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Sample records for carbon paste electrodes

  1. Electroanalysis with carbon paste electrodes

    CERN Document Server

    Svancara, Ivan; Walcarius, Alain; Vytras, Karel

    2011-01-01

    Introduction to Electrochemistry and Electroanalysis with Carbon Paste-Based ElectrodesHistorical Survey and GlossaryField in Publication Activities and LiteratureCarbon Pastes and Carbon Paste ElectrodesCarbon Paste as the Binary MixtureClassification of Carbon Pastes and Carbon Paste ElectrodesConstruction of Carbon Paste HoldersCarbon Paste as the Electrode MaterialPhysicochemical Properties of Carbon PastesElectrochemical Characteristics of Carbon PastesTesting of Unmodified CPEsIntera

  2. Carbon paste electrodes in electroanalytical chemistry

    Directory of Open Access Journals (Sweden)

    KAREL VYTŘAS

    2009-09-01

    Full Text Available An overview is given dealing with the applications of carbon paste electrodes in equilibrium potentiometry as well as in electrochemical stripping analysis using both voltammetric and potentiometric modes. Various modifications of carbon pastes and carbon paste-based biosensors are also mentioned. The main emphasis in this article is directed at summarizing recent results of the authors’ research group during the past few years.

  3. Amperometric determination of rutin on carbon paste electrodes

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    Pavla Macikova

    2010-12-01

    Full Text Available Three different carbon paste electrodes (i.e. unmodified, ironphthalocyanine and ionic liquid modified were tested to determinerutin by amperometry. The widest linear concentration range andlowest detection limit were obtained with unmodified carbon pasteelectrode.

  4. All-solid-state carbonate-selective electrode based on screen-printed carbon paste electrode

    Science.gov (United States)

    Li, Guang; Lyu, Xiaofeng; Wang, Zhan; Rong, Yuanzhen; Hu, Ruifen; Luo, Zhiyuan; Wang, You

    2017-02-01

    A novel disposable all-solid-state carbonate-selective electrode based on a screen-printed carbon paste electrode using poly(3-octylthiophene-2,5-diyl) (POT) as an ion-to-electron transducer has been developed. The POT was dropped onto the reaction area of the carbon paste electrode covered by the poly(vinyl chloride) (PVC) membrane, which contains N,N-Dioctyl-3α,12α-bis(4-trifluoroacetylbenzoyloxy)-5β-cholan-24-amide as a carbonate ionophore. The electrode showed a near-Nernstian slope of  -27.5 mV/decade with a detection limit of 3.6 * 10-5 mol l-1. Generally, the detection time was 30 s. Because these electrodes are fast, convenient and low in cost, they have the potential to be mass produced and used in on-site testing as disposable sensors. Furthermore, the repeatability, reproducibility and stability have been studied to evaluate the properties of the electrodes. Measurement of the carbonate was also conducted in a human blood solution and achieved good performance.

  5. Voltammetric determination of Arbutin on carbon paste electrode

    OpenAIRE

    Libánský, Milan; Zima, Jiří; Barek, Jiří; Dejmková, Hana

    2011-01-01

    Arbutin (hydroquinone- -D-glukopyranoside) belongs among the most frequent active substances in skin-whitening cosmetics. In this matrix, its content does not require sensitive, but rather simple, quick and cheap methods of determination, which can be supplied by electrochemical methods. Method for determination of Arbutin was developed using differential pulse voltammetry at a carbon paste electrode in Britton-Robinson buffer (pH 2). The concentration dependence proved a linear respons...

  6. Ion-selective carbon-paste electrodes for halides and silver(I) ions

    NARCIS (Netherlands)

    Mesaric, S.; Dahmen, E.A.M.F.

    1973-01-01

    The behaviour of a simple type of ion-selective electrode for halogens and silver has been studied. The electrode consists of a plastic body filled with carbon paste, the surface of which can be easily renewed. The paste composition is based on carbon-nujol (5:1, w/v) or carbon-paraffin wax (3:1,w/w

  7. Imprinted zeolite modified carbon paste electrode as a potentiometric sensor for uric acid

    Science.gov (United States)

    Khasanah, Miratul; Widati, Alfa Akustia; Fitri, Sarita Aulia

    2016-03-01

    Imprinted zeolite modified carbon paste electrode (carbon paste-IZ) has been developed and applied to determine uric acid by potentiometry. The imprinted zeolite (IZ) was synthesized by the mole ratio of uric acid/Si of 0.0306. The modified electrode was manufactured by mass ratio of carbon, IZ and solid paraffin was 40:25:35. The modified electrode had shown the measurement range of 10-5 M to 10-2 M with Nernst factor of 28.6 mV/decade, the detection limit of 5.86 × 10-6 M and the accuracy of 95.3 - 105.0%. Response time of the electrode for uric acid 10-5 M - 10-2 M was 25 - 44 s. The developed electrode showed the high selectivity toward uric acid in the urea matrix. Life time of the carbon paste-IZ electrode was 10 weeks.

  8. Magnetite nanoparticles-chitosan composite containing carbon paste electrode for glucose biosensor application.

    Science.gov (United States)

    Kavitha, A L; Prabu, H Gurumallesh; Babu, S Ananda; Suja, S K

    2013-01-01

    This work was aimed to develop reusable magnetite chitosan composite containing carbon paste electrode for biosensor application. Glucose oxidase (GOx) enzyme was used to prepare GOx-magnetite-chitosan nanocomposite containing carbon paste electrode for sensitive detection of glucose. The immobilized enzyme retained its bioactivity, exhibited a surface confined reversible electron transfer reaction, and had good stability. The surface parameters like surface coverage (tau), Diffusion coefficient (D0), and rate constant (kS) were studied. The carbon paste modified electrode virtually eliminated the interference during the detection of glucose. The excellent performance of the biosensor is attributed to large surface-to-volume ratio, high conductivity and good biocompatibility of chitosan, which enhances the enzyme absorption and promotes electron transfer between redox enzymes and the surface of electrode. The shelf life of the developed electrode system is about 12 weeks under refrigerated conditions. We report for the first time in the fabrication of carbon paste bioelectrode containing magnetite-chitosan-GOx.

  9. Brain Tissue Oxygen: In Vivo Monitoring with Carbon Paste Electrodes

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    John P. Lowry

    2005-11-01

    Full Text Available In this communication we review selected experiments involving the use ofcarbon paste electrodes (CPEs to monitor and measure brain tissue O2 levels in awakefreely-moving animals. Simultaneous measurements of rCBF were performed using the H2clearance technique. Voltammetric techniques used include both differential pulse (O2 andconstant potential amperometry (rCBF. Mild hypoxia and hyperoxia produced rapidchanges (decrease and increase respectively in the in vivo O2 signal. Neuronal activation(tail pinch and stimulated grooming produced similar increases in both O2 and rCBFindicating that CPE O2 currents provide an index of increases in rCBF when such increasesexceed O2 utilization. Saline injection produced a transient increase in the O2 signal whilechloral hydrate produced slower more long-lasting changes that accompanied the behavioralchanges associated with anaesthesia. Acetazolamide increased O2 levels through an increasein rCBF.

  10. Single electrode heat effects. I. Peltier entropies of gas electrodes in carbonate paste electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Jacobsen, T. (Technical Univ. of Denmark, Lyngby); Broers, G.H.J.

    1977-02-01

    Standard Peltier entropies for the reactions /sup 1///sub 2/O/sub 2/ + CO/sub 2/ + 2e/sup -/ ..-->.. CO/sub 3//sup - -/ and 2CO/sub 2/ + 2e/sup -/ ..-->.. CO + CO/sub 3//sup - -/ in molten carbonate paste elctrolytes at 1000/sup 0/K have been determined from thermogalvanic measurements. The results are -217 and -118 J/mole/sup 0/K, respectively. No dependence on electrolyte composition is observed. The reversible part of the Peltier entropy for the oxygen electrode reaction is estimated from thermodynamic data and reasonable agreement with the experimental results is found. It is concluded that the main contribution to the Peltier entropy arises from the transition from gaseous to liquid state, whereas the transfer entropies of the ionic species are of minor importance.

  11. IMPROVED SELECTIVE ELECTROCATALYTIC OXIDATION OF PHENOLS BY TYROSINASE-BASED CARBON PASTE ELECTRODE BIOSENSOR

    Science.gov (United States)

    Tyrosinase-based carbon paste electrodes are evaluated with respect to the viscosity and polarity of the binder liquids. The electrodes constructed using a lower viscosity mineral oil yielded a greater response to phenol and catechol than those using a higher viscosity oil of s...

  12. Electrochemical behaviorof carbon paste electrode modified with Carbon Nanofibers: Application to detection of Bisphenol A

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    N.Achargui

    2016-12-01

    Full Text Available The electrochemical behavior of carbon paste electrode modified with carbon nanofibers has been studied using cyclic voltammetry (CV, electrochemical impedance spectroscopy (EIS and scaning electron microscopy. The response of modified electrodein ferroferricyanidesolutionshows reversible behavior and significant increment in current value compared to the bare CPE indicating that CNFs act as efficient electron mediator to catalyze reactions at the surface. The modified electrode has been used to study the electrochemical response of bisphenol Ausing different electrochemical techniques such as cyclic voltammetry, linear sweep voltammetry, differential pulse voltammetry and square wave voltammetry. The oxidation peak of BPA was observed at about 0.53 V in phosphate buffer solution at pH 6.7. The oxidation peak current of BPA varied linearly with concentration over a wide range of 5µmol L-1 to 400 µmol L-1 and the detection limit of this method was found to be 0.55 µmol L-1

  13. Electrocatalytic amperometric determination of amitrole using a cobalt-phthalocyanine-modified carbon paste electrode.

    Science.gov (United States)

    Chicharro, Manuel; Zapardiel, Antonio; Bermejo, Esperanza; Moreno, Mónica; Madrid, Elena

    2002-07-01

    Cobalt-phthalocyanine-modified carbon paste electrodes are shown to be excellent indicators for electrocatalytic amperometric measurements of triazolic herbicides such as amitrole, at low oxidation potentials (+0.40 V). The detection and determination of amitrole in flow injection analysis with a modified carbon paste electrode with Co-phthalocyanine is described. The concentrations of amitrole in 0.1 M NaOH solutions were determined using the electrocatalytic oxidation signal corresponding to the Co(II)/Co(III) redox process. A detection limit of 0.04 microg mL(-1) (4 ng amitrole) was obtained for a sample loop of 100 microL at a fixed potential of +0.55 V (vs. Ag/AgCl) in 0.1 M NaOH and a flow rate of 4.0 mL min(-1). Furthermore, the modified carbon paste electrodes offers reproducible responses in such a system, and the relative standard deviation was 3.3% using the same surface, 5.1% using different surface, and 6.9% using different pastes. The performance of the cobalt-phthalocyanine-modified carbon paste electrodes is illustrated here for the determination of amitrole in commercial formulations. The response of the electrodes is stable, with more than 80% of the initial retained activity after 50 min of continuous use.

  14. Antimony trifluoride-modified carbon paste electrode for electrochemical stripping analysis of selected heavy metals

    OpenAIRE

    Stočes, Matěj; Hočevar, Samo B.; Švancara, Ivan

    2011-01-01

    In this article, a new typ of non-mercury metal-based electrode, antimony trifluoridebulk- modified carbon paste electrode (SbF3-CPE) is for the first time reported and examined for electrochemical stripping analysis of selected heavy metal ions at their trace concentration level. In the role of bulk modifier and a source of antimony film generated in state nascenti, SbF3 in a content of 3% (w/w) in the carbon paste mixture was the ultimate choice. All important experimental parameters hav...

  15. Studies on the potentiometric thallium(III)-selective carbon paste electrode and its possible applications

    Energy Technology Data Exchange (ETDEWEB)

    Vytras, K.; Khaled, E.; Jezkova, J. [Dept. of Analytical Chemistry, University of Pardubice (Czech Republic); Hassan, H.N.A. [Microanalytical Lab., National Research Centre, Dokki, Cairo (Egypt); Barsoum, B.N. [Dept. of Chemistry, Faculty of Science, Cairo University, Giza (Egypt)

    2000-05-01

    Construction, performance characteristics and applications of a carbon paste thallium(III) ion-selective electrode are described. The electrode, which is based on ion-associate compounds formed between cetylpyridinium and chlorothallate(III) complexes dissolved in tricresyl phosphate as pasting liquid, showed near-Nernstian response over the concentration range of 5.8 x 10{sup -6}-2.9 x 10{sup -3}mol/L. Potentiometric titrations of thallium(III) with cetylpyridinium chloride were affected by higher concentrations of excess halides, probably due to the formation of higher halogenothallates. (orig.)

  16. Electrochemical Investigation of Catechol at Poly(niacinamide Modified Carbon Paste Electrode: A Voltammetric Study

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    A. B. Teradale

    2016-01-01

    Full Text Available A polymeric thin film modified electrode, that is, poly(niacinamide modified carbon paste electrode (MCPE, was developed for the electrochemical determination of catechol (CC by using cyclic voltammetric technique. Compared to bare carbon paste electrode (BCPE, the poly(niacinamide MCPE shows good electrocatalytic activity towards the oxidation of catechol in phosphate buffer solution (PBS of physiological pH 7.4. All experimental parameters were optimized. Poly(niacinamide modified carbon paste electrode gave a linear response between concentration of CC and its anodic peak current in the range within 20.6–229.0 μM. The limit of detection (3S/M and limit of quantification (10S/M were 1.497 μM and 4.99 μM, respectively. From the study of scan rate variation, the electrode process was found to be adsorption-controlled. The involvement of protons and electrons in the oxidation of CC was found to be equal. The probable electropolymerisation mechanism of niacinamide was proposed. Finally, this method can be used in development of a sensor for sensitive determination of CC.

  17. Voltammetric copper(II) determination with a montmorillonite-modified carbon paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Kula, P. [Institute of Geonics, Academy of Sciences of Czech Republic, Studertska 1768, 708 00 Ostrava (Czech Republic); Navratilova, Z. [Institute of Geonics, Academy of Sciences of Czech Republic, Studertska 1768, 708 00 Ostrava (Czech Republic)

    1996-03-01

    The clay mineral montmorillonite has been tested as modifier for the carbon paste electrode with a novel electrode modification technique. The differential pulse voltammetric determination of copper(II) by means of this modified carbon paste electrode has been studied. A detection limit of 4 x 10{sup -8} mol/l has been achieved after 10 min preconcentration under open circuit conditions with subsequent anodic stripping voltammetry. The calibration curve for Cu(II) is linear in the range of 4 x 10{sup -8}-8 x 10{sup -7} mol/l. Pb interferes in a 10-fold molar and Cd and Hg in a 100-fold molar excess. The interference by humic ligands is significant. (orig.). With 5 figs., 1 tab.

  18. Enzyme-free ethanol sensor based on electrospun nickel nanoparticle-loaded carbon fiber paste electrode.

    Science.gov (United States)

    Liu, Yang; Zhang, Lei; Guo, Qiaohui; Hou, Haoqing; You, Tianyan

    2010-03-24

    We have developed a novel nickel nanoparticle-loaded carbon fiber paste (NiCFP) electrode for enzyme-free determination of ethanol. An electrospinning technique was used to prepare the NiCF composite with large amounts of spherical nanoparticles firmly embedded in carbon fibers (CF). In application to electroanalysis of ethanol, the NiCFP electrode exhibited high amperometric response and good operational stability. The calibration curve was linear up to 87.5 mM with a detection limit of 0.25 mM, which is superior to that obtained with other transition metal based electrodes. For detection of ethanol present in liquor samples, the values obtained with the NiCFP electrode were in agreement with the ones declared on the label. The attractive analytical performance and simple preparation method make this novel material promising for the development of effective enzyme-free sensors.

  19. Cyclam Modified Carbon Paste Electrode as a Potentiometric Sensor For Determination of Cobalt(Ⅱ) Ions

    Institute of Scientific and Technical Information of China (English)

    Hamid Reza POURETEDAL; Mohammad Hossein KESHAVARZ

    2005-01-01

    A new modified carbon paste electrode based on cyclam as a modifier was prepared for the determination of Co(Ⅱ) ions. The proposed electrode shows a Nernstian slope 28.4 mV per decade over a wide concentration range 5.0×10-6_1.0×10-1 mol/L of Co2+ ions with detection limit 2.5×10-6 mol/L. The sensor exhibits good selectivities for Co2+ over a wide variety of other cations. It can be used as an indicator electrode in potentiometric titration of cobalt(Ⅱ) ions as well as in direct determination of cobalt(Ⅱ) ions in wastewater of acidic cobalt electroplating bath. The electrode shows Nernestian behavior in a solution of 25% ethanol.

  20. Electrochemical behavior of an anticancer drug 5-fluorouracil at methylene blue modified carbon paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Bukkitgar, Shikandar D.; Shetti, Nagaraj P., E-mail: dr.npshetti@gmail.com

    2016-08-01

    A novel sensor for the determination of 5-fluorouracil was constructed by electrochemical deposition of methylene blue on surface of carbon paste electrode. The electrode surface morphology was studied using Atomic force microscopy and XRD. The electrochemical activity of modified electrode was characterized using cyclic voltammetry and differential pulse method. The developed sensor shows impressive enlargement in sensitivity of 5-fluorouracil determination. The peak currents obtained from differential pulse voltammetry was linear with concentration of 5-fluorouracil in the range 4 × 10{sup −5}–1 × 10{sup −7} M and detection limit and quantification limit were calculated to be 2.04 nM and 6.18 nM respectively. Further, the sensor was successfully applied in pharmaceutical and biological fluid sample analysis. - Highlights: • Electrochemical oxidation of 5-fluorouracil has been investigated for first time at methylene blue modified carbon paste electrode • The electrode process was irreversible and diffusion controlled • Probable electrochemical mechanism was proposed which involved two proton and two electron transfer reaction • The LOD and LOQ values were calculated to be 2.04 nM and 6.18 nM, respectively, with good selectivity and sensitivity. • Proposed method was applied to 5-Fluorouracil determination in pharmaceutical and spiked human urine samples.

  1. Maize tassel-modified carbon paste electrode for voltammetric determination of Cu(II).

    Science.gov (United States)

    Moyo, Mambo; Okonkwo, Jonathan O; Agyei, Nana M

    2014-08-01

    The preparation and application of a practical electrochemical sensor for environmental monitoring and assessment of heavy metal ions in samples is a subject of considerable interest. In this paper, a carbon paste electrode modified with maize tassel for the determination of Cu(II) has been proposed. Scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) were used to study morphology and identify the functional groups on the modified electrode, respectively. First, Cu(II) was adsorbed on the carbon paste electrode surface at open circuit and voltammetric techniques were used to investigate the electrochemical performances of the sensor. The electrochemical sensor showed an excellent electrocatalytic activity towards Cu(II) at pH 5.0 and by increasing the amount of maize tassel biomass, a maximum response at 1:2.5 (maize tassel:carbon paste; w/w) was obtained. The electrocatalytic redox current of Cu(II) showed a linear response in the range (1.23 μM to 0.4 mM) with the correlation coefficient of 0.9980. The limit of detection and current-concentration sensitivity were calculated to be 0.13 (±0.01) μM and 0.012 (±0.001) μA/μM, respectively. The sensor gave good recovery of Cu(II) in the range from 96.0 to 98.0 % when applied to water samples.

  2. Electrochemical Behavior and Determination of Rutin on Modified Carbon Paste Electrodes

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    Pavla Macikova

    2012-01-01

    Full Text Available The performances of ionic liquid (1-hexyl-3-methylimidazolium-bis(trifluoromethylsulfonylimide, IL/CPE and iron phthalocyanine (IP/CPE modified carbon paste electrodes in electroanalytical determinations of rutin were evaluated and compared to the performance of unmodified carbon paste electrode (CPE. Cyclic voltammetry (CV, differential pulse voltammetry (DPV, differential pulse adsorptive stripping voltammetry (DPAdSV, and amperometry were used for rutin analysis. The best current responses of rutin were obtained at pH 4.0 for all tested techniques. IL/CPE electrode was found to perform best with DPAdSV technique, where a detection limit (LOD as low as 5 nmol L-1 of rutin was found. On the other hand, IP/CPE showed itself to be an optimum choice for DPV technique, where LOD of 80 nmol L-1 was obtained. Analytical applicability of newly prepared electrodes was demonstrated on determination of rutin in the model samples and the extracts of buckwheat seeds. To find an optimum method for buckwheat seeds extraction, a boiling water extraction (BWE, Soxhlet extraction (SE, pressurized solvent extraction (PSE, and supercritical fluid extraction (SFE were tested.

  3. A zeolite modified carbon paste electrode as useful sensor for voltammetric determination of acetaminophen

    Energy Technology Data Exchange (ETDEWEB)

    Ahmadpour-Mobarakeh, Leila; Nezamzadeh-Ejhieh, Alireza, E-mail: arnezamzadeh@iaush.ac.ir

    2015-04-01

    The voltammetric behavior of a carbon paste electrode modified with Co(II)-exchanged zeolite A (Co(II)-A/ZMCPE) for determination of acetaminophen was studied. The proposed electrode showed a diffusion controlled reaction with the electron transfer rate constant (K{sub s}) of 0.44 s{sup −1} and charge transfer coefficient of 0.73 in the absence of acetaminophen. A linear voltammetric response was obtained in the range of 0.1 to 190 μmol L{sup −1} of acetaminophen [r{sup 2} = 0.9979, r = 0.9989 (n = 10)] with a detection limit of 0.04 μmol L{sup −1}. The method was successfully applied to the analysis of acetaminophen in some drugs. - Highlights: • Modified carbon paste electrode with Co(II)-zeolite A improved the voltammetric current in determination of acetaminophen. • Modified electrode is applicable for acetaminophen in real samples. • The proposed method has good reproducibility and repeatability.

  4. Electrochemical detection of carbidopa using a ferrocene-modified carbon nanotube paste electrode

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    FATEMEH KARIMI

    2009-12-01

    Full Text Available A chemically modified carbon paste electrode (MCPE containing ferrocene (FC and carbon nanotubes (CNT was constructed. The electrochemical behavior and stability of the MCPE were investigated by cyclic voltammetry. The electrocatalytic activity of the MCPE was investigated and it showed good characteristics for the oxidation of carbidopa (CD in phosphate buffer solution (PBS. A linear concentration range of 5 to 600 μM CD, with a detection limit of 3.6±0.17 μM CD, was obtained. The diffusion coefficient of CD and the transfer coefficient ( were also determined. The MCPE showed good reproducibility, remarkable long-term stability and especially good surface renewability by simple mechanical polishing. The results showed that this electrode could be used as an electrochemical sensor for the determination of CD in real samples, such as urine samples.

  5. Voltammetric determination of carbidopa and folic acid using a modified carbon nanotubes paste electrode

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    Keshtkar Nasrin

    2015-01-01

    Full Text Available A novel electrochemical sensor for the selective and sensitive detection of carbidopa in presence of large excess of folic acid at physiological pH was developed by the bulk modification of carbon paste electrode (CPE with carbon nanotubes (CNTs and vinylferrocene. Large peak separation, good sensitivity and stability allow this modified electrode to analyze carbidopa individually and simultaneously along with folic acid. Applying square wave voltammetry (SWV, a linear dynamic range of 1.0×10-6- 7.0×10-4 M with detection limit of 2.0×10-7 M was obtained for carbidopa. Finally, the proposed method was applied to the determination of carbidopa and folic acid in urine sample.

  6. Electrochemical sensor for ranitidine determination based on carbon paste electrode modified with oxovanadium (IV) salen complex.

    Science.gov (United States)

    Raymundo-Pereira, Paulo A; Teixeira, Marcos F S; Fatibello-Filho, Orlando; Dockal, Edward R; Bonifácio, Viviane Gomes; Marcolino, Luiz H

    2013-10-01

    The preparation and electrochemical characterization of a carbon paste electrode modified with the N,N-ethylene-bis(salicyllideneiminato)oxovanadium (IV) complex ([VO(salen)]) as well as its application for ranitidine determination are described. The electrochemical behavior of the modified electrode for the electroreduction of ranitidine was investigated using cyclic voltammetry, and analytical curves were obtained for ranitidine using linear sweep voltammetry (LSV) under optimized conditions. The best voltammetric response was obtained for an electrode composition of 20% (m/m) [VO(salen)] in the paste, 0.10 mol L(-1) of KCl solution (pH 5.5 adjusted with HCl) as supporting electrolyte and scan rate of 25 mV s(-1). A sensitive linear voltammetric response for ranitidine was obtained in the concentration range from 9.9×10(-5) to 1.0×10(-3) mol L(-1), with a detection limit of 6.6×10(-5) mol L(-1) using linear sweep voltammetry. These results demonstrated the viability of this modified electrode as a sensor for determination, quality control and routine analysis of ranitidine in pharmaceutical formulations.

  7. Electrochemical behavior of labetalol at an ionic liquid modified carbon paste electrode and its electrochemical determination

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    Zhang Yan-Mei

    2013-01-01

    Full Text Available Electrochemical behavior of labetalol (LBT at carbon paste electrode (CPE and an ionic liquid1-benzyl-3-methylimidazolehexafluorophosphate([BnMIM]PF6modified carbon paste electrode([BnMIM]PF6/CPEin Britton-Robinson buffer solution (pH 2.0 was investigated by cyclic voltammetry (CV and square wave voltammetric (SWV. The experimental results showed that LBT at both the bare CPE and [BnMIM]PF6/CPEshowed an irreversible oxidation process, but at [BnMIM]PF6/CPE its oxidation peak current increased greatly and the oxidation peak potential shifted negatively. The electrode reaction process is a diffusion-controlled process involving one electron transferring accompanied by a participation of one proton at [BnMIM]PF6/CPE. At the same time, the electrochemical kinetic parameters were determined. Under the optimized electrochemical experimental conditions, the oxidation peak currents were proportional to LBT concentration in the range of 7.0 x 10-6-1.0 x 10-4 mol L-1 with the limit of detection(LOD, S/N=3 of 4.810 x 10-8 mol L-1and the limit of quantification(LOQ, S/N=10 of 1.60 x 10-7 mol L-1, respectively. The proposed method was successfully applied in the determination of LBT content in commercial tablet samples.

  8. Molecularly imprinted polymer based electrochemical detection of L-cysteine at carbon paste electrode.

    Science.gov (United States)

    Aswini, K K; Vinu Mohan, A M; Biju, V M

    2014-04-01

    A methacrylic acid (MAA) based molecularly imprinted polymer (MIP) modified carbon paste electrode (CPE) was developed for electrochemical detection of L-cysteine (Cys). Characterisation of MIP was done with FTIR and the modified electrode with cyclic voltammetry (CV) and differential pulse voltammetry (DPV). CV, DPV and impedance analysis demonstrated that the modified electrode is responsive towards the target molecule. The optimum percentage composition of MIP for MIP/CPE and the effect of pH towards the electrode response for Cys were studied. The detection of Cys in the range of 2×10(-8) to 18×10(-8)M at MIP/CPE was monitored by DPV with a limit of detection of 9.6nM and R(2) of 0.9974. Also, various physiological interferents such as ascorbic acid, L-tryptophan, D-glucose, D-cysteine and L-cysteine were found to have little effect on DPV response at MIP/CPE. The utility of the electrode was proved by the effective detection of Cys from tap water and human blood plasma samples with reproducible results.

  9. Optimization of the use of carbon paste electrodes (CPE for electrochemical study of the chalcopyrite

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    Daniela G. Horta

    2009-01-01

    Full Text Available The use of carbon paste electrodes (CPE of mineral sulfides can be useful for electrochemical studies to overcome problems by using massive ones. Using CPE-chalcopyrite some variables were electrochemically evaluated. These variables were: (i the atmosphere of preparation (air or argon of CPE and elapsed time till its use; (ii scan rate for voltammetric measurements and (iii chalcopyrite concentration in the CPE. Based on cyclic voltammetry, open-circuit potential and electrochemical impedance results the recommendations are: oxygen-free atmosphere to prepare and kept the CPE until around two ours, scan rates from 10 to 40 mV s-1, and chalcopyrite concentrations > 20%.

  10. Electrochemical Oxidation of Fragrances 4-Allyl and 4-Propenylbenzenes on Platinum and Carbon Paste Electrodes

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    Lai-Hao Wang

    2015-03-01

    Full Text Available The electrochemical oxidation behaviors of 4-allylbenzenes (estragole, safrole and eugenol and 4-propenylbenzenes (anethole, asarone and isoeugenol on platinum and carbon paste electrodes were investigated in a Britton-Robinson buffer (pH = 2.93 and 10.93, acetate buffer, phosphate buffer solutions (pH = 2.19 and 6.67, and acetonitrile containing various supporting electrolytes examined lithium perchlorate. Their oxidation potential with Hammett (free-energy relationships and possible reaction mechanisms were discussed.

  11. Stripping voltammetric determination of mercury(II) at antimony-coated carbon paste electrode.

    Science.gov (United States)

    Ashrafi, Amir M; Vytřas, Karel

    2011-10-15

    A new procedure was elaborated to determine mercury(II) using an anodic stripping square-wave voltammetry at the antimony film carbon paste electrode (SbF-CPE). In highly acidic medium of 1M hydrochloric acid, voltammetric measurements can be realized in a wide potential window. Presence of cadmium(II) allows to separate peaks of Hg(II) and Sb(III) and apparently catalyses reoxidation of electrolytically accumulated mercury, thus allowing its determination at ppb levels. Calibration dependence was linear up to 100 ppb Hg with a detection limit of 1.3 ppb. Applicability of the method was tested on the real river water sample.

  12. A zeolite modified carbon paste electrode as useful sensor for voltammetric determination of acetaminophen.

    Science.gov (United States)

    Ahmadpour-Mobarakeh, Leila; Nezamzadeh-Ejhieh, Alireza

    2015-04-01

    The voltammetric behavior of a carbon paste electrode modified with Co(II)-exchanged zeolite A (Co(II)-A/ZMCPE) for determination of acetaminophen was studied. The proposed electrode showed a diffusion controlled reaction with the electron transfer rate constant (Ks) of 0.44s(-1) and charge transfer coefficient of 0.73 in the absence of acetaminophen. A linear voltammetric response was obtained in the range of 0.1 to 190μmolL(-1) of acetaminophen [r(2)=0.9979, r=0.9989 (n=10)] with a detection limit of 0.04μmolL(-1). The method was successfully applied to the analysis of acetaminophen in some drugs.

  13. SBA-15 Modified Carbon Paste Electrode for Rapid cTnI Detection with Enhanced Sensitivity

    Institute of Scientific and Technical Information of China (English)

    Nong Yue HE; Hui Shi GUO; Di YANG; Chun Rong GU; Ji Nan ZHANG

    2006-01-01

    A novel electrochemical immunoassay for cardiac troponin I (cTnI) combining the concepts of the dual monoclonal antibody "sandwich" principle, the silver enhancement on the nano-gold particle, and the SBA-15 mesoporous modified carbon paste electrode (SBA-MCPE) is described. Four main steps were carried out to obtain the analytical signal, i.e., electrode preparation, immunoreaction, silver enhancement, and anodic stripping voltammetric detection.A linear relationship between the anodic stripping peak current and concentration of cTnI from 0.5 to 5.0 ng/mL and a limit of detection of 0.2 ng/mL of cTnI were obtained.

  14. Inorganic-Organic Hybrid 18-Molybdodiphosphate Nanoparticles Bulk-modified Carbon Paste Electrode and Its Electrocatalysis

    Institute of Scientific and Technical Information of China (English)

    WANG,Xiu-Li(王秀丽); KANG,Zhen-Hui(康振辉); WANG,En-Bo(王恩波); HU,Chang-Wen(胡长文)

    2002-01-01

    A kind of inorganic- organic hybrid 18-molybdodiphosphate nanoparticles ([(C4H9)4N]6P2Mo18O62 @4H2O) was firstly used as a bulk-modifier to fabricate a three-dimensional chemically modified carbon paste electrode (CPE) by direct mixing. The electrochemical behavior of the solid nanoparticles dispersed in the CPE in acidic aqueous solution was characterized by cyclic and square-wave voltammetry. The hybrid 18-molybdodiphosphate nanoparticles bulk-modified CPE (MNP-CPE) displayed a high electrocatalytic activity towards the reduction of nitrite,bromate and hydrogen peroxide. The remarkable advantages of the MNP-CPE over the traditional polyoxometalates-modified electrodes are their excellent reproducibility of surface-renewal and high stability owing to the insolubility of the hybrid 18-molybdodiphosphate nanoparticles.

  15. Voltammetric Determination of Estrogens Based on the Enhancement Effect of Surfactant at Carbon Paste Electrode

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Highly sensitive voltammetric method for the determination of estrogens, based on the enhancement effect of cetyltrimethylammonium bromide (CTAB) has been described. In the presence of CTAB, the oxidation peak currents of estrogens (estradiol, estrone, estriol, estradiol valerate and diethylstilbestrol) at the carbon paste electrode (CPE) increased significantly after open-circuit accumulation. The peak current was proportional to the concentration of estradiol over the range from 5×10-9 to 2.5×10-6 mol\\5L-1. The detection limit was 8×10-10 mol\\5L-1 at 6 min of accumulation. The total amounts of estrogens in the blood serums were determined and the average recovery was 104.92%. Under the conditions used, the electrode process of estradiol was examined and the mechanism for peak current enhancement was also discussed.

  16. TYROSINASE-BASED CARBON PASTE ELECTRODE BIOSENSOR FOR DETECTION OF PHENOLS: BINDER AND PRE-OXIDATION EFFECTS

    Science.gov (United States)

    Tyrosinase-based carbon paste electrodes are evaluated with respect to the viscosity and polarity of the binder liquids. The electrodes constructed using a lower viscosity mineral oil or paraffin wax oil yielded a greater response to phenol and catechol than those using the hi...

  17. Voltammetric detection of As(III) with Porphyridium cruentum based modified carbon paste electrode biosensor.

    Science.gov (United States)

    Zaib, M; Saeed, A; Hussain, I; Athar, M M; Iqbal, M

    2014-12-15

    A novel biosensor based on carbon paste electrode modified with Porphyridium cruentum biomass was developed for the determination of As(III) in contaminated water. As(III) was first biosorbed-accumulated on the electrode surface at open circuit potential and then stripped off by applying anodic scan range of -0.8 to +0.8 V using differential pulse anodic stripping voltammetric technique. The best result was obtained at pH 6.0 with 0.1M HNO3 solution as stripping medium, allowing biosorption-accumulation time of 8 min using 5% P. cruentum biomass in graphite-mineral oil paste. Linear range for As(III) detection with the modified electrode-biosensor was observed between 2.5 and 20 µg L(-1). The FTIR spectrum of P. cruentum biomass confirmed the presence of active functional groups that participate in the binding of As(III). Scanning Electron Microscopy (SEM) indulged the surface morphology of modified electrode-biosensor before and after As(III) adsorption. Similarly, Atomic Force Microscopy (AFM) showed that the average roughness of the modified electrode decreased indicating the successful incorporation of P. cruentum biomass. Efficiency of the biosensor in the presence of different interfering metal (Na(+), K(+), Ca(2+), and Mg(2+)) ions were also evaluated. The application of P. cruentum modified biosensor was successfully used for the detection of As(III) in the binary metal (Fe(3+), Mn(2+), Cd(2+), Cu(2+), Ni(2+), Hg(2+), and Pb(2+)) contaminated system. The accuracy of application of biosorption based biosensor for the detection of As(III) is as low as 2.5 µg L(-1).

  18. Application of graphene oxide/lanthanum-modified carbon paste electrode for the selective determination of dopamine

    Energy Technology Data Exchange (ETDEWEB)

    Ye, Fengying; Feng, Chenqi; Fu, Ning; Wu, Huihui; Jiang, Jibo, E-mail: jibojiang0506@163.com; Han, Sheng, E-mail: hansheng654321@sina.com

    2015-12-01

    Highlights: • The effective surface area of the modified CPE has been expanded after self-assembly. • The GO–La composite exhibited excellent electrocatalytic activity toward DA. • The GO–La/CPE presented high selectivity, sensitivity, excellent stability and repeatability. - Abstract: A home-made carbon paste electrode (CPE) was reformed by graphene oxide (GO)/lanthanum (La) complexes, and a modified electrode, called GO–La/CPE, was fabricated for the selective determination of dopamine (DA) by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Several factors affecting the electrocatalytic performance of the modified sensor were investigated. Owning to the combination of GO and La ions, the GO–La/CPE sensor exhibited large surface area, well selectivity, good repeatability and stability in the oxidation reaction of DA. At optimal conditions, the response of the GO–La/CPE electrode for determining DA was linear in the region of 0.01–0.1 μM and 0.1–400.0 μM. The limit of detection was down to 0.32 nM (S/N = 3). In addition, this modified electrode was successfully applied to the detection of DA in real urine and serum samples by using standard adding method, showing its promising application in the electroanalysis of real samples.

  19. Catalytic Adsorptive Stripping Voltammetry at a Carbon Paste Electrode for the Determination of Amiodarone

    Institute of Scientific and Technical Information of China (English)

    LIU Ning; GAO Wei; SONG Jun-Feng

    2006-01-01

    Voltammetry using solid electrodes usually suffers from the contamination due to the deposition of the redox products of analytes on the electrode surface. The contamination has resulted in poor reproducibility and overelaborate operation procedures. The use of the chemical catalysis of oxidant on the reduction product of analyte not only can eliminate the contamination of analyte to solid electrodes but also can improve the faradaic response of analyte. This work introduced both the catalysis of oxidant K2S2O8 and the enhancement of surfactant Triton X-100 on the faraday response of amiodarone into an adsorptive stripping voltammetry at a carbon paste electrode for the determination of amiodarone. The method exhibits high sensitivity, good reproducibility and simple operation procedure. In 0.2 mol·L-1 HOAc-NaOAc buffer (pH=5.3) containing 2.2 × 10-2 mol·L-1 K2S2O8 and 0.002% Triton X-100, the 2.5th-order derivative stripping peak current of the catalytic wave at 0.3 V (vs. Ag/AgCl) is rectilinear to amiodarone concentration in the range of 2.0× 10-10-2.3× 10-8 mol·L-1 with a detection limit of 1.5× l0-10 mol·L-1 after accumulation at 0 V for 30 s.

  20. Determination of Trace Antimony (III by Adsorption Voltammetry at Carbon Paste Electrode

    Directory of Open Access Journals (Sweden)

    Nongyue He

    2005-05-01

    Full Text Available This work presents a sensitive method for the determination of trace antimonybased on the antimony-pyrogallol red (PGR adsorption at a carbon paste electrode (CPE.The optimal conditions were to use an electrode containing 25% paraffin oil and 75%high purity graphite powder as working electrode, a 0.10 mol/L HCl solution containing3.0×10-5 mol/L PGR as accumulation medium and a 0.20 mol/L HCl solution aselectrolyte with an accumulation time of 150 s and a reduction time of 60 s at -0.50 Vfollowed with a sweep from -0.50 V to 0.20 V. The mechanism of the electrode reactionwas discussed. Interferences of other metal ions were studied as well. The detection limitwas 1×10-9 mol/L. The linear range was from 2.0×10-9 mol/L to 5.0×10-7 mol/L.Application of the proposed method to the determination of antimony in water andhuman hair samples gave good results.

  1. Simultaneous determination of Sunset yellow and Tartrazine in soft drinks using gold nanoparticles carbon paste electrode.

    Science.gov (United States)

    Ghoreishi, Sayed Mehdi; Behpour, Mohsen; Golestaneh, Mahshid

    2012-05-01

    The monitoring of synthetic dyes in foods is very important due to their potential harmfulness to human beings. Herein, a carbon-paste electrode (CPE) that is chemically modified with gold nanoparticles (nAu) was fabricated and used for the determination of Sunset yellow (SY) and Tartrazine (Tz). Cyclic and differential pulse voltammetry (CV and DPV) results revealed two well-resolved anodic peaks for SY and Tz with remarkably increase in oxidation signals of these colourants. Based on this, a novel electrochemical method was developed for the simultaneous determination of SY and Tz. High sensitivity and selectivity, sub-micromolar detection limit, high reproducibility and regeneration of the electrode surface by simple polishing make the nAu-CPE electrode very suitable for the determination of SY and Tz in commercially available soft drinks. The detection limits was 3.0×10(-8) and 2.0×10(-9)moll(-1) for SY and Tz, respectively, which are remarkably lower than those reported previously for SY and Tz using other modified electrodes.

  2. Study on the adsorptive catalytic voltammetry of aloe-emodin at a carbon paste electrode

    Institute of Scientific and Technical Information of China (English)

    LI; Ju'nan; GAO; Peng; LI; Xiangling; YAN; Zhihong; MAO; Xu

    2005-01-01

    A new catalytic voltammetric method for the determination of anthraqunone medicines at a carbon paste electrode (CPE) was described for the first time. The mechanism of the catalytic reaction was investigated by using linear sweep voltammetry, cyclic voltammetry, constant potential electrolysis and so on. The experiment results indicate that aloe-emodin was efficiently accumulated at a CPE by adsorption. In the following potential scan, aloe-emodin was reduced to homologous anthrahydroquinone compound, then the compound was immediately oxidized to aloe-emodin by the dissolved oxygen, and the aloe-emodin was again reduced at the CPE. As a result, a cyclic catalytic reaction was established. But a reversible redox reaction of aloe-emodin can only be observed at a mercury electrode, no catalytic reaction occurs there. A sensitive catalytic voltammetric peak of aloe-emodin was obtained at about -0.60 V (vs. SCE) in 0.56 mol/L NH3-NH4Cl buffer (pH 8.9). The proposed method was applied to the determination of aloe-emodin in the Radix Rhei with satisfactory results. The determination results were in good agreement with reference values obtained by the HPLC. The adsorptive catalytic voltammetry for the determination of organic compound at CPE, chemically modified electrode and other solid electrodes could be significant in the studies on pharmacology, pharmacodynamics, toxicity of medicine, clinical medicine and biochemistry.

  3. Electrocatalytic behavior of modified carbon paste electrode with Ni(ii-zeolite for oxidation of methanol in a basic solution

    Directory of Open Access Journals (Sweden)

    Maryam Abrishamkar

    2014-12-01

    Full Text Available In this research, the electrochemical behavior of Ni-zeolite modified carbon paste electrode in the form of Ni/NiZSM-5/CPE and unmodified carbon paste electrode were studied using cyclic voltammetry and chronoamperometric techniques. It was found that methanol was oxidized by NiOOH generated with further electrooxidation of Ni ions which were doped in modified electrode during the anodic sweep. Also, the rate constant for the catalytic reaction (K of methanol was calculated 2.64* 10⁵cm³s⁻¹mol⁻¹ via Cottrell equation.

  4. Electrocatalytic behavior of modified carbon paste electrode with Ni(ii)-zeolite for oxidation of methanol in a basic solution

    OpenAIRE

    Maryam Abrishamkar; Nassrin Kiamehr

    2014-01-01

    In this research, the electrochemical behavior of Ni-zeolite modified carbon paste electrode in the form of Ni/NiZSM-5/CPE and unmodified carbon paste electrode were studied using cyclic voltammetry and chronoamperometric techniques. It was found that methanol was oxidized by NiOOH generated with further electrooxidation of Ni ions which were doped in modified electrode during the anodic sweep. Also, the rate constant for the catalytic reaction (K) of methanol was calculated 2.64* 10⁵cm³s⁻¹mo...

  5. Ionic liquid modified carbon paste electrode and investigation of its electrocatalytic activity to hydrogen peroxide

    Indian Academy of Sciences (India)

    Erhan Canbay; Hayati Türkmen; Erol Akyilmaz

    2014-05-01

    This paper reports on the preparation and advantages of novel amperometric biosensors in the presence of hydrophobic ionic liquid (IL), 1-methyl-3-butylimidazolium bromide ([MBIB]). Carbon paste bio-sensor has been constructed by entrapping horseradish peroxidase in graphite and IL mixed with paraffin oil as a binder. The resulting IL/graphite material brings new capabilities for electrochemical devices by combining the advantages of ILs composite electrodes. Amounts of H2O2 were amperometrically detected by monitoring current values at reduction potential (–0.15 V) of K3Fe(CN)6. Decrease in biosensor responses were linearly related to H2O2 concentrations between 10 and 100 M with 2 s response time. Limit of detection of the biosensor were calculated to be 3.98 M for H2O2. In the optimization studies of the biosensor some parameters such as optimum pH, optimum temperature, enzyme amount, interference effects of some substances on the biosensor response, reproducibility and storage stability were carried out. The promising results are ascribed to the use of an ionic liquid, which forms an excellent charge-transfer bridge and wide electrochemical windows in the bulk of carbon paste electrode.

  6. Cathodic stripping voltammetric determination of arsenic in sugarcane brandy at a modified carbon nanotube paste electrode.

    Science.gov (United States)

    Teixeira, Meryene C; Tavares, Elisângela de F L; Saczk, Adelir A; Okumura, Leonardo L; Cardoso, Maria das Graças; Magriotis, Zuy M; de Oliveira, Marcelo F

    2014-07-01

    We have developed an eletroanalytical method that employs Cu(2+) solutions to determine arsenic in sugarcane brandy using an electrode consisting of carbon paste modified with carbon nanotubes (CNTPE) and polymeric resins. We used linear sweep (LSV) and differential-pulse (DPV) voltammetry with cathodic stripping for CNTPE containing mineral oil or silicone as binder. The analytical curves were linear from 30 to 110μgL(-1) and from 10 to 110μgL(-1) for LSV and DPV, respectively. The limits of detection (L.O.D.) and quantification (L.O.Q.) of CNTPE were 10.3 and 34.5μgL(-1) for mineral oil and 3.4 and 11.2μgL(-1) for silicone. We applied this method to determine arsenic in five commercial sugarcane brandy samples. The results agreed well with those obtained by hydride generation combined with atomic absorption spectrometry (HG AAS).

  7. Simultaneous determination of dopamine, uric acid, and tryptophan using an MWCNT modified carbon paste electrode by square wave voltammetry

    OpenAIRE

    BEITOLLAHI, Hadi; Mohadesi, Alireza; MAHANI, Saeedeh KHALILIZADEH

    2012-01-01

    A highly sensitive method was investigated for the simultaneous determination of dopamine (DA), uric acid (UA), and tryptophan (TRP) using a multiwall carbon nanotubes/5-amino-3',4'-dimethoxy-biphenyl-2-ol modified carbon paste electrode (5ADMBCNPE). The 5ADMBCNPE displayed excellent electrochemical catalytic activities towards the oxidation of DA, UA, and TRP. The electrochemical profile of the proposed modified electrode was analyzed by cyclic voltammetry (CV), which showe...

  8. Pristine multi-walled carbon nanotubes/SDS modified carbon paste electrode as an amperometric sensor for epinephrine.

    Science.gov (United States)

    Thomas, Tony; Mascarenhas, Ronald J; D' Souza, Ozma J; Detriche, Simon; Mekhalif, Zineb; Martis, Praveen

    2014-07-01

    An amperometric sensor for the determination of epinephrine (EP) was fabricated by modifying the carbon paste electrode (CPE) with pristine multi-walled carbon nanotubes (pMWCNTs) using bulk modification followed by drop casting of sodium dodecyl sulfate (SDS) onto the surface for its optimal potential application. The modified electrode showed an excellent electrocatalytic activity towards EP by decreasing the overpotential and greatly enhancing the current sensitivity. FE-SEM images confirmed the dispersion of pMWCNTs in the CPE matrix. EDX analysis ensured the surface coverage of SDS. A comparative study of pMWCNTs with those of oxidized MWCNTs (MWCNTsOX) modified electrodes reveals that the former is the best base material for the construction of the sensor with advantages of lower oxidation overpotential and the least background current. The performance of the modified electrode was impressive in terms of the least charge transfer resistance (Rct), highest values for diffusion coefficient (DEP) and standard heterogeneous electron transfer rate constant (k°). Analytical characterization of the modified electrode exhibited two linear dynamic ranges from 1.0×10(-7) to 1.0×10(-6)M and 1.0×10(-6) to 1.0×10(-4)M with a detection limit of (4.5±0.18)×10(-8)M. A 100-fold excess of serotonin, acetaminophen, folic acid, uric acid, tryptophan, tyrosine and cysteine, 10-fold excess of ascorbic acid and twofold excess of dopamine do not interfere in the quantification of EP at this electrode. The analytical applications of the modified electrode were demonstrated by determining EP in spiked blood serum and adrenaline tartrate injection. The modified electrode involves a simple fabrication procedure, minimum usage of the modifier, quick response, excellent stability, reproducibility and anti-fouling effects.

  9. Gold nanoparticles modified carbon paste electrode for differential pulse voltammetric determination of eugenol.

    Science.gov (United States)

    Afzali, Daryoush; Zarei, Somaye; Fathirad, Fariba; Mostafavi, Ali

    2014-10-01

    In the present study, a carbon paste electrode chemically modified with gold nanoparticles was used as a sensitive electrochemical sensor for determination of eugenol. The differential pulse voltammetric method was employed to study the behavior of eugenol on this modified electrode. The effect of variables such as percent of gold nanoparticles, pH of solution, accumulation potential and time on voltammogram peak current were optimized. The proposed electrode showed good oxidation response for eugenol in 0.1 mol L(-1) phosphate buffer solution (pH8) and the peak potential was about +285 mV (vs. Ag/AgCl). The peak current increased linearly with the eugenol concentration in the range of 5-250 μmol L(-1). The detection limit was found to be 2.0 μmol L(-1) and the relative standard deviation was 1.2% (n=7). The effect of interferences on the eugenol peak current was studied. The method has been applied to the determination of eugenol in different real samples, spiked recoveries were in the range of 96%-99%.

  10. Inorganic arsenic speciation by differential pulse anodic stripping voltammetry using thoria nanoparticles-carbon paste electrodes.

    Science.gov (United States)

    Pereira, F J; Vázquez, M D; Debán, L; Aller, A J

    2016-05-15

    Two novel thoria (ThO2) nanoparticles-carbon paste electrodes were used to evaluate an anodic stripping voltammetric method for the direct determination of arsenite and total inorganic arsenic (arsenite plus arsenate) in water samples. The effect of Ag((I)), Cu((II)), Hg((II)), Sb((III)) and Se((IV)) ions on the electrochemical response of arsenic was assayed. The developed electroanalytical method offers a rapid procedure with improved analytical characteristics including good repeatability (3.4%) at low As((III)) concentrations, high selectivity, lower detection limit (0.1 μg L(-1)) and high sensitivity (0.54 μA μg(-1) L). The analytical capability of the optimized method was demonstrated by the determination of arsenic in certified reference materials (trace elements in natural water, trace elements in water and coal fly ash).

  11. Characterization by electrochemical impedance spectroscopy of magnetite nanoparticles supported on carbon paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Rodriguez-Lopez, A.; Torres-Torres, D.; Mojica-Gomez, J.; Estrada-Arteaga, C. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, S. C., Parque Tecnologico Queretaro - Sanfandila, C.P. 76703, Pedro Escobedo, Queretaro (Mexico); Antano-Lopez, R., E-mail: rantano@cideteq.mx [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, S. C., Parque Tecnologico Queretaro - Sanfandila, C.P. 76703, Pedro Escobedo, Queretaro (Mexico)

    2011-09-30

    Magnetite nanoparticles were supported on carbon paste electrode and characterized by low scan rate voltammetry and electrochemical impedance spectroscopy (EIS) to obtain mechanistic information related to its oxidation and reduction in acid media. The voltammograms showed only one reduction and one oxidation peak for the supported magnetite, which were attributed to formation of ferrous ion and ferric oxide, respectively. Both peaks are fairly wide, indicating complex mechanisms. Using EIS, a mechanism showing up to three time constants, capacitive all of them, was evidenced, both in anodic and cathodic domain. These were attributed to charge transfer at the highest frequencies, adsorption of generated species at intermediate frequencies, and proton adsorption at low frequencies. Discussion about the nature of the adsorbed species and the concerned mechanism for each domain is developed.

  12. A study of quasi reversible nitro radical anion from -nitrostyrene at wax-impregnated carbon paste electrode

    Indian Academy of Sciences (India)

    Ronald J Mascarenhas; Irishi N Namboothiri; B S Sherigara; Vijayakumar K Reddy

    2006-05-01

    A comprehensive study of the electrochemical reduction of -nitrostyrene and the corresponding heterocyclic analogue has been carried out in aprotic media using wax-impregnated carbon paste electrodes. Nitrostyrene exhibits quasi-reversible reduction process in aprotic medium at the waximpregnated carbon paste electrodes as compared to other electrodes reported in the literature. The nitroradical anion couple detected in the presence of tetrabutyl ammonium perchlorate is found to be stable only in aprotic media. Though, as reported, the pharmacological activity related to this nitro radical anion and its therapeutic value are related to the stability of the nitro radical anion, the stability itself depends on the electrode system employed. Added benzoic acid is found to bring about a positive shift in cathodic peak potential.

  13. Simultaneous determination of hydroquinone and catechol at gold nanoparticles mesoporous silica modified carbon paste electrode.

    Science.gov (United States)

    Tashkhourian, J; Daneshi, M; Nami-Ana, F; Behbahani, M; Bagheri, A

    2016-11-15

    A new electrochemical sensor based on gold nanoparticles mesoporous silica modified carbon paste electrode (AuNPs-MPS) was developed for simultaneous determination of hydroquinone and catechol. Morphology and structure of the AuNPs-MPS were characterized by transmission electron microscopy, X-ray diffraction and Fourier transform infrared spectroscopy. The electrochemical behavior of hydroquinone and catechol were investigated using square wave voltammetry and the results indicate that the electrochemical responses are improved significantly at the modified electrode. The observed oxidative peaks separation of about 120mV made possible the simultaneous determination of hydroquinone and catechol in their binary-mixture. Under the optimized condition, a linear dynamic range of 10.0μM-1.0mM range for hydroquinone with the detection limit of 1.2μM and from 30.0μM-1.0mM for catechol with the detection limit of 1.1μM were obtained. The applicability of the method was demonstrated by the recovery studies of hydroquinone and catechol in spiked tap water samples.

  14. Amperometric Metronidazole Sensor Based on the Supermolecular Recognition by Metalloporphyrin Incorporated In Carbon Paste Electrode

    Directory of Open Access Journals (Sweden)

    Ru-Qin Yu

    2003-03-01

    Full Text Available An amperometric metronidazole (MTZ sensor using a glycosylated metalloporphyrin as a recognition element, which was incorporated in a carbon paste electrode, is reported. For the preparation of a MTZ-sensitive active material, 5, 10, 15, 20-tetrakis [2-(2, 3, 4, 6-tetraacetyl-β-D-glucopyranosyl-1-O-phenyl]porphyrin (T(oglu PPH2 and its Mn(III complex MnT(o-gluPPCl were synthesized from the reaction of pyrrole with ortho-acetylglycosylated benzaldehyde by Lindsay’s method. The MnT(oglu PPCl-modified electrode showed excellent selectivity toward MTZ with respect to a number of interferents and exhibited stable response. The calibration graph obtained with the proposed sensor was linear over the range of 2.9×10-3-5.8×10-8 M/L, with a detection limit of 5.8×10-8 M/L for MTZ. Cyclic voltammetric measurements indicated that MnT(oglu PPCl included in graphite-epoxy resin matrices could efficiently mediate electron transfer from the base electrode to MTZ causing a decrease of reduction potential for MTZ detection. The sensor could be regenerated by simply polishing with an alumina paper, with an excellent reproducibility (RSD=1.6%. The experimental conditions such as pH and applied working potential were optimized. The prepared sensor is applied for the determination of MTZ in pharmaceutical preparations and the results agreed with the values obtained by the pharmacopoeia method.

  15. Electrocatalytic and simultaneous determination of isoproterenol, uric acid and folic acid at molybdenum (VI) complex-carbon nanotube paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Beitollahi, Hadi, E-mail: h.beitollahi@yahoo.com [Environment Department, Research Institute of Environmental Sciences, International Center for Science, High Technology and Environmental Sciences, Kerman (Iran, Islamic Republic of); Sheikhshoaie, Iran [Department of Chemistry, Faculty of Science, Shahid Bahonar University of Kerman, Kerman 76175-133 (Iran, Islamic Republic of)

    2011-11-30

    Highlights: > A molybdenum (VI) complex-carbon nanotube paste electrode have been fabricated. > This electrode reduced the oxidation potential of isoproterenol by about 175 mV. > It resolved the voltammetric waves of isoproterenol, uric acid and folic acid. - Abstract: This paper describes the development, electrochemical characterization and utilization of a novel modified molybdenum (VI) complex-carbon nanotube paste electrode for the electrocatalytic determination of isoproterenol (IP). The electrochemical profile of the proposed modified electrode was analyzed by cyclic voltammetry (CV) that showed a shift of the oxidation peak potential of IP at 175 mV to less positive value, compared with an unmodified carbon paste electrode. Differential pulse voltammetry (DPV) in 0.1 M phosphate buffer solution (PBS) at pH 7.0 was performed to determine IP in the range from 0.7 to 600.0 {mu}M, with a detection limit of 35.0 nM. Then the modified electrode was used to determine IP in an excess of uric acid (UA) and folic acid (FA) by DPV. Finally, this method was used for the determination of IP in some real samples.

  16. VISCOSITY AND BINDER COMPOSITION EFFECTS ON TYROSINASE-BASED CARBON PASTE ELECTRODE FOR DETECTION OF PHENOL AND CATECHOL

    Science.gov (United States)

    The systematic study of the effect of binder viscosity on the sensitivity of a tyrosinase-based carbon paste electrode (CPE) biosensor for phenol and catechol is reported. Silicon oil binders with similar (polydimethylsiloxane) chemical composition were used to represent a wid...

  17. Carbon paste electrode in a solid-contact minicavity; Eletrodo de pasta de carbono em minicavidade de contato solido

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Antonio Ap. Pupim; Ribeiro, Sidney Jose Lima; Fugivara, Cecilio Sadao; Caiut, Jose Mauricio Almeida; Sargentelli, Vagner; Benedetti, Assis Vicente [UNESP - Universidade Estadual Paulista, Instituto de Quimica, Araraquara SP (Brazil)

    2011-07-01

    This work describes the preparation of carbon paste electrode (EPC) in a solid-contact minicavity and its evaluation when containing carbon paste without and with SiO{sub 2}(Eu{sup 3+} 2%) and SiO{sub 2}(Eu{sup 3+} 2%)-lysine sub-micrometrics particles. For this study cyclic voltammetry and electrochemical impedance measurements were performed at pH 7.4 in 0.1 mol L{sup -1} PBS containing Fe(CN){sub 6}{sup -3}/{sup -4} redox species. The impedance results were interpreted based on a charge-transfer reaction involving Fe(CN){sub 6}{sup -3}/{sup -4} species and/or oxygen at higher frequencies and, diffusion of the electroactive species and carbon paste characteristics at lower frequencies. EPC-minicavity is suitable for electroanalysis using modified carbon paste. (author)

  18. Trace Determination of Zirconium(Ⅳ) by Anodic Adsorptive Voltammetry at a Carbon Paste Electrode

    Institute of Scientific and Technical Information of China (English)

    Xun MAO; Huan Xin LAI; Ju Nan LI; Peng GAO; Zhi Hong YAN

    2004-01-01

    A new sensitive adsorptive voltammetric method was described for the determination of zirconium at a carbon paste electrode (CPE) in the presence of alizarin complexone (ALC). Optimal analytical conditions are: 1.0×10-6 or 5.0×10-7 mol/L ALC, 0. 20 mol/L HAC-NaAc (pH 4.3), accumulation for 60 s at 0 V (vs. SCE), and linear scanning from 0 V to 1.0 V at 250 mV/s. The peak potential of the complex is at 0.81 V. By using a model JP-303 polarographic analyzer, 2.0×10-10 mol/L (S/N=3) zirconium can be detected with a 90 s accumulation, when the 2nd-order derivative linear sweep technique is used, and the linear range is 6.0×10-10-2.0×10-8 mol/L (5.0×10-7 mol/L ALC) and 2.0×10-8-2.0×10-7 mol/L (1.0×10-6 mol/L ALC), respectively. The developed method was applied to the determination of trace zirconium in the ore samples with satisfactory results.

  19. Sensitive Voltammetric Determination of Captopril Using a Carbon Paste Electrode Modified with Nano-TiO2/Ferrocene Carboxylic Acid

    Institute of Scientific and Technical Information of China (English)

    Jahan Bakhsh RAOOF; Reza OJANI; Mehdi BAGHAYERI

    2011-01-01

    A carbon paste electrode (CPE) modified with ferrocene carboxylic acid (FcCA) and TiO2 nanoparticles was constructed by incorporating TiO2 nanoparticles and ferrocene carboxylic acid into the carbon paste matrix.The electrochemical behavior of captopril (CAP) at the surface of the modified electrode was investigated using electroanalytical methods.The modified electrode showed excellent electrocatalytic activity for the oxidation of CAP in aqueous solutions at physiological pH values.Cyclic voltammetric curves showed that the oxidation of CAP at the surface of the modified electrode reduced its overpotential by more than 290 mV.The modified electrode was used for detecting captopril using cyclic voltammetry and square wave voltammetry techniques.A calibration curve in the range of 0.03 to 2400μmol/L was obtained that had a detection limit of 0.0096 μmol/L (3σ) under the optimized conditions.The modified electrode was successfully used for the determination of captopril in pharmaceutical and biological samples.

  20. Electrochemical oxidation of 4-chloro phenol over a carbon paste electrode modified with Zn Al layered double hydroxides

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez F, D.; Palomar P, M.; Licona S, T. de J.; Romero R, M. [Universidad Autonoma Metropolitana, Unidad Azcapotzalco, Departamento de Materiales, Av. San Pablo 180, Col. Reynosa-Tamaulipas, 02200 Mexico D. F. (Mexico); Valente, Jaime S., E-mail: mepp@correo.azc.uam.mx [Instituto Mexicano del Petroleo, Eje Central No. 152, 07730 Mexico D. F. (Mexico)

    2014-07-01

    A study is presented on the electrochemical oxidation of 4-chloro phenol (4cp) in aqueous solution using a bare carbon paste electrode, Cpe, and another one that was modified with Zn Al layered double hydroxides (Cpe/Zn Al-LDH). The electro-oxidation was effected at ph values ranging from 3 up to 11. It was found through cyclic voltammetry that this process was irreversible, namely, there were no reduction peaks, and that depending on the nature of the electrode, the anodic current was limited either by adsorption (Cpe) or diffusion (Cpe/Zn Al-LDH). The energy required and the oxidation reaction rate depended on the ph and on the nature of the electrode, such that the greater rates were obtained when the Cpe/Zn Al-LDH electrode and acid ph were used. The Zn Al-LDH was characterized by means of X-ray diffraction. (Author)

  1. Potentiometric stripping analysis of antimony based on carbon paste electrode modified with hexathia crown ether and rice husk

    Energy Technology Data Exchange (ETDEWEB)

    Gadhari, Nayan S.; Sanghavi, Bankim J. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400098 (India); Srivastava, Ashwini K., E-mail: aksrivastava@chem.mu.ac.in [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400098 (India)

    2011-10-03

    Highlights: {yields} Potentiometric stripping analysis (PSA) employed for the determination of antimony. {yields} Hexathia-18C6 and rice husk modified carbon paste electrode developed for the analysis. {yields} Lowest detection limit obtained for the determination of Sb(III) using PSA. {yields} Analysis of Sb in pharmaceutical formulations, human hair, blood serum, urine and sea water. {yields} Rice husk used as a modifier for the first time in electrochemistry. - Abstract: An electrochemical method based on potentiometric stripping analysis (PSA) employing a hexathia 18C6 (HT18C6) and rice husk (RH) modified carbon paste electrode (HT18C6-RH-CPE) has been proposed for the subnanomolar determination of antimony. The characterization of the electrode surface has been carried out by means of scanning electron microscopy, cyclic voltammetry, electrochemical impedance spectroscopy and chronocoulometry. By employing HT18C6-RH-CPE, a 12-fold enhancement in the PSA signal (dt/dE) was observed as compared to plain carbon paste electrode (PCPE). Under the optimized conditions, dt/dE (s V{sup -1}) was proportional to the Sb(III) concentration in the range of 1.42 x 10{sup -8} to 6.89 x 10{sup -11} M (r = 0.9944) with the detection limit (S/N = 3) of 2.11 x 10{sup -11} M. The practical analytical utilities of the modified electrode were demonstrated by the determination of antimony in pharmaceutical formulations, human hair, sea water, urine and blood serum samples. The prepared modified electrode showed several advantages, such as simple preparation method, high sensitivity, very low detection limit and excellent reproducibility. Moreover, the results obtained for antimony analysis in commercial and real samples using HT18C6-RH-CPE and those obtained by inductively coupled plasma-atomic emission spectrometry (ICP-AES) are in agreement at the 95% confidence level.

  2. Preparation of magnetic TNT-imprinted polymer nanoparticles and their accumulation onto magnetic carbon paste electrode for TNT determination.

    Science.gov (United States)

    Alizadeh, Taher

    2014-11-15

    In this study, the TNT-imprinted polymer shell was created on nano-sized Fe3O4 cores in order to construct the nano-sized magnetic molecularly imprinted polymer (nano-MMIP). For this purpose, the surface of the synthesized magnetic nanoparticles was modified with methacrylic acid. The modified particles were then utilized as the core on which the TNT-imprinted polymeric shell was synthesized. The synthesized materials were then characterized by scanning electron microscopy, FT-IR and thermal gravimetric analysis (TGA). The resulting nano-MMIP particles were suspended in TNT solution and then collected on the surface of a carbon paste electrode via a permanent magnet, situated within the CP electrode. The extracted TNT was analyzed on the CP electrode by applying square wave voltammetry (SWV). It was found that the oxidative signal of TNT is much favorable for TNT detection on the resulting magnetic carbon paste electrode. The electrode with nano-MMIP showed distinctly higher signal to TNT, compared to that containing magnetic non-imprinted polymer (MNIP) nanoparticles. All parameters influencing the method performance including extraction pH, extraction time and sorbent amount were evaluated and optimized. The developed method showed a dynamic linear concentration range of 1.0-130.0 nM for TNT measurement. The detection limit of the method was calculated to be 0.5 nM. The method showed appropriate capability for TNT analysis in real water samples.

  3. A Hydrogen Peroxide Sensor Prepared by Electropolymerization of Pyrrole Based on Screen-Printed Carbon Paste Electrodes

    OpenAIRE

    Hui Xu; You Wang; Guang Li

    2007-01-01

    A disposable amperometric biosensor for commercial use to detect hydrogen peroxide has been developed. The sensor is based on screen-printed carbon paste electrodes modified by electropolymerization of pyrrole with horseradish peroxidase (HRP) entrapped. The facture techniques of fabricating the enzyme electrodes are suitable for mass production and quality control. The biosensor shows a linear amperometric response to H2O2 from 0.1 to 2.0 mM, with a sensitivity of 33.24 µA mM-1 cm-2. Differe...

  4. Electrocatalytic oxidation and determination of homocysteine at carbon nanotubes modified paste electrode using dopamine as a mediator

    OpenAIRE

    Mohammadzadeh Safoora; Fouladgar Masoud

    2013-01-01

    A carbon paste electrode modified with multiwall carbon nanotubes (MWCNTPE) was prepared to study the electrocatalytic activity of dopamine (DP) in the presence of homocysteine (HCy) and it was used for determination of HCy. The diffusion coefficient of HCy (D = 6.79×10−6 cm2 s−1), and the kinetic parameters of its oxidation such as electron transfer coefficient (α = 0.46), and rate constant (kh = 7.44×102 dm3 mol-1 s-1) were also determined using electroch...

  5. A New Sensitive Sensor for Simultaneous Differential Pulse Voltammetric Determination of Codeine and Acetaminophen Using a Hydroquinone Derivative and Multiwall Carbon Nanotubes Carbon Paste Electrode

    Directory of Open Access Journals (Sweden)

    Elahe Garazhian

    2015-01-01

    Full Text Available A new sensitive sensor was fabricated for simultaneous determination of codeine and acetaminophen based on 4-hydroxy-2-(triphenylphosphoniophenolate (HTP and multiwall carbon nanotubes paste electrode at trace levels. The sensitivity of codeine determination was deeply affected by spiking multiwall carbon nanotubes and a modifier in carbon paste. Electron transfer coefficient, α, catalytic electron rate constant, k, and the exchange current density, j0, for oxidation of codeine at the HTP-MWCNT-CPE were calculated using cyclic voltammetry. The calibration curve was linear over the range 0.2–844.7 μM with two linear segments, and the detection limit of 0.063 μM of codeine was obtained using differential pulse voltammetry. The modified electrode was separated codeine and acetaminophen signals by differential pulse voltammetry. The modified electrode was applied for the determination of codeine and acetaminophen in biological and pharmaceutical samples with satisfactory results.

  6. A Sensitive Voltammetric Sensor for Determination of Glutathione Based on Multiwall Carbon Nanotubes Paste Electrode Incorporating Pyrogallol Red

    Directory of Open Access Journals (Sweden)

    Mohsen Keyvanfard

    2014-06-01

    Full Text Available A new sensitive and selective electrochemical sensor was developed for determination of glutathione (GSH at the surface of carbon paste electrode (CPE modified with multi-wall carbon nanotubes (MWCNTs as a sensor and pyrogallol red (PGR as a mediator. The mechanism of GSH electrochemical behavior at the modified electrode surface was investigated by various electrochemical techniques including chronoamperometry, cyclic voltammetry (CV and square wave voltammetry (SWV. A linear calibration curve was obtained in the concentration range of GSH of 0.3–500 μmol L–1, with a limit of detection of 0.19 μmol L–1. The method was applied to the determination of GSH in urine samples with satisfactory results.

  7. Simultaneous determination of cysteamine and folic acid in pharmaceutical and biological samples using modified multiwall carbon nanotube paste electrode

    Institute of Scientific and Technical Information of China (English)

    Ali Taherkhani; Hassan Karimi-Maleh; Ali A.Ensafi; Hadi Beitollahi; Ahmad Hosseini; Mohammad A.Khalilzadeh; Hassan Bagheri

    2012-01-01

    A carbon paste electrode (CPE) chemically modified with multiwall carbon nanotubes and ferrocene (FC) was used as a selective electrochemical sensor for the simultaneous determination of trace amounts of cysteamine (CA) and folic acid (FA).This modified electrode showed very efficient electrocatalytic activity for the anodic oxidation of CA.The peak current of differential pulse voltammograms of CA and FA increased linearly with their concentration in the ranges of 0.7-200 μmol/L CA and 5.0-700 μmol/L FA.The detection limits for CA and FA were 0.3 μmol/L and 2.0 μ mol/L,respectively.The diffusion coefficient (D) and transfer coefficient (α) of CA were also determined.These conditions are sufficient to allow determination of CA and FA both individually and simultaneously.

  8. An Ionic Liquid Bulk-Modified Carbon Paste Electrode and Its Electrocatalytic Activity toward p-Aminophenol

    Institute of Scientific and Technical Information of China (English)

    ZHANG Ya; ZHENG Jian-Bin

    2007-01-01

    An ionic liquid bulk-modified carbon paste electrode (M-CPE) has been fabricated by using 1-heptyl-3-methylimidazolium bromide as a modifier. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were used to evaluate the electrocatalytic activity of the proposed electrode by choosing p-aminophenol (p-AP) as a model compound. Both at a bare carbon paste electrode (CPE) and the M-CPE, p-AP yielded a pair of redox peaks was 0.233 V, while at the M-CPE the AEp was decreased to 0.105 V. Furthermore, the current response to p-AP at the M-CPE was 10.2 times of that at the CPE by DPV. The electron transfer rate constant (ks) of p-AP at the M-CPE was 13.3 times of that at the CPE. Under the optimal condition, a linear dependence of the catalytic current versus advantages of simple prapartion, surface renewal, good reproducibility and good stability. It has been used to determine p-AP in simulated wastewater samples.

  9. A novel and simple electrochemical sensor for electrocatalytic reduction of nitrite and oxidation of phenylhydrazine based on poly (o-anisidine) film using ionic liquid carbon paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Ojani, Reza, E-mail: fer-o@umz.ac.ir [Electroanalytical Chemistry Research Laboratory, Faculty of Chemistry, University of Mazandaran, Babolsar (Iran, Islamic Republic of); Raoof, Jahan-Bakhsh; Zamani, Saeed [Electroanalytical Chemistry Research Laboratory, Faculty of Chemistry, University of Mazandaran, Babolsar (Iran, Islamic Republic of)

    2013-04-15

    In this study, nitrite electroreduction and phenylhydrazine electrooxidation were investigated on poly(o-anisidine) formed by cyclic voltammetry at the surface of ionic liquid carbon paste electrode. The films were characterized by cyclic voltammetry and scanning electron microscopy (SEM) and were contrasted with poly(o-anisidine) prepared under identical conditions in the absence of ionic liquid in carbon paste electrode. This carbon paste modified electrode exhibits a good electrocatalytic capability (via an EC’ mechanism) for both electrooxidation and electroreduction of some important molecules. The obtained results showed that the catalytic oxidation peak currents of phenylhydrazine and catalytic reduction peak currents of nitrite at the surface of this simple (unfunctionalized) polymeric electrode were linearly dependent on their concentrations. Electrode was successfully applied for determination of nitrite and phenylhydrazine in real samples.

  10. Silver nanoparticle decorated poly(2-aminodiphenylamine) modified carbon paste electrode as a simple and efficient electrocatalyst for oxidation of formaldehyde

    Institute of Scientific and Technical Information of China (English)

    Reza Ojani; Saeid Safshekan; Jahan-Bakhsh Raoof

    2014-01-01

    This work describes the promising activity of silver nanoparticles on the surface of a poly(2-amino diphenylamine) modified carbon paste electrode (CPE) towards formaldehyde oxidation. Electro-deposition of the conducting polymer film on the CPE was carried out using consecutive cyclic voltammetry in an aqueous solution of 2-aminodiphenylamine and HCl. Nitrogen groups in the polymer backbone had a Ag ion accumulating effect, allowing Ag nanoparticles to be electrochemi-cally deposited on the surface of the electrode. The electrochemical and morphological characteris-tics of the modified electrode were investigated. The electro-oxidation of formaldehyde on the sur-face of electrode was studied using cyclic voltammetry and chronoamperometry in aqueous solu-tion of 0.1 mol/L NaOH. The electro-oxidation onset potential was found to be around-0.4 V, which is unique in the literature. The effect of different concentrations of formaldehyde on the electrocat-alytic activity of the modified electrode was investigated. Finally, the diffusion coefficient of formal-dehyde in alkaline media was calculated to be 0.47 × 10-6 cm2/s using chronoamperometry.

  11. Direct electron transfer at a glucose oxidase-chitosan-modified Vulcan carbon paste electrode for electrochemical biosensing of glucose.

    Science.gov (United States)

    Mutyala, Sankararao; Mathiyarasu, Jayaraman

    2014-02-01

    This article describes the investigation of direct electron transfer (DET) between glucose oxidase (GOD) and the electrode materials in an enzyme-catalyzed reaction for the development of improved bioelectrocatalytic system. The GOD pedestal electrochemical reaction takes place by means of DET in a tailored Vulcan carbon paste electrode surfaces with GOD and chitosan (CS), allowing efficient electron transfer between the electrode and enzyme. The key understanding of the stability, biocatalytic activity, selectivity, and redox properties of these enzyme-based glucose biosensors is studied without using any reagents, and the properties are characterized using electrochemical techniques like cyclic voltammogram, amperometry, and electrochemical impedance spectroscopy. Furthermore, the interaction between the enzyme and the electrode surface is studied using ultraviolet-visible (UV-Vis) and Fourier transform infrared (FTIR) spectroscopy. The present glucose biosensor exhibited better linearity, limit of detection (LOD = 0.37 ± 0.02 mol/L) and a Michaelis-Menten constant of 0.40 ± 0.01 mol/L. The proposed enzyme electrode exhibited excellent sensitivity, selectivity, reproducibility, and stability. This provides a simple "reagent-less" approach and efficient platform for the direct electrochemistry of GOD and developing novel bioelectrocatalytic systems.

  12. Electrochemical detection of E. coli O157:H7 using porous pseudo-carbon paste electrode modified with carboxylic multi-walled carbon nanotubes, glutaraldehyde and 3-aminopropyltriethoxysilane.

    Science.gov (United States)

    Xu, Lijian; Du, Jingjing; Deng, Yan; He, Nongyue

    2012-12-01

    Fabrication of three different electrodes based on functional porous pseudo-carbon paste electrodes (PPCPEs) was described. PPCPEs were modified with carboxylic multi-walled carbon nanotubes (PPCPE-COOH), glutaraldehyde (PPCPE-CHO) and 3-aminopropyltriethoxysilane (PPCPE-NH2). The modified electrodes were applied in detection of E. coli O157:H7, it was showed that the electrochemical signal of PPCPE-CHO was the strongest among those three kinds of electrodes. A linear relationship between the anodic stripping peak current and the concentration of E. coli O157:H7 from 1.0 x 10(3) to 1.0 x 10(7) cells/mL and a limit of detection as low as 8.0 x 10(2) cells/mL were obtained when PPCPE-CHO was used.

  13. Electrocatalytic oxidation and determination of homocysteine at carbon nanotubes modified paste electrode using dopamine as a mediator

    Directory of Open Access Journals (Sweden)

    Mohammadzadeh Safoora

    2013-01-01

    Full Text Available A carbon paste electrode modified with multiwall carbon nanotubes (MWCNTPE was prepared to study the electrocatalytic activity of dopamine (DP in the presence of homocysteine (HCy and it was used for determination of HCy. The diffusion coefficient of HCy (D = 6.79×10−6 cm2 s−1, and the kinetic parameters of its oxidation such as electron transfer coefficient (α = 0.46, and rate constant (kh = 7.44×102 dm3 mol-1 s-1 were also determined using electrochemical approaches. Under the optimum pH of 5.0, the peak current of oxidation of HCy at MWCNTPE in the presence of DP occurs at a potential about 530 mV and the results showed that the oxidation peak current of HCy at the modified carbon nanotubes electrode was higher than on unmodified electrode. The peak current of differential pulse voltammograms of HCy solutions increased linearly in the range of 3.0-600.0 μM HCy with the detection limit of 2.08 μM HCy. This method was also examined for determination of HCy in physiological serum and urine samples.

  14. A Hydrogen Peroxide Sensor Prepared by Electropolymerization of Pyrrole Based on Screen-Printed Carbon Paste Electrodes

    Directory of Open Access Journals (Sweden)

    Hui Xu

    2007-03-01

    Full Text Available A disposable amperometric biosensor for commercial use to detect hydrogenperoxide has been developed. The sensor is based on screen-printed carbon paste electrodesmodified by electropolymerization of pyrrole with horseradish peroxidase (HRP entrapped.The facture techniques of fabricating the enzyme electrodes are suitable for mass productionand quality control. The biosensor shows a linear amperometric response to H2O2 from 0.1to 2.0 mM, with a sensitivity of 33.24 μA mM-1 cm-2. Different operational parameters ofelectropolymerization are evaluated and optimized.

  15. Ni(II) decorated nano silicoaluminophosphate molecular sieves-modified carbon paste electrode as an electrocatalyst for electrooxidation of methanol

    Indian Academy of Sciences (India)

    SEYED KARIM HASSANINEJAD-DARZI; MOSTAFA RAHIMNEJAD; SEYEDEH ELHAM MOKHTARI

    2016-06-01

    In this work, we reported amethod for the synthesis of nanosized silicoaluminophosphate (SAPO) molecular sieves that are important members of zeolites family. The synthesized SAPO was characterized using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) as well as infrared (IR) techniques. Then, the modified carbon paste electrode was prepared by nano SAPO molecular sieves and nickel (II) ion incorporated at this electrode. The electrochemical behaviour of the modified electrode (Ni-SAPO/CPE) towards the oxidation of methanol was investigated by cyclic voltammetry and hronoamperometry methods. It has been found that the oxidation current is extremely increased by using Ni-SAPO/CPE compared to the unmodified Ni-CPE, it seems that Ni$^{2+}$ inclusion into nano SAPO channels provides the active sites for catalysis of methanol oxidation. The effect of some parameters such as scan rate of potential, concentration of methanol, amount of SAPO was investigated on the oxidation of methanol at the surface of modified electrode. The values of electron transfer coefficient, charge-transfer rate constant and electrode surface coverage for the Ni(II)/Ni(III) couple in the surface of Ni-SAPO/CPE were found to be 0.555, 0.022 s$^{−1}$ and 5.995 $\\times$ 10$^{−6}$ mol cm$^{−2}$, respectively. Also, the diffusion coefficient and the mean value of catalytic rate constant for methanol and redox sites of modified electrode were obtained to be $1.16\\times 10^{−5}$ cm$^2$ s$^{−1}$ and $4.62\\times 10^4$ cm$^3$ mol$^{−1} s$^{−1}$, respectively. The good catalytic activity, high sensitivity, good selectivity and stability and easy in preparation rendered the Ni-SAPO/CPE to be a capable electrode for electrocatalytic oxidation of methanol.

  16. A novel amperometric catechol biosensor based on α-Fe2O3 nanocrystals-modified carbon paste electrode.

    Science.gov (United States)

    Sarika, C; Shivakumar, M S; Shivakumara, C; Krishnamurthy, G; Narasimha Murthy, B; Lekshmi, I C

    2017-05-01

    In this work, we designed an amperometric catechol biosensor based on α-Fe2O3 nanocrystals (NCs) incorporated carbon-paste electrode. Laccase enzyme is then assembled onto the modified electrode surface to form a nanobiocomposite enhancing the electron transfer reactions at the enzyme's active metal centers for catechol oxidation. The biosensor gave good sensitivity with a linear detection response in the range of 8-800 μM with limit of detection 4.28 μM. We successfully employed the sensor for real water sample analysis. The results illustrate that the metal oxide NCs have enormous potential in the construction of biosensors for sensitive determination of phenol derivatives.

  17. Comparative Study of PVC-Free All-Solid-State, PVC Membrane, and Carbon Paste Ion-Selective Electrodes for the Determination of Dapoxetine Hydrochloride in Pharmaceutical Formulation.

    Science.gov (United States)

    Aziz, Azza; Khamees, Nesrin; Mohamed, Tagreed Abdel-Fattah; Derar, Abeer Rashad

    2016-11-01

    The potentiometric response characteristics and analytical applications of a poly(vinyl chloride) (PVC)-free all-solid-state ion-selective electrode for dapoxetine hydrochloride (DAP) are examined. The Nernstian response of the electrode was evaluated by comparison with PVC-based liquid membrane and carbon paste electrodes. The PVC-free electrode is prepared by direct incorporation of dapoxetine-tetraphenyl borate (DAP-TPB) as a sensing element into a commercial nail varnish containing cellulose acetate propionate. The composite was applied onto a 3 mm diameter graphite disk electrode. The electrode exhibited a Nernstian slope of 56.0 mV/decade in the concentration range of 1 × 10-4 to 1 × 10-2 mol/L with an LOD of 2 × 10-5 mol/L. The electrode is independent of pH in the range of 2 to 6 and showed good selectivity for DAP with respect to a large number of inorganic cations and amino acids. Comparable Nernstian slope, sensitivity, pH range, and selectivity pattern were obtained with a PVC membrane and a carbon paste incorporating DAP-TPB as a sensing element and dioctylphthalate as a solvent mediator. The electrodes were used for the determination of DAP in pure solution and in tablets without extraction with high accuracy and precision (RSD ≤ 2%). The nail varnish solid-state electrode is simple, economical, and rapid when compared with PVC membrane and carbon paste electrodes.

  18. A novel cysteine sensor based on modification of carbon paste electrode by Fe(II)-exchanged zeolite X nanoparticles.

    Science.gov (United States)

    Hashemi, Habibeh-Sadat; Nezamzadeh-Ejhieh, Alireza; Karimi-Shamsabadi, Maryam

    2016-01-01

    An electrochemical sensor based on carbon paste electrode (CPE) modified with iron(II) doped into a synthesized nano-particles of zeolite X (Fe(II)-NX/ZCME) was constructed, which is highly sensitive for detection of cysteine (Cys). The modified electrode showed an excellent electro-activity for oxidation of Cys in phosphate buffer at pH7.4. It has been found that anodic peak potential of Cys oxidation, compared with the unmodified CPE (UCPE), was shifted towards negative values at the surface of the modified electrode under the optimum condition. The peak current increased linearly with the Cys concentration in the wide range of 5.0 × 10(-9)-3.0 × 10(-3) mol L(-1). The very low detection limit was obtained to be 1.5 × 10(-10) mol L(-1). Finally, the modified electrode was used as a selective, simple and precise new electrochemical sensor for the determination of Cys in the real samples, such as pharmaceutical and biological fluids.

  19. New Modified-Multiwall Carbon Nanotubes Paste Electrode for Electrocatalytic Oxidation and Determination of Hydrazine Using Square Wave Voltammetry

    Institute of Scientific and Technical Information of China (English)

    Ali A. ENSAF; Mahsa LOTFI; Hassan KARIMI-MALEH

    2012-01-01

    The application of p-aminophenol as a suitable mediator, as a sensitive and selective voltammetric sensor for the determination of hydrazine using square wave voltammetric method were described. The modified multiwall carbon nanotubes paste electrode exhibited a good electrocatalytic activity for the oxidation of hydrazine at pH = 7.0. The catalytic oxidation peak currents showed a linear dependence of the peaks current to the hydrazine concentrations in the range of 0.5–175 μmol/L with a correlation coefficient of 0.9975. The detection limit (S/N = 3) was estimated to be 0.3 μmol/L of hydrazine. The relative standard deviations for 0.7 and 5.0 μmol/L hydrazine were 1.7 and 1.1%, respectively. The modified electrode showed good sensitivity and selectivity. The diffusion coefficient (D = 9.5 × 10–4 cm2/s) and the kinetic parameters such as the electron transfer coefficient (α = 0.7) of hydrazine at the surface of the modified electrode were determined using electrochemical approaches. The electrode was successfully applied for the determination of hydrazine in real samples with satisfactory results.

  20. Voltammetric Determination of Homocysteine Using Multiwall Carbon Nanotube Paste Electrode in the Presence of Chlorpromazine as a Mediator

    Directory of Open Access Journals (Sweden)

    Fathali Gholami-Orimi

    2012-01-01

    Full Text Available We propose chlorpromazine (CHP as a new mediator for the rapid, sensitive, and highly selective voltammetric determination of homocysteine (Hcy using multiwall carbon nanotube paste electrode (MWCNTPE. The experimental results showed that the carbon nanotube paste electrode has a highly electrocatalytic activity for the oxidation of Hcy in the presence of CHP as a mediator. Cyclic voltammetry, double potential step chronoamperometry, and square wave voltammetry (SWV are used to investigate the suitability of CHP at the surface of MWCNTPE as a mediator for the electrocatalytic oxidation of Hcy in aqueous solutions. The kinetic parameters of the system, including electron transfer coefficient, and catalytic rate constant were also determined using the electrochemical approaches. In addition, SWV was used for quantitative analysis. SWV showed wide linear dynamic range (0.1–210.0 μM Hcy with a detection limit of 0.08 μM Hcy. Finally, this method was also examined as a selective, simple, and precise electrochemical sensor for the determination of Hcy in real samples.

  1. Potentiometric stripping analysis of bismuth based on carbon paste electrode modified with cryptand [2.2.1]and multiwalled carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Gadhari, Nayan S.; Sanghavi, Bankim J. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400 098 (India); Karna, Shashi P. [U.S. Army Research Laboratory, Weapons and Materials Research Directorate, ATTN: RDRL-WM, Aberdeen Proving Ground, MD 21005-5069 (United States); Srivastava, Ashwini K., E-mail: aksrivastava@chem.mu.ac.i [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400 098 (India)

    2010-12-30

    An electrochemical method based on potentiometric stripping analysis (PSA) employing a cryptand [2.2.1](CRY) and carbon nanotube (CNT) modified paste electrode (CRY-CNT-PE) has been proposed for the subnanomolar determination of bismuth. The characterization of the electrode surface has been carried out by means of scanning electron microscopy (SEM), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and chronocoulometry (CC). It was observed that by employing CRY-CNT-PE, a 9-fold enhancement in the PSA signal (dt/dE) was observed as compared to plain carbon paste electrode (PCPE). Under the optimized conditions, dt/dE (s/V) was proportional to the Bi(III) concentration in the range of 5.55 x 10{sup -8} to 9.79 x 10{sup -11} M (r = 0.9990) with the detection limit (S/N = 3) of 3.17 x 10{sup -11} M. The practical analytical utilities of the modified electrode were demonstrated by the determination of bismuth in pharmaceutical formulations, human hair, sea water, urine and blood serum samples. The prepared modified electrode showed several advantages, such as a simple preparation method, high sensitivity, very low detection limits and excellent reproducibility. Moreover, the results obtained for bismuth analysis in commercial and real samples using CRY-CNT-PE and those obtained by atomic absorption spectroscopy (AAS) are in agreement at the 95% confidence level.

  2. Determination of dopamine in presence of ascorbic acid and uric acid using poly (Spands Reagent) modified carbon paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Veera Manohara Reddy, Y.; Prabhakara Rao, V.; Vijaya Bhaskar Reddy, A.; Lavanya, M.; Venu, M.; Lavanya, M.; Madhavi, G., E-mail: gmchem01@gmail.com

    2015-12-01

    In this paper, we have fabricated a modified carbon paste electrode (CPE) by electropolymerisation of spands reagent (SR) onto surface of CPE using cyclic voltammetry (CV). The developed electrode was abbreviated as poly(SR)/CPE and the surface morphology of the modified electrode was studied by using scanning electron microscopy (SEM). The developed electrode showed higher electrocatalytic properties towards the detection of dopamine (DA) in 0.1 M phosphate buffer solution (PBS) at pH 7.0. The effect of pH, scan rate, accumulation time and concentration of dopamine was studied at poly(SR)/CPE. The poly(SR)/CPE was successfully used as a sensor for the selective determination of DA in presence of ascorbic acid (AA) and uric acid (UA) without any interference. The poly(SR)/CPE showed a good detection limit of 0.7 μM over the linear dynamic range of 1.6 μM to 16 μM, which is extremely lower than the reported methods. The prepared poly(SR)/CPE exhibited good stability, high sensitivity, better reproducibility, low detection limit towards the determination of DA. The developed method was also applied for the determination of DA in real samples. - Highlights: • Electropolymerization of spands reagent was fabricated by cyclic voltammetry • The Poly (spands reagent) electrode shows excellent electrocatalytic activity for the detection of dopamine. • The detection limit for dopamine was found to be 0.7 μM. • The proposed method can be applied for DA in injection and human blood serum samples.

  3. Nickel (II) incorporated AlPO-5 modified carbon paste electrode for determination of thioridazine in human serum

    Energy Technology Data Exchange (ETDEWEB)

    Amiri, Mandana, E-mail: mandanaamiri@uma.ac.ir [Department of Chemistry, University of Mohaghegh Ardabili, Ardabil (Iran, Islamic Republic of); Sohrabnezhad, Shabnam [Department of Chemistry, Faculty of Science, University of Guilan, P.O. Box 1914, Rasht. Iran (Iran, Islamic Republic of); Rahimi, Azad [Department of Chemistry, University of Mohaghegh Ardabili, Ardabil (Iran, Islamic Republic of)

    2014-04-01

    In this approach, synthesis of nickel (II) incorporated aluminophosphate (NiAlPO-5) was performed by using hydrothermal method. The diffuse reflectance spectroscopy (DRS), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR) techniques were applied in order to characterize synthesized compounds. The NiAlPO-5 was used as a modifier in carbon paste electrode for the selective determination of thioridazine which is an antidepressant drug. This research is the first example of an aluminophosphate being employed in electroanalysis. The effective catalytic role of the modified electrode toward thioridazine oxidation can be attributed to the electrocatalytic activity of nickel (II) in the aluminaphosphate matrix. In addition, NiAlPO-5 has unique properties such as the high specific surface area which increases the electron transfer of thioridazine. The effects of varying the percentage of modifier, pH and potential sweep rate on the electrode response were investigated. Differential pulse voltammetry was used for quantitative determination as a sensitive method. A dynamic linear range was obtained in the range of 1.0 × 10{sup −7}–1.0 × 10{sup −5} mol L{sup −1}. The determination of thioridazine in real samples such as commercial tablets and human serum was demonstrated. - Highlights: • Nickel aluminophosphate (NiAlPO-5) has been synthesized and characterized. • Nickel (II) in modified electrode shows electrocatalytic activity. • High specific surface area of NiAlPO-5 increases electron transfer of thioridazine. • Modified electrode has very good applicability for determination of thioridazine.

  4. Fabrication of gallium hexacyanoferrate modified carbon ionic liquid paste electrode for sensitive determination of hydrogen peroxide and glucose

    Energy Technology Data Exchange (ETDEWEB)

    Haghighi, Behzad, E-mail: haghighi@iasbs.ac.ir; Khosravi, Mehdi; Barati, Ali

    2014-07-01

    Gallium hexacyanoferrate (GaHCFe) and graphite powder were homogeneously dispersed into n-dodecylpyridinium hexafluorophosphate and paraffin to fabricate GaHCFe modified carbon ionic liquid paste electrode (CILPE). Mixture experimental design was employed to optimize the fabrication of GaHCFe modified CILPE (GaHCFe-CILPE). A pair of well-defined redox peaks due to the redox reaction of GaHCFe through one-electron process was observed for the fabricated electrode. The fabricated GaHCFe-CILPE exhibited good electrocatalytic activity towards reduction and oxidation of H{sub 2}O{sub 2}. The observed sensitivities for the electrocatalytic oxidation and reduction of H{sub 2}O{sub 2} at the operating potentials of + 0.8 and − 0.2 V were about 13.8 and 18.3 mA M{sup −1}, respectively. The detection limit (S/N = 3) for H{sub 2}O{sub 2} was about 1 μM. Additionally, glucose oxidase (GOx) was immobilized on GaHCFe-CILPE using two methodology, entrapment into Nafion matrix and cross-linking with glutaraldehyde and bovine serum albumin, in order to fabricate glucose biosensor. Linear dynamic rage, sensitivity and detection limit for glucose obtained by the biosensor fabricated using cross-linking methodology were 0.1–6 mM, 0.87 mA M{sup −1} and 30 μM, respectively and better than those obtained (0.2–6 mM, 0.12 mA M{sup −1} and 50 μM) for the biosensor fabricated using entrapment methodology. - Highlights: • Gallium hexacyanoferrate modified carbon ionic liquid paste electrode was fabricated. • Mixture experimental design was used to optimize electrode fabrication. • Response trace plot was used to show the effect of electrode materials on response. • The sensor exhibited electrocatalytic activity towards H{sub 2}O{sub 2} reduction and oxidation. • Glucose biosensor was fabricated by immobilization of glucose oxidase on sensor.

  5. Preparation of alanine and tyrosine functionalized graphene oxide nanoflakes and their modified carbon paste electrodes for the determination of dopamine

    Science.gov (United States)

    Kumar, Mohan; Swamy, B. E. Kumara; Asif, M. H. Mohammed; Viswanath, C. C.

    2017-03-01

    Herein, established the synthesis of graphene oxide (GO) by Hummers Method with addition of KMnO4 followed by thermal heating at 80 °C. The obtained GO was further functionalized by alanine and tyrosine. The prepared GO, alanine functionalized GO nanoflakes (AGONF) and tyrosine functionalized GO nanoflakes (TGONF) were characterized by spectroscopic technique using energy-dispersive spectroscopy (EDS), quantitatively by scanning electron microscopy (SEM) and structural studies along with interlayer distance verified through X-ray diffraction technique. Afterwards, the prepared AGONF and TGONF were used as the modifier for the carbon paste electrode (CPE). The electrochemical behavior of the AGONF and TGONF modified carbon paste electrodes (MCPEs) towards dopamine (DA) in phosphate buffer solution (PBS) were examined by cyclic voltammetric (CV) technique and the obtained consequences showed good electrocatalytic activity of MCPEs by increasing the redox peak current with a lower potential difference compared to the bare CPE (BCPE). The AGONF and TGONF MCPEs were further used for the optimization studies. From the pH studies, it was found that the equal number of proton and electron transfer reaction involved in both the modified electrodes. The scan rate studies demonstrate the adsorption controlled electrode process at AGONF MCPE and diffusion controlled at TGONF MCPE. The oxidation peak current increased linearly with two concentration interval of DA at a range of 2-7 μM and 10-30 μM in presence of PBS (pH 7.4) at MCPEs and the limit of detection (LOD) were found to be 0.84 μM and 0.96 μM for first interval DA concentration range (2-7 μM) at AGONF and TGONF MCPE. The stability, repeatability and reproducibility of functionalized GO nanoflakes MCPEs at DA were studied and established excellent characteristics. The newly developed functionalized GO nanoflake electrodes were successfully tested in DA injection sample. Furthermore the functionalized GO and

  6. Sensitive and reproducible quantification of Cu2+ by stripping with a carbon paste electrode modified with humic acid.

    Science.gov (United States)

    Thobie-Gautier, Christine; da Silva, Wilson T Lopes; Rezende, Maria O O; El Murr, Nabil

    2003-09-01

    The preparation of a humic acid modified carbon paste electrode (HA-MCPE) as well as the behavior of its surface as complexing agent toward Cu2+ cations are described. Electrochemical studies of the reduction of the complexed cations and of the anodic stripping oxidation of the resulting copper are outlined. The anodic stripping current was correlated to the Cu2+ concentrations. A well-defined method for the preparation of reproducible electrodes is described. The effects on the current response obtained by cyclic voltammetry of the humic acid ratio, the pH, the accumulation time, and the speed scan rate were studied. Calibration graphs were linear over the range 3 x 10(-8)-10(-5) mol L(-1) Cu2+ and the relative standard deviation (R.S.D.) was 1.2% (n=5) for [Cu2+] = 1.6 x 10(-5) mol L(-1). 5 min accumulation time for [Cu2+] > 10(-7) mol L(-1) and 10 min for [Cu2+] < 10(-7) mol L(-1) were sufficient to permit sensitive and reproducible measurements. The electrode was successfully used to measure Cu2+ in real samples and the results were compared to those obtained by the standard method with differential pulse anodic stripping voltammetry.

  7. 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.

  8. Electrochemical determination of paraquat in citric fruit based on electrodeposition of silver particles onto carbon paste electrode

    Directory of Open Access Journals (Sweden)

    Abdelfettah Farahi

    2015-09-01

    Full Text Available Carbon paste electrodes (CPEs modified with silver particles present an interesting tool in the determination of paraquat (PQ using square wave voltammetry. Metallic silver particle deposits have been obtained via electrochemical deposition in acidic media using cyclic voltammetry. Scanning electron microscopy and X-ray diffraction measurements show that the silver particles are deposited onto carbon surfaces in aggregate form. The response of PQ with modified electrode (Ag-CPE related to Ag/CP loading, preconcentration time, and measuring solution pH was investigated. The result shows that the increase in the two cathodic peak currents (Peak 1 and Peak 2, under optimized conditions, was linear with the increase in PQ concentration in the range 1.0 × 10−7 mol/L to 1.0 × 10−3 mol/L. The detection limit and quantification limit were 2.01 × 10−8 mol/L and 6.073 × 10−8 mol/L, respectively for Peak 1. The precision expressed as relative standard deviation for the concentration level 1.0 × 10−5 mol/L (n = 8 was found to be 1.45%. The methodology was satisfactorily applied for the determination of PQ in citric fruit cultures.

  9. In situ modified screen printed and carbon paste ion selective electrodes for potentiometric determination of naphazoline hydrochloride in its formulation

    Institute of Scientific and Technical Information of China (English)

    Gehad G. Mohamed; F.A. Nour El-Dien; Eman Y.Z. Frag; Marwa El-Badry Mohamed

    2013-01-01

    The construction and performance characteristics of new sensitive and selective in situ modified screen printed (ISPE) and carbon paste (ICPE) electrodes for determination of naphazoline hydrochloride (NPZ-HCl) have been developed. The electrodes under investigation show potentiometric response for NPZ-HCl in the concentration range from 7.0 Â 10-7 to 1.0 Â 10-2 M at 25 1C and the electrode response is independent of pH in the range of 3.1-7.9. These sensors have slope values of 59.770.6 and 59.270.2 mV decade−1 with detection limit values of 5.6 Â 10-7 and 5.9 Â 10-7 M NPZ-HCl using ISPE and ICPE, respectively. These electrodes show fast response time of 4-7 s and 5-8 s and exhibits lifetimes of 28 and 30 days for ISPE and ICPE, respectively. Selectivity for NPZ-HCl with respect to a number of interfering materials was also investigated. It was found that there is no interference from the investigated inorganic cations, anions, sugars and other pharmaceutical excipients. The proposed sensors were applied for the determination of NPZ-HCl in pharmaceutical formulation using the direct potentiometric method. It showed a mean average recovery of 100.2%and 102.6%for ISPE and ICPE, respectively. The obtained results using the proposed sensors were in good agreement with those obtained using the official method. The proposed sensors show significantly high selectivity, response time, accuracy, precision, limit of detection (LOD) and limit of quantification (LOQ) compared with other proposed methods.

  10. Sensitive amperometric determination of hydrazine using a carbon paste electrode modified with silver-doped zeolite L nanoparticles

    Indian Academy of Sciences (India)

    NEDA SALEK GILANI; SEYED NASER AZIZI; SHAHRAM GHASEMI

    2017-02-01

    Silver-loaded nanozeolite-L-modified carbon paste electrode (Ag/L–CPE) was used as a novel sensing platform for enhanced electrocatalytic oxidation and determination of hydrazine. Zeolite L nanoparticles were synthesized via hydrothermal approach and then characterized using various techniques such as X-ray diffraction (XRD), Fourier transform infrared (FTIR), scanning electronic microscopy (SEM) and Brunauer–Emmett–Teller (BET). Silver-exchanged nanozeolite L (Ag/L) was prepared and mixed with carbon paste to prepare the modified electrode. Cyclic voltammetry studies revealed the high performance of Ag/L–CPE for electrocatalytic oxidation of hydrazine. Two linear ranges were detected in the amperometric detection of hydrazine. The first range was from10 $\\mu$M to 0.4 mM with sensitivity of 103.13 $\\mu$A mM$^{−1}$ and the second one was from 0.4 to 4mM with sensitivity of 58.131 $\\mu$A mM$^{−1}$. The response time and detection limit ($S/N = 3$) of this sensor were determined to be 2 s and 1.5 $\\mu$M, respectively. The unique porous structure of nanozeolite L offers a promising catalyst support candidate for efficient electrochemical sensing of hydrazine. The sensor exhibited appreciable repeatability, reproducibility and stability, and was able to detect hydrazine in the presence of even 500-fold excess concentrations of interfering species. Also, the sensor was used to determine hydrazine concentration in water samples with satisfactory results.

  11. Construction of a carbon ionic liquid paste electrode based on multi-walled carbon nanotubes-synthesized Schiff base composite for trace electrochemical detection of cadmium

    Energy Technology Data Exchange (ETDEWEB)

    Afkhami, Abbas, E-mail: afkhami@basu.ac.ir [Faculty of Chemistry, Bu-Ali Sina University, Hamedan (Iran, Islamic Republic of); Khoshsafar, Hosein [Faculty of Chemistry, Bu-Ali Sina University, Hamedan (Iran, Islamic Republic of); Bagheri, Hasan [Chemical Injuries Research Center, Baqiyatallah University of Medical Sciences, Tehran (Iran, Islamic Republic of); Madrakian, Tayyebeh [Faculty of Chemistry, Bu-Ali Sina University, Hamedan (Iran, Islamic Republic of)

    2014-02-01

    A simple, highly sensitive and selective carbon nanocomposite electrode has been developed for the electrochemical trace determination of cadmium. This sensor was designed by incorporation of multi-walled carbon nanotubes (MWCNTs) and a new synthesized Schiff base into the carbon paste ionic liquid electrode (CPE{sub IL}) which provides remarkably improved sensitivity and selectivity for the electrochemical stripping assay of Cd(II). The detection limit of the method was found to be 0.08 μg L{sup −1} (S/N = 3) that is lower than the maximum contaminant level of Cd(II) allowed by the Environmental Protection Agency (EPA) in standard drinking waters. The proposed electrode exhibits good applicability for monitoring Cd(II) in various real samples. - Highlights: • A new nanocomposite was prepared and applied to the modification of CPE. • The prepared nanocomposite was characterized by scanning electron microscopy. • The electrode was used to the rapid and selective determination of Cd(II)

  12. Mixed ion-exchanger chemically modified carbon paste ion-selective electrodes for determination of triprolidine hydrochloride

    Directory of Open Access Journals (Sweden)

    Yousry M. Issa

    2010-01-01

    Full Text Available Triprolidine hydrochloride (TpCl ion-selective carbon paste electrodes were constructed using Tp-TPB/Tp-CoN and Tp-TPB/Tp-PTA as ion-exchangers. The two electrodes revealed Nernstian responses with slopes of 58.4 and 58.1 mV decade−1 at 25 °C in the ranges 6 × 10−6–1 × 10−2 and 2 × 10−5–1 × 10−2 M for Tp-TPB/Tp-CoN and Tp-TPB/Tp-PTA, respectively. The potentials of these electrodes were independent of pH in the ranges of 2.5–7.0 and 4.5–7.0, and detection limits were 6 × 10−6 and 1 × 10−5 M for Tp-TPB/Tp-CoN and Tp-TPB/Tp-PTA, respectively. The electrodes showed a very good selectivity for TpCl with respect to a large number of inorganic cations and compounds. The standard addition, potentiometric titration methods and FIA were applied to the determination of TpCl in pure solutions and pharmaceutical preparations. The results obtained were in close agreement with those found by the official method. The mean recovery values were 100.91% and 97.92% with low coefficient of variation values of 0.94%, and 0.56% in pure solutions, 99.82% and 98.53% with coefficient of variation values of 2.20%, and 0.73% for Actifed tablet and Actifed syrup, respectively, using the Tp-TPB/Tp-CoN electrode, and 98.85%, and 99.18% with coefficient of variation values of 0.48% and 0.85% for Actifed tablet and Actifed syrup, respectively, using the Tp-TPB/Tp-PTA electrode.

  13. Multi-walled carbon nanotube/poly(glycine) modified carbon paste electrode for the determination of dopamine in biological fluids and pharmaceuticals.

    Science.gov (United States)

    Thomas, Tony; Mascarenhas, Ronald J; Swamy, B E Kumara; Martis, Praveen; Mekhalif, Zineb; Sherigara, B S

    2013-10-01

    A modified carbon paste electrode (CPE) for the selective detection of dopamine (DA) in presence of large excess of ascorbic acid (AA) and uric acid (UA) at physiological pH has been fabricated by bulk modification of CPE with multi-walled carbon nanotubes (MWCNTs) followed by electropolymerization of glycine (Gly). The surface morphology is compared using SEM images. The presence of nitrogen was confirmed by the energy dispersion X-ray spectroscopy (EDS) indicating the polymerization of Gly on the surface of the modified electrode. The impedance study indicates a better charge transfer kinetics for DA at CPE modified with MWCNT/polyglycine electrode. The presence of MWCNTs in carbon paste matrix triggers the extent of electropolymerization of Gly and imparts more selectivity towards DA by electrochemically not sensing AA below a concentration of 3.1×10(-4)M. Due to the exclusion of the signal for AA, the interference of AA in the determination of DA is totally ruled out by DPV method which is used for its detection at lower concentrations. Large peak separation, good sensitivity, reproducibility and stability allow this modified electrode to analyze DA individually and simultaneously along with AA and UA. Detection limit of DA was determined from differential pulse voltammetric (DPV) study and found to be 1.2×10(-8)M with a linear dynamic range of 5.0×10(-7)M to 4.0×10(-5)M. The practical analytical application of this electrode was demonstrated by measurement of DA content in dopamine hydrochloride injection and human blood serum.

  14. Voltammetric sensor based on carbon paste electrode modified with molecular imprinted polymer for determination of sulfadiazine in milk and human serum.

    Science.gov (United States)

    Sadeghi, Susan; Motaharian, Ali

    2013-12-01

    A new sensitive voltammetric sensor for determination of sulfadiazine is described. The developed sensor is based on carbon paste electrode modified with sulfadiazine imprinted polymer (MIP) as a recognition element. For comparison, a non-imprinted polymer (NIP) modified carbon paste electrode was prepared. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) methods were performed to study the binding event and electrochemical behavior of sulfadiazine at the modified carbon paste electrodes. The determination of sulfadiazine after its extraction onto the electrode surface was carried out by DPV at 0.92 V vs. Ag/AgCl owing to oxidation of sulfadiazine. Under the optimized operational conditions, the peak current obtained at the MIP modified carbon paste electrode was proportional to the sulfadiazine concentration within the range of 2.0×10(-7)-1.0×10(-4) mol L(-1) with a detection limit and sensitivity of 1.4×10(-7) mol L(-1) and 4.2×10(5) μA L mol(-1), respectively. The reproducibility of the developed sensor in terms of relative standard deviation was 2.6%. The sensor was successfully applied for determination of sulfadiazine in spiked cow milk and human serum samples with recovery values in the range of 96.7-100.9%.

  15. Determination of buprenorphine by differential pulse voltammetry on carbon paste electrode using SDS as an enhancement factor.

    Science.gov (United States)

    Behpour, Mohsen; Valipour, Akram; Keshavarz, Mahin

    2014-09-01

    In the present study, a facile electrochemical approach is proposed for the determination of buprenorphine (BPR) in the presence of sodium dodecyl sulfate (SDS). SDS was applied for amplification of oxidation signal. Carbon paste electrode (CPE) used as working electrode and cyclic voltammetry (CV), differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS) were carried out in phosphate buffer solution (pH3.0). Under optimal experimental conditions, the oxidation current increased with the addition of BPR in the sample and two dynamic ranges obtained from 4.00 nM to 0.126 μM and from 0.126 to 0.317 μM by DPV and exhibited a low detection limit (LOD) of 1.33 nM (S/N=3). This offered method has been used for the determination of BPR in the real samples and has validated with the recovery test for BPR spiked urine samples. The result demonstrated that this method is a simple, sensitive, rapid, low-cost, and stable method for BPR detection.

  16. 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.

  17. Simple and rapid determination of iodide in table salt by stripping potentiometry at a carbon-paste electrode.

    Science.gov (United States)

    Svancara, Ivan; Ogorevc, Bozidar; Nović, Milko; Vytras, Karel

    2002-04-01

    A simple and rapid procedure, utilising constant-current stripping analysis (CCSA) at a carbon-paste electrode containing tricresyl phosphate as a pasting liquid (TCP-CPE), has been developed for the determination of iodide in table salt. Because of a synergistic accumulation mechanism based on ion-pairing and extraction of iodide in combination with electrolytic pretreatment of the TCP-CPE, the method is selective for iodide and enables direct determination of iodide in samples of table salt containing anti-caking agents such as K(4)[Fe(CN)(6)] (food additive "E 536") or MgO. The iodide content (calculated as KI) can be determined in a concentration range of 2 to 100 mg kg(-1) salt, with a detection limit (S/N=3) of 1 mg kg(-1), and a recovery from 90 to 115%. The proposed method has been used to determine iodide in several types of artificially iodised table salt and in one sample of natural sea salt. The results obtained agreed well with those obtained by use of three independent reference methods (titration, spectrophotometry, and ICP-MS) used to validate the CCSA method, indicating that the developed method is applicable as a routine procedure for rapid testing in salt production process control and in the analysis of marketed table salts.

  18. Development of a selective and sensitive voltammetric sensor for propylparaben based on a nanosized molecularly imprinted polymer-carbon paste electrode.

    Science.gov (United States)

    Gholivand, Mohammad Bagher; Shamsipur, Mojtaba; Dehdashtian, Sara; Rajabi, Hamid Reza

    2014-03-01

    The design and construction of a selective voltammetric sensor for propylparaben (PP) in cosmetics by using a molecularly imprinted polymer (MIP) as recognition element was introduced. The MIP was synthesized by using PP as template and methacrylic acid as functional monomer and then incorporated in the carbon paste electrode as PP sensor. The molecularly imprinted polymer-carbon paste electrode (MIP-CPE) showed very high recognition ability in comparison to non-imprinted polymer-carbon paste electrode (NIP-CPE). It was shown that electrode washing after PP extraction, led to enhanced selectivity, without noticeably decreasing the sensitivity. Some parameters affecting sensor response were optimized, and a calibration curve was then plotted using differential pulse voltammetric (DPV) technique. A dynamic linear range of 1 nM to 100 nM was obtained. The detection limit of the sensor was calculated to be equal to 0.32 nM. The imprinted electrode also displayed good selectivity for PP and selectivity coefficients were 2.29 and 1.66 for methylparaben (MP) and ethylparaben (EP) respectively. Structural analogs, such as phenol and p-hydroxybenzoic acid had almost no response. This sensor was used successfully for propylparaben determination in cosmetic sample.

  19. Amperometric Biosensors Based on Carbon Paste Electrodes Modified with Nanostructured Mixed-valence Manganese Oxides and Glucose Oxidase

    Energy Technology Data Exchange (ETDEWEB)

    Cui, Xiaoli; Liu, Guodong; Lin, Yuehe

    2005-06-01

    Nanostructured multivalent manganese oxides octahedral molecular sieve (OMS), including cryptomelane-type manganese oxides and todorokite-type manganese oxides, were synthesized and evaluated for chemical sensing and biosensing at low operating potential. Both cryptomelane-type manganese oxides and todorokite-type manganese oxides are nanofibrous crystals with sub-nanometer open tunnels that provide a unique property for sensing applications. The electrochemical and electrocatalytic performance of OMS for the oxidation of H2O2 have been compared. Both cryptomelane-type manganese oxides and todorokite-type manganese oxides can be used to fabricate sensitive H2O2 sensors. Amperometric glucose biosensors are constructed by bulk modification of carbon paste electrodes (CPEs) with glucose oxidase as a biocomponent and nanostructured OMS as a mediator. A Nafion thin film was applied as an immobilization/encapsulation and protective layer. The biosensors were evaluated as an amperometric glucose detector at phosphate buffer solution with a pH 7.4 at an operating potential of 0.3 V (vs. Ag/AgCl). The biosensor is characterized by a well-reproducible amperometric response, linear signal-to-glucose concentration range up to 3.5 mM and 1.75 mM, and detection limits (S/N = 3) of 0.1 mM and 0.05 mM for todorokite-type manganese oxide and cryptomelane-type manganese oxide modified electrodes, respectively. The biosensors based on OMS exhibit considerable good reproducibility and stability, and the construction and renewal are simple and inexpensive.

  20. Amperometric biosensors based on carbon paste electrodes modified with nanostructured mixed-valence manganese oxides and glucose oxidase.

    Science.gov (United States)

    Cui, Xiaoli; Liu, Guodong; Lin, Yuehe

    2005-06-01

    Nanostructured, multivalent, manganese-oxide octahedral molecular sieves (OMS), including cryptomelane-type manganese oxides and todorokite-type manganese oxides, were synthesized and evaluated for chemical sensing and biosensing at low operating potential. Both cryptomelane-type manganese oxides and todorokite-type manganese oxides are nanofibrous crystals with subnanometer open tunnels that provide a unique property for sensing applications. The electrochemical and electrocatalytic performance of OMS for the oxidation of H2O2 have been compared. Both cryptomelane-type manganese oxides and todorokite-type manganese oxides can be used to fabricate sensitive H2O2 sensors. With glucose oxidase (GOx) as an enzyme model, amperometric glucose biosensors are constructed by bulk modification of carbon paste electrodes with GOx as a biocomponent and nanostructured OMS as a mediator. A Nafion thin film was applied as an immobilization/encapsulation and protective layer. The biosensors were evaluated as an amperometric glucose detector at phosphate buffer solution with a pH 7.4 at an operating potential of 0.3 V (vs Ag/AgCl). The biosensor is characterized by a well-reproducible amperometric response, linear signal-to-glucose concentration range up to 3.5 mmol/L and 1.75 mmol/L, and detection limits (S/N = 3) of 0.1 mmol/L and 0.05 mmol/L for todorokite-type manganese oxide and cryptomelane-type manganese oxide-modified electrodes, respectively. The biosensors based on OMS exhibit considerable good reproducibility and stability, and the construction and renewal are simple and inexpensive.

  1. Gold Nanoparticle-based Layer-by-Layer Enhancement of DNA Hybridization Electrochemical Signal at Carbon Nanotube Modified Carbon Paste Electrode

    Institute of Scientific and Technical Information of China (English)

    Li Bo NIE; Jian Rong CHEN; Yu Qing MIAO; Nong Yue HE

    2006-01-01

    Colloid gold nanoparticle-based layer-by-layer amplification approach was applied to enhance the electrochemical detection sensitivity of DNA hybridization at carbon nanotube modified carbon paste electrodes (CNTPEs). Streptavidin was immobilized onto the surface of CNTPEs, and the conjugation of biotin labeled target oligonucleotides to the above immobilized streptavidin was performed, followed by the hybridization of target oligonucleotides with the gold nanoparticle-labeled DNA probe and then the layer-by-layer enhanced connection of gold nanoparticles, on which oligonucleotides complementary to the DNA probe were attached, to the hybridization system. The differential pulse voltammetry (DPV) signal of total gold nanoparticles was monitored. It was found that the layer-by-layer colloidal gold DPV detection enhanced the sensitivity by about one order of magnitude compared with that of one-layer detection. One-base mismatched DNA and complementary DNA could be distinguished clearly.

  2. A voltammetric sensor based on NiO/CNTs ionic liquid carbon paste electrode for determination of morphine in the presence of diclofenac

    Energy Technology Data Exchange (ETDEWEB)

    Sanati, Afsaneh L. [Department of Chemistry, Graduate University of Advanced Technology, Kerman (Iran, Islamic Republic of); Karimi-Maleh, Hassan, E-mail: h.karimi.maleh@gmail.com [Department of Chemistry, Graduate University of Advanced Technology, Kerman (Iran, Islamic Republic of); Badiei, Alireza [School of Chemistry, College of Science, University of Tehran, Tehran (Iran, Islamic Republic of); Biparva, Pourya [Department of Basic Sciences, Sari Agricultural Sciences and Natural Resources University, Sari (Iran, Islamic Republic of); Ensafi, Ali A. [Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111 (Iran, Islamic Republic of)

    2014-02-01

    A novel ionic liquid modified NiO/CNTs carbon paste electrode (IL/NiO/CNTCPE) had been fabricated by using hydrophilic ionic liquid 1-methyl-3-butylimidazolium chloride [MBIDZ]Cl as a binder. The cyclic voltammogram showed an irreversible oxidation peak at 0.61 V (vs. Ag/AgCl{sub sat}), which corresponded to the oxidation of morphine. Compared to common carbon paste electrode, the electrochemical response was greatly improved for morphine electrooxidation. This modified electrode exhibited a potent and persistent electron mediating behavior followed by well separated oxidation peaks of morphine and diclofenac. Detection limit of morphine was found to be 0.01 μM using square wave voltammetry (SWV) method. The proposed sensor was successfully applied for the determination of morphine in human urine and pharmaceutical samples. - Graphical abstract: Diclofenac as a nonsteroidal anti-inflammatory drug has been shown to decrease morphine consumption after operation in adults. The addition of regular doses of diclofenac may reduce the need for morphine after abdominal surgery. Therefore, in this study we describe a sensitive electrochemical sensor for simultaneous determination of morphine and diclofenac. - Highlights: • Electrochemical behavior of morphine study using modified carbon paste electrode • The sensor resolved the overlap of morphine and diclofenac • This sensor is also used for the determination of morphine in real samples.

  3. Voltammetric determination of norepinephrine in the presence of acetaminophen using a novel ionic liquid/multiwall carbon nanotubes paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Salmanpour, Sadegh [Department of Chemistry, Sari Branch, Islamic Azad University, Sari (Iran, Islamic Republic of); Tavana, Toktam [Department of Chemistry, Qaemshahr Branch, Islamic Azad University, Qaemshahr (Iran, Islamic Republic of); Pahlavan, Ali [Department of Physics, Science and Research Branch, Islamic Azad University, Mazandaran (Iran, Islamic Republic of); Khalilzadeh, Mohammad A., E-mail: khalilzadeh73@yahoo.com [Department of Chemistry, Science and Research Branch, Islamic Azad University, Mazandaran (Iran, Islamic Republic of); Ensafi, Ali A. [Department of Chemistry, Isfahan University of Technology, Isfahan (Iran, Islamic Republic of); Karimi-Maleh, Hassan, E-mail: h.karimi.maleh@gmail.com [Department of Chemistry, Science and Research Branch, Islamic Azad University, Mazandaran (Iran, Islamic Republic of); Beitollahi, Hadi [Environment Department, Research Institute of Environmental Sciences, International Center for Science, High Technology and Environmental Sciences, Kerman (Iran, Islamic Republic of); Kowsari, Elaheh [Department of Chemistry, Amirkabir University of Technology, No. 424, Hafez Avenue, Tehran (Iran, Islamic Republic of); Zareyee, Daryoush [Department of Chemistry, Qaemshahr Branch, Islamic Azad University, Qaemshahr (Iran, Islamic Republic of)

    2012-10-01

    A novel multiwall carbon nanotubes (MWCNTs) modified carbon ionic liquid electrode (CILE) was fabricated and used to investigate the electrochemical behavior of norepinephrine (NP). MWCNTs/CILE was prepared by mixing hydrophilic ionic liquid, 1-methyl-3-butylimidazolium bromide (MBIDZBr), with graphite powder, MWCNTs, and liquid paraffin. The fabricated MWCNTs/CILE showed great electrocatalytic ability to the oxidation of NE. The electron transfer coefficient, diffusion coefficient, and charge transfer resistant (R{sub ct}) of NE at the modified electrode were calculated. Differential pulse voltammetry of NE at the modified electrode exhibited two linear dynamic ranges with slopes of 0.0841 and 0.0231 {mu}A/{mu}M in the concentration ranges of 0.3 to 30.0 {mu}M and 30.0 to 450.0 {mu}M, respectively. The detection limit (3{sigma}) of 0.09 {mu}M NP was achieved. This modified electrode exhibited a good ability for well separated oxidation peaks of NE and acetaminophen (AC) in a buffer solution, pH 7.0. The proposed sensor was successfully applied for the determination of NE in human urine, pharmaceutical, and serum samples. Highlights: Black-Right-Pointing-Pointer Electrochemical behavior of norepinephrine study using carbon ionic liquid electrode Black-Right-Pointing-Pointer This sensor resolved the overlap response of norepinephrine and acetaminophen. Black-Right-Pointing-Pointer This sensor is also used for the determination of above compounds in real samples.

  4. Application of a nanostructured sensor based on NiO nanoparticles modified carbon paste electrode for determination of methyldopa in the presence of folic acid

    Science.gov (United States)

    Fouladgar, Masoud; Ahmadzadeh, Saeid

    2016-08-01

    A new method for determination of methyldopa in the presence of folic acid has been described in this work. This method is based on modification of carbon paste electrode with NiO nanoparticles and an ionic liquid (1-Butyl-3-methylimidazolium hexafluorophosphate). Electrochemical studies showed that on the surface of modified electrode, oxidation current of methyldopa has been enhanced and shifted to negative potentials. The fabricated electrode exhibited a linear response to concentration of methyldopa from 0.1 to 700.0 μmol L-1. The sensitivity of the modified electrode to methyldopa not changed in the presence of folic acid and simultaneous or independent measurements of them are possible. The performance of proposed method was investigated by determination of methyldopa in real samples.

  5. Optimization of modified carbon paste electrode with multiwalled carbon nanotube/ionic liquid/cauliflower-like gold nanostructures for simultaneous determination of ascorbic acid, dopamine and uric acid.

    Science.gov (United States)

    Afraz, Ahmadreza; Rafati, Amir Abbas; Najafi, Mojgan

    2014-11-01

    We describe the modification of a carbon paste electrode (CPE) with multiwalled carbon nanotubes (MWCNTs) and an ionic liquid (IL). Electrochemical studies by using a D-optimal mixture design in Design-Expert software revealed an optimized composition of 60% graphite, 14.2% paraffin, 10.8% MWCNT and 15% IL. The optimal modified CPE shows good electrochemical properties that are well matched with model prediction parameters. In the next step, the optimized CPE was modified with gold nanostructures by applying a double-pulse electrochemical technique. The resulting electrode was characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction, and electrochemical impedance spectroscopy. It gives three sharp and well-separated oxidation peaks for ascorbic acid (AA), dopamine (DA), and uric acid (UA). The sensor enables simultaneous determination of AA, DA and UA with linear responses from 0.3 to 285, 0.08 to 200, and 0.1 to 450 μM, respectively, and with 120, 30 and 30 nM detection limits (at an S/N of 3). The method was successfully applied to the determination of AA, DA, and UA in spiked samples of human serum and urine.

  6. Electrocatalytic determination of dopamine in the presence of uric acid using an indenedione derivative and multiwall carbon nanotubes spiked in carbon paste electrode.

    Science.gov (United States)

    Nasirizadeh, Navid; Shekari, Zahra; Zare, Hamid R; Makarem, Somayeh

    2013-04-01

    In the present study, a modified carbon paste electrode (CPE) containing multi-wall carbon nanotubes and an indenedione derivative(IMWCNT-CPE) was constructed and was successfully used for dopamine(DA) electrocatalytic oxidation and simultaneous determination of DA and uric acid (UA). Cyclic voltammograms of the IMWCNT-CPE show a pair of well-defined and reversible redox. The obtained results indicate that the peak potential of DA oxidation at IMWCNT-CPE shifted by about 65 and 185 mV toward the negative values compared with that at a MWCNT and indenedione modified CPE, respectively. The electron transfer coefficient, α, and the heterogeneous electron transfer rate constant, k', for the oxidation of DA at IMWCNT-CPE were calculated 0.4±0.01 and (1.13±0.03)×10(-3) cm s(-1), respectively. Furthermore, differential pulse voltammetry (DPV) exhibits two linear dynamic ranges of 1.9-79.4 μM, and 79.4-714.3 μM and a detection limit of 0.52 μM for DA determination. Then IMWCNT-CPE was applied to the simultaneous determination of DA and UA with DPV. Finally, the activity of the modified electrode was also investigated for determination of DA and UA in real samples, such as injection solution of DA and urine, with satisfactory results.

  7. Electrocatalytic determination of L-cysteine using a modified carbon nanotube paste electrode: Application to the analysis of some real samples

    Institute of Scientific and Technical Information of China (English)

    Malihe Ahmadipour; Mohammad Ali Taher; Hadi Beitollahi; Rahman Hosseinzadeh

    2012-01-01

    The electrooxidation of L-cysteine (L-Cys) was studied using a benzoylferrocene (BF) modified multi-wall carbon nanotube paste electrode (BFCNPE) using cyclic voltammetry (CV),square wave voltammetry (SWV) and chronoamperometry (CHA).Under optimum pH in CV the oxidation of L-Cys occurs at a potential about 215 mV less positive than that at the surface of unmodified carbon paste electrode.The catalytic oxidation peak currents were dependent on the L-Cys concentration and a linearcalibration curve was obtained in the range 0.7-350.0 μmol/L of L-Cys with SWV method.The detection limit (3σ) was determined as 0.1 μmolL.This method was also used for the determination of L-Cys in some real samples.

  8. Trace analysis of cefotaxime at carbon paste electrode modified with novel Schiff base Zn(II) complex.

    Science.gov (United States)

    Nigam, Preeti; Mohan, Swati; Kundu, Subir; Prakash, Rajiv

    2009-02-15

    Cefotaxime a third generation cephalosporin drug estimation in nanomolar concentration range is demonstrated for the first time in aqueous and human blood samples using novel Schiff base octahedral Zn(II) complex. The cefotaxime electrochemistry is studied over graphite paste and Zn(II) complex modified graphite paste capillary electrodes in H(2)SO(4) (pH 2.3) using cyclic voltammetry and differential pulse voltammetry. Cefotaxime enrichment is observed over Zn(II) complex modified graphite paste electrode probably due to interaction of functional groups of cefotaxime with Zn(II) complex. Possible interactions between metal complex and cefotaxime drug is examined by UV-vis and electrochemical quartz crystal microbalance (EQCM) techniques and further supported by voltammetric analysis. Differential pulse voltammetry (DPV) with modified electrode is applied for the determination of cefotaxime in acidified aqueous and blood samples. Cefotaxime estimation is successfully demonstrated in the range of 1-500 nM for aqueous samples and 0.1-100 microM in human blood samples. Reproducibility, accuracy and repeatability of the method are checked by triplicate reading for large number of samples. The variation in the measurements is obtained less than 10% without any interference of electrolyte or blood constituents.

  9. Electrochemical response of carbon paste electrode modified with mixture of titanium dioxide/zirconium dioxide in the detection of heavy metals: lead and cadmium.

    Science.gov (United States)

    Nguyen, Phuong Khanh Quoc; Lunsford, Suzanne K

    2012-11-15

    A novel carbon modified electrode was developed by incorporating titanium dioxide/zirconium dioxide into the graphite carbon paste electrode to detect heavy metals-cadmium and lead. In this work, the development of the novel titanium dioxide/zirconium dioxide modified carbon paste electrode was studied to determine the optimum synthesis conditions related to the temperature, heating duration, amount and ratio of titanium dioxide/zirconium dioxide, and amount of surfactant, to create the most reproducible results. Using cyclic voltammetric (CV) analysis, this study has proven that the novel titanium dioxide/zirconium dioxide can be utilized to detect heavy metals-lead and cadmium, at relatively low concentrations (7.6×10(-6) M and 1.1×10(-5) M for Pb and Cd, respectively) at optimum pH value (pH=3). From analyzing CV data the optimal electrodes surface area was estimated to be 0.028 (±0.003) cm(2). Also, under the specific experimental conditions, electron transfer coefficients were estimated to be 0.44 and 0.33 along with the heterogeneous electron transfer rate constants of 5.64×10(-3) and 2.42×10(-3) (cm/s) for Pb and Cd, respectively.

  10. Construction and evaluation of a carbon paste electrode modified with polyaniline-co-poly(dithiodianiline) for enhanced stripping voltammetric determination of metal ions

    OpenAIRE

    Somerset, Vernon; Silwana, Bongiwe; Horst, Charlton van der; Iwuoha, Emmanuel

    2014-01-01

    A modified carbon paste electrodes (MCPE) have been prepared in this study as an alternative “mercury-free” electrochemical sensor for the determination of Pb2+ and Cd2+ metal ions in aqueous solutions. CPE containing a conducting copolymer of polyaniline-co-poly(2,2'- dithiodianiline) (PANI-co-PDTDA) was used as a modified substrate transducer to achieve enhanced selectivity in stripping voltammetric analysis. The experimental conditions optimised included the supporting electrolyte pH, d...

  11. Comparison of lead dioxide and cerium dioxide as mediators for carbon paste electrodes in flow injection-amperometric detection of hydrogen peroxide

    OpenAIRE

    Mihić-Necin, Bojana; Guzsvány, Valéria; Kalcher, Kurt

    2010-01-01

    Carbon paste electrodes (graphite / paraffin oil), bulk-modified with lead dioxide and cerium dioxide, were used as sensors for the amperometric determination of hydrogen peroxide in flow injection analysis. Experimental parameters, such as applied working potential, flow rate of the carrier and injection volume were optimized with a thin-layer flow-through cell. The method was validated with respect to calibration curve, linear dynamic range, detection limit, repeatability and...

  12. Optimization of modified carbon paste electrode with multiwalled carbon nanotube/ionic liquid/cauliflower-like gold nanostructures for simultaneous determination of ascorbic acid, dopamine and uric acid

    Energy Technology Data Exchange (ETDEWEB)

    Afraz, Ahmadreza [Department of Physical Chemistry, Faculty of Chemistry, Bu-Ali Sina University, P.O. Box 65174, Hamedan (Iran, Islamic Republic of); Rafati, Amir Abbas, E-mail: aa_rafati@basu.ac.ir [Department of Physical Chemistry, Faculty of Chemistry, Bu-Ali Sina University, P.O. Box 65174, Hamedan (Iran, Islamic Republic of); Najafi, Mojgan [Department of Materials Engineering, Hamedan University of Technology (HUT), 65169 Hamedan (Iran, Islamic Republic of)

    2014-11-01

    We describe the modification of a carbon paste electrode (CPE) with multiwalled carbon nanotubes (MWCNTs) and an ionic liquid (IL). Electrochemical studies by using a D-optimal mixture design in Design-Expert software revealed an optimized composition of 60% graphite, 14.2% paraffin, 10.8% MWCNT and 15% IL. The optimal modified CPE shows good electrochemical properties that are well matched with model prediction parameters. In the next step, the optimized CPE was modified with gold nanostructures by applying a double-pulse electrochemical technique. The resulting electrode was characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction, and electrochemical impedance spectroscopy. It gives three sharp and well-separated oxidation peaks for ascorbic acid (AA), dopamine (DA), and uric acid (UA). The sensor enables simultaneous determination of AA, DA and UA with linear responses from 0.3 to 285, 0.08 to 200, and 0.1 to 450 μM, respectively, and with 120, 30 and 30 nM detection limits (at an S/N of 3). The method was successfully applied to the determination of AA, DA, and UA in spiked samples of human serum and urine. - Highlights: • New method for simultaneous determination of AA, DA and UA was developed. • MWCNT/ionic liquid/cauliflower-like Au nanostructure was used for CPE modification. • Optimization of electrode composition was done by Design-Expert software. • The pH effect, peak separation mechanism and real samples was thoroughly studied.

  13. Composite carbon foam electrode

    Energy Technology Data Exchange (ETDEWEB)

    Mayer, S.T.; Pekala, R.W.; Kaschmitter, J.L.

    1997-05-06

    Carbon aerogels used as a binder for granulated materials, including other forms of carbon and metal additives, are cast onto carbon or metal fiber substrates to form composite carbon thin film sheets. The thin film sheets are utilized in electrochemical energy storage applications, such as electrochemical double layer capacitors (aerocapacitors), lithium based battery insertion electrodes, fuel cell electrodes, and electrocapacitive deionization electrodes. The composite carbon foam may be formed by prior known processes, but with the solid particles being added during the liquid phase of the process, i.e. prior to gelation. The other forms of carbon may include carbon microspheres, carbon powder, carbon aerogel powder or particles, graphite carbons. Metal and/or carbon fibers may be added for increased conductivity. The choice of materials and fibers will depend on the electrolyte used and the relative trade off of system resistivity and power to system energy. 1 fig.

  14. Composite carbon foam electrode

    Energy Technology Data Exchange (ETDEWEB)

    Mayer, Steven T. (San Leandro, CA); Pekala, Richard W. (Pleasant Hill, CA); Kaschmitter, James L. (Pleasanton, CA)

    1997-01-01

    Carbon aerogels used as a binder for granularized materials, including other forms of carbon and metal additives, are cast onto carbon or metal fiber substrates to form composite carbon thin film sheets. The thin film sheets are utilized in electrochemical energy storage applications, such as electrochemical double layer capacitors (aerocapacitors), lithium based battery insertion electrodes, fuel cell electrodes, and electrocapacitive deionization electrodes. The composite carbon foam may be formed by prior known processes, but with the solid particles being added during the liquid phase of the process, i.e. prior to gelation. The other forms of carbon may include carbon microspheres, carbon powder, carbon aerogel powder or particles, graphite carbons. Metal and/or carbon fibers may be added for increased conductivity. The choice of materials and fibers will depend on the electrolyte used and the relative trade off of system resistivty and power to system energy.

  15. Carbon paste electrode incorporating multi-walled carbon nanotube/ferrocene as a sensor for the electroanalytical determination of -acetyl--cysteine in the presence of tryptophan

    Indian Academy of Sciences (India)

    Jahan Bakhsh Raoof; Fereshteh Chekin; Reza Ojani; Saeideh Barari

    2013-03-01

    The preparation and electrochemical performance of the carbon nanotube paste electrode modified with ferrocene (FCMCNPE) was investigated for electrocatalytic behaviour toward oxidation of -acetyl--cysteine (NAC) in the presence of tryptophan (Trp) using cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The results showed an efficient electrocatalytic activity of FCMCNPE toward oxidation of NAC and Trp, as the electrooxidation of NAC and Trp together gave two well-defined anodic peaks, revealing the applicability of this modified electrode for simultaneous voltammetric detection of mentioned compounds in the same solution. The values of catalytic rate constant () and the apparent diffusion coefficient (Dapp) were also calculated using chronoamperometry. The DPV method was applied as a sensitive method for the quantitative detection of trace amounts of NAC and Trp. A linear dynamic range from 1.0 to 18.0 M for NAC and 2.0 to 150.0 M for Trp was obtained using DPV method in pH 7.00 buffered solution and the detection limit (3) was determined as 0.49 M and 0.54 M for NAC and Trp, respectively. The proposed method was also applied for analysis of NAC tablet, investigating the applicability of the proposed voltammetric method for determination of NAC in real sample.

  16. A simple and efficient electrochemical sensor for folic acid determination in human blood plasma based on gold nanoparticles–modified carbon paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Arvand, Majid, E-mail: arvand@guilan.ac.ir; Dehsaraei, Mohammad

    2013-08-01

    Folic acid (FA) is a water soluble vitamin that exists in many natural species. The lack of FA causes some deficiencies in human body, so finding a simple and sensitive method for determining the FA is important. A new chemically modified electrode was fabricated for determination of FA in human blood plasma using gold nanoparticles (AuNPs) and carbon paste electrode (CPE). Gold nanoparticles–modified carbon paste electrode (AuNPs/CPE) was characterized by transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The experimental parameters such as pH, scan rate (ν) and amount of modifier were studied by cyclic voltammetry and the optimized values were chosen. The electrochemical parameters such as diffusion coefficient of FA (D{sub FA}), electrode surface area (A) and electron transfer coefficient (α) were calculated. Square wave voltammetry as an accurate technique was used for quantitative calculations. A good linear relation was observed between anodic peak current (i{sub pa}) and FA concentration (C{sub FA}) in the range of 6 × 10{sup −8} to 8 × 10{sup −5} mol L{sup −1}, and the detection limit (LOD) achieved 2.7 × 10{sup −8} mol L{sup −1}, that is comparable with recently studies. This paper demonstrated a novel, simple, selective and rapid sensor for determining the FA in the biological samples. - Highlights: • We examine a AuNPs/CPE for direct electrooxidation behavior and determination of FA. • Characterization of the electrode showed an obvious increase in surface area and porosity after modification. • The modified electrode showed good ability to distinguish the electrochemical response of FA. • The results were attributed to the specific characteristics of AuNPs present in the AuNPs/CPE. • This paper demonstrated a simple and rapid sensor for determination of FA in plasma.

  17. Electrocatalytic determination of dopamine in the presence of uric acid using an indenedione derivative and multiwall carbon nanotubes spiked in carbon paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Nasirizadeh, Navid, E-mail: nasirizadeh@yahoo.com [Scientific Society of Nanotechnology, Yazd Branch, Islamic Azad University, Yazd (Iran, Islamic Republic of); Department of Textile Engineering, Yazd Branch, Islamic Azad University, Yazd (Iran, Islamic Republic of); Shekari, Zahra [Scientific Society of Nanotechnology, Yazd Branch, Islamic Azad University, Yazd (Iran, Islamic Republic of); Zare, Hamid R. [Department of Chemistry, Yazd University, P.O. Box 89195-741, Yazd (Iran, Islamic Republic of); Makarem, Somayeh [Department of Chemistry, Faculty of Sciences, ShahidBeheshti University, G. C., P. O. Box 19839-4716, Tehran (Iran, Islamic Republic of)

    2013-04-01

    In the present study, a modified carbon paste electrode (CPE) containing multi-wall carbon nanotubes and an indenedione derivative(IMWCNT−CPE) was constructed and was successfully used for dopamine(DA) electrocatalytic oxidation and simultaneous determination of DA and uric acid (UA). Cyclic voltammograms of the IMWCNT−CPE show a pair of well-defined and reversible redox. The obtained results indicate that the peak potential of DA oxidation at IMWCNT−CPE shifted by about 65 and 185 mV toward the negative values compared with that at a MWCNT and indenedione modified CPE, respectively. The electron transfer coefficient, α, and the heterogeneous electron transfer rate constant, k′, for the oxidation of DA at IMWCNT−CPE were calculated 0.4 ± 0.01 and (1.13 ± 0.03) × 10{sup −3} cm s{sup −1}, respectively. Furthermore, differential pulse voltammetry (DPV) exhibits two linear dynamic ranges of 1.9–79.4 μM, and 79.4–714.3 μM and a detection limit of 0.52 μM for DA determination. Then IMWCNT−CPE was applied to the simultaneous determination of DA and UA with DPV. Finally, the activity of the modified electrode was also investigated for determination of DA and UA in real samples, such as injection solution of DA and urine, with satisfactory results. - Highlights: ► According to referee's comment we have omitted references 33–35. ► Fig. 1 of the revised manuscript was improved based on referee comment. ► We have calculated the effective areas of MWCNT−CPE and unmodified CPE. ► Differential pulse voltammetry was used to estimate the quantitative parameters. ► Based on referee comment, the necessary corrections at the references list were mad.

  18. Voltammetric sensor for D-penicillamine determination based on its electrocatalytic oxidation at the surface of ferrocenes modified carbon paste electrodes

    Indian Academy of Sciences (India)

    Jahan-Bakhsh Raoof; Reza Ojani; Fereshteh Chekin

    2009-11-01

    Electrocatalytic oxidation of D-penicillamine (D-PA) at the surface of ferrocene modified carbon paste electrode (FCCPE) was thoroughly investigated in aqueous solution with various pH. The performance of this modified electrode was compared with those of 2,7-bis(ferrocenyl ethyl) fluoren-9-one modified carbon paste electrode (2,7-BFEFMCPE). In the optimum condition, the oxidation of D-PA at the surface of FCCPE and 2,7-BFEFMCPE is occurred about 480 and 320 mV less positive than that unmodified carbon paste electrode, respectively. The linear dynamic ranges 6 × 10-5 M-2 × 10-3 M, 6.5 × 10-5 M-1.1 × 10-3 M and 7 × 10-6 M-1.6 × 10-4M, 7 × 10-6 M-2 × 10-4 M of D-PA are obtained from CV and DPV methods for FCCPE and 2,7-BFEFMCPE, respectively. The detection limits (3) were determined as 5.4 × 10-5 M and 6.3 × 10-5 M in CV and 6.2 × 10-6 M and 6.8 × 10-6 M in DPV determinations for FCCPE and 2,7-BFEFMCPE, respectively. The proposed method was applied in a highly sensitive determination of D-PA in drug and human synthetic serum samples by standard addition and recovery methods, respectively.

  19. Voltammetric determination of isoproterenol using a 5-amino-2′,4′-dimethoxybiphenyl-2-ol modified carbon nanotube paste electrode

    Institute of Scientific and Technical Information of China (English)

    Hadi Beitollahi; Hojatollah Khabazzadeh; Hassan Karimi-Maleh; Ali Akbari

    2012-01-01

    A new electrochemical sensor for determination ofisoproterenol (IP) is described.The sensor is based on carbon paste electrode (CPE) modified with 5-amino-2',4'-dimethoxybiphenyl-2-ol (5ADMB) and takes the advantages of carbon nanotubes (CNTs).Under the optimum pH of 7.0,the oxidation of IP occurs at a potential about 210 mV less positive than that of the unmodified CPE.The oxidation currents increased linearly with two concentration intervals of IP,one is 0.09 to 20.0 μmol/L and,the other is 20.0 to 400.0 μmol/L.The detection limit (3σ) obtained by square wave voltammetry (SWV) was 39.0 nmol/L.The practical application of the modified electrode was demonstrated by determining IP in IP ampoule,urine and human blood serum samples.

  20. Determination of Lead Ion by a Modified Carbon Paste Electrode Based on Multi-Walled Carbon Nanotubes (MWCNTs and Ligand (N-(4-Hydroxyphenyl Ethanamide

    Directory of Open Access Journals (Sweden)

    Marzieh Bagheri

    2015-06-01

    Full Text Available The preparation of a new modified carbon paste electrode (CPE to measure lead ion has been reported in this study. Lead is a highly toxic element which can have a negative impact on the environment. Therefore, measurement of lead in aquatic environments is very important. Although several methods have been developed for determination of lead ion in aquatic environments, there is no a cheap, simple, accurate and rapid method to measure this ion. Aim of this study is to develop a new method to measure the lead based on using multi walls carbon nanotubes (MWCNTs and Paracetamol as an ionophore for modification of a CPE. The optimum composition of modified CPE was determined as 64% of graphite powder, 20% of paraffin oil, 12% of nanotube and 4% of ionophore. This optimum composition was shown high selectivity, with appropriate Nernestian slope (-29.73 mV/decade, linear range (from 1.0×10-1to 1.0×10-8M, low lead concentration detection limit (7.5×10-9M and good response time (equal of 25 sec.The results of this study to introduce a cheap, accurate and simple method for determination of lead ion in aquatic environments.

  1. Determination of Lead Ion by a Modified Carbon Paste Electrode Based on Multi-Walled Carbon Nanotubes (MWCNTs andLigand (N-(4-Hydroxyphenyl Ethanamide

    Directory of Open Access Journals (Sweden)

    Marzieh Bagheri

    2015-06-01

    Full Text Available The preparation of a new modified carbon paste electrode (CPEto measure lead ion has been reported in this study. Lead is a highly toxic element which can have a negative impact on the environment. Therefore, measurement of lead in aquatic environments is very important. Although several methods have been developed for determination of lead ion in aquatic environments, there is no a cheap, simple, accurate and rapid method to measure this ion. Aim of this study is to develop a new method to measure the lead based on using multi walls carbon nanotubes (MWCNTs and Paracetamol as an ionophore for modificationof a CPE.The optimum composition of modified CPE was determined as 64% of graphite powder, 20% of paraffin oil, 12% of nanotube and 4% of ionophore.This optimum composition was shown high selectivity, with appropriate Nernestian slope (-29.73 mV/decade, linear range (from 1.0×10-1to 1.0×10-8M, low lead concentration detection limit (7.5×10-9M and good response time (equal of 25 sec.The results of this study to introduce a cheap, accurate and simple method for determination of lead ion in aquatic environments.

  2. 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.

  3. Homogeneous and nanomolar detection of hydrazine by indigocarmine as a mediator at the surface of TiO2 nanoparticles modified carbon paste electrode

    Institute of Scientific and Technical Information of China (English)

    Mohammad Mazloum-Ardakani; Hossein Rajabi; Hadi Beitollahi

    2012-01-01

    The homogeneous electrocatalytic oxidation of hydrazine (HZ) has been studied by indigocarmine (IND) as a mediator at the surface of TiO2 nanoparticles modified carbon paste electrode (TNMCPE).Cyclic voltammetry was used to study the electrochemical behavior of IND at different scan rates.The voltammetric response of the modified electrode was linear against the concentration of HZ in the ranges of 3.0 × 10-8-7.0 × 10 -6 mol/L with differential pulse voltammetry method.The detection limit (3σ) was determined as 27.3 nmoL/L.To evaluate the applicability of the proposed method to real samples,the modified CPE was applied to the determination of HZ in water samples.

  4. Study on electrochemical behaviors and the reaction mechanisms of dopamine and epinephrine at the pre-anodized inlaying ultrathin carbon paste electrode with nichrome as a substrate.

    Science.gov (United States)

    Huo, Jing'e; Li, Jing; Li, Quanmin

    2013-01-01

    In this paper, nichrome was adopted as a substrate, to fabricate the pre-anodized inlaying ultrathin carbon paste electrode (PAIUCPE). The electrochemical behaviors of dopamine (DA) and epinephrine (EP) at the electrode were investigated by cyclic voltammetry (CV). The reaction mechanisms of DA and EP have also been put forward. It was found that the electrode showed an excellent electrochemical behavior for electrode reaction of DA and EP. The cathodic potential difference of DA and EP was about 370 mV and the simultaneous determination of DA and EP was achieved based on it. The reduction peak current was proportional to the DA and EP concentrations in the range of 8.0×10(-7)-3.0×10(-4) M and 2.0×10(-6)-1.5×10(-4) M with the detection limits of 1.70×10(-7) M and 3.27×10(-7) M, respectively. Because the oxidation of ascorbic acid (AA) is an irreversible reaction at the PAIUCPE, the interferences of AA for determining DA and EP were eliminated. The method has been successfully applied to the determination of DA and EP in hydrochloride injection with satisfactory results.

  5. Simultaneous trace-levels determination of Hg(II) and Pb(II) ions in various samples using a modified carbon paste electrode based on multi-walled carbon nanotubes and a new synthesized Schiff base

    Energy Technology Data Exchange (ETDEWEB)

    Afkhami, Abbas, E-mail: afkhami@basu.ac.ir [Faculty of Chemistry, Bu-Ali Sina University, Hamedan (Iran, Islamic Republic of); Bagheri, Hasan [Department of Chemistry, Takestan Branch, Islamic Azad University, Takestan (Iran, Islamic Republic of); Khoshsafar, Hosein [Faculty of Chemistry, Bu-Ali Sina University, Hamedan (Iran, Islamic Republic of); Saber-Tehrani, Mohammad [Department of Chemistry, Science and Research Branch, Islamic Azad University, Tehran (Iran, Islamic Republic of); Tabatabaee, Masoumeh [Department of Chemistry, Yazd Branch, Islamic Azad University, Yazd (Iran, Islamic Republic of); Shirzadmehr, Ali [Faculty of Chemistry, Bu-Ali Sina University, Hamedan (Iran, Islamic Republic of)

    2012-10-09

    Highlights: Black-Right-Pointing-Pointer A new chemically modified carbon paste electrode was constructed and used. Black-Right-Pointing-Pointer A new Schiff base and multi-walled carbon nanotube was used as a modifier. Black-Right-Pointing-Pointer The electrochemical properties of the modified electrode were studied. Black-Right-Pointing-Pointer The electrode was used to the simultaneous determination of Pb{sup 2+} and Hg{sup 2+}. - Abstract: A modified carbon paste electrode based on multi-walled carbon nanotubes (MWCNTs) and 3-(4-methoxybenzylideneamino)-2-thioxothiazolodin-4-one as a new synthesized Schiff base was constructed for the simultaneous determination of trace amounts of Hg(II) and Pb(II) by square wave anodic stripping voltammetry. The modified electrode showed an excellent selectivity and stability for Hg(II) and Pb(II) determinations and for accelerated electron transfer between the electrode and the analytes. The electrochemical properties and applications of the modified electrode were studied. Operational parameters such as pH, deposition potential and deposition time were optimized for the purpose of determination of traces of metal ions at pH 3.0. Under optimal conditions the limits of detection, based on three times the background noise, were 9.0 Multiplication-Sign 10{sup -4} and 6.0 Multiplication-Sign 10{sup -4} {mu}mol L{sup -1} for Hg(II) and Pb(II) with a 90 s preconcentration, respectively. In addition, the modified electrode displayed a good reproducibility and selectivity, making it suitable for the simultaneous determination of Hg(II) and Pb(II) in real samples such as sea water, waste water, tobacco, marine and human teeth samples.

  6. A novel sensor based on electropolymerization of β-cyclodextrin and L-arginine on carbon paste electrode for determination of fluoroquinolones

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Fenfen [School of Materials Science and Engineering, Shanghai University, Shanghai 200444 (China); Gu, Shuqing [Department of Chemistry, Shanghai University, Shanghai 200444 (China); School of Materials Science and Engineering, Shanghai University, Shanghai 200444 (China); Ding, Yaping, E-mail: wdingyp@sina.com [Department of Chemistry, Shanghai University, Shanghai 200444 (China); School of Materials Science and Engineering, Shanghai University, Shanghai 200444 (China); Zhang, Zhen [School of Materials Science and Engineering, Shanghai University, Shanghai 200444 (China); School of Chemistry and Chemical Engineering, Linyi University, 18 TongDa Road, Linyi 276005 (China); Li, Li [Department of Chemistry, Shanghai University, Shanghai 200444 (China)

    2013-04-03

    Graphical abstract: The inner cavities of β-CD could restrain fluoroquinolones to form stable host–guest inclusion complexes, and the guanidyl group of L-arg could enable L-arg to form electrostatic interactions with negatively charged groups -COO{sup −} of fluoroquinolones. Highlights: ► Electropolymerization of β-cyclodextrin and L-arginine on carbon paste electrode. ► The electrooxidation and reaction of FQs on the modified CPE were surmised. ► The sensor is used to detect ciprofloxacin, ofloxacin, norfloxacin and gatifloxacin. ► Determine FQs drugs in pharmaceutical formulations and human serum samples. ► It showed high stability, repeatability, reproducibility, good sensitivity. -- Abstract: An electrochemical sensor for fluoroquinolones (FQs) based on polymerization of β-cyclodextrin (β-CD) and L-arginine (L-arg) modified carbon paste electrode (CPE) (P-β-CD-L-arg/CPE) was built for the first time. Synergistic effect of L-arg and β-CD was used to construct this sensor for quantification of these important antibiotics. Scanning electron microscope (SEM) image shows that polymer of β-CD and L-arg has been successfully modified on electrode. Electrochemical impedance spectroscopy (EIS) and cyclic voltammograms (CV) further indicate that polymer of β-CD and L-arg efficiently decreased the charge transfer resistance value of electrode and improved the electron transfer kinetic between analyte and electrode. Under the optimized conditions, this modified electrode was utilized to determine the concentrations of ciprofloxacin, ofloxacin, norfloxacin and gatifloxacin. The differential pulse voltammogram (DPV) exhibits the oxidation peak currents were linearly proportional to their concentration in the range of 0.05–100 μM for ciprofloxacin, 0.1–100 μM for ofloxacin, 0.1–40 μM for norfloxacin and 0.06–100 μM for gatifloxacin, respectively. This method was also successfully used to detect the concentrations of each drug in

  7. Voltammetric Detection of Diquat at the Carbon Paste Electrode Containing a Ca10(PO46(OH2

    Directory of Open Access Journals (Sweden)

    Moulay Abderrahim EL MHAMMEDI

    2007-01-01

    Full Text Available We report a sensitive electrochemical voltammetric method for analyzing diquat (DQ ions using a carbon paste electrochemical (CPE modified by porous material, such as hydroxyapatite (HAP. Diquat strongly adsorbed on a HAP-CPE surface and provides facile electrochemical quantitative methods for electroactive DQ ions. Operational parameters have been optimized, and the stripping voltammetric performance has been studied using square wave voltammetry. The peaks current intensity are highly linear over the 7×10-7–3×10-4 mol L-1 diquat range examined (10-min accumulation time, with a good sensitivity. These findings can lead to a widespread use of electrochemical sensors to detect DQ contaminates.Scanning electron microscopy was used for morphology observation and in particular the X-ray diffraction analysis (XRD and Fourier transformed infrared spectroscopy (FTIR analysis for characterization of synthesis powder.

  8. A solid paraffin-based carbon paste electrode modified with 2-aminothiazole organofunctionalized silica for differential pulse adsorptive stripping analysis of nickel in ethanol fuel

    Energy Technology Data Exchange (ETDEWEB)

    Takeuchi, Regina M. [Departamento de Quimica Analitica, Instituto de Quimica, UNESP, CP 355, 14801-970 Araraquara, SP (Brazil)]. E-mail: takeuchi@iq.unesp.br; Santos, Andre L. [Departamento de Quimica Analitica, Instituto de Quimica, UNESP, CP 355, 14801-970 Araraquara, SP (Brazil); Padilha, Pedro M. [Departamento de Quimica e Bioquimica-IB/UNESP, CP 510, 18618-000 Botucatu, SP (Brazil); Stradiotto, Nelson R. [Departamento de Quimica Analitica, Instituto de Quimica, UNESP, CP 355, 14801-970 Araraquara, SP (Brazil)

    2007-02-19

    A solid paraffin-based carbon paste electrode modified with 2-aminothiazole organofunctionalized silica (SiAt-SPCPE) was applied to Ni{sup 2+} determination in commercial ethanol fuel samples. The proposed method comprised four steps: (1) Ni{sup 2+} preconcentration at open circuit potential directly in the ethanol fuel sample, (2) transference of the electrode to an electrochemical cell containing DMG, (3) differential pulse voltammogram registering and (4) surface regeneration by polishing the electrode. The proposed method combines the high Ni{sup 2+} adsorption capacity presented by 2-aminothiazole organofunctionalized silica with the electrochemical properties of the Ni(DMG){sub 2} complex, whose electrochemical reduction provides the analytical signal. All experimental parameters involved in the proposed method were optimized. Using a preconcentration time of 20 min, it was obtained a linear range from 7.5 x 10{sup -9} to 1.0 x 10{sup -6} mol L{sup -1} with detection limit of 2.0 x 10{sup -9} mol L{sup -1}. Recovery values between 96.5 and 102.4% were obtained for commercial samples spiked with 1.0 {mu}mol L{sup -1} Ni{sup 2+} and the developed electrode was totally stable in ethanolic solutions. The contents of Ni{sup 2+} found in the commercial samples using the proposed method were compared to those obtained by graphite furnace atomic absorption spectroscopy by using the F- and t-test. Neither the F- nor t-values exceeded the critical values at 95% confidence level, confirming that there are not statistical differences between the results obtained by both methods. These results indicate that the developed electrode can be successfully employed to reliable Ni{sup 2+} determination in commercial ethanol fuel samples without any sample pretreatment or dilution step.

  9. Electroanalysis and simultaneous determination of dopamine and epinephrine at poly(isonicotinic acid)-modified carbon paste electrode in the presence of ascorbic acid

    Institute of Scientific and Technical Information of China (English)

    Yuan Zhen Zhou; Li Juan Zhang; Shuang Li Chen; She Ying Dong; Xiao Hui Zheng

    2009-01-01

    A carbon paste electrode modified with electropolymerized fills of isonicotinic acid was developed.The modified electrode shows excellent electrocatalytic activity toward the oxidation of both dopamine(DA)and epinephrine(EP).Separation of the reduction peak potentials for dopamine and epinephrine was about 357 mV in pH 5.3 phosphate buffer solution(PBS)and the character was used for the detection DA and EP simultaneously.The peak currents increase linearly with DA and EP concentration over the range of 8.0×10-5 to 7.0×10-4 mol/L and 5.0×10-6 to 1.0×10-4 mol/L with detection limits of 2 × 10-5 and 1×10-6 mol/L,respectively.The interference studies showed that the modified electrode exhibits excellent selectivity in the presence of large excess of ascorbic acid(AA).

  10. Adsorptive stripping voltammetric determination of imipramine, trimipramine and desipramine employing titanium dioxide nanoparticles and an Amberlite XAD-2 modified glassy carbon paste electrode.

    Science.gov (United States)

    Sanghavi, Bankim J; Srivastava, Ashwini K

    2013-03-07

    An Amberlite XAD-2 (XAD2) and titanium dioxide nanoparticles (TNPs) modified glassy carbon paste electrode (XAD2-TNP-GCPE) was developed for the determination of imipramine (IMI), trimipramine (TRI) and desipramine (DES). The electrochemical behavior of these molecules was investigated employing cyclic voltammetry (CV), chronocoulometry (CC), electrochemical impedance spectroscopy (EIS) and adsorptive stripping differential pulse voltammetry (AdSDPV). After optimization of analytical conditions using a XAD2-TNP-GCPE electrode at pH 6.0 phosphate buffer (0.1 M), the peak currents were found to vary linearly with its concentration in the range of 1.30 × 10(-9) to 6.23 × 10(-6) M for IMI, 1.16 × 10(-9) to 6.87 × 10(-6) M for TRI and 1.43 × 10(-9) to 5.68 × 10(-6) M for DES. The detection limits (S/N = 3) of 3.93 × 10(-10), 3.51 × 10(-10) and 4.35 × 10(-10) M were obtained for IMI, TRI and DES respectively using AdSDPV. The prepared modified electrode showed several advantages such as a simple preparation method, high sensitivity, very low detection limits and excellent reproducibility. The proposed method was employed for the determination of IMI, TRI and DES in pharmaceutical formulations, blood serum and urine samples.

  11. Electroanalysis and simultaneous determination of 6-thioguanine in the presence of uric acid and folic acid using a modified carbon nanotube paste electrode.

    Science.gov (United States)

    Beitollahi, Hadi; Raoof, Jahan-Bakhsh; Hosseinzadeh, Rahman

    2011-01-01

    The present work describes the preparation and characterization of a carbon nanotube paste electrode modified with 2,7-bis(ferrocenyl ethyl)fluoren-9-one (2,7-BF). This electrode showed an efficient catalytic activity for the electro-oxidation of 6-thioguanine (6-TG), which leads to lowering 6-TG overpotential by more than 610 mV. Also, the values of catalytic rate constant (k = 2.7 × 10(3) mol(-1) L s(-1)), and diffusion coefficient (D = 2.7 × 10(-5) cm(2) s) were calculated. In 0.1 M phosphate buffer solution of pH 7.0, the oxidation current increased linearly with two concentration intervals of 6-TG, one is 0.06 to 10.0 µmol L(-1) and the other is 10.0 to 160.0 µmol L(-1). The detection limit (3σ) obtained by differential pulse voltammetry (DPV) was 22.0 nmol L(-1). DPV was used for simultaneous determination of 6-TG, uric acid (UA) and folic acid (FA) at the modified electrode, and for quantification of 6-TG, UA and FA in some real samples by the standard addition method.

  12. Multivariate curve resolution-alternating least squares assisted by voltammetry for simultaneous determination of betaxolol and atenolol using carbon nanotube paste electrode.

    Science.gov (United States)

    Khoobi, Asma; Ghoreishi, Sayed Mehdi; Masoum, Saeed; Behpour, Mohsen

    2013-12-01

    In the present work differential pulse voltammetry coupled with multivariate curve resolution-alternating least squares (MCR-ALS) was applied for simultaneous determination of betaxolol (Bet) and atenolol (Ate) in 0.20 M Britton-Robinson (B-R) buffer solution at the surface of a multi-walled carbon nanotube modified carbon paste electrode (MWCNT/CPE). Characterization of the modified electrode was carried out by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). A strategy based on experimental design was followed. Operating conditions were improved with central composite rotatable design (CCRD) and response surface methodology (RSM), involving several chemical and instrumental parameters. Then second order data were built from variable pulse heights of DPV and after correction in potential shift analyzed by MCR-ALS. Analytical parameters such as linearity, repeatability, and stability were also investigated and a detection limit (DL) of 0.19 and 0.29 μM for Bet and Ate was achieved, respectively. The proposed method was successfully applied in simultaneous determining the two analytes in human plasma.

  13. A novel electrochemical sensor based on magneto Au nanoparticles/carbon paste electrode for voltammetric determination of acetaminophen in real samples

    Energy Technology Data Exchange (ETDEWEB)

    Haghshenas, Esmaeel; Madrakian, Tayyebeh, E-mail: madrakian@basu.ac.ir; Afkhami, Abbas

    2015-12-01

    An electrochemical magneto Au nanoparticles/carbon paste electrodes (MAuNP/CPE) which is used for the determination of acetaminophen (AC) in real samples was developed. Initially, Au nanoparticles were immobilized at the surface of Fe{sub 3}O{sub 4} (AuNPs@Fe{sub 3}O{sub 4}), which was used as a sorbent for capturing AC molecules. After adding AuNPs@Fe{sub 3}O{sub 4} to the AC solution and stirring for 20 min, the AuNPs@Fe{sub 3}O{sub 4} was gathered on the magneto electrode based on its magnetic field. The AC molecules which became adsorbed at AuNPs@Fe{sub 3}O{sub 4} were analyzed by differential pulse voltammetry (DPV). For characterization and investigation of the performance of AuNPs@Fe{sub 3}O{sub 4} and MAuNPs/CPE, various methods, including scanning electron microscopy, X-ray diffraction, UV–Vis spectroscopy, electrochemical impedance spectroscopy, cyclic voltammetry and DPV were used. Under the optimized conditions, the anodic peak current was linear to the concentration of AC in the range of 0.1 to 70.0 μmol L{sup −1} with the detection limit of 4.5 × 10{sup −2} μmol L{sup −1}. This method was also successfully used to detect the concentration of AC in pharmaceutical formulations and human serum samples. In addition, the proposed magneto sensor exhibited good reproducibility, long-term stability and fast current response. - Highlights: • Magneto Au nanoparticle/carbon paste electrode was fabricated. • Au nanoparticles were immobilized at the surface of Fe{sub 3}O{sub 4} (AuNPs@Fe{sub 3}O{sub 4}). • It is the first time AuNPs@Fe{sub 3}O{sub 4} and magneto electrode are used for the determination of AC. • The proposed sensor showed a wide linear range, low detection limit, and high sensitivity. • This sensor is also used for the determination of AC in real samples.

  14. Determination of ultra-trace amounts of silver in water by differential pulse anodic stripping voltammetry using a new modified carbon paste electrode.

    Science.gov (United States)

    El-Mai, Hafida; Espada-Bellido, Estrella; Stitou, Mostafa; García-Vargas, Manuel; Galindo-Riaño, Maria Dolores

    2016-05-01

    A highly sensitive and selective new procedure for the determination of silver in aqueous media was developed using a modified carbon paste electrode (MCPE) by differential pulse anodic stripping voltammetry (DPASV). The modified electrode was based on the incorporation of 2-hydroxybenzaldehyde benzoylhydrazone (2-HBBH) in the carbon paste electrode. Silver ions were preconcentrated on the modified electrode at open-circuit by complexation with the ligand and reduced to zero valent at a potential of 0V, and followed by the reoxidation of adsorbed ions onto the electrode by scanning the potential in a positive direction. The oxidation peak of Ag(I) was observed at 0.2V (versus Ag/AgCl). The analysis of Ag(I) was carried out in a cell containing the sample solution (20mL) buffered by 0.1molL(-1) K2HPO4/NaOH at pH 5.5 in aqueous solution and nitric acid (pH 1) in real water samples. The optimum conditions for the analysis of silver include a reduction potential of 0V and a pulse amplitude of 100mV, among others. The optimum carbon paste composition was found to be 14.1% (w/w) 2-HBBH, 56.2% (w/w) graphite powder and 29.7% (w/w) paraffin oil. Differential pulse anodic stripping voltammetric response was used as the analytical signal. Under the selected conditions, the voltammetric signal was proportional to the Ag(I) concentration in the range of 0.001-100μgL(-1) with favorable limits of detection and quantification of 1.1ngL(-1) and 3.7ngL(-1) after 3min of accumulation time, respectively. By increasing the accumulation time to 10min, detection and quantification limits can be further improved up to 0.1ngL(-1) and 0.34ngL(-1), respectively. In addition, the results showed a highly reproducible procedure showing a relative standard deviation of 1.5% for 12 replicate measurements. Many coexisting metal ions were investigated and very few interferences were found on the determination of Ag(I). The proposed method was validated using certified reference estuarine waters

  15. Contact dermatitis caused by ECG electrode paste.

    Science.gov (United States)

    Cochran, R J; Rosen, T

    1980-12-01

    A case of contact dermatitis caused by ECG electrode cream is presented and the pertinent literature is reviewed. Our patient was found to be allergic to propylene glycol. Patch-testing remains an invaluable tool in the evaluation of patients suspected of being allergic to ECG paste, creams, and gels.

  16. Effect of cobalt doping level of ferrites in enhancing sensitivity of analytical performances of carbon paste electrode for simultaneous determination of catechol and hydroquinone.

    Science.gov (United States)

    Lakić, Mladen; Vukadinović, Aleksandar; Kalcher, Kurt; Nikolić, Aleksandar S; Stanković, Dalibor M

    2016-12-01

    This work presents the simultaneous determination of catechol (CC) and hydroquinone (HQ), employing a modified carbon paste electrode (CPE) with ferrite nanomaterial. Ferrite nanomaterial was doped with different amount of cobalt and this was investigated toward simultaneous oxidation of CC and HQ. It was shown that this modification strongly increases electrochemical characteristics of the CPE. Also, electrocatalytic activity of such materials strongly depends on the level of substituted Co in the ferrite nanoparticles. The modified electrodes, labeled as CoFerrite/CPE, showed two pairs of well-defined redox peaks for the electrochemical processes of catechol and hydroquinone. Involving of ferrite material in the structure of CPE, cause increase in the potentials differences between redox couples of the investigated compounds, accompanied with increases in peaks currents. Several important parameters were optimized and calibration curves, with limits of detection (LOD) of 0.15 and 0.3µM for catechol and hydroquinone, respectively, were constructed by employing amperometric detection. Effect of possible interfering compounds was also studied, and proposed method was successfully applied for CC and HQ quantification in real samples.

  17. Voltammetric determination of hydroxylamine in water and waste water samples using a NiO nanoparticle/new catechol derivative modified carbon paste electrode

    Directory of Open Access Journals (Sweden)

    Mahbobeh Moazampour

    2014-12-01

    Full Text Available A (9,10-dihydro-9,10-ethanoanthracene-11,12-dicarboximido-4-ethylbenzene-1,2-diol (DED mo­di­fied NiO/NPs carbon paste electrode “(DED/NiO nanoparticle (NiO/NPs/CPE was constructed for determination of hydroxylamine (HX. The cyclic voltammogram showed that the electro­catalytic oxidation of HX at the surface of DED/NiO/NPs/CPE occurs at a potential of about 800 mV less positive than with an unmodified electrode. Square-wave voltammetry results presented that the electrocatalytic oxidation peak currents of HX in pH 8.0 had two linear dynamic ranges in the range of 0.1 to 2.0 and 2.0 to 400.0 µM HX, with a detection limit of 0.07 µM. The kinetic parameters such as electron transfer coefficient a (0.47 and rate constant (2.454 × 103 M-1 s-1 were determined for the chemical reaction between HX and DED. Finally, this method was evaluated for the determination of HX in water and waste water samples.

  18. Modification of carbon paste electrode with Fe(III)-clinoptilolite nano-particles for simultaneous voltammetric determination of acetaminophen and ascorbic acid.

    Science.gov (United States)

    Sharifian, Samira; Nezamzadeh-Ejhieh, Alireza

    2016-01-01

    A novel carbon paste electrode (CPE) modified with Fe(III)-exchanged clinoptilolite nano-particles (Fe(III)-NClino/CPE) was constructed and used for simultaneous voltammetric (CV, SqW and chronoamperometry) determination of ascorbic acid and acetaminophen. Raw and modified zeolites were characterized by X-ray diffraction (XRD) and transmission electron microscope (TEM). The square wave peak current was linearly increased in the concentration ranges of 1.0 × 10(-9)-1.0 × 10(-2) mol L(-1) for ascorbic acid and 1.0 × 10(-10-)1.0 × 10(-2) mol L(-1) for acetaminophen with detection limits of 1.8 × 10(-9) mol L(-1) and 9.9 × 10(-10) mol L(-1), respectively. The detection limits of 2.4 × 10(-10) mol L(-1) and 2.5 × 10(-11) mol L(-1) were also obtained for AA and AC in chronoamperometric measurements, respectively. The diffusion coefficients of 7.5 × 10(-5) cm(2) s(-1) and 2.4 × 10(-5) cm(2) s(-1) were respectively calculated for the oxidation of AC and AA by chronoamperometry. The proposed electrode exhibited high sensitivity and good stability, and would be valuable for the clinical assay of ascorbic acid and acetaminophen.

  19. Electroanalytical Performance of a Carbon Paste Electrode Modified by Coffee Husks for the Quantification of Acetaminophen in Quality Control of Commercialized Pharmaceutical Tablets

    Directory of Open Access Journals (Sweden)

    Serge Foukmeniok Mbokou

    2016-01-01

    Full Text Available Electrochemical determination of acetaminophen (APAP was successfully performed using a carbon paste electrode (CPE modified with coffee husks (CH-CPE. Scanning electron microscopy (SEM and SEM-energy dispersive X-ray spectroscopy (SEM-EDX were, respectively, used for the morphological and elemental characterization of coffee husks prior to their utilization. The electrochemical oxidation of APAP was investigated by cyclic voltammetry (CV, differential pulse voltammetry (DPV, and square wave voltammetry (SWV. SWV technique appeared to be more sensitive since the oxidation current of APAP was twofold higher with the CH-CPE sensor than with the bare CPE, in relation to the increase in the organophilic character of the electrode surface. Furthermore, on CH-CPE, the current response of APAP varied linearly with its concentration in the range of 6.6 μM to 0.5 mM, leading to a detection limit of 0.66 μM (S/N=3. Finally, the proposed CH-CPE sensor was successfully used to determine the amount of APAP in commercialized tablets (Doliprane® 500 and Doliprane 1000, with a recovery rate ranging from 98% to 103%. This novel sensor opens the way for the development of low-cost and reliable devices for the electroanalysis of pharmaceutical formulations in developing countries.

  20. Simultaneous trace-levels determination of Hg(II) and Pb(II) ions in various samples using a modified carbon paste electrode based on multi-walled carbon nanotubes and a new synthesized Schiff base.

    Science.gov (United States)

    Afkhami, Abbas; Bagheri, Hasan; Khoshsafar, Hosein; Saber-Tehrani, Mohammad; Tabatabaee, Masoumeh; Shirzadmehr, Ali

    2012-10-09

    A modified carbon paste electrode based on multi-walled carbon nanotubes (MWCNTs) and 3-(4-methoxybenzylideneamino)-2-thioxothiazolodin-4-one as a new synthesized Schiff base was constructed for the simultaneous determination of trace amounts of Hg(II) and Pb(II) by square wave anodic stripping voltammetry. The modified electrode showed an excellent selectivity and stability for Hg(II) and Pb(II) determinations and for accelerated electron transfer between the electrode and the analytes. The electrochemical properties and applications of the modified electrode were studied. Operational parameters such as pH, deposition potential and deposition time were optimized for the purpose of determination of traces of metal ions at pH 3.0. Under optimal conditions the limits of detection, based on three times the background noise, were 9.0×10(-4) and 6.0×10(-4) μmol L(-1) for Hg(II) and Pb(II) with a 90 s preconcentration, respectively. In addition, the modified electrode displayed a good reproducibility and selectivity, making it suitable for the simultaneous determination of Hg(II) and Pb(II) in real samples such as sea water, waste water, tobacco, marine and human teeth samples.

  1. A novel electrochemical DNA biosensor based on a modified magnetic bar carbon paste electrode with Fe3O4NPs-reduced graphene oxide/PANHS nanocomposite.

    Science.gov (United States)

    Jahanbani, Shahriar; Benvidi, Ali

    2016-11-01

    In this study, we have designed a label free DNA biosensor based on a magnetic bar carbon paste electrode (MBCPE) modified with nanomaterial of Fe3O4/reduced graphene oxide (Fe3O4NP-RGO) as a composite and 1- pyrenebutyric acid-N- hydroxysuccinimide ester (PANHS) as a linker for detection of DNA sequences. Probe (BRCA1 5382 insC mutation detection) strands were immobilized on the MBCPE/Fe3O4-RGO/PANHS electrode for the exact incubation time. The characterization of the modified electrode was studied using different techniques such as scanning electron microscopy (SEM), infrared spectroscopy (IR), vibrating sample magnetometer (VSM), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry methods. Some experimental parameters such as immobilization time of probe DNA, time and temperature of hybridization process were investigated. Under the optimum conditions, the immobilization of the probe and its hybridization with the target DNA (Complementary DNA) were tested. This DNA biosensor revealed a good linear relationship between ∆Rct and logarithm of the complementary target DNA concentration ranging from 1.0×10(-18)molL(-1) to 1.0×10(-8)molL(-1) with a correlation coefficient of 0.9935 and a detection limit of 2.8×10(-19)molL(-1). In addition, the mentioned biosensor was satisfactorily applied for discriminating of complementary sequences from non-complementary sequences. The constructed biosensor (MBCPE/Fe3O4-RGO/PANHS/ssDNA) with high sensitivity, selectivity, stability, reproducibility and low cost can be used for detection of BRCA1 5382 insC mutation.

  2. Role of heat on the development of electrochemical sensors on bare and modified Co{sub 3}O{sub 4}/CuO composite nanopowder carbon paste electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Mohan; Kumara Swamy, B.E., E-mail: kumaraswamy21@yahoo.com

    2016-01-01

    The Co{sub 3}O{sub 4}/CuO composite nanopowder (NP) was synthesized by a mechanochemical method and characterized by using powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and energy-dispersive spectroscopy (EDS). The synthesized Co{sub 3}O{sub 4}/CuO NP was used as a modified carbon paste electrode (MCPE) and further the bare carbon paste and Co{sub 3}O{sub 4}/CuO NP modified carbon paste was heated at different temperatures (100, 150, 200 and 250 °C) for 10 min. The Co{sub 3}O{sub 4}/CuO NP MCPE was used to study the consequences of scan rate and dopamine concentration. Furthermore the preheated modified electrodes were used to study the electrochemical response to dopamine (DA), ascorbic acid (AA) and uric acid (UA). - Highlights: • Co{sub 3}O{sub 4}/CuO composite nanopowders (NPs) are prepared by the mechanochemical method. • Co{sub 3}O{sub 4}/CuO was used as a modified electrode for detection of DA, AA and UA. • The role of temperature on the sensor development was studied. • The modified carbon paste electrode shows good sensitivity to DA and UA.

  3. Coated magnetic particles in electrochemical systems: Synthesis, modified electrodes, alkaline batteries, and paste electrodes

    Science.gov (United States)

    Unlu, Murat

    Magnetic field effects on electrochemical reactions have been studied and shown to influence kinetics and dynamics. Recently, our group has introduced a novel method to establish magnetic field effects by incorporating inert, magnetic microparticles onto the electrode structure. This modification improved several electrochemical systems including modified electrodes, alkaline batteries, and fuel cells. This dissertation describes the applicability of magnetic microparticles and the understanding of magnetic field effects in modified electrodes, alkaline batteries, and paste electrodes. Magnetic effects are studied on electrodes that are coated with an ion exchange polymer that embeds chemically inert, commercial, magnetic microparticles. The flux (electrolysis current) of redox probe to the magnetically modified system is compared to a similar non-magnetic electrode. Flux enhancements of 60% are achieved at magnetically modified electrode as compared to non-magnetic controls. In addition to modifying electrode surfaces, the incorporation of magnetic microparticles into the electrode material itself establishes a 20% increase in flux. Possible magnetic field effects are evaluated. Study of samarium cobalt modified electrolytic manganese dioxide, EMD electrodes further establish a magnetic effect on alkaline cathode performance. Magnetic modification improves alkaline battery performance in primary and secondary applications. The reaction mechanism is examined through voltammetric methods. This work also includes coating protocols to produce inert magnetic microparticles with high magnetic content. Magnetite powders are encapsulated in a polymer matrix by dispersion polymerization. Composite particles are examined in proton exchange membrane fuel cells to study carbon monoxide tolerance.

  4. Biosensor for direct determination of fenitrothion and EPN using recombinant Pseudomonas putida JS444 with surface-expressed organophosphorous hydrolase. 2. Modified carbon paste electrode.

    Science.gov (United States)

    Lei, Yu; Mulchandani, Priti; Chen, Wilfred; Mulchandani, Ashok

    2007-03-01

    A whole cell-based amperometric biosensor for highly selective, sensitive, rapid, and cost-effective determination of the organophosphate pesticides fenitrothion and ethyl p-nitrophenol thio-benzene phosphonate (EPN) is discussed. The biosensor comprised genetically engineered p-nitrophenol (PNP)-degrading bacteria Pseudomonas putida JS444 anchoring and displaying organophosphorous hydrolase (OPH) on its cell surface as biological sensing element and carbon paste electrode as the amperometric transducer. Surface-expressed OPH catalyzed the hydrolysis of organophosphorous pesticides such as fenitrothion and EPN to release PNP and 3-methyl-4- nitrophenol, respectively, which were subsequently degraded by the enzymatic machinery of P. putida JS444 through electrochemically active intermediates to the TCA cycle. The electro-oxidization current of the intermediates was measured and correlated to the concentration of organophosphates. Operating at optimum conditions, 0.086 mg dry wt of cell operating at 600 mV of applied potential (vs Ag/AgCl reference) in 50 mM citrate phosphate buffer, pH 7.5, with 50 muM CoCl2 at room temperature, the biosensor measured as low as 1.4 ppb of fenitrothion and 1.6 ppb of EPN. There was no interference from phenolic compounds, carbamate pesticides, triazine herbicides, or organophosphate pesticides without nitrophenyl substituent. The service life of the biosensor and the applicability to lake water were also demonstrated.

  5. Why is the electroanalytical performance of carbon paste electrodes involving an ionic liquid binder higher than paraffinic binders? A simulation investigation.

    Science.gov (United States)

    Ghatee, M H; Namvar, S; Zolghadr, A R; Moosavi, F

    2015-10-14

    Recently, carbon paste electrodes (CPE) fabricated using an ionic liquid (IL) binder have shown enhanced electroanalytical performance over conventional paraffinic binders. Molecular dynamics (MD) simulations of graphite mixed with ionic liquid and with paraffin binder can unravel the potential atomistic factors responsible for such enhancement. Based on an experimentally optimized binder/graphite mass ratio, which has been reported to be crucial for such a performance, comprehensive simulations (at 323 K) are performed with the ensembles involving an ionic liquid binder (1-butyl-3-methylimidazolium hexafluorophosphate, [C4mim]PF6) and a paraffin binder (n-C20H42) mixed with graphite comprising large-size hexagonal-shaped double graphene plates. Structural analysis indicates both binders form only a monolayer on the graphite surface, covering the surface locally by IL but all-encompassing by paraffin. With charged and uncharged graphite, the IL monolayer tends to cover mainly the graphite center without approaching the edge planes. On the contrary, a monolayer of the paraffin binder covers uniformly the center, near the center, and the edge planes. Cations and anions of the IL form well-defined two dimensional pentagonal matrixes with characteristic high adsorption energy, almost 2.4 times higher than paraffin adsorption. The cation and anion coordination ability of the IL is responsible for such a local distribution. The simulation of these phenomena under experimental conditions unravels strong two-dimensional coordination properties inherent to the ionic liquid when distributed over the graphite surface. This direct MD simulation comparison of the IL properties with an organic liquid counterpart, made for the first time, can be used to explain the high electroanalytical performance (electron transfer) of CPEs involving an IL binder over paraffin binders.

  6. A voltammetric sensor with a multiwall carbon nanotube paste electrode and naphthol green as a mediator for the determination of N-actylcysteine in the presence of tryptophan

    Institute of Scientific and Technical Information of China (English)

    Mohsen Keyvanfard; Maryam Tahmasbi; Hassan Karimi-Maleh; Khadijeh Alizad

    2014-01-01

    A multiwall carbon nanotube modified electrode prepared by incorporating multiwall carbon nanotubes in the electrode of a sensor and naphthol green as a homogeneous mediator was used as a voltammetric sensor for the determination of N-actylcysteine (N-AC) in the presence of tryptophan (Trp). The voltammograms of differential pulse voltammetry of N-AC in a mixture with Trp were separated from each other by a potential difference of 200 mV, which allowed the determination of both N-AC and Trp simultaneously. Under the optimum conditions, the electrocatalytic currents increased linearly with N-AC concentration in the range of 0.25-400 μmol/L (two linear segments with different slopes). The detection limit for N-AC was 0.08 μmol/L. The kinetic parameters of the system were determined using electrochemical methods. The method was applied for the determination of N-AC in drug and urine samples.

  7. Iron nanoparticles decorated multi-wall carbon nanotubes modified carbon paste electrode as an electrochemical sensor for the simultaneous determination of uric acid in the presence of ascorbic acid, dopamine and L-tyrosine.

    Science.gov (United States)

    Bhakta, Arvind K; Mascarenhas, Ronald J; D'Souza, Ozma J; Satpati, Ashis K; Detriche, Simon; Mekhalif, Zineb; Dalhalle, Joseph

    2015-12-01

    Iron nanoparticles decorated multi-wall carbon nanotubes modified carbon paste electrode (Fe-MWCNTs/MCPE) was prepared by bulk-modification method. The electrochemical impedance spectroscopy (EIS) suggests least charge transfer resistance at the modified electrode. The electrochemical behavior of UA was studied in 0.1M phosphate buffer solution (PBS) of pH3.0 using cyclic voltammetry (CV) while differential pulse voltammetry (DPV) was used for quantification. The spectroelectrochemial study of oxidation of UA at Fe-MWCNTs/MCPE showed a decrease in the absorbance of two peaks with time, which are ascribed to π to π(⁎) and n to π(⁎) transitions. Under optimum condition, the DPV response offered two linear dynamic ranges for UA in the concentration range 7.0×10(-8)M-1.0×10(-6)M and 2.0×10(-6)M-1.0×10(-5)M with detection limit (4.80±0.35)×10(-8)M (S/N=3). The practical analytical application of this sensor was successfully evaluated by determination of spiked UA in clinical samples, such as human blood serum and urine with good percentage recovery. The proposed electrochemical sensor offers a simple, reliable, rapid, reproducible and cost effective analysis of a quaternary mixture of biomolecules containing AA, DA, UA and Tyr which was free from mutual interferences.

  8. Coated carbon nanotube array electrodes

    Science.gov (United States)

    Ren, Zhifeng; Wen, Jian; Chen, Jinghua; Huang, Zhongping; Wang, Dezhi

    2008-10-28

    The present invention provides conductive carbon nanotube (CNT) electrode materials comprising aligned CNT substrates coated with an electrically conducting polymer, and the fabrication of electrodes for use in high performance electrical energy storage devices. In particular, the present invention provides conductive CNTs electrode material whose electrical properties render them especially suitable for use in high efficiency rechargeable batteries. The present invention also provides methods for obtaining surface modified conductive CNT electrode materials comprising an array of individual linear, aligned CNTs having a uniform surface coating of an electrically conductive polymer such as polypyrrole, and their use in electrical energy storage devices.

  9. A high sensitive biosensor based on FePt/CNTs nanocomposite/N-(4-hydroxyphenyl)-3,5-dinitrobenzamide modified carbon paste electrode for simultaneous determination of glutathione and piroxicam.

    Science.gov (United States)

    Karimi-Maleh, Hassan; Tahernejad-Javazmi, Fahimeh; Ensafi, Ali A; Moradi, Reza; Mallakpour, Shadpour; Beitollahi, Hadi

    2014-10-15

    This study describes the development, electrochemical characterization and utilization of novel modified N-(4-hydroxyphenyl)-3,5-dinitrobenzamide-FePt/CNTs carbon paste electrode for the electrocatalytic determination of glutathione (GSH) in the presence of piroxicam (PXM) for the first time. The synthesized nanocomposite was characterized with different methods such as TEM and XRD. The modified electrode exhibited a potent and persistent electron mediating behavior followed by well-separated oxidation peaks of GSH and PXM. The peak currents were linearly dependent on GSH and PXM concentrations in the range of 0.004-340 and 0.5-550 µmol L(-1), with detection limits of 1.0 nmol L(-1) and 0.1 µmolL(-1), respectively. The modified electrode was successfully used for the determination of the analytes in real samples with satisfactory results.

  10. An installation for pressing pasted electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Matsudzava, S.; Sugimoto, K.

    1983-07-13

    The active mass is placed on the current outlet and the electrode is pressed and its thickness is regulated by passing it through rollers. The water and the adhering particles of the active mass are continuously sucked off during rotation of the rollers.

  11. Peltier effects in electrode carbon

    Science.gov (United States)

    Hansen, Ellen Marie; Egner, Espen; Kjelstrup, Signe

    1998-02-01

    The thermoelectric power of a cell with platinum electrodes and a carbon conductor was determined. The electromotive force (emf) was measured as a function of the temperature difference between the electrodes at temperatures varying from 310 °C to 970 °C. From these measurements, the transported entropy of electric charge in carbon was found to vary from -1.7 to -1.9 J/(K mole) at temperatures around 300 °C, from -2.0 to -2.3 J/(K mole) at temperatures around 550 °C, and from -3.4 to -3.7 J/(K mole) at temperatures around 950 °C. This transported entropy had not before been determined for temperatures above 550 °C. Also, it is shown how the previously neglected surface properties can be taken into account to interpret the measurements. In the Hall-Héroult cell, the anode is made of a similar kind of carbon. Hence, the transported entropy found above can be used to describe the often neglected coupling between transport of heat and electric charge in this electrode. It is shown that the calculated electric potential profile through a coal sample will change significantly if the coupling is neglected, but the calculated temperature profile is independent of whether the coupling is neglected. New equations are also developed that can be used to evaluate the importance of the coupling in other systems.

  12. 用固体石蜡山梨酸碳糊电极电位法测定食品中山梨酸%Potentiometric Determination of Sorbic Acid with Solid Paraffin Sorbic Acid Modified Carbon Paste Electrode

    Institute of Scientific and Technical Information of China (English)

    李东辉; 李潇; 于秋泓; 岳京立; 陈连山; 鄂义峰

    2011-01-01

    制备了一种以山梨酸根与乙基紫形成的缔合物为电活性物的固体石蜡山梨酸碳糊电极,并对其性能做了测定.结果显示该电极对山梨酸有较好的能斯特响应.山梨酸的线性范围为2.2×10-5~1.0× 10-1mol·L-1,检出限为1.6×10-5mol·L-1.该电极用于食品中山梨酸根的测定,结果与分光光度法结果相符.%Solid paraffin sorbic acid modified carbon paste electrode based on the complex of ethyl violet with sorbic acid as electroactive material was prepared and its electrochemical properties were studied.Good response of this ion selective electrode against sorbic acid was obtained giving linearity range from 2.2 × 10-5 to 1.0 × 10-1 mol · L-1, with detection limit of 1.6 × 10-5 mol · L-1.The modified electrode was used in the potentiometric determination of sorbic acid in food, and results obtained were found to be checked quite well with those obtained by spectrophotometry.

  13. Graphene-doped carbon paste electrode:preparation and its electrochemical properties%石墨烯碳糊电极的制备及其性能研究

    Institute of Scientific and Technical Information of China (English)

    王小萍; 刘娇; 龚晨晨; 刘桂亭; 李黎; 杨海峰; 文颖

    2014-01-01

    A graPhene doPed carbon Paste electrode( GPE)was PrePared by mixing graPhene with graPhite Powder and mineral oil. The electrochemical behavior at the as-PrePared electrode was studied using cy-clic voltammetry in a Fe( CN)6 3-/4- solution. The electrocatalytic ProPerties of GPE toward the oxidation of nitrite were also analyzed. The result showed that the resulting electrode disPlayed high electro-catalytic activity,attributing to the unique structure,tunable oPtical ProPerties and electrical conductivity of gra-Phene.%将石墨烯掺杂在石墨粉和矿物油的混合物中,制备基于石墨烯的碳糊电极( GPE),采用循环伏安法研究了GPE的电化学性质,并对其应用进行了初步的探索。结果表明,石墨烯对GPE电极表面上的电子转移起到了明显的促进作用,对亚硝酸( NO2-)有良好的电化学响应。

  14. Desalination with carbon aerogel electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, J.C.; Richardson, J.H.; Fix, D.V.

    1996-10-21

    An electrically regenerated electrosorption process known as carbon aerogel CDI was developed for continuously removing ionic impurities from aqueous streams. A salt solution flows in a channel formed by pairs of parallel carbon aerogel electrodes. Each electrode has a very high BET surface area and very low resistivity. After polarization, anions and cations are removed from electrolyte by the electric field and electrosorbed onto the carbon aerogel. The solution is thus separated into two streams, brine and water. Based on this, carbon aerogel CDI appears to be an energy-efficient alternative to evaporation, electrodialysis, and reverse osmosis. The energy required by this process is about QV/2, plus losses. Estimated energy requirement for sea water desalination is 18-27 Wh gal{sup -1}, depending on cell voltage and flow rate. The requirement for brackish water desalination is less, 1.2-2.5 Wh gal{sup -1} at 1600 ppM. This is assuming that stored electrical energy is reclaimed during regeneration.

  15. Carbon aerogel electrodes for direct energy conversion

    Science.gov (United States)

    Mayer, Steven T.; Kaschmitter, James L.; Pekala, Richard W.

    1997-01-01

    A direct energy conversion device, such as a fuel cell, using carbon aerogel electrodes, wherein the carbon aerogel is loaded with a noble catalyst, such as platinum or rhodium and soaked with phosphoric acid, for example. A separator is located between the electrodes, which are placed in a cylinder having plate current collectors positioned adjacent the electrodes and connected to a power supply, and a pair of gas manifolds, containing hydrogen and oxygen positioned adjacent the current collectors. Due to the high surface area and excellent electrical conductivity of carbon aerogels, the problems relative to high polarization resistance of carbon composite electrodes conventionally used in fuel cells are overcome.

  16. Voltammetric Response of Epinephrine at Carbon Nanotube Modified Glassy Carbon Electrode and Activated Glassy Carbon Electrode

    Institute of Scientific and Technical Information of China (English)

    WANG Juan; TANG Ping; ZHAO Fa-qiong; ZENG Bai-zhao

    2005-01-01

    The electrochemical behavior of epinephrine at activated glassy carbon electrode and carbon nanotube-coated glassy carbon electrode was studied. Epinephrine could exhibit an anodic peak at about 0.2 V (vs. SCE) at bare glassy carbon electrode, but it was very small.However, when the electrode was activated at certain potential (i. e. 1.9V) or modified with carbon nanotube, the peak became more sensitive,resulting from the increase in electrode area in addition to the electrostatic attraction. Under the selected conditions, the anodic peak current was linear to epinephrine concentration in the range of 3.3 × 10-7-1.1 × 10-5mol/L at activated glassy carbon electrode and in the range of 1.0 × 10-6-5.0 × 10-5 mol/L at carbon nanotube-coated electrode. The correlation coefficients were 0. 998 and 0. 997, respectively. The determination limit was 1.0 × 10-7 mol/L. The two electrodes have been successfully applied for the determination of epinephrine in adrenaline hydrochloride injection with recovery of 95%-104%.

  17. Capacitor with a composite carbon foam electrode

    Energy Technology Data Exchange (ETDEWEB)

    Mayer, S.T.; Pekala, R.W.; Kaschmitter, J.L.

    1999-04-27

    Carbon aerogels used as a binder for granularized materials, including other forms of carbon and metal additives, are cast onto carbon or metal fiber substrates to form composite carbon thin film sheets. The thin film sheets are utilized in electrochemical energy storage applications, such as electrochemical double layer capacitors (aerocapacitors), lithium based battery insertion electrodes, fuel cell electrodes, and electrocapacitive deionization electrodes. The composite carbon foam may be formed by prior known processes, but with the solid particles being added during the liquid phase of the process, i.e. prior to gelation. The other forms of carbon may include carbon microspheres, carbon powder, carbon aerogel powder or particles, graphite carbons. Metal and/or carbon fibers may be added for increased conductivity. The choice of materials and fibers will depend on the electrolyte used and the relative trade off of system resistivity and power to system energy. 1 fig.

  18. Capacitor with a composite carbon foam electrode

    Energy Technology Data Exchange (ETDEWEB)

    Mayer, Steven T. (San Leandro, CA); Pekala, Richard W. (Pleasant Hill, CA); Kaschmitter, James L. (Pleasanton, CA)

    1999-01-01

    Carbon aerogels used as a binder for granularized materials, including other forms of carbon and metal additives, are cast onto carbon or metal fiber substrates to form composite carbon thin film sheets. The thin film sheets are utilized in electrochemical energy storage applications, such as electrochemical double layer capacitors (aerocapacitors), lithium based battery insertion electrodes, fuel cell electrodes, and electrocapacitive deionization electrodes. The composite carbon foam may be formed by prior known processes, but with the solid partides being added during the liquid phase of the process, i.e. prior to gelation. The other forms of carbon may include carbon microspheres, carbon powder, carbon aerogel powder or particles, graphite carbons. Metal and/or carbon fibers may be added for increased conductivity. The choice of materials and fibers will depend on the electrolyte used and the relative trade off of system resistivity and power to system energy.

  19. Potentiometric Determination of Lidocaine with Solid Paraffin Lidocaine Modified Carbon Paste Electrode%固体石蜡利多卡因碳糊电极电位法测定利多卡因

    Institute of Scientific and Technical Information of China (English)

    李东辉; 李潇

    2012-01-01

    Solid paraffin lidocaine modified carbon paste electrode based on the complex of HgI42- with lidoeaine as electroactive material was prepared and its electrochemical properties were studied. Good response of this ion selective electrode against lidocaine was obtained giving linearity range from 5.0× 10-5 to 1.6 × 10-2 mol · L-1 , with a slope of 29 mV/pc and lower limit of determination of 1.3× 10-5mol · L-1. The modified electrode was used in the potentiometric determination of lidocaine in lidocaine injection, and results obtained were found to be checked quite well with those found by the pharmacopoeia method.%制备了一种以利多卡因与HgI42-形成的缔合物为电活性物质的固体石蜡利多卡因碳糊电极,并对其性能做了测定。结果显示:电极对利多卡因有较好的能斯特响应。利多卡因的线性范围为5.0×10-5~1.6×10-2mol·L-1,极差电位为29mY/pc,测定下限为1.3×10-5mol·L-1。电极用于盐酸利多卡因注射液中利多卡因含量的测定,结果与药典法测定值相符。

  20. 掺杂硒碳糊电极阳极溶出法测定铋%Determination of bismuth at carbon paste electrodes doped with selenium by anodic stripping voltammetry

    Institute of Scientific and Technical Information of China (English)

    韦革; 魏小平; 李建平

    2011-01-01

    A new anodic stripping voltammetric method for the determination trace bismuth of was developed by using carbon paste electrodes doped with selenium as a working electrode. In 0.1 mol/L HC1, a sensitive oxidation peak of the Bi3+ were obtained with the peak potential of + 0.05 V (vs. Ag/AgCl). The oxidation peak current linearly changed with the logarithmic value of bismuth ion concentration in the range of 1.0 × 10-9 ~ 1. 0 × 10-5 mol/L. The detection limit was 1. 0 × 10 -10 mol/L. The method has been applied to the determination of the content of bismuth in water samples and the drugs of Bismuth Potassium Citrate Granules. The recoveries were found to be in the range of 93.3% ~ 105.4%. The proposed electrode is simple in fabrication, and cheap renewal in use. It is valuable in practical application.%建立了一种测定痕量铋的新方法,即利用掺杂硒碳糊电极作为工作电极的阳极溶出法.在0.1 mol/L的HCl底液中,Bi3+于+0.05V(vs.Ag/AgCl)出现灵敏的氧化溶出峰,铋离子的浓度在1.0×10-5~1.0×10-9 mol/L范围内其对数值lgc与铋的氧化峰电流值呈线性关系,检出限达1.0×10 -10 mol/L.本法已用于药物枸橼铋钾颗粒中铋含量的测定,回收率为95.5%~104.9%.

  1. 预阳极化碳糊电极同时测定对乙酰氨基酚和多巴胺%The simultaneous determination of acetaminophen and dopamine at a pre-anodized carbon paste electrode

    Institute of Scientific and Technical Information of China (English)

    孙瑶; 上官恩波; 李晶; 李全民

    2013-01-01

    A pre-anodized carbon paste electrode was prepared by cyclic voltammetry.The electrochemical behaviors of acetaminophen and dopamine were investigated on the modified electrode.The experimental results showed that the electrode had excellent electrocatalytic activity to acetaminophen and dopamine.The oxidation peak currents were proportional to the concentrations of acetaminophen and dopamine both in the range of 2.0 ×106-5.0 × 104mol/L,and the detection limits were 6.3 × 10-7moL/L and 2.5 × 10-7mol/L,respectively.The proposed method was applied to the determination of acetaminophen and dopamine in commercial pharmaceutical samples with satisfactory results.%采用循环伏安法制备了预阳极化碳糊电极,研究了对乙酰氨基酚和多巴胺在该修饰电极上的电化学行为.结果表明,预阳极化碳糊电极对对乙酰氨基酚和多巴胺的电化学行为具有良好的电催化作用.对乙酰氨基酚和多巴胺的氧化峰电流与其浓度在2.0×10-6~5.0×10-4mol/L的范围内呈良好的线性关系,检出限分别为6.3×10-7 mol/L,2.5×10-7 mol/L.方法已用于药物样品中对乙酰氨基酚和多巴胺的测定.

  2. Fabricating solid carbon porous electrodes from powders

    Energy Technology Data Exchange (ETDEWEB)

    Kaschmitter, James L. (Pleasanton, CA); Tran, Tri D. (Livermore, CA); Feikert, John H. (Livermore, CA); Mayer, Steven T. (San Leandro, CA)

    1997-01-01

    Fabrication of conductive solid porous carbon electrodes for use in batteries, double layer capacitors, fuel cells, capacitive dionization, and waste treatment. Electrodes fabricated from low surface area (<50 m.sup.2 /gm) graphite and cokes exhibit excellent reversible lithium intercalation characteristics, making them ideal for use as anodes in high voltage lithium insertion (lithium-ion) batteries. Electrodes having a higher surface area, fabricated from powdered carbon blacks, such as carbon aerogel powder, carbon aerogel microspheres, activated carbons, etc. yield high conductivity carbon compositives with excellent double layer capacity, and can be used in double layer capacitors, or for capacitive deionization and/or waste treatment of liquid streams. By adding metallic catalysts to be high surface area carbons, fuel cell electrodes can be produced.

  3. Fabricating solid carbon porous electrodes from powders

    Energy Technology Data Exchange (ETDEWEB)

    Kaschmitter, J.L.; Tran, T.D.; Feikert, J.H.; Mayer, S.T.

    1997-06-10

    Fabrication is described for conductive solid porous carbon electrodes for use in batteries, double layer capacitors, fuel cells, capacitive deionization, and waste treatment. Electrodes fabricated from low surface area (<50 m{sup 2}/gm) graphite and cokes exhibit excellent reversible lithium intercalation characteristics, making them ideal for use as anodes in high voltage lithium insertion (lithium-ion) batteries. Electrodes having a higher surface area, fabricated from powdered carbon blacks, such as carbon aerogel powder, carbon aerogel microspheres, activated carbons, etc. yield high conductivity carbon composites with excellent double layer capacity, and can be used in double layer capacitors, or for capacitive deionization and/or waste treatment of liquid streams. By adding metallic catalysts to high surface area carbons, fuel cell electrodes can be produced. 1 fig.

  4. Photocatalytic, antimicrobial activities of biogenic silver nanoparticles and electrochemical degradation of water soluble dyes at glassy carbon/silver modified past electrode using buffer solution.

    Science.gov (United States)

    Khan, Zia Ul Haq; Khan, Amjad; Shah, Afzal; Chen, Yongmei; Wan, Pingyu; Khan, Arif Ullah; Tahir, Kamran; Muhamma, Nawshad; Khan, Faheem Ullah; Shah, Hidayat Ullah

    2016-03-01

    In the present research work a novel, nontoxic and ecofriendly procedure was developed for the green synthesis of silver nano particle (AgNPs) using Caruluma edulis (C. edulis) extract act as reductant as well as stabilizer agents. The formation of AgNPs was confirmed by UV/Vis spectroscopy. The small and spherical sizes of AgNPs were conformed from high resolution transmission electron microscopy (HRTEM) analysis and were found in the range of 2-10nm, which were highly dispersion without any aggregation. The crystalline structure of AgNPs was conformed from X-ray diffraction (XRD) analysis. For the elemental composition EDX was used and FTIR helped to determine the type of organic compounds in the extract. The potential electrochemical property of modified silver electrode was also studied. The AgNPs showed prominent antibacterial motion with MIC values of 125 μg/mL against Bacillus subtilis and Staphylococcus aureus while 250 μg/mL against Escherichia coli. High cell constituents' release was exhibited by B. subtilis with 2 × MIC value of silver nanoparticles. Silver nanoparticles also showed significant DPPH free radical scavenging activity. This research would have an important implication for the synthesis of more efficient antimicrobial and antioxidant agent. The AgNP modified electrode (GC/AgNPs) exhibited an excellent electro-catalytic activity toward the redox reaction of phenolic compounds. The AgNPs were evaluated for electrochemical degradation of bromothymol blue (BTB) dyes which showed a significant activity. From the strong reductive properties it is obvious that AgNPs can be used in water sanitization and converting some organic perilous in to non-hazardous materials. The AgNPs showed potential applications in the field of electro chemistry, sensor, catalyst, nano-devices and medical.

  5. Voltammetric Determination of Acetaminophen Using Carbon Paste Modified Electrode Doped with Selenium%掺杂硒修饰碳糊电极伏安法测定对乙酰氨基酚

    Institute of Scientific and Technical Information of China (English)

    谭君林; 张连明; 胡存杰; 魏小平

    2014-01-01

    Carbon paste modified electrode doped with selenium was prepared by cyclic voltammetry,and the electrochemical behavior of acetaminophen (ACOP)at this electrode was studied by cyclic voltammetry and differential pulse voltammetry.A cyclic voltammetric method for the determination of ACOP with carbon paste modified electrode doped with selenium was established.In 0.1 mol·L-1 HOAc-NaOAc buffer solution of pH 4.6, a sensitive oxidation peak of ACOP at +0.61 V (vs.SCE)was observed.Linear relationship between values of oxidation peak current and concentration of ACOP was kept in the range of 6.0×10-7 -1.5×10-4 mol·L-1 with detection limit (3s/k)of 2.8×10-7 mol·L-1 .The proposed method was applied to the analysis of tablet samples, giving results in consistency with the values obtained by pharmacopoeia method with RSD′s (n=5)in the range of 2.1%-2.5%.%采用循环伏安法制备了掺杂硒修饰碳糊电极,用循环伏安法和差分脉冲伏安法研究了对乙酰氨基酚在掺杂硒修饰碳糊电极上的电化学行为,建立了掺杂硒修饰碳糊电极测定对乙酰氨基酚的电化学方法。在 pH 4.6的0.1 mol ·L-1乙酸-乙酸钠缓冲溶液中,对乙酰氨基酚在+0.61 V呈现一个灵敏的氧化峰。对乙酰氨基酚的浓度在6.0×10-7~1.5×10-4 mol·L-1范围内与其氧化峰电流呈线性关系,检出限(3s/k)为2.8×10-7 mol·L-1。方法用于药品中对乙酰氨基酚的测定,测定结果与药典法测定值相符,测定值的相对标准偏差(n=5)在2.1%~2.5%之间。

  6. Electrohemical properties of carbon nanotube paste electrodes modified with redox cationic dyes=Propriedades eletroquímicas de eletrodos a base de pasta de nanotubo de carbono modificados com corantes redox catiônicos

    Directory of Open Access Journals (Sweden)

    Arnaldo César Pereira

    2012-07-01

    Full Text Available The present work describes the electrochemical behavior of methylene blue and toluidine blue as electron mediators adsorbed in the multiwall carbon nanotubes paste. Based on midpoint potential and separation of cathodic and anodic peaks (ΔE, it was not observed interaction of different eletrolytes with the cationic dyes by an ion exchange reaction and, as a consequence, absence of leaching of cationic dyes to the solution phase. The kinetics of electron transfer on the surface electrode was not sufficiently fast showing a fairly resistence of carbon nanotube paste modified with the mediators. The midpoint potential and ΔE also were insentive to the pH range (4-8, confirming the protective effect of carbon nanotubes matrix, owing to strong interaction of between the latter and the nitrogen of nitrogen of cationic dyes with carbon nanotube matrix, minimizing the proton interaction under cationic dye. This result is very important for sensor/biosensor preparation, because the eletrooxidation behavior of the analyte will be only affected by its formal potencial shifting. Carbon nanotubes proved to be an efficient solid matrix for the adsorption of mediator electron in comparison to the electrochemical behavior of free cationic dyes in solution phase.O presente trabalho descreve o comportamento eletroquímico de azul de metileno e azul de toluidina como mediadores de elétrons adsorvidos em pasta de nanotubo de carbono multiparede. Com base no potencial médio e na separação de pico catódico e anódico (ΔE, não foi observada interação de diferentes eletrólitos com os corantes catiônicos por meio de reação de troca iônica e, como consequência, ausência de lixiviação dos corantes para solução. A cinética de transferência de elétron na superfície do eletrodo não foi suficientemente rápida, mostrando razoável resistência da pasta de nanotubo de carbono modificada com os mediadores. O potencial médio e ΔE também foram insens

  7. Improved technology for manufacture of carbon electrodes

    Indian Academy of Sciences (India)

    A Platon; A Dumbrava; N Iutes-Petrescu; Luzia Simionescu

    2000-02-01

    Current industrial carbon electrodes are typically manufactured by blending petroleum coke particles (the filler) with molten coal tar pitch (the binder) and extruding the resultant mix to form the `green electrode’. This is then baked under controlled conditions. In case of usage as anodes in steel electric furnaces (or as other carbon and graphite products), the electrodes could undergo further processing like pitch impregnation or graphitization. During heat treatment, some of the organics are destructively distilled, vaporized or decomposed, resulting in carbon deposition in the electrode. As the vaporized materials exit the body of the electrode they cause porosity in the walls, which results in reduction in density, current carrying capacity and flexural strength. The paper presents investigations to improve some physico-chemical characteristics of these electrodes (such as coefficient of thermal expansion, mechanical strengths, density, pore volume, porosity etc.), obtained in different manufacture steps, by addition of varieties of coal tar pitch. These include attempts to improve the chemical compatibility of the coke-pitch system in the mixture and establish the method and the point of introduction of additive, the concentration required and appropriate analytical control during the entire manufacture. Methods of analysis used include thermogravimetry and porosimetry. The microstructure of the electrodes is investigated through a wide range and the data obtained include pore size and pore volume distribution, surface area, porosity, particle size distribution and type of pores. The overall results clearly indicate better characteristics and performance for electrodes with additives as against electrodes without them, such as lower porosity, lower thermal expansion coefficients and greater mechanical strength. These data are analyzed with respect to the process step and electrode type.

  8. Characteristics of Arcs Between Porous Carbon Electrodes

    OpenAIRE

    Carvou, Erwann; Le Garrec, Jean-Luc; Mitchell, Brian

    2013-01-01

    International audience; Arcs between carbon electrodes present some specific differences compared with metallic arcs. The arc voltage is higher, but does not attain a stable value displaying large fluctuations. Indeed, the arcs are produced by the direct sublimation of the electrodes, without passing through a molten phase. The arc production is also facilitated by both circuit breaking and electric field breakdown. In this paper, arcing has been examined under various conditions (voltage, cu...

  9. Nucleation and electrolytic deposition of lead on model carbon electrodes

    Science.gov (United States)

    Cericola, D.; Spahr, M.

    2016-08-01

    There is a general consensus in the lead acid battery industry for the use of carbon additives as a functional component in the negative paste to boost the battery performance with regards to charge acceptance and cycle life especially for upcoming automotive and energy storage applications. Several mechanisms are discussed in the scientific literature and the affinity of the carbon surfaces to lead species seems to play a key role. With a set of experiments on model carbon electrodes we gave evidence to the fact that some carbon materials promote spontaneous nucleation of lead crystals. We propose a mechanism such that the carbon, as soon as in a lead containing environment, immobilizes some lead on its surface. Such immobilized lead acts as nucleation seed for the deposition of lead when a current is passed through the material. It is therefore possible to differentiate and select the carbon materials based on their ability to form nucleation seeds.

  10. 染料木素在碳糊电极上的电化学行为及其测定%Eletrochemical Behavior of Genistein at Carbon Paste Electrode and Its Determination

    Institute of Scientific and Technical Information of China (English)

    白敏

    2016-01-01

    在pH=3.0的磷酸盐缓冲液中,通过循环伏安法研究了染料木素在碳糊电极( CPE)上的电化学行为,并探讨了其电化学反应机理。结果表明:染料木素在+1.14 V和+0.746 V处出现了两个氧化峰。氧化峰电流( Ip1)在浓度范围为4.0Χ10-9~2.0Χ10-6 mol/L内呈线性关系,检出限为6.5Χ10-9 mol/L。对8.0Χ10-7 mol/L的染料木素平行测定6次的相对标准偏差为2.8%。该方法可用于对人体内服用过染料木素后的药物代谢含量进行测定,回收率在97%~102%之间。%The electrochemical behavior of genistein on carbon paste electrode ( CPE ) was studied by cyclic voltammetry in pH=3. 0 phosphate buffer solution. The results showed that two oxidation peaks occurred in the +1. 14 V and +0. 746 V. Oxidation peak current ( Ip1 ) in the concentration range of 4. 0Χ10-9 ~2. 0Χ10-6 mol/L, the detection limit was 6. 5Χ10-9 mol/L. The relative standard deviation of 6 times of the 8. 0Χ10-7 mol/L of genistein was 2. 8%. The method can be used for the determination of drug metabolism in the human body after taking over genistein, and the recovery rate was between 97% ~102%.

  11. 离子液体BMIMPF6修饰碳糊电极电化学测定维生素E%Electrochemical determination of vitamin E at ionic liquid BMIMPF6 modified carbon paste electrode

    Institute of Scientific and Technical Information of China (English)

    顾玲; 贺亚梅; 张苗

    2012-01-01

    摘要:用疏水性离子液体1-丁基-3-甲基咪唑六氟磷酸([BMIM] PF6)作粘合剂制备了离子液体修饰碳糊电极(IL/CPE).采用循环伏安法(CV)研究了维生素E( vitamin E,VE)的氧化产物生育酚红在IL/CPE和未修饰碳糊电极(CPE)上的电化学行为,结果表明生育酚红在IL/CPE上氧化过程更易于进行,峰电流响应ip也明显增加,表明IL/CPE对生育酚红的氧化还原反应具有良好的电催化作用.同时测定了电极过程的动力学参数:电荷转移系数c=0.8746,扩散系数D=1.65×10-3cm2/s,电极反应速率常数kt=6.64× 10-2cm/s.采用方波伏安法(SWV)发现生育酚红氧化峰电流与其浓度在1.53× 10-4mol/L~8.39×10-7mol/L范围内呈线性关系,检出限为1.58× 10-8mol/L.该法可用于VE实际样品的分析测定.%An ionic liquid modified carbon paste electrode( IL/CPE) was fabricated by employing hydrophobia ionic liquid 1-butyl-3-melhylinudazolmm hexafluorophosphate( [BMIM]PF5)as a binder. The electrochemical behavior of tecored(the oxidation product of vitamin E) at the IL/CPE and non-modified CPE was investigated by cyclic voltamnietry( CV). The experimental results show that the oxidation process of tecored at the IL/CPE was much more easier,while peak current ipwas significantly increased,which indicated that IL/CPE had electrocatalytic activity toward the redox of vitamin E. At the same time some kinetics parameters of the vitamin E were determined at IL/CPE;electron transfer coefficient a is 0.8746Tthe Diffusion coefficient D is 1. 65×10-3cmVs and the e-lectrode reaction rate constant kf is 6.64×10-2cm/s. The linear relationship between values of oxidation peak current and concentra-tion of vitamin E was found in the range from l,53×10-4mol/L to 8.39×10-7mol/L with a detection limit of 1.58×10-8mol/L(S/ N=3)by Square Wave Voltametry(SWV)method. The proposed method was applied to directly analysis and determines vitamin E samples.

  12. ELECTROCHEMICAL PROPERTIES OF NANOPOROUS CARBON ELECTRODES

    Directory of Open Access Journals (Sweden)

    P.Nigu

    2002-01-01

    Full Text Available Electrical double layer and electrochemical characteristics at the nanoporous carbon | (C2H54NBF4 + acetonitrile interface have been studied by the cyclic voltammetry and impedance spectroscopy methods. The value of zero charge potential (0.23 V vs. SCE in H2O, the region of ideal polarizability and other characteristics have been established. Analysis of complex plane plots shows that the nanoporous carbon | x M (C2H54NBF4 + acetonitrile interface can be simulated by the equivalent circuit, in which the two parallel conduction parts in the solid and liquid phases are interconnected by the double layer capacitance in parallel with the complex admittance of hindered reaction of the charge transfer process. The values of the characteristic frequency depend on the electrolyte concentration and on the electrode potential, i.e. on the nature of ions adsorbed at the surface of nanoporous carbon electrode.

  13. Electrochemical storage of hydrogen on carbon electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Jurewicz, K.; Frackowiak, E. [ICTE, Poznan University of Technology (Poland); Gautier, S.; Beguin, F. [CRMD, CNRS Universite, 45 - Orleans (France)

    2000-07-01

    Amount of hydrogen reversibly stored on an activated carbon electrode using electro-decomposition of 6 mol.l{sup -1} KOH aqueous solution has been investigated and compared data obtained under a high pressure of dihydrogen (70 bars) at 273 K. In the electrochemical method, 1.5 wt% of hydrogen was released from carbon during the oxidation process, with a well-defined plateau at ca. - 0.5 V vs Hg/HgO. Relatively smaller values were obtained for the sorption ability under a high pressure of gas. This means that the formation of nascent hydrogen during water reduction favours its easy penetration in the carbon nano-structure, even at ambient pressure and temperature. Our results show that not only carbon nano-tubes should be considered for hydrogen reservoir and that low cost materials such as activated carbons could be convenient in appropriate conditions.

  14. Electrochemical behavior of tylosin at carbon paste electrode and its electroanalytical application%泰乐星在碳糊电极上的伏安行为研究及应用

    Institute of Scientific and Technical Information of China (English)

    犹卫; 高作宁

    2009-01-01

    目的 研究表面活性剂增敏作用下泰乐星(TLS)在碳糊电极(CPE)上的电化学行为,建立一种测定TLS的电化学分析方法 .方法 用循环伏安法(cyclic voltammetry,CV)和线性扫描伏安法(linear sweep voltammetry,LSV)探讨了TLS在CPE上的电化学行为及其影响因素.结果 阴离子表面活性剂十二烷基苯磺酸钠(SDBS)存在下TLS在CPE上有一显著的不可逆氧化峰,峰电位(Ep)为0.735V.结论 TLS氧化峰电流与其浓度在1.2×10-5~1.0 × 10-3mol/L范围内呈良好的线性关系,r=0.9974,检出限1.7×10-7mol/L,以此建立TLS含量的电化学分析方法 .测定结果 RSD1.6~2.4%,加样回收率98.6%~101.1%.该方法 简便快捷,测定结果 令人满意.%Objective To research the electrochemical behaviors of tylosin (TLS) based on the enhanced effect of surfactant at carbon paste electrode (CPE), an electroanalytic method of content determination of TLS was established. Methods Electrochemical behaviors and influence factor of TLS had been investigated by cyclic voltammetry (CV) and linear sweep voltammetry (LSV). Results Electrochemical results showed that the electrochemical behavior of TLS on surfactant of sodium dodecyl benzene sulfonate in aqueous 0. 10 mol/L PBS exhibited an irreversible electrochemical redox process at CPE, the oxidation peak potential (Ep) was 0.735 V. Conclusion The oxidation peak currents of TLS versus its concentration had a good linear relationship in the concentration range of 1.2 × 10-5~1.0 × 10-3 mol/L with the correlation coefficient of 0.9974 and the detection limit of 1.7 × 10-7 mol/L by LSV response. The relative standard deviation was between 1.6%~2.4 % and recovery was in the range of 98.6%~101.1%. The method could be applied in the determination of TLS in samples with the satisfied results.

  15. Air Brush Fabricated Carbon Nanotube Supercapacitor Electrodes

    Science.gov (United States)

    2010-09-01

    dispersant is not contributing to the capacitance. The electrochemical, cyclic voltametry , measurements were made using a Keithley 4200 Semiconductor...reference electrode. The cyclic voltamogram (CV) was performed in potential ranges of anywhere between –0.9–0.5 V at scan rates ranging from 1–100 mV...Symbols, Acronyms, and Abbreviations AL aluminum CNT carbon nanotube Cu copper CV cyclic voltamogram ESEM environmental scanning electron microscope

  16. Carbon nanotube based multi electrode arrays for neuronal interfacing: progress and prospects

    OpenAIRE

    Yael eHanein; Lilach eBareket-Keren

    2013-01-01

    Carbon nanotube coatings have been demonstrated over the past several years as a promising material for neuronal interfacing applications. In particular, in the realm of neuronal implants, carbon nanotubes have major advantages owing to their unique mechanical and electrical properties. Here we review recent investigations utilizing carbon nanotubes in neuro-interfacing applications. Cell adhesion, neuronal engineering and multi electrode recordings with carbon nanotubes are described. We als...

  17. Electrochemistry of ABTS at Glassy Carbon Electrodes

    Institute of Scientific and Technical Information of China (English)

    Han Zeng; Zhi-qiang Tang; Ling-wen Liao; Jing Kang; Yan-xia Chen

    2011-01-01

    The electrochemical and the mass transport behavior of ABTS2-/ABTS- (2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonate)) redox couple at glassy carbon electrode (GCE) in phosphate buffer solution (PBS,pH=4.4) is studied in detail by cyclic voltammetry combined with rotating disk electrode system.From the i-E curves recorded at different electrode rotating rate,rate constant,and transfer coefficient for ABTS 2-(≒)ABTS-+e reaction at GCE electrode and the diffusion coefficient of ABTS2- in PBS are estimated to be 4.6× 10-3 cm/s,0.28,and 4.4× 10-6 cm2/s,respectively.The transfer coefficient with a value of ca.0.28 differs largely from the value of 0.5 that is always assumed in the literature.The origins for the difference of the rate constant determined and the challenges for estimating the standard rate constant are discussed.The performance for such ABTS2- mediated bio-cathode toward oxygen reduction reaction is discussed according to the over-potential drop as well as current output limit associated with the charge transfer kinetics of ABTS2- (≒)ABTS- +e redox reaction and/or the mass transport effect.

  18. Desalination with carbon aerogel electrodes. Revision 1

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, J.C.; Richardson, J.H.; Fix, D.V. [Lawrence Livermore National Lab., CA (United States); Thomson, S.L.; May, S.C. [Bechtel National, Inc., San Francisco, CA (United States)

    1996-12-04

    Electrically regenerated electrosorption process (carbon aerogel CDI) was developed by LLNL for continuously removing ionic impurities from aqueous streams. A salt solution flows in a channel formed by numerous pairs of parallel carbon aerogel electrodes. Each electrode has a very high BET surface area (2-5.4x10{sup 6}ft{sup 2}lb{sup -1} or 400-1100 m{sup 2}g{sup -1}) and very low electrical resistivity ({le}40 m{Omega}). Ions are removed from the electrolyte by the electric field and electrosorbed onto the carbon aerogel. It is concluded that carbon aerogel CDI may be an energy-efficient alternative to electrodialysis and reverse osmosis for desalination of brackish water ({le}5000 ppM). The intrinsic energy required by this process is about QV/2, where Q is the stored electrical charge and V is the voltage between the electrodes, plus losses. Estimated requirement for desalination of a 2000 ppM feed is -0.53-2.5 Wh/gal{sup -1} (0.5-2.4 kJ L{sup -1}), depending on voltage, flow rate, cell dimensions, aerogel density, recovery ratio, etc. This assumes that 50-70% of the stored electrical energy is reclaimed during regeneration (electrical discharge). Though the energy requirement for desalination of sea water is also low, this application will be much more difficult. Additional work will be required for desalination of streams that contain more than 5000 ppM total dissolved solids (2000 ppM will require electrochemical cells with extremely tight, demanding tolerances). At this present time, the process is best suited for streams with dilute impurities, as recently demonstrated during a field test at LLNL Treatment Facility C.

  19. Carbon-based electrode materials for DNA electroanalysis.

    Science.gov (United States)

    Kato, Dai; Niwa, Osamu

    2013-01-01

    This review addresses recent studies of newly developed carbon-based electrode materials and their use for DNA electroanalysis. Recently, new carbon materials including carbon nanotubes (CNT), graphene and diamond-based nanocarbon electrodes have been actively developed as sensing platforms for biomolecules, such as DNA and proteins. Electrochemical techniques using these new material-based electrodes can provide very simple and inexpensive sensing platforms, and so are expected to be used as one of the "post-light" DNA analysis methods, which include coulometric detection, amperometric detection with electroactive tags or intercalators, and potentiometric detection. DNA electroanalysis using these new carbon materials is summarized in view of recent advances on electrodes.

  20. Consistency Research of Negative Electrode Pasting for MH/Ni High Power Battery

    Institute of Scientific and Technical Information of China (English)

    Zhang Zhong; Liu Dong; Cao Shengbiao; Li Jianping; Jia Chunming

    2004-01-01

    It is discovered that the consistency of negative electrode is one of the main influences on battery performance, since the main raw material in negative electrode is metal hydride powder, ingredients, particle distribution and density of the powder could influence the pasting consistency in some aspects.With the study of MH powder characteristics, through the modification of the coating die, the consistency of negative electrode is improved efficiently.

  1. Electrocatalytic Oxidation of H2O2 at a Carbon Paste Electrode Modified with a Nickel (Ⅱ)-5, 11,17, 23-Tetra-Tert-Butyl-25,27-Bis ( Diethylcarbamoylmethoxy ) Calix[ 4 ] Arene Complex and Its Application

    Institute of Scientific and Technical Information of China (English)

    LiChun-ya; ChertYong; WangChang-fa; LiHai-bing; ChenYuan-yin

    2003-01-01

    Electrochemical behavior of a carbon paste elec-trode (CPE) modified with nickel(Ⅱ)-5, 11, 17, 23-tetra-tert-butyl-25, 27-bis (diethylcarhamoylmethoxy) calix[4] arene (Ni(Ⅱ)-L) complex and its electrocatalytic activity towards the oxidation of hydrogen peroxide were investigated by cyclic voham-metric technique in a 5.0 × 10-2 mol/L NaClO4 + 1. 0× 10-3 mol/L NaOH solution. It was found that Ni(Ⅱ)-L acts as an effective catalyst for the oxidation of hydrogen peroxide. The modified electrode exhibited a linear response over a hydrogen peroxide concentrations in the range of 2. 0 × 10-6--1.0 × 10-4 mol/L with a detection limit as low as 1.0× 10-6 mol/L. The relative standard deviation was 3. 5% for 5 successive determi-nations of H2O2 at 1.0×10-5 mol/L. The modified electrode was used successfully in rainwater analysis.

  2. Performance characteristics of lead oxides in pasted lead/acid battery electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Afifi, S.E. (Electrometallurgy Lab., Central Metallurgical Research and Development Inst., Cairo (Egypt)); Saba, A.E. (Electrometallurgy Lab., Central Metallurgical Research and Development Inst., Cairo (Egypt)); Shenouda, A.Y. (Electrometallurgy Lab., Central Metallurgical Research and Development Inst., Cairo (Egypt))

    1993-10-15

    The performance characteristics of lead oxides used for the pasted type of lead/acid battery plate have been investigated. The [alpha]- and [beta]-PbO polymorphs have been prepared carefully and used for pasting model electrodes. The factors that may affect the electrical capacity of such electrodes have been studied. These are: the type of oxide; percentage of free lead; additives such as carboxymethyl cellulose, zeolite and graphite. Lead hydroxide has also been studied with special attention. Photomicrographs have been taken to examine the crystal forms that develop on the electrode surface. Finally, some industrial samples have been investigated. (orig.)

  3. Carbon nanotube nanocomposite-modified paper electrodes for supercapacitor applications

    Science.gov (United States)

    Korivi, Naga S.; Vangari, Manisha; Jiang, Li

    2017-02-01

    This paper describes the evaluation of carbon paper electrodes for supercapacitor applications. The electrodes are based on carbon micro-fiber paper modified with active material consisting of layers of silver nano-particulate ink and a nanocomposite of multi-walled carbon nanotubes and silver nano-particulate ink. The electrodes were characterized microscopically and electrically. Current-voltage studies revealed a consistent Ohmic behavior of the electrode when modified with different nanostructured active material. Among the active materials incorporated into the electrode, a nanocomposite of carbon nanotubes and silver nano-particulate ink significantly improved capacitance. The paper electrodes can be used for lightweight and ultrathin supercapacitors and other portable energy applications.

  4. Carbon nanotube nanocomposite-modified paper electrodes for supercapacitor applications

    Science.gov (United States)

    Korivi, Naga S.; Vangari, Manisha; Jiang, Li

    2016-12-01

    This paper describes the evaluation of carbon paper electrodes for supercapacitor applications. The electrodes are based on carbon micro-fiber paper modified with active material consisting of layers of silver nano-particulate ink and a nanocomposite of multi-walled carbon nanotubes and silver nano-particulate ink. The electrodes were characterized microscopically and electrically. Current-voltage studies revealed a consistent Ohmic behavior of the electrode when modified with different nanostructured active material. Among the active materials incorporated into the electrode, a nanocomposite of carbon nanotubes and silver nano-particulate ink significantly improved capacitance. The paper electrodes can be used for lightweight and ultrathin supercapacitors and other portable energy applications.

  5. Silver-functionalized carbon nanofiber composite electrodes for ibuprofen detection

    NARCIS (Netherlands)

    Manea, F.; Motoc, S.; Pop, A.; Remes, A.; Schoonman, J.

    2012-01-01

    The aim of this study is to prepare and characterize two types of silver-functionalized carbon nanofiber (CNF) composite electrodes, i.e., silver-decorated CNF-epoxy and silver-modified natural zeolite-CNF-epoxy composite electrodes suitable for ibuprofen detection in aqueous solution. Ag carbon nan

  6. Carbon nanotube based multi electrode arrays for neuronal interfacing: progress and prospects

    Directory of Open Access Journals (Sweden)

    Yael eHanein

    2013-01-01

    Full Text Available Carbon nanotube coatings have been demonstrated over the past several years as a promising material for neuronal interfacing applications. In particular, in the realm of neuronal implants, carbon nanotubes have major advantages owing to their unique mechanical and electrical properties. Here we review recent investigations utilizing carbon nanotubes in neuro-interfacing applications. Cell adhesion, neuronal engineering and multi electrode recordings with carbon nanotubes are described. We also highlight prospective advances in this field, in particular, progress towards flexible, bio-compatible carbon nanotubes technology.

  7. NUCLEATION STUDIES OF GOLD ON CARBON ELECTRODES

    Directory of Open Access Journals (Sweden)

    S. SOBRI

    2008-04-01

    Full Text Available Interest has grown in developing non-toxic electrolytes for gold electrodeposition to replace the conventional cyanide-based bath for long term sustainability of gold electroplating. A solution containing thiosulphate and sulphite has been developed specially for microelectronics applications. However, at the end of the electrodeposition process, the spent electrolyte can contain a significant amount of gold in solution. This study has been initiated to investigate the feasibility of gold recovery from a spent thiosulphate-sulphite electrolyte. We have used flat-plate glassy carbon and graphite electrodes to study the mechanism of nucleation and crystal growth of gold deposition from the spent electrolyte. It was found that at the early stages of reduction process, the deposition of gold on glassy carbon exhibits an instantaneous nucleation of non-overlapping particles. At longer times, the particles begin to overlap and the deposition follows a classic progressive nucleation phenomenon. On the other hand, deposition of gold on graphite does not follow the classical nucleation phenomena.

  8. Electroanalysis of NADH Using Conducting and Redox Active Polymer/Carbon Nanotubes Modified Electrodes-A Review

    Directory of Open Access Journals (Sweden)

    Shen-Ming Chen

    2008-01-01

    Full Text Available Past few decades, conducting and redox active polymers play a critical role in the development of transducers for biosensing. It has been evidenced by increasing numerous reports on conducting and redox active polymers incorporated electrodes for assay of biomolcules. This review highlights the potential uses of electrogenerated polymer modified electrodes and polymer/carbon nanotubes composite modified electrodes for electroanalysis of reduced form of nicotinamide adenine dinuceltoide (NADH. In addition, carbon electrodes modified with organic and inorganic materials as modifier have been discussed in detail for the quantification of NADH based on mediator or mediator-less methods.

  9. Carbon nanotube electrodes for effective interfacing with retinal tissue.

    Science.gov (United States)

    Shoval, Asaf; Adams, Christopher; David-Pur, Moshe; Shein, Mark; Hanein, Yael; Sernagor, Evelyne

    2009-01-01

    We have investigated the use of carbon nanotube coated microelectrodes as an interface material for retinal recording and stimulation applications. Test devices were micro-fabricated and consisted of 60, 30 mum diameter electrodes at spacing of 200 mum. These electrodes were coated via chemical vapor deposition of carbon nanotubes, resulting in conducting, three dimensional surfaces with a high interfacial area. These attributes are important both for the quality of the cell-surface coupling as well as for electro-chemical interfacing efficiency. The entire chip was packaged to fit a commercial multielectrode recording and stimulation system. Electrical recordings of spontaneous spikes from whole-mount neonatal mouse retinas were consistently obtained minutes after retinas were placed over the electrodes, exhibiting typical bursting and propagating waves. Most importantly, the signals obtained with carbon nanotube electrodes have exceptionally high signal to noise ratio, reaching values as high as 75. Moreover, spikes are marked by a conspicuous gradual increase in amplitude recorded over a period of minutes to hours, suggesting improvement in cell-electrode coupling. This phenomenon is not observed in conventional commercial electrodes. Electrical stimulation using carbon nanotube electrodes was also achieved. We attribute the superior performances of the carbon nanotube electrodes to their three dimensional nature and the strong neuro-carbon nanotube affinity. The results presented here show the great potential of carbon nanotube electrodes for retinal interfacing applications. Specifically, our results demonstrate a route to achieve a reduction of the electrode down to few micrometers in order to achieve high efficacy local stimulation needed in retinal prosthetic devices.

  10. Structure engineering of hole-conductor free perovskite-based solar cells with low-temperature-processed commercial carbon paste as cathode.

    Science.gov (United States)

    Zhang, Fuguo; Yang, Xichuan; Wang, Haoxin; Cheng, Ming; Zhao, Jianghua; Sun, Licheng

    2014-09-24

    Low-temperature-processed (100 °C) carbon paste was developed as counter electrode material in hole-conductor free perovskite/TiO2 heterojunction solar cells to substitute noble metallic materials. Under optimized conditions, an impressive PCE value of 8.31% has been achieved with this carbon counter electrode fabricated by doctor-blading technique. Electrochemical impedance spectroscopy demonstrates good charge transport characteristics of low-temperature-processed carbon counter electrode. Moreover, this carbon counter electrode-based perovskite solar cell exhibits good stability over 800 h.

  11. Mutagens in urine of carbon electrode workers

    Energy Technology Data Exchange (ETDEWEB)

    Pasquini, R.; Monarca, S.; Sforzolini, G.S.; Conti, R.; Fagioli, F.

    1982-01-01

    Following previous work carried out in an Italian factory producing carbon electrodes and evaluating the occupational mutagenic-carcinogenic hazards, the authors studied the presence of mutagen metabolites in the urine of workers in the same factory who were exposed to petroleum coke and pitch and in the urine of a control group of unexposed workers. The urine samples were concentrated by absorption on XAD-2 columns and were tested using the Salmonella/microsome assay (strain TA98, TA100, TA1535, TA1538) with and without the addition of beta-glucuronidase and metabolizing system. The collection of urine samples was carried out twice, with an interval of 2 months; 'before working time', 'after working time', and also during Sunday. The results showed that urine samples collected 'before' occupational exposure (upon waking) or on Sunday revealed no mutagenic activity in either worker groups and that the urine samples collected after or during occupational exposure revealed high mutagenic activity in the exposed workers, with a statistically significant difference between the mean of the revertants/plate values for exposed and unexposed workers. On the basis of the previous and the present research, the authors suggest that application of the Salmonella/microsome test to work environments could offer useful and suitable tool for evaluating the health hazards due to mutagenic/carcinogenic substances from occupational exposure.

  12. Wireless desalination using inductively powered porous carbon electrodes

    NARCIS (Netherlands)

    Kuipers, J.; Porada, S.

    2013-01-01

    Water desalination by capacitive deionization (CDI) uses electrochemical cell pairs formed of porous carbon electrodes, which are brought in contact with the water that must be desalinated. Upon applying a cell voltage or current between the electrodes, ions are electrosorbed and water is produced o

  13. Carbon nanotube electrodes for effective interfacing with retinal tissue

    Directory of Open Access Journals (Sweden)

    Asaf Shoval

    2009-04-01

    Full Text Available We have investigated the use of carbon nanotube microelectrodes as an interface material for retinal recording and stimulation applications. Test devices were micro-fabricated and consisted of 60 pristine 30 um electrodes coated with chemical vapor deposited carbon nanotubes, resulting in conducting, three dimensional surfaces with a high effective interfacial area. These attributes are important both for the quality of the cell-surface coupling as well as for electro-chemical interfacing efficiency. The entire chip was packaged to fit a commercial multielectrode recording and stimulation system. Electrical recordings of spontaneous spikes from whole-mount neonatal mouse retinas were consistently obtained minutes after retinas were placed over the electrodes, exhibiting typical bursting and propagating waves. Most importantly, the signals obtained with carbon nanotube electrodes have exceptionally high signal to noise ratio, reaching values as high as 75. Moreover, spikes are marked by a conspicuous gradual increase in amplitude recorded over a period of minutes to hours, suggesting improvement in cell-electrode coupling. This phenomenon is not observed in conventional commercial electrodes. Electrical stimulation using carbon nanotube electrodes was also achieved. We attribute the superior performances of the carbon nanotube electrodes to their three dimensional nature and the strong neuro-carbon nanotube affinity. The results presented here show the great potential of carbon nanotube electrodes for retinal interfacing applications. Specifically, our results demonstrate a route to achieve a reduction in the electrode size down to few micrometers in order to achieve high efficacy local stimulation needed in retinal prosthetic devices.

  14. Carbon Nanotube Electrodes for Effective Interfacing with Retinal Tissue

    OpenAIRE

    Shoval, Asaf; Adams, Christopher; David-Pur, Moshe; Shein, Mark; Hanein, Yael; Sernagor, Evelyne

    2009-01-01

    We have investigated the use of carbon nanotube coated microelectrodes as an interface material for retinal recording and stimulation applications. Test devices were micro-fabricated and consisted of 60, 30 μm diameter electrodes at spacing of 200 μm. These electrodes were coated via chemical vapor deposition of carbon nanotubes, resulting in conducting, three dimensional surfaces with a high interfacial area. These attributes are important both for the quality of the cell-surface coupling as...

  15. Effect of oxidation of carbon material on suspension electrodes for flow electrode capacitive deionization.

    Science.gov (United States)

    Hatzell, Kelsey B; Hatzell, Marta C; Cook, Kevin M; Boota, Muhammad; Housel, Gabrielle M; McBride, Alexander; Kumbur, E Caglan; Gogotsi, Yury

    2015-03-03

    Flow electrode deionization (FCDI) is an emerging area for continuous and scalable deionization, but the electrochemical and flow properties of the flow electrode need to be improved to minimize energy consumption. Chemical oxidation of granular activated carbon (AC) was examined here to study the role of surface heteroatoms on rheology and electrochemical performance of a flow electrode (carbon slurry) for deionization processes. Moreover, it was demonstrated that higher mass densities could be used without increasing energy for pumping when using oxidized active material. High mass-loaded flow electrodes (28% carbon content) based on oxidized AC displayed similar viscosities (∼21 Pa s) to lower mass-loaded flow electrodes (20% carbon content) based on nonoxidized AC. The 40% increased mass loading (from 20% to 28%) resulted in a 25% increase in flow electrode gravimetric capacitance (from 65 to 83 F g(-1)) without sacrificing flowability (viscosity). The electrical energy required to remove ∼18% of the ions (desalt) from of the feed solution was observed to be significantly dependent on the mass loading and decreased (∼60%) from 92 ± 7 to 28 ± 2.7 J with increased mass densities from 5 to 23 wt %. It is shown that the surface chemistry of the active material in a flow electrode effects the electrical and pumping energy requirements of a FCDI system.

  16. Capacitive, deionization with carbon aerogel electrodes: Carbonate, sulfate, and phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, J.C.; Fix, D.V.; Mack, G.V.; Pekala, R.W.; Poco, J.F.

    1995-07-24

    A process for the capacitive deionization (CDI) of water with a stack of carbon aerogel electrodes has been developed by Lawrence Livermore National Laboratory. Unlike ion exchange, one of the more conventional deionization processes, no chemicals are required for regeneration of the system. Electricity is used instead. Water with various anions and cations is pumped through the electrochemical cell. After polarization, ions are electrostatically removed from the water and held in the electric double layers formed at the surfaces of electrodes. The water leaving the cell is purified, as desired. The effects of cell voltage on the electrosorption capacities for Na{sub 2}SO{sub 4}, Na{sub 3}PO{sub 4}, and Na{sub 2}CO{sub 3} have been investigated and are reported here. Results for NaCl and NaNO{sub 3} have been reported previously. Possible applications for CDI are as a replacement for ion exchange processes which remove heavy metals and radioisotopes from process and waste water in various industries, as well as to remove inorganic ions from feedwater for fossil and nuclear power plants.

  17. Fabrication, Characterization and Electrocatalysis of an Ordered Carbon Nanotube Electrode

    Institute of Scientific and Technical Information of China (English)

    陈静; 包建春; 蔡称心

    2003-01-01

    A method for fabrication of ordered carbon nanotube (CNT) film,which was template-synthesized within the highly ordered pores of a commercially available alumina template membrane,modified glassy carbon(CNT/GC) electrode was established.The CNT/GC electrode showed excellent electrocatalytic activity toward dopamine electrochemical reaction without introducing any electrochemically active group into CNT film or activating any electrochemically active group into CNT film or activating the electrode electrochemically.DA undergoes ideal reversible electrochemical reaction on CNT/GC electrode at low scan rate(≤20mV/s) with an excellent reproducibility and stability.The CNT/GC electrode might be used in biosensors because the highly ordered CNT may present a steric effect on more efficient redox reactions of biomolecules.

  18. Cupric Hexacyanoferrate Nanoparticle Modified Carbon Ceramic Composite Electrodes

    Institute of Scientific and Technical Information of China (English)

    WANG,Peng(王鹏); ZHU,Guo-Yi(朱果逸)

    2002-01-01

    Graphite powder-supported cupric hexacyanoferrate (CuHCF)nanoparticles were dispersed into methyltrimethoxysilane-based gels to produce a conducting carbon ceramic composite, which was used as electrode material to fabricate surface-renewable CuHCF-modified electrodes. Electrochemical behavior of the CuHCF-modified carbon ceramic composite electrodes was characterized using cyclic and square-wave voitammetry.Cyclic voltammograms at various scan rates indicated that peak currents were surface-confined at low scan rates. In the presence of glutathione, a clear electrocatalytic response was observed at the CuHCF-modified composite electrodes. In addition, the electrodes exhibited a distinct advantage of reproducible surface-renewal by simple mechanical polishing on emery paper, as well as ease of preparation, and good chemical and mechanical stability in a flowing stream.

  19. Cupric Hexacyanoferrate Nanoparticle Modified Carbon Ceramic Composite Electrodes

    Institute of Scientific and Technical Information of China (English)

    WANG,Peng; ZHU,Guo-Yi

    2002-01-01

    Graphite powder-supported cupric hexacyanoferrate(CuHCF) nanoparticles were dispersed into methyltrimethoxysilane-based gels to produce a conducting carbon ceramic composite,which was used as electrode materials to fabricate surface-renewable CuHCF-modified electrodes.Electrochemical behavior of the CuHCF-modified carbon ceramic composite electrodes was characterized using cyclic and square-wave voltammetry. Cyclinc voltammograms at various scan rates indicated that peak currents were suface-confined at low scan rates.In the presence of glutathione,a clear electrocatalytic response was observed at the CuHCF-modified composite electrodes.In addition,the electrodes exhibited a distinct advantage of reproducible surface-renewal by simple mechanical polishing on emery paper,as well as ease of preparation,and good chemical and mechanical stability in a flowing stream.

  20. A Reliable Reference Electrode in Molten Carbonate and Its Applications

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    A Ag|AgCl reference electrode which can be used in molten carbonate media has been described in this paper.It consists of a silver wire immersed in a solution of AgCl(1mol%) in (Li0.62,K0.38)2CO3,with a zirconia junction.The main properties of reference electrode,such as reproducibility ,stability and reversibility, were checked.The results have demonstrated that the reference electrode is reliable.With such reference electrode catalysis of various electrode materials to oxygen reduction in molten alkali carbonate media was investigated.It is found that as catalysts for oxygen reduction oxidized nickel-niobium alloy is superior to nickel oxide.

  1. Sensitive voltammetric determination of tryptophan using an acetylene black paste electrode modified with a Schiff's base derivative of chitosan.

    Science.gov (United States)

    Deng, Peihong; Fei, Junjie; Feng, Yonglan

    2011-12-21

    Chitosan was modified by salicylaldehyde via Schiff's base reaction and the resulting product was modified on the surface of an acetylene black paste electrode (ABPE) by the drop-coating method. In 0.5 mol L(-1) acetate buffer (pH 4.2), a substantial increase in the anodic stripping peak current of tryptophan (Trp) (compared to conventional bare carbon paste electrode (CPE) and bare ABPE) is observed at the Schiff's base chitosan-modified electrode. The parameters influencing voltammetric determination of Trp have been optimized. Under the selected conditions, the linearity between the anodic peak currents and concentrations of Trp demonstrated a wide range of 6.0 × 10(-8) mol L(-1) to 2.0 × 10(-6) mol L(-1), 2.0 × 10(-6) mol L(-1) to 4.0 × 10(-5) mol L(-1) and 4.0 × 10(-5) mol L(-1) to 1.0 × 10(-4) mol L(-1), a low detection limit of 2.0 × 10(-9) mol L(-1) was obtained after a 60 s accumulation. In addition, the developed electrochemical sensor has been successfully applied for the determination of Trp in pharmaceutical and biological samples with satisfactory assay results.

  2. Coaxial fiber supercapacitor using all-carbon material electrodes.

    Science.gov (United States)

    Le, Viet Thong; Kim, Heetae; Ghosh, Arunabha; Kim, Jaesu; Chang, Jian; Vu, Quoc An; Pham, Duy Tho; Lee, Ju-Hyuck; Kim, Sang-Woo; Lee, Young Hee

    2013-07-23

    We report a coaxial fiber supercapacitor, which consists of carbon microfiber bundles coated with multiwalled carbon nanotubes as a core electrode and carbon nanofiber paper as an outer electrode. The ratio of electrode volumes was determined by a half-cell test of each electrode. The capacitance reached 6.3 mF cm(-1) (86.8 mF cm(-2)) at a core electrode diameter of 230 μm and the measured energy density was 0.7 μWh cm(-1) (9.8 μWh cm(-2)) at a power density of 13.7 μW cm(-1) (189.4 μW cm(-2)), which were much higher than the previous reports. The change in the cyclic voltammetry characteristics was negligible at 180° bending, with excellent cycling performance. The high capacitance, high energy density, and power density of the coaxial fiber supercapacitor are attributed to not only high effective surface area due to its coaxial structure and bundle of the core electrode, but also all-carbon materials electrodes which have high conductivity. Our coaxial fiber supercapacitor can promote the development of textile electronics in near future.

  3. Laser sintering of conductive carbon paste on plastic substrate

    Science.gov (United States)

    Kinzel, Edward C.; Kelkar, Rohan; Xu, Xianfan

    2010-02-01

    This work investigates fabrication of functional conductive carbon paste onto a plastic substrate using a laser. The method allows simultaneous sintering, patterning, and functionalization of the carbon paste. Experiments are carried out to optimize the laser processing parameters. It is shown that sheet resistance values obtained by laser sintering are close to the one specified by the manufacturer using conventional sintering method. Additionally, a heat transfer analysis using numerical methods is conducted to understand the relationship between the temperature during sintering and the sheet resistance values of sintered carbon wires. The process developed in this work has the potential of producing carbon-based electronic components on low cost plastic substrates.

  4. 谷胱甘肽在咖啡酸修饰碳糊电极上的电催化氧化及电分析方法%Electrocatalytic oxidation of glutathione at caffeic acid modified carbon paste electrode and its electrochemical determination

    Institute of Scientific and Technical Information of China (English)

    张艳梅; 段成茜; 高作宁

    2011-01-01

    目的:研究了谷胱甘肽(还原型,glutathione,GSH)在咖啡酸(Caffeic acid,CFA)修饰碳糊电极(CFA/CPE)上的电催化氧化行为和电化学分析方法.方法:循环伏安法(CV),计时电流法(CA)和线性扫描伏安法(LSV).结果:GSH在碳糊电极(CPE)上的直接电化学氧化过程十分迟缓,CFA/CPE对GSH电化学氧化具有良好的催化作用.同时测定了GSH在CFA/CPE上的电极过程动力学参数,用LSV法测得催化氧化峰电流与GSH在5.0×10-5~1.0×10-3 mol·L-1浓度范围内呈良好线性关系,线性回归方程为Ipa(μA) =2.003c (10-3 mol·L-1)+3.448,r=0.9989,检出限为4.0×10-5 mol·L-1.结论:CFA/CPE对GSH电化学氧化具有良好的催化作用,该方法可用于市售还原型谷胱甘肽药物含量的电化学定量测定.%Objective:Electrocatalytic oxidation behaviors and electrochemical determination of glutathione(GSH) at carbon paste electrode (CPE) and caffeic acid modified carbon paste electrode ( CFA/CPE ) were investigated. Methods:Cyclic voltammetry(CV) ,chronoamperometry(CA) and linear sweep voltammetry(LSV). Results;It was found that glutathione itself showed a poor electrochemical response at carbon paste electrode (CPE) , the electrochemical behaviors could be greatly enhanced by using CFA/CPE,which enables a sensitive electrochemical determination of the substrate glutathione. The kinetic parameters of the reaction were evaluated. The catalytic oxidation peak currents of glutathione versus its concentration had a good linear relationship in the concentration range of 5. 0 x 10-5 ~ 1.0 x 10-3 mol·L-1 with the correlation coefficient of 0. 9989, and the detection limit of 4. 0 x 10-5 mol ·L-1 by LSV. Conclusion:CFA/CPE can catalyze the oxidation of GSH well. Furthermore,the proposed method can be applied in the electrochemical determination of glutathione content with real samples with the simple manipulation.

  5. Simultaneous determination of the isomers of Ponceau 4R and Amaranth using an expanded graphite paste electrode.

    Science.gov (United States)

    Zhang, Jing; Wang, Meiling; Shentu, Chao; Wang, Wenchang; Chen, Zhidong

    2014-10-01

    A sensitive and convenient electrochemical method was developed for the simultaneous determination of the isomers of Ponceau 4R and Amaranth by an expanded graphite paste electrode (EGPE). The EGPE was prepared by mixing EG with solid paraffin. Compared with flake graphite paste and carbon paste electrodes, the EGPE showed higher electrocatalytic activity towards the oxidization of Ponceau 4R and Amaranth. Under optimal experimental conditions, the EGPE exhibited wide linear responses to Ponceau 4R and Amaranth ranging from 6×10(-8) to 4×10(-6) mol/L and 8×10(-8) to 4×10(-6)mol/L, respectively, and the detection limits for Ponceau 4R and Amaranth were 2 and 36 nmol/L, respectively, at a signal-to-noise ratio of 3. The EGPE showed good reproducibility, stability and reusability. The proposed method was successfully applied in the detection of Ponceau 4R and Amaranth in grape juice samples.

  6. Graphene/graphite paste electrode incorporated with molecularly imprinted polymer nanoparticles as a novel sensor for differential pulse voltammetry determination of fluoxetine.

    Science.gov (United States)

    Alizadeh, Taher; Azizi, Sorour

    2016-07-15

    Molecularly imprinted polymer (MIP) nanoparticles including highly selective recognition sites for fluoxetine were synthesized, utilizing precipitation polymerization. Methacrylic acid and vinyl benzene were used as functional monomers. Ethylene glycol dimethacrylate was used as cross-linker agent. The obtained polymeric nanoparticles were incorporated with carbon paste electrode (CPE) in order to construct a fluoxetine selective sensor. The response of the MIP-CP electrode to fluoxetine was remarkably higher than the electrode, modified with the non-imprinted polymer, indicating the excellent efficiency of the MIP sites for target molecule recognition. It was found that the addition of a little amount of graphene, synthesized via modified hummer's method, to the MIP-CP resulted in considerable enhancement in the sensitivity of the electrode to fluoxetine. Also, the style of electrode components mixing, before carbon paste preparation, was demonstrated to be influential factor in the electrode response. Some parameters, affecting sensor response, were optimized and then a calibration curve was plotted. A dynamic linear range of 6×10(-9)-1.0×10(-7)molL(-1) was obtained. The detection limit of the sensor was calculated equal to 2.8×10(-9)molL(-1) (3Sb/m). This sensor was used successfully for fluoxetine determination in the spiked plasma samples as well as fluoxetine capsules.

  7. Oxygen reduction on teflon-bonded carbon electrode

    Institute of Scientific and Technical Information of China (English)

    周德璧; 黄可龙; 张世民

    2004-01-01

    Oxygen reduction on Teflon-bonded carbon gas diffusion electrode without catalyst in 6 mol/L KOH solution was investigated with acimpedance spectroscopy and other electrochemical techniques. The kinetic parameters were measured with an exchange current density of J0= 3.44 × 10-9 and a Tafel slope of 46 mV/dec in low overpotential range (-0.05 --0.14 V vs SCE), which are comparable with those reported on carbon supported platinum electrode. The reaction mechanism of OR and the active effect of carbon black were examined.

  8. Towards Flexible Transparent Electrodes Based on Carbon and Metallic Materials

    Directory of Open Access Journals (Sweden)

    Minghui Luo

    2017-01-01

    Full Text Available Flexible transparent electrodes (FTEs with high stability and scalability are in high demand for the extremely widespread applications in flexible optoelectronic devices. Traditionally, thin films of indium thin oxide (ITO served the role of FTEs, but film brittleness and scarcity of materials limit its further application. This review provides a summary of recent advances in emerging transparent electrodes and related flexible devices (e.g., touch panels, organic light-emitting diodes, sensors, supercapacitors, and solar cells. Mainly focusing on the FTEs based on carbon nanomaterials (e.g., carbon nanotubes and graphene and metal materials (e.g., metal grid and metal nanowires, we discuss the fabrication techniques, the performance improvement, and the representative applications of these highly transparent and flexible electrodes. Finally, the challenges and prospects of flexible transparent electrodes will be summarized.

  9. Carbon nanotube electrodes for hot-wire electrochemistry.

    Science.gov (United States)

    Gründler, Peter; Frank, Otakar; Kavan, Ladislav; Dunsch, Lothar

    2009-02-23

    The use and preparation of single-walled carbon nanotubes (SWCNTs) at thin metallic wire electrodes for hot-wire electrochemical studies is described. The nanotubes were deposited on metal substrates such as gold by electrophoresis from a dispersion containing sodium dodecyl sulphate as an anionic surfactant. The formation of a layer of pure SWCNTs is achieved by thermal treatment at 350 degrees C. When heated in situ by a strong ac current, the electrodes can be used for electrochemical studies of nanotubes at increased temperatures. The state and functionality of the electrodes were characterized by Raman spectroscopy, scanning electron microscopy, and cyclic voltammetry with both anionic and cationic redox systems (dopamine, ferrocene carboxylic acid). First time experiments at the heated SWCNT electrodes demonstrated an excellent suitability of these as-prepared electrodes for thermoelectrochemical studies.

  10. Oxygen electrode in molten carbonate fuel cells

    Science.gov (United States)

    Dave, B. B.; White, R. E.; Srinivasan, S.; Appleby, A. J.

    1990-12-01

    During this quarter, impedance data were analyzed for an oxygen reduction process in molten carbonate electrolyte and a manuscript, Impedance Analysis for Oxygen Reduction in a Lithium Carbonate Melt: Effects of Partial Pressure of Carbon Dioxide and Temperature, was prepared to be submitted to Journal of the Electrochemical Society for publication.

  11. Study of Co-Ce coating and surface on pasted nickel electrodes substrate

    Institute of Scientific and Technical Information of China (English)

    WANG Dianlong; WANG Chunyu; DAI Changsong; SUN Dezhi

    2006-01-01

    The process of electroplating Co-Ce alloys on the nickel foam framework surface can improve electro-conductivity for active materials and nickelsubstrate interface. The results of inductive coupled plasma emission spectrometer (ICP), cyclic voltammetry (CV), scanning electron microscopy (SEM), X-ray diffraction (XRD) and electron probe microanalysis (EPMA) indicate that the Co-Ce coating chemical content of rare earth Ce 0.19wt.%-0.28wt.% can not only alter the microstructure of electroplating coating, but also accelerate the oxidation reaction of Co and improve its transfer rate of electric current conductivity to the active material particles. The grads-like distributing electro-conductive network of CoOOH is formed on the nickel substrate surface, which improves reversibility of pasted nickel electrode. The charging receptivity is improved by Co-Ce coating on the pasted nickel electrode substrate, and its specific discharging capacity is improved by 50%.

  12. Carbon electrode for desalination purpose in capacitive deionization

    Science.gov (United States)

    Endarko, Fadilah, Nurul; Anggoro, Diky

    2016-03-01

    Carbon electrodes for desalination purpose have been successfully synthesized using activated carbon powder (BET surface area=700 - 1400 m2/g), carbon black and polyvinyl alcohol (PVA) binder by cross-linking method with glutaric acid (GA) at 120 °C. The electrochemical properties of the carbon electrodes were analyzed using electrical impedance spectroscopy (EIS) and cyclic voltammetry (CV) whilst the physical properties were observed with scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM/EDX). In order to assess the desalting performance, salt removal experiments were performed by constructing a capacitive deionization unit cell with five pairs of carbon electrodes. For each pair consisted of two parallel carbon electrodes separated by a spacer. Desalination and regeneration processes were also observed in the salt-removal experiments. The salt-removal experiments were carried out in single-pass mode using a solution with 0.1 M NaCl at a flow rate of 10 mL/min. A voltage of 3 V was applied to the cell for 60 minutes for both processes in desalination and regeneration. The result showed that the percentage value of the salt-removal was achieved at 20%.

  13. Reduction of carbon monoxide. Past research summary

    Energy Technology Data Exchange (ETDEWEB)

    Schrock, R.R.

    1981-10-01

    Research programs for the year on the preparation, characterization, and reactions of binuclear tantalum complexes are described. All evidence to date suggest the following of these dimeric molecules: (1) the dimer does not break into monomers under mild conditions; (2) intermolecular hydride exchange is not negligible, but it is slow; (3) intermolecular non-ionic halide exchange is fast; (4) the ends of the dimers can rotate partially with respect to one another. The binuclear tantalum hydride complexes were found to react with carbon monoxide to give a molecule which is the only example of reduction of CO by a transition metal hydride to give a complex containing a CHO ligand. Isonitrides also reacted in a similar manner with dimeric tantalum hydride. (ATT)

  14. Electrocatalysis and simultaneous determination of dopamine and uric acid using a poly ( calconcarboxylic acid) film modified carbon paste electrode%多巴胺在聚钙羧酸膜修饰碳糊电极上的电催化及与尿酸的同时测定

    Institute of Scientific and Technical Information of China (English)

    刘静; 陈斌; 周元臻; 张海艳

    2012-01-01

    A novel poly calconcarboxylic acid ( CCA) film modified carbon paste electrode ( CPE) was fabricated and electrochemical behaviors of dopamine (DA) and uric acid ( UA) were studied. The results showed the modified electrode had excellent electrocatalytic activity toward DA and UA, and a pair of well-defined quasi-reversible redox peaks of DA was obtained. The linear response of DA was obtained in the range of 3. 0×10 -7 to 1.0 × 10-4mol/L with a detection limit ( S/N =3) of 1 × 10-7 mol/L. Furthermore, the simultaneous determination of DA and UA by differential pulse voltammetry (DPV) was investigated. The oxidation peaks of DA and UA were completely separated ( △Ep = 192 mV) and the peak currents were linear with the concentrations. The modified electrode could be used to simultaneously determine DA and UA.%采用循环伏安法(CV)制备了聚钙羧酸( PCCA)膜修饰的碳糊电极(CPE).考察了电极对多巴胺(DA)、尿酸(UA)的电氧化催化性能.结果显示,聚钙羧酸膜修饰碳糊电极( PCCA/CPE)对DA有良好的电催化效果,DA呈现出一对准可逆的氧化还原峰,氧化峰电流与DA浓度在3.0×10-7~1.0×10-4moL/L范围内呈线性关系,检出限为1×10 -7mol/L( S/N=3).使用微分脉冲伏安法(DPV),DA和UA在PCCA/CPE上的氧化峰能完全分离(△Ep=192 mV),且峰电流与浓度均呈现良好的线性关系,可实现对DA和UA的同时测定.实验还进行了实际样品测定.

  15. All-Carbon Electrode Consisting of Carbon Nanotubes on Graphite Foil for Flexible Electrochemical Applications

    Directory of Open Access Journals (Sweden)

    Je-Hwang Ryu

    2014-03-01

    Full Text Available We demonstrate the fabrication of an all-carbon electrode by plasma-enhanced chemical vapor deposition for use in flexible electrochemical applications. The electrode is composed of vertically aligned carbon nanotubes that are grown directly on a flexible graphite foil. Being all-carbon, the simple fabrication process and the excellent electrochemical characteristics present an approach through which high-performance, highly-stable and cost-effective electrochemical applications can be achieved.

  16. Using mesoporous carbon electrodes for brackish water desalination.

    Science.gov (United States)

    Zou, Linda; Li, Lixia; Song, Huaihe; Morris, Gayle

    2008-04-01

    Electrosorptive deionisation is an alternative process to remove salt ions from the brackish water. The porous carbon materials are used as electrodes. When charged in low voltage electric fields, they possess a highly charged surface that induces adsorption of salt ions on the surface. This process is reversible, so the adsorbed salt ions can be desorbed and the electrode can be reused. In the study, an ordered mesoporous carbon (OMC) electrode was developed for electrosorptive desalination. The effects of pore arrangement pattern (ordered and random) and pore size distribution (mesopores and micropores) on the desalination performance was investigated by comparing OMC and activated carbon (AC). It were revealed from X-ray diffraction and N(2) sorption measurements that AC has both micropores and mesopores, whereas ordered mesopores are dominant in OMC. Their performance as potential electrodes to remove salt was evaluated by cyclic voltammetry (CV) and galvanostatic charge/discharge tests at a range of electrolyte concentrations and sweep rates. It is deduced that under the same electrochemical condition the specific capacitance values of OMC electrode (i.e. 133 F/g obtained from CV at a sweep rate of 1 mV/s in 0.1M NaCl solution) are larger than those of AC electrode (107 F/g), suggesting that the former has a higher desalting capacity than the latter. Furthermore, the OMC electrode shows a better rate capacity than the AC electrode. In addition, the desalination capacities were quantified by the batch-mode experiment at low voltage of 1.2V in 25 ppm NaCl solution (50 micros/cm conductivity). It was found that the adsorbed ion amounts of OMC and AC electrodes were 11.6 and 4.3 micromol/g, respectively. The excellent electrosorptive desalination performance of OMC electrode might be not only due to the suitable pore size (average of 3.3 nm) for the propagation of the salt ions, but also due to the ordered mesoporous structure that facilitates desorption of the

  17. High-performance Supercapacitor cells with Activated Carbon/MWNT nanocomposite electrodes

    Science.gov (United States)

    Markoulidis, F.; Lei, C.; Lekakou, C.; Figgemeier, E.; Duff, D.; Khalil, S.; Martorana, B.; Cannavaro, I.

    2012-09-01

    The purpose of this work was to investigate and improve the performance of supercapacitor cells with carbon-based nanocomposite electrodes. The electrode structure comprised activated carbon (AC), four types of multi-wall nanotubes (MWNTs) and two alternative polymer binders, Polyvinyl alcohol (PVA) or Polyvinylidene fluoride (PVDF). Electrode fabrication involved various stages of mixing and dispersion of the AC powder and carbon nanotubes, rolling and coating of the AC/MWNT/binder paste on an aluminium substrate which also served as current collector. The organic electrolyte utilised was 1M tetraethylammonium tetrafluoroborate (TEABF4) fully dissolved in propylene carbonate (PC). All devices were of the electrochemical double layer capacitor (EDLC) type, incorporating four layers of tissue paper as separator material. The surface topography of the so fabricated electrodes was investigated with scanning electrode microscopy (SEM). Overall cell performance was evaluated with a multi-channel potentiostat/galvanostat/impedance analyser. Each supercapacitor cell was subjected to Cyclic Voltammetry (CV) at various scan rates from 0.01 V/s to 1 V/s, Charge-Discharge at a fixed current steps (2 mA) and Electrochemical Impedance Spectroscopy (EIS) with frequency range from 10 mHz to 1 MHz. It was established that an AC-based supercapacitor with 0.15%w/w MWNT content and 30 μm roll-coated, nanocomposite electrodes provided superior energy and power and energy densities while the cells was immersed in the electrolyte; well above those generated by the AC-based EDLC cells.

  18. DNA Nano-netting Intertexture on Carbon Electrodes

    Institute of Scientific and Technical Information of China (English)

    Xiang Qin LIN; Xiao Hua JIANG; Li Ping LU

    2004-01-01

    Native calf thymus double stranded DNA (ct-dsDNA) is successfully immobilized from solution onto carbon substrates by covalent linkages under an optimized deposition potential of 1.8±0.3 V vs.50 mmol/L NaCl-Ag/AgCl.The long chain DNA fabricates a layer of well conductive nano-netting intertexture, which is stable in pH 14 alkaline solution and in boiling water.The ct-dsDNA modified carbon fiber disk electrode shows two to three orders of magnitude enlarged electrode effective surface area and similarly enlarged voltammetric responses to Co(phen)33+ and dopamine.Thermal dissociated single stranded ct-DNA can also lead to similar result.This modified electrode will find wide applications in the fields of DNA-based electrochemical biosensors.

  19. Carbon nanotube yarns as strong flexible conductive capacitive electrodes

    NARCIS (Netherlands)

    Liu, F.; Wagterveld, R.M.; Gebben, B.; Otto, M.J.; Biesheuvel, P.M.; Hamelers, H.V.M.

    2015-01-01

    Carbon nanotube (CNT) yarn, consisting of 23 µm diameter CNT filaments, can be used as capacitive electrodes that are long, flexible, conductive and strong, for applications in energy and electrochemical water treatment. We measure the charge storage capacity as function of salt concentration, and u

  20. Synthesis, spectroscopic and electrochemical performance of pasted β-nickel hydroxide electrode in alkaline electrolyte

    Science.gov (United States)

    Shruthi, B.; Bheema Raju, V.; Madhu, B. J.

    2015-01-01

    β-Nickel hydroxide (β-Ni(OH)2) was successfully synthesized using precipitation method. The structure and property of the β-Ni(OH)2 were characterized by X-ray diffraction (XRD), Fourier Transform infra-red (FT-IR), Raman spectra and thermal gravimetric-differential thermal analysis (TG-DTA). The results of the FTIR spectroscopy and TG-DTA studies indicate that the β-Ni(OH)2 contains water molecules and anions. The microstructural and composition studies have been performed using Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray (EDX) analysis. A pasted-type electrode is prepared using β-Ni(OH)2 powder as the active material on a nickel sheet as a current collector. Cyclic voltammetry (CV) and Electrochemical impedance spectroscopy (EIS) studies were performed to evaluate the electrochemical performance of the β-Ni(OH)2 electrode in 6 M KOH electrolyte. CV curves showed a pair of strong redox peaks as a result of the Faradaic redox reactions of β-Ni(OH)2. The proton diffusion coefficient (D) for the present β-Ni(OH)2 electrode material is found to be 1.44 × 10-12 cm2 s-1. Further, electrochemical impedance studies confirmed that the β-Ni(OH)2 electrode reaction processes are diffusion controlled.

  1. Bismuth Modified Carbon-Based Electrodes for the Determination of Selected Neonicotinoid Insecticides

    Directory of Open Access Journals (Sweden)

    Marko Rodić

    2011-05-01

    Full Text Available Two types of bismuth modified electrodes, a bismuth-film modified glassy carbon (BiF-GCE and a bismuth bulk modified carbon paste, were applied for the determination of selected nitroguanidine neonicotinoid insecticides. The method based on an ex situ prepared BiF-GCE operated in the differential pulse voltammetric (DPV mode was applied to determine clothianidin in the concentration range from 2.5 to 23 μg cm−3 with a relative standard deviation (RSD not exceeding 1.5%. The tricresyl phosphate-based carbon paste electrodes (TCP-CPEs, bulk modified with 5 and 20 w/w% of bismuth, showed a different analytical performance in the determination of imidacloprid, regarding the peak shape, potential window, and noise level. The TCP-CPE with 5% Bi was advantageous, and the developed DPV method based on it allowed the determination in the concentration range from 1.7 to 60 μg cm−3 with an RSD of 2.4%. To get a deeper insight into the morphology of the bismuth-based sensor surfaces, scanning electron microscopic measurements were performed of both the surface film and the bulk modified electrodes.

  2. Novel Carbons as Electrodes for Electrical Energy Storage

    Science.gov (United States)

    Ruoff, Rodney S.

    2014-03-01

    In this talk I will speculate about directions for carbon materials as the electrode(s) in EES systems such as ultracapacitors and Li ion batteries. Perhaps the penultimate electrode material for ultracapacitors (based on charge storage by electrical double layer capacitance, EDLC) would be a ``negative curvature carbon'' (NCC, akin to the Schwartzite structures) with atom thick walls, and possibly substitutionally doped with, e.g., N atoms in case the all-carbon structure were limited by quantum (i.e., intrinsic) capacitance. Such an NCC would have a distribution of pore sizes that would likely (for optimal performance) span ``mesoscale'' and ``microscale'' pores, which in the parlance of porous materials means pores ``above 2-3 nanometers'' and pores ``below about 2 nanometers,'' respectively. Making such materials offers exciting challenges for materials chemists/synthetic chemists, and to date only the ``basic'' Schwarzite structures (ideal crystals studied by DFT with periodic boundary conditions and relatively simple unit cells) have been modeled in terms of properties such as their electronic states and in some cases, potential as all carbon ferromagnets. I identified the NCCs as candidates for EES for ultracapacitors, in a paper published in Science in 2011 with coauthors. We made an aperiodic carbon that had atom thick walls and surface areas as high as 3200 m2/g, along with ``good'' powder electrical conductivity, high carbon content, and apparently close to 100% trivalently bonded carbon in the walls of this very porous carbon. We have learned in one set of experiments, as published in Energy and Environmental Science, that doping with N atoms can increase the EDLC, which we suggest could be a consequence of limiting quantum capacitance in the all-carbon analogue.

  3. Enhanced performance of electrospun carbon fibers modified with carbon nanotubes: promising electrodes for enzymatic biofuel cells.

    Science.gov (United States)

    Engel, A Both; Cherifi, A; Tingry, S; Cornu, D; Peigney, A; Laurent, Ch

    2013-06-21

    New nanostructured electrodes, promising for the production of clean and renewable energy in biofuel cells, were developed with success. For this purpose, carbon nanofibers were produced by the electrospinning of polyacrylonitrile solution followed by convenient thermal treatments (stabilization followed by carbonization at 1000, 1200 and 1400° C), and carbon nanotubes were adsorbed on the surfaces of the fibers by a dipping method. The morphology of the developed electrodes was characterized by several techniques (SEM, Raman spectroscopy, electrical conductivity measurement). The electrochemical properties were evaluated through cyclic voltammetry, where the influence of the carbonization temperature of the fibers and the beneficial contribution of the carbon nanotubes were observed through the reversibility and size of the redox peaks of K3Fe(CN)6 versus Ag/AgCl. Subsequently, redox enzymes were immobilized on the electrodes and the electroreduction of oxygen to water was realized as a test of their efficiency as biocathodes. Due to the fibrous and porous structure of these new electrodes, and to the fact that carbon nanotubes may have the ability to promote electron transfer reactions of redox biomolecules, the new electrodes developed were capable of producing higher current densities than an electrode composed only of electrospun carbon fibers.

  4. 对乙酰氨基酚在离子液体修饰碳糊电极上的电化学行为及其测定%Electrochemical behavior of paracetamol at an ionic liquid modified carbon paste electrode and its detection

    Institute of Scientific and Technical Information of China (English)

    张亚; 杜芳艳

    2011-01-01

    An ionic liquid modified carbon paste electrode (IL/CPE) has been fabricated by using hydrophilic ionic liquid 1 -butyl-3-methylimidazolium tetrafluoroborate ( [C4 MIM][BF4]) as a modifier. The electrochemical behavior of paracetamol at the modified electrode was investigated in pH 4. 78 Britton-Robinson (B-R) buffer solution by cyclic voltammetry (CV) and square wave voltammetry (SWV). The IL/CPE possessed an excellent electrocatalytic activity for the redox of paracetamol. On SWV curves, a linear dependence of oxidation current on paracetamol concentration was obtained in the range of 8.0 × 10 -7 ~ 2. 0 × 10-4 mol/L( r = 0. 9998), with a detection limit of 3.0 × 10-7mol/L( S/N = 3 ). A novel method for the determination of paracetamol in tablets has been established.%用亲水性离子液体1-丁基-3-甲基咪唑四氟硼酸作修饰剂制备了离子液体修饰碳糊电极(IL/CPE).在pH4.78的Britton-Robinison缓冲溶液中,用循环伏安法和方波伏安法研究了对乙酰氨基酚在IL/CPE上的电化学行为.研究表明,IL/CPE对对乙酰氨基酚的氧化还原反应有良好的电催化作用.在方波伏安曲线上,对乙酰氨基酚的氧化电流与其浓度在8.0×10~2.0×10mol/L范围内呈线性关系,检出限为3.0×10mol/L(S/N=3).建立了测定片剂中对乙酰氨基酚含量的新方法.

  5. Voltammetric behavior of diethylstilbestrol at conductive carbon black paste electrode and its application in trace amount detection%己烯雌酚在导电炭黑糊电极上的伏安行为及其在痕量检测中的应用

    Institute of Scientific and Technical Information of China (English)

    李猛; 张旭志; 张艳; 马绍赛; 崔毅; 曲克明

    2012-01-01

    Conductive carbon black paste electrodes ( CCBPEs) displayed excellent electroanalytical ability due to the high signal/ noise ratio. The electrochemical behavior of diethylstilbestrol( DES) was studied by cyclic voltammetry( CV)and linear sweep volta-mmetry( LSV). The mechanism of electrode reaction was investigated preliminarily. Based on the results,some of important factors, including species of the supporting electrolyte, pH, accumulation potential and accumulation time, which had effect on the voltammetric response signal,were studied and optimized. Under the optimized conditions,there was a linear relationship between the oxi-dative peak value and the concentration of DES in the range of 3. 1 x 10~9 ?. 55 x 10~7 mol/L with a detection limit of 1. 55xlO~' mo)/L(signal/noise = 3). Then a rapid and highly sensitive detection method for DES was established. Satisfactory results were obtained when the new method was used to measure DES in the real fishery water samples.%由于具有较高的信/噪比,导电炭黑糊电极(CCBPE)具有优良的电分析化学性能.论文采用循环伏安(CV)及线性扫描伏安(LSV)等方法研究了己烯雌酚(DES)在CCBPE上的电化学行为,初步探讨了电极响应机理.在此基础上,对影响伏安响应信号的因素(诸如支持电解质种类、pH值、富集电位和富集时间等)进行了研究和优化.在优化条件下,DES的氧化峰电流与其浓度在3.1×10-9 ~ 1.55×10-7 mol/L范围内呈良好的线性关系,检测限为1.55×10-9mol/L( S/N=3).据此建立了一种快速、高灵敏的DES检测方法.应用于测定经过简单预处理的淡水渔业水样,得到了满意的结果.

  6. Fabrication optimisation of carbon fiber electrode with Taguchi method.

    Science.gov (United States)

    Cheng, Ching-Ching; Young, Ming-Shing; Chuang, Chang-Lin; Chang, Ching-Chang

    2003-07-01

    In this study, we describe an optimised procedure for fabricating carbon fiber electrodes using Taguchi quality engineering method (TQEM). The preliminary results show a S/N ratio improvement from 22 to 30 db (decibel). The optimised parameter was tested by using a glass micropipette (0.3 mm outer/2.5 mm inner length of carbon fiber) dipped into PBS solution under 2.9 V triangle-wave electrochemical processing for 15 s, followed by coating treatment of micropipette on 2.6 V DC for 45 s in 5% Nafion solution. It is thus shown that Taguchi process optimisation can improve cost, manufacture time and quality of carbon fiber electrodes.

  7. Preparation, applications, and digital simulation of carbon interdigitated array electrodes.

    Science.gov (United States)

    Liu, Fei; Kolesov, Grigory; Parkinson, B A

    2014-08-05

    Carbon interdigitated array (IDA) electrodes with features sizes down to 1.2 μm were fabricated by controlled pyrolysis of patterned photoresist. Cyclic voltammetry of reversible redox species produced the expected steady-state currents. The collection efficiency depends on the IDA electrode spacing, which ranged from around 2.7 to 16.5 μm, with the smaller dimensions achieving higher collection efficiencies of up to 98%. The signal amplification because of redox cycling makes it possible to detect species at relatively low concentrations (10(-5) molar) and the small spacing allows detection of transient electrogenerated species with much shorter lifetimes (submillisecond). Digital simulation software that accounts for both the width and height of electrode elements as well as the electrode spacing was developed to model the IDA electrode response. The simulations are in quantitative agreement with experimental data for both a simple fast one electron redox reaction and an electron transfer with a following chemical reaction at the IDAs with larger gaps whereas currents measured for the smallest IDA electrodes, that were larger than the simulated currents, are attributed to convection from induced charge electrokinetic flow.

  8. Preparation, Applications, and Digital Simulation of Carbon Interdigitated Array Electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Fei; Kolesov, Grigory; Parkinson, Bruce A.

    2014-12-16

    Carbon interdigitated array (IDA) electrodes with features sizes down to 1.2 μm were fabricated by controlled pyrolysis of patterned photoresist. Cyclic voltam-metry of reversible redox species produced the expected steady-state currents. The collection efficiency depends on the IDA electrode spacing, which ranged from around 2.7 to 16.5 μm, with the smaller dimensions achieving higher collection efficiencies of up to 98%. The signal amplification because of redox cycling makes it possible to detect species at relatively low concentrations (10–5 molar) and the small spacing allows detection of transient electrogenerated species with much shorter lifetimes (submillisecond). Digital simulation software that accounts for both the width and height of electrode elements as well as the electrode spacing was developed to model the IDA electrode response. The simulations are in quantitative agreement with experimental data for both a simple fast one electron redox reaction and an electron transfer with a following chemical reaction at the IDAs with larger gaps whereas currents measured for the smallest IDA electrodes, that were larger than the simulated currents, are attributed to convection from induced charge electrokinetic flow. This work was supported as part of the Center for Molecular Electrocatalysis, an Energy Frontier Research Center funded by the Department of Energy, Office of Science Office of Basic Energy Sciences.

  9. Citric acid cycle biomimic on a carbon electrode.

    Science.gov (United States)

    Sokic-Lazic, Daria; Minteer, Shelley D

    2008-12-01

    The citric acid cycle is one of the main metabolic pathways living cells utilize to completely oxidize biofuels to carbon dioxide and water. The overall goal of this research is to mimic the citric acid cycle at the carbon surface of an electrode in order to achieve complete oxidation of ethanol at a bioanode to increase biofuel cell energy density. In order to mimic this process, dehydrogenase enzymes (known to be the electron or energy producing enzymes of the citric acid cycle) are immobilized in cascades at an electrode surface along with non-energy producing enzymes necessary for the cycle to progress. Six enzymatic schemes were investigated each containing an additional dehydrogenase enzyme involved in the complete oxidation of ethanol. An increase in current density is observed along with an increase in power density with each additional dehydrogenase immobilized on an electrode, reflecting increased electron production at the bioanode with deeper oxidation of the ethanol biofuel. By mimicking the complete citric acid cycle on a carbon electrode, power density was increased 8.71-fold compared to a single enzyme (alcohol dehydrogenase)-based ethanol/air biofuel cell.

  10. Density controlled carbon nanotube array electrodes

    Science.gov (United States)

    Ren, Zhifeng F.; Tu, Yi

    2008-12-16

    CNT materials comprising aligned carbon nanotubes (CNTs) with pre-determined site densities, catalyst substrate materials for obtaining them and methods for forming aligned CNTs with controllable densities on such catalyst substrate materials are described. The fabrication of films comprising site-density controlled vertically aligned CNT arrays of the invention with variable field emission characteristics, whereby the field emission properties of the films are controlled by independently varying the length of CNTs in the aligned array within the film or by independently varying inter-tubule spacing of the CNTs within the array (site density) are disclosed. The fabrication of microelectrode arrays (MEAs) formed utilizing the carbon nanotube material of the invention is also described.

  11. Fabrication of catalytic electrodes for molten carbonate fuel cells

    Science.gov (United States)

    Smith, James L.

    1988-01-01

    A porous layer of catalyst material suitable for use as an electrode in a molten carbonate fuel cell includes elongated pores substantially extending across the layer thickness. The catalyst layer is prepared by depositing particulate catalyst material into polymeric flocking on a substrate surface by a procedure such as tape casting. The loaded substrate is heated in a series of steps with rising temperatures to set the tape, thermally decompose the substrate with flocking and sinter bond the catalyst particles into a porous catalytic layer with elongated pores across its thickness. Employed as an electrode, the elongated pores provide distribution of reactant gas into contact with catalyst particles wetted by molten electrolyte.

  12. High capacitance of coarse-grained carbide derived carbon electrodes

    Science.gov (United States)

    Dyatkin, Boris; Gogotsi, Oleksiy; Malinovskiy, Bohdan; Zozulya, Yuliya; Simon, Patrice; Gogotsi, Yury

    2016-02-01

    We report exceptional electrochemical properties of supercapacitor electrodes composed of large, granular carbide-derived carbon (CDC) particles. Using a titanium carbide (TiC) precursor, we synthesized 70-250 μm sized particles with high surface area and a narrow pore size distribution. Electrochemical cycling of these coarse-grained powders defied conventional wisdom that a small particle size is strictly required for supercapacitor electrodes and allowed high charge storage densities, rapid transport, and good rate handling ability. The material showcased capacitance above 100 F g-1 at sweep rates as high as 250 mV s-1 in organic electrolyte. 250-1000 micron thick dense CDC films with up to 80 mg cm-2 loading showed superior areal capacitances. The material significantly outperformed its activated carbon counterpart in organic electrolytes and ionic liquids. Furthermore, large internal/external surface ratio of coarse-grained carbons allowed the resulting electrodes to maintain high electrochemical stability up to 3.1 V in ionic liquid electrolyte. In addition to presenting novel insights into the electrosorption process, these coarse-grained carbons offer a pathway to low-cost, high-performance implementation of supercapacitors in automotive and grid-storage applications.

  13. Anthropogenic carbon release rate unprecedented during past 66 million years

    Science.gov (United States)

    Zeebe, R. E.; Ridgwell, A.; Zachos, J. C.

    2015-12-01

    Carbon release rates from anthropogenic sources have reached a record high of about 10 Pg C/y in 2013. However, due to uncertainties in the strength of climate system feedbacks, the full impact of the rapid carbon release on the Earth system is difficult to predict with confidence. Geologic analogues from past transient climate changes could provide invaluable constraints but only if the associated carbon release rates can be reliably reconstructed. We present a new technique - based on combined data-model analysis - to extract rates of change from the geological record, without the need for a stratigraphic age model. Given currently available records, we then show that the present anthropogenic carbon release rate is unprecedented during the Cenozoic (past 66 million years) by at least an order of magnitude. Our results have important implications for our ability to use past analogues to predict future changes, including constraints on climate sensitivity, ocean acidification, and impacts on marine and terrestrial ecosystems. For example, the fact that we have effectively entered an era of 'no analogue' state presents fundamental challenges to constraining forward modeling. Furthermore, future ecosystem disruptions will likely exceed the relatively limited extinctions observed during climate aberrations throughout the Cenozoic.

  14. Effects of binders on the performance of electric double-layer capacitors of carbon nanotube electrodes

    Institute of Scientific and Technical Information of China (English)

    LI Chensha; WANG Dazhi; ZHANG Baoyou; WANG Xiaofeng; CAO Maosheng; LIANG Ji

    2005-01-01

    Polarizable electrodes of electric double layer capacitor (EDLCs) were made from carhon nanotubes. Effects of different binders, which are phenolic resin (PF) and polytetrafluoroethylene (PTFE), on the properties of polarizable electrodes are studied. Results indicate that the microstructure, pore size distribution and specific capacitance of the electrodes with PTFE binder are superior to those electrodes with PF binder after carbonization. The suitable binder (PTFE) for carbon nanotubes electrodes is proposed.

  15. Zwitterionic Surfactant Modified Acetylene Black Paste Electrode for Highly Facile and Sensitive Determination of Tetrabromobisphenol A

    Directory of Open Access Journals (Sweden)

    Xiaoyun Wei

    2016-09-01

    Full Text Available A electrochemical sensor for the highly sensitive detection of tetrabromobisphenol A (TBBPA was fabricated based on acetylene black paste electrode (ABPE modified with 3-(N,N-Dimethylpalmitylammonio propanesulfonate (SB3-16 in this study. The peak current of TBBPA was significantly enhanced at SB3-16/ABPE compared with unmodified electrodes. To further improve the electrochemical performance of the modified electrode, corresponding experimental parameters such as the length of hydrophobic chains of zwitterionic surfactant, the concentration of SB3-16, pH value, and accumulation time were examined. The peak currents of TBBPA were found to be linearly correlated with its concentrations in the range of 1 nM to 1 µM, with a detection limit of 0.4 nM. Besides, a possible mechanism was also discussed, and the hydrophobic interaction between TBBPA and the surfactants was suggested to take a leading role in enhancing the responses. Finally, this sensor was successfully employed to detect TBBPA in water samples.

  16. Zwitterionic Surfactant Modified Acetylene Black Paste Electrode for Highly Facile and Sensitive Determination of Tetrabromobisphenol A

    Science.gov (United States)

    Wei, Xiaoyun; Zhao, Qiang; Wu, Weixiang; Zhou, Tong; Jiang, Shunli; Tong, Yeqing; Lu, Qing

    2016-01-01

    A electrochemical sensor for the highly sensitive detection of tetrabromobisphenol A (TBBPA) was fabricated based on acetylene black paste electrode (ABPE) modified with 3-(N,N-Dimethylpalmitylammonio) propanesulfonate (SB3-16) in this study. The peak current of TBBPA was significantly enhanced at SB3-16/ABPE compared with unmodified electrodes. To further improve the electrochemical performance of the modified electrode, corresponding experimental parameters such as the length of hydrophobic chains of zwitterionic surfactant, the concentration of SB3-16, pH value, and accumulation time were examined. The peak currents of TBBPA were found to be linearly correlated with its concentrations in the range of 1 nM to 1 µM, with a detection limit of 0.4 nM. Besides, a possible mechanism was also discussed, and the hydrophobic interaction between TBBPA and the surfactants was suggested to take a leading role in enhancing the responses. Finally, this sensor was successfully employed to detect TBBPA in water samples. PMID:27657078

  17. Enhanced Growth and Redox Characteristics of Some Conducting Polymers on Carbon Nanotube Modified Electrodes

    Institute of Scientific and Technical Information of China (English)

    R.Saraswathi

    2007-01-01

    1 Results Recent studies on the electrochemistry of a number of active compounds at carbon nanotube electrodes have proved beyond doubt their excellent electrocatalytic properties.Particularly,the advancements accomplished towards the functionalization of carbon nanotubes resulting in their enhanced solubilization in aqueous solutions have helped in the preparation of stable carbon nanotube electrodes.Glassy carbon has been invariably the preferred substrate for casting carbon nanotube electrodes.Such c...

  18. Modelling of cycling of lithium battery with microporous carbon electrode

    Directory of Open Access Journals (Sweden)

    D. Portnyagin

    2008-12-01

    Full Text Available Charge/discharge cycles of lithium cell with microporous carbon electrode under potentiodynamic control have been modelled. Predictions of the models with variable and constant diffusion coefficient neglecting the electric field inside the particle (CPM, DFM are compared to the predictions of the models with variable and constant diffusion coefficient in which electrostatic interaction inside the particles of carbon electrode (CPME, DFME is taken into account. There is observed a considerable difference between both. Electrostatic interactions of lithium ions with each other and the charge distributed inside the particle promote intercalation during the discharge of the cell and deintercalation during the charge. The dependance of the effect of hysteresis during the cycling of the cell on the rate of change of the applied voltage is studied. The larger is the speed of change of the applied voltage the more effective is hysteresis. We have also obtained concentration profiles at different stages of charge/discharge process.

  19. Voltammetric behaviour of oligonucleotide lipoplexes adsorbed onto glassy carbon electrodes

    OpenAIRE

    Piedade, J. A. P.; M. Mano; Lima, M. C. Pedroso de; Oretskaya, T S; Oliveira-Brett, A. M.

    2004-01-01

    The voltammetric behaviour of oligonucleotide lipoplexes (ODN-lipoplexes) prepared from short oligodeoxynucleotides (ODN), with different base compositions, and liposomes of the cationic lipid DOTAP, was studied by differential pulse voltammetry with a glassy carbon mini-electrode. It was found that the ODN base composition influences the ODN-lipoplex voltammetric response. Differential pulse voltammograms for ODN-lipoplexes of the ODN adenosine nucleotides present two different features when...

  20. ELECTROANALYTICAL APPLICATIONS OF CARBOXYL-MODIFIED CARBON NANOTUBE FILM ELECTRODES

    Institute of Scientific and Technical Information of China (English)

    C.G. Hu; W.L. Wang; K.J. Liao; W. Zhu

    2003-01-01

    The electrochemical behavior of a carboxyl-modified carbon nanotube films was investigated to explore its possibility in electroanalytical applicaton. Cyclic voltammetry of quinone was conducted in 1mol/L Na2SO4, which showed a stable, quasi-reversible voltammetric response for quinone / hydroquinone, and the anodic and the cathodic peak potentials were 0.657V and -0.029V (vs. SCE) at a scan rate of 0.1V.s-1, respectively. Both anodic and cathodic peak currents depended linearly on the square root of the scan rate over the range of 0.01-0. 5 V.s-1, which suggested that the process of the electrode reactions was diffusion-controlled. Carboxyl-modified carbon nanotube electrodes made it possible to determine low level of dopamine selectively in the presence of a large excess of ascorbic acid in acidic media using derivative voltammetry.The results obtained were discussed in details. This work demonstrates the potential of carboxyl-modified carbon nanotube electrodes for electroanalytical applications.

  1. On the molecular origin of supercapacitance in nanoporous carbon electrodes.

    Science.gov (United States)

    Merlet, Céline; Rotenberg, Benjamin; Madden, Paul A; Taberna, Pierre-Louis; Simon, Patrice; Gogotsi, Yury; Salanne, Mathieu

    2012-03-04

    Lightweight, low-cost supercapacitors with the capability of rapidly storing a large amount of electrical energy can contribute to meeting continuous energy demands and effectively levelling the cyclic nature of renewable energy sources. The excellent electrochemical performance of supercapacitors is due to a reversible ion adsorption in porous carbon electrodes. Recently, it was demonstrated that ions from the electrolyte could enter sub nanometre pores, greatly increasing the capacitance. However, the molecular mechanism of this enhancement remains poorly understood. Here we provide the first quantitative picture of the structure of an ionic liquid adsorbed inside realistically modelled microporous carbon electrodes. We show how the separation of the positive and negative ions occurs inside the porous disordered carbons, yielding much higher capacitance values (125 F g(-1)) than with simpler electrode geometries. The proposed mechanism opens the door for the design of materials with improved energy storage capabilities. It also sheds new light on situations where ion adsorption in porous structures or membranes plays a role.

  2. Measurements of Electrode Skin Impedances using Carbon Rubber Electrodes - First Results

    Science.gov (United States)

    Kaufmann, Steffen; Ardelt, Gunther; Ryschka, Martin

    2013-04-01

    Non-invasive bioimpedance measurement as a tool in biomedical engineering and life sciences allows conclusions about condition and composition of living tissue. For interfacing the electronic conduction of the instrumentation and the ionic conduction of the tissue, electrodes are needed. A crucial point is the uncertainty arising from the unknown, time-varying and current density depend Electrode Skin Impedance (ESI). This work presents ESI measurements using carbon rubber electrodes on different human test subjects. The measurements for this work are carried out by employing a high accuracy Bioimpedance Measurement System (BMS) developed by the authors group, which is based on a Field Programmable Gate Array (FPGA) System on Chip (SoC). The system is able to measure magnitude and phase of complex impedances using a two- or four-electrode setup, with excitation currents from 60 μA to 5 mA in a frequency range from about 10 kHz to 300 kHz. Achieved overall measurement uncertainties are below 1%.

  3. Electroanalysis of trimethoprim on metalloporphyrin incorporated glassy carbon electrode.

    Science.gov (United States)

    Rajith, Leena; Kumar, Krishnapillai Girish

    2010-09-01

    Trimethoprim (TMP) is a bacteriostatic antibiotic mainly used in the prophylaxis and treatment of urinary tract infections. It belongs to the class of chemotherapeutic agents known as dihydrofolate reductase inhibitors. Its use is associated with idiosyncratic reactions, including liver toxicity and agranulocytosis. In order to determine TMP electrochemically, a metalloporphyrin modified glassy carbon electrode was prepared by coating [5,10,15,20- tetrakis(4-methoxyphenyl) porphyrinato]Mn (III)chloride (TMOPPMn(III)Cl) solution on the surface of the electrode. The electrochemical behaviour of TMP in Phosphate buffer solution (PBS) on TMOPPMn(III)Cl modified glassy carbon electrode (TMOPPMn(III)Cl/GCE) was explored using differential pulse voltammetry (DPV). The voltammograms showed enhanced oxidation response at the TMOPPMn (III)Cl/GCE with respect to the bare GCE for TMP, attributable to the electrocatalytic activity of TMOPPMn(III)Cl. Electrochemical parameters of the oxidation of TMP on the modified electrode were analyzed. The electro-oxidation of TMP was found to be irreversible, pH dependent and adsorption controlled on the modified electrode. It is found that the oxidation peak current is proportional to the concentration of TMP over the range 6 × 10⁻⁸ - 1 × 10⁻⁶ M with a very low detection limit of 3 × 10⁻⁹ M at 2 min open circuit accumulation. The repeatability expressed as relative standard deviation (RSD) for n = 9 was 3.2% and the operational stability was found to be 20 days. Another striking feature is that equimolar concentration of sulfamethoxazole did not interfere in the determination of TMP. Applicability to assay the drug in urine and tablet samples has also been studied.

  4. Carbon-Nanotube-Based Electrodes for Biomedical Applications

    Science.gov (United States)

    Li, Jun; Meyyappan, M.

    2008-01-01

    A nanotube array based on vertically aligned nanotubes or carbon nanofibers has been invented for use in localized electrical stimulation and recording of electrical responses in selected regions of an animal body, especially including the brain. There are numerous established, emerging, and potential applications for localized electrical stimulation and/or recording, including treatment of Parkinson s disease, Tourette s syndrome, and chronic pain, and research on electrochemical effects involved in neurotransmission. Carbon-nanotube-based electrodes offer potential advantages over metal macroelectrodes (having diameters of the order of a millimeter) and microelectrodes (having various diameters ranging down to tens of microns) heretofore used in such applications. These advantages include the following: a) Stimuli and responses could be localized at finer scales of spatial and temporal resolution, which is at subcellular level, with fewer disturbances to, and less interference from, adjacent regions. b) There would be less risk of hemorrhage on implantation because nano-electrode-based probe tips could be configured to be less traumatic. c) Being more biocompatible than are metal electrodes, carbon-nanotube-based electrodes and arrays would be more suitable for long-term or permanent implantation. d) Unlike macro- and microelectrodes, a nano-electrode could penetrate a cell membrane with minimal disruption. Thus, for example, a nanoelectrode could be used to generate an action potential inside a neuron or in proximity of an active neuron zone. Such stimulation may be much more effective than is extra- or intracellular stimulation via a macro- or microelectrode. e) The large surface area of an array at a micron-scale footprint of non-insulated nanoelectrodes coated with a suitable electrochemically active material containing redox ingredients would make it possible to obtain a pseudocapacitance large enough to dissipate a relatively large amount of electric charge

  5. Carbon and Nickel Oxide/Carbon Composites as Electrodes for Supercapacitors

    Institute of Scientific and Technical Information of China (English)

    Liutauras Marcinauskas; Zydrunas Kavaliauskas; Vitas Valincius

    2012-01-01

    The carbon and nickel oxide/carbon composite electrodes were prepared by plasma jet and magnetron sput-tering techniques. The investigations were performed to evaluate the influence of the Ar/C2H2 ratio on the specific capacitance values of carbon and NiO/carbon electrodes. The obtained electrodes were investigated by scanning electron microscopy, Raman scattering spectroscopy (RS), and X-ray diffraction techniques. The surface of the carbon electrodes became less porous and more homogenous with increasing Ar/C2H2. The RS results indicated that the fraction of the sp2 carbon sites increased with increasing Ar/C2H2 ratio. The increase of the Ar/C2H2 ratio increased the capacitance values from 0.73 up to 3.8 F/g. Meanwhile, after the deposition of the nickel oxide on the carbon, the capacitance increased ten and more times and varied in the range of 7.6-86.1 F/g.

  6. Carbon nanotube macrofilm-based nanocomposite electrodes for energy applications

    Science.gov (United States)

    Cao, Zeyuan

    Finding new electrode materials for energy conversion and storage devices have been the focus of recent research in the fields of science and engineering. Suffering from poor electronic conductivity, chemical and mechanical stability, active electrode materials are usually coupled with different carbon nanostructured materials to form nanocomposite electrodes, showing promising electrochemical performance. Among the carbon nanostructured materials, carbon nanotube (CNT) macrofilms draw great attention owing to their extraordinary properties, such as a large specific surface area, exceptionally high conductivity, porous structure, flexibility, mechanical robustness, and adhesion. They could effectively enhance the electrochemical performance of the incorporated active materials in the nanocomposites. In this dissertation, CNT macrofilm-based nanocomposites are investigated for rechargeable lithium-ion batteries, supercapacitors, and electrocatalysts of fuel cells. The progressive research developed various nanocomposites from cathode materials to anode materials followed by a general nanocomposite solution due to the unique adhesive property of the fragmented CNT macrofilms. The in-situ synthesis strategy are explored to in-situ deposit unlithiated cathode materials V2O5 and lithiated cathode materials LiMn2O4 nanocrystals in the matrix of the CNT macrofilms as nanocomposites to be paired with metallic lithium in half cells. The presence of oxygen-containing functional groups on the surface of the CNT macrofilms after purification can enhance the association with the active materials to enable the facilitated transport of solvated ions to the electrolyte/electrode interfaces and increase the diffusion kinetics, consequently enhancing the battery performance in terms of high specific capacity, rate capability, and cycling stability. It is also significant to demonstrate a reliable, low-cost, and effective route to synthesize the family of metal oxides (MxOy (M=Fe, Co

  7. Modified glassy carbon electrodes based on carbon nanostructures for ultrasensitive electrochemical determination of furazolidone

    Energy Technology Data Exchange (ETDEWEB)

    Shahrokhian, Saeed, E-mail: shahrokhian@sharif.edu [Department of Chemistry, Sharif University of Technology, Tehran 11155-9516 (Iran, Islamic Republic of); Institute for Nanoscience and Nanotechnology, Sharif University of Technology, Tehran (Iran, Islamic Republic of); Naderi, Leila [Department of Chemistry, Sharif University of Technology, Tehran 11155-9516 (Iran, Islamic Republic of); Ghalkhani, Masoumeh [Department of Chemistry, Faculty of Science, Shahid Rajaee Teacher Training University, Lavizan, Tehran (Iran, Islamic Republic of); Institute for advanced technology, Shahid Rajaee Teacher Training University, Lavizan, Tehran, 16788 (Iran, Islamic Republic of)

    2016-04-01

    The electrochemical behavior of Furazolidone (Fu) was investigated on the surface of the glassy carbon electrode modified with different carbon nanomaterials, including carbon nanotubes (CNTs), carbon nanoparticles (CNPs), nanodiamond-graphite (NDG), graphene oxide (GO), reduced graphene oxide (RGO) and RGO-CNT hybrids (various ratios) using linear sweep voltammetry (LSV). The results of voltammetric studies exhibited a considerable increase in the cathodic peak current of Fu at the RGO modified GCE, compared to other modified electrodes and also bare GCE. The surface morphology and nature of the RGO film was thoroughly characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) techniques. The modified electrode showed two linear dynamic ranges of 0.001–2.0 μM and 2.0–10.0 μM with a detection limit of 0.3 nM for the voltammetric determination of Fu. This sensor was used successfully for Fu determination in pharmaceutical and clinical preparations. - Highlights: • The electrochemical behavior of Furazolidone (Fu) was investigated on the surface of the modified electrode with different carbon nanomaterials by Linear sweep voltammetry. • Two linear dynamic ranges and a low detection limit were obtained. • The modified electrode was applied for the detection of Fu in pharmaceutical and clinical preparations.

  8. Carbon nanopipette electrodes for dopamine detection in Drosophila.

    Science.gov (United States)

    Rees, Hillary R; Anderson, Sean E; Privman, Eve; Bau, Haim H; Venton, B Jill

    2015-04-01

    Small, robust, sensitive electrodes are desired for in vivo neurotransmitter measurements. Carbon nanopipettes have been previously manufactured and used for single-cell drug delivery and electrophysiological measurements. Here, a modified fabrication procedure was developed to produce batches of solid carbon nanopipette electrodes (CNPEs) with ∼250 nm diameter tips, and controllable lengths of exposed carbon, ranging from 5 to 175 μm. The electrochemical properties of CNPEs were characterized with fast-scan cyclic voltammetry (FSCV) for the first time. CNPEs were used to detect the electroactive neurotransmitters dopamine, serotonin, and octopamine. CNPEs were significantly more sensitive for serotonin detection than traditional carbon-fiber microelectrodes (CFMEs). Similar to CFMEs, CNPEs have a linear response for dopamine concentrations ranging from 0.1 to 10 μM and a limit of detection of 25 ± 5 nM. Recordings with CNPEs were stable for over 3 h when the applied triangle waveform was scanned between -0.4 and +1.3 V vs Ag/AgCl/Cl(-) at 400 V/s. CNPEs were used to detect endogenous dopamine release in Drosophila larvae using optogenetics, which verified the utility of CNPEs for in vivo neuroscience studies. CNPEs are advantageous because they are 1 order of magnitude smaller in diameter than typical CFMEs and have a sharp, tunable geometry that facilitates penetration and implantation for localized measurements in distinct regions of small organisms, such as the Drosophila brain.

  9. 沙丁胺醇在离子液体[BnMIM]PF6修饰碳糊电极上的电催化氧化及电分析方法%Electrocatalytic Oxidation of Salbutamol at a [BnMIM]PF6 Modified Carbon Paste Electrode and Its Electrochemical Determination

    Institute of Scientific and Technical Information of China (English)

    吴锐; 马少宁; 张艳梅; 高作宁

    2013-01-01

    The electrocatalytic oxidation and electrochemical kinetic of Salbutamol (SAL) were investigated at a 1-Benzyl-3-Methylimidazole hexafluorophosphate([BnMIM]PF6) modified carbon paste electrode([BnMIM]PF6/CPE).The experimental results showed that the [BnMIM]PF6/CPE showed an excellent electrocatalytic activity toward SAL.The reaction rate constant for catalytic oxidation k was obtained as (2.10± 0.05) × 103 (mol· L-1)-1 · s-1 by chronoamperometry(CA).The catalytic oxidation peak current of SAL and its concentration had a good linear relationship in the range of 6.0× 10-7-1.0×10-3 mol· L-1,with a detection limit of 3.7 × 10-8 mol· L 1 (S/N=3) obtained by differential pulse voltammetry (DPV).The proposed method has been successfully applied in the electrochemical quantitative determination of SAL content in the commercial inhaled salbutamol solution.%研究了沙丁胺醇(Salbutamol,SAL)在离子液体1-苄基-3-甲基咪唑六氟磷酸盐([BnMIM]PF6)修饰碳糊电极([BnMIM]PF6/CPE)上的电催化氧化行为和电化学动力学性质.实验结果表明,[BnMIM]PF6/CPE对SAL的电化学氧化具有良好的催化作用.用计时电流法(CA)测定了SAL在[BnMIM] PF6/CPE上的电催化氧化反应速率常数k为(2.10±0.05)×103(mol·L-1)1·s-1.用微分脉冲伏安法(DPV)测得催化氧化峰电流与SAL的浓度在6.0×10-7~1.0×10-3mol· L-1范围内呈良好线性关系,检测限(S/N=3)为3.27×10-8 mol·L-1,同时运用该方法对吸入用沙丁胺醇溶液中的SAL含量进行了电化学定量测定.

  10. 预镀铋膜修饰碳糊电极差分脉冲伏安法测定废水中铅和镉%Ex-situ Plating Bismuth Film Modified Carbon Paste Electrode for the Determination of Trace Lead and Cadmium by Differential Pulse Voltammetry

    Institute of Scientific and Technical Information of China (English)

    雷存喜; 刘蓉; 沈毓儒; 赵运林; 董萌; 曾戴弟

    2014-01-01

    采用预镀铋膜法制得铋膜修饰碳糊电极,当沉积时间为540 s得到最优铋膜.采用差分脉冲伏安法(DPV)实现了对痕量Pb2+、Cd2+的同时测定.优化了DPV测定条件,当富集时间为150 s、富集电位为-1.25 V、HAc-NaAc缓冲底液的pH为4.5时,Pb2+、Cd2+的峰电流最大.在最优的实验条件下,Pb2+和Cd2+的峰电流与其浓度呈良好的线性关系,线性相关系数R分别为0.9912和0.9937,线性范围分别为1~10μmol/L和5~50 μmol/L,Pb2+和Cd2+的检出限分别为0.32 μmol/L和2.01 μmol/L.对实际废水样品进行了加标回收实验,其中Pb2+和Cd2+的回收率分别为98.4%~102.6%和95.4%~104.6%.%Ex-situ plating bismuth film modified carbon paste electrode was prepared for the measurement of Pb2+ and Cd2+ by differential pulse voltammetry(DPV).Pb and Cd were deposited on the surface of bismuth and displayed well defined peaks when the preconcentration time of bismuth was 540 s.The conditions of several key operational parameters were optimized.Under the optimum conditions,the oxidation peak currents changed linearly with the concentration of Pb2+ and Cd2+ at the range of 1-10 μmol/L and 5-50 μmol/L,with the detection limits of 0.32 μmol/L for Pb2+ and 2.01 μmol/L for Cd2+,and the recoveries of Pb2+ and Cd2+ in electroplating waste water were 98.4%-102.6% and 95.4%-104.6%,respectively.

  11. Electrocatalytic oxidation of simvastatin at SDBS self-assembled monolayers and RGO modified carbon paste electrode and its electrochemical determination%SMV 在 SDBS 自组装膜与 RGO 复合修饰碳糊电极上的电催化氧化及电分析研究

    Institute of Scientific and Technical Information of China (English)

    张瑞; 张青春; 段春玲; 彭娟; 高作宁

    2013-01-01

    Electrocatalytic oxidation and electrochemical kinetics of simvastatin ( SMV) were investigated at sodium dodecyl benzene-sulfonate(SDBS)self-assembled monolayers and graphene (RGO)modified carbon paste electrode(SDBS-RGO/CPE).The experi-mental results showed that SDBS-RGO/CPE showed an excellent electrocatalytic activity towards SMV electrochemical oxida -tion.The electrochemical kinetic parameters were also determined by cyclic voltammetry ( CV) and chronoamperometry ( CA).The oxidation peak current of catalytic oxidation of SMV versus its concentration had a good linear relationship in the concentration range of 6.0 ×10-5 mol· L-1 ~4.5 ×10-4 mol· L-1 and the detection limit of 5.0 ×10-6 mol· L-1 ( S/N=3 ) by square wave voltammetry ( SWV).At the same time the supposed method have been applied in the electrochemical quantitative determination of SMV content in commercial tablet samples and the determination results meet the requirement of the quantitative determination .%研究了辛伐他汀(SMV)在表面活性剂十二烷基苯磺酸钠(SDBS)自组装膜与石墨烯(RGO)复合修饰碳糊电极(SDBS-RGO/CPE)上的电催化氧化和电化学动力学性质。实验结果表明,SDBS-RGO/CPE对SMV电化学氧化具有良好的催化作用。同时用循环伏安法(CV),计时电流法(CA)测定了SMV在SDBS-RGO/CPE上的电极反应动力学参数,用方波伏安法( SWV)测得SMV氧化峰电流( Ipa )与其浓度在6.0×10-5~4.5×10-4mol· L-1范围内呈良好线性关系,检测限(S/N=3)为5.0×10-6mol· L-1,同时运用该方法对市售辛伐他汀片剂中SMV含量进行了电化学定量测定,测定结果符合定量测定要求。

  12. Activation of glassy carbon electrodes by photocatalytic pretreatment

    Energy Technology Data Exchange (ETDEWEB)

    Dumanli, Onur [Department of Chemistry, Faculty of Science and Art, Ondokuz Mayis University, Kurupelit, 55139 Samsun (Turkey); Onar, A. Nur [Department of Chemistry, Faculty of Science and Art, Ondokuz Mayis University, Kurupelit, 55139 Samsun (Turkey)], E-mail: nonar@omu.edu.tr

    2009-11-01

    This paper describes a simple and rapid photocatalytic pretreatment procedure that removes contaminants from glassy carbon (GC) surfaces. The effectiveness of TiO{sub 2} mediated photocatalytic pretreatment procedure was compared to commonly used alumina polishing procedure. Cyclic voltammetric and chronocoulometric measurements were carried out to assess the changes in electrode reactivity by using four redox systems. Electrochemical measurements obtained on photocatalytically treated GC electrodes showed a more active surface relative to polished GC. In cyclic voltammograms of epinephrine, Fe(CN){sub 6}{sup 3-/4-} and ferrocene redox systems, higher oxidation and reduction currents were observed. The heterogeneous electron transfer rate constants (k{sup o}) were calculated for Fe(CN){sub 6}{sup 3-/4-} and ferrocene which were greater for photocatalytic pretreatment. Chronocoulometry was performed in order to find the amount of adsorbed methylene blue onto the electrode and was calculated as 0.34 pmol cm{sup -2} for photocatalytically pretreated GC. The proposed photocatalytic GC electrode cleansing and activating pretreatment procedure was more effective than classical alumina polishing.

  13. Determination of carbohydrates in honey and milk by capillary electrophoresis in combination with graphene-cobalt microsphere hybrid paste electrodes.

    Science.gov (United States)

    Liang, Peipei; Sun, Motao; He, Peimin; Zhang, Luyan; Chen, Gang

    2016-01-01

    A graphene-cobalt microsphere (CoMS) hybrid paste electrode was developed for the determination of carbohydrates in honey and milk in combination with capillary electrophoresis (CE). The performance of the electrodes was demonstrated by detecting mannitol, sucrose, lactose, glucose, and fructose after CE separation. The five analytes were well separated within 9 min in a 40 cm long capillary at a separation voltage of 12 kV. The electrodes exhibited pronounced electrocatalytic activity, lower detection potentials, enhanced signal-to-noise characteristics, and higher reproducibility. The relation between peak current and analyte concentration was linear over about three orders of magnitude. The proposed method had been employed to determine lactose in bovine milk and glucose and fructose in honey with satisfactory results. Because only electroactive substances in the samples could be detected on the paste electrode, the electropherograms of both food samples were simplified to some extent.

  14. One-step fabrication of 3D silver paste electrodes into microfluidic devices for enhanced droplet-based cell sorting

    Directory of Open Access Journals (Sweden)

    Lang Rao

    2015-05-01

    Full Text Available 3D microelectrodes are one-step fabricated into a microfluidic droplet separator by filling conductive silver paste into PDMS microchambers. The advantages of 3D silver paste electrodes in promoting droplet sorting accuracy are systematically demonstrated by theoretical calculation, numerical simulation and experimental validation. The employment of 3D electrodes also helps to decrease the droplet sorting voltage, guaranteeing that cells encapsulated in droplets undergo chip-based sorting processes are at better metabolic status for further potential cellular assays. At last, target droplet containing single cell are selectively sorted out from others by an appropriate electric pulse. This method provides a simple and inexpensive alternative to fabricate 3D electrodes, and it is expected our 3D electrode-integrated microfluidic droplet separator platform can be widely used in single cell operation and analysis.

  15. MOLECULAR DESCRIPTION OF ELECTROLYTE SOLUTION IN A CARBON AEROGEL ELECTRODE

    Directory of Open Access Journals (Sweden)

    A.Kovalenko

    2003-01-01

    Full Text Available We develop a molecular theory of aqueous electrolyte solution sorbed in a nanoporous carbon aerogel electrode, based on the replica reference interaction site model (replica RISM for realistic molecular quenched-annealed systems. We also briefly review applications of carbon aerogels for supercapacitor and electrochemical separation devices, as well as theoretical and computer modelling of disordered porous materials. The replica RISM integral equation theory yields the microscopic properties of the electrochemical double layer formed at the surface of carbon aerogel nanopores, with due account of chemical specificities of both sorbed electrolyte and carbon aerogel material. The theory allows for spatial disorder of aerogel pores in the range from micro- to macroscopic size scale. We considered ambient aqueous solution of 1 M sodium chloride sorbed in two model nanoporous carbon aerogels with carbon nanoparticles either arranged into branched chains or randomly distributed. The long-range correlations of the carbon aerogel nanostructure substantially affect the properties of the electrochemical double layer formed by the solution sorbed in nanopores.

  16. Surface behavior of pasted nickel electrodes with electrodeposited Co-Ce on substrate

    Institute of Scientific and Technical Information of China (English)

    WANG Dian-long; WANG Chun-yu; DAI Chang-song; JIANG Zhao-hua

    2006-01-01

    MH/Ni battery for electro-vehicle has become a hot topic of studies. The Co-Ce alloys were electrodeposited on the nickel substrate to modify pasted nickel electrode substrate. SEM and XRD results show that the surface of the substrate contains Co(OH)2 and CoOOH film, and CV shows that modified film can improve electron conductivity capability. The state of charge (SOC) or state of discharge (SOD) curves indicate that Co-Ce modified substrate can enhance Ni electrode charge and discharge performance at high rate. The surface analysis by XPS shows that, the Co(Ⅱ)/Co(Ⅲ) ratio is 76.80/23.19 at the SOD, but the Co(Ⅱ)/Co(Ⅲ) ratio is 57.79/42.21 at the SOC, which indicates that the conductibility of electrodeposited Co-Ce alloys on the nickel substrate is enhanced because CoOOH and Co(OH)2 are created on the substrate surface. The modified surface with CoOOH and Co(OH)2 can enhance the conductibility of electrons between the substrate and active materials, and improve the high rate SOC and SOD ability.

  17. Electrochemical reduction of imazamethabenz methyl on mercury and carbon electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Ruiz Montoya, Mercedes, E-mail: mmontoya@uhu.e [Departamento de Ingenieria Quimica, Quimica Fisica y Quimica Organica, Universidad de Huelva, Campus El Carmen, Facultad de Ciencias Experimentales, E-21071 Huelva (Spain); Pintado, Sara; Rodriguez Mellado, Jose Miguel [Departamento de Quimica Fisica y Termodinamica Aplicada, Universidad de Cordoba, Campus Universitario de Rabanales, edificio ' Marie Curie' , E-14014 Cordoba (Spain)

    2010-03-30

    This paper presents polarographic and voltammetric studies of the reduction of the herbicide imazamethabenz methyl (2/3-methyl-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-p-toluate), on mercury and carbon electrodes. The electrochemical studies were performed in strongly acidic media (0.1-2.7 M H{sub 2}SO{sub 4}) as well as in the pH range of 1-12. The overall reduction process involves the uptake of two electrons. The results obtained in polarography show that there is the reduction of two species, related via an acid-base equilibrium, and having very close reduction potentials. The voltammetric results obtained with a glassy carbon electrode were very similar to those observed on mercury electrodes. The reducible group in the molecule is the imidazolinone ring. In strongly acidic media (pH < pK{sub a}), the reaction mechanism proposed is the reduction of the protonated herbicide by an electrochemical-chemical-electrochemical (ECE) process, being the r.d.s. the second electron transfer. At pH > pK{sub a} the neutral form of the herbicide is reduced and the second electron transfer becomes reversible or quasi-reversible. In basic media, the species reduced is the deprotonated imazamethabenz methyl and the r.d.s. is the second electron transfer.

  18. Carbon nanotube prepared from carbon monoxide by CVD method and its application as electrode materials

    Institute of Scientific and Technical Information of China (English)

    AN Yuliang; YUAN Xia; CHENG Shinan; GEN Xin

    2006-01-01

    Carbon nanotubes with larger inner diameter were synthesized by the chemical vapor deposition of carbon monoxide (CO) on iron catalyst using H2S as promoting agent.It is found that the structure and morphology of carbon nanotubes can be tailored, to some degree, by varying the experimental conditions such as precursor components and process parameters.The results show that the presence of H2S may play key role for growing Y-branched carbon nanotubes.The products were characterized by SEM, TEM, and Raman spectroscopy, respectively.Furthermore, the obtained carbon nanotubes were explored as electrode materials for supercapacitor.

  19. Attractive forces in microporous carbon electrodes for capacitive deionization

    CERN Document Server

    Biesheuvel, P M; Levi, M; Bazant, M Z

    2013-01-01

    The recently developed modified Donnan (mD) model provides a simple and useful description of the electrical double layer in microporous carbon electrodes, suitable for incorporation in porous electrode theory. By postulating an attractive excess chemical potential for each ion in the micropores that is inversely proportional to the total ion concentration, we show that experimental data for capacitive deionization (CDI) can be accurately predicted over a wide range of applied voltages and salt concentrations. Since the ion spacing and Bjerrum length are each comparable to the micropore size (few nm), we postulate that the attraction results from fluctuating bare Coulomb interactions between individual ions and the metallic pore surfaces (image forces) that are not captured by meanfield theories, such as the Poisson-Boltzmann-Stern model or its mathematical limit for overlapping double layers, the Donnan model. Using reasonable estimates of the micropore permittivity and mean size (and no other fitting parame...

  20. Composite electrodes of activated carbon derived from cassava peel and carbon nanotubes for supercapacitor applications

    Science.gov (United States)

    Taer, E.; Iwantono, Yulita, M.; Taslim, R.; Subagio, A.; Salomo, Deraman, M.

    2013-09-01

    In this paper, a composite electrode was prepared from a mixture of activated carbon derived from precarbonization of cassava peel (CP) and carbon nanotubes (CNTs). The activated carbon was produced by pyrolysis process using ZnCl2 as an activation agent. A N2 adsorption-desorption analysis for the sample indicated that the BET surface area of the activated carbon was 1336 m2 g-1. Difference percentage of CNTs of 0, 5, 10, 15 and 20% with 5% of PVDF binder were added into CP based activated carbon in order to fabricate the composite electrodes. The morphology and structure of the composite electrodes were investigated by scanning electron microscopy (SEM) and X-ray diffraction (XRD) techniques. The SEM image observed that the distribution of CNTs was homogeneous between carbon particles and the XRD pattern shown the amorphous structure of the sample. The electrodes were fabricated for supercapacitor cells with 316L stainless steel as current collector and 1 M sulfuric acid as electrolyte. An electrochemical characterization was performed by using an electrochemical impedance spectroscopy (EIS) method using a Solatron 1286 instrument and the addition of CNTs revealed to improve the resistant and capacitive properties of supercapacitor cell.

  1. Electroless Co-Zn Surface-modified Nickel Hydroxide as an Active Material for Pasted Nickel Electrodes

    Institute of Scientific and Technical Information of China (English)

    SONG Quan-sheng(宋全生); TANG Zhi-yuan(唐致远); GUO He-tong(郭鹤桐); CHAN S L I

    2004-01-01

    Chemically precipitated β-type nickel hydroxide powder was surface-modified by electroless deposition of Co-Zn coatings,and physical properties of both the modified and unmodified nickel hydroxide were characterized by scanning electron microscopy (SEM), specific surface area (BET), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). It has been found that Co and Zn components of the surface electroless coatings exist in the oxidized state. Electrochemical performances of pasted nickel electrodes using the modified nickel hydroxide as an active material were investigated, and compared with those of the electrodes prepared with the unmodified nickel hydroxide. Charge/discharge tests show that the modified nickel hydroxide electrodes exhibit better performances in the charge efficiency, specific discharge capacity and active material utilization. Their resistance to swelling with cycling is also superior to that of the unmodified nickel hydroxide electrodes. Cyclic voltammetric (CV) studies indicate that the modified electrodes have a higher electrochemical activity, and the porous pasted nickel electrodes have some distinguished CV characteristics in comparison with those of the thin film nickel electrodes.

  2. High power density electrodes for Carbon supercapacitor applications

    Energy Technology Data Exchange (ETDEWEB)

    Portet, C.; Taberna, P.L.; Simon, P.; Flahaut, E.; Laberty-Robert, C. [CIRIMAT, UMR CNRS 5085, 118 Route de Narbonne 31062 Toulouse Cedex (France)

    2005-07-25

    This paper presents results obtained with 4 cm{sup 2} Carbon/Carbon supercapacitors cells in organic electrolyte. In the first approach, a surface treatment for Al current collector foil via the sol-gel route has been used in order to decrease the Al/active material interface resistance. Performances obtained with this original process are: a low equivalent series resistance (ESR) of 0.5 {omega} cm{sup 2} and a specific capacitance of 95 F g{sup -1} of activated carbon. Then, supercapacitors assembled with treated Al foil and active material containing activated carbon/carbon nanotubes (CNTs) with different compositions have been studied. Galvanostatic cycling measurements show that when CNTs content increases, both ESR and specific capacitance are decreased. Fifteen percent appears to be a good compromise between stored energy and delivered power with an ESR of 0.4 {omega} cm{sup 2} and a specific capacitance of 93 F g{sup -1} of carbonaceous active material. Finally, cells frequency behaviour has been characterized by Electrochemical Impedance Spectroscopy. The relaxation time constant of cells decreases when the CNTs content increases. For 15% of CNTs, the time constant is about 30% lower as compared to a cell using pure activated carbon-based electrodes leading to a higher delivered power. (author)

  3. Field emission properties of the graphenated carbon nanotube electrode

    Energy Technology Data Exchange (ETDEWEB)

    Zanin, H., E-mail: hudson.zanin@bristol.ac.uk [School of Chemistry, University of Bristol, Bristol BS8 1TS (United Kingdom); Faculdade de Engenharia Elétrica e Computação, Departamento de Semicondutores, Instrumentos e Fotônica, Universidade Estadual de Campinas, UNICAMP, Av. Albert Einstein N. 400, CEP 13 083-852 Campinas, São Paulo (Brazil); Ceragioli, H.J.; Peterlevitz, A.C.; Baranauskas, Vitor [Faculdade de Engenharia Elétrica e Computação, Departamento de Semicondutores, Instrumentos e Fotônica, Universidade Estadual de Campinas, UNICAMP, Av. Albert Einstein N. 400, CEP 13 083-852 Campinas, São Paulo (Brazil); Marciano, F.R.; Lobo, A.O. [Laboratory of Biomedical Nanotechnology/Institute of Research and Development at UNIVAP, Av. Shishima Hifumi, 2911, CEP 12244-000 Sao Jose dos Campos, SP (Brazil)

    2015-01-01

    Graphical abstract: - Highlights: • Facile method to prepare graphenated carbon nanotubes (g-CNTs). • The electric field emission behaviour of g-CNTs was studied. • g-CNTs show better emission current stability than non-graphenated CNTs. - Abstract: Reduced graphene oxide-coated carbon nanotubes (RGO-CNT) electrodes have been prepared by hot filament chemical vapour deposition system in one-step growth process. We studied RGO-CNT electrodes behaviour as cold cathode in field emission test. Our results show that RGO-CNT retain the low threshold voltage typical of CNTs, but with greatly improved emission current stability. The field emission enhancement value is significantly higher than that expected being caused by geometric effect (height divided by the radius of nanotube). This suggested that the field emission of this hybrid structure is not only from a single tip, but eventually it is from several tips with contribution of graphene nanosheets at CNT's walls. This phenomenon explains why the graphenated carbon nanotubes do not burn out as quickly as CNT does until emission ceases completely. These preliminaries results make nanocarbon materials good candidates for applications as electron sources for several devices.

  4. Layered double hydroxide materials coated carbon electrode: New challenge to future electrochemical power devices

    Energy Technology Data Exchange (ETDEWEB)

    Djebbi, Mohamed Amine, E-mail: mohamed.djebbi@etu.univ-lyon1.fr [Institut des Sciences Analytiques UMR CNRS 5280, Université Claude Bernard-Lyon 1, 5 rue de la Doua, 69100 Villeurbanne (France); Laboratoire de Physique des Matériaux Lamellaires et Nano-Matériaux Hybrides, Faculté des Sciences de Bizerte, Université de Carthage, 7021 Bizerte (Tunisia); Braiek, Mohamed [Institut des Sciences Analytiques UMR CNRS 5280, Université Claude Bernard-Lyon 1, 5 rue de la Doua, 69100 Villeurbanne (France); Namour, Philippe [Institut des Sciences Analytiques UMR CNRS 5280, Université Claude Bernard-Lyon 1, 5 rue de la Doua, 69100 Villeurbanne (France); Irstea, 5 rue de la Doua, 69100 Villeurbanne (France); Ben Haj Amara, Abdesslem [Laboratoire de Physique des Matériaux Lamellaires et Nano-Matériaux Hybrides, Faculté des Sciences de Bizerte, Université de Carthage, 7021 Bizerte (Tunisia); Jaffrezic-Renault, Nicole [Institut des Sciences Analytiques UMR CNRS 5280, Université Claude Bernard-Lyon 1, 5 rue de la Doua, 69100 Villeurbanne (France)

    2016-11-15

    Highlights: • MgAl and ZnAl LDH nanosheets were chemically synthesized and deposited over carbon electrode materials. • Catalytic performance of both LDHs was investigated for Fe(II) reduction reaction. • Satisfactory results have been achieved with the MgAl LDH material. • MgAl and ZnAl LDH modified carbon felt were applied in MFC as an efficient anode catalyst. • The LDH-modified anode significantly increased power performance of MFC. - Abstract: Layered double hydroxides (LDHs) have been widely used in the past years due to their unique physicochemical properties and promising applications in electroanalytical chemistry. The present paper is going to focus exclusively on magnesium-aluminum and zinc-aluminum layered double hydroxides (MgAl & ZnAl LDHs) in order to investigate the property and structure of active cation sites located within the layer structure. The MgAl and ZnAl LDH nanosheets were prepared by the constant pH co-precipitation method and uniformly supported on carbon-based electrode materials to fabricate an LDH electrode. Characterization by powder x-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy and transmission electron microscopy revealed the LDH form and well-crystallized materials. Wetting surface properties (hydrophilicity and hydrophobicity) of both prepared LDHs were recorded by contact angle measurement show hydrophilic character and basic property. The electrochemical performance of these hybrid materials was investigated by mainly cyclic voltammetry, electrochemical impedance spectroscopy and chronoamperometry techniques to identify the oxidation/reduction processes at the electrode/electrolyte interface and the effect of the divalent metal cations in total reactivity. The hierarchy of the modified electrode proves that the electronic conductivity of the bulk material is considerably dependent on the divalent cation and affects the limiting parameter of the overall redox process. However

  5. Direct prediction of the desalination performance of porous carbon electrodes for capacitive deionization

    NARCIS (Netherlands)

    Porada, S.; Borchardt, D.; Oschatz, M.; Bryjak, M.; Atchison, J.S.; Keesman, K.J.; Kaskel, S.; Biesheuvel, P.M.; Presser, V.

    2013-01-01

    Desalination by capacitive deionization (CDI) is an emerging technology for the energy- and cost-efficient removal of ions from water by electrosorption in charged porous carbon electrodes. A variety of carbon materials, including activated carbons, templated carbons, carbon aerogels, and carbon nan

  6. Layered double hydroxide materials coated carbon electrode: New challenge to future electrochemical power devices

    Science.gov (United States)

    Djebbi, Mohamed Amine; Braiek, Mohamed; Namour, Philippe; Ben Haj Amara, Abdesslem; Jaffrezic-Renault, Nicole

    2016-11-01

    Layered double hydroxides (LDHs) have been widely used in the past years due to their unique physicochemical properties and promising applications in electroanalytical chemistry. The present paper is going to focus exclusively on magnesium-aluminum and zinc-aluminum layered double hydroxides (MgAl & ZnAl LDHs) in order to investigate the property and structure of active cation sites located within the layer structure. The MgAl and ZnAl LDH nanosheets were prepared by the constant pH co-precipitation method and uniformly supported on carbon-based electrode materials to fabricate an LDH electrode. Characterization by powder x-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy and transmission electron microscopy revealed the LDH form and well-crystallized materials. Wetting surface properties (hydrophilicity and hydrophobicity) of both prepared LDHs were recorded by contact angle measurement show hydrophilic character and basic property. The electrochemical performance of these hybrid materials was investigated by mainly cyclic voltammetry, electrochemical impedance spectroscopy and chronoamperometry techniques to identify the oxidation/reduction processes at the electrode/electrolyte interface and the effect of the divalent metal cations in total reactivity. The hierarchy of the modified electrode proves that the electronic conductivity of the bulk material is considerably dependent on the divalent cation and affects the limiting parameter of the overall redox process. However, MgAl LDH shows better performance than ZnAl LDH, due to the presence of magnesium cations in the layers. Following the structural, morphological and electrochemical behavior studies of both synthesized LDHs, the prepared LDH modified electrodes were tested through microbial fuel cell configuration, revealing a remarkable, potential new pathway for high-performance and cost-effective electrode use in electrochemical power devices.

  7. Direct Electrochemistry of Catalase on Single Wall Carbon Nanotubes Modified Glassy Carbon Electrode

    Institute of Scientific and Technical Information of China (English)

    Qiang ZHAO; Lun Hui GUAN; Zhen Nan GU; Qian Kun ZHUANG

    2005-01-01

    Direct electrochemistry of catalase (Ct) has been studied on single wall carbon nanotubes (SWNTs) modified glassy carbon (GC) electrode. A pair of well-defined nearly reversible redox peaks is given at --0.48 V (vs. SCE) in 0.1 mol/L phosphate solution (pH 7.0).The peak current in cyclic voltammogram is proportional to the scan rate. The peak potential of catalase is shifted to more negative value when the pH increases. Catalase can adsorb on the SWNTs modified electrode.

  8. Enhancing the capacitances of electric double layer capacitors based on carbon nanotube electrodes by carbon dioxide activation and acid oxidization

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Polarizable electrodes of electric double layer capacitors(EDLCs) were made from carbon nanotubes(CNTs).Effect of carbon dioxide activation together with acid oxidation for the electrodes on the characteristics and performances of electrodes and EDLCs was studied.Carbon dioxide activation changed the microstructure of the electrodes,increased the effective surface area of CNTs and optimized the distribution of apertures of the electrodes.Acid oxidization modified the surface characteristics of CNTs.Based on the polarizable electrodes treated by carbon dioxide activation and acid oxidization,the performances of EDLCs were greatly enhanced.The specific capacitance of the electrodes with organic electrolyte was increased from 21.8 F/g to 60.4 F/g.

  9. Single-walled Carbon Nanotubes as Electrode Materials for Supercapacitors

    Institute of Scientific and Technical Information of China (English)

    XU Bina; WU Feng; WANG Fang; CHEN Shi; CAO Gao-Ping; YANG Yu-Sheng

    2006-01-01

    Large-scale synthesized single-walled carbon nanotubes (SWNT) prepared by electric arc discharge method and a mixture of NiO and Y2O3 as catalyst have been used as electrode materials for supercapacitors. N2 adsorption/desorption measurement shows that the SWNT is a microporous and mesoporous material with specific surface area 435 m2g1.Thespecific capacitance of the nitric acid treated SWNT in aqueous electrolyte reaches as high as 105 F/g, which is a combination of electric double layer capacitance and pseudocapacitance. The SWNT-based capacitors also have good charge/discharge reversibility and cycling perdurability.

  10. Vertically Aligned Carbon Nanotube Electrodes for Lithium-Ion Batteries

    Science.gov (United States)

    2011-01-01

    37] Z. Yang, H. Wu, Mater. Chem. Phys. 71 (2001) 7. [38] D. Linden , T.B. Reddy, Handbook of Batteries , 3rd ed., McGraw-Hill Co., Inc., New York, 2005. ...Lithium-ion Energy storage Battery a b s t r a c t As portable electronics becomemore advanced and alternative energy demands becomemore prevalent, the...aligned carbon nanotube electrodes for lithium-ion batteries 5a. CONTRACT NUMBER 5b. GRANT NUMBER 5c. PROGRAM ELEMENT NUMBER 6. AUTHOR( S ) 5d. PROJECT

  11. Catalase-Modified Carbon Electrodes: Persuading Oxygen To Accept Four Electrons Rather Than Two.

    Science.gov (United States)

    Sepunaru, Lior; Laborda, Eduardo; Compton, Richard G

    2016-04-18

    We successfully exploited the natural highly efficient activity of an enzyme (catalase) together with carbon electrodes to produce a hybrid electrode for oxygen reduction, very appropriate for energy transformation. Carbon electrodes, in principle, are cheap but poor oxygen reduction materials, because only two-electron reduction of oxygen occurs at low potentials, whereas four-electron reduction is key for energy-transformation technology. With the immobilization of catalase on the surface, the hydrogen peroxide produced electrochemically is decomposed back to oxygen by the enzyme; the enzyme natural activity on the surface regenerates oxygen, which is further reduced by the carbon electrode with no direct electron transfer between the enzyme and the electrode. Near full four-electron reduction of oxygen is realised on a carbon electrode, which is modified with ease by a commercially available enzyme. The value of such enzyme-modified electrode for energy-transformation devices is evident.

  12. Conducting polymer/carbon nanocoil composite electrodes for efficient supercapacitors

    KAUST Repository

    Baby, Rakhi Raghavan

    2012-01-01

    Herein, we report for the first time, conducting polymer (polyaniline (PANI) and polypyrrole (PPY)) coated carbon nanocoils (CNCs) as efficient binder-free electrode materials for supercapacitors. CNCs act as a perfect backbone for the uniform distribution of the conducting polymers in the composites. In two electrode configuration, the samples exhibited high specific capacitance with the values reaching up to 360 and 202 F g -1 for PANI/CNCs and PPY/CNCs respectively. The values obtained for specific capacitance and maximum storage energy per unit mass of the composites were found to be comparable to one of the best reported values for polymer coated multi-walled carbon nanotubes. In addition, the fabricated PANI/CNC based supercapacitors exhibited a high value of 44.61 Wh kg -1 for maximum storage energy per unit mass. Although the devices exhibit an initial capacitance loss due to the instability of the polymer, the specific capacitance stabilizes at a fixed value after 500 charge-discharge cycles. © 2012 The Royal Society of Chemistry.

  13. A novel palygorskite-modified carbon paste amperometric sensor for catechol determination

    Energy Technology Data Exchange (ETDEWEB)

    Kong Yong [School of Chemistry and Chemical Engineering, Changzhou University, No. 1 Gehu Road, Changzhou 213164, Jiangsu Province (China); Key Lab of Analytical Chemistry for Life Science, Ministry of Education, Nanjing University, Nanjing 210093 (China); Chen Xiaohui; Wang Wenchang [School of Chemistry and Chemical Engineering, Changzhou University, No. 1 Gehu Road, Changzhou 213164, Jiangsu Province (China); Chen Zhidong, E-mail: czd_chen@yahoo.com.cn [School of Chemistry and Chemical Engineering, Changzhou University, No. 1 Gehu Road, Changzhou 213164, Jiangsu Province (China)

    2011-03-04

    A palygorskite-modified carbon paste electrode (CPE) was constructed using graphite powder mixed with palygorskite particles. Compared with the unmodified CPE, the resulting palygorskite-modified CPE remarkably increases the peak currents of catechol, and greatly lowers the peak potential separation. Therefore, the palygorskite exhibits catalytic activity to catechol and significantly improves the determining sensitivity. The electrocatalytic activity of palygorskite is attributed to its high adsorption capability and the -OH groups on its surface, which plays an important role in the electron transfer between the modified CPE and the catechol in the solution. The sensor shows a linear response range between 5 and 100 {mu}M catechol with a correlation coefficient of 0.998. The detection limit was calculated as 0.57 {mu}M (s/n = 3).

  14. Particulate inverse opal carbon electrodes for lithium-ion batteries.

    Science.gov (United States)

    Kang, Da-Young; Kim, Sang-Ok; Chae, Yu Jin; Lee, Joong Kee; Moon, Jun Hyuk

    2013-01-29

    Inverse opal carbon materials were used as anodes for lithium ion batteries. We applied particulate inverse opal structures and their dispersion in the formation of anode electrodes via solution casting. We prepared aminophenyl-grafted inverse opal carbons (a-IOC), inverse opal carbons with mesopores (mIOC), and bare inverse opal carbons (IOC) and investigated the electrochemical behavior of these samples as anode materials. Surface modification by aminophenyl groups was confirmed by XPS measurements. TEM images showed mesopores, and the specific area of mIOC was compared with that of IOC using BET analysis. A half-cell test was performed to compare a-IOC with IOC and mIOC with IOC. In the case of the a-IOC structure, the cell test revealed no improvement in the reversible specific capacity or the cycle performance. The mIOC cell showed a reversible specific capacity of 432 mAh/g, and the capacity was maintained at 88%-approximately 380 mAh/g-over 20 cycles.

  15. Electrochemical Reduction of Carbon Dioxide to Methanol by Direct Injection of Electrons into Immobilized Enzymes on a Modified Electrode.

    Science.gov (United States)

    Schlager, Stefanie; Dumitru, Liviu Mihai; Haberbauer, Marianne; Fuchsbauer, Anita; Neugebauer, Helmut; Hiemetsberger, Daniela; Wagner, Annika; Portenkirchner, Engelbert; Sariciftci, Niyazi Serdar

    2016-03-21

    We present results for direct bio-electrocatalytic reduction of CO2 to C1 products using electrodes with immobilized enzymes. Enzymatic reduction reactions are well known from biological systems where CO2 is selectively reduced to formate, formaldehyde, or methanol at room temperature and ambient pressure. In the past, the use of such enzymatic reductions for CO2 was limited due to the necessity of a sacrificial co-enzyme, such as nicotinamide adenine dinucleotide (NADH), to supply electrons and the hydrogen equivalent. The method reported here in this paper operates without the co-enzyme NADH by directly injecting electrons from electrodes into immobilized enzymes. We demonstrate the immobilization of formate, formaldehyde, and alcohol dehydrogenases on one-and-the-same electrode for direct CO2 reduction. Carbon felt is used as working electrode material. An alginate-silicate hybrid gel matrix is used for the immobilization of the enzymes on the electrode. Generation of methanol is observed for the six-electron reduction with Faradaic efficiencies of around 10%. This method of immobilization of enzymes on electrodes offers the opportunity for electrochemical application of enzymatic electrodes to many reactions in which a substitution of the expensive sacrificial co-enzyme NADH is desired.

  16. Electrochemical behaviors of Fenbendazole at graphene and[ Bupy] PF6 modified carbon paste electrode and its electrochemical determination%芬苯达唑在石墨烯与[ Bupy ] PF6复合修饰碳糊电极上的电化学性质及电分析方法研究

    Institute of Scientific and Technical Information of China (English)

    田碧桃; 李金来; 王维; 犹卫; 彭娟; 高作宁

    2015-01-01

    本文研究了芬苯达唑( Fenbendazole,FBZ)在石墨烯( RGO)与离子液体( N-丁基吡啶六氟磷酸盐)复合修饰碳糊电极上的电催化氧化及电化学动力学性质。同时用CC法(计时库仑法)、计时电流法( CA)测定FBZ在RGO-[ Bupy] PF6/CPE上的电极反应动力学参数,并用方波伏安法( SWV)测定FBZ氧化峰电流( Ip )与其浓度c在4.0×10-8~1.0×10-5mol·L-1范围内呈良好线性关系,线性回归方程为Ip(μA)=1.471+5220.78c (10-3mol·L-1),R=0.9995,检测限(S/N=3)为1.4×10-9mol·L-1,在此基础上用SWV法对FBZ片剂中FBZ含量进行了电化学定量测定,RSD在0.2%~0.9%之间,回收率在99.0%~101.4%之间。%Objective:Electrocatalytic oxidation and its electrochemical kinetics of fenbendazole( FBZ) were investigated by Cyclic voltammetry(CV)method at carbon paste electrode(CPE)which modified by graphene(RGO)and [Bupy]PF6. The experiment re-sults indicated that FBZ electrochemical behaviors exhibits an irreversible electrochemical oxidation progress at RGO-[ Bupy] PF6/CPE,The electrochemical kinetic parameters were determined by chronocoulometry ( CC) and chronoamperometry ( CA) at RGO-[ Bupy] PF6/CPE. The oxidation peak current of FBZ versus its concentration had a good linear relationship in the concentration range of 4. 0 × 10-8 ~1. 0 × 10-5 mol·L-1and the detection limit(S/N=3)was 1. 4 × 10-9mol·L-1 by square wave voltammetric (SWV)method. The equation of linear regression was Ip(μA)=1. 471+5220. 78c(10-3mol·L-1),R=0. 9995,Also the proposed method have been applied in electrochemical quantitative determination of FBZ content in commercial tablet samples,with their rel-ative standard deviations of 0. 2% ~0. 9%and recoveries of 99. 0% ~101. 4%.

  17. Intra-operative micro-electrode recording in functional neurosurgery: Past, present, future.

    Science.gov (United States)

    Maiti, Tanmoy K; Konar, Subhas; Bir, Shyamal; Kalakoti, Piyush; Nanda, Anil

    2016-10-01

    The field of functional neurosurgery has experienced a rise, fall and lastly a renaissance over the past 75years. Micro-electrode recording (MER) played a key role during this eventful journey. However, as the intra-operative MRI continues to evolve, a pertinent question about the utility of MER has been raised in recent years. In this article, we critically review these current controversies. The English literature is reviewed and the complex technique of MER is discussed in a simplified manner. The improvement of neuroimaging and its application in functional neurosurgery, especially in deep brain stimulation, is discussed. Finally, the current controversies and technical advances which can direct the future are reviewed. The results of existing meta-analyses addressing the controversies are summarized. Wide variations of pre-operative and intra-operative targeting methods have been described in the literature. Though functional neurosurgery is generally safe, complications do occur and multiple passes during MER can certainly add to the risk of inadvertent hemorrhage and infection. Additionally, the recent introduction of newer MRI modalities has ensured better delineation of the target. However, MER is still useful to address brain shift, for mapping of newer targets, for ablative surgeries and in centers without an intra-operative imaging facility. In the current scenario, it is nearly impossible to conduct a prospective study to decide the utility of MER. The importance of MER may further diminish in the future as a routine procedure, but its role as a gold standard procedure may still persist.

  18. Polymyxin-coated Au and carbon nanotube electrodes for stable [NiFe]-hydrogenase film voltammetry.

    NARCIS (Netherlands)

    Hoeben, F.J.M.; Heller, I.; Albracht, S.P.J.; Dekker, C.; Lemay, S.G.; Heering, H.A.

    2008-01-01

    We report on the use of polymyxin (PM), a cyclic cationic lipodecapeptide, as an electrode modifier for studying protein film voltammetry (PFV) on Au and single-walled carbon nanotube (SWNT) electrodes. Pretreating the electrodes with PM allows for the subsequent immobilization of an active submonol

  19. Carbon Fiber-gold/mercury Dual-electrode Detection for Capillary Electrophoresis

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A carbon fiber-gold/mercury dual-electrode for capillary electrophoresis is constructed. Cysteine, glutathione, ascorbic acid and uric acid can be detected simultaneously and selectively at the dual-electrode, respectively. The capillary electrophoresis / dual-electrode detection system has been used to determine these compounds in human blood samples.

  20. Hierarchical Porous Carbon Counter Electrode for Dye-Sensitized Solar Cells

    Institute of Scientific and Technical Information of China (English)

    WANG Gui-Qiang; HUANG Cong-Gong; XING Wei; ZHUO Shu-Ping

    2011-01-01

    Hierarchical porous carbon is prepared by a combination of self-organization and chemical activation and explored as counter electrode for dye-sensitized solar cells.Pore structure analysis shows that micropores generated within the mesopore wall and the pristine mesopore structure of mesoporous carbon are preserved during KOH activation. Electrochemical impedance spectroscopy studies demonstrate a relatively high electrocatalytic activity of hierarchical porous carbon electrode for triiodide reduction, as compared with a pristine mesoporous carbon electrode. This enhanced electrocatalytic activity is beneficial for improving the photovoltaic performance of dyesensitized solar cells. The overall conversion efficiency of dye-sensitized solar cells with the hierarchical porous carbon electrode increased by 11.5% compared with that of the cell with a pristine mesoporous carbon electrode.

  1. Influence of carbonisation on selected engineering properties of carbon resin electrodes for electrochemical treatment of wastewater

    Energy Technology Data Exchange (ETDEWEB)

    Oke, I.A. [Obafemi Awolowo Univ., Ile-Ife (Nigeria). Dept. of Civil Engineering

    2009-10-15

    Carbon resin electrodes (CRE) developed using a non-heat treatment process were investigated in an effort to determine the influence of several properties on electrode performance. These included density; electrical resistance; microstructure; hydroscopy; stability moisture content; and compressive and flexural strength. The influences of carbonization temperature, carbon particle size, and compaction pressure were also analyzed. Results of the study showed that the electrical resistance and density of the CRE decreased with increases in carbonization temperatures. Particle size, compacting pressure, and the percentage of resin used in the electrodes also influenced electrical resistance. The carbonization of the CREs from 30 to 220 degrees C reduced specific electrical resistance and density. The carbonization temperature did not have a significant effect on wetness, compressive and flexural strength, or on the stability and moisture content of the electrodes. It was concluded that the cost of producing the CREs is significantly cheaper than the cost of heat-treated electrodes. 78 refs., 9 tabs., 8 figs.

  2. Polymer-Assisted Direct Deposition of Uniform Carbon Nanotube Bundle Networks for High Performance Transparent Electrodes

    KAUST Repository

    Hellstrom, Sondra L.

    2009-06-23

    Flexible transparent electrodes are crucial for touch screen, flat panel display, and solar cell technologies. While carbon nanotube network electrodes show promise, characteristically poor dispersion properties have limited their practicality. We report that addition of small amounts of conjugated polymer to nanotube dispersions enables straightforward fabrication of uniform network electrodes by spin-coating and simultaneous tuning of parameters such as bundle size and density. After treatment in thionyl chloride, electrodes have sheet resistances competitive with other reported carbon nanotube based transparent electrodes to date. © 2009 American Chemical Society.

  3. Composite supercapacitor electrodes made of activated carbon/PEDOT:PSS and activated carbon/doped PEDOT

    Indian Academy of Sciences (India)

    T S Sonia; P A Mini; R Nandhini; Kalluri Sujith; Balakrishnan Avinash; S V Nair; K R V Subramanian

    2013-08-01

    In this paper, we report on the high electrical storage capacity of composite electrodes made from nanoscale activated carbon combined with either poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) or PEDOT doped with multiple dopants such as ammonium persulfate (APS) and dimethyl sulfoxide (DMSO). The composites were fabricated by electropolymerization of the conducting polymers (PEDOT:PSS, doped PEDOT) onto the nanoscale activated carbon backbone, wherein the nanoscale activated carbon was produced by ball-milling followed by chemical and thermal treatments. Activated carbon/PEDOT:PSS yielded capacitance values of 640 F g-1 and 26mF cm-2, while activated carbon/doped PEDOT yielded capacitances of 1183 F g-1 and 42 mF cm-2 at 10 mV s-1. This is more than five times the storage capacity previously reported for activated carbon–PEDOT composites. Further, use of multiple dopants in PEDOT improved the storage performance of the composite electrode well over that of PEDOT:PSS. The composite electrodes were characterized for their electrochemical behaviour, structural and morphological details and electronic conductivity and showed promise as high-performance energy storage systems.

  4. Characterization of Transition-Metal Oxide Deposition on Carbon Electrodes of a Supercapacitor

    Directory of Open Access Journals (Sweden)

    Ying-Chung Chen

    2016-12-01

    Full Text Available In order to fabricate the composite electrodes of a supercapacitor, transition-metal oxide materials NiO and WO3 were deposited on carbon electrodes by electron beam evaporation. The influences of various transition-metal oxides, scan rates of cyclic voltammograms (CVs, and galvanostatic charge/discharge tests on the characteristics of supercapacitor were studied. The charge/discharge efficiency and the lifetime of the composite electrodes were also investigated. It was found that the composite electrodes exhibited more favorable capacitance properties than those of the carbon electrodes at high scan rates. The results revealed the promotion of the capacitance property of the supercapacitor with composite electrode and the improving of the decay property in capacitance at high scan rate. In addition, the charge/discharge efficiency is close to 100% after 5000 cycles, and the composite electrode retains strong adhesion between the electrode material and the substrate.

  5. Self-Templated Synthesis of Mesoporous Carbon from Carbon Tetrachloride Precursor for Supercapacitor Electrodes.

    Science.gov (United States)

    Tang, Duihai; Hu, Shi; Dai, Fang; Yi, Ran; Gordin, Mikhail L; Chen, Shuru; Song, Jiangxuan; Wang, Donghai

    2016-03-23

    A high-surface-area mesoporous carbon material has been synthesized using a self-templating approach via reduction of carbon tetrachloride by sodium potassium alloy. The advantage is the reduction-generated salt templates can be easily removed with just water. The produced mesoporous carbon has a high surface area and a narrow pore size distribution. When used as a supercapacitor electrode, this material exhibits a high specific capacitance (259 F g(-1)) and excellent cycling performance (>92% capacitance retention for 6000 cycles).

  6. Electrochemical determination of hydrochlorothiazide and folic acid in real samples using a modified graphene oxide sheet paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Beitollahi, Hadi, E-mail: h.beitollahi@yahoo.com [Environment Department, Institute of Science and High Technology and Environmental Sciences, Graduate University of Advanced Technology, Kerman (Iran, Islamic Republic of); Hamzavi, Mozhdeh [Department of Chemistry, Graduate University of Advanced Technology, Kerman (Iran, Islamic Republic of); Torkzadeh-Mahani, Masoud [Biotechnology Department, Institute of Science and High Technology and Environmental Sciences, Graduate University of Advanced Technology, Kerman (Iran, Islamic Republic of)

    2015-07-01

    A new ferrocene-derivative compound, 2-chlorobenzoyl ferrocene, was synthesized and used to construct a modified graphene oxide sheet paste electrode. The electrooxidation of hydrochlorothiazide at the surface of the modified electrode was studied. Under optimized conditions, the square wave voltammetric (SWV) peak current of hydrochlorothiazide increased linearly with hydrochlorothiazide concentration in the range of 5.0 × 10{sup −8} to 2.0 × 10{sup −4} M and a detection limit of 20.0 nM was obtained for hydrochlorothiazide. The diffusion coefficient and kinetic parameters (such as electron transfer coefficient and the heterogeneous rate constant) for hydrochlorothiazide oxidation were also determined. The prepared modified electrode exhibits a very good resolution between the voltammetric peaks of hydrochlorothiazide and folic acid which makes it suitable for the detection of hydrochlorothiazide in the presence of folic acid in real samples. - Highlights: • A novel modified-graphene oxide nanosheet paste electrode has been fabricated. • This electrode reduced the oxidation potential of hydrochlorothiazide by about 315 mV. • Hydrochlorothiazide was measured in the range of 5.0 × 10{sup −8} to 2.0 × 10{sup −4} M. • The detection limit for hydrochlorothiazide was obtained at 20.0 nM. • It resolved the voltammetric waves of hydrochlorothiazide and folic acid.

  7. Direct electrochemistry of hemoglobin entrapped in dextran film on carbon ionic liquid electrode

    Indian Academy of Sciences (India)

    Xiaoqing Li; Yan Wang; Xiaoying Sun; Tianrong Zhan; Wei Sun

    2010-03-01

    Direct electrochemistry of hemoglobin (Hb) entrapped in the dextran (De) film on the surface of a room temperature ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF6) modified carbon paste electrode (CILE) has been investigated. UV-Vis and FT-IR spectroscopy showed that Hb retained its native structure in the De film. Scanning electron microscopy (SEM) indicated an uniform film was formed on the electrode surface. Cyclic voltammetric experiments indicated that the electron transfer efficiency between Hb and the electrode was greatly improved due to the presence of the De film and ionic liquid, which provided a biocompatible and higher conductive interface. A pair of well-defined and quasi-reversible redox peak was obtained with the anodic and cathodic peaks located at -0.195 V and -0.355 V in pH 7.0 phosphate buffer solution, respectively. The electrochemical parameters were calculated by investigating the relationship of the peak potential with the scan rate. The fabricated De/Hb/CILE showed good electrocatalytic ability to the reduction of H2O2 with the linear concentration range from 4.0 × 10-6 to 1.5 × 10-5 mol/L and the apparent Michaelis-Menten constant ($K_{M}^{\\text{app}}$) for the electrocatalytic reaction was calculated as 0.17 M.

  8. Fabrication and electrochemical behavior of single-walled carbon nanotube/graphite-based electrode

    Energy Technology Data Exchange (ETDEWEB)

    Moghaddam, Abdolmajid Bayandori [Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran P.O. Box 14155-6455, Tehran (Iran, Islamic Republic of); Medical Nanotechnology Research Centre, Medical Sciences/University of Tehran, P.O. Box 14155-6451, Tehran (Iran, Islamic Republic of); Ganjali, Mohammad Reza [Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran P.O. Box 14155-6455, Tehran (Iran, Islamic Republic of)], E-mail: Ganjali@khayam.ut.ac.ir; Dinarvand, Rassoul [Medical Nanotechnology Research Centre, Medical Sciences/University of Tehran, P.O. Box 14155-6451, Tehran (Iran, Islamic Republic of); Razavi, Taherehsadat [Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran P.O. Box 14155-6455, Tehran (Iran, Islamic Republic of); Riahi, Siavash [Institute of Petroleum Engineering, Faculty of Engineering, University of Tehran, Tehran (Iran, Islamic Republic of); Rezaei-Zarchi, Saeed [Department of Biology, Payam-e-Noor University, Yazd (Iran, Islamic Republic of); Norouzi, Parviz [Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran P.O. Box 14155-6455, Tehran (Iran, Islamic Republic of)

    2009-01-01

    An electrochemical method for determining the dihydroxybenzene derivatives on glassy carbon (GC) has been developed. In this method, the performance of a single-walled carbon nanotube (SWCNT)/graphite-based electrode, prepared by mixing SWCNTs and graphite powder, was described. The resulting electrode shows an excellent behavior for redox of 3,4-dihydroxybenzoic acid (DBA). SWCNT/graphite-based electrode presents a significant decrease in the overvoltage for DBA oxidation as well as a dramatic improvement in the reversibility of DBA redox behavior in comparison with graphite-based and glassy carbon (GC) electrodes. In addition, scanning electron microscopy (SEM) and atomic force microscopy (AFM) procedures performed for used SWCNTs.

  9. Novel Conductive Carbon Black and Polydimethlysiloxane ECG Electrode: A Comparison with Commercial Electrodes in Fresh, Chlorinated, and Salt Water.

    Science.gov (United States)

    Noh, Yeonsik; Bales, Justin R; Reyes, Bersain A; Molignano, Jennifer; Clement, Amanda L; Pins, George D; Florian, John P; Chon, Ki H

    2016-08-01

    In this study, we evaluated the performance of two novel conductive carbon black (CB) and polydimethlysiloxane (PDMS) bio-potential electrodes, with and without an integrated flexible copper mesh, against commercially available electrodes (Polar(®) textile, Silver-coated textile, and carbon rubber). The electrodes were tested in three types of water (fresh/unfiltered, chlorinated, and salt water). Our testing revealed that our CB/PDMS electrode with integrated copper mesh provided a high-fidelity ECG signal morphologies without any amplitude degradation in all of the types of water tested (N = 10). The non-meshed CB/PDMS electrodes were also subjected to a long-term durability test by the US Navy SCUBA divers during which the electrodes maintained ECG signal quality for a 6 h period of continuous use. The results of a material degradation analysis revealed the CB/PDMS composite material does not exhibit significant changes in physical integrity after prolonged exposure to the test conditions. The newly developed meshed CB/PDMS electrodes have the potential to be used in a wide variety of both dry and wet environments including the challenge of obtaining ECG signals in salt water environments.

  10. Electron Cyclotron Resonance-Sputtered Nanocarbon Film Electrode Compared with Diamond-Like Carbon and Glassy Carbon Electrodes as Regards Electrochemical Properties and Biomolecule Adsorption

    Science.gov (United States)

    Xue, Qiang; Kato, Dai; Kamata, Tomoyuki; Umemura, Shigeru; Hirono, Shigeru; Niwa, Osamu

    2012-09-01

    The electrochemical properties and biocompatible characteristics at an electron cyclotron resonance (ECR)-sputtered nanocarbon film electrode, a diamond-like carbon (DLC) electrode and a glassy carbon (GC) electrode have been studied. The three carbon electrodes show significant current reductions with increased peak separations as a result of protein fouling before oxygen plasma treatment, but the current reductions of the ECR-sputtered nanocarbon and DLC film electrodes are smaller than that of the GC electrode due to their superior surface flatness. The oxygen plasma pretreated ECR-sputtered nanocarbon film electrode exhibits a significant improvement in anti-fouling performance with an improved electron transfer. This is because the pretreated ECR-sputtered nanocarbon film enabled the surface to introduce surface oxygen functionalities that not only improve the interaction between the analytes and the electrode surface but also make the film surface more hydrophilic, which is important for the suppression of biomolecule adsorption. At the same time, the pretreated ECR-sputtered nanocarbon film also retained an ultraflat surface even after pretreatment as a result of the low background current. This excellent performance can only be achieved with our ECR-sputtered nanocarbon film, indicating that our film is promising for application to electrochemical detectors for various biomolecular analytes.

  11. Carbon felt and carbon fiber - A techno-economic assessment of felt electrodes for redox flow battery applications

    Science.gov (United States)

    Minke, Christine; Kunz, Ulrich; Turek, Thomas

    2017-02-01

    Carbon felt electrodes belong to the key components of redox flow batteries. The purpose of this techno-economic assessment is to uncover the production costs of PAN- and rayon-based carbon felt electrodes. Raw material costs, energy demand and the impact of processability of fiber and felt are considered. This innovative, interdisciplinary approach combines deep insights into technical, ecologic and economic aspects of carbon felt and carbon fiber production. Main results of the calculation model are mass balances, cumulative energy demands (CED) and the production costs of conventional and biogenic carbon felts supplemented by market assessments considering textile and carbon fibers.

  12. Study on Utilization of Carboxyl Group Decorated Carbon Nanotubes and Carbonation Reaction for Improving Strengths and Microstructures of Cement Paste

    Directory of Open Access Journals (Sweden)

    Xiantong Yan

    2016-08-01

    Full Text Available Carbon nanotubes (CNTs have excellent mechanical properties and can be used to reinforce cement-based materials. On the other hand, the reaction product of carbonation with hydroxides in hydrated cement paste can reduce the porosity of cement-based materials. In this study, a novel method to improve the strength of cement paste was developed through a synergy of carbon nanotubes decorated with carboxyl group and carbonation reactions. The experimental results showed that the carboxyl group (–COOH of decorated carbon nanotubes and the surfactant can control the morphology of the calcium carbonate crystal of carbonation products in hydrated cement paste. The spindle-like calcium carbonate crystals showed great morphological differences from those observed in the conventional carbonation of cement paste. The spindle-like calcium carbonate crystals can serve as fiber-like reinforcements to reinforce the cement paste. By the synergy of the carbon nanotubes and carbonation reactions, the compressive and flexural strengths of cement paste were significantly improved and increased by 14% and 55%, respectively, when compared to those of plain cement paste.

  13. The Effect of Anodic Surface Treatment on the Oxidation of Catechols at Ultrasmall Carbon Ring Electrodes

    Science.gov (United States)

    1991-07-09

    selectivity. A model of the surface formed following anodic oxidation is consistent with previous models involving both surface cleanliness and carbon...involving both surface cleanliness and carbon structure orientation. 2 INTRODUCTION Because of the vast electroanalytical utility of carbon electrodes...of the electron transfer rate following treatment are a function of the surface cleanliness and the orientation of the carbon structure

  14. Electroadsorption Desalination with Carbon Nanotube/PAN-Based Carbon Fiber Felt Composites as Electrodes

    Directory of Open Access Journals (Sweden)

    Yang Liu

    2014-01-01

    Full Text Available The chemical vapor deposition method is used to prepare CNT (carbon nanotube/PCF (PAN-based carbon fiber felt composite electrodes in this paper, with the surface morphology of CNT/PCF composites and electroadsorption desalination performance being studied. Results show such electrode materials with three-dimensional network nanostructures having a larger specific surface area and narrower micropore distribution, with a huge number of reactive groups covering the surface. Compared with PCF electrodes, CNT/PCF can allow for a higher adsorption and desorption rate but lower energy consumption; meanwhile, under the condition of the same voltage change, the CNT/PCF electrodes are provided with a better desalination effect. The study also found that the higher the original concentration of the solution, the greater the adsorption capacity and the lower the adsorption rate. At the same time, the higher the solution’s pH, the better the desalting; the smaller the ions’ radius, the greater the amount of adsorption.

  15. Pore structure and carbonation in blended lime-cement pastes

    Directory of Open Access Journals (Sweden)

    Álvarez, J. I.

    2006-06-01

    Full Text Available The present study aims to gain a fuller understandingof the curing process in lime pastes (100, 90, 80, 70,60, 50 and 40% lime blended with cement by analyzingcarbonation in these materials. A hydrated, airslaked lime powder and CEM II A/L 32.5 Portlandcement were used for the blends. These materialswere singled out for research primarily because theymay be used in the restoration of heritage monuments.Variation in weight was used as an indicator for carbonation.A new parameter, A, was found to vary inverselywith the percentage of the cement because of theprevalence of Knudsen diffusion in the paste, in turndue to the characteristics of the pore structure, whichwas studied by mercury intrusion porosimetry (MIP.The hygroscopic study conducted on the different pastesprovided information on water content at a givenhumidity and its location, i.e., adsorbed on the surfaceof the pores or condensed inside them, obstructing thediffusion of CO2. The conclusion drawn from this studyof the curing process was that neither drying nor C3Shydration retarded lime carbonation.En este trabajo se estudia el proceso de carbonatacionen pastas mixtas de cal y cemento (100, 90, 80, 70, 60,50 y 40% de cal con el objeto de obtener un mejorconocimiento del proceso de curado en estos materiales.Para ello se ha empleado una cal aerea hidratada en polvoy un cemento Portland del tipo CEM II A/L 32,5. Enparticular, este estudio investiga estos materiales ya quepueden ser utilizados en la restauracion del PatrimonioCultural. Se ha utilizado la variacion de peso como indicadordel proceso de carbonatacion. Se ha establecidoun nuevo parametro, A, que varia inversamente con elporcentaje de cemento en la pasta, debido al predominiode la difusion de Knudsen como consecuencia de laestructura porosa, que ha sido estudiada por medio deporosimetria de intrusion de mercurio (PIM. El estudiohigroscopico realizado sobre las diversas pastas permiteconocer el contenido en agua a una

  16. Electrochemical investigation of NO at single-wall carbon nanotubes modified electrodes

    Indian Academy of Sciences (India)

    Tingliang Xia; Hongmei Bi; Keying Shi

    2010-05-01

    The NO electro-oxidation was investigated at various single-wall carbon nanotubes (SWCNTs) modified electrodes by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Compared with the glassy carbon electrode, the SWCNTs modified electrodes possess higher electro-catalytic activity to NO electro-oxidation. CV results indicate that the peak current density of NO electro-oxidation at the SWCNT-COOH (SWCNTs with carboxyl groups) modified electrode is the highest and the peak potential is the most negative among the four kinds of electrodes. EIS indicates that the charge transfer resistance of NO electro-oxidation at the SWCNT-COOH modified electrode is the least. The determined factors (charge transfer and mass transfer of diffusion) of NO electro-oxidation are different in varied potential region. The mechanism of NO electro-oxidation reaction at the SWCNTs modified electrodes is also discussed.

  17. Electrochemical Determination of Glycoalkaloids Using a Carbon Nanotubes-Phenylboronic Acid Modified Glassy Carbon Electrode

    Directory of Open Access Journals (Sweden)

    Huiying Wang

    2013-11-01

    Full Text Available A versatile strategy for electrochemical determination of glycoalkaloids (GAs was developed by using a carbon nanotubes-phenylboronic acid (CNTs-PBA modified glassy carbon electrode. PBA reacts with α-solanine and α-chaconine to form a cyclic ester, which could be utilized to detect GAs. This method allowed GA detection from 1 μM to 28 μM and the detection limit was 0.3 μM. Affinity interaction of GAs and immobilized PBA caused an essential change of the peak current. The CNT-PBA modified electrodes were sensitive for detection of GAs, and the peak current values were in quite good agreement with those measured by the sensors.

  18. Electrochemical Determination of Glycoalkaloids Using a Carbon Nanotubes-Phenylboronic Acid Modified Glassy Carbon Electrode

    Science.gov (United States)

    Wang, Huiying; Liu, Mingyue; Hu, Xinxi; Li, Mei; Xiong, Xingyao

    2013-01-01

    A versatile strategy for electrochemical determination of glycoalkaloids (GAs) was developed by using a carbon nanotubes-phenylboronic acid (CNTs-PBA) modified glassy carbon electrode. PBA reacts with α-solanine and α-chaconine to form a cyclic ester, which could be utilized to detect GAs. This method allowed GA detection from 1 μM to 28 μM and the detection limit was 0.3 μM. Affinity interaction of GAs and immobilized PBA caused an essential change of the peak current. The CNT-PBA modified electrodes were sensitive for detection of GAs, and the peak current values were in quite good agreement with those measured by the sensors. PMID:24287539

  19. Electrooxidation of DNA at glassy carbon electrodes modified with multiwall carbon nanotubes dispersed in polyethylenimine

    Energy Technology Data Exchange (ETDEWEB)

    Luque, Guillermina L.; Ferreyra, Nancy F. [INFIQC, Departamento de Fisico Quimica, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba, Ciudad Universitaria, 5000 Cordoba (Argentina); Granero, Adrian [INFIQC, Departamento de Fisico Quimica, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba, Ciudad Universitaria, 5000 Cordoba (Argentina); Departamento de Quimica, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Rio Cuarto (Argentina); Bollo, Soledad [Laboratorio de Bioelectroquimica, Facultad de Ciencias Quimicas y Farmaceuticas, Universidad de Chile, P.O. Box 233, Santiago (Chile); Rivas, Gustavo A., E-mail: grivas@fcq.unc.edu.ar [INFIQC, Departamento de Fisico Quimica, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba, Ciudad Universitaria, 5000 Cordoba (Argentina)

    2011-10-30

    This work reports the electrochemical response of the complex between dsDNA and PEI formed in solution and at the surface of glassy carbon electrodes (GCE) modified with a dispersion of multi-walled carbon nanotubes in polyethylenimine (CNT-PEI). Scanning Electron Microscopy and Scanning Electrochemical Microscopy demonstrate that the dispersion covers the whole surface of the electrode although there are areas with higher density of CNT and, consequently, with higher electrochemical reactivity. The adsorption of DNA at GCE/CNT-PEI is fast and it is mainly driven by electrostatic forces. A clear oxidation signal is obtained either for dsDNA or a heterooligonucleotide of 21 bases (oligoY) at potentials smaller than those for the oxidation at bare GCE. The comparison of the behavior of DNA before and after thermal treatment demonstrated that the electrochemical response highly depends on the 3D structure of the nucleic acid.

  20. Improved Manufacturing Performance of Screen Printed Carbon Electrodes through Material Formulation.

    Science.gov (United States)

    Jewell, Eifion; Philip, Bruce; Greenwood, Peter

    2016-06-27

    Printed carbon graphite materials are the primary common component in the majority of screen printed sensors. Screen printing allows a scalable manufacturing solution, accelerating the means by which novel sensing materials can make the transition from laboratory material to commercial product. A common bottleneck in any thick film printing process is the controlled drying of the carbon paste material. A study has been undertaken which examines the interaction between material solvent, printed film conductivity and process consistency. The study illustrates that it is possible to reduce the solvent boiling point to significantly increase process productivity while maintaining process consistency. The lower boiling point solvent also has a beneficial effect on the conductivity of the film, reducing the sheet resistance. It is proposed that this is a result of greater film stressing increasing charge percolation through greater inter particle contact. Simulations of material performance and drying illustrate that a multi layered printing provides a more time efficient manufacturing method. The findings have implications for the volume manufacturing of the carbon sensor electrodes but also have implications for other applications where conductive carbon is used, such as electrical circuits and photovoltaic devices.

  1. Improved Manufacturing Performance of Screen Printed Carbon Electrodes through Material Formulation

    Directory of Open Access Journals (Sweden)

    Eifion Jewell

    2016-06-01

    Full Text Available Printed carbon graphite materials are the primary common component in the majority of screen printed sensors. Screen printing allows a scalable manufacturing solution, accelerating the means by which novel sensing materials can make the transition from laboratory material to commercial product. A common bottleneck in any thick film printing process is the controlled drying of the carbon paste material. A study has been undertaken which examines the interaction between material solvent, printed film conductivity and process consistency. The study illustrates that it is possible to reduce the solvent boiling point to significantly increase process productivity while maintaining process consistency. The lower boiling point solvent also has a beneficial effect on the conductivity of the film, reducing the sheet resistance. It is proposed that this is a result of greater film stressing increasing charge percolation through greater inter particle contact. Simulations of material performance and drying illustrate that a multi layered printing provides a more time efficient manufacturing method. The findings have implications for the volume manufacturing of the carbon sensor electrodes but also have implications for other applications where conductive carbon is used, such as electrical circuits and photovoltaic devices.

  2. Carbon nanofibers grafted on activated carbon as an electrode in high-power supercapacitors.

    Science.gov (United States)

    Gryglewicz, Grażyna; Śliwak, Agata; Béguin, François

    2013-08-01

    A hybrid electrode material for high-power supercapacitors was fabricated by grafting carbon nanofibers (CNFs) onto the surface of powdered activated carbon (AC) through catalytic chemical vapor deposition (CCVD). A uniform thin layer of disentangled CNFs with a herringbone structure was deposited on the carbon surface through the decomposition of propane at 450 °C over an AC-supported nickel catalyst. CNF coating was controlled by the reaction time and the nickel content. The superior CNF/AC composite displays excellent electrochemical performance in a 0.5 mol L(-1) solution of K2 SO4 due to its unique structure. At a high scan rate (100 mV s(-1) ) and current loading (20 A g(-1) ), the capacitance values were three- and fourfold higher than those for classical AC/carbon black composites. Owing to this feature, a high energy of 10 Wh kg(-1) was obtained over a wide power range in neutral medium at a voltage of 0.8 V. The significant enhancement of charge propagation is attributed to the presence of herringbone CNFs, which facilitate the diffusion of ions in the electrode and play the role of electronic bridges between AC particles. An in situ coating of AC with short CNFs (below 200 nm) is a very attractive method for producing the next generation of carbon composite materials with a high power performance in supercapacitors working in neutral medium.

  3. A new strategy for determination of bisphenol A in the presence of Sudan I using a ZnO/CNTs/ionic liquid paste electrode in food samples.

    Science.gov (United States)

    Najafi, Maryam; Khalilzadeh, Mohammad A; Karimi-Maleh, Hassan

    2014-09-01

    The electrochemistry of bisphenol A (BPA) was studied by voltammetric methods at a surface of carbon paste electrode modified by a ZnO/CNTs nanocomposite and room-temperature ionic liquid of 1,3-dipropylimidazolium bromide. The ratio of ZnO/CNTs and ionic liquid (IL) on the surface of the electrode has to be controlled carefully because the charging currents. The anodic peaks of BPA and Sudan I in their mixture can be well separated. At pH 7.0 the two peaks are separated ca. 0.47 and 0.70 V, respectively; hence BPA can be determined in the presence of Sudan I and more than 8.7 times current excess of BPA. The peaks current of square wave voltammograms (SWV) of BPA and Sudan I increased linearly with their concentration in the ranges of 0.002-700 μmol L(-1)BPA and 0.2-800 μmol L(-1) Sudan I. The detection limits for BPA and Sudan I were 9.0 nmol L(-1) and 80 nmol L(-1), respectively. The modified electrode has been successfully applied for the assay of BPA in food samples. This study provides a simple and easy approach to selectively detect BPA in the presence of Sudan I.

  4. Comparative study of multi walled carbon nanotubes-based electrodes in micellar media and their application to micellar electrokinetic capillary chromatography.

    Science.gov (United States)

    Chicharro, Manuel; Arribas, Alberto Sánchez; Moreno, Mónica; Bermejo, Esperanza; Zapardiel, Antonio

    2007-12-15

    This work reports on a comparative study of the electrochemical performance of carbon nanotubes-based electrodes in micellar media and their application for amperometric detection in micellar electrokinetic capillary chromatography (MEKC) separations. These electrodes were prepared in two different ways: immobilization of a layer of carbon nanotubes dispersed in polyethylenimine (PEI), ethanol or Nafion onto glassy carbon electrodes or preparation of paste electrodes using mineral oil as binder. Scanning electron microscopy (SEM) was employed for surface morphology characterization while cyclic voltammetry of background electrolyte was used for capacitance estimation. The amperometric responses to hydrogen peroxide, amitrol, diuron and 2,3-dichlorophenol (2,3CP) in the presence and in the absence of sodium dodecylsulphate (SDS) were studied by flow injection analysis (FIA), demonstrating that the electrocatalytic activity, background current and electroanalytical performance were strongly dependent on the electrodes preparation procedure. Glassy carbon electrodes modified with carbon nanotubes dispersed in PEI (GC/(CNT/PEI)) displayed the most adequate performance in micellar media, maintaining good electrocatalytic properties combined with acceptable background currents and resistance to passivation. The advantages of using GC/(CNT/PEI) as detectors in capillary electrophoresis were illustrated for the MEKC separations of phenolic pollutants (phenol, 3-chlorophenol, 2,3-dichlorophenol and 4-nitrophenol) and herbicides (amitrol, asulam, diuron, fenuron, monuron and chlortoluron).

  5. Plasma Activation of Integrated Carbon Nanotube Electrodes for Electrochemical Detection of Catechol

    Institute of Scientific and Technical Information of China (English)

    WANG Shenggao; WANG Tao; LI Yanqiong; ZHAO Xiujian; HAN Jianjun; WANG Jianhua

    2007-01-01

    In this study,integrated multi-wall carbon nanotube (MWCNT) electrodes were prepared in the holes of glass directly by microwave plasma chemical vapour deposition (MWPCVD).The electrochemical behaviour of catechol at the integrated MWCNT electrodes was investigated.The oxygen plasma treated CNT electrodes had better electrochemical performance for the analysis of catechol than that of as-synthesized CNT electrodes.Both the as-synthesized CNTs and plasma treated CNTs were characterized by TEM(transmission electron microscopy,XPS(X-ray photoelectron spectroscopy) and Raman spectroscopy.The results revealed that the oxygen plasma activation is an effective method to enhance the electrochemical properties of CNT electrodes.

  6. In-situ Raman spectroscopy as a characterization tool for carbon electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Panitz, J.-C.; Joho, F.B.; Novak, P. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1999-08-01

    Lithium intercalation and de-intercalation into/from graphite electrodes in a nonaqueous electrolyte has been studied using in-situ Raman spectroscopy. Our experiments give information on the electrode-electrolyte interface with improved spatial resolution. The spectra taken from the electrode surface change with electrode potential. In this way, information on the nature of the chemical species present during charging and discharging half cycles is gained. For the first time, mapping techniques were applied to investigate if lithium intercalation proceeds homogeneously on the carbon electrode. (author) 3 figs., 1 tab., 4 refs.

  7. Porous carbon-coated graphite electrodes for energy production from salinity gradient using reverse electrodialysis

    Science.gov (United States)

    Lee, Su-Yoon; Jeong, Ye-Jin; Chae, So-Ryong; Yeon, Kyeong-Ho; Lee, Yunkyu; Kim, Chan-Soo; Jeong, Nam-Jo; Park, Jin-Soo

    2016-04-01

    Performance of graphite foil electrodes coated by porous carbon black (i.e., Vulcan) was investigated in comparison with metal electrodes for reverse electrodialysis (RED) application. The electrode slurry that was used for fabrication of the porous carbon-coated graphite foil is composed of 7.2 wt% of carbon black (Vulcan X-72), 0.8 wt% of a polymer binder (polyvinylidene fluoride, PVdF), and 92.0 wt% of a mixing solvent (dimethylacetamide, DMAc). Cyclic voltammograms of both the porous carbon (i.e., Vulcan)-coated graphite foil electrode and the graphite foil electrode without Vulcan showed good reversibility in the hexacyanoferrate(III) (i.e., Fe(CN)63-) and hexacyanoferrate(II) (i.e., Fe(CN)64-) redox couple and 1 M Na2SO4 at room temperature. However, anodic and cathodic current of the Vulcan-coated graphite foil electrode was much higher than those of the graphite foil electrode. Using a bench-scale RED stack, the current-voltage polarization curve of the Vulcan-coated graphite electrode was compared to that of metal electrodes such as iridium (Ir) and platinum (Pt). From the results, it was confirmed that resistance of four different electrodes increased with the following order: the Vulcan-coated graphite foilVulcan-coated graphite foil showed 5-10% higher power density than the metal mesh electrodes. From the polarization curve of the Vulcan-coated graphite foil electrode, it was found that total resistance decreased as thickness and geometric surface area of the electrode increased.

  8. Self-heating function of carbon nanofiber cement pastes

    Directory of Open Access Journals (Sweden)

    Galao, O.

    2014-05-01

    Full Text Available The viability of carbon nanofiber (CNF composites incement matrices as a self-heating material is reported in this paper. This functional application would allow the use of CNF cement composites as a heating element in buildings, or for deicing pavements of civil engineering transport infrastructures, such as highways or airport runways. Cement pastes with the addition of different CNF dosages (from 0 to 5% by cement mass have been prepared. Afterwards, tests were run at different fixed voltages (50, 100 and 150V, and the temperature of the specimens was registered. Also the possibility of using a casting method like shotcrete, instead of just pouring the fresh mix into the mild (with no system’s efficiency loss expected was studied. Temperatures up to 138 °C were registered during shotcrete-5% CNF cement paste tests (showing initial 10 °C/min heating rates. However a minimum voltage was required in order to achieve a proper system functioning.En este artículo se estudia la viabilidad del uso de matrices cementicias con adición de nanofibras de carbono (NFC como elementos calefactores. Esto permitiría aumentar la temperatura de estancias en edificación o el deshielo de pavimentos en obras civiles. Se han fabricado pastas de cemento con distintas dosificaciones de NFC (0, 1, 2 y 5% respecto masa del cemento y sometidas al paso de corriente continua a distintos potenciales fijos (50, 100 y 150 V, mientras se controlaba la temperatura en distintos puntos. Se ha estudiado la viabilidad de utilizar la proyección de la pasta fresca como método de puesta en obra, sin perjudicar la eficiencia del sistema. Se consiguieron temperaturas de hasta 138 °C (con velocidades iniciales de 10 °C/min para pasta proyectada con 5% NFC. Además se ha detectado la necesidad de un potencial mínimo para que la densidad de corriente resultante sea suficiente para producir el efecto esperado.

  9. A Multiwall Carbon Nanotube-chitosan Modified Electrode for Selective Detection of Dopamine in the Presence of Ascorbic Acid

    Institute of Scientific and Technical Information of China (English)

    Ling Yan JIANG; Chuan Yin LIU; Li Ping JIANG; Guang Han LU

    2005-01-01

    A novel multiwall carbon nanotube-chitosan modified electrode has been prepared.The modified electrode resolves the overlapping voltammetric response of dopamine and ascorbic acid into two well-defined peak by 212 mY. The mechanism of discrimination of dopamine from ascorbic acid is discussed. Dopamine can be determined selectively with the carbon nanotube-chitosan modified electrode. The electrode shows good sensitivity, selectivity and stability.keywords: Nanotube-chitosan modified electrode, dopamine, ascorbic acid.

  10. The performance of supercapacitor electrodes developed from chemically activated carbon produced from waste tea

    Science.gov (United States)

    Inal, I. Isil Gurten; Holmes, Stuart M.; Banford, Anthony; Aktas, Zeki

    2015-12-01

    Highly microporous and mesoporous activated carbons were produced from waste tea for application as supercapacitor electrodes, utilising a chemical activation method involving treatment with either K2CO3 or H3PO4. The area, pore structure characteristics and surface functionality of the activated carbons were evaluated to investigate the influence on electrochemical performance. The performance of the activated carbons as supercapacitor electrodes was tested by cyclic voltammetry (CV), impedance spectroscopy (EIS) and galvanostatic charge-discharge (GCD) measurements, in an aqueous electrolyte. The results showed that the pore structure and type of the activated carbon have significant impact on the supercapacitor performance. Both waste tea-based activated carbon electrodes showed good cyclic stability. However, despite its lower specific surface area the highly microporous activated carbon produced with K2CO3, exhibited much better capacitive performance than that of the mesoporous activated carbon produced with H3PO4.

  11. Characterization of Carbon Nanotube/Graphene on Carbon Cloth as an Electrode for Air-Cathode Microbial Fuel Cells

    Directory of Open Access Journals (Sweden)

    Hung-Yin Tsai

    2015-01-01

    Full Text Available Microbial fuel cells (MFCs, which can generate low-pollution power through microbial decomposition, have become a potentially important technology with applications in environmental protection and energy recovery. The electrode materials used in MFCs are crucial determinants of their capacity to generate electricity. In this study, we investigate the performance of using carbon nanotube (CNT and graphene-modified carbon-cloth electrodes in a single-chamber MFC. We develop a process for fabricating carbon-based modified electrodes and Escherichia coli HB101 in an air-cathode MFC. The results show that the power density of MFCs can be improved by applying a coat of either graphene or CNT to a carbon-cloth electrode, and the graphene-modified electrode exhibits superior performance. In addition, the enhanced performance of anodic modification by CNT or graphene was greater than that of cathodic modification. The internal resistance decreased from 377 kΩ for normal electrodes to 5.6 kΩ for both electrodes modified by graphene with a cathodic catalyst. Using the modified electrodes in air-cathode MFCs can enhance the performance of power generation and reduce the associated costs.

  12. Electroanalysis of some common pesticides using conducting polymer/multiwalled carbon nanotubes modified glassy carbon electrode.

    Science.gov (United States)

    Manisankar, P; Sundari, Pl Abirama; Sasikumar, R; Palaniappan, Sp

    2008-09-15

    The cyclic voltammetric behaviour of three common pesticides such as isoproturon (ISO), voltage (VOL) and dicofol (DCF) was investigated at glassy carbon electrode (GCE), multiwalled carbon nanotubes modified GCE (MWCNTs/GCE), polyaniline (PANI) and polypyrrole (PPY) deposited MWCNT/GCE. The modified electrode film was characterized by scanning electron microscopy (SEM) and X-ray diffraction analysis (XRD). The electroactive behaviour of the pesticides was realized from the cyclic voltammetric studies. The differential pulse voltammetric principle was used to analyze the above-mentioned pesticides using MWCNT/GCE, PANI/MWCNT/GCE and PPY/MWCNT/GCE. Effects of accumulation potential, accumulation time, Initial scan potential, amplitude and pulse width were examined for the optimization of stripping conditions. The PANI/MWCNT/GCE performed well among the three electrode systems and the determination range obtained was 0.01-100 mgL(-1) for ISO, VOL and DCF respectively. The limit of detection (LOD) was 0.1 microgL(-1) for ISO, 0.01 microgL(-1) for VOL and 0.05 microgL(-1) for DCF on PANI/MWCNT/GCE modified system. It is significant to note that the PANI/MWCNT/GCE modified system results in the lowest LOD in comparison with the earlier reports. Suitability of this method for the trace determination of pesticide in spiked samples was also realized.

  13. A highly permeable and enhanced surface area carbon-cloth electrode for vanadium redox flow batteries

    Science.gov (United States)

    Zhou, X. L.; Zhao, T. S.; Zeng, Y. K.; An, L.; Wei, L.

    2016-10-01

    In this work, a high-performance porous electrode, made of KOH-activated carbon-cloth, is developed for vanadium redox flow batteries (VRFBs). The macro-scale porous structure in the carbon cloth formed by weaving the carbon fibers in an ordered manner offers a low tortuosity (∼1.1) and a broad pore distribution from 5 μm to 100 μm, rendering the electrode a high hydraulic permeability and high effective ionic conductivity, which are beneficial for the electrolyte flow and ion transport through the porous electrode. The use of KOH activation method to create nano-scale pores on the carbon-fiber surfaces leads to a significant increase in the surface area for redox reactions from 2.39 m2 g-1 to 15.4 m2 g-1. The battery assembled with the present electrode delivers an energy efficiency of 80.1% and an electrolyte utilization of 74.6% at a current density of 400 mA cm-2, as opposed to an electrolyte utilization of 61.1% achieved by using a conventional carbon-paper electrode. Such a high performance is mainly attributed to the combination of the excellent mass/ion transport properties and the high surface area rendered by the present electrode. It is suggested that the KOH-activated carbon-cloth electrode is a promising candidate in redox flow batteries.

  14. Ultra low Pt-loading electrode prepared by displacement of electrodeposited Cu particles on a porous carbon electrode

    Energy Technology Data Exchange (ETDEWEB)

    Liao, M.J. [The State Key Laboratory of Power Transmission Equipment and System Security and New Technology, School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044 (China); Wei, Z.D.; Li, L. [The State Key Laboratory of Power Transmission Equipment and System Security and New Technology, School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044 (China); School of Material Science and Engineering, Chongqing University, Chongqing 400044 (China); Chen, S.G.; Ji, M.B.; Wang, Y.Q. [School of Material Science and Engineering, Chongqing University, Chongqing 400044 (China)

    2010-08-15

    Ultra low Pt-loading and high Pt utilization electrodes were prepared by displacement of electrodeposited Cu on a porous carbon electrode. Copper particles were electrodeposited on a porous carbon electrode (PCE) by four-step deposition (FSD) at first. The size and dispersion of deposited Cu particles were markedly improved with application of the FSD. The Cu deposits were then displaced by platinum as dipping a Cu/PCE in a platinum salt solution. Sequentially, Pt particles supported on the PCE were obtained. The Pt/PCE electrode prepared via the FSD of Cu overcomes the problem of the hydrogen evolution reaction accompanied with direct platinum electrochemical deposition, and has a high Pt dispersion. The single cell consisting of the electrodes Pt/PCE via the FSD of Cu outputs a power of 0.45 W cm{sup -2} with ultra low Pt loadings of 0.196 mg cm{sup -2} MEA (0.098 mg cm{sup -2} per each side of the MEA) at no backpressure of reactant gases. (author)

  15. Development of electrochemical oxidase biosensors based on carbon nanotube-modified carbon film electrodes for glucose and ethanol

    Energy Technology Data Exchange (ETDEWEB)

    Gouveia-Caridade, Carla; Pauliukaite, Rasa; Brett, Christopher M.A. [Departamento de Quimica, Faculdade de Ciencias e Tecnologia, Universidade de Coimbra, 3004-535 Coimbra (Portugal)

    2008-10-01

    Functionalised multi-walled carbon nanotubes (MWCNTs) were cast on glassy carbon (GC) and carbon film electrodes (CFE), and were characterised electrochemically and applied in a glucose-oxidase-based biosensor. MWCNT-modified carbon film electrodes were then used to develop an alcohol oxidase (AlcOx) biosensor, in which AlcOx-BSA was cross-linked with glutaraldehyde and attached by drop-coating. The experimental conditions, applied potential and pH, for ethanol monitoring were optimised, and ethanol was determined amperometrically at -0.3 V vs. SCE at pH 7.5. Electrocatalytic effects of MWCNT were observed with respect to unmodified carbon film electrodes. The sensitivity obtained was 20 times higher at carbon film/MWCNT-based biosensors than without MWCNT. (author)

  16. Metal-electrode-free Window-like Organic Solar Cells with p-Doped Carbon Nanotube Thin-film Electrodes

    Science.gov (United States)

    Jeon, Il; Delacou, Clement; Kaskela, Antti; Kauppinen, Esko I.; Maruyama, Shigeo; Matsuo, Yutaka

    2016-08-01

    Organic solar cells are flexible and inexpensive, and expected to have a wide range of applications. Many transparent organic solar cells have been reported and their success hinges on full transparency and high power conversion efficiency. Recently, carbon nanotubes and graphene, which meet these criteria, have been used in transparent conductive electrodes. However, their use in top electrodes has been limited by mechanical difficulties in fabrication and doping. Here, expensive metal top electrodes were replaced with high-performance, easy-to-transfer, aerosol-synthesized carbon nanotubes to produce transparent organic solar cells. The carbon nanotubes were p-doped by two new methods: HNO3 doping via ‘sandwich transfer’, and MoOx thermal doping via ‘bridge transfer’. Although both of the doping methods improved the performance of the carbon nanotubes and the photovoltaic performance of devices, sandwich transfer, which gave a 4.1% power conversion efficiency, was slightly more effective than bridge transfer, which produced a power conversion efficiency of 3.4%. Applying a thinner carbon nanotube film with 90% transparency decreased the efficiency to 3.7%, which was still high. Overall, the transparent solar cells had an efficiency of around 50% that of non-transparent metal-based solar cells (7.8%).

  17. Metal-electrode-free Window-like Organic Solar Cells with p-Doped Carbon Nanotube Thin-film Electrodes.

    Science.gov (United States)

    Jeon, Il; Delacou, Clement; Kaskela, Antti; Kauppinen, Esko I; Maruyama, Shigeo; Matsuo, Yutaka

    2016-08-16

    Organic solar cells are flexible and inexpensive, and expected to have a wide range of applications. Many transparent organic solar cells have been reported and their success hinges on full transparency and high power conversion efficiency. Recently, carbon nanotubes and graphene, which meet these criteria, have been used in transparent conductive electrodes. However, their use in top electrodes has been limited by mechanical difficulties in fabrication and doping. Here, expensive metal top electrodes were replaced with high-performance, easy-to-transfer, aerosol-synthesized carbon nanotubes to produce transparent organic solar cells. The carbon nanotubes were p-doped by two new methods: HNO3 doping via 'sandwich transfer', and MoOx thermal doping via 'bridge transfer'. Although both of the doping methods improved the performance of the carbon nanotubes and the photovoltaic performance of devices, sandwich transfer, which gave a 4.1% power conversion efficiency, was slightly more effective than bridge transfer, which produced a power conversion efficiency of 3.4%. Applying a thinner carbon nanotube film with 90% transparency decreased the efficiency to 3.7%, which was still high. Overall, the transparent solar cells had an efficiency of around 50% that of non-transparent metal-based solar cells (7.8%).

  18. Nanostructured membranes and electrodes with sulfonic acid functionalized carbon nanotubes

    KAUST Repository

    Tripathi, Bijay Prakash

    2011-02-01

    Herein we report the covalent functionalization of multiwall carbon nanotubes by grafting sulfanilic acid and their dispersion into sulfonated poly(ether ether ketone). The nanocomposites were explored as an option for tuning the proton and electron conductivity, swelling, water and alcohol permeability aiming at nanostructured membranes and electrodes for application in alcohol or hydrogen fuel cells and other electrochemical devices. The nanocomposites were extensively characterized, by studying their physicochemical and electrochemical properties. They were processed as self-supporting films with high mechanical stability, proton conductivity of 4.47 × 10 -2 S cm-1 at 30 °C and 16.8 × 10-2 S cm-1 at 80 °C and 100% humidity level, electron conductivity much higher than for the plain polymer. The methanol permeability could be reduced to 1/20, keeping water permeability at reasonable values. The ratio of bound water also increases with increasing content of sulfonated filler, helping in keeping water in the polymer in conditions of low external humidity level. © 2010 Elsevier B.V.

  19. Nanostructured membranes and electrodes with sulfonic acid functionalized carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Tripathi, Bijay P. [Electro-Membrane Processes Division, Central Salt and Marine Chemicals Research Institute, Council of Scientific and Industrial Research (CSIR), G.B. Marg, Bhavnagar 364002, Gujarat (India); Department of Membranes for Sustainable Energy, GKSS Research Centre Geesthacht GmbH, Max Planck Str. 1, D-21502 Geesthacht (Germany); Schieda, M. [Department of Membranes for Sustainable Energy, GKSS Research Centre Geesthacht GmbH, Max Planck Str. 1, D-21502 Geesthacht (Germany); Shahi, Vinod K. [Electro-Membrane Processes Division, Central Salt and Marine Chemicals Research Institute, Council of Scientific and Industrial Research (CSIR), G.B. Marg, Bhavnagar 364002, Gujarat (India); Nunes, Suzana P. [King Abdullah University of Science and Technology, Thuwal 23955-6900 (Saudi Arabia)

    2011-02-01

    Herein we report the covalent functionalization of multiwall carbon nanotubes by grafting sulfanilic acid and their dispersion into sulfonated poly(ether ether ketone). The nanocomposites were explored as an option for tuning the proton and electron conductivity, swelling, water and alcohol permeability aiming at nanostructured membranes and electrodes for application in alcohol or hydrogen fuel cells and other electrochemical devices. The nanocomposites were extensively characterized, by studying their physicochemical and electrochemical properties. They were processed as self-supporting films with high mechanical stability, proton conductivity of 4.47 x 10{sup -2} S cm{sup -1} at 30 C and 16.8 x 10{sup -2} S cm{sup -1} at 80 C and 100% humidity level, electron conductivity much higher than for the plain polymer. The methanol permeability could be reduced to 1/20, keeping water permeability at reasonable values. The ratio of bound water also increases with increasing content of sulfonated filler, helping in keeping water in the polymer in conditions of low external humidity level. (author)

  20. Nanostructured membranes and electrodes with sulfonic acid functionalized carbon nanotubes

    Science.gov (United States)

    Tripathi, Bijay P.; Schieda, M.; Shahi, Vinod K.; Nunes, Suzana P.

    Herein we report the covalent functionalization of multiwall carbon nanotubes by grafting sulfanilic acid and their dispersion into sulfonated poly(ether ether ketone). The nanocomposites were explored as an option for tuning the proton and electron conductivity, swelling, water and alcohol permeability aiming at nanostructured membranes and electrodes for application in alcohol or hydrogen fuel cells and other electrochemical devices. The nanocomposites were extensively characterized, by studying their physicochemical and electrochemical properties. They were processed as self-supporting films with high mechanical stability, proton conductivity of 4.47 × 10 -2 S cm -1 at 30 °C and 16.8 × 10 -2 S cm -1 at 80 °C and 100% humidity level, electron conductivity much higher than for the plain polymer. The methanol permeability could be reduced to 1/20, keeping water permeability at reasonable values. The ratio of bound water also increases with increasing content of sulfonated filler, helping in keeping water in the polymer in conditions of low external humidity level.

  1. Resistive random access memory enabled by carbon nanotube crossbar electrodes.

    Science.gov (United States)

    Tsai, Cheng-Lin; Xiong, Feng; Pop, Eric; Shim, Moonsub

    2013-06-25

    We use single-walled carbon nanotube (CNT) crossbar electrodes to probe sub-5 nm memory domains of thin AlOx films. Both metallic and semiconducting CNTs effectively switch AlOx bits between memory states with high and low resistance. The low-resistance state scales linearly with CNT series resistance down to ∼10 MΩ, at which point the ON-state resistance of the AlOx filament becomes the limiting factor. Dependence of switching behavior on the number of cross-points suggests a single channel to dominate the overall characteristics in multi-crossbar devices. We demonstrate ON/OFF ratios up to 5 × 10(5) and programming currents of 1 to 100 nA with few-volt set/reset voltages. Remarkably low reset currents enable a switching power of 10-100 nW and estimated switching energy as low as 0.1-10 fJ per bit. These results are essential for understanding the ultimate scaling limits of resistive random access memory at single-nanometer bit dimensions.

  2. Bulk Mechanical Properties of Single Walled Carbon Nanotube Electrodes

    Science.gov (United States)

    Giarra, Matthew; Landi, Brian; Cress, Cory; Raffaelle, Ryne

    2007-03-01

    The unique properties of single walled carbon nanotubes (SWNTs) make them especially well suited for use as electrodes in power devices such as lithium ion batteries, hydrogen fuel cells, solar cells, and supercapacitors. The performances of such devices are expected to be influenced, at least in part, by the mechanical properties of the SWNTs used in composites or in stand alone ``papers.'' Therefore, the elastic moduli and ultimate tensile strengths of SWNT papers were measured as functions of temperature, SWNT purity, SWNT length, and SWNT bundling. The SWNTs used to produce the papers were synthesized in an alexandrite laser vaporization reactor at 1100^oC and purified using conventional acid-reflux conditions. Characterization of the SWNTs was performed using SEM, BET, TGA, and optical and Raman spectroscopy. The purified material was filtered and dried to yield papers of bundled SWNTs which were analyzed using dynamic mechanical analysis (DMA). It was observed that the mechanical properties of acid-refluxed SWNT papers were significantly improved by controlled thermal oxidation and strain-hardening. Elastic moduli of SWNT papers were measured between 3 and 6 GPa. Ultimate (breaking) tensile stresses were measured between 45 and 90 MPa at 1-3% strain. These results and their implications in regard to potential applications in power devices will be discussed.

  3. Electrochemical Impedance Characterization of Nafion-Coated Carbon Film Resistor Electrodes for Electroanalysis

    OpenAIRE

    Gouveia-Caridade, Carla; Brett, Christopher M. A.

    2005-01-01

    Carbon film disk electrodes with Nafion coatings have been characterized by electrochemical impedance spectroscopy (EIS) with a view to a better understanding of their advantages and limitations in electroanalysis, particularly in anodic stripping voltammetry of metal ions. After initial examination by cyclic voltammetry, spectra were recorded over the full potential range in acetate buffer solution at the bare electrodes, electrodes electrochemically pretreated in acid solution, and Nafion-c...

  4. Anthocyanin-sensitized solar cells using carbon nanotube films as counter electrodes

    Science.gov (United States)

    Zhu, Hongwei; Zeng, Haifeng; Subramanian, Venkatachalam; Masarapu, Charan; Hung, Kai-Hsuan; Wei, Bingqing

    2008-11-01

    Carbon nanotube (CNT) films have been used as counter electrodes in natural dye-sensitized (anthocyanin-sensitized) solar cells to improve the cell performance. Compared with conventional cells using natural dye electrolytes and platinum as the counter electrodes, cells with a single-walled nanotube (SWNT) film counter electrode show comparable conversion efficiency, which is attributed to the increase in short circuit current density due to the high conductivity of the SWNT film.

  5. Electrocatalytic Study of Paracetamol at a Single-Walled Carbon Nanotube/Nickel Nanocomposite Modified Glassy Carbon Electrode

    OpenAIRE

    Koh Sing Ngai; Wee Tee Tan; Zulkarnain Zainal; Ruzniza Mohd Zawawi; Joon Ching Juan

    2015-01-01

    A rapid, simple, and sensitive method for the electrochemical determination of paracetamol was developed. A single-walled carbon nanotube/nickel (SWCNT/Ni) nanocomposite was prepared and immobilized on a glassy carbon electrode (GCE) surface via mechanical attachment. This paper reports the voltammetry study on the effect of paracetamol concentration, scan rate, pH, and temperature at a SWCNT/Ni-modified electrode in the determination of paracetamol. The characterization of the SWCNT/Ni/GCE w...

  6. Recent development of carbon electrode materials and their bioanalytical and environmental applications.

    Science.gov (United States)

    Zhang, Wei; Zhu, Shuyun; Luque, Rafael; Han, Shuang; Hu, Lianzhe; Xu, Guobao

    2016-02-07

    Carbon materials have been extensively investigated due to their diversity, favorable properties, and active applications including electroanalytical chemistry. This critical review discusses new synthetic methods, novel carbon materials, new properties and electroanalytical applications of carbon materials particularly related to the preparation as well as bioanalytical and environmental applications of highly oriented pyrolytic graphite, graphene, carbon nanotubes, various carbon films (e.g. pyrolyzed carbon films, boron-doped diamond films and diamond-like carbon films) and screen printing carbon electrodes. Future perspectives in the field have also been discussed (366 references).

  7. Effects of Co Species on the Performance of Pasted Ni Electrode

    Institute of Scientific and Technical Information of China (English)

    Xianxia YUAN; Yindong WANG; Feng ZHAN

    2001-01-01

    Effects of various Co species added by mechanically mixing with Ni(OH)2 on the performance of Ni electrode were studied and the results were interpreted by means of cyclic voltammetry (CV)and electrochemical impedance spectroscopy (EIS). It was found that CoO, Co and CoO+Co all can improve the performance of Ni electrode to some extent and the effect of CoO was the most obvious. This could be attributed to several causes: all three forms of additives increased the reversibility of Ni(Ⅱ)/Ni(Ⅲ) redox reaction, enhanced the oxygen evolution polarization, improved the charging efficiency of Ni electrode, improved the lattice imperfection of Ni hydroxide and made it more beneficial to charge transfer and H+ diffusion processes.

  8. Arsenic removal from groundwater using low-cost carbon composite electrodes for capacitive deionization.

    Science.gov (United States)

    Lee, Ju-Young; Chaimongkalayon, Nantanee; Lim, Jinho; Ha, Heung Yong; Moon, Seung-Hyeon

    2016-01-01

    Affordable carbon composite electrodes were developed to treat low-concentrated groundwater using capacitive deionization (CDI). A carbon slurry prepared using activated carbon powder (ACP), poly(vinylidene fluoride), and N-methyl-2-pyrrolidone was employed as a casting solution to soak in a low-cost porous substrate. The surface morphology of the carbon composite electrodes was investigated using a video microscope and scanning electron microscopy. The capacitance and electrical conductivity of the carbon composite electrodes were then examined using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), respectively. According to the CV and EIS measurements, the capacitances and electrical conductivities of the carbon composite electrodes were in the range of 8.35-63.41 F g(-1) and 0.298-0.401 S cm(-1), respectively, depending on ACP contents. A CDI cell was assembled with the carbon composite electrodes instead of with electrodes and current collectors. The arsenate removal test included an investigation of the optimization of several important operating parameters, such as applied voltage and solution pH, and it achieved 98.8% removal efficiency using a 1 mg L(-1) arsenate solution at a voltage of 2 V and under a pH 9 condition.

  9. Tribology of Carbon-Based Coatings : Past, Present, and Future

    OpenAIRE

    Broitman, Esteban; Hultman, Lars

    2013-01-01

    In this talk, the development of carbon-based coatings will be reviewed. The most recent findings in the synthesis, characterization and application of carbon-based coatings will be highlighted. Future perspectives of new fullerene-like carbon-based tribological coatings will be discussed. Novel applications of fullerene-like CNx, CPx, and CFx will be envisioned.

  10. Electrochemical Investigation of Carbon as Additive to the Negative Electrode of Lead-Acid Battery

    Directory of Open Access Journals (Sweden)

    Fernandez Matthew M.

    2015-01-01

    Full Text Available The increasing demand of cycle life performance of Pb-acid batteries requires the improvement of the negative Pb electrode’s charge capacity. Electrochemical investigations were performed on Pb electrode and Pb+Carbon (Carbon black and Graphite electrodes to evaluate the ability of the additives to enhance the electrochemical faradaic reactions that occur during the cycle of Pb-acid battery negative electrode. The electrodes were characterized through Cyclic Voltammetry (CV, Potentiodynamic Polarization (PP, and Electrochemical Impedance Spectroscopy (EIS. CV revealed that the addition of carbon on the Pb electrode increased anodic and cathodicreactions by tenfold. The kinetics of PbSO4 passivation measured through PPrevealed that the addition of Carbon on the Pb electrode accelerated the oxide formation by tenfold magnitude. The Nyquist plot measured through EIS suggest that the electrochemical mechanism and reaction kinetics is under charge-transfer. From the equivalent circuit and physical model, Pb+CB1 electrode has the lowest EIS parameters while Pb+G has the highest which is attributed to faster faradaic reaction.The Nyquist plot of the passivated Pb+CB1 electrode showed double semicircular shape. The first layer represents to the bulk passive PbSO4 layer and the second layer represents the Carbon+PbSO4 layer. The enhancements upon addition of carbon on the Pb electrode were attributed to the additive’s electrical conductivity and total surface area. The electrochemical active sites for the PbSO4 to nucleate and spread increases upon addition of electrical conductive and high surface area carbon additives.

  11. Integration of UV-cured Ionogel Electrolyte with Carbon Paper Electrodes

    Directory of Open Access Journals (Sweden)

    Stephanie Flores Zopf

    2014-02-01

    Full Text Available A test bed with a coplanar architecture is employed to investigate the integration of an in situ cross-linked, polymer-supported ionogel with several commercially available, high surface area carbon paper electrodes. Specifically, a UV-cured poly(ethylene glycol diacrylate (PEGDA-supported ionogel electrolyte film is formed in situ against a variety of porous electrodes comprising: a carbon fiber paper, a carbon aerogel paper, and four carbon nanotube-based papers. Electrochemical impedance spectroscopy measurements reveal that the relative performance of a particular carbon paper with the neat ionic liquid is not necessarily indicative of its behavior when integrated with the solid ionogel electrolyte. The coplanar test bed can therefore serve as a useful tool to help guide the selection of suitable carbon-based electrode structures for supercapacitors that incorporate UV-cured ionogels created in situ for wearable energy storage applications.

  12. The dependence of the electronic conductivity of carbon molecular sieve electrodes on their charging states.

    Science.gov (United States)

    Pollak, Elad; Genish, Isaschar; Salitra, Gregory; Soffer, Abraham; Klein, Lior; Aurbach, Doron

    2006-04-13

    The dependence of the electronic conductivity of activated carbon electrodes on their potential in electrolyte solutions was examined. Kapton polymer films underwent carbonization (1000 degrees C), followed by a mild oxidation process (CO(2) at 900 degrees C) for various periods of time, to obtain carbons of different pore structures. A specially designed cell was assembled in order to measure the conductivity of carbon electrodes at different potentials in solutions. When the carbon electrodes possessed molecular sieving properties, a remarkable dependence of their conductivity on their charging state was observed. Aqueous electrolyte solutions containing ions of different sizes were used in order to demonstrate this phenomenon. As the average pore size of the activated carbons was larger, their molecular sieving ability was lower, and the dependence of their conductivity on their charging state regained its classical form. This behavior is discussed herein.

  13. Platinum-polyaniline-modified carbon fiber electrode for the electrooxidation of methanol

    Institute of Scientific and Technical Information of China (English)

    WU Kezhong; MENG Xu; WANG Xindong; LI Jingling

    2005-01-01

    Platinum was electrodeposited onto a polyaniline-modified carbon fiber electrode by the cyclic voltammetric method in sulfuric acid, which may enable an increase in the level of platinum u tilization currently achieved in electrocatalyric systems. This electrode preparation consists of a two-step procedure: first electropolymerization of aniline onto carbon fiber and then electrodeposition of platinum. The catalytic activity of the platinum-polyaniline-modified carbon fiber electrode (Pt/PAni/C) was compared with that of a bare carbon fiber electrode (Pt/C) by the oxidation of methanol. The maximum oxidation current of methanol on Pt/PAni/C is 50.7 mA.cm-2, which is 6.7 times higher than 7.6 mA.cm-2 on the Pt/C.Scanning electron microscopy was used to investigate the dispersion of the platinum particles of about 0.4 μm.

  14. Inkjet printed multiwall carbon nanotube electrodes for dielectric elastomer actuators

    Science.gov (United States)

    Baechler, Curdin; Gardin, Samuele; Abuhimd, Hatem; Kovacs, Gabor

    2016-05-01

    Dielectric elastomers (DE’s) offer promising applications as soft and light-weight electromechanical actuators. It is known that beside the dielectric material, the electrode properties are of particular importance regarding the DE performance. Therefore, in recent years various studies have focused on the optimization of the electrode in terms of conductivity, stretchability and reliability. However, less attention was given to efficient electrode processing and deposition methods. In the present study, digital inkjet printing was used to deposit highly conductive and stretchable electrodes on silicone. Inkjet printing is a versatile and cost effective deposition method, which allows depositing complex-shaped electrode patterns with high precision. The electrodes were printed using an ink based on industrial low-cost MWCNT. Experiments have shown that the strain-conductivity properties of the printed electrode are strongly depended on the deposition parameters like drop-spacing and substrate temperature. After the optimization of the printing parameters, thin film electrodes could be deposited showing conductivities of up to 30 S cm-1 without the need of any post-treatment. In addition, electromechanical tests with fabricated DE actuators have revealed that the inkjet printed MWCNT electrodes are capable to self-clear in case of a dielectric breakdown.

  15. Cobalt hexacyanoferrate modified multi-walled carbon nanotubes/graphite composite electrode as electrochemical sensor on microfluidic chip

    Energy Technology Data Exchange (ETDEWEB)

    Li Xinchun [School of Pharmaceutical Sciences, Sun Yat-sen University, 132 Waihuan East Road of Higher Education Mega Centre, Guangzhou 510006 (China); Chen Zuanguang, E-mail: chenzg@mail.sysu.edu.cn [School of Pharmaceutical Sciences, Sun Yat-sen University, 132 Waihuan East Road of Higher Education Mega Centre, Guangzhou 510006 (China); Zhong Yuwen, E-mail: yu0106@163.com [Center for Disease Control and Prevention of Guangdong Province, 176 Xingangxi, Guangzhou 510300 (China); Yang Fan; Pan Jianbin; Liang Yajing [School of Pharmaceutical Sciences, Sun Yat-sen University, 132 Waihuan East Road of Higher Education Mega Centre, Guangzhou 510006 (China)

    2012-01-13

    Highlights: Black-Right-Pointing-Pointer CoHCF nanoparticles modified MWCNTs/graphite electrode use for electrochemistry on electrophoresis microchip for the first time. Black-Right-Pointing-Pointer Simultaneous, rapid, and sensitive electrochemical detection of hydrazine and isoniazid in real samples. Black-Right-Pointing-Pointer An exemplary work of CME sensor assembly onto microchip for determination of analytes with environmental significance. Black-Right-Pointing-Pointer Manifestation of the applicability and flexibility of CME sensor for electroanalysis on microfluidic chip. - Abstract: Nanomaterial-based electrochemical sensor has received significant interest. In this work, cobalt hexacyanoferrate modified multi-walled carbon nanotubes/graphite composite electrode was electrochemically prepared and exploited as an amperometric detector for microchip electrophoresis. The prepared sensor displayed rapid and sensitive response towards hydrazine and isoniazid oxidation, which was attributed to synergetic electrocatalytic effect of cobalt hexacyanoferrate and multi-walled carbon nanotubes. The sensitivity enhancement with nearly two orders of magnitude was gained, compared with the bare carbon paste electrode, with the detection limit of 0.91 {mu}M (S/N = 3) for hydrazine. Acceptable repeatability of the microanalysis system was verified by consecutive eleven injections of hydrazine without chip and electrode treatments, the RSDs for peak current and migration time were 3.4% and 2.1%, respectively. Meanwhile, well-shaped electrophoretic peaks were observed, mainly due to fast electron transfer of electroactive species on the modified electrode. The developed microchip-electrochemistry setup was successfully applied to the determination of hydrazine and isoniazid in river water and pharmaceutical preparation, respectively. Several merits of the novel electrochemical sensor coupled with microfluidic platform, such as comparative stability, easy fabrication and

  16. Electrochemical Reduction of Oxygen on Multi-walled Carbon Nanotubes Electrode in Alkaline Solution

    Institute of Scientific and Technical Information of China (English)

    You Qun CHU; Chun An MA; Feng Ming ZHAO; Hui HUANG

    2004-01-01

    The multi-walled carbon nanotubes (MWNTs) electrode was constructed using poly- tetrafluoroethylene as binder, and the electrochemical reductive behavior of oxygen in alkaline solution was first examined on this electrode. Compared with other carbon materials, MWNTs show higher electrocatalytic activity, and the reversibility of O2 reduction reaction is greatly improved. The experiments reveal that the electrochemical reduction of O2 to HO2- is controlled by adsorption. The preliminary results illustrate the potential application of MWNTs in fuel cells.

  17. Cathodic stripping voltammetry of trace Mn(II) at carbon film electrodes

    OpenAIRE

    Filipe, Olga M. S.; Brett,Christopher M.A.

    2003-01-01

    A sensitive voltammetric method is presented for the determination of tract levels of Mn (II) using carbon film electrodes fabricated from carbon resistors of 2 [Omega]. Determination of manganese was made by square wave cathodic stripping voltammetry (CSV), with deposition of manganese as manganese dioxide. Chronoamperometric experiments were made to study MnO2 nucleation and growth. As a result, it was found to be necessary to perform electrode conditioning at a more positive potential to i...

  18. Effects of the transcutaneous electrode temperature on the accuracy of transcutaneous carbon dioxide tension

    DEFF Research Database (Denmark)

    Sørensen, Line C; Brage-Andersen, Lene; Greisen, Gorm

    2011-01-01

    The harmful effect of hypocapnia on the neonatal brain emphasizes the importance of monitoring arterial carbon dioxide tension (PaCO2). Transcutaneous monitoring of carbon dioxide (tcPCO2) reduces the need for arterial blood sampling. Drawbacks are high electrode temperature causing risks of skin...... burning. The aim was to determine the accuracy and precision of tcPCO2 at reduced electrode temperature....

  19. Electrochemical Reduction of Oxygen on Anthraquinone/Carbon Nanotubes Nanohybrid Modified Glassy Carbon Electrode in Neutral Medium

    Directory of Open Access Journals (Sweden)

    Zheng Gong

    2013-01-01

    Full Text Available The electrochemical behaviors of monohydroxy-anthraquinone/multiwall carbon nanotubes (MHAQ/MWCNTs nanohybrid modified glassy carbon (MHAQ/MWCNTs/GC electrodes in neutral medium were investigated; also reported was their application in the electrocatalysis of oxygen reduction reaction (ORR. The resulting MHAQ/MWCNTs nanohybrid was characterized by scanning electron microscope (SEM and transmission electron microscope (TEM. It was found that the ORR at the MHAQ/MWCNTs/GC electrode occurs irreversibly at a potential about 214 mV less negative than at a bare GC electrode in pH 7.0 buffer solution. Cyclic voltammetric and rotating disk electrode (RDE techniques indicated that the MHAQ/MWCNTs nanohybrid has high electrocatalytic activity for the two-electron reduction of oxygen in the studied potential range. The kinetic parameters of ORR at the MHAQ/MWCNTs nanohybrid modified GC electrode were also determined by RDE and EIS techniques.

  20. Voltammetric determination of theophylline at a Nafion/multi-wall carbon nanotubes composite film-modified glassy carbon electrode

    Indian Academy of Sciences (India)

    Suling Yang; Ran Yang; Gang Li; Jianjun Li; Lingbo Qu

    2010-11-01

    A Nafion/multi-wall carbon nanotubes (MWNTs) composite film-modified electrode was fabricated and applied to the sensitive and convenient determination of theophylline (TP). Multi-wall carbon nanotubes (MWNTs) were easily dispersed homogeneously into 0.1% Nafion methanol solution by sonication. Appropriate amount of Nafion/MWNTs suspension was coated on a glassy carbon electrode. After evaporating methanol, a Nafion/MWNTs composite film-modified electrode was achieved. TP could effectively accumulate at Nafion/MWNTs composite film-modified electrode and cause a sensitive anodic peak at around 1180 mV (vs SCE) in 0.01 mol/L H2SO4 medium (pH 1.8). In contrast with the bare glassy carbon electrode, Nafion film-modified electrode, Nafion/MWNTs film-modified electrode could remarkably increase the anodic peak current and decreased the overpotential of TP oxidation. Under the optimized conditions, the anodic peak current was proportional to TP concentration in the range of 8.0 × 10-8-6.0 × 10-5 mol/L, with a detection limit of 2.0 × 10-8 mol/L. This newly developed method was used to determine TP in drug samples with good percentage of recoveries.

  1. Study on electroactive and electrocatalytic surfaces of single walled carbon nanotube-modified electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Salinas-Torres, David [Departamento de Quimica Fisica and Instituto Universitario de Materiales de Alicante, Universidad de Alicante, Apdo. de Correos 99, E-03080 Alicante (Spain); Huerta, Francisco [Departamento de Ingenieria Textil y Papelera, Universidad Politecnica de Valencia, Plaza Ferrandiz y Carbonell, 1. E-03801 Alcoy (Spain); Montilla, Francisco, E-mail: francisco.montilla@ua.e [Departamento de Quimica Fisica and Instituto Universitario de Materiales de Alicante, Universidad de Alicante, Apdo. de Correos 99, E-03080 Alicante (Spain); Morallon, Emilia [Departamento de Quimica Fisica and Instituto Universitario de Materiales de Alicante, Universidad de Alicante, Apdo. de Correos 99, E-03080 Alicante (Spain)

    2011-02-01

    An investigation of the electrocatalysis of single-walled carbon nanotubes modified electrodes has been performed in this work. Nanotube-modified electrodes present a surface area much higher than the bare glassy carbon surfaces as determined by capacitance measurements. Several redox probes were selected for checking the reactivity of specific sites at the carbon nanotube surface. The presence of carbon nanotubes on the electrode improves the kinetics for all the reactions studied compared with the bare glassy carbon electrode with variations of the heterogeneous electron transfer rate constant up to 5 orders of magnitude. The most important effects are observed for the benzoquinone/hydroquinone and ferrocene/ferricinium redox couples, which show a remarkable improvement of their electron transfer kinetics on SWCNT-modified electrodes, probably due to strong {pi}-{pi} interaction between the organic molecules and the walls of the carbon nanotubes. For many of the reactions studied, less than 1% of the nanotube-modified electrode surface is transferring charge to species in solution. This result suggests that only nanotube tips are active sites for the electron transfer in such cases. On the contrary, the electroactive surface for the reactions of ferrocene and quinone is higher indicating that the electron transfer is produced also from the nanotube walls.

  2. Water Desalination Using Capacitive Deionization with Microporous Carbon Electrodes

    NARCIS (Netherlands)

    Porada, S.; Weinstein, L.; Dash, R.; Wal, van der A.F.; Bryjak, M.; Gogotsi, Y.; Biesheuvel, P.M.

    2012-01-01

    Capacitive deionization (CDI) is a water desalination technology in which salt ions are removed from brackish water by flowing through a spacer channel with porous electrodes on each side. Upon applying a voltage difference between the two electrodes, cations move to and are accumulated in electrost

  3. Electrochemical Oxidation of Paracetamol Mediated by MgB2 Microparticles Modified Glassy Carbon Electrode

    OpenAIRE

    Mohammed Zidan; Tan Wee Tee; A. Halim Abdullah; Zulkarnain Zainal; Goh Joo Kheng

    2011-01-01

    A MgB2 microparticles modified glassy carbon electrode (MgB2/GCE) was fabricated by adhering microparticles of MgB2 onto the electrode surface of GCE. It was used as a working electrode for the detection of paracetamol in 0.1 M KH2PO4 aqueous solution during cyclic voltammetry. Use of the MgB2/GCE the oxidation process of paracetamol with a current enhancement significantly by about 2.1 times. The detection limit of this modified electrode was found to be 30 μM. The sensitivity under conditio...

  4. Preparation of porous carbon nanofibers derived from PBI/PLLA for supercapacitor electrodes

    Science.gov (United States)

    Jung, Kyung-Hye; Ferraris, John P.

    2016-10-01

    Porous carbon nanofibers were prepared by electrospinning blend solutions of polybenzimidazole/poly-L-lactic acid (PBI/PLLA) and carbonization. During thermal treatment, PLLA was decomposed, resulting in the creation of pores in the carbon nanofibers. From SEM images, it is shown that carbon nanofibers had diameters in the range of 100-200 nm. The conversion of PBI to carbon was confirmed by Raman spectroscopy, and the surface area and pore volume of carbon nanofibers were determined using nitrogen adsorption/desorption analyses. To investigate electrochemical performances, coin-type cells were assembled using free-standing carbon nanofiber electrodes and ionic liquid electrolyte. cyclic voltammetry studies show that the PBI/PLLA-derived porous carbon nanofiber electrodes have higher capacitance due to lower electrochemical impedance compared to carbon nanofiber electrode from PBI only. These porous carbon nanofibers were activated using ammonia for further porosity improvement and annealed to remove the surface functional groups to better match the polarity of electrode and electrolyte. Ragone plots, correlating energy density with power density calculated from galvanostatic charge-discharge curves, reveal that activation/annealing further improves energy and power densities.

  5. Carbon nanotube detectors for microchip CE: comparative study of single-wall and multiwall carbon nanotube, and graphite powder films on glassy carbon, gold, and platinum electrode surfaces.

    Science.gov (United States)

    Pumera, Martin; Merkoçi, Arben; Alegret, Salvador

    2007-04-01

    The performance of microchip electrophoresis/electrochemistry system with carbon nanotube (CNT) film electrodes was studied. Electrocatalytic activities of different carbon materials (single-wall CNT (SWCNT), multiwall CNT (MWCNT), carbon powder) cast on different electrode substrates (glassy carbon (GC), gold, and platinum) were compared in a microfluidic setup and their performance as microchip electrochemical detectors was assessed. An MWCNT film on a GC electrode shows electrocatalytic effect toward oxidation of dopamine (E(1/2) shift of 0.09 V) and catechol (E(1/2) shift of 0.19 V) when compared to a bare GC electrode, while other CNT/carbon powder films on the GC electrode display negligible effects. Modification of a gold electrode by graphite powder results in a strong electrocatalytic effect toward oxidation of dopamine and catechol (E(1/2) shift of 0.14 and 0.11 V, respectively). A significant shift of the half-wave potentials to lower values also provide the MWCNT film (E(1/2) shift of 0.08 and 0.08 V for dopamine and catechol, respectively) and the SWCNT film (E(1/2) shift of 0.10 V for catechol) when compared to a bare gold electrode. A microfluidic device with a CNT film-modified detection electrode displays greatly improved separation resolution (R(s)) by a factor of two compared to a bare electrode, reflecting the electrocatalytic activity of CNT.

  6. Carbonation of low heat portland cement paste procured in water for different time

    Institute of Scientific and Technical Information of China (English)

    Deping Chen; Etsuo Sakai; Masaki Daimon; Yoko Ohba

    2007-01-01

    The carbonation technique was applied to accelerate the hydration of low heat portland cement (LHC). Before carbonation, the demoulded pastes were precured in water for 0, 2, 7, and 21 d, respectively. The results show that procuring time in water strongly influences the carbonation process. The phenolphthalein test indicates that the paste precured in water for a shorter time is more quickly carbonated than that for a longer time. The content of calcium hydroxide increases with increasing the procuring time in water, whereas, the amount of absorbed carbon dioxide changes contrarily. Scanning electron microscope (SEM) observation shows that portlandite always fills up big air bubbles in the paste during precuring in water, and the mercury intrusion porosimetry (MIP) results show that there are less large capillary pores in the paste precured in water for a longer time. It is found that the paste without precuring in water has more carbon dioxide absorption during curing in carbon dioxide atmosphere, and its total pore volume decreases remarkably with an increase in the carbonation time than that precured in water. X-ray diffraction (XRD) and Brunauer-Emmett-Teller (BET) surface area analyses indicate that the carbonate products are vaterite and calcite; CxSHy,, formed from carbonation has low BET surface area in comparison with that of C-S-H formed from curing in water.

  7. Fabrication and electrical properties of single wall carbon nanotube channel and graphene electrode based transistors arrays

    Energy Technology Data Exchange (ETDEWEB)

    Seo, M.; Kim, H.; Kim, Y. H.; Yun, H.; McAllister, K.; Lee, S. W., E-mail: leesw@konkuk.ac.kr [Division of Quantum Phases and Devices, School of Physics, Konkuk University, Seoul 143-701 (Korea, Republic of); Na, J.; Kim, G. T. [School of Electrical Engineering, Korea University, Seoul 136-701 (Korea, Republic of); Lee, B. J.; Kim, J. J.; Jeong, G. H. [Department of Nano Applied Engineering, Kangwon National University, Kangwon-do 200-701 (Korea, Republic of); Lee, I.; Kim, K. S. [Department of Physics and Graphene Research Institute, Sejong University, Seoul 143-747 (Korea, Republic of)

    2015-07-20

    A transistor structure composed of an individual single-walled carbon nanotube (SWNT) channel with a graphene electrode was demonstrated. The integrated arrays of transistor devices were prepared by transferring patterned graphene electrode patterns on top of the aligned SWNT along one direction. Both single and multi layer graphene were used for the electrode materials; typical p-type transistor and Schottky diode behavior were observed, respectively. Based on our fabrication method and device performances, several issues are suggested and discussed to improve the device reliability and finally to realize all carbon based future electronic systems.

  8. Effect of acid oxidization of carbon nanotube electrode on the capacitances of double layer capacitors

    Institute of Scientific and Technical Information of China (English)

    LI; Chensha; WANG; Dazhi; LIANG; Tongxiang; WANG; Xiaofen

    2004-01-01

    Polarizable electrode of electric double layer capacitor was made from carbon nanotubes. The effect of acid oxidation of electrode on the specific capacitance was studied. Oxidation removed the redundant carbon, expanded the pore size and introduced some kinds of functional groups on the surface of CNTs. The specific capacit ance of the electrodes with organic electrolyte was increased from 21.4 to 49.6 F/gafter being oxidized at a volume ratio of H2SO4 to HNO3 of 3:1.

  9. Carbon nanotubes paste sensor modified with bismuth film for determination of metallic ions in ethanol fuel

    Directory of Open Access Journals (Sweden)

    Felipe Augusto Gorla

    2015-05-01

    Full Text Available In the present study an anodic stripping voltammetric method using a bismuth film modified carbon nanotubes paste electrode for simultaneous determination of metals Zn2+, Cd2+and Pb2+in ethanol fuel is described. The metallic ions were preconcentrated on the bismuth film in the time and deposition potential of 500 s and -1.2 V and the stripping step was carried out by square wave voltammetry (frequency of 15 Hz, pulse amplitude of 25 mV and potential step of 5 mV. Acetate buffer at 0.1 mol L-1concentration and pH 4.5 was used as support electrolyte. The method showed linearity including the analytical blank up to 48.39 ?g L-1 for the metals and the obtained limits of detection were 3.36, 0.32 and 0.47 ?g L-1for Zn2+, Cd2+and Pb2+, respectively. The proposed method was applied in ethanol fuel samples.

  10. Electroanalysis of cationic species at membrane-carbon electrodes modified by polysaccharides. Bioaccumulation at microorganism-modified electrodes.

    Science.gov (United States)

    Lojou, E; Bianco, P

    2000-05-01

    Membrane-carbon electrodes modified with polysaccharides suspensions entrapped between a dialysis membrane and the carbon surface were used for electroanalysis of various cationic species. Cationic complexes of ruthenium and cobalt, metallic cations (Cu(2+), Fe(3+), UO(2)(2+)) as well as methylviologen were considered. By investigating various parameters (concentration of the suspension, pH) binding of the cations by the polysaccharides was demonstrated. Comparison of cations uptake by different kinds of polysaccharides such as alginic acid, polygalacturonic acid, pectin, dextran and agar was performed. This study has been extended to natural biomaterials, alga and lichen, which are known to contain polysaccharides. The interest of the membrane-electrode strategy is described.

  11. Chemistry of carbon polymer composite electrode - An X-ray photoelectron spectroscopy study

    Science.gov (United States)

    Andersen, Shuang Ma; Dhiman, Rajnish; Skou, Eivind

    2015-01-01

    Surface chemistry of the electrodes in a proton exchange membrane fuel cell is of great importance for the cell performance. Many groups have reported that electrode preparation condition has a direct influence on the resulting electrode properties. In this work, the oxidation state of electrode components and the composites (catalyst ionomer mixtures) in various electrode structures were systematically studied with X-ray photoelectron spectroscopy (XPS). Based on the spectra, when catalyst is physically mixed with Nafion ionomer, the resulting electrode surface chemistry is a combination of the two components. When the electrode is prepared with a lamination procedure, the ratio between fluorocarbon and graphitic carbon is decreased. Moreover, ether type oxide content is decreased although carbon oxide is slightly increased. This indicates structure change of the catalyst layer due to an interaction between the ionomer and the catalyst and possible polymer structural change during electrode fabrication. The surface of micro porous layer was found to be much more influenced by the lamination, especially when it is in contact with catalysts in the interphase. Higher amount of platinum oxide was observed in the electrode structures (catalyst ionomer mixture) compared to the catalyst powder. This also indicates a certain interaction between the functional groups in the polymer and platinum surface.

  12. Bioelectrocatalytic mediatorless dioxygen reduction at carbon ceramic electrodes modified with bilirubin oxidase

    Energy Technology Data Exchange (ETDEWEB)

    Nogala, Wojciech; Celebanska, Anna; Szot, Katarzyna [Institute of Physical Chemistry, Polish Academy of Sciences, Warsaw (Poland); Wittstock, Gunther, E-mail: gunther.wittstock@uni-oldenburg.d [Carl von Ossietzky University of Oldenburg, Faculty of Mathematics and Science, Center of Interface Science (CIS), Department of Pure and Applied Chemistry, D-26111 Oldenburg (Germany); Opallo, Marcin, E-mail: mopallo@ichf.edu.p [Institute of Physical Chemistry, Polish Academy of Sciences, Warsaw (Poland)

    2010-08-01

    Carbon ceramic electrodes were prepared by sol-gel processing of a hydrophobic precursor - methyltrimethoxysilane (MTMOS) - together with dispersed graphite microparticles according to a literature procedure. Bilirubin oxidase (BOx) was adsorbed on this electrode from buffer solution and this process was followed by atomic force microscopy (AFM). The electrodes exhibited efficient mediatorless electrocatalytic activity towards dioxygen reduction. The activity depends on the time of adsorption of the enzyme and the pH. The electrode remains active in neutral solution. The bioelectrocatalytic activity is further increased when a fraction of the carbon microparticles is replaced by sulfonated carbon nanoparticles (CNPs). This additive enhances the electrical communication between the enzyme and the electronic conductor. At pH 7 the carbon ceramic electrode modified with bilirubin oxidase retains ca. half of its highest activity. The role of the modified nanoparticles is confirmed by experiments in which a film embedded in a hydrophobic silicate matrix also exhibited efficient mediatorless biocatalytic dioxygen reduction. Scanning electrochemical microscopy (SECM) of the studied electrodes indicated a rather even distribution of the catalytic activity over the electrode surface.

  13. Nitrogen Doped Macroporous Carbon as Electrode Materials for High Capacity of Supercapacitor

    Directory of Open Access Journals (Sweden)

    Yudong Li

    2017-01-01

    Full Text Available Nitrogen doped carbon materials as electrodes of supercapacitors have attracted abundant attention. Herein, we demonstrated a method to synthesize N-doped macroporous carbon materials (NMC with continuous channels and large size pores carbonized from polyaniline using multiporous silica beads as sacrificial templates to act as electrode materials in supercapacitors. By the nice carbonized process, i.e., pre-carbonization at 400 °C and then pyrolysis at 700/800/900/1000 °C, NMC replicas with high BET specific surface areas exhibit excellent stability and recyclability as well as superb capacitance behavior (~413 F ⋅ g−1 in alkaline electrolyte. This research may provide a method to synthesize macroporous materials with continuous channels and hierarchical pores to enhance the infiltration and mass transfer not only used as electrode, but also as catalyst somewhere micro- or mesopores do not work well.

  14. Graphene as conductive additives in binderless activated carbon electrodes for power enhancement of supercapacitor

    Science.gov (United States)

    Nor, N. S. M.; Deraman, M.; Suleman, M.; Norizam, M. D. M.; Basri, N. H.; Sazali, N. E. S.; Hamdan, E.; Hanappi, M. F. Y. M.; Tajuddin, N. S. M.; Othman, M. A. R.; Shamsudin, S. A.; Omar, R.

    2016-11-01

    Carbon based supercapacitor electrodes from composite of binderless activated carbon and graphene as a conductive additive were fabricated with various amount of graphene (0, 2, 4, 6, 8 and 10 wt%). Graphene was mixed in self-adhesive carbon grains produced from pre-carbonized powder derived from fibers of oil palm empty fruit bunches and converted into green monoliths (GMs). The GMs were carbonized (N2) and activated (CO2) to produce activated carbon monoliths (ACMs) electrodes. Porosity characterizations by nitrogen adsorption-desorption isotherm method shows that the pore characteristics of the ACMs are influenced by the graphene additive. The results of galvanostatic charge-discharge tests carried out on the supercapacitor cells fabricated using these electrodes shows that the addition of graphene additive (even in small amount) decreases the equivalent series resistance and enhances the specific power of the cells but significantly lowers the specific capacitance. The supercapacitor cell constructed with the electrode containing 4 wt % of graphene offers the maximum power (175 W kg-1) which corresponds to an improvement of 55%. These results demonstrate that the addition of graphene as conductive additive in activated carbon electrodes can enhance the specific power of the supercapacitor.

  15. Electrochemical and Optical Evaluation of Noble Metal-and Carbon-ITO Hybrid Optically Transparent Electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Zudans, Imants; Paddock, Jean R.; Kuramitz, Hideki; Maghasi, Anne T.; Wansapura, Chamika M.; Conklin, Sean D.; Kaval, Necati; Shtoyko, Tanya; Monk, David J.; Bryan, Samuel A.; Hubler, Timothy L.; Richardson, John N.; Seliskar, Carl J.; Heineman, William R.

    2004-04-15

    Optically transparent hybrid electrodes were constructed by sputtering or thermally evaporating layers of varying thickness of Au, Pd, Pt, or C onto an existing conductive indium-tin oxide (ITO) layer on glass. These electrodes were characterized using UV-Vis spectroscopy and cyclic voltammetry; redox probes examined were potassium ferricyanide, tris-(2, 2'-bipyridyl)ruthenium(II) chloride, hydroquinone, and para-aminophenol (PAP). Each type of hybrid was evaluated and compared with other hybrids, as well as with bare ITO electrodes and commercially available Au, Pt, and glassy carbon disk electrodes. Our results indicated that these hybrid electrodes are reasonably robust, easy to prepare, and extend the capabilities of bare ITO surfaces with respect to the electrochemical response (especially for organic redox probes), while giving up little in the way of optical transparency. Because of these characteristics, hybrid electrodes should be especially suited to many spectroelectrochemical applications.

  16. Carbon Nanotubes Counter Electrode for Dye-Sensitized Solar Cells Application

    Directory of Open Access Journals (Sweden)

    Drygała A.

    2016-06-01

    Full Text Available The influence of the carbon nanotubes counter electrode deposited on the FTO glass substrates on the structure and optoelectrical properties of dye-sensitized solar cells counter electrode (CE was analysed. Carbon materials have been applied in DSSC s in order to produce low-cost solar cells with reasonable efficiency. Platinum is a preferred material for the counter electrode because of its high conductivity and catalytic activity. However, the costs of manufacturing of the platinum counter electrode limit its use to large-scale applications in solar cells. This paper presents the results of examining the structure and properties of the studied layers, defining optical properties of conductive layers and electrical properties of dye-sensitized solar cells manufactured with the use of carbon nanotubes.

  17. Graphene-carbon nanotube hybrid materials and use as electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Tour, James M.; Zhu, Yu; Li, Lei; Yan, Zheng; Lin, Jian

    2016-09-27

    Provided are methods of making graphene-carbon nanotube hybrid materials. Such methods generally include: (1) associating a graphene film with a substrate; (2) applying a catalyst and a carbon source to the graphene film; and (3) growing carbon nanotubes on the graphene film. The grown carbon nanotubes become covalently linked to the graphene film through carbon-carbon bonds that are located at one or more junctions between the carbon nanotubes and the graphene film. In addition, the grown carbon nanotubes are in ohmic contact with the graphene film through the carbon-carbon bonds at the one or more junctions. The one or more junctions may include seven-membered carbon rings. Also provided are the formed graphene-carbon nanotube hybrid materials.

  18. Changes in Carbon Electrode Morphology Affect Microbial Fuel Cell Performance with Shewanella oneidensis MR-1

    Directory of Open Access Journals (Sweden)

    David V. P. Sanchez

    2015-03-01

    Full Text Available The formation of biofilm-electrodes is crucial for microbial fuel cell current production because optimal performance is often associated with thick biofilms. However, the influence of the electrode structure and morphology on biofilm formation is only beginning to be investigated. This study provides insight on how changing the electrode morphology affects current production of a pure culture of anode-respiring bacteria. Specifically, an analysis of the effects of carbon fiber electrodes with drastically different morphologies on biofilm formation and anode respiration by a pure culture (Shewanella oneidensis MR-1 were examined. Results showed that carbon nanofiber mats had ~10 fold higher current than plain carbon microfiber paper and that the increase was not due to an increase in electrode surface area, conductivity, or the size of the constituent material. Cyclic voltammograms reveal that electron transfer from the carbon nanofiber mats was biofilm-based suggesting that decreasing the diameter of the constituent carbon material from a few microns to a few hundred nanometers is beneficial for electricity production solely because the electrode surface creates a more relevant mesh for biofilm formation by Shewanella oneidensis MR-1.

  19. Novel air electrode for metal-air battery with new carbon material and method of making same

    Science.gov (United States)

    Ross, P.N. Jr.

    1988-06-21

    This invention relates to a rechargeable battery or fuel cell. More particularly, this invention relates to a novel air electrode comprising a new carbon electrode support material and a method of making same. 3 figs.

  20. Determination of L- and D-fucose using amperometric electrodes based on diamond paste.

    Science.gov (United States)

    Stefan-van Staden, Raluca-Ioana; Nejem, R'afat Mahmoud; van Staden, Jacobus Frederick; Aboul-Enein, Hassan Y

    2012-02-21

    Monocrystalline diamond (natural diamond, synthetic-1 and synthetic-2) based electrochemical electrodes were designed for the analysis of L- and D-fucose. Response characteristics of the electrochemical electrodes were determined using cyclic voltammetry and differential pulse voltammetry (DPV). L-fucose was determined using DPV with electrodes based on natural diamond, synthetic-1 and synthetic-2, respectively, at 240 mV using NaCl as the electrolyte (pH 3.0); at 160 mV using KNO(3) (pH 10.0) and at 80 mV using KCl as the electrolyte (pH 10.0) while D-fucose was analyzed at 120 mV using KCl as the electrolyte (pH 1.0); at 140 mV using KNO(3) as the electrolyte (pH 1.0) and at 160 mV using NaNO(3) as the electrolyte (pH 3.0). The linear concentration ranges for L-fucose were between 10(-13) and 10(-9) mol L(-1) (natural diamond), 10(-11) and 10(-8) mol L(-1) (synthetic-1) and 10(-6) and 10(-3) mol L(-1) (synthetic-2) with detection limits of 10(-14), 10(-12) and 10(-8) mol L(-1) magnitude order, respectively. For D-fucose, the linear concentration ranges were 10(-6) to 10(-3) mol L(-1) (natural diamond), 10(-5) to 10(-3) mol L(-1) (synthetic-1) and 10(-9) to 10(-3) mol L(-1) (synthetic-2) with detection limits of 10(-7), 10(-7) and 10(-10) mol L(-1) magnitude order, respectively. The sensors were used for the assay of L-fucose in serum and urine samples.

  1. Facile preparation of nickel/carbonized wood nanocomposite for environmentally friendly supercapacitor electrodes

    Science.gov (United States)

    Yaddanapudi, Haritha Sree; Tian, Kun; Teng, Shiang; Tiwari, Ashutosh

    2016-09-01

    We are reporting a facile way to prepare nickel/carbon nanocomposites from wood as a novel electrode material for supercapacitors. The surface morphology and the structure of the as-prepared electrodes were studied by using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The results indicate that after high-temperature carbonization process, the wood is converted into graphitic carbon with nickel nanoparticles uniformly distributed within the three dimensional structure of the wood. Electrochemical characterization such as cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and galvanostatic charge-discharge measurements were conducted. These results showed that the introduction of nickel into the carbonized wood improves the specific capacitance and the cyclic stability of the nanocomposite electrode over that of the pure carbonized wood electrode. The composite electrode displayed an enhanced capacitive performance of 3616 F/g at 8 A/g, and showed an excellent capacitance retention after 6000 charge-discharge cycles. These results endow the nickel nanoparticles impregnated carbonized wood with a great potential for future application in supercapacitors.

  2. Copper-decorated carbon nanotubes-based composite electrodes for nonenzymatic detection of glucose

    NARCIS (Netherlands)

    Pop, A.; Manea, F.; Orha, C.; Motoc, S.; Llinoiu, E.; Vaszilcsin, N.; Schoonman, J.

    2012-01-01

    The aim of this study was to prepare three types of multiwall carbon nanotubes (CNT)-based composite electrodes and to modify their surface by copper electrodeposition for nonenzymatic oxidation and determination of glucose from aqueous solution. Copper-decorated multiwall carbon nanotubes composite

  3. Effects of the transcutaneous electrode temperature on the accuracy of transcutaneous carbon dioxide tension

    DEFF Research Database (Denmark)

    Sørensen, Line C; Brage-Andersen, Lene; Greisen, Gorm

    2011-01-01

    The harmful effect of hypocapnia on the neonatal brain emphasizes the importance of monitoring arterial carbon dioxide tension (PaCO2). Transcutaneous monitoring of carbon dioxide (tcPCO2) reduces the need for arterial blood sampling. Drawbacks are high electrode temperature causing risks of skin...

  4. Nucleation and aggregative growth of palladium nanoparticles on carbon electrodes: Experiment and kinetic model

    NARCIS (Netherlands)

    Kim, Yang-Rae; Lai, Stanley C.S.; McKelvey, Kim; Zhang, Guohui; Perry, David; Miller, Thomas S.; Unwin, Patrick R.

    2015-01-01

    The mechanism and kinetics of the electrochemical nucleation and growth of palladium (Pd) nanoparticles (NPs) on carbon electrodes have been investigated using a microscale meniscus cell on both highly oriented pyrolytic graphite (HOPG) and a carbon-coated transmission electron microscopy (TEM) grid

  5. [Research on treatment of high salt wastewater by the graphite and activated carbon fiber composite electrodes].

    Science.gov (United States)

    Zhou, Gui-Zhong; Wang, Zhao-Feng; Wang, Xuan; Li, Wen-Qian; Li, Shao-Xiang

    2014-05-01

    High salinity wastewater is one of the difficulties in the field of wastewater treatment. As a new desalination technology, electrosorption technology has many advantages. This paper studied a new type of carbon-based electrodes, the graphite and activated carbon fiber composite electrodes. And the influencing factors of electrosorption and its desalination effect were investigated. The electrosorption device had optimal desalination effect when the voltage was 1. 6 V, the retention time was 60 min and the plate spacing was 1 cm. The graphite and activated carbon fiber composite electrodes were used to treat the black liquor of refined cotton and sodium copper chlorophyll wastewater to investigate its desalination effect. When the electrodes were used to treat the black liquor of refined cotton after acid treatment, the removal rate of conductivity and COD reached 58. 8% and 75. 6% respectively when 8 pairs of electrodes were used. And when the electrode was used to treat the sodium copper chlorophyll wastewater, the removal rate of conductivity and COD reached higher than 50. 0% and 13. 5% respectively when 6-8 pairs of electrodes were used.

  6. Polynuclear Nickel Hexacyanoferrate/Graphitized Mesoporous Carbon Hybrid Chemically Modified Electrode for Selective Hydrazine Detection

    OpenAIRE

    Palani Barathi; Annamalai Senthil Kumar; Minnal Ranjan Babu Karthick

    2011-01-01

    A hybrid polynuclear nickel hexacyanoferrate (NiHCFe)/graphitized mesoporous carbon- (GMC-) modified glassy carbon electrode (GCE/NiHCFe@GMC) has been prepared by a sequential method using electrodeposited Ni on a GMC-modified glassy carbon electrode (GCE/Ni@GMC) as a template and [Fe(CN)6]3− as an in-situ chemical precipitant, without any additional interlinking agent. Physicochemical and electrochemical characterizations reveal the presence of NiHCFe units within the porous sites of the GM...

  7. Grafted, cross-linked carbon black as a double-layer capacitor electrode material

    Energy Technology Data Exchange (ETDEWEB)

    Richner, R.; Mueller, S.; Wokaun, A.

    2001-03-01

    Isocyanate prepolymers readily react with oxidic functional groups on carbon black. On carbon black grafted with diisocyanates, reactive isocyanate groups are available for cross-linking to a polyurethane system. This cross-linked carbon black was considered as a new active material for electrochemical electrodes. Active material for electric double-layer capacitor electrodes was produced which had values of specific capacitance of up to 200 F/g. Cross-linking efficiencies of up to 58 % of the polymers utilised were achieved. (author)

  8. Metal/Diamond Composite Thin-Film Electrodes: New Carbon Supported Catalytic Electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Greg M. Swain, PI

    2009-03-10

    The DOE-funded research conducted by the Swain group was focused on (i) understanding structure-function relationships at boron-doped diamond thin-film electrodes, (ii) understanding metal phase formation on diamond thin films and developing electrochemical approaches for producing highly dispersed electrocatalyst particles (e.g., Pt) of small nominal particle size, (iii) studying the electrochemical activity of the electrocatalytic electrodes for hydrogen oxidation and oxygen reduction and (iv) conducting the initial synthesis of high surface area diamond powders and evaluating their electrical and electrochemical properties when mixed with a Teflon binder. (Note: All potentials are reported versus Ag/AgCl (sat'd KCl) and cm{sup 2} refers to the electrode geometric area, unless otherwise stated).

  9. Aqueous solutions of acidic ionic liquids for enhanced stability of polyoxometalate-carbon supercapacitor electrodes

    Science.gov (United States)

    Hu, Chenchen; Zhao, Enbo; Nitta, Naoki; Magasinski, Alexandre; Berdichevsky, Gene; Yushin, Gleb

    2016-09-01

    Nanocomposites based on polyoxometalates (POMs) nanoconfined in microporous carbons have been synthesized and used as electrodes for supercapacitors. The addition of the pseudocapacitance from highly reversible redox reaction of POMs to the electric double-layer capacitance of carbon lead to an increase in specific capacitance of ∼90% at 1 mV s-1. However, high solubility of POM in traditional aqueous electrolytes leads to rapid capacity fading. Here we demonstrate that the use of aqueous solutions of protic ionic liquids (P-IL) as electrolyte instead of aqueous sulfuric acid solutions offers an opportunity to significantly improve POM cycling stability. Virtually no degradation in capacitance was observed in POM-based positive electrode after 10,000 cycles in an asymmetric capacitor with P-IL aqueous electrolyte. As such, POM-based carbon composites may now present a viable solution for enhancing energy density of electrical double layer capacitors (EDLC) based on pure carbon electrodes.

  10. Carbonized chicken eggshell membranes with 3D architectures as high-performance electrode materials for supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Li, Zhi; Zhang, Li; Amirkhiz, Babak Shalchi; Tan, Xuehai; Xu, Zhanwei; Wang, Huanlei; Olsen, Brian C.; Holt, Chris M.B.; Mitlin, David [Chemical and Materials Engineering, University of Alberta, Edmonton, AB (Canada); National Institute for Nanotechnology (NINT), NRC, Edmonton, AB (Canada)

    2012-04-15

    Supercapacitor electrode materials are synthesized by carbonizing a common livestock biowaste in the form of chicken eggshell membranes. The carbonized eggshell membrane (CESM) is a three-dimensional macroporous carbon film composed of interwoven connected carbon fibers containing around 10 wt% oxygen and 8 wt% nitrogen. Despite a relatively low surface area of 221 m{sup 2} g{sup -1}, exceptional specific capacitances of 297 F g{sup -1} and 284 F g{sup -1} are achieved in basic and acidic electrolytes, respectively, in a 3-electrode system. Furthermore, the electrodes demonstrate excellent cycling stability: only 3% capacitance fading is observed after 10 000 cycles at a current density of 4 A g{sup -1}. These very attractive electrochemical properties are discussed in the context of the unique structure and chemistry of the material. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  11. Converting biowaste corncob residue into high value added porous carbon for supercapacitor electrodes.

    Science.gov (United States)

    Qu, Wen-Hui; Xu, Yuan-Yuan; Lu, An-Hui; Zhang, Xiang-Qian; Li, Wen-Cui

    2015-08-01

    In this report, corncob residue, the main by-product in the furfural industry, is used as a precursor to prepare porous carbon by a simple and direct thermal treatment: one-step activation without pre-carbonization. As a consequence, the corncob residue derived porous carbon achieves a high surface area of 1210 m(2) g(-1) after ash-removal. The carbon material has the advantages of low cost and low environmental impact, with a superior electrochemical performance compared to those polymer-based synthetic carbons as electrode material for a supercapacitor. The carbon electrode exhibits a high capacitance of 314 F g(-1) in 6M KOH electrolyte. The corresponding sample also shows a superb cycling stability. Almost no capacitance decay was observed after 100,000 cycles. The excellent electrochemical performance is due to the combination of a high specific surface area with a fraction of mesopores and highly stable structure.

  12. Cooperation of micro- and meso-porous carbon electrode materials in electric double-layer capacitors

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Cheng [State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022, Jilin Province (China); Graduate University of Chinese Academy of Sciences, Beijing 100039 (China); Qi, Li; Wang, Hongyu [State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022, Jilin Province (China); Yoshio, Masaki [Advanced Research Center, Saga University, 1341 Yoga-machi, Saga 840-0047 (Japan)

    2010-07-01

    The capacitive characteristics of micro- and meso-porous carbon materials have been compared in cyclic voltammetric studies and galvanostatic charge-discharge tests. Meso-porous carbon can keep certain high capacitance values at high scan rates, whereas micro-porous carbon possesses very high capacitance values at low scan rates but fades quickly as the scan rate rises up. For better performance of electric double-layer capacitors (EDLCs), the cooperative application of both kinds of carbon materials has been proposed in the following two ways: mixing both kinds of carbons in the same electrode or using the asymmetric configuration of carbon electrodes in the same EDLC. The cooperative effect on the electrochemical performance has also been addressed. (author)

  13. Amperometric choline biosensor based on multiwalled carbon nanotubes/zirconium oxide nanoparticles electrodeposited on glassy carbon electrode.

    Science.gov (United States)

    Pundir, S; Chauhan, N; Narang, J; Pundir, C S

    2012-08-01

    A bienzymatic choline biosensor was constructed by coimmobilizing acetylcholinesterase (AChE) and choline oxidase (ChO) onto nanocomposite of carboxylated multiwalled carbon nanotubes (c-MWCNTs) and zirconium oxide nanoparticles (ZrO(2)NPs) electrodeposited on the surface of a glassy carbon electrode (GCE) and using it (AChE-ChO/c-MWCNT/ZrO(2)NPs/GCE) as working electrode, Ag/AgCl as reference electrode, and Pt wire as auxiliary electrode connected through a potentiostat. The enzyme electrode was characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, and cyclic voltammetry (CV) studies, optimized, and evaluated. The biosensor exhibited optimum response within 4 s at +0.2V, pH 7.4, and 25 °C. The detection limit and working range of the biosensor were 0.01 μM and 0.05 to 200 μM, respectively. The half-life of the enzyme electrode was 60 days at 4 °C. The serum choline level, as measured by the biosensor, was 9.0 to 12.8 μmol/L (with a mean of 10.81 μmol/L) in apparently healthy persons and 5.0 to 8.4 μmol/L (with a mean of 6.53 μmol/L) in persons suffering from Alzheimer's disease. The enzyme electrode was unaffected by a number of serum substances.

  14. Hierarchical porous carbon aerogel derived from bagasse for high performance supercapacitor electrode.

    Science.gov (United States)

    Hao, Pin; Zhao, Zhenhuan; Tian, Jian; Li, Haidong; Sang, Yuanhua; Yu, Guangwei; Cai, Huaqiang; Liu, Hong; Wong, C P; Umar, Ahmad

    2014-10-21

    Renewable, cost-effective and eco-friendly electrode materials have attracted much attention in the energy conversion and storage fields. Bagasse, the waste product from sugarcane that mainly contains cellulose derivatives, can be a promising candidate to manufacture supercapacitor electrode materials. This study demonstrates the fabrication and characterization of highly porous carbon aerogels by using bagasse as a raw material. Macro and mesoporous carbon was first prepared by carbonizing the freeze-dried bagasse aerogel; consequently, microporous structure was created on the walls of the mesoporous carbon by chemical activation. Interestingly, it was observed that the specific surface area, the pore size and distribution of the hierarchical porous carbon were affected by the activation temperature. In order to evaluate the ability of the hierarchical porous carbon towards the supercapacitor electrode performance, solid state symmetric supercapacitors were assembled, and a comparable high specific capacitance of 142.1 F g(-1) at a discharge current density of 0.5 A g(-1) was demonstrated. The fabricated solid state supercapacitor displayed excellent capacitance retention of 93.9% over 5000 cycles. The high energy storage ability of the hierarchical porous carbon was attributed to the specially designed pore structures, i.e., co-existence of the micropores and mesopores. This research has demonstrated that utilization of sustainable biopolymers as the raw materials for high performance supercapacitor electrode materials is an effective way to fabricate low-cost energy storage devices.

  15. Enzymatic electrodes nanostructured with functionalized carbon nanotubes for biofuel cell applications.

    Science.gov (United States)

    Nazaruk, E; Sadowska, K; Biernat, J F; Rogalski, J; Ginalska, G; Bilewicz, R

    2010-10-01

    Nanostructured bioelectrodes were designed and assembled into a biofuel cell with no separating membrane. The glassy carbon electrodes were modified with mediator-functionalized carbon nanotubes. Ferrocene (Fc) and 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonate) diammonium salt (ABTS) bound chemically to the carbon nanotubes were found useful as mediators of the enzyme catalyzed electrode processes. Glucose oxidase from Aspergillus niger AM-11 and laccase from Cerrena unicolor C-139 were incorporated in a liquid-crystalline matrix-monoolein cubic phase. The carbon nanotubes-nanostructured electrode surface was covered with the cubic phase film containing the enzyme and acted as the catalytic surface for the oxidation of glucose and reduction of oxygen. Thanks to the mediating role of derivatized nanotubes the catalysis was almost ten times more efficient than on the GCE electrodes: catalytic current of glucose oxidation was 1 mA cm(-2) and oxygen reduction current exceeded 0.6 mA cm(-2). The open circuit voltage of the biofuel cell was 0.43 V. Application of carbon nanotubes increased the maximum power output of the constructed biofuel cell to 100 μW cm(-2) without stirring of the solution which was ca. 100 times more efficient than using the same bioelectrodes without nanotubes on the electrode surface.

  16. Carbon nanotube/graphene nanocomposite as efficient counter electrodes in dye-sensitized solar cells.

    Science.gov (United States)

    Velten, Josef; Mozer, Attila J; Li, Dan; Officer, David; Wallace, Gordon; Baughman, Ray; Zakhidov, Anvar

    2012-03-02

    We demonstrated the replacement of the Pt catalyst normally used in the counter electrode of a dye-sensitized solar cell (DSSC) by a nanocomposite of dry spun carbon multi-walled nanotube (MWNT) sheets with graphene flakes (Gr-F). The effectiveness of this counter electrode on the reduction of the triiodide in the iodide/triiodide redox (I(-)/I(3)(-)) redox reaction was studied in parallel with the use of the dry spun carbon MWNT sheets alone and graphene flakes used independent of each other. This nanocomposite deposited onto fluorinated tin-oxide-coated glass showed improved catalytic behavior and power conversion efficiency (7.55%) beyond the use of the MWNTs alone (6.62%) or graphene alone (4.65%) for the triiodide reduction reaction in DSSC. We also compare the use of the carbon MWNT/Gr-F composite counter electrode with a DSSC using the standard Pt counter electrode (8.8%). The details of increased performance of graphene/MWNT composite electrodes as studied are discussed in terms of increased catalytic activity permitted by sharp atomic edges that arise from the structure of graphene flakes or the defect sites in the carbon MWNT and increased electrical conductivity between the carbon MWNT bundles by the graphene flakes.

  17. Stability of carbon electrodes for aqueous lithium-air secondary batteries

    Science.gov (United States)

    Ohkuma, Hirokazu; Uechi, Ichiro; Matsui, Masaki; Takeda, Yasuo; Yamamoto, Osamu; Imanishi, Nobuyuki

    2014-01-01

    The air electrode performance of various carbon materials, such as Ketjen black (KB), acetylene black (AB and AB-S), Vulcan XC-72R (VX), and vapor grown carbon fiber (VGCF) with and without La0.6Sr0.4Co0.2Fe0.8O3 (LSCF) catalyst were examined in an aqueous solution of saturated LiOH with 10 M LiCl in the current density range 0.2-2.0 mA cm-2. The best performance for oxygen reduction and evolution reactions was observed for the KB electrode, which has the highest surface area among the carbon materials examined. A steady over-potential of 0.2 V was obtained for the oxygen reduction reaction using the KB electrode without the catalyst, while the over-potential was 0.15 V for KB with the LSCF catalyst at 2.0 mA cm-2. The over-potentials for the oxygen evolution reaction were slightly higher than those for the oxygen reduction reaction, and gradually increased with the polarization period. Analysis of the gas in the cell after polarization above 0.4 V revealed the evolution of a small amount of CO during the oxygen evolution reaction by the decomposition of carbon in the electrode. The amount of CO evolved was significantly decreased by the addition of LSCF to the carbon electrode.

  18. Enzymatic electrodes nanostructured with functionalized carbon nanotubes for biofuel cell applications

    Energy Technology Data Exchange (ETDEWEB)

    Nazaruk, E.; Bilewicz, R. [University of Warsaw, Faculty of Chemistry, Warsaw (Poland); Sadowska, K.; Biernat, J.F. [Gdansk University of Technology, Chemical Faculty, Gdansk (Poland); Rogalski, J. [Maria Curie Sklodowska University, Department of Biochemistry, Lublin (Poland); Ginalska, G. [Medical University of Lublin, Department of Biochemistry, Lublin (Poland)

    2010-10-15

    Nanostructured bioelectrodes were designed and assembled into a biofuel cell with no separating membrane. The glassy carbon electrodes were modified with mediator-functionalized carbon nanotubes. Ferrocene (Fc) and 2,2{sup '}-azino-bis (3-ethylbenzothiazoline-6-sulfonate) diammonium salt (ABTS) bound chemically to the carbon nanotubes were found useful as mediators of the enzyme catalyzed electrode processes. Glucose oxidase from Aspergillus niger AM-11 and laccase from Cerrena unicolor C-139 were incorporated in a liquid-crystalline matrix-monoolein cubic phase. The carbon nanotubes-nanostructured electrode surface was covered with the cubic phase film containing the enzyme and acted as the catalytic surface for the oxidation of glucose and reduction of oxygen. Thanks to the mediating role of derivatized nanotubes the catalysis was almost ten times more efficient than on the GCE electrodes: catalytic current of glucose oxidation was 1 mA cm{sup -2} and oxygen reduction current exceeded 0.6 mA cm{sup -2}. The open circuit voltage of the biofuel cell was 0.43 V. Application of carbon nanotubes increased the maximum power output of the constructed biofuel cell to 100 {mu}W cm{sup -2} without stirring of the solution which was ca. 100 times more efficient than using the same bioelectrodes without nanotubes on the electrode surface. (orig.)

  19. Effect of nano-scale characteristics of graphene on electrochemical performance of activated carbon supercapacitor electrodes

    Science.gov (United States)

    Jasni, M. R. M.; Deraman, M.; Suleman, M.; Hamdan, E.; Sazali, N. E. S.; Nor, N. S. M.; Shamsudin, S. A.

    2016-02-01

    Graphene with its typical nano-scale characteristic properties has been widely used as an additive in activated carbon electrodes in order to enhance the performance of the electrodes for their use in high performance supercapacitors. Activated carbon monoliths (ACMs) electrodes have been prepared by carbonization and activation of green monoliths (GMs) of pre-carbonized fibers of oil palm empty fruit bunches or self-adhesive carbon grains (SACGs) and SACGs added with 6 wt% of KOH-treated multi-layer graphene. ACMs electrodes have been assembled in symmetrical supercapacitor cells that employed aqueous KOH electrolyte (6 M). The cells have been tested with cyclic voltammetry, electrochemical impedance spectroscopy and galvanostatic charge discharge methods to investigate the effect of graphene addition on the specific capacitance (Csp), specific energy (E), specific power (P), equivalent series resistance (ESR) and response time (τo) of the supercapacitor cells. The results show that the addition of graphene in the GMs change the values of Csp, Emax, Pmax, ESR and τo from (61-96) F/g, 2 Wh/kg, 104 W/kg, 2.6 Ω and 38 s, to the respective values of (110-124) F/g, 3 Wh/kg, 156 W/kg, 3.4 Ω and 63 s. This study demonstrates that the graphene addition in the GMs has a significant effect on the electrochemical behavior of the electrodes.

  20. Electrical impedance properties of carbon nanotube composite electrodes for chemical and biosensor.

    Science.gov (United States)

    So, Dae-Sup; Kang, Inpil; Huh, Hoon; Lee, Haiwon

    2010-05-01

    Electrical impedance properties of different type of carbon nanotubes based bulk electrodes have been investigated to develop chemical and biosensors. The bulk composite electrodes were fabricated with single-wall and multi-wall carbon nanotubes involving ionic conducting host polymer, Nafion, by using traditional solution-casting techniques. Under the various amounts of buffer solution, resistance and capacitance of the electrodes were measured with LCR meter and their characteristics due to ionic conducting host polymer were investigated by means of electrokinetic analysis. The capacitance values showed drastic change while the resistances only changed within few percent ranges. Electrical impedance measurement provided rapid and simple sensing mechanism to develop chemical sensor and biosensors with bulk nano electrodes.

  1. Electrochemical energy storage devices using electrodes incorporating carbon nanocoils and metal oxides nanoparticles

    KAUST Repository

    Baby, Rakhi Raghavan

    2011-07-28

    Carbon nanocoil (CNC) based electrodes are shown to be promising candidates for electrochemical energy storage applications, provided the CNCs are properly functionalized. In the present study, nanocrystalline metal oxide (RuO 2, MnO2, and SnO2) dispersed CNCs were investigated as electrodes for supercapacitor applications using different electrochemical methods. In the two electrode configuration, the samples exhibited high specific capacitance with values reaching up to 311, 212, and 134 F/g for RuO2/CNCs, MnO2/CNCs, and SnO2/CNCs, respectively. The values obtained for specific capacitance and maximum storage energy per unit mass of the composites were found to be superior to those reported for metal oxide dispersed multiwalled carbon nanotubes in two electrode configuration. In addition, the fabricated supercapacitors retained excellent cycle life with ∼88% of the initial specific capacitance retained after 2000 cycles. © 2011 American Chemical Society.

  2. Decrease of contact resistance at the interface of carbon nanotube/electrode by nanowelding

    Science.gov (United States)

    Zhao, Bo; Wang, Yanfang; Zhang, Yafei

    2017-03-01

    Reliable interconnection between carbon nanotubes (CNTs) and external circuit is one of the prerequisite in CNT electronics. In this work, ultrasonic nanowelding was used to bond CNTs with metal electrodes. By exerting ultrasonic energy at the interface of CNT/electrode, a reliable joint with negligible contact resistance was obtained between CNTs and electrodes. The performance of welding is susceptible to the ultrasonic parameters such as ultrasonic power and clamping force, as well as the metal type. It is found that the metals with good ductility or low melting point are easier to achieve effective joints. Moreover, interfacial compounds are formed at the welded surface of metal Al and Fe, which is resulted from the interacting and chemical bonding of carbon and metal atoms. After nanowelding, the contact resistance between CNTs and electrode is decreased dramatically, and the two-terminal resistance of the sample approximates to the intrinsic resistance of the CNT itself.

  3. Hydrogen peroxide biosensor based on electrodeposition of zinc oxide nanoflowers onto carbon nanotubes film electrode

    Institute of Scientific and Technical Information of China (English)

    Hui Ping Bai; Xu Xiao Lu; Guang Ming Yang; Yun Hui Yang

    2008-01-01

    A new amperometric biosensor for hydrogen peroxide was developed based on adsorption of horseradish peroxidase at the glassy carbon electrode modified with zinc oxide nanoflowers produced by electrodeposition onto multi-walled carbon nanotubes (MWNTs) firm. The morphology of the MWNTs/nano-ZnO electrode has been investigated by scanning electron microscopy (SEM), and the electrochemical performance of the electrode has also been studied by amperometric method. The resulting electrode offered an excellent detection for hydrogen peroxide at -0.11 V with a linear response range of 9.9 × 10(-7) to 2.9 × 10(-3) mol/L with a correlation coefficient of 0.991, and response time <5 s. The biosensor displays rapid response and expanded linear response range, and excellent stability.

  4. Hybrid Electrodes of Carbon Nanotube and Reduced Graphene Oxide for Energy Storage Applications.

    Science.gov (United States)

    Choi, Eunmi; Chae, Su Jin; Kim, Areum; Kang, Keun Won; Oh, Min Seok; Kwon, Soon Hyeong; Yoon, Sung Pil; Pyo, Sung Gyu

    2015-11-01

    The choice of electrode materials in lithium ion batteries and supercapacitors is important for the stability, capacity, and cycle life of the device. Despite its low capacity, graphite has often been used as an electrode material due to its inherent stability. Due to an increasing demand for large-capacity energy storage systems, there is also a demand for the development of large-capacity Li ion batteries and supercapacitors. Therefore, carbonaceous materials like graphene and carbon nanotubes (CNTs), which have high stability as well as excellent electrical conductivity and mechanical strength, are receiving attention as new electrode materials. Recently, starting from simply applying graphene and CNTs as electrode materials and progressing to the development of hybrid materials, there have been increasing research efforts in enhancing the performance of Li ion batteries and supercapacitors through the use of carbonaceous materials. This paper will discuss new composite materials and electrode structures that use graphene and CNTs for applications in Li ion batteries and supercapacitors.

  5. Effect of Paste Composition on the Microstructure of NiO Electrode%浆料成分对NiO电极微观结构的影响

    Institute of Scientific and Technical Information of China (English)

    王敏; 夏风; 王晓昳; 鄢文超; 肖建中

    2012-01-01

    NiO paste, Ni paste and Ni/YSZ paste were used to prepare NiO sensing electrodes, respectively. Ni/YSZ paste was fabricated by adding 15 vol% YSZ powder into Ni paste. The results indicated that the NiO electrodes made by NiO paste using ordinary sintering are compact and contained a lot of cracks. By contrast, the NiO electrodes and NiO/YSZ composite electrodes prepared by Ni paste and Ni/YSZ paste adopting reaction sintering, respectively, are porous and no cracks are observed. The addition of YSZ in pastes have a strong particle refining effect on NiO grains, enhance interface adhesion between NiO electrode and YSZ electrolyte and increase the amount and length of three phase boundary.%分别采用NiO浆料、Ni浆料和Ni/YSZ浆料制备NiO敏感电极.其中Ni/YSZ浆料是由在Ni浆料中添加15vol% YSZ粉末制备的.结果表明,采用NiO浆料普通烧结得到的NiO电极致密且有裂纹;采用Ni浆料和Ni/YSZ浆料反应烧结分别制备的NiO电极和NiO/YSZ复合电极则疏松多孔且无裂纹.浆料中添加的YSZ不仅能够细化NiO电极晶粒,同时能增强电极和基底的界面附着,增加三相界面的数量和长度.

  6. Arsenic species interactions with a porous carbon electrode as determined with an electrochemical quartz crystal microbalance

    Science.gov (United States)

    Morallón, Emilia; Arias-Pardilla, Joaquín; Calo, J.M.; Cazorla-Amorós, D.

    2009-01-01

    The interactions of arsenic species with platinum and porous carbon electrodes were investigated with an electrochemical quartz crystal microbalance (EQCM) and cyclic voltammetry in alkaline solutions. It is shown that the redox reactions in arsenic-containing solutions, due to arsenic reduction/deposition, oxidation/desorption, and electrocatalyzed oxidation by Pt can be readily distinguished with the EQCM. This approach was used to show that the arsenic redox reactions on the carbon electrode are mechanistically similar to that on the bare Pt electrode. This could not be concluded with just classical cyclic voltammetry alone due to the obfuscation of the faradaic features by the large capacitative effects of the carbon double layer. For the porous carbon electrode, a continual mass loss was always observed during potential cycling, with or without arsenic in the solution. This was attributed to electrogasification of the carbon. The apparent mass loss per cycle was observed to decrease with increasing arsenic concentration due to a net mass increase in adsorbed arsenic per cycle that increased with arsenic concentration, offsetting the carbon mass loss. Additional carbon adsorption sites involved in arsenic species interactions are created during electrogasification, thereby augmenting the net uptake of arsenic per cycle. It is demonstrated that EQCM, and in particular the information given by the behavior of the time derivative of the mass vs. potential, or massogram, is very useful for distinguishing arsenic species interactions with carbon electrodes. It may also prove to be effective for investigating redox/adsorption/desorption behavior of other species in solution with carbon materials as well. PMID:20161369

  7. Arsenic species interactions with a porous carbon electrode as determined with an electrochemical quartz crystal microbalance.

    Science.gov (United States)

    Morallón, Emilia; Arias-Pardilla, Joaquín; Calo, J M; Cazorla-Amorós, D

    2009-06-30

    The interactions of arsenic species with platinum and porous carbon electrodes were investigated with an electrochemical quartz crystal microbalance (EQCM) and cyclic voltammetry in alkaline solutions. It is shown that the redox reactions in arsenic-containing solutions, due to arsenic reduction/deposition, oxidation/desorption, and electrocatalyzed oxidation by Pt can be readily distinguished with the EQCM. This approach was used to show that the arsenic redox reactions on the carbon electrode are mechanistically similar to that on the bare Pt electrode. This could not be concluded with just classical cyclic voltammetry alone due to the obfuscation of the faradaic features by the large capacitative effects of the carbon double layer.For the porous carbon electrode, a continual mass loss was always observed during potential cycling, with or without arsenic in the solution. This was attributed to electrogasification of the carbon. The apparent mass loss per cycle was observed to decrease with increasing arsenic concentration due to a net mass increase in adsorbed arsenic per cycle that increased with arsenic concentration, offsetting the carbon mass loss. Additional carbon adsorption sites involved in arsenic species interactions are created during electrogasification, thereby augmenting the net uptake of arsenic per cycle.It is demonstrated that EQCM, and in particular the information given by the behavior of the time derivative of the mass vs. potential, or massogram, is very useful for distinguishing arsenic species interactions with carbon electrodes. It may also prove to be effective for investigating redox/adsorption/desorption behavior of other species in solution with carbon materials as well.

  8. A Novel Cholesterol Oxidase Biosensor Based on Pt-nanoparticle /Carbon Nanotube Modified Electrode

    Institute of Scientific and Technical Information of China (English)

    Qiao Cui SHI; Tu Zhi PENG

    2005-01-01

    A Pt-nanoparticle/carbon nanotube modified graphite electrode immobilized with cholesterol oxidase/sol-gel layer was developed for monitoring cholesterol. Using this electrode,cholesterol concentration (4.0×10-6 to 1.0×10 mol/L) could be determined accurately in the presence of ascorbic or uric acid, and the response time was rapid (< 20 s). This biosensor has high sensitivity and selectivity.

  9. Layer-by-layer Assembly of Noble Metal Nanoparticles on Glassy Carbon Electrode

    Institute of Scientific and Technical Information of China (English)

    CHEN Da; ZHENG Long-Zhen

    2008-01-01

    Silver,gold,platinum and palladium nanoparticles were initially prepared in the AOT[sodium bis(2-ethylhexyl)-sulfosuccinate]micelle and characterized by ultraviolet-visible spectroscopy,transmission electron macroscopy,X-ray diffraction,Fourier transform-infrared spectroscopy,and zeta potential analysis.The negatively charged Pt nanoparticles were self-assembled on a glassy carbon electrode by a layer-by-layer method and the modified electrode electrocatalytic reactivity toward methanol oxidation was studied.

  10. Preconcentration and electroanalysis of copper at glassy carbon electrode modified with poly(2-aminothiazole)

    OpenAIRE

    Çiftçi, Hakan; Testereci, Hasan Nur; Öktem, Zeki

    2011-01-01

    Conducting poly(2-aminothiazole), PAT, was synthesized in acetonitrile with tetrabutylammonium tetrafluoroborate, TBAFB, as supporting electrolyte via constant potential electrolysis, CPE. Glassy carbon, GC, electrode was modified by immersing the electrode in a DMSO solution of PAT. Preconcentration of copper on polymer matrix was carried out at -0.7 V. The effects of preconcentration time and pH and Cu(II) concentration of the preconcentration solution on the stripping peak current of coppe...

  11. Use of the optical lithography in the development of disposable carbon based electrodes - doi: 10.4025/actascitechnol.v35i1.11915

    Directory of Open Access Journals (Sweden)

    Lucilene Dornelles Mello

    2013-01-01

    Full Text Available In this study, carbon-based electrodes for disposable use were constructed using the technique of optical lithography. The process consisted in the irradiation of UV light on a layer of photosensitive resin (SU-8 50 deposited on a substrate of PVC. The pattern obtained electrode was filled with carbon paste. The electrodes were characterized by cyclic voltammetric using the reversible system Fe(CN63-/Fe(CN64- in KCl 0.1 mol L-1 and electrochemical impedance spectroscopy (EIS. The electrodes showed an E°’ = ½ (Epa + Epc » 229 (± 2 mV vs SCE (n = 4, with DEp » 235 (± 14 mV (n = 4. Other studies showed a linear behavior of the peak current (Ip both anode and cathode with v1/2, probably due to diffuse contribution and/or electron transfer kinetics of the reaction. These parameters are in accordance to with those obtained for screen-printed electrode described in the literature. The good results obtained show the suitability of the electrodes for analytical applications such as development of sensors.  

  12. Electrocatalytic reduction of nitrite on tetraruthenated metalloporphyrins/Nafion glassy carbon modified electrode

    Energy Technology Data Exchange (ETDEWEB)

    Calfuman, Karla [Facultad de Ciencias, Departamento de Quimica, Universidad de Chile, Las Palmeras 3425, Casilla 653, Nunoa, Santiago (Chile); Aguirre, Maria Jesus [Facultad de Quimica y Biologia, Departamento de Quimica de los Materiales, Universidad de Santiago de Chile, Santiago (Chile); Canete-Rosales, Paulina; Bollo, Soledad [Facultad de Ciencias Quimicas y Farmaceuticas, Departamento de Quimica Farmacologica y Toxicologica, Universidad de Chile, Santiago (Chile); Llusar, Rosa [Departamento de Quimica Fisica y Analitica, Universidad de Jaume I, Castellon (Spain); Isaacs, Mauricio, E-mail: misaacs@uchile.cl [Facultad de Ciencias, Departamento de Quimica, Universidad de Chile, Las Palmeras 3425, Casilla 653, Nunoa, Santiago (Chile)

    2011-10-01

    Highlights: > Preparation and characterization of modified electrodes with M(II) Tetraruthenated porphyrins onto a Nafion film. > The electrodes were characterized by SEM, TEM, AFM and SECM techniques. > The modified electrodes are active in the electrochemical reduction of nitrite at -660 mV vs Ag/AgCl. > GC/Nf/CoTRP modified electrode is more electrochemically active than their Ni and Zn analogues. - Abstract: This paper describes the electrochemical reduction of nitrite ion in neutral aqueous solution mediated by tetraruthenated metalloporphyrins (Co(II), Ni(II) and Zn(II)) electrostatically assembled onto a Nafion film previously adsorbed on glassy carbon or ITO electrodes. Scanning electron microscope (SEM-EDX) and transmission electron microscopy (TEM) results have shown that on ITO electrodes the macrocycles forms multiple layers with a disordered stacking orientation over the Nafion film occupying hydrophobic and hydrophilic sites in the polyelectrolyte. Atomic force microscopy (AFM) results demonstrated that the Nafion film is 35 nm thick and tetraruthenated metalloporphyrins layers 190 nm thick presenting a thin but compacted morphology. Scanning electrochemical microscopy (SECM) images shows that the Co(II) tetraruthenated porphyrins/Nf/GC modified electrode is more electrochemically active than their Ni and Zn analogues. These modified electrodes are able to reduce nitrite at -660 mV showing enhanced reduction current and a decrease in the required overpotential compared to bare glassy carbon electrode. Controlled potential electrolysis experiments verify the production of ammonia, hydrazine and hydroxylamine at potentials where reduction of solvent is plausible demonstrating some selectivity toward the nitrite ion. Rotating disc electrode voltammetry shows that the factor that governs the kinetics of nitrite reduction is the charge propagation in the film.

  13. Thin, Flexible Supercapacitors Made from Carbon Nanofiber Electrodes Decorated at Room Temperature with Manganese Oxide Nanosheets

    Directory of Open Access Journals (Sweden)

    S. K. Nataraj

    2013-01-01

    Full Text Available We report the fabrication and electrochemical performance of a flexible thin film supercapacitor with a novel nanostructured composite electrode. The electrode was prepared by in situ coprecipitation of two-dimensional (2D MnO2 nanosheets at room temperature in the presence of carbon nanofibers (CNFs. The highest specific capacitance of 142 F/g was achieved for CNFs-MnO2 electrodes in sandwiched assembly with PVA-H4SiW12O40·nH2O polyelectrolyte separator.

  14. Application of N-doped graphene modified carbon ionic liquid electrode for direct electrochemistry of hemoglobin

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Wei, E-mail: swyy26@hotmail.com [College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158 (China); Dong, Lifeng, E-mail: donglifeng@qust.edu.cn [College of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Department of Physics, Astronomy, and Materials Science, Missouri State University, Springfield, MO 65897 (United States); Deng, Ying; Yu, Jianhua [College of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Wang, Wencheng [College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158 (China); Zhu, Qianqian [College of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China)

    2014-06-01

    Nitrogen-doped graphene (NG) was synthesized and used for the investigation on direct electrochemistry of hemoglobin (Hb) with a carbon ionic liquid electrode as the substrate electrode. Due to specific characteristics of NG such as excellent electrocatalytic property and large surface area, direct electron transfer of Hb was realized with enhanced electrochemical responses appearing. Electrochemical behaviors of Hb on the NG modified electrode were carefully investigated with the electrochemical parameters calculated. The Hb modified electrode exhibited excellent electrocatalytic reduction activity toward different substrates, such as trichloroacetic acid and H{sub 2}O{sub 2}, with wider dynamic range and lower detection limit. These findings show that NG can be used for the preparation of chemically modified electrodes with improved performance and has potential applications in electrochemical sensing. - Graphical abstract: The utilization of N-doped graphene enables direct electrochemistry of hemoglobin with a pair of well-defined redox peaks appearing. - Highlights: • Nitrogen-doped graphene (NG) was synthesized by a solvothermal method. • NG was used for the investigation on direct electrochemistry of hemoglobin with carbon ionic liquid electrode. • The Hb modified electrode exhibited excellent electrocatalytic activity toward different substrates.

  15. Vertical electric field stimulated neural cell functionality on porous amorphous carbon electrodes.

    Science.gov (United States)

    Jain, Shilpee; Sharma, Ashutosh; Basu, Bikramjit

    2013-12-01

    We demonstrate the efficacy of amorphous macroporous carbon substrates as electrodes to support neuronal cell proliferation and differentiation in electric field mediated culture conditions. The electric field was applied perpendicular to carbon substrate electrode, while growing mouse neuroblastoma (N2a) cells in vitro. The placement of the second electrode outside of the cell culture medium allows the investigation of cell response to electric field without the concurrent complexities of submerged electrodes such as potentially toxic electrode reactions, electro-kinetic flows and charge transfer (electrical current) in the cell medium. The macroporous carbon electrodes are uniquely characterized by a higher specific charge storage capacity (0.2 mC/cm(2)) and low impedance (3.3 kΩ at 1 kHz). The optimal window of electric field stimulation for better cell viability and neurite outgrowth is established. When a uniform or a gradient electric field was applied perpendicular to the amorphous carbon substrate, it was found that the N2a cell viability and neurite length were higher at low electric field strengths (≤ 2.5 V/cm) compared to that measured without an applied field (0 V/cm). While the cell viability was assessed by two complementary biochemical assays (MTT and LDH), the differentiation was studied by indirect immunostaining. Overall, the results of the present study unambiguously establish the uniform/gradient vertical electric field based culture protocol to either enhance or to restrict neurite outgrowth respectively at lower or higher field strengths, when neuroblastoma cells are cultured on porous glassy carbon electrodes having a desired combination of electrochemical properties.

  16. Microwave enhanced electroanalysis of formulations: processes in micellar media at glassy carbon and at platinum electrodes.

    Science.gov (United States)

    Ghanem, Mohamed A; Compton, Richard G; Coles, Barry A; Canals, Antonio; Marken, Frank

    2005-10-01

    The direct electroanalysis of complex formulations containing alpha-tocopherol (vitamin E) is possible in micellar solution and employing microwave-enhanced voltammetry. In the presence of microwave radiation substantial heating and current enhancement effects have been observed at 330 microm diameter glassy carbon electrodes placed into a micellar aqueous solution and both hydrophilic and highly hydrophobic redox systems are detected. For the water soluble Fe(CN)(6)(3-/4-) redox system in micellar aqueous solutions of 0.1 M NaCl and 0.1 M sodium dodecylsulfate (SDS) at low to intermediate microwave power, thermal effects and convection effects are observed. At higher microwave power, thermal cavitation is induced and dominates the mass transport at the electrode surface. For the micelle-soluble redox systems tert-butylferrocene and 2,5-di-tert-butyl-1,4-benzoquinone, strong and concentration dependent current responses are observed only in the presence of microwave radiation. For the oxidation of micelle-soluble alpha-tocopherol current responses at glassy carbon electrodes are affected by adsorption and desorption processes whereas at platinum electrodes, analytical limiting currents are obtained over a wide range of alpha-tocopherol concentrations. However, for the determination of alpha-tocopherol in a commercial formulation interference from proteins is observed at platinum electrodes and direct measurements are possible only over a limited concentration range and at glassy carbon electrodes.

  17. Lead-carbon electrode designed for renewable energy storage with superior performance in partial state of charge operation

    Science.gov (United States)

    Zhang, Wen-Li; Yin, Jian; Lin, Zhe-Qi; Shi, Jun; Wang, Can; Liu, De-Bo; Wang, Yue; Bao, Jin-Peng; Lin, Hai-Bo

    2017-02-01

    Renewable energy storage is a key issue in our modern electricity-powered society. Lead acid batteries (LABs) are operated at partial state of charge in renewable energy storage system, which causes the sulfation and capacity fading of Pb electrode. Lead-carbon composite electrode is a good solution to the sulfation problem of LAB. In this paper, a rice-husk-derived hierarchically porous carbon with micrometer-sized large pores (denoted as RHC) has been used as the component of lead-carbon composite electrode. Scanning electron microscopy was used to characterize the morphology of lead-carbon composite electrode. Electrochemical impedance spectroscopy was used to determine the charge transfer capability of lead-carbon composite electrode. Both full charge-discharge method and charge-discharge method operating at harsh partial state of charge condition have been used to prove the superior energy storage capability of lead-carbon composite electrode. Experiment results prove that the micrometer-sized pores of RHC are beneficial to the construction and stability of lead-carbon composite electrode. Microporous carbon material with high surface area is not suitable for the construction of lead-carbon electrode due to the ruin of lead-carbon structure caused by severe electrochemical hydrogen evolution.

  18. The Impact of Surface Chemistry on Bio-derived Carbon Performance as Supercapacitor Electrodes

    KAUST Repository

    Alshareef, Niman H.

    2016-12-23

    In this study, we demonstrate that highly functionalized and porous carbons can be derived from palm-leaf waste using the template-free facile synthesis process. The derived carbons have high content of nitrogen dopant, high surface area, and various defects. Moreover, these carbons exhibit a high electrical conductivity (107 S m−1). Thanks to the high content of edge N (64.3%) and highly microporous nature (82% of microspores), these biomass-derived carbons show promising performance when used as supercapacitor electrodes. To be specific, these carbonaceous materials show a specific capacitance as high as 197 and 135 F g−1 at 2 and 20 A g−1 in three-electrode configuration, respectively. Furthermore, the symmetrical cells using palm-leaf-derived carbon show an energy density of 8.4 Wh Kg−1 at a power density of 0.64 kW Kg−1, with high cycling life stability (∼8% loss after 10,000 continuous charge–discharge cycles at 20 A g−1). Interestingly, as the power density increases from 4.4 kW kg−1 to 36.8 kW kg−1, the energy density drops slowly from 8.4 Wh kg−1 to 3.4 Wh kg−1. Getting such extremely high power density without significant loss of energy density indicates that these palm-leaf-derived carbons have excellent electrode performance as supercapacitor electrodes.

  19. Transduction mechanism of carbon nanotubes in solid-contact ion-selective electrodes.

    Science.gov (United States)

    Crespo, Gastón A; Macho, Santiago; Bobacka, Johan; Rius, F Xavier

    2009-01-15

    Porous carbon materials and carbon nanotubes were recently used as solid contacts in ion-selective electrodes (ISE), and the signal transduction mechanism of these carbon-based materials is therefore of great interest. In this work the ion-to-electron transduction mechanism of carbon nanotubes is studied by using electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). Single-walled carbon nanotubes (SWCNT) are deposited on glassy carbon (GC) disk electrodes by repetitive spraying, resulting in SWCNT layers with thicknesses of 10, 35, and 50 mum. The impedance spectra of these GC/SWCNT electrodes in contact with aqueous electrolyte solution show a very small resistance and a large bulk capacitance that is related to a large effective double layer at the SWCNT/electrolyte interface. Interestingly, the impedance response of GC/SWCNT is very similar to that of poly(3,4-ethylenedioxythiophene) (PEDOT) film electrodes studied earlier under the same experimental conditions. The same equivalent circuit is valid for both types of materials. The reason is that both materials can be described schematically as an asymmetric capacitor where one side is formed by electronic charge (electrons/holes) in the SWCNT wall or along the conjugated polymer chain of PEDOT and the other side is formed by ions (anions/cations) in the solution (or in the ion-selective membrane when used as a solid contact in ISE).

  20. The Impact of Surface Chemistry on Bio-derived Carbon Performance as Supercapacitor Electrodes

    Science.gov (United States)

    Alshareef, Niman H.; Whitehair, Daniel; Xia, Chuan

    2016-12-01

    In this study, we demonstrate that highly functionalized and porous carbons can be derived from palm-leaf waste using the template-free facile synthesis process. The derived carbons have high content of nitrogen dopant, high surface area, and various defects. Moreover, these carbons exhibit a high electrical conductivity (107 S m-1). Thanks to the high content of edge N (64.3%) and highly microporous nature (82% of microspores), these biomass-derived carbons show promising performance when used as supercapacitor electrodes. To be specific, these carbonaceous materials show a specific capacitance as high as 197 and 135 F g-1 at 2 and 20 A g-1 in three-electrode configuration, respectively. Furthermore, the symmetrical cells using palm-leaf-derived carbon show an energy density of 8.4 Wh Kg-1 at a power density of 0.64 kW Kg-1, with high cycling life stability (˜8% loss after 10,000 continuous charge-discharge cycles at 20 A g-1). Interestingly, as the power density increases from 4.4 kW kg-1 to 36.8 kW kg-1, the energy density drops slowly from 8.4 Wh kg-1 to 3.4 Wh kg-1. Getting such extremely high power density without significant loss of energy density indicates that these palm-leaf-derived carbons have excellent electrode performance as supercapacitor electrodes.

  1. The Impact of Surface Chemistry on Bio-derived Carbon Performance as Supercapacitor Electrodes

    Science.gov (United States)

    Alshareef, Niman H.; Whitehair, Daniel; Xia, Chuan

    2017-03-01

    In this study, we demonstrate that highly functionalized and porous carbons can be derived from palm-leaf waste using the template-free facile synthesis process. The derived carbons have high content of nitrogen dopant, high surface area, and various defects. Moreover, these carbons exhibit a high electrical conductivity (107 S m-1). Thanks to the high content of edge N (64.3%) and highly microporous nature (82% of microspores), these biomass-derived carbons show promising performance when used as supercapacitor electrodes. To be specific, these carbonaceous materials show a specific capacitance as high as 197 and 135 F g-1 at 2 and 20 A g-1 in three-electrode configuration, respectively. Furthermore, the symmetrical cells using palm-leaf-derived carbon show an energy density of 8.4 Wh Kg-1 at a power density of 0.64 kW Kg-1, with high cycling life stability (˜8% loss after 10,000 continuous charge-discharge cycles at 20 A g-1). Interestingly, as the power density increases from 4.4 kW kg-1 to 36.8 kW kg-1, the energy density drops slowly from 8.4 Wh kg-1 to 3.4 Wh kg-1. Getting such extremely high power density without significant loss of energy density indicates that these palm-leaf-derived carbons have excellent electrode performance as supercapacitor electrodes.

  2. Study on hydrogen evolution performance of the carbon supported PtRu alloy film electrodes

    Institute of Scientific and Technical Information of China (English)

    YANG; Bin; LI; Yang; ZAN; Lin-han

    2005-01-01

    The carbon supported PtRu alloy film electrodes having Pt about 0.10 mg/cm2 or even less were prepared by ion beam sputtering method (IBSM). It was valued on the hydrogen analyse performance, the temperature influence factor and the stability by electroanalysis hydrogen analyse method. It was found that the carbon supported PtRu alloy film electrodes had higher hydrogen evolution performance and stability, such as the hydrogen evolution exchange current density (j0) was increase as the temperature (T) rised, and it overrun 150 mA/cm2 as the trough voltage in about 0.68V, and it only had about 2.8% decline in 500 h electrolytic process. The results demonstrated that the carbon supported PtRu alloy film electrodes kept highly catalytic activity and stability, and it were successfully used in pilot plant for producing H2 on electrolysis of H2S.

  3. Electro-catalytic effect of manganese oxide on oxygen reduction at teflonbonded carbon electrode

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Oxygen reduction(OR)on Teflon-bonded carbon electrodes with manganese oxide as catalyst in 6 mol/L KOH solution was investigated using AC impedance spectroscopy combined with other techniques. For OR at this electrode, the Tafel slope is-0.084V/dec and the apparent exchange current density is (1.02-3.0)×10-7 A/cm2. In the presence of manganese oxide on carbon electrode,the couple Mn3+/Mn4+ reacts with the O2 adsorbed on carbon sites forming O2- radicals and acceletes the dismutation of O2-, which contributes to the catalytic effect of manganese oxide for OR reaction.

  4. Electrochemical Determination of Brilliant Blue and Tartrazine Based on an Ionic Liquid-Modified Expanded Graphite Paste Electrode.

    Science.gov (United States)

    Wang, Wenchang; Chen, Ye; Zhang, Jing; Wang, Xue; Chen, Zhidong

    2015-01-01

    A sensitive electrochemical method was developed for the simultaneous determination of Brilliant Blue (BB) and tartrazine (Tz) using an ionic liquid-modified expanded graphite paste electrode (IL-EGPE). The IL-EGPE was prepared by mixing ionic liquid-expanded graphite composite (IL-EG) with solid paraffin. Compared with the EGPE, the IL-EGPE remarkably enhanced the electrocatalytic oxidation signals of BB and Tz. Under optimal experimental conditions, the designed IL-EGPE exhibited wide linear responses to BB and Tz ranging from 5.0×10(-9) to 4.0×10(-6) M and 1.0×10(-8) to 1.0×10(-6) M, respectively. The detection limits for BB and Tz were 2.0×10(-9) M (1.6 ng/mL) and 3.3×10(-9) M (1.8 ng/mL) at an S/N of 3, respectively. This electrode showed good reproducibility, stability, and reusability. The proposed method was successfully applied in the simultaneous determination of BB and Tz in a soft drink with satisfactory results.

  5. Glassy carbon electrodes modified with multiwalled carbon nanotubes for the determination of ascorbic acid by square-wave voltammetry

    Directory of Open Access Journals (Sweden)

    Sushil Kumar

    2012-05-01

    Full Text Available Multiwalled carbon nanotubes were used to modify the surface of a glassy carbon electrode to enhance its electroactivity. Nafion served to immobilise the carbon nanotubes on the electrode surface. The modified electrode was used to develop an analytical method for the analysis of ascorbic acid (AA by square-wave voltammetry (SWV. The oxidation of ascorbic acid at the modified glassy carbon electrode showed a peak potential at 315 mV, about 80 mV lower than that observed at the bare (unmodified electrode. The peak current was about threefold higher than the response at the bare electrode. Replicate measurements of peak currents showed good precision (3% rsd. Peak currents increased with increasing ascorbic acid concentration (dynamic range = 0.0047–5.0 mmol/L and displayed good linearity (R2 = 0.994. The limit of detection was 1.4 μmol/L AA, while the limit of quantitation was 4.7 μmol/L AA. The modified electrode was applied to the determination of the amount of ascorbic acid in four brands of commercial orange-juice products. The measured content agreed well (96–104% with the product label claim for all brands tested. Recovery tests on spiked samples of orange juice showed good recovery (99–104%. The reliability of the SWV method was validated by conducting parallel experiments based on high-performance liquid chromatography (HPLC with absorbance detection. The observed mean AA contents of the commercial orange juice samples obtained by the two methods were compared statistically and were found to have no significant difference (P = 0.05.

  6. New Electrochemically-Modified Carbon Paste Inclusion β-Cyclodextrin and Carbon Nanotubes Sensors for Quantification of Dorzolamide Hydrochloride

    Directory of Open Access Journals (Sweden)

    Nawal Ahmad Alarfaj

    2016-12-01

    Full Text Available The present article introduces a new approach to fabricate carbon paste sensors, including carbon paste, modified carbon paste inclusion β-cyclodextrin, and carbon nanotubes for the quantification of dorzolamide hydrochloride (DRZ. This study is mainly based on the construction of three different carbon paste sensors by the incorporation of DRZ with phosphotungstic acid (PTA to form dorzolamide-phosphotungstate (DRZ-PT as an electroactive material in the presence of the solvent mediator ortho-nitrophenyloctyl ether (o-NPOE. The fabricated conventional carbon paste sensor (sensor I, as well as the other modified carbon paste sensors using β-cyclodextrin (sensor II and carbon nanotubes (sensor III, have been investigated. The sensors displayed Nernstian responses of 55.4 ± 0.6, 56.4 ± 0.4 and 58.1 ± 0.2 mV·decade−1 over concentration ranges of 1.0 × 10−5–1.0 × 10−2, 1.0 × 10−6–1.0 × 10−2, and 5.0 × 10−8–1.0 × 10−2 mol·L−1 with lower detection limits of 5.0 × 10−6, 5.0 × 10−7, and 2.5 × 10−9 mol·L−1 for sensors I, II, and III, respectively. The critical performance of the developed sensors was checked with respect to the effect of various parameters, including pH, selectivity, response time, linear concentration relationship, lifespan, etc. Method validation was applied according to the international conference on harmonisation of technical requirements for registration of pharmaceuticals for human use ICH guidelines. The developed sensors were employed for the determination of DRZ in its bulk and dosage forms, as well as bio-samples. The observed data were statistically analyzed and compared with those obtained from other published methods.

  7. High-performance supercapacitor electrode from cellulose-derived, inter-bonded carbon nanofibers

    Science.gov (United States)

    Cai, Jie; Niu, Haitao; Wang, Hongxia; Shao, Hao; Fang, Jian; He, Jingren; Xiong, Hanguo; Ma, Chengjie; Lin, Tong

    2016-08-01

    Carbon nanofibers with inter-bonded fibrous structure show high supercapacitor performance when being used as electrode materials. Their preparation is highly desirable from cellulose through a pyrolysis technique, because cellulose is an abundant, low cost natural material and its carbonization does not emit toxic substance. However, interconnected carbon nanofibers prepared from electrospun cellulose nanofibers and their capacitive behaviors have not been reported in the research literature. Here we report a facile one-step strategy to prepare inter-bonded carbon nanofibers from partially hydrolyzed cellulose acetate nanofibers, for making high-performance supercapacitors as electrode materials. The inter-fiber connection shows considerable improvement in electrode electrochemical performances. The supercapacitor electrode has a specific capacitance of ∼241.4 F g-1 at 1 A g-1 current density. It maintains high cycling stability (negligible 0.1% capacitance reduction after 10,000 cycles) with a maximum power density of ∼84.1 kW kg-1. They may find applications in the development of efficient supercapacitor electrodes for energy storage applications.

  8. Electrochemical study of oxidation process of promethazine using sensor based on carbon nanotubes paste containing immobilized DNA on inorganic matrix

    Directory of Open Access Journals (Sweden)

    João Paulo Marco

    2014-10-01

    Full Text Available In the present work the voltammetric behavior and the oxidation process of promethazine (PHZ in electrochemical sensor based on carbon nanotubes paste containing DNA immobilized on the inorganic matrix prepared by sol-gel process (SiO2/Al2O3/Nb2O5. The method of Laviron verified that the system is irreversible and high speed of electron transfer between the electrode and DNA. The study of the oxidation of PHZ and influence of pH showed slope of 0.054 V / pH (near the nernstian system: 0.0592 V / pH suggesting that it involves the transfer of two protons and two electrons.

  9. Surface morphology changes of polymer membrane and carbon paste sertraline sensors.

    Science.gov (United States)

    Khater, M M; Hassib, H B; Issa, Y M; Mohammed, S H

    2015-03-01

    Polymer membrane and chemically modified carbon paste (CMCP) sensors for determination of sertraline HCl (Ser-Cl) incorporating sertraline tetraphenylborate (Ser-TPB) as an electro-active material were constructed. They showed a rapid and linear response for Ser-ion over the concentration range 0.01-10.00 mmol L(-1). The limits of detection were 2.80 and 9.55 μmol L(-1), and Nernastian slopes were 56.60, 59.60 mV decade(-1) for membrane and CMCP sensors for batch method. In flow injection analysis (FIA), the electrodes revealed comparatively good selectivity for Ser-ion with regard to a wide variety of different cations, sugars, and amino acids. The addition of different anionic additives, namely sodium tetraphenylborate (NaTPB), potassium tetraphenylborate (KTPB), potassium tetrakis[3,5-bis-(triflouromethyl)phenyl]borate (KTFMPB), and sodium tetrakis[3,5-bis(trifluoro-methyl)phenyl]borate (NaTFMPB), to the prepared mixture improved their response characteristics. The surface morphologies of membrane films containing PVC only (blank), plasticizer+PVC, Ser-TPB+plasticizer+PVC, and Ser-TPB +plasticizer+PVC+additive were studied using scanning and atomic force electron microscopes. These sensors had been used in the potentiometric titration of Ser-ion against NaTPB. Standard addition method for the pure raw material and some of its pharmaceutical tablets was used for Ser-Cl determination. The obtained results were tested for their repeatability and reproducibility and were statistically treated by F- and t- tests.

  10. Highly porous activated carbons from resource-recovered Leucaena leucocephala wood as capacitive deionization electrodes.

    Science.gov (United States)

    Hou, Chia-Hung; Liu, Nei-Ling; Hsi, Hsing-Cheng

    2015-12-01

    Highly porous activated carbons were resource-recovered from Leucaena leucocephala (Lam.) de Wit. wood through combined chemical and physical activation (i.e., KOH etching followed by CO2 activation). This invasive species, which has severely damaged the ecological economics of Taiwan, was used as the precursor for producing high-quality carbonaceous electrodes for capacitive deionization (CDI). Carbonization and activation conditions strongly influenced the structure of chars and activated carbons. The total surface area and pore volume of activated carbons increased with increasing KOH/char ratio and activation time. Overgasification induced a substantial amount of mesopores in the activated carbons. In addition, the electrochemical properties and CDI electrosorptive performance of the activated carbons were evaluated; cyclic voltammetry and galvanostatic charge/discharge measurements revealed a typical capacitive behavior and electrical double layer formation, confirming ion electrosorption in the porous structure. The activated-carbon electrode, which possessed high surface area and both mesopores and micropores, exhibited improved capacitor characteristics and high electrosorptive performance. Highly porous activated carbons derived from waste L. leucocephala were demonstrated to be suitable CDI electrode materials.

  11. Fabrication and characterization of three-dimensional carbon electrodes for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Teixidor, Genis Turon; Zaouk, Rabih B.; Park, Benjamin Y.; Madou, Marc J. [Department of Mechanical and Aerospace Engineering, 4200 Engineering Gateway Building, University of California, Irvine, Irvine, CA 92697 (United States)

    2008-09-01

    This paper presents fabrication and testing results of three-dimensional carbon anodes for lithium-ion batteries, which are fabricated through the pyrolysis of lithographically patterned epoxy resins. This technique, known as Carbon-MEMS, provides great flexibility and an unprecedented dimensional control in shaping carbon microstructures. Variations in the pattern density and in the pyrolysis conditions result in anodes with different specific and gravimetric capacities, with a three to six times increase in specific capacity with respect to the current thin-film battery technology. Newly designed cross-shaped Carbon-MEMS arrays have a much higher mechanical robustness (as given by their moment of inertia) than the traditionally used cylindrical posts, but the gravimetric analysis suggests that new designs with thinner features are required for better carbon utilization. Pyrolysis at higher temperatures and slower ramping up schedules reduces the irreversible capacity of the carbon electrodes. We also analyze the addition of Meso-Carbon Micro-Beads (MCMB) particles on the reversible and irreversible capacities of new three-dimensional, hybrid electrodes. This combination results in a slight increase in reversible capacity and a big increase in the irreversible capacity of the carbon electrodes, mostly due to the non-complete attachment of the MCMB particles. (author)

  12. A novel method of fabricating carbon nanotubes-polydimethylsiloxane composite electrodes for electrocardiography.

    Science.gov (United States)

    Liu, Benyan; Chen, Yingmin; Luo, Zhangyuan; Zhang, Wenzan; Tu, Quan; Jin, Xun

    2015-01-01

    Polymer-based flexible electrodes are receiving much attention in medical applications due to their good wearing comfort. The current fabrication methods of such electrodes are not widely applied. In this study, polydimethylsiloxane (PDMS) and conductive additives of carbon nanotubes (CNTs) were employed to fabricate composite electrodes for electrocardiography (ECG). A three-step dispersion process consisting of ultrasonication, stirring, and in situ polymerization was developed to yield homogenous CNTs-PDMS mixtures. The CNTs-PDMS mixtures were used to fabricate CNTs-PDMS composite electrodes by replica technology. The influence of ultrasonication time and CNT concentration on polymer electrode performance was evaluated by impedance and ECG measurements. The signal amplitude of the electrodes prepared using an ultrasonication time of 12 h and CNT content of 5 wt% was comparable to that of commercial Ag/AgCl electrodes. The polymer electrodes were easily fabricated by conventional manufacturing techniques, indicating a potential advantage of reduced cost for mass production.

  13. Functional Single-walled Carbon Nanotube Electrodes for Solar Energy Conversion

    Science.gov (United States)

    Blackburn, Jeffrey

    2010-03-01

    In this presentation, we discuss our progress in producing high surface area electrodes from single-walled carbon nanotubes (SWNTs) and the utilization of these electrodes in solar energy conversion devices. SWNTs have several fundamental properties that make them attractive for functional electrodes, including high electron and hole mobilities, a tunable work function with an energy range relevant to many photovoltaic devices, and optical transitions in the visible and near infrared that may be useful for solar driven photochemical reactions. Additionally, they possess numerous properties amenable to practical, scalable, and economic electrode deposition including abundant source material, a natural disposition for solution processing, and high surface area and flexibility. All of these features make them extremely attractive for replacing conventional electrodes, such as tin-doped indium oxide (ITO), which suffer from questionable world supply, high temperature/low pressure deposition requirements, and brittleness. We will present our development of a versatile and scalable ultrasonic spray process for producing SWNT electrodes with high transparency, high conductivity, and very low surface roughness. This method can be adapted for aqueous and organic solvents, allowing SWNT electrodes to be sprayed on a variety of different substrates, including directly on photovoltaic devices. The performance of PV devices incorporating our electrodes is nearly equivalent to devices incorporating traditional transparent conducting oxides. Finally, we demonstrate that this method can be extended to the production of a variety of different functional SWNT electrodes, including bio-hybrid electrodes for the production of hydrogen fuel. These electrodes achieve electrolytic current densities close to that of platinum at a fraction of the cost. We will discuss devices incorporating bulk SWNTs as well as SWNTs enriched in specific electronic structures.

  14. Energy storage capability of the dye sensitized solar cells via utilization of highly porous carbon electrodes

    Science.gov (United States)

    Rahimi, Fatemeh; Takshi, Arash

    2016-09-01

    Dye sensitized solar cells (DSSCs) have shown promising results in the field of renewable energy owing to their low cost and portable features. In practical applications, their harvested energy could be stored in a supercapacitor once it exceeds the regular consumption. Various methods of manipulation of the active electrode have been examined to facilitate the energy storage of the system, whereas the counter electrode has always been known for its catalytic functionality and its contribution to the capacitive response of the device left a well-oriented study to be desired. In this work, the substitution of the platinum electrode with a specific porous electrode resulted in a supercapacitive behavior of the device. The photoactive electrode was fabricated using zinc oxide nanowires (ZnO) grown on a conductive transparent substrate with hydrothermal deposition method. The electrode was used to make a standard DSSC using a ruthenium dye, iodide/triiodide standard redox electrolyte, and a platinum counter electrode. The cyclic voltammetry (CV) study of the device showed a low capacitance with 350 mV open circuit voltage. Replacing the platinum counter electrode with a particularly designed porous paper-based carbon nanotube electrode resulted in a considerable difference in the CV response. A capacitive behavior was observed due to the large surface area of the counter electrode and the ZnO nanostructures on the photoactive electrode. Due to the large capacitance and relatively small photocurrent, the change in the open circuit voltage was limited. However, enhancement of the photocurrent could improve both the energy harvesting and charge storage in the device.

  15. Nitrogen-doped porous carbon monoliths from polyacrylonitrile (PAN) and carbon nanotubes as electrodes for supercapacitors

    Science.gov (United States)

    Wang, Yanqing; Fugetsu, Bunshi; Wang, Zhipeng; Gong, Wei; Sakata, Ichiro; Morimoto, Shingo; Hashimoto, Yoshio; Endo, Morinobu; Dresselhaus, Mildred; Terrones, Mauricio

    2017-01-01

    Nitrogen-doped porous activated carbon monoliths (NDP-ACMs) have long been the most desirable materials for supercapacitors. Unique to the conventional template based Lewis acid/base activation methods, herein, we report on a simple yet practicable novel approach to production of the three-dimensional NDP-ACMs (3D-NDP-ACMs). Polyacrylonitrile (PAN) contained carbon nanotubes (CNTs), being pre-dispersed into a tubular level of dispersions, were used as the starting material and the 3D-NDP-ACMs were obtained via a template-free process. First, a continuous mesoporous PAN/CNT based 3D monolith was established by using a template-free temperature-induced phase separation (TTPS). Second, a nitrogen-doped 3D-ACM with a surface area of 613.8 m2/g and a pore volume 0.366 cm3/g was obtained. A typical supercapacitor with our 3D-NDP-ACMs as the functioning electrodes gave a specific capacitance stabilized at 216 F/g even after 3000 cycles, demonstrating the advantageous performance of the PAN/CNT based 3D-NDP-ACMs. PMID:28074847

  16. Nitrogen-doped porous carbon monoliths from polyacrylonitrile (PAN) and carbon nanotubes as electrodes for supercapacitors

    Science.gov (United States)

    Wang, Yanqing; Fugetsu, Bunshi; Wang, Zhipeng; Gong, Wei; Sakata, Ichiro; Morimoto, Shingo; Hashimoto, Yoshio; Endo, Morinobu; Dresselhaus, Mildred; Terrones, Mauricio

    2017-01-01

    Nitrogen-doped porous activated carbon monoliths (NDP-ACMs) have long been the most desirable materials for supercapacitors. Unique to the conventional template based Lewis acid/base activation methods, herein, we report on a simple yet practicable novel approach to production of the three-dimensional NDP-ACMs (3D-NDP-ACMs). Polyacrylonitrile (PAN) contained carbon nanotubes (CNTs), being pre-dispersed into a tubular level of dispersions, were used as the starting material and the 3D-NDP-ACMs were obtained via a template-free process. First, a continuous mesoporous PAN/CNT based 3D monolith was established by using a template-free temperature-induced phase separation (TTPS). Second, a nitrogen-doped 3D-ACM with a surface area of 613.8 m2/g and a pore volume 0.366 cm3/g was obtained. A typical supercapacitor with our 3D-NDP-ACMs as the functioning electrodes gave a specific capacitance stabilized at 216 F/g even after 3000 cycles, demonstrating the advantageous performance of the PAN/CNT based 3D-NDP-ACMs.

  17. Characterisation of porous carbon electrode materials used in proton exchange membrane fuel cells via gas adsorption

    Science.gov (United States)

    Watt-Smith, M. J.; Rigby, S. P.; Ralph, T. R.; Walsh, F. C.

    Porous carbon materials are typically used in both the substrate (typically carbon paper) and the electrocatalyst supports (often platinised carbon) within proton exchange membrane fuel cells. Gravimetric nitrogen adsorption has been studied at a carbon paper substrate, two different Pt-loaded carbon paper electrodes and three particulate carbon blacks. N 2 BET surface areas and surface fractal dimensions were determined using the fractal BET and Frenkel-Halsey-Hill models for all but one of the materials studied. The fractal dimensions of the carbon blacks obtained from gas adsorption were compared with those obtained independently by small angle X-ray scattering and showed good agreement. Density functional theory was used to characterise one of the carbon blacks, as the standard BET model was not applicable.

  18. Selective Voltammetric Determination of Uric Acid in the Presence of Ascorbic Acid at Ordered Mesoporous Carbon Modified Electrodes

    Institute of Scientific and Technical Information of China (English)

    WEN,Yan-Li; JIA,Neng-Qin; WANG,Zhi-Yong; SHEN,He-Bai

    2008-01-01

    A novel chemically modified electrode was fabricated by immobilizing ordered mesoporous carbon (OMC)onto a glassy carbon (GC) electrode.The electrocatalytic behavior of the OMC modified electrode towards the oxidation of uric acid (UA) and ascorbic acid (AA) was studied.Compared to a glassy carbon electrode,the OMC modified electrode showed a faster electron transfer rate and reduced the overpotentials greatly.Furthermore,the OMC modified electrode resolved the overlapping voltammetric responses of UA and AA into two well-defined voltammetric peaks with peak separation of ca.0.38 V.All results show that the OMC modified electrode has a good electrocatalytic ability to UA and AA,and has an excellent response towards UA even in the presence of high concentration AA.

  19. Electrochemical oxidation of organic carbonate based electrolyte solutions at lithium metal oxide electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Imhof, R.; Novak, P. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1999-08-01

    The oxidative decomposition of carbonate based electrolyte solutions at practical lithium metal oxide composite electrodes was studied by differential electrochemical mass spectrometry. For propylene carbonate (PC), CO{sub 2} evolution was detected at LiNiO{sub 2}, LiCoO{sub 2}, and LiMn{sub 2}O{sub 4} composite electrodes. The starting point of gas evolution was 4.2 V vs. Li/Li{sup +} at LiNiO{sub 2}, whereas at LiCoO{sub 2} and LiMn{sub 2}O{sub 4}, CO{sub 2} evolution was only observed above 4.8 V vs. Li/Li{sup +}. In addition, various other volatile electrolyte decomposition products of PC were detected when using LiCoO{sub 2}, LiMn{sub 2}O4, and carbon black electrodes. In ethylene carbonate / dimethyl carbonate, CO{sub 2} evolution was only detected at LiNiO{sub 2} electrodes, again starting at about 4.2 V vs. Li/Li{sup +}. (author) 3 figs., 2 refs.

  20. UNIFORMITY ASSESSMENT OF CARBON FIBRES DISPERSION IN CEMENT PASTE BY IMPEDANCE MEASUREMENTS

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    An alternating current was applied to measure the impedance of a hardened cement paste with various contents of carbon fibres.When the free water content in the hardened cement paste is 90%-98%,and the measuring frequency 500Hz,an approximate linear relationship was found between fibre content and impedance of the composite.Based on this relationship,a new attempt was made to evaluate the dispersion uniformity of carbon fibres in cement paste by impedance measurement.The standard deviation S and the coefficient of vriation S/(X-)i of impedance of the fibre-cement specimens randomly taken locating in different points were used as main parameters for the uniformity assessment.As a case,four different mixing processes were designed for dispersing carbon fibres into the cement paste.The results demonstrate that the relative longer mixing time increases the dispersion uniformity of carbon fibres in cement paste,and the addition of the water reducer dramatically improves the uniformity due to the change of the fluidity of the paste.The ground fly ash can increase the uniformity to a certain extent.

  1. Electrocatalytic oxidation of deferiprone and its determination on a carbon nanotube-modified glassy carbon electrode

    Energy Technology Data Exchange (ETDEWEB)

    Yadegari, H. [Department of Chemistry, Faculty of Science, K.N. Toosi University of Technology, P.O. Box 16315-1618, Tehran (Iran, Islamic Republic of); Jabbari, A. [Department of Chemistry, Faculty of Science, K.N. Toosi University of Technology, P.O. Box 16315-1618, Tehran (Iran, Islamic Republic of)], E-mail: jabbari@kntu.ac.ir; Heli, H.; Moosavi-Movahedi, A.A. [Institute of Biochemistry and Biophysics, University of Tehran, Tehran (Iran, Islamic Republic of); Karimian, K. [Arasto Pharmaceutical Chemicals Inc., Tehran (Iran, Islamic Republic of); Khodadadi, A. [Department of Chemical Engineering, Faculty of Engineering, University of Tehran, Tehran (Iran, Islamic Republic of)

    2008-02-15

    The electrochemical behavior of the anti-thalassemia and anti-HIV replication drug, deferiprone, was investigated on a carbon nanotube-modified glassy carbon (GC-CNT) electrode in phosphate buffer solution, pH 7.40 (PBS). During oxidation of deferiprone, two irreversible anodic peaks, with E{sub 1}{sup 0}=452 and E{sub 2}{sup 0}=906mV, appeared, using GC-CNT. Cyclic voltammetric study indicated that the oxidation process is irreversible and diffusion controlled. The number of exchanged electrons in the electro-oxidation process was obtained, and the data indicated that deferiprone is oxidized via two two-electron steps. The results revealed that carbon nanotube (CNT) promotes the rate of oxidation by increasing the peak current, so that deferiprone is oxidized at lower potentials, which thermodynamically is more favorable. This result was confirmed by impedance measurements. The diffusion coefficient, electron-transfer coefficient and heterogeneous electron-transfer rate constant of deferiprone were found to be 1.49 x 10{sup -6} cm{sup 2} s{sup -1}, 0.44, and 3.83 x 10{sup -3} cm s{sup -1}, respectively. A sensitive, simple and time-saving differential-pulse voltammetric procedure was developed for the analysis of deferiprone. Using the proposed method, deferiprone can be determined with a detection limit of 5.25 x 10{sup -7} M. The applicability of the method to direct assays of spiked human serum and urine fluids is described.

  2. Electrochemical impedance spectroscopy on nanostructured carbon electrodes grown by supersonic cluster beam deposition

    Energy Technology Data Exchange (ETDEWEB)

    Bettini, Luca Giacomo; Bardizza, Giorgio; Podesta, Alessandro; Milani, Paolo; Piseri, Paolo, E-mail: piseri@mi.infn.it [Universita degli Studi di Milano, Dipartimento di Fisica and CIMaINa (Italy)

    2013-02-15

    Nanostructured porous films of carbon with density of about 0.5 g/cm{sup 3} and 200 nm thickness were deposited at room temperature by supersonic cluster beam deposition (SCBD) from carbon clusters formed in the gas phase. Carbon film surface topography, determined by atomic force microscopy, reveals a surface roughness of 16 nm and a granular morphology arising from the low kinetic energy ballistic deposition regime. The material is characterized by a highly disordered carbon structure with predominant sp2 hybridization as evidenced by Raman spectroscopy. The interface properties of nanostructured carbon electrodes were investigated by cyclic voltammetry and electrochemical impedance spectroscopy employing KOH 1 M solution as aqueous electrolyte. An increase of the double layer capacitance is observed when the electrodes are heat treated in air or when a nanostructured nickel layer deposited by SCBD on top of a sputter deposited film of the same metal is employed as a current collector instead of a plain metallic film. This enhancement is consistent with an improved charge injection in the active material and is ascribed to the modification of the electrical contact at the interface between the carbon and the metal current collector. Specific capacitance values up to 120 F/g have been measured for the electrodes with nanostructured metal/carbon interface.

  3. Glucose biosensor based on a glassy carbon electrode modified with polythionine and multiwalled carbon nanotubes.

    Directory of Open Access Journals (Sweden)

    Wenwei Tang

    Full Text Available A novel glucose biosensor was fabricated. The first layer of the biosensor was polythionine, which was formed by the electrochemical polymerisation of the thionine monomer on a glassy carbon electrode. The remaining layers were coated with chitosan-MWCNTs, GOx, and the chitosan-PTFE film in sequence. The MWCNTs embedded in FAD were like "conductive wires" connecting FAD with electrode, reduced the distance between them and were propitious to fast direct electron transfer. Combining with good electrical conductivity of PTH and MWCNTs, the current response was enlarged. The sensor was a parallel multi-component reaction system (PMRS and excellent electrocatalytic performance for glucose could be obtained without a mediator. The glucose sensor had a working voltage of -0.42 V, an optimum working temperature of 25°C, an optimum working pH of 7.0, and the best percentage of polytetrafluoroethylene emulsion (PTFE in the outer composite film was 2%. Under the optimised conditions, the biosensor displayed a high sensitivity of 2.80 µA mM(-1 cm(-2 and a low detection limit of 5 µM (S/N = 3, with a response time of less than 15 s and a linear range of 0.04 mM to 2.5 mM. Furthermore, the fabricated biosensor had a good selectivity, reproducibility, and long-term stability, indicating that the novel CTS+PTFE/GOx/MWCNTs/PTH composite is a promising material for immobilization of biomolecules and fabrication of third generation biosensors.

  4. Ion-selective electrodes using carbon nanotubes as ion-to-electron transducers.

    Science.gov (United States)

    Crespo, Gastón A; Macho, Santiago; Rius, F Xavier

    2008-02-15

    This study developed a new type of all-solid-state ion-selective electrode based on a transducing layer of a network of single-walled carbon nanotubes. The extraordinary capacity of carbon nanotubes to promote electron transfer between heterogeneous phases made the presence of electroactive polymers or any other ion-to-electron-transfer promoter unnecessary. The new transducer layer was characterized by environmental scanning electron microscopy and electrochemical impedance spectroscopy. The stability of the electrical potential of the new solid-contact electrode was examined by performing current-reversal chronopotentiometry, and the influence of the interfacial water film was assessed by the potentiometric water layer test. The performance of the new electrode was evaluated by determining K+ with an ion-selective membrane that contained the well-known valinomycin ion carrier. The new electrode had a Nernstian slope (58.4 mV/decade), dynamic ranges of four logarithmic units, and selectivities and limits of detection comparable to other solid-contact electrodes. The short response time (less than 10 s for activities higher than 10(-5.5) M) and the stability of the signal over several days makes these new electrodes very promising candidates for attaining true miniaturization.

  5. Graphene-coated carbon fiber cloth for flexible electrodes of glucose fuel cells

    Science.gov (United States)

    Hoshi, Kazuki; Muramatsu, Kazuo; Sumi, Hisato; Nishioka, Yasushiro

    2016-02-01

    In this work, we fabricated flexible electrodes for a miniaturized, simple structured, and flexible glucose biofuel cell (BFC) using a graphene-coated carbon fiber cloth (GCFC). The areas of the anode and cathode electrodes were 3 × 10 mm2. The anode area was coated with the enzyme glucose oxidase, and the cathode area was coated with the enzyme bilirubin oxidase. No ion-exchange film was needed because glucose oxidase selectively oxidizes glucose and bilirubin oxidase selectively reduces oxygen. The power density of the BFC with GCFC electrodes in a phosphate buffer solution of 200 mM glucose solution at room temperature was 34.3 µW/cm2 at 0.43 V. The power density of a BFC using carbon fiber cloth (CFC) without graphene modification was 18.5 µW/cm2 at 0.13 V. The BFC with the GCFC electrode continued to function longer than 24 h with a power density higher than 5 µW/cm2. These effects were attributed to the much larger effective surface areas of the GCFC electrodes that maintain more enzymes than those of the CFC electrodes.

  6. Lithium-ion capacitors with 2D Nb2CTx (MXene) - carbon nanotube electrodes

    Science.gov (United States)

    Byeon, Ayeong; Glushenkov, Alexey M.; Anasori, Babak; Urbankowski, Patrick; Li, Jingwen; Byles, Bryan W.; Blake, Brian; Van Aken, Katherine L.; Kota, Sankalp; Pomerantseva, Ekaterina; Lee, Jae W.; Chen, Ying; Gogotsi, Yury

    2016-09-01

    There is a growing interest to hybrid energy storage devices, such as lithium-ion capacitors, in which battery-type electrodes are combined with capacitor-type ones. It is anticipated that the energy density (either gravimetric or volumetric) of lithium-ion capacitors is improved if pseudocapacitive or fast insertion materials are used instead of conventional activated carbon (AC) in the capacitor-type electrode. MXenes, a new family of two-dimensional transition metal carbides, demonstrate metallic conductivity and fast charge-discharge behavior that make them suitable for this application. In this study, we move beyond single electrodes, half-cell studies and demonstrate three types of hybrid cells using Nb2CTx-carbon nanotube (CNT) films. It is shown that lithiated graphite/Nb2CTx-CNT, Nb2CTx-CNT/LiFePO4 and lithiated Nb2CTx-CNT/Nb2CTx-CNT cells are all able to operate within 3 V voltage windows and deliver capacities of 43, 24 and 36 mAh/g (per total weight of two electrodes), respectively. Moreover, the polarity of the electrodes can be reversed in the symmetric Nb2CTx-CNT cells from providing a positive potential between 0 and 3 V to a negative one from -3 to 0 V. It is shown that the volumetric energy density (50-70 Wh/L) of our first-generation devices with MXene electrodes exceeds that of a lithium titanate/AC capacitor.

  7. Study on the Highly Sensitive AChE Electrode Based on Multiwalled Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    Shuping Zhang

    2014-01-01

    Full Text Available Using chitosan (CS as carrier, the method named layer-by-layer (LBL self-assembly modification to modify the glassy carbon electrode (GCE with multiwalled carbon nanotubes (MWNTs and acetylcholine esterase (AChE was proposed to prepare the acetylcholine esterase electrode with high sensitivity and stability. The modified electrode was used to detect pesticide of aldicarb, and the enzyme inhibition rate of the electrode showed good linearity with pesticide concentrations in the range of 10−10 g·L−1 to 10−3 g·L−1. The detection limit was 10−11 g·L−1. The modified electrode was also used to detect the actual sample, and the recovery rate range was from 97.72% to 107.15%, which could meet the rapid testing need of the aldicarb residue. After being stored in the phosphate buffer solution (PBS in 4°C for 30 days, the modified electrode showed good stability with the response current that was 80% of the original current.

  8. Electrospun carbon nanofibers/electrocatalyst hybrids as asymmetric electrodes for vanadium redox flow battery

    Science.gov (United States)

    Wei, Guanjie; Fan, Xinzhuang; Liu, Jianguo; Yan, Chuanwei

    2015-05-01

    To improve the electrochemical activity of polyacrylonitrile (PAN)-based electrospun carbon nanofibers (ECNFs) toward vanadium redox couples, the multi-wall carbon nanotubes (CNTs) and Bi-based compound as electrocatalyst have been embedded in the ECNFs to make composite electrode, respectively. The morphology and electrochemical properties of pristine ECNFs, CNTs/ECNFs and Bi/ECNFs have been characterized. Among the three kinds of electrodes, the CNTs/ECNFs show best electrochemical activity toward VO2+/VO2+ redox couple, while the Bi/ECNFs present the best electrochemical activity toward V2+/V3+ redox couple. Furthermore, the high overpotential of hydrogen evolution on Bi/ECNFs makes the side-reaction suppressed. Because of the large property difference between the two composite electrodes, the CNTs/ECNFs and Bi/ECNFs are designed to act as positive and negative electrode for vanadium redox flow battery (VRFB), respectively. It not only does improve the kinetics of two electrode reactions at the same time, but also reduce the kinetics difference between them. Due to the application of asymmetric electrodes, performance of the cell is improved greatly.

  9. Gold nanoparticle decorated multi-walled carbon nanotubes as counter electrode for dye sensitized solar cells.

    Science.gov (United States)

    Kaniyoor, Adarsh; Ramaprabhu, Sundara

    2012-11-01

    A novel counter electrode material for dye sensitized solar cells (DSSCs) composed of nanostructured Au particles decorated on functionalized multi-walled carbon nanotubes (f-MWNTs) is demonstrated for the first time. MWNTs synthesized by catalytic chemical vapor deposition technique are purified and functionalized by treating with concentrated acids. Au nanoparticles are decorated on f-MWNTs by a rapid and facile microwave assisted polyol reduction method. The materials are characterized by X-ray diffractometry, Fourier transform infra red spectroscopy and electron microscopy. The DSSC fabricated with Au/f-MWNTs based counter electrode shows enhanced power conversion efficiency (eta) of 4.9% under AM 1.5G simulated solar radiation. In comparison, the reference DSSCs fabricated with f-MWNTs and Pt counter electrodes show eta of 2.1% and 4.5%. This high performance of Au/f-MWNTs counter electrode is investigated using electrochemical impedance spectroscopy and cyclic voltammetry studies.

  10. Electrocatalytic Oxidation of Dopamine by Ferrocene in Lipid Film Cast on a Glassy Carbon Electrode

    Institute of Scientific and Technical Information of China (English)

    WANG,Jian-Guo(王建国); WU,Zheng-Yan(吴正岩); TANG,Ji-Lin(唐纪琳); TENG,Ren-Rui(滕人瑞); WANG,Er-Kang(汪尔康)

    2002-01-01

    The ferrocene-lipid film electrode was successfully prepared by means of casting the solution of ferrocene and lipid in chloroform onto a glassy carbon (GC) electrode surface. Ferrocene saved in the biological membrane gave a couple of quasi-reversble peaks of cyclic voltammmogram. The electrode displays a preferential electrocatalytic oxidation of dopamine (DA).The effect of electrocatalytic oxidation of DA depends on the solution pH and the negative charge lipid is in favor of catalytic oxidation of DA. The charistic was employed for separating the electrochemical responses of DA and ascorbic acid (AA). The electrode was assessed for the voltammtric differentiation of DA and AA. The measurement of DA can be achieved with differential pulse voltammetry in the presence of high conentration of AA. The catalytic peak current was proportional to the concentration of DA in the range of 1 ×10- 4-3 × 10-3 mol/L.

  11. Carbon-based Composite Electrodes: Preparation, Characterization and Application in Electroanalysis

    Directory of Open Access Journals (Sweden)

    Joop Schoonman

    2007-11-01

    Full Text Available Electrodes based on carbon, i.e., expanded graphite (20%, wt.-epoxy composite(20EG-Epoxy and expanded graphite (20%, wt.-polystyrene composite (20EG-PS havebeen prepared, characterized using scanning electron microscopy (SEM and cyclicvoltammetry (CV, and tested as anodic sensors. The electrodes exhibited good mechanicalresistance and low electrical resistances. Scan rate dependent cyclic voltammetry responsesat 20EG-Epoxy and 20EG-PS composite electrodes, which were exemplified for thiourea(TU, a toxic sulphur organic compound selected as testing target analyte in 0.1 M Na2SO4 supporting electrolyte, were investigated. The obtained voltammetric data were inaccordance with those for a random array of microelectrodes. The voltammetric andchronoamperometric detection results of TU in tap water samples, without a supplementaryaddition of supporting electrolyte, at 20EG-Epoxy electrode proved its use for directanalysis of environmental samples.

  12. Flexible supercapacitor electrodes with vertically aligned carbon nanotubes grown on aluminum foils

    Directory of Open Access Journals (Sweden)

    Itir Bakis Dogru

    2016-06-01

    Full Text Available In this work, vertically aligned carbon nanotubes (VACNTs grown on aluminum foils were used as flexible supercapacitor electrodes. Aluminum foils were used as readily available, cheap and conductive substrates, and VACNTs were grown directly on these foils through chemical vapor deposition (CVD method. Solution based ultrasonic spray pyrolysis (USP method was used for the deposition of the CNT catalyst. Direct growth of VACNTs on aluminum foils ruled out both the internal resistance of the supercapacitor electrodes and the charge transfer resistance between the electrode and electrolyte. A specific capacitance of 2.61 mF/cm2 at a scan rate of 800 mV/s was obtained from the fabricated electrodes, which is further improved through the bending cycles.

  13. ENOBIO - first tests of a dry electrophysiology electrode using carbon nanotubes.

    Science.gov (United States)

    Ruffini, Giulio; Dunne, Stephen; Farrés, Esteve; Watts, Paul C P; Mendoza, Ernest; Silva, S Ravi P; Grau, Carles; Marco-Pallarés, Josep; Fuentemilla, Lluís; Vandecasteele, B Jorn

    2006-01-01

    We describe the development and first tests of ENOBIO, a dry electrode sensor concept for biopotential applications. In the proposed electrodes the tip of the electrode is covered with a forest of multi-walled carbon nanotubes (CNTs) that can be coated with Ag/AgCl to provide ionic-electronic transduction. The CNT brush-like structure is to penetrate the outer layers of the skin improving electrical contact as well as increase the contact surface area. In this paper we report the results of the first tests of this concept--immersion on saline solution and pig skin signal detection. These indicate performance on a par with state of the art research-oriented wet electrodes.

  14. Preparation,Electrochemical Behavior and Electrocatalytic Activity of a Copper Hexacyanoferrate Modified Ceramic Carbon Electrode

    Institute of Scientific and Technical Information of China (English)

    YU,Hao; ZHENG,Jian-Bin

    2007-01-01

    A copper hexacyanoferrate modified ceramic carbon electrode(CuHCF/CCE)had been prepared by two-step sol-gel technique and characterized using electrochemical methods.The resulting modified electrode showed a pair of well-defined surface waves in the potential range of 0.40 to 1.0 V with the formal potential of 0.682 V (vs.SCE)in 0.050 mol·dm-3 HOAc-NaOAc buffer containing 0.30 mol·dm-3 KCI.The charge transfer coefficient (α) and charge transfer rate constant(Ks)for the modified electrode were calculated.The electrocatalytic activity of this modified electrode to hydrazine was also investigated,and chronoamperometry was exploited to conveniently determine the diffusion coefficient(D)of hydrazine in solution and the catalytic rate constant(Kcat).Finally,hydrazine was determined with amperometry using the resulting modified electrode.The calibration plot for hydrazine determination was linear in 3.0×10-6-7.5×10-4 mol·dm-3 with the detection limit of 8.0×10-7 mol·dm-3.This modified electrode had some advantages over the modified film electrodes constructed by the conventional methods,such as renewable surface,good long-term stability,excellent catalytic activity and short response time to hydrazine.

  15. Electrochemical determination of ascorbic acid at p-phenylenediamine film-holes modified glassy carbon electrode

    Directory of Open Access Journals (Sweden)

    Olana Bikila Nagasa

    2015-01-01

    Full Text Available In this work the determination of ascorbic acid (AA at glassy carbon electrode (GCE modified with a perforated film produced by reduction of diazonium generated in situ from p-phenylenediamine (PD is reported. Holes were intentionally created in the modifier film by stripping a pre-deposited gold nanoparticles. The modified electrodes were electrochemically characterized by common redox probes: hydroquinone, ferrocyanide and hexamineruthenium(III. The cyclic voltammetric and amperometric response of AA using the modified electrodes was compared with that of bare GCE. The bare GCE showed a linear response to AA in the concentration range of 5 mM to 45 mM with detection limit of 1.656 mM and the modified GCE showed a linear response to AA in the concentration range of 5 μM to 45 μM with detection limit of 0.123 μM. The effect of potential intereferents on amperometric signal of AA at the modified GCE was examined and found to be minimal. The inter-electrode reproducibility, stability, and accuracy were determined. The modified electrode showed excellent inter-electrode reproducibility, accuracy and stability. The modified electrode reported is a promising candidate for use in electroanalysis of AA.

  16. Fast redox of composite electrode of nitroxide radical polymer and carbon with polyacrylate binder

    Science.gov (United States)

    Komaba, Shinichi; Tanaka, Tatsuya; Ozeki, Tomoaki; Taki, Takayuki; Watanabe, Hiroaki; Tachikawa, Hiroyuki

    For organic radical batteries, poly(2,2,6,6-tetramethylpiperidinyloxy-4-yl methacrylate) (PTMA) has been reported as a promising positive electrode material. The PTMA/C composite electrode prepared with polyacrylate binder demonstrated the fast redox performance for the application to aprotic secondary batteries. When the variation in discharge capacities of the PTMA/C composite electrode was tested galvanostatically at 20 C rates, the electrode retained 96% of the initial capacity after 1000 cycles. This is attributed to the fact that the redox of PTMA is a simple reaction to form the oxoammonium salt doped with ClO 4 - anions in the electrolyte. When the PTMA/C composite electrode was discharged at different C rates, the electrode retained 81% of the theoretical capacity even at 50 C rates. This remarkably high rate capability originates from the fast electron-transfer kinetic of the 2,2,6,6-tetramethylpiperidine- N-oxyl (so-called TEMPO) radical, partially jelled polyacrylate binder, and the improved conductivity throughout the electrode by thoroughly mixing with carbon.

  17. Dithiooxamide Modified Glassy Carbon Electrode for the Studies of Non-Aqueous Media: Electrochemical Behaviors of Quercetin on the Electrode Surface

    Directory of Open Access Journals (Sweden)

    Ecir Yılmaz

    2012-03-01

    Full Text Available Electrochemical oxidation of quercetin, as an important biological molecule, has been studied in non-aqueous media using cyclic voltammetry, electrochemical impedance spectroscopy and scanning electron microscopy. To investigate the electrochemical properties of quercetin, an important flavonoid derivative, on a different surface, a new glassy carbon electrode has been developed using dithiooxamide as modifier in non-aqueous media. The surface modification of glassy carbon electrode has been performed within the 0.0 mV and +800 mV potential range with 20 cycles using 1 mM dithioxamide solution in acetonitrile. However, the modification of quercetin to both bare glassy carbon and dithiooxamide modified glassy carbon electrode surface was carried out in a wide +300 mV and +2,800 mV potential range with 10 cycles. Following the modification process, cyclic voltammetry has been used for the surface characterization in aqueous and non-aqueous media whereas electrochemical impedance spectroscopy has been used in aqueous media. Scanning electron microscopy has also been used to support the surface analysis. The obtained data from the characterization and modification studies of dithioxamide modified and quercetin grafted glassy carbon electrode showed that the developed electrode can be used for the quantitative determination of quercetin and antioxidant capacity determination as a chemical sensor electrode.

  18. Assessment of Carbon/Salt/Adhesive Electrodes for Surface Electromyography Measurements.

    Science.gov (United States)

    Posada-Quintero, Hugo; Rood, Ryan; Burnham, Ken; Pennace, John; Chon, Ki

    2016-01-01

    This paper presents the evaluation of novel electrodes for surface electromyography (sEMG) measurements. The electrodes are based on the mixture of carbon powder, quaternary salt, and viscoelastic polymeric adhesive (carbon/salt/adhesive or simply CSA), which when combined, provide the unique advantages of having longer (theoretically infinite) shelf life and potentially lower cost than Ag/AgCl hydrogel electrodes, consistent with FLEXcon's Patent #8 673 184. The 20 subjects were recruited to collect simultaneous recordings of sEMG signals using Ag/AgCl and CSA electrodes, side-by-side on triceps brachii, tibial anterior muscles, biceps brachii, and quadriceps femoris. Although CSA sEMG electrodes showed higher electrode-skin contact impedance for the frequency range of 4 Hz-2 kHz, no significant differences were found in the signals' amplitude between the two electrodes either during relaxation or contraction stages. Furthermore, correlations of the computed linear envelopes (>0.91), rms value envelopes (>0.91), and power spectral densities (>0.95) of the signals were found to be high between the two media. Detected ON- and OFF-times of contraction were also highly correlated (>0.9) and interchangeable (ON-time: bias = -0.02, variance = 0.11; OFF-time: bias = -0.04, variance = 0.23) between the two media. However, CSA sEMG electrodes exhibited a significantly better response to noise (38.3 ± 10.6 dB versus 32.7 ± 15.6 dB) and motion artifacts (24.1 ± 12.1 dB versus 16.6 ± 8.52 dB), and a significantly lower spectral deformation (1.32 ± 0.2 versus 1.46 ± 0.4). Ag/AgCl electrodes showed a significantly more peaked and sensitive response to EMG amplitude (67.9 ± 13.9 dB versus 65.4 ± 14.6 dB). Given no significant differences in many of the measures described earlier and the fact that CSA electrodes have an infinite shelf-life are potentially lower cost, and are more resistant to motion artifacts, the new electrodes provide an attractive alternative to Ag

  19. Synthesis of mesoporous carbon as electrode material for supercapacitor by modified template method

    Institute of Scientific and Technical Information of China (English)

    ZHAO Jia-chang; LAI Chun-yan; DAI Yang; XIE Jing-ying

    2005-01-01

    The pore structures and electrochemical performances of mesoporous carbons prepared by silica sol template method as electrode material for supercapacitor were investigated. The mean pore size and mass specific capacitance of the mesoporous carbons increase with the increase of mass ratio of silica sol to carbon source (glucose). A modified template method, combining silica sol template method and ZnCl2 chemical activation method, was proposed to improve the mass specific capacitance of the mesoporous carbon with an improved BET surface area. The correlation of rate capability and pore structure was studied by constant current discharge and electrochemical impedance spectroscopy. A commercially available microporous carbon was used for comparison. The result shows that mesoporous carbon with a larger pore size displays a higher rate capability. Mesoporous carbon synthesized by modified template method has both high mass specific capacitance and good rate capability.

  20. Simultaneous Determination of Hydroquinone, Catechol and Resorcinol at Graphene Doped Carbon Ionic Liquid Electrode

    Directory of Open Access Journals (Sweden)

    Li Ma

    2012-01-01

    Full Text Available A new composite electrode has been prepared with doping graphene into the paste consisting graphite and ionic liquid, n-octyl-pyridinum hexafluorophosphate (OPFP. This electrode shows an excellent electrochemical activity for the redox of hydroquinone (HQ, catechol (CC, and resorcinol (RS. In comparison with bare paste electrode, the redox peaks of three isomers of dihydroxybenzene can be obviously, simultaneously observed at graphene doping paste electrode. Under the optimized condition, the simultaneous determination of HQ, CC, and RS in their ternary mixture can be carried out with a differential pulse voltammetric technique. The peak currents are linear to the concentration of HQ, CC, and RS in the range form 1×10−5 to 4×10−4, 1×10−5 to 3×10−4, and 1×10−6 to 1.7×10−4 mol L−1, respectively. The limits of detection are 1.8×10−6 mol L−1 for HQ, 7.4×10−7 mol L−1 for CC, and 3.6×10−7 M for RS, respectively.

  1. Operation of a Segmented Hall Thruster with Low-sputtering Carbon-velvet Electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Raitses, Y.; Staack, D.; Dunaevsky, A.; Fisch, N.J.

    2005-12-01

    Carbon fiber velvet material provides exceptional sputtering resistance properties exceeding those for graphite and carbon composite materials. A 2 kW Hall thruster with segmented electrodes made of this material was operated in the discharge voltage range of 200–700 V. The arcing between the floating velvet electrodes and the plasma was visually observed, especially, during the initial conditioning time, which lasted for about 1 h. The comparison of voltage versus current and plume characteristics of the Hall thruster with and without segmented electrodes indicates that the magnetic insulation of the segmented thruster improves with the discharge voltage at a fixed magnetic field. The observations reported here also extend the regimes wherein the segmented Hall thruster can have a narrower plume than that of the conventional nonsegmented thruster.

  2. Fe3O4/carbon coated silicon ternary hybrid composite as supercapacitor electrodes

    Science.gov (United States)

    Oh, Ilgeun; Kim, Myeongjin; Kim, Jooheon

    2015-02-01

    In this study, Fe3O4/carbon-coated Si ternary hybrid composites were fabricated. A carbon layer was directly formed on the surface of Si by the thermal vapor deposition. The carbon-coating layer not only prevented the contact between Si and reactive electrolyte but also provided anchoring sites for the deposition of Fe3O4. Fe3O4 nanoparticles were deposited on the surface of carbon-coated Si by the hydrazine reducing method. The morphology and structure of Fe3O4 and carbon layer were characterized via X-ray diffractometry, field emission scanning electron microscopy, field emission transmission electron microscopy, X-ray photoelectron spectroscopy, and thermogravimetric analyses. These characterizations indicate that a carbon layer was fully coated on the Si particles, and Fe3O4 particles were homogeneously deposited on the carbon-coated Si particles. The Fe3O4/carbon-coated Si electrode exhibited enhanced electrochemical performance, attributed to the high conductivity and stability of carbon layer and pseudocapacitive reaction of Fe3O4. The proposed ternary-hybrid composites may be potentially useful for the fabrication of high-performance electrodes.

  3. Integration of a gate electrode into carbon nanotube devices for scanning tunneling microscopy

    NARCIS (Netherlands)

    Kong, J.; LeRoy, B.J.; Lemay, S.G.; Dekker, C.

    2005-01-01

    We have developed a fabrication process for incorporating a gate electrode into suspended single-walled carbon nanotube structures for scanning tunneling spectroscopy studies. The nanotubes are synthesized by chemical vapor deposition directly on a metal surface. The high temperature (800 °C) involv

  4. Carbon-based Composite Electrodes: Preparation, Characterization and Application in Electroanalysis

    NARCIS (Netherlands)

    Corb, I.; Manea, F.; Radovan, C.; Pop, A.; Burtica, G.; Malchev, P.G.; Picken, S.J.; Schoonman, J.

    2007-01-01

    Electrodes based on carbon, i.e., expanded graphite (20%, wt.)-epoxy composite (20EG-Epoxy) and expanded graphite (20%, wt.)-polystyrene composite (20EG-PS) have been prepared, characterized using scanning electron microscopy (SEM) and cyclic voltammetry (CV), and tested as anodic sensors. The elect

  5. Peptide nanowires for coordination and signal transduction of peroxidase biosensors to carbon nanotube electrode arrays.

    Science.gov (United States)

    Yeh, J I; Lazareck, A; Kim, J Ho; Xu, J; Du, S

    2007-11-30

    A strategy of metallizing peptides to serve as conduits of electronic signals that bridge between a redox enzyme and a carbon-nanotube electrode has been developed with enhanced results. In conjunction, a protocol to link the biological elements to the tips of carbon nanotubes has been developed to optimize contact and geometry between the redox enzyme and the carbon nanotube electrode array. A peptide nanowire of 33 amino acids, comprised of a leucine zipper motif, was mutated to bind divalent metals, conferring conductivity into the peptide. Reaction between a thiolate of the peptide with the sulfenic acid of the NADH peroxidase enzyme formed a peptide-enzyme assembly that are fully primed to transduce electrons out of the enzyme active site to an electrode. Scanning electron microscopy shows immobilization and linking of the assembly specifically to the tips of carbon nanotube electrodes, as designed. Isothermal titration calorimetry and mass spectrometry indicate a binding stoichiometry of at least three metals bound per peptide strand. Overall, these results highlight the gain that can be achieved when the signal tranducing units of a biosensor are aligned through directed peptide chemistry.

  6. A self-template strategy for the synthesis of mesoporous carbon nanofibers as advanced supercapacitor electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Li, Wei; Zhang, Fan; Dou, Yuqian; Wu, Zhangxiong; Liu, Haijing; Qian, Xufang; Gu, Dong; Xia, Yongyao; Tu, Bo; Zhao, Dongyuan [Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials and Laboratory of Advanced Materials, Fudan University, Shanghai 200433 (China)

    2011-05-15

    Self-construction: A facile self-templating strategy is presented for the synthesis of mesoporous carbon nanofibers by using zinc glycolate fibers as the built-in template. The spectacular architectures show excellent performances as recommended electrode material for electrochemical capacitors. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  7. High surface area carbon for bifunctional air electrodes applied in zinc-air batteries

    Energy Technology Data Exchange (ETDEWEB)

    Arai, H. [on leave from NTT Laboratories (Japan); Mueller, S.; Haas, O. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1999-08-01

    Bifunctional air electrodes with high surface area carbon substrates showed low reduction overpotential, thus are promising for enhancing the energy efficiency and power capability of zinc-air batteries. The improved performance is attributed to lower overpotential due to diffusion of the reaction intermediate, namely the peroxide ion. (author) 1 fig., 2 refs.

  8. Preparation and Electrochemistry of Hydrous Ruthenium Oxide/Active Carbon Electrode materials for Supercapacitor

    Institute of Scientific and Technical Information of China (English)

    Zhang; Jianrong

    2001-01-01

    In this paper, we reported a new method to directly prepare the amorphous hydrous ruthenium oxide/active carbon powders. The relationship between the specific capacitance and ruthenium content in powders was studied in detail. Physical properties of the powders such as crystallinity、 particle size, and electrochemical characteristics of electrodes were reported along with the capacitor performance.  ……

  9. Preparation and Electrochemistry of Hydrous Ruthenium Oxide/Active Carbon Electrode materials for Supercapacitor

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    @@ In this paper, we reported a new method to directly prepare the amorphous hydrous ruthenium oxide/active carbon powders. The relationship between the specific capacitance and ruthenium content in powders was studied in detail. Physical properties of the powders such as crystallinity、 particle size, and electrochemical characteristics of electrodes were reported along with the capacitor performance.

  10. Cement Pastes and Mortars Containing Nitrogen-Doped and Oxygen-Functionalized Multiwalled Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    Mauricio Martínez-Alanis

    2016-01-01

    Full Text Available Cement pastes and mortars based on ordinary Portland cement containing nitrogen-doped multiwalled carbon nanotubes (MWCNT-Nx or oxygen-functionalized multiwalled carbon nanotubes (MWCNT-Ox are investigated. To incorporate MWCNTs into the cementitious matrix, the as-produced carpets are dispersed over periods of 1 and 2 hours in distilled water at pH levels of 1 and 7. The cement pastes are prepared by adding 0.1 wt% of MWCNTs to cement powder, followed by characterization with SEM and X-ray diffraction (XRD at an early age (first hours of hydration. The mortars are mechanically characterized during the hydration process for a period of 28 days. SEM characterization of cement pastes revealed that the carbon nanotubes are well incorporated in the cementitious matrix, with the hydrated cement grains interconnected by long carbon nanotubes. XRD characterizations demonstrated that, during the hydration of cement pastes, different peaks emerged that were associated with ettringite, hydrated calcium silicate, and calcium hydroxide, among other structures. Results of the compressive strength measurements for mortars simultaneously mixed with MWCNT-Nx and MWCNT-Ox reached an increment of approximately 30% in compressive strength. In addition, density functional theory calculations were performed in nitrogen-doped and oxygen-functionalized carbon nanotubes interacting with a cement grain.

  11. Simultaneous voltammetric determination of tramadol and acetaminophen using carbon nanoparticles modified glassy carbon electrode

    Energy Technology Data Exchange (ETDEWEB)

    Ghorbani-Bidkorbeh, Fatemeh [Department of Chemistry, Sharif University of Technology, Tehran 11155-9516 (Iran, Islamic Republic of); Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Shahrokhian, Saeed, E-mail: shahrokhian@sharif.ed [Department of Chemistry, Sharif University of Technology, Tehran 11155-9516 (Iran, Islamic Republic of); Institute for Nanoscience and Technology, Sharif University of Technology, Tehran (Iran, Islamic Republic of); Mohammadi, Ali [Department of Drug and Food Control, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Dinarvand, Rassoul [Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Nanotechnology Research Centre, Faculty of Pharmacy, Tehran University of Medical Sciences, P.O. Box 14155-6451, Tehran (Iran, Islamic Republic of)

    2010-03-01

    A sensitive and selective electrochemical sensor was fabricated via the drop-casting of carbon nanoparticles (CNPs) suspension onto a glassy carbon electrode (GCE). The application of this sensor was investigated in simultaneous determination of acetaminophen (ACE) and tramadol (TRA) drugs in pharmaceutical dosage form and ACE determination in human plasma. In order to study the electrochemical behaviors of the drugs, cyclic and differential pulse voltammetric studies of ACE and TRA were carried out at the surfaces of the modified GCE (MGCE) and the bare GCE. The dependence of peak currents and potentials on pH, concentration and the potential scan rate were investigated for these compounds at the surface of MGCE. Atomic force microscopy (AFM) was used for the characterization of the film modifier and its morphology on the surface of GCE. The results of the electrochemical investigations showed that CNPs, via a thin layer model based on the diffusion within a porous layer, enhanced the electroactive surface area and caused a remarkable increase in the peak currents. The thin layer of the modifier showed a catalytic effect and accelerated the rate of the electron transfer process. Application of the MGCE resulted in a sensitivity enhancement and a considerable decrease in the anodic overpotential, leading to negative shifts in peak potentials. An optimum electrochemical response was obtained for the sensor in the buffered solution of pH 7.0 and using 2 muL CNPs suspension cast on the surface of GCE. Using differential pulse voltammetry, the prepared sensor showed good sensitivity and selectivity for the determination of ACE and TRA in wide linear ranges of 0.1-100 and 10-1000 muM, respectively. The resulted detection limits for ACE and TRA was 0.05 and 1 muM, respectively. The CNPs modified GCE was successfully applied for ACE and TRA determinations in pharmaceutical dosage forms and also for the determination of ACE in human plasma.

  12. Biochips Containing Arrays of Carbon-Nanotube Electrodes

    Science.gov (United States)

    Li, Jun; Meyyappan, M.; Koehne, Jessica; Cassell, Alan; Chen, Hua

    2008-01-01

    Biochips containing arrays of nanoelectrodes based on multiwalled carbon nanotubes (MWCNTs) are being developed as means of ultrasensitive electrochemical detection of specific deoxyribonucleic acid (DNA) and messenger ribonucleic acid (mRNA) biomarkers for purposes of medical diagnosis and bioenvironmental monitoring. In mass production, these biochips could be relatively inexpensive (hence, disposable). These biochips would be integrated with computer-controlled microfluidic and microelectronic devices in automated hand-held and bench-top instruments that could be used to perform rapid in vitro genetic analyses with simplified preparation of samples. Carbon nanotubes are attractive for use as nanoelectrodes for detection of biomolecules because of their nanoscale dimensions and their chemical properties.

  13. Towards ultrathick battery electrodes: aligned carbon nanotube-enabled architecture.

    Science.gov (United States)

    Evanoff, Kara; Khan, Javed; Balandin, Alexander A; Magasinski, Alexandre; Ready, W Jud; Fuller, Thomas F; Yushin, Gleb

    2012-01-24

    Vapor deposition techniques were utilized to synthesize very thick (∼1 mm) Li-ion battery anodes consisting of vertically aligned carbon nanotubes coated with silicon and carbon. The produced anode demonstrated ultrahigh thermal (>400 W·m(-1) ·K(-1)) and high electrical (>20 S·m(-1)) conductivities, high cycle stability, and high average capacity (>3000 mAh·g(Si) (-1)). The processes utilized allow for the conformal deposition of other materials, thus making it a promising architecture for the development of Li-ion anodes and cathodes with greatly enhanced electrical and thermal conductivities.

  14. Fabrication of free-standing carbon nanotube electrode arrays on a quartz wafer

    Energy Technology Data Exchange (ETDEWEB)

    Chang, W.S., E-mail: paul@kimm.re.k [Division of Nano-Mechanical Systems, Korea Institute of Machinery and Materials, 104 Sinseongno, Yuseong-gu, Daejeon, 305-343 (Korea, Republic of); Kim, J.W. [Gyeongbuk Hybrid Technology Institute, 36 Goeyeon-dong, Yeongcheon, Gyeongbuk, 770-170 (Korea, Republic of); Choi, D.G. [Division of Nano-Mechanical Systems, Korea Institute of Machinery and Materials, 104 Sinseongno, Yuseong-gu, Daejeon, 305-343 (Korea, Republic of); Han, C.S. [Gyeongbuk Hybrid Technology Institute, 36 Goeyeon-dong, Yeongcheon, Gyeongbuk, 770-170 (Korea, Republic of)

    2010-09-01

    For this paper, the fabrication of nano-electrodes by the synthesis of multi-wall carbon nanotubes (MWCNTs) has been investigated. MWCNTs were grown on a TiN coated quartz plate with Fe catalysts patterned by UV nano-imprint lithography (NIL). The proposed study is the realization of a simple, inexpensive and reproducible method to produce nano-scale electrode arrays in large areas. The patterns were defined by an array of circles 200 nm in diameter, and 500 nm in pitch. The nano-patterned master and Fe catalyst are observed with good pattern fidelity over a large area by atomic force microscope (AFM) and scanning electron microscopy (SEM). Among various synthesis methods for carbon nanotube growth, plasma-enhanced chemical-vapor deposition (PECVD) was used for the growth of vertically aligned multi-wall carbon nanotube arrays. Ammonia (NH{sub 3}) and acetylene (C{sub 2}H{sub 2}) were used as the etchant gases and the carbon source, respectively. The carbon nanotubes were vertically aligned in high density on a large area of the plain quartz substrates. High-resolution transmission electron microscopy analysis reveals that the synthesized CNTs are multi-walled with a bamboo-like structure. Patterned catalysts made it possible to allow the precise placement of individual CNT electrodes on the substrate. These electrodes have diameters ranging from 50 nm to 100 nm and lengths of about 300 nm. A field emission test using isolated CNTs on quartz plates showed the ability of CNTs as nano-electrodes. Bio-compatibility was also investigated by cell culturing on the fabricated CNTs/quartz template for potential bio-applications.

  15. Influence of KOH activation techniques on pore structure and electrochemical property of carbon electrode materials

    Institute of Scientific and Technical Information of China (English)

    LI Jing; LI Jie; LAI Yan-qing; SONG Hai-sheng; ZHANG Zhi-an; LIU Ye-xiang

    2006-01-01

    Taking the selection of coal-tar pitch as precursor and KOH as activated agent, the activated carbon electrode material was fabricated for supercapacitor. The surface area and the pore structure of activated carbon were analyzed by Nitro adsorption method. The electrochemical properties of the activated carbons were determined using two-electrode capacitors in 6 mol/L KOH aqueous electrolytes. The influences of activated temperature and mass ratio ofKOH to C on the pore structure and electrochemical property of porous activated carbon were investigated in detail. The reasons for the changes of pore structure and electrochemical performance of activated carbon prepared under different conditions were also discussed theoretically. The results indicate that the maximum specific capacitance of 240 F/g can be obtained in alkaline medium, and the surface area, the pore structure and the specific capacitance of activated carbon depend on the treatment methods; the capacitance variation of activated carbon cannot be interpreted only by the change of surface area and pore structure, the lattice order and the electrolyte wetting effect of the activated carbon should also be taken into account.

  16. Immobilization of Nafion-ordered mesoporous carbon on a glassy carbon electrode: Application to the detection of epinephrine

    Energy Technology Data Exchange (ETDEWEB)

    Zhou Ming [Faculty of Chemistry, Northeast Normal University, Renmin Street 5268, Changchun 130024 (China); Guo Liping [Faculty of Chemistry, Northeast Normal University, Renmin Street 5268, Changchun 130024 (China)], E-mail: guolp078@nenu.edu.cn; Hou Ying; Peng Xiaojuan [Faculty of Chemistry, Northeast Normal University, Renmin Street 5268, Changchun 130024 (China)

    2008-05-01

    A stable suspension of ordered mesoporous carbon (OMC) was obtained by dispersing OMC in a solution of Nafion. By coating the suspension onto glassy carbon (GC) electrode, cyclic voltammetry was used to evaluate the electrochemical behaviors of Nafion-OMC-modified GC (Nafion-OMC/GC) electrode in 0.1 mmol L{sup -1} hexaammineruthenium(III) chloride (Ru(NH{sub 3}){sub 6}Cl{sub 3})/0.1 mol L{sup -1} KCl solution, where Nafion-OMC/GC electrode shows a faster electron transfer rate as compared with OMC/GC, Nafion/GC and GC electrodes. Due to the unique properties of Nafion-OMC, an obvious decrease in the overvoltage of the epinephrine (EP) oxidation (ca. 100 mV at pH 4.1 and 115 mV at pH 7.0) as well as a dramatic increase in the peak current (12 times at pH 4.1 and 6 times at pH 7.0) was observed at Nafion-OMC/GC electrode compared to that seen at GC electrode. By combining the advantages of OMC with those of Nafion, the anodic peak of EP and that of ascorbic acid (AA) were separated successfully (by ca. 144-270 mV) in the pH range of 2.0-10.0, which may make Nafion-OMC/GC electrode potential for selective determination of EP in the presence of AA at a broad pH range. As an EP sensor, the EP amperometric response at Nafion-OMC/GC electrode in pH 7.0 PBS is extremely stable, with 99% of the initial activity remaining (compared to 32% at GC surface) after 120 min stirring of 0.20 mmol L{sup -1} EP. And Nafion-OMC/GC electrode can be used to readily detect the physiological concentration of EP at pH 7.0. These make Nafion-OMC/GC electrode potential candidates for stable and efficient electrochemical sensor for the detection of EP. The solubilization of OMC by Nafion may provide a route to more precise manipulation, and functionalization for the construction of OMC-based sensors, as well as allowing OMC to be introduced to biologically relevant systems.

  17. Electrochemical reduction of dilute chromate solutions on carbon felt electrodes

    NARCIS (Netherlands)

    Frenzel, Ines; Holdik, Hans; Barmashenko, Vladimir; Stamatialis, Dimitrios F.; Wessling, Matthias

    2006-01-01

    Carbon felt is a potential material for electrochemical reduction of chromates. Very dilute solutions may be efficiently treated due to its large specific surface area and high porosity. In this work, the up-scaling of this technology is investigated using a new type of separated cell and once-throu

  18. Characterization of Microporous Activated Carbon Electrodes for Electric Double-layer Capacitors

    Institute of Scientific and Technical Information of China (English)

    MENG Qing-han; LIU Ling; SONG Huai-he

    2004-01-01

    Activated carbons (ACs) with a wide range of surface areas were made from petroleum coke by means of KOH activation. The electrochemical characterization was carried out for several activated carbons used as polariz able electrodes of electric double-layer capacitors (EDLCs) in an aqueous electrolytic solution. The porous structures and electrochemical double-layer capacitance of the activated carbons were investigated by virtue of nitrogen gas adsorption and constant current cycling(CCC) methods. The relationship among the surface area, pore volume of the activated carbons and specific double-layer capacitance was discussed. It was found that the specific capacitance of ACs increased linearly with the increase of surface area. The presence of mesopores in the activated carbons with very high surface area(>2000 m2/g) was not very effective for them to be used as EDLCs. The influence of chemical characteristics of the activated carbons on the double layer formation could be considered to be negligible.

  19. Disposable planar reference electrode based on carbon nanotubes and polyacrylate membrane.

    Science.gov (United States)

    Rius-Ruiz, F Xavier; Bejarano-Nosas, Diego; Blondeau, Pascal; Riu, Jordi; Rius, F Xavier

    2011-07-15

    In this technical note, we report a new all-solid-state planar reference electrode based on single-walled carbon nanotubes and photocured poly(n-butylacrylate) (poly(nBA)) membrane containing the Ag/AgCl/Cl(-) ion system. Single-walled carbon nanotubes functionalized with octadecylamide (SWCNT-ODA) and deposited by drop-casting onto a disposable screen-printed electrode are an excellent all-solid-state transducer. The novel potentiometric planar reference electrode shows low potential variability (calibration slopes inferior to 2 mV/dec) for a wide range of chemical species (i.e., ions, small molecules, proteins) in a wide calibration range, redox pairs, changes in pH, and changes in ambient light. Potentiometric medium-term signal stability (-0.9 ± 0.2 mV/h) and electrochemical impedance characterization confirm the correct solid contact between the SWCNT-ODA layer and photocured poly(nBA) membrane. Overall, the materials used and the simple fabrication by screen-printing and drop-casting enable a high throughput and highly parallel and cost-effective mass manufacture of the new disposable reference electrode. Moreover, the reference electrode has a long shelf life, a characteristic that can be of special interest in decentralized and multiplexing potentiometric analysis.

  20. Graphene and carbon nanotube composite electrodes for supercapacitors with ultra-high energy density.

    Science.gov (United States)

    Cheng, Qian; Tang, Jie; Ma, Jun; Zhang, Han; Shinya, Norio; Qin, Lu-Chang

    2011-10-21

    We describe a graphene and single-walled carbon nanotube (SWCNT) composite film prepared by a blending process for use as electrodes in high energy density supercapacitors. Specific capacitances of 290.6 F g(-1) and 201.0 F g(-1) have been obtained for a single electrode in aqueous and organic electrolytes, respectively, using a more practical two-electrode testing system. In the organic electrolyte the energy density reached 62.8 Wh kg(-1) and the power density reached 58.5 kW kg(-1). The addition of single-walled carbon nanotubes raised the energy density by 23% and power density by 31% more than the graphene electrodes. The graphene/CNT electrodes exhibited an ultra-high energy density of 155.6 Wh kg(-1) in ionic liquid at room temperature. In addition, the specific capacitance increased by 29% after 1000 cycles in ionic liquid, indicating their excellent cyclicity. The SWCNTs acted as a conductive additive, spacer, and binder in the graphene/CNT supercapacitors. This work suggests that our graphene/CNT supercapacitors can be comparable to NiMH batteries in performance and are promising for applications in hybrid vehicles and electric vehicles.

  1. Low-dimensional carbon and MXene-based electrochemical capacitor electrodes

    Science.gov (United States)

    Yoon, Yeoheung; Lee, Keunsik; Lee, Hyoyoung

    2016-04-01

    Due to their unique structure and outstanding intrinsic physical properties such as extraordinarily high electrical conductivity, large surface area, and various chemical functionalities, low-dimension-based materials exhibit great potential for application in electrochemical capacitors (ECs). The electrical properties of electrochemical capacitors are determined by the electrode materials. Because energy charge storage is a surface process, the surface properties of the electrode materials greatly influence the electrochemical performance of the cell. Recently, graphene, a single layer of sp2-bonded carbon atoms arrayed into two-dimensional carbon nanomaterial, has attracted wide interest as an electrode material for electrochemical capacitor applications due to its unique properties, including a high electrical conductivity and large surface area. Several low-dimensional materials with large surface areas and high conductivity such as onion-like carbons (OLCs), carbide-derived carbons (CDCs), carbon nanotubes (CNTs), graphene, metal hydroxide, transition metal dichalcogenides (TMDs), and most recently MXene, have been developed for electrochemical capacitors. Therefore, it is useful to understand the current issues of low-dimensional materials and their device applications.

  2. Past explosive outbursts of entrapped carbon dioxide in salt mines provide a new perspective on the hazards of carbon dioxide

    DEFF Research Database (Denmark)

    Hedlund, Frank Huess

    2013-01-01

    This paper reports on a source of past carbon dioxide accidents which so far has only been sporadically mentioned in the literature. Violent and highly destructive outbursts of hundreds of tons of CO2 occurred regularly, if not routinely, in the now closed salt mines of the former DDR....... The Menzengraben mine experienced an extreme outburst in 1953, possibly involving a several thousand tons of carbon dioxide. This source of accidents fills an important gap in the available carbon dioxide accident history and may provide a unique empirical perspective on the hazards of handling very large amounts...

  3. Electrochemical impedance-based DNA sensor using a modified single walled carbon nanotube electrode

    Energy Technology Data Exchange (ETDEWEB)

    Weber, Jessica E. [Department of Mechanical Engineering, University of South Florida, Tampa, FL (United States); Nanomaterials and Nanomanufacturing Research Center, University of South Florida, Tampa, FL (United States); Pillai, Shreekumar [Center for NanoBiotechnology Research, Alabama State University, Montgomery, AL (United States); Ram, Manoj Kumar, E-mail: mkram@usf.edu [Department of Mechanical Engineering, University of South Florida, Tampa, FL (United States); Nanomaterials and Nanomanufacturing Research Center, University of South Florida, Tampa, FL (United States); Kumar, Ashok [Department of Mechanical Engineering, University of South Florida, Tampa, FL (United States); Nanomaterials and Nanomanufacturing Research Center, University of South Florida, Tampa, FL (United States); Singh, Shree R. [Center for NanoBiotechnology Research, Alabama State University, Montgomery, AL (United States)

    2011-07-20

    Carbon nanotubes have become promising functional materials for the development of advanced electrochemical biosensors with novel features which could promote electron-transfer with various redox active biomolecules. This paper presents the detection of Salmonella enterica serovar Typhimurium using chemically modified single walled carbon nanotubes (SWNTs) with single stranded DNA (ssDNA) on a polished glassy carbon electrode. Hybridization with the corresponding complementary ssDNA has shown a shift in the impedance studies due to a higher charge transfer in ssDNA. The developed biosensor has revealed an excellent specificity for the appropriate targeted DNA strand. The methodologies to prepare and functionalize the electrode could be adopted in the development of DNA hybridization biosensor.

  4. Carbon nanotubes functionalized by salts containing stereogenic heteroatoms as electrodes in their battery cells

    Directory of Open Access Journals (Sweden)

    Zdanowska Sandra

    2016-12-01

    Full Text Available This paper concentrates on electrochemical properties of groups of multi-walled carbon nanotubes (MWCNT functionalized with substituents containing a stereogenic heteroatom bonded covalently to the surface of the carbon nanotube. This system was tested in Swagelok-type cells. The cells comprised a system (functionalized CNT with salts containing S and P atoms with a working electrode, microfiber separators soaked with electrolyte solution, and a lithium foil counter/reference (commercial LiCoO2 electrode. The electrolyte solution was 1 M LiPF6 in propylene carbonate. Using standard techniques (cyclic voltammetry/chronopotentiometry, galvanostatic cycling was performed on the cells at room temperature with a CH Instruments Model 600E potentiostat/galvanostat electrochemical measurements. Methods of functionalization CNT were compared in terms of the electrochemical properties of the studied systems. In all systems, the process of charge/discharge was observed.

  5. CO2 Activated Carbon Aerogel with Enhanced Electrochemical Performance as a Supercapacitor Electrode Material.

    Science.gov (United States)

    Lee, Eo Jin; Lee, Yoon Jae; Kim, Jeong Kwon; Hong, Ung Gi; Yi, Jongheop; Yoon, Jung Rag; Song, In Kyu

    2015-11-01

    Carbon aerogel (CA) was prepared by a sol-gel polymerization of resorcinol and formaldehyde in ambient conditions. A series of activated carbon aerogels (ACA-X, X = 1, 2, 3, 4, 5, and 6 h) were then prepared by CO2 activation of CA with a variation of activation time (X) for use as an electrode material for supercapacitor. Specific capacitances of CA and ACA-X electrodes were measured by cyclic voltammetry and galvanostatic charge/discharge methods in 6 M KOH electrolyte. Among the samples, ACA-5 h showed the highest BET surface area (2574 m2/g) and the highest specific capacitance (100 F/g). It was found that CO2 activation was a very efficient method for enhancing physicochemical property and supercapacitive electrochemical performance of activated carbon aerogel.

  6. Simulation of capacity loss in carbon electrode for lithium-ion cells during storage

    Science.gov (United States)

    Ramasamy, Ramaraja P.; Lee, Jong-Won; Popov, Branko N.

    A mathematical model was developed which simulates the self-discharge capacity losses in the carbon anode for a SONY 18650 lithium-ion battery. The model determines the capacity loss during storage on the basis of a continuous reduction of organic solvent and de-intercalation of lithium at the carbon/electrolyte interface. The state of charge, open circuit potential, capacity loss and film resistance on the carbon electrode were calculated as a function of storage time using different values of rate constant governing the solvent reduction reaction.

  7. Fabrication, characterization, and functionalization of dual carbon electrodes as probes for scanning electrochemical microscopy (SECM).

    Science.gov (United States)

    McKelvey, Kim; Nadappuram, Binoy Paulose; Actis, Paolo; Takahashi, Yasufumi; Korchev, Yuri E; Matsue, Tomokazu; Robinson, Colin; Unwin, Patrick R

    2013-08-01

    Dual carbon electrodes (DCEs) are quickly, easily, and cheaply fabricated by depositing pyrolytic carbon into a quartz theta nanopipet. The size of DCEs can be controlled by adjusting the pulling parameters used to make the nanopipet. When operated in generation/collection (G/C) mode, the small separation between the electrodes leads to reasonable collection efficiencies of ca. 30%. A three-dimensional finite element method (FEM) simulation is developed to predict the current response of these electrodes as a means of estimating the probe geometry. Voltammetric measurements at individual electrodes combined with generation/collection measurements provide a reasonable guide to the electrode size. DCEs are employed in a scanning electrochemical microscopy (SECM) configuration, and their use for both approach curves and imaging is considered. G/C approach curve measurements are shown to be particularly sensitive to the nature of the substrate, with insulating surfaces leading to enhanced collection efficiencies, whereas conducting surfaces lead to a decrease of collection efficiency. As a proof-of-concept, DCEs are further used to locally generate an artificial electron acceptor and to follow the flux of this species and its reduced form during photosynthesis at isolated thylakoid membranes. In addition, 2-dimensional images of a single thylakoid membrane are reported and analyzed to demonstrate the high sensitivity of G/C measurements to localized surface processes. It is finally shown that individual nanometer-size electrodes can be functionalized through the selective deposition of platinum on one of the two electrodes in a DCE while leaving the other one unmodified. This provides an indication of the future versatility of this type of probe for nanoscale measurements and imaging.

  8. Electrochemical Oxidation of Paracetamol Mediated by MgB2 Microparticles Modified Glassy Carbon Electrode

    Directory of Open Access Journals (Sweden)

    Mohammed Zidan

    2011-01-01

    Full Text Available A MgB2 microparticles modified glassy carbon electrode (MgB2/GCE was fabricated by adhering microparticles of MgB2 onto the electrode surface of GCE. It was used as a working electrode for the detection of paracetamol in 0.1 M KH2PO4 aqueous solution during cyclic voltammetry. Use of the MgB2/GCE the oxidation process of paracetamol with a current enhancement significantly by about 2.1 times. The detection limit of this modified electrode was found to be 30 μM. The sensitivity under conditions of cyclic voltammetry is significantly dependent on pH, supporting electrolyte, temperature and scan rate. The current enhancement observed in different electrolytic media varied in the following order: KH2PO4 > KCl > K2SO4 > KBr. Interestingly, the oxidation of paracetamol using modified GC electrode remain constant even after 15 cycling. It is therefore evident that the MgB2 modified GC electrode possesses some degree of stability. A slope of 0.52 dependent of scan rate on current indicates that the system undergoes diffusion-controlled process.

  9. Spontaneous adsorption and electrochemical behaviour of safranine O at electrochemically activated glassy carbon electrode

    Energy Technology Data Exchange (ETDEWEB)

    Abdessamad, NourElHouda [Laboratoire de Chimie Analytique et d' Electrochimie, Institut National des Sciences Appliquees et de Technologie, Centre Urbain Nord B.P. No. 676, 1080 Tunis Cedex (Tunisia); Adhoum, Nafaa, E-mail: Nafaa.adhoum@insat.rnu.tn [Laboratoire de Chimie Analytique et d' Electrochimie, Institut National des Sciences Appliquees et de Technologie, Centre Urbain Nord B.P. No. 676, 1080 Tunis Cedex (Tunisia)

    2009-08-15

    The adsorption behaviour of safranine O (SO) at electrochemically pretreated glassy carbon electrodes has been studied. It was found that SO adsorption depended on the properties of the electrode surface, as determined by the nature and duration of the activation step. It was noticed that SO was adsorbed spontaneously and strongly on the surface of anodically pretreated electrode. The electrochemical behaviour of the modified electrode was investigated in H{sub 2}SO{sub 4} (0.25 M) using cyclic voltammetry (CV). A reversible two electron, two proton wave was observed at -180 mV vs. SCE and the formal potential was found to be decreasing upon increasing the solution pH (-56.8 mV pH{sup -1}). The modified electrode exhibited good stability on repeated scanning between -500 and 200 mV vs. SCE, causing only 5% decrease in the peak height after 100 cycles at a scan rate of 20 mV s{sup -1}. The surface coverage was calculated to be 0.812 nmol cm{sup -2} and the electron transfer rate constant (k{sub s}{sup 0}=1.45s{sup -1}) and transfer coefficient ({alpha} = 0.43) for the adsorbed SO were evaluated using the Laviron method. The modified electrode clearly showed good electrocatalytic ability for oxygen reduction to H{sub 2}O{sub 2}.

  10. Determination of Mercury (II Ion on Aryl Amide-Type Podand-Modified Glassy Carbon Electrode

    Directory of Open Access Journals (Sweden)

    Sevgi Güney

    2011-01-01

    Full Text Available A new voltammetric sensor based on an aryl amide type podand, 1,8-bis(o-amidophenoxy-3,6-dioxaoctane, (AAP modified glassy carbon electrode, was described for the determination of trace level of mercury (II ion by cyclic voltammetry (CV and differential pulse voltammetry (DPV. A well-defined anodic peak corresponding to the oxidation of mercury on proposed electrode was obtained at 0.2 V versus Ag/AgCl reference electrode. The effect of experimental parameters on differential voltammetric peak currents was investigated in acetate buffer solution of pH 7.0 containing 1 × 10−1 mol L−1 NaCl. Mercury (II ion was preconcentrated at the modified electrode by forming complex with AAP under proper conditions and then reduced on the surface of the electrode. Interferences of Cu2+, Pb2+, Fe3+, Cd2+, and Zn2+ ions were also studied at two different concentration ratios with respect to mercury (II ions. The modified electrode was applied to the determination of mercury (II ions in seawater sample.

  11. Thermo-Electrochemical Cells Based on Carbon Nanotube Electrodes by Electrophoretic Deposition

    Institute of Scientific and Technical Information of China (English)

    Weijin Qian; Mingxuan Cao; Fei Xie; Changkun Dong

    2016-01-01

    Drawbacks of low efficiency and high cost of the electrode materials have restricted the wide applications of the thermo-electrochemical cells (TECs). Due to high specific areas and electrical conductivities, the low cost multi-walled carbon nanotubes (MWNTs) are promising alternative electrode materials. In this work, the MWNT films of up to 16 cm2 were synthesized on stainless steel substrates by the electrophoretic deposition (EPD) to make the thermo-electrochemical electrodes. MWNT electrodes based on TECs were characterized by cyclic voltammetry and the long-term stability tests with the potassium ferri/ferrocyanide electrolyte. The TECs reached the current density of 45.2 A m-2 and the maximum power density of 0.82 W m-2. The relative power conversion efficiency of the MWNT electrode is 50%higher than that for the Pt electrode. Meanwhile, the TECs was operated continuously for 300 h without performance degradation. With the priorities of low cost and simple fabrication, EPD-based MWNT TECs may become commercially viable.

  12. Electrodeposited nickel oxide and graphene modified carbon ionic liquid electrode for electrochemical myglobin biosensor

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Wei, E-mail: swyy26@hotmail.com [College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158 (China); Gong, Shixing; Deng, Ying; Li, Tongtong; Cheng, Yong [College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Wang, Wencheng [College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158 (China); Wang, Lei [College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China)

    2014-07-01

    By using ionic liquid 1-hexylpyridinium hexafluorophosphate based carbon ionic liquid electrode (CILE) as the substrate electrode, graphene (GR) and nickel oxide (NiO) were in situ electrodeposited step by step to get a NiO/GR nanocomposite modified CILE. Myoglobin (Mb) was further immobilized on the surface of NiO/GR/CILE with a Nafion film to get the electrochemical sensor denoted as Nafion/Mb/NiO/GR/CILE. Cyclic voltammetric experiments indicated that a pair of well-defined quasi-reversible redox peaks appeared in pH 3.0 phosphate buffer solution with the formal peak potential (E{sup 0′}) located at − 0.188 V (vs. SCE), which was the typical characteristics of Mb Fe(III)/Fe(II) redox couples. So the direct electron transfer of Mb was realized and promoted due to the presence of the NiO/GR nanocomposite on the electrode. Based on the cyclic voltammetric data, the electrochemical parameters of Mb on the modified electrode were calculated. The Mb modified electrode showed an excellent electrocatalytic activity towards the reduction of different substrates including trichloroacetic acid and H{sub 2}O{sub 2}. Therefore a third-generation electrochemical Mb biosensor based on NiO/GR/CILE was constructed with good stability and reproducibility. - Highlights: • Graphene and nickel oxide nanocomposites were prepared by electrodeposition. • Electrochemical myoglobin sensor was prepared on a nanocomposite modified electrode. • Direct electrochemistry and electrocatalysis of myglobin were realized.

  13. Solid-contact pH-selective electrode using multi-walled carbon nanotubes.

    Science.gov (United States)

    Crespo, Gastón A; Gugsa, Derese; Macho, Santiago; Rius, F Xavier

    2009-12-01

    Multi-walled carbon nanotubes (MWCNT) are shown to be efficient transducers of the ionic-to-electronic current. This enables the development of a new solid-contact pH-selective electrode that is based on the deposition of a 35-microm thick layer of MWCNT between the acrylic ion-selective membrane and the glassy carbon rod used as the electrical conductor. The ion-selective membrane was prepared by incorporating tridodecylamine as the ionophore, potassium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate as the lipophilic additive in a polymerized methylmethacrylate and an n-butyl acrylate matrix. The potentiometric response shows Nernstian behaviour and a linear dynamic range between 2.89 and 9.90 pH values. The response time for this electrode was less than 10 s throughout the whole working range. The electrode shows a high selectivity towards interfering ions. Electrochemical impedance spectroscopy and chronopotentiometry techniques were used to characterise the electrochemical behaviour and the stability of the carbon-nanotube-based ion-selective electrodes.

  14. Electrochemical performance of porous diamond-like carbon electrodes for sensing hormones, neurotransmitters, and endocrine disruptors.

    Science.gov (United States)

    Silva, Tiago A; Zanin, Hudson; May, Paul W; Corat, Evaldo J; Fatibello-Filho, Orlando

    2014-12-10

    Porous diamond-like carbon (DLC) electrodes have been prepared, and their electrochemical performance was explored. For electrode preparation, a thin DLC film was deposited onto a densely packed forest of highly porous, vertically aligned multiwalled carbon nanotubes (VACNT). DLC deposition caused the tips of the carbon nanotubes to clump together to form a microstructured surface with an enlarged surface area. DLC:VACNT electrodes show fast charge transfer, which is promising for several electrochemical applications, including electroanalysis. DLC:VACNT electrodes were applied to the determination of targeted molecules such as dopamine (DA) and epinephrine (EP), which are neurotransmitters/hormones, and acetaminophen (AC), an endocrine disruptor. Using simple and low-cost techniques, such as cyclic voltammetry, analytical curves in the concentration range from 10 to 100 μmol L(-1) were obtained and excellent analytical parameters achieved, including high analytical sensitivity, good response stability, and low limits of detection of 2.9, 4.5, and 2.3 μmol L(-1) for DA, EP, and AC, respectively.

  15. Carbon nanotube modification of microbial fuel cell electrodes.

    Science.gov (United States)

    Yazdi, Alireza Ahmadian; D'Angelo, Lorenzo; Omer, Nada; Windiasti, Gracia; Lu, Xiaonan; Xu, Jie

    2016-11-15

    The use of carbon nanotubes (CNTs) for energy harvesting devices is preferable due to their unique mechanical, thermal, and electrical properties. On the other hand, microbial fuel cells (MFCs) are promising devices to recover carbon-neutral energy from the organic matters, and have been hindered with major setbacks towards commercialization. Nanoengineered CNT-based materials show remarkable electrochemical properties, and therefore have provided routes towards highly effective modification of MFC compartments to ultimately reach the theoretical limits of biomass energy recovery, low-cost power production, and thus the commercialization of MFCs. Moreover, these CNT-based composites offer significant flexibility in the design of MFCs that enable their use for a broad spectrum of applications ranging from scaled-up power generation to medically related devices. This article reviews the recent advances in the modification of MFCs using CNTs and CNT-based composites, and the extent to which each modification route impacts MFC power and current generation.

  16. The use of capacitive deionization with carbon aerogel electrodes to remove inorganic contaminants from water

    Energy Technology Data Exchange (ETDEWEB)

    Farmer, J.C.; Fix, D.V.; Mack, G.V.; Pekala, R.W.; Poco, J.F.

    1995-02-17

    The capacitive deionization of water with a stack of carbon aerogel electrodes has been successfully demonstrated for the first time. Unlike ion exchange, one of the more conventional deionization processes, no chemicals were required for regeneration of the system. Electricity was used instead. Water with various anions and cations was pumped through the electrochemical cell. After polarization, ions were electrostatically removed from the water and held in the electric double layers formed at electrode surfaces. The water leaving the cell was purified, as desired.

  17. Fabrication of a carbon nanotube protruding electrode array for a retinal prosthesis

    Science.gov (United States)

    Wang, Ke; Dai, Hongjie; Fishman, Harvey A.; Harris, James S.

    2005-01-01

    Implantable retinal prosthetic devices consisting of microelectrode arrays are being built in attempts to restore vision. Current retinal prostheses use metal planar electrodes. We are developing a novel electro-neural interface using carbon nanotube (CNT) bundles as flexible, protruding microelectrodes. We have synthesized vertically self-assembled, multi-walled CNT bundles by thermal chemical vapor deposition. Using conventional silicon-based micro-fabrication processes, these CNT bundles were integrated onto pre-patterned circuits. CNT protruding electrodes have significant potentials in providing safer stimulation for retinal prostheses. They could also act as recording units to sense electrical and chemical activities in neural systems for fundamental neuroscience research.

  18. Tracing organic matter sources and carbon burial in mangrove sediments over the past 160 years

    Science.gov (United States)

    Gonneea, Meagan Eagle; Paytan, Adina; Herrera-Silveira, Jorge A.

    2004-10-01

    Mangrove ecosystems may be a source of organic carbon and nutrients to adjacent coastal systems on one hand and provide a sedimentary sink for organic carbon on the other. The balance between these two functions may be sensitive to both natural and anthropogenically induced variability, yet these effects have not been thoroughly evaluated in mangrove ecosystems. We determine organic matter sources and carbon burial rates over the past 160 years in three lagoons on the Yucatan Peninsula, Mexico. Carbon isotopes and C/N elemental ratios are utilized to trace the three sources contributing to sedimentary organic matter, mangroves, seagrasses and phytoplankton, while nitrogen isotopes are used to elucidate potential post-depositional biogeochemical transformations in mangrove lagoon sediments. All three organic matter sources contribute to organic carbon burial. Phytoplankton and mangroves are the dominant sources of organic matter in lagoon bank sediments and seagrasses are a significant source to central lagoon sediments. Organic carbon burial rates are higher at the lagoon fringes, where mangrove vegetation dominates, than in seagrass-dominated mid-lagoon areas. A reduction in mangrove contribution to the sedimentary organic matter pool concurrent with reduced total organic carbon burial rates is observed in the recent past at all three lagoons studied. Natural cycles in sediment organic matter source over the past 160 years are observed in a high-resolution core. These fluctuations correspond to climatic variability in this region, as recorded in deep-sea foraminiferal assemblages. Additional work is required in order to differentiate between recent anthropogenic perturbations and natural variability in organic carbon sources and burial rates within these ecosystems.

  19. Effects of atmospheric air plasma treatment of graphite and carbon felt electrodes on the anodic current from Shewanella attached cells.

    Science.gov (United States)

    Epifanio, Monica; Inguva, Saikumar; Kitching, Michael; Mosnier, Jean-Paul; Marsili, Enrico

    2015-12-01

    The attachment of electrochemically active microorganisms (EAM) on an electrode is determined by both the chemistry and topography of the electrode surface. Pre-treatment of the electrode surface by atmospheric air plasma introduces hydrophilic functional groups, thereby increasing cell attachment and electroactivity in short-term experiments. In this study, we use graphite and carbon felt electrodes to grow the model EAM Shewanella loihica PV-4 at oxidative potential (0.2 V vs. Ag/AgCl). Cell attachment and electroactivity are measured through electrodynamic methods. Atmospheric air plasma pre-treatment increases cell attachment and current output at graphite electrodes by 25%, while it improves the electroactivity of the carbon felt electrodes by 450%. Air plasma pre-treatment decreased the coulombic efficiency on both carbon felt and graphite electrodes by 60% and 80%, respectively. Microbially produced flavins adsorb preferentially at the graphite electrode, and air plasma pre-treatment results in lower flavin adsorption at both graphite and carbon felt electrodes. Results show that air plasma pre-treatment is a feasible option to increase current output in bioelectrochemical systems.

  20. Electrocatalysis of chemically synthesized noble metal nanoparticles on carbon electrodes

    DEFF Research Database (Denmark)

    Zhang, Ling; Ulstrup, Jens; Zhang, Jingdong

    Noble metal nanoparticles (NPs), such as platinum (Pt) and palladium (Pd) NPs are promising catalysts for dioxygen reduction and oxidation of molecules such as formic acid and ethanol in fuel cells. Carbon nanomaterials are ideal supporting materials for electrochemical catalysts due to their good...... microscopy (AFM) which have proved to be highly efficient techniques to map the in situ structures of selfassembled molecular monolayers at molecular or sub-molecular resolution. Electrocatalysis of the Pd NPs immobilized on atomically flat, highly oriented pyrolytic graphite (HOPG) will be investigated...

  1. Multi-walled carbon nanotubes (MWCNT) as compliant electrodes for dielectric elastomer actuators

    Science.gov (United States)

    Chua, Soo-Lim; Neo, Xin-Hui; Lau, Gih-Keong

    2011-04-01

    A stacked dielectric elastomer actuator (DEA) consists of multiple layers of elastomeric dielectrics interleaved with compliant electrodes. It is capable of taking a tensile load if only the interleaving compliant electrodes provide a good bonding and enough elasticity. However, the stacked configuration of DEA was found to produce less actuation strain as compared to a single-layer configuration of pre-stretched membrane. It is believed the binder for compliant electrodes has a significant influence on the actuation strain. Yet, there has yet systematic study on the effect of binder. In this paper, we will study the effects of binder, solvent, and surface fictionalization on the compliant electrodes using the conductive filler of Multi-Walled Carbon Nanotube (MWCNT). Two types of binders are used, namely a soft silicone rubber (Mold Max 10T) and a soft silicone gel (Sylgard 527 gel). The present experiments show that the actuators using binders in the compliant electrodes produce a much lower areal strain as compared to the ones without binders in them. It is found that introducing a binder in the electrodes decreases the conductivity. The MWCNT compliant electrode with binder remains conductive (<1TΩ) up to a strain of 300%, whereas the one without binder remains conductive up to a strain of 800%. Changing the type of binder to a softer and less-viscous one increases the percolation ratio for MWCNT-COOH filler from 5% to 15% but this does not significantly increase the actuation strain. In addition, this study investigates the effect of MWCNT functionalization on the dielectric elastomeric actuation. The compliant electrodes using the MWCNT functionalized with (-COOH) group was also found to have a lower electrical conductivity and areal actuation strain, in comparison to the ones using the pristine MWCNT filler. In addition to binder, solvent for dispersing MWCNT-COOH was found to affect the actuation strain even though the solvent is eventually removed by

  2. Morphological and Electrochemical Properties of the Lactose-derived Carbon Electrode Materials

    Directory of Open Access Journals (Sweden)

    I.F. Myronyuk

    2016-11-01

    Full Text Available The article explores the morphological and electrochemical properties of carbon electrode materials derived from D-lactose by mixing of carbon precursor with activating reagent selected from a number КОН, K2CO3, ZnCl2, SnCl2∙2H2O, and calcining the composite mixture at 800 °С. After dissolution and removal of K2O, ZnO or SnO from volume of prototypes specific surface of carbon materials increases in 1,7-4,2 times, and electrical conductivity - in 1,4-2,8 times. The activating reagents for effective influence on the properties of carbon structures can be placed in the following order: ZnCl2  КОН  K2CO3  SnCl2∙2H2O. It is set that the highest specific capacity as an electrode material for supercapacitor has a sample with the highest electrical conductivity (78 Оhm – 1∙m – 1 obtained using KOH activating reagent. The electrode material capacity was 176-157 F∙g – 1 at discharge currents of 10-100 mA. It was found that the difference in the values of capacitance of prototypes caused by different chemical state of their surface.

  3. Morphological and Electrochemical Properties of the Lactose-derived Carbon Electrode Materials

    Directory of Open Access Journals (Sweden)

    I.F. Myronyuk

    2016-10-01

    Full Text Available The article explores the morphological and electrochemical properties of carbon electrode materials derived from D-lactose by mixing of carbon precursor with activating reagent selected from a number КОН, K2CO3, ZnCl2, SnCl2∙2H2O, and calcining the composite mixture at 800 °С. After dissolution and removal of K2O, ZnO or SnO from volume of prototypes specific surface of carbon materials increases in 1,7-4,2 times, and electrical conductivity - in 1,4-2,8 times. The activating reagents for effective influence on the properties of carbon structures can be placed in the following order: ZnCl2 > КОН > K2CO3 > SnCl2∙2H2O. It is set that the highest specific capacity as an electrode material for supercapacitor has a sample with the highest electrical conductivity (78 Оhm – 1∙m – 1 obtained using KOH activating reagent. The electrode material capacity was 176-157 F∙g – 1 at discharge currents of 10-100 mA. It was found that the difference in the values of capacitance of prototypes caused by different chemical state of their surface.

  4. Transparent Electrodes: A Review of the Use of Carbon-Based Nanomaterials

    Directory of Open Access Journals (Sweden)

    Edgar J. López-Naranjo

    2016-01-01

    Full Text Available Transparent conducting electrodes (TCE are extensively applied in a great range of optoelectronic and photovoltaic equipment (e.g., solar cells, touch panels, and flexible devices. Carbon-based nanomaterials are considered as suitable replacements to substitute traditional materials to manufacture TCE due to their remarkable characteristics, for example, high optical transmittance and outstanding electrical properties. In comparison with traditional indium tin oxide electrodes, carbon-based electrodes show good mechanical properties, chemical stability, and low cost. Nevertheless, major issues related to the development of good quality manufacture methods to produce carbon-based nanomaterials have to be overcome to meet massive market requirements. Hence, the development of alternative TCE materials as well as appropriate large production techniques that meet the requirements of a proper sheet resistance along with a high optical transparency is a priority. Therefore, in this work, we summarize and discuss novel production and synthesis methods, chemical treatments, and hybrid materials developed to satisfy the worldwide request for carbon-based nanomaterials.

  5. Direct Electrochemical Oxidation of NADPH at a Low Potential on the Carbon Nanotube Modified Glassy Carbon Electrode

    Institute of Scientific and Technical Information of China (English)

    CHEN, Jing(陈静); CAI, Chen-Xin(蔡称心)

    2004-01-01

    NADPH can be directly oxidized on a carbon nanotube modified glassy carbon (CNT/GC) electrode in phosphate buffer solution (pH=6.0) with a diminution of the overpotential of more than 700 mV. The anodic peak currents increase linearly with the increase of concentration of NADPH in the range of 5×10-7 to 1×10-3 mol/L with a detection limit of about 1×10-7 mol/L. The CNT/GC electrode exhibits high sensitivity, low potential and stability in detecting NADPH and thus might be used in biosensors to study the electrocatalytic reaction of important dehydrogenase-based biological systems.

  6. Application of multi-walled carbon nanotubes modified carbon ionic liquid electrode for electrocatalytic oxidation of dopamine.

    Science.gov (United States)

    Li, Yonghong; Liu, Xinsheng; Liu, Xiaoying; Mai, Nannan; Li, Yuandong; Wei, Wanzhi; Cai, Qingyun

    2011-11-01

    A simple, sensitive, and reliable method based on a multi-walled carbon nanotubes (MWNTs) modified carbon ionic liquid electrode (CILE) has been successfully developed for determination of dopamine (DA) in the presence of ascorbic acid (AA). The acid-treated MWNTs with carboxylic acid functional groups could promote the electron-transfer reaction of DA and inhibit the voltammetric response of AA. Due to the good performance of the ionic liquid, the electrochemical response of DA on the MWNTs/CILE was better than that of other MWNTs modified electrodes. Under the optimum conditions a linear calibration plot was obtained in the range 5.0×10(-8) to 2.0×10(-4) mol L(-1) and the detection limit was 1.0×10(-8) mol L(-1).

  7. Carbon deposition behaviour in metal-infiltrated gadolinia doped ceria electrodes for simulated biogas upgrading in solid oxide electrolysis cells

    Science.gov (United States)

    Duboviks, V.; Lomberg, M.; Maher, R. C.; Cohen, L. F.; Brandon, N. P.; Offer, G. J.

    2015-10-01

    One of the attractive applications for reversible Solid Oxide Cells (SOCs) is to convert CO2 into CO via high temperature electrolysis, which is particularly important for biogas upgrading. To improve biogas utility, the CO2 component can be converted into fuel via electrolysis. A significant issue for SOC operation on biogas is carbon-induced catalyst deactivation. Nickel is widely used in SOC electrodes for reasons of cost and performance, but it has a low tolerance to carbon deposition. Two different modes of carbon formation on Ni-based electrodes are proposed in the present work based on ex-situ Raman measurements which are in agreement with previous studies. While copper is known to be resistant towards carbon formation, two significant issues have prevented its application in SOC electrodes - namely its relatively low melting temperature, inhibiting high temperature sintering, and low catalytic activity for hydrogen oxidation. In this study, the electrodes were prepared through a low temperature metal infiltration technique. Since the metal infiltration technique avoids high sintering temperatures, Cu-Ce0.9Gd0.1O2-δ (Cu-CGO) electrodes were fabricated and tested as an alternative to Ni-CGO electrodes. We demonstrate that the performance of Cu-CGO electrodes is equivalent to Ni-CGO electrodes, whilst carbon formation is fully suppressed when operated on biogas mixture.

  8. Application of Polyaniline Incorporated Carbon Particles Coated Platinum Electrode in Coulometric Titration to Determination of Polyisoprene Alcohol

    Institute of Scientific and Technical Information of China (English)

    ZHAO Ge; LIU Meng; LIU Kuai-zhi; QU Jiang-ying; CHENG Gang; DU Zu-ling

    2003-01-01

    The feasibility of using electrodes modified with polyaniline incorporated carbon particles films for improving the precision of coulometric titration is demonstrated. The problem of large deviation produced during determining polyisoprene by coulometric titration with direct titration technique(double Pt electrodes indicating electrode) has been solved. In the titration process, polyisoprene alcohol, an electro-inactive species, is adsorbed on the surface of the bare Pt electrode, which inhibits the electrode reaction of Br- and Br2. Therefore, when the titration reaches the end-point, the detected current will slowly change with time, which can make the repeatability of end-point poor. The atomic force microscopic images show the morphology of the electrode surface of adsorbing polyisoprene alcohol. The application of the chemically modified electrode instead of the bare Pt electrode to indicating the end-point has been investigated. The results show that the Pt electrode coated with polyaniline incorporated carbon particles films is an excellent indicator electrode. This electrode has advantages that the indicating signals are sharp and repeatable at end-point. The precision and the accuracy of the determination of polyisoprene alcohol are satisfactory.

  9. Electrochemical behavior of adrenaline at the carbon atom wire modified electrode

    Energy Technology Data Exchange (ETDEWEB)

    Xue Kuanhong [Chemistry Department, Nanjing Normal University, Jiangsu Engineering Research Center for Bio-medical Function Materials, 122 NingHai Road, Nanjing, JiangSu 210097 (China)], E-mail: khxue@njnu.edu.cn; Liu Jiamei [Chemistry Department, Nanjing Normal University, Jiangsu Engineering Research Center for Bio-medical Function Materials, 122 NingHai Road, Nanjing, JiangSu 210097 (China); Wei Ribing [Chemistry Department, Nanjing Normal University, Jiangsu Engineering Research Center for Bio-medical Function Materials, 122 NingHai Road, Nanjing, JiangSu 210097 (China); Chen Shaopeng [Chemistry Department, Nanjing Normal University, Jiangsu Engineering Research Center for Bio-medical Function Materials, 122 NingHai Road, Nanjing, JiangSu 210097 (China)

    2006-09-11

    Electrochemical behavior of adrenaline at an electrode modified by