Directory of Open Access Journals (Sweden)

    Davood Kaviani

    2016-09-01

    Full Text Available Background & Aims of the Study:  Soil and water pollution to heavy metals is a serious threat for environment and human health. Finding an effective way for refining water from these metals is very important. The aim of this study was modifying electrospun polymeric nano fibers and studying its efficiency for copper ion omission in water solutions. Materials & Methods: In this study, nano fiber was produced by solution electrospun polystyrene in DMF/THF solvent and produced nano fiber was used for copper pre-concentration in waste water sample. In this study, an investigation of primary PH of solution, adsorption particle size, cleaning solvent volume, salt supply, contact time duration of adsorption material on copper ion adsorption supply was done, using modified nano fiber. Results: According to this study, copper adsorption process with correlation coefficient of (R2 in scope of 0.986 by Langmuir and Freundlich are describable. Findings show that, pH optimized amount for isolating copper ion on absorbent level is 7, absorbent particle size is 0.006 g/l, salt 1.3, potassium nitrate and the contact time of absorbent material on copper ion adsorption is 10 minutes. Copper ion adsorbate was cleaned, using 0.7 ml methanol. Most of obtrusive ions didn't have any inconvenience for copper ion isolation and measuring. The mean of the method was 2.7 µg/l and standard deviation was lower than %4. Conclusions: this method was done on actual samples which findings show that, this method has the ability of cooper adsorption and can use this method for measuring heavy metals like copper in different tissues. This method because of having the privilege for isolating and pre concentrating different kind of mineral and organic is used successfully in different samples.

  19. Bioactive and Antibacterial Glass Powders Doped with Copper by Ion-Exchange in Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Marta Miola

    2016-05-01

    Full Text Available In this work, two bioactive glass powders (SBA2 and SBA3 were doped with Cu by means of the ion-exchange technique in aqueous solution. SBA2 glass was subjected to the ion-exchange process by using different Cu salts (copper(II nitrate, chloride, acetate, and sulphate and concentrations. Structural (X-ray diffraction-XRD, morphological (Scanning Electron Microscopy-SEM, and compositional (Energy Dispersion Spectrometry-EDS analyses evidenced the formation of crystalline phases for glasses ion-exchanged in copper(II nitrate and chloride solutions; while the ion-exchange in copper(II acetate solutions lead to the incorporation of higher Cu amount than the ion-exchange in copper(II sulphate solutions. For this reason, the antibacterial test (inhibition halo towards S. aureus was performed on SBA2 powders ion-exchanged in copper(II acetate solutions and evidenced a limited antibacterial effect. A second glass composition (SBA3 was developed to allow a greater incorporation of Cu in the glass surface; SBA3 powders were ion-exchanged in copper(II acetate solutions (0.01 M and 0.05 M. Cu-doped SBA3 powders showed an amorphous structure; morphological analysis evidenced a rougher surface for Cu-doped powders in comparison to the undoped glass. EDS and X-ray photoelectron spectroscopy (XPS confirmed the Cu introduction as Cu(II ions. Bioactivity test in simulated body fluid (SBF showed that Cu introduction did not alter the bioactive behaviour of the glass. Finally, inhibition halo test towards S. aureus evidenced a good antimicrobial effect for glass powders ion-exchanged in copper(II acetate solutions 0.05 M.

  20. Effective inhibition of the early copper ion burst release with ultra-fine grained copper and single crystal copper for intrauterine device application.

    Science.gov (United States)

    Xu, X X; Nie, F L; Wang, Y B; Zhang, J X; Zheng, W; Li, L; Zheng, Y F

    2012-02-01

    To solve the main problems of existing coarse grained copper (CG Cu) intrauterine devices (IUD)-namely burst release and a low transfer efficiency of the cupric ions during usage-ultra-fine grained copper (UFG Cu) and single crystal copper (SC Cu) have been investigated as potential substitutes. Their corrosion properties with CG Cu as a control have been studied in simulated uterine fluid (SUF) under different conditions using electrochemical measurement methods. Long-term immersion of UFG Cu, SC Cu and CG Cu samples in SUF at 37 °C have been studied for 300 days. A lower copper ion burst release and a higher efficiency release of cupric ions were observed for UFG Cu and SC Cu compared with CG Cu in the first month of immersion and 2 months later. The respective corrosion mechanisms for UFG Cu, SC Cu and CG Cu in SUF are proposed. In vitro biocompatibility tests show a better cellular response to UFG Cu and SC Cu than CG Cu. In terms of instantaneous corrosion behavior, long-term corrosion performance and in vitro biocompatibility, the three pure copper materials follow the order: UFG Cu>SC Cu>CG Cu, which indicates that UFG Cu could be the most suitable candidate material for intrauterine devices.

  1. Recovery of copper ion by flotation with potassium amylxanthate; Recuperacion de iones cobre por flotacion con amilxantato de potasio

    Energy Technology Data Exchange (ETDEWEB)

    Ramirez-Serrano, B.; Coello-Velazquez, A. L.; Bernardo, A.; Afif, E.; Menendez-Aguado, J. M.

    2012-11-01

    In this paper a study about the column flotation process of copper ion employing potassium amylxanthate as collector reagent is carried out. The effect on the recovery of copper ion by the modification of variables such as collector/metal relation and surface velocity of gas and liquid was determined experimentally by the analysis of the statistic-mathematical model of the copper flotation process, as well as the physico-chemical phenomena that take place, showing the effect of the collector/metal relation in the process. The effect of pH as the main properties of the chemical system in the recovery and the kinetic of the flotation process is made too. The experimental results shows that the recovery of copper in the pH range of 4,5 - 12 is possible with prevalence of precipitate flotation. (Author) 43 refs.

  2. Electrochemical removal of copper ions from dilute solutions using packed bed electrode. Part ІІ

    Directory of Open Access Journals (Sweden)

    I.A. Khattab

    2013-06-01

    Full Text Available Conversion of soluble precious copper ions into a solid form in dilute wastewater effluents for further reuse was studied by using a packed-bed cell. The cathode packing consisted of graphite particles that have an average particle size of 0.125 cm. The effects of electrolysis time and initial copper concentration were studied. The cell was found to be effective in reducing metal ion concentration to less than 0.05% of the initial concentration and maximum current efficiency reached upto 96.2% for dilute copper solution (100 mg/l. It was observed that using this cell was effective in reducing copper ion concentration from 100 mg/l to less than 4 mg/l.

  3. Magnetic Interactions in the Copper Complex (L-Aspartato)(1,10-phenanthroline)copper(II) Hydrate. An Exchange-Coupled Extended System with Two Dissimilar Copper Ions.

    Science.gov (United States)

    Brondino, Carlos D.; Calvo, Rafael; Atria, Ana María; Spodine, Evgenia; Nascimento, Otaciro R.; Peña, Octavio

    1997-07-02

    We report EPR measurements in single-crystal samples at the microwave frequencies 9.8 and 34.3 GHz and magnetic susceptibility measurements in polycrystalline samples for the ternary complex of copper with aspartic acid and phenanthroline, (L-aspartato)(1,10-phenanthroline)copper(II) hydrate. The crystal lattice of this compound is composed of two dissimilar copper ions identified as Cu(A) and Cu(B), which are in two types of copper chains called A and B, respectively, running parallel to the b crystal axis. The copper ions in the A chains are connected by the aspartic acid molecule, and those in the B chains by a chemical path that involves a carboxylate bridge and a hydrogen bond. Both chains are held together by a complex network of hydrogen bonds and by hydrophobic interactions between aromatic amines. Magnetic susceptibility data indicate a Curie-Weiss behavior in the studied temperature range (2-300 K). The EPR spectra at 9.8 GHz display a single exchange collapsed resonance for any magnetic field orientation, in the so-called strong exchange regime. Those at 34.3 GHz are within the so-called weak exchange regime and display two resonances which belong to each type of copper ion chain. The decoupling of the spectra at 34.3 GHz using a theory based on Anderson's model for the case of two weakly exchange coupled spins S = (1)/(2) allows one to obtain the angular variation of the squares of the g-factor and the peak-to-peak line width of each resonance. This model also allows one to evaluate the exchange parameter |J(AB)/k| = 2.7(6) mK associated with the chemical path connecting dissimilar copper ions. The line width data obtained for each component of the spectra at 34.3 GHz are analyzed in terms of a model based on Kubo and Tomita's theory, to obtain the exchange parameters |J(A)/k| = 0.77(2) K and |J(B)/k| = 1.44(2) K associated with the chemical paths connecting the similar copper ions of types A and B, respectively.

  4. Mixed matrix membranes for efficient adsorption of copper ions from aqueous solutions

    NARCIS (Netherlands)

    Tetala, K.K.R.; Stamatialis, Dimitrios

    2013-01-01

    This work presents adsorption of copper (Cu2+) ions from aqueous solutions using mixed matrix membrane (MMM) and its elution afterwards. The developed flat sheet MMM, comprises of chitosan beads incorporated in Ethylene vinyl alcohol (EVAL) polymer porous matrix and exhibits static Cu2+ ion

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

    Science.gov (United States)

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

    2014-07-15

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

  6. Effect of Lithium Ions on Copper Nanoparticle Size, Shape, and Distribution

    Directory of Open Access Journals (Sweden)

    Kyung-Deok Jang

    2012-01-01

    Full Text Available Copper nanoparticles were synthesized using lithium ions to increase the aqueous electrical conductivity of the solution and precisely control the size, shape, and size distribution of the particles. In this study, the conventional approach of increasing particle size by the concentration of copper ions and PGPPE in a copper chloride solution was compared to increasing the concentration of lithium chloride when the copper chloride concentration was held constant. Particle size and shape were characterized by TEM, and the size distribution of the particles at different concentrations was obtained by particle size analysis. Increasing the concentration of copper ion in the solution greatly increased the aqueous electric conductivity and the size of the particles but led to a wide size distribution ranging from 150 nm to 400 nm and rough particle morphology. The addition of lithium ions increased the size of the particles, but maintains them in a range of 250 nm. In addition the particles exhibited spherical shape as determined by TEM. The addition of lithium ions to the solution has the potential to synthesize nanoparticles with optimal characteristics for printing applications by maintaining a narrow size range and spherical shape.

  7. [Electrooptical properties of soil nitrogen-fixing bacterium Azospirillum brasilense: effect of copper ions].

    Science.gov (United States)

    Ignatov, O V; Kamnev, A A; Markina, L N; Antoniuk, L P; Kolina, M; Ignatov, V V

    2001-01-01

    The effects of copper ions on the uptake of some essential metals in the biomass and the electrooptical properties of cell suspensions of the nitrogen-fixing soil bacterium Azospirillum brasilense sp. 245 were studied. Copper cations were shown to be effectively taken up by the cell biomass from the culture medium. The addition of copper ions increased the rate of uptake of some other metals present in the culture medium. This was accompanied by changes in the electrooptical characteristics of cell suspension as measured within the orienting electric field frequency range of 10 to 10,000 kHz. The effects observed during short-term incubation of A. brasilense in the presence of copper cations were less significant than during long-term incubation. These results can be used for rapid screening of microbial cultures for enhanced efficiency of sorption and uptake of metals.

  8. Determination of copper(I) and copper(II) ions after complexation with bicinchoninic acid by CE.

    Science.gov (United States)

    Basheer, Chanbasha; Lee, Hian Kee

    2007-10-01

    A facile, sensitive, and selective method was developed for the simultaneous separation and determination of copper(I) [Cu(+)] and copper(II) [Cu(2+)] ions using CE with direct UV detection. The copper ions were complexed with a 1.5 mM bicinchoninic acid disodium salt solution at pH 8.7 prior to analysis. Acetate buffer (2 mM) was used as the CE running buffer. Parameters affecting CE separation such as sample pH, applied voltage, concentration of complexing agent, nature of the buffer solution, and interferences by other metal ions, were evaluated. The LODs for Cu(+) and Cu(2+) were 3.0 and 2.5 microg/mL (S/N = 3), respectively. The developed method allows the simultaneous determination of Cu(+) and Cu(2+) in less than 5 min with RSDs of between 5.3 and 9.5% for migration time and between 3.4 and 9.7% for peak areas, respectively. At optimum conditions, the percentage recoveries of Cu(+) and Cu(2+) were found to be 99.4 and 99.5%.

  9. Evaluation of copper ion of antibacterial effect on Pseudomonas aeruginosa, Salmonella typhimurium and Helicobacter pylori and optical, mechanical properties

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Young-Hwan [School of Materials Science and Engineering, University of Yonsei, Seoul (Korea, Republic of); Choi, Yu-ri; Kim, Kwang-Mahn [Department and Research Institute of Dental Biomaterials and Bioengineering, College of Dentistry, University of Yonsei, Seoul (Korea, Republic of); Choi, Se-Young, E-mail: sychoi@yonsei.ac.kr [School of Materials Science and Engineering, University of Yonsei, Seoul (Korea, Republic of)

    2012-02-01

    Antibacterial effect on Pseudomonas aeruginosa, Salmonella typhimurium and Helicobacter pylori of copper ion was researched. Also, additional effects of copper ion coating on optical and mechanical properties were researched as well. Copper ion was coated on glass substrate as a thin film to prevent bacteria from growing. Cupric nitrate was used as precursors for copper ion. The copper ion contained sol was deposited by spin coating process on glass substrate. Then, the deposited substrates were heat treated at the temperature range between 200 Degree-Sign C and 250 Degree-Sign C. The thickness of deposited copper layer on the surface was 63 nm. The antibacterial effect of copper ion coated glass on P. aeruginosa, S. typhimurium and H. pylori demonstrated excellent effect compared with parent glass. Copper ion contained layer on glass showed a similar value of transmittance compared with value of parent glass. The 3-point bending strength and Vickers hardness were 209.2 MPa, 540.9 kg/mm{sup 2} which were about 1.5% and 1.3% higher than the value of parent glass. From these findings, it is clear that copper ion coating on glass substrate showed outstanding effect not only in antibacterial activity but also in optical and mechanical properties as well.

  10. Evaluation of copper ion of antibacterial effect on Pseudomonas aeruginosa, Salmonella typhimurium and Helicobacter pylori and optical, mechanical properties

    Science.gov (United States)

    Kim, Young-Hwan; Choi, Yu-ri; Kim, Kwang-Mahn; Choi, Se-Young

    2012-02-01

    Antibacterial effect on Pseudomonas aeruginosa, Salmonella typhimurium and Helicobacter pylori of copper ion was researched. Also, additional effects of copper ion coating on optical and mechanical properties were researched as well. Copper ion was coated on glass substrate as a thin film to prevent bacteria from growing. Cupric nitrate was used as precursors for copper ion. The copper ion contained sol was deposited by spin coating process on glass substrate. Then, the deposited substrates were heat treated at the temperature range between 200 °C and 250 °C. The thickness of deposited copper layer on the surface was 63 nm. The antibacterial effect of copper ion coated glass on P. aeruginosa, S. typhimurium and H. pylori demonstrated excellent effect compared with parent glass. Copper ion contained layer on glass showed a similar value of transmittance compared with value of parent glass. The 3-point bending strength and Vickers hardness were 209.2 MPa, 540.9 kg/mm2 which were about 1.5% and 1.3% higher than the value of parent glass. From these findings, it is clear that copper ion coating on glass substrate showed outstanding effect not only in antibacterial activity but also in optical and mechanical properties as well.

  11. SOURCES OF COPPER IONS AND SELECTED METHODS OF THEIR REMOVAL FROM WASTEWATER FROM THE PRINTED CIRCUITS BOARD PRODUCTION

    Directory of Open Access Journals (Sweden)

    Maciej Thomas

    2014-10-01

    Full Text Available This paper presents the issues related to the presence and removal of copper compounds from industrial effluents with including wastewater from plants involved in the production of printed circuit boards. Characterized the toxicological properties of selected copper compounds, described the applicable technological processes, sources of copper ions in the effluents and selected methods for their removal.

  12. Combined effects of water temperature and copper ion concentration on catalase activity in Crassostrea ariakensis

    Science.gov (United States)

    Wang, Hui; Yang, Hongshuai; Liu, Jiahui; Li, Yanhong; Liu, Zhigang

    2015-07-01

    A central composite experimental design and response surface method were used to investigate the combined effects of water temperature (18-34°C) and copper ion concentration (0.1-1.5 mg/L) on the catalase (CAT) activity in the digestive gland of Crassostrea ariakensis. The results showed that the linear effects of temperature were significant ( P0.05), and the quadratic effects of copper ion concentration were significant ( P0.05), and the effect of temperature was greater than that of copper ion concentration. A model equation of CAT enzyme activity in the digestive gland of C. ariakensis toward the two factors of interest was established, with R 2, Adj. R 2 and Pred. R 2 values as high as 0.943 7, 0.887 3 and 0.838 5, respectively. These findings suggested that the goodness of fit to experimental data and predictive capability of the model were satisfactory, and could be practically applied for prediction under the conditions of the study. Overall, the results suggest that the simultaneous variation of temperature and copper ion concentration alters the activity of the antioxidant enzyme CAT by modulating active oxygen species metabolism, which may be utilized as a biomarker to detect the effects of copper pollution.

  13. Simultaneous removal of copper and lead ions from a binary solution by sono-sorption process

    Energy Technology Data Exchange (ETDEWEB)

    Entezari, M.H. [Department of Chemistry, Ferdowsi University of Mashhad, 91775 Mashhad (Iran, Islamic Republic of)], E-mail: moh_entezari@yahoo.com; Soltani, T. [Department of Chemistry, Ferdowsi University of Mashhad, 91775 Mashhad (Iran, Islamic Republic of)

    2008-12-15

    The aim of this work is to compare the simultaneous sorption of copper and lead ions from a binary aqueous solution in the presence and in the absence of ultrasound. The experiments under sonication were carried out by 20-kHz apparatus. Results indicated that the removal of copper and lead ions from a binary aqueous solution was greater in the presence of ultrasound than in control method. The removal of these ions was examined by varying experimental conditions such as the amount of sorbent, contact time, and temperature. In addition, the competitive sorption of ions was considered with different concentrations of each ion under the constant total concentration. The Langmuir isotherm model fits adequately the experimental data. In point of kinetics, the second-order kinetic model describes the sorption process for both ions. It was found that more than 90% of the lead and 60% of the copper ions was removed in less than 2 min from the solution under sonication. The thermodynamic parameters such as {delta}G{sup o}, {delta}H{sup o}, and {delta}S{sup o} were determined for the sorption of Cu{sup 2+} and Pb{sup 2+} from the temperature dependence of the sorption process.

  14. Biosorption effects of copper ions on Candida utilis under negative pressure cavitation

    Institute of Scientific and Technical Information of China (English)

    ZU Yuan-gang; ZHAO Xiu-hua; HU Mao-sheng; REN Yuan; XIAO Peng; ZHU Lei; CAO Yu-jie; ZHANG Yao

    2006-01-01

    Under the optimal condition of copper ions adsorption on yeast, we found some different effects among static adsorption,shaking adsorption and negative pressure cavitation adsorption, and the methods of yeast with different pretreatments also affect adsorption of copper ions. At the same time, the change of intercellular pH before and after adsorption of copper with BCECF was studied. The copper distribution was located by using PhenGreen (dipotassium salt and diacetate), and the surface of yeast was observed by an atomic force microscope. The results showed that negative pressure cavitation can improve bioadsorption capacity of copper ions on yeast. However, the yeasts' pretreatment has a higher effect on bioadsorption. It indicates that heavy metal bioadsorption on yeast has much relation with its cellular molecule basis. With the adsorping, the intercellular pH of yeast increased gradually and changed from acidity to alkalescence. These results may suggest that negative pressure cavitation can compel heavy metals to transfer from the cell surface into inside cell and make the surface of yeast coarse.

  15. Development of a four-zone carousel process packed with metal ion-imprinted polymer for continuous separation of copper ions from manganese ions, cobalt ions, and the constituent metal ions of the buffer solution used as eluent.

    Science.gov (United States)

    Jo, Se-Hee; Park, Chanhun; Yi, Sung Chul; Kim, Dukjoon; Mun, Sungyong

    2011-08-19

    A three-zone carousel process, in which Cu(II)-imprinted polymer (Cu-MIP) and a buffer solution were employed as adsorbent and eluent respectively, has been developed previously for continuous separation of Cu²⁺ (product) from Mn²⁺ and Co²⁺ (impurities). Although this process was reported to be successful in the aforementioned separation task, the way of using a buffer solution as eluent made it inevitable that the product stream included the buffer-related metal ions (i.e., the constituent metal ions of the buffer solution) as well as copper ions. For a more perfect recovery of copper ions, it would be necessary to improve the previous carousel process such that it can remove the buffer-related metal ions from copper ions while maintaining the previous function of separating copper ions from the other 2 impure heavy-metal ions. This improvement was made in this study by proposing a four-zone carousel process based on the following strategy: (1) the addition of one more zone for performing the two-step re-equilibration tasks and (2) the use of water as the eluent of the washing step in the separation zone. The operating conditions of such a proposed process were determined on the basis of the data from a series of single-column experiments. Under the determined operating conditions, 3 runs of carousel experiments were carried out. The results of these experiments revealed that the feed-loading time was a key parameter affecting the performance of the proposed process. Consequently, the continuous separation of copper ions from both the impure heavy-metal ions and the buffer-related metal ions could be achieved with a purity of 91.9% and a yield of 92.8% by using the proposed carousel process based on a properly chosen feed-loading time.

  16. Metal ions to control the morphology of semiconductor nanoparticles: copper selenide nanocubes.

    Science.gov (United States)

    Li, Wenhua; Zamani, Reza; Ibáñez, Maria; Cadavid, Doris; Shavel, Alexey; Morante, Joan Ramon; Arbiol, Jordi; Cabot, Andreu

    2013-03-27

    Morphology is a key parameter in the design of novel nanocrystals and nanomaterials with controlled functional properties. Here, we demonstrate the potential of foreign metal ions to tune the morphology of colloidal semiconductor nanoparticles. We illustrate the underlying mechanism by preparing copper selenide nanocubes in the presence of Al ions. We further characterize the plasmonic properties of the obtained nanocrystals and demonstrate their potential as a platform to produce cubic nanoparticles with different composition by cation exchange.

  17. Copper ions stimulate the proliferation of hepatic stellate cells via oxygen stress in vitro.

    Science.gov (United States)

    Xu, San-qing; Zhu, Hui-yun; Lin, Jian-guo; Su, Tang-feng; Liu, Yan; Luo, Xiao-ping

    2013-02-01

    This study examined the effect of copper ions on the proliferation of hepatic stellate cells (HSCs) and the role of oxidative stress in this process in order to gain insight into the mechanism of hepatic fibrosis in Wilson's disease. LX-2 cells, a cell line of human HSCs, were cultured in vitro and treated with different agents including copper sulfate, N-acetyl cysteine (NAC) and buthionine sulfoximine (BSO) for different time. The proliferation of LX-2 cells was measured by non-radioactive cell proliferation assay. Real-time PCR and Western blotting were used to detect the mRNA and protein expression of platelet-derived growth factor receptor β subunit (PDGFβR), ELISA to determine the level of glutathione (GSH) and oxidized glutathione (GSSG), dichlorofluorescein assay to measure the level of reactive oxygen species (ROS), and lipid hydroperoxide assay to quantify the level of lipid peroxide (LPO). The results showed that copper sulfate over a certain concentration range could promote the proliferation of LX-2 cells in a time- and dose-dependent manner. The effect was most manifest when LX-2 cells were treated with copper sulfate at a concentration of 100 μmol/L for 24 h. Additionally, copper sulfate could dose-dependently increase the levels of ROS and LPO, and decrease the ratio of GSH/GSSG in LX-2 cells. The copper-induced increase in mRNA and protein expression of PDGFβR was significantly inhibited in LX-2 cells pre-treated with NAC, a precursor of GSH, and this phenomenon could be reversed by the intervention of BSO, an inhibitor of NAC. It was concluded that copper ions may directly stimulate the proliferation of HSCs via oxidative stress. Anti-oxidative stress therapies may help suppress the copper-induced activation and proliferation of HSCs.

  18. Biodynamics of copper oxide nanoparticles and copper ions in an oligochaete, Part I

    DEFF Research Database (Denmark)

    Ramskov, Tina; Thit, Amalie; Croteau, Marie-Noelle

    2015-01-01

    Copper oxide (CuO) nanoparticles (NPs) are widely used, and likely released into the aquatic environment. Both aqueous (i.e., dissolved Cu) and particulate Cu can be taken up by organisms. However, how exposure routes influence the bioavailability and subsequent toxicity of Cu remains largely...

  19. Copper ions removal from water using functionalized carbon nanotubes–mullite composite as adsorbent

    Energy Technology Data Exchange (ETDEWEB)

    Tofighy, Maryam Ahmadzadeh; Mohammadi, Toraj, E-mail: torajmohammadi@iust.ac.ir

    2015-08-15

    Highlights: • CNTs–mullite composite was prepared via chemical vapor deposition (CVD) method. • The prepared composite was modified with concentrated nitric acid and chitosan. • The modified CNTs–mullite composites were used as novel adsorbents. • Copper ion removal from water by the prepared adsorbents was performed. • Langmuir and Freundlich isotherms and two kinetic models were applied to fit the experimental data. - Abstract: Carbon nanotubes–mullite composite was synthesized by direct growth of carbon nanotubes on mullite particles via chemical vapor deposition method using cyclohexanol and ferrocene as carbon precursor and catalyst, respectively. The carbon nanotubes–mullite composite was oxidized with concentrated nitric acid and functionalized with chitosan and then used as a novel adsorbent for copper ions removal from water. The results demonstrated that modification with concentrated nitric acid and chitosan improves copper ions adsorption capacity of the prepared composite, significantly. Langmuir and Freundlich isotherms and two kinetic models were applied to fit the experimental data. The carbon nanotubes growth on mullite particles to form the carbon nanotubes–mullite composite with further modification is an inherently safe approach for many promising environmental applications to avoid some concerns regarding environment, health and safety. It was found that the modified carbon nanotubes–mullite composite can be considered as an excellent adsorbent for copper ions removal from water.

  20. A copper-catalyzed bioleaching process for enhancement of cobalt dissolution from spent lithium-ion batteries.

    Science.gov (United States)

    Zeng, Guisheng; Deng, Xiaorong; Luo, Shenglian; Luo, Xubiao; Zou, Jianping

    2012-01-15

    A copper-catalyzed bioleaching process was developed to recycle cobalt from spent lithium-ion batteries (mainly LiCoO(2)) in this paper. The influence of copper ions on bioleaching of LiCoO(2) by Acidithiobacillus ferrooxidans (A.f) was investigated. It was shown that almost all cobalt (99.9%) went into solution after being bioleached for 6 days in the presence of 0.75 g/L copper ions, while only 43.1% of cobalt dissolution was obtained after 10 days without copper ions. EDX, XRD and SEM analyses additionally confirmed that the cobalt dissolution from spent lithium-ion batteries could be improved in the presence of copper ions. The catalytic mechanism was investigated to explain the enhancement of cobalt dissolution by copper ions, in which LiCoO(2) underwent a cationic interchange reaction with copper ions to form CuCo(2)O(4) on the surface of the sample, which could be easily dissolved by Fe(3+).

  1. Level of Copper Ion in Cervical Mucus of Various Duration after Inserting VCu200 IUD

    Institute of Scientific and Technical Information of China (English)

    刘庆喜; 黄祝姈; 潘琢如

    1996-01-01

    The purpose of the study was to test the effective period of VCu200 IUD. The concentration of copper ion was measured with non-flame atomic absorption s pectrophotometer HITACHI- 180. The average concentration of copper ion(x±sx) was 2.66±0.58 μg/g cervical mucus wet weight (μg/g · M·W·W) in the first year, then gradually decreasing to 0.91±0. 16 μg/g·M·W·W in the fifteenth-year group of VCu200 IUD. There was an average of 0.35±0.08~0. 56±0. 14 μg/g·M·W·W in the control group. It showed that the concentration of copper ion was decreasing with prolongation of use of VCu200 IUD and there was statistically significant difference between VCu200 IUD group, on the one hand, and the stainless steel ring group and the control group (P<0.05~0. 01) on the other hand. No difference was found between the stainless steel ring group and the control group (P>0. 05). It was reported in the literature that the concentration of copper ion in 1.0 μg/ml had the action of anti fertility, and it was found that the concentration of copper ion was higher than 1.0 μg/ml in the tenth year after insertion of VCu200 IUD. It suggested that effective period of VCu200 IUD was at least ten years.

  2. Ion-beam-induced modifications in the structural and electrical properties of copper oxide selenite nanowires

    Energy Technology Data Exchange (ETDEWEB)

    Rana, Pallavi, E-mail: prana.phy@gmail.com; Chauhan, R.P.

    2015-04-15

    Highlights: •Nanowires were synthesized via template-assisted electrodeposition method. •Copper oxide selenite nanowires were irradiated with 160 MeV, Ni{sup +12} ion beam. •XRD confirmed no change in phase of irradiated nanowires. •Electrical resistivity of nanowires was found to decrease with the ion fluence. -- Abstract: Irradiation with swift heavy ions (SHIs) with energy in the MeV range is a unique tool for engineering the properties of materials. In this context, the objective of the present work is to study the conduction of charge carriers in pre- and post-ion-irradiated semiconducting nanowires. Copper oxide selenite nanowires were synthesized using a template-assisted electrodeposition technique from an aqueous solution of 0.8 M CuSO{sub 4}·5H{sub 2}O and 8 mM SeO{sub 2}. The synthesized nanowires were observed to have a monoclinic structure with linear I–V characteristics (IVC). The effect of irradiation with 160 MeV Ni{sup +12} ions on the properties of the copper oxide selenite nanowires was investigated for fluences varying from 10{sup 11} to 10{sup 13} ions/cm{sup 2}. XRD spectra confirmed no change in the phase of the swift-heavy-ion-irradiated nanowires, but a modification in the orientation of the planes was observed that depended on the ion fluence. The electrical resistivity of the semiconducting nanowires also varied with the ion fluence. Simultaneous irradiation-induced modifications to the electro-chemical potential gradient and the granular properties of the material may have been the origin of the alteration in the structural and electrical properties of the nanowires.

  3. New Class of Antimicrobial Agents: SBA-15 Silica Containing Anchored Copper Ions

    Directory of Open Access Journals (Sweden)

    Lukasz Laskowski

    2017-01-01

    Full Text Available The paper is about a new class of antimicrobial functional nanomaterials. Proposed compounds are based on SBA-15 porous silica matrices and contain anchored copper ions. Thanks to the immobilization of functional groups the compounds are safer for environment than commonly used disinfectant agents. We prepared and examined silica based materials containing two concentrations of copper-containing groups: 10 and 5%. For the reference we prepared samples containing free-standing CuO molecules in the structure and checked their antimicrobial properties. Antibacterial effect of considered SBA-15-Cu material was tested on Escherichia coli bacteria. Antimicrobial tests were applied for the pure form of the material and as modifying agents for plastics. The obtained results showed that the sample with lower concentration of active copper-containing groups has stronger antimicrobial properties than the one with higher concentration of copper. Interestingly, silica containing free-standing CuO molecules has no antimicrobial properties. Considering the obtained results, we can conclude that the most probable antimicrobial mechanism in this case is an oxidation stress. When a plastic modifier is applied the material is enriched with bacterial inhibitory properties. It seems that SBA-15 silica containing low concentration of anchored copper ions is promising in terms of its antibacterial property and biomaterial potential for commercial use.

  4. Effect of copper (II) ion against elongation behavior of amyloid {beta} fibrils on liposome membranes

    Energy Technology Data Exchange (ETDEWEB)

    Shimanouchi, T.; Onishi, R.; Kitaura, N.; Umakoshi, H.; Kuboi, R. [Division of Chemical Engineering, Graduate School of Engineering Science, Osaka University, 1-3 Machikaneyama-cho, Toyonaka, Osaka (Japan)

    2012-01-15

    The fibril growth behavior of amyloid {beta} protein (A{beta}) on cell membranes is relating to the progression of Alzheimer's disease. This growth behavior of A{beta} fibrils is sensitively affected by the metal ions, neurotransmitters, or bioreactive substrate. The inhibitory effect of those materials was quantitatively estimated from the viewpoints of ''crystal growth''. In a bulk aqueous solution, copper (II) ion showed the strong inhibitory effect on the growth of A{beta} fibrils. Meanwhile, the addition of a closed-phospholipid bilayer membrane (liposome) could reduce the above inhibitory effect of copper (II) ion. (copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  5. Cancer Therapy by Catechins Involves Redox Cycling of Copper Ions and Generation of Reactive Oxygen Species

    Directory of Open Access Journals (Sweden)

    Mohd Farhan

    2016-02-01

    Full Text Available Catechins, the dietary phytochemicals present in green tea and other beverages, are considered to be potent inducers of apoptosis and cytotoxicity to cancer cells. While it is believed that the antioxidant properties of catechins and related dietary agents may contribute to lowering the risk of cancer induction by impeding oxidative injury to DNA, these properties cannot account for apoptosis induction and chemotherapeutic observations. Catechin (C, epicatechin (EC, epigallocatechin (EGC and epigallocatechin-3-gallate (EGCG are the four major constituents of green tea. In this article, using human peripheral lymphocytes and comet assay, we show that C, EC, EGC and EGCG cause cellular DNA breakage and can alternatively switch to a prooxidant action in the presence of transition metals such as copper. The cellular DNA breakage was found to be significantly enhanced in the presence of copper ions. Catechins were found to be effective in providing protection against oxidative stress induced by tertbutylhydroperoxide, as measured by oxidative DNA breakage in lymphocytes. The prooxidant action of catechins involved production of hydroxyl radicals through redox recycling of copper ions. We also determined that catechins, particularly EGCG, inhibit proliferation of breast cancer cell line MDA-MB-231 leading to a prooxidant cell death. Since it is well established that tissue, cellular and serum copper levels are considerably elevated in various malignancies, cancer cells would be more subject to redox cycling between copper ions and catechins to generate reactive oxygen species (ROS responsible for DNA breakage. Such a copper dependent prooxidant cytotoxic mechanism better explains the anticancer activity and preferential cytotoxicity of dietary phytochemicals against cancer cells.

  6. Effect of Some Heterocyclic Derivatives on the Removal of Copper Ions from Wastewater by Cementation

    Institute of Scientific and Technical Information of China (English)

    A.A. Taha; M.G.Marei; D.E.Abd El-khalek

    2004-01-01

    Removal of copper ions from copper sulphate solutions on a rotating zinc rod in absence and in presence of 3(2H)-furanones and 4H-pyran-4-one derivatives was investigated experimentally. Variables studied were initial copper ions concentration,rotational speed of the zinc rod, temperature and concentration of organic additives. It was found that cementation reaction is first order in presence and in absence of additives. Increasing concentration of initial copper ions, rotational speed of the zinc rod and temperature were found to increase the rate of cementation. In presence of organic additives an enhancement of the rate was observed, except in presence of methoxyfuranone the rate was found to decrease by an amount ranging from 11.74% to 33.79%. Rate acceleration or inhibition is associated mainly with changes in the structure of the additives as well as its concentration. The apparent activation energy for the cementation process in presence of different additives was estimated and was found to be ranged between 11.8 k J/mol and 25.95 k J/mol. These values suggest that the copper removal process in presence of these additives is controlled by diffusion. A scanning electron microscopy study of copper deposits obtained in presence of tolylfuranone, phenylpyrone and methoxyfuranone correlate with their behaviour during the kinetic study. Different reaction conditions and the physical properties of solutions were studied to obtain dimensionless correlation among all these parameters. It was found that on applying cementation reaction on a sample from industrial wastewater in presence of phenylpyrone about 91.9% of Cu2+ are removed.

  7. Cancer Therapy by Catechins Involves Redox Cycling of Copper Ions and Generation of Reactive Oxygen species.

    Science.gov (United States)

    Farhan, Mohd; Khan, Husain Yar; Oves, Mohammad; Al-Harrasi, Ahmed; Rehmani, Nida; Arif, Hussain; Hadi, Sheikh Mumtaz; Ahmad, Aamir

    2016-02-04

    Catechins, the dietary phytochemicals present in green tea and other beverages, are considered to be potent inducers of apoptosis and cytotoxicity to cancer cells. While it is believed that the antioxidant properties of catechins and related dietary agents may contribute to lowering the risk of cancer induction by impeding oxidative injury to DNA, these properties cannot account for apoptosis induction and chemotherapeutic observations. Catechin (C), epicatechin (EC), epigallocatechin (EGC) and epigallocatechin-3-gallate (EGCG) are the four major constituents of green tea. In this article, using human peripheral lymphocytes and comet assay, we show that C, EC, EGC and EGCG cause cellular DNA breakage and can alternatively switch to a prooxidant action in the presence of transition metals such as copper. The cellular DNA breakage was found to be significantly enhanced in the presence of copper ions. Catechins were found to be effective in providing protection against oxidative stress induced by tertbutylhydroperoxide, as measured by oxidative DNA breakage in lymphocytes. The prooxidant action of catechins involved production of hydroxyl radicals through redox recycling of copper ions. We also determined that catechins, particularly EGCG, inhibit proliferation of breast cancer cell line MDA-MB-231 leading to a prooxidant cell death. Since it is well established that tissue, cellular and serum copper levels are considerably elevated in various malignancies, cancer cells would be more subject to redox cycling between copper ions and catechins to generate reactive oxygen species (ROS) responsible for DNA breakage. Such a copper dependent prooxidant cytotoxic mechanism better explains the anticancer activity and preferential cytotoxicity of dietary phytochemicals against cancer cells.

  8. In vitro release of cupric ion from intrauterine devices: influence of frame, shape, copper surface area and indomethacin.

    Science.gov (United States)

    Zhang, Shuangshuang; Li, Ying; Yu, Panpan; Chen, Tong; Zhou, Weisai; Zhang, Wenli; Liu, Jianping

    2015-02-01

    The release of cupric ion from copper intrauterine device (Cu-IUD) in human uterus is essential for contraception. However, excessive cupric ion will cause cytotoxic effect. In this paper, we investigated the influence of device characteristics (frame, copper surface area, shape, copper type and indomethacin) on copper release for the efficacy and adverse effects vary with IUD types which may correlate to their different release behaviors. Nine types of Cu-IUDs were selected and incubated in simulated uterine fluid. They were paired for comparison based on the device properties and the release of cupric ion was determined by flame atomic absorption spectrometer for about 160 days. The result showed that there was a burst release during the first month and the release rate tends to slow down and become steady afterwards. In addition, the copper release was mainly influenced by frame, indomethacin and copper type (copper wire and copper sleeve) while the shape variation had little effect on copper release throughout the experiment. Moreover, the influence of copper surface area was only noticeable during the first month. These findings were seldom reported before and may provide some useful information for the design of Cu-IUDs.

  9. Fragmentation of copper current collectors in Li-ion batteries during spherical indentation

    Science.gov (United States)

    Wang, Hsin; Watkins, Thomas R.; Simunovic, Srdjan; Bingham, Philip R.; Allu, Srikanth; Turner, John A.

    2017-10-01

    Large, areal, brittle fracture of copper current collector foils has been observed by 3D x-ray computed tomography (XCT) of a spherically indented Li-ion cell. This fracture is hidden and non-catastrophic to a degree because the graphite layers deform plastically, and hold the materials together so that the cracks in the foils cannot be seen under optical and electron microscopy. The cracking of copper foils could not be immediately confirmed when the cell is opened for post-mortem examination. However, 3D XCT on the indented cell reveals "mud cracks" within the copper layer and an X-ray radiograph on a single foil of the Cu anode shows clearly that the copper foil has broken into multiple pieces. This failure mode of anodes in Li-ion cell has very important implications on the behavior of Li-ion cells under mechanical abuse conditions. The fragmentation of current collectors in the anode must be taken into consideration for the electrochemical responses which may lead to capacity loss and affect thermal runaway behavior of the cells.

  10. Copper(II) ions and the Alzheimer's amyloid-β peptide: Affinity and stoichiometry of binding

    Science.gov (United States)

    Tõugu, Vello; Friedemann, Merlin; Tiiman, Ann; Palumaa, Peep

    2014-10-01

    Deposition of amyloid beta (Aβ) peptides into amyloid plaques is the hallmark of Alzheimer's disease. According to the amyloid cascade hypothesis this deposition is an early event and primary cause of the disease, however, the mechanisms that cause this deposition remain elusive. An increasing amount of evidence shows that the interactions of biometals can contribute to the fibrillization and amyloid formation by amyloidogenic peptides. From different anions the copper ions deserve the most attention since it can contribute not only toamyloid formation but also to its toxicity due to the generation of ROS. In this thesis we focus on the affinity and stoichiometry of copper(II) binding to the Aβ molecule.

  11. The ligational behavior of an isatinic quinolyl hydrazone towards copper(II- ions

    Directory of Open Access Journals (Sweden)

    Mousa Marwa A

    2011-04-01

    Full Text Available Abstract Background The importance of the isatinic quinolyl hydrazones arises from incorporating the quinoline ring with the indole ring. Quinoline ring has therapeutic and biological activities whereas, the indole ring occurs in Jasmine flowers and Orange blossoms. As a ligand, the isatin moiety is potentially ambidentate and can coordinate the metal ions either through its lactam or lactim forms. In a previous study, the ligational behavior of a phenolic quinolyl hydrazone towards copper(II- ions has been studied. As continuation of our interest, the present study is planned to check the ligational behavior of an isatinic quinolyl hydrazone. Results New homo- and heteroleptic copper(II- complexes were obtained from the reaction of an isatinic quinolyl hydrazone (HL with several copper(II- salts viz. Clˉ, Brˉ, NO3ˉ, ClO4-, SO42- and AcO-. The obtained complexes have Oh, Td and D4h- symmetry and fulfill the strong coordinating ability of Clˉ, Brˉ, NO3ˉ and SO42- anions. Depending on the type of the anion, the ligand coordinates the copper(II- ions either through its lactam (NO3ˉ and ClO4- or lactim (the others forms. Conclusion The effect of anion for the same metal ion is obvious from either the geometry of the isolated complexes (Oh, Td and D4h or the various modes of bonding. Also, the obtained complexes fulfill the strong coordinating ability of Clˉ, Brˉ, NO3ˉ and SO42- anions in consistency with the donor ability of the anions. In case of copper(II- acetate, a unique homoleptic complex (5 was obtained in which the AcO- anion acts as a base enough to quantitatively deprotonate the hydrazone. The isatinic hydrazone uses its lactim form in most complexes.

  12. Removal of copper, nickel, and zinc ions from electroplating rinse water

    Energy Technology Data Exchange (ETDEWEB)

    Revathi, Meyyappan; Saravanan, Mohan; Velan, Manickam [Department of Chemical Engineering, AC Tech, Anna University, Chennai, Tamil Nadu (India); Chiya, Ahmed Basha [Department of Chemical Engineering, Industrial Liaison Research Institute, Kyang Hee University, Gyeonggi (Korea, Republic of)

    2012-01-15

    Removal of copper, nickel, and zinc ions from synthetic electroplating rinse water was investigated using cationic exchange resin (Ceralite IR 120). Batch ion exchange studies were carried out to optimize the various experimental parameters (such as contact time, pH, and dosage). Influence of co-existing cations, chelating agent EDTA on the removal of metal ion of interest was also studied. Sorption isotherm data obtained at different experimental conditions were fitted with Langmuir, Freundlich, Redlich-Peterson, and Toth models. A maximum adsorption capacity of 164 mg g{sup -1} for Cu(II), 109 mg g{sup -1} for Ni(II), and 105 mg g{sup -1} for Zn(II) was observed at optimum experimental conditions according to Langmuir model. The kinetic data for metal ions adsorption process follows pseudo second-order. Presence of EDTA and co-ions markedly alters the metal ion removal. Continuous column ion exchange experiments were also conducted. The breakeven point of the column was obtained after recovering effectively several liters of rinse water. The treated rinse water could be recycled in rinsing operations. The Thomas and Adams-Bohart models were applied to column studies and the constants were evaluated. Desorption of the adsorbed metal ions from the resin column was studied by conducting a model experiments with Cu(II) ions loaded ion exchange resin column using sulfuric acid as eluant. A novel lead oxide coated Ti substrate dimensionally stable (DSA) anode was prepared for recovery of copper ions as metal foil from regenerated liquor by electro winning at different current densities (50-300 A cm{sup -2}). (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  13. A spectrophotometric method for the determination of zinc, copper, and cobalt ions in metalloproteins using Zincon.

    Science.gov (United States)

    Säbel, Crystal E; Neureuther, Joseph M; Siemann, Stefan

    2010-02-15

    Zincon (2-carboxy-2'-hydroxy-5'-sulfoformazylbenzene) has long been known as an excellent colorimetric reagent for the detection of zinc and copper ions in aqueous solution. To extend the chelator's versatility to the quantification of metal ions in metalloproteins, the spectral properties of Zincon and its complexes with Zn(2+), Cu(2+), and Co(2+) were investigated in the presence of guanidine hydrochloride and urea, two common denaturants used to labilize metal ions in proteins. These studies revealed the detection of metals to be generally more sensitive with urea. In addition, pH profiles recorded for these metals indicated the optimal pH for complex formation and stability to be 9.0. As a consequence, an optimized method that allows the facile determination of Zn(2+), Cu(2+), and Co(2+) with detection limits in the high nanomolar range is presented. Furthermore, a simple two-step procedure for the quantification of both Zn(2+) and Cu(2+) within the same sample is described. Using the prototypical Cu(2+)/Zn(2+)-protein superoxide dismutase as an example, the effectiveness of this method of dual metal quantification in metalloproteins is demonstrated. Thus, the spectrophotometric determination of metal ions with Zincon can be exploited as a rapid and inexpensive means of assessing the metal contents of zinc-, copper-, cobalt-, and zinc/copper-containing proteins.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-07-15

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

  15. Interaction of ions in water system containing copper-zinc alloy for boiler energy saving

    Institute of Scientific and Technical Information of China (English)

    MING Xing; LIANG Jinsheng; OU Xiuqin; TANG Qingguo; DING Yan

    2006-01-01

    Copper-zinc alloy element for boiler energy saving was put in the intake of simulated boiler system to investigate the interaction and transfer of ions in water system both theoretically and experimentally. The fouling was analyzed by scanning electron microscopy (SEM) and energy dispersive X-ray detector (EDX). The results show that the transfer of calcium and magnesium ions in heat-transfer-surface-water system is affected by zinc ions dissolved from the alloy because of primary battery reaction. Some calcium ions of calcium carbonate crystal are replaced by zinc ions, the growth of aragonite crystal nucleus is retarded, and the transition of calcium carbonate from aragonite to calcite is hampered.

  16. Electrochemical removal of copper ions from dilute solutions using packed bed electrode. Part І

    Directory of Open Access Journals (Sweden)

    I.A. Khattab

    2013-06-01

    Full Text Available Removal of some hazardous waste like copper from effluent streams has an industrial importance. In this field, this paper is directed towards electrochemical removal of copper ions from sulfate solution using packed bed electrode. The cathode packing is in static mode, consisted of graphite particles, with mean particle size equal to 0.125 cm. The high surface area of this cell is expected to give high current efficiency and removal percent. The effect of current density and liquid flow rate were tested. Experimental results obtained indicate that the efficiencies are in direct proportional with current density while inversely proportional with liquid flow rate. It was observed that, using this cell was effective in reducing copper concentration to less than 4 mg/l with R.E of 96.2% during 30 min electrolysis time.

  17. Free cupric ions in contaminated agricultural soils around a copper mine in eastern Nanjing City, China

    Institute of Scientific and Technical Information of China (English)

    LUO Xiao-san; ZHOU Dong-mei; WANG Yu-jun

    2006-01-01

    To determine the environmental free metal ion activity was a recent hot issue. A method to measure low-level free cupric ion activity in soil solution extracted with 0.01 mol/L KNO3 was developed by using cupric ion-selective electrode (ISE) and calibrating with Cu-buffer solution. Three copper buffers including iminodiacetic acid (IDA), ethylenediamine (EN), and glycine (Gly)were compared for calibrating the Cu-ISE curves in the range of free cupric ions (pCu2+) 7-13. The Cu-EN buffer showed the best electrode response and thus was applied as the calibration buffer. The pCu2+ of 39 contaminated agricultural soils around a copper mine was measured, ranging from 5.03 to 9.20. Most Cu in the soil solutions was found to be complexed with dissolved soil organic matters, averaging 98.1%. The proportion of free Cu2+ ions in the soil solutions decreased with the increasing of solution pH. Soluble Cu and free Cu2+ ions concentrations were analyzed by multiple linear regressions to evaluate the effects of soil properties on metal levels and speciation. The results showed that soil solution pH was the most significant factor influencing pCu2+ (with R2 value of 0.76), while not important for the soluble Cu concentration.

  18. Flotation of traces of silver and copper(II) ions with a methyl cellosolve solution of dithizone.

    Science.gov (United States)

    Hiraide, M; Mizuike, A

    1975-06-01

    Microgram quantities of silver and copper(II) ions in aqueous solutions are collected on dithizone precipitates, which are then floated with the aid of small nitrogen bubbles. This separation technique has been successfully applied to the atomic-absorption spectrophotometric determination of down to a tenth ppm of silver and copper in high-purity lead and zinc metals.

  19. Effects of copper oxide nanoparticles and copper ions to zebrafish (Danio rerio) cells, embryos and fry

    DEFF Research Database (Denmark)

    Thit, Amalie; Skjolding, Lars Michael; Selck, Henriette

    2017-01-01

    with similar concentration-response relationships, whereas only Cu ions affected fry mortality (24h LC50≈30μM, ≈2mgCuL-1 for Cu ions and no significant mortality observed at up to 200μM, 12.7mgCuL-1 for CuO NP). Both Cu forms increased fry swimming activity during light cycles and decreased activity during......) and fry locomotion. In the ZFL tests, no significant cytotoxicity (cell death, decreased metabolic or cell membrane integrity) was detected for either treatment, though both significantly affected reactive oxygen species (ROS) production. Embryo mortality was affected by both Cu ions and CuO NPs...... dark cycles: Cu ions had significant impact at lower concentrations than CuO NPs. The implications are that Cu ions generally are more toxic than CuO NPs to embryos and fry but there is a marked difference in toxicity among the different zebrafish model systems. Metal NPs release into the environment...

  20. Disulfiram and Copper Ions Kill Mycobacterium tuberculosis in a Synergistic Manner.

    Science.gov (United States)

    Dalecki, Alex G; Haeili, Mehri; Shah, Santosh; Speer, Alexander; Niederweis, Michael; Kutsch, Olaf; Wolschendorf, Frank

    2015-08-01

    Tuberculosis is a severe disease affecting millions worldwide. Unfortunately, treatment strategies are hampered both by the prohibitively long treatment regimen and the rise of drug-resistant strains. Significant effort has been expended in the search for new treatments, but few options have successfully emerged, and new treatment modalities are desperately needed. Recently, there has been growing interest in the synergistic antibacterial effects of copper ions (Cu(II/I)) in combination with certain small molecular compounds, and we have previously reported development of a drug screening strategy to harness the intrinsic bactericidal properties of Cu(II/I). Here, we describe the copper-dependent antimycobacterial properties of disulfiram, an FDA-approved and well-tolerated sobriety aid. Disulfiram was inhibitory to mycobacteria only in the presence of Cu(II/I) and exerted its bactericidal activity well below the active concentration of Cu(II/I) or disulfiram alone. No other physiologically relevant bivalent transition metals (e.g., Fe(II), Ni(II), Mn(II), and Co(II)) exhibited this effect. We demonstrate that the movement of the disulfiram-copper complex across the cell envelope is porin independent and can inhibit intracellular protein functions. Additionally, the complex is able to synergistically induce intracellular copper stress responses significantly more than Cu(II/I) alone. Our data suggest that by complexing with disulfiram, Cu(II/I) is likely allowed unfettered access to vulnerable intracellular components, bypassing the normally sufficient copper homeostatic machinery. Overall, the synergistic antibacterial activity of Cu(II/I) and disulfiram reveals the susceptibility of the copper homeostasis system of Mycobacterium tuberculosis to chemical attacks and establishes compounds that act in concert with copper as a new class of bacterial inhibitors.

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

    Directory of Open Access Journals (Sweden)

    Marcia T. Veit

    2007-10-01

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

  2. Irradiation damage in aluminium single crystals produced by 50-keV aluminium and copper ions

    DEFF Research Database (Denmark)

    Henriksen, L.; Johansen, A.; Koch, J.

    1968-01-01

    Aluminium single crystals, thin enough to be examined by electron microscopy, have been irradiated with 50-keV aluminium and copper ions. The irradiation fluxes were in the range 1011–1014 cm−2 s−1 and the doses were from 6 × 1012 to 6 × 1014 cm−2. Irradiation along either a or a direction produc...

  3. Micronized Copper Wood Preservatives: Efficacy of Ion, Nano, and Bulk Copper against the Brown Rot Fungus Rhodonia placenta.

    Directory of Open Access Journals (Sweden)

    Chiara Civardi

    Full Text Available Recently introduced micronized copper (MC formulations, consisting of a nanosized fraction of basic copper (Cu carbonate (CuCO3·Cu(OH2 nanoparticles (NPs, were introduced to the market for wood protection. Cu NPs may presumably be more effective against wood-destroying fungi than bulk or ionic Cu compounds. In particular, Cu- tolerant wood-destroying fungi may not recognize NPs, which may penetrate into fungal cell walls and membranes and exert their impact. The objective of this study was to assess if MC wood preservative formulations have a superior efficacy against Cu-tolerant wood-destroying fungi due to nano effects than conventional Cu biocides. After screening a range of wood-destroying fungi for their resistance to Cu, we investigated fungal growth of the Cu-tolerant fungus Rhodonia placenta in solid and liquid media and on wood treated with MC azole (MCA. In liquid cultures we evaluated the fungal response to ion, nano and bulk Cu distinguishing the ionic and particle effects by means of the Cu2+ chelator ammonium tetrathiomolybdate (TTM and measuring fungal biomass, oxalic acid production and laccase activity of R. placenta. Our results do not support the presence of particular nano effects of MCA against R. placenta that would account for an increased antifungal efficacy, but provide evidence that attribute the main effectiveness of MCA to azoles.

  4. Effect of Phosphorylation and Copper(II or Iron(II Ions Enrichment on Some Physicochemical Properties of Spelt Starch

    Directory of Open Access Journals (Sweden)

    Jacek Rożnowski

    Full Text Available ABSTRACT: This paper provides an assessment of the effect of saturation of spelt starch and monostarch phosphate with copper or iron ions on selected physicochemical properties of the resulting modified starches. Native and modified spelt starch samples were analyzed for selected mineral element content using Atomic Absorption Spectroscopy (AAS. Thermodynamic properties were measured using DSC, and pasting properties by RVA. Flow curves of 5% pastes were plotted and described using the Herschel-Bulkley model. The structure recovery ratio was measured. AAS analysis established the presence of iron(II and copper(II ions in the samples of modified starches and that potassium and magnesium ions had leached from them. In comparison to unfortified samples, enriching native starch with copper(II ions decreases value of all temperatures of phase transformation about 1.3-2.7 °C, but in case of monostarch phosphates bigger changes (2.8-3.7 °C were observed. Fortified native spelt starch with copper(II ions caused increasing the final viscosity of paste from 362 to 429 mPa·s. However, presence iron(II ions in samples caused reduced its final viscosity by 170 (spelt starch and 103 mPa·s (monostarch phosphate. Furthermore, enriching monostarch phosphate contributed to reduce degree of structure recovery of pastes from 70.9% to 66.6% in case of copper(II ions and to 59.9% in case of iron(II ions.

  5. Synthesis and evaluation of a new colorimetric and ratiometric fluorescence probe for copper ions

    Energy Technology Data Exchange (ETDEWEB)

    Chawla, Har Mohindra, E-mail: hmchawla@chemistry.iitd.ernet.in; Munjal, Priyanka; Goel, Preeti

    2015-08-15

    Synthesis and spectroscopic evaluation of compounds 3a, 3b and 4 reveal that cone conformer of 25,27-bis(o-aminothiophenyl propyloxy) -tetra-p-tert-butylcalix[4]arene 3a can function as a highly selective ratiometric and colorimetric fluorescence probe for copper ions. - Highlights: • We have synthesized a new calixarene based receptor 3 for Cu{sup 2+}. • 3 Showed ratiometric changes with Cu{sup 2+} in emission spectrum. • Reference compound 4 showed quenching with Cu{sup 2+} in emission spectrum. • Importance of calix[4]arene platform in ion recognition.

  6. Electrochemical determination of copper ions in spirit drinks using carbon paste electrode modified with biochar.

    Science.gov (United States)

    Oliveira, Paulo Roberto; Lamy-Mendes, Alyne C; Rezende, Edivaltrys Inayve Pissinati; Mangrich, Antonio Sálvio; Marcolino, Luiz Humberto; Bergamini, Márcio F

    2015-03-15

    This work describes for first time the use of biochar as electrode modifier in combination with differential pulse adsorptive stripping voltammetric (DPAdSV) techniques for preconcentration and determination of copper (II) ions in spirit drinks samples (Cachaça, Vodka, Gin and Tequila). Using the best set of the experimental conditions a linear response for copper ions in the concentration range of 1.5 × 10(-6) to 3.1 × 10(-5) mol L(-1) with a Limit of Detection (LOD) of 4.0 × 10(-7) mol L(-1). The repeatability of the proposed sensor using the same electrode surface was measured as 3.6% and 6.6% using different electrodes. The effect of foreign species on the voltammetric response was also evaluated. Determination of copper ions content in different samples of spirit drinks samples was also realized adopting inductively coupled plasma optical emission spectroscopy (ICP-OES) and the results achieved are in agreement at a 95% of confidence level.

  7. Polyacrylamide hydrogel encapsulated E. coli expressing metal-sensing green fluorescent protein as a potential tool for copper ion determination.

    Science.gov (United States)

    Tantimongcolwat, Tanawut; Isarankura-Na-Ayudhya, Chartchalerm; Srisarin, Apapan; Galla, Hans-Joachim; Prachayasittikul, Virapong

    2014-01-01

    A simple, inexpensive and field applicable metal determination system would be a powerful tool for the efficient control of metal ion contamination in various sources e.g. drinking-water, water reservoir and waste discharges. In this study, we developed a cell-based metal sensor for specific and real-time detection of copper ions. E. coli expressing metal-sensing green fluorescent protein (designated as TG1/(CG)6GFP and TG1/H6CdBP4GFP) were constructed and served as a metal analytical system. Copper ions were found to exert a fluorescence quenching effect, while zinc and cadmium ions caused minor fluorescence enhancement in the engineered bacterial suspension. To construct a user-friendly and reagentless metal detection system, TG1/H6CdBP4GFP and TG1/(CG)6GFP were encapsulated in polyacrylamide hydrogels that were subsequently immobilized on an optical fiber equipped with a fluorescence detection module. The sensor could be applied to measure metal ions by simply dipping the encapsulated bacteria into a metal solution and monitoring fluorescence changes in real time as a function of the metal concentration in solution. The sensor system demonstrated high specificity toward copper ions. The fluorescence intensities of the encapsulated TG1/(CG)6GFP and TG1/H6CdBP4GFP were quenched by approximately 70 % and 80 % by a high-dose of copper ions (50 mM), respectively. The level of fluorescence quenching exhibited a direct correlation with the copper concentration, with a linear correlation coefficient (r) of 0.99. The cell-based metal sensor was able to efficiently monitor copper concentrations ranging between 5 M and 50 mM, encompassing the maximum allowed copper contamination in drinking water (31.15 M) established by the WHO. Furthermore, the cell-based metal sensor could undergo prolonged storage for at least 2 weeks without significantly influencing the copper sensitivity.

  8. Uptake of copper ion by activated sludge and its bacterial community variation analyzed by 16S rDNA

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The effect and uptake of copper ion on SBR(sequence batch reactor) biological treatment system was studied in this paper. Special nutrient and powder activated carbon(PAC) additive were tested as uptake stimulation technique. Results showed that copper ion had higher effect on unacclimated activated sludge system than on acclimated one. The special nutrient adding could enhance the uptake of copper significantly, while PAC adding could improve the sludge settling and decrease the turbidity of effluent. The variation of bacterial community analyzed by 16S rDNA method showed the acclimation of copper could increase copper resistance species, and excess accumulation could cause some species diminish. It was confirmed that acclimation could improve the resistance and uptake ability of microorganism to heavy metal.

  9. Reduction of microbial pathogens during apple cider production using sodium hypochlorite, copper ion, and sonication.

    Science.gov (United States)

    Rodgers, Stephanie L; Ryser, Elliot T

    2004-04-01

    Sodium hypochlorite (100 ppm), copper ion water (1 ppm), and sonication (22 to 44 kHz and 44 to 48 kHz) were assessed individually and in combination for their ability to reduce populations of Escherichia coli O157:H7 and Listeria monocytogenes on apples and in apple cider. Commercial unpasteurized cider was inoculated to contain approximately 10(6) CFU/ml of either pathogen and then sonicated at 44 to 48 kHz, with aliquots removed at intervals of 30 to 60 s for up to 5 min and plated to determine numbers of survivors. Subsequently, whole apples were inoculated by dipping to contain approximately 10(6) CFU/g E. coli O157:H7 or L. monocytogenes, held overnight, and then submerged in 1 ppm copper ion water with or without 100 ppm sodium hypochlorite for 3 min with or without sonication at 22 to 44 kHz and examined for survivors. Treated apples were also juiced, with the resulting cider sonicated for 3 min. Populations of both pathogens decreased 1 to 2 log CFU/ml in inoculated cider following 3 min of sonication. Copper ion water alone did not significantly reduce populations of either pathogen on inoculated apples. However, when used in combination with sodium hypochlorite, pathogen levels decreased approximately 2.3 log CFU/g on apples. Sonication of this copper ion-sodium hypochlorite solution at 22 to 44 kHz did not further improve pathogen reduction on apples. Numbers of either pathogen in the juice fraction were approximately 1.2 log CFU/ml lower after being juiced, with sonication (44 to 48 kHz) of the expressed juice decreasing L. monocytogenes and E. coli O157:H7 populations an additional 2 log. Hence, a 5-log reduction was achievable for both pathogens with the use of copper ion water in combination with sodium hypochlorite followed by juicing and sonication at 44 to 48 kHz.

  10. Extraction of copper ions by supercritical carbon dioxide

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Complexation combined with supercritical fluid extraction was used to extract Cu2+ in this study. The effects of pressure, temperature, volume of CO2 on the efficiency of extraction were systematically investigated. At the optimum condition a 57.32% recovery was achieved. Addition of suitable amount of methanol(v/v = 5 % ) to the supercritical CO2 can increase in the extraction of Cu2+ (72.69 %, RSD = 2.12 %, n = 3). And the recovery can further increase in the presence of non-ionic surfactant Triton X-100 because of its function of solubilization. Surfactant was first used in the extraction of metal ions in the present study, and the results are satisfied (90.52%, RSD=2.20%, n =3).

  11. Two-step flash light sintering process for enhanced adhesion between copper complex ion/silane ink and a flexible substrate

    Energy Technology Data Exchange (ETDEWEB)

    Jeon, Eun-Beom; Joo, Sung-Jun [Department of Mechanical Convergence Engineering, Hanyang University, Haengdang-dong, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Ahn, Heejoon [Department of Organic and Nano Engineering, Hanyang University, Haengdang-dong, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Kim, Hak-Sung, E-mail: kima@hanyang.ac.kr [Department of Mechanical Convergence Engineering, Hanyang University, Haengdang-dong, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Institute of Nano Science and Technology, Hanyang University, Seoul 133-791 (Korea, Republic of)

    2016-03-31

    A copper complex ion ink (including copper nanoparticles, a copper precursor and a silane coupling agent) was synthesized to enhance the adhesion between the copper pattern and a polyimide (PI) substrate. Oxygen plasma treatment was performed on the polyimide substrate to initiate a chemical reaction between the complex ion ink and the polyimide. Then, a two-step flash light sintering method (consisting of preheating and main sintering) was used to sinter the copper complex ion ink. The copper complex ion patterns were characterized as a function of the weight fraction of silane coupling agent using scanning electron microscopy (SEM), a four-point probe method and adhesion testing. In addition, a bending fatigue test was performed to evaluate the reliability of the conductive copper pattern under cyclic bending. The copper pattern fabricated with copper complex ion ink containing 3 wt% silane coupling agent exhibited the highest adhesion level (5B), the lowest resistivity (7.6 μΩ·cm) and a low resistance change (18%) after the bending fatigue test. The two-step sintering method used to enhance the adhesion between the copper complex ion ink and polyimide substrate was also studied using X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). - Highlights: • The copper complex ion ink with copper nanoparticles and copper precursor was fabricated. • The copper complex ion ink was sintered by two-step flash light sintering method. • The sintered copper pattern exhibited the highest adhesion level (5B). • The resistivity of sintered copper pattern was 7.6 μΩ·cm.

  12. Size-Controlled Synthesis of Copper Oxide Particles on Reduced Graphene Oxide for Lithium-Ion Battery Anode Applications.

    Science.gov (United States)

    Jang, Haneul; Kim, Kyungbae; Chang, Hyejung; Kim, Jae-Hun; Choi, Hyunjoo

    2015-11-01

    Copper oxide/reduced graphene oxide (rGO) hybrids have been successfully synthesized by attaching copper ions onto the functional groups of GO by means of a solution process, which causes precipitation and agglomeration of copper oxides during subsequent thermal reduction of the GO. The resulting copper oxide/rGO hybrid exhibited improved electrochemical performance compared to monolithic CuO, which is presumed to be due to rGO acting as a mechanical support that buffers the volume change in copper oxides that occurs as a result of the conversion reaction during charge/discharge cycling. Furthermore, it was found that the size of the copper oxide particles can be optimized by adjusting the annealing time, with a hybrid annealed for 30 min achieving a reversible capacity of 544 mA h g(-1) and an initial coulombic efficiency of 62.7%.

  13. Montmorillonite modified with copper ions: Efficient adsorbent for aflatoxin B1

    Directory of Open Access Journals (Sweden)

    Daković Aleksandra

    2008-01-01

    Full Text Available In this paper, the results of preparation of material for adsorption of aflatoxin B1, based on modification of montmorillonite with copper ions (Cu-MONT, are presented. The bentonite clay from Sokolac deposit (Šipovo, Bosnia was used as the starting raw material. After modification of concentrate of montmorillonite (MONT with copper, the content of copper in Cu-MONT, was 2.65%. It was shown that MONT, as well as the Cu-MONT were efficient in adsorption of aflatoxin B1, at different mass ratios of adsorbent : toxin, and at different pH values. It was determined that for MONT, at the mass ratio adsorbent : toxin = 5000 : 1, aflatoxin B1 adsorption index was 100% at pH 3, 98% at pH 7 and 96% at pH 9. For Cu-MONT, at the same mass ratio, the following aflatoxin B1 adsorption indexes were achieved: 98% at pH 3, 98% at pH 7 and 96% at pH 9. No differences in adsorption of this toxin by both montmorillonites with decreasing the mass ratio of adsorbent : toxin (250 : 1 were observed. That means that ion exchange of inorganic cations in montmorillonite with copper ions did not cause any changes in aflatoxin B1 adsorption, at pH 3, as well as at pH 7 and 9. It was also noticed that adsorption of aflatoxin B1 by MONT and Cu-MONT was not pH dependent.

  14. Strategy for copper speciation in white wine by differential pulse anodic stripping voltammetry, potentiometry with an ion-selective electrode and kinetic photometric determination

    Energy Technology Data Exchange (ETDEWEB)

    Wiese, C. [Inst. fuer Anorganische und Analytische Chemie, Technische Univ. Clausthal, Clausthal-Zellerfeld (Germany); Schwedt, G. [Inst. fuer Anorganische und Analytische Chemie, Technische Univ. Clausthal, Clausthal-Zellerfeld (Germany)

    1997-07-01

    Differential pulse anodic stripping voltammetry (DPASV), potentiometry with a copper ion-selective electrode and a kinetic photometric method were used to determine copper species in white wines. The kinetic method is based on the catalytic effect of labile copper(II) species on the oxidation of 3-hydroxybenzaldehyde azine by potassium peroxidisulfate in an ammonical medium at room temperature. The total copper concentrations were determined by flame atomic absorption spectrometry. Free copper(II) ions, labile and tightly bound copper species could be quantified in 16 non pre-treated wine samples. (orig.). With 3 figs., 5 tabs.

  15. Electrochemical Behavior of Nano-grained Pure Copper in Dilute Alkaline Solution with Chloride Ion Trace

    Science.gov (United States)

    Fattah-Alhosseini, Arash; Imantalab, Omid; Attarzadeh, Farid Reza

    2016-10-01

    Effect of nano-grained structure on the interface behavior of pure copper in 0.01M KOH solution with chloride ion trace is investigated by various electrochemical techniques. Nano-grained structure was achieved by accumulative roll bonding (ARB) technique. Before any electrochemical measurements, microstructure was evaluated by means of optical microscopy and transmission electron microscopy (TEM). TEM observations showed that nano-grains (with an average size of below 100 nm) appeared after eight passes of ARB. Polarization curves revealed that increasing chloride ion concentration leads to a decrease in the corrosion and pitting potentials of both annealed and nano-grained pure copper samples. Electrochemical impedance spectroscopy revealed that chloride ion trace lowers passive film resistance and charge-transfer resistance in both annealed and nano-grained samples. Mott-Schottky analysis showed that the surface films formed on annealed and nano-grained samples in KOH solution with and without NaCl addition are of p-type semiconducting behavior. Moreover, this analysis showed that the acceptor density increases by increasing chloride ion concentration.

  16. Effect of Mo Ion Implantation on Stability of Nanocrystalline Copper Surface Layers

    Directory of Open Access Journals (Sweden)

    XI Yang

    2016-08-01

    Full Text Available The surface of pure copper was modified using the surface mechanical attrition treatment (SMAT method, and molybdenum ions were implanted in the nanosurface using a metal vapor vacuum arc (MEVVA. The results of the SMAT were observed by optical microscopy (OM, X-ray diffraction (XRD and scanning electron microscopy (SEM. An obvious nanocrystalline layer and a deformation region exist on the surface. The size of the nanocrystalline layer was characterized using atomic force microscopy (AFM. The results indicate remarkable suppression on grain size, the nanocrystalline layer grows to 163nm after annealing and reduces to only 72nm due to the Mo ion implantation. In addition, the hardness of the topmost surface of the material is 3.5 times that of the SMATed copper, which is about 7 times of the value of the matrix. The above improvements most likely result from the dispersion of the Mo ions and the reactions of the crystal defects due to the SMAT and ion implantation.

  17. Chloride-Ion Penetrability and Mechanical Analysis of High Strength Concrete with Copper Slag

    Directory of Open Access Journals (Sweden)

    Savaş Erdem

    2014-05-01

    Full Text Available The use of waste materials and industrial by-products in high-strength concrete could increase the sustainability of the construction industry. In this study, the potential of using copper slag as coarse aggregate in high-strength concrete was experimentally investigated. The effects of replacing gravel coarse aggregate by copper slag particles on the compressive strength, chloride ion- migration, water permeability and impact resistance of high-strength concretes were evaluated. Incorporating copper slag coarse particles resulted in a compressive strength increase of about 14 % on average partly due to the low Ca/Si ratio through the interface area of this concrete (more homogenous internal structure as confirmed by the energy dispersive X-ray micro chemical analysis. It was also found that the copper slag high-strength concrete provided better ductility and had much greater load carrying capacity compared to gravel high-strength concrete under dynamic conditions. Finally, it was observed that in comparison to the high strength concrete with slag, the chloride migration coefficient from non-steady state migration was approximately 30 % greater in the gravel high-strength concrete.

  18. Two different modes for copper(II ion coordination to quinine-type ligands

    Directory of Open Access Journals (Sweden)

    Rey Nicolás A.

    2006-01-01

    Full Text Available Three new copper(II complexes with the ligands quinuclidine [Cu(C7H13N2(OH2Cl]Cl.2H 2O (1, quinine [Cu(C20H23O2N2(OH 22]ClO4 (2, and hydroquinidine [Cu(C20H27O2N2(OH 2 Cl2]Cl.fraction one-halfH2O (3 have been isolated and characterized. The binding sites were assigned on the basis of vibrational spectroscopy, electron paramagnetic resonance, and thermal analysis results. The possibility of the involvement of the quinuclidinic nitrogen in the coordination was evidenced in complex 1, in which copper(II is coordinated to two quinuclidine molecules. In the case of quinine-type ligands, if the starting material is deprotonated in both nitrogens, copper(II coordination occurs through the quinuclidinic nitrogen, as in complex 2. In contrast, if the starting material is protonated in the quinuclidinic nitrogen the binding site is the quinolinic nitrogen, as in complex 3. Therefore, both nitrogens of quinine-type ligands constitute binding sites for copper(II ions.

  19. Immobilization of Magnetic Nanoparticles onto Amine-Modified Nano-Silica Gel for Copper Ions Remediation

    Directory of Open Access Journals (Sweden)

    Marwa Elkady

    2016-06-01

    Full Text Available A novel nano-hybrid was synthesized through immobilization of amine-functionalized silica gel nanoparticles with nanomagnetite via a co-precipitation technique. The parameters, such as reagent concentrations, reaction temperature and time, were optimized to accomplish the nano-silica gel chelating matrix. The most proper amine-modified silica gel nanoparticles were immobilized with magnetic nanoparticles. The synthesized magnetic amine nano-silica gel (MANSG was established and characterized using X-ray diffraction (XRD, transmission electron microscopy (TEM, scanning electron microscopy (SEM, Fourier transform infrared (FTIR, thermal gravimetric analysis (TGA, differential scanning calorimetry (DSC and vibrating sample magnetometry (VSM. The feasibility of MANSG for copper ions’ remediation from wastewater was examined. MANSG achieves a 98% copper decontamination from polluted water within 90 min. Equilibrium sorption of copper ions onto MANSG nanoparticles obeyed the Langmuir equation compared to the Freundlich, Temkin, Elovich and Dubinin-Radushkevich (D-R equilibrium isotherm models. The pseudo-second-order rate kinetics is appropriate to describe the copper sorption process onto the fabricated MANSG.

  20. THE EFFECTS OF COPPER AND ZINC IONS DURING THEIR BINDING WITH HUMAN SERUM γ-GLOBULIN

    Directory of Open Access Journals (Sweden)

    S. B. Cheknev

    2006-01-01

    Full Text Available Abstract. Conformational changes of human serum γ-globulin were studied during and after its binding with copper and zinc ions, using molecular ultrafiltration and differential spectrophotometry. The contents of nonbound metals in the filtrate were evaluated, resp., with sodium diethyl thyocarbamate and o-phenanthroline. It has been shown that copper and zinc exhibited common biological properties during their interactions with protein, but the binding differed sufficiently under similar experimental conditions. E.g., it was confirmed that copper was more active at the external sites of γ-globulin molecule, whereas zinc demonstrated tropicity for the areas of protein intraglobular compartments. The metal-binding sites have been described that differ in their parameters of interactions with cations and their spatial location within globular domains. Approaches are suggested for dynamic analysis of saturation for these differently located sites by the metal ions. We discuss the issues of altered conformational state of the γ-globulin molecule during the binding of cations, as well as potential usage of these data in clinical immunology.

  1. Ion exchange in KTiOPO4 crystals irradiated by copper and hydrogen ions.

    Science.gov (United States)

    Zhang, Ruifeng; Lu, Fei; Lian, Jie; Liu, Hanping; Liu, Xiangzhi; Lu, Qingming; Ma, Hongji

    2008-05-12

    Cs(+)-K+ ion exchanges were produced on KTiOPO4 crystals which is prior irradiated by Cu+ can H+ ions. The energy and dose of implanted Cu+ ions are 1.5 MeV and 0.5 x 10(14) ions/cm2, and that of H+ are 300 keV and 1 x 10(16) ions/cm2, respectively. The temperature of ions exchange is 430 degrees C, and the time range from 15 minutes to 30 minutes. The prism coupling method is used to measure the dark mode spectra of the samples. Compared with results of ion exchange on the sample without irradiations, both the number of guided mode and its corresponding effective refractive index are decreased. The experimental results indicate that the ion exchange rate closely related with the lattice damage and the damage layers formed in the depth of maximum nuclear energy deposition act as a barrier to block the ions diffuse into the sample and the concentration of defects can modify the speed of ion exchange..

  2. Membrane Anchoring and Ion-Entry Dynamics in P-type ATPase Copper Transport

    DEFF Research Database (Denmark)

    Grønberg, Christina; Sitsel, Oleg; Lindahl, Erik

    2016-01-01

    Cu(+)-specific P-type ATPase membrane protein transporters regulate cellular copper levels. The lack of crystal structures in Cu(+)-binding states has limited our understanding of how ion entry and binding are achieved. Here, we characterize the molecular basis of Cu(+) entry using molecular......-dynamics simulations, structural modeling, and in vitro and in vivo functional assays. Protein structural rearrangements resulting in the exposure of positive charges to bulk solvent rather than to lipid phosphates indicate a direct molecular role of the putative docking platform in Cu(+) delivery. Mutational analyses...... and simulations in the presence and absence of Cu(+) predict that the ion-entry path involves two ion-binding sites: one transient Met148-Cys382 site and one intramembranous site formed by trigonal coordination to Cys384, Asn689, and Met717. The results reconcile earlier biochemical and x-ray absorption data...

  3. Rapid determination of trace level copper in tea infusion samples by solid contact ion selective electrode

    Directory of Open Access Journals (Sweden)

    Aysenur Birinci

    2016-07-01

    Full Text Available A new solid contact copper selective electrode with a poly (vinyl chloride (PVC membrane consisting of o-xylylenebis(N,N-diisobutyldithiocarbamate as ionophore has been prepared. The main novelties of constructed ion selective electrode concept are the enhanced robustness, cheapness, and fastness due to the use of solid contacts. The electrode exhibits a rapid (< 10 seconds and near-Nernstian response to Cu2+ activity from 10−1 to 10−6 mol/L at the pH range of 4.0–6.0. No serious interference from common ions was found. The electrode characterizes by high potential stability, reproducibility, and full repeatability. The electrode was used as an indicator electrode in potentiometric titration of Cu(II ions with EDTA and for the direct assay of tea infusion samples by means of the calibration graph technique. The results compared favorably with those obtained by the atomic absorption spectroscopy (AAS.

  4. Influence of copper ions on the viability and cytotoxicity of Pseudomonas aeruginosa under conditions relevant to drinking water environments.

    Science.gov (United States)

    Dwidjosiswojo, Zenyta; Richard, Jessica; Moritz, Miriam M; Dopp, Elke; Flemming, Hans-Curt; Wingender, Jost

    2011-11-01

    Copper plumbing materials can be the source of copper ions in drinking water supplies. The aim of the current study was to investigate the influence of copper ions on the viability and cytotoxicity of the potential pathogen Pseudomonas aeruginosa that presents a health hazard when occurring in building plumbing systems. In batch experiments, exposure of P. aeruginosa (10(6)cells/mL) for 24h at 20°C to copper-containing drinking water from domestic plumbing systems resulted in a loss of culturability, while total cell numbers determined microscopically did not decrease. Addition of the chelator diethyldithiocarbamate (DDTC) to copper-containing water prevented the loss of culturability. When suspended in deionized water with added copper sulfate (10 μM), the culturability of P. aeruginosa decreased by more than 6 log units, while total cell counts, the concentration of cells with intact cytoplasmic membranes, determined with the LIVE/DEAD BacLight kit, and the number of cells with intact 16S ribosomal RNA, determined by fluorescent in situ hybridization, remained unchanged. When the chelator DDTC was added to copper-stressed bacteria, complete restoration of culturability was observed to occur within 14 d. Copper-stressed bacteria were not cytotoxic towards Chinese hamster ovary (CHO-9) cells, while untreated and resuscitated bacteria caused an almost complete decrease of the concentration of viable CHO-9 cells within 24 h. Thus, copper ions in concentrations relevant to drinking water in plumbing systems seem to induce a viable but non-culturable (VBNC) state in P. aeruginosa accompanied by a loss of culturability and cytotoxicity, and VBNC cells can regain both culturability and cytotoxicity, when copper stress is abolished.

  5. Development and tests of molybdenum armored copper components for MITICA ion source

    Science.gov (United States)

    Pavei, Mauro; Böswirth, Bernd; Greuner, Henri; Marcuzzi, Diego; Rizzolo, Andrea; Valente, Matteo

    2016-02-01

    In order to prevent detrimental material erosion of components impinged by back-streaming positive D or H ions in the megavolt ITER injector and concept advancement beam source, a solution based on explosion bonding technique has been identified for producing a 1 mm thick molybdenum armour layer on copper substrate, compatible with ITER requirements. Prototypes have been recently manufactured and tested in the high heat flux test facility Garching Large Divertor Sample Test Facility (GLADIS) to check the capability of the molybdenum-copper interface to withstand several thermal shock cycles at high power density. This paper presents both the numerical fluid-dynamic analyses of the prototypes simulating the test conditions in GLADIS as well as the experimental results.

  6. Development and tests of molybdenum armored copper components for MITICA ion source

    Energy Technology Data Exchange (ETDEWEB)

    Pavei, Mauro, E-mail: mauro.pavei@igi.cnr.it; Marcuzzi, Diego; Rizzolo, Andrea; Valente, Matteo [Consorzio RFX, Corso Stati Uniti, 4, I-35127 Padova (Italy); Böswirth, Bernd; Greuner, Henri [Max-Planck-Institut für Plasmaphysik, Boltzmannstrasse 2, D-85748 Garching (Germany)

    2016-02-15

    In order to prevent detrimental material erosion of components impinged by back-streaming positive D or H ions in the megavolt ITER injector and concept advancement beam source, a solution based on explosion bonding technique has been identified for producing a 1 mm thick molybdenum armour layer on copper substrate, compatible with ITER requirements. Prototypes have been recently manufactured and tested in the high heat flux test facility Garching Large Divertor Sample Test Facility (GLADIS) to check the capability of the molybdenum-copper interface to withstand several thermal shock cycles at high power density. This paper presents both the numerical fluid-dynamic analyses of the prototypes simulating the test conditions in GLADIS as well as the experimental results.

  7. Non-invasive nano-imaging of ion implanted and activated copper in silicon

    Science.gov (United States)

    Ballout, Fouad; Samson, Jean-Sébastien; Schmidt, Diedrich A.; Bründermann, Erik; Mathis, Yves-Laurent; Gasharova, Biliana; Dirk Wieck, Andreas; Havenith, Martina

    2011-07-01

    Using vibrational imaging techniques including Fourier-transform infrared (FTIR) synchrotron microscopy, Raman microscopy, and scattering scanning near-field infrared microcscopy (s-SNIM), we mapped a sample of phosphor and copper ions implanted in a high-purity silicon wafer. While Raman microscopy monitors the structural disorder within the implantation fields, the aforementionedinfrared techniques provide a detailed picture of the distribution of the free carriers. On a large scale (tens of micrometers), we visualized the channeling effects of phosphor dopants in silicon using FTIR microscopy. In comparison, using s-SNIM we were able to image, on a nanometer scale, local variations of the dielectric properties of the silicon substrate due to the activation of copper dopants.

  8. Comparative toxicity and biodistribution of copper nanoparticles and cupric ions in rats

    Directory of Open Access Journals (Sweden)

    Lee IC

    2016-06-01

    Full Text Available In-Chul Lee,1 Je-Won Ko,1 Sung-Hyeuk Park,1 Je-Oh Lim,1 In-Sik Shin,1 Changjong Moon,1 Sung-Hwan Kim,2 Jeong-Doo Heo,3 Jong-Choon Kim1 1College of Veterinary Medicine BK21 Plus Project Team, Chonnam National University, Gwangju, 2Jeonbuk Department of Inhalation Research, Korea Institute of Toxicology, Jeongeup, 3Gyeongnam Department of Environment and Toxicology, Korea Institute of Toxicology, Gyeongnam, Republic of Korea Abstract: Despite widespread use and prospective biomedical applications of copper nanoparticles (Cu NPs, their biosafety issues and kinetics remain unclear. Thus, the aim of this study was to compare the detailed in vivo toxicity of Cu NPs and cupric ions (CuCl2; Cu ions after a single oral dose. We determined the physicochemical characteristics of Cu NPs, including morphology, hydrodynamic size, zeta potential, and dissolution in gastric (pH 1.5, vehicle (pH 6.5, and intestinal (pH 7.8 conditions. We also evaluated the kinetics of Cu following a single equivalent dose (500 mg/kg of Cu NPs and Cu ions. Cu NPs had highest dissolution (84.5% only in gastric conditions when compared with complete dissolution of Cu ions under various physiological milieus. Kinetic analysis revealed that highest Cu levels in blood and tested organs of Cu NP-treated rats were 15%–25% lower than that of Cu ions. Similar to the case of Cu ions, Cu levels in the tested organs (especially liver, kidney, and spleen of Cu NP-treated rats increased significantly when compared with the vehicle control. However, delay in reaching the highest level and biopersistence of Cu were observed in the blood and tested organs of Cu NP-treated rats compared with Cu ions. Extremely high levels of Cu in feces indicated that unabsorbed Cu NPs or absorbed Cu ions were predominantly eliminated through liver/feces. Cu NPs exerted apparent toxicological effects at higher dose levels compared with Cu ions and showed sex-dependent differences in mortality, biochemistry, and

  9. Extraction of copper(II) ions from aqueous solutions with a methimazole-based ionic liquid.

    Science.gov (United States)

    Reyna-González, Juan M; Torriero, Angel A J; Siriwardana, Amal I; Burgar, Iko M; Bond, Alan M

    2010-09-15

    The recently synthesized ionic liquid (IL) 2-butylthiolonium bis(trifluoromethanesulfonyl)amide, [mimSBu][NTf(2)], has been used for the extraction of copper(II) from aqueous solution. The pH of the aqueous phase decreases upon addition of [mimSBu](+), which is attributed to partial release of the hydrogen attached to the N(3) nitrogen atom of the imidazolium ring. The presence of sparingly soluble water in [mimSBu][NTf(2)] also is required in solvent extraction studies to promote the incorporation of Cu(II) into the [mimSBu][NTf(2)] ionic liquid phase. The labile copper(II) system formed by interacting with both the water and the IL cation component has been characterized by cyclic voltammetry as well as UV-vis, Raman, and (1)H, (13)C, and (15)N NMR spectroscopies. The extraction process does not require the addition of a complexing agent or pH control of the aqueous phase. [mimSBu][NTf(2)] can be recovered from the labile copper-water-IL interacting system by washing with a strong acid. High selectivity of copper(II) extraction is achieved relative to that of other divalent cobalt(II), iron(II), and nickel(II) transition-metal cations. The course of microextraction of Cu(2+) from aqueous media into the [mimSBu][NTf(2)] IL phase was monitored in situ by cyclic voltammetry using a well-defined process in which specific interaction with copper is believed to switch from the ionic liquid cation component, [mimSBu], to the [NTf(2)] anion during the course of electrochemical reduction from Cu(II) to Cu(I). The microextraction-voltammetry technique provides a fast and convenient method to determine whether an IL is able to extract electroactive metal ions from an aqueous solution.

  10. Separation of metalloproteins using a novel metal ion contaminant sweeping technique and detection of protein-bound copper by a metal ion probe in polyacrylamide gel electrophoresis: distribution of copper in human serum.

    Science.gov (United States)

    Saito, Shingo; Kawashima, Mitsuyoshi; Ohshima, Hiroki; Enomoto, Kazuki; Sato, Makoto; Yoshimura, Hajime; Yoshimoto, Keitaro; Maeda, Mizuo; Shibukawa, Masami

    2013-10-21

    A polyacrylamide gel electrophoresis (PAGE)-based method has been developed, consisting of two types of gel electrophoresis, to obtain an accurate distribution of protein-bound metal ions in biological samples. First, proteins are separated by PAGE without the uptake of contaminant metal ions in the separation field and dissociation of metal ions from the proteins. This is followed by another PAGE for the separation and detection of protein-bound metal ions in small volume samples with high sensitivity in the ppt range using a fluorescent metal probe. The former is a new technique using blue-native (BN) PAGE to electrophoretically sweep all metal contaminants by employing two kinds of chelating agents. These agents form complexes with contaminants in the gel and the separation buffer solution, which migrate towards opposite pole directions, thus lowering the contaminants to below the ppt level during separation. This is termed "Metal Ion Contaminant Sweeping BN-PAGE (MICS-BN-PAGE)". After the separation of proteins under these first metal-free conditions, the metal ions in the gel fractions are eluted, followed by derivatization of copper ions into the metal probe complexes to be separated and determined by fluorescence detection in the second PAGE. In this PAGE-based method, the copper ions bound to ceruloplasmin and superoxide dismutase were quantitatively determined, in addition to the exchangeable albumin-bound copper ions. This system successfully provided distribution maps of protein-copper in human serum. The precise distribution of copper in human serum was investigated, and found to be different from that which is widely accepted.

  11. MECHANICAL PROPERTIES OF PVA NANOFIBER TEXTILES WITH INCORPORATED NANODIAMONDS, COPPER AND SILVER IONS

    Directory of Open Access Journals (Sweden)

    Kateřina Indrová

    2015-02-01

    Full Text Available The unique properties of nanotextiles based on poly(vinyl-alcohol (PVA manufactured using electrospinning method have been known and exploited for many years. Recently, the enrichment of nanofiber textiles with nanoparticles, such as ions or nanodiamond particles (NDP, has become a popular way to modify the textile mechanical, chemical and physical properties. The aim of our study is to investigate the macromechanical properties of PVA nanotextiles enriched with NDP, silver (Ag and copper (Cu ions. The nanofiber textiles of a various surface weight were prepared from 16% PVA solution, while glyoxal and phosphoric acid were used as cross-linking agents. The copper and silver ions were diluted in aqueous solution and NDP were dispersed into the fibers by ultrasound homogenization. All but one set of samples were exposed to the temperature of 140 °C for 10 minutes. The samples without thermal stabilization exhibited significantly lower elastic stiffness and tensile strength. Moreover, the results of tensile testing indicate that the addition of dispersed nanoparticles has a minor effect on the mechanical properties of textiles and contributes rather to their reinforcement. On the other hand, the lack of thermal stabilization results in a poor interconnection of individual nanofiber layers and the non-stabilized textiles exhibit a lower elastic stiffness and reduced tensile strength.

  12. Comparative toxicity and biodistribution of copper nanoparticles and cupric ions in rats.

    Science.gov (United States)

    Lee, In-Chul; Ko, Je-Won; Park, Sung-Hyeuk; Lim, Je-Oh; Shin, In-Sik; Moon, Changjong; Kim, Sung-Hwan; Heo, Jeong-Doo; Kim, Jong-Choon

    2016-01-01

    Despite widespread use and prospective biomedical applications of copper nanoparticles (Cu NPs), their biosafety issues and kinetics remain unclear. Thus, the aim of this study was to compare the detailed in vivo toxicity of Cu NPs and cupric ions (CuCl2; Cu ions) after a single oral dose. We determined the physicochemical characteristics of Cu NPs, including morphology, hydrodynamic size, zeta potential, and dissolution in gastric (pH 1.5), vehicle (pH 6.5), and intestinal (pH 7.8) conditions. We also evaluated the kinetics of Cu following a single equivalent dose (500 mg/kg) of Cu NPs and Cu ions. Cu NPs had highest dissolution (84.5%) only in gastric conditions when compared with complete dissolution of Cu ions under various physiological milieus. Kinetic analysis revealed that highest Cu levels in blood and tested organs of Cu NP-treated rats were 15%-25% lower than that of Cu ions. Similar to the case of Cu ions, Cu levels in the tested organs (especially liver, kidney, and spleen) of Cu NP-treated rats increased significantly when compared with the vehicle control. However, delay in reaching the highest level and biopersistence of Cu were observed in the blood and tested organs of Cu NP-treated rats compared with Cu ions. Extremely high levels of Cu in feces indicated that unabsorbed Cu NPs or absorbed Cu ions were predominantly eliminated through liver/feces. Cu NPs exerted apparent toxicological effects at higher dose levels compared with Cu ions and showed sex-dependent differences in mortality, biochemistry, and histopathology. Liver, kidney, and spleen were the major organs affected by Cu NPs. Collectively, the toxicity and kinetics of Cu NPs are most likely influenced by the release of Cu dissociated from Cu NPs under physiological conditions.

  13. Transport Measurements in the Mixed Ion-Electron Conductor Copper(x) Carbon-Disulfide

    Science.gov (United States)

    Kuo, Hung-Jen

    (sigma)(,i), (sigma)(,e), and the chemical diffusion coefficient, (')D, of highly-disordered Cu(,x)CS(,2) were investigated using a dc 4-lead technique employing Pt electrodes. The experiments were performed at various copper concentrations from x = 2.87 to 3.60 and various temperatures from 260 K to 350 K. The results were interpreted by Yokota's and ionic hopping diffusion theories. (sigma)(,i) and (sigma)(,e) are comparable at room temperature, 4.18 x 10('-3) (OMEGA)('-1)cm('-1) and 1.55 x 10('-3) (OMEGA)('-1)cm('-1) respectively at X = 3.60 and 300 K. Both (sigma)(,i) and (sigma)(,e) follow a simple Arrhenius form with activation energies (TURN)0.40 eV and (TURN)0.29 eV respectively. The exponential dependence of (sigma)(,i) on X is explained in terms of the activation entropy associated with the motion of ions. Electronic conduction is by hopping. Results show that it is reasonable to assume that all the copper ions are mobile. The mobility and the diffusivity of copper ions were found to be 0.71 x 10('-6) cm('2)V(' -1)sec('-1) and 1.83 x 10('-8) cm('2)/sec respectively at X = 3.6 and 300 K. The diffusivity is much less than the chemical diffusion coefficient evaluated from the diffusion time constant, (')D = 0.829 x 10('-5) cm('2)/sec at X = 3.60 and 300 K. This is because of a large enhancement factor W (TURN) 453, or a large (PAR-DIFF)m(,e)/(PAR-DIFF)N. The change in galvanic cell potential E with X, -(PAR-DIFF)E/(PAR -DIFF)X, calculated from the measurements of (sigma)(,i), (sigma)(,e), and (')D, is 14 Volt.

  14. A novel zerovalent manganese for removal of copper ions: synthesis, characterization and adsorption studies

    Science.gov (United States)

    Dada, A. O.; Adekola, F. A.; Odebunmi, E. O.

    2015-11-01

    Synthesis of nanoscale zerovalent manganese (nZVMn) by chemical reduction was carried out in a single pot system under inert environment. nZVMn was characterized using a combination of analytical techniques: Ultraviolet-Visible Spectroscopy, Fourier Transform Infrared Spectroscopy, Scanning Electron Microscopy, Transmission Electron Microscopy, Energy Dispersive X-ray, BET surface area and Point of Zero Charge. The adsorption physicochemical factors: pH, contact time, adsorbent dose, agitation speed, initial copper ion concentration and temperature were optimized. The kinetic data fitted better to Pseudo second-order, Elovich, fractional power and intraparticle diffusion models and their validity was tested by three statistical models: sum of square error, Chi-square (χ 2) and normalized standard deviation (Δq). Seven of the two-parameter isotherm models [Freundlich, Langmuir, Temkin, Dubinin-Kaganer-Raduskevich (DKR), Halsey, Harkin-Jura and Flory-Huggins] were used to analyse the equilibrium adsorption data. The Langmuir monolayer adsorption capacity (Q max = 181.818 mg/g) obtained is greater than other those of nano-adsorbents utilized in adsorption of copper ions. The equilibrium adsorption data were better described by Langmuir, Freundlich, Temkin, DKR and Halsey isotherm models considering their coefficient of regression (R 2 > 0.90). The values of the thermodynamic parameters: standard enthalpy change ∆H° (+50.27848 kJ mol-1), standard entropy change ∆S° (203.5724 J mol-1 K-1) and the Gibbs free energy change ∆G° revealed that the adsorption process was feasible, spontaneous, and endothermic in nature. The performance of this novel nanoscale zerovalent manganese (nZVMn) suggested that it has a great potential for effective removal of copper ions from aqueous solution.

  15. A novel zerovalent manganese for removal of copper ions: synthesis, characterization and adsorption studies

    Science.gov (United States)

    Dada, A. O.; Adekola, F. A.; Odebunmi, E. O.

    2017-06-01

    Synthesis of nanoscale zerovalent manganese (nZVMn) by chemical reduction was carried out in a single pot system under inert environment. nZVMn was characterized using a combination of analytical techniques: Ultraviolet-Visible Spectroscopy, Fourier Transform Infrared Spectroscopy, Scanning Electron Microscopy, Transmission Electron Microscopy, Energy Dispersive X-ray, BET surface area and Point of Zero Charge. The adsorption physicochemical factors: pH, contact time, adsorbent dose, agitation speed, initial copper ion concentration and temperature were optimized. The kinetic data fitted better to Pseudo second-order, Elovich, fractional power and intraparticle diffusion models and their validity was tested by three statistical models: sum of square error, Chi-square ( χ 2) and normalized standard deviation (Δ q). Seven of the two-parameter isotherm models [Freundlich, Langmuir, Temkin, Dubinin-Kaganer-Raduskevich (DKR), Halsey, Harkin-Jura and Flory-Huggins] were used to analyse the equilibrium adsorption data. The Langmuir monolayer adsorption capacity ( Q max = 181.818 mg/g) obtained is greater than other those of nano-adsorbents utilized in adsorption of copper ions. The equilibrium adsorption data were better described by Langmuir, Freundlich, Temkin, DKR and Halsey isotherm models considering their coefficient of regression ( R 2 > 0.90). The values of the thermodynamic parameters: standard enthalpy change ∆ H° (+50.27848 kJ mol-1), standard entropy change ∆ S° (203.5724 J mol-1 K-1) and the Gibbs free energy change ∆ G° revealed that the adsorption process was feasible, spontaneous, and endothermic in nature. The performance of this novel nanoscale zerovalent manganese (nZVMn) suggested that it has a great potential for effective removal of copper ions from aqueous solution.

  16. Removal of Copper (II Ions from Aqueous Solutions by Adsorption with Low Cost Acid Activated Cynodon Dactylon Carbon

    Directory of Open Access Journals (Sweden)

    U. Gayathri

    2011-01-01

    Full Text Available The main purpose of this work was to exploit low cost and efficient sorbents for the removal of copper from aqueous solution using Cynodon dactylon carbon. It was observed from the experimental results that almost 90-100% copper can be removed from the aqueous solution. Adsorption kinetics and equilibrium have been investigated as a function of initial copper ion concentration. pH, contact time and adsorbent dosage. Kinetics studies suggested that the adsorption allowed first order reaction. Equilibrium data were analyzed using Langmuir and Freundlich isotherm models. On the basis of experimental results and the model parameters, it can be concluded that the carbonaceous Cynodon dactylon is effective for the removal of copper ion from aqueous solution.

  17. Rapid determination of trace level copper in tea infusion samples by solid contact ion selective electrode

    OpenAIRE

    2016-01-01

    A new solid contact copper selective electrode with a poly (vinyl chloride) (PVC) membrane consisting of o-xylylenebis(N,N-diisobutyldithiocarbamate) as ionophore has been prepared. The main novelties of constructed ion selective electrode concept are the enhanced robustness, cheapness, and fastness due to the use of solid contacts. The electrode exhibits a rapid (< 10 seconds) and near-Nernstian response to Cu2+ activity from 10−1 to 10−6 mol/L at the pH range of 4.0–6.0. No serious interfer...

  18. Silicon-Copper Helical Arrays for New Generation Lithium Ion Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Polat, B. D.; Keles, O; Amine, K

    2015-09-22

    The helical array (with 10 atom % Cu) exhibits 3130 mAh g–1 with 83% columbic efficiency and retains 83% of its initial discharge capacity after 100th cycle. Homogeneously distributed interspaces between the helical arrays accommodate high volumetric changes upon cycling and copper atoms form a conductive network to buffer the mechanical stress generated in the electrode while minimizing electrochemical agglomeration of Si. Also, ion assistance is believed to enhance the density of the helices at the bottom thus increasing the adhesion

  19. Mathematical modeling of copper(II) ion inhibition on COD removal in an activated sludge unit.

    Science.gov (United States)

    Pamukoglu, M Yunus; Kargi, Fikret

    2007-07-19

    A mathematical model was developed to describe the Cu(II) ion inhibition on chemical oxygen demand (COD) removal from synthetic wastewater containing 15 mg l(-1) Cu(II) in an activated sludge unit. Experimental data obtained at different sludge ages (5-30 days) and hydraulic residence times (HRT) (5-25 h) were used to determine the kinetic, stoichiometric and inhibition constants for the COD removal rate in the presence and absence of Cu(II) ions. The inhibition pattern was identified as non-competitive, since Cu(II) ion inhibitions were observed both on maximum specific substrate removal rate (k) and on the saturation constant (Ks) with the inhibition constants of 97 and 18 mg l(-1), respectively, indicating more pronounced inhibition on Ks. The growth yield coefficient (Y) decreased and the death rate constant (b) increased in the presence of Cu(II) ions due to copper ion toxicity on microbial growth with inhibition constants of 29 and 200 mg l(-1), respectively indicating more effective inhibition on the growth yield coefficient or higher maintenance requirements. The mathematical model with the predetermined kinetic constants was able to predict the system performance reasonably well especially at high HRT operations.

  20. Fabrication of Chitosan-complexed Electrode and Evaluation of Its Efficiency in Removal of Copper Ion from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Yoon Young-Chan

    2016-01-01

    Full Text Available In this study, we fabricated chitosan/PVA/activated carbon complexed electrode to remove copper ion from aqueous solution. The prepared composite electrode was analyzed by BET and SEM to investigate its physicochemical properties. Electrochemical properties of prepared composite electrodes were analyzed via cyclic voltammetry. Adsorption performance of copper ion on chitosan composite complexed electrodes was evaluated. Almost similar pore size distribution results were observed in the series of ACP not included electrodes while observed differences in pore size distribution for the ACP included one. Cyclic voltammetry results exhibited that oxidation-reduction reaction does not occur in a potential range of -1.0 ~ 1.0 V. The amount of copper ion during adsroption reaction is increase according to increase of adsorption potential to 1.0 V.

  1. EFFECTS OF COPPER ION IMPLANTATION ON ANTIBACTERIAL ACTIVITY OF AISI420 STAINLESS STEEL

    Institute of Scientific and Technical Information of China (English)

    Z.G. Dan; H.W. Ni; B.F. Xu; J. Xiong; P. Y. Xiong

    2005-01-01

    Antibacterial activity of AISI420 stainless steel (SS) implanted by copper was investigated. Ions extracted from a metal vapor vacuum arc (MEVVA) are sourced with 100keV energy and a dose range from 0.2×1017 to 2.0×1017ions .cm-2. The saturation dose of Cu implantation in AISI420 SS and Cu surface concentration were calculated at the energy of 100keV. The effect of dose on the antibacterial activity was analyzed. Results of antibacterial test show that the saturation dose is the optimum implantation dose for best antibacterial activity, which is above 99% against both Escherichia coli and Staphylococcus aureus. Novel phases such as Fe4Cu3 and Cu9.9Fe0.1 were found in the implanted layer by glancing angle X-ray diffraction (GXRD). The antibacterial activity of AISI420 SS attributes to Cu-contained phase.

  2. Colorimetric and fluorimetric response of salicylaldehyde dithiosemicarbazone towards fluoride, cyanide and copper ions: Spectroscopic and TD-DFT studies

    Science.gov (United States)

    Harikrishnan, Vengayil K.; Basheer, Sabeel M.; Joseph, Nithin; Sreekanth, Anandaram

    2017-07-01

    The sensing mechanism of salicylaldehyde phenyldithiosemicarbazone (SDTSC) chemosensor has been investigated by spectroscopic and TD-DFT methods. The SDTSC shows colourimetric and spectral changes towards fluoride, cyanide and copper ions. The interaction between SDTSC with fluoride, cyanide and copper ions was examined through their absorption and fluorescence behaviour, and found that SDTSC has more sensing ability towards Cu2 + ion than CN- and F- ions. The 1H NMR titration with SDTSC and F- gives the structural changes in the sensing process. The reversibility of SDTSC was also evaluated and thus it is confirmed as a reusable chemosensor which can be clarified by the ;Read-Erase-Read-Write; logic system. The DFT and TD-DFT calculations give the detailed sensing mechanism of SDTSC towards fluoride ion. The potential energy surface (PES) analysis confirms the excited state electron transfer mechanism.

  3. Real-time monitoring of copper ions-induced cytotoxicity by EIS cell chips.

    Science.gov (United States)

    Primiceri, Elisabetta; Chiriacò, Maria Serena; D'Amone, Eliana; Urso, Emanuela; Ionescu, Rodica Elena; Rizzello, Antonia; Maffia, Michele; Cingolani, Roberto; Rinaldi, Ross; Maruccio, Giuseppe

    2010-08-15

    An important goal of biomedical research is the development of tools for high-throughput evaluation of drug effects and cytotoxicity tests. Here we demonstrate EIS cell chips able to monitor cell growth, morphology, adhesion and their changes as a consequence of treatment with drugs or toxic compounds. As a case study, we investigate the uptake of copper ions and its effect on two cell lines: B104 and HeLa cells. For further understanding, we also carried out in parallel with EIS studies, a complete characterization of cell morphology and changes induced by copper ions through complementary methodologies (including state-of-the-art AFM, viability test and Western blot). Our results reveal a strong correlation between EIS data and both MTT test and AFM characterization so our chip can be used as powerful tools in all biology lab in combination with other standard methods giving additional information that can be useful in a complete and deep investigation of a biological process. This chip can be used even alone replacing in vitro drug tests based on conventional biochemical methods, being very cheap and reusable and allowing to perform cytotoxicity tests without using any expensive reagent or equipment.

  4. Estimation of free copper ion concentrations in blood serum using T1 relaxation rates

    Science.gov (United States)

    Blicharska, Barbara; Witek, Magdalena; Fornal, Maria; MacKay, Alex L.

    2008-09-01

    The water proton relaxation rate constant R1 = 1/ T1 (at 60 MHz) of blood serum is substantially increased by the presence of free Cu 2+ ions at concentrations above normal physiological levels. Addition of chelating agents to serum containing paramagnetic Cu 2+ nulls this effect. This was demonstrated by looking at the effect of adding a chelating agent—D-penicillamine (D-PEN) to CuSO 4 and CuCl 2 aqueous solutions as well as to rabbit blood serum. We propose that the measurement of water proton spin-lattice relaxation rate constants before and after chelation may be used as an alternative approach for monitoring the presence of free copper ions in blood serum. This method may be used in the diagnosis of some diseases (leukaemia, liver diseases and particularly Wilson's disease) because, in contrast to conventional methods like spectrophotometry which records the total number of both bound and free ions, the proton relaxation technique is sensitive solely to free paramagnetic ions dissolved in blood serum. The change in R1 upon chelation was found to be less than 0.06 s -1 for serum from healthy subjects but greater than 0.06 s -1 for serum from untreated Wilson's patients.

  5. PERIODATE AND HYPOBROMITE MODIFICATION OF SOUTHERN PINE WOOD TO IMPROVE SORPTION OF COPPER ION

    Directory of Open Access Journals (Sweden)

    James D. McSweeny

    2008-02-01

    Full Text Available Milled southern pine wood was modified with sequential treatments of sodium periodate and sodium hypobromite for the purpose of improving copper ion (Cu2+ sorption capacity of the wood when tested in 24-h equilibrium batch tests. The modified wood provided additional carboxyl groups to those in the native wood and substantially increased Cu2+ uptake over that of unmodified wood. Sorption capacity (qe measured with an unbuffered standard solution increased to a maximum of 7.8 mg Cu2+ ion per gram of wood (treated from 3.1 mg Cu2+ ion/g wood (untreated. Samples tested were first sodium ion exchanged to keep the pH of the standard solution from declining during the sorption test. The treatment necessary for maximum qe was 3% (w/v periodate for 24 h and 0.8% (w/v bromine (as hypobromite for 24 h; both treatments were at room temperature. These conditions corresponded to the maximum periodate concentration and treatment times tested. To further evaluate the efficacy of modification treatments, weight change after each treatment was determined. Weight loss after the periodate stage for any concentration and time used was minor, indicating the selective nature of this reaction. However, most of the weight loss was incurred after hypobromite treatment. Weight loss corresponding to the greatest increase in sorption capacity was 12.6% total from the combined periodate and hypobromite stages. The increase of carboxylate functional groups in the wood was monitored using FTIR/ATR spectroscopy.

  6. Activation of oxygen-mediating pathway using copper ions: fine-tuning of growth kinetics in gold nanorod overgrowth.

    Science.gov (United States)

    Liu, Wenqi; Zhang, Hui; Wen, Tao; Yan, Jiao; Hou, Shuai; Shi, Xiaowei; Hu, Zhijian; Ji, Yinglu; Wu, Xiaochun

    2014-10-21

    Growth kinetics plays an important role in the shape control of nanocrystals (NCs). Herein, we presented a unique way to fine-tune the growth kinetics via oxidative etching activated by copper ions. For the overgrowth of gold nanorods (Au NRs), competitive adsorption of dissolved oxygen on rod surface was found to slow down the overgrowth rate. Copper ions were able to remove the adsorbed oxygen species from the Au surface via oxidative etching, thus exposing more reaction sites for Au deposition. In this way, copper ions facilitated the overgrowth process. Furthermore, Cu(2+) rather than Cu(+) acted as the catalyst for the oxidative etching. Comparative study with Ag(+) indicated that Cu(2+) cannot regulate NC shapes via an underpotential deposition mechanism. In contrast, Ag(+) led to the formation of Au tetrahexahedra (THH) and a slight decrease of the growth rate at similar growth conditions. Combining the distinct roles of the two ions enabled elongated THH to be produced. Copper ions activating the O2 pathway suggested that dissolved oxygen has a strong affinity for the Au surface. Moreover, the results of NC-sensitized singlet oxygen ((1)O2) indicated that the absorbed oxygen species on the surface of Au NCs bounded with low-index facets mainly existed in the form of molecular O2.

  7. Study of coagulation processes of selected humic acids under copper ions influence*

    Science.gov (United States)

    Boguta, Patrycja; Sokolowska, Zofia

    2013-04-01

    Humic acids have limited sorption capacity and big dose of metal or other mineral component which can be sorbed on humic acids, can cause saturation of negative, surface charge of humic acids leading to destabilization of dissolved humic acids compounds. Destabilisation can be observed as coagulation and floculation proces of humic acids. However there are a lot of mechanisms which causing precipitation of humic acids. Thereby, in order to full description of coagulation process, different methods should be applied. Ordinarily, humic acids coagulation is studied by measurement of absorbance, transmittance or carbon loss in solution. Meanwhile, very significant information is also variation of metal content in soil solution and information whether metal goes to precipitate together with humic acids or stays in dissolved form in solution. So, that, from one side, processes of stronger accumulation of metal can lead to soil degradation and micronutrient deficiency for plants. However, there is also possibility to stay metal in solution in toxic and bioavailable form for plants. Main aim of this paper was to study coagulation process of different humic acids extracted from mucking peats under copper ions influence at adjusted pH to 5. In order to this, four peaty-muck soils were taken from selected places in east part of Poland (meadows and river valleys). These soils differed by humification degree, secondary transformation, density and pH. At next step, humic acids were extracted from soils using sodium hydroxide (NaOH) extractant. After exact purification by washing with HF-HCl mixture and water, humic acids were liofilized. Solutions of humic acids were prepared at concentration 40 mg/dm3 with addition of different amount of copper ions to obtain final concentration of Cu(II) ranged from 0-40mg/dm3. After 24 hours solutions were investigated using measurements of absorbance at 470nm (UV-VIS spectrometer Jasco V-530), measurements of organic carbon in solution

  8. Controlled growth of few-layer hexagonal boron nitride on copper foils using ion beam sputtering deposition.

    Science.gov (United States)

    Wang, Haolin; Zhang, Xingwang; Meng, Junhua; Yin, Zhigang; Liu, Xin; Zhao, Yajuan; Zhang, Liuqi

    2015-04-01

    Ion beam sputtering deposition (IBSD) is used to synthesize high quality few-layer hexagonal boron nitride (h-BN) on copper foils. Compared to the conventional chemical vapor deposition, the IBSD technique avoids the use of unconventional precursors and is much easier to control, which should be very useful for the large-scale production of h-BN in the future.

  9. Possible wave formation and martensitic transformation of iron particles in copper single crystals during argon ion bombardment

    DEFF Research Database (Denmark)

    Thölén, Anders Ragnar; Li, Chang-Hai; Easterling, K.E.

    1983-01-01

    Thin single crystal copper specimens (thickness ~250 nm) containing coherent iron particles (diameter 40–50 nm) have been bombarded with argon ions (5, 80, and 330 keV). During this process some of the iron particles transform to martensite. The transformation was observed near the exposed surface...

  10. Electron Paramagnetic Resonance and Optical Absorption Studies on Copper Ions in Mixed Alkali Cadmium Phosphate Glasses

    Institute of Scientific and Technical Information of China (English)

    G.Giridhar; M.Rangacharyulu; R.V.S.S.N.Ravikumar; P.Sambasiva Rao

    2009-01-01

    Electron paramagnetic resonance (EPR) and optical absorption studies were carried out at room temperature on copper doped mixed alkali cadmium phosphate (LiNaCdP) glasses to understand the nature and symmetry of dopant. Three samples with varying concentrations of alkali ions have been prepared. The spin Hamiltonian parameters obtained from room temperature EPR spectra are: g||=2.437, g⊥=2.096, A||=117×10-4 cm-1, A⊥=26×10-4 cm-1 for LiNaCdP1, g||=2.441, g⊥=2.088, A||=121×10-4 cm-1, A⊥=25×10-4 cm-1 for LiNaCdP2 and g||=2.433, g⊥=2.096, A||=125×10-4 cm-1, A⊥=32×10-4 cm-1 for LiNaCdP3. These EPR results indicate that the dopant Cu2+ ion enters the glass matrix into a tetragonally elongated octahedral site. The bonding parameters evaluated by correlating optical and EPR data suggest that bonding between the central metal ion and ligands is partially covalent. The mixed alkali effect in cadmium phosphate glasses was reported.

  11. DNA cleavage system of nanosized graphene oxide sheets and copper ions.

    Science.gov (United States)

    Ren, Hongliu; Wang, Chong; Zhang, Jiali; Zhou, Xuejiao; Xu, Dafeng; Zheng, Jing; Guo, Shouwu; Zhang, Jingyan

    2010-12-28

    The exploration of efficient DNA intercalative agents (intercalators) is essential for understanding DNA scission, repair, and signal transduction. In this work, we explored systematically the graphene oxide (GO) interaction with DNA molecules using fluorescence spectroscopic (FL) and circular dichroism (CD) studies, gel electrophoresis, and DNA thermal denaturation. We demonstrated that the GO nanosheets could intercalate efficiently into DNA molecules. Significantly, we illustrated that the scission of DNA by GO sheets combining with copper ions could take place pronouncedly. The scission of DNA by the GO/Cu(2+) system is critically dependent on the concentrations of GO and Cu(2+) and their ratio. DNA cleavage ability exhibited by the GO with several other metal ions and the fact that GO/Cu(2+)-cleaved DNA fragments can be partially relegated suggest that the mechanism of DNA cleavage by the GO/metal ion system is oxidative and hydrolytic. The result reveals that the GO/Cu(2+) could be used as a DNA cleaving system that should find many practical applications in biotechnology and as therapeutic agents.

  12. D-penicillamine-templated copper nanoparticles via ascorbic acid reduction as a mercury ion sensor.

    Science.gov (United States)

    Lin, Shu Min; Geng, Shuo; Li, Na; Li, Nian Bing; Luo, Hong Qun

    2016-05-01

    Mercury ion is one of the most hazardous metal pollutants that can cause deleterious effects on human health and the environment even at low concentrations. It is necessary to develop new mercury detection methods with high sensitivity, specificity and rapidity. In this study, a novel and green strategy for synthesizing D-penicillamine-capped copper nanoparticles (DPA-CuNPs) was successfully established by a chemical reduction method, in which D-penicillamine and ascorbic acid were used as stabilizing agent and reducing agent, respectively. The as-prepared DPA-CuNPs showed strong red fluorescence and had a large Stoke's shift (270nm). Scanning electron microscopy, transmission electron microscopy, Fourier-transform infrared spectroscopy, fluorescence spectroscopy, and ultraviolet-visible spectrophotometry were utilized to elucidate the possible fluorescence mechanism, which could be aggregation-induced emission effect. Based on the phenomenon that trace mercury ion can disperse the aggregated DPA-CuNPs, resulting in great fluorescence quench of the system, a sensitive and selective assay for mercury ion in aqueous solution with the DPA-CuNPs was developed. Under optimum conditions, this assay can be applied to the quantification of Hg(2+) in the 1.0-30μM concentration range and the detection limit (3σ/slope) is 32nM. The method was successfully applied to determine Hg(2+) in real water samples.

  13. Effect of halide ions on passivation and pitting corrosion of copper in alkaline solutions

    Energy Technology Data Exchange (ETDEWEB)

    Gad Allah, A.G.; Abou-Romia, M.M.; Badawy, W.A.; Rehan, H.H. (Cairo Univ., Gizeh (Egypt). Dept. of Chemistry)

    1991-11-01

    The passivity of copper in NaOH and borate buffer solutions containing chloride, bromide and fluoride ions was studied by using cyclic voltammetry and potentiostatic current transient measurements. At scan rates >> 20 mVs{sup -1}, the addition of halide ions does not nearly affect the cyclic voltammograms in the absence of pitting. But they differ considerably in presence of pitting. The pitting potential was found to depend on the solution pH and decreased linearly with increase of logarithm of halide ion concentration. The current transients in the passivity as well as in the pitting potential regions were analyzed. Before the pitting, i-time curves were rather similar to those obtained in the plain solutions. At times > 20 seconds, the current varies linearly with the reciprocal of the square root of time indicating diffusional characteristics of the metal corrosion through the passive layer. In presence of pitting, the pitting current versus time relations fit the Engell-Stolica equation. (orig.).

  14. Copper ion implanted aluminum nitride dilute magnetic semiconductors (DMS) prepared by molecular beam epitaxy

    Energy Technology Data Exchange (ETDEWEB)

    Shah, A., E-mail: attaullah77@yahoo.com [National Institute of Lasers and Optronics (NILOP), PO Nilore, Islamabad (Pakistan); DMME, Pakistan Institute of Engineering and Applied Science (PIEAS), PO Nilore, Islamabad (Pakistan); Ahmad, Jamil [DMME, Pakistan Institute of Engineering and Applied Science (PIEAS), PO Nilore, Islamabad (Pakistan); Ahmad, Ishaq [Experimental Physics Lab, National Center for Physics (NCP), Islamabad (Pakistan); Mehmood, Mazhar [DMME, Pakistan Institute of Engineering and Applied Science (PIEAS), PO Nilore, Islamabad (Pakistan); Mahmood, Arshad [National Institute of Lasers and Optronics (NILOP), PO Nilore, Islamabad (Pakistan); Rasheed, Muhammad Asim [DMME, Pakistan Institute of Engineering and Applied Science (PIEAS), PO Nilore, Islamabad (Pakistan)

    2014-10-30

    Highlights: • AlN:Cu dilute magnetic semiconductors were successfully prepared by molecular beam epitaxy followed by Cu{sup +} implantation. • Room temperature ferromagnetism was observed after annealing the samples at appropriate temperature. • XRD and Raman spectrometry excluded the possibility of formation of any secondary phases. • By doping intrinsically nonmagnetic dopants (Cu), it has been proved experimentally that their precipitates do not contribute to ferromagnetism. • The reason for ferromagnetism in Cu-doped AlN as observed was explained on the basis of p–d hybridization mechanism (Wu et al.). - Abstract: Diluted magnetic semiconductor (DMS) AlN:Cu films were fabricated by implanting Cu{sup +} ions into AlN thin films at various ion fluxes. AlN films were deposited on c-plane sapphire by molecular beam epitaxy followed by Cu{sup +} ion implantation. The structural and magnetic characterization of the samples was performed through Rutherford backscattering and channeling spectrometry (RBS/C), X-ray diffraction (XRD), Raman spectroscopy, vibrating sample magnetometer (VSM) and SQUID. Incorporation of copper into the AlN lattice was confirmed by RBS, while XRD revealed that no new phase was formed as a result of ion implantation. RBS also indicated formation of defects as a result of implantation process and the depth and degree of damage increased with an increase in ion fluence. Raman spectra showed only E{sub 2} (high) and A{sub 1} (LO) modes of wurtzite AlN crystal structure and confirmed that no secondary phases were formed. It was found that both Raman modes shift with Cu{sup +} fluences, indicating that Cu ion may go to interstitial or substitutional sites resulting in distortion or damage of lattice. Although as implanted samples showed no magnetization, annealing of the samples resulted in appearance of room temperature ferromagnetism. The saturation magnetization increased with both the annealing temperature as well as with ion

  15. DNA degradation by aqueous extract of Aloe vera in the presence of copper ions.

    Science.gov (United States)

    Naqvi, Shoa; Ullah, M F; Hadi, S M

    2010-06-01

    The plant Aloe vera has long been used in medicine, as dietary supplements and for cosmetic purposes. Aloe vera extracts are a rich source of polyphenols, such as aloin and aloe emodin and have shown a wide range of pharmacological properties, including anti-inflammatory and anti-cancer properties. The bioactive component aloe emodin has been reported to induce apoptosis in various cancer cell lines. Many of the biological activities of Aloe vera have been attributed to its antioxidant properties. However, most plant-derived polyphenols that are also present in Aloe vera may exhibit pro-oxidant properties either alone or in the presence of transition metals, such as copper. Previous reports from this laboratory have implicated the pro-oxidant action as one of the mechanisms for their anti-cancer properties. In the present paper, we show that aqueous extract of Aloe vera is also able to cause DNA degradation in the presence of copper ions. Further, the extract is also able to reduce Cu(II) to Cu(I) and generate reactive oxygen species, such as superoxide anion and hydroxyl radicals in a dose-dependent manner, which correlates with ability of the extract to cause DNA breakage. Thus, the study shows that in addition to antioxidant activity, Aloe vera extract also possess pro-oxidant properties, leading to oxidative DNA breakage.

  16. Negative ion photoelectron spectroscopy of the copper-aspartic acid anion and its hydrated complexes

    Science.gov (United States)

    Li, Xiang; Wang, Haopeng; Bowen, Kit H.; Martínez, Ana; Salpin, Jean-Yves; Schermann, Jean-Pierre

    2010-08-01

    Negative ions of copper-aspartic acid Cu(Asp)- and its hydrated complexes have been produced in the gas phase and studied by anion photoelectron spectroscopy. The vertical detachment energies (VDE) of Cu(Asp)- and Cu(Asp)-(H2O)1,2 were determined to be 1.6, 1.95, and 2.20 eV, respectively. The spectral profiles of Cu(Asp)-(H2O)1 and Cu(Asp)-(H2O)2 closely resembled that of Cu(Asp)-, indicating that hydration had not changed the structure of Cu(Asp)- significantly. The successive shifts to higher electron binding energies by the spectra of the hydrated species provided measures of their stepwise solvation energies. Density functional calculations were performed on anionic Cu(Asp)- and on its corresponding neutral. The agreement between the calculated and measured VDE values implied that the structure of the Cu(Asp)- complex originated with a zwitterionic form of aspartic acid in which a copper atom had inserted into the N-H bond.

  17. Application of magnetic particles modified with amino groups to adsorb copper ions in aqueous solution

    Institute of Scientific and Technical Information of China (English)

    Yafen Lin; Huawei Chen; Kaelong Lin; Boryann Chen; Chyowsan Chiou

    2011-01-01

    A magnetic adsorbent can be easily recovered from treated water by magnetic force, without requiring further downstream treatment.In this research, amine-functionalized silica magnetite has been synthesized using N-[3-(trimethoxysilyl)propyl]-ethylenediamine (TPED) as a surface modification agent.The synthesized magnetic amine adsorbents were used to adsorb copper ions in an aqueous solution in a batch system, and the maximum adsorption was found to occur at pH 5.5 ± 0.1.The adsorption equilibrium data fitted the Langmuir isotherm equation reasonably well, with a maximum adsorption capacity of 10.41 mg/g.A pseudo second-order model could best describe the adsorption kinetics, and the derived activation energy was 26.92 kJ/mol.The optimum condition to desorb Cu2+ from NH2/SiO2/Fe3O4 was provided by a solution with 0.1 mol/L HNO3.

  18. Colorimetric detection of trace copper ions based on catalytic leaching of silver-coated gold nanoparticles.

    Science.gov (United States)

    Lou, Tingting; Chen, Lingxin; Chen, Zhaopeng; Wang, Yunqing; Chen, Ling; Li, Jinhua

    2011-11-01

    A colorimetric, label-free, and nonaggregation-based silver coated gold nanoparticles (Ag/Au NPs) probe has been developed for detection of trace Cu(2+) in aqueous solution, based on the fact that Cu(2+) can accelerate the leaching rate of Ag/Au NPs by thiosulfate (S(2)O(3)(2-)). The leaching of Ag/Au NPs would lead to dramatic decrease in the surface plasmon resonance (SPR) absorption as the size of Ag/Au NPs decreased. This colorimetric strategy based on size-dependence of nanoparticles during their leaching process provided a highly sensitive (1.0 nM) and selective detection toward Cu(2+), with a wide linear detection range (5-800 nM) over nearly 3 orders of magnitude. The cost-effective probe allows rapid and sensitive detection of trace Cu(2+) ions in water samples, indicating its potential applicability for the determination of copper in real samples.

  19. Synthesis and characteristics of a novel artificial hapten using the copper mercaptide of penicillenic acid from penicillin G for immunoassay of heavy metal ions.

    Science.gov (United States)

    Xu, Wu; Xie, Peng; Fan, Liuyin; Cao, Chengxi; Xi, Tao; Zhou, Pei

    2011-09-01

    In this paper, we describe the synthesis of a novel copper ion hapten using the copper mercaptide of penicillenic acid (CMPA) derived from penicillin. Results from tests with immune rabbits indicate that: (i) A new antigen synthesized with CMPA has good stability and is safe for immunizing animals with no toxic phenomena being found in animal experiments; (ii) the immunogenic antigen (CMPA-BSA) can stimulate the immune system to produce specific antibodies with high titrations, up to 150000; and (iii) antibodies in antisera showed higher affinity to OVA-GSH-CuCl than OVA-GSH, which indicates that the antibodies have specific affinity towards copper ions. These results confirm that the novel hapten and relevant antigen for copper ion have been successfully synthesized, giving progress towards an immunoassay for copper ions in environmental and food samples.

  20. Rat liver mitochondrial dysfunction by addition of copper(II) or iron(III) ions.

    Science.gov (United States)

    Saporito-Magriñá, Christian; Musacco-Sebio, Rosario; Acosta, Juan M; Bajicoff, Sofía; Paredes-Fleitas, Paola; Boveris, Alberto; Repetto, Marisa G

    2017-01-01

    Increased copper (Cu) and iron (Fe) levels in liver and brain are associated to oxidative stress and damage with increased phospholipid oxidation process. The aim of this work was to assess the toxic effects of Cu(2+) and Fe(3+) addition to rat liver mitochondria by determining mitochondrial respiration in states 3 (active respiration) and 4 (resting respiration), and phospholipid peroxidation. Both, Cu(2+) and Fe(3+) produced decreases in O2 consumption in a concentration-dependent manner in active state 3: both ions by 42% with malate-glutamate as complex I substrate (concentration for half maximal response (C50) 60μM Cu(2+) and 1.25mM Fe(3+)), and with succinate as complex II substrate: 64-69% with C50 of 50μM Cu(2+) and with C50 of 1.25mM of Fe(3+). Respiratory control decreased with Cu(2+) (C50 50μM) and Fe(3+) (C50 1.25-1-75mM) with both substrates. Cu(2+) produced a 2-fold increase and Fe(3+) a 5-fold increase of thiobarbituric acid-reactive substances (TBARS) content from 25μM Cu(2+) (C50 40μM) and from 100μM Fe(3+) (C50 1.75mM). Supplementations with Cu(2+) and Fe(3+) ions induce mitochondrial dysfunction with phospholipid peroxidation in rat liver mitochondria. Although is proved that a Fenton/Haber Weiss mechanism of oxidative damage occurs in metal-ion induced mitochondrial toxicity, slightly different responses to the metal ions suggest some differences in the mechanism of intracellular toxicity. The decreased rates of mitochondrial respiration and the alteration of mitochondrial function by phospholipid and protein oxidations lead to mitochondrial dysfunction, cellular dyshomeostasis and cell death.

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

    Directory of Open Access Journals (Sweden)

    M. G. A. Vieira

    2014-06-01

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

  2. Femtomole level photoelectrochemical aptasensing for mercury ions using quercetin-copper(II) complex as the DNA intercalator.

    Science.gov (United States)

    Li, Hongbo; Xue, Yan; Wang, Wei

    2014-04-15

    An ultrasensitive and selective photoelectrochemical (PEC) aptasensor for mercury ions was first fabricated based on perylene-3, 4, 9, 10-tetracarboxylic acid/graphene oxide (PTCA/GO) heterojunction using quercetin-copper(II) complex intercalated into the poly(dT)-poly(dA) duplexes. Both the PTCA/GO heterojunction and the quercetin-copper(II) complex are in favor of the sensitivity for the fabricated PEC aptasensor due to band alignment and strong reduction capability, respectively. And they efficiently promote the separation of photoexcited carriers and enhance the photocurrent. The formation of thymine-Hg(2+)-thymine coordination chemistry resulted in the dehybridization of poly(dT)-poly(dA) duplexes and then the intercalator quercetin-copper(II) complex broke away from the surface of the PEC aptasensor. As the concentration of mercury ions increased, the photocurrent gradually decreased. The electrode response for mercury ions detection was in the linear range from 0.01 pmol L(-1) to 1.00 pmol L(-1) with the detection limit of 3.33 fmol L(-1). The label-free PEC aptasensor has excellent performances with ultrasensitivity and good selectivity besides the advantage of economic and facile fabrication. The strategy of quercetin-copper(II) complex as a novel DNA intercalator paves a new way to improve the performances for PEC sensors. © 2013 Published by Elsevier B.V.

  3. Solid-phase extraction of copper, iron and zinc ions on Bacillus thuringiensis israelensis loaded on Dowex optipore V-493

    Energy Technology Data Exchange (ETDEWEB)

    Tuzen, Mustafa; Melek, Esra [Gaziosmanpasa University, Faculty of Science and Arts, Chemistry Department, 60250 Tokat (Turkey); Soylak, Mustafa [Erciyes University, Faculty of Science and Arts, Chemistry Department, 38039 Kayseri (Turkey)], E-mail: msoylak@gmail.com

    2008-11-30

    Bacillus thuringiensis israelensis loaded on Dowex optipore V-493 as new adsorbent for the separation-preconcentration of heavy metal ions has been proposed. The analytical conditions for the quantitative recoveries of copper(II), iron(III) and zinc(II) including pH, amounts of adsorbent, sample volume, etc. were investigated. The influences of alkaline and earth alkaline ions were also reported. The recovery values for the analytes are generally higher than 95%. The preconcentration factor was 37. The limit of detections of the analyte ions (k = 3, N = 21) were 1.14 {mu}g L{sup -1} for copper, 2.01 {mu}g L{sup -1} for iron and 0.14 {mu}g L{sup -1} for zinc. The relative standard deviations of the determinations were found to be lower than 9%. The procedure was validated by analyzing copper, iron and zinc contents in two certified reference materials, NRCC-SLRS-4 Riverine water and NIST SRM 1515 Apple leaves. Agreements between the obtained results and the certified values were achieved. The developed preconcentration method was applied in the flame atomic absorption spectrometric determination of copper, iron and zinc in several samples including a multivitamin-multimineral tablet, dialysis solutions, natural waters and some food samples.

  4. 铜粉处理酸性镀铜溶液中氯离子的机理%Mechanism of Treating Chloride Ion in Acidic Copper Plating Bath with Copper Powder

    Institute of Scientific and Technical Information of China (English)

    郭崇武

    2011-01-01

    阐明了用铜粉处理酸性镀铜溶液中氯离子的机理,理论分析和实验表明,在酸性镀铜溶液中,Cu2+离子与铜粉反应生成Cu+离子,同时氯离子与Cu+离子反应生成氯化亚铜沉淀.向镀液中加铜粉1g/L,氯离子的起始质量浓度为174mg/L时,氯离子的去除率为58.9%,而向镀液中加锌粉1g/L,氯离子的去除率为47.0%,用铜粉处理氯离子的效率较高.%The mechanism of treating chloride ion in acidic copper plating bath by using copper powder was illustrated. Theoretical analyses and experimental tests indicated that in acidic copper plating solution Cu2+ ion could react with copper powder to form Cu + ion and the Cu + ion could react with chloride ion in the solution to produce cuprous chloride precipitation. When the initial mass concentration of the chloride ions in the acidic copper plating solution was 174 mg/L, the elimination rate of chloride ions after adding 1 g/L copper powders to the solution was 58.9% while that after adding 1 g/L zinc powders was 47.0%. This indicates that the treatment efficiency of chloride ion in the acidic copper plating solution with copper powders is higher than that with zinc powders.

  5. CYCLIC VOLTAMMETRY STUDIES OF COPPER (II AND TELLURIUM (IV IONS IN ACIDIC AQUEOUS SOLUTIONS FOR THIN FILM DEPOSITION

    Directory of Open Access Journals (Sweden)

    SARAVANAN NAGALINGAM

    2014-05-01

    Full Text Available Cyclic voltammetry studies of copper (II and tellurium (IV ions in acidic aqueous solutions were carried out to determine the optimum condition for copper telluride thin film deposition. The voltammetry studies include reversible scans at different solution pH. Based on the voltammogram, suitable deposition conditions was determined to be in the range of -0.35 V to -0.45 V versus Ag/AgCl at pH values between 2.0 to 2.2 under non diffusion-limited conditions.

  6. Recovery of Copper Ions from Wastewater by Hollow Fiber Supported Emulsion Liquid Membrane

    Institute of Scientific and Technical Information of China (English)

    郑辉东; 陈晶晶; 王碧玉; 赵素英

    2013-01-01

    Recovery of copper ions from wastewater using a hollow fiber supported emulsion liquid membrane (HFSELM) was studied with LIX984N as carrier, kerosene as diluents, and sulfuric acid solution as stripping phase. Effects of compositions of feed and emulsion liquid phase, flow rates on both sides of membrane, and hollow fiber module parameters were investigated. The stability of the emulsion liquid phase without surfactant and the effect of buffer in the feed phase on the extraction rate were also evaluated. It is found that the stability of the emulsion phase without surfactant is poor. Higher flow velocity gives shorter residence time for the emulsion liquid phase on the tube side, reducing the effect of particle coalescence on the separation process. The extraction rate increases with the increase of feed phase pH, carrier concentration, hydrogen ion concentration in the stripping phase, and ef-fective hollow fiber area. The phase ratio in the emulsion liquid phase has a negative effect on extraction rate. The flow rates on both sides have little influence on the extraction performance of the HFSELM, while buffer addition in the feed solution improves the extraction efficiency.

  7. Multipath colourimetric assay for copper(II) ions utilizing MarR functionalized gold nanoparticles

    Science.gov (United States)

    Wang, Yulong; Wang, Limin; Su, Zhenhe; Xue, Juanjuan; Dong, Jinbo; Zhang, Cunzheng; Hua, Xiude; Wang, Minghua; Liu, Fengquan

    2017-02-01

    We use the multiple antibiotic resistance regulator (MarR), as a highly selective biorecognition elements in a multipath colourimetric sensing strategy for the fast detection of Cu2+ in water samples. The colourimetric assay is based on the aggregation of MarR-coated gold nanoparticles in the presence of Cu2+ ions, which induces a red-to-purple colour change of the solution. The colour variation in the gold nanoparticle aggregation process can be used for qualitative and quantitative detection of Cu2+ by the naked eye, and with UV–vis and smartphone-based approaches. The three analysis techniques used in the multipath colourimetric assay complement each other and provide greater flexibility for differing requirements and conditions, making the assay highly applicable for Cu2+ detection. Under optimal conditions, the Cu2+ concentration was quantified in less than 5 min with limits of detection for the naked eye, UV–vis and smartphone-based approaches of 1 μM, 405 nM and 61 nM, respectively. Moreover, the sensing system exhibited excellent selectivity and practical application for Cu2+ detection in real water samples. Thus, our strategy has great potential for application in on-site monitoring of Cu2+, and the unique response of MarR towards copper ions may provide a new approach to Cu2+ sensing.

  8. Multipath colourimetric assay for copper(II) ions utilizing MarR functionalized gold nanoparticles

    Science.gov (United States)

    Wang, Yulong; Wang, Limin; Su, Zhenhe; Xue, Juanjuan; Dong, Jinbo; Zhang, Cunzheng; Hua, Xiude; Wang, Minghua; Liu, Fengquan

    2017-01-01

    We use the multiple antibiotic resistance regulator (MarR), as a highly selective biorecognition elements in a multipath colourimetric sensing strategy for the fast detection of Cu2+ in water samples. The colourimetric assay is based on the aggregation of MarR-coated gold nanoparticles in the presence of Cu2+ ions, which induces a red-to-purple colour change of the solution. The colour variation in the gold nanoparticle aggregation process can be used for qualitative and quantitative detection of Cu2+ by the naked eye, and with UV–vis and smartphone-based approaches. The three analysis techniques used in the multipath colourimetric assay complement each other and provide greater flexibility for differing requirements and conditions, making the assay highly applicable for Cu2+ detection. Under optimal conditions, the Cu2+ concentration was quantified in less than 5 min with limits of detection for the naked eye, UV–vis and smartphone-based approaches of 1 μM, 405 nM and 61 nM, respectively. Moreover, the sensing system exhibited excellent selectivity and practical application for Cu2+ detection in real water samples. Thus, our strategy has great potential for application in on-site monitoring of Cu2+, and the unique response of MarR towards copper ions may provide a new approach to Cu2+ sensing. PMID:28155905

  9. Study of the interaction mechanism in the biosorption of copper(II) ions onto posidonia oceanica and peat

    Energy Technology Data Exchange (ETDEWEB)

    Izquierdo, Marta; Marzal, Paula; Gabaldon, Carmen [Departamento de Ingenieria Quimica, Escuela Tecnica Superior de Ingenieria, Universitat de Valencia, Valencia (Spain); Silvetti, Margherita; Castaldi, Paola [Dipartimento di Scienze Ambientali e Agrarie e Biotecnologie Agro-Alimentari, Sez. Chimica Agraria ed Ambientale, University of Sassari, Sassari (Italy)

    2012-04-15

    A systematic approach was used to characterize the biosorption of copper(II) onto two biosorbents, Posidonia oceanica and peat, focusing on the interaction mechanisms, the copper(II) sorption-desorption process and the thermal behavior of the biosorbents. Sorption isotherms at pH 4-6 were obtained and the experimental data were fitted to the Langmuir model with a maximum uptake (q{sub max}) at pH 6 of 85.78 and 49.69 mg g{sup -1}, for P. oceanica and peat, respectively. A sequential desorption (SD) with water, Ca(NO{sub 3}){sub 2}, and EDTA was applied to copper-saturated biosorbents. Around 65-70% copper(II) were desorbed with EDTA, indicating that this heavy metal was strongly bound. The reversibility of copper(II) sorption was obtained by desorption with HCl and SD. Fourier transform IR spectroscopy (FTIR) analysis detected the presence of peaks associated with OH groups in aromatic and aliphatic structures, CH, CH{sub 2}, and CH{sub 3} in aliphatic structures, COO{sup -} and COOH groups and unsaturated aromatic structures on the surface of both biosorbents, as well as peaks corresponding to Si-O groups on the surface of peat. The results of SEM-EDX and FTIR analysis of copper-saturated samples demonstrated that ion exchange was one of the mechanisms involved in copper(II) retention. Thermal analysis of biosorbent samples showed that copper(II) sorption-desorption processes affected the thermal stability of the biosorbents. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  10. Releasing of Cupric Ion of Three types of Copper-bearing Intrauterine Contraceptive Device in Simulated Uterine Fluid

    Institute of Scientific and Technical Information of China (English)

    Jie GAO; Ying LI; Jian-ping LIU; Xuan GU

    2007-01-01

    Objective To compare the cupric ion releasing in vitro of the three IUDs.Methods The stability of cupric ion releasing of IUDs including TCu 380A IUD (TCu 380A), Multiload Cu375 IUD (MCu 375) and Yuangong 365 copper-bearing indomethacin-releasing IUD (Yuangong 365) by the determination of cupric ion releasing in simulated uterine fluid. The simulated uterine fluid was used for releasing media. Copper ion was determined by flame atomic absorption spectrometerResults The cupric ion releasing of three IUDs were instable at the beginning and tend to be stable gradually. In the stable phase, the average level of cupric ion releasing of TCu380A, MCu375 and Yuangong 365 were 4.25±2.71 -7.62±6.42 μg,4.92±1.23 -8.62±3.08 μg and 2.19±0.40-4.68±1.66 μg, respectively. TCu380A had higher instable releasing level than those of Yuangong 365 (P<0. 05).Conclusion TCu 380A and MCu 375 showed a "burst release" during the first few days and the former was of great significance(P<0. 05). The initial cupric ion releasing of Yuangong 365 appeared to be the lowest, followed by MCu375 and TCu380A in a releasing order.

  11. Simultaneous and sensitive analysis of aliphatic carboxylic acids by ion-chromatography using on-line complexation with copper(II) ion.

    Science.gov (United States)

    Kemmei, Tomoko; Kodama, Shuji; Yamamoto, Atsushi; Inoue, Yoshinori; Hayakawa, Kazuichi

    2015-01-02

    A new approach to ion chromatography is proposed to improve the UV detection of aliphatic carboxylic acids separated by anion-exchange chromatography. When copper(II) ion added to the mobile phase, it forms complexes with carboxylic acids that can be detected at 240 nm. The absorbance was found to increase with increasing copper(II) ion concentration. The retention times of α-hydroxy acids were also found to depend on the copper(II) ion concentration. Addition of acetonitrile to the mobile phase improved the separation of aliphatic carboxylic acids. The detection limits of the examined carboxylic acids (formate, glycolate, acetate, lactate, propionate, 3-hydroxypropionate, n-butyrate, isobutyrate, n-valerate, isovalerate, n-caproate) calculated at S/N=3 ranged from 0.06 to 3 μM. The detector signal was linear over three orders of magnitude of carboxylic acid concentration. The proposed method was successfully applied to analyze aliphatic carboxylic acids in rainwater and bread.

  12. Bio sorption of copper ions with biomass of algae and dehydrated waste of olives; Biosorcion de iones cobre con biomasa de algas y orujos deshidratados

    Energy Technology Data Exchange (ETDEWEB)

    Tapia, P.; Santander, M.; Pavez, O.; Valderrama, L.; Guzman, D.; Romero, L.

    2011-07-01

    They were carried out experiments of biosorption batch and in continuous to remove copper from aqueous solutions using as adsorbents green algae and olive residues under virgins conditions and chemically activated. The results of batch bio sorption indicate that the algae present mayor elimination capacities than the waste of olives, with uptakes of copper of the order of 96 % using activated algae with dissolution of Na{sub 2}SO{sub 4} under the optimum conditions. The results of the columns tests show that the virgin algae permits the removal of more copper ions than the activate algae, with removal efficiency of 98 % during the firth 20 min, a breakthrough time of 240 min and a saturation at time of 600 min. In the second cycle the regenerated biomass showed a best performance indicating that they can be used for another bio sorption cycle. (Author) 42 refs.

  13. [Study on the release of copper ion and corrosion for intrauterine contraceptive device with two kinds of Cu-containing stent].

    Science.gov (United States)

    Zou, Fengping; Huang, Shuze; Ji, Rong; Ding, Biao; Yao, Tianping

    2014-05-01

    Two kinds of Cu-containing intrauterine contraceptive device (Cu-IUD) has been evaluated through the study on the release of copper ion and corrosion of copper surface in artificially formulated fluid. The result showed that the copper ions were released profusely from the stainless steel stents Cu-IUD in the first week of soak (25-12 microg/d), and then it became slowly and steady. The release of the copper ions from the titanium nickel shape memory alloy stents Cu-IUD were always slowly and steady in two months (0.5-5 microg/d). It obviously shows that the corrosion on copper surface of stainless steel stents Cu-IUD were more serious than titanium nickel shape memory alloy stents Cu-IUD by using 200 times microscope testing before and after soaking in formulated fluid.

  14. Cloud point extraction and flame atomic absorption spectrometry combination for copper(II) ion in environmental and biological samples

    Energy Technology Data Exchange (ETDEWEB)

    Shokrollahi, Ardeshir [Chemistry Department, Yasouj University, Yasouj 75914-353 (Iran, Islamic Republic of)], E-mail: ashokrollahi@mail.yu.ac.ir; Ghaedi, Mehrorang [Chemistry Department, Yasouj University, Yasouj 75914-353 (Iran, Islamic Republic of)], E-mail: m_ghaedi@mail.yu.ac.ir; Hossaini, Omid; Khanjari, Narges [Chemistry Department, Yasouj University, Yasouj 75914-353 (Iran, Islamic Republic of); Soylak, Mustafa [Chemistry Department, University of Erciyes, 38039 Kayseri (Turkey)

    2008-12-30

    A cloud point extraction procedure was presented for the preconcentration of copper(II) ion in various samples. After complexation by 4-(phenyl diazenyl) benzene-1,3-diamine (PDBDM) (chrysoidine), copper(II) ions were quantitatively recovered in Triton X-114 after centrifugation. 0.5 ml of methanol acidified with 1.0 mol L{sup -1} HNO{sub 3} was added to the surfactant-rich phase prior to its analysis by flame atomic absorption spectrometry (FAAS). The influence of analytical parameters including ligand, Triton X-114 and HNO{sub 3} concentrations, bath temperature, heating time, centrifuge rate and time were optimized. The effect of the matrix ions on the recovery of copper(II) ions was investigated. The detection limit (3S.D.{sub b}/m, n = 10) of 0.6 ng mL{sup -1} along with preconcentration factor of 30 and enrichment factor of 41.1 with R.S.D. of 1.0% for Cu was achieved. The proposed procedure was applied to the analysis of various environmental and biological samples.

  15. Thin copper oxide films prepared by ion beam sputtering with subsequent thermal oxidation: Application in chemiresistors

    Science.gov (United States)

    Horak, P.; Bejsovec, V.; Vacik, J.; Lavrentiev, V.; Vrnata, M.; Kormunda, M.; Danis, S.

    2016-12-01

    Copper oxide films were prepared by thermal oxidation of thin Cu films deposited on substrates by ion beam sputtering. The subsequent oxidation was achieved in the temperature range of 200 °C-600 °C with time of treatment from 1 to 7 h (with a 1-h step) in a furnace open to air. At temperatures 250 °C-600 °C, the dominant phase formed was CuO, while at 200 °C mainly the Cu2O phase was identified. However, the oxidation at 200 °C led to a more complicated composition - in the depth Cu2O phase was observed, though in the near-surface layer the CuO dominant phase was found with a significant presence of Cu(OH)2. A limited amount of Cu2O was also found in samples annealed at 600 °C. The sheet resistance RS of the as-deposited Cu sample was 2.22 Ω/□, after gradual annealing RS was measured in the range 2.64 MΩ/□-2.45 GΩ/□. The highest RS values were obtained after annealing at 300 °C and 350 °C, respectively. Oxygen depth distribution was studied using the 16O(α,α) nuclear reaction with the resonance at energy 3032 keV. It was confirmed that the higher oxidation degree of copper is located in the near-surface region. Preliminary tests of the copper oxide films as an active layer of a chemiresistor were also performed. Hydrogen and methanol vapours, with a concentration of 1000 ppm, were detected by the sensor at an operating temperature of 300 °C and 350 °C, respectively. The response of the sensors, pointed at the p-type conductivity, was improved by the addition of thin Pd or Au catalytic films to the oxidic film surface. Pd-covered films showed an increased response to hydrogen at 300 °C, while Au-covered films were more sensitive to methanol vapours at 350 °C.

  16. Use of ligand-modified micellar-enhanced ultrafiltration to selectively separate copper ions from wastewater streams

    Energy Technology Data Exchange (ETDEWEB)

    Shadizadeh, S.B.

    1992-12-31

    The selective removal of target ions from an aqueous solution containing ions of like charge by ligand-modified micellar-enhanced ultrafiltration (LM-MEUF), is presented. In LM-MEUF, surfactant and specially tailored ligand are added to the contaminated stream. The surfactant forms aggregates called micelles, the hydrocarbon core of which the ligand complexed with the target species will solubilize. The surfactant is chosen to have the same charge type as the target ion; therefore, other ions (with similar charge) will not associate with the micelle, which makes the separation of the target ion selective. The solution is then processed by ultrafiltration, using a membrane with pore size small enough to block the passage of the micelles. In this study the divalent copper is the target ion in the solution containing divalent calcium. The surfactant is cetylpyridinium chloride (CPC) and the ligand is 4-hexadecyloxybenzyliminodiacetic acid (C{sub 16}BIDA). Experiments were conducted with batch stirred cells and the results have been compared to separation that take place under a variety of conditions in the LM-MEUF process. Rejections of copper of up to 99.8% are observed, with almost no rejection of calcium, showing that LM-MEUF has excellent selectivity and separation efficiency.

  17. Removal of Copper(II and Zinc(II Ions From Aqueous Solution by Chemical Treatment of Coal Fly Ash

    Directory of Open Access Journals (Sweden)

    Eleonora Sočo

    2015-12-01

    Full Text Available The aim of this study was to investigate the chemical modifications of coal fly ash (CFA treated with HNO3 or ammonium acetate (AcNH4 or NaOH or sodium diethyldithiocarbamate (NaDDTC as an adsorbent for the removal of copper(II and zinc(II ions from aqueous solution. The morphology of fly ash grains before and after modification was examined via X-ray diffraction (XRD and images of scanning electron microscope (SEM. Adsorption of copper(II and zinc(II ions was conducted under batch process at different duration, concentrations and temperature of the suspension. Equilibrium experiments shows that the selectivity of CFA-NaOH nanoparticles towards Cu(II ions is greater than that of Zn(II ions, which is related to their hydrated ionic radius and first hydrolysis equilibrium constant. The adsorption isotherms were described by Langmuir and Freundlich models. Kinetic data revealed that the adsorption fits well by the pseudo-second-order rate model with high regression coefficients. Thermodynamic parameters suggested that the immobilization Cu(II and Zn(II ions onto CFA-NaOH is a spontaneous process. Results demonstrated that the treating coal fly ash with alkaline solution was a promising way to enhance Cu(II and Zn(II ions adsorption.

  18. Facile preparation of carbon wrapped copper telluride nanowires as high performance anodes for sodium and lithium ion batteries

    Science.gov (United States)

    Yu, Hong; Yang, Jun; Geng, Hongbo; Chao Li, Cheng

    2017-04-01

    Uniform carbon wrapped copper telluride nanowires were successfully prepared by using an in situ conversion reaction. The length of these nanowires is up to several micrometers and the width is around 30–40 nm. The unique one dimensional structure and the presence of conformal carbon coating of copper telluride greatly accommodate the large volumetric changes during cycling, significantly increase the electrical conductivity and reduce charge transfer resistance. The copper telluride nanowires show promising performance in a lithium ion battery with a discharge capacity of 130.2 mA h g‑1 at a high current density of 6.0 A g‑1 (26.74 C) and a stable cycling performance of 673.3 mA h g‑1 during the 60th cycle at 100 mA g‑1. When evaluated as anode material for a sodium ion battery, the copper telluride nanowires deliver a reversible capacity of 68.1 mA h g‑1 at 1.0 A g‑1 (∼4.46 C) and have a high capacity retention of 177.5 mA h g‑1 during the 500th cycle at 100 mA g‑1.

  19. A new disubstituted polyacetylene bearing 6-benzylaminopurine moieties: postfunctional synthetic strategy and sensitive chemosensor towards copper and cobalt ions.

    Science.gov (United States)

    Ou, Daxin; Zhang, Liang; Huang, Yanfen; Lou, Xiaoding; Qin, Jingui; Li, Zhen

    2013-05-14

    A new 6-benzylaminopurine-functionalized disubstituted polyacetylene (P2) with strong green fluorescence is successfully synthesized by utilizing the postfunctional method. The polymer is soluble in common organic solvents, and its strong green fluorescence can be quenched by copper and cobalt ions with a detection limit down to 1.0 × 10(-8) (0.64 ppb) and 3.3 × 10(-8) mol L(-1) (1.94 ppb), respectively. Moreover, not much interference is observed from other metal ions, including Li(+) , Na(+) , K(+) , Fe(3+) , Fe(2+) , Ni(2+) , Hg(2+) , Mg(2+) , Al(3+) , Zn(2+) , Mn(2+) , Pb(2+) , Ba(2+) , Ca(2+) , Cd(2+) , Ag(+) , and Cr(3+) . Furthermore, P2 can be put into application using test strips, making P2 a practical, sensitive, and selective copper and cobalt probe.

  20. Comparative time-courses of copper-ion-mediated protein and lipid oxidation in low-density lipoprotein

    DEFF Research Database (Denmark)

    Knott, Heather M; Baoutina, Anna; Davies, Michael Jonathan

    2002-01-01

    Free radicals damage both lipids and proteins and evidence has accumulated for the presence of both oxidised lipids and proteins in aged tissue samples as well as those from a variety of pathologies including atherosclerosis, diabetes, and Parkinson's disease. Oxidation of the protein and lipid...... moieties of low-density lipoprotein is of particular interest due to its potential role in the unregulated uptake of lipids and cholesterol by macrophages; this may contribute to the initial stage of foam cell formation in atherosclerosis. In the study reported here, we examined the comparative time......-courses of lipid and protein oxidation during copper-ion-mediated oxidation of low-density lipoprotein. We show that there is an early, lipid-mediated loss of 40-50% of the Trp residues of the apoB100 protein. There is no comparable loss over an identical period during the copper-ion-mediated oxidation of lipid...

  1. SBA-15 mesoporous silica free-standing thin films containing copper ions bounded via propyl phosphonate units - preparation and characterization

    Science.gov (United States)

    Laskowski, Lukasz; Laskowska, Magdalena; Jelonkiewicz, Jerzy; Dulski, Mateusz; Wojtyniak, Marcin; Fitta, Magdalena; Balanda, Maria

    2016-09-01

    The SBA-15 silica thin films containing copper ions anchored inside channels via propyl phosphonate groups are investigated. Such materials were prepared in the form of thin films, with hexagonally arranged pores, laying rectilinear to the substrate surface. However, in the case of our thin films, their free standing form allowed for additional research possibilities, that are not obtainable for typical thin films on a substrate. The structural properties of the samples were investigated by X-ray reflectometry, atomic force microscopy (AFM) and transmission electron microscopy (TEM). The molecular structure was examined by Raman spectroscopy supported by numerical simulations. Magnetic measurements (SQUID magnetometry and EPR spectroscopy) showed weak antiferromagnetic interactions between active units inside silica channels. Consequently, the pores arrangement was determined and the process of copper ions anchoring by propyl phosphonate groups was verified in unambiguous way. Moreover, the type of interactions between magnetic atoms was determined.

  2. Highly selective and sensitive determination of copper ion by two novel optical sensors

    Directory of Open Access Journals (Sweden)

    Mehrorang Ghaedi

    2017-05-01

    Full Text Available New optical sensors for the determination of copper ion by incorporation of 1,1′-(4-nitro-1,2-phenylenebis(azan-1-yl-1-ylidenebis(methan-1-yl-1-lidenedinaphthalen-2-ol(L1, 1,1′-2,2′-(1,2-phenylenebis(ethene-2,1-diyldinaphthalen-2-ol 1(L2, dibutylphthalate (DBP and sodium tetraphenylborate (Na-TPB to the plasticized polyvinyl chloride matrices were prepared. The tendency of both ionophores (L2 and L1 as chromoionophore was significantly enhanced by the addition of DBP to the membrane. The proposed sensors benefit from advantages such as high stability, reproducibility and relatively long lifetime, good selectivity for Cu2+ ion determination over a large number of alkali, alkaline earth, transition and heavy metal ions. At optimum values of membrane compositions and experimental conditions, both sensors’ response was linear over a concentration range of 7.98 × 10−6 to 1.31 × 10−4mol L−1 and 1.99 × 10−6 to 5.12 × 10−5 mol L−1 for L2 and L1, respectively. Sensor detection limit based on the definition that the concentration of the sample leads to a signal equal to the blank signal plus three times of its standard deviation was found to be 3.99 × 10−7 and 5.88 × 10−7 mol L−1 for L2 and L1, respectively. The response time of the optodes (defined as the time required reaching the 90% of the peak signal was found to be 5–8 min for L2 and 20–25 min for L1 based sensor. The proposed optical sensors were applied successfully for the determination of Cu2+ ion content in water samples.

  3. Biological Effects of Drug-Free Alginate Beads Cross-Linked by Copper Ions Prepared Using External Ionotropic Gelation.

    Science.gov (United States)

    Pavelková, M; Kubová, K; Vysloužil, J; Kejdušová, M; Vetchý, D; Celer, V; Molinková, D; Lobová, D; Pechová, A; Vysloužil, J; Kulich, P

    2016-08-08

    External ionotropic gelation offers a unique possibility to entrap multivalent ions in a polymer structure. The aim of this experimental study was to prepare new drug-free sodium alginate (ALG) particles cross-linked by Cu(2+) ions and to investigate their technological parameters (particle size, sphericity, surface topology, swelling capacity, copper content, release of Cu(2+) ions, mucoadhesivity) and biological activity (cytotoxicity and efficiency against the most common vaginal pathogens-Herpes simplex, Escherichia coli, Candida albicans) with respect to potential vaginal administration. Beads prepared from NaALG dispersions (3 or 4%) were cross-linked by Cu(2+) ions (0.5 or 1.0 M CuCl2) using external ionotropic gelation. Prepared mucoadhesive beads with particle size over 1000 μm exhibited sufficient sphericity (all ˃0.89) and copper content (214.8-249.07 g/kg), which increased with concentration of polymer and hardening solution. Dissolution behaviour was characterized by extended burst effect, followed by 2 h of copper release. The efficiency of all samples against the most common vaginal pathogens was observed at cytotoxic Cu(2+) concentrations. Anti-HSV activity was demonstrated at a Cu(2+) concentration of 546 mg/L. Antibacterial activity of beads (expressed as minimum inhibition concentration, MIC) was influenced mainly by the rate of Cu(2+) release which was controlled by the extent of swelling capacity. Lower MIC values were found for E. coli in comparison with C. albicans. Sample ALG-3_1.0 exhibited the fastest copper release and was proved to be the most effective against both bacteria. This could be a result of its lower polymer concentration in combination with smaller particle size and thus larger surface area.

  4. Copper and silver ion implantation of aluminium oxide-blasted titanium surfaces: proliferative response of osteoblasts and antibacterial effects.

    Science.gov (United States)

    Fiedler, Jörg; Kolitsch, Andreas; Kleffner, Bernhard; Henke, Dietmar; Stenger, Steffen; Brenner, Rolf E

    2011-09-01

    Implant infection still represents a major clinical problem in orthopedic surgery. We therefore tested the in vitro biocompatibility and antibacterial effects of copper (Cu)- and silver (Ag)-ion implantation. Discs of a commonly used titanium alloy (Ti6AlV4) with an aluminium oxide-blasted surface were treated by Cu- or Ag-ion implantation with different dosage regimen (ranging from 1e15-17 ions cm(-2) at energies of 2-20 keV). The samples were seeded with primary human osteoblasts and cell attachment and proliferation was analyzed by an MTT-assay. In comparison to the reference titanium alloy there was no difference in the number of attached viable cells after two days. After seven days the number of viable cells was increased for Cu with 1e17 ions cm(-2) at 2 and 5 keV, and for Ag with 1e16 ions cm(-2) at 5 keV while it was reduced for the highest amount of Ag deposition (1e17 ions cm(-2) at 20 keV). Antibacterial effects on S.aureus and E.coli were marginal for the studied dosages of Cu but clearly present for Ag with 1e16 ions cm(-2) at 2 and 5 keV and 1e17 ions cm(-2) at 20 keV. These results indicate that Ag-ion implantation may be a promising methodological approach for antibacterial functionalization of titanium implants.

  5. Focused ion beam sectioning and lift-out method for copper and resist vias in organic low-k dielectrics.

    Science.gov (United States)

    Crawford, E J; Gignac, L; Barth, K; Petrus, J; Levine, E

    2002-12-01

    The focused ion beam lift-out technique for scanning electron microscope (SEM) and transmission electron microscope (TEM) sample preparation was shown to be applicable to copper/low-k dielectric semiconductor technology. High resolution SEM, TEM, and scanning transmission electron microscope analyses were performed on metal contacts and resist vias with no evidence of the interface damage or metal smearing commonly observed with mechanical polishing. Ion milling of the sample ex situ to the substrate provided decoration and adjustment of the exposed plane of the section when necessary for SEM analysis.

  6. Combined effects of temperature and copper ion concentration on the superoxide dismutase activity inCrassostrea ariakensis

    Institute of Scientific and Technical Information of China (English)

    WANG Hui; YANG Hongshuai; LIU Jiahui; LI Yanhong; LIU Zhigang

    2016-01-01

    Superoxide dismutase (SOD) is a crucial antioxidant enzyme playing the first defense line in antioxidant pathways against reactive oxygen species in various organisms including marine invertebrates. There exist mainly two specific forms, Cu/Zn-SOD (SOD1) and Mn-SOD (SOD2), in eukaryotes. SODs are known to be concurrently modulated by a variety of environmental stressors. By using central composite experimental design and response surface method, the joint effects of water temperature (18–34°C) and copper ion concentration (0.1–1.5 mg/L) on the total SOD activity in the digestive gland ofCrassostrea ariakensis were studied. The results showed that the linear effect of temperature was highly significant (P0.05), while the quadratic effect of copper ion concentration was highly significant (P0.05); the effect of temperature was greater than that of copper ion concentration. The model equation of digestive gland SOD enzyme activity towards the two factors of interest was established, withR2 and predictiveR2 as high as 0.961 6 and 0.820 7, respectively, suggesting that the goodness-of-fit to experimental data be very satisfactory, and could be applied to prediction of digestive gland SOD activity in C. ariakensis under the conditions of the experiment. Our results would be conducive to addressing the health of aquatic animals and/or to detecting environmental problems by taking SOD as a potential bioindicator.

  7. Silica nanoparticles functionalized with polyamidoamine (PAMAM) dendrimers as platforms for photoluminescence (PL) sensing of copper and cyanide ions.

    Science.gov (United States)

    Gerrans, Kateryna; Luhrs, Alicia; Feider, Clara; Margerum, Lawrence D

    2016-05-15

    Functionalized nanoparticles for photoluminescence (PL) applications are a promising technology for biomedical imaging and as sensors for small molecules. This work presents a new method to modify silica nanoparticles (SNP) using the bifunctional linker 1,1'-carbonyldiimidazole (CDI) with a series of polyamidoamine (PAMAM) dendrimer molecules followed by grafting of fluorescein isothiocyanate (FITC) or rhodamine B isothiocyanate (RITC) to create platforms for photoluminescence (PL) sensors. A dendrimer size and charge-variable response to only copper(II) ions confirmed the prediction of a selective turn-off sensor via proximity quenching. Both dye density and Cu(2+) quenching efficiency peaked with SNP-dendrimer generation 4 (64 terminal amines). In addition, changing the terminal dendrimer arms to carboxylic acid end groups increased the copper quenching suggesting that more metal ion binding sites were created in close proximity to the dyes. Of the small anions tested for a turn-off sensor, only cyanide ion fully restored the PL when reaching a 2:1 CN(-):Cu(2+) ratio, while EDTA was not as effective at the same ratio. Therefore, dendrimer size and surface charge on the nanoparticles controlled the dye loading and copper quenching efficiency, while creating multiple binding sites for cyanide over other metal binding anions. Copyright © 2016 Elsevier Inc. All rights reserved.

  8. Copper Nanoparticle-Incorporated Carbon Fibers as Free-Standing Anodes for Lithium-Ion Batteries.

    Science.gov (United States)

    Han, Pan; Yuan, Tao; Yao, Long; Han, Zhuo; Yang, Junhe; Zheng, Shiyou

    2016-12-01

    Copper-incorporated carbon fibers (Cu/CF) as free-standing anodes for lithium-ion batteries are prepared by electrospinning technique following with calcination at 600, 700, and 800 °C. The structural properties of materials are characterized by X-ray diffraction (XRD), Raman, thermogravimetry (TGA), scanning electron microscopy (SEM), transmission electron microscope (TEM), and energy dispersive X-ray spectrometry (EDS). It is found that the Cu/CF composites have smooth, regular, and long fibrous morphologies with Cu nanoparticles uniformly dispersed in the carbon fibers. As free-standing anodes, the unique structural Cu/CF composites show stable and high reversible capacities, together with remarkable rate and cycling capabilities in Li-ion batteries. The Cu/CF calcined at 800 °C (Cu/CF-800) has the highest charge/discharge capacities, long-term stable cycling performance, and excellent rate performance; for instance, the Cu/CF-800 anode shows reversible charge/discharge capacities of around 800 mAh g(-1) at a current density of 100 mA g(-1) with stable cycling performance for more than 250 cycles; even when the current density increases to 2 A g(-1), the Cu/CF-800 anode can still deliver a capacity of 300 mAh g(-1). This excellent electrochemical performance is attributed to the special 1D structure of Cu/CF composites, the enhanced electrical conductivity, and more Li(+) active positions by Cu nanoinclusion.

  9. Di(2-ethylhexyl)phosphoric acid-coconut oil supported liquid membrane for the separation of copper ions from copper plating wastewater

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Permeation of Cu(II) from its aqueous solution through a supported liquid membrane (SLM) containing di(2-ethylhexyl)phosphoric acid (D2EHPA) carrier dissolved in coconut oil has been studied. The effects of Cu(II), pH (in feed), H2SO4 (stripping) and D2EHPA (in membrane) concentrations have been investigated. The stability of the D2EHPA-coconutoil has also been evaluated. High Cu(II) concentration in the feed leads to an increase in flux from 4.1 × 10-9 to 8.9 × 10-9 mol/(m2·s) within the Cu(II) concentration range 7.8×10-4-78.6×10-4 mol/L at pH of 4.0 in the feed and 12.4 × 10-4 mol/L D2EHPA in the membrane phase. Increase in H2SO4 concentration in strip solution leads to an increase in copper ions flux up to 0.25 mol/L H2SO4, providing a maximum flux of 7.4 × 10-9 mol/(m2·s). The optimum conditions for Cu(II) transport are, pH of feed 4.0, 0.25 mol/L H2SO4 in strip phase and 12.4 × 10-4 mol/L D2EHPA (membrane) in 0.5 (m pore size polytetrafluoroethylene (PTFE) membrane. It has been observed that Cu(II) flux across the membrane tends to increase with the concentration of copper ions. Application of the method developed to copper plating bath rinse solutions has been found to be successful in the recovery of Cu(II). rane. It

  10. Copper-ion-assisted self-assembly of silicate clays in rod- and disklike morphologies.

    Science.gov (United States)

    Tsai, Wei-Cheng; Lin, Jiang-Jen

    2010-06-15

    Self-assembled rodlike (0.3-2.5 microm in diameter and 5.3-31 microm in length) and disklike microstructures (1.8-10.6 microm in width and 0.1-1.0 microm in thickness) are uniquely present in amorphous clay aggregates. Clay units were prepared by intercalation of Na(+)-montmorillonite (Na(+)-MMT) with copper ions (Cu(2+)) and poly(oxypropylene)-amine salt (POP) in simultaneous or stepwise ionic exchange reactions. Differences in process control during incorporation of Cu(2+) and hydrophobic POP greatly affected the layer structure of the clay units (d spacing of 12-53 A) and consequently their amphiphilic dispersion properties. By controlling the dispersion in water and drying at 80 degrees C, highly ordered self-assembly structures were obtained, presumably as a result of self-piling of clay units in competing vertical and horizontal directions. In general, association with Cu(2+) yielded units with a disklike microstructure, in contrast to the rod-like structure obtained for POP-intercalated clay. The self-assembled structures were characterized using X-ray diffraction, UV adsorption, thermal gravimetric analysis, zeta potential, scanning electron microscopy, and energy-dispersive X-ray spectroscopy techniques. Control of the clay self-piling process provides a new synthetic route for the fabrication of bottom-up microstructures that are potentially useful for templates, sensors, and electronic devices.

  11. Role of zinc and copper ions in the pathogenetic mechanisms of Alzheimer's and Parkinson's diseases.

    Science.gov (United States)

    Stelmashook, E V; Isaev, N K; Genrikhs, E E; Amelkina, G A; Khaspekov, L G; Skrebitsky, V G; Illarioshkin, S N

    2014-05-01

    Disbalance of zinc (Zn2+) and copper (Cu2+) ions in the central nervous system is involved in the pathogenesis of numerous neurodegenerative disorders such as multisystem atrophy, amyotrophic lateral sclerosis, Creutzfeldt-Jakob disease, Wilson-Konovalov disease, Alzheimer's disease, and Parkinson's disease. Among these, Alzheimer's disease (AD) and Parkinson's disease (PD) are the most frequent age-related neurodegenerative pathologies with disorders in Zn2+ and Cu2+ homeostasis playing a pivotal role in the mechanisms of pathogenesis. In this review we generalized and systematized current literature data concerning this problem. The interactions of Zn2+ and Cu2+ with amyloid precursor protein (APP), β-amyloid (Abeta), tau-protein, metallothioneins, and GSK3β are considered, as well as the role of these interactions in the generation of free radicals in AD and PD. Analysis of the literature suggests that the main factors of AD and PD pathogenesis (oxidative stress, structural disorders and aggregation of proteins, mitochondrial dysfunction, energy deficiency) that initiate a cascade of events resulting finally in the dysfunction of neuronal networks are mediated by the disbalance of Zn2+ and Cu2+.

  12. Studies on the Interactions of Copper and Zinc Ions with β-Amyloid Peptides by a Surface Plasmon Resonance Biosensor

    Directory of Open Access Journals (Sweden)

    He Tian

    2012-09-01

    Full Text Available The aggregation of β-amyloid peptide (Aβ into fibrils plays an important role in the pathogenesis of Alzheimer’s disease (AD. Metal ions including copper and zinc are closely connected to the precipitation and toxicity of Aβ. In this study, a surface plasmon resonance (SPR biosensor was constructed to investigate the interactions between Aβ and metal ions. Aβ peptide was immobilized on the SPR chip surface through a preformed alkanethiol self-assembled monolayer (SAM. Our observations indicate that the immobilized Aβ undergoes a conformational change upon exposure to the metal ions. A difference in metal binding affinity between Aβ1–28 and Aβ1–42 was also detected. The results suggest that SPR is an effective method to characterize the interactions between Aβ and metal ions.

  13. Studies on the interactions of copper and zinc ions with β-amyloid peptides by a surface plasmon resonance biosensor.

    Science.gov (United States)

    Yao, Fujun; Zhang, Ruiping; Tian, He; Li, Xiangjun

    2012-01-01

    The aggregation of β-amyloid peptide (Aβ) into fibrils plays an important role in the pathogenesis of Alzheimer's disease (AD). Metal ions including copper and zinc are closely connected to the precipitation and toxicity of Aβ. In this study, a surface plasmon resonance (SPR) biosensor was constructed to investigate the interactions between Aβ and metal ions. Aβ peptide was immobilized on the SPR chip surface through a preformed alkanethiol self-assembled monolayer (SAM). Our observations indicate that the immobilized Aβ undergoes a conformational change upon exposure to the metal ions. A difference in metal binding affinity between Aβ(1-28) and Aβ(1-42) was also detected. The results suggest that SPR is an effective method to characterize the interactions between Aβ and metal ions.

  14. Preparation of 3D nanoporous copper-supported cuprous oxide for high-performance lithium ion battery anodes.

    Science.gov (United States)

    Liu, Dequan; Yang, Zhibo; Wang, Peng; Li, Fei; Wang, Desheng; He, Deyan

    2013-03-01

    Three-dimensional (3D) nanoporous architectures can provide efficient and rapid pathways for Li-ion and electron transport as well as short solid-state diffusion lengths in lithium ion batteries (LIBs). In this work, 3D nanoporous copper-supported cuprous oxide was successfully fabricated by low-cost selective etching of an electron-beam melted Cu(50)Al(50) alloy and subsequent in situ thermal oxidation. The architecture was used as an anode in lithium ion batteries. In the first cycle, the sample delivered an extremely high lithium storage capacity of about 2.35 mA h cm(-2). A high reversible capacity of 1.45 mA h cm(-2) was achieved after 120 cycles. This work develops a promising approach to building reliable 3D nanostructured electrodes for high-performance lithium ion batteries.

  15. Effect of copper ions implantation on the corrosion behavior of ZIRLO alloy in 1 mol/L H2SO4

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    In order to study the effect of copper ion implantation on the aqueous corrosion behavior of ZIRLO alloy, specimens were implanted with copper ions with fluences ranging from l×l016 to 1×1017 ions/cm2, using a metal vapor vacuum arc source (MEVVA) at an extraction voltage of 40 kV.The valence states and depth distributions of elements in the surface layer of the samples were analyzed by X-ray photoelectron spectroscopy (XPS) and Auger electron spectroscopy (AES), respectively.Glancing angle X-ray diffraction(GAXRD) was employed to examine the phase transformation due to the copper ion implantation.The potentiodynamic polarization technique was used to evaluate the aqueous corrosion resistance of implanted ZIRLO alloy in a l mol/L H2SO4 solution.It was found that a significant improvement was achieved in the aqueous corrosion resistance of ZIRLO alloy implanted with copper ions when the fluence is 5×1016 ions/cm2.When the fluence is l×l016 or l×l017 ions/cm2, the corrosion resistance of implanted samples was bad..Finally, the mechanism of the corrosion behavior of copper-implanted ZIRLO alloy was discussed.

  16. Metalloselenonein, the selenium analogue of metallothionein: synthesis and characterization of its complex with copper ions.

    OpenAIRE

    Oikawa, T; Esaki, N; Tanaka, H.; Soda, K

    1991-01-01

    We used an automated peptide synthesizer to produce a peptide, metalloselenonein, that contains selenocysteine residues substituted for all cysteine residues in Neurospora crassa copper metallothionein. Metalloselenonein binds 3 mol of Cu(I) per mol. This adduct shows a broad absorption band between 230 and 400 nm and a fluorescence band at 395 nm, which can be attributed to copper-selenolate coordination. The circular dichroism spectrum of the copper-metalloselenonein complex shows a positiv...

  17. [Study on the orientation of liquid crystals presented on the glass substrates spin-coated and functionalized with copper ions].

    Science.gov (United States)

    Wang, Shiming; Xiong, Xingliang; Zhang, Yan; Li, Guang; Chen, Mengmeng

    2013-06-01

    A stable, uniform, easily implemented, LC-based chemical and biological sensor substrate for orientations of liquid crystals (LCs) for a long-term is urgently needed for medical applications of the sensors. We proposed a use of spin-coating of copper perchlorate (Cu(ClO4)2), with five different concentrations(0-100mmol/L), directly on glass slides for fabricating a layer of chemically-sensitive copper ions. Observing the transmitted light with a polarized microscope, we found the luminosity of the light propagated through sensors deposited with copper ions started to weaken gradually after a certain time. The higher was the concentration of copper ions covered on the glass substrates of the sensors, the faster the weakening occurred, and the less time was needed for transmitted light to turn completely dark. But there was no change in luminosity of the transmitted light for the sensors without Cu(ClO4)2 spin-coating even after stored at room temperature (25 degrees C) for a whole day. When the Cu(ClO4)2 deposited sensors were stored within a drying oven at room temperature (25 degrees C) for 2 months, it was found that there vas almost no change in luminosity of the transmitted lights. The results showed that all the thin films of LC on glass slides functionalized with Cu(ClO4)2 could keep homeotropic and stable orientation for a long time; the concentration of Cu (ClO4)2I has an influence on the orientation response speed of LC from planar to perpendicular orientation.

  18. An Optical Fiber-Based Sensor Array for the Monitoring of Zinc and Copper Ions in Aqueous Environments

    Directory of Open Access Journals (Sweden)

    Steven Kopitzke

    2014-02-01

    Full Text Available Copper and zinc are elements commonly used in industrial applications as aqueous solutions. Before the solutions can be discharged into civil or native waterways, waste treatment processes must be undertaken to ensure compliance with government guidelines restricting the concentration of ions discharged in solution. While currently there are methods of analysis available to monitor these solutions, each method has disadvantages, be it high costs, inaccuracy, and/or being time-consuming. In this work, a new optical fiber-based platform capable of providing fast and accurate results when performing solution analysis for these metals is described. Fluorescent compounds that exhibit a high sensitivity and selectivity for either zinc or copper have been employed for fabricating the sensors. These sensors demonstrated sub-part-per-million detection limits, 30-second response times, and the ability to analyze samples with an average error of under 10%. The inclusion of a fluorescent compound as a reference material to compensate for fluctuations from pulsed excitation sources has further increased the reliability and accuracy of each sensor. Finally, after developing sensors capable of monitoring zinc and copper individually, these sensors are combined to form a single optical fiber sensor array capable of simultaneously monitoring concentration changes in zinc and copper in aqueous environments.

  19. A new approach to copper ion removal from water by polymeric nanocomposite membrane embedded with γ-alumina nanoparticles

    Science.gov (United States)

    Ghaemi, Negin

    2016-02-01

    The ability of alumina (Al2O3) nanoparticles in adsorption of heavy metals was employed in improving the copper removal efficiency of PES membranes. Mixed matrix membranes were prepared using PES and different amounts of alumina nanoparticles by phase inversion method. The fabricated membranes were characterized in terms of morphology and performance using scanning electron microscopy (SEM) and atomic force microscopy (AFM) analyses, water contact angle and porosity measurements, determination of pure water flux, copper ion removal, and reusability test. Mixed matrix membranes revealed higher water permeation compared with the pristine PES membrane just by adding small amounts of nanoparticles (≤ 1.0 wt. %) as a result of increasing the membrane porosity and hydrophilicity after addition of alumina nanoparticles into the membrane matrix. Moreover, copper ion removal efficiency of alumina mixed membranes was improved. Membrane performance tests as well as adsorptive nature of alumina nanoparticles proposed that adsorption was the most possible separation mechanism by mixed matrix membranes. Reusability test of membrane confirmed the durability of removal efficiency even after four cycles of filtration.

  20. In vitro efficacy of copper and silver ions in eradicating Pseudomonas aeruginosa, Stenotrophomonas maltophilia and Acinetobacter baumannii: implications for on-site disinfection for hospital infection control.

    Science.gov (United States)

    Huang, Hsin-I; Shih, Hsiu-Yun; Lee, Chien-Ming; Yang, Thomas C; Lay, Jiunn-Jyi; Lin, Yusen E

    2008-01-01

    Pseudomonas aeruginosa, Stenotrophomonas maltophilia and Acinetobacter baumannii are major opportunistic waterborne pathogens causing hospital-acquired infections. Copper-silver ionization has been shown to be effective in controlling Legionella colonization in hospital water systems. The objective was to determine the efficacy of copper and silver ions alone and in combination in eradicating P. aeruginosa, S. maltophilia and A. baumannii at the concentration applied to Legionella control. Kill curve experiments and mathematical modeling were conducted at copper and silver ion concentrations of 0.1, 0.2, 0.4, 0.8 and 0.01, 0.02, 0.04, 0.08 mg/L, respectively. The combinations of copper and silver ions were tested at concentrations of 0.2/0.02 and 0.4/0.04 mg/L, respectively. Initial organism concentration was ca. of 3 x 10(6)cfu/mL, and viability of the test organisms was assessed at predetermined time intervals. Samples (0.1 mL) withdrawn were mixed with 10 microL neutralizer solution immediately, serially diluted and plated in duplicate onto blood agar plates. The culture plates were incubated for 48 h at 37 degrees C and enumerated for the cfu (detection limit 10 cfu/mL). The results showed all copper ion concentrations tested (0.1-0.8 mg/L) achieved more than 99.999% reduction of P. aeruginosa which appears to be more susceptible to copper ions than S. maltophilia and A. baumannii. Silver ions concentration of 0.08 mg/L achieved more than 99.999% reduction of P. aeruginosa, S. maltophilia and A. baumannii in 6, 12 and 96 h, respectively. Combination of copper and silver ions exhibited a synergistic effect against P. aeruginosa and A. baumannii while the combination exhibited an antagonistic effect against S. maltophilia. Ionization may have a potential to eradicate P. aeruginosa, S. maltophilia and A. baumannii from hospital water systems.

  1. Catalytic therapy of cancer by ascorbic acid involves redox cycling of exogenous/endogenous copper ions and generation of reactive oxygen species.

    Science.gov (United States)

    Hadi, S M; Ullah, M F; Shamim, U; Bhatt, S H; Azmi, A S

    2010-01-01

    Catalytic therapy is a cancer treatment modality based on the generation of reactive oxygen species (ROS) through administration of ascorbate/medicinal herbal extracts and copper. It is known that antioxidants such as ascorbate also exhibit prooxidant activity in the presence of transition metals such as copper. Based on our work and that in the literature, in this review we propose a mechanism for the cytotoxic action of ascorbate against cancer cells. It involves redox cycling of exogenous/endogenous copper ions and the consequent generation of ROS leading to oxidative DNA breakage. Using human peripheral lymphocytes and the Comet assay, we have shown that ascorbic acid is able to cause oxidative breakage in cellular DNA. Such DNA degradation is inhibited by neocuproine (a Cu(I) sequestering agent) and scavengers of ROS indicating that the cellular DNA breakage involves the generation of Cu(I) and formation of ROS. Similar results are also obtained with plant polyphenol antioxidants that are important constituents of medicinal herbal extracts. Copper is an essential component of chromatin and can take part in redox reactions. It is well established that tissue, cellular and serum copper levels are considerably elevated in various malignancies. Therefore, cancer cells may be more subject to electron transfer between copper ions and ascorbate/plant polyphenols to generate ROS. In this review we cite evidence to indicate that in catalytic therapy cytotoxic action against cancer cells involves redox cycling of exogenous/endogenous copper ions.

  2. EVALUATION OF APPLICATION OF COAGULANTS CONTAINING DIVALENT AND TRIVALENT IRON TO ENHANCE REMOVAL OF ORGANIC COMPOUNDS AND COMPLEXED COPPER AND TIN IONS FROM INDUSTRIAL EFFLUENTS

    Directory of Open Access Journals (Sweden)

    Maciej Thomas

    2014-10-01

    Full Text Available The article presents the issues concerning physical and chemical parameters of raw sewage from the production of printed circuit boards and the composition of the bath used technology in terms of meeting the requirements for the introduction of treated wastewater into surface waters, ground or the municipal sewage system. Showed test results for the removal of organic compounds and ions complexed copper (II and tin (II and (IV using coagulants containing ions of Fe (II and Fe (III. The studies showed the high efficiency of removal of organic compounds and tin compounds. Explained the possible causes of the difficulties of precipitation complexed copper ions (II.

  3. Biosorption of copper ions from aqueous solutions by Spirulina platensis biomass

    Directory of Open Access Journals (Sweden)

    Ali A. Al-Homaidan

    2014-01-01

    Full Text Available In this study, the economically important micro-alga (cyanobacterium Spirulina platensis was used as biosorbent for the removal of copper from aqueous solutions. The cyanobacterium was exposed to various concentrations of copper and adsorption of copper by the biomass was evaluated under different conditions that included pH, contact time, temperature, concentration of adsorbate and the concentration of dry biomass. Increased adsorption of copper by the non-living biomass was recorded with gradually increasing pH, and a maximal uptake by the biomass was observed at pH 7. The adsorption of copper was found to increase gradually along with decrease in biomass concentration. Biosorption was found to be at a maximum (90.6%, in a solution containing 100 mg copper/L, at pH 7, with 0.050 g dry biomass and at 37 °C with 90 min of contact time. Analysis of the spectrum obtained with atomic absorption spectrophotometer (AAS, indicated that the adsorbent has a great potential to remove copper from aqueous media contributing to an eco-friendly technology for efficient bioremediation in the natural environment.

  4. Metalloselenonein, the selenium analogue of metallothionein: synthesis and characterization of its complex with copper ions.

    Science.gov (United States)

    Oikawa, T; Esaki, N; Tanaka, H; Soda, K

    1991-01-01

    We used an automated peptide synthesizer to produce a peptide, metalloselenonein, that contains selenocysteine residues substituted for all cysteine residues in Neurospora crassa copper metallothionein. Metalloselenonein binds 3 mol of Cu(I) per mol. This adduct shows a broad absorption band between 230 and 400 nm and a fluorescence band at 395 nm, which can be attributed to copper-selenolate coordination. The circular dichroism spectrum of the copper-metalloselenonein complex shows a positive band around 245 nm attributable to asymmetry in metal coordination. PMID:1826562

  5. Ion release from copper phosphate cement and influence on Streptococcus mutans growth in vitro: a comparative study.

    Science.gov (United States)

    Foley, Jennifer; Blackwell, Alison

    2003-01-01

    The aim of this study was to compare the effects of a black copper cement (BCC), an established restorative material (a conventional glass ionomer cement) and two temporary restorative materials (a zinc phosphate and a zinc polycarboxylate cement) on the growth of Streptococcus mutans in vitro, and to correlate bacterial growth with ion release from each material. Test specimens were eluted in either 0.1 M lactic acid, pH 4, or 0.1 M sodium chloride, pH 7. At 2 days, 7 days, 28 days and 6 months, eluates were inoculated with S. mutans and bacterial growth was recorded. Metal ion (Cu(2+), Zn(2+ )and Mg(2+)) and fluoride release were measured. At most immersion times, the different materials had a statistically significant inhibitory effect on bacterial growth compared to the respective control, at both pH levels. The inhibitory effect decreased with time and in most cases was associated with high levels of ion release at the beginning of the experimental period, followed by significantly lower levels. For BCC, there were statistically significant relationships between the median rates of growth of S. mutans in the presence of BCC eluates and the median values for release of copper and zinc, although not magnesium. Of the different materials, BCC demonstrated greatest antibacterial activity.

  6. Acid-base characterization, coordination properties towards copper(II) ions and DNA interaction studies of ribavirin, an antiviral drug.

    Science.gov (United States)

    Nagaj, Justyna; Starosta, Radosław; Jeżowska-Bojczuk, Małgorzata

    2015-01-01

    We have studied processes of copper(II) ion binding by ribavirin, an antiviral agent used in treating hepatitis C, which is accompanied usually by an increased copper level in the serum and liver tissue. Protonation equilibria and Cu(II) binding were investigated using the UV-visible, EPR and NMR spectroscopic techniques as well as the DFT (density functional theory) calculations. The spectroscopic data suggest that the first complex is formed in the water solution at pH as low as 0.5. In this compound Cu(II) ion is bound to one of the nitrogen atoms from the triazole ring. Above pH6.0, the metal ion is surrounded by two nitrogen and two oxygen atoms from two ligand molecules. The DFT calculations allowed to determine the exact structure of this complex. We found that in the lowest energy isomer two molecules of the ligand coordinate via O and N4 atoms in trans positions. The hypothetical oxidative properties of the investigated system were also examined. It proved not to generate plasmid DNA scission products. However, the calf thymus (CT)-DNA binding studies showed that it reacts with ribavirin and its cupric complex. Moreover, the interaction with the complex is much more efficient.

  7. Aminobenzenesulfonamide functionalized SBA-15 nanoporous molecular sieve: A new and promising adsorbent for preconcentration of lead and copper ions

    Institute of Scientific and Technical Information of China (English)

    Leila Hajiaghababaei; Babak Ghasemi; Alireza Badiei; Hassan Goldooz; Mohammad Reza Ganjali; Ghodsi Mohammadi Ziarani

    2012-01-01

    A rapid method for the extraction and monitoring of nanogram level of Pb2+ and Cu2+ ions using uniform silanized mesopor (SBA-15) functionalized with aminobenzenesulfonamide groups and flame atomic absorption spectrometry (FAAS) is presented.Aminobenzenesulfonamide functionalized SBA-15 was synthesized according to procedure in the literature and the presence of organic groups in the silica framework was demonstrated by FT-IR spectra.The functionalized product showed the BET surface area 110 m2/g and pore diameter 5.1 nm,based on adsorption-desorption of N2 at 77 K.The effect of several variables such as (amount of adsorbent,stirring time,pH and presence of other ions in the medium) has been studied.Lead and copper were completely extracted at pH greater than 3 after stirring for 10 min.The maximum capacity of the adsorbent was found to be 191.3 ± 1.4 and 155.0 ± 1.0 μg of lead and copper ions/mg functionalized SBA-15,respectively.The preconcentration factor of the method was found to be 200.The detection limit of the technique was 3.4 and 0.4 ng/mL for Pb2+ and Cu2+,respectively.The applications of this methodology for real samples were examined by various water type,black tea and pepper samples.

  8. Characteristics of copper removal and ion release during copper biosorption by Stenotrophomonas maltophilia in presence of benzo[a]pyrene

    Institute of Scientific and Technical Information of China (English)

    田云; 叶锦韶; 尹华; 彭辉; 李取生; 白洁琼; 谢丹平

    2013-01-01

    The ability of Stenotrophomonas maltophilia was demonstrated to selectively remove Cu2+from Cu(NO3)2 solution under the circumstance that 1 mg/L benzo[a]pyrene(BaP) was either present or not. The removal ratios of 2 and 10 mg/L Cu2+by 0.25 g/L biosorbent are up to 80% and 49% at 10 min, respectively. The biosorption includes ion exchange, NO3 reduction, ion release, and cell oxidation by Cu2+. BaP does not significantly affect Cu2+removal and ion release. Although 2 mg/L Cu2+increases the release of PO4 3, K+, NH4 +and Ca2+, 10 mg/L Cu2+has strong oxidation on cell, and then decreases NO3 reduction and hinders the release of K+, NH4 +and Ca2+. Exogenous cations inhibit the Cu2+biosorption, while additional anions increase the removal ratios of 10 mg/L Cu2+from 52% to 88%.

  9. Sorption of diuron, atrazine, and copper ion on chars with long-term natural oxidation in soils

    Science.gov (United States)

    Cheng, C.; Lin, T.; Lai, C.

    2011-12-01

    Biochar has been proposed as a measure to sequestrate carbon (C) and to increase soil fertility in sustainable agriculture. However, its sorption characteristics to herbicides, such as lowing herbicides efficacy, may constrain its agricultural application. This assertion may be arguable because most studies so far were conducted with the newly produced char and barely considered the "ageing effect" of old char since it could be oxidized over long time. In this study, historical char samples were collected and compared with the newly produced char. Batch sorption studies of diuron, atrazine, and copper ion onto chars was performed. Greater sorption of Cu was observed on the historical char samples and reached a saturated sorption at 30 mg g-1 for Cu, much higher adsorption value than newly produced char at 4 mg g-1. In contrast, sorption of diuron and atrazine on newly produced char had the highest sorption capacity than the historical char samples. The historical chars also had much higher negative charge than the newly produced char, but its surface area were lower than the new char. The results indicated that change in surface functional groups through natural oxidation rather than the change of surface area may have more pronounced influences on sorption characteristics, in which the negative charge on the historical chars' surface could hinder the adsorption of diuron and atrazine while enhance the sorption to copper ion. Biological assay to test the toxicity of diuron and copper ion for both historical and new chars on rye seed were conducted and will be presented in our poster.

  10. Studies on Zinc and Copper Ion in Relation to Wound Healing in ...

    African Journals Online (AJOL)

    olayemitoyin

    of both male and female goats could also be a factor for wound healing in the animals. Keywords: Wound ... and healing of wounds. The direct role of copper in facilitating angiogenesis .... well as activities of fibroblasts and skin immune cells.

  11. Analytical application of solid contact ion-selective electrodes for determination of copper and nitrate in various food products and drinking water.

    Science.gov (United States)

    Wardak, Cecylia; Grabarczyk, Malgorzata

    2016-08-02

    A simple, fast and cheap method for monitoring copper and nitrate in drinking water and food products using newly developed solid contact ion-selective electrodes is proposed. Determination of copper and nitrate was performed by application of multiple standard additions technique. The reliability of the obtained results was assessed by comparing them using the anodic stripping voltammetry or spectrophotometry for the same samples. In each case, satisfactory agreement of the results was obtained, which confirms the analytical usefulness of the constructed electrodes.

  12. Static secondary ion mass spectrometry investigation of corrosion inhibitor Irgamet®39 on copper surfaces treated in power transformer insulating oil

    OpenAIRE

    Facciotti, Marco; Amaro, Pedro S.; Brown, Richard C. D.; Paul L. Lewin; Pilgrim, James A.; Wilson, Gordon; Jarman, Paul N.; Fletcher, Ian W.

    2015-01-01

    Static secondary ion mass spectrometry was used to study the corrosion inhibitor Irgamet®39 on the surface of copper treated in insulating oils and the effect of temperature changes, by means of temperature programmed desorption experiments under vacuum, on metal coverage. Four commercial oils, both corrosive and non-corrosive, showed no significant influence on the stability of the tolyltriazole layer and the energy of its main desorption event from copper was calculated around 100 kJ mol?1....

  13. Biodynamics of copper oxide nanoparticles and copper ions in an oligochaete - Part II: Subcellular distribution following sediment exposure

    Science.gov (United States)

    Thit, Amalie; Ramskov, Tina; Croteau, Marie-Noele; Selck, Henriette

    2016-01-01

    The use and likely incidental release of metal nanoparticles (NPs) is steadily increasing. Despite the increasing amount of published literature on metal NP toxicity in the aquatic environment, very little is known about the biological fate of NPs after sediment exposures. Here, we compare the bioavailability and subcellular distribution of copper oxide (CuO) NPs and aqueous Cu (Cu-Aq) in the sediment-dwelling worm Lumbriculus variegatus. Ten days (d) sediment exposure resulted in marginal Cu bioaccumulation in L. variegatus for both forms of Cu. Bioaccumulation was detected because isotopically enriched 65Cu was used as a tracer. Neither burrowing behavior or survival was affected by the exposure. Once incorporated into tissue, Cu loss was negligible over 10 d of elimination in clean sediment (Cu elimination rate constants were not different from zero). With the exception of day 10, differences in bioaccumulation and subcellular distribution between Cu forms were either not detectable or marginal. After 10 d of exposure to Cu-Aq, the accumulated Cu was primarily partitioned in the subcellular fraction containing metallothionein-like proteins (MTLP, ≈40%) and cellular debris (CD, ≈30%). Cu concentrations in these fractions were significantly higher than in controls. For worms exposed to CuO NPs for 10 d, most of the accumulated Cu was partitioned in the CD fraction (≈40%), which was the only subcellular fraction where the Cu concentration was significantly higher than for the control group. Our results indicate that L. variegatus handle the two Cu forms differently. However, longer-term exposures are suggested in order to clearly highlight differences in the subcellular distribution of these two Cu forms.

  14. Structural Studies of the Alzheimer's Amyloid Precursor Protein Copper-Binding Domain Reveal How It Binds Copper Ions

    Energy Technology Data Exchange (ETDEWEB)

    Kong, G.K.-W.; Adams, J.J.; Harris, H.H.; Boas, J.F.; Curtain, C.C.; Galatis, D.; Master, C.L.; Barnham, K.J.; McKinstry, W.J.; Cappai, R.; Parker, M.W.; /Sydney U.

    2007-07-09

    Alzheimer's disease (AD) is the major cause of dementia. Amyloid {beta} peptide (A {beta}), generated by proteolytic cleavage of the amyloid precursor protein (APP), is central to AD pathogenesis. APP can function as a metalloprotein and modulate copper (Cu) transport, presumably via its extracellular Cu-binding domain (CuBD). Cu binding to the CuBD reduces A{beta} levels, suggesting that a Cu mimetic may have therapeutic potential. We describe here the atomic structures of apo CuBD from three crystal forms and found they have identical Cu-binding sites despite the different crystal lattices. The structure of Cu[2+]-bound CuBD reveals that the metal ligands are His147, His151, Tyrl68 and two water molecules, which are arranged in a square pyramidal geometry. The site resembles a Type 2 non-blue Cu center and is supported by electron paramagnetic resonance and extended X-ray absorption fine structure studies. A previous study suggested that Met170 might be a ligand but we suggest that this residue plays a critical role as an electron donor in CuBDs ability to reduce Cu ions. The structure of Cu[+]-bound CuBD is almost identical to the Cu[2+]-bound structure except for the loss of one of the water ligands. The geometry of the site is unfavorable for Cu[+], thus providing a mechanism by which CuBD could readily transfer Cu ions to other proteins.

  15. Experimental and numerical optical characterization of plasmonic copper nanoparticles embedded in ZnO fabricated by ion implantation and annealing

    Energy Technology Data Exchange (ETDEWEB)

    Le, Khai Q. [Faculty of Science and Technology, Hoa Sen University, Ho Chi Minh City (Viet Nam); Department of Physics, Faculty of Science, Jazan University, P.O. Box 114, 45142 Jazan (Saudi Arabia); Nguyen, Hieu P.T. [Department of Electrical and Computer Engineering, New Jersey Institute of Technology, NJ 07102 (United States); Ngo, Quang Minh [Institute of Material Sciences, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Cau Giay, Hanoi (Viet Nam); Canimoglu, Adil [Nigde University, Faculty of Arts and Sciences, Physics Department, Nigde (Turkey); Can, Nurdogan, E-mail: cannurdogan@yahoo.com [Celal Bayar University, Faculty of Arts and Sciences, Department of Physics, Muradiye, Manisa (Turkey); Department of Physics, Faculty of Science, Jazan University, P.O. Box 114, 45142 Jazan (Saudi Arabia)

    2016-06-05

    Here we describe the successfully fabrication of metal nanoparticle crystals by implanting copper (Cu) ions into single zinc oxide (ZnO) crystals with ion energy of 400 keV at ion doses of 1 × 10{sup 16} to 1 × 10{sup 17} ions/cm{sup 2}. After implantation and post-annealing treatment, the Cu implanted ZnO produces a broad range of luminescence emissions, ranging from green to yellow. A green luminescence peak at 550 nm could be ascribed to the isolated Cu ions. The changes in luminescence emission bands between the initial implant and annealed suggest that the implants give rise to clustering Cu nanoparticles in the host matrix but that the annealing process dissociates these. Numerical modelling of the Cu nanoparticles was employed to simulate their optical properties including the extinction cross section, electron energy loss spectroscopy and cathodoluminescence. We demonstrate that the clustering of nanoparticles generates Fano resonances corresponding to the generation of multiple resonances, while the isolation of nanoparticles results in intensity amplification. - Highlights: • We present the fabrication of metal nanoparticle crystals by implanting Cu into ZnO. • The luminescence properties were studied at different annealing temperature. • Numerical modelling of the Cu nanoparticles was employed. • We demonstrate that the clustering of nanoparticles generates Fano resonances.

  16. A highly selective and sensitive fluorescence assay for determination of copper(II) and cobalt(II) ions in environmental water and toner samples.

    Science.gov (United States)

    Tsai, Chia-Yi; Lin, Yang-Wei

    2013-02-21

    In this study, a highly selective and sensitive fluorescence assay has been proposed for the determination of copper(II) and cobalt(II) ions in environmental water and toner samples. In the presence of hydrogen peroxide, copper(II) reacted with a new fluorescence reagent Amplex® UltraRed (AUR), forming a fluorescence product only at pH 7.0, while the fluorescence product of cobalt(II) with AUR formed only at pH 9.0. The fluorescence signal obtained was linear with respect to the copper(II) concentration over the range of 1.6-12.0 μM (R(2) = 0.988) and was linear with respect to the cobalt(II) concentration over the range of 45.0 nM to 1.0 μM (R(2) = 0.992). The limits of detection (at a signal-to-noise ratio of 3) for copper(II) and cobalt(II) were 0.17 μM and 14.0 nM, respectively. Our present approach is simpler, faster, and more cost-effective than other techniques for the detection of copper(II) and cobalt(II) ions in environmental water samples and that of copper(II) ions in toner samples.

  17. Biosorption of copper(II) ions onto powdered waste sludge in a completely mixed fed-batch reactor: estimation of design parameters.

    Science.gov (United States)

    Pamukoglu, Yunus; Kargi, Fikret

    2007-04-01

    Biosorption of Cu(II) ions onto pre-treated powdered waste sludge (PWS) was investigated using a fed-batch operated completely mixed reactor. Fed-batch adsorption experiments were performed by varying the feed flow rate ( 0.075-0.325 l h(-1)), feed copper (II) ion concentrations (50-300 mg l(-1)) and the amount of adsorbent (1-6 g PWS) using fed-batch operation. Breakthrough curves describing the variations of effluent copper ion concentrations with time were determined for different operating conditions. Percent copper ion removals from the aqueous phase decreased, but the biosorbed (solid phase) copper ion concentrations increased with increasing the feed flow rate and Cu(II) concentration. A modified Bohart-Adams equation was used to determine the biosorption capacity of PWS and the rate constant for Cu(II) ion biosorption. Adsorption rate constant in fed-batch operation was an order of magnitude larger than those obtained in adsorption columns because of elimination of mass transfer limitations encountered in the column operations while the biosorption capacity of PWS was comparable with powdered activated (PAC) in column operations. Therefore, a completely mixed reactor operated in fed-batch mode was proven to be more advantageous as compared to adsorption columns due to better contact between the phases yielding faster adsorption rates.

  18. Microanalysis of oligodeoxynucleotides by cathodic stripping voltammetry at amalgam-alloy surfaces in the presence of copper ions.

    Science.gov (United States)

    Hason, Stanislav; Vetterl, Vladimír

    2006-05-15

    The application of gold amalgam-alloy electrode (AuAE) for a sensitive voltammetric detection of different oligodeoxynucleotides (ODNs) containing the purine units within the ODN-chains in the presence of copper is described. The detection of ODNs is based on the following procedure: (i) the first step includes an acidic hydrolysis of the ODN (ahODN) samples performing the release of the purine bases from ODN-chain; (ii) the second step includes an electrochemical accumulation of the complex of the purine base residues released from ODN-chain with copper ions Cu(I) (ahODN-Cu(I) complex) at the potential of reduction of copper ions Cu(II) on the amalgam-alloy electrode surfaces; (iii) finally followed the cathodic stripping of the electrochemically accumulated ahODN-Cu(I) complex from the electrode surface. The proposed electrochemical method was used for: (a) detection of different ODN lengths containing only adenine units (the number of adenine units within the ODN-chains was changed from 10 to 80), and (b) determination of the number of purine units within the 30-mer ODNs containing a random sequence segments involving both the purine and pyrimidine units. The intensity of the cathodic stripping current density peak (j(CSP)) of the electrochemically accumulated ahODN-Cu(I) complex increased linearly with the increasing number of purine units within the ODN-chains. We observed a good correlation between the percentage content of purine units to the whole length of different 30-mer ODNs and the percentage content of the intensity of the j(CSP) of the electrochemically accumulated 30-mer ahODN-Cu(I) complexes. The detection of acid hydrolysed 80-mer (A(80)) in the bulk solution and in a 20-mul volume is possible down to 200pM and 2nM at the AuAE, respectively. For the shortest 10-mer (A(10)) a detectable value of 5nM in the bulk solution on the AuAE was observed. The sensitive detection of different ODNs containing the purine units in their chains in the presence of

  19. The Formation of Polycomplexes of Poly(Methyl Vinyl Ether-Co-Maleic Anhydride and Bovine Serum Albumin in the Presence of Copper Ions

    Directory of Open Access Journals (Sweden)

    Karahan Mesut

    2014-09-01

    Full Text Available The binary and ternary complex formations of poly(methyl vinyl ether-co-maleic anhydride (PMVEMA with copper ions and with bovine serum albumin (BSA in the presence of copper ions in phosphate buffer solution at pH = 7 were examined by the techniques of UV-visible, fluorescence, dynamic light scattering, atomic force microscopy measurements. In the formation of binary complexes of PMVEMA-Cu(II, the addition of copper ions to the solution of PMVEMA in phosphate buffer solution at pH = 7 forms homogeneous solutions when the molar ratio of Cu(II/MVEMA is 0.5. Then the formations of ternary complexes of PMVEMA-Cu(II-BSA were examined. Study analysis revealed that the toxicities of polymer-metal and polymer-metal-protein mixture solutions depend on the nature and ratio of components in mixtures.

  20. Effect of sorption conditions on the state of copper(II) ions in the phase of AN-31 ion exchange resin, according to data from ESR and UV-vis diffuse reflectance spectroscopy

    Science.gov (United States)

    Stroganova, E. A.; Anufrienko, V. F.; Larina, T. V.; Vasenin, N. T.; Lebedev, Yu. A.; Parmon, V. N.

    2017-08-01

    It is found that the sorption recovery of copper ions from water solutions in the phase of AN-31 low basicity anion exchanger has a mixed character. It is established via diffuse reflectance spectroscopy that ions are stabilized through complexation with the participation of the functional groups of the sorbent with the formation of structures [Cu(NR3)2(OH)2(H2O)2], [Cu(NR3)3(OH)(H2O)2], and as a result of the physical adsorption of oxide dimers and planar-squared copper clusters. It is shown that increasing the ionic strength of a solution by introducing sodium chloride into the system greatly improves the capacity of the sorbent and leads to the uniform distribution of copper ions in the resin matrix. The similarity between the ESR spectrum parameters of copper-containing samples of the ion exchanger, obtained in a wider range of pH, is determined via ESR and testifies to the homogeneity of the stabilization positions of Cu2+ ions. The crystalline field of tetragonal-elongated octahedron is typical of all Cu2+ ions. All of the complexes have Cu(NO3)2 coordination nodes with the covalent bonding of Cu2+ ions and the amine groups of the sorbent.

  1. Carboxymethyl-{beta}-cyclodextrin conjugated magnetic nanoparticles as nano-adsorbents for removal of copper ions: Synthesis and adsorption studies

    Energy Technology Data Exchange (ETDEWEB)

    Badruddoza, A.Z.M.; Tay, A.S.H.; Tan, P.Y.; Hidajat, K. [Department of Chemical and Biomolecular Engineering, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260 (Singapore); Uddin, M.S., E-mail: cheshahb@nus.edu.sg [Department of Chemical and Biomolecular Engineering, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260 (Singapore)

    2011-01-30

    A novel nano-adsorbent, carboxymethyl-{beta}-cyclodextrin modified Fe{sub 3}O{sub 4} nanoparticles (CMCD-MNPs) is fabricated for removal of copper ions from aqueous solution by grafting CM-{beta}-CD onto the magnetite surface via carbodiimide method. The characteristics results of FTIR, TEM, TGA and XPS show that CM-{beta}-CD is grafted onto Fe{sub 3}O{sub 4} nanoparticles. The grafted CM-{beta}-CD on the Fe{sub 3}O{sub 4} nanoparticles contributes to an enhancement of the adsorption capacity because of the strong abilities of the multiple hydroxyl and carboxyl groups in CM-{beta}-CD to adsorb metal ions. The adsorption of Cu{sup 2+} onto CMCD-MNPs is found to be dependent on pH and temperature. Adsorption equilibrium is achieved in 30 min and the adsorption kinetics of Cu{sup 2+} is found to follow a pseudo-second-order kinetic model. Equilibrium data for Cu{sup 2+} adsorption are fitted well by Langmuir isotherm model. The maximum adsorption capacity for Cu{sup 2+} ions is estimated to be 47.2 mg/g at 25 {sup o}C. Furthermore, thermodynamic parameters reveal the feasibility, spontaneity and exothermic nature of the adsorption process. FTIR and XPS reveal that Cu{sup 2+} adsorption onto CMCD-MNPs mainly involves the oxygen atoms in CM-{beta}-CD to form surface-complexes. In addition, the copper ions can be desorbed from CMCD-MNPs by citric acid solution with 96.2% desorption efficiency and the CMCD-MNPs exhibit good recyclability.

  2. Carboxymethyl-β-cyclodextrin conjugated magnetic nanoparticles as nano-adsorbents for removal of copper ions: synthesis and adsorption studies.

    Science.gov (United States)

    Badruddoza, A Z M; Tay, A S H; Tan, P Y; Hidajat, K; Uddin, M S

    2011-01-30

    A novel nano-adsorbent, carboxymethyl-β-cyclodextrin modified Fe(3)O(4) nanoparticles (CMCD-MNPs) is fabricated for removal of copper ions from aqueous solution by grafting CM-β-CD onto the magnetite surface via carbodiimide method. The characteristics results of FTIR, TEM, TGA and XPS show that CM-β-CD is grafted onto Fe(3)O(4) nanoparticles. The grafted CM-β-CD on the Fe(3)O(4) nanoparticles contributes to an enhancement of the adsorption capacity because of the strong abilities of the multiple hydroxyl and carboxyl groups in CM-β-CD to adsorb metal ions. The adsorption of Cu(2+) onto CMCD-MNPs is found to be dependent on pH and temperature. Adsorption equilibrium is achieved in 30 min and the adsorption kinetics of Cu(2+) is found to follow a pseudo-second-order kinetic model. Equilibrium data for Cu(2+) adsorption are fitted well by Langmuir isotherm model. The maximum adsorption capacity for Cu(2+) ions is estimated to be 47.2mg/g at 25 °C. Furthermore, thermodynamic parameters reveal the feasibility, spontaneity and exothermic nature of the adsorption process. FTIR and XPS reveal that Cu(2+) adsorption onto CMCD-MNPs mainly involves the oxygen atoms in CM-β-CD to form surface-complexes. In addition, the copper ions can be desorbed from CMCD-MNPs by citric acid solution with 96.2% desorption efficiency and the CMCD-MNPs exhibit good recyclability. Copyright © 2010 Elsevier B.V. All rights reserved.

  3. Synergistic inhibition effect of L-phenylalanine and rare earth Ce(IV) ion on the corrosion of copper in hydrochloric acid solution

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Daquan, E-mail: zhangdaquan@shiep.edu.cn [Department of Environmental Engineering, Shanghai University of Electric Power, Shanghai 200090 (China); Wu Huan; Gao Lixin [Department of Environmental Engineering, Shanghai University of Electric Power, Shanghai 200090 (China)

    2012-04-16

    Highlights: Black-Right-Pointing-Pointer Synergistic effect of L-phenylalanine (L-Phe) and Ce(SO{sub 4}){sub 2} on the corrosion of copper on the corrosion inhibition of copper in 0.5 M HCl solution. Black-Right-Pointing-Pointer Structure of the complex film formed by the interaction of L-phenylalanine (L-Phe) and Ce(SO{sub 4}){sub 2} on the copper surface. Black-Right-Pointing-Pointer Mechanism of the improvement of the inhibition property of amino acids by the addition of rare earth compound. - Abstract: The synergistic inhibition effect of L-phenylalanine (L-Phe) and Ce(SO{sub 4}){sub 2} on the corrosion of copper in 0.5 M HCl solution was investigated by weight-loss, electrochemical methods and surface analysis. The electrochemical results showed that L-Phe has definite inhibition effects for copper, while Ce(IV) promoted the anodic process of copper corrosion. The combination L-Phe with Ce(IV) ion produced strong synergistic effect on corrosion inhibition for copper. The maximum inhibition efficiency was 82.7% for 5 mM L-Phe + 2 mM Ce(IV). The results of EIS and potentiodynamic polarization are in good agreement. SEM showed that L-Phe and Ce(IV) can form a dense protective film on the copper surface.

  4. Ligandless-dispersive liquid-liquid microextraction of trace amount of copper ions

    Energy Technology Data Exchange (ETDEWEB)

    Mohammadi, Sayed Zia, E-mail: szmohammadi@yahoo.com [Department of Chemistry, Payame Noor University (PNU), Kerman (Iran, Islamic Republic of); Afzali, Daryoush [Environment Department, Institute Research of Environmental Sciences, International Center for Science, High Technology and Environmental Sciences, Kerman (Iran, Islamic Republic of); Baghelani, Yar Mohammad [Department of Chemistry, Payame Noor University (PNU), Kerman (Iran, Islamic Republic of)

    2009-10-27

    In the present work, a new ligandless-dispersive liquid-liquid microextraction (LL-DLLME) method has been developed for preconcentration trace amounts of copper as a prior step to its determination by flame atomic absorption spectrometry. In the proposed approach 1,2-dicholorobenzene and ethanol were used as extraction and dispersive solvents, respectively. Some factors influencing on the extraction efficiency of copper and its subsequent determination were studied and optimized, such as the extraction and dispersive solvent type and volume, pH of sample solution, extraction time and salting out effect. Under the optimal conditions, the calibration curve was linear in the range of 1.0 ng mL{sup -1}-0.6 {mu}g mL{sup -1} of copper with R{sup 2} = 0.9985. Detection limit was 0.5 ng mL{sup -1} in original solution (3S{sub b}/m) and the relative standard deviation for seven replicate determination of 0.2 {mu}g mL{sup -1} copper was {+-}1.4%. The proposed method has been applied for determination of copper in standard and water samples with satisfactory results.

  5. A Copper Coordination Compound Produced by a Marine Fungus Fusarium sp. ZZF51 with Biosorption of Cu(Ⅱ) Ions

    Institute of Scientific and Technical Information of China (English)

    TAN Ni; PAN Jia-Hui; PENG Guang-Tian; MOU Cheng-Bo; TAO Yi-Wen; SHE Zhi-Gang; YANG Ze-Liang; ZHOU Shi-Ning; LIN Yong-Cheng

    2008-01-01

    A copper coordination compound ZZF51 (A) named bis(5-butyl-2-pyridinecarboxylato-N1,O2)-copper, the first time found in the nature, was isolated from a marine endophytic fungus Fusarium sp. ZZF51 from the South China Sea coast. Its structure was elucidated using spectroscopic methods and single crystal X-ray diffraction analysis.The antimicrobial cytotoxicity experiments exhibited that ZZF51(A) had mutagenicity activities against four aerobic reference strains Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Salmonella enteritidis with respective MIC values of 12.5, 25, 12.5, and 50 μg/mL. The anti-cancer tests showed that the compound had strong inhibitory activities against three human cancer lines KB, KBv200, and HepG2 with IC50 values of 3.54, 3.68 and 25.12 μg/mL respectively. In the course of investigating the source of ZZF51(A) in biomass, it was found that the output of ZZF51(A) was largely influenced by the amount of CuCl2 in the liquid medium, and the fungus (No.ZZF51) had two notable characteristics: endurance of high concentration Cu(Ⅱ) ions and biosorption of Cu(Ⅱ) ions.

  6. Formation of TiO2 photoanodes by simultaneous electrophoretic deposition of anatase and rutile particles for photoassisted electrolytic copper ions removal

    Directory of Open Access Journals (Sweden)

    Yeimmy Y. Peralta-Ruiz

    2012-01-01

    Full Text Available The influence of Anatasa/Rutile ratio on TiO2 films, grown by electrophoretic deposition was studied in the photoassisted electrolytic copper ions removal from cyanide solutions. The proper dispersant dosage allowing the simultaneous electrophoretic deposition of Anatase and Rutile was chosen based on electrokinetic measurements; evidenced by the XRD spectra of the formed films. The evaluation of films photoassisted electrolytic copper ion removal showeds that it is possible to enhance the activity of Anatase films by adding some Rutile exploiting the synergetic interaction between these two materials, achieve by its proper deposition.

  7. Synthesis and characterization of novel ion-imprinted polymeric nanoparticles for very fast and highly selective recognition of copper(II) ions.

    Science.gov (United States)

    Shamsipur, Mojtaba; Besharati-Seidani, Abbas; Fasihi, Javad; Sharghi, Hashem

    2010-12-15

    This work reports the preparation of new Cu(2+) ion-imprinted polymeric nanoparticles using 1-hydroxy-4-(prop-2'-enyloxy)-9,10-anthraquinone (AQ) as a vinylated chelating agent. The Cu(2+) ion found to form a stable 1:1 complex with AQ in methanol solution. The resulting Cu(2+)-AQ complex was copolymerized with ethyleneglycol dimethacrylate, as a cross-linking monomer, via precipitation polymerization method. The imprint copper ion was removed from the polymeric matrix using a 0.1 mol L(-1) HNO(3) solution. The Cu(2+)-imprinted polymeric nanoparticles were characterized by IR spectroscopy, scanning electron microscopy (SEM) and N(2) adsorption-desorption isotherms. The SEM micrographs showed colloidal nanoparticles of 60-100 nm in diameter and slightly irregular in shape. Optimum pH for maximum sorption was 7.0. Sorption and desorption of Cu(2+) ion on the IIP nanoparticles were quite fast and achieved completely over entire investigated time periods of 2-30 min. Maximum sorbent capacity and enrichment factor of the prepared IIP for Cu(2+) were 73.8 μmol g(-1) and 56.5, respectively. The relative standard deviation and limit of detection (C(LOD)=3S(b)/m) of the method were evaluated as 2.6% and 0.1 ng mL(-1), using inductively coupled plasma-atomic emission spectrometry, respectively. It was found that the imprinting technology results in increased affinity of the prepared material toward Cu(2+) ion over other metal ions with the same charge and close ionic radius. The relative standard deviations for six and twenty replicates with the same nanoparticles were found to be 1.7% and 2.1%, respectively. Copyright © 2010 Elsevier B.V. All rights reserved.

  8. Interaction between Langmuir and Langmuir-Blodgett films of two calix[4]arenes with aqueous copper and lithium ions.

    Science.gov (United States)

    Supian, Faridah L; Richardson, Tim H; Deasy, Mary; Kelleher, Fintan; Ward, James P; McKee, Vickie

    2010-07-06

    The binding interactions between aqueous copper (Cu(2+)) and lithium (Li(+)) ions and Langmuir monolayers and Langmuir-Blodgett (LB) multilayers have been investigated by studying surface pressure-area (Pi-A) isotherms and surface potential-area (DeltaV-A) behavior in order to find the effective dipole moment, mu(perpendicular), of the calixarene molecules in the uncomplexed and complexed states. The orientation of both calix[4]arenes, namely, 5,11,17,23-tetra-tert-butyl-25,27-diethoxycarbonyl methyleneoxy-26,28-dihydroxycalix[4]arene and 5,17-(9H-fluoren-2-yl)methyleneamino)-11,23-di-tert-butyl-25,27-diethoxycarbonyl methyleneoxy-26,28-dihydroxycalix[4]arene, is such that the plane of the calix ring is parallel with the plane of the water surface regardless of the ion content of the subphase. The Gibbs equation was used to interpret the adsorption of ions with both calix[4]arenes as a function of the concentration. Effective dipole moments have been calculated from surface potential values using the Helmholtz equation. In this work, new LB films have been prepared employing two novel amphiphilic calix[4]arene derivatives bearing different upper rim substituents. Thus, the effect of modifiying the upper rim has been observed. The results have shown that these calixarenes may be useful components of ion sensors.

  9. Impact of manganese, copper and zinc ions on the transcriptome of the nosocomial pathogen Enterococcus faecalis V583.

    Directory of Open Access Journals (Sweden)

    Marta Coelho Abrantes

    Full Text Available Mechanisms that enable Enterococcus to cope with different environmental stresses and their contribution to the switch from commensalism to pathogenicity of this organism are still poorly understood. Maintenance of intracellular homeostasis of metal ions is crucial for survival of these bacteria. In particular Zn(2+, Mn(2+ and Cu(2+ are very important metal ions as they are co-factors of many enzymes, are involved in oxidative stress defense and have a role in the immune system of the host. Their concentrations inside the human body vary hugely, which makes it imperative for Enterococcus to fine-tune metal ion homeostasis in order to survive inside the host and colonize it. Little is known about metal regulation in Enterococcus faecalis. Here we present the first genome-wide description of gene expression of E. faecalis V583 growing in the presence of high concentrations of zinc, manganese or copper ions. The DNA microarray experiments revealed that mostly transporters are involved in the responses of E. faecalis to prolonged exposure to high metal concentrations although genes involved in cellular processes, in energy and amino acid metabolisms and genes related to the cell envelope also seem to play important roles.

  10. Handling of Copper and Copper Oxide Nanoparticles by Astrocytes.

    Science.gov (United States)

    Bulcke, Felix; Dringen, Ralf

    2016-02-01

    Copper is an essential trace element for many important cellular functions. However, excess of copper can impair cellular functions by copper-induced oxidative stress. In brain, astrocytes are considered to play a prominent role in the copper homeostasis. In this short review we summarise the current knowledge on the molecular mechanisms which are involved in the handling of copper by astrocytes. Cultured astrocytes efficiently take up copper ions predominantly by the copper transporter Ctr1 and the divalent metal transporter DMT1. In addition, copper oxide nanoparticles are rapidly accumulated by astrocytes via endocytosis. Cultured astrocytes tolerate moderate increases in intracellular copper contents very well. However, if a given threshold of cellular copper content is exceeded after exposure to copper, accelerated production of reactive oxygen species and compromised cell viability are observed. Upon exposure to sub-toxic concentrations of copper ions or copper oxide nanoparticles, astrocytes increase their copper storage capacity by upregulating the cellular contents of glutathione and metallothioneins. In addition, cultured astrocytes have the capacity to export copper ions which is likely to involve the copper ATPase 7A. The ability of astrocytes to efficiently accumulate, store and export copper ions suggests that astrocytes have a key role in the distribution of copper in brain. Impairment of this astrocytic function may be involved in diseases which are connected with disturbances in brain copper metabolism.

  11. Removal of copper ions from aqueous solution by adsorption onto novel polyelectrolyte film-coated nanofibrous silk fibroin non-wovens

    Science.gov (United States)

    Zhou, Weitao; Huang, Haitao; Du, Shan; Huo, Yingdong; He, Jianxin; Cui, Shizhong

    2015-08-01

    In this approach, polyelectrolyte film-coated nanofibrous silk fibroin (SF) nonwovens were prepared from the alternate deposition of positively charged polyethylenimine (PEI) and negatively charged SF using electrostatic layer-by-layer (LBL) self-assembled technology. The composite membranes were characterized by scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectrometer. The SF-PEI multilayer-assembled nanofibers (less than five layers) were fine and uniform with the fiber diameter from 400 nm to 600 nm, and had very large surface area and high porosity (more than 70%). The amino groups of PEI were proved to be deposited onto SF nonwovens, which granted the coated nonwovens with potential applicability for copper ions adsorption. The PEI films coated SF substrate showed much higher copper ions adsorption capacity than that of ethanol treated SF nanofibers. Adding the number of PEI coated could enhance the Cu2+ adsorption capacity significantly. The maximum milligrams per gram of copper ions adsorbed reached 59.7 mg/g when the SF substrate was coated with 5 bilayers of SF-PEI. However, the copper ions adsorption capacity had no obvious change as the number of PEI continued to increase. These results suggest potential for PEL film-coated nanofibrous nonwovens as a new adsorbent for metal ions.

  12. The effect of copper ions, aluminium ions and their mixtures on separation of pectin from the sugar beet juice

    Directory of Open Access Journals (Sweden)

    Kuljanin Tatjana A.

    2013-01-01

    Full Text Available In sugar industry there is a problem of the presence of undesirable macromolecules compounds such as pectin in sugar beet juice. The affinity of calcium ions commonly used in the sugar industry for the removal of pectin from the sugar beet juice is relatively small. Coagulation and precipitation of pectin can be performed by process of discharging that is chemically induced. Compounds with di- and trivalent cations such as pure CuSO4, Al2(SO43 or their mixtures can be applied for clarification of pectin colloidal systems. According to data from the order of pectin selectivity to divalent metal ions, Cu2+ ions are the first order of ion binding. Also, aluminum sulfate is commonly used in the waste water treatment. Two model solutions of pectin whose concentration corresponds to the concentration of these macromolecules in sugar beet juice (0.1% w/w are investigated. Using a method of measuring zeta potential, it was proven for both investigated pectin that fewer quantities of Cu2+ ions compared to the values of Al3+ ions are needed to reach zero zeta potential. In all the investigated coagulants and their mixtures, zeta potential has changed the sign. In experiments with mixtures has been shown that pure salts showed better coagulation properties. The reduced strength of binding of cations in the case of most of the applied mixture of Cu2+ and Al3+ ions, can be explained by the mutual competition of these ions for the adsorption site (COO- groups on the surface of macromolecules. Mixture with approximately equal shares of ions Cu2+ and Al3+ had the most unfavorable coagulation ability (ion antagonism. Mechanism of discharge as well as the model of double electric layer surrounding pectin macromolecules in the presence of mixtures of Cu2+ and Al3+ ions are suggested. However, due to possible undesirable effects of CuSO4 on food processing, Al2(SO43 is proposed instead of traditional coagulant CaO, not only because of lower consumptions of

  13. Copper-transporting P-type ATPases use a unique ion-release pathway

    DEFF Research Database (Denmark)

    Andersson, Magnus; Mattle, Daniel; Sitsel, Oleg

    2014-01-01

    Heavy metals in cells are typically regulated by PIB-type ATPases. The first structure of the class, a Cu(+)-ATPase from Legionella pneumophila (LpCopA), outlined a copper transport pathway across the membrane, which was inferred to be occluded. Here we show by molecular dynamics simulations...

  14. Removal of copper ions from aqueous solution by adsorption onto novel polyelectrolyte film-coated nanofibrous silk fibroin non-wovens

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Weitao, E-mail: weitao_zhou@yahoo.com [Key Laboratory of Functional Textiles, The Education Department of Henan Province, Zhongyuan University of Technology, Zhengzhou 450007 (China); Huang, Haitao [School of Textile, Henan Institute of Engineering, Zhengzhou 451191 (China); Du, Shan [Australian Future Fibers Research and Innovation Centre for Frontier Materials, Deakin University, Geelong, VIC 3217 (Australia); Huo, Yingdong; He, Jianxin [Key Laboratory of Functional Textiles, The Education Department of Henan Province, Zhongyuan University of Technology, Zhengzhou 450007 (China); Cui, Shizhong, E-mail: snowballer@163.com [Key Laboratory of Functional Textiles, The Education Department of Henan Province, Zhongyuan University of Technology, Zhengzhou 450007 (China)

    2015-08-01

    Graphical abstract: - Highlights: • Polyethylenimine coated silk fibroin nanofibrous nonwovens were fabricated. • The characteristics such as the fiber shape and porous structure were well maintained. • The structure and adsorption properties were studied. The adsorption property for copper ions is good. - Abstract: In this approach, polyelectrolyte film-coated nanofibrous silk fibroin (SF) nonwovens were prepared from the alternate deposition of positively charged polyethylenimine (PEI) and negatively charged SF using electrostatic layer-by-layer (LBL) self-assembled technology. The composite membranes were characterized by scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) spectrometer. The SF-PEI multilayer-assembled nanofibers (less than five layers) were fine and uniform with the fiber diameter from 400 nm to 600 nm, and had very large surface area and high porosity (more than 70%). The amino groups of PEI were proved to be deposited onto SF nonwovens, which granted the coated nonwovens with potential applicability for copper ions adsorption. The PEI films coated SF substrate showed much higher copper ions adsorption capacity than that of ethanol treated SF nanofibers. Adding the number of PEI coated could enhance the Cu{sup 2+} adsorption capacity significantly. The maximum milligrams per gram of copper ions adsorbed reached 59.7 mg/g when the SF substrate was coated with 5 bilayers of SF-PEI. However, the copper ions adsorption capacity had no obvious change as the number of PEI continued to increase. These results suggest potential for PEL film-coated nanofibrous nonwovens as a new adsorbent for metal ions.

  15. Magnetic Graphene Nanosheet-Based Microfluidic Device for Homogeneous Real-Time Electronic Monitoring of Pyrophosphatase Activity Using Enzymatic Hydrolysate-Induced Release of Copper Ion.

    Science.gov (United States)

    Lin, Youxiu; Zhou, Qian; Li, Juan; Shu, Jian; Qiu, Zhenli; Lin, Yuping; Tang, Dianping

    2016-01-01

    A novel flow-through microfluidic device based on a magneto-controlled graphene sensing platform was designed for homogeneous electronic monitoring of pyrophosphatase (PPase) activity; enzymatic hydrolysate-induced release of inorganic copper ion (Cu(2+)) from the Cu(2+)-coordinated pyrophosphate ions (Cu(2+)-PPi) complex was assessed to determine enzyme activity. Magnetic graphene nanosheets (MGNS) functionalized with negatively charged Nafion were synthesized by using the wet-chemistry method. The Cu(2+)-PPi complexes were prepared on the basis of the coordination reaction between copper ion and inorganic pyrophosphate ions. Upon target PPase introduction into the detection system, the analyte initially hydrolyzed pyrophosphate ions into phosphate ions and released the electroactive copper ions from Cu(2+)-PPi complexes. The released copper ions could be readily captured through the negatively charged Nafion on the magnetic graphene nanosheets, which could be quantitatively monitored by using the stripping voltammetry on the flow-through detection cell with an external magnet. Under optimal conditions, the obtained electrochemical signal exhibited a high dependence on PPase activity within a dynamic range from 0.1 to 20 mU mL(-1) and allowed the detection at a concentration as low as 0.05 mU mL(-1). Coefficients of variation for reproducibility of the intra-assay and interassay were below 7.6 and 9.8%, respectively. The inhibition efficiency of sodium fluoride (NaF) also received good results in pyrophosphatase inhibitor screening research. In addition, the methodology afforded good specificity and selectivity, simplification, and low cost without the need of sample separations and multiple washing steps, thus representing a user-friendly protocol for practical utilization in a quantitative PPase activity.

  16. Effect of copper content in the new conductive material Cu-SPB used in low-temperature Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Yaqub, Adnan; Pervez, Syed Atif; Farooq, Umer; Saleem, Mohsin; Doh, Chilhoon [Korea Electro-technology Research Institute, Changwon (Korea, Republic of); University of Science and Technology, Daejeon (Korea, Republic of); Lee, Youjin; Hwang, Minji; Choi, Jeonghee; Kim, Doohun [Korea Electro-technology Research Institute, Changwon (Korea, Republic of)

    2014-08-15

    A new conductive material, copper/Super-P carbon black composite (Cu-SPB), is prepared via an efficient ion reducing method for use in low-temperature lithium-ion batteries (LIBs). The present study investigated the effects of copper content on the low-temperature performance of LIBs. Electrodes prepared with a high-copper-content conductive material (Cu = 18.54%) showed remarkably improved performance in terms of capacity retention (around 40%), cycling stability, and columbic efficiency. The electrochemical impedance spectroscopy (EIS) analysis revealed that the presence of higher Cu contents could reduce the cell's impedance. The results were also confirmed by using a coin-type full cell's improved capacity retention, which indicated the significance of Cu particles in enhancing the low-temperature performance of LIBs.

  17. Coumarin-Based Fluorescent Probes for Dual Recognition of Copper(II and Iron(III Ions and Their Application in Bio-Imaging

    Directory of Open Access Journals (Sweden)

    Olimpo García-Beltrán

    2014-01-01

    Full Text Available Two new coumarin-based “turn-off” fluorescent probes, (E-3-((3,4-dihydroxybenzylideneamino-7-hydroxy-2H-chromen-2-one (BS1 and (E-3-((2,4-dihydroxybenzylideneamino-7-hydroxy-2H-chromen-2-one (BS2, were synthesized and their detection of copper(II and iron(III ions was studied. Results show that both compounds are highly selective for Cu2+ and Fe3+ ions over other metal ions. However, BS2 is detected directly, while detection of BS1 involves a hydrolysis reaction to regenerate 3-amino-7-hydroxycoumarin (3 and 3,4-dihydroxybenzaldehyde, of which 3 is able to react with copper(II or iron(III ions. The interaction between the tested compounds and copper or iron ions is associated with a large fluorescence decrease, showing detection limits of ca. 10−5 M. Preliminary studies employing epifluorescence microscopy demonstrate that Cu2+ and Fe3+ ions can be imaged in human neuroblastoma SH-SY5Y cells treated with the tested probes.

  18. Coumarin-based fluorescent probes for dual recognition of copper(II) and iron(III) ions and their application in bio-imaging.

    Science.gov (United States)

    García-Beltrán, Olimpo; Cassels, Bruce K; Pérez, Claudio; Mena, Natalia; Núñez, Marco T; Martínez, Natalia P; Pavez, Paulina; Aliaga, Margarita E

    2014-01-13

    Two new coumarin-based "turn-off" fluorescent probes, (E)-3-((3,4-dihydroxybenzylidene)amino)-7-hydroxy-2H-chromen-2-one (BS1) and (E)-3-((2,4-dihydroxybenzylidene)amino)-7-hydroxy-2H-chromen-2-one (BS2), were synthesized and their detection of copper(II) and iron(III) ions was studied. Results show that both compounds are highly selective for Cu²⁺ and Fe³⁺ ions over other metal ions. However, BS2 is detected directly, while detection of BS1 involves a hydrolysis reaction to regenerate 3-amino-7-hydroxycoumarin (3) and 3,4-dihydroxybenzaldehyde, of which 3 is able to react with copper(II) or iron(III) ions. The interaction between the tested compounds and copper or iron ions is associated with a large fluorescence decrease, showing detection limits of ca. 10⁻⁵ M. Preliminary studies employing epifluorescence microscopy demonstrate that Cu²⁺ and Fe³⁺ ions can be imaged in human neuroblastoma SH-SY5Y cells treated with the tested probes.

  19. Disposable competitive-type immunoassay for determination of aflatoxin B1 via detection of copper ions released from Cu-apatite.

    Science.gov (United States)

    Wang, Huan; Zhang, Yihe; Chu, Yanguang; Ma, Hongmin; Li, Yan; Wu, Dan; Du, Bin; Wei, Qin

    2016-01-15

    A disposable electrochemical immunosensor was developed for detection of aflatoxin B1 (AFB1) based on stripping voltammetric detection of copper ions released from Cu-apatite. AFB1 antibody (Ab) was firstly fixed on the gold nanoparticle (Au NPs) modified screen-printed carbon electrode (SPCE). AFB1-bovine serum albumin (AFB1-BSA) conjugate was labeled with Cu-apatite, and then competed with AFB1 for binding to the Ab. Copper ions were released from Cu-apatite through acidolysis and stripping voltammetry signal of the copper ions was used for the detection. The Cu-apatite increased the amount of loaded copper ions, and the anodic stripping strategy performed in the micro electrolytic cell of the SPCE simplified the detection procedure and further amplified the electrochemical signal. This immunosensor could detect AFB1 over a wide concentration range from 0.001 to 100ng mL(-1) with a detection limit of 0.2pg mL(-1). The low cost, high sensitive, rapid and accurate method may find widely potential application in the detection of other toxic or harmful substances.

  20. Fluorescent sensor for selective determination of copper ion based on N-acetyl-L-cysteine capped CdHgSe quantum dots.

    Science.gov (United States)

    Wang, Qingqing; Yu, Xiangyang; Zhan, Guoqing; Li, Chunya

    2014-04-15

    Using N-acetyl-L-cysteine as a stabilizer, well water-dispersed, high-quality and stable CdHgSe quantum dots were facilely synthesized via a simple aqueous phase method. The as-prepared N-acetyl-L-cysteine capped CdHgSe quantum dots were thoroughly characterized by transmission electron microscopy, X-ray diffraction spectroscopy and FTIR. A fluorescent sensor for selective determination of copper ions was developed using N-acetyl-L-cysteine capped CdHgSe quantum dots as fluorescent probe. The fluorescence intensity of N-acetyl-L-cysteine capped CdHgSe quantum dots decreased when interacted with copper ions due to the formation of coordination complex and aggregates. The method possesses high selectivity and is not influenced by some potential interferences such as Ag(+), Zn(2+), Co(2+) and Ni(2+). Under the optimal conditions, the change of fluorescence intensity (ΔI) was linearly proportional to the concentration of copper ions in the range of 1.0×10(-9)-4.0×10(-7) mol L(-1), with a detection limit as low as 2.0×10(-10) mol L(-1) (S/N=3). The developed method had been successfully employed to determine Cu(2+) in shrimp and South-lake water samples, and the results were verified by atomic absorption spectroscopy. The fluorescent sensor was demonstrated to be selective, sensitive and simple for copper ion determination, and promise for practical applications.

  1. Simple Colorimetric Detection of Amyloid β-peptide (1-40) based on Aggregation of Gold Nanoparticles in the Presence of Copper Ions.

    Science.gov (United States)

    Zhou, Yanli; Dong, Hui; Liu, Lantao; Xu, Maotian

    2015-05-13

    A simple method for specific colorimetric sensing of Alzheimer's disease related amyloid-β peptide (Aβ) is developed based on the aggregation of gold nanoparticles in the presence of copper ion. The detection of limit for Aβ(1-40) is 0.6 nM and the promising results from practical samples (human serum) indicate the great potential for the routine detection.

  2. Biosorption of copper ions from dilute aqueous solutions on base treated rubber (Hevea brasiliensis) leaves powder: kinetics, isotherm, and biosorption mechanisms

    Institute of Scientific and Technical Information of China (English)

    W. S. Wan Ngah; M. A. K. M. Hanafiah

    2008-01-01

    The efficiency of sodium hydroxide treated rubber (Hevea brasiliensis) leaves powder (NHBL) for removing copper ions fromaqueous solutions has been investigated. The effects of physicochemical parameters on biosorption capacities such as stirring speed,pH, biosorbent dose, initial concentrations of copper, and ionic strength were studied. The biosorption capacities of NHBL increasedwith increase in pH, stirring speed and copper concentration hut decreased with increase in biosorbent dose and ionic strength. Theisotherm study indicated that NHBL fitted well with Langmuir model compared to Freundlich and Dubinin-Radushkevich models. Themaximum biosorption capacity determined from Langmuir isotherm was 14.97 mg/g at 27~C. The kinetic study revealed that pseudo-second order model fitted well the kinetic data, while Boyd kinetic model indicated that film diffusion was the main rate determiningstep in biosorption process. Based on surface area analysis, NHBL has low surface area and categorized as macroporous. Fouriertransform infrared (FT-IR) analyses revealed that hydroxyl, carboxyl, and amino are the main functional groups involved in the bindingof copper ions. Complexation was one of the main mechanisms for the removal of copper ions as indicated by FT-IR spectra. Ionexchange was another possible mechanism since the ratio of adsorbed cations (Cu2+ and H+) to the released cations (Na, Ca, andMg) from NHBL was almost unity. Copper ions bound on NHBL were able to be desorbed at>99% using 0.05 mol/L HCI, 0.01mol/L HNO, and 0.01 mol/L EDTA solutions.

  3. Photophysical studies of the interactions of poly(amidoamine) generation zero (PAMAM G0) with copper and zinc ions

    Energy Technology Data Exchange (ETDEWEB)

    López-Cabaña, Z.E. [Laboratory of Asymmetric Synthesis, Chemistry Institute of Natural Resources, University of Talca (Chile); Valdés, O. [Nanobiotechnology Division at University of Talca, Fraunhofer Chile Research Foundation – Center for Systems Biotechnology, FCR-CSB, P.O. Box 747 Talca (Chile); Vergara, C.E. [Laboratory of Asymmetric Synthesis, Chemistry Institute of Natural Resources, University of Talca (Chile); Camarada, M.B. [Universidad Andrés Bello, Facultad de Biología, Center for Bioinformatics and Integrative Biology (CBIB), República 239, Santiago (Chile); Fundación Fraunhofer Chile Research, M. Sánchez Fontecilla 310 piso 14, Las Condes (Chile); Nachtigall, F.M. [Nanobiotechnology Division at University of Talca, Fraunhofer Chile Research Foundation – Center for Systems Biotechnology, FCR-CSB, P.O. Box 747 Talca (Chile); González-Nilo, F.D. [Universidad Andrés Bello, Facultad de Biología, Center for Bioinformatics and Integrative Biology (CBIB), República 239, Santiago (Chile); Fundación Fraunhofer Chile Research, M. Sánchez Fontecilla 310 piso 14, Las Condes (Chile); Santos, Leonardo S., E-mail: lssantos@utalca.cl [Laboratory of Asymmetric Synthesis, Chemistry Institute of Natural Resources, University of Talca (Chile); Nanobiotechnology Division at University of Talca, Fraunhofer Chile Research Foundation – Center for Systems Biotechnology, FCR-CSB, P.O. Box 747 Talca (Chile)

    2015-08-15

    This study reports the photophysical behavior of poly(amidoamine) generation zero (PAMAM G0) in the presence of Cu(II) and Zn(II) ions in aqueous solutions using absorption and fluorescence spectroscopy. Theoretical and experimental results confirmed the presence of a strong covalent metal–ligand interaction between PAMAM G0 and copper ion that favored the formation of a ligand–metal charge transfer band coordination complex. In the case of Zn(II), no complex formation with PAMAM G0 was registered. Structure analysis identified the presence of aggregate like PAMAM G0–Zn moieties that generated an enhancement in the fluorescence emission of PAMAM G0. - Highlights: • Photophysical behavior of PAMAM G0 dendrimer with Cu and Zn ions was studied. • Strong covalent metal–ligand interaction was confirmed between PAMAM G0–Cu(II). • No complex formation with PAMAM G0 was registered in the case of Zn(II). • Dendrimer aggregate generated an enhancement in fluorescence emission.

  4. Trapping of muscle relaxant methocarbamol degradation product by complexation with copper(II) ion: Spectroscopic and quantum chemical studies

    Science.gov (United States)

    Mansour, Ahmed M.; Shehab, Ola R.

    2014-07-01

    Structural properties of methocarbamol (Mcm) were extensively studied both experimentally and theoretically using FT IR, 1H NMR, UV-Vis., geometry optimization, Mulliken charge, and molecular electrostatic potential. Stability arises from hyper-conjugative interactions, charge delocalization and H-bonding was analyzed using natural bond orbital (NBO) analysis. Mcm was decomposed in ethanol/water mixture at 80 °C to guaifenesin [(RS)-3-(2-methoxyphenoxy)propane-1,2-diol] and carbamate ion [NH2COO-], where the degradation mechanism was explained by trapping the carbamate ion via the complexation with copper(II) ion. The structure of the isolated complex ([Cu(NH2COO)2(H2O)]ṡ4H2O) was elucidated by spectral, thermal, and magnetic tools. Electronic spectra were discussed by TD-DFT and the descriptions of frontier molecular orbitals and the relocations of the electron density were determined. Calculated g-tensor values showed best agreement with experimental values from EPR when carried out using both the B3LYP and B3PW91 functional.

  5. Extended adsorption transport models for permeation of copper ions through nanocomposite chitosan/polyvinyl alcohol thin affinity membranes

    Institute of Scientific and Technical Information of China (English)

    Ehsan Salehi; Leila Bakhtiari; Mahdi Askari

    2016-01-01

    Transport of copper ions through nanocomposite chitosan/polyvinyl alcohol thin adsorptive membranes has been mathematical y investigated in the current study. Unsteady-state diffusive transport model was coupled with the Freundlich isotherm to predict the concentration of the ions in dialysis permeation operation. Pristine model was not successful in predicting the experimental data based upon its low coefficients of determination (0.1﹤R2﹤0.65). Well-behaved polynomial and exponential functions were used to describe time-dependency of the inlet-concentration in the first extension of the model with a little improvement in the model adjustment (0.4﹤R2﹤0.69). Similar time-dependent functions were employed for tracking the ion diffusivity and then applied in combination with the optimized functions of inlet-concentration in the second extension of the model. A sensible enhancement was obtained in the adjustment of the second extended models as a result of this combination (0.73﹤R2﹤0.93). APRE, AAPRE, RSME, RMSE, STD and R-square statistical analyses were per-formed to verify the agreement of the models with the experimental results. Concentration distribution versus time and location (inside the membrane) was obtained as 3D plots with the help of the optimized models. Modeling results emphasized on the transiency of diffusivity and feed-side concentration in dialysis permeation through chitosan membranes.

  6. Cloud point extraction for the determination of copper, nickel and cobalt ions in environmental samples by flame atomic absorption spectrometry.

    Science.gov (United States)

    Ghaedi, M; Shokrollahi, A; Ahmadi, F; Rajabi, H R; Soylak, M

    2008-02-11

    A cloud point extraction procedure was presented for the preconcentration of copper, nickel and cobalt ions in various samples. After complexation with methyl-2-pyridylketone oxime (MPKO) in basic medium, analyte ions are quantitatively extracted to the phase rich in Triton X-114 following centrifugation. 1.0 mol L(-1) HNO(3) nitric acid in methanol was added to the surfactant-rich phase prior to its analysis by flame atomic absorption spectrometry (FAAS). The adopted concentrations for MPKO, Triton X-114 and HNO(3), bath temperature, centrifuge rate and time were optimized. Detection limits (3 SDb/m) of 1.6, 2.1 and 1.9 ng mL(-1) for Cu(2+), Co(2+) and Ni(2+) along with preconcentration factors of 30 and for these ions and enrichment factor of 65, 58 and 67 for Cu(2+), Ni(2+) and Co(2+), respectively. The high efficiency of cloud point extraction to carry out the determination of analytes in complex matrices was demonstrated. The proposed procedure was applied to the analysis of biological, natural and wastewater, soil and blood samples.

  7. Cloud point extraction for the determination of copper, nickel and cobalt ions in environmental samples by flame atomic absorption spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Ghaedi, M. [Chemistry Department, University of Yasouj, Yasouj 75914-353 (Iran, Islamic Republic of)], E-mail: m_ghaedi@mail.yu.ac.ir; Shokrollahi, A.; Ahmadi, F.; Rajabi, H.R. [Chemistry Department, University of Yasouj, Yasouj 75914-353 (Iran, Islamic Republic of); Soylak, M. [Chemistry Department, University of Erciyes, 38039 Kayseri (Turkey)

    2008-02-11

    A cloud point extraction procedure was presented for the preconcentration of copper, nickel and cobalt ions in various samples. After complexation with methyl-2-pyridylketone oxime (MPKO) in basic medium, analyte ions are quantitatively extracted to the phase rich in Triton X-114 following centrifugation. 1.0 mol L{sup -1} HNO{sub 3} nitric acid in methanol was added to the surfactant-rich phase prior to its analysis by flame atomic absorption spectrometry (FAAS). The adopted concentrations for MPKO, Triton X-114 and HNO{sub 3}, bath temperature, centrifuge rate and time were optimized. Detection limits (3 SDb/m) of 1.6, 2.1 and 1.9 ng mL{sup -1} for Cu{sup 2+}, Co{sup 2+} and Ni{sup 2+} along with preconcentration factors of 30 and for these ions and enrichment factor of 65, 58 and 67 for Cu{sup 2+}, Ni{sup 2+} and Co{sup 2+}, respectively. The high efficiency of cloud point extraction to carry out the determination of analytes in complex matrices was demonstrated. The proposed procedure was applied to the analysis of biological, natural and wastewater, soil and blood samples.

  8. Non-noble metal graphene oxide-copper (II) ions hybrid electrodes for electrocatalytic hydrogen evolution reaction

    KAUST Repository

    Muralikrishna, S.

    2015-08-25

    Non-noble metal and inexpensive graphene oxide-copper (II) ions (GO-Cu2+) hybrid catalysts have been explored for the hydrogen evolution reaction (HER). We were able to tune the binding abilities of GO toward the Cu2+ ions and hence their catalytic properties by altering the pH. We have utilized the oxygen functional moieties such as carboxylate, epoxide, and hydroxyl groups on the edge and basal planes of the GO for binding the Cu2+ ions through dative bonds. The GO-Cu2+ hybrid materials were characterized by cyclic voltammetry in sodium acetate buffer solution. The morphology of the hybrid GO-Cu2+ was characterized by atomic force microscopy. The GO-Cu2+ hybrid electrodes show good electrocatalytic activity for HER with low overpotential in acidic solution. The Tafel slope for the GO-Cu2+ hybrid electrode implies that the primary discharge step is the rate determining step and HER proceed with Volmer step. © 2015 American Institute of Chemical Engineers Environ Prog.

  9. REMOVAL OF COPPER IONS USING ALIQUAT 336/TBP BASED SUPPORTED LIQUID MEMBRANE

    Directory of Open Access Journals (Sweden)

    Baghdad Medjahed

    2014-03-01

    Full Text Available The sorption of copper (II present in an aqueous media using a supported liquid membrane (SLM by chloride tri-N-octylmethylammonium (Aliquat 336 and Tri-n-butylphosphate (TBP from molar ratio 1:1, with polytetrafluoroethylene (PTFE as a membrane support was studied. The effects of various parameters as initial pH, KSCN concentration and ammonium acetate concentration on the extraction yield were carried out. By a calculation program using CHEAQS V. L20.1, the determination of the percentages of the present species before and after extraction were given, in aqueous medium and on the membrane to be able to determine the relation between the nature of the extracted species and the extraction yield. The 23 factorial design achieve the best conditions of recovery procedure. The recovery of copper (II is almost quantitative (94 %, in one step.

  10. Simultaneous spectrophotometric determination of trace copper, nickel, and cobalt ions in water samples using solid phase extraction coupled with partial least squares approaches

    Science.gov (United States)

    Guo, Yugao; Zhao, He; Han, Yelin; Liu, Xia; Guan, Shan; Zhang, Qingyin; Bian, Xihui

    2017-02-01

    A simultaneous spectrophotometric determination method for trace heavy metal ions based on solid-phase extraction coupled with partial least squares approaches was developed. In the proposed method, trace metal ions in aqueous samples were adsorbed by cation exchange fibers and desorbed by acidic solution from the fibers. After the ion preconcentration process, the enriched solution was detected by ultraviolet and visible spectrophotometer (UV-Vis). Then, the concentration of heavy metal ions were quantified by analyzing ultraviolet and visible spectrum with the help of partial least squares (PLS) approaches. Under the optimal conditions of operation time, flow rate and detection parameters, the overlapped absorption peaks of mixed ions were obtained. The experimental data showed that the concentration, which can be calculated through chemometrics method, of each metal ion increased significantly. The heavy metal ions can be enriched more than 80-fold. The limits of detection (LOD) for the target analytes of copper ions (Cu2 +), cobalt ions (Co2 +) and nickel ions (Ni2 +) mixture was 0.10 μg L- 1, 0.15 μg L- 1 and 0.13 μg L- 1, respectively. The relative standard deviations (RSD) were less than 5%. The performance of the solid-phase extraction can enrich the ions efficiently and the combined method of spectrophotometric detection and PLS can evaluate the ions concentration accurately. The work proposed here is an interesting and promising attempt for the trace ions determination in water samples and will have much more applied field.

  11. Removal of copper (II), iron (III) and lead (II) ions from Mono ...

    African Journals Online (AJOL)

    EJIRO

    The adsorption of Pb (II) was found to be maximum (94%±3.2) at pH 5, temperature of 100°C, metal ion concentration of ... Key words: Metal ions, adsorption, simulated effluent, coconut husk. INTRODUCTION ..... activated carbon and zeolite.

  12. A Room Temperature Nitric Oxide Gas Sensor Based on a Copper-Ion-Doped Polyaniline/Tungsten Oxide Nanocomposite

    Science.gov (United States)

    Wang, Shih-Han; Shen, Chi-Yen; Su, Jian-Ming; Chang, Shiang-Wen

    2015-01-01

    The parts-per-billion-level nitric oxide (NO) gas sensing capability of a copper-ion-doped polyaniline/tungsten oxide nanocomposite (Cu2+/PANI/WO3) film coated on a Rayleigh surface acoustic wave device was investigated. The sensor developed in this study was sensitive to NO gas at room temperature in dry nitrogen. The surface morphology, dopant distribution, and electric properties were characterized using scanning electron microscopy, energy-dispersive X-ray spectroscopy mapping, and Hall effect measurements, respectively. The Cu2+/PANI/WO3 film exhibited high NO gas sensitivity and selectivity as well as long-term stability. At 1 ppb of NO, a signal with a frequency shift of 4.3 ppm and a signal-to-noise ratio of 17 was observed. The sensor exhibited distinct selectivity toward NO gas with no substantial response to O2, NH3 and CO2 gases. PMID:25811223

  13. Highly sensitive detection of copper ions by densely grafting fluorescein inside polyethyleneimine core-silica shell nanoparticles.

    Science.gov (United States)

    Qiao, Yali; Zheng, Xingwang

    2015-12-21

    In this work, polyethyleneimine (PEI) core-silica shell nanoparticles were synthesized and used for densely grafting fluorescent receptor units inside the core of these particles to result in multi-receptor units collectively sensing a target. Herein, copper ion quenching of the fluorescence intensity of a fluorescein isothiocyanate (FITC) system was selected as a model to confirm our proof-of-concept strategy. Our results showed that, compared to free FITC in solution, a 10-fold enhancement of the Stern-Volmer constant value for Cu(2+) quenching of the fluorescence intensity of the grafted state of FITC in PEI core-silica shell nanoparticles was achieved. Furthermore, compared to a previous collective sensing scheme by densely grafting fluorescent receptor units on a silica nanoparticle surface, the proposed scheme, which grafted fluorescent receptor units inside a polymer nano-core, was simple, highly efficient and presented higher sensitivity.

  14. A Room Temperature Nitric Oxide Gas Sensor Based on a Copper-Ion-Doped Polyaniline/Tungsten Oxide Nanocomposite

    Directory of Open Access Journals (Sweden)

    Shih-Han Wang

    2015-03-01

    Full Text Available The parts-per-billion-level nitric oxide (NO gas sensing capability of a copper-ion-doped polyaniline/tungsten oxide nanocomposite (Cu2+/PANI/WO3 film coated on a Rayleigh surface acoustic wave device was investigated. The sensor developed in this study was sensitive to NO gas at room temperature in dry nitrogen. The surface morphology, dopant distribution, and electric properties were characterized using scanning electron microscopy, energy-dispersive X-ray spectroscopy mapping, and Hall effect measurements, respectively. The Cu2+/PANI/WO3 film exhibited high NO gas sensitivity and selectivity as well as long-term stability. At 1 ppb of NO, a signal with a frequency shift of 4.3 ppm and a signal-to-noise ratio of 17 was observed. The sensor exhibited distinct selectivity toward NO gas with no substantial response to O2, NH3 and CO2 gases.

  15. A room temperature nitric oxide gas sensor based on a copper-ion-doped polyaniline/tungsten oxide nanocomposite.

    Science.gov (United States)

    Wang, Shih-Han; Shen, Chi-Yen; Su, Jian-Ming; Chang, Shiang-Wen

    2015-03-24

    The parts-per-billion-level nitric oxide (NO) gas sensing capability of a copper-ion-doped polyaniline/tungsten oxide nanocomposite (Cu(2+)/PANI/WO3) film coated on a Rayleigh surface acoustic wave device was investigated. The sensor developed in this study was sensitive to NO gas at room temperature in dry nitrogen. The surface morphology, dopant distribution, and electric properties were characterized using scanning electron microscopy, energy-dispersive X-ray spectroscopy mapping, and Hall effect measurements, respectively. The Cu(2+)/PANI/WO3 film exhibited high NO gas sensitivity and selectivity as well as long-term stability. At 1 ppb of NO, a signal with a frequency shift of 4.3 ppm and a signal-to-noise ratio of 17 was observed. The sensor exhibited distinct selectivity toward NO gas with no substantial response to O2, NH3 and CO2 gases.

  16. New insights into single-compound and binary adsorption of copper and lead ions on a treated sea mango shell: experimental and theoretical studies.

    Science.gov (United States)

    Sellaoui, Lotfi; Edi Soetaredjo, Felycia; Ismadji, Suryadi; Cláudio Lima, Éder; Dotto, Guilherme L; Ben Lamine, Abdelmottaleb; Erto, Alessandro

    2017-09-21

    Herein, adsorption isotherms of Pb(ii) and Cu(ii) ions on treated sea mango fruit in both single-compound and binary systems were experimentally realized at different temperatures in the range of 30-50 °C. Experimental results show that adsorption of Pb(ii) was more as compared to that of Cu(ii) ions; however, for both ions, a significant reduction in the adsorption capacity was observed in the binary system as compared to that in the single-compound systems. Moreover, under all the investigated conditions, adsorption seems to be promoted by an increase in temperature. To understand and interpret the experimental evidences, the Hill and competitive Hill models developed on the basis of the grand canonical ensemble were applied for the analysis of adsorption equilibrium data. These models contain some physicochemical parameters that allow an exhaustive analysis of the dynamics of single-compound and binary adsorptions. Based on the fitting results, in particular, through the evaluation of the number of ions bonded per site (n and ni), it was found that lead and copper ions interacted by inclined and horizontal positions on treated sea mango in single-compound and binary systems, respectively. In addition, based on the same parameters, a significant interaction between ions was retrieved. A study focused on the saturation adsorption capacity in single-compound and binary systems affirmed that the adsorbent was more selective for lead than for copper. The reduction of the adsorbed capacity ratio between the binary and single-compound systems (i.e. Qb/Qs) explained and confirmed that an inhibition effect between copper and lead ions at the same receptor site occurred. Finally, based on the energetic investigations, it was deduced that the adsorption energy represented the dominant factor promoting the greater adsorption of lead than that of copper in both systems.

  17. Adsorption characteristics of copper, lead, zinc and cadmium ions by tourmaline

    Institute of Scientific and Technical Information of China (English)

    JIANG Kan; SUN Tie-heng; SUN Li-na; LI Hai-bo

    2006-01-01

    The adsorption characteristics of heavy metals: Cu(Ⅱ), Pb(Ⅱ), Zn(Ⅱ) and Cd(Ⅱ) ions on tourmaline were studied. Adsorption equilibrium was established. The adsorption isotherms of all the four metal ions followed well Langmuir equation. Tourmaline was found to remove heavy metal ions efficiently fiom aqueous solution with selectivity in the order of Pb(Ⅱ)>Cu(Ⅱ)>Cd(Ⅱ)>Zn(Ⅱ).The adsorption of metal ions by tourmaline increased with the initial concentration of metal ions increasing in the medium.Tourmaline could also increase pH value of metal solution. Themaximum heavy metal ions adsorbed by tourmaline was found to be 78.86, 154.08, 67.25, and 66.67 mg/g for Cu(Ⅱ), Pb(Ⅱ), Zn(Ⅱ) and Cd(Ⅱ), respectively. The temperature (25-55℃) had a small effect on the adsorption capacity of tourmaline. Competitive adsorption of Cu(Ⅱ), Pb(Ⅱ), Zn(Ⅱ) and Cd(Ⅱ) ions was also studied. The adsorption capacity of tourmaline for single metal decreased in the order of Pb>Cu>Zn>Cd and inhibition dominance observed in two metal systems was Pb>Cu, Pb>Zn, Pb>Cd, Cu>Zn, Cu>Cd, and Cd>Zn.

  18. Energy distribution of metal and noble gas ions traversing single-crystal copper films

    Science.gov (United States)

    Isakhanov, Z. A.

    2012-09-01

    A comparative investigation of the energy distribution of ions that traversed single-crystal cooper films reveals that the energy loss of channeled and nonchanneled particles depends not only on the mass but also on the radius of bombarding ions. It is established that the energy spectra of transmitted ions are highly sensitive to a change in the composition and structure of the films. From the change in these spectra, one can estimate the degree of disordering in thin films under various applied forces.

  19. Engineering Short Preorganized Peptide Sequences for Metal Ion Coordination: Copper(II) a Case Study.

    Science.gov (United States)

    Lima, L M P; Iranzo, O

    2016-01-01

    Peptides are multidentate chiral ligands capable of coordinating different metal ions. Nowadays, they can be obtained with high yield and purity, thanks to the advances on peptide/protein chemistry as well as in equipment (peptide synthesizers). Based on the identity and length of their amino acid sequences, peptides can present different degrees of flexibility and folding. Although short peptide sequences (ion coordination. Based on our experience, we present a general scheme for the design, synthesis, and characterization of these peptidic scaffolds and provide protocols for the study of their metal ion coordination properties.

  20. Cadmium Sulphide-Reduced Graphene Oxide-Modified Photoelectrode-Based Photoelectrochemical Sensing Platform for Copper(II Ions.

    Directory of Open Access Journals (Sweden)

    I Ibrahim

    Full Text Available A photoelectrochemical (PEC sensor with excellent sensitivity and detection toward copper (II ions (Cu2+ was developed using a cadmium sulphide-reduced graphene oxide (CdS-rGO nanocomposite on an indium tin oxide (ITO surface, with triethanolamine (TEA used as the sacrificial electron donor. The CdS nanoparticles were initially synthesized via the aerosol-assisted chemical vapor deposition (AACVD method using cadmium acetate and thiourea as the precursors to Cd2+ and S2-, respectively. Graphene oxide (GO was then dip-coated onto the CdS electrode and sintered under an argon gas flow (50 mL/min for the reduction process. The nanostructured CdS was adhered securely to the ITO by a continuous network of rGO that also acted as an avenue to intensify the transfer of electrons from the conduction band of CdS. The photoelectrochemical results indicated that the ITO/CdS-rGO photoelectrode could facilitate broad UV-visible light absorption, which would lead to a higher and steady-state photocurrent response in the presence of TEA in 0.1 M KCl. The photocurrent decreased with an increase in the concentration of Cu2+ ions. The photoelectrode response for Cu2+ ion detection had a linear range of 0.5-120 μM, with a limit of detection (LoD of 16 nM. The proposed PEC sensor displayed ultra-sensitivity and good selectivity toward Cu2+ ion detection.

  1. Technical note: removal of metal ion inhibition encountered during DNA extraction and amplification of copper-preserved archaeological bone using size exclusion chromatography.

    Science.gov (United States)

    Matheson, Carney D; Marion, Travis E; Hayter, Shana; Esau, Neal; Fratpietro, Renee; Vernon, Kim K

    2009-10-01

    A novel technique for the removal of metal ions inhibiting DNA extraction and PCR of archaeological bone extracts is presented using size exclusion chromatography. Two case studies, involving copper inhibition, demonstrate the effective removal of metal ion inhibition. Light microscopy, SEM, elemental analysis, and genetic analysis were used to demonstrate the effective removal of metal ions from samples that previously exhibited molecular inhibition. This research identifies that copper can cause inhibition of DNA polymerase during DNA amplification. The use of size exclusion chromatography as an additional purification step before DNA amplification from degraded bone samples successfully removes metal ions and other inhibitors, for the analysis of archaeological bone. The biochemistry of inhibition is explored through chemical and enzymatic extraction methodology on archaeological material. We demonstrate a simple purification technique that provides a high yield of purified DNA (>95%) that can be used to address most types of inhibition commonly associated with the analysis of degraded archaeological and forensic samples. We present a new opportunity for the molecular analysis of archaeological samples preserved in the presence of metal ions, such as copper, which have previously yielded no DNA results.

  2. Neutron production from 158 GeV/c per nucleon lead ions on thin copper and lead targets in the angular range 30-135 degree

    CERN Document Server

    Silari, Marco; Birattari, C; Foglio-Para, A; Gini, L; Mitaroff, Angela; Ulrici, L

    2002-01-01

    The neutron emission from 5, 10 and 20 mm thick lead and 10 and 20 mm thick copper targets bombarded by a lead ion beam with momentum of 158 GeV/c per nucleon were measured at the CERN Super Proton Synchrotron. The neutron yield and spectral fluence per incident ion on target were measured with an extended range Bonner sphere spectrometer in the angular range 30-135 degree with respect to beam direction. Monte Carlo simulations with the FLUKA code were performed to establish a guess spectrum for the unfolding of the experimental data. The results have shown that, lacking Monte Carlo radiation transport codes dealing with ions with masses larger than 1 amu, a reasonable prediction can be carried out by scaling the result of a Monte Carlo calculation for protons by the projectile mass number to the power of 0.85-0.95 for a lead target and 0.88-1.03 for a copper target.

  3. Ion beam analysis of copper selenide thin films prepared by chemical bath deposition

    Science.gov (United States)

    Andrade, E.; García, V. M.; Nair, P. K.; Nair, M. T. S.; Zavala, E. P.; Huerta, L.; Rocha, M. F.

    2000-03-01

    Analyses of Rutherford back scattered (RBS) 4He+-particle spectra of copper selenide thin films deposited on glass slides by chemical bath were carried out to determine the changes brought about in the thin film by annealing processes. The atomic density per unit area and composition of the films were obtained from these measurements. This analysis shows that annealing in a nitrogen atmosphere at 400°C leads to the conversion of Cu xSe thin film to Cu 2Se. Results of X-ray diffraction, optical, and electrical characteristics on the films are presented to supplement the RBS results.

  4. Effect of copper ions on voltammetric signals of aminopurines at a carbon electrode

    Directory of Open Access Journals (Sweden)

    Frantisek Jelen

    2010-12-01

    Full Text Available Electrochemical oxidations of aminopurines (adenine–Ade, 2–aminopurine, 2AP, 2,6–diaminopurine, 2,6–DAP and theircomplexes with Cu(I on carbon electrodes (pencil–PeGE wereinvestigated by means of linear sweep voltammetry (LSV andelimination voltammetry with linear scan (EVLS. We found thatthe Cu(I–purine complex was formed not only by aminopurines butalso by purine. On the other hand the complex is not formed in thecase of imidazol or cytosine. The results showed that carbonelectrodes in connection with EVLS can be an excellent prototypefor cheap and fast working sensor for aminopurines in the presenceof copper.

  5. Fluorescence Quenching of Pheo-phytin-a by Copper(Ⅱ)Ions

    Institute of Scientific and Technical Information of China (English)

    HU,Mingbo; LI,Huaixiang; CHEN,Lusheng; ZHANG,Huaibin; DONG,Chuan

    2009-01-01

    A method was developed for determination of Cu(Ⅱ)ions quantitatively by measuring fluorescent intensity of pheophytin-a(Pheoa)solution.The Pheoa was obtained by de-intercalation of magnesium from the porphyrin ring of chlorophyll-a(Chla)extracted from fresh spinach leaves.Its two UV-Vis absorption peaks at 505 and 535 am in acetone solution have been observed but disappeared When the acetone solution of Pheoa was mixed with a Cu(Ⅱ)ion aqueous solution.A fluorescence quenching phenomenon was thus observed when the acetone solution of Pheoa was mixed with an aqueous solution of Cu(Ⅱ)ions.However,other physiologically relevant cations rarely caused any quenching fluorescence of Pheoa under the same experimental conditions.Kinetics of the fluorescence fading process Was investigated by measuring the effects of Cu(Ⅱ)ion concentration,reaction time and reaction temperature on the fluorescence intensity of the Pheoa acetone solution.An activation energy of(10±1)kJ·mol-1 was estimated from Arrhenius empirical relation assuming that the interaction between the Pheoa and the Cu(Ⅱ)ions was the first order reaction.The calibration graph obtained with the fluorescence Was linear over the Cu(Ⅱ)concentration range of 8.0×10-5-8.0×10-7 mol·dm-3 with a detection limit of 8.0×10-7 mool·dm-3 for Cu(Ⅱ)ion.

  6. Fabrication of new carbon paste electrodes based on gold nano-particles self-assembled to mercapto compounds as suitable ionophores for potentiometric determination of copper ions

    Directory of Open Access Journals (Sweden)

    Rasoul Pourtaghavi Talemi

    2013-12-01

    Full Text Available In the present study, we investigate the potentiometric behavior of Cu2+ carbon paste electrodes based on two mercapto compounds 2-ethylmino-5-mercapto-1,3,4-thiadiazole (EAMT and 2-acetylamino-5-mercapto-1,3,4-thiadiazole (AAMT self-assembled on gold nano-paricle (GNP as ionophore. Then, the obtained results from the modified electrodes are compared. The self-assembled ionophores exhibit a high selectivity for copper ion (Cu2+, in which the sulfur and nitrogen atoms in their structure play a significant role as the effective coordination donor site for the copper ion. Among these electrodes, the best performance was obtained with the sensor with a EAMT/graphite powder/paraffin oil weight ratio of 4.0/68/28 with 200 µL of GNP which exhibits the working concentration range of 1.6×10−9 to 6.3×10−2 M and a nernstian slope of 28.9±0.4 mVdecade−1 of copper(II activity. The detection limit of electrode was 2.9(±0.2×10−10M and potential response was pH ; in other words, it was independent across the range of 2.8–6.3. The proposed electrode presented very good selectivity and sensitivity towards the Cu2+ ions over a wide variety of cations including alkali, alkaline earth, transition and heavy metal ions. Moreover, the proposed electrode was successfully applied as an indicator electrode in the potentiometric titration of Cu(II ions with EDTA and also the potentiometric determination of copper ions in spiked water samples.

  7. Thermodynamics of the formation of complexes of copper(II) ions and glycylglycine in aqueous solutions at 298 K according to calorimetry data

    Science.gov (United States)

    Kochergina, L. A.; Emel'yanov, A. V.

    2015-04-01

    Heat effects of the interaction between glycylglycine and copper(II) nitrate solutions are measured by direct calorimetry at a [metal] : [ligand] ratio of 1 : 5 and at different pH values of the solution. The measurements are made at a temperature of 298.15 K and ionic strengths of 0.25, 0.50, and 0.75. KNO3 is used as a background electrolyte. The thermodynamic characteristics of complex formation by the peptide and copper(II) ions in aqueous solutions are determined. Standard enthalpies of the formation of complex particles in aqueous solutions are calculated.

  8. [Flotation spectrophotometric determination of copper on isochromatic dye ion pair with crystal violet and bromopnenol blue].

    Science.gov (United States)

    Liu, B; Chen, C; Zuo, B

    1999-02-01

    Bromophenol blue (BPB) was produced and entered into the aqueous phase when NaOH solution of pH = 10 was added to Cu(biq)2BPB by trichloromethane and isoamyl alcohol (20:1) extractive. And then CV x BPB was floated by crystal violet (CV) with benzene solution. The flotation was dissolved in ethanol and the absorbance of the solution measured at 590 nm. The sensitivity was raised because of the two dyes assistant effect. The molar absorptivity was 1.45 x 10(5) L x mol(-1) x cm(-1). Copper in the sample was separated first by extracting the Cu(biq)2BPB complex with trichloromethane and isoamyl alcohol, thus achieving a high selectivity. Beer's law was obeyd in the range of 0-0. 4 mg/L with a relative standard deviation of 3.6%. For 4.8 x 10(-8) g/mL copper solution, the recoveries were 97.8%-101.7%.

  9. ELECTRODEPOSITION OF COPPER IONS ON FIXED BED ELECTRODES: KINETIC AND HYDRODYNAMIC STUDY

    Directory of Open Access Journals (Sweden)

    L.A.M. Ruotolo

    2002-03-01

    Full Text Available The kinetic and hydrodynamic behaviour of a fixed-bed electrochemical reactor was studied in terms of current efficiency (CE and energy efficiency (EE. In the kinetic experiments the effects of fixed bed thickness (L, current density (i and initial concentration of copper (C0 were studied. In the hydrodynamic experiments the permeability (k of the electrode and the coefficient for inertial forces (c were also studied as functions of the applied current density. At low current densities and bed thicknesses greater than 1.0 cm, negative CE and EE were observed as a consequence of the dissolution of the porous matrix. At high current densities low CE and EE were observed and a powdery deposit was formed on the surface of the particles. From the results of the kinetic study bed thickness and the range of current densities employed in the hydrodynamic experiments were chosen. In these experiments the electrodeposition process continued until the whole electrode had been clogged and no more electrolyte could pass through it. The relationship between pressure drop and flow rate was well described by the Forchheimer equation. It was observed that the reduction in porosity due to copper electrodeposition causes the flow rate to decrease because of the decrease in electrode permeability, but it had no influence on current efficiency.

  10. Bioinspired, direct synthesis of aqueous CdSe quantum dots for high-sensitive copper(II) ion detection.

    Science.gov (United States)

    Bu, Xiaohai; Zhou, Yuming; He, Man; Chen, Zhenjie; Zhang, Tao

    2013-11-21

    Luminescent CdSe semiconductor quantum dots (QDs), which are coated with a denatured bovine serum albumin (dBSA) shell, have been directly synthesized via a bioinspired approach. The dBSA coated CdSe QDs are ultrasmall (d CdSe QDs. The luminescent QDs are used for copper(II) ion detection due to their highly sensitive and selective fluorescence quenching response to Cu(2+). The concentration dependence of the quenching effect can be best described by the typical Stern-Volmer equation in a linearly proportional concentration of Cu(2+) ranging from 10 nM to 7.5 μM with a detection limit of 5 nM. As confirmed by various characterization results, a possible quenching mechanism is given: Cu(2+) ions are first reduced to Cu(+) by the dBSA shell and then chemical displacement between Cu(+) and Cd(2+) is performed at the surface of the ultrasmall metallic core to impact the fluorescence performance.

  11. Ion pair formation in copper sulfate aqueous solutions at high temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Mendez De Leo, Lucila P. [Unidad de Actividad Quimica, Comision Nacional de Energia, Avenida del Libertador 8250, 1429 Ciudad de Buenos Aires (Argentina); Escuela de Ciencia y Tecnologia, Universidad Nacional General San Martin, Alem 3901, 1653 Villa Ballester (Argentina); Bianchi, Hugo L. [Unidad de Actividad Quimica, Comision Nacional de Energia, Avenida del Libertador 8250, 1429 Ciudad de Buenos Aires (Argentina); Escuela de Ciencia y Tecnologia, Universidad Nacional General San Martin, Alem 3901, 1653 Villa Ballester (Argentina); Fernandez-Prini, Roberto [Unidad de Actividad Quimica, Comision Nacional de Energia, Avenida del Libertador 8250, 1429 Ciudad de Buenos Aires (Argentina) and INQUIMAE, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pabellon II, 1428 Ciudad de Buenos Aires (Argentina)]. E-mail: rfprini@cnea.gov.ar

    2005-05-15

    Ionic association between Cu{sup 2+}(aq) and SO42-(aq) has been studied in the temperature range (298 to 473) K using a spectrophotometric technique. Experiments were designed to minimize the contribution of other protolytic equilibria in solution. The values of the ionic association equilibrium constant at different temperatures and pressures were fitted to an appropriate equation that allows the calculation of the thermodynamic quantities for states close to the saturation line. Using Bjerrum's model for ionic association evidence for two ion pair populations was obtained. The process of ion pairing is discussed and a possibility to reconcile the continuum model (Bjerrum) with molecular simulation results is suggested.

  12. Sulfated chitosan/PVA absorbent membrane for removal of copper and nickel ions from aqueous solutions-Fabrication and sorption studies.

    Science.gov (United States)

    Abu-Saied, M A; Wycisk, Ryszard; Abbassy, Moustafa M; El-Naim, G Abd; El-Demerdash, F; Youssef, M E; Bassuony, H; Pintauro, Peter N

    2017-06-01

    Novel absorbents for the removal of Cu(2+) and Ni(2+) ions from aqueous solutions were prepared from solution cast sulfated chitosan/polyvinyl alcohol membranes (SCS/PVA) and their properties were investigated. FTIR, SEM, XRD and TGA analyses were used to determine membrane structure. The effect of environmental parameters on absorption was studied, including pH, contact time, temperature and the initial concentration of Ni(2+) and Cu(2+) ions. Freundlich and Langmuir absorption isotherms were fitted to experimental data and a pseudo-second order rate equation was employed to model the kinetics of uptake for several copper and nickel ion concentrations. The results indicate that the affinity of an SCS/PVA membrane for Cu(2+) ions was higher than that for Ni(2+) ions. The study demonstrated that the SCS/PVA system can be utilized as highly efficient sorbents, to extract Ni(2+) and Cu(2+) from aqueous feed solutions.

  13. Modelling the effects of copper on soil organisms and processes using the free ion approach: towards a multi-species toxicity model.

    Science.gov (United States)

    Lofts, Stephen; Criel, Peggy; Janssen, Colin R; Lock, Koen; McGrath, Steve P; Oorts, Koen; Rooney, Corinne P; Smolders, Erik; Spurgeon, David J; Svendsen, Claus; Van Eeckhout, Hilde; Zhao, Fang-Zie

    2013-07-01

    The free ion approach has been previously used to calculate critical limit concentrations for soil metals based on point estimates of toxicity. Here, the approach was applied to dose-response data for copper effects on seven biological endpoints in each of 19 European soils. The approach was applied using the concept of an effective dose, comprising a function of the concentrations of free copper and 'protective' major cations, including H(+). A significant influence of H(+) on the toxicity of Cu(2+) was found, while the effects of other cations were inconsistent. The model could be generalised by forcing the effect of H(+) and the slope of the dose-response relationship to be equal for all endpoints. This suggests the possibility of a general bioavailability model for copper effects on organisms. Furthermore, the possibility of such a model could be explored for other cationic metals such as nickel, zinc, cadmium and lead.

  14. Preparation and copper ions adsorption properties of thiosemicarbazide chitosan from squid pens.

    Science.gov (United States)

    Lin, Yue-Cheng; Wang, Hong-Peng; Gohar, Faryal; Ullah, Muhammad Haseeb; Zhang, Xiang; Xie, Dong-Fang; Fang, Hui; Huang, Jun; Yang, Jun-Xing

    2017-02-01

    Chitosan was prepared by alkaline N-deacetylation of β-chitin from squid pens. Thiosemicarbazide group was introduced to chitosan via formaldehyde-derived linkages, and thiosemicarbazide chitosan (TSFCS) with different degrees of substitution (DS) was synthesized. The DS values of TSFCS calculated by elemental analysis were 0.19, 0.36 and 0.63. The structure of the TSFCS was confirmed by elemental analysis, FTIR, XRD, TGA and SEM. The adsorption capacity of Cu(II) ions by TSFCS showed good correlation with the DS and pH (pH range 2.2-5.8). The maximum Cu(II) ions adsorption capacity of all three TSFCS samples reached 134.0mgg(-1) at pH 3.6, but chitosan showed no adsorption at this pH. The adsorption equilibrium process of Cu(II) ions onto TSFCS was better described by the Langmuir model than the Freundlich isotherm model. Cu(II) ions adsorbed by TSFCS could be released using 0.01M Na2EDTA and the adsorption capacity could retain above 80% after five adsorption-desorption cycles. TSFCS exhibited good potential for heavy metal removal because of its high adsorption capacity at the low pH.

  15. Antioxidant properties of carnosine re-evaluated with oxidizing systems involving iron and copper ions.

    Science.gov (United States)

    Mozdzan, Monika; Szemraj, Janusz; Rysz, Jacek; Nowak, Dariusz

    2005-05-01

    Carnosine has antioxidant properties and is efficient in the treatment of chemically-induced inflammatory lesions in animals. However, some studies question its biological significance as antioxidant and show lack of protection and even pro-oxidant effect of carnosine in systems containing nickel and iron ions. The ability of carnosine to: (1) reduce Fe(3+) into Fe(2+) ions; (2) protect deoxyribose from oxidation by Fe(2+)-, Fe(3+)-, and Cu(2+)-H(2)O(2)-EDTA systems; (3) protect DNA from damage caused by Cu(2+)-, and Fe(2+)-H(2)O(2)-ascorbate systems; (4) inhibit HClO- and H(2)O(2)-peroxidase-induced luminol dependent chemiluminescence was tested in vitro. At concentration 10 mM carnosine reduced 16.6+/-0.5 nmoles of Fe(3+) into Fe(2+) ions during 20 min. incubation and added to plasma significantly increased its ferric reducing ability. Inhibition of deoxyribose oxidation by 10 mM carnosine reached 56+/-5, 40+/-11 and 30+/-11% for systems containing Fe(2+), Fe(3+) and Cu(2+) ions, respectively. The damage to DNA was decreased by 84+/-9 and 61+/-14% when Cu(2+)-, and Fe(2+)-H(2)O(2)-ascorbate systems were applied. Combination of 10 mM histidine with alanine or histidine alone (but not alanine) enhanced 1.3 and 2.3 times (Peffect on DNA. Carnosine at 10 and 20 mM decreased by more than 90% light emission from both chemiluminescent systems. It is concluded that carnosine has significant antioxidant activity especially in the presence of transition metal ions. However, hydrolysis of carnosine with subsequent histidine release may be responsible for some pro-oxidant effects.

  16. The formation of copper sulphide semiconductors inside Langmuir–Blodgett films of Cu(II) ion complexes

    NARCIS (Netherlands)

    Werkman, P.J.; Wieringa, R.H.; Schouten, A.J.

    1998-01-01

    The fabrication of layers of copper sulphide within multilayers of copper complexes of the amphiphile 4-(10,12-pentacosadiynamido methyl pyridine, by diffusion of H2S into the multilayers, was studied by UV–VIS spectroscopy. XPS measurements revealed that copper sulphides can be synthesised which di

  17. H4octapa: highly stable complexation of lanthanide(III) ions and copper(II).

    Science.gov (United States)

    Kálmán, Ferenc Krisztián; Végh, Andrea; Regueiro-Figueroa, Martín; Tóth, Éva; Platas-Iglesias, Carlos; Tircsó, Gyula

    2015-03-02

    The acyclic ligand octapa(4-) (H4octapa = 6,6'-((ethane-1,2-diylbis((carboxymethyl)azanediyl))bis(methylene))dipicolinic acid) forms stable complexes with the Ln(3+) ions in aqueous solution. The stability constants determined for the complexes with La(3+), Gd(3+), and Lu(3+) using relaxometric methods are log KLaL = 20.13(7), log KGdL = 20.23(4), and log KLuL = 20.49(5) (I = 0.15 M NaCl). High stability constants were also determined for the complexes formed with divalent metal ions such as Zn(2+) and Cu(2+) (log KZnL = 18.91(3) and log KCuL = 22.08(2)). UV-visible and NMR spectroscopic studies and density functional theory (DFT) calculations point to hexadentate binding of the ligand to Zn(2+) and Cu(2+), the donor atoms of the acetate groups of the ligand remaining uncoordinated. The complexes formed with the Ln(3+) ions are nine-coordinated thanks to the octadentate binding of the ligand and the presence of a coordinated water molecule. The stability constants of the complexes formed with the Ln(3+) ions do not change significantly across the lanthanide series. A DFT investigation shows that this is the result of a subtle balance between the increased binding energies across the 4f period, which contribute to an increasing complex stability, and the parallel increase of the absolute values of the hydration free energies of the Ln(3+) ions. In the case of the [Ln(octapa)(H2O)](-) complexes the interaction between the amine nitrogen atoms of the ligand and the Ln(3+) ions is weakened along the lanthanide series, and therefore the increased electrostatic interaction does not overcome the increasing hydration energies. A detailed kinetic study of the dissociation of the [Gd(octapa)(H2O)](-) complex in the presence of Cu(2+) shows that the metal-assisted pathway is the main responsible for complex dissociation at pH 7.4 and physiological [Cu(2+)] concentration (1 μM).

  18. Effects of ion beam treatment on atomic and macroscopic adhesion of copper to different polymer materials

    Science.gov (United States)

    Zaporojtchenko, V.; Zekonyte, J.; Faupel, F.

    2007-12-01

    Low-energy ion irradiation of polymer induces different phenomena in the near surface layer, which effect strongly the metal-polymer interface formation and promotes adhesion of polymers to metals. Low-energy argon and oxygen ion beams were used to alter the chemical and physical properties of different polymers (PS (polystyrene), PαMS (poly(α-methylstyrene), BPA-PC (bisphenol-A-polycarbonate) and PMMA (poly(methyl methacrylate)), in order to understand the adhesion phenomena between a deposited Cu layer and the polymers. The resulting changes were investigated by various techniques including X-ray photoelectron spectroscopy, measurements of the metal condensation coefficient and a new technique to measure cross-linking at the polymer surface. Two types of practical adhesion strengths of Cu-polymer systems, measured using 90° peel tests, were observed: (i) peel strength increased at low ion fluences, reached a maximum and then decreased after prolonged treatment and (ii) no improvement in the peel strength on treated polymer surfaces was recorded. The improvement in the metal-polymer adhesion in the ion fluence range of 10 13-10 15 cm -2 is attributed to the creation of a large density of new adsorption sites resulting in a larger contact area and incorporation of chemically active groups that lead to increased interaction between metal and polymer by metal-oxygen-polymer species formation. XPS analysis of peeled-off surfaces showed that in most cases the failure location changed from interfacial for untreated polymers to cohesive failure in the polymer for treated surfaces. These observations and measurements of the metal condensation coefficients suggest that bonding is improved at the metal-polymer interface for all metal-polymer systems. However, the decrease in the peel strength at high ion fluences is attributed to the formation of a weak boundary layer in polymers. The correlation between sputter rate of polymers and altering in the peel strength for

  19. 氯化银浊度法测定铜电解液中氯离子%Determination of Chlorine Ion in Copper Electrolyte Using Chloride Turbidimetric Method

    Institute of Scientific and Technical Information of China (English)

    巫来富

    2012-01-01

    在丙酮存在的条件下,铜电解液中的氯离子与硝酸银反应,形成氯化银乳浊液,用铜电解液的原液(即实验中铜电解液原液没有加硝酸银的试液)作参比,于分光光度计500nm处测定其吸光度,从而得出铜电解液中氯离子的含量.%In the condition of Acetone existence,Chloride ion in Copper electrolyte reacted with Silver nitrate,forming the Silver Chloride emulsion.And then we used the initial copper electrolyte solution(i.e.,copper electrolyte solution without the addition of silver nitrate solution) as reference to determine its absorbance at 500nm in spectrophotometer.Finally,we got the content of Chloride ion in Copper electrolyte.

  20. Detection and investigation of the molecular nature of low-molecular-mass copper ions in isolated rheumatoid knee-joint synovial fluid.

    Science.gov (United States)

    Naughton, D P; Knappitt, J; Fairburn, K; Gaffney, K; Blake, D R; Grootveld, M

    1995-03-20

    Low-molecular-mass copper(II) species have been detected and quantified in ultrafiltrates (n = 7) of rheumatoid synovial fluid (SF) by a highly-sensitive HPLC-based assay system with the ability to determine Cu(II) concentrations of ultrafiltrates resulted in complexation by histidine > alanine > formate > threonine > lactate > tyrosine > phenylalanine, their effectiveness in this context being in the given order. CD spectra of Cu(II)-treated samples of intact SF exhibited absorption bands typical of copper(II)-albumin complexes, in addition to a band attributable to a low-molecular-mass histidinate complex (lambda min 610 nm). Since both albumin and histidine are potent radical scavengers, these results indicate that any .OH radical generated from bound copper ions will be 'site-specifically' scavenged. Hence, low-molecular-mass copper complexes with the ability to promote the generation of .OH radical which can then escape from the metal ion co-ordination sphere (and in turn, cause damage to critical biomolecules) appear to be absent from inflammatory SF.

  1. Immobilization of Trichosporon cutaneum R 57 Cells onto Methylcellulose/SiO2 Hybrids and Biosorption of Cadmium and Copper Ions

    Directory of Open Access Journals (Sweden)

    Georgieva N.

    2009-12-01

    Full Text Available Methylcellulose/Silica (MC/SiO2 hybrids were synthesized via poly step sol-gel method. SiO2 was included into the hybrids from two silica precursors - methyltriethoxysilane (MTES and ethyltrimethoxysilane (ETMS with different quantity of organic part-5, 20 and 50 wt.%. The filamentous yeasts Trichosporon cutaneum strain R 57 was immobilized onto the synthesized MC/SiO2 hybrids. After immobilization the hybrid materials were used in the processes of sorption of cadmium and copper ions. The obtained results of protein content analysis indicated that the amount of protein increased with increasing of MC in the hybrids. It was established that the maximal efficiency of copper and cadmium removal were observed for hybrid materials containing MTES and 50 wt.% MC - 66% and 26% respectively. For ETMS and 50 wt.% MC a high value of copper removal was 56% and for cadmium - 45% removal, respectively. FTIR analysis of free and immobilized cells with metal ions was conducted. SEM images showed successful immobilization of the yeasts cells. Second order model was employed in order to investigate the kinetics of copper and cadmium biosorption.

  2. Synergistic inhibition effect of benzotriazole (BTA) and oxalate ions on the corrosion of copper, zinc and brass in NaCl and HCl solutions

    Energy Technology Data Exchange (ETDEWEB)

    Yanardag, T.; Aksut, A.A. [Ankara Univ., Science Faculty, Dept. of Chemistry, Ankara (Turkey)

    2009-07-01

    Inhibition of corrosion is of high technological importance and progress made in this field has been phenomenal in recent years. Zinc is more active compared to copper. Copper is a valuable material, especially in electronics, solar cell fittings, household products, structural engineering, art and decoration, coinage and biomedical application. Even though copper is corrosion resistant due to its natural oxide film, it is prone to corrode in solutions that contain oxygen and high concentration of chloride, sulphate, sulphide and nitrate ions. A variety of potentially damaging environments require versatile inhibition actions. Although an inhibitor is sometimes added to avoid tarnishing, in the majority of cases the inhibitor's purpose is to prevent or postpone corrosion attack. The corrosion inhibition of copper, zinc and brass in 0.5 M NaCl and 0.5 M HCl solutions in the presence of BTA and sodium oxalate have been investigated using polarization, AC-impedance and current-potential methods. Inhibition effect depends to the pretreatment of electrode. For this reason, the electrodes were pretreated in 0.15 M HCl solution for 20 seconds in order to obtain better surface prone to form coatings on the electrode surface before immersing into the studied solutions. Results showed BTA and oxalate to have synergistic inhibition effect on the corrosion of copper and brass. All the methods employed showed good correlation between each other revealing a mean efficiency of 99% in neutral medium and 88% in acidic medium for brass. (authors)

  3. Surface reaction of Bacillus cereus biomass and its biosorption for lead and copper ions

    Institute of Scientific and Technical Information of China (English)

    PAN Jian-hua; LIU Rui-xia; TANG Hong-xiao

    2007-01-01

    In this study, the Fourier transform infrared (FTIR) analytical technique identified the surface chemical functional groups of Bacillus cereus biomass. B. Cereus cells mainly contained carboxyl, hydroxyl, phosphate, amino, and amide functional groups. In order to explain the surface acid-base properties of aqueous B. Cereus biomass, the potentiometric titration was conducted . The computer program FITEQL 4.0 was used to perform the model calculations. The optimization results indicated that three sites-three pKas model, which assumed the cell surface to have three distinct types of surface organic functional groups based on IR analysis results, simulated the experimental results very well. Moreover, batch adsorption experiments were performed to investigate biosorption behavior of Cu (Ⅱ) and Pb (Ⅱ) ions onto the biomass. Obviously, the adsorption equilibrium data for the two ions were reasonably described by typical Langmuir isotherm.

  4. A novel method for thermodynamic study on binding of copper ion with Alzheimer's amyliod β peptide

    Institute of Scientific and Technical Information of China (English)

    BEHBEHANI G. Rezaei

    2009-01-01

    The interaction of Cu2+ with the first 16 residues of the Alzheimer's amyliod β peptide, Afl(1-16), was studied by employing isothermal titration calorimetry at pH 7.2 and 37℃ in aqueous solution. The Gholamreza Rezaei Behbehani (GRB) solvation model was used to reproduce the enthalpies of Cu2++Aβ(1-16) interaction over the whole Cu++concentrations. The binding parameters recovered from the solvation model were attributed to the structural change of Aβ(1-16) due to the metal ion interaction. It was found that there is a set of two identical and non interacting binding sites for Cu2+ ions. The molar enthalpy of binding is △H=27.895 kJ/mol. The association binding constants are 1.895 μM-1 and 1.891 μM-1 for the first and second binding sites respectively.

  5. Oxidative degradation of propachlor by ferrous and copper ion activated persulfate.

    Science.gov (United States)

    Liu, C S; Shih, K; Sun, C X; Wang, F

    2012-02-01

    The process of in situ chemical oxidation (ISCO) by persulfate (S(2)O(8)(2-)) can be accelerated by metal ion activation, which more effectively degrades subsurface pollutants by enhancing sulfate radical (SO(4)(-)) generation. This study compared the results of propachlor degradation by Cu(2+) and Fe(2+) activated persulfate and revealed differing degradation kinetics and mechanisms between the two types of activation system. The activation of persulfate by Fe(2+) ions generally resulted in rapid degradation in the early stage, but was accompanied by a dramatic decrease in efficiency due to the rapid depletion of Fe(2+) by the sulfate radicals generated. In contrast, the Cu(2+) activated persulfate had a longer lasting degradation effect and a proportionally greater degradation enhancement at elevated Cu(2+) concentrations. An optimal Fe(2+) concentration should be sought to activate the persulfate, as a high Fe(2+) concentration of 2.5mM or above, as was used in this study, may inhibit propachlor degradation due to the competitive consumption of sulfate radicals by the excess Fe(2+) ions. Higher temperatures (55°C compared with 30°C) resulted in enhanced metal activation, particularly with the Cu(2+) activated system. Furthermore, acidic conditions were found to be more favorable for propachlor degradation by metal activated persulfate. The ecotoxicity of degraded propachlor samples, which was indicated by average well color development (AWCD) for its microbial community activity, was confirmed to be decreased during the degradation processes with these two ions activated persulfate. Copyright © 2011 Elsevier B.V. All rights reserved.

  6. The structure and phase composition of the surface layer of the samples during the processing of VT-10 titanium alloys by copper ions

    Science.gov (United States)

    Kalashnikov, Mark P.; Fedorischeva, Marina V.; Nikonenko, Alisa V.; Bozhko, Irina A.; Sergeev, Victor P.

    2016-11-01

    The phase composition, structure and morphology of the surface of VT-10 titanium modified by copper ions have been investigated by X-ray, SEM and TEM. It has been established that there are intermetallide phases of Cu-Ti equilibrium diagram in the surface layer during the treatment of VT-10 titanium by copper ions. The modified surface layer in the cross section is divided into two layers: up to 1 µm in thickness and from 1µm up to 4.5-5.0 µm, depending on the treatment time. Two-level micro and nanoporous nanocrystalline structure was formed in the modified layer. It was found that the phase structure and the morphology of the surface layers of VT-10 alloys depend on the treatment time.

  7. Sputtering of copper atoms by keV atomic and molecular ions A comparison of experiment with analytical and computer based models

    CERN Document Server

    Gillen, D R; Goelich,

    2002-01-01

    Non-resonant multiphoton ionisation combined with quadrupole and time-of-flight analysis has been used to measure energy distributions of sputtered copper atoms. The sputtering of a polycrystalline copper target by 3.6 keV Ar sup + , N sup + and CF sub 2 sup + and 1.8 keV N sup + and CF sub 2 sup + ion bombardment at 45 deg. has been investigated. The linear collision model in the isotropic limit fails to describe the high energy tail of the energy distributions. However the TRIM.SP computer simulation has been shown to provide a good description. The results indicate that an accurate description of sputtering by low energy, molecular ions requires the use of computer simulation rather than analytical approaches. This is particularly important when considering plasma-surface interactions in plasma etching and deposition systems.

  8. EPR study of complex formation between copper (II) ions and sympathomimetic amines in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Preoteasa, E.A. [Inst. of Atomic Physics, IFIN, Bucharest (Romania); Duliu, O.G.; Grecu, V.V. [Bucharest, Univ. (Romania). Dept. of Atomic and Nuclear Physics

    1997-07-01

    The complex formation between sympathomimetic amines (SA): adrenaline (AD), noradrenaline (NA), dopamine (DA), ephedrine (ED) and p-tyramine (pTA), and Cu(II) ion in aqueous solution has been studied by X-band EPR at room temperature. Excepting pTA, all investigated SA yielded two types of complexes in different pH domains. All complexes consistent with a ligand fields having a distorted octahedral symmetry, i.e., hexacoordination of Cu(II). The covalence coefficient calculated from the isotropic g and A values has shown strong ionic sigma-type ligand bonds. A structural model with the Cu(II) ion bound by four catecholic O(hydroxy) atoms for the low pH complexes of AD, NA and DA is proposed. For the high pH complexes of the former compounds as well as for both Ed complexes, the authors suppose Cu(II) bound by two N (amino) and two O (hydroxy) atoms. The spectra are consistent to water binding on the longitudinal octahedron axis in all compounds excepting the high pH complex of Ed, where OH2- ions are bound. Possible implications for the SA-cell receptors interactions are discussed.

  9. Characterisation and Optical Studies of Copper Oxide Nanostructures Doped with Lanthanum Ions

    Directory of Open Access Journals (Sweden)

    Varughese G.

    2014-12-01

    Full Text Available Copper Oxide is an extensively studied group II-VI semiconductor with optical properties. It exhibits a wide variety of morphologies in the nano regime that can be grown by tuning the growth habit of the CuO crystal. CuO nano materials with an average particle size of 15-27 nm are synthesized by chemical route. XRD, SEM, FTIR UV-Vis and EDS characterize the samples. The percentage of doping material is confirmed from the EDS spectra. The average crystal size of the prepared CuO: La nanopowder is determined by XRD. The UV absorption spectra revealed the absorption edge at wavelength 389 nm indicating the smaller size of CuO:La nano particle. The optical direct band gap energy of doped CuO nanoparticle is found to be in the range 3.149 eV. The increasing red shift with decreasing particle size suggests that the defects responsible for the intra gap states are primarily surface defect. The La doped CuO is highly effective and can significantly enhance the photo catalytic degradation.

  10. Removal of copper (II) from aqueous solutions by flotation using polyaluminum chloride silicate (PAX-XL60 S) as coagulant and carbonate ion as activator.

    Science.gov (United States)

    Ghazy, S E; Mahmoud, I A; Ragab, A H

    2006-01-01

    Flotation is a separation technology for removing toxic heavy metal ions from aqueous solutions. Here a simple and rapid flotation procedure is presented for the removal of copper(II) from aqueous solutions. It is based on the use of polyaluminum chloride silicate (PAX-XL60 S) as coagulant and flocculent, carbonate ion as activator and oleic acid (HOL) as surfactant. Both ion and precipitate flotation are included depending on the solution pH. Ion and precipitate flotation in the aqueous HOL-PAX-XL60 S-Cu2+-CO3(2-) system gave powerful preferential removal of Cu2+ (F -100%) over the HOL-PAX-XL60 S-Cu2+ system containing no CO3(2+) ion (F approximately 86%). The role of CO3(2-) ion is also evident from decreasing the dose of PAX-XL60 S from 700 mg l(-1) to 200 mg l(-1). The other parameters, influencing the flotation process, namely: metal ion, surfactant and PAX-XL60 S concentrations, ionic strength, temperature and foreign ions were examined. Moreover, the procedure was successfully applied to recover Cu2+ ions from different volumes up to 11 and from natural water samples.

  11. Copper ion-mediated liposomal encapsulation of mitoxantrone: the role of anions in drug loading, retention and release.

    Science.gov (United States)

    Li, Chunlei; Cui, Jingxia; Li, Yingui; Wang, Caixia; Li, Yanhui; Zhang, Lan; Zhang, Li; Guo, Wenmin; Wang, Jinxu; Zhang, Hongwu; Hao, Yanli; Wang, Yongli

    2008-08-01

    Besides pH gradient, other transmembrane gradients such as metal ion gradient could be also employed to load drugs into liposomes. In pH gradient method, anions have an important role since they could form specific aggregates with drugs, and then affect drug release kinetics from vesicles. To explore the role of anions in metal ion gradient method, copper ion-mediated mitoxantrone (MIT) loading was investigated systematically. When empty liposomes exhibiting a transmembrane copper ion gradient (300 mM) were mixed with MIT in a molar ratio of 0.2:1, after 5 min incubation at 60 degrees C, >95% MIT could be loaded into vesicles and the encapsulation was stable, regardless of the kinds of anions and initial intraliposomal pH values. The encapsulation ratio decreased with increased MIT/lipid molar ratio. But even when the molar ratio increased to 0.4, >90% encapsulation could still be achieved. In the presence of nigericin and ammonium, the drug loading profiles were affected to different degree with respect to both drug loading rate and encapsulation ratio. Relative to CuSO(4)-containing systems, CuCl(2) mediated MIT loading was unstable. Both nigericin and ammonium could alter the absorption spectra of liposomal MITs loaded with CuSO(4) gradient. In vitro release studies were performed in glucose/histidine buffer and in 50% human plasma using a dialysis method. In both of release media, CuCl(2)-containing vesicles displayed rapid release kinetics in comparison with CuSO(4) systems; and during the experiment period, MIT was lost from the vesicles continuously. When the formulations were injected into BDF1 mice at a dose of 4 mg/kg, all the liposomal formulations exhibited enhanced blood circulation time, with half-life values of 6.8-7.2h, significantly compared to the rapid clearance of free-MIT. In L1210 ascitic model, CuCl(2) formulation was more therapeutically active than CuSO(4) formulation. At a dose of 6 mg/kg, the treatment with CuCl(2) formulation resulted in

  12. Binding of transition metal ions [cobalt, copper, nickel and zinc] with furanyl-, thiophenyl-, pyrrolyl-, salicylyl- and pyridyl-derived cephalexins as potent antibacterial agents.

    Science.gov (United States)

    Chohan, Zahid H; Pervez, Humayun; Khan, Khalid Mohammed; Rauf, A; Supuran, Claudiu T

    2004-02-01

    A method is described for the preparation of novel cephalexin-derived furanyl-, thiophenyl-, pyrrolyl-, salicylyl- and pyridyl-containing compounds showing potent antibacterial activity. The binding of these newly synthesized antibacterial agents with metal ions such as cobalt(II), copper(II), nickel(II) and zinc(II) has been studied and their inhibitory properties against various bacterial species such as Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, and Klebsiella pneumoniae are also reported. These results suggest that metal ions to possess an important role in the designing of metal-based antibacterials and that such complexes are more effective against infectious diseases compared to the uncomplexed drugs.

  13. Oxygen and hydrogen peroxide reduction catalyses in neutral aqueous media using copper ion loaded glassy carbon electrode electrolyzed in ammonium carbamate solution

    Energy Technology Data Exchange (ETDEWEB)

    Watanabe, Hiroaki; Yamazaki, Haruhito [Department of Materials Science and Engineering, Graduate School of Engineering, Saitama Institute of Technology, 1690 Fusaiji Fukaya, Saitama 369-0293 (Japan); Wang, Xiuyun [School of Chemical Engineering, University of Science and Technology Liaoning, Anshan, Liaoning, 114051 (China); Uchiyama, Shunichi [Department of Materials Science and Engineering, Graduate School of Engineering, Saitama Institute of Technology, 1690 Fusaiji Fukaya, Saitama 369-0293 (Japan)], E-mail: uchiyama@sit.ac.jp

    2009-01-30

    An aminated glassy carbon electrode (AGCE) can be obtained by the electrode oxidation of glassy carbon electrode in ammonium carbamate solution. In the cyclic voltammetric experiments, the electrode reduction of the dissolved oxygen began from -0.15 V vs. Ag/AgCl in neutral aqueous media when the aminated glassy carbon electrode was used as a working electrode although it began from -0.40 V vs. Ag/AgCl when a polished GCE was used. The nitrogen containing groups introduced by the electrode oxidation of carbamic acid must be related with the acceleration of the electron transfer rate of oxygen. Moreover, the new reduction wave of the dissolved oxygen appeared at +0.15 V vs. Ag/AgCl when copper (II) ion was coordinated to AGCE surface. This reduction potential of oxygen coincided with that of copper (II) ion and this fact suggests that the coordinated copper ion to the aminated carbon surface works as a redox mediator of oxygen. The reduction product of oxygen was monitored by rotating platinum ring - aminated glassy carbon disk electrode, and it was found that most of oxygen was reduced to water in a potential range negative than -0.4 V vs. Ag/AgCl. By using AGCE, it was recognized that the catalytic reduction of hydrogen peroxide was also taken place as well as oxygen reduction.

  14. Polyacrylamide-phytic acid-polydopamine conducting porous hydrogel for rapid detection and removal of copper (II) ions.

    Science.gov (United States)

    Zhao, Zhen; Chen, Hongda; Zhang, Hua; Ma, Lina; Wang, Zhenxin

    2017-05-15

    In this work, a conducting porous polymer hydrogel-based electrochemical sensor has been developed for rapid detection of copper (II) ions (Cu(2+)). The polymer (termed as PAAM/PA/PDA) hydrogel is prepared through multi-interactions of the monomers dopamine (DA), acrylamide (AAM) and phytic acid (PA) under mild ambient conditions: the AAM polymerizes through free-radical polymerization, DA occurs poly coupling reaction, and PA crosslinks polydopamine (PDA) and polyacrylamide (PAAM) by hydrogen bonds. The three dimensional (3D) network nanostructured PAAM/PA/PDA hydrogel not only provides a large surface area for increasing the amount of immobilized molecules/ions, but also exhibits a good conductivity. The PAAM/PA/PDA hydrogel-based electrochemical sensor exhibits a low detection limit (1nmolL(-)(1), S/N=3) and wide linear range (from 1nmolL(-)(1) to 1µmolL(-1)) for Cu(2+) detection in aqueous samples. Furthermore, the Cu(2+) can be sensitively detected by the electrochemical sensor in different sample matrices, indicating that the electrochemical sensor could be used to monitor Cu(2+) with reasonable assay performance in practical samples. The PAAM/PA/PDA hydrogel also exhibits a good capacity to remove Cu(2+)(231.36±4.70mgg(-1)), which is superior to those of other adsorption materials reported in the literature. The facile synthesized PAAM/PA/PDA hydrogel provides a novel and regenerable platform for monitoring and removing Cu(2+) in real samples. Copyright © 2016 Elsevier B.V. All rights reserved.

  15. Copper and Zinc Ions Specifically Promote Nonamyloid Aggregation of the Highly Stable Human γ-D Crystallin.

    Science.gov (United States)

    Quintanar, Liliana; Domínguez-Calva, José A; Serebryany, Eugene; Rivillas-Acevedo, Lina; Haase-Pettingell, Cameron; Amero, Carlos; King, Jonathan A

    2016-01-15

    Cataract is the leading cause of blindness in the world. It results from aggregation of eye lens proteins into high-molecular-weight complexes, causing light scattering and lens opacity. Copper and zinc concentrations in cataractous lens are increased significantly relative to a healthy lens, and a variety of experimental and epidemiological studies implicate metals as potential etiological agents for cataract. The natively monomeric, β-sheet rich human γD (HγD) crystallin is one of the more abundant proteins in the core of the lens. It is also one of the most thermodynamically stable proteins in the human body. Surprisingly, we found that both Cu(II) and Zn(II) ions induced rapid, nonamyloid aggregation of HγD, forming high-molecular-weight light-scattering aggregates. Unlike Zn(II), Cu(II) also substantially decreased the thermal stability of HγD and promoted the formation of disulfide-bridged dimers, suggesting distinct aggregation mechanisms. In both cases, however, metal-induced aggregation depended strongly on temperature and was suppressed by the human lens chaperone αB-crystallin (HαB), implicating partially folded intermediates in the aggregation process. Consistently, distinct site-specific interactions of Cu(II) and Zn(II) ions with the protein and conformational changes in specific hinge regions were identified by nuclear magnetic resonance. This study provides insights into the mechanisms of metal-induced aggregation of one of the more stable proteins in the human body, and it reveals a novel and unexplored bioinorganic facet of cataract disease.

  16. Simple PEG Modification of DNA Aptamer Based on Copper Ion Coordination for Tumor Targeting.

    OpenAIRE

    Takafuji, Yoshimasa; Jo, Jun-ichiro; Tabata, Yasuhiko

    2011-01-01

    A simple modification of a DNA aptamer with poly(ethylene glycol) (PEG) based on metal coordination was developed. N, N-bis(carboxymethyl)-L-lysine (NTA) of a metal chelate residue was chemically introduced to one terminus of PEG. The NTA-introduced PEG (PEG-NTA) chelated Cu(2+) ions form a Cu(2+)-chelated PEG (PEG-Cu). When PEG-Cu was mixed with a DNA aptamer of anti-tumor activity (AS1411) in aqueous solution, a complex of PEG-Cu and AS1411 based on metal coordination was formed. The comple...

  17. Use of Composite Sorbents for the Removal of Copper (II ions from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Rebecca Oyedoyin Adeeyo

    2015-01-01

    Full Text Available Composite adsorbents are synthesized from two or more materials with different chemical and physical properties in order to increase their selectivity and the reusability. Researchers have developed and applied several novel composite materials for enhancing the removal of heavy metal. In this review, extensive list of composites developed via advanced technologies with specified characteristics for the removal of Cu (II ion are discussed. Emphases on their adsorption capacities, reusability, desorption and regeneration with improved mechanical strengths are presented. Conclusively, prospects and other challenges to be checked and addressed in future are outlined.

  18. Determination of trace labile copper in environmental waters by magnetic nanoparticle solid phase extraction and high-performance chelation ion chromatography.

    Science.gov (United States)

    Wei, Z; Sandron, S; Townsend, A T; Nesterenko, P N; Paull, B

    2015-04-01

    Cobalt magnetic nanoparticles surface functionalised with iminodiacetic acid were evaluated as a nano-particulate solid phase extraction absorbent for copper ions (Cu(2+)) from environmental water samples. Using an external magnetic field, the collector nanoparticles could be separated from the aqueous phase, and adsorbed ions simply decomplexed using dilute HNO3. Effects of pH, buffer concentration, sample and sorbent volume, extraction equilibrium time, and interfering ion concentration on extraction efficiency were investigated. Optimal conditions were then applied to the extraction of Cu(2+) ions from natural water samples, prior to their quantitation using high-performance chelation ion chromatography. The limits of detection (LOD) of the combined extraction and chromatographic method were ~0.1 ng ml(-1), based upon a 100-fold preconcentration factor (chromatographic performance; LOD=9.2 ng ml(-1) Cu(2+)), analytical linear range from 20 to 5000 ng mL(-1), and relative standard deviations=4.9% (c=1000 ng ml(-1), n=7). Accuracy and precision of the combined approach was verified using a certified reference standard estuarine water sample (SLEW-2) and comparison of sample determinations with sector field inductively coupled plasma mass spectrometry. Recoveries from the addition of Cu(2+) to impacted estuarine and rain water samples were 103.5% and 108.5%, respectively. Coastal seawater samples, both with and without prior UV irradiation and dissolved organic matter removal were also investigated using the new methodology. The effect of DOM concentration on copper availability was demonstrated.

  19. Mobilization of Copper ions by Flavonoids in Human Peripheral Lymphocytes Leads to Oxidative DNA Breakage: A Structure Activity Study

    Directory of Open Access Journals (Sweden)

    Hussain Arif

    2015-11-01

    Full Text Available Epidemiological studies have linked dietary consumption of plant polyphenols with lower incidence of various cancers. In particular, flavonoids (present in onion, tomato and other plant sources induce apoptosis and cytotoxicity in cancer cells. These can therefore be used as lead compounds for the synthesis of novel anticancer drugs with greater bioavailability. In the present study, we examined the chemical basis of cytotoxicity of flavonoids by studying the structure–activity relationship of myricetin (MN, fisetin (FN, quercetin (QN, kaempferol (KL and galangin (GN. Using single cell alkaline gel electrophoresis (comet assay, we established the relative efficiency of cellular DNA breakage as MN > FN > QN > KL > GN. Also, we determined that the cellular DNA breakage was the result of mobilization of chromatin-bound copper ions and the generation of reactive oxygen species. The relative DNA binding affinity order was further confirmed using molecular docking and thermodynamic studies through the interaction of flavonoids with calf thymus DNA. Our results suggest that novel anti-cancer molecules should have ortho-dihydroxy groups in B-ring and hydroxyl groups at positions 3 and 5 in the A-ring system. Additional hydroxyl groups at other positions further enhance the cellular cytotoxicity of the flavonoids.

  20. Imprint Molding of a Microfluidic Optical Cell on Thermoplastics with Reduced Surface Roughness for the Detection of Copper Ions.

    Science.gov (United States)

    Wu, Jing; Lee, Nae Yoon

    2016-01-01

    Here, we introduce a simple and facile technique for fabricating microfluidic optical cells by utilizing a micropatterned polymer mold, followed by imprinting on thermoplastic substrates. This process has reduced the surface roughness of the microchannel, making it suitable for microscale optical measurements. The micropatterned polymer mold was fabricated by first micromilling on a poly(methylmethacrylate) (PMMA) substrate, and then transferring the micropattern onto an ultraviolet (UV)-curable optical adhesive. After an anti-adhesion treatment of the polymer mold fabricated using the UV-curable optical adhesive, the polymer mold was used repeatedly for imprinting onto various thermoplastics, such as PMMA, polycarbonate (PC), and poly(ethyleneterephthalate) (PET). The roughness values for the PMMA, PC, and PET microchannels were approximately 11.3, 20.3, and 14.2 nm, respectively, as compared to those obtained by micromilling alone, which were 15.9, 76.8, and 207.5 nm, respectively. Using the imprint-molded thermoplastic optical cell, rhodamine B and copper ions were successfully quantified. The reduced roughness of the microchannel surface resulted in improved sensitivity and reduced noise, paving the way for integration of the detection module so as to realize totally integrated microdevices.

  1. Creatinine and urea biosensors based on a novel ammonium ion-selective copper-polyaniline nano-composite.

    Science.gov (United States)

    Zhybak, M; Beni, V; Vagin, M Y; Dempsey, E; Turner, A P F; Korpan, Y

    2016-03-15

    The use of a novel ammonium ion-specific copper-polyaniline nano-composite as transducer for hydrolase-based biosensors is proposed. In this work, a combination of creatinine deaminase and urease has been chosen as a model system to demonstrate the construction of urea and creatinine biosensors to illustrate the principle. Immobilisation of enzymes was shown to be a crucial step in the development of the biosensors; the use of glycerol and lactitol as stabilisers resulted in a significant improvement, especially in the case of the creatinine, of the operational stability of the biosensors (from few hours to at least 3 days). The developed biosensors exhibited high selectivity towards creatinine and urea. The sensitivity was found to be 85 ± 3.4 mAM(-1)cm(-2) for the creatinine biosensor and 112 ± 3.36 mAM(-1)cm(-2) for the urea biosensor, with apparent Michaelis-Menten constants (KM,app), obtained from the creatinine and urea calibration curves, of 0.163 mM for creatinine deaminase and 0.139 mM for urease, respectively. The biosensors responded linearly over the concentration range 1-125 µM, with a limit of detection of 0.5 µM and a response time of 15s. The performance of the biosensors in a real sample matrix, serum, was evaluated and a good correlation with standard spectrophotometric clinical laboratory techniques was found.

  2. Copper Ferrocyanide Functionalized Core-Shell Magnetic Silica Composites for the Selective Removal of Cesium Ions from Radioactive Liquid Waste.

    Science.gov (United States)

    Lee, Hyun Kyu; Yang, Da Som; Oh, Wonzin; Choi, Sang-June

    2016-06-01

    The copper ferrocyanide functionalized core-shell magnetic silica composite (mag@silica-CuFC) was prepared and was found to be easily separated from aqueous solutions by using magnetic field. The synthesized mag@silica-CuFC composite has a high sorption ability of Cs owing to its strong affinity for Cs as well as the high surface area of the supports. Cs sorption on the mag@silica-CuFC composite quickly reached the sorption equilibrium after 2 h of contact time. The effect of the presence of salts with a high concentration of up to 3.5 wt% on the efficiency of Cs sorption onto the composites was also studied. The maximum sorption ability was found to be maintained in the presence of up to 3.5 wt% of NaCl in the solution. Considering these results, the mag@silica-CuFC composite has great potential for use as an effective sorbent for the selective removal of radioactive Cs ions.

  3. Solvothermal syntheses and characterization of three new silver(I)/copper(I)-thioarsenates based on As2+/As3+ ions

    Science.gov (United States)

    Yao, Hua-Gang; Tang, Cheng-Fei; An, Yong-Lin; Ou, Zi-Jian; Wu, Guo-Hao; Lan, Pei; Zheng, Yi-Long

    2017-02-01

    Three new silver(I)/copper(I)-thioarsenates KAgAsIIS2 (1), RbCu2AsIIIS3 (2) and RbCu4AsIIIS4 (3) have been solvothermally synthesized and structurally characterized. 1 exhibits a two-dimensional anionic network built up by As-As bond connecting the left- and right-handed helical [AgS2]4- chains, and represents the first examples of thioarsenates(II). The structure of 2 consists of two kinds of helical [Cu2S3]4- chains linked by the arsenic atoms to form double layers with rubidium ions between the layers. Compound 3 is built up of infinite [Cu2S2]2- chain and layered [Cu6As2S6] linked to form a three-dimensional anionic framework, [Cu4AsS4]-, and containing channels in which the rubidium cations reside. The optical properties of 1-3 have been investigated by UV-vis spectroscopy.

  4. Polyethyleneimine-templated copper nanoclusters via ascorbic acid reduction approach as ferric ion sensor

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Jie; Ju, Yuyun; Liu, Juanjuan; Zhang, Huige [State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000 (China); Department of Chemistry, Lanzhou University, Lanzhou 730000 (China); Chen, Xingguo, E-mail: chenxg@lzu.edu.cn [State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000 (China); Department of Chemistry, Lanzhou University, Lanzhou 730000 (China); Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province, Lanzhou 730000 (China)

    2015-01-07

    Highlights: • A new method for synthesis of the BPEI-CuNCs is established. • A facile approach for Fe{sup 3+} ion sensing by fluorescence quenching is developed. • The method for Fe{sup 3+} sensing has high sensitivity and excellent selectivity. - Abstract: In this report we reported a facile one-pot method for synthesis of water-soluble and stable fluorescent CuNCs at room temperature, in which branched polyethyleneimine (BPEI) served as capping scaffold and ascorbic acid as reducing agent. The prepared BPEI-CuNCs exhibited excellent properties such as good water-solubility, photostability and high stability toward high ionic strength. Based on the electron transfer induced fluorescence quenching mechanism, this fluorescence probe was used for the sensitive and selective determination of ferric ions (Fe{sup 3+}) in aqueous solution. The limit of detection was 340 nM in the linear range of 0.5–1000 μM, which was lower than the maximum level of Fe{sup 3+} permitted in drinking water by the U.S. Environmental Protection Agency. The method was successfully applied to the detection of Fe{sup 3+} in tap water, Yellow River water and human urine samples with the quantitative spike recoveries ranging from 95.3% to 112.0%.

  5. Self-assembly of core-satellite gold nanoparticles for colorimetric detection of copper ions.

    Science.gov (United States)

    Weng, Ziqing; Wang, Hongbin; Vongsvivut, Jitraporn; Li, Runqing; Glushenkov, Alexey M; He, Jin; Chen, Ying; Barrow, Colin J; Yang, Wenrong

    2013-11-25

    Molecule-coated nanoparticles are hybrid materials which can be engineered with novel properties. The molecular coating of metal nanoparticles can provide chemical functionality, enabling assembly of the nanoparticles that are important for applications, such as biosensing devices. Herein, we report a new self-assembly of core-satellite gold nanoparticles linked by a simple amino acid l-Cysteine for biosensing of Cu(2+). The plasmonic properties of core-satellite nano-assemblies were investigated, a new red shifted absorbance peak from about 600 to 800 nm was found, with specific wavelength depending on ratios with assembly of large and small gold nanoparticles. The spectral features obtained using surface-enhanced Raman spectroscopy (SERS) provided strong evidence for the assembly of the Cu(2+) ions to the L-Cysteine molecules leading to the successful formation of the core-satellite Cu(l-Cysteine) complex on the gold surfaces. In addition, a linear relationship between the concentration of mediating Cu(2+) and absorbance of self-assembled gold nanoparticles (GNPs) at 680 nm was obtained. These results strongly address the potential strategy for applying the functionalized GNPs as novel biosensing tools in trace detections of certain metal ions.

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

    Science.gov (United States)

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

    2016-06-01

    Cu2-xTe nanocubes were used as starting seeds to access metal telluride nanocrystals by cation exchanges at room temperature. The coordination number of the entering cations was found to play an important role in dictating the reaction pathways. The exchanges with tetrahedrally coordinated cations (i.e., with coordination number 4), such as Cd(2+) or Hg(2+), yielded monocrystalline CdTe or HgTe nanocrystals with Cu2-xTe/CdTe or Cu2-xTe/HgTe Janus-like heterostructures as intermediates. The formation of Janus-like architectures was attributed to the high diffusion rate of the relatively small tetrahedrally coordinated cations, which could rapidly diffuse in the Cu2-xTe NCs and nucleate the CdTe (or HgTe) phase in a preferred region of the host structure. Also, with both Cd(2+) and Hg(2+) ions the exchange led to wurtzite CdTe and HgTe phases rather than the more stable zinc-blende ones, indicating that the anion framework of the starting Cu2-xTe particles could be more easily deformed to match the anion framework of the metastable wurtzite structures. As hexagonal HgTe had never been reported to date, this represents another case of metastable new phases that can only be accessed by cation exchange. On the other hand, the exchanges involving octahedrally coordinated ions (i.e., with coordination number 6), such as Pb(2+) or Sn(2+), yielded rock-salt polycrystalline PbTe or SnTe nanocrystals with Cu2-xTe@PbTe or Cu2-xTe@SnTe core@shell architectures at the early stages of the exchange process. In this case, the octahedrally coordinated ions are probably too large to diffuse easily through the Cu2-xTe structure: their limited diffusion rate restricts their initial reaction to the surface of the nanocrystals, where cation exchange is initiated unselectively, leading to core@shell architectures. Interestingly, these heterostructures were found to be metastable as they evolved to stable Janus-like architectures if annealed at 200 °C under vacuum.

  7. MODIFICATION OF KELUD VOLCANIC ASH 2014 AS SELECTIVE ADSORBENT MATERIAL FOR COPPER(II METAL ION

    Directory of Open Access Journals (Sweden)

    Susila Kristianingrum

    2017-01-01

      This research aims to prepare an adsorbent from Kelud volcanic ash for better Cu(II adsorption efficiency than Kiesel gel 60G E'Merck. Adsorbent synthesis was done by dissolving 6 grams of volcanic ash activated 700oC 4 hours and washed with HCl 0.1 M into 200 ml of 3M sodium hydroxide with stirring and heating of 100 °C for 1 hour. The filtrate sodium silicate was then neutralized using sulfuric acid. The mixture was allowed to stand for 24 hours then filtered and washed with aquaDM, then dried and crushed. The procedure is repeated for nitric acid, acetic acid and formic acid with a contact time of 24 hours. The products were then characterized using FTIR and XRD, subsequently determined acidity, moisture content, and tested for its adsorption of the ion Cu (II with AAS. The results showed that the type of acid that produced highest rendemen is AK-H2SO4-3M ie 36.93%, acidity of the adsorbent silica gel synthesized similar to Kiesel gel 60G E'Merck ie adsorbent AK-CH3COOH-3M and the water content of the silica gel adsorbent synthesized similar to Kiesel gel 60G E'Merck ie adsorbent AK-H2SO4-2 M. The character of the functional groups of silica gel synthesized all have similarities with Kiesel gel 60G E'Merck as a comparison. Qualitative analysis by XRD for all modified adsorbent showed a dominant peak of SiO2 except adsorbent AK-H2SO4 amorphous and chemical bonds with FTIR indicates that it has formed a bond of Si-O-Si and Si-OH. The optimum adsorption efficiency of the metal ions Cu(II obtained from AK-H2SO4-5M adsorbent that is equal to 93.2617% and the optimum adsorption capacity of the Cu(II metal ions was obtained from the adsorbent AK-CH3COOH-3M is equal to 2.4919 mg/ g.   Keywords: adsorbents, silica gel, adsorption, kelud volcanic ash

  8. In vivo detection of copper ions by magnetic resonance imaging using a prion-based contrast agent.

    Science.gov (United States)

    Makino, Satoshi; Umemoto, Tomohiro; Yamada, Hiroshi; Yezdimer, Eric M; Tooyama, Ikuo

    2012-10-01

    Abnormal distributions of transition metals inside the body are potential diagnostic markers for several diseases, including Alzheimer's disease, Parkinson's disease, Wilson's disease, and cancer. In this article, we demonstrate that P57/Gd, a novel prion-based contrast agent, can selectively image tissues with excessive copper accumulation using magnetic resonance imaging (MRI). P57/Gd selectivity binds copper(II) over other physiologically relevant cations such as zinc, iron, manganese, and calcium. To simulate a metabolic copper disorder, we treated mice with an intraperitoneal injection of a CuSO(4) solution to induce a renal copper overload. The MRI signal intensities from the renal cortex and medulla of copper spiked animals that were administered P57/Gd were found to correlate with the ex vivo copper concentrations determined by inductively coupled plasma mass spectrometry.

  9. Iron sulfide attenuates the methanogenic toxicity of elemental copper and zinc oxide nanoparticles and their soluble metal ion analogs.

    Science.gov (United States)

    Gonzalez-Estrella, Jorge; Gallagher, Sara; Sierra-Alvarez, Reyes; Field, Jim A

    2016-04-01

    Elemental copper (Cu(0)) and zinc oxide (ZnO) nanoparticle (NP) toxicity to methanogens has been attributed to the release of soluble metal ions. Iron sulfide (FeS) partially controls the soluble concentration of heavy metals and their toxicity in aquatic environments. Heavy metals displace the Fe from FeS forming poorly soluble metal sulfides in the FeS matrix. Therefore, FeS may be expected to attenuate the NP toxicity. This work assessed FeS as an attenuator of the methanogenic toxicity of Cu(0) and ZnO NPs and their soluble salt analogs. The toxicity attenuation capacity of fine (25-75μm) and coarse (500 to 1200μm) preparations of FeS (FeS-f and FeS-c respectively) was tested in the presence of highly inhibitory concentrations of CuCl2, ZnCl2 Cu(0) and ZnO NPs. FeS-f attenuated methanogenic toxicity better than FeS-c. The results revealed that 2.5× less FeS-f than FeS-c was required to recover the methanogenic activity to 50% (activity normalized to uninhibited controls). The results also indicated that a molar FeS-f/Cu(0) NP, FeS-f/ZnO NP, FeS-f/ZnCl2, and FeS-f/CuCl2 ratio of 2.14, 2.14, 4.28, and 8.56 respectively, was necessary to recover the methanogenic activity to >75%. Displacement experiments demonstrated that CuCl2 and ZnCl2 partially displaced Fe from FeS. As a whole, the results indicate that not all the sulfide in FeS was readily available to react with the soluble Cu and Zn ions which may explain the need for a large stoichiometric excess of FeS to highly attenuate Cu and Zn toxicity. Overall, this study provides evidence that FeS attenuates the toxicity caused by Cu(0) and ZnO NPs and their soluble ion analogs to methanogens.

  10. Removal of copper ions from aqueous solution by calcium alginate immobilized kaolin.

    Science.gov (United States)

    Li, Yanhui; Xia, Bing; Zhao, Quansheng; Liu, Fuqiang; Zhang, Pan; Du, Qiuju; Wang, Dechang; Li, Da; Wang, Zonghua; Xia, Yanzhi

    2011-01-01

    Kaolin has been widely used as an adsorbent to remove heavy metal ions from aqueous solutions. However, the lower heavy metal adsorption capacity of kaolin limits its practical application. A novel environmental friendly material, calcium alginate immobilized kaolin (kaolin/CA), was prepared using a sol-gel method. The effects of contact time, pH, adsorbent dose, and temperature on Cu2+ adsorption by kaolin/CA were investigated. The Langmuir isotherm was used to describe the experimental adsorption, the maximum Cu2+ adsorption capacity of the kaolin/CA reached up to 53.63 mg/g. The thermodynamic studies showed that the adsorption reaction was a spontaneous and endothermic process.

  11. Removal of copper ions from aqueous solution by calcium alginate immobilized kaolin

    Institute of Scientific and Technical Information of China (English)

    Yanhui Li; Yanzhi Xia; Bing Xia; Quansheng Zhao; Fuqiang Liu; Pan Zhang; Qiuju Du; Dechang Wang; Da Li; Zonghua Wang

    2011-01-01

    Kaolin has been widely used as an adsorbent to remove heavy metal ions from aqueous solutions. However, the lower heavy metal adsorption capacity of kaolin limits its practical application. A novel environmental friendly material, calcium alginate immobilized kaolin (kaolin/CA), was prepared using a sol-gel method. The effects of contact time, pH, adsorbent dose, and temperature on Cu2+ adsorption by kaolin/CA were investigated. The Langmuir isotherm was used to describe the experimental adsorption, the maximum Cu2+ adsorption capacity of the kaolin/CA reached up to 53.63 mg/g. The thermodynamic studies showed that the adsorption reaction was a spontaneous and endothermic process.

  12. Understanding the Photoluminescence Mechanism of Nitrogen-Doped Carbon Dots by Selective Interaction with Copper Ions.

    Science.gov (United States)

    Ganiga, Manjunatha; Cyriac, Jobin

    2016-08-04

    Doped fluorescent carbon dots (CDs) have drawn widespread attention because of their diverse applications and attractive properties. The present report focusses on the origin of photoluminescence in nitrogen-doped CDs (NCDs), which is unraveled by the interaction with Cu(2+) ions. Detailed spectroscopic and microscopic studies reveal that the broad steady-state photoluminescence emission of the NCDs originates from the direct recombination of excitons (high energy) and the involvement of defect states (low energy). In addition, highly selective detection of Cu(2+) is achieved, with a detection limit of 10 μm and a dynamic range of 10 μm-0.4 mm. The feasibility of the present sensor for the detection of Cu(2+) in real water samples is also presented. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. Copper(II) ions interactions in the systems with triamines and ATP. Potentiometric and spectroscopic studies.

    Science.gov (United States)

    Hoffmann, S K; Goslar, J; Bregier-Jarzebowska, R; Gasowska, A; Zalewska, A; Lomozik, L

    2017-09-09

    The mode of interaction and thermodynamic stability of complexes formed in binary and ternary Cu(II)/ATP/triamines systems were studied using potentiometric and spectroscopic (NMR, EPR, UV-Vis) methods. It was found that in binary metal-free systems ATP/HxPA species are formed (PA: Spd=spermidine or 3,3-tri=1,7-diamino-4-azaheptane) where the phosphate groups from nucleotides are preferred negative centers and protonated amine groups of amines are positive centers of reaction. In the ternary systems Cu/ATP/Hx(PA) as well as Cu/(ATP)(PA) species are formed. The type of the formed Cu(II) complexes depends on pH of the solution. For a low pH value the complexation appears between Cu(II) and ATP molecules via oxygen atoms of phosphate groups. For a very high pH value, where ATP is hydrolyzed, the Cu(II) ions are bound to the nitrogen atoms of polyamine molecules. We did not detect any direct coordination of the N7 nitrogen atom of adenosine to Cu(II) ions. It means that the CuN7 interaction is an indirect type and can be due to noncovalent interplay including water molecule. EPR studies were performed at glassy state (77K) after a fast freezing both for binary and ternary systems. The glassy state EPR spectra do not reflect species identified in titration studies indicating significant effect of rapid temperature decrease on equilibrium of Cu(II) complexes. We propose the molecular structure of all the studied complexes at the glassy state deduced from EPR and optical spectroscopy results. Copyright © 2017 Elsevier Inc. All rights reserved.

  14. ADSORPTION OF ION EXCHANGE RESIN FOR COPPER ION IN ORGANIC WASTE WATER%离子交换树脂对有机废水中铜离子的吸附

    Institute of Scientific and Technical Information of China (English)

    张剑波; 王维敬; 祝乐

    2001-01-01

    Different ion exchange resins were selected to adsorb the copperion in organic wastewater. The absorption rate of resin for copper was determined. The impact of copper ion concentration and pH value on absorption rate, and the regenesis capability of the resin were tested. Results showed "zhengguang", "Qiangsuan 1#" and PK208 resin possess outstanding performance, which should be used in decontamination of wastewater that contains copper ion.%选用多种大孔强酸型离子交换树脂,用于吸附浓集含有机物废水中的铜离子,通过测定各种树脂对铜离子的去除率、不同铜离子浓度和溶液pH值对去除率的影响,以及各树脂再生性能的比较,表明“争光”、“强酸1号”和PK208树脂性能最为突出,效果明显优于其它几种树脂,可用于吸附处理有机废水中的铜离子。

  15. Removal of copper, nickel and zinc ions from aqueous solution by chitosan-8-hydroxyquinoline beads

    Energy Technology Data Exchange (ETDEWEB)

    Barros, Francisco C.F.; Dias, Francisco S.; Vasconcellos, Luiz C.G. [Departamento de Quimica Organica e Inorganica, Campus do Pici - Universidade Federal do Ceara, Fortaleza (Brazil); Sousa, Francisco W. [Departamento de Engenharia Hidraulica e Ambiental, Campus do Pici - Universidade Federal do Ceara, Fortaleza (Brazil); Cavalcante, Rivelino M.; Carvalho, Tecia V.; Queiroz, Danilo C. [Departamento de Quimica Analitica e Fisico Quimica, Campus do Pici - Universidade Federal do Ceara, Fortaleza (Brazil); Nascimento, Ronaldo F.

    2008-03-15

    In this work, 8-hydroxyquinoline is used as the active sites in cross-linked chitosan beads with epichlorohydrin (CT-8HQ). The CT-8HQ material was shaped in bead form and used for heavy metal removal from aqueous solution. The study was carried out at pH 5.0 with both batch and column methods and the maximum adsorption capacity of metal ions by the CT-8HQ was attained in 4 h in the batch experiment. The adsorption capacity order was: Cu{sup 2+} > Ni{sup 2+} > Zn{sup 2+} for both mono- and multi-component systems with batch conditions. From breakthrough curves with column conditions, the adsorption capacity followed the order Cu{sup 2+} > Zn{sup 2+} > Ni{sup 2+} for both mono- and multi-component systems. The CT-8HQ beads maintained good metal adsorption capacity for all five cycles with absorbent restoration achieved with the use of 1.0 mol L{sup -1} HCl solution, with 90% regeneration. (Abstract Copyright [2008], Wiley Periodicals, Inc.)

  16. Increased Uptake of Chelated Copper Ions by Lolium perenne Attributed to Amplified Membrane and Endodermal Damage

    Directory of Open Access Journals (Sweden)

    Anthea Johnson

    2015-10-01

    Full Text Available The contributions of mechanisms by which chelators influence metal translocation to plant shoot tissues are analyzed using a combination of numerical modelling and physical experiments. The model distinguishes between apoplastic and symplastic pathways of water and solute movement. It also includes the barrier effects of the endodermis and plasma membrane. Simulations are used to assess transport pathways for free and chelated metals, identifying mechanisms involved in chelate-enhanced phytoextraction. Hypothesized transport mechanisms and parameters specific to amendment treatments are estimated, with simulated results compared to experimental data. Parameter values for each amendment treatment are estimated based on literature and experimental values, and used for model calibration and simulation of amendment influences on solute transport pathways and mechanisms. Modeling indicates that chelation alters the pathways for Cu transport. For free ions, Cu transport to leaf tissue can be described using purely apoplastic or transcellular pathways. For strong chelators (ethylenediaminetetraacetic acid (EDTA and diethylenetriaminepentaacetic acid (DTPA, transport by the purely apoplastic pathway is insufficient to represent measured Cu transport to leaf tissue. Consistent with experimental observations, increased membrane permeability is required for simulating translocation in EDTA and DTPA treatments. Increasing the membrane permeability is key to enhancing phytoextraction efficiency.

  17. Increased Uptake of Chelated Copper Ions by Lolium perenne Attributed to Amplified Membrane and Endodermal Damage.

    Science.gov (United States)

    Johnson, Anthea; Singhal, Naresh

    2015-10-23

    The contributions of mechanisms by which chelators influence metal translocation to plant shoot tissues are analyzed using a combination of numerical modelling and physical experiments. The model distinguishes between apoplastic and symplastic pathways of water and solute movement. It also includes the barrier effects of the endodermis and plasma membrane. Simulations are used to assess transport pathways for free and chelated metals, identifying mechanisms involved in chelate-enhanced phytoextraction. Hypothesized transport mechanisms and parameters specific to amendment treatments are estimated, with simulated results compared to experimental data. Parameter values for each amendment treatment are estimated based on literature and experimental values, and used for model calibration and simulation of amendment influences on solute transport pathways and mechanisms. Modeling indicates that chelation alters the pathways for Cu transport. For free ions, Cu transport to leaf tissue can be described using purely apoplastic or transcellular pathways. For strong chelators (ethylenediaminetetraacetic acid (EDTA) and diethylenetriaminepentaacetic acid (DTPA)), transport by the purely apoplastic pathway is insufficient to represent measured Cu transport to leaf tissue. Consistent with experimental observations, increased membrane permeability is required for simulating translocation in EDTA and DTPA treatments. Increasing the membrane permeability is key to enhancing phytoextraction efficiency.

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

    CERN Document Server

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

    2016-01-01

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

  19. Simple PEG modification of DNA aptamer based on copper ion coordination for tumor targeting.

    Science.gov (United States)

    Takafuji, Yoshimasa; Jo, Jun-ichiro; Tabata, Yasuhiko

    2011-01-01

    A simple modification of a DNA aptamer with poly(ethylene glycol) (PEG) based on metal coordination was developed. N,N-bis(carboxymethyl)-L-lysine (NTA) of a metal chelate residue was chemically introduced to one terminus of PEG. The NTA-introduced PEG (PEG-NTA) chelated Cu(2+) ions form a Cu(2+)-chelated PEG (PEG-Cu). When PEG-Cu was mixed with a DNA aptamer of anti-tumor activity (AS1411) in aqueous solution, a complex of PEG-Cu and AS1411 based on metal coordination was formed. The complex inhibited in vitro tumor growth in a dose-dependent manner. A body distribution study with tumor-bearing mice revealed that PEG-Cu-AS1411 complexes injected intravenously had a significant longer lifetime in the blood circulation and 1.5-2.0-fold higher accumulation in the tumor tissue than free AS1411. Intravenous injection of complexes suppressed the in vivo growth of tumor mass to a significantly greater extent compared with that of free AS1411. The Cu(2+)-coordinated PEG modification is a simple and promising method to enhance accumulation of the aptamer in the tumor, resulting in the augmented anti-tumor effect.

  20. A New Rhodamine B Derivative As a Colorimetric Chemosensor for Recognition of Copper(II) Ion

    Energy Technology Data Exchange (ETDEWEB)

    Tang, Lijun; Li, Fangfang; Liu, Minghui [Bohai University, Jinzhou (China); Nandhakumar, Raju [Karunya University, TamilNadu (India)

    2010-11-15

    A new rhodamine-based sensor 1 was designed and synthesized by incorporating rhodamine B and benzimidazole moieties. Sensor 1 exhibits high selectivity and sensitivity to Cu{sup 2+} in CH{sub 3}CN-water solution (HEPES buffer, pH = 7.0) with an obvious color change from colorless to pink. Other metal ions such as Hg{sup 2+}, Ag{sup +}, Pb{sup 2+}, Sr{sup 2+}, Ba{sup 2+}, Cd{sup 2+}, Ni{sup 2+}, Co{sup 2+}, Fe{sup 2+}, Mn{sup 2+}, Cu{sup 2+}, Zn{sup 2+}, Ce{sup 3+}, Mg{sup 2+}, K{sup +} and Na{sup +} had no such color change and have no significant influence on Cu{sup 2+} recognition process. The interaction of Cu{sup 2+} and sensor 1 was proven to adopt a 1:1 binding stoichiometry and the recognition process is reversible.

  1. Copper Ion Attenuated the Antiproliferative Activity of Di-2-pyridylhydrazone Dithiocarbamate Derivative; However, There Was a Lack of Correlation between ROS Generation and Antiproliferative Activity.

    Science.gov (United States)

    Wang, Tingting; Fu, Yun; Huang, Tengfei; Liu, Youxun; Wu, Meihao; Yuan, Yanbin; Li, Shaoshan; Li, Changzheng

    2016-08-20

    The use of chelators for cancer treatment has been an alternative option. Dithiocarbamates have recently attracted considerable attention owning to their diverse biological activities; thus, the preparation of new dithiocarbamate derivatives with improved antitumor activity and selectivity as well as probing the underlying molecular mechanism are required. In this study, di-2-pyridylhydrazone dithiocarbamate S-propionic acid (DpdtpA) and its copper complex were prepared and characterized, and its antiproliferative activity was evaluated. The proliferation inhibition assay showed that DpdtpA exhibited excellent antiproliferative effect in hepatocellular carcinoma (IC50 = 1.3 ± 0.3 μM for HepG2, and 2.5 ± 0.6 μM for Bel-7402). However, in the presence of copper ion, the antiproliferative activity of DpdtpA was dramatically attenuated (20-30 fold) owing to the formation of copper chelate. A preliminarily mechanistic study revealed that reactive oxygen species (ROS) generation mediated the antiproliferative activity of DpdtpA, and accordingly induced apoptosis, DNA cleavage, and autophagy. Surprisingly, the cytotoxicity of DpdtpA copper complex (DpdtpA-Cu) was also involved in ROS generation; however, a paradoxical relation between cellular ROS level and cytotoxicity was observed. Further investigation indicated that DpdtpA could induce cell cycle arrest at the S phase; however, DpdtpA-Cu lacked this effect, which explained the difference in their antiproliferative activity.

  2. Copper Ion Attenuated the Antiproliferative Activity of Di-2-pyridylhydrazone Dithiocarbamate Derivative; However, There Was a Lack of Correlation between ROS Generation and Antiproliferative Activity

    Directory of Open Access Journals (Sweden)

    Tingting Wang

    2016-08-01

    Full Text Available The use of chelators for cancer treatment has been an alternative option. Dithiocarbamates have recently attracted considerable attention owning to their diverse biological activities; thus, the preparation of new dithiocarbamate derivatives with improved antitumor activity and selectivity as well as probing the underlying molecular mechanism are required. In this study, di-2-pyridylhydrazone dithiocarbamate S-propionic acid (DpdtpA and its copper complex were prepared and characterized, and its antiproliferative activity was evaluated. The proliferation inhibition assay showed that DpdtpA exhibited excellent antiproliferative effect in hepatocellular carcinoma (IC50 = 1.3 ± 0.3 μM for HepG2, and 2.5 ± 0.6 μM for Bel-7402. However, in the presence of copper ion, the antiproliferative activity of DpdtpA was dramatically attenuated (20–30 fold owing to the formation of copper chelate. A preliminarily mechanistic study revealed that reactive oxygen species (ROS generation mediated the antiproliferative activity of DpdtpA, and accordingly induced apoptosis, DNA cleavage, and autophagy. Surprisingly, the cytotoxicity of DpdtpA copper complex (DpdtpA–Cu was also involved in ROS generation; however, a paradoxical relation between cellular ROS level and cytotoxicity was observed. Further investigation indicated that DpdtpA could induce cell cycle arrest at the S phase; however, DpdtpA–Cu lacked this effect, which explained the difference in their antiproliferative activity.

  3. Development of two highly sensitive immunoassays for detection of copper ions and a suite of relevant immunochemicals

    Energy Technology Data Exchange (ETDEWEB)

    Zhao Hongwei [College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193 (China); Department of Molecular Biosciences and Bioengineering, University of Hawaii at Manoa, Honolulu, HI 96822 (United States); Nan Tiegui; Tan Guiyu; Gao Wei; Cao Zhen; Sun Shuo; Li Zhaohu [College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193 (China); Li, Qing X., E-mail: qingl@hawaii.edu [Department of Molecular Biosciences and Bioengineering, University of Hawaii at Manoa, Honolulu, HI 96822 (United States); Wang Baomin, E-mail: wbaomin@263.com [College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193 (China)

    2011-09-19

    Highlights: {center_dot} Two highly sensitive immunoassays for determination of Cu(II) at sub ppb levels. {center_dot} The heterologous competitive enzyme linked immunosorbent assay for heavy metals. {center_dot} Haptenated protein directly conjugated with HRP can reduce the loss of HRP activity. - Abstract: Availability of highly sensitive assays for metal ions can help monitor and manage the environmental and food contamination. In the present study, a monoclonal antibody against Copper(II)-ethylenediaminetetraacetic acid was used to develop two sensitive ELISAs for Cu(II) analysis. Cobalt(II)-EDTA-BSA was the coating antigen in a heterologous indirect competitive ELISA (hicELISA), whereas Co(II)-EDTA-BSA-horseradish peroxidase (HRP) was the enzyme tracer in a heterologous direct competitive ELISA (hdcELISA). Both ELISAs were validated for detecting the content of Cu(II) in environmental waters. The ELISA data agreed well with those from graphite furnace atomic absorption spectroscopy. The methods of developing the Cu(II) hicELISA and hdcELISA are potentially applicable for developing ELISAs for other metals. The chelator-protein complexes such as EDTA-BSA and EDTA-BSA-HRP can form a suite of metal complexes having the consistent hapten density, location and orientation on the conjugates except the difference of the metal core, which can be used as ideal reagents to investigate the relationship between assay sensitivity and antibody affinities for the haptens and the analytes. The strategy of conjugating a haptenated protein directly with HRP can reduce the loss of HRP activity during the conjugation reaction and thus can be applicable for the development of ELISAs for small molecules.

  4. New force field parameters for metalloproteins I: Divalent copper ion centers including three histidine residues and an oxygen-ligated amino acid residue.

    Science.gov (United States)

    Wise, Olivia; Coskuner, Orkid

    2014-06-30

    Transition metal ion complexation with proteins is ubiquitous across such diverse fields as neurodegenerative and cardiovascular diseases and cancer. In this study, the structures of divalent copper ion centers including three histidine and one oxygen-ligated amino acid residues and the relative binding affinities of the oxygen-ligated amino acid residues with these metal ion centers, which are debated in the literature, are presented. Furthermore, new force field parameters, which are currently lacking for the full-length metal-ligand moieties, are developed for metalloproteins that have these centers. These new force field parameters enable investigations of metalloproteins possessing these binding sites using molecular simulations. In addition, the impact of using the atom equivalence and inequivalence atomic partial charge calculation procedures on the simulated structures of these metallopeptides, including hydration properties, is described.

  5. A novel solidified floating organic drop microextraction method for preconcentration and determination of copper ions by flow injection flame atomic absorption spectrometry.

    Science.gov (United States)

    Sahin, Ciğdem Arpa; Tokgöz, Ilknur

    2010-05-14

    A rapid, simple and cost effective solidified floating organic drop microextraction (SFODME) and flow injection flame atomic absorption spectrometric determination (FI-FAAS) method for copper was developed. In this method, a free microdrop of 1-undecanol containing 1,5-diphenyl carbazide (DPC) as the complexing agent was transferred to the surface of an aqueous sample including Cu(II) ions, while being agitated by a stirring bar in the bulk of the solution. Under the proper stirring conditions, the suspended microdrop can remain at the top-center position of the aqueous sample. After the completion of the extraction, the sample vial was cooled by placing it in a refrigerator for 10min. The solidified microdrop was then transferred into a conical vial, where it melted immediately and diluted to 300microL with ethanol. Finally, copper ions in 200microL of diluted solution were determined by FI-FAAS. Several factors affecting the microextraction efficiency, such as type of extraction solvent, pH, complexing agent concentration, extraction time, stirring rate, sample volume and temperature were investigated and optimized. Under optimized conditions for 100mL of solution, the preconcentration factor was 333 and the enrichment factor was 324. The limit of detection (3s) was 0.4ngmL(-1), the limit of quantification (10s) was 1.1ngmL(-1) and the relative standard deviation (RSD) for 10 replicate measurements of 10ngmL(-1) copper was 0.9%. The proposed method was successfully applied to the determination of copper in different water samples.

  6. Selective extraction and release using (EDTA-Ni)-layered double hydroxide coupled with catalytic oxidation of 3,3',5,5'-tetramethylbenzidine for sensitive detection of copper ion.

    Science.gov (United States)

    Tang, Sheng; Chang, Yuepeng; Chia, Guo Hui; Lee, Hian Kee

    2015-07-23

    Copper is an important heavy metal in various biological processes. Many methods have been developed for detecting of copper ions (Cu(2+)) in aqueous samples. However, an easy, cheap, selective and sensitive method is still desired. In this study, a selective extraction-release-catalysis approach has been developed for sensitive detection of copper ion. Ethylenediaminetetraacetic acid (EDTA) chelated with nickel ion (Ni(2+)) were intercalated in a layered double hydroxide via a co-precipitation reaction. The product was subsequently applied as sorbent in dispersive solid-phase extraction for the enrichment of Cu(2+) at pH 6. Since Cu(2+) has a stronger complex formation constant with EDTA, Ni(2+) exchanged with Cu(2+) selectively. The resulting sorbent containing Cu(2+) was transferred to catalyze the 3,3',5,5'-tetramethylbenzidine oxidation reaction, since Cu(2+) could be released by the sorbent effectively and has high catalytic ability for the reaction. Blue light emitted from the oxidation product was measured by ultraviolet-visible spectrophotometry for the determination of Cu(2+). The extraction temperature, extraction time, and catalysis time were optimized. The results showed that this method provided a low limit of detection of 10nM, a wide linear range (0.05-100μM) and good linearity (r(2)=0.9977). The optimized conditions were applied to environmental water samples. Using Cu(2+) as an example, this work provided a new and interesting approach for the convenient and efficient detection of metal cations in aqueous samples. Copyright © 2015 Elsevier B.V. All rights reserved.

  7. Integrated miniature fluorescent probe to leverage the sensing potential of ZnO quantum dots for the detection of copper (II) ions.

    Science.gov (United States)

    Ng, Sing Muk; Wong, Derrick Sing Nguong; Phung, Jane Hui Chiun; Chin, Suk Fun; Chua, Hong Siang

    2013-11-15

    Quantum dots are fluorescent semiconductor nanoparticles that can be utilised for sensing applications. This paper evaluates the ability to leverage their analytical potential using an integrated fluorescent sensing probe that is portable, cost effective and simple to handle. ZnO quantum dots were prepared using the simple sol-gel hydrolysis method at ambient conditions and found to be significantly and specifically quenched by copper (II) ions. This ZnO quantum dots system has been incorporated into an in-house developed miniature fluorescent probe for the detection of copper (II) ions in aqueous medium. The probe was developed using a low power handheld black light as excitation source and three photo-detectors as sensor. The sensing chamber placed between the light source and detectors was made of 4-sided clear quartz windows. The chamber was housed within a dark compartment to avoid stray light interference. The probe was operated using a microcontroller (Arduino Uno Revision 3) that has been programmed with the analytical response and the working algorithm of the electronics. The probe was sourced with a 12 V rechargeable battery pack and the analytical readouts were given directly using a LCD display panel. Analytical optimisations of the ZnO quantum dots system and the probe have been performed and further described. The probe was found to have a linear response range up to 0.45 mM (R(2)=0.9930) towards copper (II) ion with a limit of detection of 7.68×10(-7) M. The probe has high repeatable and reliable performance.

  8. Facilitated Transport of Ethylene in Poly (Amide 12-Block Tetramethylenoxide) Copolymer/AgBF4 Membranes Containing Silver (I) and Copper (I) Ions as Carriers

    Science.gov (United States)

    Ben Hamouda, Sofiane; Trong Nguyen, Quang; Langevin, Dominique; Roudesli, Sadok

    Metal-incorporated poly(amide 12-block-tetramethylenoxide) (PA12-co-PTMO) copolymer was used for studying facilitated transport of olefines through new composite membranes. The metals incorporated were silver {Ag(I)} and copper {Cu(I)}. Tests were carried out at room temperature (25±2°C) to determine the selectivity and permeability of these membranes to ethylene and ethane gas. The membranes prepared by mixing in solution the copolymer with silver (AgBF4) or copper (CuBF4) salt show a ethylene/ethane selectivity much higher than that of pure PA12-co-PTMO. The membranes were also characterized by Fourier Transform Infra Red (FTIR) spectroscopy and Scanning Electron Microscopy (SEM) in order to understand the structural feature responsible for the observed behaviour. The IRFT spectrum indicate that Ag+ and Cu+ ions are developing interactions with the copolymer. The permeation results obtained with copper containing membranes show that CuBF4 salt introduction in the copolymer tends to reduce ethane permeability. This phenomenon is explained by a diminution of the free volume caused by a decrease of the interchain distance due to the formation of metal ions-polymer matrix complexes. At the same time, for ethylene, the decrease in permeability observed at low salt content is recouped rapidly, when the salt content increases, by a dramatic increase of the permeability which attains 10 times that of the pure PA12-co-PTMO. This behaviour is attributed to the facilitated transport mechanism of the ethylene molecules able to develop specific interactions with the incorporated metal ions. It results from these two antagonistic phenomena a multiplication by 18 of the ethylene/ethane selectivity of the pure copolymer when the CuBF4 content of the composite attains 60%.

  9. Fluorescence enhancement of CdTe/CdS quantum dots by coupling of glyphosate and its application for sensitive detection of copper ion

    Energy Technology Data Exchange (ETDEWEB)

    Liu Zhengqing; Liu Shaopu; Yin Pengfei [Key Laboratory on Luminescence and Real-Time Analysis, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715 (China); He Youqiu, E-mail: heyq@swu.edu.cn [Key Laboratory on Luminescence and Real-Time Analysis, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715 (China)

    2012-10-01

    Graphical abstract: Glyphosate (Glyp) had been used to modify the surface of CdTe/CdS QDs, resulting in the enhancement of fluorescence intensity. The Glyp-functionalized QDs fluorescent probe offers good sensitivity and selectivity for detecting Cu{sup 2+} based on the fluorescence quenching. Highlights: Black-Right-Pointing-Pointer Water soluble CdTe/CdS quantum dots capped with glyphosate were firstly synthesized. Black-Right-Pointing-Pointer The fluorescence of the Glyp-functionalized QDs was quenched by copper ion. Black-Right-Pointing-Pointer A new fluorescent sensor for copper ion was developed based on the prepared QDs. Black-Right-Pointing-Pointer The sensor exhibited high sensitivity and good selectivity for copper ion. - Abstract: A novel fluorescent probe for Cu{sup 2+} determination based on the fluorescence quenching of glyphosate (Glyp)-functionalized quantum dots (QDs) was firstly reported. Glyp had been used to modify the surface of QDs to form Glyp-functionalized QDs following the capping of thioglycolic acid on the core-shell CdTe/CdS QDs. Under the optimal conditions, the response was linearly proportional to the concentration of Cu{sup 2+} between 2.4 Multiplication-Sign 10{sup -2} {mu}g mL{sup -1} and 28 {mu}g mL{sup -1}, with a detection limit of 1.3 Multiplication-Sign 10{sup -3} {mu}g mL{sup -1} (3{delta}). The Glyp-functionalized QDs fluorescent probe offers good sensitivity and selectivity for detecting Cu{sup 2+}. The fluorescent probe was successfully used for the determination of Cu{sup 2+} in environmental samples. The mechanism of reaction was also discussed.

  10. Chromate (CrO(4)(2-)) and copper (Cu2+) adsorption by dual-functional ion exchange resins made from agricultural by-products.

    Science.gov (United States)

    Marshall, Wayne E; Wartelle, Lynda H

    2006-07-01

    Ion exchange resins commonly have a single functionality for either cations or anions. Resins that have a dual functionality for both cations and anions are uncommon. The objective of this study was to create dual-functional ion exchange resins derived from soybean hulls, sugarcane bagasse and corn stover. Dual-functional resins were prepared by two separate two-step processes. In the first two-step process, by-products were reacted with a solution of citric acid in order to impart additional negative charge, and then reacted with the cross-linking reagent dimethyloldihydroxyethylene urea (DMDHEU) and a quaternary amine (choline chloride) to add positive charge to the lignocellulosic material. In the second two-step process, the order of reaction was reversed, with positive charge added first, followed by the addition of negative charge. These combined reactions added both cationic and anionic character to the by-products as evidenced by the increased removal from solution of copper (Cu(2+)) cation and the chromate (CrO(4)(2-)) anion compared to unmodified by-products. The order of reaction appeared to slightly favor the functionality that was added last. That is, if negative charge was added last, the resulting resin sequestered more copper ion than a comparable resin where the negative charge was added first and vice-versa. Cu(2+) and CrO(4)(2-) were used as marker ions in a solution that contained both competing cations and anions. The dual-functional resins adsorbed as much as or more of the marker ions compared to commercial cation or anion exchange resins used for comparison. None of the commercial resins exhibited dual-functional properties to the same extent as the by-product-based resins.

  11. Tailor-made ion-imprinted polymer based on functionalized graphene oxide for the preconcentration and determination of trace copper in food samples.

    Science.gov (United States)

    Liu, Yan; Qiu, Jian; Liu, Zhanchao; Ni, Liang; Jiang, Yinhua; Gong, Chongying; Meng, Xiangguo; Liu, Fangfang; Zhong, Guoxing

    2016-04-01

    A tailor-made Cu(II) ion-imprinted polymer based on large-surface-area graphene oxide sheets has been synthesized for the preconcentration and determination of trace copper from food samples by solid-phase extraction. Attributed to the ultrahigh surface area and hydrophilicity of graphene oxide, the Cu(II) ion-imprinted polymer prepared by the surface ion-imprinting technique exhibited a high binding capacity and a fast adsorption rate under the optimized experimental conditions. In the static adsorption experiments, the maximum adsorption capacity of Cu(II) ion-imprinted polymer is 109.38 mg/g at 25°C, which is much higher than that of the nonimprinted polymer (32.12 mg/g). Meanwhile, the adsorption is very rapid and equilibrium is reached after approximately 30 min. The adsorption mechanism is found to follow Langmuir adsorption model and the pseudo-second-order adsorption process. The Cu(II) ion-imprinted polymer was used for extracting and detecting Cu(II) in food samples combined with graphite flame atomic adsorption spectrometry with high recoveries in the range of 97.6-103.3%. The relative standard deviation and limit of detection of the method were evaluated as 1.2% and 0.37 μg/L, respectively. The results showed that the novel absorbent can be utilized as an effective material for the selective enrichment and determination of Cu(II) from food samples.

  12. Copper nanowall array grown on bulk Fe-Co-Ni alloy substrate at room temperature as lithium-ion battery current collector

    Energy Technology Data Exchange (ETDEWEB)

    Hu Yingying, E-mail: yyhu@phy.ccnu.edu.cn; Liu Jinping; Ding Ruimin; Wang Kai; Jiang Jian; Ji Xiaoxu; Li Yuanyuan; Huang Xintang, E-mail: xthuang@phy.ccnu.edu.c

    2010-09-30

    Large-scale copper nanowall array on the bulk Fe-Co-Ni alloy substrate has been prepared in aqueous solution at room temperature via an electroless deposition method. The thickness of the nanowalls is about 15 nm. A possible growth mechanism of the nanowalls was proposed. The effects of reaction temperature, reaction time and the amount of critical agent (Fe{sup 3+}) on the morphology and crystalline phase of the nanowalls were investigated. Furthermore, the electrochemical performance of Sn film supported on the as-prepared copper nanowalls current collector is enhanced in comparison with that on the commercial copper foil when used as anode for Li-ion batteries with the operating voltage window of 0.01-2.0 V (vs. Li). After 20 cycles, the discharge capacity of Sn-Cu nanowalls anode still remained 365.9 mAh g{sup -1}, that is, 40% retention of the reversible capacity, while the initial charge capacity of Sn film cast on commercial Cu foil was 590 mAh g{sup -1}, dropping rapidly to 260 mAh g{sup -1} only after 10 cycles.

  13. Influence of divalent copper, manganese and zinc ions on fibril nucleation and elongation of the amyloid-like yeast prion determinant Sup35p-NM.

    Science.gov (United States)

    Suhre, Michael H; Hess, Simone; Golser, Adrian V; Scheibel, Thomas

    2009-12-01

    There is a large body of evidence that divalent metal ions, particularly copper, might play a role in several protein folding pathologies like Alzheimer's disease, Parkinson's disease or the prion diseases. However, contribution of metal ions on pathogenesis and their molecular influence on the formation of amyloid structures is not clear. Therefore, the general influence of metals on the formation of amyloids is still controversially discussed. We have utilized the well established system of yeast Sup35p-NM to investigate the role of three different metal ions, Cu(2+), Mn(2+) and Zn(2+), on amyloidogenesis. Recently, it has been shown that the prion determining region NM of the Saccharomyces cerevisiae prion protein Sup35p, which is responsible for the yeast prion phenotype [PSI(+)], specifically binds Cu(2+) ions. We further characterized the affinity of NM for Cu(2+), which were found to be comparable to that of other amyloidogenic proteins like the mammalian prion protein PrP. The specific binding sites could be located in the aminoterminal N-region which is known to initiate formation of amyloidogenic nuclei. In the presence of Cu(2+), fibril nucleation was significantly delayed, probably due to influences of copper on the oligomeric ensemble of soluble Sup35p-NM, since Cu(2+) altered the tertiary structure of soluble Sup35p-NM, while no influences on fibril elongation could be detected. The secondary structure of soluble or fibrous protein and the morphology of the fibrils were apparently not altered when assembled in presence of Cu(2+). In contrast, Mn(2+) and Zn(2+) did not bind to Sup35p-NM and did not exhibit significant effects on the formation of NM amyloid fibrils.

  14. Fragmentation of mitochondrial cardiolipin by copper ions in the Atp7b-/- mouse model of Wilson's disease.

    Science.gov (United States)

    Yurkova, Irina L; Arnhold, Juergen; Fitzl, Guenther; Huster, Dominik

    2011-07-01

    Cellular copper overload as found in Wilson's disease may disturb mitochondrial function and integrity. Atp7b(-/-) mice accumulate copper in the liver and serve as an animal model for this inherited disease. The molecular mechanism of copper toxicity in hepatocytes is poorly understood. Total mitochondrial lipids from liver of wild-type mice were subjected to oxidative stress by the Cu(2+)/H(2)O(2)/ascorbate system. Phosphatidic acid (PA) and phosphatidylhydroxyacetone (PHA) were detected as cardiolipin fragmentation products by thin-layer chromatography combined with MALDI-TOF mass spectrometry in oxidized samples, but not in unperturbed ones. The formation of PA and PHA in copper-treated model membrane correlated well with the decrease of cardiolipin. Mitochondrial lipids from Atp7b(-/-) mice of different age were analyzed for the presence of PA. While 32-weeks old wild-type (control) and Atp7b(-/-) mice did not show any PA, there was a steady increase in the amount of this lipid in Atp7b(-/-) mice in contrast to control with increasing age. Hepatocytes from elder Atp7b(-/-)mice contained morphologically changed mitochondria unlike cells from wild-type animals of the same age. We concluded that free-radical fragmentation of cardiolipin with the formation of PA is a likely mechanism that damages mitochondria under conditions of oxidative stress due to copper overload. Our findings are relevant for better understanding of molecular mechanisms for liver damage found in Wilson's disease.

  15. A 9,10-anthraquinone derivative having two propenyl arms as a neutral ionophore for highly selective and sensitive membrane sensors for copper(II) ion.

    Science.gov (United States)

    Shamsipur, Mojtaba; Avanes, Armen; Javanbakht, Mehran; Ganjali, Mohammad Reza; Sharghi, Hashem

    2002-08-01

    New polymeric membrane (PME) and coated graphite (CGE) copper(II)-selective electrodes based on 1-hydroxy-2-(prop-2'-enyl)-4-(prop-2'-enyloxy)-9,10-anthraquinone were prepared. The electrodes reveal linear emf-pCu2+ responses over wide concentration ranges (1.0 x 10(-5)-1.0 x 10(-1) M with a slope of 27.3 mV decade-1 for PME and 8.0 x 10(-8)-5.0 x 10(-2) M with a slope of 29.1 mV decade-1 for CGE) and very low limits of detection (8.0 x 10(-6) M for PME and 5.0 x 10(-8) M for CGE). The potentiometric response is independent of the pH of the test solution in the pH range 3.0-6.0. The proposed electrodes possess very good selectivities over a wide variety of other cations, including alkali, alkaline earth, transition and heavy metal ions, the selectivity coefficients for the CGE being much improved over those for the PME. The electrodes were used as indicator electrodes in the potentiometric titration of Cu2+ and in the recovery of copper ions from wastewater.

  16. Effect of copper ions on the degradation of thiram in aqueous solution: identification of degradation products by HPLC-MS/MS.

    Science.gov (United States)

    Filipe, Olga M S; Santos, Sónia A O; Domingues, M Rosário M; Vidal, Maria M; Silvestre, Armando J D; Santos, Eduarda B H

    2014-08-30

    The aim of this work was to examine the effect of Cu(II) on the degradation of thiram (Thi) in aqueous solutions, since the literature focused on this effect is scarce and copper based fungicides can be applied together with thiram or during the same season to agricultural crops. The effect of Cu(II) on the degradation of thiram was followed by both UV-vis and HPLC-MS/MS. When thiram is dissolved in pure water its degradation occurs very slowly, being negligible during the first 7 days. However, the presence of Cu(II) has a strong influence on the thiram degradation in aqueous solutions along time. In the presence of an excess of Cu(II), a [CuThi](2+) complex is initially formed which degrades into a complex formed between the dimethyldithiocarbamate anion (DMDTC) and Cu(II) ion, [Cu(DMDTC)](+). This complex further degrades leading to other copper complexes which were identified for the first time, by MS(n). The results obtained in the present work also demonstrated that a redox reaction involving DMDTC anions and Cu(II) ions gives rise to the formation of a Thi-Cu(I) complex. Finally, some of the complexes resulting from the degradation of [CuThi](2+) are quite persistent in solution for long periods of time (>1 month).

  17. Polyetheretherketone (PEEK) surface functionalization by low-energy ion-beam irradiation under a reactive O2 environment and its effect on the PEEK/copper adhesives.

    Science.gov (United States)

    Kim, Sehyun; Lee, Ki-Jun; Seo, Yongsok

    2004-01-06

    A low-energy Ar+ ion beam was used to modify the surface of a polyetheretherketone (PEEK) film. The modification reaction proceeded with or without oxygen gas injected during the irradiation. The surface functional groups of the modified PEEK were confirmed with X-ray photoelectron spectroscopy as increasing various oxygen-containing functional groups. The concentration of the functional groups varied rapidly with the irradiation time, reached a maximum value, and then slowly decreased. The surface morphology of PEEK was substantially changed by ion-beam irradiation. Surface smoothening occurred so that the surface roughness reached almost constant value after some irradiation time. The incorporation of functional groups on the PEEK surface and the surface topology change had opposite effects on the adhesion strength between PEEK and copper. Dominance of the former was evident because the lap-shear strength initially increased with the irradiation. The special surface features significantly enhanced the adhesion strength between the evaporated copper layer and the modified PEEK surface. However, the decrease in the surface roughness with a long time irradiation implies a decrease in adhesion strength due to a smaller contact area, and the shear strength due to topology change also slowly decreased after a long time irradiation.

  18. Semax, an ACTH4-10 peptide analog with high affinity for copper(II) ion and protective ability against metal induced cell toxicity.

    Science.gov (United States)

    Tabbì, Giovanni; Magrì, Antonio; Giuffrida, Alessandro; Lanza, Valeria; Pappalardo, Giuseppe; Naletova, Irina; Nicoletti, Vincenzo Giuseppe; Attanasio, Francesco; Rizzarelli, Enrico

    2015-01-01

    Heptapeptide Semax, encompassing the sequence 4-7 of N-terminal domain of the adrenocorticotropic hormone (ACTH) and a C-terminal Pro-Gly-Pro tripeptide, belongs to a short regulatory peptides family. This compound has been found to affect learning processes and to exert marked neuroprotective activities on cognitive brain functions. Dys-homeostasis of metal ions is involved in several neurodegenerative disorders and growing evidences have showed that brain is a specialized organ able to concentrate metal ions. In this work, the metal binding ability and protective activity of Semax and its metal complexes were studied. The equilibrium study clearly demonstrated the presence of three complex species. Two minor species [CuL] and [CuLH-1]- co-exist together with the [CuLH-2]2- in the pH range from 3.6 to 5. From pH5 the [CuLH-2]2- species becomes predominant with the donor atoms around copper arranged in a 4N planar coordination mode. Noteworthy, a reduced copper induced cytotoxicity was observed in the presence of Semax by MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assay on a SHSY5Y neuroblastoma and RBE4 endothelial cell lines.

  19. CaMac1, a Candida albicans Copper Ion-sensing Transcription Factor, Pro- motes Filamentous and Invasive Growth in Saccharomyces cerevisiae

    Institute of Scientific and Technical Information of China (English)

    Guang-Hua HUANG; Xin-Yi NIE; Jiang-Ye CHEN

    2006-01-01

    Molecular mechanisms of morphogenesis share many common components between Candida albicans and Saccharomyces cerevisiae. The Kssl-associated MAPK cascade and the cAMP/PKA pathway are two important signal transduction pathways that control morphogenesis in S. cerevisiae. A C. albicans copper ion-sensing transcription factor gene, CaMAC1, was cloned from C. albicans SC5314. Ectopic expression of CaMAC1 in S. cerevisiae promoted filamentous and invasive growth. In diploid cells, CaMacl could suppress the filamentous growth defect of mutants in the Kss 1-associated MAPK pathway and the cAMP/PKA pathway. In haploid strains, ectopic expression of CaMAC1 suppressed the invasive growth defect of mutants in the MAPK pathway (ste7, stel2 and tecl), but failed to suppress the invasive growth defect of thefio8 mutant. Our results suggest that the activation of CaMacl is independent of the MAPK and cAMP/PKA pathways in filament formation, but requires Flo8 factor for invasive growth. In the media containing a high concentration of CuSO4, the yeast filamentous and invasive growth was blocked. The activating effect of CaMacl is inhibited by copper ions.

  20. Preparation of Granulated Adsorption Material of Water-quenched Slag/rectorite Composite for Removal of Cu (Ⅱ) Ions from Copper Smelter Wastewater

    Institute of Scientific and Technical Information of China (English)

    WANG Hukun; GONG Wenqi

    2008-01-01

    The preparation of granulated adsorption material of water-quenched slag/rectorite composite and the treatment of Cu (Ⅱ)-containing copper smelter wastewater with the adsorption material were studied. The experimental results showed that under the conditions with the mass ratio of water-quenched slag to rectorite of 1:1, 10% additive of industrial starch (IS), and 50% water, and a calcination temperature of 400℃, the granulated adsorption material prepared had a density of 1.06kg/m3, a porosity of 62.29%, water absorption rate of 58.82%, and compressive strength of 2.22MPa. The efficiency of wastewater treatment was the best, whereas the rate of spallation loss was low. Under the conditions of natural pH, with the addition of the granulated adsorption material of 0.05g/mL, a reaction time of 40 minutes, and temperature of 25℃, the efficiency of the granulated adsorption material for the removal of Cu (Ⅱ) ions from the copper smelter wastewater attained 98.2%, and the quality indexes of the wastewater after treatment conformed with the first level of integrated wastewater discharge standard (GB8978-1996). The reclamation of the used granulated adsorption material was carried out by de-sorption of the Cu (Ⅱ) ions from the surface with 1mol/L sodium chloride solution. The de-sorption rate was 96.4%, and the adsorption material can be reused many times to treat copper smelter wastewater.

  1. An approach by using near-infrared diffuse reflectance spectroscopy and resin adsorption for the determination of copper, cobalt and nickel ions in dilute solution.

    Science.gov (United States)

    Sheng, Nan; Cai, Wensheng; Shao, Xueguang

    2009-07-15

    Near-infrared spectroscopy (NIRS) has been proved to be a powerful analytical tool and used in various fields, it is seldom, however, used in the analysis of metal ions in solutions. A method for quantitative determination of metal ions in solution is developed by using resin adsorption and near-infrared diffuse reflectance spectroscopy (NIRDRS). The method makes use of the resin adsorption for gathering the analytes from a dilute solution, and then NIRDRS of the adsorbate is measured. Because both the information of the metal ions and their interaction with the functional group of resin can be reflected in the spectrum, quantitative determination is achieved by using multivariate calibration technique. Taking copper (Cu(2+)), cobalt (Co(2+)) and nickel (Ni(2+)) as the analyzing targets and D401 resin as the adsorbent, partial least squares (PLS) model is built from the NIRDRS of the adsorbates. The results show that the concentrations that can be quantitatively detected are as low as 1.00, 1.98 and 1.00 mg L(-1) for Cu(2+), Co(2+) and Ni(2+), respectively, and the coexistent ions do not influence the determination.

  2. Electrochemical detection of copper ions leached from CuO nanoparticles in saline buffers and biological media using a gold wire working electrode

    Science.gov (United States)

    Baldisserri, Carlo; Costa, Anna Luisa

    2016-04-01

    We performed explorative cyclic voltammetry in phosphate-buffered saline buffers, Dulbecco's modified Eagle's medium (DMEM), and fetal bovine serum-added DMEM using Au wire as working electrode, both in the absence and in the presence of known nominal concentrations of Cu2+ ions or 15 nm CuO nanoparticles. Addition of either Cu2+ ions or aqueous suspension of CuO nanoparticles caused a single anodic peak to appear in the double-layer region of all three pristine media. The height of the anodic peak was found to increase in a monotonic fashion vs. Cu2+ concentration in Cu2+-added media, and versus time since CuO addition in CuO-added media. Stepwise addition of glycine to Cu2+-added phosphate-buffered saline buffer caused an increasing cathodic shift of the anodic peak accompanied by decreasing peak currents. Results indicate that preparing Cu2+-free suspensions of CuO nanoparticles in such media is difficult, owing to the presence of leached copper ions. The implications on results of experiments in which CuO nanoparticle-added biological media are used as cell culture substrates are discussed. Literature data on the interactions between Cu2+ ions, dissolved carbon dioxide in aqueous CuO suspensions, and amino acids present in such media are compared to our results.

  3. EVALUATING THE ROLE OF ION COMPOSITION ON THE TOXICITY OF COPPER TO CERIODAPHNIA DUBIA IN VERY HARD WATERS

    Science.gov (United States)

    The mitigating effect of increasing hardness on metal toxicity is reflected in water quality criteria in the United States. - - - Copper toxicity did not consistently vary as a function of hardness, but likely as a function of other water quality characteristics (e.g. alkalinity ...

  4. The removal of toxic metals from liquid effluents by ion exchange resins. Part lll:Copper(ll/Sulphate/Amberlite 200

    Directory of Open Access Journals (Sweden)

    Alguacil, F. J.

    2003-06-01

    Full Text Available Copper(II adsorption from aqueous sulphate media on Amberlite 200 was investigated. The influence of operating variables such as aqueous pH, temperature and copper concentration on the metal adsorption kinetics was measured. The copper{II uptake is best fitted to the film-diffusion controlled process. The resin has been used in minicolumns to investigate its performance under dynamics conditions. Copper(II desorption from the resin is accomplished using sulphuric acid solutions.

    Se estudia la adsorción de cobre(II, de disoluciones en medio sulfato, en la resina Amberlite 200. La cinética de adsorción del metal se ha estudiado en función de una serie de variables experimentales: pH de la fase acuosa, temperatura y concentración del metal en el medio acuoso. La adsorción de cobre(II se puede correlacionar como controlada por un proceso de difusión en capa límite. Se ha utilizado la resina en minicolumnas para estudiar su comportamiento bajo condiciones dinámicas. La desorción del cobre(II se lleva a cabo con disoluciones de ácido sulfúrico.

  5. Application of a metal ion-imprinted polymer based on salen-Cu complex to flow injection preconcentration and FAAS determination of copper.

    Science.gov (United States)

    Walas, Stanisław; Tobiasz, Anna; Gawin, Marta; Trzewik, Bartosz; Strojny, Marcin; Mrowiec, Halina

    2008-06-30

    A new Cu(II)-imprinted polymer (Cu-IIP) for preconcentration of copper by liquid-solid extraction via flow injection technique has been proposed. Cu-IIP was obtained by copolymerization of salen-Cu(II) complex with styrene and divinylbenzene using suspension polymerization technique. Granules fraction of 60-80 microm in diameter was used as a microcolumn packing. Cu(II) sorption was proved to be the most effective from solutions of pH 7, whereas similar elution effectiveness was observed when applying as eluents hydrochloric or nitric acid in the concentration range of 0.5-10% (v/v). The system exhibited good long-term stability and acid resistance. Batch sorbent capacity was found to be 0.11 mmol g(-1) of a dry polymer. Enrichment factor (EF) for 30 s loading time was 16. Preconcentration of Cu(II) and potentially interfering metal ions is strongly pH dependent. Examination of Cu(II) sorption in the presence of Pb(II), Cd(II), Zn(II) and Ag(I) showed significant influence of cadmium and zinc ions only and that was for the interferent concentrations above 0.5 mg L(-1) (Cu-IIP mass of ca. 35 mg). The interference effect was reduced with the sorbent mass increase. Fe(III) and Mn(II) ions, present in treated tap water in relatively high concentrations, did not interfere. Effective pH adjusting of the loaded solution in on-line mode, when applying diluted Clark-Lubs buffering solution, allowed accurate copper determination in tap water (compared to graphite furnace atomic absorption spectrometry, GFAAS) using standard addition or combination calibration method.

  6. Studies on Zinc and Copper Ion in Relation to Wound Healing in Male and Female West African Dwarf Goats.

    Science.gov (United States)

    Olaifa, A K; Fadason, S T

    2017-03-06

    Wound healing remains a challenging clinical problem for which precise and efficient management is essential in order to curtail morbidity and mortality. Wound healing has been shown to depend upon the availability of appropriate trace elements like copper and zinc which serve as enzyme cofactors and structural components in tissue repair. This study aims at evaluating the distribution of zinc and copper found in the hair as well as skin during epidermal wound healing. Adult and healthy West African dwarf (WAD) goats of both sexes fed with concentrate, grass, cassava peel and water ad libitum were used. The animals were housed for three weeks before commencement of the experiments. Epidermal wounds were created on the trunks of all the goats using cardboard template of 1cm². Progressive changes in wound contraction were monitored grossly by placing clean and sterile venier calliper on the wound margin. Hair and skin elemental (copper and zinc) analyses were done using atomic absorption spectroscopy (AAS). Significant increases in Cu level were observed in the female hair compared with that of males. There were significant increases in the Zn levels of the females' hair compared with the males. The wound healed faster in female goat compared with the males. The ratio of copper to zinc is clinically more important than the concentration of either of these trace metals. The pattern of distribution between zinc and copper concentration in the skin and hair of the male and female goats observed in this study could be added factor responsible for early wound healing in female. Therefore, our findings suggest that the distribution in the Cu and Zinc level in skin and hair of both male and female goats could also be a factor for wound healing in the animals.

  7. Biodynamics of copper oxide nanoparticles and copper ions in an oligochaete: Part I: relative importance of water and sediment as exposure routes

    Science.gov (United States)

    Ramskov, Tina; Thit, Amalie; Croteau, Marie-Noele; Selck, Henriette

    2015-01-01

    Copper oxide (CuO) nanoparticles (NPs) are widely used, and likely released into the aquatic environment. Both aqueous (i.e., dissolved Cu) and particulate Cu can be taken up by organisms. However, how exposure routes influence the bioavailability and subsequent toxicity of Cu remains largely unknown. Here, we assess the importance of exposure routes (water and sediment) and Cu forms (aqueous and nanoparticulate) on Cu bioavailability and toxicity to the freshwater oligochaete, Lumbriculus variegatus, a head-down deposit-feeder. We characterize the bioaccumulation dynamics of Cu in L. variegatus across a range of exposure concentrations, covering both realistic and worst-case levels of Cu contamination in the environment. Both aqueous Cu (Cu-Aq; administered as Cu(NO3)2) and nanoparticulate Cu (CuO NPs), whether dispersed in artificial moderately hard freshwater or mixed into sediment, were weakly accumulated by L. variegatus. Once incorporated into tissues, Cu elimination was negligible, i.e., elimination rate constants were in general not different from zero for either exposure route or either Cu form. Toxicity was only observed after waterborne exposure to Cu-Aq at very high concentration (305 µgL-1), where all worms died. There was no relationship between exposure route, Cu form or Cu exposure concentration on either worm survival or growth. Slow feeding rates and low Cu assimilation efficiency (approximately 30%) characterized the uptake of Cu from the sediment for both Cu forms. In nature, L. variegatus is potentially exposed to Cu via both water and sediment. However, sediment progressively becomes the predominant exposure route for Cu in L. variegatus as Cu partitioning to sediment increases.

  8. Biodynamics of copper oxide nanoparticles and copper ions in an oligochaete - Part I: Relative importance of water and sediment as exposure routes.

    Science.gov (United States)

    Ramskov, Tina; Thit, Amalie; Croteau, Marie-Noële; Selck, Henriette

    2015-07-01

    Copper oxide (CuO) nanoparticles (NPs) are widely used, and likely released into the aquatic environment. Both aqueous (i.e., dissolved Cu) and particulate Cu can be taken up by organisms. However, how exposure routes influence the bioavailability and subsequent toxicity of Cu remains largely unknown. Here, we assess the importance of exposure routes (water and sediment) and Cu forms (aqueous and nanoparticulate) on Cu bioavailability and toxicity to the freshwater oligochaete, Lumbriculus variegatus, a head-down deposit-feeder. We characterize the bioaccumulation dynamics of Cu in L. variegatus across a range of exposure concentrations, covering both realistic and worst-case levels of Cu contamination in the environment. Both aqueous Cu (Cu-Aq; administered as Cu(NO3)2) and nanoparticulate Cu (CuO NPs), whether dispersed in artificial moderately hard freshwater or mixed into sediment, were weakly accumulated by L. variegatus. Once incorporated into tissues, Cu elimination was negligible, i.e., elimination rate constants were in general not different from zero for either exposure route or either Cu form. Toxicity was only observed after waterborne exposure to Cu-Aq at very high concentration (305μgL(-1)), where all worms died. There was no relationship between exposure route, Cu form or Cu exposure concentration on either worm survival or growth. Slow feeding rates and low Cu assimilation efficiency (approximately 30%) characterized the uptake of Cu from the sediment for both Cu forms. In nature, L. variegatus is potentially exposed to Cu via both water and sediment. However, sediment progressively becomes the predominant exposure route for Cu in L. variegatus as Cu partitioning to sediment increases. Copyright © 2015 Elsevier B.V. All rights reserved.

  9. Electrochemical in-situ impregnation of wood using a copper nail as source for copper

    DEFF Research Database (Denmark)

    Ottosen, Lisbeth M.; Block, Thomas; Nymark, Morten

    2011-01-01

    A new method for copper impregnation of wood in structures was suggested and tested in laboratory scale with specimen of new pine sapwood. A copper nail and a steel screw were placed in the wood, and an electric direct current field was applied, so the copper nail was anode and the screw...... was cathode. At the anode, copper ions were generated. The copper ions were transported into the wood by electromigration (movement of ions in an applied electric field) towards the cathode, and a volume between the two electrodes was thereby impregnated. Copper also moved to a lesser degree in the opposite...

  10. Adding high time resolution to charge-state-specific ion energy measurements for pulsed copper vacuum arc plasmas

    CERN Document Server

    Tanaka, Koichi; Zhou, Xue; Anders, André

    2015-01-01

    Charge-state-resolved ion energy-time-distributions of pulsed Cu arc plasma were obtained by using direct (time dependent) acquisition of the ion detection signal from a commercial ion mass-per-charge and energy-per-charge analyzer. We find a shift of energies of Cu2+, Cu3+ and Cu4+ ions to lower values during the first few hundred microseconds after arc ignition, which is evidence for particle collisions in the plasma. The generation of Cu1+ ions in the later part of the pulse, measured by the increase of Cu1+ signal intensity and an associated slight reduction of the mean charge state point to charge exchange reactions between ions and neutrals. At the very beginning of the pulse, when the plasma expands into vacuum and the plasma potential strongly fluctuates, ions with much higher energy (over 200 eV) were observed. Early in the pulse, the ion energies observed are approximately proportional to the ion charge state, and we conclude that the acceleration mechanism is primarily based on acceleration in an e...

  11. Preparation of chitosan/poly(acrylic acid) magnetic composite microspheres and applications in the removal of copper(II) ions from aqueous solutions.

    Science.gov (United States)

    Yan, Han; Yang, Lingyun; Yang, Zhen; Yang, Hu; Li, Aimin; Cheng, Rongshi

    2012-08-30

    In this current work, the magnetic composite microspheres (MCM), consisting of Fe(3)O(4) nanoparticles and poly(acrylic acid) (PAA) blended chitosan (CS), were prepared successfully by a simple method, co-precipitation of the compounds in alkaline solution. SEM, FTIR and TG techniques have been applied to investigate the structures of the MCM materials. The vibrating-sample magnetometer (VSM) measurement illustrated a paramagnetic property as well as a fast magnetic response, which indicated the significant separability of the MCM in the aqueous suspensions. Then, the MCM materials were employed as absorbents for removal of copper(II) (Cu(II)) ions from aqueous solutions. The fundamental adsorption behaviors of MCM were studied also. Experimental results revealed that the CS/PAA-MCM had greater adsorption capacity than CS-MCM, and PAA played an important role for the adsorption of Cu(II) ions. Moreover, the adsorption isotherms were all well described by the Langmuir model, while the adsorption kinetics followed the pseudo-second order equation. Furthermore, the adsorbent could be easily regenerated at lower pH and reused almost without any loss of adsorption capacity. On the contrary, the Cu(II) ions loaded CS-MCM and CS/PAA-MCM were stable enough at pH higher than 4.0, and both exhibited efficient phosphate removal with maximal uptakes around 63.0 and 108.0 mg Pg(-1), respectively. Copyright © 2012 Elsevier B.V. All rights reserved.

  12. Biodynamics of copper oxide nanoparticles and copper ions in an oligochaete – Part I: Relative importance of water and sediment as exposure routes

    Energy Technology Data Exchange (ETDEWEB)

    Ramskov, Tina, E-mail: tramskov@hotmail.com [Department of Environmental, Social and Spatial Change, Roskilde University, PO Box 260, Universitetsvej 1, DK-4000 Roskilde (Denmark); US Geological Survey, 345 Middlefield Road, Menlo Park, CA 94025 (United States); Thit, Amalie, E-mail: athitj@ruc.dk [Department of Environmental, Social and Spatial Change, Roskilde University, PO Box 260, Universitetsvej 1, DK-4000 Roskilde (Denmark); Croteau, Marie-Noële, E-mail: mcroteau@usgs.gov [US Geological Survey, 345 Middlefield Road, Menlo Park, CA 94025 (United States); Selck, Henriette, E-mail: selck@ruc.dk [Department of Environmental, Social and Spatial Change, Roskilde University, PO Box 260, Universitetsvej 1, DK-4000 Roskilde (Denmark); US Geological Survey, 345 Middlefield Road, Menlo Park, CA 94025 (United States)

    2015-07-15

    Highlights: • Both aqueous and nanoparticulate Cu forms are available for uptake by L. variegatus. • Cu accumulation is driven by both water and sediment uptake. • Cu form weakly influences Cu biodynamics in L. variegatus. • Food ingestion rate is a sensitive endpoint for dietborne Cu exposure. • Stable isotope tracers allow detecting accumulation after environmentally relevant exposures. - Abstract: Copper oxide (CuO) nanoparticles (NPs) are widely used, and likely released into the aquatic environment. Both aqueous (i.e., dissolved Cu) and particulate Cu can be taken up by organisms. However, how exposure routes influence the bioavailability and subsequent toxicity of Cu remains largely unknown. Here, we assess the importance of exposure routes (water and sediment) and Cu forms (aqueous and nanoparticulate) on Cu bioavailability and toxicity to the freshwater oligochaete, Lumbriculus variegatus, a head-down deposit-feeder. We characterize the bioaccumulation dynamics of Cu in L. variegatus across a range of exposure concentrations, covering both realistic and worst-case levels of Cu contamination in the environment. Both aqueous Cu (Cu-Aq; administered as Cu(NO{sub 3}){sub 2}) and nanoparticulate Cu (CuO NPs), whether dispersed in artificial moderately hard freshwater or mixed into sediment, were weakly accumulated by L. variegatus. Once incorporated into tissues, Cu elimination was negligible, i.e., elimination rate constants were in general not different from zero for either exposure route or either Cu form. Toxicity was only observed after waterborne exposure to Cu-Aq at very high concentration (305 μg L{sup −1}), where all worms died. There was no relationship between exposure route, Cu form or Cu exposure concentration on either worm survival or growth. Slow feeding rates and low Cu assimilation efficiency (approximately 30%) characterized the uptake of Cu from the sediment for both Cu forms. In nature, L. variegatus is potentially exposed to Cu

  13. New Insight in Copper-Ion Binding to Human Islet Amyloid: The Contribution of Metal-Complex Speciation To Reveal the Polypeptide Toxicity.

    Science.gov (United States)

    Magrì, Antonio; La Mendola, Diego; Nicoletti, Vincenzo Giuseppe; Pappalardo, Giuseppe; Rizzarelli, Enrico

    2016-09-05

    Type-2 diabetes (T2D) is considered to be a potential threat on a global level. Recently, T2D has been listed as a misfolding disease, such as Alzheimer's and Parkinson's diseases. Human islet amyloid polypeptide (hIAPP) is a molecule cosecreted in pancreatic β cells and represents the main constituent of an aggregated amyloid found in individuals affected by T2D. The trace-element serum level is significantly influenced during the development of diabetes. In particular, the dys-homeostasis of Cu(2+) ions may adversely affect the course of the disease. Conflicting results have been reported on the protective role played by complex species formed by Cu(2+) ions with hIAPP or its peptide fragments in vitro. The histidine (His) residue at position 18 represents the main binding site for the metal ion, but contrasting results have been reported on other residues involved in metal-ion coordination, in particular those toward the N or C terminus. Sequences that encompass regions 17-29 and 14-22 were used to discriminate between the two models of the hIAPP coordination mode. Due to poor solubility in water, poly(ethylene glycol) (PEG) derivatives were synthesized. A peptide fragment that encompasses the 17-29 region of rat amylin (rIAPP) in which the arginine residue at position 18 was substituted by a histidine residue was also obtained to assess that the PEG moiety does not alter the peptide secondary structure. The complex species formed by Cu(2+) ions with Ac-PEG-hIAPP(17-29)-NH2 , Ac-rIAPP(17-29)R18H-NH2 , and Ac-PEG-hIAPP(14-22)-NH2 were studied by using potentiometric titrations coupled with spectroscopic methods (UV/Vis, circular dichroism, and EPR). The combined thermodynamic and spectroscopic approach allowed us to demonstrate that hIAPP is able to bind Cu(2+) ions starting from the His18 imidazole nitrogen atom toward the N-terminus domain. The stability constants of copper(II) complexes with Ac-PEG-hIAPP(14-22)-NH2 were used to simulate the different

  14. A Novel n-Type Organosilane-Metal Ion Hybrid of Rhodamine B and Copper Cation for Low-Temperature Thermoelectric Materials.

    Science.gov (United States)

    Bertram, John R; Penn, Aubrey; Nee, Matthew J; Rathnayake, Hemali

    2017-03-29

    An n-type organosilane-metal ion hybrid of Rhodamine B-silane and copper cation (Cu-RBS) was investigated as a low-temperature thermoelectric material. Computational analysis revealed the most likely localized binding site of Cu(2+) was to the Rhodamine B core and provided predictions of molecular orbitals and electrostatic potentials upon complexation. The concentration-dependent optical absorption and emission spectra confirmed the effective metal-ligand charge transfer from Cu(2+) to the xanthene core of RBS, indicating the potential for improved electrical properties for the complex relative to RBS. The electrical conductivity and Seebeck thermoelectric (TE) behavior were evaluated and compared with its precursor complex of Rhodamine B and copper cation. While a moderately high electrical conductivity of 4.38 S m(-1) was obtained for the Cu-RBS complex, the relatively low Seebeck coefficient of -26.2 μV/K resulted in a low TE power factor. However, compared to other organic doped materials, these results were promising toward developing n-type thermoelectric materials with no doping agents. Both phase segregation and thin film heterogeneity remain to be optimized; thus, the balance between Cu(2+) domains and RBS domain phases will likely yield higher Seebeck coefficients and improved power factors.

  15. Application of artificial neural network to simultaneous potentiometric determination of silver(I), mercury(II) and copper(II) ions by an unmodified carbon paste electrode.

    Science.gov (United States)

    Shamsipur, Mojtaba; Tashkhourian, Javad; Hemmateenejad, Bahram; Sharghi, Hashem

    2004-10-20

    The response characteristics and selectivity coefficients of an unmodified carbon paste electrode (CPEs) towards Ag(+), Cu(2+) and Hg(2+) were evaluated. The electrode was used as an indicator electrode for the simultaneous determination of the three metal ions in their mixtures via potentiometric titration with a standard thiocyanate solution. A three-layered feed-forward artificial neural network (ANN) trained by back-propagation learning algorithm was used to model the complex non-linear relationship between the concentration of silver, copper and mercury in their different mixtures and the potential of solution at different volumes of the added titrant. The network architecture and parameters were optimized to give low prediction errors. The optimized networks were able to precisely predict the concentrations of the three cations in synthetic mixtures.

  16. Copper Silicate Hydrate Hollow Spheres Constructed by Nanotubes Encapsulated in Reduced Graphene Oxide as Long-Life Lithium-Ion Battery Anode.

    Science.gov (United States)

    Wei, Xiujuan; Tang, Chunjuan; Wang, Xuanpeng; Zhou, Liang; Wei, Qiulong; Yan, Mengyu; Sheng, Jinzhi; Hu, Ping; Wang, Bolun; Mai, Liqiang

    2015-12-09

    Hierarchical copper silicate hydrate hollow spheres-reduced graphene oxide (RGO) composite is successfully fabricated by a facile hydrothermal method using silica as in situ sacrificing template. The electrochemical performance of the composite as lithium-ion battery anode was studied for the first time. Benefiting from the synergistic effect of the hierarchical hollow structure and conductive RGO matrix, the composite exhibits excellent long-life performance and rate capability. A capacity of 890 mAh/g is achieved after 200 cycles at 200 mA/g and a capacity of 429 mAh/g is retained after 800 cycles at 1000 mA/g. The results indicate that the strategy of combining hierarchical hollow structures with conductive RGO holds the potential in addressing the volume expansion issue of high capacity anode materials.

  17. Effect of organic complexation on copper accumulation and toxicity to the estuarine red macroalga Ceramium tenuicorne: a test of the free ion activity model.

    Science.gov (United States)

    Ytreberg, Erik; Karlsson, Jenny; Hoppe, Sabina; Eklund, Britta; Ndungu, Kuria

    2011-04-01

    Current water quality criteria (WQC) regulations on copper toxicity to biota are still based on total dissolved (MINTEQ incorporating the Stockholm Humic Model) show that copper accumulation in C. tenuicorne only correlates linearly well to [Cu2+] at relatively high [Cu2+] and in the absence of fulvic acid. Thus the FIAM fails to describe copper accumulation in C. tenuicorne at copper and DOC concentrations typical of most marine waters. These results seem to indicate that at ambient total dissolved copper concentration in coastal and estuarine waters, C. tenuicorne might be able to access a sizable fraction of organically complexed copper when free copper concentration to the cell membrane is diffusion limited.

  18. Copper(II)-mediated thermolysis of alginates: a model kinetic study on the influence of metal ions in the thermochemical processing of macroalgae.

    Science.gov (United States)

    Rowbotham, J S; Dyer, P W; Greenwell, H C; Selby, D; Theodorou, M K

    2013-02-06

    Thermochemical processing methods such as pyrolysis are of growing interest as a means of converting biomass into fuels and commodity chemicals in a sustainable manner. Macroalgae, or seaweed, represent a novel class of feedstock for pyrolysis that, owing to the nature of the environments in which they grow coupled with their biochemistry, naturally possess high metal contents. Although the impact of metals upon the pyrolysis of terrestrial biomass is well documented, their influence on the thermochemical conversion of marine-derived feeds is largely unknown. Furthermore, these effects are inherently difficult to study, owing to the heterogeneous character of natural seaweed samples. The work described in this paper uses copper(II) alginate, together with alginic acid and sodium alginate as model compounds for exploring the effects of metals upon macroalgae thermolysis. A thermogravimetric analysis-Fourier transform infrared spectroscopic study revealed that, unusually, Cu(2+) ions promote the onset of pyrolysis in the alginate polymer, with copper(II) alginate initiating rapid devolatilization at 143°C, 14°C lower than alginic acid and 61°C below the equivalent point for sodium alginate. Moreover, this effect was mirrored in a sample of wild Laminaria digitata that had been doped with Cu(2+) ions prior to pyrolysis, thus validating the use of alginates as model compounds with which to study the thermolysis of macroalgae. These observations indicate the varying impact of different metal species on thermochemical behaviour of seaweeds and offer an insight into the pyrolysis of brown macroalgae used in phytoremediation of metal-containing waste streams.

  19. Synthesis and application of ion-imprinted polymer nanoparticles for the extraction and preconcentration of copper ions in environmental water samples.

    Science.gov (United States)

    Roushani, Mahmoud; Abbasi, Shahryar; Khani, Hossein

    2015-04-01

    Novel Cu(II) ion-imprinted polymers (Cu-IIP) nanoparticles were prepared by using Cu(II) ion-thiosemicarbazide complex as the template molecule and methacrylic acid, ethylene glycol dimethacrylate (EGDMA), and 2,2'azobisisobutyronitrile (AIBN) as the functional monomer, cross-linker, and the radical initiator, respectively. The synthesized polymer nanoparticles were characterized by using infrared spectroscopy (IR), thermo gravimetric analysis (TGA), X-ray diffraction (XRD), and scanning electron microscopic (SEM) techniques. Some parameters such as pH, weight of the polymer, adsorption time, elution time, eluent type, and eluent volume which affect the extraction efficiency of the polymer were studied. In the proposed method, the maximum sorbent capacity of the ion-imprinted polymer was calculated to be 38.8 mg g(-1). The preconcentration factor, relative standard deviation, and limit of detection of the method were found to be 80, 1.7%, and 0.003 μg mL(-1), respectively. The prepared ion-imprinted polymer nanoparticles have an increased selectivity toward Cu(II) ions over a range of competing metal ions with the same charge and similar ionic radius. The method was applied to the determination of ultra trace levels of Cu2+ in environmental water samples with satisfactory results.

  20. Micelles entrapped Cresyl Violet can selectively detect copper and mercury ions in solution: A fluorescence Correlation Spectroscopy investigation

    Science.gov (United States)

    Das, Nirmal Kumar; Ghosh, Subhadip; Jaiswal, Sunidhi; Tewary, Anu; Mukherjee, Saptarshi

    2017-08-01

    The dynamic interaction of Cresyl Violet (CV) in different micellar systems has been demonstrated in single molecular level by FCS studies. The SDS micelle entrapped CV efficiently detected Cu2+ ions in solution with a limit of detection (LOD) of 70 nM, which is further substantiated with the gradual enhancement of the translational motion. The CV entrapped in the DTAB micelles could selectively detect Hg2+ ions in solution with a LOD of 35 nM. The micelle encapsulated CV was effective in detecting these metal ions in real water samples from different sources.

  1. Free Cu2+ Ions, Cu Fractionation and Microbial Parameters in Soils from Apple Orchards Following Long-Term Application of Copper Fungicides

    Institute of Scientific and Technical Information of China (English)

    ZHOU Dong-Mei; WANG Quan-Ying; CANG Long

    2011-01-01

    Soil samples were collected from apple orchards 5, 15, 20, 30, and 45 years old, and one adjacent forest soil was used as reference to investigate the free Cu2+ ion activity in soil solution and the soil Cu fractionation in the solid phase following long-term application of copper fungicide, Bordeaux mixture, in apple orchards and to investigate the relationships among soil free Cu2+ ions, Cu fractionation and soil microbial parameters. The total Cu concentration in the orchard soils varied from 21.8 to 141 mg kg-l, increasing with the orchard age, and the value for the reference soil was 12.5 mg kg-1. The free Cu2+ ion concentrations in the soil solutions extracted by 0.01 mol L-1 KNO3 ranged from 3.13 × 10-8 (reference) to 4.08 × 10-6 mol L-1 (45 years-old orchard). The concentration of Cu complexed in the fulvic fraction increased with orchard age from 5.16 to 52.5 mg kg-1. This was also the case for other soil Cu fractions except the residual one. The residual soil Cu remained practically constant, ranging from 4.28 to 5.66 mg kg-1, suggesting that anthropogenic soil Cu mainly existed in the more labile active fractions. Regression analyses revealed that both the free Cu2+ ions in the soil solution and the humic acid-complexed Cu fraction in the solid phase were strongly related with soil microbial parameters.

  2. Condition Monitoring of Corrosive Sulfur Reaction in Transformer by Copper Ion Analysis%利用铜离子质量分数监测变压器中硫腐蚀状态的研究

    Institute of Scientific and Technical Information of China (English)

    万涛; 钱晖; 冯兵; 周舟; 龚尚昆

    2013-01-01

    In order to investigate monitoring methods of sulfur corrosion in transformer,the copper content in oil and the sulfur-corrosion test results of 40 operating transformers were compared.Moreover,dynamic copper strip corrosion was tested by simulation in transformer oil samples filled with nitrogen,air and oxygen,respectively,and the change of copper content in oil and copper sulfide on copper strip and the influence of oxygen in the corrosion process were determined.The results showed that the consistency between the copper content tests and the corrosive sulfur tests exceeded 70%.The amounts of copper ion in oil and cuprous sulfide on copper strip both increased while the corrosion developed,indicating that copper corrosion of a transformer could be effectively monitored through copper content analysis.Meanwhile,corrosive sulfur tests could accurately reflect the accumulation of cuprous sulfide on copper strip from the color of copper strip.In the absence of oxygen,the main copper corrosion process should be copper→copper complex ion→cuprous sulfide,and the oxygen-contained copper corrosion process includes both copper→ copper oxide→copper complex ion→cuprous sulfide and copper→copper complex ion→cuprous sulfide.%为了研究变压器中硫腐蚀作用的监测方法,考察了40台运行变压器油中铜离子质量分数与腐蚀性硫测试结果的关系.将变压器油样品充入氮气、空气和氧气条件下进行了腐蚀过程动态模拟试验,确定了铜腐蚀过程中油中铜离子和铜片表面元素含量变化的规律和氧气含量的影响.结果表明,铜离子质量分数检测与腐蚀性硫试验一致性>70%,油中铜离子和铜片表面硫化亚铜离子质量分数随腐蚀过程不断增加,通过铜离子质量分数检测能够有效监测变压器铜腐蚀状态;腐蚀性硫试验中铜片颜色能够准确反映硫化亚铜离子质量分数变化.不含氧气时,铜的腐蚀过程主

  3. New dinuclear copper(II) and zinc(II) complexes for the investigation of sugar-metal ion interactions.

    Science.gov (United States)

    Bera, Manindranath; Patra, Ayan

    2011-10-18

    We have studied the binding interactions of biologically important carbohydrates (D-glucose, D-xylose and D-mannose) with the newly synthesized five-coordinate dinuclear copper(II) complex, [Cu(2)(hpnbpda)(μ-OAc)] (1) and zinc(II) complex, [Zn(2)(hpnbpda)(μ-OAc)] (2) [H(3)hpnbpda=N,N'-bis(2-pyridylmethyl)-2-hydroxy-1,3-propanediamine-N,N'-diacetic acid] in aqueous alkaline solution. The complexes 1 and 2 are fully characterized both in solid and solution using different analytical techniques. A geometrical optimization was made of the ligand H(3)hpnbpda and the complexes 1 and 2 by molecular mechanics (MM+) method in order to establish the stable conformations. All carbohydrates bind to the metal complexes in a 1:1 molar ratio. The binding events have been investigated by a combined approach of FTIR, UV-vis and (13)C NMR spectroscopic techniques. UV-vis spectra indicate a significant blue shift of the absorption maximum of complex 1 during carbohydrate coordination highlighting the sugar binding ability of complex 1. The apparent binding constants of the substrate-bound copper(II) complexes have been determined from the UV-vis titration experiments. The binding ability and mode of binding of these sugar substrates with complex 2 are indicated by their characteristic coordination induced shift (CIS) values in (13)C NMR spectra for carbon atoms C1, C2, and C3 of sugar substrates.

  4. Application of L-Aspartic Acid-Capped ZnS:Mn Colloidal Nanocrystals as a Photosensor for the Detection of Copper (II Ions in Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Jungho Heo

    2016-04-01

    Full Text Available Water-dispersible ZnS:Mn nanocrystals (NCs were synthesized by capping the surface with polar L-aspartic acid (Asp molecules. The obtained ZnS:Mn-Asp NC product was optically and physically characterized using the corresponding spectroscopic methods. The ultra violet-visible (UV-VIS absorption spectrum and photoluminescence (PL emission spectrum of the NCs showed broad peaks at 320 and 590 nm, respectively. The average particle size measured from the obtained high resolution-transmission electron microscopy (HR-TEM image was 5.25 nm, which was also in accordance with the Debye-Scherrer calculations using the X-ray diffraction (XRD data. Moreover, the surface charge and degree of aggregation of the ZnS:Mn-Asp NCs were determined by electrophoretic and hydrodynamic light scattering methods, respectively. These results indicated the formation of agglomerates in water with an average size of 19.8 nm, and a negative surface charge (−4.58 mV in water at ambient temperature. The negatively-charged NCs were applied as a photosensor for the detection of specific cations in aqueous solution. Accordingly, the ZnS:Mn-Asp NCs showed an exclusive luminescence quenching upon addition of copper (II cations. The kinetic mechanism study on the luminescence quenching of the NCs by the addition of the Cu2+ ions proposed an energy transfer through the ionic binding between the two oppositely-charged ZnS:Mn-Asp NCs and Cu2+ ions.

  5. Upon exposure to Cu nanoparticles, accumulation of copper in the isopod Porcellio scaber is due to the dissolved Cu ions inside the digestive tract.

    Science.gov (United States)

    Golobič, Miha; Jemec, Anita; Drobne, Damjana; Romih, Tea; Kasemets, Kaja; Kahru, Anne

    2012-11-06

    The fate of nanoparticles in organisms is of significant interest. In the current work, we used a test system with terrestrial isopods (Porcellio scaber) fed with food spiked with Cu NPs or soluble Cu salt for 14 days. Two different doses were used for spiking to yield final concentrations of 2000 and 5000 μg Cu/g dry food. After the exposure period, part of the exposed group of animals was transferred to clean food to depurate. Cu content was analyzed in the digestive glands, gut, and the 'rest' of the body. Similar patterns of (i) assimilated and depurated amounts of Cu, (ii) Cu body distribution, and (iii) effect on isopods feeding behavior were observed regardless of whether the animals were fed with Cu NPs or soluble Cu salt spiked food. Thus, Cu ions and not Cu NPs were assimilated by the digestive gland cells. Solubilization of the Cu NPs applied to the leaves was also analyzed with chemical methods and recombinant Cu-sensing bacteria. The comparison of the in vitro data on solubilization of Cu NPs and in vivo data on Cu accumulation in the animal tissues showed that about 99% of accumulated copper ions was dissolved from ingested Cu NPs in the digestive system of isopods.

  6. One-pot fabrication of FRET-based fluorescent probe for detecting copper ion and sulfide anion in 100% aqueous media

    Science.gov (United States)

    Lv, Kun; Chen, Jian; Wang, Hong; Zhang, Peisheng; Yu, Maolin; Long, Yunfei; Yi, Pinggui

    2017-04-01

    The design of effective tools for detecting copper ion (Cu2 +) and sulfide anion (S2 -) is of great importance due to the abnormal level of Cu2 + and S2 - has been associated with an increase in risk of many diseases. Herein, we report on the fabrication of fluorescence resonance energy transfer (FRET) based fluorescent probe PF (PEI-FITC) for detecting Cu2 + and S2 - in 100% aqueous media via a facile one-pot method by covalent linking fluorescein isothiocyanate (FITC) with branched-polyethylenimine (b-PEI). PF could selectively coordinate with Cu2 + among 10 metal ions to form PF-Cu2 + complex, resulting in fluorescence quenching through FRET mechanism. Furthermore, the in situ generated PF-Cu2 + complex can be used to selectively detect S2 - based on the displacement approach, resulting in an off-on type sensing. There is no obvious interference from other anions, such as Cl-, NO3-, ClO4-, SO42 -, HCO3-, CO32 -, Br-, HPO42 -, F- and S2O32 -. In addition, PF was successfully used to determine Cu2 + and S2 - in human serum and tap water samples. Therefore, the FRET-based probe PF may provide a new method for selective detection of multifarious analysts in biological and environmental applications, and even hold promise for application in more complicated systems.

  7. Insight into the electroreduction of nitrate ions at a copper electrode, in neutral solution, after determination of their diffusion coefficient by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Aouina, Nizar; Cachet, Hubert [Laboratoire Interfaces et Systemes Electrochimiques - UPR15 du CNRS, Universite Pierre et Marie Curie - Paris 6, 4, place Jussieu, F-75005 Paris (France); Debiemme-chouvy, Catherine, E-mail: catherine.debiemme-chouvy@upmc.f [Laboratoire Interfaces et Systemes Electrochimiques - UPR15 du CNRS, Universite Pierre et Marie Curie - Paris 6, 4, place Jussieu, F-75005 Paris (France); Tran, Thi Tuyet Mai [Laboratoire Interfaces et Systemes Electrochimiques - UPR15 du CNRS, Universite Pierre et Marie Curie - Paris 6, 4, place Jussieu, F-75005 Paris (France)

    2010-10-01

    The electrochemical reduction of nitrate ions at a copper electrode in an unbuffered neutral aqueous solution is studied. Using a two compartment electrochemical cell, three stationary cathodic waves, noted P1, P2 and P3, were evidenced by cyclic voltammetry at -0.9, -1.2 and -1.3 V/SCE, respectively. By comparing the electrochemical response of nitrate and nitrite containing solutions, P1 was attributed to the reduction of nitrate to nitrite. In order to assign P2 and P3 features by determining the number of electrons involved at the corresponding potential, rotating disk electrode experiments at various rotation speeds, combined with linear sweep voltammetry, were performed. Current data analysis at a given potential was carried out using Koutecky-Levich treatment taking into account water reduction. Confident values of the diffusion coefficient D of nitrate ions were assessed by electrochemical impedance spectroscopy for nitrate concentrations of 10{sup -3}, 10{sup -2} and 10{sup -1} M. For a nitrate concentration of 10{sup -2} M, D was found to be 1.31 x 10{sup -5} cm{sup 2} s{sup -1} allowing the number of electrons to be determined as 6 for P2 and 8 for P3, in accordance with nitrate reduction into hydroxylamine and ammonia, respectively. The formation of hydroxylamine was confirmed by the observation of its reoxidation at a Pt microelectrode present at the Cu electrode/nitrate solution interface.

  8. Adsorption of divalent copper, zinc, cadmium and lead ions from aqueous solution by waste tea and coffee adsorbents.

    Science.gov (United States)

    Djati Utomo, H; Hunter, K A

    2006-01-01

    The adsorption of the divalent cations of Cu, Zn, Cd and Pb by tea leaves and coffee grounds from aqueous solutions is described. Both adsorbents exhibited strong affinity for these ions which could be described by a simple single-site equilibrium model. For coffee, the order of increasing adsorption equilibrium constant K was Cu 10, probably because of anion formation in the case of Zn2+ and also increased leaching of metal-binding soluble materials. The effect of metal ion concentration on the adsorptive equilibria indicated a threshold concentration above which overall adsorption became limited by saturation of the adsorption sites. Competition between two metal ions for the same sites was not observed with Cu(II) and Pb(II), however Zn(II) reacted competitively with Cd(II) binding sites on both tea and coffee. If fresh coffee or tea adsorbents were used, the fraction of metal ion taken up by the adsorbent was diminished by the competitive effects of soluble metal-binding ligands released by the tea or coffee. Experiments with coffee showed that roasting temperature controls the formation of metal ion adsorption sites for this adsorbent.

  9. Adsorption of copper (II), chromium (III), nickel (II) and lead (II) ions from aqueous solutions by meranti sawdust.

    Science.gov (United States)

    Rafatullah, M; Sulaiman, O; Hashim, R; Ahmad, A

    2009-10-30

    The present study proposed the use of meranti sawdust in the removal of Cu(II), Cr(III), Ni(II) and Pb(II) ions from synthetic aqueous solutions. Batch adsorption studies showed that meranti sawdust was able to adsorb Cu(II), Cr(III), Ni(II) and Pb(II) ions from aqueous solutions in the concentration range 1-200mg/L. The adsorption was favoured with maximum adsorption at pH 6, whereas the adsorption starts at pH 1 for all metal ions. The effects of contact time, initial concentration of metal ions, adsorbent dosage and temperature have been reported. The applicability of Langmuir, Freundlich, and Dubinin-Radushkevich (D-R) isotherm was tried for the system to completely understand the adsorption isotherm processes. The adsorption kinetics tested with pseudo-first-order and pseudo-second-order models yielded high R(2) values from 0.850 to 0.932 and from 0.991 to 0.999, respectively. The meranti sawdust was found to be cost effective and has good efficiency to remove these toxic metal ions from aqueous solution.

  10. The sorption of lead, cadmium, copper and zinc ions from aqueous solutions on a raw diatomite from Algeria.

    Science.gov (United States)

    Safa, Messaouda; Larouci, Mohammed; Meddah, Boumediene; Valemens, Pierre

    2012-01-01

    The adsorption of Cu(2+), Zn(2+), Cd(2+) and Pb(2+) ions from aqueous solution by Algerian raw diatomite was studied. The influences of different sorption parameters such as contact pH solution, contact time and initial metal ions concentration were studied to optimize the reaction conditions. The metals ions adsorption was strictly pH dependent. The maximum adsorption capacities towards Cu(2+), Zn(2+), Cd(2+) and Pb(2+) were 0.319, 0.311, 0.18 and 0.096 mmol g(-1), respectively. The kinetic data were modelled using the pseudo-first-order and pseudo-second-order kinetic equations. Among the kinetic models studied, the pseudo-second-order equation was the best applicable model to describe the sorption process. Equilibrium isotherm data were analysed using the Langmuir and the Freundlich isotherms; the results showed that the adsorption equilibrium was well described by both model isotherms. The negative value of free energy change ΔG indicates feasible and spontaneous adsorption of four metal ions on raw diatomite. According to these results, the high exchange capacities of different metal ions at high and low concentration levels, and given the low cost of the investigated adsorbent in this work, Algerian diatomite was considered to be an excellent adsorbent.

  11. mRNA Expression and activity of ion-transporting proteins in gills of the blue crab Callinectes sapidus: effects of waterborne copper.

    Science.gov (United States)

    Martins, Camila M G; Almeida, Daniela Volcan; Marins, Luis Fernando Fernandes; Bianchini, Adalto

    2011-01-01

    Waterborne Cu effects on the transcription of genes encoding ion-transporting proteins and the activities of these proteins were evaluated in gills of the blue crab Callinectes sapidus acclimated to diluted (2‰) and full (30‰) seawater. Crabs were exposed (96 h) to an environmentally relevant concentration of dissolved Cu (0.78 µM) and had their posterior (osmoregulating) gills dissected for enzymatic and molecular analysis. Endpoints analyzed were the activity of key enzymes involved in crab osmoregulation (sodium-potassium adenosine triphosphatase [Na(+)/K(+)-ATPase], hydrogen adenosine triphosphatase [H(+)-ATPase], and carbonic anhydrase [CA]) and the mRNA expression of genes encoding these enzymes and the sodium-potassium-chloride (Na(+)/K(+)/2Cl⁻) cotransporter. Copper effects were observed only in crabs acclimated to diluted seawater (hyperosmoregulating crabs) and were associated with an inhibition of the expression of mRNA of genes encoding the Na(+)/K(+)-ATPase and the Na(+)/K(+)/2Cl⁻ cotransporter. However, Cu did not affect Na(+)/K(+)-ATPase activity, indicating that the gene transcription is downregulated before a significant inhibition of the enzyme activity can be observed. This also suggests the existence of a compensatory response of this enzyme to prevent osmoregulatory disturbances after short-term exposure to environmentally relevant Cu concentrations. These findings suggest that Cu is a potential ionoregulatory toxicant in blue crabs C. sapidus acclimated to low salinity. The lack of Cu effect on blue crabs acclimated to full seawater would be due to the reduced ion uptake needed for the regulation of the hemolymph osmotic concentration in full seawater (30‰). Also, this could be explained considering the lower bioavailability of toxic Cu (free ion) associated with the higher ionic content and dissolved organic matter concentration in high salinity (30‰) than in diluted seawater (2‰). © 2010 SETAC.

  12. Target-Triggered Switching on and off the Luminescence of Lanthanide Coordination Polymer Nanoparticles for Selective and Sensitive Sensing of Copper Ions in Rat Brain.

    Science.gov (United States)

    Huang, Pengcheng; Wu, Fangying; Mao, Lanqun

    2015-07-01

    Copper ions (Cu(2+)) in the central nervous system play a crucial role in the physiological and pathological events, so simple, selective, and sensitive detection of cerebral Cu(2+) is of great importance. In this work, we report a facile yet effective fluorescent method for sensing of Cu(2+) in rat brain using one kind of lanthanide coordination polymer nanoparticle, adenosine monophosphate (AMP) and terbium ion (Tb(3+)), i.e., AMP-Tb, as the sensing platform. Initially, a cofactor ligand, 5-sulfosalicylic acid (SSA), as the sensitizer, was introduced into the nonluminescent AMP-Tb suspension, resulting in switching on the luminescence of AMP-Tb by the removal of coordinating water molecules and concomitant energy transfer from SSA to Tb(3+). The subsequent addition of Cu(2+) into the resulting SSA/AMP-Tb can strongly quench the fluorescence because the specific coordination interaction between SSA and Cu(2+) rendered energy transfer from SSA to Tb(3+) inefficient. The decrease ratio of the fluorescence intensities of SSA/AMP-Tb at 550 nm show a linear relationship for Cu(2+) within the concentration range from 1.5 to 24 μM with a detection limit of 300 nM. The method demonstrated here is highly selective and is free from the interference of metal ions, amino acids, and the biological species commonly existing in the brain such as dopamine, lactate, and glucose. Eventually, by combining the microdialysis technique, the present method has been successfully applied in the detection of cerebral Cu(2+) in rat brain with the basal dialysate level of 1.91 ± 0.40 μM (n = 3). This method is very promising to be used for investigating the physiological and pathological events that cerebral Cu(2+) participates in.

  13. New hybrid nanocomposite of copper terephthalate MOF-graphene oxide: synthesis, characterization and application as adsorbents for toxic metal ion removal from Sungun acid mine drainage.

    Science.gov (United States)

    Rahimi, Esmaeil; Mohaghegh, Neda

    2017-08-11

    The application of a hybrid Cu(tpa).GO (Cu(tpa) copper terephthalate metal organic framework, GO graphene oxide) composite as a new adsorbent for the removal of toxic metal ions was reported. New hybrid nanocomposite with excellent dispersibility and stability was successfully fabricated by the simple and effective ultrasonication method. The synthesized composite was characterized by scanning electron microscopy (SEM), UV-Vis and Fourier-transform infrared (FT-IR) techniques. The characterization results concluded that the binding mechanism of the Cu(tpa) and GO was related to both π-π packing and hydrogen bonding. For scrutinizing the sorption activity, the prepared adsorbents were assessed for the removal of Mn(2+), Cu(2+), Zn(2+), Cd(2+), Pb(2+) and Fe(3+) metal ions from aqueous synthetic solution and also acid mine drainage (AMD) wastewater. The sorption experiments demonstrated that the removal efficiency was significantly improved by modified hybrid Cu(tpa).GO composite, owing to the significant number of active binding sites and unique structure formed based on π-conjugated networks. Also, it was shown that the adsorption reaction was mainly attributed to the chemical interactions between metal ions and the surface functional groups. Moreover, kinetic and adsorption studies clarified that the adsorption process onto the Cu(tpa).GO follows a pseudo-second-order kinetics and fits the Langmuir and Freundlich adsorption models. Holistically, the results of this research represent that applying Cu(tpa).GO can be remarked as an effective adsorbent with high possibility at conventional water treatment.

  14. Impact of manganese, copper and zinc ions on the transcriptome of the nosocomial pathogen Enterococcus faecalis V583

    NARCIS (Netherlands)

    Abrantes, Marta Coelho; Lopes, Maria de Fátima; Kok, Jan

    2011-01-01

    Mechanisms that enable Enterococcus to cope with different environmental stresses and their contribution to the switch from commensalism to pathogenicity of this organism are still poorly understood. Maintenance of intracellular homeostasis of metal ions is crucial for survival of these bacteria. In

  15. Detection of Copper(II) Ions Using Glycine on Hydrazine-Adsorbed Gold Nanoparticles via Raman Spectroscopy

    Science.gov (United States)

    Ly, Nguyễn Hoàng; Seo, Chulhun; Joo, Sang-Woo

    2016-01-01

    A facile, selective, and sensitive detection method for the Cu2+ ions in environmental and biological solutions has been newly developed by observing the unique CN stretching peaks at ~2108 cm−1 upon the dissociative adsorption of glycine (GLY) in hydrazine buffer on gold nanoparticles (AuNPs). The relative abundance of Cu species on AuNPs was identified from X-ray photoelectron spectroscopy analysis. UV-Vis spectra also indicated that the Au particles aggregated to result in the color change owing to the destabilization induced by the GLY-Cu2+ complex. The CN stretching band at ~2108 cm−1 could be observed to indicate the formation of the CN species from GLY on the hydrazine-covered AuNP surfaces. The other ions of Fe3+, Fe2+, Hg2+, Mg2+, Mn2+, Ni2+, Zn2+, Cr3+, Co2+, Cd2+, Pb2+, Ca2+, NH4+, Na+, and K+ at high concentrations of 50 µM did not produce such spectral changes. The detection limit based on the CN band for the determination of the Cu2+ ion could be estimated to be as low as 500 nM in distilled water and 1 µM in river water, respectively. We attempted to apply our method to estimate intracellular ion detection in cancer cells for more practical purposes. PMID:27792178

  16. Integrated Solid/Nanoporous Copper/Oxide Hybrid Bulk Electrodes for High-performance Lithium-Ion Batteries

    Science.gov (United States)

    Hou, Chao; Lang, Xing-You; Han, Gao-Feng; Li, Ying-Qi; Zhao, Lei; Wen, Zi; Zhu, Yong-Fu; Zhao, Ming; Li, Jian-Chen; Lian, Jian-She; Jiang, Qing

    2013-01-01

    Nanoarchitectured electroactive materials can boost rates of Li insertion/extraction, showing genuine potential to increase power output of Li-ion batteries. However, electrodes assembled with low-dimensional nanostructured transition metal oxides by conventional approach suffer from dramatic reductions in energy capacities owing to sluggish ion and electron transport kinetics. Here we report that flexible bulk electrodes, made of three-dimensional bicontinuous nanoporous Cu/MnO2 hybrid and seamlessly integrated with Cu solid current collector, substantially optimizes Li storage behavior of the constituent MnO2. As a result of the unique integration of solid/nanoporous hybrid architecture that simultaneously enhances the electron transport of MnO2, facilitates fast ion diffusion and accommodates large volume changes on Li insertion/extraction of MnO2, the supported MnO2 exhibits a stable capacity of as high as ~1100 mA h g−1 for 1000 cycles, and ultrahigh charge/discharge rates. It makes the environmentally friendly and low-cost electrode as a promising anode for high-performance Li-ion battery applications. PMID:24096928

  17. Impact of manganese, copper and zinc ions on the transcriptome of the nosocomial pathogen Enterococcus faecalis V583

    NARCIS (Netherlands)

    Abrantes, Marta Coelho; Lopes, Maria de Fátima; Kok, Jan

    2011-01-01

    Mechanisms that enable Enterococcus to cope with different environmental stresses and their contribution to the switch from commensalism to pathogenicity of this organism are still poorly understood. Maintenance of intracellular homeostasis of metal ions is crucial for survival of these bacteria. In

  18. Binding selectivity of vitamin K3 based chemosensors towards nickel(II) and copper(II) metal ions

    Science.gov (United States)

    Patil, Amit; Lande, Dipali N.; Nalkar, Archana; Gejji, Shridhar P.; Chakrovorty, Debamitra; Gonnade, Rajesh; Moniz, Tânia; Rangel, Maria; Pereira, Eulália; Salunke-Gawali, Sunita

    2017-09-01

    The vitamin K3 derivatives 2-methyl-3-[(pyridin-2-ylmethyl)-amino]-1,4-naphthoquinone (M-1), 2-methyl-3-[(pyridin-2-ylethyl)-amino]-1,4-naphthoquinone (M-2), 2-methyl-3-((2-(thiophen-2-yl)methyl)amino)naphthalene-1,4-dione (M-3) and 2-methyl-3-((2-(thiophen-2-yl)ethyl)amino)naphthalene-1,4-dione (M-4) have been synthesized, characterized and studied for their chemosensor abilities towards transition metal ions. Crystal structures of M-1 to M-4 revealed a variety of Nsbnd H⋯O, Csbnd H⋯O, Csbnd H⋯π and π⋯π interactions. Minor variations in such interactions by chemical stimuli such as metal ions, results in change in color that can be visualized by naked eyes. It has been shown that electronic structure and 1H NMR, vibrational as well as electronic spectra from the density functional theory agree well with the experiments. The metal ion binding in ethanol, ethanol-water and in mild base triethylamine brings forth recognizing ability of M-1 toward Ni2+ whereas M-2 exhibits large sensing ability for Cu2+ ion. Interestingly M-1 display varying metal ion binding specificity in different solvents with the association constant in ethanol being 11,786 M-1 for Ni2+ compared to 9462 M-1 for the Cu2+. A reversal in preferential binding of M-2 with the respective association constants being 4190 M-1 and 6370 M-1 is discernible.

  19. New Technology for Preparation of High Purity Silver by Electrolysis Using Copper-ions Free Electrolyte%无铜离子电解制备高纯银新技术

    Institute of Scientific and Technical Information of China (English)

    王日; 黄绍勇; 聂华平

    2013-01-01

    Aiming at the problems of copper being hard to be further removed from electrolytic silver product ,the electrolytic silver using copper-ions free electrolyte was studied based on the copper ions action mechanism in silver electrolysis process .T he results show that no copper ions but adding reagents A and B in electrolyte ,the conductive properties of electrolyte and precipitation properties of electrolytic silver powder can be obviously improved ,current efficiency increases by 6 .5% ,and high purity silver product in which copper content is lower than 0 .000 5% can be acquired .%针对以电解法生产高纯银过程中杂质铜难以深度去除这一难题,在探明铜离子在银电解过程中的作用机制基础上,研究了以无铜离子电解体系电解银。试验结果表明:电解体系中无铜离子,通过添加试剂A、B,可以明显改善电解液的导电性能和电银粉的析出性能,电流效率提高6.5%,电银粉中铜质量分数低于0.0005%,产品质量符合IC-Ag99.99国家标准。

  20. Technical feasibility of using silver and copper ions electro generated in the microbiological control of cooling systems; Factibilidad tecnica para emplear iones plata y cobre electrogenerados en el control microbiologico de los sistemas de enfriamiento

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Susana M; Martinez Meza, Esteban; Alvarez Gallegos, Alberto [Instituto de Investigaciones Electricas, Temixco, Morelos (Mexico)

    2001-07-01

    The objective of this work is to determine the technical feasibility of replacing the chlorine use by another biocida (ionization of silver or copper) non dangerous in cooling waters. This technique of ionization could be used to treat the water of industrial processes in general. The used water came from the make up water of the cooling system of the Thermoelectric Power Station of Valle de Mexico (CTEVM) and residual water of the treatment plants of the Instituto Mexicano de Tecnologia del Agua (IMTA) (Mexican Institute of WaterTechnology) and the Instituto de Investigaciones Electricas (IIE). The three types of water used have similar physical, chemical and biological characteristics. The used methodology was the jar tests and by continuous system. The bacteriological analysis is indicated reaching the conclusion. The metallic systems studied in the establishment of the microbiological control in the residual water and make up water are silver, silver/copper and copper in the concentration intervals of 200 mg/l to 3000 mg/l of silver and 200 mg/l to 1200 mg/l of copper. The experiments performed in the jar tests (closed system) were carried out at two temperatures (25 {+-} 0.5 and 32 {+-} 0.5 ) without pH control; whereas in the continuous system the pH was maintained in the pH interval of 7 to 8 by means of the sulfuric acid addition and a delta temperature of 10 was maintained (27 {+-} 5 ). The pH, the conductivity and the temperature were continuously measured. Graphs are shown on the effect silver/copper ions on the annihilation of total coliform bacteria and fecal coliforms the effect of the concentration of the silver metallic ion is given as a figure on the annihilation of bacteria related to iron. It is possible to conclude that the plant systems studied of silver/copper and copper turned out to be a good alternative with a minimum environmental impact to replace chlorine in the cooling systems. These systems managed microbiologically to lower the

  1. Technical feasibility of using silver and copper ions electro generated in the microbiological control of cooling systems; Factibilidad tecnica para emplear iones plata y cobre electrogenerados en el control microbiologico de los sistemas de enfriamiento

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Susana M; Martinez Meza, Esteban; Alvarez Gallegos, Alberto [Instituto de Investigaciones Electricas, Temixco, Morelos (Mexico)

    2001-07-01

    The objective of this work is to determine the technical feasibility of replacing the chlorine use by another biocida (ionization of silver or copper) non dangerous in cooling waters. This technique of ionization could be used to treat the water of industrial processes in general. The used water came from the make up water of the cooling system of the Thermoelectric Power Station of Valle de Mexico (CTEVM) and residual water of the treatment plants of the Instituto Mexicano de Tecnologia del Agua (IMTA) (Mexican Institute of WaterTechnology) and the Instituto de Investigaciones Electricas (IIE). The three types of water used have similar physical, chemical and biological characteristics. The used methodology was the jar tests and by continuous system. The bacteriological analysis is indicated reaching the conclusion. The metallic systems studied in the establishment of the microbiological control in the residual water and make up water are silver, silver/copper and copper in the concentration intervals of 200 mg/l to 3000 mg/l of silver and 200 mg/l to 1200 mg/l of copper. The experiments performed in the jar tests (closed system) were carried out at two temperatures (25 {+-} 0.5 and 32 {+-} 0.5 ) without pH control; whereas in the continuous system the pH was maintained in the pH interval of 7 to 8 by means of the sulfuric acid addition and a delta temperature of 10 was maintained (27 {+-} 5 ). The pH, the conductivity and the temperature were continuously measured. Graphs are shown on the effect silver/copper ions on the annihilation of total coliform bacteria and fecal coliforms the effect of the concentration of the silver metallic ion is given as a figure on the annihilation of bacteria related to iron. It is possible to conclude that the plant systems studied of silver/copper and copper turned out to be a good alternative with a minimum environmental impact to replace chlorine in the cooling systems. These systems managed microbiologically to lower the

  2. The Number and Surviral Rate of Corn Root Border Cells under the Stress of Copper Ions%铜离子胁迫下玉米根边缘细胞数量及存活率

    Institute of Scientific and Technical Information of China (English)

    刘婷婷; 李锋; 张曦; 施积炎; 陈英旭

    2012-01-01

    采用悬空培养及离体培养的方式,观察玉米的根边缘细胞在铜离子胁迫下发生的形态、数量及存活率变化情况,结果表明,在玉米根长为32 mm的时候,边缘细胞的数量达到最大,为4125个,但其存活率此时最低.玉米的根边缘细胞随着铜离子浓度的增加,边缘细胞的数量发生变化.当处理浓度为50 μmol·L-1时,边缘细胞的死细胞数量达到758个(存活率为24.80%),随后铜离子处理浓度增加到100 μmol·L-1时,存活率降低了17.54%.玉米根边缘细胞的数量随着铜离子浓度的增加呈现出逐渐减少的趋势,而存活率逐渐降低,说明在重金属铜离子胁迫下,根边缘细胞的释放起到对根际区域的保护作用.%By using the hanging air culture and in vitro culture with different concentrations of copper ions stress, we observed the changes of corn root border cells's shape, numbers and survival rates. The result showed that, when the corn root was 32 mm, the number of border cells reached a maximum of 4 125, but its survival rate was the lowest at this time. The number of border cells showed some changes accompany with the copper ions increased. When the copper concentration was 50 umol·L-1, the number of dead border cells reached 758 (the survival rate was 24.80%). Followed by the concentration of copper ions increased to 100 umol·L-1, the survival rate declined 17.54%. The number of corn root border cells were showed an gradually reducing trend with the increase of the concentration of copper ions, the surviral rate decreased gradually. Thus, under the stress of the copper ions, the release of root border cells played the role of protection the rhizosphere region.

  3. A novel isotachophoresis of cobalt and copper complexes by metal ion substitution reaction in a continuous moving chelation boundary.

    Science.gov (United States)

    Zhang, Wei; Chen, Jian-Feng; Fan, Liu-Yin; Cao, Cheng-Xi; Ren, Ji-Cun; Li, Si; Shao, Jing

    2010-01-01

    A novel separation mode of isotachophoresis (ITP) was advanced for the study on the continuous moving chelation boundary (MCB) formed with EDTA and two metal ions of Co(II) and Cu(II). The experiments were performed systemically. The relevant results indicated that: (1) there were three boundaries in the whole system, viz., a sharp MCB, a wide moving substitution boundary (MSB) and a sharp complex boundary (CB); (2) within the MSB, an ion substitution reaction occurred between [Co-EDTA](2-) and Cu(II), and the reaction resulted in the release of Co(II) and EDTA from [Co-EDTA](2-) and the binding of Cu(II) with the released EDTA due to log K(Cu(II)) (= 18.80) > log K(Co(II)) (= 16.31); (3) because of the novel ITP mode induced by the MSB as well as the merging of the MCB and CB, the original low concentration Co(II) and Cu(II) were chemically separated as two characteristic coloured zones of pink [Co-EDTA](2-) and blue [Cu-EDTA](2-), and the sensitivities for detection of the two metal ions were greatly enhanced. The quantitative analyses of the zone composition by ICP-AES and UV-vis spectrophotometry supported the mechanism of the novel separation mode induced by the MSB. The further theoretical and experimental results indicated that the separation mode was a novel ITP relied on moving reaction boundary (MRB), rather than a classic ITP based on the moving boundary system developed about 60 years ago. These findings provide guidance for the development of the MRB and the MCB-based ITP separation of metal ions in environmental and biological matrices.

  4. Hierarchical micro-lamella-structured 3D porous copper current collector coated with tin for advanced lithium-ion batteries

    Science.gov (United States)

    Park, Hyeji; Um, Ji Hyun; Choi, Hyelim; Yoon, Won-Sub; Sung, Yung-Eun; Choe, Heeman

    2017-03-01

    A Novel 3D porous Sn-Cu architecture is prepared as an anode material for use in an advanced lithium-ion battery. Micro-lamellar-structured 3D porous Cu foam, which is electroless-plated with Sn as an active material, is used as anode current collector. Compared to Sn-coated Cu foil, the 3D Sn-Cu foam exhibits superior Li-ion capacity and stable capacity retention, demonstrating the advantage of 3D porous architecture by preserving its structural integrity. In addition, the effect of heat-treatment after Sn plating is investigated. Sn/Sn6Cu5 and SnO2/Cu10Sn3 were formed on and in the 3D Sn-Cu foam under the heat-treatment at 150 °C and 500 °C, respectively. The development of Cu10Sn3 in the 3D Sn-Cu foam heat-treated at 500 °C can be a key factor for the enhanced cyclic stability because the Cu10Sn3 inactively reacts with Li-ion and alleviates the volume expansion of SnO2 as an inactive matrix.

  5. Copper L X-ray spectra measured by a high resolution ion-induced X-ray spectrometer

    Energy Technology Data Exchange (ETDEWEB)

    Takahashi, Ryohei; Hamaguchi, Dai; Kageyama, Hiroyoshi [Kyoto Inst. of Tech. (Japan)] [and others

    1997-03-01

    High resolution L X-ray emission spectra of Cu have been measured by 0.75 MeV/u H, He, and F, 0.73 MeV/u Ar, 0.64 MeV/u Si, and 0.073 MeV/u Si ion impacts with a crystal spectrometer. The X-ray transition energies in the Cu target for L{iota}, L{eta}, L{alpha}{sub 1,2}, L{beta}{sub 1}, and L{beta}{sub 3,4} diagram lines induced by light ion impacts are determined, which are in good agreement with those given in the reference. The difference in L X-ray emission spectra produced by H, He, F, Si, and Ar ions are considered and the L{alpha}{sub 1,2} and L{beta}{sub 1} emission spectra are compared with the calculated ones based on the multiconfiguration Dirac-Fock method. (author)

  6. Preparation and Evaluation of Acetabularia-Modified Carbon Paste Electrode in Anodic Stripping Voltammetry of Copper and Lead Ions

    Directory of Open Access Journals (Sweden)

    Muhammad Raziq Rahimi Kooh

    2013-01-01

    Full Text Available Seaweed is well known about for potential in chelating heavy metals. In this study, carbon paste electrodes were fabricated with siphonous seaweed Acetabularia acetabulum as the modifiers to sense lead (II and copper (II by square-wave anodic stripping voltammetry. Various scan rates and deposition potentials were measured to obtain the optimal peak current for Pb(II and Cu(II. Optimum conditions of Acetabularia-CPE for sensing Pb(II were at the scan rate of 75 mV/s and deposition potential of −800 mV, while for Cu(II sensing were at 100 mV/s and −300 mV, respectively. The electrodes were characterized by the duration of accumulation time, preconcentration over a range of standards, supporting electrolyte, and standard solutions of various pH values. Interference studies were carried out. Both Zn(II and Cu(II were found to interfere with Pb(II sensing, whereas only Zn(II causes interference with Cu(II sensing. The electrode was found to have good regeneration ability via electrochemical cleaning. Preliminary testing of complex samples such as NPK fertilisers, black soil, and sea salt samples was included.

  7. Single step synthesis of amine-functionalized mesoporous magnetite nanoparticles and their application for copper ions removal from aqueous solution.

    Science.gov (United States)

    Gao, Jining; He, Yingjuan; Zhao, Xianying; Ran, Xinze; Wu, Yonghui; Su, Yongping; Dai, Jianwu

    2016-11-01

    Amine-functionalized mesoporous superparamagnetic Fe3O4 nanoparticles with an average size of 70nm have been synthesized using a single step solvothermal method by the introduction of triethylenetetramine (TETA), a chelating agent recommended for the removal of excess copper in patients with Wilson's disease. The synthesized nanoparticles were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, nitrogen adsorption/desorption isotherm, vibrating sample magnetometer (VSM), and Fourier transform infrared spectroscopy (FTIR). It is confirmed that the magnetic nanoparticles have been functionalized with TETA during the synthetic process, and the concentration of TETA is crucial for the formation of monodisperse mesoporous nanoparticles. The obtained single-crystal magnetic nanoparticles have a high magnetization, which enhances their response to external magnetic field and therefore should greatly facilitate the manipulation of the particles in practical uses. Reaction parameters affecting the formation of mesoporous structure were explored, and a possible formation mechanism involving templated aggregation and recrystallization processes was proposed. The capacity of the synthesized amine-functionalized Fe3O4 nanoparticles toward Cu(II) removal from aqueous solution was investigated. The adsorption rate of Cu(II) on amine-functionalized Fe3O4 nanoparticles followed a pseudo-second order kinetic model. The results of this study demonstrated that the amine-functionalized mesoporous superparamagnetic Fe3O4 nanoparticles could be used as an efficient adsorbent in water treatment and would also find potential application for Cu(II) removal in vivo.

  8. Mass transfer study on the electrochemical removal of copper ions from synthetic effluents using reticulated vitreous carbon.

    Science.gov (United States)

    Britto-Costa, Pedro H; Ruotolo, Luís Augusto M

    2013-01-01

    Porous electrodes have been successfully used for metal electrodeposition from diluted aqueous solution due to their high porosity and specific surface area, which lead to high mass transfer rates. This work studies the mass transfer of copper electrodeposition on reticulated vitreous carbon in a flow reactor without membrane. The flow configuration, otherwise the filter-press electrochemical reactors, was designed in order to minimize the pressure drop. The mass transfer coefficient was determined by voltammetric and galvanostatic electrodeposition. In the voltammetric experiments a Luggin capillary was used to measure the current-potential curves and to determine the limiting current (and, consequently, the mass transfer coefficient). In the galvanostatic experiments the concentration-time curves were obtained and considering a limiting current kinetics model, the mass transfer coefficient (k(m)) was determined for different flow velocities. The results showed that both methods give similar values of k(m), thus the voltammetric method can be recommended because it is faster and simpler. Finally, the reactor performance was compared with others from literature, and it was observed that the proposed reactor design has high Sherwood numbers similar to other reactor configurations using membranes and reticulated vitreous carbon electrodes.

  9. Combustion synthesized copper-ion substituted FeAl2O4 (Cu0.1Fe0.9Al2O4): A superior catalyst for methanol steam reforming compared to its impregnated analogue

    Science.gov (United States)

    Maiti, Sayantani; Llorca, Jordi; Dominguez, Montserrat; Colussi, Sara; Trovarelli, Alessandro; Priolkar, Kaustubh R.; Aquilanti, Giuliana; Gayen, Arup

    2016-02-01

    A series of copper ion substituted MAl2O4 (M = Mg, Mn, Fe and Zn) spinels is prepared by a single step solution combustion synthesis (SCS) and tested for methanol steam reforming (MSR). The copper ion substituted Cu0.1Fe0.9Al2O4 appears to be the most active, showing ∼98% methanol conversion at 300 °C with ∼5% CO selectivity at GHSV = 30,000 h-1 and H2O:CH3OH = 1.1. The analogous impregnated catalyst, CuO (10 at%)/FeAl2O4, is found to be much less active. These materials are characterized by XRD, H2-TPR, BET, HRTEM, XPS and XANES analyses. Spinel phase formation is highly facilitated upon Cu-ion substitution and Cu loading beyond 10 at% leads to the formation of CuO as an additional phase. The ionic substitution of copper in FeAl2O4 leads to the highly crystalline SCS catalyst containing Cu2+ ion sites that are shown to be more active than the dispersed CuO nano-crystallites on the FeAl2O4 impregnated catalyst, despite its lower surface area. The as prepared SCS catalyst contains also a portion of copper as Cu1+ that increases when subjected to reforming atmosphere. The MSR activity of the SCS catalyst decreases with time-on-stream due to the sintering of catalyst crystallites as established from XPS and HRTEM analyses.

  10. 赤泥吸附剂的制备及其对铜离子的吸附性能%Preparation of red mud adsorbent and its adsorption properties for copper ion

    Institute of Scientific and Technical Information of China (English)

    李德贵; 李奇幸

    2014-01-01

    In order to explore the adsorption properties of red mud adsorbent for copper ion,red mud ad-sorbent had been prepared by granulating-calcinations with red mud as raw materials. Several influencing factors of copper ion removal performance have been studied,such as adsorption time,calcinations temper-ature,calcinations time,pH value and dosing quantity,and so on. The results showed that the adsorbent prepared by red mud with granulating-calcinations method has good removal performance for copper ions, and the concentration of copper ion could be reduced from 64. 00 mg/L to 0. 22 mg/L,and adsorbent ca-pacity could reach 1. 595 mg/g,the removal rate could reach more than 98%.%以赤泥为原料,通过造粒、焙烧的方法制备赤泥吸附剂,探讨赤泥吸附剂对铜离子的吸附性能。研究了吸附时间、焙烧温度、焙烧时间、pH值、吸附剂投入量等对赤泥吸附剂除铜性能的影响。结果表明,赤泥经过造粒、焙烧后制备的吸附剂对铜离子具有很好的去除效果,铜离子的浓度可以从64.00 mg/L降低到0.22 mg/L,吸附剂对铜的吸附容量可达1.595 mg/g,对铜离子的吸附率达98%以上。

  11. Electroleaching of Copper Waste with Recovery of Copper by Electrodialysis

    Directory of Open Access Journals (Sweden)

    Nuñez P.

    2013-04-01

    Full Text Available A new process to leach and recover copper from solid waste using electric fields was designed. The leaching with electro migration is presented as an alternative to traditional leaching. Preliminary data indicate that the copper ion migration is facilitated by using the electrical potential difference; therefore applying a potential difference in the processes of leaching facilitates the removal of copper. This is especially useful when mineral concentrations are very low. Different phenomena associated with transport of copper in solution are studied to generate a model able predict the state of the copper ion concentration in time. A kinetic model for the process was developed and fitted very well the experimental data.

  12. 铜离子对葡萄酒发酵中硫化氢产量的影响%Effects of Copper Ions on Hydrogen Sulfide Production in the Fermentation of Grape Wine

    Institute of Scientific and Technical Information of China (English)

    刘富兵; 殷向静; 何娟; 刘延琳

    2012-01-01

    The quantitative determination of the residual S2-concentration in grape wine and the amount of hydrogen sulfide produced in the fermentation process was carried out in the conditions of different copper ions concentration by use of methylene-blue colorimetric method with white rose from Jingyang Shanxi as raw materials.The results suggested that appropriate copper ions concentration(0~0.8 mg/L) in fermenting liquid could inhibit the production of hydrogen sulfide and the best effects could be achieved as the addition level of copper ions was 0.4 mg/L.%以陕西泾阳县的小白玫瑰为材料,根据亚甲基兰比色法,在不同铜离子浓度条件下定量测定发酵过程中产生的硫化氢气体量,以及酒中残留的S2-浓度。结果表明,发酵液中适当浓度的铜离子(0~0.8 mg/L)可以抑制发酵过程中硫化氢气体的生成,当添加0.4 mg/L铜离子浓度时,综合效果最佳。

  13. Suspended nanoparticles in surfactant media as a microextraction technique for simultaneous separation and preconcentration of cobalt, nickel and copper ions for electrothermal atomic absorption spectrometry determination.

    Science.gov (United States)

    Dadfarnia, Shayessteh; Shakerian, Farid; Shabani, Ali Mohammad Haji

    2013-03-15

    The aim of this study was to describe a new method of microextraction based on the suspension of alumina nanoparticles in the surfactant media for simultaneous separation and preconcentration of the ultra-traces of cobalt, nickel and copper ions. In this technique, the alumina nanoparticles were suspended in the non-ionic surfactant solution of Triton X-114. The analytes in the sample solution were adsorbed onto the nanoparticles. After the phase separation based on the cloud point of the mixture at 40 °C, the nanoparticles settled down in the surfactant rich phase. Then 120 μL of nitric acid (3.0 mol L(-1)) was added to the surfactant rich phase which caused desorption of the analytes. Finally, the liquid phase was separated by centrifugation from the nanoparticles and was used for the quantification of the analytes by the electrothermal atomic absorption spectrometry (ETAAS). The parameters affecting the extraction and detection processes were optimized. Under the optimized experimental conditions (i.e. pH∼8, Triton X-114, 0.05% (v/v); temperature 40 °C), a sample volume of 25 mL resulted in the enhancement factors of 198, 205 and 206 and detection limits (defined as 3Sb/m) of 2.5, 2.8 and 2.6 ng L(-1) for Co(II), Ni(II) and Cu(II) respectively. The sorbent showed high capacity for these metal ions (30-40 mg g(-1) sorbent). The method was successfully applied to the determination of the analytes in natural water samples.

  14. Effects of salinity on metal uptake and metallothionein mRNA levels in the organs of tilapia exposed to cadmium, copper, and zinc ions.

    Science.gov (United States)

    Shek, Alex C S; Chan, King Ming

    2015-05-01

    This study aimed to determine the effects of salinity on metal uptake and metallothionein (MT) mRNA levels in tilapia exposed to three metal ions. Male Oreochromis niloticus × O. aureus juveniles (hereafter, "tilapia") were exposed to various concentrations (100, 500, and 1 ppm) of metal ions (Cd(2+), Cu(2+) and Zn(2+)) in freshwater and water with two levels of salinity (10 and 20 ppt) for 7 days. Tests were then performed to investigate the effects of salinity on metal concentrations and MT mRNA induction in the test subjects' organs. Saline decreased cadmium (Cd) uptake and MT mRNA fold induction in various internal organs, but it did not enhance MT mRNA induction in the gills. Exposure to Cu(2+) caused greater copper (Cu) levels in the brains, intestines and livers, but Cu uptake in the intestines and kidneys occurred only at 10 ppm. MT mRNA induction caused by Cu(2+) was observed in various internal organs, but it occurred in the gills only at greater levels of salinity. Exposure at greater salinities also decreased zinc (Zn) uptake and MT mRNA induction in all organs except the gills. Although greater salinity decreased Cd and Zn uptake, the metal content in the water correlated with the MT mRNA levels in most of the organs, except for the intestines. In conclusion, metal accumulations in the livers and kidneys of tilapia correlated with MT mRNA levels. The levels of MT mRNA in the livers and kidneys of tilapia might therefore be used as biomarkers of exposure to Cd(2+), Cu(2+) and Zn(2+) in water of various salinities.

  15. Bifunctional sensor of pentachlorophenol and copper ions based on nanostructured hybrid films of humic acid and exfoliated layered double hydroxide via a facile layer-by-layer assembly.

    Science.gov (United States)

    Yuan, Shuang; Peng, Dinghua; Hu, Xianluo; Gong, Jingming

    2013-06-27

    A new, highly sensitive bifunctional electrochemical sensor for the simultaneous determination of pentachlorophenol (PCP) and copper ions (Cu(2+)) has been developed, where organic-inorganic hybrid ultrathin films were fabricated by alternate assembly of humic acid (HA) and exfoliated Mg-Al-layered double hydroxide (LDH) nanosheets onto ITO substrates via a layer-by-layer (LBL) approach. The multilayer films were then characterized by means of UV-vis spectrometry, scanning electron microscopy (SEM), and atomic force microscope (AFM). These films were found to have a relatively smooth surface with almost equal amounts of HA incorporated in each cycle. Its electrochemical performance was systematically investigated. Our results demonstrate that such a newly designed (LDH/HA)n multilayer films, combining the individual properties of HA (dual recognition ability for organic herbicides and metal ions) together with LDH nanosheets (a rigid inorganic matrix), can be applied to the simultaneous analysis of PCP and Cu(II) without interference from each other. The LBL assembled nanoarchitectures were further investigated by X-ray photoelectron spectroscopy (XPS) and infrared spectroscopy (IR), which provides insight for bifunctional sensing behavior. Under the optimized conditions, the detection limit was found to be as low as 0.4 nM PCP, well below the guideline value of PCP in drinking water (3.7 nM) set by the United States Environmental Protection Agency (U.S. EPA), and 2.0 nM Cu(2+), much below the guideline value (2.0 mg L(-1), ~31.2 nM) from the World Health Organization (WHO), respectively. Toward the goal for practical applications, this simple and cost-effective probe was further evaluated by monitoring PCP and Cu(II) in water samples.

  16. Study of Silicon Nitrate and Tin Dioxide carbon nanotube composite as lithium-ion battery anode, gas sensor and the self-assembly of carbon nanotubes on copper substrates

    Science.gov (United States)

    Hernandez-Lugo, Dionne M.

    Carbon nanotubes since their discovery have been used for many applications. They are predicted to reinforce novel composite materials because of their structural perfection, excellent mechanical properties and low density. CNT can be made into nanowires of different materials or as part of a composite making them beneficial for the incorporation into electrochemical devices. Carbon nanotubes in this study were gown directly on a copper substrate employing hot filament chemical vapor deposition (HFCVD). Bamboo-like carbon nanotubes were made into electrodes reducing the use of inactive materials on the development of working electrodes for electrochemical application. This BCNT were tested as lithium-ion battery anodes assembled together with high capacity materials such as Silicon and Tin Oxide (4200mAh/g and 782 mAh/g). On this study BCNT served as a conductive matrix as well as buffer matrix for the volume expansion brought by cycling silicon and tin oxide. The composite structural properties enhance the surface-to-volume ratio of the electrode demonstrating a desirable electrochemical performance for a lithium-ion battery anode. As a gas sensor electrode CNT was assembled with tin-oxide directly on a copper substrate for the detection of ethanol, methanol, ammonia and H2S. CNT gave a higher surface area and a conductive matrix aiding to the sensing capabilities of the SnO2 increasing the effectiveness of the matrix material for gas detection. Copper is known to produce CNT with a disturb structure. To develop an electrode on copper with well-ordered CNT other techniques need to be used. One way to do this is by chemical modification of the copper substrate with a molecule able to react with the carbon nanotube. For the attachment of well-ordered carbon nanotubes such as SWCNT a self-assembly monolayer technique is chosen. On this study 4-aminothiophenol served as the linker between the copper substrate and the carbon nanotubes. This study let to chemically

  17. Copper hypersensitivity.

    Science.gov (United States)

    Fage, Simon W; Faurschou, Annesofie; Thyssen, Jacob P

    2014-10-01

    The world production of copper is steadily increasing. Although humans are widely exposed to copper-containing items on the skin and mucosa, allergic reactions to copper are only infrequently reported. To review the chemistry, biology and accessible data to clarify the implications of copper hypersensitivity, a database search of PubMed was performed with the following terms: copper, dermatitis, allergic contact dermatitis, contact hypersensitivity, contact sensitization, contact allergy, patch test, dental, IUD, epidemiology, clinical, and experimental. Human exposure to copper is relatively common. As a metal, it possesses many of the same qualities as nickel, which is a known strong sensitizer. Cumulative data on subjects with presumed related symptoms and/or suspected exposure showed that a weighted average of 3.8% had a positive patch test reaction to copper. We conclude that copper is a very weak sensitizer as compared with other metal compounds. However, in a few and selected cases, copper can result in clinically relevant allergic reactions.

  18. Removal of copper (II) ion from aqueous solution using zeolite Y synthesized from rice husk ash: Equilibrium and kinetic study

    Science.gov (United States)

    Tuyen, Nguyen Thi Kim; Nhan, Do Nguyen Thanh; Nhat, Trieu Thi; An, Ngo Thanh; Long, Nguyen Quang

    2017-09-01

    Zeolite Y was synthesized from silica of rice-husk ash using hydrothermal process. The crystalline structure FAU of zeolite Y was characterized by X-ray diffraction (XRD). Surface's area of the catalyst was determined by physic-adsorption method using BET model. The zeolite was examined for possibility of Cu2+ adsorbent by an ion-exchange mechanism. Various adsorption isotherm models, such as Langmuir, Freundlich and Dubinin-Radushkevich were tested for equilibrium study. The integration method was applied to find out the possible kinetic equation of the Cu2+ adsorption on the zeolite Y which obtained from cheap and locally available rice husk ash.

  19. Experimental study of the removal of copper ions using hydrogels of xanthan, 2-acrylamido-2-methyl-1-propane sulfonic acid, montmorillonite: Kinetic and equilibrium study.

    Science.gov (United States)

    Aflaki Jalali, Marzieh; Dadvand Koohi, Ahmad; Sheykhan, Mehdi

    2016-05-20

    In this paper, removal of copper ions from aqueous solution using novel xanthan gum (XG) hydrogel, xanthan gum-graft-2-acrylamido-2-methyl-1-propane sulfonic acid (XG-g-P(AMPS)) hydrogel and xanthan gum-graft-2-acrylamido-2-methyl-1-propane sulfonic acid/montmorillonite (XG-g-P(AMPS)/MMT) hydrogel composite were studied. The structure and morphologies of the xanthan-based hydrogels were characterized by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). Adsorbents comprised a porous crosslink structure with side chains that carried carboxyl, hydroxyl and sulfonate. Maximum adsorption was observed in the pH=5.2, initial concentrations of Cu(2+)=321.8 mg/L, Temperature=45 °C, contact time=5 h with 0.2 g/50 mL of the hydrogels. Adsorption process was found to follow Langmuir isotherm model with maximum adsorption capacity of 24.57, 39.06 and 29.49 mg/g for the XG, XG-g-P(AMPS) and XG-g-P(AMPS)/MMT, respectively. Adsorption kinetics data fitted well with pseudo second order model. The negative ΔG° values and the positive ΔS° confirmed that the adsorption was a spontaneous process. The positive ΔH° values suggested that the adsorption was endothermic in nature.

  20. Cap for copper(I) ions! Metallosupramolecular solid and solution state structures on the basis of the dynamic tetrahedral [Cu(phenAr2)(py)2]+ motif.

    Science.gov (United States)

    Schmittel, Michael; He, Bice; Fan, Jian; Bats, Jan W; Engeser, Marianne; Schlosser, Marc; Deiseroth, Hans-Jörg

    2009-09-07

    The tetrahedral [Cu(phenAr(2))(py)(2)](+) coordination motif (phen = 1,10-phenanthroline; py = pyridine) conceived on the basis of the HETPYP concept (heteroleptic pyridyl and phenanthroline metal complexes) is a versatile dynamic unit for constructing various heteroleptic metallosupramolecular pseudo-1D, 2D, and 3D structures, both in solution and the solid state. The 2,9-diaryl substituted phenanthroline (phenAr(2)) serves as a capping ligand for copper(I) ions, as its bulky nature prevents formation of the homoleptic complex [Cu(phenAr(2))(2)](+). Combination of the dynamic and concave metal ligand building block [Cu(phenAr(2))](+) with various pyridine (py) ligands, such as bi-, tri-, and tetra-pyridines, opened the way to infinite 1D helicates, 2D networks, and discrete 3D hexanuclear cages, whereas spatial integration of both phenAr(2) and py units into a single ligand resulted in the formation of a Borromean-ring-type hexanuclear cage.

  1. Effects of Calcium and Magnesium Ions on Acute Copper Toxicity to Glochidia and Early Juveniles of the Chinese Pond Mussel Anodonta woodiana.

    Science.gov (United States)

    Liu, Hongbo; Chen, Xiubao; Su, Yanping; Kang, Ik Joon; Qiu, Xuchun; Shimasaki, Yohei; Oshima, Yuji; Yang, Jian

    2016-10-01

    We evaluated the effects of calcium (Ca(2+)) and magnesium (Mg(2+)) ions on copper (Cu) toxicity to glochidia and newly-transformed juvenile mussels (age 1-2 days) of the Chinese pond mussel (Anodonta woodiana). Acute Cu toxicity tests were performed with glochidia for 24 h and juveniles for 96 h with measured Ca(2+) concentrations of 1.1, 14, 26, 51, and 99 mg L(-1), or measured Mg(2+) concentrations of 2.6, 11, 21, and 39 mg L(-1). The Ca(2+) and Mg(2+) cations provided no statistically significant protection against Cu toxicity to glochidia or juveniles. The 24-h EC50 value for glochidia was 82 μg L(-1) Cu, and contrastly, 96-h EC50 value for newly-transformed juvenile mussels was as low as 12 μg L(-1) Cu, implying that the juveniles of A. woodiana are more vulnerable to Cu contamination at concentrations close to currently-accepted levels.

  2. Measurements of plasma temperature and electron density in laser-induced copper plasma by time-resolved spectroscopy of neutral atom and ion emissions

    Indian Academy of Sciences (India)

    V K Unnikrishnan; Kamlesh Alti; V B Kartha; C Santhosh; G P Gupta; B M Suri

    2010-06-01

    Plasma produced by a 355 nm pulsed Nd:YAG laser with a pulse duration of 6 ns focussed onto a copper solid sample in air at atmospheric pressure is studied spectroscopically. The temperature and electron density characterizing the plasma are measured by time-resolved spectroscopy of neutral atom and ion line emissions in the time window of 300–2000 ns. An echelle spectrograph coupled with a gated intensified charge coupled detector is used to record the plasma emissions. The temperature is obtained using the Boltzmann plot method and the electron density is determined using the Saha– Boltzmann equation method. Both parameters are studied as a function of delay time with respect to the onset of the laser pulse. The results are discussed. The time window where the plasma is optically thin and is also in local thermodynamic equilibrium (LTE), necessary for the laser-induced breakdown spectroscopy (LIBS) analysis of samples, is deduced from the temporal evolution of the intensity ratio of two Cu I lines. It is found to be 700–1000 ns.

  3. 离子选择电极法测定冰铜中氟%Determination of Fluorine in Copper Matte by Ion -Selective Electrode

    Institute of Scientific and Technical Information of China (English)

    谢立进; 刘在美; 刘江

    2014-01-01

    研究了柠檬酸钠-三乙醇胺体系应用于冰铜中氟量测定的离子选择电极法,讨论了熔剂用量和熔解时间的选择,及该体系测定时pH范围、缓冲溶液的用量、铝量及铁量的影响。该方法测定的标准偏差小于0.01%,回收率为97%~103%。%The fluorine in copper matte was determined by the ion -selective electrode method in the system of sldium citrate and tri -alcoholic amine . The influencing factors were investigated , including dosage of fluxes , selection of melting time , pH ,TISAB addition amount , aluminum and iron . The results show that standard deviation is less than 0 .01% and recovery ratio is in the range of 97% ~103% .

  4. Magnesite tailing as low-cost adsorbent for the removal of copper (II) ions from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Kipcak, Ilker; Isiyel, Turgut Giray [Eskisehir Osmangazi University, Eskisehir (Turkmenistan)

    2015-08-15

    The removal of Cu(II) ions from aqueous solution using magnesite tailing was investigated. Batch kinetic and equilibrium experiments were conducted to study the effects of initial pH, adsorbent dosage, contact time, initial concentration and temperature. The pseudo-first-order, pseudo-second-order and intraparticle diffusion models were used to study the kinetic data. The experimental data were best fitted by the pseudo-second-order kinetic model. The linear Langmuir and Freundlich adsorption equations were applied to describe the equilibrium isotherms. The equilibrium data fit very well the Langmuir model, and the maximum adsorption capacity was estimated as 12.18mg/g at 45 .deg. C. Thermodynamic parameters such as enthalpy change (ΔH{sup o}), free energy change (ΔG{sup o}) and entropy change (ΔS{sup o}) were calculated, and it was found that the adsorption process was spontaneous and endothermic. The results showed that magnesite tailing is a suitable adsorbent for the removal of Cu(II) ions from aqueous solutions.

  5. Hair copper in intrauterine copper device users.

    Science.gov (United States)

    Thiery, M; Heyndrickx, A; Uyttersprot, C

    1984-03-01

    The antifertility effect of copper-bearing IUDs is based on continuous release of copper, which is a result of the reaction between the metal and the uterine secretions. Released cupric ions collect in the endometrium and in the uterine fluid but significant accumulation has not been found in the bloodstream or elsewhere. Following Laker's suggestion that hair be used for monitoring essential trace elements, e.g., copper, we checked the copper content of the hair of women wearing copper-bearing IUDs. Samples of untreated pubic hair removed by clipping before diagnostic curettage were obtained from 10 young (24-34 years old), white caucasian females who until then had been wearing an MLCu250 IUD for more than 1 year. Pubes from 10 comparable (sex, age, race) subjects who had never used a Cu-containing device served as controls. The unwashed material was submitted to the toxicology laboratory, where the copper content was assessed by flameless atomic absorption, a technique whose lower limit of measurement lies at a concentration of 0.05 mcg Cu/ml fluid (50 ppb). Hair samples were washed to remove extraneous traces of metal according to the prescriptions of the International Atomic Energy Agency, weighed, and mineralized, after which a small volume (10 mcl) of the diluted fluid was fed into the graphite furnace. Each sample (75-150 mg) was analyzed 4 times, both before and after washing. Since the cleaning procedure reduces the weight of the sample (mainly by the removal of fat, dust, etc.) this explains why the percentage copper content of washed hair is higher than that of unwashed hair belonging to the same subject. The results indicate that there was no significant difference (Mann-Whitney U test) between the mean copper levels of both unwashed and washed pubes from women who were using or had never used an MLCu250 IUD. We therefore conclude that the use of this copper-containing device is not associated with significant accumulation of copper in (pubic) hair.

  6. Copper transport.

    Science.gov (United States)

    Linder, M C; Wooten, L; Cerveza, P; Cotton, S; Shulze, R; Lomeli, N

    1998-05-01

    In adult humans, the net absorption of dietary copper is approximately 1 mg/d. Dietary copper joins some 4-5 mg of endogenous copper flowing into the gastrointestinal tract through various digestive juices. Most of this copper returns to the circulation and to the tissues (including liver) that formed them. Much lower amounts of copper flow into and out of other major parts of the body (including heart, skeletal muscle, and brain). Newly absorbed copper is transported to body tissues in two phases, borne primarily by plasma protein carriers (albumin, transcuprein, and ceruloplasmin). In the first phase, copper goes from the intestine to the liver and kidney; in the second phase, copper usually goes from the liver (and perhaps also the kidney) to other organs. Ceruloplasmin plays a role in this second phase. Alternatively, liver copper can also exit via the bile, and in a form that is less easily reabsorbed. Copper is also present in and transported by other body fluids, including those bathing the brain and central nervous system and surrounding the fetus in the amniotic sac. Ceruloplasmin is present in these fluids and may also be involved in copper transport there. The concentrations of copper and ceruloplasmin in milk vary with lactational stage. Parallel changes occur in ceruloplasmin messenger RNA expression in the mammary gland (as determined in pigs). Copper in milk ceruloplasmin appears to be particularly available for absorption, at least in rats.

  7. A Solid-Contact Ion Selective Electrode for Copper(II Using a Succinimide Derivative as Ionophore

    Directory of Open Access Journals (Sweden)

    Mihaela Dana Tutulea-Anastasiu

    2013-04-01

    Full Text Available All-solid-state sensors with polyvinyl chloride (PVC-based membranes using off-the-shelf N-hydroxysuccinimide (NHS and succinimide (Succ ionophores were prepared using DOP (dioctyl phthalate and NPOE (ortho-nitrophenyloctyl ether as plasticizers. Good responses were obtained when NHS was used. The potentiometric response of the proposed electrode is independent of pH over the range 2–6. The electrode shows a fast response time of 0.25 s. The electrode exhibits a Super-Nernstian response, with 37.5 mV/decade, with a potentiometric detection limit of 4.4 µM. The proposed sensor revealed good selectivity towards a group of transition metal ions.

  8. 3D amorphous silicon on nanopillar copper electrodes as anodes for high-rate lithium-ion batteries.

    Science.gov (United States)

    Kim, Gyutae; Jeong, Sookyung; Shin, Ju-Hyeon; Cho, Jaephil; Lee, Heon

    2014-02-25

    We present an amorphous Si anode deposited on a Cu nanopillar current collector, fabricated using a thermal roll-to-roll process followed by electroformation and LPCVD, for application in high-rate Li-ion batteries. Cu nanopillar current collectors with diameters of 250 and 500 nm were patterned periodically with 1 μm pitch and 2 μm height to optimize the diameters of the pillars for better electrochemical performance. Void spaces between Cu nanopillars allowed not only greater effective control of the strain caused by the Si expansion during lithiation than that allowed by a nonpatterned electrode but also significantly improved cycle performance even at 20 C measured after the same rate test: After 100 cycles at 0.5 C, the patterned electrodes with 250 and 500 nm diameter nanopillars showed high capacity retentions of 86% and 84%, respectively. These electrodes retained discharge capacities of 1057 and 780 mAh/g even at 20 C, respectively.

  9. Synthesis, characterization, and catalytic properties of cationic hydrogels containing copper(II) and cobalt(II) ions.

    Science.gov (United States)

    Lombardo Lupano, Lucía Victoria; Lázaro Martínez, Juan Manuel; Piehl, Lidia Leonor; Rubín de Celis, Emilio; Torres Sánchez, Rosa María; Campo Dall' Orto, Viviana

    2014-03-18

    Here, we report the synthesis and characterization of a hydrogel based on ethylene glycol diglycidyl ether (EGDE) and 1,8-diamino-3,6-dioxaoctane (DA). Chemically stable Co(II) and Cu(II) coordination complexes were prepared with this nonsoluble polyelectrolyte, poly(EGDE-DA), and studied by ss-NMR, FT-IR, thermogravimetry, and microscopy. Mesopores were found in all the samples, the thermal stability of the polymer matrix was highly affected by the presence of metal ions, and the (13)C CP-MAS spectrum for the Cu(II)-complex evidenced a significant increase in the reticulation degree by Cu(II) ions. The catalytic activity of these materials on H2O2 activation was studied by electron spin resonance (ESR). The Co(II)-poly(EGDE-DA)/H2O2 heterogeneous system produced O2, an anion superoxide (O2(•)¯), and a hydroxyl radical (OH(•)), which diffused into the solution at the time that a decrease in pH was detected. In the same way, the Cu(II)-poly(EGDE-DA)/H2O2 heterogeneous system produced O2 and OH(•). H2O2 activation by the poly(EGDE-DA) complexes with Co(II) and Cu(II) were applied on the decolorization of solutions of the azo-dye methyl orange (MO). In the presence of 63 mM H2O2, 87% of MO was removed in 10 min with Cu(II)-poly(EGDE-DA) and in 110 min with Co(II)-poly(EGDE-DA). In addition, the pharmaceutical product epinephrine was partially oxidized to adrenochrome by the O2(•)¯ released from the Co(II)-poly(EGDE-DA)/H2O2 heterogeneous system.

  10. Study on the antibacterial mechanism of copper ion- and neodymium ion-modified α-zirconium phosphate with better antibacterial activity and lower cytotoxicity.

    Science.gov (United States)

    Cai, Xiang; Zhang, Bin; Liang, Yuanyuan; Zhang, Jinglin; Yan, Yinghui; Chen, Xiaoyin; Wu, Zhimin; Liu, Hongxi; Wen, Shuiping; Tan, Shaozao; Wu, Ting

    2015-08-01

    To improve the antibacterial activity of Cu(2+), a series of Cu(2+) and/or Nd(3+)-modified layered α-zirconium phosphate (ZrP) was prepared and characterized, and the antibacterial activities of the prepared Cu(2+) and/or Nd(3+)-modified ZrP on Gram-negative Escherichia coli were investigated. The results showed that the basal spacing of ZrP was not obviously affected by the incorporation of Cu(2+), but the basal spacing of the modified ZrP changed into an amorphous state with increasing additions of Nd(3+). An antibacterial mechanism showed that Cu(2+) and Nd(3+) could enter into E. coli cells, leading to changes in ion concentrations and leakage of DNA, RNA and protein. The Cu(2+)- and Nd(3+)-modified ZrP, combining the advantages of Cu(2+) and Nd(3+), displayed excellent additive antibacterial activity and lower cytotoxicity, suggesting the great potential application as an antibacterial powder for microbial control.

  11. Copper hypersensitivity

    DEFF Research Database (Denmark)

    Fage, Simon W; Faurschou, Annesofie; Thyssen, Jacob P

    2014-01-01

    hypersensitivity, a database search of PubMed was performed with the following terms: copper, dermatitis, allergic contact dermatitis, contact hypersensitivity, contact sensitization, contact allergy, patch test, dental, IUD, epidemiology, clinical, and experimental. Human exposure to copper is relatively common...

  12. Measurements of the Backstreaming Proton IONS in the Self-Magnetic Pinch (SMP) Diode Utilizing Copper Activation Technique

    Science.gov (United States)

    Mazarakis, Michael; Cuneo, Michael; Fournier, Sean; Johnston, Mark; Kiefer, Mark; Leckbee, Joshua; Simpson, Sean; Renk, Timothy; Webb, Timothy; Bennett, Nichelle

    2016-10-01

    The results presented here were obtained with an SMP diode mounted at the front high voltage end of the 8-10-MV RITS Self-Magnetically Insulated Transmission Line (MITL) voltage adder. Our experiments had two objectives: first, to measure the contribution of the back-streaming proton currents emitted from the anode target, and second, to evaluate the energy of those ions and hence the actual Anode-Cathode (A-K) gap voltage. The accelerating voltage quoted in the literature is estimated utilizing para-potential flow theories. Thus, it is interesting to have another independent measurement of the A-K voltage. We have measured the back-streaming protons emitted from the anode and propagating through a hollow cathode tip for various diode configurations and different techniques of target cleaning treatment, namely, heating at very high temperatures with DC and pulsed current, with RF plasma cleaning, and with both plasma cleaning and heating. We have also evaluated the A-K gap voltage by energy filtering techniques. Sandia is operated by Sandia Corporation, a subsidiary of Lockheed Martin Company, for the US DOE NNSA under Contract No. DE-AC04-94AL85000.

  13. Effect of copper ion on adsorption of chlorinated phenols and 1-naphthylamine to surface-modified carbon nanotubes.

    Science.gov (United States)

    Wang, Fang; Zhu, Dongqiang; Chen, Wei

    2012-01-01

    Understanding the adsorptive interactions between organic contaminants and carbon nanotubes (CNTs) is critical to both environmental applications and risk management of CNTs. The objective of the present study was to understand how transitional metal ions with strong complexing capabilities might affect the adsorption of hydroxyl- and amino-substituted aromatics to surface O-functionality-rich single-walled CNTs (O-SWNT) and N-functionality-rich single-walled CNTs (N-SWNT). Adsorption of 2,4-dichlorophenol, pentachlorophenol, and 1-naphthylamine to O-SWNT and N-SWNT can be significantly enhanced in the presence of Cu(II) (50 mg/L), whereas adsorption of 1,2-dichlorobenzene is essentially unaffected. The most likely mechanism for the Cu-enhanced adsorption is that Cu(II) serves as a bridging agent between organic solutes and the functional groups on CNT surfaces. For the adsorption of 1-naphthylamine to N-SWNT, an additional mechanism might be possible; that is, the complexation of Cu(II) with the N-functional groups of N-SWNT can change these groups from strong Lewis bases to Lewis acids and thereby significantly enhance adsorption via the mechanism of Lewis acid-base interactions. In addition, adsorption of Cu(II) can be significantly enhanced by the adsorption of organic cosolutes.

  14. The Effective Electrolytic Recovery of Dilute Copper from Industrial Wastewater

    Directory of Open Access Journals (Sweden)

    Teng-Chien Chen

    2013-01-01

    Full Text Available Electroplating copper industry was discharged huge amount wastewater and cause serious environmental and health damage in Taiwan. This research applied electrical copper recovery system to recover copper metal. In this work, electrotreatment of a industrial copper wastewater ([Cu] = 30000 mg L−1 was studied with titanium net coated with a thin layer of RuO2/IrO2 (DSA reactor. The optimal result for simulated copper solution was 99.9% copper recovery efficiency in current density 0.585 A/dm2 and no iron ion. Due to high concentration of iron and chloride ions in real industrial wastewater, the copper recovery efficiency was down to 60%. Although, the copper recovery efficiency was not high as simulated copper solution, high environmental economic value was included in the technology. The possibility of pretreating the wastewater with iron is the necessary step, before the electrical recovery copper system.

  15. The effects of copper proximity on oxalate production in Fibroporia radiculosa

    Science.gov (United States)

    Katie M. Jenkins; Carol A. Clausen; Frederick Green III

    2014-01-01

    Copper remains a key component used in wood preservatives available today. However, the observed tolerance of several critical wood rotting organisms continues to be problematic. Tolerance to copper has been linked to the production and accumulation of oxalate, which precipitates copper into insoluble copper-oxalate crystals, thus inactivating copper ions. The purpose...

  16. Preparation of Copper Telluride Films by Co-Reduction of Cu(I) and Te(IV) Ions in Choline Chloride: Ethylene Glycol Ionic Liquid

    Science.gov (United States)

    Golgovici, Florentina; Catrangiu, Adriana-Simona; Stoian, Andrei Bogdan; Anicai, Liana; Visan, Teodor

    2016-07-01

    Cathodic processes of direct co-reduction of Cu+ and Te4+ ions on Pt electrode at 60°C were investigated using cyclic voltammetry and electrochemical impedance spectroscopy techniques. The ionic liquid as background electrolyte consisted of a mixture of choline chloride and ethylene glycol (ChCl-EG 1:2 mol ratio) in which 5-20 mM CuCl and 8 mM TeO2 were dissolved. The voltammograms exhibited the following successive cathodic processes: Cu2+/Cu+ reduction, Te underpotential deposition, simultaneous deposition of Cu metal and CuTe compound, and deposition of Te-rich CuTe compound at the most negative potentials (from -0.5 V to -0.8 V). Corresponding dissolution or oxidation peaks were recorded on the anodic branch. The voltammetric results were confirmed by electrochemical impedance spectra. Copper telluride films have been synthesized on platinum substrate via potentiostatic electrodeposition at 60°C. It was found from atomic force microscopy that CuTe film samples prepared from ChCl-EG + 5 mM CuCl + 8 mM TeO2 ionic liquid have high growth rates. The x-ray diffraction patterns of the deposited films from ChCl-EG + 10 mM CuCl + 8 mM TeO2 ionic liquid indicated the presence of a Cu2Te phase for film deposited at -0.7 V and a Cu0.656Te0.344 phase for film deposited at -0.6 V.

  17. Efficient On-Off Ratiometric Fluorescence Probe for Cyanide Ion Based on Perturbation of the Interaction between Gold Nanoclusters and a Copper(II)-Phthalocyanine Complex.

    Science.gov (United States)

    Shojaeifard, Zahra; Hemmateenejad, Bahram; Shamsipur, Mojtaba

    2016-06-22

    A new ratiometric fluorescent sensor was developed for the sensitive and selective detection of cyanide ion (CN(-)) in aqueous media. The ratiometric sensing system is based on CN(-) modulated recovery of copper(II) phthalocyanine (Cu(PcTs)) fluorescence signal at the expense of diminished fluorescence intensity of gold nanoclusters (AuNCs). Preliminary experiments revealed that the AuNCs and Cu(PcTs) possess a turn-off effect on each other, the interaction of which being verified through studying their interactions by principle component analysis (PCA) and multivariate cure resolution-alternating least-squares (MCR-ALS) methods. In the presence of CN(-) anion, the AuNCs and Cu(PcTs) interaction was perturbed, so that the fluorescence of Cu (PcTs), already quenched by AuNCs, was found to be efficiently recovered, while the fluorescence intensity of AuNCs was quenched via the formation of a stable [Au(CN)2](-) species. The ratiometric variation of AuNCs and Cu(PcTs) fluorescence intensities leads to designing a highly sensitive probe for CN(-) ion detection. Under the optimal conditions, CN(-) anion was detected without needing any etching time, over the concentration range of 100 nM-220 μM, with a detection limit of 75 nM, which is much lower than the allowable level of CN(-) in water permitted by the World Health Organization (WHO). Moreover, the detection of CN(-) was developed based on the CN(-) effects on the blue and red florescent colors of Cu(PcTs) and AuNCs, respectively. The designed probe displays a continuous color change from red to blue by addition of CN(-), which can be clearly observed by the naked eye in the range of 7-350 μM, under UV lamp. The prepared AuNCs/Cu(PcTs) probe was successfully utilized for the selective and sensitive determination of CN(-) anion in two different types of natural water (Rodbal dam and rainwater) and also in blood serum as a biological sample.

  18. Electrochemical behaviour of alkaline copper complexes

    Indian Academy of Sciences (India)

    C L Aravinda; S M Mayanna; V R Muralidharan

    2000-10-01

    A search for non-cyanide plating baths for copper resulted in the development of alkaline copper complex baths containing trisodium citrate [TSC] and triethanolamine [TEA]. Voltammetric studies were carried out on platinum to understand the electrochemical behaviour of these complexes. In TSC solutions, the deposition of copper involves the slow formation of a monovalent species. Adsorption of this species obeys Langmuir isotherm. In TEA solutions the deposition involves the formation of monovalent ions obeying the non-activated Temkin isotherm. Conversion of divalent to monovalent copper is also slow. In TEA and TSC alkaline copper solutions, the predominant species that undergo stepwise reduction contain only TEA ligands

  19. Cellular copper distribution: a mechanistic systems biology approach.

    Science.gov (United States)

    Banci, Lucia; Bertini, Ivano; Cantini, Francesca; Ciofi-Baffoni, Simone

    2010-08-01

    Copper is an essential but potentially harmful trace element required in many enzymatic processes involving redox chemistry. Cellular copper homeostasis in mammals is predominantly maintained by regulating copper transport through the copper import CTR proteins and the copper exporters ATP7A and ATP7B. Once copper is imported into the cell, several pathways involving a number of copper proteins are responsible for trafficking it specifically where it is required for cellular life, thus avoiding the release of harmful free copper ions. In this study we review recent progress made in understanding the molecular mechanisms of copper transport in cells by analyzing structural features of copper proteins, their mode of interaction, and their thermodynamic and kinetic parameters, thus contributing to systems biology of copper within the cell.

  20. A sensitive and selective sensing platform based on CdTe QDs in the presence of l-cysteine for detection of silver, mercury and copper ions in water and various drinks.

    Science.gov (United States)

    Gong, Tingting; Liu, Junfeng; Liu, Xinxin; Liu, Jie; Xiang, Jinkun; Wu, Yiwei

    2016-12-15

    Water soluble CdTe quantum dots (QDs) have been prepared simply by one-pot method using potassium tellurite as stable tellurium source and thioglycolic acid (TGA) as stabilizer. The fluorescence of CdTe QDs can be improved 1.3-fold in the presence of l-cysteine (Cys), however, highly efficiently quenched in the presence of silver or mercury or copper ions. A sensitive and selective sensing platform for analysis of silver, mercury and copper ions has been simply established based on CdTe QDs in the presence of l-cysteine. Under the optimum conditions, excellent linear relationships exist between the quenching degree of the sensing platform and the concentrations of Ag(+), Hg(2+) and Cu(2+) ranging from 0.5 to 40ngmL(-1). By using masking agents of sodium diethyldithiocarbamate (DDTC) for Ag(+) and Cu(2+), NH4OH for Ag(+) and Hg(2+) and 1-(2-Pyridylazo)-2-naphthol (PAN) for Hg(2+) and Cu(2+), Hg(2+), Cu(2+) and Ag(+) can be exclusively detected in coexistence with other two ions, and the detection limits (3σ) were 0.65, 0.063 and 0.088ngmL(-1) for Ag(+), Hg(2+) and Cu(2+), respectively. This effective sensing platform has been used to detection of Ag(+), Hg(2+) and Cu(2+) in water and various drinks with satisfactory results.

  1. 铜离子转运蛋白家族与肺癌顺铂耐药的研究进展%Research progress on copper ion transport protein family and cisplatin drug resistance in lung cancer

    Institute of Scientific and Technical Information of China (English)

    阳甜; 陈天君; 陈明伟

    2012-01-01

    铂类药作为化疗一种关键药之一,被广泛用于治疗各种恶性肿瘤,如卵巢、膀胱、头颈部肿瘤及肺癌.但铂类耐药的发生限制了化疗反应,影响了患者的预后.目前在铂类耐药的机制方面已经有一些重要的发展,其中之一是肿瘤铂类耐药与细胞内浓度的蓄积之间的相关性,摄入的减少和泵出过多均可减少药物在细胞内的聚积,导致耐药.但是具体耐药机制尚不清楚.铜离子动态平衡是由铜离子转运蛋白及其分子伴侣来维持.铜离子转运蛋白家族包括铜离子转运蛋白和铜离子转运磷酸化ATP酶.本文将就铜离子转运蛋白家族与肺癌顺铂耐药作一综述.%Cisplatin is one of the most important chemotherapeutic agents,commonly used for treatment of various cancers including ovary,endometrial,lung and gastric cancer.The secondary drugresistance,however,limits the efficacy of chemotherapy and consequently compromises the prognosis of patients.Recently,there have been some important developments in the understanding of mechanisms of tumor resistance to cisplatin.One of them is concerning the association between the tumor resistance to platinum drugs and the reduced intracellular accumulation owing to impaired drug intake and enhanced outward transport.However,mechanisms for transporting platinum drugs were not known until recently studies have shown that copper transporters may be involved in the transport of platinum-based anticancer drugs.Body copper homeostasis is maintained by a group of proteins including copper transporters and chaperones.Copper transporters include copper transporter 1 and copper-transporting P-type adenosine triphosphatase.This paper will state copper ion transport protein family and cisplatin drug resistance in lung cancer.

  2. Sorption mechanisms of iodide ions on oxides and divided copper sulfides; environmental outlook; Mecanismes de sorption des ions iodure sur les oxydes et les sulfures de cuivre divises; perspectives environnementales

    Energy Technology Data Exchange (ETDEWEB)

    Lefevre, G

    1999-10-15

    The radioactive iodine released in environment is a great risk for health. Copper compounds have a sufficient affinity for tracking this element inside a solid phase. These researches are useful in 1)the obtention of a hatch material hindering the iodine 129, released by nuclear wastes, to reach the biosphere, 2)the development of decontamination processes, 3)the forecast of the becoming of iodine in the environment, and 4)the design of analyses methods based on a iodine preconcentration on a solid. Three copper systems have been used: Cu{sub 2}O, copper sulfides (Cu{sub 2}S, CuFeS{sub 2} and CuS) and the mixture metallic copper/copper(II)carbonate. CuI is formed on Cu{sub 2}O in acid solutions. The adsorption of iodines occur in basic solutions, by exchange with Cu{sub 2}O surface hydroxyls, which losses its fixation properties if a reduction potential transforms it into metallic copper. An electrochemical analysis method of the iodine by preconcentration on Cu{sub 2}O in acid solution has been developed; its detection limit is of 5.10{sup -7} M. The three sulfide used (Cu{sub 2}S, CuFeS{sub 2} and CuS) adsorb the iodides. The similarity of their reactivity is due to the presence of copper(I). The stability of Cu{sub 2}S and CuFeS{sub 2} could allow to these compounds to keep their efficiency to the reducing potentials of the underground medium. At last, when they are into contact with a metallic copper/azurite mixture, the iodides precipitate to the copper surface. This study is then a synthesis of the properties of the copper(I) systems towards iodides in high concentration ({>=}10{sup -4} M). (O.M.)

  3. Trace elements in human physiology and pathology. Copper.

    Science.gov (United States)

    Tapiero, H; Townsend, D M; Tew, K D

    2003-11-01

    Copper is a trace element, important for the function of many cellular enzymes. Copper ions can adopt distinct redox states oxidized Cu(II) or reduced (I), allowing the metal to play a pivotal role in cell physiology as a catalytic cofactor in the redox chemistry of enzymes, mitochondrial respiration, iron absorption, free radical scavenging and elastin cross-linking. If present in excess, free copper ions can cause damage to cellular components and a delicate balance between the uptake and efflux of copper ions determines the amount of cellular copper. In biological systems, copper homeostasis has been characterized at the molecular level. It is coordinated by several proteins such as glutathione, metallothionein, Cu-transporting P-type ATPases, Menkes and Wilson proteins and by cytoplasmic transport proteins called copper chaperones to ensure that it is delivered to specific subcellular compartments and thereby to copper-requiring proteins.

  4. The Amyloid Precursor Protein of Alzheimer's Disease in the Reduction of Copper(II) to Copper(I)

    Science.gov (United States)

    Multhaup, Gerd; Schlicksupp, Andrea; Hesse, Lars; Beher, Dirk; Ruppert, Thomas; Masters, Colin L.; Beyreuther, Konrad

    1996-03-01

    The transition metal ion copper(II) has a critical role in chronic neurologic diseases. The amyloid precursor protein (APP) of Alzheimer's disease or a synthetic peptide representing its copper-binding site reduced bound copper(II) to copper(I). This copper ion-mediated redox reaction led to disulfide bond formation in APP, which indicated that free sulfhydryl groups of APP were involved. Neither superoxide nor hydrogen peroxide had an effect on the kinetics of copper(II) reduction. The reduction of copper(II) to copper(I) by APP involves an electron-transfer reaction and could enhance the production of hydroxyl radicals, which could then attack nearby sites. Thus, copper-mediated toxicity may contribute to neurodegeneration in Alzheimer's disease.

  5. Study on copper adsorption on olivine

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The copper adsorption on olivine supplied by A/S Olivine production plant at Aheim in western Norway has been studied. The factors which affect the uptake of copper have been evaluated. The results reveal that the equilibrium pH in aqueous solution has the greatest influence on the copper adsorption thanks to the competitive adsorption between proton and copper ions, and the adsorption of copper to olivine increases rapidly with the pH increasing from 4 to 6. The initial copper concentration and olivine dose also possess significant effect on copper adsorption. The adsorption efficieny of copper increases with the increase of olivine dose or the decrease of initial copper concentration at the same pH. The ionic strength effect on the adsorption has also been investigated, but it owns little effect on the adsorption process of copper due to the formation of inner sphere surface complexation of copper on olivine. The experimental data show that olivine has a high acid buffer capacity and is an effective adsorbent for copper.

  6. 铜(II)离子对橙皮素清除自由基作用的影响%Study on effect of copper (II) ion on radical scavenging of hesperetin

    Institute of Scientific and Technical Information of China (English)

    邹淑君; 许树军; 张蕾; 徐暘

    2015-01-01

    为探讨Cu2+存在对橙皮素( Hsp)清除自由基作用的影响.将Hsp与Cu2+混合即生成不稳定配合物(Hsp-Cu),利用UV-Vis光谱测定Hsp及Hsp-Cu对1,1-二苯基-2-三硝基苯肼自由基( DPPH·)、羟基自由基(· OH)、超氧阴离子自由基( O2-·)的清除作用.在实验条件下Hsp-Cu对DPPH·及· OH有一定的清除作用,但清除能力不如Hsp.Hsp-Cu不能有效清除O2-·,且在邻苯三酚自氧化过程中表现出促氧化作用.表明Hsp作为抗氧化剂使用时,应避免与Cu2+接触,以免影响其抗氧化能力.%To study the affection of Copper ( II ) ions on radical scavenging of hesperetin . Unstable hesperetin -copper ( II ) complex was generated when hesperetin was mixed with copper ( II ) chloride dihydrate .By the contrast tests on the scavenging reaction to DPPH radical, hydroxyl radical (· OH), and superoxide free radical (O2 -· ) of hesperetin -copper ( II) complex and hesperetin , proves that the scavenging activity of DPPH · and · OH of hesperetin-copper ( II) complex was weaker than that of hesperetin .The hesperetin-copper (II) complex can’t scavenge O2 -· showing accelerated oxidation in the process of pyrogallol autoxidation .Hesperetin was used as an antioxidant , cannot coexist with Cu 2+, so as not to affect the antioxidant capacity of hesperetin .

  7. Comparative genomic analyses of copper transporters and cuproproteomes reveal evolutionary dynamics of copper utilization and its link to oxygen.

    Directory of Open Access Journals (Sweden)

    Perry G Ridge

    Full Text Available Copper is an essential trace element in many organisms and is utilized in all domains of life. It is often used as a cofactor of redox proteins, but is also a toxic metal ion. Intracellular copper must be carefully handled to prevent the formation of reactive oxygen species which pose a threat to DNA, lipids, and proteins. In this work, we examined patterns of copper utilization in prokaryotes by analyzing the occurrence of copper transporters and copper-containing proteins. Many organisms, including those that lack copper-dependent proteins, had copper exporters, likely to protect against copper ions that inadvertently enter the cell. We found that copper use is widespread among prokaryotes, but also identified several phyla that lack cuproproteins. This is in contrast to the use of other trace elements, such as selenium, which shows more scattered and reduced usage, yet larger selenoproteomes. Copper transporters had different patterns of occurrence than cuproproteins, suggesting that the pathways of copper utilization and copper detoxification are independent of each other. We present evidence that organisms living in oxygen-rich environments utilize copper, whereas the majority of anaerobic organisms do not. In addition, among copper users, cuproproteomes of aerobic organisms were larger than those of anaerobic organisms. Prokaryotic cuproproteomes were small and dominated by a single protein, cytochrome c oxidase. The data are consistent with the idea that proteins evolved to utilize copper following the oxygenation of the Earth.

  8. Tuning of copper nanocrystals optical properties with their shapes.

    Science.gov (United States)

    Salzemann, C; Brioude, A; Pileni, M-P

    2006-04-13

    Copper nanocrystals are obtained by chemical reduction of copper ions in mixed reverse micelles. A large excess of reducing agent favors producing a new generation of shaped copper nanocrystals as nanodisks, elongated nanocrystals, and cubes. By using UV-Visible spectroscopy and numerical optical simulations we demonstrate that the optical properties are tuned by the relative proportions of spheres and nanodisks.

  9. Molecular responses of mouse macrophages to copper and copper oxide nanoparticles inferred from proteomic analyses.

    Science.gov (United States)

    Triboulet, Sarah; Aude-Garcia, Catherine; Carrière, Marie; Diemer, Hélène; Proamer, Fabienne; Habert, Aurélie; Chevallet, Mireille; Collin-Faure, Véronique; Strub, Jean-Marc; Hanau, Daniel; Van Dorsselaer, Alain; Herlin-Boime, Nathalie; Rabilloud, Thierry

    2013-11-01

    The molecular responses of macrophages to copper-based nanoparticles have been investigated via a combination of proteomic and biochemical approaches, using the RAW264.7 cell line as a model. Both metallic copper and copper oxide nanoparticles have been tested, with copper ion and zirconium oxide nanoparticles used as controls. Proteomic analysis highlighted changes in proteins implicated in oxidative stress responses (superoxide dismutases and peroxiredoxins), glutathione biosynthesis, the actomyosin cytoskeleton, and mitochondrial proteins (especially oxidative phosphorylation complex subunits). Validation studies employing functional analyses showed that the increases in glutathione biosynthesis and in mitochondrial complexes observed in the proteomic screen were critical to cell survival upon stress with copper-based nanoparticles; pharmacological inhibition of these two pathways enhanced cell vulnerability to copper-based nanoparticles, but not to copper ions. Furthermore, functional analyses using primary macrophages derived from bone marrow showed a decrease in reduced glutathione levels, a decrease in the mitochondrial transmembrane potential, and inhibition of phagocytosis and of lipopolysaccharide-induced nitric oxide production. However, only a fraction of these effects could be obtained with copper ions. In conclusion, this study showed that macrophage functions are significantly altered by copper-based nanoparticles. Also highlighted are the cellular pathways modulated by cells for survival and the exemplified cross-toxicities that can occur between copper-based nanoparticles and pharmacological agents.

  10. Molecular Responses of Mouse Macrophages to Copper and Copper Oxide Nanoparticles Inferred from Proteomic Analyses*

    Science.gov (United States)

    Triboulet, Sarah; Aude-Garcia, Catherine; Carrière, Marie; Diemer, Hélène; Proamer, Fabienne; Habert, Aurélie; Chevallet, Mireille; Collin-Faure, Véronique; Strub, Jean-Marc; Hanau, Daniel; Van Dorsselaer, Alain; Herlin-Boime, Nathalie; Rabilloud, Thierry

    2013-01-01

    The molecular responses of macrophages to copper-based nanoparticles have been investigated via a combination of proteomic and biochemical approaches, using the RAW264.7 cell line as a model. Both metallic copper and copper oxide nanoparticles have been tested, with copper ion and zirconium oxide nanoparticles used as controls. Proteomic analysis highlighted changes in proteins implicated in oxidative stress responses (superoxide dismutases and peroxiredoxins), glutathione biosynthesis, the actomyosin cytoskeleton, and mitochondrial proteins (especially oxidative phosphorylation complex subunits). Validation studies employing functional analyses showed that the increases in glutathione biosynthesis and in mitochondrial complexes observed in the proteomic screen were critical to cell survival upon stress with copper-based nanoparticles; pharmacological inhibition of these two pathways enhanced cell vulnerability to copper-based nanoparticles, but not to copper ions. Furthermore, functional analyses using primary macrophages derived from bone marrow showed a decrease in reduced glutathione levels, a decrease in the mitochondrial transmembrane potential, and inhibition of phagocytosis and of lipopolysaccharide-induced nitric oxide production. However, only a fraction of these effects could be obtained with copper ions. In conclusion, this study showed that macrophage functions are significantly altered by copper-based nanoparticles. Also highlighted are the cellular pathways modulated by cells for survival and the exemplified cross-toxicities that can occur between copper-based nanoparticles and pharmacological agents. PMID:23882024

  11. Biological Role of Cobalt(II), Copper(II) and Nickel(II) Metal Ions on the Antibacterial Properties of Some Nicotinoyl-Hydrazine Derived Compounds

    OpenAIRE

    Chohan, Zahid H.; Sherazi, Syed K. A.

    1997-01-01

    Several cobalt(II), copper(II) and nickel(II) complexes of nicotinoylhydrazine-derived compounds were prepared and characterised by physical, spectral and analytical data. These compounds and their complexes have proven to be antibacterial. The screening data show the metal complexes to be more potential/bactericidal than the uncomplexed compounds against one or more bacterial species.

  12. Structure of a copper-isoniazid complex.

    Science.gov (United States)

    Hanson, J C; Camerman, N; Camerman, A

    1981-11-01

    It is well-known that complex formation with copper ions increases the in vitro mycobactericidal action of the antituberculosis agent isoniazid. We report here the preparation and structure of a copper(II)-isoniazid complex. Unit cell parameters are a = 9.575, b = 14.855, and c = 7.056 A and space group P2(1)2(1)2(1). Copper bonding geometry is square planar with the isoniazid carbonyl oxygen and hydrazide amino nitrogen atoms and two chlorines occupying coordination positions. Complexing with copper(II) does not significantly alter the isoniazid molecular conformation.

  13. Synthesis zeolite from Na2CO3 activated flyash for copper ions removal%Na2 CO3活化粉煤灰合成沸石及去除Cu2+性能

    Institute of Scientific and Technical Information of China (English)

    曹月坤; 陈文艺; 邓慧; 白云; 张志强

    2015-01-01

    Zeolites were synthesized through high temperature melting method,hydrothermal method and hydrothermal assisted pressure method based on fly ash as a matrix material with Na2 CO3 as alkaline acti-vating reagent,and their removal effect of copper ions were compared. Influence of hydrothermal tempera-ture,autogenous pressure,Na2 CO3 concentration,liquid to solid ratio,hydrothermal time and other factors on Na2 CO3 alkaline activation of fly ash were investigated. Results showed that the hydrothermal assisted pressure synthesis of zeolite adsorption of copper ions was the best,removal rate for 200 mg/L copper ion reached 92% when temperature was 90 ℃,self-generated pressure was 0. 038 MPa,Na2 CO3 was 2. 0 mol/L,liquid-solid ratio was 10∶1 and hydrothermal time was 2 h. XRD and SEM description sugges-ted that synthesic zeolite was NaP.%以粉煤灰为基质材料,Na2 CO3为碱性活化试剂,比较了高温熔融法、水热法和加压水热法合成沸石对铜离子的去除效果。研究了水热温度及压力、Na2 CO3浓度、液固比、水热时间等因素对Na2 CO3碱性活化粉煤灰的影响。结果表明,加压水热法合成的沸石对铜离子的吸附效果最好,温度90℃,自生压0.038 MPa,Na2 CO32.0 mol/L,液固比10∶1、水热时间2 h时合成的沸石对初始浓度200 mg/L的铜离子的去除率可达92%,XRD表征说明合成的沸石为NaP型。

  14. Adsorption Treatment of Copper Ion and Corrosive Sulfur in Transformer Oil%变压器油中腐蚀性硫与铜离子综合处理研究

    Institute of Scientific and Technical Information of China (English)

    万涛; 周舟; 冯兵; 钱晖; 何铁祥

    2016-01-01

    Corrosive sulfur and copper ion often exist in transformer oils. It is extremely dangerous to the safety and stability operation of transformers. In view of this technical problem, we used an effective adsorbent to remove the corrosive sulfur and copper ion. The results show that after adsorption treatment for 84 h, the copper ion decreases from 1.2 mg/kg to 0.2 mg/kg, the dielectric loss factor decreases from 1.57% to 0.057%, the volume resistivity increases from 3.6 × 1010Ω·m to 1.96 × 1011Ω·m, the total sulfur decreases from 550.1 mg/kg to 380.8 mg/kg, and the corrosive sulfur decreases from 51.6 mg/L to 18.1 mg/L. The insulation resistance of transformer winding increases about three times, and the absorp-tion ratio return to normal. Moreover, the treatment process has no harmful effect to the antioxidant T501 content, water, interfacial tension acid value, and breakdown voltage.%变压器油中存在腐蚀性硫和铜离子会严重威胁变压器的安全稳定运行.针对腐蚀性硫和铜离子综合治理这一技术难题,采用吸附法对变压器油进行脱除处理.结果表明:经过84 h吸附处理,油中铜离子含量从1.2 mg/kg降至0.2 mg/kg,介质损耗因数从1.57%降至0.057%,体积电阻率从3.6 × 1010Ω·m升至1.96 × 1012Ω·m,总硫含量从550.1 mg/kg降至380.8 mg/kg,腐蚀性硫含量从51.6 mg/L降至18.1 mg/L.绕组绝缘电阻提高约3倍,吸收比恢复正常.处理过程对抗氧剂T501含量、水分、酸值、界面张力和击穿电压没有不良影响.

  15. Copper Ion Accumulation in Litopenaeus Vannamei and the Effect on Metallothionein in Different Aquaculture Systems%铜离子在养殖对虾组织中的积累及其对金属硫蛋白含量的影响

    Institute of Scientific and Technical Information of China (English)

    李湘萍; 程波; 程江峰; 刘鹰

    2011-01-01

    为考察铜在循环水与静水养殖系统的凡纳滨对虾组织中的积累,本实验在两种养殖系统中分别添加硫酸铜,并使其浓度保持一致,经过92 d的培养,对铜在虾组织中的积累量进行了测定.结果表明,在两种系统中养殖的对虾,其组织中铜浓度依次为:肝胰t>鳃丝>甲壳>肌肉,肝胰腺中金属硫蛋白(MT)与肝胰腺中铜的积累有相似变化趋势.循环水系统与静水系统中虾肝胰腺和甲壳中铜的积累量有显著差异,而两种系统中虾鳃丝中铜的积累量差异不明显.%In order to study the accumulation of copper ion in shrimp of different aqua-culture systems, we added a certain concentration of sulfate copper in aquaculture systems and kept in the same level during the experiment. After 92 d, the accumulation of copper ion in different tissues and systems were analyzed. The copper accumulation in different tissues both in recirculating aquaculture system (RAS) and static aquaculture system (SAS) had the same accumulation currence: hepatopancreas > lamella > cara-pace> muscle. The concentration of metallothionein(MT) in hepatopancreas had the same change with the copper accumulation. The accumulation of copper in hepatopancreas and carapace in different aquaculture systems had significant difference, while copper ion in lamella changed insignificantly.

  16. Antimicrobial properties of zeolite-X and zeolite-A ion-exchanged with silver, copper, and zinc against a broad range of microorganisms.

    Science.gov (United States)

    Demirci, Selami; Ustaoğlu, Zeynep; Yılmazer, Gonca Altın; Sahin, Fikrettin; Baç, Nurcan

    2014-02-01

    Zeolites are nanoporous alumina silicates composed of silicon, aluminum, and oxygen in a framework with cations, water within pores. Their cation contents can be exchanged with monovalent or divalent ions. In the present study, the antimicrobial (antibacterial, anticandidal, and antifungal) properties of zeolite type X and A, with different Al/Si ratio, ion exchanged with Ag(+), Zn(2+), and Cu(2+) ions were investigated individually. The study presents the synthesis and manufacture of four different zeolite types characterized by scanning electron microscopy and X-ray diffraction. The ion loading capacity of the zeolites was examined and compared with the antimicrobial characteristics against a broad range of microorganisms including bacteria, yeast, and mold. It was observed that Ag(+) ion-loaded zeolites exhibited more antibacterial activity with respect to other metal ion-embedded zeolite samples. The results clearly support that various synthetic zeolites can be ion exchanged with Ag(+), Zn(2+), and Cu(2+) ions to acquire antimicrobial properties or ion-releasing characteristics to provide prolonged or stronger activity. The current study suggested that zeolite formulations could be combined with various materials used in manufacturing medical devices, surfaces, textiles, or household items where antimicrobial properties are required.

  17. Site Preference in Multimetallic Nanoclusters: Incorporation of Alkali Metal Ions or Copper Atoms into the Alkynyl-Protected Body-Centered Cubic Cluster [Au7 Ag8 (C≡C(t) Bu)12 ]().

    Science.gov (United States)

    Wang, Yu; Su, Haifeng; Ren, Liting; Malola, Sami; Lin, Shuichao; Teo, Boon K; Häkkinen, Hannu; Zheng, Nanfeng

    2016-11-21

    The synthesis, structure, substitution chemistry, and optical properties of the gold-centered cubic monocationic cluster [Au@Ag8 @Au6 (C≡C(t) Bu)12 ](+) are reported. The metal framework of this cluster can be described as a fragment of a body-centered cubic (bcc) lattice with the silver and gold atoms occupying the vertices and the body center of the cube, respectively. The incorporation of alkali metal atoms gave rise to [Mn Ag8-n Au7 (C≡C(t) Bu)12 ](+) clusters (n=1 for M=Na, K, Rb, Cs and n=2 for M=K, Rb), with the alkali metal ion(s) presumably occupying the vertex site(s), whereas the incorporation of copper atoms produced [Cun Ag8 Au7-n (C≡C(t) Bu)12 ](+) clusters (n=1-6), with the Cu atom(s) presumably occupying the capping site(s). The parent cluster exhibited strong emission in the near-IR region (λmax =818 nm) with a quantum yield of 2 % upon excitation at λ=482 nm. Its photoluminescence was quenched upon substitution with a Na(+) ion. DFT calculations confirmed the superatom characteristics of the title compound and the sodium-substituted derivatives. © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. A novel solidified floating organic drop microextraction method for preconcentration and determination of copper ions by flow injection flame atomic absorption spectrometry in water samples

    Directory of Open Access Journals (Sweden)

    Arpa Şahin Ç.

    2013-04-01

    Full Text Available A simple, rapid and inexpensive solidified floating organic drop microextraction (SFODME and flow injection flame atomic absorption spectrometric determination (FI-FAAS method for copper was developed. 3-amino-7-dimethylamino-2-methylphenazine (Neutral red, NR was used as the complexing agent. Several factors affecting the microextraction efficiency, such as, pH, NR and sodium dodecylbenzenesulfonate (SDBS concentration, extraction time, stirring rate, and temperature were investigated and optimized. Under optimized experimental conditions an enrichment factor of 541 was obtained for 100 mL of sample solution. The calibration graph was linear in the range of 0.5 – 20.0 ng mL–1 and the limit of detection (3s was 0.18 ng mL–1, the limit of quantification (10s was 0.58 ng mL–1. The relative standard deviation (RSD for 10 replicate measurements of 10 ng mL–1 copper was 2.7%. The developed method was successfully applied to the extraction and determination of copper in different certified reference materials (Estuarine water, Slew 3 and fortified water, TM 23.2 and real water samples and satisfactory results were obtained.

  19. Synthesis of nano-sized stereoselective imprinted polymer by copolymerization of (S)-2-(acrylamido) propanoic acid and ethylene glycol dimethacrylate in the presence of racemic propranolol and copper ion.

    Science.gov (United States)

    Alizadeh, Taher; Bagherzadeh, Azam; Shamkhali, Amir Nasser

    2016-06-01

    A new chiral functional monomer of (S)-2-(acrylamido) propanoic acid was obtained by reaction of (l)-alanine with acryloyl chloride. The resulting monomer was characterized by FT-IR and HNMR and then utilized for the preparation of chiral imprinted polymer (CIP). This was carried out by copolymerization of (l)-alanine-derived chiral monomer and ethylene glycol dimethacrylate, in the presence of racemic propranolol and copper nitrate, via precipitation polymerization technique, resulting in nano-sized networked polymer particles. The polymer obtained was characterized by scanning electron microscopy and FT-IR. The non-imprinted polymer was also synthesized and used as blank polymer. Density functional theory (DFT) was also employed to optimize the structures of two diasterometric ternary complexes, suspected to be created in the pre-polymerization step, by reaction of optically active isomers of propranolol, copper ion and (S)-2-(acrylamido) propanoic acid. Relative energies and other characteristics of the described complexes, calculated by the DFT, predicted the higher stability of (S)-propranolol involved complex, compared to (R)-propranolol participated complex. Practical batch extraction test which employed CIP as solid phase adsorbent, indicated that the CIP recognized selectively (S)-propranolol in the racemic mixture of propranolol; whereas, the non-imprinted polymer (NIP) showed no differentiation capability between two optically active isomers of propranolol. Copyright © 2016 Elsevier B.V. All rights reserved.

  20. Accumulation and hyperaccumulation of copper in plants

    Science.gov (United States)

    Adam, V.; Trnkova, L.; Huska, D.; Babula, P.; Kizek, R.

    2009-04-01

    Copper is natural component of our environment. Flow of copper(II) ions in the environment depends on solubility of compounds containing this metal. Mobile ion coming from soil and rocks due to volcanic activity, rains and others are then distributed to water. Bio-availability of copper is substantially lower than its concentration in the aquatic environment. Copper present in the water reacts with other compounds and creates a complex, not available for organisms. The availability of copper varies depending on the environment, but moving around within the range from 5 to 25 % of total copper. Thus copper is stored in the sediments and the rest is transported to the seas and oceans. It is common knowledge that copper is essential element for most living organisms. For this reason this element is actively accumulated in the tissues. The total quantity of copper in soil ranges from 2 to 250 mg / kg, the average concentration is 30 mg / kg. Certain activities related to agriculture (the use of fungicides), possibly with the metallurgical industry and mining, tend to increase the total quantity of copper in the soil. This amount of copper in the soil is a problem particularly for agricultural production of food. The lack of copper causes a decrease in revenue and reduction in quality of production. In Europe, shows the low level of copper in total 18 million hectares of farmland. To remedy this adverse situation is the increasing use of copper fertilizers in agricultural soils. It is known that copper compounds are used in plant protection against various illnesses and pests. Mining of minerals is for the development of human society a key economic activity. An important site where the copper is mined in the Slovakia is nearby Smolníka. Due to long time mining in his area (more than 700 years) there are places with extremely high concentrations of various metals including copper. Besides copper, there are also detected iron, zinc and arsenic. Various plant species

  1. Comparative proteomic analysis of the molecular responses of mouse macrophages to titanium dioxide and copper oxide nanoparticles unravels some toxic mechanisms for copper oxide nanoparticles in macrophages.

    Directory of Open Access Journals (Sweden)

    Sarah Triboulet

    Full Text Available Titanium dioxide and copper oxide nanoparticles are more and more widely used because of their catalytic properties, of their light absorbing properties (titanium dioxide or of their biocidal properties (copper oxide, increasing the risk of adverse health effects. In this frame, the responses of mouse macrophages were studied. Both proteomic and targeted analyses were performed to investigate several parameters, such as phagocytic capacity, cytokine release, copper release, and response at sub toxic doses. Besides titanium dioxide and copper oxide nanoparticles, copper ions were used as controls. We also showed that the overall copper release in the cell does not explain per se the toxicity observed with copper oxide nanoparticles. In addition, both copper ion and copper oxide nanoparticles, but not titanium oxide, induced DNA strands breaks in macrophages. As to functional responses, the phagocytic capacity was not hampered by any of the treatments at non-toxic doses, while copper ion decreased the lipopolysaccharide-induced cytokine and nitric oxide productions. The proteomic analyses highlighted very few changes induced by titanium dioxide nanoparticles, but an induction of heme oxygenase, an increase of glutathione synthesis and a decrease of tetrahydrobiopterin in response to copper oxide nanoparticles. Subsequent targeted analyses demonstrated that the increase in glutathione biosynthesis and the induction of heme oxygenase (e.g. by lovastatin/monacolin K are critical for macrophages to survive a copper challenge, and that the intermediates of the catecholamine pathway induce a strong cross toxicity with copper oxide nanoparticles and copper ions.

  2. Comparative proteomic analysis of the molecular responses of mouse macrophages to titanium dioxide and copper oxide nanoparticles unravels some toxic mechanisms for copper oxide nanoparticles in macrophages.

    Science.gov (United States)

    Triboulet, Sarah; Aude-Garcia, Catherine; Armand, Lucie; Collin-Faure, Véronique; Chevallet, Mireille; Diemer, Hélène; Gerdil, Adèle; Proamer, Fabienne; Strub, Jean-Marc; Habert, Aurélie; Herlin, Nathalie; Van Dorsselaer, Alain; Carrière, Marie; Rabilloud, Thierry

    2015-01-01

    Titanium dioxide and copper oxide nanoparticles are more and more widely used because of their catalytic properties, of their light absorbing properties (titanium dioxide) or of their biocidal properties (copper oxide), increasing the risk of adverse health effects. In this frame, the responses of mouse macrophages were studied. Both proteomic and targeted analyses were performed to investigate several parameters, such as phagocytic capacity, cytokine release, copper release, and response at sub toxic doses. Besides titanium dioxide and copper oxide nanoparticles, copper ions were used as controls. We also showed that the overall copper release in the cell does not explain per se the toxicity observed with copper oxide nanoparticles. In addition, both copper ion and copper oxide nanoparticles, but not titanium oxide, induced DNA strands breaks in macrophages. As to functional responses, the phagocytic capacity was not hampered by any of the treatments at non-toxic doses, while copper ion decreased the lipopolysaccharide-induced cytokine and nitric oxide productions. The proteomic analyses highlighted very few changes induced by titanium dioxide nanoparticles, but an induction of heme oxygenase, an increase of glutathione synthesis and a decrease of tetrahydrobiopterin in response to copper oxide nanoparticles. Subsequent targeted analyses demonstrated that the increase in glutathione biosynthesis and the induction of heme oxygenase (e.g. by lovastatin/monacolin K) are critical for macrophages to survive a copper challenge, and that the intermediates of the catecholamine pathway induce a strong cross toxicity with copper oxide nanoparticles and copper ions.

  3. Comparative Proteomic Analysis of the Molecular Responses of Mouse Macrophages to Titanium Dioxide and Copper Oxide Nanoparticles Unravels Some Toxic Mechanisms for Copper Oxide Nanoparticles in Macrophages

    Science.gov (United States)

    Triboulet, Sarah; Aude-Garcia, Catherine; Armand, Lucie; Collin-Faure, Véronique; Chevallet, Mireille; Diemer, Hélène; Gerdil, Adèle; Proamer, Fabienne; Strub, Jean-Marc; Habert, Aurélie; Herlin, Nathalie; Van Dorsselaer, Alain; Carrière, Marie; Rabilloud, Thierry

    2015-01-01

    Titanium dioxide and copper oxide nanoparticles are more and more widely used because of their catalytic properties, of their light absorbing properties (titanium dioxide) or of their biocidal properties (copper oxide), increasing the risk of adverse health effects. In this frame, the responses of mouse macrophages were studied. Both proteomic and targeted analyses were performed to investigate several parameters, such as phagocytic capacity, cytokine release, copper release, and response at sub toxic doses. Besides titanium dioxide and copper oxide nanoparticles, copper ions were used as controls. We also showed that the overall copper release in the cell does not explain per se the toxicity observed with copper oxide nanoparticles. In addition, both copper ion and copper oxide nanoparticles, but not titanium oxide, induced DNA strands breaks in macrophages. As to functional responses, the phagocytic capacity was not hampered by any of the treatments at non-toxic doses, while copper ion decreased the lipopolysaccharide-induced cytokine and nitric oxide productions. The proteomic analyses highlighted very few changes induced by titanium dioxide nanoparticles, but an induction of heme oxygenase, an increase of glutathione synthesis and a decrease of tetrahydrobiopterin in response to copper oxide nanoparticles. Subsequent targeted analyses demonstrated that the increase in glutathione biosynthesis and the induction of heme oxygenase (e.g. by lovastatin/monacolin K) are critical for macrophages to survive a copper challenge, and that the intermediates of the catecholamine pathway induce a strong cross toxicity with copper oxide nanoparticles and copper ions. PMID:25902355

  4. Two novel Krebs-type polyoxoanions [Cu I2(WO 2) 2(β-XW 9O 33) 2] 12- (X = Sb III, Bi III) resulting in 2D layer structures linked by copper(I) ions and copper(II) complex groups

    Science.gov (United States)

    Zhang, Wei; Liu, Shuxia; Feng, Dan; Zhang, Chundan; Sun, Ping; Ma, Fengji

    2009-11-01

    Two sandwich-type organic-inorganic hybrid polyoxotungstates [enH 2] 5[Cu II(en) 2][Cu I2(WO 2) 2(β-SbW 9O 33) 2]·16H 2O ( 1) and [enH 2] 5[Cu II(en) 2][Cu I2(WO 2) 2(β-BiW 9O 33) 2]·22H 2O ( 2) (en = ethylenediamine) have been synthesized hydrothermally and structurally characterized by elemental analyses, IR spectra, thermal stability analyses, X-ray powder diffraction, and single-crystal X-ray diffraction. The polyoxoanions in 1 and 2 are composed of two trivacant (B-β-XW 9O 33) 9- (X = Sb III ( 1), Bi III ( 2)) subunits joined together by two Cu(I) ions and two W(VI) ions resulting in two novel Krebs-type sandwich structures. These polyoxoanions are further connected by Cu(I) ions and [Cu II(en) 2] 2+ coordination cations, and afford the first copper(I)-linked 2D layer structure constructed from Krebs-type polyoxotungstates. Additionally, the electrochemical behavior and electrocatalysis of 1 and 2 modified carbon paste electrodes (CPEs) have been studied. The results indicate that they have good electrocatalytic activities toward the reduction of nitrite.

  5. Síntese da zeólita ZSM-5 e suas propriedades estruturais após troca iônica com cobre Synthesis of the ZSM-5 zeolite and its structural properties after copper ion-exchange

    Directory of Open Access Journals (Sweden)

    E. L. Foletto

    2000-12-01

    Full Text Available A zeólita ZSM-5 foi sintetizada utilizando sílica "Aerosil-Degussa -- 380 m²/g" como fonte de silício, em substituição ao trisilicato de sódio, que é normalmente utilizado na síntese dessa zeólita. Subseqüentemente, foi incorporado cobre à ZSM-5 através do método convencional de troca iônica. Técnicas de difração de raios X, microscopia eletrônica de varredura, área superficial e análise elementar por absorção atômica foram utilizadas para verificar a formação da zeólita sintetizada e suas propriedades após troca com cobre. Os resultados mostraram que houve a formação da ZSM-5 nas condições de síntese empregadas e que a amostra modificada pelo processo de troca manteve as propriedades da zeólita original.The ZSM-5 zeolite was synthesized using silica "Aerosil-Degussa -- 380 m²/g" as silicon source, in substitution to the sodium trisilicate, which is usually employed in the zeolite synthesis. Subsequently, the copper was incorporated to ZSM-5 by conventional ion-exchange method. X-ray diffraction, scanning electron microscopy, surface area and elemental analysis by atomic absorption have been used to verify ZSM-5 formation and its properties after copper exchange. The results presented ZSM-5 formation in the employed synthesis conditions. The ion-exchanged sample conserved the original ZSM-5 properties.

  6. The role of natural zeolite and of zeolite modified with ammnonium ions to reduce the uptake of lead, zinc, copper and iron ions in Hieracium aurantium and Rumex acetosella grown on tailing ponds

    OpenAIRE

    Anca PETER; Mihaly-Cozmuta, Leonard; Anca MIHALY-COZMUTA; Camelia NICULA

    2011-01-01

    The objective of this research is to determine if zeolite modified with ammonium ions has a higher capacity than natural zeolite to protect Hieracium aurantium and Rumex acetosella growing on tailing ponds, by reducing the quantity of metal ions these plants would accumulate in their roots and leaves. The influence of the amount of zeolite in the substrate (5% and 10% mass percentage) was also studied. The experiments were carried out in laboratory and the concentration of the ions of heavy m...

  7. Effect of water pollutants to copper ion removal bv using cation exchange membrane%水中污染物对阳离子交换膜分离去除Cu2+的影响

    Institute of Scientific and Technical Information of China (English)

    谢德华; 施周; 陈世洋

    2012-01-01

    Baesd on Donnan dialysis mechanism, copper ion separation and removing experiments in raw water using exchange membrane was conducted under voltage free condition. The copper ion removing effects of cation exchange membrane cuased by various potential pollutants in raw water such as inorganic particles, organic matters, EDTA acid, ammonia, ferric ion and surfacatant etc, were studied. The results showed that upon addition any one of the above pollutants to raw water, would influence on the copper ions removing effects more or less after a long time operation procedure. To pollutants with no physical and chemical interaction with copper ion and membrane, such as silica and non-ionic surfactant, there were little influences on the copper ion separation of the cation exchange membrane and the Cu2+ removal decreased only by about 4% compared to that of blank control experiments; Cu2+ could be precipitated by ammonia and anionic surfaceactive agent, or adsorbed by humic acid which made the concentration of free Cu2+ in the solution reduce by about 50%; While to pollutants which could form complex compounds with Cu2+, serious effects on Cu2+ removal efficiency were observed. For EDTA acid, ammonia and anionic surfaceactive agent, the Cu2+ removal effects decreased by approximately 100%, 78% and 56% respectively; Cationic surfactants may occupy a lot of space of film render Cu2+ remove difficulty; ferric ion easily hydrolyzed into iron hydroxide colloids in weak acid or neutral solution induced Cu2+ removal effect decreased to certain extend, by about 12% compared to the blank.%基于Donnan dialysis原理,在无外加电压作用下采用阳离子交换膜分离去除原水中的Cu2+,研究原水中可能出现的无机颗粒物,有机物质,EDTA酸、氨水、Fe3+、表面活性剂等对阳离子交换膜分离去除Cu2+效果的影响.研究表明:原水中添加二氧化硅、腐殖酸、EDTA酸、氨水、Fe3+、表面活性剂等物质,在长时间运行后均

  8. Molecular mechanisms of the epithelial transport of toxic metal ions, particularly mercury, cadmium, lead, arsenic, zinc and copper. Progress report, January 1, 1980-December 31, 1980

    Energy Technology Data Exchange (ETDEWEB)

    Wasserman, R H

    1980-01-01

    Investigations were continued to elucidate the mode of transepithelial transport of toxic metal ions across the gastrointestinal tract, as well as their interactions with biological processes and other metal ions. All experimental details that are either published, submitted for publication or in press during this report period are included in the Appendix. Primary attention for this report has been given to the intestinal absorption of lead and its interaction with other biological moieties.

  9. Formation of copper oxychloride and reactive oxygen species as causes of uterine injury during copper oxidation of Cu-IUD.

    Science.gov (United States)

    Beltran-Garcia, M J; Espinosa, A; Herrera, N; Perez-Zapata, A J; Beltran-Garcia, C; Ogura, T

    2000-02-01

    The lining of the uterus and cervix might be injured by a variety of oxidation products of Cu in a Cu-IUD, including cuprous ions, dissolved and precipitated cupric ions, and reactive oxygen species such as superoxide radicals, hydrogen peroxide, and hydroxyl radicals. In this study, the human amnious WISH cell line was employed as a model of uterine cells in the presence of copper. The cell viability was decreased by elemental copper, which was alleviated up to 70% by the addition of catalase. The addition of copper oxychloride caused cell death in a dose-dependent manner. Hydroxyl radicals in the presence of copper were determined by the formation of malondialdehyde. Soluble cuprous chloride complexes are formed in the uterus by slowly entering oxygen. The complexes are partly oxidized to insoluble copper oxychloride. which damages the endometrium. Unoxidized cuprous ions migrate to the oxygen-rich cervix and are oxidized to copper oxychloride, causing cervix damage.

  10. Role of copper oxides in contact killing of bacteria.

    Science.gov (United States)

    Hans, Michael; Erbe, Andreas; Mathews, Salima; Chen, Ying; Solioz, Marc; Mücklich, Frank

    2013-12-31

    The potential of metallic copper as an intrinsically antibacterial material is gaining increasing attention in the face of growing antibiotics resistance of bacteria. However, the mechanism of the so-called "contact killing" of bacteria by copper surfaces is poorly understood and requires further investigation. In particular, the influences of bacteria-metal interaction, media composition, and copper surface chemistry on contact killing are not fully understood. In this study, copper oxide formation on copper during standard antimicrobial testing was measured in situ by spectroscopic ellipsometry. In parallel, contact killing under these conditions was assessed with bacteria in phosphate buffered saline (PBS) or Tris-Cl. For comparison, defined Cu2O and CuO layers were thermally generated and characterized by grazing incidence X-ray diffraction. The antibacterial properties of these copper oxides were tested under the conditions used above. Finally, copper ion release was recorded for both buffer systems by inductively coupled plasma atomic absorption spectroscopy, and exposed copper samples were analyzed for topographical surface alterations. It was found that there was a fairly even growth of CuO under wet plating conditions, reaching 4-10 nm in 300 min, but no measurable Cu2O was formed during this time. CuO was found to significantly inhibit contact killing, compared to pure copper. In contrast, thermally generated Cu2O was essentially as effective in contact killing as pure copper. Copper ion release from the different surfaces roughly correlated with their antibacterial efficacy and was highest for pure copper, followed by Cu2O and CuO. Tris-Cl induced a 10-50-fold faster copper ion release compared to PBS. Since the Cu2O that primarily forms on copper under ambient conditions is as active in contact killing as pure copper, antimicrobial objects will retain their antimicrobial properties even after oxide formation.

  11. 胺基接枝纤维的制备及其对铜离子吸附的应用研究%Study on Preparation and Application of Adsorption Copper Ions by Amino-grafted Fiber

    Institute of Scientific and Technical Information of China (English)

    卫威; 石美玲; 朱红祥

    2013-01-01

    以漂白蔗渣浆纤维素为基体,二乙烯三胺为单体,硝酸铈铵为引发剂,制备胺基接枝纤维,得到高效重金属吸附剂。研究了单体用量、引发剂用量、温度、时间等反应因素对胺基接枝纤维制备的影响。采用红外光谱、X射线衍射和扫描电镜分析表征胺基接枝纤维的结构。从温度、时间、pH值、接枝纤维加入量和铜离子溶液初始浓度方面对胺基接枝纤维吸附二价铜离子进行研究,探究较好的吸附条件。结果表明,当绝干蔗渣纤维∶单体二乙烯三胺=1∶1(质量比),硝酸铈铵的用量为25%,温度为70℃,时间为2h时,可以获得较高的吸附量,其吸附量可以达到12.8 mg·g-1。通过红外光谱和扫描电镜分析手段对接枝纤维的结构进行表征。胺基接枝纤维对铜离子溶液吸附的较优条件为:时间20min,温度为30℃,pH值为4.5,初始浓度为400mg·L-1。对吸附过程进行动力学研究,拟合得到Lagrange二级动力学方程y=0.0116x+0.021。%In this paper, using bleaching bagasse pulp cellulose as substrate, diethylene triamine as monomer and cerium ammonium nitrate as initiator, amino-grafted fiber was prepared, then it attained efficient heavy metals adsorbent. The influence of monomer dosage, initia-tor dosage, temperature, time and other factors on the preparation of amino-grated fiber were investigated. The structure of amino-grafted fiber was characterized by FTIR spectra, X-ray diffraction and scanning electron microscope analysis. In addition, it studied amino-grafted fiber absorbent on Cu (Ⅱ) ions, which did adsorption research to explore better adsorption conditions from the following aspects including temperature, time, pH value, grafted fiber content and the initial concentration of copper ions solution. The results showed that mass ratio both oven dried bagasse fiber and monomer diethylene triamine was 1:1, the dosage of ammonium ceric

  12. Sodium dodecyl sulfate coated γ-alumina support modified by a new Schiff base for solid phase extraction and flame-AAS determination of lead and copper ions

    Directory of Open Access Journals (Sweden)

    Ardeshir Shokrollahi

    2013-01-01

    Full Text Available A simple and fast approach for solid phase extraction is herein described, and used to determine trace amounts of Pb2+ and Cu2+ metal ions. The solid phase support is sodium dodecyl sulfate (SDS-coated γ-alumina modified with bis(2-hydroxy acetophenone-1,6-hexanediimine (BHAH ligand. The adsorbed ions were stripped from the solid phase by 6 mL of 4 M nitric acid as eluent. The eluting solution was analyzed by flame atomic absorption spectrometry (FAAS. The sorption recovery of metal ions was investigated with regard to the effects of pH, amount of ligand, γ-alumina and surfactant and the amount and type of eluent. Complexation of BHAH with Pb2+ or Cu2+ ions was examined via spectrophotometry using the HypSpec program. The detection limit for Cu2+ was 7.9 µg L-1 with a relative standard deviation of 1.67%, while that for Pb2+ was 6.4 µg L-1 with a relative standard deviation of 1.64%. A preconcentration factor of 100 was achieved for these ions. The method was successfully applied to determine analyte concentrations in samples of liver, parsley, cabbage, and water.

  13. Irradiation route to aqueous synthesis of highly luminescent ZnSe quantum dots and its function as a copper ion fluorescence sensor

    Energy Technology Data Exchange (ETDEWEB)

    Rao, Yeluri Narayana; Datta, Aparna [UGC-DAE Consortium for Scientific Research, Kolkata Centre, III/LB-8 Bidhannagar, Kolkata 700 098 (India); Das, Satyendra K. [Radiochemistry Division, Variable Energy Cyclotron Centre, 1/AF Bidhannagar, Kolkata 700 064 (India); Saha, Abhijit, E-mail: abhijit@alpha.iuc.res.in [UGC-DAE Consortium for Scientific Research, Kolkata Centre, III/LB-8 Bidhannagar, Kolkata 700 098 (India)

    2016-08-15

    Highlights: • Radiation chemical technique can provide a useful route for synthesis of ZnSe QDs. • Chelating nature of ethylene diamine is exploited for capping nanoparticles. • ZnSe QDs can be a suitable sensitive alternative to toxic cadmium-based system. • Cu(II) ion is probed by QDs in the presence of other physiologically relevant ions. - Abstract: Size-controlled synthesis of stable ZnSe QDs with narrow distribution in aqueous environment through conventional soft chemical method still poses a challenge. The proposed radiation assisted strategy demonstrates aqueous synthesis of stable, monodisperse and luminescent ZnSe QDs capped with chelating ethylene diamine under ambient conditions and at room temperature. Radiation chemical method facilitates in slow and in-situ release of selenium ion from sodium selenosulfate. The concentrations of precursors, such as zinc salt, selenium source, ethylene diamine and absorbed radiation (7–90 kGy) dose were optimized for obtaining good quality particles. Selective quenching of luminescence of as-synthesized quantum dots (QDs) by Cu{sup 2+} ions vis-à-vis other physiologically important cations provide evidence for use of ZnSe quantum dots as alternative to toxic Cd-based quantum dots to probe Cu{sup 2+} ions. The linear relation of ratio of loss in emission intensity as a function of concentration of Cu(II) indicates detection limit in nano-molar range.

  14. An Effective Secondary Electron Emission Suppression Treatment For Copper MDC

    Science.gov (United States)

    Curren, Arthur N.; Long, Kenwyn J.; Jensen, Kenneth A.; Roman, Robert F.

    1993-01-01

    Untreated oxygen-free, high-conductivity (OFHC) copper, commonly used for MDC electrodes, exhibits relatively high secondary electron emission characteristics. This paper describes a specialized ion-bombardment procedure for texturing copper surfaces which sharply reduces the emission properties relative to untreated copper. The resulting surface is a particle-free, robust, uniformly highly-textured all-metal structure. The use of this process requires no modifications to copper machining, brazing, or other MDC normal fabrication procedures. The flight TWT for a planned NASA deep space probe, the Cassini Mission, will incorporate copper MDC electrodes treated with the method described here.

  15. COORDINATION POLYMERIZATION OF BENZOTRIAZOLE ON THE SURFACE OF METALLIC COPPER

    Institute of Scientific and Technical Information of China (English)

    XUE Gi; DAI Qinpin; DING Jianfu; WU Peiyi

    1989-01-01

    The coordination polymerization of benzotriazole with metallic copper has been investigated by infrared and X-ray photoelectron spectroscopies. We found that benzotriazole could react with copper (0) under mild conditions to form bis ( benzotriazolato ) copper (Ⅱ) and benzotriazolato copper(Ⅰ)which covered the surface of copper metal in the shape of polymeric materials. Since benzotriazole is of great interest as a ligand in that its presence in many biological system with metal ions ,and is considered as a corrosion inhibitor, this work will be in favour of the study of protective corrosion.

  16. The role of natural zeolite and of zeolite modified with ammnonium ions to reduce the uptake of lead, zinc, copper and iron ions in Hieracium aurantium and Rumex acetosella grown on tailing ponds

    Directory of Open Access Journals (Sweden)

    Anca PETER

    2011-11-01

    Full Text Available The objective of this research is to determine if zeolite modified with ammonium ions has a higher capacity than natural zeolite to protect Hieracium aurantium and Rumex acetosella growing on tailing ponds, by reducing the quantity of metal ions these plants would accumulate in their roots and leaves. The influence of the amount of zeolite in the substrate (5% and 10% mass percentage was also studied. The experiments were carried out in laboratory and the concentration of the ions of heavy metal in roots and leaves, after 38 days of growth was established by Flame Atomic Adsorption Spectroscopy. The pH, conductivity and redox potential for each of the substrate considered were measured. The results were statistically processed using the one-way analysis of variance (one-way ANOVA. FTIR analyses were performed to establish the structural differences between the natural and modified zeolite. Hieracium aurantium and Rumex acetosella accumulate a smaller quantity of metal ions in roots and leaves in the presence of zeolite modified with ammonium ions than in the presence of natural zeolite. Laboratory tests showed that Hieracium aurantium is more tolerant to ions of heavy metals than Rumex acetosella, as demonstrated by their translocation factors.In terms of reducing the uptake of ions of heavy metals, only the zeolite modified with ammonium has a significant protective effecton Hieracium aurantium, while both natural zeolite and zeolite modified demonstrate a significant role for Rumex acetosella, asrevealed by statistical tests.

  17. Diffusion of copper in porous silicon

    Energy Technology Data Exchange (ETDEWEB)

    Andsager, D.; Hetrick, J.M.; Hilliard, J.; Nayfeh, M.H. [Department of Physics, 1110 West Green Street, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801 (United States)

    1995-05-01

    We present a study on the nature of diffusion of copper in {ital p}-type porous silicon. The diffusion of evaporated copper in porous silicon and deposition of metal ions in aqueous solution through the porous network was measured by monitoring the metal concentration depth profile as a function of time using Auger electron spectroscopy. We observed that increasing metal penetration from copper evaporated samples correlates with quenching of photoluminescence, in agreement with previous ion quenching results. We extracted a diffusion coefficient from Auger concentration depth profiles which was seven orders of magnitude lower than that expected for diffusion of copper in bulk crystalline Si at room temperature. Deposition of ionic species cannot be characterized as a simple diffusion process. The observed deposition rates were strongly dependent on the solution concentration.

  18. Comparison of copper speciation in the Zhujiang River Estuary between summer and winter: implication for upwelling current

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    The contents of total copper, total dissolved copper, particulate copper, and free ion copper in the Zhujiang River Estuary were investigated in July 2002 and January 2003 respectively, and the spatial distribution trend of these species of copper were compared in two cruises. It was found that, in summer, the total copper content in the Zhujiang River Estuary increased with salinity, while the content of free ion copper decreased with salinity. However, in winter, the contents of total copper and free ion copper both decreased with salinity. So, it could be concluded that, copper content and speciation in the Zhujiang River Estuary were regulated by other factors than runoffdiffusion such as upwelling current. In order to prove the spatial trend of free ion copper content in the Zhujiang River Estuary, the cultivation of Dunaliella tertiolecta in waters obtained from sampling stations with different salinities was carried out, and the copper uptake by algae cells was measured then. It was found that, the cells' uptake of copper increased with free ion copper, not the content of total copper.

  19. Evaluation of immobilized metal-ion affinity chromatography and electrospray ionization tandem mass spectrometry for recovery and identification of copper(II-binding ligands in seawater using the model ligand 8-hydroxyquinoline

    Directory of Open Access Journals (Sweden)

    Richard L Nixon

    2016-11-01

    Full Text Available Complexation by organic ligands dominates the speciation of iron (Fe, copper (Cu, and other bioactive trace metals in seawater, controlling their bioavailability and distribution in the marine environment. Several classes of high-affinity Fe-binding ligands (siderophores have been identified in seawater but the chemical structures of marine Cu-complexing ligands remain unknown. Immobilized metal-ion affinity chromatography (IMAC allows Cu ligands to be isolated from bulk dissolved organic matter (DOM in seawater and separated into fractions which can be characterized independently using electrochemical and spectroscopic techniques. Attempts have been made to combine IMAC with electrospray ionization mass spectrometry (ESI-MS to characterize marine Cu ligands, but results have proven inconclusive due to the lack of tandem mass spectrometry (MS/MS data to confirm ligand recovery. We used 8-hydroxyquinoline (8-HQ, a well-characterized model ligand that forms strong 1:2 metal:ligand complexes with Cu2+ at pH 8 (log β2 = 18.3, to evaluate Cu(II-IMAC and ESI-MS/MS for recovery and identification of copper(II-complexing ligands in seawater. One-litre samples of 0.45µm-filtered surface seawater were spiked with 8-HQ at low concentrations (up to 100 nM and fractionated by IMAC. Fractions eluted with acidified artificial seawater were desalted and re-suspended in methanol via solid-phase extraction (SPE to obtain extracts suitable for ESI-MS analysis. Recovery of 8-HQ by Cu(II-IMAC was confirmed unambiguously by MS/MS and found to average 81% based upon accurate quantitation via multiple reaction monitoring (MRM. Cu(II-IMAC fractionation of unspiked seawater using multiple UV detection wavelengths suggests an optimal fraction size of 2 mL for isolating and analyzing Cu ligands with similar properties.

  20. Synthesis of nano-sized stereoselective imprinted polymer by copolymerization of (S)-2-(acrylamido) propanoic acid and ethylene glycol dimethacrylate in the presence of racemic propranolol and copper ion

    Energy Technology Data Exchange (ETDEWEB)

    Alizadeh, Taher, E-mail: talizadeh@ut.ac.ir [Department of Analytical Chemistry, Faculty of Chemistry, University College of Science, University of Tehran, P.O. Box 14155-6455, Tehran (Iran, Islamic Republic of); Bagherzadeh, Azam; Shamkhali, Amir Nasser [Department of Applied Chemistry, Faculty of Science, University of Mohaghegh Ardabili, Ardabil (Iran, Islamic Republic of)

    2016-06-01

    A new chiral functional monomer of (S)-2-(acrylamido) propanoic acid was obtained by reaction of (L)-alanine with acryloyl chloride. The resulting monomer was characterized by FT-IR and HNMR and then utilized for the preparation of chiral imprinted polymer (CIP). This was carried out by copolymerization of (L)-alanine-derived chiral monomer and ethylene glycol dimethacrylate, in the presence of racemic propranolol and copper nitrate, via precipitation polymerization technique, resulting in nano-sized networked polymer particles. The polymer obtained was characterized by scanning electron microscopy and FT-IR. The non-imprinted polymer was also synthesized and used as blank polymer. Density functional theory (DFT) was also employed to optimize the structures of two diasterometric ternary complexes, suspected to be created in the pre-polymerization step, by reaction of optically active isomers of propranolol, copper ion and (S)-2-(acrylamido) propanoic acid. Relative energies and other characteristics of the described complexes, calculated by the DFT, predicted the higher stability of (S)-propranolol involved complex, compared to (R)-propranolol participated complex. Practical batch extraction test which employed CIP as solid phase adsorbent, indicated that the CIP recognized selectively (S)-propranolol in the racemic mixture of propranolol; whereas, the non-imprinted polymer (NIP) showed no differentiation capability between two optically active isomers of propranolol. - Highlights: • A new chiral functional monomer of (S)-2-(acrylamido) propanoic acid was synthesized. • (S)-propranolol-selective imprinted polymer was synthesized using the chiral monomer. • Racemic propranolol mixed with Cu(II) was used as template in the imprinting. • Density functional theory was employed to clarify the imprinting mechanism. • (S)-propranolol-Cu(II) complex was shown to conduct the imprinting process.

  1. Mono-nuclear copper complexes mimicking the intermediates for the binuclear copper center of the subunit II of cytochrome oxidase: a peptide based approach.

    Science.gov (United States)

    Dutta Gupta, Dwaipayan; Usharani, Dandamudi; Mazumdar, Shyamalava

    2016-11-28

    Three stable copper complexes of peptides derived from the copper ion binding loop of the subunit II of cytochrome c oxidase have been prepared and characterized by various spectroscopic techniques. These stable copper complexes of peptides were found to exhibit cysteine, histidine and/or methionine ligation, which has predominant σ-contribution in the Cys-Cu charge transfer. The copper(ii) peptide complexes showed type-2 EPR spectra, which is uncommon in copper-cysteinate complexes. UV-visible spectra, Raman and EPR results support a tetragonal structure of the coordination geometry around the copper ion. The copper complex of the 9-amino acid peptide suggested the formation of a 'red' copper center while the copper complexes of the 12- and 11-amino acid peptides showed the formation of a 'green' copper center. The results provide insights on the first stable models of the copper complexes formed in the peptide scaffold that mimic the mono-nuclear copper bound protein intermediates proposed during the formation of the binuclear Cu2S2 core of the enzyme. These three copper complexes of peptides derived from the metal ion binding loop of the CuA center of the subunit II of cytochrome c oxidase showed novel spectroscopic properties which have not so far been reported in any stable small complex.

  2. Microporous spongy chitosan monoliths doped with graphene oxide as highly effective adsorbent for methyl orange and copper nitrate (Cu(NO3)2) ions.

    Science.gov (United States)

    Wang, Ying; Liu, Xu; Wang, Hongfang; Xia, Guangmei; Huang, Wei; Song, Rui

    2014-02-15

    In the current study, microporous spongy chitosan monoliths doped with small amount of graphene oxide (CSGO monoliths) with high porosity (96-98%), extraordinary high water absorption (more than 2000%) and low density (0.0436-0.0607 g cm(-3)) were prepared by the freeze-drying method and used as adsorbents for anionic dyes methyl orange (MO) and Cu(2+) ions. The adsorption behavior of the CSGO monoliths and influencing factors such as pH value, graphene oxide (GO) content, concentration of pollutants as well as adsorption kinetics were studied. Specifically, the saturated adsorption capacity for MO is 567.07 mg g(-1), the highest comparing with other publication results, and it is 53.69 mg g(-1) for Cu(2+) ions. Since they are biodegradable, non-toxic, efficient, low-cost and easy to prepare, we believe that these microporous spongy CSGO monoliths will be the promising candidates for water purification.

  3. Transition-metal prion protein attachment: Competition with copper

    Science.gov (United States)

    Hodak, Miroslav; Bernholc, Jerry

    2012-02-01

    Prion protein, PrP, is a protein capable of binding copper ions in multiple modes depending on their concentration. Misfolded PrP is implicated in a group of neurodegenerative diseases, which include ``mad cow disease'' and its human form, variant Creutzfeld-Jacob disease. An increasing amount of evidence suggests that attachment of non-copper metal ions to PrP triggers transformations to abnormal forms similar to those observed in prion diseases. In this work, we use hybrid Kohn-Sham/orbital-free density functional theory simulations to investigate copper replacement by other transition metals that bind to PrP, including zinc, iron and manganese. We consider all known copper binding modes in the N-terminal domain of PrP. Our calculations identify modes most susceptible to copper replacement and reveal metals that can successfully compete with copper for attachment to PrP.

  4. Ghezeljeh nanoclay as a new natural adsorbent for the removal of copper and mercury ions:Equilibrium, kinetics and thermodynamics studies

    Institute of Scientific and Technical Information of China (English)

    Majid Soleimani⁎; Zahra Hassanzadeh Siahpoosh

    2015-01-01

    Heavy metal determination was carried out by applying the solid phase extraction (SPE) method in batch mode followed by atomic absorption spectroscopy (AAS) and inductively coupled plasma atomic emission spectrosco-py (ICP-AES) from aqueous solutions using Ghezeljeh montmoril onite nanoclay as a new natural adsorbent. The Ghezeljeh clay is characterized by using Fourier Transform Infrared (FT-IR) Spectroscopy, Scanning Electron Mi-croscopy–Energy Dispersive Spectrometry (SEM–EDS) and X-ray Diffractometry (XRD) and X-ray Fluorescence (XRF). The results of XRD and FT-IR of nanoclay confirm that montmoril onite is the dominant mineral phase. Based on SEM images of Ghezeljeh clay, it can be seen that the distance between the plates is Nano. The effects of varying parameters such as initial concentration of metal ions, pH and type of buffer solutions, amount of ad-sorbent, contact time, and temperature on the adsorption process were examined. The effect of various interfer-ing ions was studied. The adsorption data correlated with Freundlich, Langmuir, Dubinin–Radushkevich (D–R), and Temkin isotherms. The Langmuir and Freundlich isotherms showed the best fit to the equilibrium data for Hg(I ), but the equilibrium nature of Cu(II) adsorption has been described by the Langmuir isotherm. The kinetic data were described with pseudo-first-order, pseudo-second-order and double-exponential models. The adsorp-tion process follows a pseudo-second-order reaction scheme. Calculation ofΔG0,ΔH0 andΔS0 showed that the nature of Hg(II) ion sorption onto the Ghezeljeh nanoclay was endothermic and was favored at higher temper-ature, and the nature of Cu(II) ion sorption was exothermic and was favored at lower temperature.

  5. Transverse momentum distribution of. pi. sup - from 14. 6A GeV/c silicon ion interactions in copper and gold

    Energy Technology Data Exchange (ETDEWEB)

    Ahmad, S.; Bonner, B.E.; Buchanan, J.A.; Chiou, C.N.; Clement, J.M.; Mutchler, G.S. (Rice Univ., Houston, TX (United States)); Chan, C.S.; Kramer, M.A. (City Coll., New York, NY (United States)); Eiseman, S.E.; Etkin, A.; Foley, K.J.; Hackenburg, R.W.; Longacre, R.S.; Love, W.A.; Morris, T.W.; Platner, E.D.; Saulys, A.C. (Brookhaven National Lab., Upton, NY (United States)); Hallman, T.J.; Madansky, L. (Johns Hopkins Univ., Baltimore, MD (United States)); Lindenbaum, S.J. (Brookhaven National Lab., Upton, NY (United States) City Coll., New York, NY (United States))

    1992-05-07

    A measurement of the transverse momentum spectra of negatively charged tracks from AGS energy silicon ion collisions is presented. The spectrum has a different shape than that of nucleon-nucleon collisions at approximately the same energy. The transverse mass spectrum is well represented by a sum of two exponentials with different slopes and may be reasonably well accounted for by a model of pion production in interacting nuclear matter that includes resonance production and decay. (orig.).

  6. Removal of Pb(II) ions from aqueous solution by a waste mud from copper mine industry: equilibrium, kinetic and thermodynamic study.

    Science.gov (United States)

    Ozdes, Duygu; Gundogdu, Ali; Kemer, Baris; Duran, Celal; Senturk, Hasan Basri; Soylak, Mustafa

    2009-07-30

    The objective of this study was to assess the adsorption potential of a waste mud (WM) for the removal of lead (Pb(II)) ions from aqueous solutions. The WM was activated with NaOH in order to increase its adsorption capacity. Adsorption studies were conducted in a batch system as a function of solution pH, contact time, initial Pb(II) concentration, activated-waste mud (a-WM) concentration, temperature, etc. Optimum pH was specified as 4.0. The adsorption kinetic studies indicated that the overall adsorption process was best described by pseudo-second-order kinetics. The equilibrium adsorption capacity of a-WM was obtained by using Langmuir and Freundlich isotherm models and both models fitted well. Adsorption capacity for Pb(II) was found to be 24.4 mg g(-1) for 10 g L(-1) of a-WM concentration. Thermodynamic parameters including the Gibbs free energy (Delta G degrees), enthalpy (Delta H degrees), and entropy (DeltaS degrees) indicated that the adsorption of Pb(II) ions on the a-WM was feasible, spontaneous and endothermic, at temperature range of 0-40 degrees C. Desorption studies were carried out successfully with diluted HCl solutions. The results indicate that a-WM can be used as an effective and no-cost adsorbent for the treatment of industrial wastewaters contaminated with Pb(II) ions.

  7. Preconcentration and determination of copper and cadmium ions with 1,6-bis(2-carboxy aldehyde phenoxy)butane functionalized Amberlite XAD-16 by flame atomic absorption spectrometry.

    Science.gov (United States)

    Oral, Elif V; Dolak, Ibrahim; Temel, Hamdi; Ziyadanogullari, Berrin

    2011-02-15

    A new chelating resin, covalently linked 1,6-bis(2-carboxy aldehyde phenoxy)butane with the Amberlite XAD-16 was synthesized and used for preconcentration of Cu(II) and Cd(II) prior to their determination by flame atomic absorption spectrometry (FAAS). It was characterized by elemental analyses and Fourier Transform Infrared Spectroscopy (FT-IR). Cu(II) and Cd(II) ions were quantitatively preconcentrated on minicolumn loaded with synthesised resin at pH 4.00 and 6.00, respectively. They were eluated with 5 mL of 0.5 mol L(-1) HCl. Recoveries of Cu(II) and Cd(II) were found to be 100±2.15, 100±1.40 (N=5), the limits of detection of Cu(II) and Cd(II) in the determination by FAAS (3s, N=20) were found to be 0.33 and 1.19 μg L(-1), respectively. The effect of foreign ions on the recovery has been investigated. The proposed method has been applied for the determination of Cu(II) and Cd(II) ions to the real samples collected from Tigris river water in Diyarbakir and Elaziğ cities in Turkey. Standard addition method and analysis of the certified reference material (NCS-DC 73350) was employed to check the accuracy of the method.

  8. Base Catalytic Approach: A Promising Technique for the Activation of Biochar for Equilibrium Sorption Studies of Copper, Cu(II Ions in Single Solute System

    Directory of Open Access Journals (Sweden)

    Sharifah Bee Abdul Hamid

    2014-04-01

    Full Text Available This study examines the feasibility of catalytically pretreated biochar derived from the dried exocarp or fruit peel of mangostene with Group I alkali metal hydroxide (KOH. The pretreated char was activated in the presence of carbon dioxide gas flow at high temperature to upgrade its physiochemical properties for the removal of copper, Cu(II cations in single solute system. The effect of three independent variables, including temperature, agitation time and concentration, on sorption performance were carried out. Reaction kinetics parameters were determined by using linear regression analysis of the pseudo first, pseudo second, Elovich and intra-particle diffusion models. The regression co-efficient, R2 values were best for the pseudo second order kinetic model for all the concentration ranges under investigation. This implied that Cu(II cations were adsorbed mainly by chemical interactions with the surface active sites of the activated biochar. Langmuir, Freundlich and Temkin isotherm models were used to interpret the equilibrium data at different temperature. Thermodynamic studies revealed that the sorption process was spontaneous and endothermic. The surface area of the activated sample was 367.10 m2/g, whereas before base activation, it was only 1.22 m2/g. The results elucidated that the base pretreatment was efficient enough to yield porous carbon with an enlarged surface area, which can successfully eliminate Cu(II cations from waste water.

  9. One-Pot Synthesis of Copper Sulfide Nanowires/Reduced Graphene Oxide Nanocomposites with Excellent Lithium-Storage Properties as Anode Materials for Lithium-Ion Batteries.

    Science.gov (United States)

    Feng, Caihong; Zhang, Le; Yang, Menghuan; Song, Xiangyun; Zhao, Hui; Jia, Zhe; Sun, Kening; Liu, Gao

    2015-07-29

    Copper sulfide nanowires/reduced graphene oxide (CuSNWs/rGO) nanocompsites are successfully synthesized via a facile one-pot and template-free solution method in a dimethyl sulfoxide (DMSO)-ethyl glycol (EG) mixed solvent. It is noteworthy that the precursor plays a crucial role in the formation of the nanocomposites structure. SEM, TEM, XRD, IR and Raman spectroscopy are used to investigate the morphological and structural evolution of CuSNWs/rGO nanocomposites. The as-fabricated CuSNWs/rGO nanocompsites show remarkably improved Li-storage performance, excellent cycling stability as well as high-rate capability compared with pristine CuS nanowires. It obtains a reversible capacity of 620 mAh g(-1) at 0.5C (1C = 560 mA g(-1)) after 100 cycles and 320 mAh g(-1) at a high current rate of 4C even after 430 cycles. The excellent lithium storage performance is ascribed to the synergistic effect between CuS nanowires and rGO nanosheets. The as-formed CuSNWs/rGO nanocomposites can effectively accommodate large volume changes, supply a 2D conducting network and trap the polysulfides generated during the conversion reaction of CuS.

  10. Mesophilic leaching of copper sulphide sludge

    Directory of Open Access Journals (Sweden)

    VLADIMIR B. CVETKOVSKI

    2009-02-01

    Full Text Available Copper was precipitated using a sodium sulphide solution as the precipitation agent from an acid solution containing 17 g/l copper and 350 g/l sulphuric acid. The particle size of nearly 1 µm in the sulphide sludge sample was detected by optical microscopy. Based on chemical and X-ray diffraction analyses, covellite was detected as the major sulphide mineral. The batch bioleach amenability test was performed at 32 °C on the Tk31 mine mesophilic mixed culture using a residence time of 28 days. The dissolution of copper sulphide by direct catalytic leaching of the sulphides with bacteria attached to the particles was found to be worthy, although a small quantity of ferrous ions had to be added to raise the activity of the bacteria and the redox potential of the culture medium. Throughout the 22-day period of the bioleach test, copper recovery based on residue analysis indicated a copper extraction of 95 %, with copper concentration in the bioleach solution of 15 g/l. The slope of the straight line tangential to the exponential part of the extraction curve gave a copper solubilisation rate of 1.1 g/l per day. This suggests that a copper extraction of 95 % for the period of bioleach test of 13.6 days may be attained in a three-stage bioreactor system.

  11. Bacterial leaching of discarded copper ores from Yongping, China

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    The elementary and phase analysis of discarded copper ores from Yongping of China has been performed. The experiments of extracting copper from the discarded copper ores were done with the mixed bacteria obtained through a series of enrichment,separation, domestication and combination tests. The results show that in the process of bioleaching, the pH value rises at first and drops gradually. The Eh value keeps rising along with the time and the appropriate Eh value varying between 750 and 800 mV will benefit the bioleaching copper. The high concentration of ferric ions is detrimental to the bioleaching copper. The results of bioleaching copper are good. That is, the copper recovery is 31.8% after 27 days.

  12. Mitochondrial dysfunction in neurodegenerative diseases associated with copper imbalance.

    Science.gov (United States)

    Rossi, Luisa; Lombardo, Marco F; Ciriolo, Maria R; Rotilio, Giuseppe

    2004-03-01

    Copper is an essential transition metal ion for the function of key metabolic enzymes, but its uncontrolled redox reactivity is source of reactive oxygen species. Therefore a network of transporters strictly controls the trafficking of copper in living systems. Deficit, excess, or aberrant coordination of copper are conditions that may be detrimental, especially for neuronal cells, which are particularly sensitive to oxidative stress. Indeed, the genetic disturbances of copper homeostasis, Menkes' and Wilson's diseases, are associated with neurodegeneration. Furthermore, copper interacts with the proteins that are the hallmarks of neurodegenerative disorders, such as Alzheimer's disease, Parkinson's disease, prion diseases, and familial amyotrophic lateral sclerosis. In all cases, copper-mediated oxidative stress is linked to mitochondrial dysfunction, which is a common feature of neurodegeneration. In particular we recently demonstrated that in copper deficiency, mitochondrial function is impaired due to decreased activity of cytochrome c oxidase, leading to production of reactive oxygen species, which in turn triggers mitochondria-mediated apoptotic neurodegeneration.

  13. Copper allergy from dental copper amalgam?

    Science.gov (United States)

    Gerhardsson, Lars; Björkner, Bert; Karlsteen, Magnus; Schütz, Andrejs

    2002-05-06

    A 65-year-old female was investigated due to a gradually increasing greenish colour change of her plastic dental splint, which she used to prevent teeth grinding when sleeping. Furthermore, she had noted a greenish/bluish colour change on the back of her black gloves, which she used to wipe her tears away while walking outdoors. The investigation revealed that the patient had a contact allergy to copper, which is very rare. She had, however, had no occupational exposure to copper. The contact allergy may be caused by long-term exposure of the oral mucosa to copper from copper-rich amalgam fillings, which were frequently used in childhood dentistry up to the 1960s in Sweden. The deposition of a copper-containing coating on the dental splint may be caused by a raised copper intake from drinking water, increasing the copper excretion in saliva, in combination with release of copper due to electrochemical corrosion of dental amalgam. The greenish colour change of the surface of the splint is probably caused by deposition of a mixture of copper compounds, e.g. copper carbonates. Analysis by the X-ray diffraction technique indicates that the dominant component is copper oxide (Cu2O and CuO). The corresponding greenish/bluish discoloration observed on the back of the patient's gloves may be caused by increased copper excretion in tears.

  14. Potassium-doped copper oxide nanoparticles synthesized by a solvothermal method as an anode material for high-performance lithium ion secondary battery

    Energy Technology Data Exchange (ETDEWEB)

    Thi, Trang Vu; Rai, Alok Kumar; Gim, Jihyeon; Kim, Jaekook, E-mail: jaekook@chonnam.ac.kr

    2014-06-01

    A simple and efficient approach was developed to synthesize CuO nanoparticles with improved electrochemical performance. Potassium (K{sup +})-doped CuO nanoparticles were synthesized by a simple and cost-effective solvothermal method followed by annealing at 500 °C for 5 h under air atmosphere. For comparison, an undoped CuO sample was also synthesized under the same conditions. X-ray diffraction analysis demonstrates that the K{sup +} ion doping caused no change in the phase structure, and highly crystalline K{sub x}Cu{sub 1−x}O{sub 1−δ} (x = 0.10) powder without any impurity was obtained. As an anode material for a lithium ion battery, the K{sup +}-doped CuO nanoparticle electrode exhibited better capacity retention with a reversible capacity of over 354.6 mA h g{sup −1} for up to 30 cycles at 0.1 C, as well as a high charge capacity of 162.3 mA h g{sup −1} at a high current rate of 3.2 C, in comparison to an undoped CuO electrode (275.9 mA h g{sup −1} at 0.1 C and 68.9 mA h g{sup −1} at 3.2 C). The high rate capability and better cycleability of the doped electrode can be attributed to the influence of the K{sup +} ion nanostructure on the increased electronic conductivity, diffusion efficiency, and kinetic properties of CuO during the lithiation and delithiation process.

  15. Potassium-doped copper oxide nanoparticles synthesized by a solvothermal method as an anode material for high-performance lithium ion secondary battery

    Science.gov (United States)

    Thi, Trang Vu; Rai, Alok Kumar; Gim, Jihyeon; Kim, Jaekook

    2014-06-01

    A simple and efficient approach was developed to synthesize CuO nanoparticles with improved electrochemical performance. Potassium (K+)-doped CuO nanoparticles were synthesized by a simple and cost-effective solvothermal method followed by annealing at 500 °C for 5 h under air atmosphere. For comparison, an undoped CuO sample was also synthesized under the same conditions. X-ray diffraction analysis demonstrates that the K+ ion doping caused no change in the phase structure, and highly crystalline KxCu1-xO1-δ (x = 0.10) powder without any impurity was obtained. As an anode material for a lithium ion battery, the K+-doped CuO nanoparticle electrode exhibited better capacity retention with a reversible capacity of over 354.6 mA h g-1 for up to 30 cycles at 0.1 C, as well as a high charge capacity of 162.3 mA h g-1 at a high current rate of 3.2 C, in comparison to an undoped CuO electrode (275.9 mA h g-1 at 0.1 C and 68.9 mA h g-1 at 3.2 C). The high rate capability and better cycleability of the doped electrode can be attributed to the influence of the K+ ion nanostructure on the increased electronic conductivity, diffusion efficiency, and kinetic properties of CuO during the lithiation and delithiation process.

  16. Molecular mechanisms of the epithelial transport of toxic metal ions, particularly mercury, cadmium, lead, arsenic, zinc, and copper. Comprehensive progress report, October 1, 1975--December 31, 1978

    Energy Technology Data Exchange (ETDEWEB)

    Wasserman, R. H.

    1978-10-01

    Investigations were undertaken to elucidate the mode of transepithelial transport of potentially toxic metal ions across the gastrointestinal tract, with primary attention given to cadmium, zinc, and arsenic. In addition, the toxic effects of cadmium on the metabolism of vitamin D and calcium have been investigated in some detail. Several approaches have been taken, including studies on the localization of heavy metals in the intestinal mucosa, the effects of cadmium on various parameters of calcium metabolism, the modes of intestinal absorption of cadmium, arsenate, and zinc, and the interactions of heavy metals with each other and with calcium, phosphorus, and vitamin D. Details of these experiments are attached in the Comprehensive Progress Report.

  17. Exploiting 1,2,3-Triazolium Ionic Liquids for Synthesis of Tryptanthrin and Chemoselective Extraction of Copper(II Ions and Histidine-Containing Peptides

    Directory of Open Access Journals (Sweden)

    Hsin-Yi Li

    2016-10-01

    Full Text Available Based on a common structural core of 4,5,6,7-tetrahydro[1,2,3]triazolo[1,5-a]pyridine, a number of bicyclic triazolium ionic liquids 1–3 were designed and successfully prepared. In our hands, this optimized synthesis of ionic liquids 1 and 2 requires no chromatographic separation. Also in this work, ionic liquids 1, 2 were shown to be efficient ionic solvents for fast synthesis of tryptanthrin natural product. Furthermore, a new affinity ionic liquid 3 was tailor-synthesized and displayed its effectiveness in chemoselective extraction of both Cu(II ions and, for the first time, histidine-containing peptides.

  18. Exploiting 1,2,3-Triazolium Ionic Liquids for Synthesis of Tryptanthrin and Chemoselective Extraction of Copper(II) Ions and Histidine-Containing Peptides.

    Science.gov (United States)

    Li, Hsin-Yi; Chen, Chien-Yuan; Cheng, Hui-Ting; Chu, Yen-Ho

    2016-10-13

    Based on a common structural core of 4,5,6,7-tetrahydro[1,2,3]triazolo[1,5-a]pyridine, a number of bicyclic triazolium ionic liquids 1-3 were designed and successfully prepared. In our hands, this optimized synthesis of ionic liquids 1 and 2 requires no chromatographic separation. Also in this work, ionic liquids 1, 2 were shown to be efficient ionic solvents for fast synthesis of tryptanthrin natural product. Furthermore, a new affinity ionic liquid 3 was tailor-synthesized and displayed its effectiveness in chemoselective extraction of both Cu(II) ions and, for the first time, histidine-containing peptides.

  19. Coordination modes of a schiff base pentadentate derivative of 4-aminoantipyrine with cobalt(II), nickel(II) and copper(II) metal ions: synthesis, spectroscopic and antimicrobial studies.

    Science.gov (United States)

    Chandra, Sulekh; Jain, Deepali; Sharma, Amit Kumar; Sharma, Pratibha

    2009-01-01

    Transition metal complexes of Co(II), Ni(II) and Cu(II) metal ions with general stoichiometry [M(L)X]X and [M(L)SO(4)], where M = Co(II), Ni(II) and Cu(II), L = 3,3'-thiodipropionic acid bis(4-amino-5-ethylimino-2,3-dimethyl-1-phenyl-3-pyrazoline) and X = NO(3)(-), Cl(-) and OAc(-), have been synthesized and structurally characterized by elemental analyses, molar conductance measurements, magnetic susceptibility measurements and spectral techniques like IR, UV and EPR. The nickel(II) complexes were found to have octahedral geometry, whereas cobalt(II) and copper(II) complexes were of tetragonal geometry. The covalency factor (beta) and orbital reduction factor (k) suggest the covalent nature of the complexes. The ligand and its complexes have been screened for their antifungal and antibacterial activities against three fungi, i.e. Alternaria brassicae, Aspergillus niger and Fusarium oxysporum and two bacteria, i.e. Xanthomonas compestris and Pseudomonas aeruginosa.

  20. Coordination mode of pentadentate ligand derivative of 5-amino-1,3,4-thiadiazole-2-thiol with nickel(II) and copper(II) metal ions: synthesis, spectroscopic characterization, molecular modeling and fungicidal study.

    Science.gov (United States)

    Chandra, Sulekh; Gautam, Seema; Kumar, Amit; Madan, Molly

    2015-02-01

    Complexes of nickel(II), and copper(II) were synthesized with pantadentate ligand i.e. 3,3'-thiodipropionicacid-bis(5-amino-1,3,4-thiadiazole-2-thiol) (L). The ligand was synthesized by the condensation of thiodipropionic acid and 5-amino-1,3,4-thiadiazole-2-thiol in 1:2 ratio, respectively. Synthesized ligand was characterized by elemental analysis, mass, (1)H NMR, IR, and molecular modeling. All the complexes were characterized by elemental analysis, molar conductance, magnetic moment, IR, electronic spectra, ESR, and molecular modeling. The newly synthesized complexes possessed general composition [M(L)X2] where M = Ni(II), Cu(II), L = pantadentate ligand and X = Cl(-), CH3COO(-). The IR spectral data indicated that the ligand behaved as a pantadentate ligand and coordinated to the metal ion through N2S3 donor atoms. The molar conductance value of Ni(II), and Cu(II) complexes in DMSO corresponded to their electrolytic behavior. On the basis of spectral study, octahedral and tetragonal geometry was assigned for Ni(II) and Cu(II) complexes, respectively. In vitro fungicidal study of ligand and its complexes was investigated against fungi Candida albicans, Candida parapsilosis, Candidia krusei, and Candida tropicalis by means of well diffusion method.

  1. Study on synthesis of new dinuclear copper macrocyclic complex by template reaction involving lead ion as templating agent%模板法合成大环单核铅及双核铜(Ⅱ)配合物

    Institute of Scientific and Technical Information of China (English)

    王小波; 姜治平; 候波涛; 胡学雷; 潘志权

    2011-01-01

    采用Pb2+作为模板离子,以2,6-二甲酰基对甲苯酚与2-羟基-1,3-丙二胺为原料通过[2+2]缩合反应,得到单核铅配合物[Pb(H2L)](ClO4)2(H2L为中性大环配体),进一步通过金属置换反应合成了一个新的希夫碱大环双核铜(Ⅱ)配合物[Cu2L](ClO4)2,并对中间体大环单核铅配合物及其双核铜(Ⅱ)配合物的结构进行了表征.%A new dinuclear copper macrocyclic complex was synthesized by metal transferred reaction of the mononuclear lead complex as the precursor which was obtained based on the [2+2]condensation between 2,6-diacetyl-4-methylphenol and 1,3-diamino- 2-propanol in the presence of Pb2+ ion.Both structure of two complexes were characterized by several methods.

  2. Development and Industrialization of Silver Electrolysis Process at a High Current Density in Copper Ions -free Electrolyte%无铜离子高电流密度银电解工艺的开发与产业化

    Institute of Scientific and Technical Information of China (English)

    谢太李; 黄强; 王日

    2012-01-01

    对贵溪冶炼厂传统银电解工艺存在的问题进行了分析,同时针对高电流密度下银电解工艺需解决的关键问题提出了解决方法,研发出无铜离子高电流密度(1000A/m2)银电解集成技术,并在贵溪冶炼厂工业生产中稳定运行多年.生产实践证明,此工艺具有简单、操作方便、产品质量稳定、单槽产能高、作业环境友好等优点.%In this paper, the existing problems in traditional silver electrolysis process are analyzed and the corresponding solutions are proposed. The author proposes solutions for the key problems in the traditional silver electrolysis process with high current density, which are supposed to be solved. A new process for silver electrolysis at the high current density of 1000 A/m2 in copper ions -free electrolyte was developed, and has been applied to industrial production in Guixi smelter for many years. The production practice shows that this process has advantages of being simple and environmentally - friendly with high capacity of single cell, and produces the product of high quality.

  3. Diffusion behavior of copper atoms under Cu(II) reduction in Cucurbit[8]uril cavity at elevated temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Bakovets, Vladimir V., E-mail: becambe@niic.nsc.ru [Nikolaev Institute of Inorganic Chemistry SB RAS, 630090 Novosibirsk, Prospekt Akademika Lavrent’eva 3 (Russian Federation); Nadolinnii, Vladimir A.; Kovalenko, Ekaterina A.; Plyusnin, Pavel E.; Dolgovesova, Irina P. [Nikolaev Institute of Inorganic Chemistry SB RAS, 630090 Novosibirsk, Prospekt Akademika Lavrent’eva 3 (Russian Federation); Zaikovskii, Vladimir I. [Boreskov Institute of Catalysis SB RAS, 630090 Novosibirsk, Pospekt Akademika Lavrent’eva 5 (Russian Federation)

    2015-01-15

    In this paper we describe copper clusters and nanoparticles formation by the reduction of copper (II) ions inside cavities of macrocycle molecules using supramolecular compound [Cu(Cyclen)(H{sub 2}O)@CB[8

  4. Incorporation of copper histidine complexes into a zeolite Y matrix

    NARCIS (Netherlands)

    Mesu, J.G.; Baute, D.; Tromp, H.J.; Faassen, E.E.H. van; Weckhuysen, B.M.

    2003-01-01

    Preformed copper-histidine complexes were loaded into zeolite Y by ion exchange. The zeolite was found to contain a mixture of two different encaged complexes: a mono-histidine complex (A) and a bis-histidine complex (B). The initial copper concentration affects the composition of this mixture, with

  5. Copper Products Capacity Expansion Stimulate the Copper Consumption

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    <正>The dramatic growth of copper consumption in China can directly be seen from the expansion of copper products capacity.According to sta- tistics,in the past 4 years,the improvement on the balance of trade on copper bar,copper,and copper alloy and copper wire & cable has driven the growth of copper consumption a lot.

  6. Excitation-Energy Transfer Paths from Tryptophans to Coordinated Copper Ions in Engineered Azurins: a Source of Observables for Monitoring Protein Structural Changes

    Science.gov (United States)

    Di Rocco, Giulia; Bernini, Fabrizio; Borsari, Marco; Martinelli, Ilaria; Bortolotti, Carlo Augusto; Battistuzzi, Gianantonio; Ranieri, Antonio; Caselli, Monica; Sola, Marco; Ponterini, Glauco

    2016-09-01

    The intrinsic fluorescence of recombinant proteins offers a powerful tool to detect and characterize structural changes induced by chemical or biological stimuli. We show that metal-ion binding to a hexahistidine tail can significantly broaden the range of such structurally sensitive fluorescence observables. Bipositive metal-ions as Cu2+, Ni2+ and Zn2+ bind 6xHis-tag azurin and its 6xHis-tagged R129W and W48A-R129W mutants with good efficiency and, thereby, quench their intrinsic fluorescence. Due to a much more favourable spectral overlap, the 6xHis-tag/Cu2+ complex(es) are the most efficient quenchers of both W48 and W129 emissions. Based on simple Förster-type dependence of energy-transfer efficiency on donor/acceptor distance, we can trace several excitation-energy transfer paths across the protein structure. Unexpected lifetime components in the azurin 6xHis-tag/Cu2+ complex emission decays reveal underneath complexity in the conformational landscape of these systems. The new tryptophan emission quenching paths provide additional signals for detecting and identifying protein structural changes.

  7. Green Synthesis of Silver Nanoparticles Stabilized with Mussel-Inspired Protein and Colorimetric Sensing of Lead(II and Copper(II Ions

    Directory of Open Access Journals (Sweden)

    Ja Young Cheon

    2016-11-01

    Full Text Available This articles reports a simple and green method for preparing uniform silver nanoparticles (AgNPs, for which self-polymerized 3,4-dihydroxy-l-phenylalanine (polyDOPA is used as the reducing and stabilizing agent in aqueous media. The AgNPs functionalized by polyDOPA were analyzed by UV–Vis spectroscopy, high-resolution transmission electron microscopy (HR-TEM, Fourier transform infrared spectroscopy (FT-IR, thermogravimetric analysis (TGA, Raman spectrophotometry, and X-ray diffraction (XRD techniques. The results revealed that the polyDOPA-AgNPs with diameters of 25 nm were well dispersed due to the polyDOPA. It was noted that the polyDOPA-AgNPs showed selectivity for Pb2+ and Cu2+ detection with the detection limits for the two ions as low as 9.4 × 10−5 and 8.1 × 10−5 μM, respectively. Therefore, the polyDOPA-AgNPs can be applied to both Pb2+ and Cu2+ detection in real water samples. The proposed method will be useful for colorimetric detection of heavy metal ions in aqueous media.

  8. Green Synthesis of Silver Nanoparticles Stabilized with Mussel-Inspired Protein and Colorimetric Sensing of Lead(II) and Copper(II) Ions

    Science.gov (United States)

    Cheon, Ja Young; Park, Won Ho

    2016-01-01

    This articles reports a simple and green method for preparing uniform silver nanoparticles (AgNPs), for which self-polymerized 3,4-dihydroxy-l-phenylalanine (polyDOPA) is used as the reducing and stabilizing agent in aqueous media. The AgNPs functionalized by polyDOPA were analyzed by UV–Vis spectroscopy, high-resolution transmission electron microscopy (HR-TEM), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), Raman spectrophotometry, and X-ray diffraction (XRD) techniques. The results revealed that the polyDOPA-AgNPs with diameters of 25 nm were well dispersed due to the polyDOPA. It was noted that the polyDOPA-AgNPs showed selectivity for Pb2+ and Cu2+ detection with the detection limits for the two ions as low as 9.4 × 10−5 and 8.1 × 10−5 μM, respectively. Therefore, the polyDOPA-AgNPs can be applied to both Pb2+ and Cu2+ detection in real water samples. The proposed method will be useful for colorimetric detection of heavy metal ions in aqueous media. PMID:27916894

  9. Isolation and characterization of bacteria resistant to metallic copper surfaces.

    Science.gov (United States)

    Santo, Christophe Espírito; Morais, Paula Vasconcelos; Grass, Gregor

    2010-03-01

    Metallic copper alloys have recently attracted attention as a new antimicrobial weapon for areas where surface hygiene is paramount. Currently it is not understood on a molecular level how metallic copper kills microbes, but previous studies have demonstrated that a wide variety of bacteria, including Escherichia coli, Staphylococcus aureus, and Clostridium difficile, are inactivated within minutes or a few hours of exposure. In this study, we show that bacteria isolated from copper alloy coins comprise strains that are especially resistant against the toxic properties exerted by dry metallic copper surfaces. The most resistant of 294 isolates were Gram-positive staphylococci and micrococci, Kocuria palustris, and Brachybacterium conglomeratum but also included the proteobacterial species Sphingomonas panni and Pseudomonas oleovorans. Cells of some of these bacterial strains survived on copper surfaces for 48 h or more. Remarkably, when these dry-surface-resistant strains were exposed to moist copper surfaces, resistance levels were close to those of control strains and MICs for copper ions were at or below control strain levels. This suggests that mechanisms conferring resistance against dry metallic copper surfaces in these newly isolated bacterial strains are different from well-characterized copper ion detoxification systems. Furthermore, staphylococci on coins did not exhibit increased levels of resistance to antibiotics, arguing against coselection with copper surface resistance traits.

  10. Detoxification of copper fungicide using EDTA-modified cellulosic ...

    African Journals Online (AJOL)

    STORAGESEVER

    2009-02-04

    Feb 4, 2009 ... ugh the R2 values are high (and good), for the Longmuir isotherm, the .... mass transfer resistance and the third is intraparticle ... Chromium and Copper ions from aqueous solutions by shea Butter ... Batch nickel removal from.

  11. Antwerp Copper Plates

    DEFF Research Database (Denmark)

    Wadum, Jørgen

    1999-01-01

    In addition to presenting a short history of copper paintings, topics detail artists’ materials and techniques, as well as aspects of the copper industry, including mining, preparation and trade routes.......In addition to presenting a short history of copper paintings, topics detail artists’ materials and techniques, as well as aspects of the copper industry, including mining, preparation and trade routes....

  12. Magnetic field effects on copper metal deposition from copper sulfate aqueous solution.

    Science.gov (United States)

    Udagawa, Chikako; Maeda, Aya; Katsuki, Akio; Maki, Syou; Morimoto, Shotaro; Tanimoto, Yoshifumi

    2014-05-01

    Effects of a magnetic field (≤0.5 T) on electroless copper metal deposition from the reaction of a copper sulfate aqueous solution and a zinc thin plate were examined in this study. In a zero field, a smooth copper thin film grew steadily on the plate. In a 0.38 T field, a smooth copper thin film deposited on a zinc plate within about 1 min. Then, it peeled off repeatedly from the plate. The yield of consumed copper ions increased about 2.1 times compared with that in a zero field. Mechanism of this magnetic field effect was discussed in terms of Lorentz force- and magnetic force-induced convection and local volta cell formation.

  13. Copper removal using electrosterically stabilized nanocrystalline cellulose.

    Science.gov (United States)

    Sheikhi, Amir; Safari, Salman; Yang, Han; van de Ven, Theo G M

    2015-06-03

    Removal of heavy metal ions such as copper using an efficient and low-cost method with low ecological footprint is a critical process in wastewater treatment, which can be achieved in a liquid phase using nanoadsorbents such as inorganic nanoparticles. Recently, attention has turned toward developing sustainable and environmentally friendly nanoadsorbents to remove heavy metal ions from aqueous media. Electrosterically stabilized nanocrystalline cellulose (ENCC), which can be prepared from wood fibers through periodate/chlorite oxidation, has been shown to have a high charge content and colloidal stability. Here, we show that ENCC scavenges copper ions by different mechanisms depending on the ion concentration. When the Cu(II) concentration is low (C0≲200 ppm), agglomerates of starlike ENCC particles appear, which are broken into individual starlike entities by shear and Brownian motion, as evidenced by photometric dispersion analysis, dynamic light scattering, and transmission electron microscopy. On the other hand, at higher copper concentrations, the aggregate morphology changes from starlike to raftlike, which is probably due to the collapse of protruding dicarboxylic cellulose (DCC) chains and ENCC charge neutralization by copper adsorption. Such raftlike structures result from head-to-head and lateral aggregation of neutralized ENCCs as confirmed by transmission electron microscopy. As opposed to starlike aggregates, the raftlike structures grow gradually and are prone to sedimentation at copper concentrations C0≳500 ppm, which eliminates a costly separation step in wastewater treatment processes. Moreover, a copper removal capacity of ∼185 mg g(-1) was achieved thanks to the highly charged DCC polyanions protruding from ENCC. These properties along with the biorenewability make ENCC a promising candidate for wastewater treatment, in which fast, facile, and low-cost removal of heavy metal ions is desired most.

  14. Transfer of Copper from an Amyloid to a Natural Copper-Carrier Peptide with a Specific Mediating Ligand.

    Science.gov (United States)

    Nguyen, Michel; Bijani, Christian; Martins, Nathalie; Meunier, Bernard; Robert, Anne

    2015-11-16

    The oxidative stress that arises from the catalytic reduction of dioxygen by Cu(II/I)-loaded amyloids is the major pathway for neuron death that occurs in Alzheimer's disease. In this work, we show that bis-8(aminoquinoline) ligands, copper(II) specific chelators, are able to catalytically extract Cu(II) from Cu-Aβ1-16 and then completely release Cu(I) in the presence of glutathione to provide a Cu(I)-glutathione complex, a biological intermediate that is able to deliver copper to apo forms of copper-protein complexes. These data demonstrate that bis-8(aminoquinolines) can perform the transfer of copper ions from the pathological Cu-amyloid complexes to regular copper-protein complexes. These copper-specific ligands assist GSH to recycle Cu(I) in an AD brain and consequently slow down oxidative damage that is due to copper dysregulation in Alzheimer's disease. Under the same conditions, we have shown that the copper complex of PBT2, a mono(8-hydroxyquinoline) previously used as a drug candidate, does not efficiently release copper in the presence of GSH. In addition, we report that GSH itself was unable to fully abstract copper ions from Cu-β-amyloid complexes.

  15. Copper and copper proteins in Parkinson's disease.

    Science.gov (United States)

    Montes, Sergio; Rivera-Mancia, Susana; Diaz-Ruiz, Araceli; Tristan-Lopez, Luis; Rios, Camilo

    2014-01-01

    Copper is a transition metal that has been linked to pathological and beneficial effects in neurodegenerative diseases. In Parkinson's disease, free copper is related to increased oxidative stress, alpha-synuclein oligomerization, and Lewy body formation. Decreased copper along with increased iron has been found in substantia nigra and caudate nucleus of Parkinson's disease patients. Copper influences iron content in the brain through ferroxidase ceruloplasmin activity; therefore decreased protein-bound copper in brain may enhance iron accumulation and the associated oxidative stress. The function of other copper-binding proteins such as Cu/Zn-SOD and metallothioneins is also beneficial to prevent neurodegeneration. Copper may regulate neurotransmission since it is released after neuronal stimulus and the metal is able to modulate the function of NMDA and GABA A receptors. Some of the proteins involved in copper transport are the transporters CTR1, ATP7A, and ATP7B and the chaperone ATOX1. There is limited information about the role of those biomolecules in the pathophysiology of Parkinson's disease; for instance, it is known that CTR1 is decreased in substantia nigra pars compacta in Parkinson's disease and that a mutation in ATP7B could be associated with Parkinson's disease. Regarding copper-related therapies, copper supplementation can represent a plausible alternative, while copper chelation may even aggravate the pathology.

  16. Electrodeposition of copper on a Pt(111) electrode in sulfuric acid containing poly(ethylene glycol) and chloride ions as probed by in situ STM.

    Science.gov (United States)

    Fu, YunLin; Pao, Te; Chen, Sih-Zih; Yau, ShuehLin; Dow, Wei-Ping; Lee, Yuh-Lang

    2012-07-03

    This study employed real-time in situ STM imaging to examine the adsorption of PEG molecules on Pt(111) modified by a monolayer of copper adatoms and the subsequent bulk Cu deposition in 1 M H(2)SO(4) + 1 mM CuSO(4)+ 1 mM KCl + 88 μM PEG. At the end of Cu underpotential deposition (~0.35 V vs Ag/AgCl), a highly ordered Pt(111)-(√3 × √7)-Cu + HSO(4)(-) structure was observed in 1 M H(2)SO(4) + 1 mM CuSO(4). This adlattice restructured upon the introduction of poly(ethylene glycol) (PEG, molecular weight 200) and chloride anions. At the onset potential for bulk Cu deposition (~0 V), a Pt(111)-(√3 × √3)R30°-Cu + Cl(-) structure was imaged with a tunneling current of 0.5 nA and a bias voltage of 100 mV. Lowering the tunneling current to 0.2 nA yielded a (4 × 4) structure, presumably because of adsorbed PEG200 molecules. The subsequent nucleation and deposition processes of Cu in solution containing PEG and Cl(-) were examined, revealing the nucleation of 2- to 3-nm-wide CuCl clusters on an atomically smooth Pt(111) surface at overpotentials of less than 50 mV. With larger overpotential (η > 150 mV), Cu deposition seemed to bypass the production of CuCl species, leading to layered Cu deposition, starting preferentially at step defects, followed by lateral growth to cover the entire Pt electrode surface. These processes were observed with both PEG200 and 4000, although the former tended to produce more CuCl nanoclusters. Raising [H(2)SO(4)] to 1 M substantiates the suppressing effect of PEG on Cu deposition. This STM study provided atomic- or molecular-level insight into the effect of PEG additives on the deposition of Cu.

  17. The changes in the chloroplast membranes of pea leaves under the influence of carbonic anhydrase inhibitors (ions of copper and zinc

    Directory of Open Access Journals (Sweden)

    M.V. Vodka

    2014-04-01

    Full Text Available Тhe effects of carbonic anhydrase inhibitors, such as ions Cu2+ and Zn2+, on the membrane system of chloroplasts in pea leaves were investigated. After treatment of pea leaves with 250 mM Cu2+ or 400 mM Zn2+ we observed changes in the granal structure and compactness of the thylakoids in granae. It was shown that the thickness of granal thylakoids and the interspace between thylakoids increased comparing to control. Changes of the size and structure of thylakoids and granae in treated leaves may be associated with the enhanced accumulation of CO2 in the membrane. It is suggested that the carbonic anhydrase may also play a structural role in chloroplast granae.

  18. Cysteamine capped CdS quantum dots as a fluorescence sensor for the determination of copper ion exploiting fluorescence enhancement and long-wave spectral shifts

    Science.gov (United States)

    Boonmee, Chanida; Noipa, Tuanjai; Tuntulani, Thawatchai; Ngeontae, Wittaya

    2016-12-01

    We described a turn-on fluorescence sensor for the determination of Cu2 + ions, utilizing the quantum confinement effect of cadmium sulfide quantum dots capped with cysteamine (Cys-CdS QDs). The fluorescence intensity of the Cys-CdS QDs was both enhanced and red shifted (from blue-green to yellow) in the presence of Cu2 +. Fluorescence enhancement was linearly proportional to the concentration of Cu2 + in the concentration range 2 to 10 μM. Other cations at the same concentration level did not significantly change the intensity and spectral maxima of Cys-CdS QDs, except Ag+. The limit of detection was 1.5 μM. The sensor was applied to the determination of Cu2 + in (spiked) real water samples and gave satisfactory results, with recoveries ranging from 96.7 to 108.2%, and with RSDs ranging from 0.3 to 2.6%.

  19. β-amyloid fibrils in Alzheimer disease are not inert when bound to copper ions but can degrade hydrogen peroxide and generate reactive oxygen species.

    Science.gov (United States)

    Mayes, Jennifer; Tinker-Mill, Claire; Kolosov, Oleg; Zhang, Hao; Tabner, Brian J; Allsop, David

    2014-04-25

    According to the "amyloid cascade" hypothesis of Alzheimer disease, the formation of Aβ fibrils and senile plaques in the brain initiates a cascade of events leading to the formation of neurofibrillary tangles, neurodegeneration, and the symptom of dementia. Recently, however, emphasis has shifted away from amyloid fibrils as the predominant toxic form of Aβ toward smaller aggregates, referred to as "soluble oligomers." These oligomers have become one of the prime suspects for involvement in the early oxidative damage that is evident in this disease. This raises the question whether or not Aβ fibrils are actually "inert tombstones" present at the end of the aggregation process. Here we show that, when Aβ(1-42) aggregates, including fibrils, are bound to Cu(II) ions, they retain their redox activity and are able to degrade hydrogen peroxide (H2O2) with the formation of hydroxyl radicals and the consequent oxidation of the peptide (detected by formation of carbonyl groups). We find that this ability increases as the Cu(II):peptide ratio increases and is accompanied by changes in aggregate morphology, as determined by atomic force microscopy. When aggregates are prepared in the copresence of Cu(II) and Zn(II) ions, the ratio of Cu(II):Zn(II) becomes an important factor in the degeneration of H2O2, the formation of carbonyl groups in the peptide, and in aggregate morphology. We believe, therefore, that Aβ fibrils can destroy H2O2 and generate damaging hydroxyl radicals and, so, are not necessarily inert end points.

  20. Study on the Orientation of Liquid Crystals Presented on the Glass Substrates Spin-coated and Functionalized with Copper Ions%铜离子功能化的基底表面上液晶取向的研究

    Institute of Scientific and Technical Information of China (English)

    王诗鸣; 熊兴良; 张琰; 李广; 陈萌梦

    2013-01-01

    在液晶型化学与生物传感器的研究中,构建一个能使液晶分子长时间呈稳定、均一的取向排列且制作方法简易的基底表面对于传感器的实用化至关重要.本研究通过将5种不同浓度(0~ 100 mmol/L)的高氯酸铜无水乙醇溶液直接旋转喷涂于载玻片上,制备成具有化学敏感性的铜离子基底表面;随后将5CB液晶滴加在该基底表面,制作成液晶盒(液晶传感器);利用偏光显微镜的直光和锥光模式观察液晶分子的取向排列情况.实验发现在经过较短的时间后,旋涂有高氯酸铜的所有传感器的透射光斑先后逐渐变暗;高氯酸铜的浓度越大,光斑变暗的速度越快,完全变暗所需的时间越短;而未喷涂高氯酸铜的传感器在室温环境(25℃)下静置ld后,其透射光斑亮度没有变化;室温环境下于烘箱中贮存2个月后,喷涂有高氯酸铜的传感器的透射光亮度基本没有变化.结果表明,玻璃表面上直接喷涂高氯酸铜的基底表面能使液晶分子长时间呈稳定、均一的垂直排列;高氯酸铜的浓度对液晶取向排列的响应速度有影响.%A stable,uniform,easily implemented,LC-based chemical and biological sensor substrate for orientations of liquid crystals (LCs) for a long-term is urgently needed for medical applications of the sensors.We proposed a use of spin-coating of copper perchlorate (Cu (ClO4)2),with five different concentrations (0-100mmol/L),directly on glass slides for fabricating a layer of chemically-sensitive copper ions.Observing the transmitted light with a polarized microscope,we found the luminosity of the light propagated through sensors deposited with copper ions started to weaken gradually after