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Sample records for carbon paste electrode

  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

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    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. Electrocatalytic oxidation of ethanol using zeolite modified carbon paste electrode

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    Maryam Abrishamkar

    2014-12-01

    Full Text Available In this research application of synthesized ZSM-5 zeolite to prepare the modified carbon paste electrodes was studied. To prepare of modified electrode, the nickel ions as mediator for electrochemical oxidation of ethanol were doped to ZSM-5 zeolite framework through ion exchange mechanism and oxidation of ethanol on the surface of proposed electrode in the alkaline solution was investigated using cyclic voltammetry and chronoamperometry methods. Also, the catalytic rate constant for oxidation of ethanol (k was reported.

  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. Comparative investigation on electrochemical behavior of hydroquinone at carbon ionic liquid electrode, ionic liquid modified carbon paste electrode and carbon paste electrode

    International Nuclear Information System (INIS)

    Ionic liquid, 1-heptyl-3-methylimidazolium hexafluorophosphate (HMIMPF6), has been used to fabricate two new electrodes, carbon ionic liquid electrode (CILE) and ionic liquid modified carbon paste electrode (IL/CPE), using graphite powder mixed with HMIMPF6 or the mixture of HMIMPF6/paraffin liquid as the binder, respectively. The electrochemical behaviors of hydroquinone at the CILE, the IL/CPE and the CPE were investigated in phosphate buffer solution. At all these electrodes, hydroquinone showed a pair of redox peaks. The order of the current response and the standard rate constant of hydroquinone at these electrodes were as follows: CILE > IL/CPE > CPE, while the peak-to-peak potential separation was in an opposite sequence: CILE < IL/CPE < CPE. The results show the superiority of CILE to IL/CPE and CPE, and IL/CPE to CPE in terms of promoting electron transfer, improving reversibility and enhancing sensitivity. The CILE was chosen as working electrode to determine hydroquinone by differential pulse voltammetry, which can be used for sensitive, simple and rapid determination of hydroquinone in medicated skin cosmetic cream

  7. Determination of ascorbic acid in pharmaceutical preparation and fruit juice using modified carbon paste electrode

    OpenAIRE

    Simona Žabčíková; Dai Long Vu; Libor Červenka; Vojtěch Tambor; Martina Vašatová

    2016-01-01

    Acrobic acid is key substance in the human metabolism and the rapid and accurate determination in food is of a great interest. Ascorbic acid is an electroactive compound, however poorly responded on the bare carbon paste electrodes. In this paper, brilliant cresyl blue and multi-walled carbon nanotubes were used for the modification of carbon paste electrode. Brilliant cresyl blue acts as a mediator improving the transition of electrons, whereas multiwalled carbon nanotubes increased the surf...

  8. 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.

  9. Carbon Paste Electrodes Made from Different Carbonaceous Materials: Application in the Study of Antioxidants

    OpenAIRE

    Constantin Apetrei; Maria Luz Rodriguez-Mendez; Jose Antonio De Saja; Irina Mirela Apetrei

    2011-01-01

    This work describes the sensing properties of carbon paste electrodes (CPEs) prepared from three different types of carbonaceous materials: graphite, carbon microspheres and carbon nanotubes. The electrochemical responses towards antioxidants including vanillic acid, catechol, gallic acid, L-ascorbic acid and L-glutathione have been analyzed and compared. It has been demonstrated that the electrodes based on carbon microspheres show the best performances in terms of kinetics and stability, wh...

  10. 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.

  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 sensor for Baicalein using a carbon paste electrode doped with carbon nanotubes

    International Nuclear Information System (INIS)

    We report on the voltammetric determination of the flavonoid Baicalein by using a carbon paste electrode that was doped with multi-walled carbon nanotubes. The resulting sensor exhibits excellent redox activity towards Baicalein due to the large surface area and good conductivity of the electrode. Cyclic voltammetry at various scan rates was used to investigate the redox properties of Baicalein. At the optimum conditions, the sensor displays a linear current response to Baicalein in the 0.02-10 μM concentration range, with a limit of detection of 4.2 n M. The method was successfully applied to the determination of Baicalein in spiked human blood serum samples and in a Chinese oral liquid. (author)

  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. Determination of ascorbic acid in pharmaceutical preparation and fruit juice using modified carbon paste electrode

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    Simona Žabčíková

    2016-06-01

    Full Text Available Acrobic acid is key substance in the human metabolism and the rapid and accurate determination in food is of a great interest. Ascorbic acid is an electroactive compound, however poorly responded on the bare carbon paste electrodes. In this paper, brilliant cresyl blue and multi-walled carbon nanotubes were used for the modification of carbon paste electrode. Brilliant cresyl blue acts as a mediator improving the transition of electrons, whereas multiwalled carbon nanotubes increased the surface of the electrode. Both brilliant cresyl blue and multiwalled carbon nanotubes were added directly to the composite material. The electrochemical behavior of modified electode was determined in electrolyte at various pH, and the effect of the scan rate was also performed. It was shown that the electrochemical process on the surface of the modified carbon paste electrode was diffusion-controlled. The resulted modified carbon paste electrode showed a good electrocatalytic activity towards the oxidation of ascorbic acid at a reduced overpotential of +100 mV descreasing the risk of interferences. A linear response of the ascorbic acid oxidation current measured by the amperometry in the range of 0.1 - 350 µmol.L-1 was obtained applying the sensor for the standard solution. The limit of detection and limit of quantification was found to be 0.05 and 0.15 µmol.L-1, respectively. The novel method was applied for the determination of ascorbic acid in pharmaceutical vitamin preparation and fruit juice, and the results were in good agreement with the standard HPLC method. The presented modification of carbon paste electrode is suitable for the fast, sensitive and very accurate determination of ascorbic acid in fruit juices and pharmaceutical preparation.

  15. Carbon Paste Electrodes Made from Different Carbonaceous Materials: Application in the Study of Antioxidants

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    Constantin Apetrei

    2011-01-01

    Full Text Available This work describes the sensing properties of carbon paste electrodes (CPEs prepared from three different types of carbonaceous materials: graphite, carbon microspheres and carbon nanotubes. The electrochemical responses towards antioxidants including vanillic acid, catechol, gallic acid, L-ascorbic acid and L-glutathione have been analyzed and compared. It has been demonstrated that the electrodes based on carbon microspheres show the best performances in terms of kinetics and stability, whereas G-CPEs presented the smallest detection limit for all the antioxidants analyzed. An array of electrodes has been constructed using the three types of electrodes. As demonstrated by means of Principal Component Analysis, the system is able to discriminate among antioxidants as a function of their chemical structure and reactivity.

  16. Electrocatalytic determination of epinephrine and uric acid using a novel hydroquinone modified carbon paste electrode

    Institute of Scientific and Technical Information of China (English)

    Mohammad Mazloum-Ardakani; Zahra Taleat; Hadi Beitollahi; Hossein Naeimi

    2011-01-01

    A sensitive and selective electrochemical method for the determination of epinephrine (EP) was developed using a modified carbon paste electrode (MCPE) with 2,2'- [3,6-dioxa-l,8-octanediylbis(nitriloethylidyne)]-bis-hydroquinone (DOH). Cyclic vol-tammetry was used to investigate the redox properties of this modified electrode at various solution pH values and at various scan rates. In differential pulse voltammetry, the modified electrode could separate the oxidation peak potentials of EP and uric acid (UA) present in the solution but at the unmodified CPE the peak potentials were indistinguishable. This method was also examined for determination of EP in EP injection.

  17. Electrochemical determination of hydroquinone using hydrophobic ionic liquid-type carbon paste electrodes

    OpenAIRE

    Liu Hongtao; Tang Yougen; She Yiyi; He Ping

    2010-01-01

    Abstract Three types of carbon paste electrodes (CPEs) with different liquid binders were fabricated, and their electrochemical behavior was characterized via a potassium hexacyanoferrate(II) probe. 1-Octyl-3-methylimidazolium hexafluorophosphate ionic liquid (IL) as a hydrophobic conductive pasting binder showed better electrochemical performance compared with the commonly employed binder. The IL-contained CPEs demonstrated excellent electroactivity for oxidation of hydroquinone. A diffusion...

  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. Characterization of carbon pastes as matrices in composite electrodes for use in electrochemical capacitors.

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    M. Miranda-Hernandez

    2008-06-01

    Full Text Available Carbon paste electrodes (CPEs were prepared from carbon black powder with different binders (Silicon Oil or Nujol.Cyclic voltammetry, chronoamperometry and chronopotentiometry techniques and different electrolytes (1M HClO4 and 1MLiClO4 were used to characterize the capacitive response and evaluate the capacitance (F/cm2, F/g of CPEs, with andwithout surface modification. The surface modification was carried out by applying a potential pulse (1.35 V vs. saturatedcalomel electrode, SCE at a time of 300 s, where the growth of carbon-oxygen (C-O species were induced on the surface ofthe electrode. The results show that modified electrodes enhanced the capacitance and the electrolytic system has animportant influence in the stability and reactivity of electrodes. The modified electrodes shows an importantpseudocapacitive behavior as result of a diffusion processes that involved an interfacial reaction between the C-O speciesformed during the electrochemical surface treatment and the protons present in the electrolyte.

  20. 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.

  1. Mechanism of 3,4-dihydroxybenzaldehyde electropolymerization at carbon paste electrodes : catalytic detection of NADH

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    Delbem Maria Flávia

    2002-01-01

    Full Text Available Cyclic voltammetry was used to study 3,4-dihydroxybenzaldehyde (3,4-DHB electropolymerization processes on carbon paste electrodes. The characteristics of the electropolymerized films were highly dependent on pH, anodic switching potential, scan rate, 3,4-DHB concentrations and number of cycles. Film stability was determined in citrate/phosphate buffer solutions at the same pH used during the electropolymerization process. The best conditions to prepare carbon paste modified electrodes were pH 7.8; 0.0 <= Eapl <= 0.25 V; 10 mV s-1; 0.25 mmol L-1 3,4-DHB and 10 scans. These carbon paste modified electrodes were used for NADH catalytic detection at 0.23 V in the range 0.015 <= [NADH] <= 0.21 mmol L-1. Experimental data were used to propose a mechanism for the 3,4--DHB electropolymerization processes, which involves initial phenoxyl radical formation.

  2. 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. PMID:24705875

  3. 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.

  4. Electrochemical determination of hydroquinone using hydrophobic ionic liquid-type carbon paste electrodes

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    Liu Hongtao

    2010-10-01

    Full Text Available Abstract Three types of carbon paste electrodes (CPEs with different liquid binders were fabricated, and their electrochemical behavior was characterized via a potassium hexacyanoferrate(II probe. 1-Octyl-3-methylimidazolium hexafluorophosphate ionic liquid (IL as a hydrophobic conductive pasting binder showed better electrochemical performance compared with the commonly employed binder. The IL-contained CPEs demonstrated excellent electroactivity for oxidation of hydroquinone. A diffusion control mechanism was confirmed and the diffusion coefficient (D of 5.05 × 10-4 cm2 s-1 was obtained. The hydrophobic IL-CPE is promising for the determination of hydroquinone in terms of high sensitivity, easy operation, and good durability.

  5. Ultrasensitive determination of carbendazim in water and orange juice using a carbon paste electrode.

    Science.gov (United States)

    Arruda, Gilberto J; Lima, Fábio De; Cardoso, Claudia A L

    2016-08-01

    A carbon paste electrode was used for the electrochemical quantification of carbendazim in water and orange juice samples. Carbendazim oxidation on the electrode surface was found to be controlled by adsorption. The novel electrochemical procedure for carbendazim quantification employed differential pulse voltammetry using a carbon paste electrode under optimal conditions. Carbendazim oxidation currents were linear at concentrations of 2.84 to 45.44 µg L(-1), with a limit of detection of 0.96 µg L(-1). The proposed method was applied to carbendazim quantification in ultrapurified water, river water, and orange juice. Recovery rates in water and orange juice samples were in the 97%-101% range, indicating that the method can be employed to determine carbendazim in these matrices, with advantages including shorter analysis time and lower cost than routine methods such as chromatography or spectroscopy. The electrode showed good reproducibility, remarkable stability, and especially good surface renewability by simple mechanical polishing. The recovery rates observed were highly concordant with those obtained for high-performance liquid chromatography, having a relative standard deviation of less than 1.3%. PMID:27176928

  6. New triiodomercurate-modified carbon paste electrode for the potentiometric determination of mercury

    International Nuclear Information System (INIS)

    A new tetrazolium-triiodomercurate-modified carbon paste electrode has been described for the sensitive and selective determination of mercury. The electrode shows a stable, near-Nernstian response for 1x10-3 to 6x10-6 M [HgI3]- at 25 deg. C over the pH range of 4.0-9.0, with an anionic slope of 55.5±0.4 mV. The lower detection limit is 4x10-6 M with a fast response time of 30-50 s. Selectivity coefficients of a number of interfering anions and iodo complexes of some metal ions have been estimated. The interference from many of the investigated ions is negligible. The determination of 1-200 μg/ml of mercury in aqueous solutions shows an average recovery of 98.5% and a mean relative standard deviation of 1.6% at 50.0 μg/ml. The direct determination of mercury in spiked wastewater, metal amalgams and dental alloy gave results that compare favorably with those obtained by the cold vapor atomic absorption spectrometric method. Potentiometric titration of mercury and phenylmercury acetate with standard potassium iodide has been monitored using the developed triiodomercurate-carbon paste electrode (CPE) as an end point indicator electrode

  7. 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.

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

    Science.gov (United States)

    Bukkitgar, Shikandar D; Shetti, Nagaraj P

    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(-5)-1×10(-7)M and detection limit and quantification limit were calculated to be 2.04nM and 6.18nM respectively. Further, the sensor was successfully applied in pharmaceutical and biological fluid sample analysis. PMID:27157751

  9. 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.

  10. 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.

  11. 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.

  12. 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%.

  13. 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.

  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. 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...

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

    Science.gov (United States)

    Ye, Fengying; Feng, Chenqi; Fu, Ning; Wu, Huihui; Jiang, Jibo; Han, Sheng

    2015-12-01

    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.

  17. 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.

  18. 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.

  19. 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.

  20. Modified carbon paste electrode as a tool for the evaluation of oxidative stability of rapeseed oil

    Directory of Open Access Journals (Sweden)

    Simona Žabčíková

    2015-10-01

    Full Text Available Carbon paste electrode was used for evaluation of oxidative stability of rapeseed oil samples using cyclic voltammetry in 0.1 mol.L-1 HCl as a supporting electrolyte. Rapeseed oil samples were exposed to daylight and oxygen in open glass baker at the laboratory condition in order to obtain oils with accelerated primary and secondary products of oxidation. The oxidation status was determinated by peroxide value and p-anisidine value. Total oxidative stability was expressed as TOTOX index. The edible oils were used for preparation (modification of the carbon paste composite material followed by the cyclic voltammetric measurement. Peroxide values significantly increased whereas p-anisinde value rather fluctuated during 40 days of storage in all the samples. Cyclic voltammograms showed anodic current peaks at 575 - 600 mV and cathodic current peaks at 400 - 425 mV. The oxidation and reduction waves diminished at pH ≥3.0 suggesting not only phenolic compounds contributed to the electrochemical characteristic of oil samples. The peroxide value or p-anisidine value did not correlate with oxidation or reduction peak currents at the potential 575 - 600 mV and 400 - 425 mV, respectively. Both cathodic and anodic currents increased with increasing TOTOX index exhibiting positive correlation with high Spearman correlation coefficient (r = 0.894 and r = 0.914 for anodic and cathodic current, respectively. Linear relationship was found for each sample individually. A caution has to be done when interpreting results since the correlation seems to be of oil sample specific. Nevertheless, the modified carbon paste electrode with rapeseed oil represents a suitable and alternative tool for determination of the oxidative state of edible oils without use of organic solvents.

  1. 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%.

  2. 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.

  3. Electrochemical study of functionalization on the surface of a chitin/platinum-modified glassy carbon paste electrode.

    Science.gov (United States)

    Sugawara, Kazuharu; Yugami, Asako; Terui, Norifumi; Kuramitz, Hideki

    2009-11-01

    To functionalize chitin surfaces using proteins, we developed a glucose oxidase (GOD)-chitin/platinum-modified glassy carbon paste electrode (GCPE) as a model. In a weakly acidic solution, negatively charged GOD were immobilized by the protonated acetylamide groups on chitin. When the electrode was immersed in a solution containing GOD, the enzyme was readily immobilized due to the electrostatic interaction. In addition, measurements were performed using electrodes made with powders of different sizes because sensor performance depends on the particle sizes of glassy carbon powder. PMID:19907096

  4. A pyrrole quinoline quinone glucose dehydrogenase biosensor based on screen-printed carbon paste electrodes modified by carbon nanotubes

    International Nuclear Information System (INIS)

    A carbon nanotube (CNT) modified biosensor based on oxygen-independent, pyrrole quinoline quinone glucose dehydrogenase (PQQ-GDH) for monitoring glucose was studied. The disposable amperometric biosensors based on screen-printed carbon paste electrodes are low cost and suitable for mass production. Potassium ferricyanide was immobilized on the surface of the electrodes as an electron mediator, which decreased the work potential. The biosensor showed a linear amperometric response to glucose from 1 to 35 mM, with a sensitivity of 31.0 µA mM−1 cm−2. Experimentally, the compositions of PQQ-GDH, potassium ferricyanide, CNTs and other components were evaluated and optimized. Only 2 µl of sample are needed for one test, and the response time of the sensor is 20 s. The characteristics of the biosensor were studied through cyclic voltammetry, and experimental results showed that the CNTs could facilitate the electron transfer between the enzyme and electrode surface significantly. Compared with the biosensor without carbon nanotube modification, the CNTs improved the sensitivity of the biosensor up to five times

  5. Comparative voltammetric study and determination of carbamate pesticide residues in soil at carbon nanotubes paste electrodes

    Directory of Open Access Journals (Sweden)

    THOMMANDRU RAVEENDRANATH BAB

    2014-02-01

    Full Text Available In this investigation, the persistence of carbamate pesticides in soil samples was investigated. A simple and selective differential pulse adsorptive stripping voltammetry was selected for this investigation. Carbon nanotubes paste electrodes were used as working electrodes for differential pulse adsorptive stripping voltammetry and cyclic voltammetry. A symmetric study of the various operational parameters that affect the stripping response was carried out by differential pulse voltammetry. Peak currents were linear over the concentration range of 10-5 to 10-10 M with an accumulation potential of -0.6 V and a 70 s accumulation time with lower detection limits of 1.09 x 10-7 M, 1.07 × 10-7M, 1.09×10-7 M for chlorphropham, thiodicarb, aldicarb. The relative standard deviation (n=10 and correlation coefficient values were 1.15 %, 0.988; 1.13 %, 0.978; and 1.14 %, 0.987, respectively. Universal buffer with pH range 2.0 - 6.0 was used as sup­porting electrolyte. The solutions with uniform concentration (10-5 M were used in all deter­minations. Calculations were made by standard addition method.

  6. Iron-enriched natural zeolite modified carbon paste electrode for H2O2 detection

    International Nuclear Information System (INIS)

    This work demonstrates that iron-enriched natural zeolitic volcanic tuff (Paglisa deposit, Cluj county, Transilvania, Romania) resulting from a previous use as adsorbent in wastewater treatment can be recycled into effective electrode modifier applied to the electrocatalytic detection of hydrogen peroxide. After physico-chemical characterization of tuff samples using various techniques such as chemical analysis, X-ray diffraction, scanning electron microscopy, infrared spectroscopy, BET analysis and X-ray photoelectron spectroscopy, the electrochemical response of the iron-enriched zeolites was studied on the basis of solid carbon paste electrodes modified with these samples. The results indicate that iron centers in the zeolite are electroactive and that they act as electrocatalysts in the voltammetric and amperometric detection of H2O2. Best performance was achieved in phosphate buffer at pH 7, showing a sensitivity of 0.57 mA M-1 cm-2, a detection limit down to 60 μM, and a linear domain up to 100 mM H2O2.

  7. 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.

  8. 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.

  9. 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.

  10. 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...

  11. 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)

  12. Carbon paste electrode modified with duplex molecularly imprinted polymer hybrid film for metronidazole detection.

    Science.gov (United States)

    Xiao, Ni; Deng, Jian; Cheng, Jianlin; Ju, Saiqin; Zhao, Haiqing; Xie, Jin; Qian, Duo; He, Jun

    2016-07-15

    A novel electrochemical sensor based on duplex molecularly imprinted polymer (DMIP) hybrid film modified carbon paste electrode (CPE) has been developed for highly sensitive and selective determination of metronidazole (MNZ). A conductive poly(anilinomethyltriethoxysilane) film is firstly electrodeposited on the surface of a CPE, and then a molecularly imprinted polysiloxane (MIPS) membrane is covalently covered on the film via sol-gel process. The as-constructed DMIP hybrid film, combining the advantages of MIPS and conducting MIP, can make feasible the direct and efficient signal transformation between the target analyte and the transducer, as well as enhance the imprinting recognition capability, mass transfer efficiency and the detection sensitivity. Under optimized conditions, the reduction peak currents of MNZ are linear to MNZ concentrations in the range from 4.0×10(-7) to 2.0×10(-4) molL(-1) with a detection limit of 9.1×10(-8)molL(-1). The RSD values vary from 2.9% to 4.7% for intra-day and from 3.4% to 4.2% for inter-day precision. The DMIP-based sensor has been successfully applied for the determination of MNZ in biological and pharmaceutical samples. The accuracy and reliability of the method is further confirmed by high performance liquid chromatography. PMID:26921552

  13. Highly sensitive and selective determination of methylergometrine maleate using carbon nanofibers/silver nanoparticles composite modified carbon paste electrode.

    Science.gov (United States)

    Kalambate, Pramod K; Rawool, Chaitali R; Karna, Shashi P; Srivastava, Ashwini K

    2016-12-01

    A highly sensitive and selective voltammetric method for determination of Methylergometrine maleate (MM) in pharmaceutical formulations, urine and blood serum samples has been developed based on enhanced electrochemical response of MM at carbon nanofibers and silver nanoparticles modified carbon paste electrode (CNF-AgNP-CPE). The electrode material was characterized by various techniques viz., X-ray diffraction, scanning electron microscopy and energy dispersive X-ray spectroscopy. The electrocatalytic response of MM at CNF-AgNP-CPE was studied by cyclic voltammetry (CV), differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). Under optimized conditions, the proposed sensor exhibits excellent electrochemical response towards MM. The DPV study shows greatly enhanced electrochemical signal for MM at CNF-AgNP-CPE lending high sensitivity to the proposed sensor for MM detection. The peak (Ip) current for MM is found to be rectilinear in the range 4.0×10(-8)-2.0×10(-5)M with a detection limit of 7.1×10(-9)M using DPV. The feasibility of the proposed sensor in analytical applications was investigated by conducting experiments on commercial pharmaceutical formulations, human urine and blood serum samples, which yielded satisfactory recoveries of MM. The proposed electrochemical sensor offers high sensitivity, selectivity, reproducibility and practical utility. We recommend it as an authentic and productive electrochemical sensor for successful determination of MM. PMID:27612735

  14. 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)

  15. Prussian Blue Modified Solid Carbon Nanorod Whisker Paste Composite Electrodes: Evaluation towards the Electroanalytical Sensing of H2O2

    Directory of Open Access Journals (Sweden)

    Carolin Siimenson

    2012-01-01

    Full Text Available Metallic impurity free solid carbon nanorod “Whiskers” (SCNR Whiskers, a derivative of carbon nanotubes, are explored in the fabrication of a Prussian Blue composite electrode and critically evaluated towards the mediated electroanalytical sensing of H2O2. The sensitivity and detection limits for H2O2 on the paste electrodes containing 20% (w/w Prussian Blue, mineral oil, and carbon nanorod whiskers were explored and found to be 120 mA/(M cm2 and 4.1 μM, respectively, over the concentration range 0.01 to 0.10 mM. Charge transfer constant for the 20% Prussian Blue containing SCNR Whiskers paste electrode was calculated, for the reduction of Prussian Blue to Prussian White, to reveal a value of 1.8±0.2 1/s (α=0.43, N=3. Surprisingly, our studies indicate that these metallic impurity-free SCNR Whiskers, in this configuration, behave electrochemically similar to that of an electrode constructed from graphite.

  16. Influence of alkylammonium cation on multisweep cyclic voltammetry of Cu(II) on carbon paste electrode modified with montmorillonite

    OpenAIRE

    Navrátilová, Zuzana; Hranická, Zuzana

    2010-01-01

    Cyclic voltammetry of Cu2+ on the carbon paste electrode modified either with montmorillonite SAz-1 or with montmorillonite SAz-1 pretreated with hexadecyltrimethylammonium cation was performed to find the hexadecyltrimethylammonium cation influence on the Cu2+ sorption. In addition, the hexadecyltrimethylammonium presence in the sorption solution was studied, too. In this case, a significant inhibition on the Cu2+ sorption was found. The inhibition is supposed to be a conse...

  17. Application of CdS quantum dots modified carbon paste electrode for monitoring the process of acetaminophen preparation.

    Science.gov (United States)

    Pasandideh-Nadamani, M; Omrani, A; Sadeghi-Maleki, M R; Samadi-Maybodi, A

    2016-06-01

    In this research article, a novel, selective, and sensitive modified carbon paste electrode (CPE) using CdS quantum dots (QDs) is presented. The highly stable CdS QDs were successfully synthesized in an in situ process using Na2S2O3 as a precursor and thioglycolic acid as a catalyst and capping agent. The synthesis of CdS QDs was studied using X-ray diffraction (XRD) and transmission electron microscopy (TEM) techniques. The synthesized CdS QDs were used for preparation of a modified carbon paste electrode (CdS/CPE). The electrochemical behavior of the electrode toward p-aminophenol (PAP) and acetaminophen (Ac) was studied, and the results demonstrated that the CdS/CPE exhibited good electrocatalytic performance toward PAP and Ac oxidation. The oxidation peak potential of each analyte in the mixture was well separated. As a result, a selective and reliable method was developed for the determination of PAP and Ac simultaneously without any chemical separations. Application of the fabricated electrode for monitoring the process of Ac preparation from PAP was investigated. The obtained results show that CdS/CPE has satisfactory analytical performance; it could be a kind of attractive and promising nanomaterial-based sensor for process monitoring via the electrochemical approach. PMID:26945834

  18. 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.

  19. 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.

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

    International Nuclear Information System (INIS)

    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 H2O2. The observed sensitivities for the electrocatalytic oxidation and reduction of H2O2 at the operating potentials of + 0.8 and − 0.2 V were about 13.8 and 18.3 mA M−1, respectively. The detection limit (S/N = 3) for H2O2 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−1 and 30 μM, respectively and better than those obtained (0.2–6 mM, 0.12 mA M−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 H2O2 reduction and oxidation. • Glucose biosensor was fabricated by immobilization of glucose oxidase on sensor

  1. 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.

  2. 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

    International Nuclear Information System (INIS)

    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.

  3. 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.

  4. 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.

  5. Determination of Sunset Yellow using a carbon paste electrode modified with a nanostructured resorcinol-formaldehyde resin

    International Nuclear Information System (INIS)

    This article describes an electrochemical sensor for the dye additive Sunset Yellow (SY). It consists of a carbon paste electrode modified with nanostructured resorcinol-formaldehyde (RF) resin. The RF resin warrants strong signal enhancement and a strongly increased oxidation peak currents of SY at 0.66 V (vs. SCE). The effects of pH value, amount of RF polymer, accumulation potential and time were optimized. The sensor has a linear response to SY in the 0.3 to 125 nM concentration range, and the limit of detection is 0.09 nM after a 2-min accumulation time. The electrode was applied to the analysis of samples of wastewater and drinks, and the results are consistent with those obtained by HPLC. (author)

  6. Determination of Diclofenac on a Dysprosium Nanowire- Modified Carbon Paste Electrode Accomplished in a Flow Injection System by Advanced Filtering

    Directory of Open Access Journals (Sweden)

    Ali Akbar Moosavi-Movahedi

    2009-09-01

    Full Text Available A new detection technique called Fast Fourier Transform Square-Wave Voltammetry (FFT SWV is based on measurements of electrode admittance as a function of potential. The response of the detector (microelectrode, which is generated by a redox processes, is fast, which makes the method suitable for most applications involving flowing electrolytes. The carbon paste electrode was modified by nanostructures to improve sensitivity. Synthesized dysprosium nanowires provide a more effective nanotube-like surface [1-4] so they are good candidates for use as a modifier for electrochemical reactions. The redox properties of diclofenac were used for its determination in human serum and urine samples. The support electrolyte that provided a more defined and intense peak current for diclofenac determination was a 0.05 mol L−1 acetate buffer pH = 4.0. The drug presented an irreversible oxidation peak at 850 mV vs. Ag/AgCl on a modified nanowire carbon paste electrode which produced high current and reduced the oxidation potential by about 100 mV. Furthermore, the signal-to-noise ratio was significantly increased by application of a discrete Fast Fourier Transform (FFT method, background subtraction and two-dimensional integration of the electrode response over a selected potential range and time window. To obtain the much sensivity the effective parameters such as frequency, amplitude and pH was optimized. As a result, CDL of 2.0 × 10−9 M and an LOQ of 5.0 × 10−9 M were found for the determination for diclofenac. A good recovery was obtained for assay spiked urine samples and a good quantification of diclofenac was achieved in a commercial formulation.

  7. 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.

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

    Science.gov (United States)

    Veera Manohara Reddy, Y; Prabhakara Rao, V; Vijaya Bhaskar Reddy, A; Lavanya, M; Venu, M; Lavanya, M; Madhavi, G

    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 0.1M phosphate buffer solution (PBS) at pH7.0. 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. PMID:26354279

  9. 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.

  10. 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.

  11. Sensing nitric oxide with a carbon nanofiber paste electrode modified with a CTAB and nafion composite

    International Nuclear Information System (INIS)

    We describe an electrochemical sensor for nitric oxide that was obtained by modifying the surface of a nanofiber carbon paste microelectrode with a film composed of hexadecyl trimethylammonium bromide and nafion. The modified microelectrode displays excellent catalytic activity in the electrochemical oxidation of nitric oxide. The mechanism was studied by scanning electron microscopy and cyclic voltammetry. Under optimal conditions, the oxidation peak current at a working voltage of 0.75 V (vs. SCE) is related to the concentration of nitric oxide in the 2 nM to 0.2 mM range, and the detection limit is as low as 2 nM (at an S/N ratio of 3). The sensor was successfully applied to the determination of nitric oxide released from mouse hepatocytes. (author)

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

    International Nuclear Information System (INIS)

    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 10-8 to 9.79 x 10-11 M (r = 0.9990) with the detection limit (S/N = 3) of 3.17 x 10-11 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.

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

    International Nuclear Information System (INIS)

    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

  14. 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.

  15. 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.

  16. Electrochemically pretreated zeolite-modified carbon-paste electrodes for determination of linuron in an agricultural formulation and water

    International Nuclear Information System (INIS)

    Highlights: • Cyclic voltammetry, square-wave voltammetry, electrochemical impedance spectroscopic, and scanning electron microscopy were employed. • Kinetic parameters (n, α, ks, and Γ) were calculated. • High sensitivity was observed in the linear concentration range. • Excellent recovery rates were achieved for tap water samples. • The method proved applicable to the determination of linuron in the presence of potential organic and inorganic interferents, none of which affected the results. - Abstract: A simple and inexpensive, yet highly sensitive electrochemical method for quantifying linuron in tap and distilled water and in agricultural formulations was developed using electrochemically pretreated zeolite-modified carbon-paste electrodes (ZMCPEs). Compared with untreated ZMCPEs, the electrochemically pretreated electrodes showed significantly enhanced peak currents for linuron oxidation. Scanning electron microscopy and energy-dispersive x-ray spectroscopy were used to examine the structure of the zeolite-modified and unmodified carbon-paste electrodes (CPEs). ZMCPEs were electrochemically characterized using cyclic voltammetry, chronocoulometry, square-wave voltammetry, and electrochemical impedance spectroscopy. A mechanism for linuron oxidation on ZMCPE surfaces was proposed. The electrochemical variables taken into account were electrode area, number of transferred electrons, electron transfer coefficient, electrode reaction standard rate constant, surface coverage, and capacitance of the electric double layer. Zeolite was found to have a strong influence on these variables. The electrochemical procedure applied to linuron was developed using electrochemically pretreated ZMCPEs under optimal conditions. Linuron oxidation currents exhibited linear concentration in the 87.36 to 625.72 nmol L−1 range, with a limit of detection of 22.57 nmol L−1. The proposed electrochemical method was employed to quantify linuron in tap and distilled water

  17. 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.

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

    OpenAIRE

    Yousry M. Issa; Fekria M. Abu Attia; Nahla S. Ismail

    2010-01-01

    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 ...

  19. 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.

  20. Oxygen reduction in alkaline solution using mixed carbon paste/NixCo1-xO electrodes

    International Nuclear Information System (INIS)

    Hydrogen peroxide is a valuable chemical used in various applications and there is a demand for small on-site production plants. An attractive way to produce hydrogen peroxide is by electrochemical reduction of oxygen, using electrocatalytic materials that favour formation of hydrogen peroxide instead of water. Oxygen reduction on carbon in alkaline solution is known to produce mainly hydrogen peroxide but the overpotential is large and electrocatalytic materials need to be used in combination with carbon. In the present study, the mechanism of oxygen reduction in alkaline solution was studied using NiO, Ni0.75Co0.25O and CoO powders in a matrix of carbon paste. The desired product is hydrogen peroxide and the rotating ring disc technique was used to measure the amount of hydrogen peroxide formed. Two separate processes are observed with a peak shaped wave at low overpotentials and a sigmoidal process at high overpotentials. The charge involved in the first process and the heterogeneous rate constant for the second process were determined and found to be higher in the presence of oxide compared to pure carbon paste. Maximum increase was found for the NiO containing electrode with five times higher charge in the low overpotential region and 25 times higher rate constant in the high overpotential region. The mechanism of oxygen reduction comprises redox mediated electron transfer reactions involving Ni(II)/Ni(III) states on the surface. In the low overpotential region, where oxygen reduction on carbon is mediated by native quinone groups, the increased activity is explained by an interplay between the quinone and Ni(OH)2/NiOOH redox couples

  1. 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.

  2. Electrospun composite nanofibers of poly vinyl pyrrolidone and zinc oxide nanoparticles modified carbon paste electrode for electrochemical detection of curcumin.

    Science.gov (United States)

    Afzali, Moslem; Mostafavi, Ali; Shamspur, Tayebeh

    2016-11-01

    A simple and novel ferrocene-nanofiber carbon paste electrode was developed to determine curcumin in a phosphate buffer solution at pH=8. ZnO nanoparticles were produced via a sonochemical process and composite nanofibers of PVP/ZnO were prepared by electrospinning. The characterization was performed by SEM, XRD and IR. The results suggest that the electrospun composite nanofibers having a large surface area promote electron transfer for the oxidation of curcumin and hence the FCNFCPE exhibits high electrocatalytic activity and performs well in regard to the oxidation of curcumin. The proposed method was successfully applied for measurement of curcumin in urine and turmeric as real samples. PMID:27524081

  3. 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.

  4. Improving the detection of hydrogen peroxide of screen-printed carbon paste electrodes by modifying with nonionic surfactants.

    Science.gov (United States)

    Yuan, Chiun-Jye; Wang, Yen-Chi; Reiko, Ohara

    2009-10-19

    Nonionic surfactants, such as Triton X-100 and Tween-20, were shown in this study to improve the electrocatalytic activity of screen-printed carbon paste electrodes (SPCE). The electrochemical response of SPCE to hydrogen peroxide increased 8-10-fold with the modification of nonionic surfactants. In addition, the glucose biosensors fabricated from nonionic surfactant-modified SPCE exhibited 6.4-8.6-fold higher response to glucose than that fabricated from unmodified SPCE. A concentration effect is proposed for nonionic surfactant to bring neutral reactants to the surface of electrode. Moreover, nonionic surfactant-modified SPCE exhibits a capability of repetitive usage and good reproducibility (R.S.D.<5%) in the measurement of H(2)O(2). Interestingly, the nonionic surfactant-modified SPCE exhibited an opposite effect to ascorbic acid, a common electroactive agent, which causes interference during clinical diagnosis. The differential responses of nonionic surfactant-modified SPCE to H(2)O(2) and ascorbic acid suggest its potential in the development of biosensors for clinical diagnosis. PMID:19800476

  5. 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.

  6. 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.

  7. 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.

  8. 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.

  9. Determination of picomolar silver concentrations by differential pulse anodic stripping voltammetry at a carbon paste electrode modified with phenylthiourea-functionalized high ordered nanoporous silica gel

    International Nuclear Information System (INIS)

    This study introduces the design of an anodic stripping voltammetric (ASV) method for the silver ion determination at a carbon paste electrode (CPE), chemically modified with phenylthiourea-nanoporous silica gel (Tu-SBA-15-CPE). The electroanalytical pro includes two steps: preconcentration of metal ions at an electrode surface, followed by quantification of the accumulated species by differential pulse anodic stripping voltammetric methods. Factors affecting the performance of the anodic stripping were investigated, including the modifier quantity in the paste, the electrolyte concentrations, the solution pH and the accumulation potential or time. The most sensitive and reliable electrode contained 10% Tu-SBA-15 and 90% carbon paste. The accumulation potential and time were set at, -200 mV and 300 s, respectively, and the scan rate at 50 mV s-1 in the scan range of -200 to 700 mV. The resulting electrode demonstrated a linear response over range of silver ion concentration of 8.0-80 pmol/L with detection limit (S/N = 3) of 5 pmol/L. The prepared electrodes were used for the silver determination in sea and tap water samples and very good recovery results were obtained. The accuracy was assessed through recovery experiments and independent analysis by graphite furnace atomic absorption spectrometry.

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

    International Nuclear Information System (INIS)

    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 (Rct) 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 μA/μM in the concentration ranges of 0.3 to 30.0 μM and 30.0 to 450.0 μM, respectively. The detection limit (3σ) of 0.09 μM 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: ► Electrochemical behavior of norepinephrine study using carbon ionic liquid electrode ► This sensor resolved the overlap response of norepinephrine and acetaminophen. ► This sensor is also used for the determination of above compounds in real samples.

  11. 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.

  12. 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.

  13. 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.

  14. 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.

  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. Voltammetric determination of 6-thioguanine and folic acid using a carbon paste electrode modified with ZnO-CuO nanoplates and modifier.

    Science.gov (United States)

    Beitollahi, Hadi; Ivari, Susan Ghofrani; Torkzadeh-Mahani, Masoud

    2016-12-01

    ZnO-CuO nanoplates and 2-chlorobenzoyl ferrocene, were synthesized and used to construct a modified carbon paste electrode. The electrooxidation of 6-thioguanine at the surface of the modified electrode was studied. Under the optimized conditions, the square wave voltammetric (SWV) peak current of 6-thioguanine increased linearly in the concentration range 0.05 to 200.0μM and detection limit of 25±2nM was obtained for 6-thioguanine. The prepared modified electrode exhibits a very good resolution between the voltammetric peaks of 6-thioguanine and folic acid which makes it suitable for the detection of 6-thioguanine in the presence of folic acid in real samples. PMID:27612697

  17. 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.

  18. 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.

  19. 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.

  20. 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.

  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. 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.

  3. Th(IV)-hexacyanoferrate modified carbon paste electrode as a new electrocatalytic probe for simultaneous determination of ascorbic acid and dopamine from acidic media

    Energy Technology Data Exchange (ETDEWEB)

    Farhadi, Khalil; Kheiri, Farshad [Urmia University (Iran, Islamic Republic of). Faculty of Science. Dept. of Chemistry; Golzan, Mirmaqsoud [Urmia University, Urmia (Iran, Islamic Republic of). Faculty of Science. Dept. of Physics]. E-mail: khfarhadi@yahoo.com

    2008-07-01

    A stable carbon paste electrode (CPE) was prepared with Th(IV)-hexacyanoferrate (Th-HCF) ion pair and its electrochemical behavior was investigated by cyclic voltammetry. The apparent heterogeneous rate constant, k{sub s}, and transfer coefficient, alpha, for electron transfer between Th-HCF ion-pair and CPE were calculated as 3.1 +- 0.1 s{sup -1} and 0.47, respectively. The surface coverage ({gamma}) of the proposed electrode was calculated as 7.06 x 10{sup -10} mol cm{sup -2}. The proposed Th-HCF modified carbon paste electrode (THMCPE) showed a good electrocatalytic behavior with a significant shift toward negative potentials in oxidation of ascorbic acid (AA) and dopamine (DA) in acidic media (phosphate buffer solution, pH 3). The THMCPE exhibited excellent characteristics for simultaneous determination of AA and DA. Amperometric curves using the catalytic currents are linear for DA and AA concentrations in the ranges 8 x 10{sup -6} - 2 x 10{sup -3} and 1 x 10{sup -5} - 2 x 10{sup -3} mol L{sup -1} with detection limits 5.6 x 10{sup -6} mol L{sup -1} and 4.7 x 10{sup -6} mol L{sup -1}, respectively. Diffusion coefficients of AA and DA in electrocatalytic oxidation were calculated from chronoamperometric data. (author)

  4. Th(IV)-hexacyanoferrate modified carbon paste electrode as a new electrocatalytic probe for simultaneous determination of ascorbic acid and dopamine from acidic media

    International Nuclear Information System (INIS)

    A stable carbon paste electrode (CPE) was prepared with Th(IV)-hexacyanoferrate (Th-HCF) ion pair and its electrochemical behavior was investigated by cyclic voltammetry. The apparent heterogeneous rate constant, ks, and transfer coefficient, alpha, for electron transfer between Th-HCF ion-pair and CPE were calculated as 3.1 +- 0.1 s-1 and 0.47, respectively. The surface coverage (Γ) of the proposed electrode was calculated as 7.06 x 10-10 mol cm-2. The proposed Th-HCF modified carbon paste electrode (THMCPE) showed a good electrocatalytic behavior with a significant shift toward negative potentials in oxidation of ascorbic acid (AA) and dopamine (DA) in acidic media (phosphate buffer solution, pH 3). The THMCPE exhibited excellent characteristics for simultaneous determination of AA and DA. Amperometric curves using the catalytic currents are linear for DA and AA concentrations in the ranges 8 x 10-6 - 2 x 10-3 and 1 x 10-5 - 2 x 10-3 mol L-1 with detection limits 5.6 x 10-6 mol L-1 and 4.7 x 10-6 mol L-1, respectively. Diffusion coefficients of AA and DA in electrocatalytic oxidation were calculated from chronoamperometric data. (author)

  5. Simultaneous voltammetric detection of ascorbic acid and uric acid at a carbon-paste modified electrode incorporating thionine-nafion ion-pair as an electron mediator

    Energy Technology Data Exchange (ETDEWEB)

    Shahrokhian, Saeed [Department of Chemistry, Sharif University of Technology, Tehran 11365-9516 (Iran, Islamic Republic of)]. E-mail: shahrokhian@sharif.edu; Ghalkhani, Masoumeh [Department of Chemistry, Sharif University of Technology, Tehran 11365-9516 (Iran, Islamic Republic of)

    2006-03-05

    The electrochemical behavior of ascorbic acid (AA) and uric acid (UA) at the surface of a carbon-paste electrode modified with incorporate thionine-nafion ion-paired was thoroughly investigated. The results show the presence of nafion inside the matrix of modified electrode, because of the effective ion-pairing and hydrophobic interactions, significantly enhances the stability of thionine as an electron mediator inside the modified electrode. A high reproducibility in voltammetric response to analyte species results because of this enhancement. The cyclic voltammetric studies using the prepared modified electrode show the best electrocatalytic property for the electro-oxidation of AA and noticeable decrease in anodic overpotential. Although the catalytic effect is observed to some extent for UA, the property cannot be seen for other biologically reducing agents such as cysteine. The voltammetric studies using the thionine-nafion modified electrode show two well-resolved anodic peaks for AA and UA, revealing the possibility of the simultaneous electrochemical detection of these compounds in the presence of biological thiols. The detection limits of 5 x 10{sup -8} and 5 x 10{sup -7} M were obtained in differential pulse voltammetric (DPV) measurements for UA and AA, respectively. Spectrophotometric investigations were used to confirm the selective catalytic effect of thionine in oxidation of AA and to some extent, UA. The detection system is stable (R.S.D. for the slope of the calibration curves was less than 4% for six measurements in one month) and is of high selectivity for electro-oxidation of AA and UA in complex biological and clinical matrices. The prepared modified electrode is applied for the DPV measurement of AA in pharmaceutical preparations. Also, the electrode is used to determine UA in human urine and serum samples and recovery of the amounts of UA added to these complex samples.

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

    Directory of Open Access Journals (Sweden)

    Rasoul Pourtaghavi Talemi

    2013-12-01

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

  7. Synthesis and characterization of novel dopamine-derivative:Application of modified multi-wall carbon nanotubes paste electrode for electrochemical investigation

    Institute of Scientific and Technical Information of China (English)

    Shadpour Mallakpour; Mehdi Hatami; Ali A. Ensafi; Hassan Karimi-Maleh

    2011-01-01

    Novel dopamine-derivative compound, 3,5-diamino-N-(3,4-dihydroxyphenethyl)benzamide (3,5-DAB) was prepared in two steps. In the first step dopamine hydrochloride was reacted with 3,5-dinitrobenzoyl chloride in the presence of propylene oxide. In the second step reduction of nitro groups resulted in preparation of 3,5-DAB in quantitative yield. This material was characterized using conventional spectroscopic methods such as FT-IR and 1H NMR. In addition, the redox response of a modified carbon nanotubes paste electrode of 3,5-DAB was investigated in aqueous solution at a neutral pH. The result showed that the electrode process has a guasi-reversible response, with △Ep, greater than the (59/n) mV expected for a reversible system. Finally, the diffusion coefficient for redox process in paraffin oil matrix obtained using chronoamperometry methods.

  8. Ni(II)-quercetin complex modified multiwall carbon nanotube ionic liquid paste electrode and its electrocatalytic activity toward the oxidation of glucose

    Energy Technology Data Exchange (ETDEWEB)

    Zheng Li [Institute of Analytical Science, Northwest University, Xi' an, 710069 (China); College of Chemistry and Chemical Engineering, Xi' an Shiyou University, Xi' an, 710065 (China); Zhang Jiaoqiang [Department of Applied Chemistry, School of Science, Northwestern Polytechnical University, Xi' an, 710072 (China); Song Junfeng [Institute of Analytical Science, Northwest University, Xi' an, 710069 (China)], E-mail: songjunf@nwu.edu.cn

    2009-07-30

    A modified electrode Ni(II)-Qu-MWCNT-IL-PE has been fabricated by electrodepositing Ni(II)-quercetin [Ni(II)-Qu] complex on the surface of multi-wall carbon nanotube ionic liquid paste electrode (MWCNT-IL-PE) in alkaline solution. The Ni(II)-Qu-MWCNT-IL-PE exhibits the characteristic of improved reversibility and enhanced current responses of the Ni(III)/Ni(II) couple compared with Ni(II)-Qu-MWCNT-PE. It also shows good electrocatalytic activity toward the oxidation of glucose. Kinetic parameters such as the electron transfer coefficient {alpha}, rate constant k{sub s} of the electrode reaction and the catalytic rate constant k{sub cat} of the catalytic reaction are determined. Moreover, the catalytic current presents linear dependence on the concentration of glucose from 5.0 {mu}M to 2.8 mM, with a detection limit of 1.0 {mu}M by amperometry. The modified electrode for glucose determination is of the property of simple preparation, good stability, fast response and high sensitivity.

  9. Application of poly(acridine orange) and graphene modified carbon/ionic liquid paste electrode for the sensitive electrochemical detection of rutin

    International Nuclear Information System (INIS)

    A carbon/ionic liquid paste electrode (CILPE) prepared by 1-hexylpyridinium hexafluorophosphate as the binder was used as the substrate electrode. A layer of graphene oxide (GO) film was cast on CILPE surface (GO/CILPE) and the electropolymerization of acridine orange (AO) on electrode was further realized by cyclic voltammetry in the potential range from −1.40 V to 1.40 V, which could simultaneously reduce GO to graphene (GR) electrochemically. The fabricated PAO-GR/CILPE exhibited good electrochemical performances with higher conductivity and lower electron transfer resistance. Electrochemical behaviors of rutin were further investigated on the modified electrode in 0.1 mol/L pH 2.0 phosphate buffer solution by cyclic voltammetry with a pair of well-defined redox peaks appeared. The peak-to-peak separation (ΔEp) was calculated as 0.076 V, which proved a fast quasi-reversible electron transfer process and the electrochemical parameters of rutin on PAO-GR/CILPE were calculated. Under the optimal conditions, the linear relationship between the oxidation peak current of rutin and its concentration was obtained in the range from 0.03 to 800.0 μmol/L with the detection limit as 8.33 nmol/L (3σ). The PAO-GR/CILPE showed good selectivity, stability and reproducibility, which was further applied to detect rutin tablet samples with satisfactory results

  10. 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

  11. 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.

  12. A sensitive and selective on-line amperometric sulfite biosensor using sulfite oxidase immobilized on a magnetite-gold-folate nanocomposite modified carbon-paste electrode.

    Science.gov (United States)

    Sroysee, Wongduan; Ponlakhet, Kitayanan; Chairam, Sanoe; Jarujamrus, Purim; Amatatongchai, Maliwan

    2016-08-15

    We describe a novel amperometric sulfite biosensor, comprising a carbon-paste electrode (Fe3O4@Au-Cys-FA/CPE) modified with immobilized sulfite oxidase (SOx) on a gold-coated magnetite nanoparticle core, encased within a conjugated folic acid (FA) cysteine (Cys) shell. The biosensor electrode was fabricated using a polydimethylsiloxane (PDMS) and mineral oil mixture as binder, which also enhances the physical stability and sensitivity of the electrode. The developed biosensor displays good electrocatalytic activity toward oxidation of H2O2, which occurs by an enzymatic reaction between SOx and sulfite. The Fe3O4@Au-Cys-FA electrode exhibits good electrocatalytic activity, and has good retention of chemisorbed SOx on the electrode because of its large surface area. Sulfite was quantified using amperometric measurements from the Fe3O4@Au-Cys-FA/CPE biosensor, and using an in-house assembled flow cell at +0.35V (vs. Ag/AgCl), with a phosphate buffer carrier (0.10M, pH 7.0) at a flow rate of 0.8mLmin(-1). The system detects sulfite over the range 0.1-200mgL(-1) (r(2)=0.998), with a detection limit of 10µgL(-1) (3σ of blank). The system exhibits acceptable precision (%R.S.D.=3.1%), rapid sample throughput (109samplesh(-1)), and good stability (2w). The developed biosensor shows satisfactory tolerance to potential interferences, such as sugars, anions, ascorbic acid, and ethanol. We applied the developed method to the determination of sulfite content in wines and pickled food extracts, and our results are in good agreement with those obtained by the standard iodometric method. PMID:27260448

  13. 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.

  14. 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.

  15. 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).

  16. Electrohemical Properties of Carbon Nanotube Paste Electrodes Modified with Redox Cationic Dyes - doi: 10.4025/actascitechnol.v34i3.15250

    Directory of Open Access Journals (Sweden)

    Juliana Maria Ramos Antônio

    2012-05-01

    Full Text Available The present work describes the electrochemical behavior of cationic dyes (methylene blue and toluidine blue as electron mediators adsorbed in the multiwall carbon nanotubes paste in 0.5 KCl at pH 7.0 by using cyclic voltammetry. Based on midpoint potential [Em = (Eap + Ecp/2] and separation of cathodic and anodic peaks (ΔE, it was not observed interaction of different eletrolytes (LiCl, KCl, BaCl2, CaCl2, NaCl, NaNO3, Na2SO4 and NaClO4, 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 cationic dyes.  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.

  17. 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.

  18. 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.

  19. Facile stripping voltammetric determination of haloperidol using a high performance magnetite/carbon nanotube paste electrode in pharmaceutical and biological samples

    Energy Technology Data Exchange (ETDEWEB)

    Bagheri, Hasan, E-mail: h.bagheri@srbiau.ac.ir [Chemical Injuries Research Center, Baqiyatallah University of Medical Sciences, Tehran (Iran, Islamic Republic of); Afkhami, Abbas [Faculty of Chemistry, Bu-Ali Sina University, Hamedan (Iran, Islamic Republic of); Panahi, Yunes [Chemical Injuries Research Center, Baqiyatallah University of Medical Sciences, Tehran (Iran, Islamic Republic of); Khoshsafar, Hosein; Shirzadmehr, Ali [Faculty of Chemistry, Bu-Ali Sina University, Hamedan (Iran, Islamic Republic of)

    2014-04-01

    Multi-walled carbon nanotubes decorated with Fe{sub 3}O{sub 4} nanoparticles were prepared to construct a novel sensor for the determination of haloperidol (Hp) by voltammetric methods. The morphology and properties of electrode surface were characterized by scanning electron microscopy (SEM) and electrochemical impedance spectroscopy. This modified sensor was used as a selective electrochemical sensor for the determination of trace amounts of Hp. The peak currents of differential pulse and square wave voltammograms of Hp increased linearly with its concentration in the ranges of 1.2 × 10{sup −3}–0.52 and 6.5 × 10{sup −4}–0.52 μmol L{sup −1}, respectively. The detection limits for Hp were 7.02 × 10{sup −4} and 1.33 × 10{sup −4} μmol L{sup −1} for differential pulse and square wave voltammetric methods, respectively. The results show that the combination of multi-walled carbon nanotubes and Fe{sub 3}O{sub 4} nanoparticles causes a dramatic enhancement in the sensitivity of Hp quantification. This sensor was successfully applied to determine Hp in pharmaceutical samples and biological fluids. The fabricated electrode showed excellent reproducibility, repeatability and stability. - Highlights: • A sensitive paste using Fe{sub 3}O{sub 4}/multi-walled carbon nanotubes was fabricated. • Haloperidol determination is based on its adsorption on the surface of Fe{sub 3}O{sub 4}/MWCNTs. • Different electrochemical methods and impedance spectroscopy were used for this study. • Haloperidol was determined in pharmaceutical and biological samples. • In comparison to other conventional methods, this method is simple, rapid, selective and cost-effective.

  20. Graphite grains studded with silver nanoparticles: description and application in promoting direct biocatalysis between heme protein and the resulting carbon paste electrode.

    Science.gov (United States)

    ElKaoutit, Mohammed; Naggar, Ahmad H; Naranjo-Rodríguez, Ignacio; de Cisneros, José L Hidalgo-Hidalgo

    2012-04-01

    The impregnation of graphite grains with silver nanoparticles (AgNPs) is proposed for making a novel carbon paste electrode (CPE). The resulting material promotes direct electron transfer and direct biocatalysis of embedded heme protein. It is demonstrated that the impregnation of graphite grains with AgNPs of 16-25 nm, incorporated in a CPE, can promote measurable bio-electrochemical phenomena involving hemoglobin and myoglobin. Unlike other biosensors prepared with simple carbon, those based on carbon grains studded with AgNPs show well-defined and quasi-reversible voltammetric peak with heterogeneous electron transfer rate k(s) of approximately 0.037±0.007 and 0.013±0.005s(-1) for hemoglobin and myoglobin, respectively. The embedded proteins also retain their bio-catalytical activity for hydrogen peroxide and nitrite reduction with linear ranges of 0.5-3000 μM and 30-150 μM, sensitivities of 73.6±0.6nA μM(-1) and 5.72±0.11 nA μM(-1), and detection limits close to 0.08 μM and 5.80 μM, for these two analytes respectively. These results support the viability of this preliminary approach for the development of advanced third-generation biosensors. PMID:22154098

  1. Trace Determination of Scandium Using Adsorption Voltammetry of Mix-Polynuclear Complex of Scandium-Calcium-Alizarin Red S at Carbon Paste Electrode

    Institute of Scientific and Technical Information of China (English)

    黎拒难; 张军; 邓培红; 费俊杰

    2004-01-01

    A novel method was described for the determination of ultra trace amount of scandium based on the cathodic adsorptive voltammetry of the mix-polynuclear complex of scandium-calcium-alizarin red S at a carbon paste electrode (CPE).The 2nd-order derivative linear scan voltammograms of the adsorbed complex were recorded by model JP-303 polarographic analyzer from 0.0 to -1.0 V (vs.SCE).The experimental conditions of the working procedure were optimized.The results show that the complex can be adsorbed on the surface of the CPE,yielding one peak at -0.61 V,corresponding to the reduction of the alizarin red S in the mix-polynuclear complex at the electrode.The detection limit of Sc3+ is 1.0×10-10 mol·L-1 for 3 min of accumulation time.The procedure was successfully applied to the determination of trace amount of scandium in the sample ores.

  2. 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.

  3. Synthesis of nano-sized cyanide ion-imprinted polymer via non-covalent approach and its use for the fabrication of a CN(-)-selective carbon nanotube impregnated carbon paste electrode.

    Science.gov (United States)

    Alizadeh, Taher; Sabzi, Reza Emamali; Alizadeh, Hassan

    2016-01-15

    Nano-sized CN(-)-imprinted polymer was synthesized by the copolymerization of methyl methacrylic acid (MAA), vinyl pyridine (VP) and ethylene glycol dimethacrylate in the presence of cyanide ion. The obtained polymeric nanoparticles were incorporated with carbon paste electrode (CPE) to produce a CN(-)-selective electrode. Functional monomer kind had crucial influence on the efficiency of the sensor. The presence of both VP and MAA in the structure of the imprinted polymer improved the sensing characteristics of the electrode. Also, the mole ratio of MAA/VP, cross-liker kind, cross-linker amount, solvent kind and amount were found to be effective factors in the electrode behavior. Presence of little amount of multi-walled carbon nanotubes (MWCNTs) in the CPE improved the detection range and response time of the electrode at the expense of small decrease in Nernstian slope. The electrode, containing CN(-)-imprinted polymer and MWCNTs showed a dynamic linear range of 1×10(-6)-1×10(-1)mol L(-1), Nernstian slope of 46.3±(0.6) mV and detection limit of 7.5×10(-7)mol L(-1); whereas, the same electrode in the absence of MWCNTs led to linear range, Nernstian slope and detection limit of 1×10(-5)-1×10(-1)molL(-1), 55.3±(0.7) mV and 8×10(-6)mol L(-1), respectively. The utility of the electrodes was checked by determination of cyanide ion in some real samples. PMID:26592581

  4. 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. PMID:27523989

  5. Insulated electrocardiographic electrodes. [without paste electrolyte

    Science.gov (United States)

    David, R. M.; Portnoy, W. A. (Inventor)

    1975-01-01

    An integrated system is disclosed including an insulated electrode and an impedance transformer which can be assembled in a small plastic housing and used for the acquisition of electrocardiographic data. The electrode may be employed without a paste electrolyte and may be attached to the body for extended usage without producing skin reaction. The electrode comprises a thin layer of suitable nontoxic dielectric material preferably deposited by radio frequency sputtering onto a conductive substrate. The impedance transformer preferably comprises an operational amplifier having an FET input stage connected in the unity gain configuration which provides a very low lower cut-off frequency, a high input impedance with a very small input bias current, a low output impedance, and a high signal-to-noise ratio.

  6. 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.

  7. 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.

  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. Electrochemical quantification of the thermodynamic equilibrium constant of the tenoxicam-β-cyclodextrin inclusion complex formed on the surface of a poly-β cyclodextrin-modified carbon paste electrode

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • A carbon paste electrode (CPE) was modified with a β-CD polymer. • Tenoxicam oxidation on the CPE/poly-β-CD was adsorption controlled. • Influence of pH, scan rate, angular velocity and concentration was evaluated. • Fittings of i-E plots were done considering an irreversible surface reaction. • Electrochemical evaluation of the surface inclusion constant is presented. - Abstract: In this work it is shown that when a carbon paste electrode, CPE, is modified with a β-cyclodextrin polymer, the tenoxicam oxidation becomes an adsorption controlled process due to formation of a surface inclusion complex with the β-CD molecules comprising the surface of the polymer. It was found that such surface inclusion complex can be formed independently of the tenoxicam predominant species, Tenox’, in the aqueous solution namely: H2Tenox+, HTenox or Tenox−, depending on the solution pH. The electrochemical quantification of the thermodynamic constant of the equilibrium Tenox’ + β-CD (polymer) = Tenox’-β-CD (polymer) was estimated as log Kincl. = 4.26 ± 0.01. Furthermore, from the analyses of the experimental voltammograms according with Laviron's equation for an irreversible surface reaction [E. Laviron, J. Electroanal. Chem. 52 (1974) 355-393] it is shown that the surface concentration, ΓR, of tenoxicam increases as its concentration in solution does, reaching a maximum value of 1.51 × 10−10 mol cm−2 at 64 μM

  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. Exploring the electrochemical performance of graphitic paste electrodes: graphene vs. graphite

    OpenAIRE

    Figueiredo-Filho, Luiz C.S.; Brownson, Dale A.C.; Gómez Mingot, María; Iniesta Valcárcel, Jesús; Fatibello-Filho, Orlando; Banks, Craig E.

    2013-01-01

    We report the fabrication, characterisation (SEM, TEM, XPS and Raman spectroscopy) and electrochemical implementation of a graphene paste electrode. The paste electrodes utilised are constructed by simply mixing graphene with mineral oil (which acts as a binder) prior to loading the resultant paste into a piston-driven polymeric-tubing electrode-shell, where this electrode configuration allows for rapid renewal of the electrode surface. The fabricated paste electrode is electrochemically char...

  12. 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.

  13. 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%.

  14. 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.

  15. 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.

  16. 头孢氨苄在碳糊电极上的电化学行为及其分析研究%Electrochemical Behavior and Determination of Cefalexin at Carbon Paste Electrode

    Institute of Scientific and Technical Information of China (English)

    杨阿喜; 胡效亚

    2012-01-01

    用循环伏安法和线性扫描伏安法研究了头孢氨苄在碳糊电极上的电化学行为,考察了不同电解质溶液、pH以及扫描速率等的影响.实验表明:在2.0 mol·L-1 HCI支持电解质中,头孢氨苄的降解产物在-0.45 V(vs.SCE)处的电化学还原反应为2电子与2质子参加的受吸附控制的不可逆过程.还原峰电流与头孢氨苄的浓度的平方根在1.8×10-8~3.0×10-4 mol·L-1范围内呈良好的线性关系,回收率在95.7%~101.5%范围,检出限(S/N=3)为1.0×10-8 mol·L-1.并探讨了头孢氨苄在电极上的反应机理.%In this work, we studied the electrochemistry characteristic of cefalexin at a carbon paste electrode by using cyclic voltammetry(CV) and linear sweep voltammetry(LSV). The influence factors such as the electrolyte solution,pH values of the support solution and the scanning rate were discussed. Results showed that the electrochemical behavior of cefalexin hydrolysate exhibited irreversible absorption-controlled redox process of two electrons and two protons in the solution of 2. 0 mol·L-1 HCl,with irreversible reductive peak at -0. 45 V(vs. SCE). The peak currents were proportional to the square root of cefalexin concentration in the range of 1. 8× 10-8~3. 0× 10-4 mol·L-1 with a detection limit of 1.0× 10-8 mol·L-1. The range of recovery was 95. 7%-101. 5%. The reaction mechanism of cefalexin at the carbon paste electrode was discussed.

  17. Los electrodos de pasta de carbono en el estudio electroquímico de minerales metálicos The role of the carbon paste electrodes in the electrochemical study of metallic minerals

    Directory of Open Access Journals (Sweden)

    José L. Nava

    2005-10-01

    Full Text Available This paper shows the applicability of the carbon paste electrode-mineral (CPE-mineral to study the dissolution mechanisms of minerals in powder form and in flotation concentrates. A potentiodynamic strategy to find the dissolution mechanism of galena (PbS is presented. In this way, minerals less studied such as orpiment (As2S3 and realgar (As2S2 are investigated. The electrochemical activity of a more complicated mineral such as sphalerite (ZnS, containing 12.3 and 0.43% of iron in solid solution, is discussed. The mechanism of a complex zinc concentrate (containing 63.4% ZnS, 20.1% FeS2, 5% CuFeS2, 0.33% PbS, 0.45% Cu12Sb4S13 and 0.4% FeAsS is described. Finally, an electrochemical method for the detection of the different leachable and refractory silver phases (contained in two mineral concentrates is presented. This paper reviews the power of the use of CPE-mineral coupled to electrochemical techniques in hydrometallurgy.

  18. 4-methoxy-2,6-bis(3,5-dimethylpyrazoyl)-1,3,5-triazine modified carbon paste electrode for trace Cu(Ⅱ) determination by differential pulse voltammetry

    Institute of Scientific and Technical Information of China (English)

    YANG Sheng; LU Xiaoquan; XUE Zhonghua; FENG Xiaoqiang; WANG Xiaofeng

    2003-01-01

    A differential pulse voltammetric method was developed for the sensitive and selective determination of Cu(Ⅱ) at 4-methoxy-2,6-bis(3,5-dimethylpyrazoyl)-1,3,5-triazine modified carbon paste electrode in 0.05 mol/L KHC8H4O4 solution (pH = 4.02). The oxidation peak of Cu(Ⅱ) was observed at 0.065 V(vs Ag/AgC1) by scanning the potentid in positive direction. The analysis procedure consisted of an open circuit accumulation step in stirred sample solution. It was followed by medium exchange to a clean solution and subsequently an anodic potential scan was affected to obtain the voltammetric peak. The current was proportional to the concentration of the Cu(Ⅱ) ion in a range of 1 × 10-7 -1 × 10 -4 mol/L for 6 min accumulation; the most of metal ions did not interfere with the determination. The developed method was applied to Cu(Ⅱ)determination in coal-ash sample, the results agreed with that of atomic adsorption spectroscopy(AAS).

  19. Simultaneous detection of morphine and codeine in urine samples of heroin addicts using multi-walled carbon nanotubes modified SnO2-Zn2SnO4 nanocomposites paste electrode

    Science.gov (United States)

    Taei, M.; Hasanpour, F.; Hajhashemi, V.; Movahedi, M.; Baghlani, H.

    2016-02-01

    The SnO2-Zn2SnO4 nanocomposite was successfully prepared via a simple solid state method. Then, a chemically modified electrode based on incorporating SnO2-Zn2SnO4 into multi-walled carbon nanotube paste matrix (MWCNTs/SnO2-Zn2SnO4/CPE) was prepared for the simultaneous determination of morphine(MO) and codeine (CO). The measurements were carried out by application of differential pulse voltammetry (DPV), cyclic voltammetry, and chronoamperometry. The MWCNTs/SnO2-Zn2SnO4/CPE showed an efficient electrocatalytic activity for the oxidation of MO and CO. The separation of the oxidation peak potential for MO-CO was about 550 mV. The calibration curves obtained for MO and CO were in the ranges of 0.1-310 μmol L-1 and 0.1-600.0 μmol L-1, respectively. The detection limits (S/N = 3) were 0.009 μmol L-1 for both drugs. The method also successfully employed as a selective, simple, and precise method for the determination of MO and CO in pharmaceutical and biological samples.

  20. Determination of trace amount of antimony (Ⅲ) by adsorption voltammetry on carbon paste electrode%碳糊电极吸附伏安法测定痕量锑

    Institute of Scientific and Technical Information of China (English)

    郭会时; 肖鹏峰; 聂立波; 李益恒; 何农跃

    2004-01-01

    根据锑与溴邻苯三酚红(BPR)生成的络合物在碳糊电极上的吸附特性, 建立了测定痕量锑的吸附伏安法. 整个分析过程分3个步骤: 吸附富集、还原和溶出. 用单因素变化法得出最佳试验条件为: 以含40 μmol/L BPR的0.10mol/L HCl为富集底液; 富集时间150 s; 还原和溶出介质为0.20mol/L HCl; 还原电位为-0.50V; 还原时间为60 s;扫描范围为-0.5~0.20V. 考察了共存离子的影响. 二次导数溶出峰电流与锑(Ⅲ)浓度在1. 0nmol/L~0. 50μmol/L范围内呈良好的线性关系, 检出限达0.5nmol/L. 该方法已成功应用于人发和水样中锑的测定.%A sensitive method is described for the determination of trace antimony based on the antimony-bromopyrogallol red (BPR) adsorption at a carbon paste electrode (CPE). Three steps were involved in the overall analysis: preconcentration, reduction and stripping. Optimal conditions were found to be an electrode containing 25% paraffin oil and 75% high purity graphite powder as working electrode; a 0. 10mol/L HCl solution containing 40 μmol/L BPR as accumulation medium; a 0. 20mol/L HCl solution as reduction and stripping electrolyte; accumulation time, 150 s; reduction potential and time, -0. 50 V, 60 s; scan range from -0. 50 to 0. 20V. Interferences by other ions were studied as well. The detection limit was found to be 0. 5nmol/L for 150 s preconcentration. The linear range was from 1. 0nmol/L to 0. 50 μmol/L. Application of the proposed method to the determination of antimony in water and human hair samples gave good results.

  1. Magnetic core–shell Fe{sub 3}O{sub 4}@SiO{sub 2}/MWCNT nanocomposite modified carbon paste electrode for amplified electrochemical sensing of uric acid

    Energy Technology Data Exchange (ETDEWEB)

    Arvand, Majid, E-mail: arvand@guilan.ac.ir; Hassannezhad, Morassa

    2014-03-01

    A new type of nanocomposite based on multi-walled carbon nanotubes decorated with magnetic core–shell Fe{sub 3}O{sub 4}@SiO{sub 2} nanoparticles (Fe{sub 3}O{sub 4}@SiO{sub 2}/MWCNTs) was prepared and used to fabricate a modified carbon paste electrode (CPE). The nanocomposite was characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX) and Fourier transform infrared spectroscopy (FT-IR) techniques. Electrochemical behavior of uric acid (UA) was investigated on Fe{sub 3}O{sub 4}@SiO{sub 2}/MWCNTs-CPE by cyclic voltammetry (CV) and square wave voltammetry (SWV) in phosphate buffer solution (pH 6.0). Under the optimized conditions, the peak currents increased linearly with the concentration of UA in the range from 0.60 to 100.0 μM, with a detection limit of 0.13 μM. The proposed sensor was successfully applied for the determination of UA in biological fluids. - Highlights: • A simple and rapid sensor for determination of UA in human blood serum and urine was prepared. • The Fe{sub 3}O{sub 4}@SiO{sub 2}/MWCNTs-CPE showed an obvious increase in surface area and sensitivity. • The presence of Fe{sub 3}O{sub 4}@SiO{sub 2} nanoparticles showed good ability to distinguish the response of UA.

  2. 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

  3. Method for making thin carbon foam electrodes

    Energy Technology Data Exchange (ETDEWEB)

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

    1999-08-03

    A method for fabricating thin, flat carbon electrodes by infiltrating highly porous carbon papers, membranes, felts, metal fibers/powders, or fabrics with an appropriate carbon foam precursor material is disclosed. The infiltrated carbon paper, for example, is then cured to form a gel-saturated carbon paper, which is subsequently dried and pyrolyzed to form a thin sheet of porous carbon. The material readily stays flat and flexible during curing and pyrolyzing to form thin sheets. Precursor materials include polyacrylonitrile (PAN), polymethylacrylonitrile (PMAN), resorcinol/formaldehyde, catechol/formaldehyde, phenol/formaldehyde, etc., or mixtures thereof. These thin films are ideal for use as high power and energy electrodes in batteries, capacitors, and fuel cells, and are potentially useful for capacitive deionization, filtration and catalysis.

  4. Method for making thin carbon foam electrodes

    Energy Technology Data Exchange (ETDEWEB)

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

    1999-01-01

    A method for fabricating thin, flat carbon electrodes by infiltrating highly porous carbon papers, membranes, felts, metal fibers/powders, or fabrics with an appropriate carbon foam precursor material. The infiltrated carbon paper, for example, is then cured to form a gel-saturated carbon paper, which is subsequently dried and pyrolyzed to form a thin sheet of porous carbon. The material readily stays flat and flexible during curing and pyrolyzing to form thin sheets. Precursor materials include polyacrylonitrile (PAN), polymethylacrylonitrile (PMAN), resorcinol/formaldehyde, catechol/formaldehyde, phenol/formaldehyde, etc., or mixtures thereof. These thin films are ideal for use as high power and energy electrodes in batteries, capacitors, and fuel cells, and are potentially useful for capacitive deionization, filtration and catalysis.

  5. 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.

  6. 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.

  7. Exploring the electrochemical performance of graphitic paste electrodes: graphene vs. graphite.

    Science.gov (United States)

    Figueiredo-Filho, Luiz C S; Brownson, Dale A C; Gómez-Mingot, Maria; Iniesta, Jesús; Fatibello-Filho, Orlando; Banks, Craig E

    2013-11-01

    We report the fabrication, characterisation (SEM, TEM, XPS and Raman spectroscopy) and electrochemical implementation of a graphene paste electrode. The paste electrodes utilised are constructed by simply mixing graphene with mineral oil (which acts as a binder) prior to loading the resultant paste into a piston-driven polymeric-tubing electrode-shell, where this electrode configuration allows for rapid renewal of the electrode surface. The fabricated paste electrode is electrochemically characterised using both inner-sphere and outer-sphere redox probes, namely potassium ferrocyanide(ii), hexaammine-ruthenium(iii) chloride and hexachloroiridate(iii), in addition to the biologically relevant and electroactive analytes, l-ascorbic acid (AA) and uric acid (UA). Comparisons are made with a graphite paste alternative and the benefits of graphene implementation as a paste electrode within electrochemistry are explored, as well as the characterisation of their electroanalytical performances. We reveal no observable differences in the electrochemical performance and thus suggest that there are no advantages of using graphene over graphite in the fabrication of paste electrodes. Such work is highly important and informative for those working in the field of electroanalysis where electrochemistry can provide portable, rapid, reliable and accurate sensing protocols (bringing the laboratory into the field), with particular relevance to those searching for new electrode materials. PMID:24010127

  8. Supercapacitor Electrodes from Activated Carbon Monoliths and Carbon Nanotubes

    Science.gov (United States)

    Dolah, B. N. M.; Othman, M. A. R.; Deraman, M.; Basri, N. H.; Farma, R.; Talib, I. A.; Ishak, M. M.

    2013-04-01

    Binderless monoliths of supercapacitor electrodes were prepared by the carbonization (N2) and activation (CO2) of green monoliths (GMs). GMs were made from mixtures of self-adhesive carbon grains (SACG) of fibers from oil palm empty fruit bunches and a combination of 5 & 6% KOH and 0, 5 & 6% carbon nanotubes (CNTs) by weight. The electrodes from GMs containing CNTs were found to have lower specific BET surface area (SBET). The electrochemical behavior of the supercapacitor fabricated using the prepared electrodes were investigated by electrochemical impedance spectroscopy (EIS) and galvanostatic charge-discharge (GCD). In general an addition of CNTs into the GMs reduces the equivalent series resistance (ESR) value of the cells. A cell fabricated using electrodes from GM with 5% CNT and 5% KOH was found to have the largest reduction of ESR value than that from the others GMs containing CNT. The cell has steeper Warburg's slope than that from its respective non-CNT GM, which reflect the smaller resistance for electrolyte ions to move into pores of electrodes despite these electrodes having largest reduction in specific BET surface area. The cell also has the smallest reduction of specific capacitance (Csp) and maintains the specific power range despite a reduction in the specific energy range due to the CNT addition.

  9. 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.

  10. 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.

  11. Double layer capacitance of carbon foam electrodes

    Science.gov (United States)

    Delnick, F. M.; Ingersoll, D.; Firsich, D.

    We have evaluated a wide variety of microcellular carbon foams prepared by the controlled pyrolysis and carbonization of several polymers including: polyacrylonitrile (PAN), polymethacrylonitrile (PMAN), resorcinol/formaldehyde (RF), divinylbenzene/methacrylonitrile (DVB), phenolics (furfuryl/alcohol), and cellulose polymers such as Rayon. The porosity may be established by several processes including: gelation (1-5), phase separation (1-3,5-8), emulsion (1,9,10), aerogel/xerogel formation (1,11,12,13), replication (14), and activation. In this report we present the complex impedance analysis and double layer charging characteristics of electrodes prepared from one of these materials for double layer capacitor applications, namely activated cellulose derived microcellular carbon foam.

  12. Carbon additives for electrical double layer capacitor electrodes

    Science.gov (United States)

    Weingarth, D.; Cericola, D.; Mornaghini, F. C. F.; Hucke, T.; Kötz, R.

    2014-11-01

    Electrochemical double layer capacitors (EDLCs) are inherently high power devices when compared to rechargeable batteries. While capacitance and energy storage ability are mainly increased by optimizing the electrode active material or the electrolyte, the power capability could be improved by including conductive additives in the electrode formulations. This publication deals with the use of four different carbon additives - two carbon blacks and two graphites - in standard activated carbon based EDLC electrodes. The investigations include: (i) physical characterization of carbon powder mixtures such as surface area, press density, and electrical resistivity measurements, and (ii), electrochemical characterization via impedance spectroscopy and cyclic voltammetry of full cells made with electrodes containing 5 wt.% of carbon additive and compared to cells made with pure activated carbon electrodes in organic electrolyte. Improved cell performance was observed in both impedance and cyclic voltammetry responses. The results are discussed considering the main characteristics of the different carbon additives, and important considerations about electrode structure and processability are drawn.

  13. Supercapacitor carbon electrodes from pyrolyzed glycerol

    International Nuclear Information System (INIS)

    In this study pyrolyzed glycerol was explored as electrode material using a catalytic agent during pyrolysis. Here, evaporation of glycerol at high temperatures was prevented by catalyzing the formation of oligoglycerol in turn leading to carbonization above 300 °C. A one-step and tow-step pyrolysis process were developed and compared based on the suercapacitive properties of the carbon material. The pyrolysis of the glycerol was performed at 600 °C for 1 hour under nitrogen atmosphere. The product obtained was washed with 1 M HCl, and characterized using scanning electron microscopy (SEM), nitrogen adsorption (BET surface analysis), Fourier transform infrared (FTIR) spectroscopy, cyclic voltammetry, and galvanostatic charge-discharge measurements. Carbon percent yields of 4-6% were obtained for the two different processes. The one-step process was found to have slightly higher yields. FTIR spectroscopy showed that majority of the functional groups had been removed during the pyrolysis process. SEM images show no significant difference in the surface morphology and porosity from the products of the two processes. Fabricated electrodes showed specific capacitances ranging from 0.25 Fg-“1 to 1.36 Fg-“1 through cyclic voltammetry in 1 M Li2SO4 with a sweep rate of 100 mV s”-“1 and galvonostatic cycling with a current of 1 and 5 mA from 0 to 1.2 V. These results show the potential use of carbon from pyrolysis of glycerol as active component in carbon-based supercapacitors. (author)

  14. A Comparative Study of Lead Oxide Modified Graphite Paste Electrodes and Solid Graphite Electrodes with Mechanically Immobilized Lead Oxides

    OpenAIRE

    Zakharchuk, Nina; Meyer, Stefan; Lange, Britta; Scholz, Fritz

    2000-01-01

    The cyclic voltammetry of red PbO, α-PbO2, β-PbO2 and BaPbO3 was studied with two different types of electrodes in acidic and alkaline media. In one case, microcrystalline particles of lead oxides were mechanically immobilized on the surface of paraffin-impregnated graphite rod electrodes (PIGE), while in the other case, lead oxides were added to a paste of graphite and silicone oil. The overall behaviour of lead oxides in both electrodes is very similar to the well-known behaviour...

  15. 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.

  16. 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.

  17. 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.)

  18. The Printing and Firing Process of Al Paste in PTC Ohmic Contact Electrodes

    Institute of Scientific and Technical Information of China (English)

    LIANG Fei; ZHOU Dong-xiang; LU Wen-zhong; GONG Shu-ping

    2004-01-01

    Al electrodes are well known as ohmic contact electrodes for the PTC component , the influence of their thickness on final component properties was investigated by comparing their ohmic characteristics with the ones of InGa electrodes . After observing the Al paste physical and chemical behaviors during rising temperature by thermal analysis (DTA), the firing operation of Al electrodes could be divided into three main subsections: the temperature rising time (tr), the peak firing temperature (Tp) and the hold time at peak firing temperature (th). The effects of these three parameters on final component properties were discussed in detail.

  19. 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

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

    OpenAIRE

    Manea, F.; Motoc, S.; Pop, A.(National Institute for Physics and Nuclear Engineering, Bucharest, Romania); 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 nanotube composite electrode exhibited the best electroanalytical parameters through applying preconcentration/differential-pulsed voltammetry scheme.

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

    Science.gov (United States)

    Manea, Florica; Motoc, Sorina; Pop, Aniela; Remes, Adriana; Schoonman, Joop

    2012-06-01

    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 nanotube composite electrode exhibited the best electroanalytical parameters through applying preconcentration/differential-pulsed voltammetry scheme.

  2. 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.

  3. 葡萄糖在亚硝基五氰合铁酸铁修饰碳糊电极上的电化学行为研究%Study on the Electrochemical Behavior of the FePCNF Modified Carbon Paste Electrode and Its Application on the Detection of Glucose

    Institute of Scientific and Technical Information of China (English)

    刘素芹; 戴高鹏

    2012-01-01

    采用亚硝基五氰合铁酸铁(FePCNF)粉末与碳粉质量比为2∶3混合,制备了FePCNF修饰碳糊电极.研究了FePCNF修饰碳糊电极在KNO3溶液中的电化学行为和扫速、pH值及不同支持电解质的影响.该电极可用于催化氧化检测葡萄糖.实验表明:FePCNF修饰碳糊电极在0.5 mol/L KNO3溶液中有一对灵敏的氧化还原峰,峰电流与扫速呈线性关系.氧化峰电流与葡萄糖的浓度在2.0×10-6~2.4×10-5 mol/L之间有良好的线性关系(r=0.9934),检出限为6.3×10-7 mol/L.该电极具有良好的稳定性和重现性,适合于微量葡萄糖的检测.%A FePCNF modified carbon paste electrode was prepared by mixed ferrous pentacyanonitrosyl-ferrate and carbop podwer(2:3). The electrochemical behavior of the FePCNF modified carbon paste electrode in 0. 5 mol/L KNO3 solution(pH = 7. 0) was studied. Determination conditions including scan rates, pH values and supporting electrolytes were optimized and an electrochemical method for the detection of glucose was established. The peak current was significantly improved on the modified electrode. The anoidic peak currents were linear straightly with the concentration of glucose in the range of 2. 0Xl0-6~2. 4X10-5 mol/L,and the detection limit was 6. 3X10-7 mol/L.

  4. Attractive forces in microporous carbon electrodes for capacitive deionization

    NARCIS (Netherlands)

    Biesheuvel, P.M.; Porada, S.; Levi, M.; Bazant, M.Z.

    2014-01-01

    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 tha

  5. 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

  6. 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.

  7. Potentiostatic Testing of Oxygen Reduction on Polymer Carbon Electrodes

    OpenAIRE

    Sequeira, C. A. C.; D. M. F. Santos

    2011-01-01

    The preparation of polymer carbon electrocatalysts by the controlled pyrolysis of polyfurfuryl alcohol polymer is described. Potentiostatic testing in oxygen-saturated KOH electrolytes is performed, and electrokinetic properties of the electrodes prepared from the electrocatalysts are presented and discussed. It is revealed that a pure polymer carbon electrode pyrolysed in powder form possesses a very high active area, displaying higher catalytic activity than a polymer pyrolysed in bulk. Sui...

  8. 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...

  9. 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

    2015-03-01

    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. PMID:25633260

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. 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.

  15. 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. PMID:26946258

  16. 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.

  17. Reduction of Carbon Monoxide. Past Research Summary

    Science.gov (United States)

    Schrock, R. R.

    1982-01-01

    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)

  18. 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%.

  19. Lead acid battery performance and cycle life increased through addition of discrete carbon nanotubes to both electrodes

    Science.gov (United States)

    Sugumaran, Nanjan; Everill, Paul; Swogger, Steven W.; Dubey, D. P.

    2015-04-01

    Contemporary applications are changing the failure mechanisms of lead acid batteries. Sulfation at the negative electrode, acid stratification, and dendrite formation now precede positive electrode failures such as grid corrosion and active material shedding. To attenuate these failures, carbon has been explored as a negative electrode additive to increase charge acceptance, eliminate sulfation, and extend cycle life. Frequently, however, carbon incorporation decreases paste density and hinders manufacturability. Discrete carbon nanotubes (dCNT), also known as Molecular Rebar®, are lead acid battery additives which can be stably incorporated into either electrode to increase charge acceptance and cycle life with no change to paste density and without impeding the manufacturing process. Here, full-scale automotive batteries containing dCNT in the negative electrode or both negative and positive electrodes are compared to control batteries. dCNT batteries show little change to Reserve Capacity, improved Cold Cranking, increased charge acceptance, and enhanced overall system efficiency. Life cycle tests show >60% increases when dCNT are incorporated into the negative electrode (HRPSoC/SBA) and up to 500% when incorporated into both electrodes (SBA), with water loss per cycle reduced >20%. Failure modes of cycled batteries are discussed and a hypothesis of dCNT action is introduced: the dCNT/Had Overcharge Reaction Mechanism.

  20. Attractive forces in microporous carbon electrodes for capacitive deionization

    OpenAIRE

    Biesheuvel, P. M.; Porada, S.; 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 sa...

  1. Nano-Carbon Electrodes for Thermal Energy Harvesting.

    Science.gov (United States)

    Romano, Mark S; Razal, Joselito M; Antiohos, Dennis; Wallace, Gordon; Chen, Jun

    2015-01-01

    Thermogalvanic cells are capable of converting waste heat (generated as a by-product of almost all human activity) to electricity. These devices may alleviate the problems associated with the use of fossil fuels to meet the world's current demand for energy. This review discusses the developments in thermogalvanic systems attained through the use of nano-carbons as the electrode materials. Advances in cell design and electrode configuration that improve performance of these thermo converters and make them applicable in a variety of environments are also summarized. It is the aim of this review to act as a channel for further developments in thermogalvanic cell design and electrode engineering. PMID:26328301

  2. Method for making carbon super capacitor electrode materials

    Energy Technology Data Exchange (ETDEWEB)

    Firsich, David W. (Dayton, OH); Ingersoll, David (Albuquerque, NM); Delnick, Frank M. (Dexter, MI)

    1998-01-01

    A method for making near-net-shape, monolithic carbon electrodes for energy storage devices. The method includes the controlled pyrolysis and activation of a pressed shape of methyl cellulose powder with pyrolysis being carried out in two stages; pre-oxidation, preferably in air at a temperature between 200.degree.-250.degree. C., followed by carbonization under an inert atmosphere. An activation step to adjust the surface area of the carbon shape to a value desirable for the application being considered, including heating the carbon shape in an oxidizing atmosphere to a temperature of at least 300.degree. C., follows carbonization.

  3. Flexible supercapacitor yarns with coaxial carbon nanotube network electrodes

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Fabricated flexible yarn supercapacitor with coaxial electrodes. • Use of multifunctional carbon nanotube network electrodes eliminates inactive components and enables high energy/power density. • Robust structure maintains >95% of energy/power while under deformation. - Abstract: Flexible supercapacitors with a yarn-like geometry were fabricated with coaxially arranged electrodes. Carbon nanotube (CNT) network electrodes enabled the integration of the electronic conductor and active material of each electrode into a single component. CNT yarns were employed as the inner electrode to provide the supporting structure of the device. These part integration strategies eliminated the need for inactive material, which resulted in device volumetric energy and power densities among the highest reported for flexible carbon-based EDLCs. In addition, the coaxial yarn cell design provided a robust structure able to undergo flexural deformation with minimal impact on the energy storage performance. Greater than 95% of the energy density and 99% of the power density were retained when wound around an 11 cm diameter cylinder. The electrochemical properties were characterized at stages throughout the fabrication process to provide insights and potential directions for further development of these novel cell designs

  4. 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%.

  5. Electrocatalytic oxidation of glucose by poly(neutral red)/nickel modified carbon paste electrode%聚中性红/Ni2+修饰碳糊电极对葡萄糖的电催化氧化研究

    Institute of Scientific and Technical Information of China (English)

    顾玲; 张苗; 贺亚梅

    2013-01-01

    采用循环伏安法(CV)在碳糊电极(CPE)上通过共聚的方式电聚合制备了聚中性红/Ni2+修饰碳糊电极(Ni2+/PNR/CPE),该修饰电极在0.1mol·L-1NaOH溶液中扫描活化后,在0.531V/0.348V处有一对明显的氧化还原峰,表明Ni2+离子已掺杂于聚合膜中.分别运用扫描电子显微镜(SEM)和X射线能谱仪(EDS)观测并分析了聚合膜的表面形貌及组成.研究结果表明:Ni2+/PNR/CPE在碱性介质中对葡萄糖的氧化具有明显的电催化作用.探讨了最佳实验条件;计算了葡萄糖的部分动力学参数:电荷转移系数(α=0.6970)及电极反应速率常数(k=2.003×103cm3·mol-1·s-1);葡萄糖的氧化峰电流与浓度在1.0×10-5 mol·L-1~1.0×10-2mol·L-1范围内表现出良好的线性关系,检出限为5×10-6mol·L-1(S/N=3),该修饰电极制备方法简单、灵敏度高、稳定性好,用于实际样品中葡萄糖的含量分析,结果令人满意.%A poly(neutral red)/Ni2+ modified carbon paste electrode (PNR/Ni2+/CPE) is fabricated by the electrochemical polymerization on carbon paste electrode(CPE) by cyclic voltammetry(CV)with Ni(Ⅱ) ions incorporated in polymerized solution.A couple of redox current peaks are appeared at 0.531V and 0.348V after scanning in 0.1mol·L-1 NaOH solution,which indicated that Ni2+has been embedded into the polymerized film.The structural morphology and composition of the polymerized film are characterized using scanning electron microscope(SEM)and energy dispersive spectrometry (EDS).The experimental results indicate that PNR/Ni2+/CPE shows a strong electrocatalytic ability towards the oxidation of glucose in alkaline solutions.The optimal experimental conditions for the determination of glucose are discussed in detail.And some kinetic parameters such as the electron transfer coeficient(α=0.6970) and the electrode reaction rate constant(k=2.003×103cm3·mol-1·s-1)of glucose are calculated.The oxidation peak currents and concentrations of glucose

  6. PEDOT Modified Carbon Paste Microelectrodes for Scanning Electrochemical Microscopy

    OpenAIRE

    Csoka, Balazs; Mekhalif, Zineb

    2011-01-01

    Only one measuring tip was used in three different modes of operation of the Scanning Electrochemical Microscope (feed-back mode, generation-collection mode, potentiometry) to collect chemical information about copper targets. The tip was formed from 5 and 25 μm diameter conventional platinum microdisk electrode by etching a cavity, then electrochemically depositing poly(3,4-ethylenedioxythiophene) (PEDOT) layer doped with hexacyanoferrate and finally filling with modified carbon ...

  7. Electrochemical and catalytic investigation of carbon paste modified with Toluidine Blue O covalently immobilised on silica gel

    International Nuclear Information System (INIS)

    Toluidine Blue O (TBO) was covalently bound on silica gel and mixed with graphite powder and paraffin oil to produce modified carbon paste electrodes. The formal potential (E deg.') of the covalently bound TBO was found to be -100 mV versus Ag vertical bar AgCl (KCl sat.) at pH 7.0 and the E deg.' varied less than anticipated for a 2-electron-proton type mediator with pH. The bound TBO was found to act as an efficient electron acceptor for NADH as well as electron donor for oxidised horseradish peroxidase (HRP). The kinetics and the mechanism of the reaction between NADH and TBO were investigated with cyclic voltammetry and using a rotating disc electrode. Further experiments were done in the flow injection mode injecting different concentrations of NADH. Similar studies were done in the presence of hydrogen peroxide when HRP was adsorbed onto the TBO modified silica gel carbon paste electrodes

  8. Highly-Durable Carbon Electrode for Electrochemical Capacitors

    Directory of Open Access Journals (Sweden)

    Soshi Shiraishi

    2013-01-01

    Full Text Available The electric double layer capacitor (EDLC is anelectrochemical capacitor storing electric energy bycharging the electric double layer on the microporesof a nanoporous carbon electrode such as activatedcarbon. The EDLC has a fast charge-dischargeproperty and excellent cycle life, but its energydensity is lower than other electrochemical energystorage devices such as the rechargeable battery.The energy density of the EDLC can be improvedby increasing the double layer capacitance and themaximum charging voltage. In this review, the authordescribes the activated carbon electrodes for use ina durable EDLC for high voltage charging.

  9. 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.

  10. Water desalination using capacitive deionization with microporous carbon electrodes.

    Science.gov (United States)

    Porada, S; Weinstein, L; Dash, R; van der Wal, A; Bryjak, M; Gogotsi, Y; Biesheuvel, P M

    2012-03-01

    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 electrostatic double layers inside the negatively charged cathode and the anions are removed by the positively charged anode. One of the key parameters for commercial realization of CDI is the salt adsorption capacity of the electrodes. State-of-the-art electrode materials are based on porous activated carbon particles or carbon aerogels. Here we report the use for CDI of carbide-derived carbon (CDC), a porous material with well-defined and tunable pore sizes in the sub-nanometer range. When comparing electrodes made with CDC with electrodes based on activated carbon, we find a significantly higher salt adsorption capacity in the relevant cell voltage window of 1.2-1.4 V. The measured adsorption capacity for four materials tested negatively correlates with known metrics for pore structure of the carbon powders such as total pore volume and BET-area, but is positively correlated with the volume of pores of sizes <1 nm, suggesting the relevance of these sub-nanometer pores for ion adsorption. The charge efficiency, being the ratio of equilibrium salt adsorption over charge, does not depend much on the type of material, indicating that materials that have been identified for high charge storage capacity can also be highly suitable for CDI. This work shows the potential of materials with well-defined sub-nanometer pore sizes for energy-efficient water desalination. PMID:22329838

  11. Effects of carbon additives on the performance of negative electrode of lead-carbon battery

    International Nuclear Information System (INIS)

    Highlights: • The negative electrode sheets are prepared by simulating manufacture condition of negative plates. • The effect of carbon additives on negative electrode sheets is studied by electrochemical method. • Carbon additives in NAM enhance electrochemical properties of the negative sheets. • The negative sheets with 0.5 wt% carbon additive exhibit better electrochemical performance. • The charge-discharge mechanism is discussed in detail according to the experimental results. - Abstract: In this study, carbon additives such as activated carbon (AC) and carbon black (CB) are introduced to the negative electrode to improve its electrochemical performance, the negative electrode sheets are prepared by simulating the negative plate manufacturing process of lead-acid battery, the types and contents of carbon additives in the negative electrode sheets are investigated in detail for the application of lead-carbon battery. The electrochemical performance of negative electrode sheets are measured by chronopotentiometry, galvanostatic charge-discharge and electrochemical impedance spectroscopy, the crystal structure and morphology are characterized by X-ray diffraction and scanning electron microscopy, respectively. The experimental results indicate that the appropriate addition of AC or CB can enhance the discharge capacity and prolong the cycle life of negative electrode sheets under high-rate partial-state-of-charge conditions, AC additive exerts more obvious effect than CB additive, the optimum contents for the best electrochemical performance of the negative electrode sheets are determined as 0.5wt% for both AC and CB. The reaction mechanism of the electrochemical process is also discussed in this paper, the appropriate addition of AC or CB in negative electrode can promote the conversion of PbSO4 to Pb, suppress the sulfation of negative electrode sheets and reduce the electrochemical reaction resistance

  12. Conductive Carbon Coatings for Electrode Materials

    International Nuclear Information System (INIS)

    A simple method for optimizing the carbon coatings on non-conductive battery cathode material powders has been developed at Lawrence Berkeley National Laboratory. The enhancement of the electronic conductivity of carbon coating enables minimization of the amount of carbon in the composites, allowing improvements in battery rate capability without compromising energy density. The invention is applicable to LiFePO4 and other cathode materials used in lithium ion or lithium metal batteries for high power applications such as power tools and hybrid or plug-in hybrid electric vehicles. The market for lithium ion batteries in consumer applications is currently $5 billion/year. Additionally, lithium ion battery sales for vehicular applications are projected to capture 5% of the hybrid and electric vehicle market by 2010, and 36% by 2015 (http://www.greencarcongress.com). LiFePO4 suffers from low intrinsic rate capability, which has been ascribed to the low electronic conductivity (10-9 S cm-1). One of the most promising approaches to overcome this problem is the addition of conductive carbon. Co-synthesis methods are generally the most practical route for carbon coating particles. At the relatively low temperatures (4, however, only poorly conductive disordered carbons are produced from organic precursors. Thus, the carbon content has to be high to produce the desired enhancement in rate capability, which decreases the cathode energy density

  13. 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.

  14. 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

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

    OpenAIRE

    Marko Rodić; Olga Vajdle; Valéria Guzsvány; Jasmina Zbiljić; Zsigmond Papp

    2011-01-01

    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 phosp...

  16. Highly-Durable Carbon Electrode for Electrochemical Capacitors

    OpenAIRE

    Soshi Shiraishi

    2013-01-01

    [EN] The electric double layer capacitor (EDLC) is an electrochemical capacitor storing electric energy by charging the electric double layer on the micropores of a nanoporous carbon electrode such as activated carbon. The EDLC has a fast charge-discharge property and excellent cycle life, but its energy density is lower than other electrochemical energy storage devices such as the rechargeable battery. The energy density of the EDLC can be improved by increasing the double layer capacitance ...

  17. Carbon nanotube electrodes for effective interfacing with retinal tissue

    OpenAIRE

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

    2009-01-01

    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 eff...

  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. 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.

  20. 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

  1. Oxygen electrode reaction in molten carbonate fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Appleby, A.J.; White, R.E.

    1992-07-07

    Molten carbonate fuel cell system is a leading candidate for the utility power generation because of its high efficiency for fuel to AC power conversion, capability for an internal reforming, and a very low environmental impact. However, the performance of the molten carbonate fuel cell is limited by the oxygen reduction reaction and the cell life time is limited by the stability of the cathode material. An elucidation of oxygen reduction reaction in molten alkali carbonate is essential because overpotential losses in the molten carbonate fuel cell are considerably greater at the oxygen cathode than at the fuel anode. Oxygen reduction on a fully-immersed gold electrode in a lithium carbonate melt was investigated by electrochemical impedance spectroscopy and cyclic voltammetry to determine electrode kinetic and mass transfer parameters. The dependences of electrode kinetic and mass transfer parameters on gas composition and temperature were examined to determine the reaction orders and the activation energies. The results showed that oxygen reduction in a pure lithium carbonate melt occurs via the peroxide mechanism. A mass transfer parameter, D{sub O}{sup 1/2}C{sub O}, estimated by the cyclic voltammetry concurred with that calculated by the EIS technique. The temperature dependence of the exchange current density and the product D{sub O}{sup 1/2}C{sub O} were examined and the apparent activation energies were determined to be about 122 and 175 kJ/ mol, respectively.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. Hybrid capacitor with activated carbon electrode, Ni(OH) 2 electrode and polymer hydrogel electrolyte

    Science.gov (United States)

    Nohara, Shinji; Asahina, Toshihide; Wada, Hajime; Furukawa, Naoji; Inoue, Hiroshi; Sugoh, Nozomu; Iwasaki, Hideharu; Iwakura, Chiaki

    A new hybrid capacitor (HC) cell was assembled using an activated carbon (AC) negative electrode, an Ni(OH) 2 positive electrode and a polymer hydrogel electrolyte prepared from crosslinked potassium poly(acrylate) (PAAK) and KOH aqueous solution. The HC cell was characterized compared with an electric double layer capacitor (EDLC) using two AC electrodes and the polymer hydrogel electrolyte. It was found that the HC cell successfully worked in the larger voltage range and exhibited ca. 2.4 times higher capacitance than the EDLC cell. High-rate dischargeability of the HC cell was also superior to that of the EDLC cell. These improved characteristics strongly suggest that the HC cell can be a promising system of capacitors with high energy and power densities.

  9. 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.

  10. 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

  11. Composite electrode of carbon nanotubes and vitreous carbon for electron field emission

    OpenAIRE

    Matsubara, EY; Rosolen, JM; Silva, SRP

    2008-01-01

    In this work, the electron field emission behaviour of electrodes formed by carbon nanotubes (CNTs) grown onto monolithic vitreous carbon (VCarbon) substrates with microcavities is presented. Scanning electron microscopy was used to characterize the microstructure of the films. Tungsten probes, stainless steel sphere, and phosphor electrodes were employed in the electron field emission study. The CNT/VCarbon composite represents a route to inexpensive excellent large area electron emission ca...

  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. Effect of surfactants on capacitance properties of carbon electrodes

    International Nuclear Information System (INIS)

    Effect of surfactants present in alkaline solutions on the capacitance of carbon electrodes has been studied. Different types of surfactants, i.e., sodium and lithium dodecyl sulphate as anionic surfactants, tetrapropylammonium bromide and iodide as cationic surfactants and polymer of polyethylene glycol and p-t-octylophenol (commercially called Triton® X-100) as non-ionic one have been selected for this target. Concentration of these electrolyte additives was 0.005 mol L−1. Decreasing the surface tension in the electrode/electrolyte interface allows better penetration of electrolyte into the pores. However, surfactants played a different role depending on the electrode polarity. Detailed analysis of capacitance versus current load, frequency dependence as well as self-discharge, cyclability and behaviour in wider voltage range proved especially a profitable effect of Triton® X-100 on capacitor operating in alkaline solution. Influence of surfactant concentration on capacitance properties was also investigated.

  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. 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...

  16. Comparative studies of mercapto thiadiazoles self-assembled on gold nanoparticle as ionophores for Cu(II) carbon paste sensors

    Energy Technology Data Exchange (ETDEWEB)

    Mashhadizadeh, Mohammad Hossein, E-mail: mashhadizadeh@yahoo.com [Faculty of Chemistry, Tarbiat Moallem University, Tehran (Iran, Islamic Republic of); Khani, Hadi [Faculty of Chemistry, Tarbiat Moallem University, Tehran (Iran, Islamic Republic of); Foroumadi, Alireza [Department of Medicinal Chemistry, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran 14174 (Iran, Islamic Republic of); Sagharichi, Parishad [Faculty of Chemistry, Tarbiat Moallem University, Tehran (Iran, Islamic Republic of)

    2010-04-30

    Comparative studies of the potentiometric behavior of three mercapto compounds [2-((5-mercapto-1,3,4-thiadiazol-2-ylimino)methyl)phenol] (MTMP), [5-(2-methoxy benzylidene amino)-1,3,4-thiadiazole-2-thiol] (MBYT) and [5-(pyridin-2-ylmethyleneamino)-1,3,4-thiadiazole-2-thiol] (PYTT) self-assembled on gold nanoparticles (GNPs) as ionophores in carbon paste electrodes (CPEs) have been made. These mercapto thiadiazole compounds were self-assembled onto gold nanoparticles and then incorporated within carbon paste electrode. The self-assembled ionophores exhibit a high selectivity for copper ion (Cu{sup 2+}), in which the sulfur and nitrogen atoms in their structure play a role as the effective coordination donor site for the copper ion. These carbon paste electrodes were applied as indicator electrodes for potentiometric determination of copper ions. The sensor based on PYTT exhibits the working concentration range of 4.0 x 10{sup -9} to 7.0 x 10{sup -2} M and a Nernstian slope of 28.7 {+-} 0.3 mV decade{sup -1} of copper activity. The detection limit of electrode was 1.0 x 10{sup -9} M and potential response was pH independent across the range of 3.0-6.5. It exhibited a quick response time of <5 s and could be used for a period of 45 days. The ion selectivity of this electrode for Cu{sup 2+} was over 10{sup 4} times that for other metal cations. The application of prepared sensors has been demonstrated for the determination of copper ions in spiked water and natural water samples.

  17. 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.

  18. 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.

  19. 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.

  20. Measurements of Electrode Skin Impedances using Carbon Rubber Electrodes – First Results

    International Nuclear Information System (INIS)

    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%.

  1. 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%.

  2. 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.

  3. 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.

  4. 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.

  5. Low temperature growth of carbon nanotubes on printing electrodes by MPCVD

    Energy Technology Data Exchange (ETDEWEB)

    Chen, K.-C. [Department of Materials Science and Engineering, National Chiao Tung University, Taiwan (China) and Electronics Research and Service Organization (ERSO), Industrial Technology Research Institute (ITRI), Hsinchu, Taiwan (China)]. E-mail: northnose@itri.org.tw; Chen, C.-F. [Department of Materials Science and Engineering, National Chiao Tung University, Taiwan (China); Chiang, J.-S. [Union Chemica Laboratories (UCL), Industrial Technology Research Institute (ITRI), Hsinchu, Taiwan, 310 (China); Hwang, C.-L. [Union Chemica Laboratories (UCL), Industrial Technology Research Institute (ITRI), Hsinchu, Taiwan, 310 (China); Chang, Y.-Y. [Electronics Research and Service Organization (ERSO), Industrial Technology Research Institute (ITRI), Hsinchu, Taiwan (China); Lee, C.-C. [Electronics Research and Service Organization (ERSO), Industrial Technology Research Institute (ITRI), Hsinchu, Taiwan (China)

    2006-03-01

    In this work, combination of screen-printing process and microwave plasma enhanced chemical vapor deposition system (MPCVD) was applied to fabricate patterned carbon nanotubes (CNTs) on the cathode electrodes on glass substrates. Solution based Ni catalyst was well-mixed with Ag powders and organic binder materials to form screen printed paste. CNTs were then grown under the atmosphere of CH{sub 4}/H{sub 2} gas mixture below 550 deg. C. In the field emission measurement, the turn-on field was 3.2 V/{mu}m and uniform electron emission image was also observed.

  6. 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.

  7. 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

  8. 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。

  9. Fluidized bed electrodes with high carbon loading for water desalination by capacitive deionization

    NARCIS (Netherlands)

    Doornbusch, G.J.; Dykstra, J.E.; Biesheuvel, P.M.; Suss, M.E.

    2016-01-01

    The use of carbon flow electrodes has significantly impacted electrochemical energy storage and capacitive deionization (CDI), but device performance is limited as these electrodes cannot surpass ∼20 wt% carbon while maintaining flowability. We here introduce flowable fluidized bed electrodes whi

  10. Carbonation profiles in cement paste analyzed by neutron diffraction

    Science.gov (United States)

    Galan, I.; Sanchez, J.; Andrade, C.; Evans, A.

    2012-02-01

    The present work deals with the carbonation process in cement based materials such as concrete. In order to clarify the evolution of the two main phases involved in the process, portlandite and calcium carbonate as a function of depth, spatially resolved neutron diffraction experiments have been performed at SALSA diffractometer at ILL in carbonated cement paste samples. Specimens submitted to different carbonation processes, both natural and accelerated, have been analyzed with this non destructive technique. The evolution of the main diffraction peaks of portlandite and calcite has been followed by means of neutron diffraction patterns measured at different depths. The results indicate that, in specimens subjected to CO2 atmospheres for 24 and 48 hours, the amount of calcite increases from the centre of the specimen to the surface. In both type of specimens calcite is formed at all depths analyzed, with higher quantities for the ones submitted to the longest carbonation period. Regarding the evolution of portlandite in these specimens, it almost completely disappeared, with only a low amount of the phase constant throughout the sample. In specimens subjected to air in a closed chamber for 21 months, higher amounts of portlandite were observed throughout the sample and little increase of calcite in the outer part, pointing out a much less severe reaction. The absorption effects are characterized by measuring in perpendicular directions and an absorption coefficient is calculated for portlandite.

  11. 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

  12. 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.

  13. 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.

  14. Amperometric biosensor based on glassy carbon electrode modified with long-length carbon nanotube and enzyme

    Science.gov (United States)

    Furutaka, Hajime; Nemoto, Kentaro; Inoue, Yuki; Hidaka, Hiroki; Muguruma, Hitoshi; Inoue, Hitoshi; Ohsawa, Tatsuya

    2016-05-01

    An amperometric biosensor based on a glassy carbon electrode modified with long-length multiwalled carbon nanotubes (MWCNTs) and enzyme nicotinamide-adenine-dinucleotide-dependent glucose dehydrogenase (GDH) is presented. We demonstrate the effect of the MWCNT length on the amperometric response of the enzyme biosensor. The long length of MWCNT is 200 µm (average), whereas the normal length of MWCNT is 1 µm (average). The response of the long MWCNT–GDH electrode is 2 times more sensitive than that of the normal-length MWCNT–GDH electrode in the concentration range from 0.25–35 mM. The result of electrochemical impedance spectroscopy measurements suggest that the long-length MWCNT–GDH electrode formed a better electron transfer network than the normal-length one.

  15. 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.

  16. Single-wall carbon nanotube chemical attachment at platinum electrodes

    Science.gov (United States)

    Rosario-Castro, Belinda I.; Contés-de-Jesús, Enid J.; Lebrón-Colón, Marisabel; Meador, Michael A.; Scibioh, M. Aulice; Cabrera, Carlos R.

    2010-11-01

    Self-assembled monolayer (SAM) techniques were used to adsorb 4-aminothiophenol (4-ATP) on platinum electrodes in order to obtain an amino-terminated SAM as the base for the chemical attachment of single-wall carbon nanotubes (SWCNTs). A physico-chemical, morphological and electrochemical characterizations of SWCNTs attached onto the modified Pt electrodes was done by using reflection-absorption infrared spectroscopy (RAIR), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, scanning electron microscopy (SEM), atomic force microscopy (AFM), and cyclic voltammetry (CV) techniques. The SWNTs/4-ATP/Pt surface had regions of small, medium, and large thickness of carbon nanotubes with heights of 100-200 nm, 700 nm to 1.5 μm, and 1.0-3.0 μm, respectively. Cyclic voltammetries (CVs) in sulfuric acid demonstrated that attachment of SWNTs on 4-ATP/Pt is markedly stable, even after 30 potential cycles. CV in ruthenium hexamine was similar to bare Pt electrodes, suggesting that SWNTs assembly is similar to a closely packed microelectrode array.

  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. Single-wall carbon nanotube chemical attachment at platinum electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Rosario-Castro, Belinda I.; Contes-de-Jesus, Enid J. [Department of Chemistry and Center for Advanced Nanoscale Materials, University of Puerto Rico, Rio Piedras Campus, PO Box 23346, San Juan 00931-3346 (Puerto Rico); Lebron-Colon, Marisabel; Meador, Michael A. [NASA John H. Glenn Research Center, 21000 Brookpark Road, Cleveland, OH 44135 (United States); Scibioh, M. Aulice [Department of Chemistry and Center for Advanced Nanoscale Materials, University of Puerto Rico, Rio Piedras Campus, PO Box 23346, San Juan 00931-3346 (Puerto Rico); Cabrera, Carlos R., E-mail: carlos.cabrera2@uprrp.edu [Department of Chemistry and Center for Advanced Nanoscale Materials, University of Puerto Rico, Rio Piedras Campus, PO Box 23346, San Juan 00931-3346 (Puerto Rico)

    2010-11-01

    Self-assembled monolayer (SAM) techniques were used to adsorb 4-aminothiophenol (4-ATP) on platinum electrodes in order to obtain an amino-terminated SAM as the base for the chemical attachment of single-wall carbon nanotubes (SWCNTs). A physico-chemical, morphological and electrochemical characterizations of SWCNTs attached onto the modified Pt electrodes was done by using reflection-absorption infrared spectroscopy (RAIR), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, scanning electron microscopy (SEM), atomic force microscopy (AFM), and cyclic voltammetry (CV) techniques. The SWNTs/4-ATP/Pt surface had regions of small, medium, and large thickness of carbon nanotubes with heights of 100-200 nm, 700 nm to 1.5 {mu}m, and 1.0-3.0 {mu}m, respectively. Cyclic voltammetries (CVs) in sulfuric acid demonstrated that attachment of SWNTs on 4-ATP/Pt is markedly stable, even after 30 potential cycles. CV in ruthenium hexamine was similar to bare Pt electrodes, suggesting that SWNTs assembly is similar to a closely packed microelectrode array.

  19. 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.

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

    OpenAIRE

    Álvarez, J. I.; Arandigoyen, M.

    2006-01-01

    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...

  1. Glucose Biosensor Based on a Glassy Carbon Electrode Modified with Polythionine and Multiwalled Carbon Nanotubes

    OpenAIRE

    Wenwei Tang; Lei Li; Lujun Wu; Jiemin Gong; Xinping Zeng

    2014-01-01

    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 ...

  2. Electrical breakdown gas detector featuring carbon nanotube array electrodes.

    Science.gov (United States)

    Kim, Seongyul; Pal, Sunil; Ajayan, Pulickel M; Borca-Tasciuc, Theodorian; Koratkar, Nikhil

    2008-01-01

    We demonstrate here detection of dichloro-difluoro-methane and oxygen in mixtures with helium using a carbon nanotube electrical breakdown sensor device. The sensor is comprised of an aligned array of multiwalled carbon nanotubes deposited on a nickel based super-alloy (Inconel 600) as the anode; the counter electrode is a planar nickel sheet. By monitoring the electrical breakdown characteristics of oxygen and dichloro-difluoro-methane in a background of helium, we find that the detection limit for dichloro-difluoro-methane is approximately 0.1% and the corresponding limit for oxygen is approximately 1%. A phenomenologigal model is proposed to describe the trends observed in detection of the two mixtures. These results indicate that carbon nanotube based electrical breakdown sensors show potential as end detectors in gas-chromatography devices. PMID:18468093

  3. 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.

  4. New generation of hybrid carbon/Ni(OH)2 electrochemical capacitor using functionalized carbon electrode

    Science.gov (United States)

    Le Comte, Annaïg; Brousse, Thierry; Bélanger, Daniel

    2016-09-01

    Tailoring carbon based negative electrode by grafting electroactive 9,10-phenanthrenequinone molecules on porous carbon drastically improves the performance of a carbon/Ni(OH)2 hybrid electrochemical capacitor. The grafted-quinone moieties add a Faradaic contribution to the double layer capacitance of carbon leading to a significant increase of the charge stored by the full devices. Good cyclability is ensured due to the strong bond between 9,10-phenanthrenequinone molecules and the carbon surface. More importantly, by increasing the total capacity, the grafting improves the energy density of the full hybrid device while maintaining fast charge/discharge kinetics and thus without affecting the power density.

  5. 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...

  6. 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.

  7. Asymmetric electrochemical supercapacitor, based on polypyrrole coated carbon nanotube electrodes

    International Nuclear Information System (INIS)

    Highlights: • Polypyrrole (PPy) coated multiwalled carbon nanotubes (MWCNT) were prepared. • New method is based on the use of new electrochemically active dopants for PPy. • The dopans provided dispersion of MWCNT and promoted PPy coating formation. • Symmetric PPy–MWCNT supercapacitors showed high capacitance and low resistance. • Asymmetric PPy–MWCNT/VN–MWCNT devices and modules allowed larger voltage window. - Abstract: Conductive polypyrrole (PPy) polymer – multiwalled carbon nanotubes (MWCNT) composites were synthesized using sulfanilic acid azochromotrop (SPADNS) and sulfonazo III sodium salt (CHR-BS) as anionic dopants for chemical polymerization of PPy. The composites were tested for application in electrodes of electrochemical supercapacitors (ES). Sedimentation tests, electrophoretic deposition experiments and Fourier transform infrared spectroscopy (FTIR) investigations showed that strong adsorption of anionic CHR-BS on MWCNT provided MWCNT dispersion. The analysis of scanning and transmission electron microscopy data demonstrated that the use of CHR-BS allowed the formation of PPy coatings on MWCNT. As a result, the composites, prepared using CHR-BS, showed higher capacitance, compared to the composites, prepared using SPADNS. The electrodes, containing MWCNT, coated with PPy showed a capacitance of 179 F g−1 for active mass loading of 10 mg cm−2, good capacitance retention at scan rates in the range of 2–100 mV s−1 and excellent cyclic stability. Asymmetric ES devices, containing positive PPy–MWCNT electrodes and negative vanadium nitride (VN)–MWCNT electrodes showed significant improvement in energy storage performance, compared to the symmetric ES due to the larger voltage window. The low impedance and high capacitance of the individual cells paved the way to the development of modules with higher voltage, which showed good electrochemical performance

  8. Molecular imprinted polypyrrole modified glassy carbon electrode for the determination of tobramycin

    International Nuclear Information System (INIS)

    Graphical abstract: Atomic force microscopic images of (A) bare GCE and (B) TOB imprinted PPy/GCE surface. - Highlights: • Glassy carbon electrode based on molecularly imprinted polypyrrole was prepared. • The developed surfaces were characterized by AFM, FTIR, EIS and CV. • The developed nanosensor was applied to egg and milk samples. - Abstract: Over the past two decades, molecular imprinted polymers have attracted a broad interest from scientists in sensor development. In the preparation of molecular imprinted polymers the desired molecule (template) induces the creation of specific recognition sites in the polymer. In this study, the glassy carbon electrode (GCE) based on molecularly imprinted polypyrrole (PPy) was fabricated for the determination of tobramycin (TOB). The developed electrode was prepared by incorporation of a template molecule (TOB) during the electropolymerization of pyrrole on GCE in aqueous solution using cyclic voltammetry (CV) method. The performance of the imprinted and non-imprinted electrodes was evaluated by square wave voltammetry (SWV). The effect of pH, monomer and template concentrations, electropolymerization cycles on the performance of the imprinted and non-imprinted electrodes was investigated and optimized. The non-modified and TOB-imprinted surfaces were characterized by using atomic force microscopy (AFM), Fourier transform infrared spectroscopy (FTIR), electrochemical impedance spectroscopy (EIS) and CV. The linearity range of TOB was 5.0 × 10−10–1.0 × 10−8 M with the detection limit of 1.4 × 10−10 M. The developed nanosensor was applied successfully for the determination of TOB in egg and milk

  9. Carbon felt supported carbon nanotubes catalysts composite electrode for vanadium redox flow battery application

    Science.gov (United States)

    Wei, Guanjie; Jia, Chuankun; Liu, Jianguo; Yan, Chuanwei

    2012-12-01

    A modified electrode for vanadium redox flow battery (VRFB) has been developed in this paper. The electrode is based on a traditional carbon felt (CF) grafted with the short-carboxylic multi-walled carbon nanotubes (MWCNTs). The microstructure and electrochemical property of the modified electrode as well as the performance of the VRFB single cell with it have been characterized. The results show that the MWCNTs are evenly dispersed and adhere to the surface of carbon fibres in the CF. The electrochemical activities of the modified CF electrode have been improved dramatically and the reversibility of the VO2+/VO2+ and V3+/V2+ redox couples increased greatly. The VRFB single cell with the modified CF exhibits higher coulombic efficiency (93.9%) and energy efficiency (82.0%) than that with the pristine CF. The SEM analysis shows that the MWCNTs still cohere with carbon fibres after charge and discharge test, indicating the stability of the MWCNTs in flowing electrolyte. Therefore, the composite electrode presents considerable potential for the commercial application of CF in VRFB.

  10. 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)

  11. Screen printing of nucleic acid detecting carbon electrodes.

    Science.gov (United States)

    Dequaire, Murielle; Heller, Adam

    2002-09-01

    A large fraction of the presently mass-manufactured (> 10(8) units/year) electrochemical biosensors, used mostly by diabetic people to monitor their blood glucose levels, have screen-printed carbon working electrodes. An earlier study (Campbell, C. N., et al. Anal. Chem. 2002, 74, 158-162) showed that nucleic acids can be assayed at 1 nM concentrations by a sandwich-type amperometric method. The assay was performed with vitreous carbon working electrodes on which an electron-conducting polycationic redox polymer and avidin were coelectrodeposited. Because the rate of the electrodeposition increases with the surface density of the polycationic redox polymer, its practicality depends on pretreatment of the surface, which adds anionic functions. (Gao, Z., et al. Angew. Chem. Int. Ed. 2002, 41, 810-813). Here it is shown that the required conducting redox polymer films can be electrodeposited on potentially mass manufacturable electrodes made by screen-printing hydrophilic carbon inks on polyester sheets. The modified electrodes are made in two steps. First a polycationic electron-conducting redox polymer is cross-linked and electrodeposited by applying a negative potential. Next, an amine-terminated 20-base single-stranded oligonucleotide is electrodeposited by ligand-exchange. Both steps involve exchange of a labile inner sphere chloride ligand of the polymer-bound osmium-complex: Cross-linking and electrodeposition of the redox polymer result when inner-sphere chloride anions of the osmium complexes are exchanged by imidazole functions of neighboring chains. Incorporation of the oligonucleotide in the redox polymer results in the formation of a coordinative bond between the terminal amine (attached through a spacer to the oligonucleotide) and the osmium complex. In testing for the presence of a 38-base oligonucleotide, the analyte, in a 15- or 25-microL droplet of hybridization solution, is hybridized with and captured by the 20-base electrode-bound sequence; then

  12. 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.

  13. 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.

  14. 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.

  15. 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

  16. 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

  17. 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.

  18. Carbon nanofiber electrode array for electrochemical detection of dopamine using fast scan cyclic voltammetry

    OpenAIRE

    Koehne, Jessica E.; Marsh, Michael; Boakye, Adwoa; Douglas, Brandon; Kim, In Yong; Chang, Su-Youne; Jang, Dong-Pyo; Bennet, Kevin E.; Kimble, Christopher; Andrews, Russell; Meyyappan, M.; Lee, Kendall H.

    2011-01-01

    A carbon nanofiber (CNF) electrode array was integrated with the Wireless Instantaneous Neurotransmitter Sensor System (WINCS) for detection of dopamine using fast scan cyclic voltammetry (FSCV). Dopamine detection performance by CNF arrays was comparable to that of traditional carbon fiber microelectrodes (CFMs), demonstrating that CNF arrays can be utilized as an alternative carbon electrodes for neurochemical monitoring.

  19. 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.

  20. A glucose biosensor using methyl viologen redox mediator on carbon film electrodes

    OpenAIRE

    Ghica, Mariana Emilia; Christopher M. A. Brett

    2005-01-01

    A new methyl viologen-mediated amperometric enzyme electrode sensitive to glucose has been developed using carbon film electrode substrates. Carbon film electrodes from resistors fabricated by pyrolytic deposition of carbon were modified by immobilization of glucose oxidase through cross-linking with glutaraldehyde in the presence of bovine serum albumin. The mediator, methyl viologen, was directly immobilised with the enzyme together with Nafion cation-exchange polymer. The electrochemistry ...

  1. 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.

  2. 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.

  3. 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.

  4. Advantages of the Biomimetic Nanostructured Films as an Immobilization Method vs. the Carbon Paste Classical Method

    Directory of Open Access Journals (Sweden)

    Maria Luz Rodríguez-Méndez

    2012-11-01

    Full Text Available Tyrosinase-based biosensors containing a phthalocyanine as electron mediator have been prepared by two different methods. In the first approach, the enzyme and the electron mediator have been immobilized in carbon paste electrodes. In the second method, they have been introduced in an arachidic acid Langmuir-Blodgett nanostructured film that provides a biomimetic environment. The sensing properties of non-nanostructured and nanostructured biosensors towards catechol, catechin and phenol have been analyzed and compared. The enzyme retains the biocatalytic properties in both matrixes. However, the nanostructured biomimetic films show higher values of maximum reaction rates and lowest apparent Michaelis-Menten constants. In both types of sensors, the sensitivity follows the decreasing order catechol > catechin > phenol. The detection limits observed are in the range of 1.8–5.4 μM for Langmuir-Blodgett biosensors and 8.19–8.57 μM for carbon paste biosensors. In summary, it has been demonstrated that the Langmuir-Blodgett films provide a biomimetic environment and nanostructured biosensors show better performances in terms of kinetic, detection limit and stability.

  5. 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%.

  6. 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.

  7. 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.

  8. Potentiometric stripping analysis of arsenic using a graphene paste electrode modified with a thiacrown ether and gold nanoparticles

    International Nuclear Information System (INIS)

    An electrochemical method is presented for the determination of arsenic at subnanomolar levels. It is based on potentiometric stripping analysis (PSA) using a graphene paste electrode modified with the thiacrown 1,4,7-trithiacyclononane (TTCN) and gold nanoparticles (AuNPs). The electrode surface was characterized by means of cyclic voltammetry, electrochemical impedance spectroscopy, chronocoulometry and scanning electron microscopy. The modified electrode displays a 15-fold enhancement in the PSA signal (dt/dE) compared to a conventional graphene paste electrode. Under optimized conditions, the signal is proportional to the concentration of As(III) in the range from 25 pM to 34 nM (r2 = 0.9977), and the detection limit (SD/s) is as low as 8 pM. The modified electrode was successfully applied to the determination of total arsenic [i.e., As(III) and As(V)] in pharmaceutical formulations, human hair, sea water, fruits, vegetables, soil, and wine samples. (author)

  9. $MNO_2$ catalyzed carbon electrodes for dioxygen reduction in concentrated alkali

    OpenAIRE

    Manoharan, R; Shulka, AK

    1984-01-01

    A process to deposit $\\gamma-MnO_2$ catalytic oxide onto coconut-shell charcoal substrate is described. Current-potential curves for electroreduction of dioxygen with electrodes fabricated from this catalyzed substrate are obtained in 6M KOH under ambient conditions. The performance of these electrodes is competitive with platinized carbon electrodes.

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. 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.

  15. 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.

  16. Electrochemical and catalytic investigation of carbon paste modified with Toluidine Blue O covalently immobilised on silica gel

    Energy Technology Data Exchange (ETDEWEB)

    Munteanu, Florentina-Daniela; Okamoto, Yoshiyuki; Gorton, Lo

    2003-01-10

    Toluidine Blue O (TBO) was covalently bound on silica gel and mixed with graphite powder and paraffin oil to produce modified carbon paste electrodes. The formal potential (E deg.') of the covalently bound TBO was found to be -100 mV versus Ag vertical bar AgCl (KCl sat.) at pH 7.0 and the E deg.' varied less than anticipated for a 2-electron-proton type mediator with pH. The bound TBO was found to act as an efficient electron acceptor for NADH as well as electron donor for oxidised horseradish peroxidase (HRP). The kinetics and the mechanism of the reaction between NADH and TBO were investigated with cyclic voltammetry and using a rotating disc electrode. Further experiments were done in the flow injection mode injecting different concentrations of NADH. Similar studies were done in the presence of hydrogen peroxide when HRP was adsorbed onto the TBO modified silica gel carbon paste electrodes.

  17. 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. PMID:26769718

  18. 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.

  19. Activated carbon as a pseudo-reference electrode for electrochemical measurement inside concrete

    NARCIS (Netherlands)

    Abbas, Yawar; Olthuis, Wouter; Berg, van den Albert

    2015-01-01

    The application of Kynol based activated carbon (KAC) as a pseudo-reference electrode for potentiometric measurement inside concrete is presented. Due to its high surface area the activated carbons has a large electrical double layer capacitance (EDLC > 50 F g(-1)) and are used as electrode material

  20. Copper-decorated carbon nanotubes-based composite electrodes for nonenzymatic detection of glucose

    OpenAIRE

    Pop, A.(National Institute for Physics and Nuclear Engineering, Bucharest, Romania); 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 electrode (Cu/CNT-epoxy) exhibited the highest sensitivity to glucose determination.

  1. DESALINATION BY CAPACITIVE DEIONIZATION WITH CARBON-BASED MATERIALS AS ELECTRODE: A REVIEW

    OpenAIRE

    WEI HUANG; YIMIN ZHANG; SHENXU BAO; SHAOXIAN SONG

    2013-01-01

    Capacitive deionization (CDI) is a recently developed electrosorption technology for deionization using porous electrodes. The electrode materials play an important role in the efficiency. This paper highlights the current research status of carbon-based materials as the electrode and the adsorption models in the CDI. It includes the types and performances of carbon-based materials and the main influencing factors of the desalination characteristics. Also, operating parameters such as chargin...

  2. Working Electrodes

    Science.gov (United States)

    Komorsky-Lovrić, Šebojka

    In electrochemistry an electrode is an electronic conductor in contact with an ionic conductor. The electronic conductor can be a metal, or a semiconductor, or a mixed electronic and ionic conductor. The ionic conductor is usually an electrolyte solution; however, solid electrolytes and ionic melts can be used as well. The term "electrode" is also used in a technical sense, meaning the electronic conductor only. If not specified otherwise, this meaning of the term "electrode" is the subject of the present chapter. In the simplest case the electrode is a metallic conductor immersed in an electrolyte solution. At the surface of the electrode, dissolved electroactive ions change their charges by exchanging one or more electrons with the conductor. In this electrochemical reaction both the reduced and oxidized ions remain in solution, while the conductor is chemically inert and serves only as a source and sink of electrons. The technical term "electrode" usually also includes all mechanical parts supporting the conductor (e.g., a rotating disk electrode or a static mercury drop electrode). Furthermore, it includes all chemical and physical modifications of the conductor, or its surface (e.g., a mercury film electrode, an enzyme electrode, and a carbon paste electrode). However, this term does not cover the electrolyte solution and the ionic part of a double layer at the electrode/solution interface. Ion-selective electrodes, which are used in potentiometry, will not be considered in this chapter. Theoretical and practical aspects of electrodes are covered in various books and reviews [1-9].

  3. Enhancement of the carbon electrode capacitance by brominated hydroquinones

    Science.gov (United States)

    Gastol, Dominika; Walkowiak, Jedrzej; Fic, Krzysztof; Frackowiak, Elzbieta

    2016-09-01

    This paper presents supercapacitors utilizing new redox-active electrolytes with bromine species. Two sources of Br specimen were investigated, i.e. dibromodihydroxybenzene dissolved in KOH and potassium bromide dissolved in KOH with hydroxybenzene additive. KOH-activated carbon, exhibiting a well-developed porosity, was incorporated as an electrode material. The tested systems revealed a capacitance enhancement explained by Br- and partial BrO3- redox activity. The optimisation of the electrolyte concentration resulted in a capacitance value of 314 F g-1 achieved at 1.1 V voltage range. Good cyclability performance (11% capacitance loss) combined with a high capacitance value (244 F g-1) were obtained for the system operating in 0.2 mol L- 1 C6H4Br2O2 in 2 mol L-1 KOH electrolytic solution.

  4. A new amperometric glucose biosensor based on screen printed carbon electrodes with rhenium(IV) - oxide as a mediator

    OpenAIRE

    ALBANA VESELI; AHMET HAJRIZI; TAHIR ARBNESHI; KURT KALCHER

    2012-01-01

    Rhenium(IV)-oxide, ReO2, was used as a mediator for carbon paste (CPE) and screen printed carbon (SPCE) electrodes for the catalytic amperometric determination of hydro-gen peroxide, whose overpotential for the reduction could be lowered to -0.1 V vs. Ag/AgCl in flow injection analysis (FIA) using phosphate buffer (0.1 M, pH=7.5) as a carrier. For hydrogen peroxide a detection limit (3σ) of 0.8 mg L-1 could be obtained. ReO2-modified SPCEs were used to design biosensors with a template enzyme...

  5. 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

  6. 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.

  7. Carbon nanomaterials as counter electrodes for dye solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Aitola, K.

    2012-07-01

    The dye solar cell (DSC) is an interesting emerging technology for photovoltaic conversion of solar electromagnetic energy to electrical energy. The DSC is based mainly on cheap starting materials and it can be manufactured by roll-to-roll deposition techniques on flexible substrates, which is considered as one option for cost-effective large-scale solar cell production. The most expensive component of the DSC is the transparent conductive oxide glass substrate, and considerable cost reductions can be achieved by changing it to e.g. a plastic substrate. Plastic substrates are very flexible, lightweight and transparent. The state of the art DSC catalyst is thermally deposited or sputtered platinum, but platinum is a rare and expensive metal. Carbon, on the other hand, is widely available and some of its nanomaterials conduct electricity and are catalytic toward the DSC counter electrode (CE) reduction reaction. In this work, carbon nanomaterials and their composites were studied as the DSC CE active material. The materials were random network single-walled carbon nanotube (SWCNT) film on glass and plastic substrate, vertically aligned multiwalled carbon nanotube 'forest' film on steel and quartz substrate and carbon nanoparticle composite film on indium tin oxidepolyethylene terephthalate (ITO-PET) substrate. After comparison of the materials, the SWCNT network film on PET was chosen as the main CE type of this study, since it offers superior conductivity, transparency and flexibility over the other carbon-based CEs, it is also the thinnest and contains only one active material component. When a 30 % transparent SWCNT network film on PET was tested as a DSC CE, it was found out that such a film is not catalytic and conductive enough for a full 1 sun illumination DSC device, but the film could be suitable for a indoor illumination level application. The catalytic properties of a 10 % transparent SWCNT film were improved by depositing conductive PEDOT

  8. 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.

  9. 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.

  10. Synthesis and characterization of tin oxide/carbon aerogel composite electrodes for electrochemical supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Hwang, Sung-Woo; Hyun, Sang-Hoon [School of Advanced Materials Science and Engineering, Yonsei University, 134 Shinchon-dong, Seodaemun-gu, Seoul 120-749 (Korea)

    2007-10-11

    Two types of carbon aerogel-based functional electrodes for supercapacitor applications are developed. To improve the electrochemical performance of the electrodes, carbon aerogels are doped with pseudocapacitive tin oxide either by impregnating tin oxide sol into resorcinol-formaldehyde (RF) wet gels (Method I), or by impregnating tin tetrachloride solution into carbon aerogel electrodes (Method II). The electrodes are heat-treated to 450 C in air to activate the electrode surface and complete the oxidation of tin-precursors in the network structure of the aerogel. The effects of different impregnation methods on the physical/electrochemical properties of the composite electrodes are investigated. Microstructural and compositional variations of the electrodes with tin oxide doping are also examined by scanning electron microscopy and energy dispersive X-ray analysis. The tin oxide/carbon aerogel composite electrodes synthesized by both methods have similar specific capacitances (66-70 F g{sup -1}). Composite electrodes synthesized via Method II showed better cyclic stability compared with electrodes synthesized via Method I. (author)

  11. Nomex-derived activated carbon fibers as electrode materials in carbon based supercapacitors

    Science.gov (United States)

    Leitner, K.; Lerf, A.; Winter, M.; Besenhard, J. O.; Villar-Rodil, S.; Suárez-García, F.; Martínez-Alonso, A.; Tascón, J. M. D.

    Electrochemical characterization has been carried out for electrodes prepared of several activated carbon fiber samples derived from poly (m-phenylene isophthalamide) (Nomex) in an aqueous solution. Depending on the burn-off due to activation the BET surface area of the carbons was in the order of 1300-2800 m 2 g -1, providing an extensive network of micropores. Their capability as active material for supercapacitors was evaluated by using cyclic voltammetry and impedance spectroscopy. Values for the capacitance of 175 F g -1 in sulfuric acid were obtained. Further on, it was observed that the specific capacitance and the performance of the electrode increase significantly with increasing burn-off degree. We believe that this fact can be attributed to the increase of surface area and porosity with increasing burn-off.

  12. 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

  13. 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.

  14. 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.

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

    Science.gov (United States)

    Jewell, Eifion; Philip, Bruce; Greenwood, Peter

    2016-01-01

    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. PMID:27355967

  16. 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.

  17. 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.

  18. 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.

  19. Carbon Based Electrodes Modified with Horseradish Peroxidase Immobilized in Conducting Polymers for Acetaminophen Analysis

    OpenAIRE

    Cecilia Cristea; Robert Sandulescu; Anca Florea; Mihaela Tertis

    2013-01-01

    The development and optimization of new biosensors with horseradish peroxidase immobilized in carbon nanotubes-polyethyleneimine or polypyrrole nanocomposite film at the surface of two types of transducer is described. The amperometric detection of acetaminophen was carried out at −0.2 V versus Ag/AgCl using carbon based-screen printed electrodes (SPEs) and glassy carbon electrodes (GCEs) as transducers. The electroanalytical parameters of the biosensors are highly dependent on their configur...

  20. SELECTIVE VOLTAMMETRIC DETERMINATION OF HYDROXYPURINS ON ELECTRODE MODIFIED BY CARBON NANOTUBES

    OpenAIRE

    Shaidarova, L. G.; Chelnokova, I. A.; Mahmutova, G. F.; Degteva, M. A.; Gedmina, A. V.; Budnikov, H. C.

    2014-01-01

    Carbon nanotubes (CNT) deposited on the surface of glassy carbon electrode show catalytic activity in the oxidation of uric acid, xanthine and hypoxanthine that is exhibited in decreasing overvoltage and increasing oxidation current of hydroxypurins. The method of simultaneous voltammetric determination of uric acid, xanthine and hypoxanthine at the electrode modified by carbon nanotubes is suggested. The linear dependence of analytical signal from substrates concentration is observed in the ...

  1. Influence of electrode preparation on the electrochemical behaviour of carbon-based supercapacitors

    OpenAIRE

    Ruiz Ruiz, Vanesa; Blanco Rodríguez, Clara; Granda Ferreira, Marcos; Menéndez López, Rosa María; Santamaría Ramírez, Ricardo

    2007-01-01

    [EN] This work investigates the influence of electrode preparation on the electrochemical behaviour of carbon-based supercapacitors. Studies were performed using the same activated carbon and polymer polyvynilidene fluoride (PVDF) in the same proportions (10 wt.% PVDF). Only the way in which these components were mixed was modified. The procedure for mixing the activated carbon and the polymer has a significant influence on the electrochemical behaviour of the electrode used in a supercapacit...

  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. PMID:23794416

  3. 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.

  4. 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.

  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. 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).

  7. Redox Response of Reduced Graphene Oxide-Modified Glassy Carbon Electrodes to Hydrogen Peroxide and Hydrazine

    Directory of Open Access Journals (Sweden)

    Jun-ichi Anzai

    2013-05-01

    Full Text Available The surface of a glassy carbon (GC electrode was modified with reduced graphene oxide (rGO to evaluate the electrochemical response of the modified GC electrodes to hydrogen peroxide (H2O2 and hydrazine. The electrode potential of the GC electrode was repeatedly scanned from −1.5 to 0.6 V in an aqueous dispersion of graphene oxide (GO to deposit rGO on the surface of the GC electrode. The surface morphology of the modified GC electrode was characterized by scanning electron microscopy (SEM and atomic force microscopy (AFM. SEM and AFM observations revealed that aggregated rGO was deposited on the GC electrode, forming a rather rough surface. The rGO-modified electrodes exhibited significantly higher responses in redox reactions of H2O2 as compared with the response of an unmodified GC electrode. In addition, the electrocatalytic activity of the rGO-modified electrode to hydrazine oxidation was also higher than that of the unmodified GC electrode. The response of the rGO-modified electrode was rationalized based on the higher catalytic activity of rGO to the redox reactions of H2O2 and hydrazine. The results suggest that rGO-modified electrodes are useful for constructing electrochemical sensors.

  8. Compressed multiwall carbon nanotube composite electrodes provide enhanced electroanalytical performance for determination of serotonin

    International Nuclear Information System (INIS)

    Serotonin (5-HT) is an important neurochemical that is present in high concentrations within the intestinal tract. Carbon fibre and boron-doped diamond based electrodes have been widely used to date for monitoring 5-HT, however these electrodes are prone to fouling and are difficult to fabricate in certain sizes and geometries. Carbon nanotubes have shown potential as a suitable material for electroanalytical monitoring of 5-HT but can be difficult to manipulate into a suitable form. The fabrication of composite electrodes is an approach that can shape conductive materials into practical electrode geometries suitable for biological environments. This work investigated how compression of multiwall carbon nanotubes (MWCNTs) epoxy composite electrodes can influence their electroanalytical performance. Highly compressed composite electrodes displayed significant improvements in their electrochemical properties along with decreased internal and charge transfer resistance, reproducible behaviour and improved batch to batch variability when compared to non-compressed composite electrodes. Compression of MWCNT epoxy composite electrodes resulted in an increased current response for potassium ferricyanide, ruthenium hexaammine and dopamine, by preferentially removing the epoxy during compression and increasing the electrochemical active surface of the final electrode. For the detection of serotonin, compressed electrodes have a lower limit of detection and improved sensitivity compared to non-compressed electrodes. Fouling studies were carried out in 10 μM serotonin where the MWCNT compressed electrodes were shown to be less prone to fouling than non-compressed electrodes. This work indicates that the compression of MWCNT carbon-epoxy can result in a highly conductive material that can be moulded to various geometries, thus providing scope for electroanalytical measurements and the production of a wide range of analytical devices for a variety of systems

  9. Preparation of Platinum Implanted Glassy Carbon Electrode and Electro-oxidation of Formic Acid and Formaldehyde

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The glassy carbon substrates were bombarded with 5×1017 ions/cm2 of platinum.The surface composition of implanted electrode and concentration-depth profiles of various elements were measured by AES.The chemical state of Pt in glassy carbon electrode implanted with platinum (Pt/GC) was detected by X-ray Photoelectron Spectroscopy (XPS).The electro-oxidation of HCOOH and HCHO have been investigated on Pt/GC and smooth Pt electrodes.The results show that the platinum implanted into glassy carbon is much more active than the smooth platinum metal for electro-oxidation of HCOOH and HCHO.

  10. Au nanoparticles and graphene quantum dots co-modified glassy carbon electrode for catechol sensing

    Science.gov (United States)

    Zhao, Xuan; He, Dawei; Wang, Yongsheng; Hu, Yin; Fu, Chen

    2016-03-01

    In this letter, the gold nanoparticles and graphene quantum dots were applied to the modification of glassy carbon electrode for the detection of catechol. The synergist cooperation between gold nanoparticles and graphene quantum dots can increase specific surface area and enhance electronic and catalytic properties of glassy carbon electrode. The detection limit of catechol is 0.869 μmol/L, demonstrating the superior detection efficiency of the gold nanoparticles and graphene quantum dots co-modified glassy carbon electrode as a new sensing platform.

  11. 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.

  12. 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.

  13. 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.

  14. 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.

  15. Single-walled carbon nanotubes modified carbon ionic liquid electrode for sensitive electrochemical detection of rutin

    Energy Technology Data Exchange (ETDEWEB)

    Zhu Zhihong [Institute of Nano-Science and Technology Center, Huazhong Normal University, Wuhan 430079 (China); Sun Xiaoying; Zhuang Xiaoming [College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Zeng Yan [Institute of Nano-Science and Technology Center, Huazhong Normal University, Wuhan 430079 (China); Sun Wei, E-mail: sunwei@qust.edu.c [College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Huang Xintang [Institute of Nano-Science and Technology Center, Huazhong Normal University, Wuhan 430079 (China)

    2010-11-01

    The single-walled carbon nanotubes (SWCNTs) modified carbon ionic liquid electrode (CILE) was designed and further used for the voltammetric detection of rutin in this paper. CILE was prepared by mixing graphite powder with ionic liquid (IL) 1-butyl-3-methylimidazolium tetrafluoroborate and liquid paraffin together. Based on the interaction of SWCNTs with IL present on the electrode surface, a stable SWCNTs film was formed on the CILE to get a modified electrode denoted as SWCNTs/CILE. The characteristics of SWCNTs/CILE were recorded by different methods including cyclic voltammetry, electrochemical impedance spectroscopy and scanning electron microscopy. The electrochemical behaviors of rutin on the SWCNTs/CILE were investigated by cyclic voltammetry and differential pulse voltammetry. Due to the specific interface provided by the SWCNTs-IL film, the electrochemical response of rutin was greatly enhanced with a pair of well-defined redox peaks appeared in pH 2.5 phosphate buffer solution. The oxidation peak currents showed good linear relationship with the rutin concentration in the range from 1.0 x 10{sup -7} to 8.0 x 10{sup -4} mol/L with the detection limit as 7.0 x 10{sup -8} mol/L (3{sigma}). The SWCNTs/CILE showed the advantages such as excellent selectivity, improved performance, good stability and it was further applied to the rutin tablets sample detection with satisfactory results.

  16. 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.

  17. 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)

  18. 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.

  19. The electrochemical behavior of Co(TPTZ){sub 2} complex on different carbon based electrodes modified with TiO{sub 2} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ortaboy, Sinem, E-mail: ortaboy@istanbul.edu.tr; Atun, Gülten, E-mail: gatun@istanbul.edu.tr

    2015-04-15

    Electrochemical behavior of cobalt (II) complex with the N-donor ligand 2,2′-bipyridyl-1,3,5-tripyridyl-s-triazine (TPTZ) was investigated to elucidate the electron-proton transfer mechanisms. The electrochemical response of the complex was studied using square-wave voltammetry (SWV) and electrochemical impedance spectroscopy (EIS) techniques. A conventional three-electrode system, consisting of glassy carbon (GCE), TiO{sub 2} modified glassy carbon (T/GCE), carbon paste (CPE) and TiO{sub 2} modified carbon paste (T/CPE) working electrodes were employed. The ligand/metal ratio and stability constant of the complex as well as the mechanisms of the electrode processes were elucidated by examining the effects of pH, ligand concentration and frequency on the voltammograms. The EIS results indicated that the samples modified with TiO{sub 2} had the higher charge transfer resistance than that of the bare electrodes and also suggested that the electroactivity of the electrode surfaces increased in the following order, T/CPE > CPE > T/GCE > GCE. The surface morphology of the working electrodes was also characterized by atomic force microscopy (AFM). The values of surface roughness parameters were found to be consistent with the results obtained by EIS experiments. - Graphical abstract: Schematic illustration of the experimental process. - Highlights: • Electrochemical behavior of Co(TPTZ){sub 2} complex studied by SWV and EIS techniques. • GCE, CPE T/GCE and T/CPE were used as working electrodes for comparative studies. • The surface morphologies of the electrodes were characterized by AFM. • Mechanisms were proposed from the effects of pH, ligand concentration and frequency. • EIS and morphologic relationships of the surfaces were established successfully.

  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. 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)

  2. 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.

  3. 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%).

  4. Physical and electrochemical properties of supercapacitor composite electrodes prepared from biomass carbon and carbon from green petroleum coke

    Science.gov (United States)

    Awitdrus, Deraman, M.; Talib, I. A.; Farma, R.; Omar, R.; Ishak, M. M.; Taer, E.; Dolah, B. N. M.; Basri, N. H.; Nor, N. S. M.

    2015-04-01

    The green monoliths (GMs) were prepared from the mixtures of pre-carbonized fibers of oil palm empty fruit bunches (or self-adhesive carbon grains (SACG)) and green petroleum coke (GPC) with the mixing ratio of 0, 10, 30, 50 and 70 % GPC, respectively. The GMs were carbonized in N2 environment at 800°C to produce carbon monoliths (CM00, CM10, CM30, CM50 and CM70). The CMs were CO2 activated at 800°C for 1 hour to produced activated carbon monolith electrodes (ACM00, ACM10, ACM30, ACM50 and ACM70). For each percentage of GPC, three duplicate symmetrical supercapacitor cells were fabricated using these activated carbon monolith electrodes respectively, and the capacitive performance amongst the cells was compared and analyzed in order to observe the relationship between the capacitive performance and the physical properties (microstructure and porosity) of the ACMs electrodes containing varying percentage of GPC.

  5. 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.

  6. Improved stability of redox enzyme layers on glassy carbon electrodes via covalent grafting

    Energy Technology Data Exchange (ETDEWEB)

    Pellissier, Marie; Barriere, Frederic [Universite de Rennes 1, CNRS UMR no. 6226, Sciences Chimiques de Rennes, Equipe MaCSE (France); Downard, Alison J. [MacDiarmid Institute for Advanced Materials and Nanotechnology, Department of Chemistry, University of Canterbury, Christchurch (New Zealand); Leech, Donal [School of Chemistry, National University of Ireland, Galway (Ireland)

    2008-06-15

    One of the challenges in the field of enzymatic biofuel cells is to significantly improve their current limited lifetime. In the present work, we report the covalent immobilization of enzyme layers on glassy carbon electrodes, functionalized via electrochemical reduction of in situ generated aryldiazonium salts bearing carboxylic acid groups. We present the performance and the stability over time of the modified electrodes. For glucose oxidase - modified electrodes, stable catalytic activity is observed for a minimum of 6 weeks. (author)

  7. Electrochemical Reduction of Oxygen on Anthraquinone/Carbon Nanotubes Nanohybrid Modified Glassy Carbon Electrode in Neutral Medium

    OpenAIRE

    Zheng Gong; Guoquan Zhang; Song Wang

    2013-01-01

    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 ...

  8. Surface-treated carbon electrodes with modified potential of zero charge for capacitive deionization.

    Science.gov (United States)

    Wu, Tingting; Wang, Gang; Zhan, Fei; Dong, Qiang; Ren, Qidi; Wang, Jianren; Qiu, Jieshan

    2016-04-15

    The potential of zero charge (Epzc) of electrodes can greatly influence the salt removal capacity, charge efficiency and cyclic stability of capacitive deionization (CDI). Thus optimizing the Epzc of CDI electrodes is of great importance. A simple strategy to negatively shift the Epzc of CDI electrodes by modifying commercial activated carbon with quaternized poly (4-vinylpyridine) (AC-QPVP) is reported in this work. The Epzc of the prepared AC-QPVP composite electrode is as negative as -0.745 V vs. Ag/AgCl. Benefiting from the optimized Epzc of electrodes, the asymmetric CDI cell which consists of the AC-QPVP electrode and a nitric acid treated activated carbon (AC-HNO3) electrode exhibits excellent CDI performance. For inverted CDI, the working potential window of the asymmetric CDI cell can reach 1.4 V, and its salt removal capacity can be as high as 9.6 mg/g. For extended voltage CDI, the salt removal capacity of the asymmetric CDI cell at 1.2/-1.2 V is 20.6 mg/g, which is comparable to that of membrane CDI using pristine activated carbon as the electrodes (19.5 mg/g). The present work provides a simple method to prepare highly positively charged CDI electrodes and may pave the way for the development of high-performance CDI cells. PMID:26878480

  9. 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. PMID:27332854

  10. 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.

  11. Studies on electrochemical sodium storage into hard carbons with binder-free monolithic electrodes

    Science.gov (United States)

    Hasegawa, George; Kanamori, Kazuyoshi; Kannari, Naokatsu; Ozaki, Jun-ichi; Nakanishi, Kazuki; Abe, Takeshi

    2016-06-01

    Hard carbons emerge as one of the most promising candidate for an anode of Na-ion batteries. This research focuses on the carbon monolith derived from resorcinol-formaldehyde (RF) gels as a model hard carbon electrode. A series of binder-free monolithic carbon electrodes heat-treated at varied temperatures allow the comparative investigation of the correlation between carbon nanotexture and electrochemical Na+-ion storage. The increase in carbonization temperature exerts a favorable influence on electrode performance, especially in the range between 1600 °C and 2500 °C. The comparison between Li+- and Na+-storage behaviors in the carbon electrodes discloses that the Na+-trapping in nanovoids is negligible when the carbonization temperature is higher than 1600 °C. On the other hand, the high-temperature sintering at 2500-3000 °C enlarges the resistance for Na+-insertion into interlayer spacing as well as Na+-filling into nanovoids. In addition, the study on the effect of pore size clearly demonstrates that not the BET surface area but the surface area related to meso- and macropores is a predominant factor for the initial irreversible capacity. The outcomes of this work are expected to become a benchmark for other hard carbon electrodes prepared from various precursors.

  12. 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

    2016-02-01

    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).

  13. 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.

  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. 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.

  16. 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

  17. Polarization-induced distortion of ions in the pores of carbon electrodes for electrochemical capacitors

    OpenAIRE

    Ovín Ania, María Concepción; Pernak, J.; Stefaniak, F.; Raymundo-Piñero, Encarnación; Béguin, F.

    2009-01-01

    This paper reports the effect of confining ionic species of the electrolyte inside the porosity of carbon electrodes during the performance of electrochemical capacitors. Solvent-free ionic liquids and a conventional organic medium were used as electrolytes, while two series of carbons with controlled pore sizes – one of them obtained from nanocasting procedure – were used as electrode materials. Our results demonstrate that under the effect of the electric field applied during the polarizati...

  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. Effect of unequal load of carbon xerogel in electrodes on the electrochemical performance of asymmetric supercapacitors

    OpenAIRE

    Gómez Calvo, Esther; Lufrano, F.; Arenillas de la Puente, Ana; Brigandi, A.; Menéndez Díaz, José Ángel; Staiti, P.

    2013-01-01

    This paper investigates the electrochemical performance of asymmetric supercapacitors in an environmentally friendly aqueous electrolyte (1.0 mol L−1 sodium sulfate solution). The asymmetric configuration is based on the use of a highly porous carbon xerogel as active material in both the positive and negative electrodes, but the carbon xerogel loading in each electrode has been substantially modified. This configuration leads to an increase in the operational voltage window up to values of 1...

  20. 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.

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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

  6. Preparation of porous carbon nanofibers derived from PBI/PLLA for supercapacitor electrodes.

    Science.gov (United States)

    Jung, Kyung-Hye; Ferraris, John P

    2016-10-21

    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. PMID:27632072

  7. Redox poly[Ni(saldMp)] modified activated carbon electrode in electrochemical supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Gao Fei [Department of Physical Chemistry, University of Science and Technology Beijing, 30 Xueyuan Road, Haidian District, Beijing 100083 (China); Li Jianling, E-mail: lijianling@ustb.edu.c [Department of Physical Chemistry, University of Science and Technology Beijing, 30 Xueyuan Road, Haidian District, Beijing 100083 (China); Zhang Yakun; Wang Xindong [Department of Physical Chemistry, University of Science and Technology Beijing, 30 Xueyuan Road, Haidian District, Beijing 100083 (China); Kang Feiyu [Department of Material Science and Engineering, Tsinghua University, Beijing 100083 (China)

    2010-08-01

    The complex (2,2-dimethyl-1,3-propanediaminebis(salicylideneaminato))-nickel(II), [Ni(saldMp)], was oxidatively electropolymerized on activated carbon (AC) electrode in acetonitrile solution. The poly[Ni(saldMp)] presented an incomplete coated film on the surface of carbon particles of AC electrode by field emission scanning electron microscopy. The electrochemical behaviors of poly[Ni(saldMp)] modified activated carbon (PAC) electrode were evaluated in different potential ranges by cyclic voltammetry. Counterions and solvent swelling mainly occurred up to 0.6 V for PAC electrode by the comparison of D{sup 1/2}C values calculated from chronoamperometry experiments. Both the Ohmic resistance and Faraday resistance of PAC electrode gradually approached to those of AC electrode when its potential was ranging from 1.2 V to 0.0 V. Galvanostatic charge/discharge experiments indicated that both the specific capacitance and energy density were effectively improved by the reversible redox reaction of poly[Ni(saldMp)] film under the high current density up to 10 mA cm{sup -2} for AC electrode. The specific capacitance of PAC electrode decreased during the first 50 cycles but thereafter it remained constant for the next 200 cycles. This study showed the redox polymer may be an attractive material in supercapacitors.

  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. 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.

  10. Fabrication and electrical properties of single wall carbon nanotube channel and graphene electrode based transistors arrays

    International Nuclear Information System (INIS)

    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

  11. 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.

  12. 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.

  13. Magnetism and spin transport of carbon chain between armchair graphene nanoribbon electrodes

    Science.gov (United States)

    Farghadan, R.; Yoosefi, M.

    2016-09-01

    The magnetic and spin transport properties of a carbon chain between two armchair graphene nanoribbon (AGNR) electrodes were studied using tight-binding Hamiltonian, mean-field Hubbard model and Landauer-Butikker formalism. The results showed that only odd-numbered carbon chains show intrinsic magnetic moments in chain-graphene junctions. It was also found that the electronic, magnetic and spin transport properties of carbon chain-graphene junctions strongly depend on the position and the length of the carbon chains between AGNR electrodes. Interestingly, we found a fully spin-polarized transmission near the Fermi energy in all odd-numbered carbon chain-graphene junctions, regardless of their lengths and without any magnetic field and magnetic electrodes.

  14. Electrocatalytic oxidation of hydrazine on magnetic bar carbon paste electrode modified with benzothiazole and iron oxide nanoparticles:Simultaneous determination of hydrazine and phenol%苯并噻唑和铁氧化物纳米粒子修饰的磁性棒碳糊电极上肼的电催化氧化反应:同时检测肼和苯酚

    Institute of Scientific and Technical Information of China (English)

    Ali Benvidi; Shahriar Jahanbani; Bibi-Fatemeh Mirjalili; Reza Zare

    2016-01-01

    A magnetic bar carbon paste electrode (MBCPE) modified with Fe3O4 magnetic nanoparticles (Fe3O4NPs) and 2‐(3,4‐dihydroxyphenyl) benzothiazole (DPB) for the electrochemical determina‐tion of hydrazine was developed. The DPB was firstly self‐assembled on the Fe3O4NPs, and the re‐sulting Fe3O4NPs/DPB composite was then absorbed on the designed MBCPE. The MBCPE was used to attract the magnetic nanoparticles to the electrode surface. Owing to its high conductivity and large effective surface area, the novel electrode had a very large current response for the electrocat‐alytic oxidation of hydrazine. The modified electrode was characterized by voltammetry, scanning electron microscopy, electrochemical impedance spectroscopy, infrared spectroscopy, and UV‐visible spectroscopy. Voltammetric methods were used to study the electrochemical behaviour of hydrazine on MBCPE/Fe3O4NPs/DPB in phosphate buffer solution (pH = 7.0). The MBCPE/Fe3O4NPs/DPB, acting as an electrochemical sensor, exhibited very high electrocatalytic activity for the oxidation of hydrazine. The presence of DPB was found to reduce the oxidation potential of hydrazine and increase the catalytic current. The dependence of the electrocatalytic current on the hydrazine concentration exhibited two linear ranges, 0.1–0.4 µmol/L and 0.7–12.0 µmol/L, with a detection limit of 18.0 nmol/L. Additionally, the simultaneous determination of hydrazine and phe‐nol was investigated using the MBCPE/Fe3O4NPs/DPB electrode. Voltammetric experiments showed a linear range of 100–470 µmol/L and a detection limit of 24.3 µmol/L for phenol, and the proposed electrode was applied to the determination of hydrazine and phenol in water samples.%开发了一种磁性Fe3O4纳米粒子和2-(3,4-二羟苯基)苯并噻唑(DPB)修饰的磁性棒碳糊电极(MBCPE)用于电化学检测肼.首先将DPB自组装在Fe3O4纳米粒子上,然后将此复合物吸附于设计的MBCPE上. MBCPE电极将磁性纳米粒子

  15. 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.

  16. 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.

  17. Past and present of sediment and carbon biogeochemical cycling models

    Directory of Open Access Journals (Sweden)

    F. T. Mackenzie

    2004-01-01

    Full Text Available The global carbon cycle is part of the much more extensive sedimentary cycle that involves large masses of carbon in the Earth's inner and outer spheres. Studies of the carbon cycle generally followed a progression in knowledge of the natural biological, then chemical, and finally geological processes involved, culminating in a more or less integrated picture of the biogeochemical carbon cycle by the 1920s. However, knowledge of the ocean's carbon cycle behavior has only within the last few decades progressed to a stage where meaningful discussion of carbon processes on an annual to millennial time scale can take place. In geologically older and pre-industrial time, the ocean was generally a net source of CO2 emissions to the atmosphere owing to the mineralization of land-derived organic matter in addition to that produced in situ and to the process of CaCO3 precipitation. Due to rising atmospheric CO2 concentrations because of fossil fuel combustion and land use changes, the direction of the air-sea CO2 flux has reversed, leading to the ocean as a whole being a net sink of anthropogenic CO2. The present thickness of the surface ocean layer, where part of the anthropogenic CO2 emissions are stored, is estimated as of the order of a few hundred meters. The oceanic coastal zone net air-sea CO2 exchange flux has also probably changed during industrial time. Model projections indicate that in pre-industrial times, the coastal zone may have been net heterotrophic, releasing CO2 to the atmosphere from the imbalance between gross photosynthesis and total respiration. This, coupled with extensive CaCO3 precipitation in coastal zone environments, led to a net flux of CO2 out of the system. During industrial time the coastal zone ocean has tended to reverse its trophic status toward a non-steady state situation of net autotrophy, resulting in net uptake of anthropogenic CO2 and storage of carbon in the coastal ocean, despite the significant calcification

  18. 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.

  19. 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.

  20. 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.

  1. 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.

  2. 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

    2016-01-01

    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. PMID:27651005

  3. 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).

  4. Electrodes from carbon nanotubes/NiO nanocomposites synthesized in modified Watts bath for supercapacitors

    Science.gov (United States)

    Hakamada, Masataka; Abe, Tatsuhiko; Mabuchi, Mamoru

    2016-09-01

    A modified Watts bath coupled with pulsed current electroplating is used to uniformly deposit ultrafine nickel oxide particles (diameter carbon nanotubes. The capacitance of the multiwalled carbon nanotubes/nickel oxide electrodes was as high as 2480 F g-1 (per mass of nickel oxide), which is close to the theoretical capacitance of NiO.

  5. 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

  6. 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

  7. Electrochemically reduced graphene modified carbon ionic liquid electrode for the sensitive sensing of rutin

    Energy Technology Data Exchange (ETDEWEB)

    Gao Feng [Fujian Province University Key Laboratory of Analytical Science, Department of Chemistry and Environment Science, Zhangzhou Normal University, Zhangzhou 363000 (China); Qi Xiaowei [College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Cai Xili; Wang Qingxiang; Gao Fei [Fujian Province University Key Laboratory of Analytical Science, Department of Chemistry and Environment Science, Zhangzhou Normal University, Zhangzhou 363000 (China); Sun Wei, E-mail: sunwei@qust.edu.cn [College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China)

    2012-05-31

    In this paper a graphene (GR) modified carbon ionic liquid electrode that was obtained by one-step potentiostatic electroreduction of a graphene oxide solution was described. The resulting electrode displayed excellent electrochemical performance due to the formation of highly conductive GR film on the electrode surface. Electrochemistry of rutin was carefully studied with a pair of well-defined redox peaks appeared in pH 2.5 buffer solution. Rutin exhibited a diffusion-controlled two-electron and two-proton transfer reaction on the modified electrode with the electrochemical parameters calculated. The reduction peak currents are linearly related to rutin concentration in the concentration range from 0.070 to 100.0 {mu}mol/L with a detection limit as low as 24.0 nmol/L (3{sigma}). The modified electrode displayed excellent selectivity with good stability, and was applied to the determination of rutin content in tablet, human serum and urine samples with satisfactory results. - Highlights: Black-Right-Pointing-Pointer Electroreduced graphene modified carbon ionic liquid electrode was obtained. Black-Right-Pointing-Pointer Electrochemical behaviors of rutin were investigated on the modified electrode. Black-Right-Pointing-Pointer Rutin in different samples were detected by the proposed electrode.

  8. Influence of Carbon Nanotube Clustering on Mechanical and Electrical Properties of Cement Pastes

    OpenAIRE

    Sung-Hwan Jang; Shiho Kawashima; Huiming Yin

    2016-01-01

    Given the continued challenge of dispersion, for practical purposes, it is of interest to evaluate the impact of multi-walled carbon nanotubes (MWCNTs) at different states of clustering on the eventual performance properties of cement paste. This study evaluated the clustering of MWCNTs and the resultant effect on the mechanical and electrical properties when incorporated into cement paste. Cement pastes containing different concentrations of MWCNTs (up to 0.5% by mass of cement) with/without...

  9. 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)

  10. 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.

  11. Square Wave Voltammetric Determination of Residues of Carbendazim Using a Fullerene/Multiwalled Carbon Nanotubes/Nafion/Coated Glassy Carbon Electrode

    OpenAIRE

    Djimadoum N. Teadoum; Seraphine K. Noumbo; Kamdem T. Arnaud; Temgoua T. Ranil; Antoine D. Mvondo Zé; Ignas K. Tonle

    2016-01-01

    A glassy carbon electrode (GCE) was modified with a fullerene/Multiwalled Carbon Nanotubes (MWCNTs)/Nafion composite and applied to the determination of carbendazim, a fungicide. The voltammetric behavior of the analyte was investigated using Cyclic Voltammetry (CV), on the bare GCE and on the same electrode coated by a thin film of the composite material. The electrode response was more than fourfold important on the modified electrode, due to electrical conductivity of fullerene and MWCNT a...

  12. A detective from the past called carbon 14

    International Nuclear Information System (INIS)

    The analysis is carried out using Radiometry or Accelerator mass spectrometry. After the system allowing to date the age of any organic rest - whether a fossil, a wood fragment, a parchment or a seed - is an isotope called carbon-14. An atom that comes from reactions nuclear produced in the atmosphere and cosmic-ray-induced they interact with oxygen to form carbon dioxide. This element they absorb it plants in photosynthesis and then passes to the animals remained almost unchanged during the life of the organism. to the meet the initial ratio of c-14 that had been in the atmosphere before his death, the remains that are left in it determine the elapsed time. (Author)

  13. Impact of SO 2 poisoning of platinum nanoparticles modified glassy carbon electrode on oxygen reduction

    Science.gov (United States)

    Awad, M. I.; Saleh, M. M.; Ohsaka, T.

    An extraordinary recovery characteristic of Pt-nanoparticles from SO 2 poisoning is introduced in this study. Platinum nanoparticles (nano-Pt) modified glassy carbon electrode (nano-Pt/GC) has been compared with polycrystalline platinum (poly-Pt) electrode towards SO 2 poisoning. Two procedures of recovery of the poisoned electrodes were achieved by cycling the potential in the narrow potential range (NPR, 0-0.8 V vs. Ag/AgCl/KCl (sat.)) and wide potential range (WPR, -0.2 to 1.3 V). The extent of recovery was marked using oxygen reduction reaction (ORR) as a probing reaction. SO 2 poisoning of the electrodes changed the mechanism of the oxygen reduction from the direct reduction to water to the stepwise reduction involving the formation of H 2O 2 as an intermediate, as indicated by the rotating ring-disk voltammetry. Using the WPR recovery procedure, it was found that two potential cycles were enough to recover 100% of the activity of the ORR on the nano-Pt/GC electrode. At the poly-Pt electrode, however, four potential cycles of the WPR caused only 79% in the current recovery, while the peak potential of the ORR was 130 mV negatively shifted as compared with the fresh poly-Pt electrode. Interestingly, the NPR procedure at the nano-Pt/GC electrode was even more efficient in the recovery than the WPR procedure at the poly-Pt electrode.

  14. 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)

  15. 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.

  16. 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.

  17. 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.

  18. Fabrication and electrochemical properties of free-standing single-walled carbon nanotube film electrodes

    Institute of Scientific and Technical Information of China (English)

    Niu Zhi-Qiang; Ma Wen-Jun; Dong Hai-Bo; Li Jin-Zhu; Zhou Wei-Ya

    2011-01-01

    An easily manipulative approach was presented to fabricate electrodes using free-standing single-walled carbon nanotube (SWCNT) films grown directly by chemical vapor deposition. Electrochemical properties of the electrodes were investigated. In comparison with the post-deposited SWCNT papers, the directly grown SWCNT film electrodes manifested enhanced electrochemical properties and sensitivity of sensors as well as excellent electrocatalytic activities. A transition from macroelectrode to nanoelectrode behaviours was observed with the increase of scan rate. The heat treatment of the SWCNT film electrodes increased the current signals of electrochemical analyser and background current, because the heat-treatment of the SWCNTs in air could create more oxide defects on the walls of the SWCNTs and make the surfaces of SWCNTs more hydrophilic. The excellent electrochemical properties of the directly grown and heat-treated free-standing SWCNT film electrodes show the potentials in biological and electrocatalytic applications.

  19. Carbon and Redox Tolerant Infiltrated Oxide Fuel-Electrodes for Solid Oxide Cells

    DEFF Research Database (Denmark)

    Skafte, Theis Løye; Sudireddy, Bhaskar Reddy; Blennow, P.;

    2016-01-01

    To solve issues of coking and redox instability related to the presence of nickel in typical fuel electrodes in solid oxide cells,Gd-doped CeO2 (CGO) electrodes were studied using symmetriccells. These electrodes showed high electro-catalytic activity, butlow electronic conductivity. When...... infiltrated with Sr0.99Fe0.75Mo0.25O3-δ (SFM), the electronic conductivity wasenhanced. However, polarization resistance of the cells increased,suggesting that the infiltrated material is less electro-catalyticallyactive and was partly blocking the CGO surface reaction sites. Theactivity could be regained...... by infiltrating nano-sized CGO orNiCGO on top of SFM, while still sustaining the high electronicconductivity. Ohmic resistance of the electrodes was thuspractically eliminated and performance comparable to, or betterthan, state-of-the-art fuel electrodes was achieved. The Nicontaining cells were damaged by carbon...

  20. Downsizing the pelagic carbonate factory: Impacts of calcareous nannoplankton evolution on carbonate burial over the past 17 million years

    Science.gov (United States)

    Suchéras-Marx, Baptiste; Henderiks, Jorijntje

    2014-12-01

    Cenozoic deep-sea carbonates ("calcareous oozes") are predominantly biogenic in origin and offer detailed records of the evolution of calcifying plankton groups, such as coccolithophores and foraminifera. The size and abundance of calcifying plankton determine the strength of the calcium carbonate "pump" in the open ocean, which acts as a short-term source of CO2, while the burial of pelagic carbonates serves as a long-term sink of carbon. Here, we show how the macroevolutionary size decrease in calcareous nannoplankton (coccoliths and calcareous nannoliths) has affected burial rates of calcareous ooze over the past 17 million years. We quantified nannofossil carbonate burial rates (g CaCO3/m2/yr) at five DSDP/ODP sites in the Atlantic, Indian, and Western Pacific oceans. The proportion of nannofossil-dominated fine fraction carbonate ( 38 μm fraction remained stable over the past 17 Myr. This suggests that changes in the deposition of calcareous ooze were primarily driven by calcareous nannoplankton, and that foraminifera did not compensate for the lower nannofossil-carbonate accumulation rates since the Pliocene. Despite a deepening of the lysocline over the past 4 Myr, global pelagic carbonate mass accumulation likely decreased. Whether, or how, this may relate to changes in weathering or other components within the long-term carbonate cycle remains unclear. Explanations for the macroevolutionary size decrease in calcareous nannoplankton focus on the physiological and ecological advantages of small, lightly calcified algal cells in a low-CO2 and more stratified marine environment.

  1. Fabrication of Functionalized Carbon Nanotube Buckypaper Electrodes for Application in Glucose Biosensors

    OpenAIRE

    Henry Papa; Melissa Gaillard; Leon Gonzalez; Jhunu Chatterjee

    2014-01-01

    A highly sensitive glucose detection method was developed using functionalized carbon nanotube buckypaper as a free standing electrode in an electrochemical biosensor. Glucose oxidase was immobilized onto various buckypaper samples in order to oxidize glucose resulting in a measureable current/voltage signal output of the biosensor. Cyclic voltammetry (CV) and amperometry were utilized to determine the sensitivity of these buckypaper electrodes. Sensors of three different types of buckypaper ...

  2. Asymmetric Electrodes Constructed with PAN-Based Activated Carbon Fiber in Capacitive Deionization

    OpenAIRE

    Mingzhe Li; Yingzhi Chen; Zheng-Hong Huang; Feiyu Kang

    2014-01-01

    Capacitive deionization (CDI) method has drawn much attention for its low energy consumption, low pollution, and convenient manipulation. Activated carbon fibers (ACFs) possess high adsorption ability and can be used as CDI electrode material. Herein, two kinds of PAN-based ACFs with different specific surface area (SSA) were used for the CDI electrodes. The CDI performance was investigated; especially asymmetric electrodes’ effect was evaluated. The results demonstrated that PAN-based ACFs s...

  3. 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.

  4. Carbon nanotube/Co3O4 composite for air electrode of lithium-air battery

    OpenAIRE

    Yoon, Taek Han; Park, Yong Joon

    2012-01-01

    A carbon nanotube [CNT]/Co3O4 composite is introduced as a catalyst for the air electrode of lithium-air [Li/air] batteries. Co3O4 nanoparticles are successfully attached to the sidewall of the CNT by a hydrothermal method. A high discharge capacity and a low overvoltage indicate that the CNT/Co3O4 composite is a very promising catalyst for the air electrode of Li/air batteries.

  5. 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.

  6. Large magnetoresistance in single-walled carbon nanotubes contacted different ferromagnetic metal electrodes

    International Nuclear Information System (INIS)

    Magnetoresistance (MR) in single-walled carbon nanotubes (SWNTs) with different ferromagnetic source and drain electrodes (iron and cobalt) which have different coercivity was studied. Large MR ratio of 20% could be obtained at 8 K, while 1∼2% small MR ratio could be observed for the sample with the same ferromagnetic source and drain electrodes of Co. The MR ratio of 20% is very close to the theoretically predicted value of 26% for Co-Fe system

  7. Kinetics of dioxygen reduction on gold and glassy carbon electrodes in neutral media

    OpenAIRE

    Gotti, Guillaume; Fajerwerg, Katia; Evrard, David; Gros, Pierre

    2013-01-01

    The electrochemical reduction of dioxygen (O₂) has been studied on bulk gold (Au) and glassy carbon (GC) electrodes in aqueous neutral solution close to blood ionic composition. The mechanism was found to involve two successive bielectronic steps with hydrogen peroxide (H₂O₂) as the reaction intermediate whatever the electrode material used. On Au, O₂ and H₂O₂ were reduced at close potentials. The determination of the kinetic parameters of O₂ electroreduction was thus achieved after removing ...

  8. 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

  9. 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.

  10. 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.  

  11. 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.

  12. 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.

  13. Screen-Printed Carbon Electrodes Modified by Rhodium Dioxide and Glucose Dehydrogenase

    OpenAIRE

    Vojtěch Polan; Jan Soukup; Karel Vytřas

    2011-01-01

    The described glucose biosensor is based on a screen-printed carbon electrode (SPCE) modified by rhodium dioxide, which functions as a mediator. The electrode is further modified by the enzyme glucose dehydrogenase, which is immobilized on the electrode's surface through electropolymerization with m-phenylenediamine. The enzyme biosensor was optimized and tested in model glucose samples. The biosensor showed a linear range of 500–5000 mg L−1 of glucose with a detection limit of 210 mg L−1 (es...

  14. Electroanalysis of thiocyanate using a novel glassy carbon electrode modified by aryl radicals and cobalt tetracarboxyphthalocyanine

    Energy Technology Data Exchange (ETDEWEB)

    Matemadombo, Fungisai; Nyokong, Tebello [Rhodes University, Grahamstown (South Africa). Department of Chemistry; Westbroek, Philippe [Ghent University, Ghent (Belgium). Department of Textiles

    2007-12-01

    Electrochemical grafting of 4-nitrobenzenediazonium tetrafluoroborate onto a glassy carbon electrode (GCE) results in the formation of a nitrophenyl radical, which reacts with the surface to form a covalent bond (grafting) and results in a nitrophenyl modified electrode. The nitro group is electrochemically reduced to a NH{sub 2} group. Cobalt tetracarboxyphthalocyanine (CoTCPc) complex is then attached to the NH{sub 2} group using 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) and N-hydroxysuccinimide (NHS) as coupling agents. The new CoTCPc modified electrode was characterized using cyclic voltammetry and then employed for the catalytic oxidation of thiocyanate. (author)

  15. Fabrication of functionalized carbon nanotube buckypaper electrodes for application in glucose biosensors.

    Science.gov (United States)

    Papa, Henry; Gaillard, Melissa; Gonzalez, Leon; Chatterjee, Jhunu

    2014-12-01

    A highly sensitive glucose detection method was developed using functionalized carbon nanotube buckypaper as a free standing electrode in an electrochemical biosensor. Glucose oxidase was immobilized onto various buckypaper samples in order to oxidize glucose resulting in a measureable current/voltage signal output of the biosensor. Cyclic voltammetry (CV) and amperometry were utilized to determine the sensitivity of these buckypaper electrodes. Sensors of three different types of buckypaper were prepared and compared. These modified buckypaper electrode-based sensors showed much higher sensitivity to glucose compared to other electrochemical glucose sensors. PMID:25587433

  16. Fabrication of Functionalized Carbon Nanotube Buckypaper Electrodes for Application in Glucose Biosensors

    Directory of Open Access Journals (Sweden)

    Henry Papa

    2014-11-01

    Full Text Available A highly sensitive glucose detection method was developed using functionalized carbon nanotube buckypaper as a free standing electrode in an electrochemical biosensor. Glucose oxidase was immobilized onto various buckypaper samples in order to oxidize glucose resulting in a measureable current/voltage signal output of the biosensor. Cyclic voltammetry (CV and amperometry were utilized to determine the sensitivity of these buckypaper electrodes. Sensors of three different types of buckypaper were prepared and compared. These modified buckypaper electrode-based sensors showed much higher sensitivity to glucose compared to other electrochemical glucose sensors.

  17. 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.

  18. Major carbon industries in India

    Energy Technology Data Exchange (ETDEWEB)

    Jain, P.K.

    1982-01-01

    The history of the major carbon industries in India, their growth, present status, problems and future prospects are described. Chapters cover: raw petroleum coke, calcined petroleum coke, graphite electrodes and anodes, carbon electrode paste, calcined anthracite coal, low-ash metallurgical coke, carbon black industry, activated carbon, midget electrodes, cinema arc carbons, carbon blocks and brushes for electrical machinery, and the growth of the aluminium industry and its impact on the calcined petroleum coke industry.

  19. 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.

  20. Application of N-doped graphene modified carbon ionic liquid electrode for direct electrochemistry of hemoglobin

    International Nuclear Information System (INIS)

    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 H2O2, 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

  1. Anthropogenic carbon release rate unprecedented during the past 66 million years

    Science.gov (United States)

    Zeebe, Richard E.; Ridgwell, Andy; Zachos, James C.

    2016-04-01

    Carbon release rates from anthropogenic sources reached a record high of ~10 Pg C yr-1 in 2014. Geologic analogues from past transient climate changes could provide invaluable constraints on the response of the climate system to such perturbations, but only if the associated carbon release rates can be reliably reconstructed. The Palaeocene-Eocene Thermal Maximum (PETM) is known at present to have the highest carbon release rates of the past 66 million years, but robust estimates of the initial rate and onset duration are hindered by uncertainties in age models. Here we introduce a new method to extract rates of change from a sedimentary record based on the relative timing of climate and carbon cycle changes, without the need for an age model. We apply this method to stable carbon and oxygen isotope records from the New Jersey shelf using time-series analysis and carbon cycle-climate modelling. We calculate that the initial carbon release during the onset of the PETM occurred over at least 4,000 years. This constrains the maximum sustained PETM carbon release rate to less than 1.1 Pg C yr-1. We conclude that, given currently available records, the present anthropogenic carbon release rate is unprecedented during the past 66 million years. We suggest that such a `no-analogue’ state represents a fundamental challenge in constraining future climate projections. Also, future ecosystem disruptions are likely to exceed the relatively limited extinctions observed at the PETM.

  2. 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.

  3. 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.

  4. Study on hydrogen evolution performance of the carbon supported PtRu alloy film electrodes

    Institute of Scientific and Technical Information of China (English)

    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.

  5. 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.

  6. 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.

  7. Comparison of dye solar cell counter electrodes based on different carbon nanostructures

    Energy Technology Data Exchange (ETDEWEB)

    Aitola, Kerttu, E-mail: kerttu.aitola@aalto.fi [Aalto University, Department of Applied Physics, P.O. Box 15100, 00076 Aalto (Finland); Halme, Janne [Aalto University, Department of Applied Physics, P.O. Box 15100, 00076 Aalto (Finland); Halonen, Niina [Microelectronics and Materials Physics Laboratories, Department of Electrical and Information Engineering, University of Oulu, P.O. Box 4500, FI-90014 University of Oulu (Finland); Kaskela, Antti; Toivola, Minna; Nasibulin, Albert G. [Aalto University, Department of Applied Physics, P.O. Box 15100, 00076 Aalto (Finland); Kordas, Krisztian; Toth, Geza [Microelectronics and Materials Physics Laboratories, Department of Electrical and Information Engineering, University of Oulu, P.O. Box 4500, FI-90014 University of Oulu (Finland); Kauppinen, Esko I. [Aalto University, Department of Applied Physics, P.O. Box 15100, 00076 Aalto (Finland); VTT Biotechnology, P.O. Box 1000, 02044 VTT (Finland); Lund, Peter D. [Aalto University, Department of Applied Physics, P.O. Box 15100, 00076 Aalto (Finland)

    2011-09-01

    Three characteristically different carbon nanomaterials were compared and analyzed as platinum-free counter electrodes for dye solar cells: 1) single-walled carbon nanotube (SWCNT) random network films on glass, 2) aligned multi-walled carbon nanotube (MWCNT) forest films on Inconel steel and quartz, and 3) pressed carbon nanoparticle composite films on indium tin oxide-polyethylene terephtalate plastic. Results from electrochemical impedance spectroscopy and electron microscopy were discussed in terms of the catalytic activity, conductivity, thickness, transparency and flexibility of the electrode films. The SWCNT films showed reasonable catalytic performance at similar series resistance compared to platinized fluorine doped tin oxide-coated glass. The MWCNTs had similar catalytic activity, but the electrochemical performance of the films was limited by their high porosity. Carbon nanoparticle films had the lowest charge transfer resistance resulting from a combination of high catalytic activity and dense packing of the material.

  8. All-Organic Actuator Fabricated with Single Wall Carbon Nanotube Electrodes

    Science.gov (United States)

    Lowther, Sharon E.; Harrison, Joycelyn S.; Kang, Jinho; Park, Cheol; Park, Chan Eon

    2008-01-01

    Compliant electrodes to replace conventional metal electrodes have been required for many actuators to relieve the constraint on the electroactive layer. Many conducting polymers have been proposed for the alternative electrodes, but they still have a problem of poor thermal stability. This article reports a novel all-organic actuator with single wall carbon nanotube (SWCNT) films as the alternative electrode. The SWCNT film was obtained by filtering a SWCNT solution through an anodized alumina membrane. The conductivity of the SWCNT film was about 280 S/cm. The performance of the SWCNT film electrode was characterized by measuring the dielectric properties of NASA Langley Research Center - Electroactive Polymer (LaRC-EAP) sandwiched by the SWCNT electrodes over a broad range of temperature (from 25 C to 280 C) and frequency (from 1 KHz to 1 MHz). The all-organic actuator with the SWCNT electrodes showed a larger electric field-induced strain than that with metal electrodes, under identical measurement conditions.

  9. Advantages of flattened electrode in bottom contact single-walled carbon nanotube field-effect transistor

    Energy Technology Data Exchange (ETDEWEB)

    Setiadi, Agung; Akai-Kasaya, Megumi, E-mail: kasaya@prec.eng.osaka-u.ac.jp; Saito, Akira; Kuwahara, Yuji [Department of Precision Science and Technology, Graduate School of Engineering, Osaka University, 565-0871 Suita (Japan)

    2014-09-01

    We fabricated single-walled carbon nanotube (SWNT) field-effect transistor (FET) devices on flattened electrodes, in which there are no height difference between metal electrodes and the substrate. SWNT-FET fabricated using bottom contact technique have some advantages, such that the SWNTs are free from electron irradiation, have direct contact with the desired metal electrodes, and can be functionalized before or after deposition. However, the SWNTs can be bent at the contact point with the metal electrodes leading to a different electrical characteristic of the devices. The number of SWNT direct junctions in short channel length devices is drastically increased by the use of flattened electrodes due to strong attractive interaction between SWNT and the substrate. The flattened electrodes show a better balance between their hole and electron mobility compared to that of the non-flattened electrodes, that is, ambipolar FET characteristic. It is considered that bending of the SWNTs in the non-flattened electrode devices results in a higher Schottky barrier for the electrons.

  10. Electrochemical studies on nanometal oxide-activated carbon composite electrodes for aqueous supercapacitors

    Science.gov (United States)

    Ho, Mui Yen; Khiew, Poi Sim; Isa, Dino; Chiu, Wee Siong

    2014-11-01

    In present study, the electrochemical performance of eco-friendly and cost-effective titanium oxide (TiO2)-based and zinc oxide-based nanocomposite electrodes were studied in neutral aqueous Na2SO3 electrolyte, respectively. The electrochemical properties of these composite electrodes were studied using cyclic voltammetry (CV), galvanostatic charge-discharge (CD) and electrochemical impedance spectroscopy (EIS). The experimental results reveal that these two nanocomposite electrodes achieve the highest specific capacitance at fairly low oxide loading onto activated carbon (AC) electrodes, respectively. Considerable enhancement of the electrochemical properties of TiO2/AC and ZnO/AC nanocomposite electrodes is achieved via synergistic effects contributed from the nanostructured metal oxides and the high surface area mesoporous AC. Cations and anions from metal oxides and aqueous electrolyte such as Ti4+, Zn2+, Na+ and SO32- can occupy some pores within the high-surface-area AC electrodes, forming the electric double layer at the electrode-electrolyte interface. Additionally, both TiO2 and ZnO nanoparticles can provide favourable surface adsorption sites for SO32- anions which subsequently facilitate the faradaic processes for pseudocapacitive effect. These two systems provide the low cost material electrodes and the low environmental impact electrolyte which offer the increased charge storage without compromising charge storage kinetics.

  11. Advantages of flattened electrode in bottom contact single-walled carbon nanotube field-effect transistor

    International Nuclear Information System (INIS)

    We fabricated single-walled carbon nanotube (SWNT) field-effect transistor (FET) devices on flattened electrodes, in which there are no height difference between metal electrodes and the substrate. SWNT-FET fabricated using bottom contact technique have some advantages, such that the SWNTs are free from electron irradiation, have direct contact with the desired metal electrodes, and can be functionalized before or after deposition. However, the SWNTs can be bent at the contact point with the metal electrodes leading to a different electrical characteristic of the devices. The number of SWNT direct junctions in short channel length devices is drastically increased by the use of flattened electrodes due to strong attractive interaction between SWNT and the substrate. The flattened electrodes show a better balance between their hole and electron mobility compared to that of the non-flattened electrodes, that is, ambipolar FET characteristic. It is considered that bending of the SWNTs in the non-flattened electrode devices results in a higher Schottky barrier for the electrons.

  12. 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.

  13. 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. PMID:26135977

  14. 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.

  15. Functionalization of carbon nanotube and nanofiber electrodes with biological macromolecules: Progress toward a nanoscale biosensor

    Science.gov (United States)

    Baker, Sarah E.

    The integration of nanoscale carbon-based electrodes with biological recognition and electrical detection promises unparalleled biological detection systems. First, biologically modified carbon-based materials have been shown to have superior long-term chemical stability when compared to other commonly used materials for biological detection such as silicon, gold, and glass surfaces. Functionalizing carbon electrodes for biological recognition and using electrochemical methods to transduce biological binding information will enable real-time, hand-held, lower cost and stable biosensing devices. Nanoscale carbon-based electrodes allow the additional capability of fabricating devices with high densities of sensing elements, enabling multi-analyte detection on a single chip. We have worked toward the integration of these sensor components by first focusing on developing and characterizing the chemistry required to functionalize single-walled carbon nanotubes and vertically aligned carbon nanofibers with oligonucleotides and proteins for specific biological recognition. Chemical, photochemical and electrochemical methods for functionalizing these materials with biological molecules were developed. We determined, using fluorescence and colorimetric techniques, that these biologically modified nanoscale carbon electrodes are biologically active, selective, and stable. A photochemical functionalization method enabled facile functionalization of dense arrays vertically aligned carbon nanofiber forests. We found that much of the vertically aligned carbon nanofiber sidewalls were functionalized and biologically accessible by this method---the absolute number of DNA molecules hybridized to DNA-functionalized nanofiber electrodes was ˜8 times higher than the number of DNA molecules hybridized to flat glassy carbon electrodes and implies that nanofiber forest sensors may facilitate higher sensitivity to target DNA sequences per unit area. We also used the photochemical method

  16. Electrocatalytic Reduction of NAD+ at Multi-walled Carbon Nanotubes Modified Electrode

    Institute of Scientific and Technical Information of China (English)

    陈黎明; 丁飞; 王欢; 张文; 陆嘉星

    2005-01-01

    The cyclic voltammetric (CV) behaviors of NAD+ were studied with a multi-walled carbon nanotubes (MWNTs) modified glassy carbon (GC) electrode. In 0.05 mol/L tris(hydroxymethyl)aminomethane-HCl (Tris-HCl) buffer solution (pH=6.9), the MWNTs modified electrode showed high electrocatalytic activity toward reduction of NAD+.The electroreduction of NAD+ was an irreversible diffusion controlled process. The cathodic peak current increased linearly with increasing the concentration of NAD+. The influences of scan rate, temperature and concentration were also investigated.

  17. 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.

  18. Improvement of the inter-electrode reproducibility of screen-printed carbon electrodes by oxygen plasma etching and an image color level method for quality control

    International Nuclear Information System (INIS)

    Screen-printed carbon electrodes (SPCEs) were selectively etched by oxygen plasma. The coefficient of variance (CV) of inter-electrode reproducibility was reduced from 21.6 to 4.6. Studies of the surface by color-level-indexing histogram analysis, scanning electronic microscopy (SEM) and resistance revealed that the inter-electrode reproducibility correlated with complete etching of the resin binder from the SPCE surface. The quality of the electrode was differentiated by this color level index analysis. This technique has great potential for application in on-line quality control of the SPCE plasma-treating process when integrated with suitable image processing software.

  19. Improvement of the inter-electrode reproducibility of screen-printed carbon electrodes by oxygen plasma etching and an image color level method for quality control

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Yi-Huang [Department of Food Science, Yuanpei University, Hsinchu 300, Taiwan (China); Hsu, Chuan-Liang [Department of Food Science, Tunghai University, Taichung 407, Taiwan (China); Yuan, Chiun-Jye [Department of Biological Science and Technology, National Chiao Tung University, Hsinchu 300, Taiwan (China); Tang, Shu-Fan [Department of Food Science, Yuanpei University, Hsinchu 300, Taiwan (China); Chiang, Hui-Jean [Department of Applied Science, National Hsinchu University of Education, Hsinchu 300, Taiwan (China); Jang, Hung-Der [Department of Food Science, Yuanpei University, Hsinchu 300, Taiwan (China); Chang, Ku-Shang, E-mail: tommy.first@msa.hinet.net [Department of Food Science, Yuanpei University, Hsinchu 300, Taiwan (China)

    2011-10-10

    Screen-printed carbon electrodes (SPCEs) were selectively etched by oxygen plasma. The coefficient of variance (CV) of inter-electrode reproducibility was reduced from 21.6 to 4.6. Studies of the surface by color-level-indexing histogram analysis, scanning electronic microscopy (SEM) and resistance revealed that the inter-electrode reproducibility correlated with complete etching of the resin binder from the SPCE surface. The quality of the electrode was differentiated by this color level index analysis. This technique has great potential for application in on-line quality control of the SPCE plasma-treating process when integrated with suitable image processing software.

  20. Fabrication and electrical properties of single wall carbon nanotube channel and graphene electrode based transistors; Toward all carbon electronics

    Science.gov (United States)

    Lee, Sang Wook; Seo, Miri; Na, Junhong; Kim, Yong Hyeon; Lee, Byeong-Joo; Kim, Jin-Ju; Yun, Hoyeol; Kim, Hakseong; Yoon, Ho-Ang; Kim, Keun Soo; Jeong, Goo-Hwan; Kim, Gyu Tae

    2014-03-01

    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 array on top of the pre-deposited SWNTs which were aligned along one direction. Aligned arrays of SWNTs were synthesized by thermal chemical vapor deposition (CVD) method on quartz substrate. The micro scale contact electrodes and following circuit structures were defined by photo lithography on the large area graphene produced by CVD. Both of the single and multi layer graphene were used for the electrode materials. In this presentation, the device fabrication procedure, the contact properties, and the transistor performances of the device structures were discussed. This work was supported by NRF.

  1. 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.

  2. Fabrication and electrochemical properties of carbon nanotube array electrode for supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Qiao Ling Chen; Kuan Hong Xue; Wei Shen; Fei Fei Tao; Shou Yin Yin; Wen Xu [Nanjing Normal University (China). Chemistry Dept.

    2004-09-30

    The multiwalled carbon nanotube (MWNT) array was fabricated by chemical vapor deposition (CVD) in the template of porous alumina from the carbonaceous source of C{sub 2H}2 in the presence of a catalyst of ferric metals. To utilize the external surface other than the inner surface of the carbon nanotubes, 1 mol/L sulfuric acid was applied to remove off the most part of AAO template on the carbon nanotube electrode. The electrochemical performances of the carbon nanotube array electrode were investigated by use of the cyclic voltammetry, galvanostatic charge/discharge and ac impedance methods for its application in supercapacitors. The specific capacitance of 365 F/g of the electrode was achieved with the discharge current density of 210 mA/g in the solution of 1 mol/L H{sub 2}SO{sub 4}. In addition, the carbon nanotube array electrode was found to have low equivalent series resistance (ESR) and good cycling stability. (author)

  3. Characterisation of hydrophobic carbon nanofiber-silica composite film electrodes for redox liquid immobilisation

    International Nuclear Information System (INIS)

    Carbon (50-150 nm diameter) nanofibers were embedded into easy to prepare thin films of a hydrophobic sol-gel material and cast onto tin-doped indium oxide substrate electrodes. They promote electron transport and allow efficient electrochemical reactions at solid|liquid and at liquid|liquid interfaces. In order to prevent aggregation of carbon nanofibers silica nanoparticles of 7 nm diameter were added into the sol-gel mixture as a 'surfactant' and homogeneous high surface area films were obtained. Scanning electron microscopy reveals the presence of carbon nanofibers at the electrode surface. The results of voltammetric experiments performed in redox probe-ferrocenedimethanol solution in aqueous electrolyte solution indicate that in the absence of organic phase, incomplete wetting within the hydrophobic film of carbon nanofibers can cause hemispherical diffusion regime typical for ultramicroelectrode like behaviour. The hydrophobic film electrode was modified with two types of redox liquids: pure tert-butylferrocene or dissolved in 2-nitrophenyloctylether as a water-insoluble solvent and immersed in aqueous electrolyte solution. With a nanomole deposit of pure redox liquid, stable voltammetric responses are obtained. The presence of carbon nanofibers embedded in the mesoporous matrix substantially increases the efficiency of the electrode process and stability under voltammetric conditions. Also well-defined response for diluted redox liquids is obtained. From measurements in a range of different aqueous electrolyte media a gradual transition from anion transfer dominated to cation transfer dominated processes is inferred depending on the hydrophilicity of the transferring anion or cation

  4. Fabrication and performance evaluation of hybrid supercapacitor electrodes based on carbon nanotubes and sputtered TiO2

    Science.gov (United States)

    Aravinda, L. S.; Nagaraja, K. K.; Nagaraja, H. S.; Udaya Bhat, K.; Ramachandra Bhat, B.

    2016-08-01

    We report a simple and eco-friendly method for the fabrication of a titanium dioxide/functionalized multiwalled carbon nanotube (TiO2/FMWCNT) composite electrode for use in supercapacitors. The nanocomposite electrodes were formed by depositing titanium dioxide onto FMWCNTs using reactive magnetron sputtering, thus providing a green roue for the formation of the binder-free composite electrode. It is shown that the electrochemical performance of the fabricated electrodes can be altered by tuning the thickness of the titanium dioxide overlayer. The integrated nanocomposite electrode showed an improved specific capacitance of 90 Fg‑1 in two-electrode configuration.

  5. Modelling the inorganic ocean carbon cycle under past and future climate change

    International Nuclear Information System (INIS)

    This study used a coupled ocean-atmosphere-sea ice model with an inorganic carbon component to examine the inorganic ocean carbon cycle with particular reference to how climate feedback influences future uptake. In the last 150 years, the increase in atmosphere carbon dioxide (CO2) concentrations have been higher than any time during the Earth's history. Although the oceans are the largest sink for carbon dioxide, it is not know how the ocean carbon cycle will respond to increasing anthropogenic carbon dioxide concentrations in the future. Climate feedbacks could potentially reduce further uptake of carbon by the ocean. In addition to examining past climate transitions, including both abrupt and glacial-interglacial climate transitions, this study also examined the sensitivity of the inorganic carbon cycle to increased atmospheric carbon dioxide. Atmospheric carbon dioxide levels were also projected under a range of global warming scenarios. Most simulations identified a transient weakening of the North Atlantic and increased sea surface temperatures (SST). These positive feedbacks act on the carbon system to reduce uptake. However, the ocean has the capacity to take up 65 to 75 per cent of the anthropogenic carbon dioxide increases. An analysis of climate feedback on future carbon uptake shows that oceans store 7 per cent more carbon when there are no climate feedbacks acting on the system. Sensitivity experiments using the Gent McWilliams parameterization for mixing associated with mesoscale eddies show a further 6 per cent increase in oceanic uptake. Inclusion of sea ice dynamics resulted in a 2 per cent difference in uptake. This study also examined changes in atmospheric carbon dioxide concentration that occur during abrupt climate change events. Changes in ocean circulation and carbon solubility cause significant increases in atmospheric carbon dioxide concentrations when melt water episodes are simulated in both hemispheres. The response of the carbon cycle

  6. 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.

  7. 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.

  8. 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.

  9. 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.

  10. 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.

  11. 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.

  12. Stable carbon isotopes of invertebrate remains: do they reveal past methane release from lakes?

    OpenAIRE

    van Hardenbroek-van Ammerstol, M. R.

    2010-01-01

    Lakes are a source of methane, an important greenhouse gas in the atmosphere. In order to understand increasing methane emissions in the present, it is important to study the variations of methane release during past periods of climate change. However, records of methane release from lakes over time scales longer than a few years are extremely rare. In this thesis a method is explored to reconstruct past methane availability in lakes based on the stable carbon isotope composition (delta 13C) ...

  13. Non-traditional electrode materials for detection of biomarkers

    OpenAIRE

    Barek, Jiří; Moreira, Josino C.; Wang, Joseph

    2014-01-01

    In this paper, new electrochemical methods suitable for detection of various types of biomarkers (biomarkers of exposition, tumor biomarkers, and biomarkers of medical treatment) are briefly reviewed. Attention is paid to the use of non-traditional electrode materials (various forms of amalgam electrodes, boron doped diamond film electrodes, carbon paste and carbon film electrodes, etc.) for voltammetric (batch analysis) and amperometric (flowing systems) detection of above mentio...

  14. Reactivity of NO2 and CO2 with hardened cement paste containing activated carbon

    Science.gov (United States)

    Horgnies, M.; Dubois-Brugger, I.; Krou, N. J.; Batonneau-Gener, I.; Belin, T.; Mignard, S.

    2015-07-01

    The development of building materials to reduce the concentration of NO2 is growing interest in a world where the air quality in urban areas is affected by the car traffic. The main binder in concrete is the cement paste that is partly composed of calcium hydroxide. This alkaline hydrate composing the hardened cement paste shows a high BET surface area (close to 100 m2.g-1) and can absorb low-concentrations of NO2. However, the presence of CO2 in the atmosphere limits the de-polluting effect of reference cement paste, mainly due to carbonation of the alkaline hydrates (reaction leading to the formation of calcium carbonate). The results established in this paper demonstrate that the addition of activated carbon in the cement paste, because of its very high BET surface area (close to 800 m2.g-1) and its specific reactivity with NO2, can significantly improve and prolong the de-polluting effect in presence of CO2 and even after complete carbonation of the surface of the cement paste.

  15. Carbon Based Electrodes Modified with Horseradish Peroxidase Immobilized in Conducting Polymers for Acetaminophen Analysis

    Directory of Open Access Journals (Sweden)

    Cecilia Cristea

    2013-04-01

    Full Text Available The development and optimization of new biosensors with horseradish peroxidase immobilized in carbon nanotubes-polyethyleneimine or polypyrrole nanocomposite film at the surface of two types of transducer is described. The amperometric detection of acetaminophen was carried out at −0.2 V versus Ag/AgCl using carbon based-screen printed electrodes (SPEs and glassy carbon electrodes (GCEs as transducers. The electroanalytical parameters of the biosensors are highly dependent on their configuration and on the dimensions of the carbon nanotubes. The best limit of detection obtained for acetaminophen was 1.36 ± 0.013 μM and the linear range 9.99–79.01 μM for the HRP-SWCNT/PEI in GCE configuration. The biosensors were successfully applied for the detection of acetaminophen in several drug formulations.

  16. 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.

  17. Theoretical Simulation on the Assembly of Carbon Nanotubes Between Electrodes by AC Dielectrophoresis

    Directory of Open Access Journals (Sweden)

    Yang Liu

    2008-01-01

    Full Text Available Abstract The assembly of single-walled carbon nanotubes (SWCNTs using the AC dielectrophoresis technique is studied theoretically. It is found that the comb electrode bears better position control of SWCNTs compared to the parallel electrode. In the assembly, when some SWCNTs bridge the electrode first, they can greatly alter the local electrical field so as to “screen off” later coming SWCNTs, which contributes to the formation of dispersed SWCNT array. The screening distance scales with the gap width of electrodes and the length of SWCNTs, which provides a way to estimate the assembled density of SWCNTs. The influence of thermal noise on SWCNTs alignment is also analyzed in the simulation. It is shown that the status of the array distribution for SWCNTs is decided by the competition between the thermal noise and the AC electric-field strength. This influence of the thermal noise can be suppressed by using higher AC voltage to assemble the SWCNTs.

  18. Flexible supercapacitor electrodes with vertically aligned carbon nanotubes grown on aluminum foils

    Institute of Scientific and Technical Information of China (English)

    Itir Bakis Dogru; Mete Batuhan Durukan; Onur Turel; Husnu Emrah Unalan

    2016-01-01

    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 su-percapacitor 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 elec-trodes, which is further improved through the bending cycles.

  19. 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.

  20. 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. PMID:23421212

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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

  6. 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

  7. 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.

  8. 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.

  9. Nanotextured gold coatings on carbon nanofiber scaffolds as ultrahigh surface-area electrodes

    OpenAIRE

    COLAVITA, PAULA

    2012-01-01

    PUBLISHED High surface area metal electrodes are desirable for applications in energy storage and energy conversion. Here, the formation and electrochemical characterization of a hybrid material made by electroless deposition of gold onto a scaffolding of vertically aligned carbon nanofibers is described. Vertically aligned carbon nanofibers, ~80 nm in diameter, provided mechanical support and electrical contact to the highly textured nanoscale gold coatings. By chemically functionalizing ...

  10. Stainless Steel Mesh Supported Carbon Nanofibers for Electrode in Bioelectrochemical System

    Directory of Open Access Journals (Sweden)

    Jing Wang

    2016-01-01

    Full Text Available We proposed a self-connected carbon nanofiber design for electrode in microbial bioelectrochemical system. This design was realized by direct growth of carbon nanofibers (CNFs onto stainless steel (SSM via a chemical vapor deposition process without addition of any external catalysts. In the CNFs-SSM composite electrode, the SSM acted as the conductive network and ensured efficient substrate and proton transfer, and the CNFs layer served as highly porous habitats for thick biofilm propagation. The current generated by the CNFs-SSM was 200 times higher than the bare SSM under the same experimental conditions. This provided a simple and promising method for preparation of electrode material with high performance and low-cost in bioelectrochemical system.

  11. 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.

  12. Preparation and Electrochemistry of Hydrous Ruthenium Oxide/Active Carbon Electrode materials for Supercapacitor

    Institute of Scientific and Technical Information of China (English)

    Zhang Jianrong; Jiang Dechen; Chen Bin; Zhu Junjie; Jiang Liping; Fang Huiqun

    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.

  13. 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.

  14. 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

  15. 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.  ……

  16. Electrocatalytic Hydrogen Evolution from Molybdenum Sulfide-Polymer Composite Films on Carbon Electrodes.

    Science.gov (United States)

    Lattach, Youssef; Deronzier, Alain; Moutet, Jean-Claude

    2015-07-29

    The design of more efficient catalytic electrodes remains an important objective for the development of water splitting electrolyzers. In this context a structured composite cathode material has been synthesized by electrodeposition of molybdenum sulfide (MoSx) into a poly(pyrrole-alkylammonium) matrix, previously coated onto carbon electrodes by oxidative electropolymerization of a pyrrole-alkylammonium monomer. The composite material showed an efficient electrocatalytic activity toward proton reduction and the hydrogen evolution reaction (HER). Data from Tafel plots have demonstrated that the electron transfer rate in the composite films is fast, in agreement with the high catalytic activity of this cathode material. Bulk electrolysis of acidic water at carbon foam electrodes modified with the composite have shown that the cathodes display a high catalytic activity and a reasonable operational stability, largely exceeding that of regular amorphous MoSx electrodeposited on naked carbon foam. The enhanced catalytic performances of the composite electrode material were attributed to the structuration of the composite, which led to a homogeneous distribution of the catalyst on the carbon foam network, as shown by SEM characterizations. PMID:26147828

  17. 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

  18. Oxygen electrode reaction in molten carbonate fuel cells. Final report, September 15, 1987--September 14, 1990

    Energy Technology Data Exchange (ETDEWEB)

    Appleby, A.J.; White, R.E.

    1992-07-07

    Molten carbonate fuel cell system is a leading candidate for the utility power generation because of its high efficiency for fuel to AC power conversion, capability for an internal reforming, and a very low environmental impact. However, the performance of the molten carbonate fuel cell is limited by the oxygen reduction reaction and the cell life time is limited by the stability of the cathode material. An elucidation of oxygen reduction reaction in molten alkali carbonate is essential because overpotential losses in the molten carbonate fuel cell are considerably greater at the oxygen cathode than at the fuel anode. Oxygen reduction on a fully-immersed gold electrode in a lithium carbonate melt was investigated by electrochemical impedance spectroscopy and cyclic voltammetry to determine electrode kinetic and mass transfer parameters. The dependences of electrode kinetic and mass transfer parameters on gas composition and temperature were examined to determine the reaction orders and the activation energies. The results showed that oxygen reduction in a pure lithium carbonate melt occurs via the peroxide mechanism. A mass transfer parameter, D{sub O}{sup 1/2}C{sub O}, estimated by the cyclic voltammetry concurred with that calculated by the EIS technique. The temperature dependence of the exchange current density and the product D{sub O}{sup 1/2}C{sub O} were examined and the apparent activation energies were determined to be about 122 and 175 kJ/ mol, respectively.

  19. 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

    2014-09-01

    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.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

  20. Binderless Composite Electrode Monolith from Carbon Nanotube and Biomass Carbon Activated by KOH and CO2 Gas for Supercapacitor

    Science.gov (United States)

    Farma, R.; Deraman, M.; Omar, R.; Awitdrus, Ishak, M. M.; Taer, E.; Talib, I. A.

    2011-12-01

    This paper presents a method to improve the performance of supercapacitors fabricated using binderless composite electrode monolith (BCMs) from self-adhesive carbon grains (SACG) of fibers from oil palm empty fruit bunches. The BCMs were prepared from green monoliths (GMs) contain SACG, SACG treated with KOH (5 % by weight) and SACG mixed with carbon nanotubes (CNTs) (5% by weight) and KOH (5 % by weight), respectively. These GMs were carbonized at 800 ° C under N2 environment and activated by CO2 gas at 800 ° C for 1 hour. It was found that addition of KOH and CNTs produced BCMs with higher specific capacitance and smaller internal resistance, respectively. It was also found that supercapacitor cells using these BCMs as electrodes exhibited a better specific energy and specific power. The physical properties of BCMs (density, electrical conductivity, porosity, interlayer spacing, crystallite dimension and microstructure) were affected by the addition of KOH and CNTs.

  1. Voltammetric oxidation and determination of cinnarizine at glassy carbon electrode modified with multi-walled carbon nanotubes.

    Science.gov (United States)

    Hegde, Rajesh N; Hosamani, Ragunatharaddi R; Nandibewoor, Sharanappa T

    2009-09-01

    The voltammetric oxidation of cinnarizine was investigated. In pH 2.5 Britton-Robinson buffer, cinnarizine shows an irreversible oxidation peak at about 1.20 V at a multi-walled carbon nanotube (MWCNT)-modified glassy carbon electrode. The cyclic voltammetric results indicate that MWCNT-modified glassy carbon electrode can remarkably enhance electrocatalytic activity towards the oxidation of cinnarizine. The electrocatalytic behavior was further exploited as a sensitive detection scheme for the cinnarizine determination by differential-pulse voltammetry. Under optimized conditions, the concentration range and detection limit are 9.0x10(-8) to 6.0x10(-6) M and 2.58x10(-9) M, respectively for cinnarizine. The proposed method was successfully applied to cinnarizine determination in pharmaceutical samples. The analytical performance of this sensor has been evaluated for the detection of analyte in urine as a real sample. PMID:19446444

  2. 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.

  3. 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...

  4. 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.

  5. 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.

  6. 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

  7. Electromagnetic interference shielding with Portland cement paste containing carbon materials and processed fly ash

    OpenAIRE

    Zornoza, E.; Catalá, G.; Jiménez, F.; Andión, L. Gª; Garcés, P.

    2010-01-01

    The study described in this article explored the effect of adding different types of carbon materials (graphite powder and three types of carbon fibre), fly ash (with 5.6%, 15.9% and 24.3% Fe2O3), and a mix of both on electromagnetic interference (EMI) shielding in Portland cement pastes. The parameters studied included the type and aspect ratio of the carbonic material, composite material thickness, the frequency of the incident electromagnetic r...

  8. Characterisation of carbon nanotube pastes for field emission using their sheet resistances

    Science.gov (United States)

    Floweri, Octia; Kim, Jihan; Seo, Yongho; Park, Jun-Young; Lee, Naesung

    2015-10-01

    Carbon nanotube (CNT) pastes for field emitters were fabricated by varying the milling speed, CNT amount and glass frit (GF) powder size. The CNTs remained agglomerated at lower milling speeds while they were damaged and shortened at higher speeds. Increasing the amount of CNTs improved the field emission properties, but excessive CNTs led to increased removal of the CNT paste with surface activation because of lower cohesion strength. Small GF particles were incorporated to provide a flat surface to the CNT paste, which improved its field emission uniformity and lifespan. The dispersion, density and milling damage characteristics of CNTs in the pastes were assessed by their sheet resistances under the assumption of equal printed thicknesses. Tape activation reduced the thickness of the CNT pastes by different amounts that depended on the cohesion strength of the paste. This reduction caused the sheet resistance to increase. For all cases in this study, the field emission properties of the CNT pastes were closely related to their sheet resistances, suggesting that sheet resistance could be used as a figure-of-merit for the evaluation of CNT pastes for field emission applications.

  9. Bucky-gel coated glassy carbon electrodes, for voltammetric detection of femtomolar leveled lead ions.

    Science.gov (United States)

    Wan, Qijin; Yu, Fen; Zhu, Lina; Wang, Xiaoxia; Yang, Nianjun

    2010-10-15

    Femtomolar (fM) leveled lead ions were electrochemically detected using a bucky-gel coated glassy carbon electrode and differential pulse anodic stripping voltammetry. The bucky-gel was composed of dithizone, ionic liquid (1-butyl-3-methylimidazolium hexafluorophosphate), and multi-walled carbon nanotubes (MWCNTs). The fabrication of the bucky-gel coated electrode was optimized. The modified electrode was characterized with voltammetry, electrochemical impedance spectroscopy, and chronoamperometry. After the accumulation of lead ions into the bucky-gel modified electrode at -1.2V vs. saturated calomel electrode (SCE) for 5 min in a pH 4.4 sodium acetate-acetate acid buffer solution, differential pulse anodic stripping voltammograms of the accumulated lead show an anodic wave at -0.58 V. The anodic peak current is detectable for lead ions in the concentration range from 1.0 μM down to 500 fM. The detection limit is calculated to be 100 fM. The proposed method was successfully applied for the detection of lead ions in lake water. PMID:20875583

  10. Voltammetric detection of bisphenol a by a chitosan–graphene composite modified carbon ionic liquid electrode

    International Nuclear Information System (INIS)

    In this paper 1-ethyl-3-methylimidazolium tetrafluoroborate based carbon ionic liquid electrode (CILE) was fabricated and further modified with chitosan (CTS) and graphene (GR) composite film. The fabricated CTS-GR/CILE was further used for the investigation on the electrochemical behavior of bisphenol A (BPA) by cyclic voltammetry and differential pulse voltammetry. A well-defined anodic peak appeared at 0.436 V in 0.1 mol/L pH 8.0 Britton–Robinson buffer solution, which was attributed to the electrooxidation of BPA on the modified electrode. The electrochemical parameters of BPA on the modified electrode were calculated with the results of the charge transfer coefficient (α) as 0.662 and the apparent heterogeneous electron transfer rate constant (ks) as 1.36 s−1. Under the optimal conditions, a linear relationship between the oxidation peak current of BPA and its concentration can be obtained in the range from 0.1 μmol/L to 800.0 μmol/L with the limit of detection as 2.64 × 10−8 mol/L (3σ). The CTS-GR/CILE was applied to the detection of BPA content in plastic products with satisfactory results. - Highlights: ► A graphene modified carbon ionic liquid electrode was fabricated and characterized. ► Electrochemical behaviors of bisphenol A were investigated. ► Bisphenol A was detected by the proposed electrode.

  11. 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.

  12. 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.

  13. 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.

  14. 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.

  15. 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.

  16. Ultrasensitive detection of dopamine using a carbon nanotube network microfluidic flow electrode.

    Science.gov (United States)

    Sansuk, Siriwat; Bitziou, Eleni; Joseph, Maxim B; Covington, James A; Boutelle, Martyn G; Unwin, Patrick R; Macpherson, Julie V

    2013-01-01

    The electrochemical measurement of dopamine (DA), in phosphate buffer solution (pH 7.4), with a limit of detection (LOD) of ∼5 pM in 50 μL (∼ 250 attomol) is achieved using a band electrode comprised of a sparse network of pristine single-walled carbon nanotubes (SWNTs), which covers flow injection analysis (FIA). The flow cells, have a channel (duct) geometry, with cell height of 25 μm, and are shown to be hydrodynamically well-defined, with laminar Poiseuille flow. In the arrangement where solution continuously flows over the electrode but the electrode is only exposed to the analyte for short periods of time, the SWNT electrodes do not foul and can be used repeatedly for many months. The LOD for dopamine (DA), reported herein, is significantly lower than previous reports using FIA-electrochemical detection. Furthermore, the SWNT electrodes can be used as grown, i.e., they do not require chemical modification or cleanup. The extremely low background signals of the SWNT electrodes, as a consequence of the sparse surface coverage and the low intrinsic capacitance of the SWNTs, means that no signal processing is required to measure the low currents for DA oxidation at trace levels. DA detection in artificial cerebral fluid is also possible with a LOD of ∼50 pM in 50 μL (∼2.5 fmol).

  17. 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.

  18. Au nanoparticles/poly(caffeic acid) composite modified glassy carbon electrode for voltammetric determination of acetaminophen.

    Science.gov (United States)

    Li, Tianbao; Xu, Juan; Zhao, Lei; Shen, Shaofei; Yuan, Maosen; Liu, Wenming; Tu, Qin; Yu, Ruijin; Wang, Jinyi

    2016-10-01

    An Au nanoparticles/poly(caffeic acid) (AuNPs/PCA) composite modified glassy carbon (GC) electrode was prepared by successively potentiostatic technique in pH 7.4 phosphate buffer solution containing 0.02mM caffeic acid and 1.0mM HAuCl4. Electrochemical characterization of the AuNPs/PCA-GC electrode was investigated by electrochemical impedance spectroscopy and cyclic voltammetry. The electrochemical behavior of acetaminophen (AP) at the AuNPs/PCA-GC electrode was also studied by cyclic voltammetry. Compared with bare GC and poly(caffeic acid) modified GC electrode, the AuNPs/PCA-GC electrode was exhibited excellent electrocatalytic activity toward the oxidation of AP. The plot of catalytic current versus AP concentration showed two linear segments in the concentration ranges 0.2-20µM and 50-1000µM. The detection limit of 14 nM was obtained by using the first range of the calibration plot. The AuNPs/PCA-GC electrode has been successfully applied and validated by analyzing AP in blood, urine and pharmaceutical samples. PMID:27474318

  19. 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.

  20. 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.

  1. 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.

  2. Electrodeposited nickel oxide and graphene modified carbon ionic liquid electrode for electrochemical myglobin biosensor

    International Nuclear Information System (INIS)

    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 (E0′) 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 H2O2. 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

  3. Hybrid direct carbon fuel cell anode processes investigated using a 3-electrode half-cell setup

    DEFF Research Database (Denmark)

    Deleebeeck, Lisa; Arenillas, A.; Menendez, J.A.;

    2015-01-01

    anthracite and bituminous coals, as well as carbon black, were tested, revealing similar open circuit potential and activation energies in mixed 96-4vol% N2-CO2 and 50-50vol% CO-CO2 environments between 700 and 800°C. Bituminous coal showed the highest activity, likely associated to a high O/C ratio......A 3-electrode half-cell setup consisting of a yttria-stabilized zirconia (YSZ) electrolyte support was employed to investigate the chemical and electrochemical processes occurring in the vicinity of a model hybrid direct carbon fuel cell (HDCFC) anode (Ni-YSZ) in contact with a molten carbon...

  4. Film of lignocellulosic carbon material for self-supporting electrodes in electric double-layer capacitors

    Directory of Open Access Journals (Sweden)

    Tsubasa Funabashi

    2013-09-01

    Full Text Available A novel thin, wood-based carbon material with heterogeneous pores, film of lignocellulosic carbon material (FLCM, was successfully fabricated by carbonizing softwood samples of Picea jezoensis (Jezo spruce. Simultaneous increase in the specific surface area of FLCM and its affinity for electrolyte solvents in an electric double-layer capacitor (EDLC were achieved by the vacuum ultraviolet/ozone (VUV/O3 treatment. This treatment increased the specific surface area of FLCM by 50% over that of original FLCM. The results obtained in this study confirmed that FLCM is an appropriate self-supporting EDLC electrode material without any warps and cracks.

  5. Graphene oxide-mediated electrochemistry of glucose oxidase on glassy carbon electrodes.

    Science.gov (United States)

    Castrignanò, Silvia; Valetti, Francesca; Gilardi, Gianfranco; Sadeghi, Sheila J

    2016-01-01

    Glucose oxidase (GOD) was immobilized on glassy carbon electrodes in the presence of graphene oxide (GO) as a model system for the interaction between GO and biological molecules. Lyotropic properties of didodecyldimethylammonium bromide (DDAB) were used to stabilize the enzymatic layer on the electrode surface resulting in a markedly improved electrochemical response of the immobilized GOD. Transmission electron microscopy images of the GO with DDAB confirmed the distribution of the GO in a two-dimensional manner as a foil-like material. Although it is known that glassy carbon surfaces are not ideal for hydrogen peroxide detection, successful chronoamperometric titrations of the GOD in the presence of GO with β-d-glucose were performed on glassy carbon electrodes, whereas no current response was detected upon β-d-glucose addition in the absence of GO. The GOD-DDAB-GO system displayed a high turnover efficiency and substrate affinity as a glucose biosensor. The simplicity and ease of the electrode preparation procedure of this GO/DDAB system make it a good candidate for immobilizing other biomolecules for fabrication of amperometric biosensors. PMID:25939764

  6. 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. PMID:19760402

  7. Gold nanoparticles directly modified glassy carbon electrode for non-enzymatic detection of glucose

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Gang; Shu, Honghui; Ji, Kai [Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Faculty of Materials Science and Engineering, Hubei University, No. 368 Youyi Avenue, Wuchang, Wuhan 430062 (China); Oyama, Munetaka [Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8520 (Japan); Liu, Xiong [Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Faculty of Materials Science and Engineering, Hubei University, No. 368 Youyi Avenue, Wuchang, Wuhan 430062 (China); He, Yunbin, E-mail: ybhe@hubu.edu.cn [Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials, Faculty of Materials Science and Engineering, Hubei University, No. 368 Youyi Avenue, Wuchang, Wuhan 430062 (China)

    2014-01-01

    This work describes controllable preparation of gold nanoparticles on glassy carbon electrodes by using the seed mediated growth method, which contains two steps, namely, nanoseeds attachment and nanocrystals growth. The size and the dispersion of gold nanoparticles grown on glassy carbon electrodes could be easily tuned through the growth time based on results of field-emission scanning electron microscopy. Excellent electrochemical catalytic characteristics for glucose oxidation were observed for the gold nanoparticles modified glassy carbon electrodes (AuNPs/GC), resulting from the extended active surface area provided by the dense gold nanoparticles attached. It exhibited a wide linear range from 0.1 mM to 25 mM with the sensitivity of 87.5 μA cm{sup −2} mM{sup −1} and low detection limit down to 0.05 mM for the sensing of glucose. The common interfering species such as chloride ion, ascorbic acid, uric acid and 4-acetamidophenol were verified having no interference effect on the detection of glucose. It is demonstrated that the seed mediated method is one of the facile approaches for fabricating Au nanoparticles modified substrates, which could work as one kind of promising electrode materials for the glucose nonenzymatic sensing.

  8. Voltammetric determination of adenosine and guanosine using fullerene-C(60)-modified glassy carbon electrode.

    Science.gov (United States)

    Goyal, Rajendra N; Gupta, Vinod K; Oyama, Munetaka; Bachheti, Neeta

    2007-02-28

    A fullerene-C(60)-modified glassy carbon electrode (GCE) is used for the simultaneous determination of adenosine and guanosine by differential pulse voltammetry. Compared to a bare glassy carbon electrode, the modified electrode exhibits an apparent shift of the oxidation potentials in the cathodic direction and a marked enhancement in the voltammetric peak current response for both the biomolecules. Linear calibration curves are obtained over the concentration range 0.5muM-1.0mM in 0.1M phosphate buffer solution at pH 7.2 with a detection limit of 3.02x10(-7)M and 1.45x10(-7)M for individual determination of adenosine and guanosine, respectively. The interference studies showed that the fullerene-C(60)-modified glassy carbon electrode exhibited excellent selectivity in the presence of hypoxanthine, xanthine, uric acid and ascorbic acid. The proposed procedure was successfully applied to detect adenosine and guanosine in human blood plasma and urine, without any preliminary pre-treatment. PMID:19071420

  9. Carbon Nanosheets and Nanostructured Electrodes in Organic Photovoltaic Devices: Cooperative Research and Development Final Report, CRADA Number CRD-08-321

    Energy Technology Data Exchange (ETDEWEB)

    Olson, D.

    2012-04-01

    Carbon nanosheet thin films were employed as nanostructured electrodes in organic solar cells. Due to the nanostructured texture of the carbon nanosheet electrodes, there was an increase in performance over standard ITO electrodes with very thick active layers. ZnO deposited via atomic layer deposition (ALD) was used as a hole blocking layer to provide for carrier selectivity of the carbon nanosheets.

  10. Organic carbon source and burial during the past one hundred years in Jiaozhou Bay, North China

    Institute of Scientific and Technical Information of China (English)

    LI Xuegang; YUAN Huamao; LI Ning; SONG Jinming

    2008-01-01

    Organic carbon (OC), total nitrogen (TN), and 210Pb in core sediment were measured to quantify the burial of organic carbon and the relative importance of allochthonous and autochthonous contributions during the past one hundred years in Jiaozhou Bay, North China. The core sediment was dated using 210Pb chronology, which is the most promising method for estimation of sedimentation rate on a time scale of 100-150 years. The variation of the burial flux of organic carbon in the past one hundred years can be divided into the following three stages: (1) relatively steady before 1980s; (2) increasing rapidly from the 1980s to a peak in the 1990s, and (3) decreasing from the 1990s to the present. The change is consistent with the amount of solid waste and sewage emptied into the bay. The OC:TN ratio was used to evaluate the source of organic carbon in the Jiaozhou Bay sediment. In the inner bay and bay mouth, the organic carbon was the main contributor from terrestrial sources, whereas only about half of organic carbon was contributed from terrestrial source in the outer bay. In the inner bay, the terrestrial source of organic carbon showed a steady change with an increase in the range of 69%-77% before 1990 to 93% in 2000, and then decreased from 2000 because of the decrease in the terrestrial input. In the bay mouth, the percentage of organic carbon from land reached the highest value with 94% in 1994. In the outer bay, the sediment source maintained steady for the past one hundred years.

  11. 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.

  12. 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. PMID:27213269

  13. Carbon storage in Organic Soils (COrS): Quantifying past variations in carbon accumulation in peatlands of South Wales, UK.

    Science.gov (United States)

    Carless, Donna; Kulessa, Bernd; Street-Perrott, Alayne; Davies, Siwan; Sinnadurai, Paul

    2014-05-01

    Globally, peatlands comprise a vital terrestrial carbon sink, currently estimated to be around 500 PgC (Yu et al., 2011, Gorham, 1991). Within the UK, peatlands represent the single most important terrestrial carbon store (IUCN, 2011). In particular, blanket and raised bogs account for around 23,000 square kilometres or 9.5 percent of the UK land area, with current estimates indicating that they store approximately 3.2 PgC (IUCN, 2011). Recent studies suggest that carbon-sequestration rates have been highly variable during the Holocene (Frolking & Roulet, 2007). Reconstructing these past fluctuations is essential to assess how peatlands will respond to future climate change, particularly the possibility that large amounts of respired below-ground carbon will be released as a result of enhanced rates of decomposition, causing positive climate feedback. Quantitative estimates of past variations in carbon accumulation provide valuable insights into the factors controlling carbon budgets. Recent developments have illustrated how ground-penetrating radar (GPR) can improve constraints on peat thickness (Holden et al., 2002, Warner et al., 1990), facilitating site-specific peat-volume estimates for carbon quantification. We shall present initial results from the COrS project, which brings together a novel combination of geophysical and proxy techniques to reconstruct variations in long-term carbon accumulation in 6 ombrotrophic peat bogs, located across the Brecon Beacons National Park (BBNP), South Wales, UK (51°55'30" N, 3°29'18" W). Detailed GPR surveys are being used to provide comprehensive estimates of total peat extent and thickness at these sites. Combined with surface-elevation data from LiDAR imagery, 3D models are being created, from which total peat-volume estimates will be extracted. Carbon-accumulation rates will be inferred from these bog-volume estimates, coupled with total organic carbon (TOC) measurements and high-resolution radiocarbon dating. In

  14. 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.

  15. 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...... conductivity, chemical inertness and low cost. Improvement of catalytic efficiency and stability of the NPs is, however, essential for their wider applications in electrochemical energy conversion/storage. The activities of noble metal catalysts depend not only on their size, composition, and shapes but also...

  16. Carbon nanotubes as vectors for gene therapy: past achievements, present challenges and future goals.

    Science.gov (United States)

    Bates, Katie; Kostarelos, Kostas

    2013-12-01

    Promising therapeutic and prophylactic effects have been achieved following advances in the gene therapy research arena, giving birth to the new generation of disease-modifying therapeutics. The greatest challenge that gene therapy vectors still face is the ability to deliver sufficient genetic payloads in order to enable efficient gene transfer into target cells. A wide variety of viral and non-viral gene therapy vectors have been developed and explored over the past 10years, including carbon nanotubes. In this review we will address the application of carbon nanotubes as non-viral vectors in gene therapy with the aim to give a perspective on the past achievements, present challenges and future goals. A series of important topics concerning carbon nanotubes as gene therapy vectors will be addressed, including the benefits that carbon nanotubes offer over other non-viral delivery systems. Furthermore, a perspective is given on what the ideal genetic cargo to deliver using carbon nanotubes is and finally the geno-pharmacological impact of carbon nanotube-mediated gene therapy is discussed.

  17. 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

  18. Determination of cyanide in wastewaters using modified glassy carbon electrode with immobilized silver hexacyanoferrate nanoparticles on multiwall carbon nanotube

    Energy Technology Data Exchange (ETDEWEB)

    Noroozifar, Meissam, E-mail: mnoroozifar@chem.usb.ac.ir [Analytical Research Laboratory, Department of Chemistry, University of Sistan and Baluchestan, Zahedan, P.O. Box 98155-147 (Iran, Islamic Republic of); Khorasani-Motlagh, Mozhgan [Inorganic Research Laboratory, Department of Chemistry, University of Sistan and Baluchestan, Zahedan (Iran, Islamic Republic of); Taheri, Aboozar [Analytical Research Laboratory, Department of Chemistry, University of Sistan and Baluchestan, Zahedan, P.O. Box 98155-147 (Iran, Islamic Republic of)

    2011-01-15

    Research highlights: {yields} GC electrode modified with silver hexacyanoferrate nanoparticles (SHFNPs) immobilized on MWCNT. {yields} Modified electrode use for determination of Cyanide in waste water. {yields} The detection limit of the sensor is 8.3 nM. {yields} The linear range is from 40.0 nM to 150.0 {mu}M. - Abstract: The sensitive determination of cyanide in wastewaters using modified GC electrode with silver hexacyanoferrate nanoparticles (SHFNPs) immobilized on multiwall carbon nanotube (MWCNT) was reported. The immobilization of SHFNPs on MWCNT was confirmed by transmission electron microscopy (TEM). The TEM image showed that the SHFNPs retained the spherical morphology after immobilized on MWCNT. The size of SHFNPs was examined around 27 nm. The GC/MWCNT-SHFNPs was used for the determination of cyanide in borax buffer (BB) solution (pH 8.0). Using square wave voltammetry, the current response of cyanide increases linearly while increasing its concentration from 40.0 nM to 150.0 {mu}M and a detection limit was found to be 8.3 nM (S/N = 3). The present modified electrode was also successfully used for the determination of 5.0 {mu}M cyanide in the presence of common contaminants at levels presenting in industrial wastewaters. The practical application of the present modified electrode was demonstrated by measuring the concentration of cyanide in industrial wastewater samples. Moreover, the studied sensor exhibited high sensitivity, good reproducibility and long-term stability.

  19. 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.

  20. 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.