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Sample records for chemically modified electrode

  1. Reduced chemically modified graphene oxide for supercapacitor electrode

    OpenAIRE

    Rajagopalan, Balasubramaniyan; Chung, Jin Suk

    2014-01-01

    An efficient active material for supercapacitor electrodes is prepared by reacting potassium hydroxide (KOH) with graphene oxide followed by chemical reduction with hydrazine. The electrochemical performance of KOH treated graphene oxide reduced for 24 h (reduced chemically modified graphene oxide, RCMGO-24) exhibits a specific capacitance of 253 F g-1 at 0.2 A g-1 in 2 M H2SO4 compared to a value of 141 F g-1 for graphene oxide reduced for 24 h (RGO-24), and good cyclic stability up to 3,000...

  2. Modelling Amperometric Biosensors Based on Chemically Modified Electrodes

    Science.gov (United States)

    Baronas, Romas; Kulys, Juozas

    2008-01-01

    The response of an amperometric biosensor based on a chemically modified electrode was modelled numerically. A mathematical model of the biosensor is based on a system of non-linear reaction-diffusion equations. The modelling biosensor comprises two compartments: an enzyme layer and an outer diffusion layer. In order to define the main governing parameters the corresponding dimensionless mathematical model was derived. The digital simulation was carried out using the finite difference technique. The adequacy of the model was evaluated using analytical solutions known for very specific cases of the model parameters. By changing model parameters the output results were numerically analyzed at transition and steady state conditions. The influence of the substrate and mediator concentrations as well as of the thicknesses of the enzyme and diffusion layers on the biosensor response was investigated. Calculations showed complex kinetics of the biosensor response, especially when the biosensor acts under a mixed limitation of the diffusion and the enzyme interaction with the substrate.

  3. Modelling Amperometric Biosensors Based on Chemically Modified Electrodes

    Directory of Open Access Journals (Sweden)

    Juozas Kulys

    2008-08-01

    Full Text Available The response of an amperometric biosensor based on a chemically modified electrode was modelled numerically. A mathematical model of the biosensor is based on a system of non-linear reaction-diffusion equations. The modelling biosensor comprises two compartments: an enzyme layer and an outer diffusion layer. In order to define the main governing parameters the corresponding dimensionless mathematical model was derived. The digital simulation was carried out using the finite difference technique. The adequacy of the model was evaluated using analytical solutions known for very specific cases of the model parameters. By changing model parameters the output results were numerically analyzed at transition and steady state conditions. The influence of the substrate and mediator concentrations as well as of the thicknesses of the enzyme and diffusion layers on the biosensor response was investigated. Calculations showed complex kinetics of the biosensor response, especially when the biosensor acts under a mixed limitation of the diffusion and the enzyme interaction with the substrate.

  4. Stripping voltammetric behavior of technetium at various chemically modified electrodes

    International Nuclear Information System (INIS)

    In monitoring of nuclear processing plants and storage facilities the necessity arises of assaying traces of the artificial radioactive element technetium. The oxidation states IV and VII are of particular interest. Stripping voltammetry is among the methods of assay which are suited for this purpose. It allows an enhanced selectivity to be achieved by preconcentration of the analyte and of an oxidation state of the analyte, respectively, at the electrode used. This specific enrichment is successful after appropriate chemical modification of the electrode through immobilization of a Tc-specific reagent. When various approaches of chemical modification of a glassy carbon electrode were examined, the tetraphenylarsonium chloride extractant, which is highly selective with respect to technetium, proved to be the best suited reagent, capable of fixation both by ionic and by covalent bonding on an electrodeposited polymer film. For ionic immobilization the reagent was reacted to m-sulfophenyltriphenyl arsonium and then bound to a copolymer of vinylferrocene and vinylpyridine, which had been provided with cations. It was possible to enrich Tc(VII) at such an electrode and to determine it by stripping voltammetry down to a concentration of 1x10-8 M after 5 minutes enrichment time. (orig./EF)

  5. Electrodeposition of platinum and silver into chemically modified microporous silicon electrodes

    OpenAIRE

    Koda, Ryo; Fukami, Kazuhiro; Sakka, Tetsuo; Ogata, Yukio H.

    2012-01-01

    Electrodeposition of platinum and silver into hydrophobic and hydrophilic microporous silicon layers was investigated using chemically modified microporous silicon electrodes. Hydrophobic microporous silicon enhanced the electrodeposition of platinum in the porous layer. Meanwhile, hydrophilic one showed that platinum was hardly deposited within the porous layer, and a film of platinum on the top of the porous layer was observed. On the other hand, the electrodeposition of silver showed simil...

  6. A highly stable and sensitive chemically modified screen-printed electrode for sulfide analysis

    International Nuclear Information System (INIS)

    We report here a highly stable and sensitive chemically modified screen-printed carbon electrode (CMSPE) for sulfide analysis. The CMSPE was prepared by first ion-exchanging ferricyanide into a Tosflex anion-exchange polymer and then sealing with a tetraethyl orthosilicate sol-gel layer. The sol-gel overlayer coating was crucial to stabilize the electron mediator (i.e., Fe(China)63-) from leaching. The strong interaction between the oxy-hydroxy functional group of sol-gel and the hydrophilic sites of Tosflex makes the composite highly rigid to trap the ferricyanide mediator. An obvious electrocatalytic sulfide oxidation current signal at ∼0.20 V versus Ag/AgCl in pH 7 phosphate buffer solution was observed at the CMSPE. A linear calibration plot over a wide range of 0.1 μM to 1 mM with a slope of 5.6 nA/μM was obtained by flow injection analysis. The detection limit (S/N = 3) was 8.9 nM (i.e., 25.6 ppt). Practical utility of the system was applied to the determination of sulfide trapped from cigarette smoke and sulfide content in hot spring water

  7. Developing electrodes chemically modified with cucurbit[6]uril to detect 3,4-methylenedioxymethamphetamine (MDMA) by voltammetry

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • A new stand in forensic chemistry. • Voltammetric method for the determination of MDMA in seized samples. • A new voltammetric sensor for MDMA. - Abstract: This study aimed to develop an electrode chemically modified with cucurbit[6]uril to detect 3,4-methylenedioxymethamphetamine (MDMA), the main active principle of ecstasy samples, by voltammetry. We modified the electrode surface with a film containing cucurbit[6]uril, Nafion, and methanol, using the dip coating or the spin coating technique. During analysis, we employed an electrochemical cell with a conventional three-electrode system and KCl solution (0.1 mol L−1) as the supporting electrolyte. We conducted cyclic voltammetry at concentrations ranging from 4.2 × 10−6 to 4.8 × 10−5mol L−1. We also accomplished scanning electron microscopy, to investigate the structural behavior of the film that originated on the electrode surface. We obtained the following results when we used dip coating to prepare the modified electrode: standard deviation (SD) = 0.024 μA, limit of detection (LOD) = 3.5 μmol L−1, limit of quantification (LOQ) = 11.7 μmol L−1, and amperometric sensitivity (m) = 20.9 × 103 μA L mol−1. As for spin coating, we obtained SD = 0.024 μA, LOD = 2.7 μmol L−1, LOQ = 9.1 μmol L−1 and m = 25.9 × 103 μA mol L−1. These are very promising data: the modified electrode is more sensitive than the conventional glassy carbon electrode under the studied experimental conditions

  8. Catalytic activity of platinum on ruthenium electrodes with modified (electro)chemical states.

    Science.gov (United States)

    Park, Kyung-Won; Sung, Yung-Eun

    2005-07-21

    Using Pt on Ru thin-film electrodes with various (electro)chemical states designed by the sputtering method, the effect of Ru states on the catalytic activity of Pt was investigated. The chemical and electrochemical properties of Pt/Ru thin-film samples were confirmed by X-ray photoelectron spectroscopy (XPS) and cyclic voltammetry. In addition, Pt nanoparticles on Ru metal or oxide for an actual fuel cell system showed an effect of Ru states on the catalytic activity of Pt in methanol electrooxidation. Finally, it was concluded that such an enhancement of methanol electrooxidation on the Pt is responsible for Ru metallic and/or oxidation sites compared to pure Pt without any Ru state. PMID:16852701

  9. Electron Transfer Reactivity Patterns at Chemically Modified Electrodes: Fundamentals and Application to the Optimization of Redox Recycling Amplification Systems

    Energy Technology Data Exchange (ETDEWEB)

    Adam Johan Bergren

    2006-05-01

    Electroanalytical chemistry is often utilized in chemical analysis and Fundamental studies. Important advances have been made in these areas since the advent of chemically modified electrodes: the coating of an electrode with a chemical film in order to impart desirable, and ideally, predictable properties. These procedures enable the exploitation of unique reactivity patterns. This dissertation presents studies that investigate novel reaction mechanisms at self-assembled monolayers on gold. In particular, a unique electrochemical current amplification scheme is detailed that relies on a selective electrode to enable a reactivity pattern that results in regeneration of the analyte (redox recycling). This regenerating reaction can occur up to 250 times for each analyte molecule, leading to a notable enhancement in the observed current. The requirements of electrode selectivity and the resulting amplification and detection limit improvements are described with respect to the heterogeneous and homogeneous electron transfer rates that characterize the system. These studies revealed that the heterogeneous electrolysis of the analyte should ideally be electrochemically reversible, while that for the regenerating agent should be held to a low level. Moreover, the homogeneous reaction that recycles the analyte should occur at a rapid rate. The physical selectivity mechanism is also detailed with respect to the properties of the electrode and redox probes utilized. It is shown that partitioning of the analyte into/onto the adlayer leads to the extraordinary selectivity of the alkanethiolate monolayer modified electrode. Collectively, these studies enable a thorough understanding of the complex electrode mechanism required for successful redox recycling amplification systems, Finally, in a separate (but related) study, the effect of the akyl chain length on the heterogeneous electron transfer behavior of solution-based redox probes is reported, where an odd-even oscillation

  10. Amperometric biosensors for detection of phenol using chemically modified electrodes containing immobilized bacteria.

    Science.gov (United States)

    Skládal, Petr; Morozova, Natalya O; Reshetilov, Anatoly N

    2002-10-01

    Eight strains of Pseudomonas were studied for development of phenol sensor. The immobilization of cells was performed by absorbing them on the working part of mediator-modified screen-printed electrodes (SPEs). Only three Pseudomonas strains were able to transfer electrons resulting from specific oxidation of phenol to the electrode by means of mediators; ferrocene, duroquinone and dimethyferrocene were successfully used with the strains 394 (p20), 74-III and 83-IV (working names), respectively. The lower limits for detection of phenol were 1 micro M for the strain 74-III and 10 micro M for the strain 83-IV and 394 (p20). Calibrations were obtained as the dependencies of logarithm of current changes (log deltaI) on logarithm of concentration (logC), log delta I vs. logC. Among all substrates tested (phenol, catechol, hydroquinone, ethanol, methanol, propanol, isopropanol, isobutanol, isoamylalcohol, acetate, glucose, xylose, vanillin, 2,4,6-trichlorphenol, 2,3,6-trichlorphenol, 4-hydroxy-3-methoxybenzoic acid, coumarin, pentafluorophenol), bacterial sensor demonstrated a good selectivity with respect to phenol and lower responses to catechol and hydroquinone (10-times lower). The dependence of signals on operating conditions was studied. The biosensor should be used during the day of preparation. The operational stability was satisfactory to perform up to 10 consecutive measurements. Low cost and very simple manufacturing procedure allow for bacterial sensor to be applied as disposable devices. PMID:12243905

  11. Eletrodos quimicamente modificados aplicados à eletroanálise: uma breve abordagem Chemically modified electrodes applyes to electroanalysis: a brief presentation

    Directory of Open Access Journals (Sweden)

    Maria de Fátima Brito Souza

    1997-04-01

    Full Text Available Chemically modified electrodes (CMEs have been subject of considerable attention since its inception about 23 years ago. CMEs result of a deliberate immobilization of a modifier agent onto the electrode surface obtained through chemical reactions, chemisorption, composite formation or polymer coating. This immobilization seeks transfer the physicochemical properties of the modifier to the electrode surface and thus to dictate and control the behavior of the electrode/solution interface. In recent years the interest in CMEs has increased particularly to enhance the sensitivity and/or the selectivity of electroanalytical techniques. In general higher sensitivity and/or selectivity may be achieved by exploiting one or more of the following phenomena: electrocatalysis, preconcentration and interferents exclusion. This paper deals with the application of CMEs in electroanalysis, including a brief presentation of the more general procedures that have been employed for the modification of electrode surfaces.

  12. Effect of chemically converted graphene as an electrode interfacial modifier on device-performances of inverted organic photovoltaic cells

    International Nuclear Information System (INIS)

    This study examined the effects of chemically converted graphene (CCG) materials as a metal electrode interfacial modifier on device-performances of inverted organic photovoltaic cells (OPVs). As CCG materials for interfacial layers, a conventional graphene oxide (GO) and reduced graphene oxide (rGO) were prepared, and their functions on OPV-performances were compared. The inverted OPVs with CCG materials showed all improved cell-efficiencies compared with the OPVs with no metal/bulk-heterojunction (BHJ) interlayers. In particular, the inverted OPVs with reduction form of GO showed better device-performances than those with GO and better device-stability than poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS)-based inverted solar cells, showing that the rGO can be more desirable as a metal/BHJ interfacial material for fabricating inverted-configuration OPVs. (paper)

  13. Chemically modified carbon paste electrode for fast screening of oxalic acid levels in soil solutions

    Czech Academy of Sciences Publication Activity Database

    Šestáková, Ivana; Jakl, M.; Jaklová Dytrtová, J.

    2008-01-01

    Roč. 102, - (2008), s. 140-140. E-ISSN 1213-7103. [International Conference on Electroanalysis /12./. 16.06.2008-19.06.2008, Prague] R&D Projects: GA ČR GA521/06/0496 Institutional research plan: CEZ:AV0Z40400503 Keywords : oxalic acid * carbon paste electrodes * soil solutions Subject RIV: CG - Electrochemistry

  14. Glassy carbon electrode modified with a graphene oxide/poly(o-phenylenediamine) composite for the chemical detection of hydrogen peroxide

    Energy Technology Data Exchange (ETDEWEB)

    Nguyen, Van Hoa [School of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 712-749 (Korea, Republic of); Department of Chemistry, Nha Trang University, 2 Nguyen Dinh Chieu, Nha Trang (Viet Nam); Tran, Trung Hieu [School of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 712-749 (Korea, Republic of); Shim, Jae-Jin, E-mail: jjshim@yu.ac.kr [School of Chemical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 712-749 (Korea, Republic of)

    2014-11-01

    Conducting poly(o-phenylenediamine) (POPD)/graphene oxide (GO) composites were prepared using a facile and efficient method involving the in-situ polymerization of OPD in the presence of GO in an aqueous medium. Copper sulfate was used as an oxidative initiator for the polymerization of OPD. Scanning electron microscopy and transmission electron microscopy images showed that POPD microfibrils were formed and distributed relatively uniformly with GO sheets in the obtained composites. X-ray diffraction results revealed the highly crystal structure of POPD. This composite exhibited good catalytic activity and stability. These results highlight the potential applications of POPD/GO composites as excellent electrochemical sensors. The composites were used to modify glass carbon electrodes for the chemical detection of hydrogen peroxide in aqueous media. - Highlights: • Graphene oxide/poly(o-phenylenediamine) composites were prepared efficiently. • POPD microfibrils were distributed relatively uniformly with GO sheets. • The composite exhibited good catalytic activity and stability for H{sub 2}O{sub 2} sensing.

  15. Modified nickel electrodes: a review

    International Nuclear Information System (INIS)

    Catalysts in the form of electrode surfaces offer the added dimension of the electrode potential which can be used to manage the catalyst reactivity and in some cases selectivity. The catalytic effect of nickel oxyhydroxide for the electrochemical determination of organics in alkaline media is very common. This has also received substantial thought because of the application of Ni in rechargeable alkaline batteries. This subject matter has been reviewed from different views before. The present review depicts the role of additives and the modifiers towards the enhancement of electro catalytic properties of electrode surface. (author)

  16. Electrochemical behavior of folic acid at calixarene based chemically modified electrodes and its determination by adsorptive stripping voltammetry

    Energy Technology Data Exchange (ETDEWEB)

    Vaze, Vishwanath D. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400098 (India); Srivastava, Ashwini K. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400098 (India)], E-mail: aksrivastava@chem.mu.ac.in

    2007-12-31

    Voltammetric behavior of folic acid at plain carbon paste electrode and electrode modified with calixarenes has been studied. Two peaks for irreversible oxidation were observed. Out of the three calixarenes chosen for modification of the electrodes, p-tert-butyl-calix[6]arene modified electrode (CME-6) was found to have better sensitivity for folic acid. Chronocoulometric and differential pulse voltammetric studies reveal that folic acid can assemble at CME-6 to form a monolayer whose electron transfer rate is 0.00273 s{sup -1} with 2-electron/2-proton transfer for the peak at +0.71 V against SCE. An adsorption equilibrium constant of 5 x 10{sup 3} l/mol for maximum surface coverage of 2.89 x 10{sup -10} mol/cm{sup 2} was obtained. The current is found to be rectilinear with concentration by differential pulse voltammetry. However, linearity in the lower range of concentration 8.79 x 10{sup -12} M to 1.93 x 10{sup -9} M with correlation coefficient of 0.9920 was achieved by adsorptive stripping voltammetry. The limit of detection obtained was found to be 1.24 x 10{sup -12} M. This method was used for the determination of folic acid in a variety of samples, viz. serum, asparagus, spinach, oranges and multivitamin preparations.

  17. Application of Nafion/Cobalt Hexacyanoferrate Chemically Modified Electrodes for the Determination of Electroinactive Cations by Ion Chromatography

    Institute of Scientific and Technical Information of China (English)

    徐继明; 鲜跃仲; 等

    2002-01-01

    An amperometric detector based on the chemical modification of Nafion and cobalt(Ⅱ) hexacyanoferrate(Ⅱ,Ⅲ)thin film (Nafion /Co-CN-Fe) onto a glassy carbon(GC) electrode was firstly developed for the determination of electroinactive cations (Li+,Na+,K+,Rb+,Cs+,and NH4+)in single column ion cgrinatography,A set of well-defined peaks of electroinactive cation was obtained ,The relative standard deviations (RSDs) of chromatographic peak height(nA) for these cations were all below 3.8% .The cations were detected convenivently in the linear concentration ragne of 6.0×10-6--5.0×10-3 mol/L and their correlation coefficients were all above 0.99 .The detection limits of the cations were 9.2×107 mol/L for K+,7.8×107mol/L for Rb+,6.2×107mol/L for Cs+ and 6.2×106mol/L for NH4+ ,at a signal-noise ratio of 3. The method was quick,sensitive,simple and was successfully applied to the analysis of rainwater samples,The electrode was stable for a 2 week period of operation with no evidence of chemical of mechanical deterioration.

  18. Determination of vanadium(V) by direct automatic potentiometric titration with EDTA using a chemically modified electrode as a potentiometric sensor.

    Science.gov (United States)

    Quintar, S E; Santagata, J P; Cortinez, V A

    2005-10-15

    A chemically modified electrode (CME) was prepared and studied as a potentiometric sensor for the end-point detection in the automatic titration of vanadium(V) with EDTA. The CME was constructed with a paste prepared by mixing spectral-grade graphite powder, Nujol oil and N-2-naphthoyl-N-p-tolylhydroxamic acid (NTHA). Buffer systems, pH effects and the concentration range were studied. Interference ions were separated by applying a liquid-liquid extraction procedure. The CME did not require any special conditioning before using. The electrode was constructed with very inexpensive materials and was easily made. It could be continuously used, at least two months without removing the paste. Automatic potentiometric titration curves were obtained for V(V) within 5 x 10(-5) to 2 x 10(-3)M with acceptable accuracy and precision. The developed method was applied to V(V) determination in alloys for hip prosthesis. PMID:18970248

  19. Cobalt Phthalocyanine Modified Electrodes Utilised in Electroanalysis: Nano-Structured Modified Electrodes vs. Bulk Modified Screen-Printed Electrodes

    Directory of Open Access Journals (Sweden)

    Christopher W. Foster

    2014-11-01

    Full Text Available Cobalt phthalocyanine (CoPC compounds have been reported to provide electrocatalytic performances towards a substantial number of analytes. In these configurations, electrodes are typically constructed via drop casting the CoPC onto a supporting electrode substrate, while in other cases the CoPC complex is incorporated within the ink of a screen-printed sensor, providing a one-shot economical and disposable electrode configuration. In this paper we critically compare CoPC modified electrodes prepared by drop casting CoPC nanoparticles (nano-CoPC onto a range of carbon based electrode substrates with that of CoPC bulk modified screen-printed electrodes in the sensing of the model analytes L-ascorbic acid, oxygen and hydrazine. It is found that no “electrocatalysis” is observed towards L-ascorbic acid using either of these CoPC modified electrode configurations and that the bare underlying carbon electrode is the origin of the obtained voltammetric signal, which gives rise to useful electroanalytical signatures, providing new insights into literature reports where “electrocatalysis” has been reported with no clear control experiments undertaken. On the other hand true electrocatalysis is observed towards hydrazine, where no such voltammetric features are witnessed on the bare underlying electrode substrate.

  20. 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.

  1. 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 ...

  2. Electrochemical behavior of a novel palladium pentacyanonitrosylferrate modified aluminum electrode

    International Nuclear Information System (INIS)

    Novel inorganic film modified electrodes have been prepared by chemical deposition of a thin palladium pentacyanonitrosylferrate (PdPCNF) film on the surface of aluminum substrate. The modification process including the electroless deposition of metallic palladium on the aluminum electrode surface from PdCl2+25% ammonia solution and chemical derivatization of deposited palladium to the PdPCNF film in 0.1 M Na2[Fe(CN)5NO]+0.5 M KNO3+HNO3 solution (pH 1.5-2.5), are described. The aluminum-based modified electrodes exhibit, one pair of well-defined voltammetric peaks which correspond to the Fe(III)/Fe(II) transition in complex structure. The effect of pH, ammonium, alkali metal and alkaline earth metal cations of supporting electrolyte on the electrochemical characteristics of the modified electrode was studied in detail. Diffusion coefficients of hydrated ammonium and alkali metal cations in the film (D), transfer coefficient (α) and transfer rate constant for electron (ks), were determined. The high stability of this modified electrode makes it attractive in practical application

  3. Chemical modifiers of radiotherapy

    International Nuclear Information System (INIS)

    Only two groups, anticancer drugs and radiosensitizers are discussed among many groups of chemical modifiers. In combined radiotherapy (RT) with chemotherapy (CT), sequential administration seems to be superior to concomitant administration, because simultaneous use enhances intensively normal tissue damage. In sequential administration, interruption of CT during RT causes growth of distant metastases. So, alternating scheme of RT and CT is proposed and evaluated clinically. Hypoxic cell sensitizers including well-known misonidazole and PLDR inhibitors (Ara-A etc.) are promising in radiotherapy. They should be used intermittently two or three times during RT in order to avoid neurotoxicity of misonidazole. (author) 70 refs

  4. Modified electrodes based on lipidic cubic phases.

    Science.gov (United States)

    Bilewicz, Renata; Rowiński, Paweł; Rogalska, Ewa

    2005-04-01

    The lipidic cubic phase can be characterized as a curved bilayer forming a three-dimensional, crystallographical, well-ordered structure that is interwoven by aqueous channels. It provides a stable, well-organized environment in which diffusion of both water-soluble and lipid-soluble compounds can take place. Cubic phases based on monoacylglycerols form readily and attract our interest due to their ability to incorporate and stabilize proteins. Their lyotropic and thermotropic phase behaviour has been thoroughly investigated. At hydration over 20%, lipidic cubic phases Ia3d and Pn3m are formed. The latter is stable in the presence of excess water, which is important when the cubic phase is considered as an electrode-modifying material. Due to high viscosity, the cubic phases can be simply smeared over solid substrates such as electrodes and used to host enzymes and synthetic catalysts, leading to new types of catalytically active modified electrodes as shown for the determination of cholesterol, CO(2), or oxygen. The efficiency of transport of small hydrophilic molecules within the film can be determined by voltametry using two types of electrodes: a normal-size electrode working in the linear diffusion regime, and an ultramicroelectrode working under spherical diffusion conditions. This allows determining both the concentration and diffusion coefficient of the electrochemically active probe in the cubic phase. The monoolein-based cubic phase matrices are useful for immobilizing enzymes on the electrode surface (e.g., laccases from Trametes sp. and Rhus vernicifera were employed for monitoring dioxygen). The electronic contact between the electrode and the enzyme was maintained using suitable electroactive probes. PMID:15833697

  5. A novel thin-layer amperometric detector based on chemically modified ring-disc electrode and its application for simultaneous measurements of nitric oxide and nitrite in rat brain combined with in vivo microdialysis.

    Science.gov (United States)

    Mao, L; Shi, G; Tian, Y; Liu, H; Jin, L; Yamamoto, K; Tao, S; Jin, J

    1998-08-01

    A novel thin-layer amperometric detector (TLAD) based on chemically modified ring-disc electrode and its application for simultaneous measurements of nitric oxide (NO) and nitrite (NO(2)(-)) in rat brain were demonstrated in this work. The ring-disc electrode was simultaneously sensitive to nitric oxide (NO) and nitrite (NO(2)(-)) by modifying its inner disc with electropolymerized film of cobalt(II) tetraaminophthalocyanine (polyCoTAPc)/Nafion and its outer ring with poly(vinylpyridine) (PVP), respectively. The ring-disc electrode was used to constitute a novel TLAD in radial flow cell for simultaneous measurements of NO and NO(2)(-) in rat brain combined with techniques of high performance liquid chromatography (HPLC) and in vivo microdialysis. It was found that the basal concentration of NO in the caudate nucleus of rat brain is lower than 1.0x10(-7) mol l(-1), NO(2)(-) concentration is 5.0x10(-7) mol l(-1) and NO exists in brain maybe mainly in the form of its decomposed product. PMID:18967286

  6. Determination of Thallium(I by Hybrid Mesoporous Silica (SBA-15 Modified Electrode

    Directory of Open Access Journals (Sweden)

    Geeta Rani

    2016-01-01

    Full Text Available Chemically modified mesoporous silica material (SBA-15 was used for the construction of Tl(I selective carbon paste electrode. The best response was found with the electrode containing 10% modifier as electrode material. The electrode has a lower detection limit of 6.0 × 10−9 M in a working concentration range of 1.0 × 10−8–1.0 × 10−1 M. The selectivity coefficient calculated by match potential method (MPM shows the high selectivity of electrode towards Tl(I over other tested ions. The electrode was successfully applied as an indicator electrode for the titration of 0.01 M TlNO3 solution with standards EDTA solution and for sequential titration of mixture of different anions.

  7. Synthesis of chemically modified DNA.

    Science.gov (United States)

    Shivalingam, Arun; Brown, Tom

    2016-06-15

    Naturally occurring DNA is encoded by the four nucleobases adenine, cytosine, guanine and thymine. Yet minor chemical modifications to these bases, such as methylation, can significantly alter DNA function, and more drastic changes, such as replacement with unnatural base pairs, could expand its function. In order to realize the full potential of DNA in therapeutic and synthetic biology applications, our ability to 'write' long modified DNA in a controlled manner must be improved. This review highlights methods currently used for the synthesis of moderately long chemically modified nucleic acids (up to 1000 bp), their limitations and areas for future expansion. PMID:27284032

  8. Signal amplification of dopamine using lanthanum hexacyanoferrate-modified electrode

    Indian Academy of Sciences (India)

    T Selvaraju; R Ramaraj

    2014-01-01

    A sensitive and selective electrochemical sensor has been developed using an electroactive polynuclear lanthanum hexacyanoferrate (LaHCF) complex with counter alkali cation (Na+) deposited on the glassy carbon (GC) electrode (GC/LaHCF). The GC/LaHCF-modified electrode is found to be an excellent transducer in mediating the oxidation of neurotransmitter molecule such as dopamine (DA) at physiological pH 7.2. Interestingly, the GC/LaHCF-modified electrode amplifies a 50-fold enhancement in the oxidation of DA signal compared to the bare GC electrode. Besides, the GC/LaHCF-modified electrode shows excellent selectivity in the voltammetric oxidation of DA in the presence of ascorbic acid (AA). Under optimal conditions, the GC/LaHCF modified electrode shows a linear relationship in DA oxidation between 0.1 × 10−6 and 1.0 × 10−6M with the detection limit of 1 × 10−8M (10 nM). Importantly, practical utility of the modified electrode is good in studying the real sample analysis such as dopamine hydrochloride injection assay.

  9. On the ability of metal-nitroprusside complexes as electrode modifiers: Characterization and electrochemical study of palladized aluminum electrode modified with iron pentacyanonitrosylferrate

    International Nuclear Information System (INIS)

    Highlights: • Palladized aluminum electrode was modified with ferrous nitroprusside by fully electroless procedure. • Chemical composition change of modifier on the electrode surface was investigated. • A dissociative mechanism for metal-nitroprusside type modifiers conversion was proposed. - Abstract: In this work we introduce the concept of “directed assembly” based on multiple sequential adsorption of iron pentacyanonitrosylferrate (FePCNF) multilayer on the surface of the palladized aluminum electrode (Pd-Al) by alternately exposing it to positively charged Fe2+ cations and negatively charged [Fe(CN)5NO]2− anions. The adsorbed FePCNF on the Pd-Al electrode is pure and very stable. The preliminary cyclic voltammetric studies showed that freshly prepared modified electrodes have no defined electroactivity in the potential range of −0.2–1 V/SCE, but after exerting negative potential, two couples of redox peaks are emerged at 0.17 and 0.8 V/SCE due to outer and inner Fe(II) ↔ Fe(III) redox transitions of FePCNF modifier. The pH effect of supporting electrolyte on the electrochemical behavior of the electroactivated FePCNF/Pd-Al was studied. Also, the electron transfer rate constant (ks) and charge transfer coefficient (α) were calculated. We found out that the chemical composition of adsorbed FePCNF on the electrode surface is changed by exerting negative potential. On the basis of results obtained by FT-IR spectroscopy and electrochemical techniques, a probable dissociative mechanism was proposed for the modifier conversion. We ascribe this conversion to the generation and dissociation of [Fe(CN)4NO]2− as predominant reduced species in acidic solution, which in turn releases NO and probably leads to formation of stable Prussian Blue type precipitate

  10. Modified Electrodes Used for Electrochemical Detection of Metal Ions in Environmental Analysis

    Directory of Open Access Journals (Sweden)

    Gregory March

    2015-04-01

    Full Text Available Heavy metal pollution is one of the most serious environmental problems, and regulations are becoming stricter. Many efforts have been made to develop sensors for monitoring heavy metals in the environment. This review aims at presenting the different label-free strategies used to develop electrochemical sensors for the detection of heavy metals such as lead, cadmium, mercury, arsenic etc. The first part of this review will be dedicated to stripping voltammetry techniques, on unmodified electrodes (mercury, bismuth or noble metals in the bulk form, or electrodes modified at their surface by nanoparticles, nanostructures (CNT, graphene or other innovative materials such as boron-doped diamond. The second part will be dedicated to chemically modified electrodes especially those with conducting polymers. The last part of this review will focus on bio-modified electrodes. Special attention will be paid to strategies using biomolecules (DNA, peptide or proteins, enzymes or whole cells.

  11. Copper nanoparticle modified carbon electrode for determination of dopamine

    International Nuclear Information System (INIS)

    This paper reports the synthesis and characterization of copper nanoparticles (CuNPs) and application of copper nanoparticle-modified glassy carbon electrode for the electrochemical determination of dopamine. Electrochemical measurements were performed using differently modified glassy carbon (GC) electrodes. Bare, oxidized before modification and copper nanoparticle-modified glassy carbon electrodes (bare-GC, ox-GC and CuNP/GC electrodes, respectively) were characterized by cyclic voltammetry and electrochemical impedance spectroscopy in the presence of redox probes. Atomic force microscopy was used for the visualization of electrode surfaces. The CuNP/GC electrode was found to be suitable for the selective determination of dopamine even in the presence of ascorbic acid, uric acid, and p-acetamidophenol. The observed linear range of CuNP/GC for dopamine was from 0.1 nM to 1.0 μM while the detection limit was estimated to be 50 pM. It was demonstrated that here reported glassy carbon electrode modified by copper nanoparticles is suitable for the determination of dopamine in real samples such as human blood serum.

  12. Electrochemical Biosensor Based on Boron-Doped Diamond Electrodes with Modified Surfaces

    Directory of Open Access Journals (Sweden)

    Yuan Yu

    2012-01-01

    Full Text Available Boron-doped diamond (BDD thin films, as one kind of electrode materials, are superior to conventional carbon-based materials including carbon paste, porous carbon, glassy carbon (GC, carbon nanotubes in terms of high stability, wide potential window, low background current, and good biocompatibility. Electrochemical biosensor based on BDD electrodes have attracted extensive interests due to the superior properties of BDD electrodes and the merits of biosensors, such as specificity, sensitivity, and fast response. Electrochemical reactions perform at the interface between electrolyte solutions and the electrodes surfaces, so the surface structures and properties of the BDD electrodes are important for electrochemical detection. In this paper, the recent advances of BDD electrodes with different surfaces including nanostructured surface and chemically modified surface, for the construction of various electrochemical biosensors, were described.

  13. 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

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

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Wei, E-mail: swyy26@hotmail.com [College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158 (China); Dong, Lifeng, E-mail: donglifeng@qust.edu.cn [College of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Department of Physics, Astronomy, and Materials Science, Missouri State University, Springfield, MO 65897 (United States); Deng, Ying; Yu, Jianhua [College of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Wang, Wencheng [College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158 (China); Zhu, Qianqian [College of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China)

    2014-06-01

    Nitrogen-doped graphene (NG) was synthesized and used for the investigation on direct electrochemistry of hemoglobin (Hb) with a carbon ionic liquid electrode as the substrate electrode. Due to specific characteristics of NG such as excellent electrocatalytic property and large surface area, direct electron transfer of Hb was realized with enhanced electrochemical responses appearing. Electrochemical behaviors of Hb on the NG modified electrode were carefully investigated with the electrochemical parameters calculated. The Hb modified electrode exhibited excellent electrocatalytic reduction activity toward different substrates, such as trichloroacetic acid and H{sub 2}O{sub 2}, with wider dynamic range and lower detection limit. These findings show that NG can be used for the preparation of chemically modified electrodes with improved performance and has potential applications in electrochemical sensing. - Graphical abstract: The utilization of N-doped graphene enables direct electrochemistry of hemoglobin with a pair of well-defined redox peaks appearing. - Highlights: • Nitrogen-doped graphene (NG) was synthesized by a solvothermal method. • NG was used for the investigation on direct electrochemistry of hemoglobin with carbon ionic liquid electrode. • The Hb modified electrode exhibited excellent electrocatalytic activity toward different substrates.

  15. Theory of Water Desalination by Porous Electrodes with Immobile Chemical Charge

    NARCIS (Netherlands)

    Biesheuvel, P.M.; Hamelers, H.V.M.; Suss, M.E.

    2015-01-01

    In capacitive deionization (CDI), water is desalinated by storing ions in electrical double layers (EDLs) within the micropores of charged porous carbon electrodes. Recent experiments using chemically modified electrodes have shown differing, novel phenomena such as "inverted CDI," "enhanced CDI,

  16. A modified electrode cap for EEG recordings in MRI scanners.

    Science.gov (United States)

    Baumann, S B; Noll, D C

    1999-12-01

    A stretchable electrode cap containing 64 electrodes was modified to make it compatible for functional magnetic resonance imaging (fMRI). Metallic components were individually tested for magnetic susceptibility, and those that perturbed a free-swinging magnet or moved in a strong magnetic field were replaced with non-ferromagnetic components. Studies with a phantom indicate that placement of the cables carrying signals from the cap to the amplifiers can significantly affect MR image quality. Anatomical and functional images obtained with the modified electrode cap show modest signal loss, but not enough to substantially interfere with the low-noise images required for fMRI. The cap enables faster application of large arrays of electrodes in conjunction with MRI studies, and thus makes combined EEG/fMRI studies more practical, especially those with EEG source localization as one of the goals. PMID:10616125

  17. Nanostructured metal particle-modified electrodes for electrocatalytic and sensor applications

    Indian Academy of Sciences (India)

    Ramasamy Ramaraj

    2006-11-01

    Nanotechnology has become one of the most exciting frontier fields in analytical chemistry. The huge interest in nanomaterials, for example in chemical sensors and catalysis, is driven by their many desirable properties. Although metal is a poor catalyst in bulk form, nanometre-sized particles can exhibit excellent catalytic activity due to their relative high surface area-to-volume ratio and their interface-dominated properties, which significantly differ from those of the bulk material. The integration of metal nanoparticles into thin film of permselective membrane is particularly important for various applications, for example in biological sensing and in electrocatalysis. We have already established different techniques to design permselective membrane-coated chemically modified electrodes with incorporated redox molecules for electrocatalytic, electrochromic and sensor applications. Recently, we have prepared nanostructured platinum and copper (represented Mnano, M = Pt and Cu) modified GC/Nafion electrodes (GC/Nf/Mnano) and characterized by using AFM, XPS, XRD and electrochemical techniques. The nanostructured Mnano modified electrodes were utilized for efficient electrocatalytic selective oxidation of neurotransmitter molecules in the presence of interfering species such as ascorbic acid (AA) and uric acid (UA). It has been also shown that the modified electrodes could be used as sensors for the detection of submicromolar concentrations of biomolecules with practical applications to real samples such as blood plasma and dopamine hydrochloride injection solution. The GC/Cunano electrode has been used for catalytic reduction of oxygen.

  18. Graphene oxide-modified electrodes for sensitive determination of diethylstilbestrol

    Science.gov (United States)

    Yu, Chunmei; Ji, Wanyu; Wang, Yidan; Bao, Ning; Gu, Haiying

    2013-03-01

    This paper reports an electrochemical sensor fabricated with graphene oxide (GO) modified on a chitosan-coated glassy carbon electrode (GO-CS/GCE) and its application for the detection of diethylstilbestrol (DES). It was observed that the effective electrochemical surface area of the GO modified electrode was nearly 10 times that of the bare GCE. This could be used to explain the results that the oxidation peak current of DES on the GO-CS/GCE was much larger than on the bare GCE. Under optimized conditions, the prepared electrode could be used to electrochemically detect DES according to the oxidation of the DES. Based on the technique of differential pulse voltammetry and the accumulation of DES on GO modified electrodes, the calibration curve for DES determination could be obtained with a linear range of 1.5 × 10-8-3.0 × 10-5 M and an estimated detection limit of 3.0 × 10-9 M (S/N = 3). The feasibility of the developed electrode for tablet sample analysis was investigated. Our investigation revealed that GO could significantly improve the analytical performance of electrochemical sensors.

  19. Graphene oxide-modified electrodes for sensitive determination of diethylstilbestrol

    International Nuclear Information System (INIS)

    This paper reports an electrochemical sensor fabricated with graphene oxide (GO) modified on a chitosan-coated glassy carbon electrode (GO-CS/GCE) and its application for the detection of diethylstilbestrol (DES). It was observed that the effective electrochemical surface area of the GO modified electrode was nearly 10 times that of the bare GCE. This could be used to explain the results that the oxidation peak current of DES on the GO-CS/GCE was much larger than on the bare GCE. Under optimized conditions, the prepared electrode could be used to electrochemically detect DES according to the oxidation of the DES. Based on the technique of differential pulse voltammetry and the accumulation of DES on GO modified electrodes, the calibration curve for DES determination could be obtained with a linear range of 1.5 × 10−8–3.0 × 10−5 M and an estimated detection limit of 3.0 × 10−9 M (S/N = 3). The feasibility of the developed electrode for tablet sample analysis was investigated. Our investigation revealed that GO could significantly improve the analytical performance of electrochemical sensors. (paper)

  20. Facile direct electron transfer in glucose oxidase modified electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Wang Dan [Department of Chemistry and Biochemistry, Ohio University, Athens, OH 45701 (United States); Chen Liwei [Department of Chemistry and Biochemistry, Ohio University, Athens, OH 45701 (United States); Suzhou Institute of Nano Tech and Nano Bionics, Chinese Academy of Sciences, 398 Ruoshui Road, Suzhou Industrial Park, Suzhou, Jiangsu 215125 (China)], E-mail: lwchen2008@sinano.ac.cn

    2009-07-15

    Glucose oxidase (GOx) is widely used in the glucose biosensor industry. However, mediatorless direct electron transfer (DET) from GOx to electrode surfaces is very slow. Recently, mediatorless DET has been reported via the incorporation of nanomaterials such as carbon nanotubes and nanoparticles in the modification of electrodes. Here we report GOx electrodes showing DET without the need for any nanomaterials. The enzyme after immobilization with poly-L-lysine (PLL) and Nafion retains the biocatalytic activities and oxidizes glucose efficiently. The amperometric response of Nafion-PLL-GOx modified electrode is linearly proportional to the concentration of glucose up to 10 mM with a sensitivity of 0.75 {mu}A/mM at a low detection potential (-0.460 V vs. Ag/AgCl). The methodology developed in this study will have impact on glucose biosensors and biofuel cells and may potentially simplify enzyme immobilization in other biosensing systems.

  1. 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.

  2. 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%.

  3. Enzyme monolayer- and bilayer-modified tin oxide electrodes for the determination of hydrogen peroxide and glucose

    Energy Technology Data Exchange (ETDEWEB)

    Tatsuma, Tetsu; Okawa, Yusuke; Watanabe, Tadashi (Univ. of Tokyo (Japan))

    1989-11-01

    An enzyme-based amperometric biosensor for hydrogen peroxide was developed, employing a horseradish peroxidase (HRP) monolayer covalently attached to a tin oxide electrode and a dissolved electron mediator. The sensor can determine hydrogen peroxide at levels down to 10{sup {minus}8} M and can be applied to a flow system. Stability of the electrode, kinetics of the surface process, and the efficiencies of different mediators were studied. As an extension, glucose oxidase (GOx) was chemically bound to the HRP-modified electrode. A GOx/HRP bilayer-modified electrode thus obtained exhibits much better performance in glucose detection limit, sensitivity, and response speed than previously reported GOx monolayer-modified electrodes.

  4. Electrochemical Degradation of Surfactants in Wastewater Using Ti/SnO2-PbO2 Modified Electrode

    International Nuclear Information System (INIS)

    This study deals with the possibility of using Ti/SnO2-PbO2 modified electrode for the electrocatalytic oxidation process of surfactants in wastewater. The electrode was prepared by electrodeposition of Sn and Pb from fluoborate bath on the pre-anodized Ti substrates and anodization of the prepared Ti/Sn-Pb electrode in the oxalic acid (100 g/l) at high current density to obtain the Ti/SnO2-PbO2 modified electrode. The results of the electrocatalytic degradation were expressed in term of chemical oxygen demand (COD) removal. The highest electrocatalytic activity was obtained in the presence of NaCl as a conductive electrolyte. The different operating conditions of the electrocatalytic oxidation process were studied which include current density, pH, electrolysis time, temperature, initial surfactant concentration and conductive electrolyte concentration. The optimum operating conditions for the modified electrode were determined

  5. Diffusional transport to and through thin-layer nanoparticle film modified electrodes: capped CdSe nanoparticle modified electrodes.

    Science.gov (United States)

    Hepburn, William G; Batchelor-McAuley, Christopher; Tschulik, Kristina; Barnes, Edward O; Kachoosangi, Roohollah Torabi; Compton, Richard G

    2014-09-01

    We present a simple and general theoretical model which accounts fully for the influence of an electrode modifying non-electroactive layer on the voltammetric response of a diffusional redox probe. The layer is solely considered to alter the solubilities and diffusion coefficients of the electroactive species within the thin layer on the electrode surface. On this basis it is demonstrated how, first, the apparent electrochemical rate constant can deviate significantly from that measured at an unmodified electrode. Second, depending on the conditions within the layer the modification of the electrode may lead to either apparent 'negative' or 'positive' electrocatalytic effects without the true standard electrochemical rate constant for the electron transfer at the electrode surface being altered. Having presented the theoretical model three experimental cases are investigated, specifically, the reductions of ruthenium(III) hexaamine, oxygen and boric acid on a gold macro electrode with and without a multi-layer organic capped nanoparticle film. In the latter case of the reduction of boric acid the voltammetric reduction is found to be enhanced by the presence of the organic layer. This result is interpreted as being due to an increase in the solubility of the analyte within the non-electroactive layer and not due to an alteration of the standard electrochemical rate constant. PMID:25050481

  6. 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.

  7. Voltammetry of Os(VI)-modified polysaccharides at carbon electrodes

    Czech Academy of Sciences Publication Activity Database

    Trefulka, Mojmír; Paleček, Emil

    2009-01-01

    Roč. 21, č. 15 (2009), s. 1763-1766. ISSN 1040-0397 R&D Projects: GA ČR(CZ) GA301/07/0490; GA MŠk(CZ) LC06035 Institutional research plan: CEZ:AV0Z50040507; CEZ:AV0Z50040702 Keywords : chemical modification of polysaccharides * Os(VI)L-polysaccharide adducts * pyrolytic graphite electrodes Subject RIV: BO - Biophysics Impact factor: 2.630, year: 2009

  8. 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.

  9. Electrochemical detection of phenolic estrogenic compounds at clay modified carbon paste electrode

    Science.gov (United States)

    Belkamssa, N.; Ouattara, L.; Kawachi, A.; Tsujimura, M.; Isoda, H.; Chtaini, A.; Ksibi, M.

    2015-04-01

    A simple and sensitive electroanalytical method was developed to determine the Endocrine Disrupting chemical 4-tert-octylphenol on clay modified carbon paste electrode (Clay/CPE). The electrochemical response of the proposed electrode was studied by means of cyclic and square wave voltammetry. It has found that the oxidation of 4-tert-octylphenol on the clay/CPE displayed a well-defined oxidation peak. Under these optimal conditions, a linear relation between concentrations of 4-tert-octylphenol current response was obtained over range of 7.26×10-6 to 3.87×10-7 with a detection and quantification limit of 9.2×10-7 M and 3.06×10-6 M, respectively. The correlation coefficient is 0.9963. The modified electrode showed suitable sensitivity, high stability and an accurate detection of 4-tert-octylphenol. The modified electrode also relevant suitable selectivity for various phenolic estrogenic compounds.

  10. Electrochemical detection of hydrogen peroxide at a waxed graphite electrode modified with platinum-decorated carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    SHI Qiao-cui; ZENG Wen-fang; ZHU Yunu

    2009-01-01

    Platinum-decorated carbon nanotubes (CNT-Pt) were produced by the chemical reduction method. A novel modified electrode was fabricated by intercalated CNT-Pt in the surface of waxed graphite, which provided excellent electro-catalytic activity and selectivity for both oxidation and reduction of hydrogen peroxide. The current response of the modified electrode for hydrogen peroxide was very rapid and the detection limits in amperometry are 2.5×10-6 mol/L at reduction potential and 4.8×10-6 mol/L at oxidation potential. It was desmonstrated that the electrode with high electro-activity was a suitable basic electrode for preparing enzyme electrode.

  11. 化学修饰丝网印刷薄片碳电极测定痕量铜%Determination of the Copper(Ⅱ) by A Chemically Modified Screen-printing Carbon Electrode

    Institute of Scientific and Technical Information of China (English)

    屠一锋; 许健

    2001-01-01

    采用丝网印刷技术制备一次性薄片碳电极,并在此电极上进行化学修饰,于邻苯二酚-甲醛-NaOH溶液中,在-0.1 V~1.2V电位范围内,循环伏安法进行电聚合,可获得性能良好的修饰电极,该电极可用于阳极溶出伏安法测量痕量铜,其响应灵敏度较裸碳电极提高50倍以上;线性范围为2.5~50 μg/L;测量的RSD为2.7%。用该电极可直接测定当地自来水中铜的含量为6.27μg/L。%The technique for developing a screen-printing disposabl e carbonelectrode and modifying its surface with electropolymer of catechol- formaldehyde was described. This modified electrode could be used to determine the Cu2+ with high selectivity. The linear range of the determination was from 2.5 μg/L to 50 μg/L. The linear regression coefficient and the RSD were 0.9992 and 2.7%, respectively. The content of Cu2+in local tap water was determined by this modified electrode for 6.27 μg/L.

  12. Application of an exfoliated graphite nanoplatelet-modified electrode for the determination of quintozen

    Energy Technology Data Exchange (ETDEWEB)

    Ion, Ion; Ion, Alina Catrinel, E-mail: ac_ion@yahoo.com; Culetu, Alina

    2011-10-10

    A chitosan-grafted exfoliated graphite nanoplatelet (xGnP) hybrid chemically modified electrode was developed and characterized for the determination of organochlorine pesticides with nitro groups using quintozen as a representative. The hybrid material was characterized by Fourier transform infrared spectroscopy (FTIR), ultraviolet-visible spectroscopy (UV-VIS) and scanning electron microscopy (SEM). The electrochemical properties of the chitosan-xGnP modified electrode were characterized by a physical deposition method for depositing it on a graphite electrode. Because of the affinity of the xGnP for nitro groups, nitroaromatic organophosphate pesticides are attached to the surface, allowing the extraction of quintozen within a short time (4 min). The differential pulse response was linear over the quintozen concentration range of 10{sup -12}-10{sup -6} M, and the current linearly increased with the quintozen concentrations in two concentration ranges: from 10{sup -12} to 10{sup -8} M with the linear regression equation of y = 0.0423x + 0.6451, R{sup 2} = 0.9964 and from 10{sup -8} to 10{sup -6} M with the linear regression equation of y = 0.0085x + 0.303, R{sup 2} = 0.9952, with a detection limit of 10{sup -11} M. Highlights: {yields} The first attempt to use graphitic nanoplatelets in an electrochemical sensor for quintozen and to characterize the obtained electrode. {yields} The studied sensor exhibits good sensitivity and stability, xGnP representing a good candidate of advanced electrode materials. {yields} We concluded that a simple method for the production of cheap xGnP-chit/GC modified electrodes for pesticides with nitro groups can be established, further study on developing this methods being envisaged.

  13. Metallization of cyanide-modified Pt(111) electrodes with copper

    DEFF Research Database (Denmark)

    Escribano, Maria Escudero; Wildi, Christopher; Mwanda, Jonathan A.;

    2016-01-01

    The reduction of Cu2+ ions irreversibly attached to the surface of a cyanide-modified Pt(111) electrode via non-covalent or weakly covalent interactions with the N atom of adsorbed cyanide was studied using cyclic voltammetry (CV) and in situ scanning tunneling microscopy (STM). Both CV and STM...... provide evidence that the reduction of irreversibly adsorbed Cu2+ to Cu in Cu2+-free sulfuric acid solutions does not result in the stripping of the cyanide adlayer. This strongly suggests that the reduction process results in the metallization of the cyanide adlayer on Pt(111), yielding a platinum...

  14. Amperometric sensing of hydrogen peroxide using glassy carbon electrode modified with copper nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Sophia, J.; Muralidharan, G., E-mail: muraligru@gmail.com

    2015-10-15

    In this paper, fabrication of glassy carbon electrode (GCE) modified with nano copper particles is discussed. The modified electrode has been tested for the non-enzymatic electrochemical detection of hydrogen peroxide (H{sub 2}O{sub 2}). The copper nanoparticles (Cu NPs) were prepared employing a simple chemical reduction method. The presence of Cu NPs was confirmed through UV–visible (UV–vis) absorption spectroscopy and X-ray diffraction (XRD) analysis. The size and morphology of the particles were investigated using transmission electron microscopy (TEM). The electrochemical properties of the fabricated sensor were studied via cyclic voltammetry (CV), chronoamperometry and electrochemical impedance spectroscopy (EIS). The electrochemical sensor displayed excellent performance features towards H{sub 2}O{sub 2} detection exhibiting wide linear range, low detection limit, swift response time, good reproducibility and stability.

  15. Amperometric sensing of hydrogen peroxide using glassy carbon electrode modified with copper nanoparticles

    International Nuclear Information System (INIS)

    In this paper, fabrication of glassy carbon electrode (GCE) modified with nano copper particles is discussed. The modified electrode has been tested for the non-enzymatic electrochemical detection of hydrogen peroxide (H2O2). The copper nanoparticles (Cu NPs) were prepared employing a simple chemical reduction method. The presence of Cu NPs was confirmed through UV–visible (UV–vis) absorption spectroscopy and X-ray diffraction (XRD) analysis. The size and morphology of the particles were investigated using transmission electron microscopy (TEM). The electrochemical properties of the fabricated sensor were studied via cyclic voltammetry (CV), chronoamperometry and electrochemical impedance spectroscopy (EIS). The electrochemical sensor displayed excellent performance features towards H2O2 detection exhibiting wide linear range, low detection limit, swift response time, good reproducibility and stability

  16. Platinum Nanoparticles Modified Electrode for Rapid Electrochemical Detection of Escherichia coli

    Institute of Scientific and Technical Information of China (English)

    CHENG Yu-Xiao; LIU Ya-Jun; HUANG Jing-Jing; FENG Zhen; XIAN Yue-Zhong; WU Zi-Rong; ZHANG Wen; JIN Li-Tong

    2008-01-01

    A platinum nanoparticles chemically modified electrode (PtNP/GCE) was fabricated by electro-deposition and used to detection of Escherichia coli (E.coli).The detection principle was based on determination of p-aminophenol that was produced by an enzymatic reaction in E.coli solution.The sensitivity of the detection was improved by the platinum nanoparticle modified electrode and optimization of the detection system.The current responses were proportional to the density of E.coli ranging from 50 to 1.0× 105 cfu/mL, with detection limit of 20 cfu/mL, and the detection time was less than 4 h.Compared with conventional methods, the electrochemical technology described here could be suitable for rapid detection of E.coli in the fields of food industry, environmental monitoring and clinic biomedicine.

  17. 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.

  18. Modified silver nanowire transparent electrodes with exceptional stability against oxidation

    Science.gov (United States)

    Idier, J.; Neri, W.; Labrugère, C.; Ly, I.; Poulin, P.; Backov, R.

    2016-03-01

    We report an easy method to prepare thin, flexible and transparent electrodes that show enhanced inertness toward oxidation using modified silver nanowires (Ag NWs). Stabilization is achieved through the adsorption of triphenylphosphine (PPh3) onto the Ag NW hybrid dispersions prior to their 2D organization as transparent electrodes on polyethylene terephtalate (PET) films. After 110 days in air (20 °C) under atmospheric conditions, the transmittance of the PET/Ag NW/PPh3 based films is nearly unchanged, while the transmittance of the PET/Ag NW-based films decreases by about 5%. The sheet resistance increases for both materials as time elapses, but the rate of increase is more than four times slower for films stabilized by PPh3. The improved transmittance and conductivity results in a significantly enhanced stability for the figure of merit σ dc/σ op. This phenomenon is highlighted in highly oxidative nitric acid vapor. The tested stabilized films in such conditions exhibit a decrease to σ dc/σ op of only 38% after 75 min, whereas conventional materials exhibit a relative loss of 71%. In addition, by contrast to other classes of stabilizers, such as polymer or graphene-based encapsulants, PPh3 does not alter the transparency or conductivity of the modified films. While the present films are made by membrane filtration, the stabilization method could be implemented directly in other liquid processes, including industrially scalable ones.

  19. Fabrication of ferrocenyl glutathione modified electrode and its application for detection of cadmium ions

    Institute of Scientific and Technical Information of China (English)

    WANG Fang-bin; FAN Mei-yi; LIU You-nian; WANG Jian-xiu; ZENG Dong-ming; HUANG Ke-long

    2008-01-01

    1'-eysteaminecarbonyl-1-glutathionecarbonyl-ferrucene (Fc-GSH) was synthesized from ferrocene dicarboxylic acid and reduced glutathione (GSH) with 4 steps. IR and 1H-NMR were used to characterize the products. Then Fe-GSH was immobilized on the surface of gold electrode. Cyclic votammetry (CV) was adopted to investigate the electrochemical properties of this Fc-GSHmodified electrode in the absence and presence of Cd2+ aqueous solutions. The peak oxidation potential (Ea) and reduction potential(Ec) of Fc-GSH modified electrode were observed at Ea= 0.74 V and Ec= 0.64 V (vs Ag/AgCl) before the accumulation of Cd2+. This redox process is a monoelectron chemical reaction. The anodic shift is about 80 mV in the presence of 20 nmol/L of Cd2+ aqueous solution. Moreover, this shift is in proportion to the concentration of Cd2+ when the concentration of Cd2+ is lower than 20 nmol/L. So the modified electrode can be used as probes to detect cadmium ions with the limit of 0.1 nmol/L by cyclic voltammetry.

  20. 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.

  1. From clay- to organoclay-film modified electrodes: tuning charge selectivity in ion exchange voltammetry

    International Nuclear Information System (INIS)

    The surface of two natural smectite-type clay samples was chemically modified by covalent grafting of amine groups, by reaction with γ-aminopropyltriethoxysilane, which were easily protonated in HCl medium. Multisweep cyclic voltammograms of clay-film modified glassy carbon electrodes made of either the raw clays or the propylammonium-functionalized samples exposed to Ru(NH3)63+ or Fe(CN)63- electroactive probes were obtained. The results indicated a permselective behavior of these clay and organoclay-films based on either favorable or unfavorable electrostatic interactions. The cation-exchanging raw clay film modified electrodes exhibited accumulation properties for Ru(NH3)63+ species while rejecting Fe(CN)63-, whereas the anion-exchanging organoclay coatings acted as a barrier against Ru(NH3)63+ while increasing dramatically the concentration of Fe(CN)63- species at the electrode surface. Strong binding of the probe to the organoclays resulted in a potential shift of ca. 0.1 V of the voltammetric signals characteristic of the Fe(CN)63-/4- couple in the anodic direction. Their good preconcentration efficiency at low analyte concentration highlighted their interest for electroanalytical applications

  2. Microdetermination of human serum albumin by differential pulse voltammetry at a L-cysteine modified silver electrode

    Indian Academy of Sciences (India)

    Liyuan Lu; Yanqin Zi; Hongling Wang

    2008-07-01

    A simple and highly sensitive electrochemical method for the determination of human serum albumin (HSA) using differential pulse voltammetry (DPV), based on a silver electrode modified with a self-assembled monolayer of L-cysteine, was developed. L-cysteine can be modified onto a silver electrode by covalent bonding through the sulfur to give stable and long-lived chemical electrodes. This electrode showed good sensitivity, selectivity, reproducibility and time stability in the determination of trace amounts of HSA by DPV technique. The detection limit can be as low as 4 × 10-17 mol/L. The optimum conditions for the determination were carefully investigated. This method had been applied to the determination of HSA in human serum samples. The results were in agreement with those given in standard method.

  3. Photoinduced Electron Accumulation of Titanium Dioxide Nanoparticles Modified Electrodes

    Science.gov (United States)

    Miyoshi, Hirokazu; Sakamoto, Kensho; Kurashina, Masaru; Kanezaki, Eiji

    Titanium dioxide (TiO2) nanoparticles (Nps) were prepared by the hydrolysis of titanium tetraisopropoxide (TTIP) in 2-propanol with different water contents (0.5 vol% to 7.2 vol%) at 45 °C. The diameter of the Nps was estimated to be 1.5±0.5 nm (L-TiO2) and 3.0±0.6 nm (S-TiO2) from the onset wavelength in the absorption spectra and by transmission electron microscopy (TEM). A modified Pt electrode with a three-layered sandwich structure was prepared; the outermost and innermost layers were composed of S-TiO2 and L-TiO2, respectively, and the middle layer contained 1, 1'-dimethyl-4,4'-bipyridyl (MV2+)/Nafion®. Irradiation by a 500 W superhigh-pressure mercury lamp produced electrons in the conduction band of TiO2. An anodic current was observed after turning off the light. The mechanism by which anodic current is generated after turning off the radiation involves the reduction of MV2+ to MV+. by photogenerated electrons on the Nps and the diffusion of MV+. in the middle layer. After turning off the irradiation, MV+. transferred an electron to the Pt electrode via holes in the innermost layer or the conduction band of S-TiO2 coincidentally localized on the Pt electrode, resulting in the generation of the anodic current. The generation of MV+. was confirmed by the absorption spectra of MV+.. As a sacrificial reagent, 2-propanol (0.1 M) was used.

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

    Directory of Open Access Journals (Sweden)

    FATEMEH KARIMI

    2009-12-01

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

  5. Electrochemical impedance-based DNA sensor using a modified single walled carbon nanotube electrode

    International Nuclear Information System (INIS)

    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.

  6. 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.

  7. Investigation of a Nanophotonic Sensor with Electrode Modified by Semiconductor Quantum Dots

    Directory of Open Access Journals (Sweden)

    O.A. Sushko

    2014-10-01

    Full Text Available This paper focuses on optical sensors, namely nanophotonic ones intended for liquid media contained polynuclear aromatics assay. Developed by us nanophotonic sensor includes optically transparent working electrode modified by quantum-dimensional structures such as spherical semiconductor quantum dots (QDs. Monomolecular layer of QDs is plotted onto the electrode by Langmuir-Blodgett technology. Particular attention is paid to the processes of assay in nanophotonic sensor. As an analyte we used polycyclic aromatic hydrocarbon (PAH such as benzo[a]pyrene (BP, which is known for its carcinogenic properties. The developed nanophotonic sensor can be used in ecology for organic carcinogens detection in water objects of environment as well as for biomedical, physical chemical assays and some others.

  8. 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.

  9. A novel amperometric sensor for peracetic acid based on a polybenzimidazole-modified gold electrode

    Energy Technology Data Exchange (ETDEWEB)

    Hua, Mu-Yi, E-mail: huamy@mail.cgu.edu.t [Green Research Center, Department of Chemical and Materials Engineering, Chang Gung University, 259 Wen-Hwa 1st Rd., Kuei-Shan, Tao-Yuan 33302, Taiwan (China); Biosensor Group, Biomedical Engineering Research Center, Chang Gung University, 259 Wen-Hwa 1st Rd., Kuei-Shan, Tao-Yuan 33302, Taiwan (China); Chen, Hsiao-Chien [Green Research Center, Department of Chemical and Materials Engineering, Chang Gung University, 259 Wen-Hwa 1st Rd., Kuei-Shan, Tao-Yuan 33302, Taiwan (China); Biosensor Group, Biomedical Engineering Research Center, Chang Gung University, 259 Wen-Hwa 1st Rd., Kuei-Shan, Tao-Yuan 33302, Taiwan (China); Tsai, Rung-Ywan [Electronics and Optoelectronics Research Laboratories, Industrial Technology Research Institute, 195, Sec. 4, Chung Hsing Rd., Hsinchu 31040, Taiwan (China); Lin, Yu-Chen [Green Research Center, Department of Chemical and Materials Engineering, Chang Gung University, 259 Wen-Hwa 1st Rd., Kuei-Shan, Tao-Yuan 33302, Taiwan (China); Biosensor Group, Biomedical Engineering Research Center, Chang Gung University, 259 Wen-Hwa 1st Rd., Kuei-Shan, Tao-Yuan 33302, Taiwan (China)

    2011-04-30

    We have developed a peracetic acid (PAA) sensor based on a polybenzimidazole-modified gold (PBI/Au) electrode. Fourier transform infrared and X-ray photoelectron spectroscopy indicated that PAA oxidized 69.4% of the imine in PBI to form PBI N-oxide, increasing the electrochemical reduction current during cyclic voltammetry. The chemical oxidation of the PBI/Au electrode by PAA, followed by its electrochemical reduction, allowed PAA to be detected directly and consecutively by assessing its reduction current. The PAA sensor had a broad linear detection range (3.1 {mu}M-1.5 mM) and a rapid response time (3.9 s) at an applied potential of -0.3 V. Potentially interfering substances, such as hydrogen peroxide, acetic acid, and oxygen, had no effect on the ability of the probe to detect PAA, indicating high selectivity of the probe. Furthermore, the detection range, response time, and sensitivity of the sensor could all be improved by modification of the smooth planar electrode surface to a porous three-dimensional configuration. When compared to the analytical characteristics of other PAA sensors operating under optimal conditions, the three-dimensional PBI/Au electrode offers a rapid detection time, a usable linear range, and a relatively low detection limit.

  10. CO oxidation on Pt-modified Rh(111) electrodes.

    Science.gov (United States)

    Housmans, T H M; Feliu, J M; Gómez, R; Koper, M T M

    2005-08-12

    The CO electro-oxidation reaction was studied on platinum-modified Rh(111) electrodes in 0.5 M H2SO4 using cyclic voltammetry and chronoamperometry. The Pt-Rh(111) electrodes were generated during voltammetric cycles at 50 mV s(-1) in a 30 microM H2PtCl6 and 0.5 M H2SO4 solution. Surfaces generated by n deposition cycles were investigated (Ptn-Rh(111) with n=2, 4, 6, 8, 10, and 16). The blank cyclic voltammograms of these surfaces are characterized by a pronounced sharpening of the hydrogen/(bi)sulfate adsorption/desorption peaks, typical for Rh(111), and the appearance of contributions between 0.1 and 0.4 V, which were ascribed to hydrogen/(bi)sulfate adsorption/desorption on the deposited platinum. At higher potentials, the surface oxidation of Rh(111) is enhanced by the presence of platinum. The structure of the Pt-modified electrodes was investigated by STM imaging. At low Pt coverages (Pt2-Rh(111)), monoatomically high islands are formed, which grow three dimensionally as the number of deposition cycles increases. After eight cycles, the monolayer islands have grown in diameter and range from mono- to multiatomic height. At even higher Pt coverage (Pt16-Rh(111)), the islands grow to particles of approx. 10 nm in diameter, which are 5-6 atoms high. The CO stripping voltammetry on these surfaces is characterized by two peaks: A low-potential, structure-insensitive peak, ascribed to CO reacting at the platinum monolayer islands, whose onset is shifted 150, 250, and 100 mV negatively with respect to pure Rh(111), Pt(111), and polycrystalline Pt, respectively, indicating the enhanced CO electro-oxidation properties of the Pt overlayer system. A peak at higher potentials displays strong structure sensitivity (particle-size effect) and was ascribed to CO reacting on the islands of multiatomic height. Current-time transients recorded on the surface with the highest amount of monolayer islands (Pt4-Rh(111)) also indicate enhanced CO-oxidation kinetics. Comparison of

  11. Single-Layer Pentacene Field-Effect Transistors Using Electrodes Modified With Self-assembled Monolayers

    NARCIS (Netherlands)

    Asadi, Kamal; Wu, Yu; Gholamrezaie, Fatemeh; Rudolf, Petra; Blom, Paul W. M.

    2009-01-01

    Pentacene field-effect transistor performance can be improved by modifying metal electrodes with self-assembled monolayers. The dominant role in performance is played by pentacene morphology rather than the work function of the modified electrodes. With optimized processing conditions, hysteresis-fr

  12. Electrocatalytic Evolution of Oxygen Gas at Cobalt Oxide Nanoparticles Modified Electrodes

    OpenAIRE

    Sadiek, Ibrahim M.; Mohammad, Ahmad M.; El-Shakre, Mohamed E.; Awad, M. Ismail; Mohamed S. El-Deab; Anadouli, Bahgat E.

    2012-01-01

    The electrocatalysis of oxygen evolution reaction (OER) at cobalt oxide nanoparticles (nano-CoOx) modified GC, Au and Pt electrodes has been examined using cyclic voltammetry. The OER is significantly enhanced upon modification of the electrodes with nano-CoOx, as demonstrated by a negative shift in the polarization curves at the nano-CoOx modified electrodes compared to that obtained at the unmodified ones. Scanning electron microscopy (SEM) revealed the electrodeposition of nanometer-size C...

  13. 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.

  14. EUGENOL POLYMER MODIFIED TITANIUM ELECTRODE FOR THE ANALYSIS OF CARBOCYSTEINE

    OpenAIRE

    S. EL QOUATLI; R. T. NGONO; R. NAJIH; A. CHTAINI

    2012-01-01

    A eugenol polymer immobilized electrode was developed for the assay of the carbocysteine compound. The electrochemical sensor was made by in situ electropolymerization of eugenol at titanium electrode. Cyclic voltamperometry at prepared electrode permitted to point out a reversible pattern for carbocysteine electrooxidation.

  15. EUGENOL POLYMER MODIFIED TITANIUM ELECTRODE FOR THE ANALYSIS OF CARBOCYSTEINE

    Directory of Open Access Journals (Sweden)

    S. EL QOUATLI

    2012-06-01

    Full Text Available A eugenol polymer immobilized electrode was developed for the assay of the carbocysteine compound. The electrochemical sensor was made by in situ electropolymerization of eugenol at titanium electrode. Cyclic voltamperometry at prepared electrode permitted to point out a reversible pattern for carbocysteine electrooxidation.

  16. Study of enzyme biosensor based on carbon nanotubes modified electrode for detection of pesticides residue

    Institute of Scientific and Technical Information of China (English)

    Shu Ping Zhang; Lian Gang Shan; Zhen Ran Tian; Yi Zheng; Li Yi Shi; Deng Song Zhang

    2008-01-01

    The paper describes a controllable layer-by-layer (LBL) self-assembly modification technique of multi-walled carbon nanotubes(MWNTs) and poly(diallyldimethylammonium chloride) (PDDA) towards glassy carbon electrode (GCE), Acetylcholinesterase(ACHE) was immobilized directly to the modified GCE by LBL self-assembly method, the activity value of AChE was detected byusing i-t technique based on the modified Ellman method. Then the composition of carbaryl were detected by the enzyme electrodewith 0.01U activity value and the detection limit of carbaryl is 10-12 g L-1 so the enzyme biosensor showed good properties forpesticides residue detection.2008 Shu Ping Zhang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.

  17. Electrochemical oxidation of ascorbic acid mediated by carbon nano tubes/ Li+/ carbon paste modified solid electrode

    International Nuclear Information System (INIS)

    Multi-walled carbon nano tube (MWCNT) was used to modify BPPG electrode because of its unique structure and extraordinary properties. MWCNT modified electrode exhibited obvious enhancing and electro catalyzing effects to the oxidation of ascorbic acid using cyclic voltammetry technique. MWCNT was bonded on BPPG electrode surface using carbon paste with ratio of 30 % (w/ W) carbon paste (binder): 70 % (w/ w) MWCNT. This method of modification has lowered the capacitance background current and enabled lower detection limit of ascorbic acid concentration. The electrical conductivity property of MWCNT modified electrode was further improved with the intercalation with lithium ion and resulted in current enhancement of 2 times on the oxidation current of ascorbic acid. Parameters of pH and temperature showed significant relation to the sensitivity of MWCNT modified electrode. Under the optimized parameters, the calibration curve constructed was linear up from 50 μM to 5 mM with sensitivity of 34.5 mA M-1. The practical application of MWCNT modified electrode was demonstrated with Vitamin C pill and orange juice. Good reproducibility and recovery of ascorbic acid concentration showed the feasibility of MWCNT modified electrode to be used in the detection of ascorbic acid in aqueous solution. This also proposed MWCNT modified BPPG electrode possessed advantages such as low detection limit, high stability, low cost and simplicity in fabrication. (author)

  18. 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.

  19. Study of the electrochemical properties of a transition metallic ions modified electrode in acidic VOSO4 solution

    Institute of Scientific and Technical Information of China (English)

    WANG Wenhong; WANG Xindong

    2007-01-01

    Graphite material was used as the electrode for an all-vanadium redox flow battery, and the electrode was modified by transition metallic ions to enhance its electrochemical behavior. An porous graphite composite electrode has high specific surface area and high current density. The electrode modified by transition metallic ions has improved catalysis behavior that can catalyze the V(Ⅱ)-V(Ⅴ) redox reaction showed by cyclic voltammograms. This article studied the impedance of the modified electrode by electrochemical impedance spectroscopy (EIS), and approved that the electrode modified by Co2+ and Mn2+ has a lower charge transfer resistance than the non-modified electrode. The effect of average particle size distribution is at lower frequencies that the slope of Warburg impedance is reduced by large particle size distribution. The voltage efficiency of the Co2+ modified electrode test cell is 81.5%, which is higher than that of the non-modified electrode.

  20. Enhancing biocompatibility of some cation selective electrodes using heparin modified bacterial cellulose.

    Science.gov (United States)

    Badr, Ibrahim H A; Abdel-Sattar, R; Keshk, Sherif M A S

    2015-12-10

    Bacterial cellulose (BC) and heparin-modified bacterial cellulose (HBC) were utilized to enhance the biocompatibility of highly thrombogenic PVC-based potassium and calcium membrane electrodes. Three types of membrane electrodes were prepared: (1) conventional PVC electrode (control), (2) PVC-based electrode sandwiched with bacterial cellulose membrane (BC-PVC), and (3) PVC-based electrode sandwiched with heparin-modified bacterial cellulose membrane (HBC-PVC). The potentiometric response characteristics of the modified potassium and calcium membrane electrodes (BC-PVC and HBC-PVC) were compared with those of the control PVC-based potassium and calcium selective electrode, respectively. Response characteristics of the modified membrane electrodes were comparable to the control PVC membrane electrode. The platelet adhesion investigations indicated that (BC) and (HBC) layers are less thrombogenic compared to PVC. Therefore, use of BC or HBC would enable the enhancement of the biocompatibility of PVC-based membrane electrodes for potassium and calcium while practically maintaining the overall electrochemical performance of the PVC sensing film. PMID:26428173

  1. Nanostructured copper particles-incorporated Nafion-modified electrode for oxygen reduction

    Indian Academy of Sciences (India)

    T Selvaraju; R Ramaraj

    2005-10-01

    The electrocatalytic activity of nanostructured copper particles (represented as Cunano) incorporated Nafion (Nf) film-coated glassy carbon (GC) electrode (GC/Nf/Cunano) towards oxygen reduction was investigated in oxygenated 0.1 M phosphate buffer (pH 7.2). The electrodeposited Cunano in Nf film was characterized by atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS). The electrocatalytic activity of Cunano at the modified electrode towards oxygen reduction was studied using cyclic voltammetry technique. The molecular oxygen reduction at the GC/Nf/Cunano-modified electrode started at a more positive potential than at a bare GC electrode. A possible reaction mechanism was proposed in which oxygen reduction may proceed through two-step two-electron processes at the GC/Nf/Cunano electrode. The GC/Nf/Cunano electrode shows higher stability for oxygen reduction in neutral solution and the electrode may find applications in fuel cells.

  2. Preparation of Ti/SnO2-Sb electrodes modified by carbon nanotube for anodic oxidation of dye wastewater and combination with nanofiltration

    International Nuclear Information System (INIS)

    Highlights: • Ti/SnO2-Sb-CNT electrodes were prepared by pulse electrodeposition technology. • The characteristics of Ti/SnO2-Sb-CNT was compared with Ti/SnO2-Sb. • We combined electro-catalytic oxidation with NF to treat dye wastewater. - Abstract: A new type of Ti/SnO2-Sb electrode modified with carbon nanotube (CNT) has been fabricated using a pulse electrodeposition method. The electrode modified with CNT versus without CNT has larger surface area and smaller crystallite particles (41.9 nm versus 46.8 nm) as seen by scanning electron microscopy (SEM), and calculated through X-ray diffraction (XRD), respectively. It means that the CNT-modified electrode can provide more active sites for electrochemical oxidation of organic pollutants. Oxygen evolution potential of the CNT-modified electrode has 0.07 V higher overpotential in the Linear sweep voltammetry (LSV) curve. The service lifetime of Ti/SnO2-Sb-CNT electrode is 4.8 times longer than that of the Ti/SnO2-Sb electrode without CNT modifying. The Ti/SnO2-Sb-CNT electrode is demonstrated to have a superior electrochemical oxidation and degradation abilities using Acid Red 73 (AR 73) as a model organic pollutant. The CNT-modified electrode has higher kinetic rate constant, chemical oxygen demand (COD) and total organic carbon (TOC) removals, and mineralization current efficiency, which is 1.93, 1.27, 1.26, and 1.38 times those of the Ti/SnO2-Sb electrode, respectively. The repeated experiments prove the reproducibility of the data. Ti/SnO2-Sb-CNT electrode is 1.15 times more effective in permeation flux than the Ti/SnO2-Sb electrode when combining electro-catalytic oxidation and nanofiltration for treating dye wastewater

  3. Properties Characterization of Chemically Modified Hemp Hurds

    Directory of Open Access Journals (Sweden)

    Nadezda Stevulova

    2014-12-01

    Full Text Available The effect of chemical treatment of hemp hurds slices in three solutions (EDTA (Ethylenediaminetetraacetic acid, NaOH and Ca(OH2 on the properties of natural material was discussed in this paper. Changes in the morphology, chemical composition and structure as well as thermal stability of hemp hurds before and after their modification were investigated by using FTIR (Fourier transform infrared spectroscopy, XRD (X-ray powder diffraction analysis and TG (thermogravimetry/DSC (differential scanning calorimetry. Size exclusion chromatography (SEC measurements were used for determination of degree of cellulose polymerization of hemp hurd samples. Chemical modification is related to the partial removal of non-cellulosic components of lignin, hemicellulose and pectin as well as waxes from the surface of hemp hurd slices. Another effect of the chemical treatment applied is connected with increasing the crystallinity index of cellulose determined by FTIR and XRD methods. Decrease in degree of cellulose polymerization and polydispersity index in chemically modified hemp hurds compared to the original sample was observed. Increase in thermal stability of treated hemp hurd was found. The most significant changes were observed in alkaline treated hemp hurds by NaOH.

  4. 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.

  5. 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.

  6. Detection of cancer cells using a peptide nanotube–folic acid modified graphene electrode

    DEFF Research Database (Denmark)

    Castillo, John J.; Svendsen, Winnie Edith; Rozlosnik, Noemi;

    2013-01-01

    This article describes the preparation of a graphene electrode modified with a new conjugate of peptide nanotubes and folic acid for the selective detection of human cervical cancer cells over-expressing folate receptors. The functionalization of peptide nanotubes with folic acid was confirmed by...... fluorescence microscopy and atomic force microscopy. The peptide nanotube–folic acid modified graphene electrode was characterized by scanning electron microscopy and cyclic voltammetry. The modification of the graphene electrode with peptide nanotube–folic acid led to an increase in the current signal. The......–folic acid modified electrode lowered the electron transfer resulting in a decrease in the measured current. A detection limit of 250 human cervical cancer cells per mL was obtained. Control experiments confirmed that the peptide nanotube–folic acid electrode specifically recognized folate receptors. The...

  7. A Biosensor Using Poly(4-Aminophenol)/acetylcholinesterase modified graphite electrode for the detection of dichlorvos

    OpenAIRE

    Edmar Isaías Melo; Diego Leoni Franco; André Santiago Afonso; Hélen Cristine Rezende; Ana Graci Brito-Madurro; João Marcos Madurro; Nívia Maria Melo Coelho

    2011-01-01

    The properties of poly(4-aminophenol) modified graphite electrode as material for the immobilization of acetylcholinesterase were investigated by the Cyclic Voltammetry, Electrochemical Impedance Spectroscopy and Atomic Force Microscopy. The polymer was deposited on graphite electrode surface by the oxidation of 4-aminophenol and then acetylcholinesterase was immobilized on the surface of the electrode. The biosensor coupled in the continuous flow system was employed for the detection of dich...

  8. Zinc phthalocyanine and silver/gold nanoparticles incorporated MCM-41 type materials as electrode modifiers.

    Science.gov (United States)

    Pal, Manas; Ganesan, Vellaichamy

    2009-11-17

    Mercaptopropyl functionalized ordered mesoporous silica spheres were prepared (MPS). Ag or Au nanoparticles (NPs) were anchored onto the MPS materials (Ag-MPS or Au-MPS). Further, zinc phthalocyanine (ZnPc) was adsorbed into the channels and surface (MPS-ZnPc, Ag-MPS-ZnPc, Au-MPS-ZnPc). Diffuse reflectance studies revealed the successful incorporation of Ag or Au NPs inside the silica spheres with and without ZnPc. TEM images showed the uniform distribution of Ag or Au NPs in the silica spheres of different size ranging from 4 to 22 nm or 6 to 31 nm, respectively. XRD pattern showed average crystallite particle size of 18 or 28 nm for Ag or Au NPs respectively which were reduced to 14 or 16 nm on introduction of ZnPc which oxidizes the metal NPs partially. Chemically modified electrodes were prepared by coating the colloidal solutions of the silica materials on the glassy carbon (GC) electrodes. Electrocatalytic reductions of O(2) and CO(2) at the modified electrodes were studied. The presence of Ag or Au NPs was found to increase the electrocatalytic efficiency of ZnPc toward O(2) reduction by 290% or 70% based on the current density measured at -0.35 V and toward CO(2) reduction by 150% or 120% based on the current density measured at -0.60 V respectively. Catalytic rate constants were increased 2-fold for O(2) reduction and 8-fold for CO(2) reduction due to Ag or Au NPs, respectively, which act as nanoelectrode ensembles. The synergic effect of ZnPc and metal NPs on the electrocatalytic reduction of O(2) is presented. PMID:19824690

  9. Electrocatalysis of chemically synthesized noble metal nanoparticles on carbon electrodes

    DEFF Research Database (Denmark)

    Zhang, Ling; Ulstrup, Jens; Zhang, Jingdong

    on their interfacial interaction with the supporting electrodes. In this work we aim at chemical production of size and shape controlled, specifically 22 nm cubic Pd NPs, and further understanding of the Pd NPs as electrocatalysts at the nanometer scale using both scanning tunneling microscopy (STM......) will be investigated by electrochemical SPM. This study offers promise for development of new high-efficiency catalyst types with low-cost for fuel cell technology...

  10. Characterization of poly(5-hydroxytryptamine)-modified glassy carbon electrode and applications to sensing of norepinephrine and uric acid in preparations and human urines

    International Nuclear Information System (INIS)

    Graphical abstract: A 5-hydroxytryptamine (5-HT) modified electrode was fabricated by electro-polymerization of 5-HT on a glassy carbon electrode (GCE) by cyclic voltammetry (CV) in 0.05 M PBS (pH 7). The characterization of the modified electrode was carried out by atomic force microscopy (AFM), voltammetry and electrochemical impedance spectroscopy (EIS). The mechanism of electro-deposition of 5-HT at GCE was discussed based on electrochemical studies and quantum chemical calculations. The poly(5-HT)-modified electrode could separately detect NE and UA, even in the presence of 10-fold concentration of ascorbic acid (AA) and was applied successfully to the analysis of NE preparations and healthy human urines. Due to the favorable functionalized groups (-NH2 and -OH), electroactivity, biocompatibility and stability, the poly(5-HT) film could be a promising immobilization matrix for anchoring interested biological molecules in the fabrication of sensors and biosensors. Highlights: ► A poly(5-HT)-modified electrode was fabricated originally by CV. ► The electro-deposition mechanism of 5-HT at GCE was proposed. ► The polymer film shows favorable electrocatalytic properties to NE and UA. ► The modified GCE was applied to the sensing analysis of real samples. -- Abstract: A poly(5-hydroxytryptamine) (poly(5-HT)) modified electrode was fabricated by electropolymerization of 5-hydroxytryptamine (5-HT) on a glassy carbon electrode (GCE) by cyclic voltammetry (CV) in 0.05 M PBS (pH 7). The characterization of poly(5-HT)-modified electrode was carried out by atomic force microscopy (AFM), voltammetry and electrochemical impedance spectroscopy (EIS). Results showed that a brown and heterogeneous film was formed on the surface of the modified electrode. The mechanism of electro-deposition of 5-HT at GCE was discussed. The modified electrode showed good affinity and electrocatalytic properties to some species, such as norepinephrine (NE) and uric acid (UA). Furthermore

  11. Efficient inverted polymer solar cells based on conjugated polyelectrolyte and zinc oxide modified ITO electrode

    International Nuclear Information System (INIS)

    Efficient inverted polymer solar cells (PSCs) were constructed by utilizing a conjugated polyelectrolyte PFEOSO3Na and zinc oxide to modify the indium tin oxide (ITO) electrode. The ITO electrode modified by PFEOSO3Na and zinc oxide possesses high transparency, increased electron mobility, smoothened surface, and lower work function. PTB7:PC71BM inverted PSCs containing the modified ITO electrode achieved a high power conversion efficiency (PCE) of 8.49%, exceeding that of the control device containing a ZnO modified ITO electrode (7.48%). Especially, PCE-10:PC71BM inverted polymer solar cells achieved a high PCE up to 9.4%. These results demonstrate a useful approach to improve the performance of inverted polymer solar cells

  12. Efficient inverted polymer solar cells based on conjugated polyelectrolyte and zinc oxide modified ITO electrode

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Tao; Zhu, Xiaoguang; Tu, Guoli, E-mail: tgl@hust.edu.cn [Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan 430074 (China); Zhou, Lingyu [State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian National Laboratory of Clean Energy, Dalian 116023 (China); Zhang, Jian, E-mail: jianzhang@guet.edu.cn [Department of Material Science and Engineering, Guangxi Key Laboratory of Information Materials, Guilin University of Electronic Technology, Guilin 541004 (China)

    2015-02-23

    Efficient inverted polymer solar cells (PSCs) were constructed by utilizing a conjugated polyelectrolyte PF{sub EO}SO{sub 3}Na and zinc oxide to modify the indium tin oxide (ITO) electrode. The ITO electrode modified by PF{sub EO}SO{sub 3}Na and zinc oxide possesses high transparency, increased electron mobility, smoothened surface, and lower work function. PTB7:PC{sub 71}BM inverted PSCs containing the modified ITO electrode achieved a high power conversion efficiency (PCE) of 8.49%, exceeding that of the control device containing a ZnO modified ITO electrode (7.48%). Especially, PCE-10:PC{sub 71}BM inverted polymer solar cells achieved a high PCE up to 9.4%. These results demonstrate a useful approach to improve the performance of inverted polymer solar cells.

  13. Electrodeposited nanostructured raspberry-like gold-modified electrodes for electrocatalytic applications

    Energy Technology Data Exchange (ETDEWEB)

    Manivannan, Shanmugam; Ramaraj, Ramasamy, E-mail: ramarajr@yahoo.com [Madurai Kamaraj University, Centre for Photoelectrochemistry, School of Chemistry (India)

    2013-10-15

    A facile method for fabrication of raspberry-like Au nanostructures (Au NRBs)-modified electrode by electrodeposition and its applications toward the electrocatalytic oxidation of methanol (MOR) in alkaline medium and oxygen reduction reaction (ORR) in both alkaline and acidic media are demonstrated. The Au NRBs are characterized by UV-Vis absorption spectra, SEM, X-ray diffraction, and electrochemical measurements. The growth of Au NRBs was monitored by recording the in-situ absorption spectral changes during electrodeposition using spectroelectrochemical technique. Here we systematically studied the MOR by varying several reaction parameters such as potential scan rate and methanol concentration. The electrocatalytic poisoning effect due to the MOR products are not observed at the Au NRBs-modified electrode. At the alkaline medium the Au NRBs-modified electrode shows the better catalytic activities toward the MOR and ORR when compared to the poly crystalline gold and bare glassy carbon electrodes. The Au NRBs-modified electrode is a promising and inexpensive electrode material for other electrocatalytic applications.Graphical AbstractRaspberry-like Au nanostructures modified electrode is prepared and used for electrocatalytic applications.

  14. Microgravimetric study of the influence of the solvent on the redox properties of polypyrrol modified electrodes

    Science.gov (United States)

    Varela, Hamilton; Malta, Marcos; Torresi, Roberto M.

    The redox behavior of the polypyrrole films in the presence of LiClO 4 salt in different solvents like propylene carbonate (PC), N, N-dimetilformamide (DMF), methanol (MetOH), ethanol (EtOH), acetonitrile (ACN) and water was investigated using simultaneous electrochemical quartz crystal microbalance and cyclic voltammetry experiments. Both charge and mass changes during redox processes were rationalized in terms of multiple regression considering some solvent parameters and ionic transport characteristics. The electroactivity of PPY modified electrodes increase in the sequence PCchemical nature on the electroactivity and electroneutralization processes.

  15. Amperometric Morphine Detection Using Pt-Co Alloy Nanowire Array-modified Electrode

    International Nuclear Information System (INIS)

    Pt-Co alloy nanowire array was directly synthesized by electrochemical deposition with polycarbonate template at -1.0V and subsequent chemical etching of the template. The use of Pt-Co alloy nanowire array-modified electrode (Pt- Co NAE) for the determination of morphine (MO) is described. The morphology of the Pt-Co alloy nanowire array has been investigated by scanning electron microscopy (SEM) and energy disperse X-ray spectroscopy (EDS) analysis), respectively. The resulting Pt-Co NAE offered a linear amperometric response for morphine ranging from 2.35 x 10-5 to 2.39 x 10-3 M with a detection limit of 7.83 x 10-6 M at optimum conditions. This sensor displayed high sensitivity and long-term stability

  16. Amperometric Morphine Detection Using Pt-Co Alloy Nanowire Array-modified Electrode

    Energy Technology Data Exchange (ETDEWEB)

    Tao, Manlan; Xu, Feng; Li, Yueting; Xu, Quanqing; Chang, Yanbing; Yang, Yunhui [Yunnan Normal University, Kunming (China); Wu, Zaisheng [Hunan University, Changsha (China)

    2010-07-15

    Pt-Co alloy nanowire array was directly synthesized by electrochemical deposition with polycarbonate template at -1.0V and subsequent chemical etching of the template. The use of Pt-Co alloy nanowire array-modified electrode (Pt- Co NAE) for the determination of morphine (MO) is described. The morphology of the Pt-Co alloy nanowire array has been investigated by scanning electron microscopy (SEM) and energy disperse X-ray spectroscopy (EDS) analysis), respectively. The resulting Pt-Co NAE offered a linear amperometric response for morphine ranging from 2.35 x 10{sup -5} to 2.39 x 10{sup -3} M with a detection limit of 7.83 x 10{sup -6} M at optimum conditions. This sensor displayed high sensitivity and long-term stability.

  17. 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.

  18. Lack of nano size effect on electrochemistry of dopamine at a gold nanoparticle modified indium tin oxide electrode

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Nanometer sized materials have been shown to possess excellent chemical and electrochemical catalytic properties.In this work,a gold nanoparticle (AuNP) modified indium tin oxide (ITO) electrode was employed for investigating its electro-catalytic property.AuNP was deposited on the 3-aminopropyltriethoxysilane (APTES) modified ITO electrode by self-assembly,and was characterized by scanning electron microscopy and cyclic voltammetry.Although the electrochemical reaction of dopamine was very sluggish on the ITO/APTES electrode,it was significantly enhanced after AuNP deposition.The cyclic voltammogram exhibited apparent dependence on the surface coverage of 11 nm AuNPs,which could be rationalized by different modes of mass diffusion.Among the different sizes of AuNP investigated,the lowest anodic peak potential was observed on 11 nm AuNP.However,the potential was still about 50 mV more positive than that obtained on a bulk gold electrode of similar geometry.It is therefore concluded that there is no nanometer size effect of AuNP modified ITO on the electrochemistry of dopamine.

  19. Antitumor activity of chemical modified natural compounds

    Directory of Open Access Journals (Sweden)

    Marilda Meirelles de Oliveira

    1991-01-01

    Full Text Available Search of new activity substances starting from chemotherapeutic agents, continously appears in international literature. Perhaps this search has been done more frequently in the field of anti-tumor chemotherapy on account of the unsuccess in saving advanced stage patients. The new point in this matter during the last decade was computer aid in planning more rational drugs. In near future "the accessibility of supercomputers and emergence of computer net systems, willopen new avenues to rational drug design" (Portoghese, P. S. J. Med. Chem. 1989, 32, 1. Unknown pharmacological active compounds synthetized by plants can be found even without this eletronic devices, as tradicional medicine has pointed out in many contries, and give rise to a new drug. These compounds used as found in nature or after chemical modifications have produced successful experimental medicaments as FAA, "flavone acetic acid" with good results as inibitors of slow growing animal tumors currently in preclinical evaluation for human treatment. In this lecture some international contributions in the field of chemical modified compounds as antineoplasic drugs will be examined, particularly those done by Brazilian researches.

  20. Silver Solid Amalgam Electrodes as Sensors for Chemical Carcinogens

    OpenAIRE

    Bogdan Yosypchuk; Karolina Peckova; Tomas Navratil; Jan Fischer; Jiri Barek

    2006-01-01

    The applicability of differential pulse voltammetry (DPV) and adsorptive stripping voltammetry (AdSV) at a non-toxic meniscus-modified silver solid amalgam electrode (m-AgSAE) for the determination of trace amounts of genotoxic substances was demonstrated on the determination of micromolar and submicromolar concentrations of 3-nitrofluoranthene using methanol - 0.01 mol L-1 NaOH (9:1) mixture as a base electrolyte and of Ostazine Orange using 0.01 mol L-1 NaOH as a base electrolyte.

  1. 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)

  2. 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...

  3. Research on PEG modified Bi-doping lead dioxide electrode and mechanism

    International Nuclear Information System (INIS)

    Bi-doping PbO2 electrode, which is called Bi-PbO2 for short, modified with different concentrations of polyethylene glycol (PEG) was prepared by electrodeposition method in this paper. The microstructure and electrochemical properties of the different modified electrodes were investigated using scanning electron microscopy, X-ray diffraction, Mott-Schottky, electrochemical impedance spectroscopy and linear sweep voltammetry techniques. The results show that adulteration of PEG has a noticeable improvement in the morphology of Bi-PbO2 electrode which can greatly decrease its particle size and enlarge its active surface area. Phenol degradation experiments reveal that the modified electrodes have excellent electro-catalytic activity and stability, and the optimal adulterate concentration of PEG is 8 g L-1. Electrochemical performance tests show that the modified electrodes exhibit more negative flatband potential (Efb), larger adsorption pseudo capacitance, lower adsorption resistance and higher oxygen evolution potential, and these characteristics promote the electro-catalytic activity of the Bi-PbO2 electrode. Finally, accelerated lifetime tests demonstrate that PEG modification can highly lengthen the service life of Bi-PbO2 electrode in its practical application.

  4. Research on PEG modified Bi-doping lead dioxide electrode and mechanism

    Energy Technology Data Exchange (ETDEWEB)

    Yang Weihua, E-mail: yangwh@hqu.edu.cn [College of Materials Science and Engineering, Huaqiao University, Xiamen 361021 (China); Yang Wutao; Lin Xiaoyan [College of Materials Science and Engineering, Huaqiao University, Xiamen 361021 (China)

    2012-05-15

    Bi-doping PbO{sub 2} electrode, which is called Bi-PbO{sub 2} for short, modified with different concentrations of polyethylene glycol (PEG) was prepared by electrodeposition method in this paper. The microstructure and electrochemical properties of the different modified electrodes were investigated using scanning electron microscopy, X-ray diffraction, Mott-Schottky, electrochemical impedance spectroscopy and linear sweep voltammetry techniques. The results show that adulteration of PEG has a noticeable improvement in the morphology of Bi-PbO{sub 2} electrode which can greatly decrease its particle size and enlarge its active surface area. Phenol degradation experiments reveal that the modified electrodes have excellent electro-catalytic activity and stability, and the optimal adulterate concentration of PEG is 8 g L{sup -1}. Electrochemical performance tests show that the modified electrodes exhibit more negative flatband potential (E{sub fb}), larger adsorption pseudo capacitance, lower adsorption resistance and higher oxygen evolution potential, and these characteristics promote the electro-catalytic activity of the Bi-PbO{sub 2} electrode. Finally, accelerated lifetime tests demonstrate that PEG modification can highly lengthen the service life of Bi-PbO{sub 2} electrode in its practical application.

  5. Determination of various insecticides and pharmaceuticals using differently modified glassy carbon electrodes

    Directory of Open Access Journals (Sweden)

    FERENC F. GAÁL

    2007-12-01

    Full Text Available The applicability of differently modified glassy carbon (GC electrodes for direct or indirect determinations of various physiologically active compounds (insecticides and pharmaceuticals in different formulations and some real samples was investigated. Samples of selected insecticides from the group of neonicotinoids with nitroguanidine (thiamethoxam and imidacloprid, cyanoimine (acetamiprid and nitromethilene (nitenpyram fragments, prepared in an appropriate manner, were determined by voltammetry on bare and surface-modified GC electrodes, while in the case of pharmaceuticals such as Trodon and Akineton, the chloride anion titration was followed using bare GC and phosphorus doped (P–GC electrodes. The P–GC was also used to monitor the chloride content in the photocatalytic degradation of the (4-chloro-2-methylphenoxyacetic acid herbicide. It was found that apart from the nature of the electrode material, the analyte and supporting electrolyte, as well as the pretreatment of the electrode surface essentially influences the applicability of the employed sensors.

  6. Electrochemical Capacitance DNA Sensing at Hairpin-Modified Au Electrodes

    OpenAIRE

    Joel Rivera-Gandía; Maria del Mar Maldonado; Yarimar De La Torre-Meléndez; Edwin O. Ortiz-Quiles; Vargas-Barbosa, Nella M.; Cabrera, Carlos R.

    2011-01-01

    An interfacial capacitance measurement electrochemical technique has been used for the sensing of self-assembled DNA hairpin probes (M. tuberculosis and B. anthracis) attached to Au electrodes. The double-layer capacitance (Cdl) was determined with electrochemical perturbations from 0.2 V to 0.5 V versus Ag/AgCl at a Au/M. tuberculosis DNA hairpin probe at surface coverage Au electrodes. The capacitance study was done at pH 7, which was necessary to maintain the M. tuberculosis and B. anthrac...

  7. Modified cermet fuel electrodes for solid oxide electrochemical cells

    Science.gov (United States)

    Ruka, Roswell J.; Spengler, Charles J.

    1991-01-01

    An exterior porous electrode (10), bonded to a solid oxygen ion conducting electrolyte (13) which is in contact with an interior electrode (14), contains coarse metal particles (12) of nickel and/or cobalt, having diameters from 3 micrometers to 35 micrometers, where the coarse particles are coated with a separate, porous, multiphase layer (17) containing fine metal particles of nickel and/or cobalt (18), having diameters from 0.05 micrometers to 1.75 micrometers and conductive oxide (19) selected from cerium oxide, doped cerium oxide, strontium titanate, doped strontium titanate and mixtures thereof.

  8. Poly(o-methoxyaniline modified electrode for detection of lithium ions

    Directory of Open Access Journals (Sweden)

    Cleber Antonio Lindino

    2012-01-01

    Full Text Available This paper reports the use of an electrode modified with poly(o-methoxyaniline for detecting lithium ions. These ions are present in drugs used for treating bipolar disorder and that requires periodical monitoring of the concentration of lithium in blood serum. Poly(o-methoxyaniline was obtained electrochemically by cyclic voltammetry on the surface of a gold electrode. The results showed that the electrode modified with a conducting polymer responded to lithium ions in the concentration range of 1 x 10-5 to 1 x 10-4 mol L-1 . The results also confirmed that the performance of the modified electrode was comparable to that of the standard method (atomic emission spectrophotometry.

  9. Poly({omicron}-methoxyaniline) modified electrode for detection of lithium ions

    Energy Technology Data Exchange (ETDEWEB)

    Lindino, Cleber Antonio; Casagrande, Marcella; Peiter, Andreia; Ribeiro, Caroline [Departamento de Quimica, Universidade Estadual do Oeste do Parana, Toledo, PR (Brazil)

    2012-07-01

    This paper reports the use of an electrode modified with poly({omicron}-methoxyaniline) for detecting lithium ions. These ions are present in drugs used for treating bipolar disorder and that requires periodical monitoring of the concentration of lithium in blood serum. Poly({omicron}-methoxyaniline) was obtained electrochemically by cyclic voltammetry on the surface of a gold electrode. The results showed that the electrode modified with a conducting polymer responded to lithium ions in the concentration range of 1 x 10{sup -5} to 1 x 10{sup -4} mol L{sup -1}. The results also confirmed that the performance of the modified electrode was comparable to that of the standard method (atomic emission spectrophotometry). (author)

  10. Poly(ο-methoxyaniline) modified electrode for detection of lithium ions

    International Nuclear Information System (INIS)

    This paper reports the use of an electrode modified with poly(ο-methoxyaniline) for detecting lithium ions. These ions are present in drugs used for treating bipolar disorder and that requires periodical monitoring of the concentration of lithium in blood serum. Poly(ο-methoxyaniline) was obtained electrochemically by cyclic voltammetry on the surface of a gold electrode. The results showed that the electrode modified with a conducting polymer responded to lithium ions in the concentration range of 1 x 10-5 to 1 x 10-4 mol L-1. The results also confirmed that the performance of the modified electrode was comparable to that of the standard method (atomic emission spectrophotometry). (author)

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

    International Nuclear Information System (INIS)

    The voltammetric behavior of a carbon paste electrode modified with Co(II)-exchanged zeolite A (Co(II)-A/ZMCPE) for determination of acetaminophen was studied. The proposed electrode showed a diffusion controlled reaction with the electron transfer rate constant (Ks) of 0.44 s−1 and charge transfer coefficient of 0.73 in the absence of acetaminophen. A linear voltammetric response was obtained in the range of 0.1 to 190 μmol L−1 of acetaminophen [r2 = 0.9979, r = 0.9989 (n = 10)] with a detection limit of 0.04 μmol L−1. The method was successfully applied to the analysis of acetaminophen in some drugs. - Highlights: • Modified carbon paste electrode with Co(II)-zeolite A improved the voltammetric current in determination of acetaminophen. • Modified electrode is applicable for acetaminophen in real samples. • The proposed method has good reproducibility and repeatability

  12. 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.

  13. Characterization of surfactant/hydrotalcite-like clay/glassy carbon modified electrodes: Oxidation of phenol

    International Nuclear Information System (INIS)

    The characteristics of hydrotalcite (HT)-like clay films containing ionic and nonionic surfactants and their ability to oxidize phenol have been examined. The HT clay (Co/Al-NO3) was synthesized by coprecipitation techniques and then modified with surfactants such as sodium dodecylbenzenesulfonate (SDBS), octylphenoxypolyethoxyethanol (TX100) or cetylpyridinium bromide (CPB). X-ray diffraction analysis revealed that the interlayer basal spacing varied depending on the type of surfactant retained by the HT. The presence of SDBS and CPB expanded the HT interlayer, which in the presence of TX100 did not show an appreciable change. Phenol oxidation is favored at surfactant-HT-GC modified electrodes, after a preconcentration time, compared to phenol oxidation at HT-GC or GC electrodes. Surfactant-HT-GC modified electrodes display good stability in continuous electrochemical phenol oxidation. At pH values between 6 and 10.8, both SDBS-HT-GC and TX100-HT-GC modified electrodes seem to be promising electrodes for the detection of phenol in water; while the CPB-HT-GC modified electrode should be affected by the inorganic anions

  14. Determination of Silver(I) by Differential Pulse Voltammetry Using a Glassy Carbon Electrode Modified with Synthesized N-(2-Aminoethyl)-4,4′-Bipyridine

    OpenAIRE

    Gabriel Lucian Radu; Bogdan Bucur; Madalina Petruta Bucur; Medeea Radulescu; Maria-Cristina Radulescu; Ana Chira

    2010-01-01

    A new modified glassy carbon electrode (GCE) based on a synthesized N-(2-aminoethyl)-4,4'-bipyridine (ABP) was developed for the determination of Ag(I) by differential pulse voltammetry (DPV). ABP was covalently immobilized on GC electrodes surface using 4-nitrobenzendiazonium (4-NBD) and glutaraldehyde (GA). The Ag(I) ions were preconcentrated by chemical interaction with bipyridine under a negative potential (−0.6 V); then the reduced ions were oxidized by differential pulse voltammetry and...

  15. Chemically modified flexible strips as electrochemical biosensors.

    Science.gov (United States)

    Thota, Raju; Ganesh, V

    2014-09-21

    A flexible and disposable strip sensor for non-enzymatic glucose detection is demonstrated in this work. The strips are prepared by using chemical modification processes followed by a simple electroless deposition of copper. Essentially, polyester overhead projector (OHP) transparent films are modified with a monolayer of 3-aminopropyltrimethoxysilane (APTMS) and polyaniline (PANI) conducting polymer. Later, nanostructured copper is deposited onto this modified film. Scanning electron microscope (SEM) and X-ray diffraction (XRD) studies are used for the structural, morphological and crystallinity characterization of the modified films. Electrochemical techniques, namely cyclic voltammetry (CV) and chronoamperometry (CA), are employed for the non-enzymatic detection of glucose. These studies clearly reveal the formation of homogeneous, close-packed spherical Cu particles converged into uniform film that exhibits a good catalytic activity towards the oxidation of glucose. The Cu/PANI/APTMS/OHP sensor displays a remarkable enhancement in the oxidation current density, a very high sensitivity value of 2.8456 mA cm(-2) per mM, and a linear concentration range from 100 μM to 6.5 mM associated with glucose detection. Detection limit is estimated to be 5 μM and the response time of the sensor is determined to be less than 5 s. For comparison, similar studies are performed without PANI, namely Cu/APTMS/OHP films for glucose detection. In this case, a sensitivity value of 2.4457 mA cm(-2) per mM and a linear concentration range of 100 μM-3 mM are estimated. The higher performance characteristics observed in the case of Cu/PANI/APTMS/OHP are attributed to the synergistic effects of the conducting polymer acting as an electron facilitator and the nanostructured Cu films. These disposable, flexible and low-cost strip sensors have also been applied to the detection of glucose in clinical blood serum samples and the results obtained agree very well with the actual glucose

  16. DNA-modified electrodes (Ⅶ)——Preparation and characterization of DNA-bonded and DNA-adsorbed SAM/Au electrodes

    Institute of Scientific and Technical Information of China (English)

    陆琪; 庞代文; 胡深; 程介克; 蔡雄伟; 施财辉; 毛秉伟; 戴鸿平

    1999-01-01

    Two kinds of DNA-modified electrodes were prepared by covalent and adsorptive immobilization of DNA onto self-assembled monolayers of 2, 2’-dithiodiethanol on gold electrodes and characterized by cyclic voltammetry, Xray photoelectron spectroscopy and scanning tunneling microscopy. The results suggest that the methods are satisfactory for the immobilization of DNA on electrodes.

  17. Reactivity study of silicon electrode modified by grafting using electrochemical reduction of diazonium salts

    International Nuclear Information System (INIS)

    The use of the hydrogenated surface of silicon is hampered by its chemical instability by surface oxidation. The researchers have attempted to modify this surface by direct grafting through the establishment of covalent silicon-carbon bonds from the reaction of chemical species on the surface. Different grafting methods can be implemented for the preparation of grafted surfaces. The choice of an electrochemical reaction allows fast grafting from the hydrogenated surface. We studied the formation of a phenyl layer by electrochemical reduction of aryl diazonium salts (BF4-,+N2-ph-OCH3) on a p-Si-H (111) electrode in an aqueous medium (0.05M H/sub 2/SO/sub 4/ + 0.05M HF). The grafting of an organic layer by reduction is confirmed by the observation of a cyclic voltammetry peak around -0.3V/SCE. In-situ infrared spectroscopy (IR) analysis allows to identify the chemical functions present on the grafted surface, allowing a direct monitoring of the grafting reaction. (author)

  18. Xanthine Biosensor Based on Didodecyldimethylammonium Bromide Modified Pyrolytic Graphite Electrode

    Institute of Scientific and Technical Information of China (English)

    TANG,Ji-Lin(唐纪琳); HAN,Xiao-Jun(韩晓军); HUANG,Wei-Min(黄卫民); WANG,Er-Kang(汪尔康)

    2002-01-01

    The vesicle of didodecyldimethylammonium bromide (DDAB)which contained tetrathiafulvalene (TTF) was mixed with xanthine oxidase, and the mixture was cast on the pyrolytic graphite electrode. The lipid films were used to supply a biological environment resembling biomembrane on the surface of the electrode. TTF was used as a mediator because of its high electron-transfer efficiency. A novel xanthine biosensor based on cast DDAB film was developed. The effects of pH and operating potential were explored for optimum analytical performance by using the amperometric method. The response time of the biosensor was less than 10 s. The detection limit of the biosensor was 3.2 × 10-7 mol/L and the liner range was from 4 × 10-7 mol/L to 2.4 × 10-6 mol/L.

  19. Study on electroactive and electrocatalytic surfaces of single walled carbon nanotube-modified electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Salinas-Torres, David [Departamento de Quimica Fisica and Instituto Universitario de Materiales de Alicante, Universidad de Alicante, Apdo. de Correos 99, E-03080 Alicante (Spain); Huerta, Francisco [Departamento de Ingenieria Textil y Papelera, Universidad Politecnica de Valencia, Plaza Ferrandiz y Carbonell, 1. E-03801 Alcoy (Spain); Montilla, Francisco, E-mail: francisco.montilla@ua.e [Departamento de Quimica Fisica and Instituto Universitario de Materiales de Alicante, Universidad de Alicante, Apdo. de Correos 99, E-03080 Alicante (Spain); Morallon, Emilia [Departamento de Quimica Fisica and Instituto Universitario de Materiales de Alicante, Universidad de Alicante, Apdo. de Correos 99, E-03080 Alicante (Spain)

    2011-02-01

    An investigation of the electrocatalysis of single-walled carbon nanotubes modified electrodes has been performed in this work. Nanotube-modified electrodes present a surface area much higher than the bare glassy carbon surfaces as determined by capacitance measurements. Several redox probes were selected for checking the reactivity of specific sites at the carbon nanotube surface. The presence of carbon nanotubes on the electrode improves the kinetics for all the reactions studied compared with the bare glassy carbon electrode with variations of the heterogeneous electron transfer rate constant up to 5 orders of magnitude. The most important effects are observed for the benzoquinone/hydroquinone and ferrocene/ferricinium redox couples, which show a remarkable improvement of their electron transfer kinetics on SWCNT-modified electrodes, probably due to strong {pi}-{pi} interaction between the organic molecules and the walls of the carbon nanotubes. For many of the reactions studied, less than 1% of the nanotube-modified electrode surface is transferring charge to species in solution. This result suggests that only nanotube tips are active sites for the electron transfer in such cases. On the contrary, the electroactive surface for the reactions of ferrocene and quinone is higher indicating that the electron transfer is produced also from the nanotube walls.

  20. 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

  1. 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.

  2. Application of a palladium hexacyanoferrate film-modified aluminum electrode to electrocatalytic oxidation of hydrazine.

    Science.gov (United States)

    Razmi, Habib; Azadbakht, Azadeh; Sadr, Moayad Hossaini

    2005-11-01

    A palladium hexacyanoferrate (PdHCF) film as an electrocatalytic material was obtained at an aluminum (Al) electrode by a simple electroless dipping method. The modified Al electrode demonstrated a well-behaved redox couple due to the redox reaction of the PdHCF film. The PdHCF film showed an excellent electrocatalytic activity toward the oxidation of hydrazine. The electrocatalytic oxidation of hydrazine was studied by cyclic voltammetry and rotating disk electrode voltammetry techniques. A calibration graph obtained for the hydrazine consisted of two segments (localized at concentration ranges 0.39-10 and 20-75 mM). The rate constant k and transfer coefficient alpha for the catalytic reaction and the diffusion coefficient of hydrazine in the solution D, were found to be 3.11 x 10(3) M(-1) s(-1), 0.52 and 8.03 x 10(-6) cm2 s(-1) respectively. The modified electrode was used to amperometric determination of hydrazine in photographic developer. The interference of ascorbic acid and thiosulfate were investigated and greatly reduced using a thin film of Nafion on the modified electrode. The modified electrode indicated reproducible behavior and a high level of stability during electrochemical experiments, making it particularly suitable for analytical purposes. PMID:16317900

  3. 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

  4. The underlying electrode causes the reported 'electro-catalysis' observed at C60-modified glassy carbon electrodes in the case of N-(4-hydroxyphenyl)ethanamide and salbutamol

    International Nuclear Information System (INIS)

    The reported 'electro-catalysis' of C60-film-modified electrodes for the electrochemical oxidation of N-(4-hydroxyphenyl)ethanamide and salbutamol has been explored at boron-doped diamond and glassy carbon electrodes. Using both C60-film-modified boron-doped diamond and glassy carbon as underlying electrode substrates no electro-catalytic response is observed using the target analytes but rather the C60 serves to block the electrode surface. A common experimental protocol used by researchers in this field is to electrochemically pre-treat the C60-film-modified electrode. The response of employing this electrochemical pre-treatment at both bare glassy carbon and boron-doped diamond electrodes using the target analytes reveals that no effect on the electrochemical responses obtained at the boron-doped diamond electrode whereas a slight but significant effect occurs on glassy carbon which is attributed to the likely introduction of surface oxygenated species. Consequently the previously reported 'electro-catalysis' using C60-film-modified electrode is not due to C60 itself being catalytic, but rather that substrate activation through electrode pre-treatment is responsible for the observed 'electro-catalysis' likely through the introduction of surface oxygenated species. This work clearly shows that substrate activation is an important parameter which researchers studying C60-film-modified electrodes, especially in electro-analysis needs to be considered

  5. Electrocatalytic response of poly(cobalt tetraaminophthalocyanine)/multi-walled carbon nanotubes-Nafion modified electrode toward sulfadiazine in urine*

    OpenAIRE

    Hong, Xiao-ping; Zhu, Yan; Zhang, Yan-zhen

    2012-01-01

    A highly sensitive amperometric sulfadiazine sensor fabricated by electrochemical deposition of poly(cobalt tetraaminophthalocyanine) (poly(CoIITAPc)) on the surface of a multi-walled carbon nanotubes-Nafion (MWCNTs-Nafion) modified electrode is described. This electrode showed a very attractive performance by combining the advantages of CoIITAPc, MWCNTs, and Nafion. Compared with the bare glassy carbon electrode (GCE) and the MWCNTs-Nafion modified electrode, the electrocatalytic activity of...

  6. Doping level influence on chemical surface of diamond electrodes

    Science.gov (United States)

    Azevedo, A. F.; Baldan, M. R.; Ferreira, N. G.

    2013-04-01

    The modification of surface bond termination promoted by the doping level on diamond electrodes is analyzed. The films were prepared by hot filament chemical vapor deposition technique using the standard mixture of H2/CH4 with an extra H2 flux passing through a bubbler containing different concentrations of B2O3 dissolved in methanol. Diamond morphology and quality were characterized by scanning electron microscopy and Raman scattering spectroscopy techniques while the changes in film surfaces were analyzed by contact angle, cyclic voltammetry and synchrotron X-ray photoelectron spectroscopy (XPS). The boron-doped diamond (BDD) films hydrophobicity, reversibility, and work potential window characteristics were related to their physical properties and chemical surface, as a function of the doping level. From the Mott-Schottky plots (MSP) and XPS analyzes, for the lightly (1018 cm-3) and highly (1020 cm-3) BDD films, the relationship between the BDD electrochemical responses and their surface bond terminations is discussed.

  7. 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

  8. A Biosensor Using Poly(4-Aminophenol/acetylcholinesterase modified graphite electrode for the detection of dichlorvos

    Directory of Open Access Journals (Sweden)

    Edmar Isaías Melo

    2011-12-01

    Full Text Available The properties of poly(4-aminophenol modified graphite electrode as material for the immobilization of acetylcholinesterase were investigated by the Cyclic Voltammetry, Electrochemical Impedance Spectroscopy and Atomic Force Microscopy. The polymer was deposited on graphite electrode surface by the oxidation of 4-aminophenol and then acetylcholinesterase was immobilized on the surface of the electrode. The biosensor coupled in the continuous flow system was employed for the detection of dichlorvos. The detection and quantification limits were 0.8 and 2.4 μmol L-1 dichlorvos, respectively. Graphite electrodes modified with the poly(4-aminophenol showed to be an efficient and promising material for immobilization of acetylcholinesterase enzyme. The proposed method requires simple parts which are easy to build, involves only one biosensor and the potentiometric detection is simple.

  9. 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

  10. 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.

  11. Role of iron oxide impurities in electrocatalysis by multiwall carbon nanotubes: An investigation using a novel magnetically modified ITO electrodes

    Indian Academy of Sciences (India)

    Kanchan M Samant; Vrushali S Joshi; Kashinath R Patil; Santosh K Haram

    2014-04-01

    The role of iron oxide impurities in the electrocatalytic properties of multiwall carbon nanotubes (MWCNTs) prepared by catalytic chemical vapour decomposition method (CCVD) is studied in detail. A novel magnetically modified electrodes have been developed by which MWCNTs were immobilized on indium-tin oxide (ITO) electrodes, without any chemical binders. The electro-catalytic oxidation of dopamine, and reduction of hydrogen peroxide have been studied by cyclic voltammetry on magnetically modified electrodes with (i) MWCNTs with occluded iron oxide impurities (Fe-MWCNTs), (ii) MWCNTs grown on iron oxide nanoparticle particulate films (Io-MWCNTs) and (iii) pristine iron oxide nanoparticle particulate film (Io-NPs). A shift towards less positive potentials for the oxidation of dopamine was observed which is in the order of Fe-MWCNTs < Io-MWCNTs < Io-NPs. Similarly, trend towards less negative potentials for the reduction of hydrogen peroxide was observed. Thus, the electrocatalytic activities displayed by MWCNTs have been attributed to the iron oxide impurities associated with it. The systematic variation was related to the nature of interaction of iron oxide nanoparticles with MWCNT surface.

  12. Protein structure-sensitive electrocatalysis at dithiothreitol-modified electrodes

    Czech Academy of Sciences Publication Activity Database

    Ostatná, Veronika; Černocká, Hana; Paleček, Emil

    2010-01-01

    Roč. 132, č. 27 (2010), s. 9408-9413. ISSN 0002-7863 R&D Projects: GA AV ČR(CZ) KJB100040901; GA ČR(CZ) GP202/07/P497; GA MŠk(CZ) LC06035 Grant ostatní: GA AV ČR(CZ) KAN400310651 Institutional research plan: CEZ:AV0Z50040507; CEZ:AV0Z50040702 Keywords : constant current chronopotentiometry * mercury and solid amalgam electrodes * structure-sensitive protein analysis Subject RIV: BO - Biophysics Impact factor: 9.019, year: 2010

  13. 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.

  14. 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 ...

  15. Glucose biosensors based on a gold nanodendrite modified screen-printed electrode

    Science.gov (United States)

    Liu, Hsi-Chien; Tsai, Chung-Che; Wang, Gou-Jen

    2013-05-01

    In this study, an enzymatic glucose biosensor based on a three-dimensional gold nanodendrite (GND) modified screen-printed electrode was developed. The GNDs were electrochemically synthesized on the working electrode component of a commercially available screen-printed electrode using a solution acquired by dissolving bulk gold in aqua regia as the precursor. The 3D GND electrode greatly enhanced the effective sensing area of the biosensor, which improved the sensitivity of glucose detection. Actual glucose detections demonstrated that the fabricated devices could perform at a sensitivity of 46.76 μA mM-1 cm-2 with a linear detection range from 28 μM-8.4 mM and detection limit of 7 μM. A fast response time (˜3 s) was also observed. Moreover, only a 20 μl glucose oxidase is required for detection owing to the incorporation of the commercially available screen-printed electrode.

  16. Glucose biosensors based on a gold nanodendrite modified screen-printed electrode

    International Nuclear Information System (INIS)

    In this study, an enzymatic glucose biosensor based on a three-dimensional gold nanodendrite (GND) modified screen-printed electrode was developed. The GNDs were electrochemically synthesized on the working electrode component of a commercially available screen-printed electrode using a solution acquired by dissolving bulk gold in aqua regia as the precursor. The 3D GND electrode greatly enhanced the effective sensing area of the biosensor, which improved the sensitivity of glucose detection. Actual glucose detections demonstrated that the fabricated devices could perform at a sensitivity of 46.76 μA mM−1 cm−2 with a linear detection range from 28 μM–8.4 mM and detection limit of 7 μM. A fast response time (∼3 s) was also observed. Moreover, only a 20 μl glucose oxidase is required for detection owing to the incorporation of the commercially available screen-printed electrode. (paper)

  17. Modified carbon nanoparticle-chitosan film electrodes: Physisorption versus chemisorption

    Energy Technology Data Exchange (ETDEWEB)

    Rassaei, Liza; Sillanpaeae, Mika [Laboratory of Applied Environmental Chemistry, Department of Environmental Sciences, University of Kuopio, Patteristonkatu 1, 50101 Mikkeli (Finland); Marken, Frank [Department of Chemistry, University of Bath, Bath BA2 7AY (United Kingdom)

    2008-08-01

    Surface functionalised carbon nanoparticles of ca. 8 nm diameter co-assemble with chitosan into stable thin film electrodes at glassy carbon surfaces. Robust electrodes for application in sensing or electrocatalysis are obtained in a simple solvent evaporation process. The ratio of chitosan binder backbone to carbon nanoparticle conductor determines the properties of the resulting films. Chitosan (a poly-D-glucosamine) has a dual effect (i) as the binder for the mesoporous carbon composite structure and (ii) as binding site for redox active probes. Physisorption due to the positively charged ammonium group (pK{sub A} {approx} 6.5) occurs, for example, with anionic indigo carmine (a reversible 2e{sup -}-2H{sup +} reduction system in aqueous media). Chemisorption at the amine functionalities is demonstrated with 2-bromo-methyl-anthraquinone in acetonitrile (resulting in a reversible 2e{sup -}-2H{sup +} anthraquinone reduction system in aqueous media). Redox processes within the carbon nanoparticle-chitosan films are studied and at sufficiently high scan rates diffusion of protons (buffer concentration depended) is shown to be rate limiting. The chemisorption process provides a much more stable interfacial redox system with a characteristic and stable pH response over a pH 2-12 range. Chemisorption and physisorption can be employed simultaneously in a complementary binding process. (author)

  18. Electrochromic properties of WO3 thin film onto gold nanoparticles modified indium tin oxide electrodes

    International Nuclear Information System (INIS)

    Gold nanoparticles (GNPs) thin films, electrochemically deposited from hydrogen tetrachloroaurate onto transparent indium tin oxide (ITO) thin film coated glass, have different color prepared by variation of the deposition condition. The color of GNP film can vary from pale red to blue due to different particle size and their interaction. The characteristic of GNPs modified ITO electrodes was studied by UV-vis spectroscopy, scanning electron microscope (SEM) images and cyclic voltammetry. WO3 thin films were fabricated by sol-gel method onto the surface of GNPs modified electrode to form the WO3/GNPs composite films. The electrochromic properties of WO3/GNPs composite modified ITO electrode were investigated by UV-vis spectroscopy and cyclic voltammetry. It was found that the electrochromic performance of WO3/GNPs composite films was improved in comparison with a single component system of WO3.

  19. 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.

  20. 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.

  1. Disposable pencil graphite electrode modified with peptide nanotubes for Vitamin B12 analysis

    Science.gov (United States)

    Pala, Betül Bozdoğan; Vural, Tayfun; Kuralay, Filiz; Çırak, Tamer; Bolat, Gülçin; Abacı, Serdar; Denkbaş, Emir Baki

    2014-06-01

    In this study, peptide nanostructures from diphenylalanine were synthesized in various solvents with various polarities and characterized with Scanning Electron Microscopy (SEM) and Powder X-ray Diffraction (PXRD) techniques. Formation of peptide nanofibrils, nanovesicles, nanoribbons, and nanotubes was observed in different solvent mediums. In order to investigate the effects of peptide nanotubes (PNT) on electrochemical behavior of disposable pencil graphite electrodes (PGE), electrode surfaces were modified with fabricated peptide nanotubes. Electrochemical activity of the pencil graphite electrode was increased with the deposition of PNTs on the surface. The effects of the solvent type, the peptide nanotube concentration, and the passive adsorption time of peptide nanotubes on pencil graphite electrode were studied. For further electrochemical studies, electrodes were modified for 30 min by immobilizing PNTs, which were prepared in water at 6 mg/mL concentration. Vitamin B12 analyses were performed by the Square Wave (SW) voltammetry method using modified PGEs. The obtained data showed linearity over the range of 0.2 μM and 9.50 μM Vitamin B12 concentration with high sensitivity. Results showed that PNT modified PGEs were highly simple, fast, cost effective, and feasible for the electro-analytical determination of Vitamin B12 in real samples.

  2. 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.

  3. Disposable pencil graphite electrode modified with peptide nanotubes for Vitamin B{sub 12} analysis

    Energy Technology Data Exchange (ETDEWEB)

    Pala, Betül Bozdoğan [Nanotechnology and Nanomedicine Division, Institute of Science, Hacettepe University, 06800 Ankara (Turkey); Vural, Tayfun [Department of Chemistry, Faculty of Science, Hacettepe University, 06800 Beytepe, Ankara (Turkey); Kuralay, Filiz [Department of Chemistry, Faculty of Science and Arts, Ordu University, 52200 Ordu (Turkey); Çırak, Tamer [Nanotechnology and Nanomedicine Division, Institute of Science, Hacettepe University, 06800 Ankara (Turkey); Bolat, Gülçin; Abacı, Serdar [Department of Chemistry, Faculty of Science, Hacettepe University, 06800 Beytepe, Ankara (Turkey); Denkbaş, Emir Baki, E-mail: denkbas@hacettepe.edu.tr [Department of Chemistry, Faculty of Science, Hacettepe University, 06800 Beytepe, Ankara (Turkey)

    2014-06-01

    In this study, peptide nanostructures from diphenylalanine were synthesized in various solvents with various polarities and characterized with Scanning Electron Microscopy (SEM) and Powder X-ray Diffraction (PXRD) techniques. Formation of peptide nanofibrils, nanovesicles, nanoribbons, and nanotubes was observed in different solvent mediums. In order to investigate the effects of peptide nanotubes (PNT) on electrochemical behavior of disposable pencil graphite electrodes (PGE), electrode surfaces were modified with fabricated peptide nanotubes. Electrochemical activity of the pencil graphite electrode was increased with the deposition of PNTs on the surface. The effects of the solvent type, the peptide nanotube concentration, and the passive adsorption time of peptide nanotubes on pencil graphite electrode were studied. For further electrochemical studies, electrodes were modified for 30 min by immobilizing PNTs, which were prepared in water at 6 mg/mL concentration. Vitamin B{sub 12} analyses were performed by the Square Wave (SW) voltammetry method using modified PGEs. The obtained data showed linearity over the range of 0.2 μM and 9.50 μM Vitamin B{sub 12} concentration with high sensitivity. Results showed that PNT modified PGEs were highly simple, fast, cost effective, and feasible for the electro-analytical determination of Vitamin B{sub 12} in real samples.

  4. Disposable pencil graphite electrode modified with peptide nanotubes for Vitamin B12 analysis

    International Nuclear Information System (INIS)

    In this study, peptide nanostructures from diphenylalanine were synthesized in various solvents with various polarities and characterized with Scanning Electron Microscopy (SEM) and Powder X-ray Diffraction (PXRD) techniques. Formation of peptide nanofibrils, nanovesicles, nanoribbons, and nanotubes was observed in different solvent mediums. In order to investigate the effects of peptide nanotubes (PNT) on electrochemical behavior of disposable pencil graphite electrodes (PGE), electrode surfaces were modified with fabricated peptide nanotubes. Electrochemical activity of the pencil graphite electrode was increased with the deposition of PNTs on the surface. The effects of the solvent type, the peptide nanotube concentration, and the passive adsorption time of peptide nanotubes on pencil graphite electrode were studied. For further electrochemical studies, electrodes were modified for 30 min by immobilizing PNTs, which were prepared in water at 6 mg/mL concentration. Vitamin B12 analyses were performed by the Square Wave (SW) voltammetry method using modified PGEs. The obtained data showed linearity over the range of 0.2 μM and 9.50 μM Vitamin B12 concentration with high sensitivity. Results showed that PNT modified PGEs were highly simple, fast, cost effective, and feasible for the electro-analytical determination of Vitamin B12 in real samples.

  5. A sensitive electrochemical sensor for paracetamole based on a glassy carbon electrode modified with multiwalled carbon nanotubes and dopamine nanospheres functionalized with gold nanoparticles

    International Nuclear Information System (INIS)

    We describe an electrochemical sensor for paracetamole that is based on a glassy carbon electrode modified with multiwalled carbon nanotubes and dopamine nanospheres functionalized with gold nanoparticles. The functionalized nanospheres were prepared by a chemical route and characterized by scanning electron microscopy. The well-dispersed gold nanoparticles were anchored on the dopamine nanosphere via a chemical reduction of the gold precursor. The stepwise fabrication of the modified electrode and its electrochemical response to paracetamole were evaluated using electrochemical impedance spectroscopy and cyclic voltammetry. The modified electrode displayed improved electrocatalytic activity towards paracetamole, a lower oxidation potential (371 mV), and a larger peak current when compared to a bare electrode or other modified electrodes. The kinetic parameters governing the electro-oxidation of paracetamole were studied, and the analytical conditions were optimized. The peak current was linearly related to the concentration of paracetamole in 0.8–400 μM range, and the detection limit was 50 nM (at an SNR of 3). The method was successfully applied to the determination of paracetamole in spiked human urine samples and gave recoveries between 95.3 and 105.2 %. (author)

  6. 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.

  7. Copper modified platinum electrode for amperometric detection of spectinomycin sulfate by anion-exchange chromatography

    Institute of Scientific and Technical Information of China (English)

    Ling Ling Xi; Pei Min Zhang; Yan Zhu

    2009-01-01

    A La~(3+)-Cu/Pt modified electrode was fabricated by electrodepositing process in CuSO_4 solution by adding a small amount of lanthium compound, and it was employed for direct current (DC) amperometric detection of spectinomycin by anion-exchange chromatography. Without derivatization, this method can simultaneously determine the main component and impurities in spectinomycin pharmaceutical raw material. Ease of preparation, being applied in DC detection mode and good catalytic stability confirmed the interests of this modified electrode as amperometric sensor for the determination of spectinomycin.

  8. Electrochemically Reduced Graphene Oxide-nafion/Au Nanoparticle Modified Electrode for Hydrogen Peroxide Sensing

    OpenAIRE

    Yajie Lv; Fang Wang; Hui Zhu; Xiaorong Zou; Cheng-an Tao; Jianfang Wang

    2016-01-01

    n this paper, a non-enzymatic hydrogen peroxide (H2O2) sensor, based on Au nanoparticles (AuNPs) electrodepos‐ ited on an electrochemically reduced graphene oxide(ER‐ GO)-Nafion modified glass carbon electrode (GCE), was reported. The graphene oxide-(GO-)Nafion nanocompo‐ sites were first assembled on the GCE surface to produce a GO-Nafion electrode. GO was then electrochemically reduced to produce an ERGO-Nafion modified GCE (to be subsequently denoted as GCE/ERGO-Nafion). Afterwards, AuNPs ...

  9. Electrochemical Preparation and Characterization of Lanthanum Hexacyanoferrate Modified Electrode

    Institute of Scientific and Technical Information of China (English)

    吴萍; 蔡称心

    2005-01-01

    An electroactive polynuclear inorganic compound of rare earth metal hexacyanoferrate, lanthanum hexacyanoferrate (LaHCF), was prepared by electrochemical deposition on the surface of a glassy carbon electrode with a potential cycling procedure. The cyclic voltammogram of LaHCF exhibits a pair of well-defined redox peaks with the formal potential of 208 mV (vs. SCE) at a scan rate of 100 mV/s in 0.2 mol/L NaCl solution and the redox peak currents increase linearly with the square root of the scan rate up to 1000 mV/s. The effects of the concentration of supporting electrolyte on the electrochemical characteristics of LaHCF were studied by voltammetry. LaHCF was also characterizated by scanning electron microscope (SEM), FTIR and XPS techniques.

  10. A 3D Microfluidic Chip for Electrochemical Detection of Hydrolysed Nucleic Bases by a Modified Glassy Carbon Electrode

    Directory of Open Access Journals (Sweden)

    Jana Vlachova

    2015-01-01

    Full Text Available Modification of carbon materials, especially graphene-based materials, has wide applications in electrochemical detection such as electrochemical lab-on-chip devices. A glassy carbon electrode (GCE modified with chemically alternated graphene oxide was used as a working electrode (glassy carbon modified by graphene oxide with sulphur containing compounds and Nafion for detection of nucleobases in hydrolysed samples (HCl pH = 2.9, 100 °C, 1 h, neutralization by NaOH. It was found out that modification, especially with trithiocyanuric acid, increased the sensitivity of detection in comparison with pure GCE. All processes were finally implemented in a microfluidic chip formed with a 3D printer by fused deposition modelling technology. As a material for chip fabrication, acrylonitrile butadiene styrene was chosen because of its mechanical and chemical stability. The chip contained the one chamber for the hydrolysis of the nucleic acid and another for the electrochemical detection by the modified GCE. This chamber was fabricated to allow for replacement of the GCE.

  11. 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.

  12. Preparation and characterization of diethylene glycol bis(2-aminophenyl) ether-modified glassy carbon electrode

    International Nuclear Information System (INIS)

    Diethylene glycol bis(2-aminophenyl) ether (DGAE) diazonium salt was covalently electrografted on a glassy carbon (GC) surface and behavior of this novel surface was investigated. Synthesis of DGAE diazonium salt (DGAE-DAS) and in situ modification of GC electrode were performed in aqueous media containing NaNO2, keeping the temperature below +4 deg. C. For the characterization of the modified electrode surface by cyclic voltammetry, dopamine (DA) was used to prove the attachment of the DGAE-DAS on the GC surface. Raman spectroscopy and electrochemical impedance spectroscopy (EIS) were used to observe the molecular bound properties of the adsorbates at the DGAE-modified GC surface (GC-DGAE). The EIS results were analyzed using the Randles equivalent circuit. The charge transfer resistance on bare GC and the modified surface were calculated using the model equivalent circuit for the ferrocene redox system. Surface coverage was found as 0.4 showing the presence of high pinhole and defects in the modified electrode. The rate constant of electron transfer through the monolayer was calculated for ferrocene. Working potential range and the stability of the DGAE-modified GC electrode was also determined

  13. Application of Multi-Walled Carbon Nanotubes Modified Glassy Carbon Electrode for Determination of Mefenamic Acid in Pharmaceutical Preparations and Biological Fluids

    International Nuclear Information System (INIS)

    A chemically modified electrode is constructed based on multi-walled carbon nanotube modified glassy carbon electrode (MWCNTs/GCE). It is demonstrated that this sensor could be used for determination of pharmaceutically important compound mefenamic acid (MEF). Differential pulse voltammetry (DPV) experiments of various concentration of MEF showed two linear dynamic ranges. The first linear dynamic range was from 2 micro M to 40 micro M, and the second linear dynamic range was between 50 micro M to 360 micro M. A detection limit of 0.21 micro M (S/N = 3) was obtained. Under optimal conditions the modified electrode exhibited high sensitivity and stability for determination of MEF, making it a suitable sensor for the submicromolar detection of MEF in solutions. The analytical performance of this sensor has been evaluated for the detection of MEF in human serum, human urine and a pharmaceutical preparation with satisfactory results. (author)

  14. Preparation, Electrochemical Property and Application in Bulk-modified Electrode of Dawson-type Phosphomolybdate-doped Polypyrrole Composite Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    A kind of inorganic-organic hybrid semiconductor composite nanoparticles: Dawson-type phosphomolybdatedoped polypyrrole (P2Mo18-PPy) was designed and prepared using microemulsion oxidation-polymerization at room temperature and characterized by TEM and IR. The P2Mo18-PPy was used as a bulk-modifier to fabricate a chemically modified carbon paste electrode(CPE) by direct mixing, which represents the example of polyoxometalates (POMs)-doped semiconductor polymer nanoparticles modified electrode. Both the advantage of POMs-doped polymer and the surface-renewal property of the CPE were fully utilized. The electrochemical behavior of the P2Mo18-PPy bulk-modified CPE(P2Mo18-PPy-CPE) was investigated with cyclic voltammetry. Three couples of reversible redox peaks were observed in the range from + 800 to 0 mV, which corresponded to the reduction and oxidation through two-, four- and six-electron processes, respectively. The P2Mo18-PPY-CPE showed a high electrocatalytic activity for the reduction of nitrite, which expanded the application of POMs-doped semiconductor polymer nanoparticles.

  15. Chemical modification approaches for improved performance of Na-ion battery electrodes

    Science.gov (United States)

    Byles, Bryan; Clites, Mallory; Pomerantseva, Ekaterina

    2015-08-01

    Na-ion batteries have received considerable attention in recent years but still face performance challenges such as limited cycle lifetime and low capacities at high current rates. In this work, we propose novel combinations of preand post-synthesis treatments to modify known Na-ion battery electrode materials to achieve enhanced electrochemical performance. We work with two model metal oxide materials to demonstrate the effectiveness of the different treatments. First, wet chemical preintercalation is combined with post-synthesis aging, hydrothermal treatment, and annealing of α-V2O5, resulting in enhanced capacity retention in a Na-ion battery system. The hydrothermal treatment resulted in an increased specific capacity of nearly 300 mAh/g. Second, post-synthesis acid leaching is performed on α- MnO2, also resulting in improved electrochemical capacity. The chemical, structural, and morphological changes brought about by the modifications are fully characterized.

  16. 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

  17. Effect of mediator added to modified paste carbon electrodes with immobilized laccase from Aspergillus oryzae

    Directory of Open Access Journals (Sweden)

    Marcelo Silva Ferreira

    2015-05-01

    Full Text Available Carbon paste electrodes based on the immobilization of laccase from Aspergillus oryzae were developed and voltammetric measurements were performed to evaluate the amperometric response. The 2,2′-azino-bis-(3-ethylbenzthiazoline-6-sulfonic acid diammonium salt  (ABTS functions as substrate and mediator for the laccase enzyme. Electrodes were modified  in two different conditions: without mediator (EPC/laccase and with mediator (EPC/laccase/ABTS. The addition of ABTS as a mediator increased eight-fold the amperometric response. The electrode was sensitive to pH variation with best response at pH 4.0. Studies on different concentrations of laccase and ABTS at different pH rates revealed that the composition 187 U mL-1 in laccase and 200 µL of ABTS obtained the highest amperometric response. The carbon paste electrode modified with ABTS proved to be a good base for the immobilization of the laccase enzyme. Moreover, it is easy to manufacture and inexpensive to produce a modified electrode with potential application in biosensors.

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

    Directory of Open Access Journals (Sweden)

    Vojtěch Polan

    2010-01-01

    Full Text Available 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 (established as 3σ and response time of 39 s. When compared with similar glucose biosensors based on glucose oxidase, the main advantage is that neither ascorbic and uric acids nor paracetamol interfere measurements with this biosensor at selected potentials.

  19. Flow injection amperometric detection of insulin at cobalt hydroxide nanoparticles modified carbon ceramic electrode.

    Science.gov (United States)

    Habibi, Esmaeil; Omidinia, Eskandar; Heidari, Hassan; Fazli, Maryam

    2016-02-15

    Cobalt hydroxide nanoparticles were prepared onto a carbon ceramic electrode (CHN|CCE) using the cyclic voltammetry (CV) technique. The modified electrode was characterized by X-ray diffraction and scanning electron microscopy. The results showed that CHN with a single-layer structure was uniformly electrodeposited on the surface of CCE. The electrocatalytic activity of the modified electrode toward the oxidation of insulin was studied by CV. CHN|CCE was also used in a homemade flow injection analysis system for insulin determination. The limit of detection (signal/noise [S/N] = 3) and sensitivity were found to be 0.11 nM and 11.8 nA/nM, respectively. Moreover, the sensor was used for detection of insulin in human serum samples. This sensor showed attractive properties such as high stability, reproducibility, and high selectivity. PMID:26686031

  20. Improved hydrogen evolution on glassy carbon electrode modified with novel Pt/cetyltrimethylammonium bromide nanoscale aggregates

    Institute of Scientific and Technical Information of China (English)

    Jahan-Bakhsh Raoof; Sayed Reza Hosseini; Seyedeh Zeinab Mousavi-Sani

    2015-01-01

    A novel, cost‐effective, and simple electrocatalyst based on a Pt‐modified glassy carbon electrode (GCE), using cetyltrimethylammonium bromide (CTAB) as a cationic surfactant, is reported. Am‐phiphilic CTAB molecules were adsorbed on GCE by immersion in a CTAB solution. The positively charged hydrophilic layer, which consisted of small aggregates of average size less than 100 nm, was used for accumulation and complexation of [PtCl6]2− anions by immersing the electrode in K2PtCl6 solution. The modified electrode was characterized using scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, impedance spectroscopy, and electrochemical methods. The electrocatalytic activity of the Pt particles in the hydrogen evolution reaction (HER) was investigat‐ed. The results show that the CTAB surfactant enhances the electrocatalytic activity of the Pt parti‐cles in the HER in acidic solution.

  1. Electroanalysis of Hydrogen Peroxide at Boron Doped Diamond Electrode Modified by Silver Nanoparticles and Haemoglobin

    International Nuclear Information System (INIS)

    The electrochemical detection of H2O2 using boron doped diamond electrode modified by silver nanoparticles and haemoglobin is reported. Silver nanoparticle obtained from electrodeposition in the presence of cetyl hexadecylthmoniom bromide (CTAB) surfactant shows the best combination of detection limit, sensitivity and reproducibility. The presence of Ag nanoparticles helps bind haemoglobin to the electrode in an active form, leading to a significantly further increase of electrode response to H2O2. Detection limits below 1 μM are achieved by a synergistic effect of both modifiers, and a good linear signal response is seen up to 8 mM. Interferences from glucose, uric acid, ascorbic acid and dopamine at typical physiological levels are shown to be negligible

  2. Screen-printed carbon electrodes modified by rhodium dioxide and glucose dehydrogenase.

    Science.gov (United States)

    Polan, Vojtěch; Soukup, Jan; Vytřas, Karel

    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) (established as 3σ) and response time of 39 s. When compared with similar glucose biosensors based on glucose oxidase, the main advantage is that neither ascorbic and uric acids nor paracetamol interfere measurements with this biosensor at selected potentials. PMID:21528113

  3. Cathodic stripping voltammetric determination of chromium in coastal waters on cubic Nano-titanium carbide loaded gold nanoparticles modified electrode

    Directory of Open Access Journals (Sweden)

    Haitao eHan

    2015-09-01

    Full Text Available The novel cubical nano-titanium carbide loaded gold nanoparticles modified electrode for selective and sensitive detection of trace chromium (Cr in coastal water was established based on a simple approach. Nano-titanium carbide is used as the typical cubical nanomaterial with wonderful catalytic activity towards the reduction of Cr(VI. Gold nanoparticles with excellent physical and chemical properties can facilitate electron transfer and enhance the catalytic activity of the modified electrode. Taking advantage of the synergistic effects of nano-titanium carbide and gold nanoparticles, the excellent cathodic signal responses for the stripping determination of Cr(VI can be obtained. The detection limit of this method is calculated as 2.08 μg L-1 with the linear calibration curve ranged from 5.2 to 1040 μg L-1. This analytical method can be used to detect Cr(VI effectively without using any complexing agent. The fabricated electrode was successfully applied for the detection of chromium in coastal waters collected from the estuary giving Cr concentrations between 12.48 and 22.88 μg L-1 with the recovery between 96% and 105%.

  4. 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.

  5. 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.

  6. Electrogenerated chemiluminesence method for the determination of riboflavin at an ionic liquid modified gold electrode

    Science.gov (United States)

    Qi, Honglan; Cao, Zongze; Hou, Lina

    2011-01-01

    A highly sensitive electrogenerated chemiluminesence (ECL) method for the determination of riboflavin was developed based on the enhancement of ECL intensity of lucigenin at room temperature ionic liquids (RTILs) modified gold electrode. RTILs modified gold electrode exhibited excellent electrochemical and ECL property to lucigenin system and the ECL intensity of lucigenin was greatly enhanced by riboflavin. The characterization of the RTILs modified electrode and the attractive performance of the sensitive ECL method for the determination of riboflavin were investigated. Under the optimized conditions, the ECL intensity was directly proportional to the concentration of riboflavin in the range from 5.0 × 10 -10 g/mL to 1.0 × 10 -8 g/mL with the detection limit of 1 × 10 -10 g/mL. The method has been applied to the determination of riboflavin in the pharmaceutical preparations with satisfactory recovery from 96% to 101%. This work demonstrates that the incorporation of ECL method with RTILs modified electrode is a promising strategy for the determination of organic compounds with high sensitivity and good reproducibility.

  7. Strain Engineering to Modify the Electrochemistry of Energy Storage Electrodes

    Science.gov (United States)

    Muralidharan, Nitin; Carter, Rachel; Oakes, Landon; Cohn, Adam P.; Pint, Cary L.

    2016-01-01

    Strain engineering has been a critical aspect of device design in semiconductor manufacturing for the past decade, but remains relatively unexplored for other applications, such as energy storage. Using mechanical strain as an input parameter to modulate electrochemical potentials of metal oxides opens new opportunities intersecting fields of electrochemistry and mechanics. Here we demonstrate that less than 0.1% strain on a Ni-Ti-O based metal-oxide formed on superelastic shape memory NiTi alloys leads to anodic and cathodic peak potential shifts by up to ~30 mV in an electrochemical cell. Moreover, using the superelastic properties of NiTi to enable strain recovery also recovers the electrochemical potential of the metal oxide, providing mechanistic evidence of strain-modified electrochemistry. These results indicate that mechanical energy can be coupled with electrochemical systems to efficiently design and optimize a new class of strain-modulated energy storage materials. PMID:27283872

  8. Strain Engineering to Modify the Electrochemistry of Energy Storage Electrodes

    Science.gov (United States)

    Muralidharan, Nitin; Carter, Rachel; Oakes, Landon; Cohn, Adam P.; Pint, Cary L.

    2016-06-01

    Strain engineering has been a critical aspect of device design in semiconductor manufacturing for the past decade, but remains relatively unexplored for other applications, such as energy storage. Using mechanical strain as an input parameter to modulate electrochemical potentials of metal oxides opens new opportunities intersecting fields of electrochemistry and mechanics. Here we demonstrate that less than 0.1% strain on a Ni-Ti-O based metal-oxide formed on superelastic shape memory NiTi alloys leads to anodic and cathodic peak potential shifts by up to ~30 mV in an electrochemical cell. Moreover, using the superelastic properties of NiTi to enable strain recovery also recovers the electrochemical potential of the metal oxide, providing mechanistic evidence of strain-modified electrochemistry. These results indicate that mechanical energy can be coupled with electrochemical systems to efficiently design and optimize a new class of strain-modulated energy storage materials.

  9. Simultaneous detection of ascorbic acid, uric acid and homovanillic acid at copper modified electrode

    Energy Technology Data Exchange (ETDEWEB)

    Selvaraju, T. [Centre for Photoelectrochemistry, School of Chemistry, Madurai Kamaraj University, Madurai 625021 (India); Ramaraj, R. [Centre for Photoelectrochemistry, School of Chemistry, Madurai Kamaraj University, Madurai 625021 (India)]. E-mail: ramarajr@yahoo.com

    2007-02-15

    The copper was deposited on glassy carbon (GC) and indium tin oxide (ITO) electrodes by electrochemical method. The copper structures on electrode were characterized by atomic force microscope, X-ray diffractometeric pattern and differential pulse voltammetric studies. Optimal conditions for uniform growth of copper structures on the electrode were established. Voltammetric sensor was fabricated using the copper deposited GC electrode for the simultaneous detection and determination of uric acid (UA) and homovanillic acid (HVA) in the presence of excess concentrations of ascorbic acid (AA). The voltammetric signals due to AA and UA oxidation were well separated with a potential difference of 400 mV and AA did not interfere with the measurement of UA and HVA at the GC/Cu electrode. Linear calibration curves were obtained in the concentration range 1-40 {mu}M for AA and 20-50 {mu}M for UA at physiological pH and a detection limit of 10 nM of UA in the presence of 10-fold excess concentrations of AA was achieved. The simultaneous detection of submicromolar concentrations of AA, UA and HVA was achieved at the GC/Cu electrode. The practical utility of the present GC/Cu modified electrode was demonstrated by measuring the AA content in Vitamin C tablet, UA content in human urine and blood serum samples with satisfactory results.

  10. Enhanced electrochemical reduction of hydrogen peroxide at metallic electrodes modified with surfactant and salt

    International Nuclear Information System (INIS)

    The enhanced electrocatalytic reduction of hydrogen peroxide brought about by the modification of noble metal electrode surfaces with a modification of surfactant and salt was assessed. A range of electrodes composed of Ag, Au and Pt, either as continuous metal films or as particulate metallic pastes were employed. Several surfactants (cationic, anionic and non-ionic), as well as a range of Group I metal halides with differing cations were all investigated to assess the contribution of these components to the reduction of hydrogen peroxide at −0.1 V vs. Ag/AgCl. It was shown that on silver paste electrodes, all surfactant/salt combinations enhanced the observed catalysis. However, the degree to which they did this appears related to the critical micellar concentration of the surfactant, the size of the Group I metal ion and the optimum formation of lamellar structures formed by the surfactant/salt combination. Metallic electrodes showed less enhancement of catalysis over particulate paste electrodes. In addition, higher grade metallic surfaces showed poorer enhancements in catalysis which may relate to the extent of surface defects amenable to surface modification, as observed by electron microscopy. Silver paste electrodes modified with dodecylbenzene sulphonic acid/KCl exhibited a catalytic rate of 5.47 × 10−2 AM−1 cm−2, which was between 2- and 4-fold less than that observed on equivalent Pt electrodes.

  11. Glassy carbon electrodes modified with gelatin functionalized reduced graphene oxide nanosheet for determination of gallic acid

    Indian Academy of Sciences (India)

    Fereshteh Chekin; Samira Bagheri; Sharifah Bee Abd Hamid

    2015-12-01

    A simple approach for the preparation of gelatin functionalized reduced graphene oxide nanosheet (Gel-RGONS) by chemical reduction of graphene oxide (GO) using gelatin as both reducing agent and stabilizing agent in an aqueous solution was developed. The morphology and structure of the Gel-RGONS were examined by X-ray diffraction, transmission electron microscopy, ultraviolet–visible spectroscopy and Raman spectroscopy. Gelatin acted as a functionalizing reagent to guarantee good dispersibility and stability of the r in distilled water. Moreover, a new electrochemical sensor was developed based on Gel-RGONS modified glassy carbon electrode (Gel-RGONS/GCE). Gel-r exhibits excellent electrocatalytic activity to gallic acid (GA) oxidation. The experimental conditions such as pH, adsorption time and scan rate were optimized for the determination of GA. Under optimum conditions, the sensor responded linearly to GA in the concentration of 1.0 × 10−6 to 1.1 × 10−4 M with detection limit of 4.7 × 10−7 M at 3 using linear sweep voltammetry (LSV). The method has been successfully applied to the determination of GA in sample of black tea.

  12. Properties Characterization of Chemically Modified Hemp Hurds

    OpenAIRE

    Nadezda Stevulova; Julia Cigasova; Adriana Estokova; Eva Terpakova; Anton Geffert; Frantisek Kacik; Eva Singovszka; Marian Holub

    2014-01-01

    The effect of chemical treatment of hemp hurds slices in three solutions (EDTA (Ethylenediaminetetraacetic acid), NaOH and Ca(OH)2) on the properties of natural material was discussed in this paper. Changes in the morphology, chemical composition and structure as well as thermal stability of hemp hurds before and after their modification were investigated by using FTIR (Fourier transform infrared spectroscopy), XRD (X-ray powder diffraction analysis) and TG (thermogravimetry)/DSC (differentia...

  13. Polymers based on chemically modified starch

    Czech Academy of Sciences Publication Activity Database

    Horák, Pavel; Kruliš, Zdeněk; Šárka, E.; Kobera, Libor

    Prague : Czech Chemical Society, 2014 - (Řápková, R.; Čopíková, J.; Šárka, E.), s. 88-90 ISBN 978-80-86238-70-8. [International Conference on Polysaccharides-Glycoscience /10./. Prague (CZ), 22.10.2014-24.10.2014] R&D Projects: GA TA ČR(CZ) TA04020853 Institutional support: RVO:61389013 Keywords : starch * chemical modification * degree of substitution Subject RIV: CD - Macromolecular Chemistry

  14. Comparing the performances of electrochemical sensors using p-aminophenol redox cycling by different reductants on gold electrodes modified with self-assembled monolayers

    International Nuclear Information System (INIS)

    Highlights: • Performances of p-AP redox cycling using different reductants on gold surface are compared. • Background current decreases in order of hydrazine, Na2SO3, NaBH4, NADH, cysteamine, and TCEP. • Chemical reaction rate with QI increases in order of NADH, TCEP, and cysteamine. • NADH, TCEP and cysteamine are suitable for p-AP redox cycling on gold electrode. -- Abstract: p-Aminophenol (p-AP) redox cycling using chemical reductants is one strategy for developing sensitive electrochemical sensors. However, most of the reported reductants are only used on indium-tin oxide (ITO) electrodes but not gold electrodes due to the high background current caused by the oxidation reaction of the reductants on the highly electrocatalytic gold electrodes. Therefore, new strategies and/or reductants are in demand for expanding the application of p-AP redox cycling on gold electrodes. In this work, we compared the performances of several reductants in p-AP redox cycling on self-assembled monolayers (SAMs)-modified gold electrodes. Among the tested reagents, nicotinamide adenine dinucleotide (NADH), tris(2-carboxyethyl)phosphine (TCEP) and cysteamine were demonstrated to be suitable for p-AP redox cycling on the alkanethiol-modified gold electrodes because of their low background current. The rate of chemical reaction between reductants and p-quinone imine (QI, the electrochemically oxidized product of p-AP) increases in the order of NADH −1 was achieved. We believe that our work will be valuable for the development of electrochemical sensors using p-AP redox cycling on gold electrodes

  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. 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.

  17. Detection of nicotine based on molecularly imprinted TiO{sub 2}-modified electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Wu, C.-T.; Chen, P.-Y.; Chen, J.-G.; Suryanarayanan, Vembu [Department of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan (China); Ho, K.-C. [Department of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan (China); Institute of Polymer Science and Engineering, National Taiwan University, Taipei 10617, Taiwan (China)], E-mail: kcho@ntu.edu.tw

    2009-02-02

    Amperometric detection of nicotine (NIC) was carried out on a titanium dioxide (TiO{sub 2})/poly(3,4-ethylenedioxythiophene) (PEDOT)-modified electrode by a molecular imprinting technique. In order to improve the conductivity of the substrate, PEDOT was coated onto the sintered electrode by in situ electrochemical polymerization of the monomer. The sensing potential of the NIC-imprinted TiO{sub 2} electrode (ITO/TiO{sub 2}[NIC]/PEDOT) in a phosphate-buffered saline (PBS) solution (pH 7.4) containing 0.1 M KCl was determined to be 0.88 V (vs. Ag/AgCl/saturated KCl). The linear detection range for NIC oxidation on the so-called ITO/TiO{sub 2}[NIC]/PEDOT electrode was 0-5 mM, with a sensitivity and limit of detection of 31.35 {mu}A mM{sup -1} cm{sup -2} and 4.9 {mu}M, respectively. When comparing with the performance of the non-imprinted one, the sensitivity ratio was about 1.24. The sensitivity enhancement was attributed to the increase in the electroactive area of the imprinted electrode. The at-rest stability of the ITO/TiO{sub 2}[NIC]/PEDOT electrode was tested over a period of 3 days. The current response remained about 85% of its initial value at the end of 2 days. The ITO/TiO{sub 2}[NIC]/PEDOT electrode showed reasonably good selectivity in distinguishing NIC from its major interferent, (-)-cotinine (COT). Moreover, scanning electrochemical microscopy (SECM) was employed to elucidate the surface morphology of the imprinted and non-imprinted electrodes using Fe(CN){sub 6}{sup 3-}/Fe(CN){sub 6}{sup 4-} as a redox probe on a platinum tip. The imprinted electrode was further characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR)

  18. Electrochemical behavior of phenol in alkaline media at hydrotalcite-like clay/anionic surfactants/glassy carbon modified electrode

    International Nuclear Information System (INIS)

    The electrochemical behavior of phenol, using glassy carbon (GC) modified electrodes containing a hydrotalcite (HT)-like clay and anionic surfactants such as sodium octyl sulfate (SOS), sodium dodecyl sulfate (SDS), or sodium dodecylbenzenesulfonate (SDBS) in alkaline media, has been examined. Phenol oxidation at the modified electrodes, after a time accumulation under open circuit conditions, promotes increments of the current and shifts the oxidation potential to less positive values, compared to phenol oxidation at HT-GC or GC electrodes. The phenol oxidation is favored by the presence of surfactants in the films. The results suggest that the surfactant molecules intercalate between the HT layers, yielding a hydrophobic clay capable of preconcentrating phenol molecules. X-ray diffraction analyses showed a larger spacing of the HT layers when the surfactant intercalates between them. Cyclic voltammograms have shown that the SOS-HT-GC modified electrode exhibits short-lived activity for phenol oxidation as a consequence of surface fouling, while the SDS-HT-GC and SDBS-HT-GC modified electrodes showed a more stable behavior. The SDBS-HT-GC modified electrode was the most effective adsorbing phenol, since the charge (Q), obtained from the integration of the anodic peak current of the phenol, is higher at this modified electrode. This is probably because the adsolubilization capacity of phenol on the SDBS-HT-GC electrode is higher than on SDS-HT-GC electrode

  19. Graphene-loaded nanofiber-modified electrodes for the ultrasensitive determination of dopamine

    International Nuclear Information System (INIS)

    Graphical abstract: -- Highlights: •A novel electrode based on electrospun graphene/polyaniline/polystyrene nanofibers has been developed. •The proposed system provides ultrahigh sensitivity, good selectivity and wide linearity for the determination of dopamine. •This system was successfully applied to determine dopamine in complex biological environment with excellent reproducibility. -- Abstract: A novel and highly sensitive electrochemical system based on electrospun graphene/polyaniline/polystyrene (G/PANI/PS) nanofiber-modified screen-printed carbon electrodes has been developed for dopamine (DA) determination. A dramatic increase (9 times) in the current signal for the redox reaction of a standard, ferri/ferrocyanide [Fe(CN)6]3−/4− couple was found when compared to an unmodified electrode. This modified electrode also exhibited favorable electron transfer kinetics and excellent electrocatalytic activity toward the oxidation of DA. When used together with square wave voltammetry (SWV), DA can be selectively determined in the presence of the common interferents (i.e. ascorbic acid and uric acid). Under optimal conditions, a very low limit of detection (0.05 nM) and limit of quantification (0.30 nM) were achieved for DA. In addition, a wide dynamic range of 0.1 nM to 100 μM was found for this electrode system. Finally, the system can be successfully applied to determine DA in complex biological environment (e.g. human serum, urine) with excellent reproducibility

  20. Graphene-loaded nanofiber-modified electrodes for the ultrasensitive determination of dopamine

    Energy Technology Data Exchange (ETDEWEB)

    Rodthongkum, Nadnudda, E-mail: Nadnudda.R@chula.ac.th [Metallurgy and Materials Science Research Institute, Chulalongkorn University, Pathumwan, Bangkok 10330 (Thailand); Ruecha, Nipapan [Program in Macromolecular Science, Faculty of Science, Chulalongkorn University, Pathumwan, Bangkok 10330 (Thailand); Rangkupan, Ratthapol [Metallurgy and Materials Science Research Institute, Chulalongkorn University, Pathumwan, Bangkok 10330 (Thailand); Center of Innovative Nanotechnology, Chulalongkorn University, Pathumwan, Bangkok 10330 (Thailand); Vachet, Richard W. [Department of Chemistry, University of Massachusetts Amherst, Amherst, MA 01002 (United States); Chailapakul, Orawon, E-mail: corawon@chula.ac.th [Electrochemistry and Optical Spectroscopy Research Unit, Department of Chemistry, Faculty of Science, Chulalongkorn University, Pathumwan, Bangkok 10330 (Thailand)

    2013-12-04

    Graphical abstract: -- Highlights: •A novel electrode based on electrospun graphene/polyaniline/polystyrene nanofibers has been developed. •The proposed system provides ultrahigh sensitivity, good selectivity and wide linearity for the determination of dopamine. •This system was successfully applied to determine dopamine in complex biological environment with excellent reproducibility. -- Abstract: A novel and highly sensitive electrochemical system based on electrospun graphene/polyaniline/polystyrene (G/PANI/PS) nanofiber-modified screen-printed carbon electrodes has been developed for dopamine (DA) determination. A dramatic increase (9 times) in the current signal for the redox reaction of a standard, ferri/ferrocyanide [Fe(CN){sub 6}]{sup 3−/4−} couple was found when compared to an unmodified electrode. This modified electrode also exhibited favorable electron transfer kinetics and excellent electrocatalytic activity toward the oxidation of DA. When used together with square wave voltammetry (SWV), DA can be selectively determined in the presence of the common interferents (i.e. ascorbic acid and uric acid). Under optimal conditions, a very low limit of detection (0.05 nM) and limit of quantification (0.30 nM) were achieved for DA. In addition, a wide dynamic range of 0.1 nM to 100 μM was found for this electrode system. Finally, the system can be successfully applied to determine DA in complex biological environment (e.g. human serum, urine) with excellent reproducibility.

  1. Amperometric oxygen sensor based on a platinum nanoparticle-modified polycrystalline boron doped diamond disk electrode.

    Science.gov (United States)

    Hutton, Laura; Newton, Mark E; Unwin, Patrick R; Macpherson, Julie V

    2009-02-01

    Pt nanoparticle (NP)-modified polycrystalline boron-doped diamond (pBDD) disk electrodes have been fabricated and employed as amperometric sensors for the determination of dissolved oxygen concentration in aqueous solution. pBDD columns were cut using laser micromachining techniques and sealed in glass, in order to make disk electrodes which were then characterized electrochemically. Electrodeposition of Pt onto the diamond electrodes was optimized so as to give the maximum oxygen reduction peak current with the lowest background signal. Pt NPs, >0-10 nm diameter, were found to deposit randomly across the pBDD electrode, with no preference for grain boundaries. The more conductive grains were found to promote the formation of smaller nanoparticles at higher density. With the use of potential step chronoamperometry, in which the potential was stepped to a diffusion-limited value, a four electron oxygen reduction process was found to occur at the Pt NP-modified pBDD electrode. Furthermore the chronoamperometric response scaled linearly with dissolved oxygen concentration, varied by changing the oxygen/nitrogen ratio of gas flowed into solution. The sensor was used to detect dissolved oxygen concentrations with high precision over the pH range 4-10. PMID:19117391

  2. 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

  3. 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.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-04-01

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

  5. Determination of nanomolar uric and ascorbic acids using enlarged gold nanoparticles modified electrode.

    Science.gov (United States)

    Kannan, P; John, S Abraham

    2009-03-01

    Individual and simultaneous determination of 50nM uric acid (UA) and ascorbic acid (AA) using enlarged, citrate-stabilized gold nanoparticles (AuNPs) self-assembled to 2,5-dimercapto-1,3,4-thiadiazole (DMT) monolayer modified Au (Au/DMT) electrode by an amperometric method is described for the first time. Self-assembly of AuNPs on the electrode surface was confirmed by atomic force microscopy (AFM), attenuated total reflectance FT-IR and diffuse reflectance spectral measurements. The electron transfer reaction (ETR) of [Fe(CN)(6)](3-/4-) was blocked at Au/DMT electrode, whereas it was restored with a peak separation of 200mV after the attachment of AuNPs on the Au/DMT (Au/DMT/AuNPs) electrode, which was confirmed from the ETR of the [Fe(CN)(6)](3-/4-) redox couple. When the self-assembled AuNPs were enlarged by hydroxylamine seeding, the ETR of [Fe(CN)(6)](3-/4-) was improved significantly with a peak separation of 100mV. Tapping mode AFM showed that the average size of the enlarged-AuNPs (E-AuNPs) was 50-70nm. The E-AuNPs modified electrode catalyzes the oxidation of AA and UA, separates their voltammetric signals by 200mV, and has excellent sensitivity towards AA and UA with a detection limit of 50nM. The practical application of the modified electrode was demonstrated by measuring the concentration of UA in blood serum and urine. PMID:19111516

  6. Antimony powder-modified carbon paste electrodes for electrochemical stripping determination of trace heavy metals

    International Nuclear Information System (INIS)

    Highlights: → New antimony powder-modified carbon paste electrode. → Combination of specific properties of carbon paste substrate and metallic antimony. → No requirement of using toxic antimony(III) salts. → Electrochemical stripping determination of trace heavy metals at ppb levels. → Anodic stripping voltammetric and stripping chronopotentiometric measurements. - Abstract: A new type of the antimony electrode based on a carbon paste bulk-modified with antimony powder (Sb-CPE) is presented for the determination of cadmium(II) and lead(II) ions at the microgram-per-liter concentration level, when using square-wave anodic stripping voltammetric or stripping chronopotentiometric protocol. The Sb-CPE was prepared by mixing fine antimony powder, carbon powder, and silicon oil, thus combining typical features of the carbon paste material with specific electrochemical properties of antimony. Key-operational parameters, including the amount of antimony powder in the carbon paste mixture, effect of the deposition potential and deposition time, were optimized and electroanalytical performance of the Sb-CPE in nondeaerated solution of 0.01 M hydrochloric acid (pH 2) was compared with related bismuth powder-modified carbon paste electrode (Bi-CPE) and with in situ prepared antimony film carbon paste electrode (SbF-CPE). The electrode of interest exhibited well-developed signals and highly linear calibration plots for both metal ions tested. In addition, favorable limits of detection were achieved; namely: 1.4 μg L-1 for Cd(II) and 0.9 μg L-1 for Pb(II). The applicability of the new electrode was demonstrated on the analysis of tap water (spiked sample). Besides voltammetric measurements, the Sb-CPE was preliminary tested also under chronopotentiometric stripping mode in deoxygenated solutions, revealing also an excellent electroanalytical performance.

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

    Directory of Open Access Journals (Sweden)

    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.

  8. Electrochemical degradation of carbamazepine using modified electrode with graphene-AuAg composite

    Science.gov (United States)

    Pogacean, F.; Biris, A. R.; Socaci, C.; Floare-Avram, V.; Rosu, M. C.; Coros, M.; Pruneanu, S.

    2015-12-01

    Carbamazepine is a pharmaceutical drug which has been detected in surface and drinking water primarily due to human usage but also from the accidental disposal of pharmaceuticals into sewers. We have developed a graphene-modified electrode which was tested at the detection and degradation of carbamazepine. The oxidation process was studied by cyclic voltammetry in aqueous and organic solutions. The electrochemical degradation of carbamazepine was performed by polarizing the working electrode at a certain potential, for different times (from 5 to 60 minutes). The degradation efficiency was highly dependent on the type of solution and on the supporting electrolyte.

  9. Electrogenerated chemiluminescence of a cationic cyclometalated iridium complex–Nafion modified electrode in neutral aqueous solution

    International Nuclear Information System (INIS)

    Electrogenerated chemiluminescence (ECL) of a cationic cyclometalated iridium complex, [(pqcm)2Ir(bpy)](PF6) (1, pqcmH=2-phenyl-quinoline-4-carboxylic acid methyl ester, bpy=2,2′-bipyridine), was investigated at a bare glassy carbon electrode in CH3CN solution and 4 ECL peaks were observed. Then, the ECL of the iridium complex was studied in neutral phosphate buffer solution (PBS) by immobilizing it on a glassy carbon electrode. Two closely located ECL peaks were obtained at 1.07 and 1.40 V when the potential was scanned from −3.00 V to 2.20 V, while only one broad ECL peak located around −2.0 V was obtained when the potential was scanned from 2.20 V to −3.00 V. In the presence of oxalate, one ECL peak located around 1.22 V could be obtained except the broad ECL peak located at −2.00 V. The ECL peak at positive potential range was enhanced more than one magnitude in the presence of Nafion and was nearly 5-times higher than that of Ru(bpy)32+–Nafion modified electrode, suggesting that the synthesized iridium complex has great application potential in ECL detection. The ECL spectra of iridium complex were identical to its photoluminescence spectrum, indicating the same metal-to-ligand charge transfer (MLCT) excited states. The mechanisms of ECL were proposed based on the experimental results. The present ECL sensor gave a linear response for the oxalate concentration from 1.0×10−6 to 1.0×10−4 mol L−1 with a detection limit (S/N=3) of 9.1×10−7 mol L−1. -- Graphical abstract: Electrochemiluminescence (ECL) of immobilized novel cationic cyclometalated iridium complex in neutral phosphate buffer solution is reported for the first time. The intensity of iridium complex ECL is 5-times higher than that of Ru(bpy)32+ ECL. Highlights: ► Cationic cyclometalated iridium complex was modified on a bare electrode. ► Electrochemiluminescence (ECL) of the modified electrode was studied. ► The ECL intensity is higher than that of Ru(bpy)32+ modified

  10. Properties of chemically modified gelatin films

    Directory of Open Access Journals (Sweden)

    R. A. de Carvalho

    2006-03-01

    Full Text Available Edible and/or biodegradable films usually have limited water vapor barriers, making it difficult to use them. Thus, the objective of this work was to evaluate the effect of a chemical reticulation treatment with formaldehyde and glyoxal on the mechanical properties, water vapor permeability, solubility and color parameters of gelatin-based films. Formaldehyde and glyoxal were added to the filmogenic solution in concentrations ranging from 3.8 to 8.8 mmoles/100 mL of filmogenic solution and 6.3 to 26.3 mmoles/100 mL of filmogenic solution, respectively. The treatments caused a reduction in permeability to water vapor and in solubility. Only the treatment with formaldehyde caused a significant increase in rupture tension for concentrations above 6.3 mmoles/100 mL of filmogenic solution. Scanning electron microscopy indicated a loss of matrix orientation due to the chemical reticulation treatment.

  11. Polymer based on chemically modified starch

    Czech Academy of Sciences Publication Activity Database

    Horák, Pavel; Kruliš, Zdeněk; Šárka, E.; Kobera, Libor

    Praha : Ústav makromolekulární chemie AV ČR, v. v. i, 2014. s. 82. ISBN 978-80-85009-81-1. [Česko-slovenská konference POLYMERY 2014 /8./. 06.10.2014-09.10.2014, Třešť] R&D Projects: GA TA ČR(CZ) TA04020853 Institutional support: RVO:61389013 Keywords : starch * chemical modification * degree of substitution Subject RIV: CD - Macromolecular Chemistry

  12. Electrocatalytic oxidation of dihydronicotineamide adenine dinucleotide on gold electrode modified with catechol-terminated alkanethiol self-assembly

    International Nuclear Information System (INIS)

    Synthesis of a mercaptoundecaneamide derivative having a terminus of catechol is described. FT-IR spectroscopic characterization showed that the new molecular entry simply undergoes molecular self-assembly on Au substrate surfaces promoting intra- and intermolecular hydrogen bonds to form well-packed monolayers. Cyclic voltammetric (CV) measurements on the monolayer-modified Au electrode revealed that the surface adlayer possesses specific electrochemical activity due to the reversible catechol/o-quinone redox reaction having characteristics of a surface process and also pH-dependence in its formal potential (59 mV per pH). Detailed analysis of CVs gave fundamental electrochemical parameters including the electroactive surface coverage (0.20-0.24 nmol cm-2), the transfer coefficients (0.24 in oxidation and 0.81 in reduction), and also the electron transfer rate constant (1.10-2.76 s-1). These data were almost consistent to those seen in literature. We have also found that the catechol monolayer modified electrode exhibits an electrocatalytic function in NADH oxidation. That is, the faradaic current appeared reinforcingly at around the same potential where catechol function is oxidized in the monolayer and increased with an increase in the NADH concentration from 1 to 5 mM, and then reached to a plateau indicating a catalyzed reaction pathway. Detailed analyses revealed that the present system could be characterized by its weak stability of the intermediate compound formed and prompt reaction rate compared with the previously reported chemically modified electrode (CME) systems. We think this type of achievement should be important for the basics of biosensors that rely on dehydrogenase enzymes

  13. Electrochemically induced chemical sensor properties in graphite screen-printed electrodes: The case of a chemical sensor for uranium

    Energy Technology Data Exchange (ETDEWEB)

    Kostaki, Vasiliki T.; Florou, Ageliki B. [Laboratory of Analytical Chemistry, Department of Chemistry, University of Ioannina, 451 10 Ioannina (Greece); Prodromidis, Mamas I., E-mail: mprodrom@cc.uoi.gr [Laboratory of Analytical Chemistry, Department of Chemistry, University of Ioannina, 451 10 Ioannina (Greece)

    2011-10-01

    Highlights: > Electrochemical treatment endows analytical characteristics to SPEs. > A sensitive chemical sensor for uranium is described. > Performance is due to a synergy between electrochemical treatment and ink's solvents. > The amount of the solvent controls the achievable sensitivity. - Abstract: We report for the first time on the possibility to develop chemical sensors based on electrochemically treated, non-modified, graphite screen-printed electrodes (SPEs). The applied galvanostatic treatment (5 {mu}A for 6 min in 0.1 M H{sub 2}SO{sub 4}) is demonstrated to be effective for the development of chemical sensors for the determination of uranium in aqueous solutions. A detailed study of the effect of various parameters related to the fabrication of SPEs on the performance of the resulting sensors along with some diagnostic experiments on conventional graphite electrodes showed that the inducible analytical characteristics are due to a synergy between electrochemical treatment and ink's solvents. Indeed, the amount of the latter onto the printed working layer controls the achievable sensitivity. The preconcentration of the analyte was performed in an electroless mode in an aqueous solutions of U(VI), pH 4.6, and then, the accumulated species was reduced by means of a differential pulse voltammetry scan in 0.1 M H{sub 3}BO{sub 3}, pH 3. Under selected experimental conditions, a linear calibration curve over the range 5 x 10{sup -9} to 10{sup -7} M U(VI) was constructed. The 3{sigma} limit of detection at a preconcentration time of 30 min, and the relative standard deviation of the method were 4.5 x 10{sup -9} M U(VI) and >12% (n = 5, 5 x 10{sup -8} M U(VI)), respectively. The effect of potential interferences was also examined.

  14. 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

  15. Graphite felt modified with bismuth nanoparticles as negative electrode in a vanadium redox flow battery.

    Science.gov (United States)

    Suárez, David J; González, Zoraida; Blanco, Clara; Granda, Marcos; Menéndez, Rosa; Santamaría, Ricardo

    2014-03-01

    A graphite felt decorated with bismuth nanoparticles was studied as negative electrode in a vanadium redox flow battery (VRFB). The results confirm the excellent electrochemical performance of the bismuth modified electrode in terms of the reversibility of the V(3+) /V(2+) redox reactions and its long-term cycling performance. Moreover a mechanism that explains the role that Bi nanoparticles play in the redox reactions in this negative half-cell is proposed. Bi nanoparticles favor the formation of BiHx , an intermediate that reduces V(3+) to V(2+) and, therefore, inhibits the competitive irreversible reaction of hydrogen formation (responsible for the commonly observed loss of Coulombic efficiency of VRFBs). Thus, the total charge consumed during the cathodic sweep in this electrode is used to reduce V(3+) to V(2+) , resulting in a highly reversible and efficient process. PMID:24520000

  16. Novel Pt nanowires modified screen-printed gold electrode by electrodeposited method

    Energy Technology Data Exchange (ETDEWEB)

    Zhao Hongli; Zhou Changxiang; Teng Yuanjie; Chen Chen [Shanghai Key Laboratory of Functional Materials Chemistry, and Research Centre of Analysis and Test, East China University of Science and Technology, Shanghai 200237 (China); Lan Minbo, E-mail: minbolan@ecust.edu.cn [Shanghai Key Laboratory of Functional Materials Chemistry, and Research Centre of Analysis and Test, East China University of Science and Technology, Shanghai 200237 (China); State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237 (China)

    2011-02-01

    In this work, the preparation and characterization of novel Pt nanowires (Pt NWs) on the screen-printed gold electrode (SPGE) surface are reported. Firstly the mesoporous template was prepared by the electro-assisted self-assembly (EASA) method on the manual SPGE. Then, in the potentiostatic condition, Pt NWs were electrodeposited in the meosoporous channel on the Au electrode surface using the chronopotentiometry (CP) method at room temperature. The synthesized Pt NWs were characterized by cyclic voltammetry (CV), transmission electron microscopy (TEM) and energy dispersive X-ray (EDX) spectrometer. The results indicated that Pt NWs were successfully electrodeposited on the SPGE substrate, even the diameter of each Pt NWs could reach 3.2 nm. Furthermore, the SPGE could be mass produced conveniently and cost low which had very promising application prospect. And it is significant that the Pt NWs modified SPGE could function as an electrode in an electrochemical biosensor.

  17. Direct electrochemistry and electrocatalysis of myoglobin in dodecyltrimethylammonium bromide film modified carbon ceramic electrode

    Institute of Scientific and Technical Information of China (English)

    Yuan Zhen Zhou; Hui Wang; She Ying Dong; An Xiang Tian; Zhi Xian He; Bin Chen

    2011-01-01

    Direct electrochemistry and electrocatalysis of myoglobin (Mb) were studied with Mb immobilized on dodecyltrimethylammonium bromide (DTAB) film modified carbon ceramic (CC) electrode. Cyclic voltammetry showed a pair of well-defined and nearly reversible redox peaks of Mb (FeⅡ/FeⅢ) at about -0.3 V vs. SCE (pH = 6.98). The currents of the redox peak were linear to scan rate, and rate constant (Ks) was estimated to be 3.03 s-1. The formal potential (E01) of Mb in the DTAB/CC electrodes shifted linearly with pH with a slope of-36.44 mV/pH, implying that the electron transfer between DTAB and CC electrodes is accompanied by proton transportation. The immobilized Mb exhibited excellent electrocatalytic response to the reduction of hydrogen peroxide (H2O2).

  18. Indirect differential pulse voltammetric determination of aluminum by a pyrocatechol violet-modified electrode

    Energy Technology Data Exchange (ETDEWEB)

    Chen, G.; Bi, S.; Dai, L.; Cao, M.; Chen, Y. Wang, X. [Nanjing Univ. (China)

    1999-03-01

    Aluminum is one of the abundant elements in the earth`s crust. It has been considered to be a causative agent for various neurological disorders such as Alzheimer Senile, presenile dementia and amyotrophic lateral sclerosis. It is also very harmful to plants and aquatic organisms. Therefore, the determination of Al is very important. A Pyrocatechol Violet (PCV) modified electrode for the voltammetric determination of aluminum is reported. The modified electrode is simply prepared by dip-coating a pyrolytic graphite electrode in a NaAc-HAc buffer solution of PCV. Optimum experimental conditions for aluminum determination include a 0.2 mol/L NaAc-HAc buffer solution of pH 4.8, a PCV concentration of 0.02 mol/L used to modify the electrode and the use of differential-pulse mode for measurement. The peak currents of differential pulse voltammograms (DPV) decrease with the addition of Al into the buffer solution while the peak potentials remain the same. The decreasing value of peak current {Delta}i{sub p} is linear with Al concentration in the range of 1{times}10{sup {minus}8} to 1{times}10{sup {minus}7} mol/L and 1{times}10{sup {minus}7} to 1{times}10{sup {minus}6} mol/L. The detection limit is 5{times}10{sup {minus}9} mol/L and the relative standard deviation for 4{times}10{sup {minus}8} mol/L Al is 2.9% (n=8). The stability of this electrode is satisfactory. No serious interference is found. This method has been applied to determine Al in drinking water samples.

  19. Obtention of chemically modified clays: organovermiculites

    International Nuclear Information System (INIS)

    The organovermiculite is obtained by incorporating the quaternary ammonium salt in the clay mineral vermiculite interlayer space. The objective of this work was to prepare organovermiculites for applications in organic contaminants adsorption. The variation of interlayer space was determined when the vermiculite was treated with an ionic salt (Praepagem WB) and a non-ionic salt (Amina Etoxilada TA50) in different concentrations. Before interacting with quaternary ammonium salt, the clay mineral was subjected to cationic change process with Na2CO3 to substitute Mg2+ by Na+. The results showed enlargement of interlayer space, reaching values up to 60.0 Å. The vermiculite pre-activated with Na2CO3 during 5 days and modified with the Praepagem WB showed the best performance. Amina Etoxilada TA50 salt was not observed significant changes with increasing concentration. The affinity of organovermiculite for organic solvents was confirmed by Foster swelling test and the best results were observed with diesel and petrol as solvents. (author)

  20. The Study of Electrochemical Behavior of Dopamine at Nano-gold Modified Carbon Fiber Electrode

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The electrochemical behaviors (cyclic voltammetry, CV and different pulse voltammetry, DPV) of dopamine (DA) were studied in this paper. The result indicated that the oxidation of dopamine was controlled by diffusion and adsorption simultaneously at nano-gold (NG) modified carbon fiber electrode (CFE). This modified electrode can separate the peak potentials of dopamine and ascorbic acid (AA). The peak current of DA in DPV curve was found to be linearly proportional to the concentration of DA at range of 2.0×10-6~1.5×10-5mol/L and 1.0×10-5~5.0×10-4mol/L, respectively.

  1. Using Poly-L-Histidine Modified Glassy Carbon Electrode to Trace Hydroquinone in the Sewage Water

    Directory of Open Access Journals (Sweden)

    Bin Wang

    2014-01-01

    Full Text Available A sensitive voltammetric method for trace measurements of hydroquinone in the sewage water is described. The poly-L-histidine is prepared to modify the glassy carbon electrode in order to improve the electrochemical catalysis of interesting substances such as hydroquinone. The influence of the base solution, pH value, and scanning speed on the tracing of hydroquinone is discussed, and the experimental procedures and conditions are optimized. The laboratory results show that it is possible to construct a linear calibration curve between the peak current of hydroquinone on modified electrode and its concentration at the level of 0.00001 mol/L. The potential limitation of the method is suggested by a linear peaking shift model as well. The method was successfully applied to the determination of hydroquinone in the actual sample of industrial waste water.

  2. A glucose/O{sub 2} biofuel cell base on nanographene platelet-modified electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, W.; Zhao, H.Y.; Zhang, J.X.; Zhou, H.M.; Xu, X.X. [Center for Biomedical Materials and Engineering, Harbin Engineering University, Harbin 150001 (China); Zheng, Y.F.; Wang, Y.B.; Cheng, Y. [Center for Biomedical Materials and Tissue Engineering, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871 (China); Jang, B.Z. [College of Engineering and Computer Science, Wright State University, 3640 Colonel Glenn Hwy., Dayton, OH 45435 (United States)

    2010-07-15

    This study demonstrated a novel nanographene platelets (NGPs)-based glucose/O{sub 2} biofuel cell (BFC) with the glucose oxidase (GOD) as the anodic biocatalysts and the laccase as the cathodic biocatalysts. The GOD/NGPs-modified electrode exhibited good catalytic activity towards glucose oxidation and the laccase/NGPs-modified electrode exhibited good catalytic activity towards O{sub 2} electroreduction. The maximum power density was ca. 57.8 {mu}W cm{sup -} {sup 2} for the assembled glucose/O{sub 2} NGPs-based BFC. These results indicated that the NGPs were very useful for the future development of novel carbon-based nanomaterials BFC device. (author)

  3. Reduced graphene oxide-yttria nanocomposite modified electrode for enhancing the sensitivity of electrochemical genosensor.

    Science.gov (United States)

    Rasheed, P Abdul; Radhakrishnan, Thulasi; Shihabudeen, P K; Sandhyarani, N

    2016-09-15

    Reduced graphene oxide-yttria nanocomposite (rGO:Y) is applied as electrochemical genosensor platform for ultrahigh sensitive detection of breast cancer 1 (BRCA1) gene for the first time. The sensor is based on the sandwich assay in which gold nanoparticle cluster labeled reporter DNA hybridize to the target DNA. Glassy carbon electrode modified with rGO-yttria serves as the immobilization platform for capture probe DNA. The sensor exhibited a fine capability of sensing BRCA1 gene with linear range of 10attomolar (aM) to 1nanomolar (nM) and a detection limit of 5.95attomolar. The minimum distinguishable response concentration is down to the attomolar level with a high sensitivity and selectivity. We demonstrated that the use of rGO:Y modified electrode along with gold nanoparticle cluster (AuNPC) label leads to the highly sensitive electrochemical detection of BRCA1 gene. PMID:27153526

  4. Direct Electrochemistry of Glucose Oxidase at a Gold Electrode Modified with Single-Wall Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    Yuan Zhuobin

    2003-12-01

    Full Text Available The direct electrochemistry of glucose oxidase (GOD was accomplished at a gold electrode modified with single-wall carbon nanotubes (SWNTs. A pair of welldefined redox peaks was obtained for GOD with the reduction peak potential at –0.465 V and a peak potential separation of 23 mV at pH 7.0. Both FT-IR spectra and the dependence of the reduction peak current on the scan rate revealed that GOD adsorbed onto the SWNT surfaces. The redox wave corresponds to the redox center of the flavin adenine dinucleotide(FAD of the GOD adsorbate. The electron transfer rate of GOD redox reaction was greatly enhanced at the SWNT-modified electrode. The peak potential was shown to be pH dependent. Verified by spectral methods, the specific enzyme activity of GOD adsorbates at the SWNTs appears to be retained.

  5. 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.

  6. Cost-effective disposable thiourea film modified copper electrode for capacitive immunosensor

    International Nuclear Information System (INIS)

    Cost-effective disposable electrodes were fabricated from copper clad laminate, usually used for printed circuit board (PCB) in electronic industries, by using dry film photoresist. Electro-oxidation (anodisation) was employed to obtain a good formation of thiourea film on the electrode surface. The affinity binding pair of carcinoembryonic antigen (CEA) and anti-carcinoembryonic antigen (anti-CEA) was used as a model system. Anti-CEA was immobilized on thiourea film via covalent coupling. This modified electrode was incorporated with a capacitive system for CEA analysis. This capacitive immunosensor provided a linear range between 0.01 and 10 ng ml-1 with a detection limit of 10 pg ml-1. When applied to analyze CEA in serum samples, the results agreed well with the enzyme linked fluorescent assay (ELFA) technique (P > 0.05). The proposed strategy for the preparation of disposable modified copper electrode is very cost effective and simple. Moreover, it provides good reproducibility. This technique can easily be applied to immobilize other biological sensing elements for biosensors development.

  7. Cost-effective disposable thiourea film modified copper electrode for capacitive immunosensor

    Energy Technology Data Exchange (ETDEWEB)

    Limbut, Warakorn, E-mail: warakorn.l@psu.ac.t [Trace Analysis and Biosensor Research Center, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Center for Innovation in Chemistry, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Department of Applied Science, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Thavarungkul, Panote [Trace Analysis and Biosensor Research Center, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Center for Innovation in Chemistry, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Department of Physics, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Kanatharana, Proespichaya [Trace Analysis and Biosensor Research Center, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Center for Innovation in Chemistry, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Department of Chemistry, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Wongkittisuksa, Booncharoen [Trace Analysis and Biosensor Research Center, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Department of Electrical Engineering, Faculty of Engineering, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Asawatreratanakul, Punnee [Trace Analysis and Biosensor Research Center, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Department of Biochemistry, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Limsakul, Chusak [Trace Analysis and Biosensor Research Center, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand); Department of Electrical Engineering, Faculty of Engineering, Prince of Songkla University, Hat Yai, Songkhla 90112 (Thailand)

    2010-03-30

    Cost-effective disposable electrodes were fabricated from copper clad laminate, usually used for printed circuit board (PCB) in electronic industries, by using dry film photoresist. Electro-oxidation (anodisation) was employed to obtain a good formation of thiourea film on the electrode surface. The affinity binding pair of carcinoembryonic antigen (CEA) and anti-carcinoembryonic antigen (anti-CEA) was used as a model system. Anti-CEA was immobilized on thiourea film via covalent coupling. This modified electrode was incorporated with a capacitive system for CEA analysis. This capacitive immunosensor provided a linear range between 0.01 and 10 ng ml{sup -1} with a detection limit of 10 pg ml{sup -1}. When applied to analyze CEA in serum samples, the results agreed well with the enzyme linked fluorescent assay (ELFA) technique (P > 0.05). The proposed strategy for the preparation of disposable modified copper electrode is very cost effective and simple. Moreover, it provides good reproducibility. This technique can easily be applied to immobilize other biological sensing elements for biosensors development.

  8. Amperometric morphine sensing using a molecularly imprinted polymer-modified electrode

    International Nuclear Information System (INIS)

    This study incorporates morphine into a molecularly imprinted polymer (MIP) for the amperometric detection of morphine. The polymer, poly(3,4-ethylenedioxythiophene), PEDOT, is an electroactive film that catalyzes morphine oxidation and lowers the oxidization potential on an indium tin oxide (ITO) electrode. The MIP-PEDOT modified electrode is prepared by electropolymerizing PEDOT onto an ITO electrode in a 0.1 M LiClO4 solution with template addition (morphine). After template molecule extraction, the oxidizing current of the MIP-PEDOT modified electrode is measured in a 0.1 M KCl solution (pH = 5.3) at 0.75 V (versus Ag/AgCl/sat'd KCl) with the morphine concentration varying in the 0.1-5 mM range. A linear range, displaying the relationship between steady-state currents and morphine concentrations, from 0.1 to 1 mM, is obtained. The proposed amperometric sensor could be used for morphine detection with a sensitivity of 91.86 μA/cm2 per mM. A detection limit of 0.2 mM at a signal-to-noise ratio of 3 is achieved. Moreover, the proposed method can discriminate between morphine and its analogs, such as codeine

  9. Amperometric morphine sensing using a molecularly imprinted polymer-modified electrode

    Energy Technology Data Exchange (ETDEWEB)

    Yeh, W.-M. [Department of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan (China); Ho, K.-C. [Department of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan (China) and Institute of Polymer Science and Engineering, National Taiwan University, Taipei 10617, Taiwan (China)]. E-mail: kcho@ntu.edu.tw

    2005-06-22

    This study incorporates morphine into a molecularly imprinted polymer (MIP) for the amperometric detection of morphine. The polymer, poly(3,4-ethylenedioxythiophene), PEDOT, is an electroactive film that catalyzes morphine oxidation and lowers the oxidization potential on an indium tin oxide (ITO) electrode. The MIP-PEDOT modified electrode is prepared by electropolymerizing PEDOT onto an ITO electrode in a 0.1 M LiClO{sub 4} solution with template addition (morphine). After template molecule extraction, the oxidizing current of the MIP-PEDOT modified electrode is measured in a 0.1 M KCl solution (pH = 5.3) at 0.75 V (versus Ag/AgCl/sat'd KCl) with the morphine concentration varying in the 0.1-5 mM range. A linear range, displaying the relationship between steady-state currents and morphine concentrations, from 0.1 to 1 mM, is obtained. The proposed amperometric sensor could be used for morphine detection with a sensitivity of 91.86 {mu}A/cm{sup 2} per mM. A detection limit of 0.2 mM at a signal-to-noise ratio of 3 is achieved. Moreover, the proposed method can discriminate between morphine and its analogs, such as codeine.

  10. 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.

  11. DNA-modified Electrodes Fabricated using Copper-Free Click Chemistry for Enhanced Protein Detection

    OpenAIRE

    Furst, Ariel L.; Hill, Michael G.; Barton, Jacqueline K.

    2013-01-01

    A method of DNA monolayer formation has been developed using copper-free click chemistry that yields enhanced surface homogeneity and enables variation in the amount of DNA assembled; extremely low-density DNA monolayers, with as little as 5% of the monolayer being DNA, have been formed. These DNA-modified electrodes (DMEs) were characterized visually, with AFM, and electrochemically, and were found to facilitate DNA-mediated reduction of a distally bound redox probe. These low-density monola...

  12. Detection of Carbofuran with Immobilized Acetylcholinesterase Based on Carbon Nanotubes-Chitosan Modified Electrode

    OpenAIRE

    Shuping Zhang; Shaoyang Li; Jie Ma; Fei Xiong; Song Qu

    2013-01-01

    A sensitive and stable enzyme biosensor based on efficient immobilization of acetylcholinesterase (AChE) to MWNTs-modified glassy carbon electrode (GCE) with chitosan (CS) by layer-by-layer (LBL) technique for rapid determination of carbofuran has been devised. According to the inhibitory effect of carbamate pesticide on the enzymatic activity of AChE, we use carbofuran as a model pesticide. The inhibitory effect of carbofuran on the biosensor was proportional to concentration of carbofuran i...

  13. Electrochemical determination of phenol at natural phosphate modified carbon paste electrode

    OpenAIRE

    Tarik EL OUAFY; Abdelilah CHTAINI; Hassan OULFAJRITE; Rachida NAJIH

    2014-01-01

    A Cyclic voltammetry (VC) and Square Wave Voltammetry methods for the determination of trace amounts of phenol at carbon paste electrode modified with Natural Phosphate (NP-CPE) is proposed. The results showed that the NP-CPE exhibited excellent electro catalytic activity to phenol. The concentration of phenol and measuring solution pH was investigated. This electrochemical sensor shows an excellent performance for detecting phenol. The sensor was successfully applied to the determination ...

  14. Electrochemical behaviour of platinum at polymer-modified glassy carbon electrodes

    Indian Academy of Sciences (India)

    Carmem L P S Zanta; C A Martínez-Huitle

    2007-07-01

    In this paper, the preparations and voltammetric characteristics of chitosan-modified glassy carbon (Ct-MGC) and platinum electrodes are studied. Ct-MGC can be used for pre-concentration and quantification of trace amounts of platinum in solution. At low pH medium, the complex of Pt with protonated group -NH3+ in the chitosan molecule has been confirmed by FT-IR spectra studies.

  15. Microbial biofuel cell operating effectively through carbon nanotube blended with gold–titania nanocomposites modified electrode

    International Nuclear Information System (INIS)

    In this study, we have explored the possibility to fabricate microbial biofuel cell operating with carbon nanotube–gold–titania nanocomposites (CNT/Au/TiO2) as anode modifier. The results demonstrate that the CNT/Au/TiO2 electrode could be utilized as a new and effective microbial fuel cell (MFC) anode, which integrate the advantages of relevant nanocomposites such as high conductivity, high specific surface area, and easy adsorption of the microorganism. It is evident that the three-dimensional network nanostructures of CNT/Au/TiO2 are propitious to improve the relevant anode surface area and thus the adsorption of the microorganism, which can efficiently promote the electronic transfer rate between the probe and electrode. Meanwhile, it is noted that open circuit voltage of the CNT/Au/TiO2 nanocomposites modified carbon paper anode increased to 0.77 V, which is more than twice that of the open circuit voltage obtained with bare carbon paper anode (0.36 V). And the MFC equipped with CNT/Au/TiO2 nanocomposites modified carbon paper anode delivers a maximum power density of 2.4 mW m−2, which is three times larger than that obtained from the MFC with bare carbon paper. This observation illustrates that the CNT/Au/TiO2 nanocomposites modified electrode could obviously increase the relevant electron transfer rate and promote the electron exchange at electrode surface, which could readily provide enhanced stability and relatively long life-span to facilitate the high electricity production efficiency, suggesting its promising prospect application in MFCs

  16. Voltammetric Determination of Herbicide Triasulfuron using Mercury Meniscus Modified Silver Solid Amalgam Electrode

    Czech Academy of Sciences Publication Activity Database

    Bandžuchová, L.; Šelešovská, R.; Chýlková, J.; Navrátil, Tomáš

    Ústí nad Labem : Best servis, 2013 - (Navrátil, T.; Fojta, M.; Pecková, K.), s. 9-13 ISBN 978-80-905221-1-4. [Moderní elektrochemické metody /33./. Jetřichovice (CZ), 20.05.2013-24.05.2013] R&D Projects: GA ČR(CZ) GAP208/12/1645 Institutional support: RVO:61388955 Keywords : Triasulfuron * Voltammetry * Mercury meniscus modified silver solid amalgam electrode Subject RIV: CG - Electrochemistry

  17. Determination of Trace Thiocyanate by a Chitosan-Modified Glassy Carbon Electrode

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A chitosan-modified glassy carbon electrode(CMGCE) was employed for the determination of thiocyanate. The measurement was carried out by means of anodic stripping voltammetry. The effects of several experimental parameters, such as pH, the amount of modifier, deposition potential and deposition time were studied for analytical application, respectively. A liner response was obtained in the concentration range of 3.5×10-8-9.3×10-7 g/mL of SCN-. The detection limit was found to be 1.9×10-8 g/mL. The method was satisfactorily used to detect SCN- in saliva.

  18. Enhanced electrochemical oxidation of methanol on copper electrodes modified by electrocorrosion and electrodeposition

    Energy Technology Data Exchange (ETDEWEB)

    Carugno, Sofía [INQUIMAE – DQIAQF, Facultad de Ciencias, Exactas y Naturales, Universidad de Buenos Aires, Consejo Nacional de Investigaciones Científicas y Técnicas, 1428 Buenos Aires (Argentina); Chassaing, Elisabeth [IRDEP (UMR7174), EDF R and D, 6 Quai Watier, 78401 Chatou (France); Rosso, Michel [LPMC (UMR7643), CNRS, Ecole Polytechnique, F91128 Palaiseau Cedex (France); González, Graciela A., E-mail: graciela@qi.fcen.uba.ar [INQUIMAE – DQIAQF, Facultad de Ciencias, Exactas y Naturales, Universidad de Buenos Aires, Consejo Nacional de Investigaciones Científicas y Técnicas, 1428 Buenos Aires (Argentina)

    2014-02-14

    In this paper, we report a study of electrocatalytic oxidation of methanol on copper electrodes subjected to different surface treatments, either electrocorrosion or electrodeposition in the absence of strong hydrogen co-deposition. The surface morphology of treated electrodes was examined by Field Emission Scanning Electron Microscopy (FE-SEM). The effect of different treatment conditions and the methanol concentration dependence were evaluated by cyclic voltammetric technique. The results indicate that the oxidation of methanol can be enhanced by a suitable micro and nano structure generated by these treatments. This enhanced electrode activity is related to an increase of the effective surface area and/or to an increase of the surface concentration of electroactive molecules or intermediates. - Highlights: • We presented simple treatments to increase the response of copper electrodes. • Copper electrodes were modified by electrocorrosion and electrodeposition. • Scanning Electron Microscopy images reveal the effects of the different treatments. • The response is enhanced by an area increase and/or intermediates concentration. • For each treatment the concentration range of the diffusion control is analyzed.

  19. Voltammetric Determination of Paraquat Using Graphite Pencil Electrode Modified with Doped Polypyrrole

    CERN Document Server

    Sayyahmanesh, Maryam; Meibodi, Azam S Emami; Ahooyi, Taha Mohseni

    2016-01-01

    Recognition and determination of paraquat (PQ) using graphite pencil electrode (GPE) modified with polypyrrole (Ppy) doped with Eriochrome blue-black B (EBB) is reported. To that end, a thin film of Ppy was deposited onto the electrode surface by electropolymerization in the presence of a functional doping ion, EBB. The Ppy/EBB-coated electrode was templated by PQ ion and then the performance of the molecularly imprinted EBB/Ppy/GPE was evaluated by voltammetric technique. The prepared electrode exhibited considerable increase in electroactivity of the sensor toward this herbicide compared to the non-imprinted electrode. To enhance the detection capability of the prepared system, the factors controlling its response were investigated and optimized using differential pulse voltammetry. The proposed analytical procedure was proved to be applicable in the concentration range of 5 to 50 {\\mu}M (R^2 = 0.9939) and detection limit of (3{\\sigma}) 0.22 {\\mu}M. Ultimately, the proposed analytical methodology was applie...

  20. Electrochemical Recognition of Metalloproteins by Bromide-modified Silver Electrode - A New Method

    Directory of Open Access Journals (Sweden)

    Abbas Ali Rostami

    2007-07-01

    Full Text Available A bromide–modified silver electrode is reported, in the present study, to catalyzethe redox reactions of metalloproteins. This study describes that the bromide ions showvery good redox behavior with silver electrode. The cathodic and anodic peak potentialswere related to the concentration of bromide ions involved in making bromide-modifiedsilver electrode. The electrode reaction in the bromine solution was a diffusion-controlledprocess. Positive potential shift of the bromide ions was seen when different proteins wereadded to the solution using a silver electrode. New cathodic and anodic peaks wereobserved at different potential ranges for myoglobin, cytochrome c and catalase. A linearlyincreasing cathodic peak current of bromide ions was seen when the concentration ofsuperoxide dismutase was increased in the test solution. However, no change for albuminwas observed when its concentration was increased in the test solution. Present data provesour methodology as an easy-to-use analysis for comparing the redox potentials of differentmetalloproteins and differentiating the metallo- from non-metalloproteins. In this study, weintroduced an interesting method for bio-electrochemical analyses.

  1. Mixed azide-terminated monolayers: a platform for modifying electrode surfaces.

    Science.gov (United States)

    Collman, James P; Devaraj, Neal K; Eberspacher, Todd P A; Chidsey, Christopher E D

    2006-03-14

    We have prepared and characterized mixed self-assembled monolayers (SAM) on gold electrodes from azido alkane thiols and various omega-functionalized alkane thiols. In the presence of copper(I) catalysts, these azide-modified surfaces are shown to react rapidly and quantitatively with terminal acetylenes forming 1,2,3-triazoles, via "click" chemistry. The initial azide substituents can be identified and monitored using both grazing-angle infrared (IR) and X-ray photoelectron spectrosopies. Acetylenes possessing redox-active ferrocene substituents react with the azide-terminated mixed SAMs and electrochemical measurements of the ferrocene-modified SAM electrodes have been used to quantify the redox centers attached to these platforms. Time-resolved electrochemical measurements have enabled us to follow the formation of these ferrocene centers and thus to measure the rate of the surface "click" reaction. Under optimal conditions this well-behaved second-order reaction takes place with a rate constant of 1 x 10(3) M(-)(1) s(-)(1). Typical reaction times of several minutes were realized using micromolar concentrations of acetylene. These techniques have been used to construct well-characterized, covalently modified monolayers that can be employed as functional electrode surfaces. PMID:16519441

  2. Silver nanoparticle-modified electrode for the determination of nitro compound-containing pesticides.

    Science.gov (United States)

    de Lima, Camila Alves; Santana, Edson Roberto; Piovesan, Jamille Valéria; Spinelli, Almir

    2016-04-01

    This paper reports the electroanalytical determination of pendimethalin and ethyl parathion by square-wave adsorptive stripping voltammetry using a material comprised of chitosan-stabilized silver nanoparticles to modify a glassy carbon electrode. Under optimized experimental conditions, the peak current was found to vary linearly with the concentration of pendimethalin in the range of 70 to 2000 nmol L(-1) and with concentration of ethyl parathion in the range of 40 to 8000 nmol L(-1). Detection limits of 36 and 40 nmol L(-1) were obtained for pendimethalin and ethyl parathion, respectively. The silver - nanoparticle-modified electrode was successfully employed for the analysis of pesticides in tap and mineral water (pendimethalin) and in lettuce and honey (ethyl parathion) samples. Pendimethalin recovery was between 94 and 100 %, and ethyl parathion recovery was between 97 and 101 %, indicating no significant matrix interference effects on the analytical results. The accuracy of the electroanalytical methodology using the proposed modified electrode was also compared to that of the UV-vis spectrophotometric method. PMID:26873207

  3. Electrochemical Glucose Oxidation Using Glassy Carbon Electrodes Modified with Au-Ag Nanoparticles: Influence of Ag Content

    Directory of Open Access Journals (Sweden)

    Nancy Gabriela García-Morales

    2015-01-01

    Full Text Available This paper describes the application of glassy carbon modified electrodes bearing Aux-Agy nanoparticles to catalyze the electrochemical oxidation of glucose. In particular, the paper shows the influence of the Ag content on this oxidation process. A simple method was applied to prepare the nanoparticles, which were characterized by transmission electron microscopy, Ultraviolet-Visible spectroscopy, X-ray diffraction spectroscopy, and cyclic voltammetry. These nanoparticles were used to modify glassy carbon electrodes. The effectiveness of these electrodes for electrochemical glucose oxidation was evaluated. The modified glassy carbon electrodes are highly sensitive to glucose oxidation in alkaline media, which could be attributed to the presence of Aux-Agy nanoparticles on the electrode surface. The voltammetric results suggest that the glucose oxidation speed is controlled by the glucose diffusion to the electrode surface. These results also show that the catalytic activity of the electrodes depends on the Ag content of the nanoparticles. Best results were obtained for the Au80-Ag20 nanoparticles modified electrode. This electrode could be used for Gluconic acid (GA production.

  4. Fabrication of alpha-Fe2O3 nanopowder modified glassy carbon electrode for applications in electrochemical sensing.

    Science.gov (United States)

    Goyal, Rajendra N; Pandey, Ashish K; Kaur, Davinder; Kumar, Ashvani

    2009-08-01

    In the present study, Fe2O3 nanopowder has been grown by Ultrasonic mist chemical vapor deposition (UM-CVD), which is a promising method for large area deposition at low temperatures taking in to account of its simplicity, inexpensiveness and safety. Room temperature XRD results revealed prominent hematite phase with intense (104) reflection and was also in agreement with the HR-TEM results. In situ high temperature X-ray diffraction (XRD) studies clearly indicated the change of phase from hematite to magnetite as the temperature increases above 300 degrees C. The surface morphology and particle size distribution of Fe2O3 nanopowder were characterized using field emission scanning electron microscope (FE-SEM) and high resolution transmission electron microscope (HR-TEM), which revealed that the particles were spherical in nature and distributed in range of 50-100 nm. SQUID magnetometry results indicate the ferromagnetic nature of the nanopowder with crystallite size of 6 nm as calculated from M-H curve. Transmittance of approximately 55% and estimated direct band gap of 2.5 eV was observed. Further, the nanopowder was used to modify glassy carbon electrode (GCE) and the modified electrode was found to exhibit electrocatalytic activity for the oxidation of dopamine. It is expected that the nanopowder will exhibit promising applications in the development of sensors. PMID:19928136

  5. Double-ion imprinted polymer @magnetic nanoparticles modified screen printed carbon electrode for simultaneous analysis of cerium and gadolinium ions.

    Science.gov (United States)

    Prasad, Bhim Bali; Jauhari, Darshika

    2015-05-22

    A typical, reproducible, and rugged screen printed carbon electrode, modified with dual-ion imprinted beads, was fabricated employing the "surface grafting from" approach. For this, the acyl chloride functionalized magnetic nanoparticles were first immobilized and chemically attached with a typical functional monomer (but-2-enedioic acid bis-[(2-amino-ethyl)-amide]) on the electrode surface. This was subsequently subjected to the thermal polymerization in the presence of template ions (Ce(IV) and Gd(III)), cross-linker (ethylene glycol dimethacrylate), initiator (AIBN), and multiwalled carbon nanotubes. The modified sensor was used for the simultaneous analysis of both template ions in aqueous, blood serum, and waste-water samples, using differential pulse anodic stripping voltammetry which revealed two oxidation peaks for respective templates with resolution as much as 950 mV, without any cross reactivity, interferences and false-positives. The detection limits realized by the proposed sensor, under optimized conditions, were found to be as low as 0.07 ng mL(-1) for Ce(IV) and 0.19 ng mL(-1) for Gd(III) (S/N=3) that could eventually be helpful for lanthanide estimation at stringent levels. PMID:25937109

  6. Theory of water desalination by porous electrodes with fixed chemical charge

    OpenAIRE

    Biesheuvel, P. M.; Suss, M. E.; Hamelers, H.V.M.

    2015-01-01

    Water desalination by capacitive deionization (CDI) is performed via electrochemical cells consisting of two porous carbon electrodes. Upon transferring charge from one electrode to the other, ions are removed from the feedwater by electrosorption into electrical double layers (EDLs) within the micropores of the porous carbon. When using electrodes containing fixed chemical charge in the micropores, various counterintuitive observations have been made, such as "inverted CDI" where upon chargi...

  7. Chemically-Modified Cellulose Paper as a Microstructured Catalytic Reactor

    Directory of Open Access Journals (Sweden)

    Hirotaka Koga

    2015-01-01

    Full Text Available We discuss the successful use of chemically-modified cellulose paper as a microstructured catalytic reactor for the production of useful chemicals. The chemical modification of cellulose paper was achieved using a silane-coupling technique. Amine-modified paper was directly used as a base catalyst for the Knoevenagel condensation reaction. Methacrylate-modified paper was used for the immobilization of lipase and then in nonaqueous transesterification processes. These catalytic paper materials offer high reaction efficiencies and have excellent practical properties. We suggest that the paper-specific interconnected microstructure with pulp fiber networks provides fast mixing of the reactants and efficient transport of the reactants to the catalytically-active sites. This concept is expected to be a promising route to green and sustainable chemistry.

  8. Highly dispersed Pd nanoparticles on chemically modified graphene with aminophenyl groups for formic acid oxidation

    Institute of Scientific and Technical Information of China (English)

    Yang Su-Dong; Shen Cheng-Min; Tong Hao; He Wei; Zhang Xiao-Gang; Gao Hong-Jun

    2011-01-01

    A novel electrode material based on chemically modified graphene (CMG) with aminophenyl groups is covalently functionalized by a nucleophilic ring-opening reaction between the epoxy groups of graphene oxide and the aminophenyl groups of p-phenylenediamine.Palladium nanoparticles with an average diameter of 4.2 nm are deposited on the CMG by a liquid-phase borohydride reduction.The electrocatalytic activity and stability of the Pd/CMG composite towards formic acid oxidation are found to be higher than those of reduced graphene oxide and commercial carbon materials such as Vulcan XC-72 supported Pd electrocatalysts.

  9. Highly dispersed Pd nanoparticles on chemically modified graphene with aminophenyl groups for formic acid oxidation

    International Nuclear Information System (INIS)

    A novel electrode material based on chemically modified graphene (CMG) with aminophenyl groups is covalently functionalized by a nucleophilic ring-opening reaction between the epoxy groups of graphene oxide and the aminophenyl groups of p-phenylenediamine. Palladium nanoparticles with an average diameter of 4.2 nm are deposited on the CMG by a liquid-phase borohydride reduction. The electrocatalytic activity and stability of the Pd/CMG composite towards formic acid oxidation are found to be higher than those of reduced graphene oxide and commercial carbon materials such as Vulcan XC-72 supported Pd electrocatalysts. (atomic and molecular physics)

  10. Chemical attachment of functionalized multiwalled carbon nanotubes on glassy carbon electrode for electrocatalytic application

    International Nuclear Information System (INIS)

    Highlights: • FMWCNTs were covalently attached on GC surface with the aid of alkyldiamine. • The attached FMWCNTs were stable for a wide potential window due to the robust C−N bond. • The composite electrode was prepared by electropolymerizing thiadiazole on FMWCNTs. • The detection limit of 0.27 μM (S/N = 3) of GMP was achieved using composite modified electrode. - Abstract: The covalent attachment of acid functionalized multiwalled carbon nanotubes (FMWCNTs) on glassy carbon (GC) electrode using 1,8-octanediamine (OD) as a linker via carbodiimide chemistry was described. The attachment of FMWCNTs on GC electrode were confirmed by attenuated total reflectance Fourier transform infra-red (ATR-FT-IR) spectroscopy, Raman, scanning electron microscopy (SEM) and electrochemical impedance studies. Raman spectrum of FMWCNTs modified surface shows the characteristic G and D bands at 1563 cm−1 and 1340 cm−1, respectively. This confirmed the successful attachment of FMWCNTs on the OD modified GC surface. Further, the attachment of FMWCNTs on OD modified surface via amide linkage was confirmed from the observed characteristic peak at 1681 cm−1 in the ATR-FT-IR spectrum. The SEM images showed that the covalently attached FMWCNTs retained their morphology similar to powder and the average diameter of them was found to be 58 nm. Unlike modification of FMWCNTs on gold substrates with the aid of conventional thiol linkers (Au−S bond), modification of them by the present method was stable for a wide positive potential window due to the robust C−N bond. To demonstrate the electrochemical stability of the MWCNTs modified electrode at more positive potential, guanosine 5′-monophosphate (GMP) was selected as a representative probe because its oxidation occurs at more than 1 V. It was found that the FMWCNTs modified electrode not only showed a stable signal for GMP but also enhanced its oxidation current when compared to bare GC electrode. Further, the present

  11. Development and characterization of fluorine tin oxide electrodes modified with high area porous thin films containing gold nanoparticles

    International Nuclear Information System (INIS)

    Different electrode materials are prepared using fluoride doped tin oxide (FTO) electrodes modified with high area porous thin films of metal oxides containing gold nanoparticles. Three different metal oxides (TiO2, MgO and SnO2) have been assayed to this end. The effect of the metal oxide nature and gold loading on the structure and performance of the modified electrodes was examined by Scanning Electron Microscopy, Transmission Electron Microscopy, X-Ray Diffraction (XRD), Diffuse Reflectance Spectroscopy and electrochemical techniques. XRD measurements reveal that MgO electrodes present the smallest gold nanoparticles after the sintering step however, the electrochemical response of these electrodes shows important problems of mass transport derived from the high porosity of these materials (Brunauer Emmett Teller area of 125 m2/g). The excellent sintering properties of titania nanoparticles result in robust films attached to the FTO electrodes which allow more reliable and reproducible results from an electroanalytical point of view.

  12. High PEC conversion efficiencies from CuSe film electrodes modified with metalloporphyrin/polyethylene matrices

    International Nuclear Information System (INIS)

    Enhancement of hole-transfer across CuSe electrode/liquid junction can be facilitated by coating with metalloporphyrin complexes embedded inside polyethylene matrices. - Highlights: • CuSe films were electrochemically deposited onto FTO/Glass • Annealing CuSe film electrodes enhanced PEC characteristics • PEC characteristics were further enhanced by metalloporphyrin/polyethylene matrices, yielding ∼15% efficiency • Matrix behavior as charge transfer mediator enhanced electrode conversion efficiency and stability - Abstract: Electrodeposited CuSe film electrodes have been prepared onto FTO/glass by a facile method based on earlier methods described for other systems. The films were characterized, modified by annealing and further characterized. The films were then modified by coating with tetra(-4-pyridyl) pophyrinato-manganese (MnTPyP) complexes embedded inside commercial polyethylene (PE) matrices. The effects of modifications on different film properties, such as X-ray diffraction (XRD) patterns, surface morphology, photoluminescence (PL) spectra and electronic absorption spectra were investigated. Compared with other thin film electrode systems, very high photoelectrochemical (PEC) conversion efficiency values have been observed here. Pre-annealing the CuSe films at 150°C for 2 h, followed by attaching the MnTPyP/PE matrices remarkably enhanced their PEC characteristics. The conversion efficiency was significantly enhanced, from less than 1.0% to more than 15%. Fill factor (FF) was also enhanced from ∼30% to ∼80%. Values of open-circuit potential (VOC) and short-circuit current (JSC) were significantly enhanced. While annealing affects uniformity, particle inter-connection and surface texture of the CuSe films, the MnTPyP complex species behaves as an additional charge-transfer mediator across the film/electrolyte junction. Optimization of PEC characteristics, using different deposition times, different annealing temperatures, different annealing

  13. Voltammetric Detection of Mn(II in Blood Sample at C60 and MWCNT Modified Glassy Carbon Electrodes

    Directory of Open Access Journals (Sweden)

    Muhammed M. Radhi

    2010-01-01

    Full Text Available Problem statement: Glassy carbon electrode GCE was modified with different microparticles to increase the efficiency of analysis Mn2+ in blood samples by cyclic voltammetry and applied for the detection of trace Mn(II by oxidation process. Approach: The structure and composition of the modified GCE processed by using Carbon Nanotubes CNT and C60 to produce two modified electrodes CNT/GCE and C60/GCE, to detect a trace Mn2+ by cyclic voltammetry for mouse blood with comparison the best modified electrode for detection the ion by the sensitivity and values of Relative Standard Deviation (RSD in calibration curve. Results: A wide linear range and good repeatability were obtained for Mn2+ detection by CNT/GCE in aqueous KCl as supporting electrolyte at different ratio of KCl: Blood using CNT/GCE and C60/GCE, the relative standard deviation of two modified electrodes are good on CNT/GCE than C60/GCE. Conclusion: The two modified electrodes CNT/GCE and C60/GCE depending on the redox current of Mn(II ions were evaluated by the determination of low concentration of Mn(II in blood samples by cyclic voltammetric method, the most modified electrode to detect the Mn(II in blood is CNT/GCE.

  14. Polyoxometalate-Graphene Nanocomposite Modified Electrode for Electrocatalytic Detection of Ascorbic Acid

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Weiying; Du, Dan; Gunaratne, Don; Colby, Robert; Lin, Yuehe; Laskin, Julia

    2013-11-15

    Phosphomolybdate functionalized graphene nanocomposite (PMo12-GS) has been successfully formed on a glassy carbon electrode (GCE) for the detection of ascorbic acid (AA). The obtained PMo12-GS modified GCE, was characterized by cyclic voltammetry, electrochemical impedance spectroscopy, scanning electron microscopy (SEM) and Fourier transform infrared (FT-IR) spectroscopy and compared with GCE, GS modified GCE, and PMo12 modified GCE. It shows an increased current and a decrease in over-potential of ~210 mV. The amperometric signals are linearly proportional to the AA concentration in a wide concentration range from 1×10-6 M to 8×10-3 M, with a detection limit of 0.5×10-6 M. Finally, the PMo12-GS modified electrode was employed for the determination of the AA level in vitamin C tablets, with recoveries between 96.3 and 100.8 %.

  15. 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.

  16. Electrogeneration of hydrogen peroxide in acidic medium using gas diffusion electrodes modified with cobalt (II) phthalocyanine

    International Nuclear Information System (INIS)

    Hydrogen peroxide (H2O2) is a commonly used oxidant with a wide variety of applications in, for example, organic synthesis and wastewater treatment. This paper describes the development of catalysts for the electrogeneration of H2O2 in acidic medium using gas diffusion electrodes (GDE). Initial experiments were performed using rotating ring-disk electrodes modified with microporous layers of Printex 6L carbon containing various amounts of cobalt (II) phthalocyanine (CoPc) in order to evaluate catalytic activities. The results showed that the current efficiency for the formation of H2O2 increased from 69.7% for Printex 6L carbon without catalyst to 81.5% when using Printex 6L carbon with CoPc, and this was accompanied by a decrease in the number of electrons involved in the oxygen reduction reaction from 2.6 to 2.3. Based on these findings, modified GDEs were constructed containing 3.0, 5.0 and 10.0% of CoPc on Printex 6L carbon. The concentration of H2O2 that formed after 90 min electrolysis with the GDE modified with Printex 6L carbon alone was 176 mg L−1, while the GDE with 5.0% CoPc on carbon produced 331 mg L−1 of H2O2, i.e. an increase in yield of 89.1% relative to Printex 6L carbon. Additionally, using GDE s modified with CoPc on carbon, the potential at which H2O2 formation attained its maximum value shifted to less negative values in comparison with electrodes without catalyst. It is concluded that CoPc is an appropriate catalyst for efficient electrogeneration of H2O2

  17. Reduced Graphene Oxide Modified the Interdigitated Chain Electrode for an Insulin Sensor

    Directory of Open Access Journals (Sweden)

    Ajay Kumar Yagati

    2016-01-01

    Full Text Available Insulin is a key regulator in glucose homeostasis and its deficiency or alternations in the human body causes various types of diabetic disorders. In this paper, we present the development of a reduced graphene oxide (rGO modified interdigitated chain electrode (ICE for direct capacitive detection of insulin. The impedance properties of rGO-ICE were characterized by equivalent circuit modeling. After an electrochemical deposition of rGO on ICE, the electrode was modified with self-assembled monolayers and insulin antibodies in order to achieve insulin binding reactions. The impedance spectra and capacitances were measured with respect to the concentrations of insulin and the capacitance change (ΔC was analyzed to quantify insulin concentration. The antibody immobilized electrode showed an increment of ΔC according to the insulin concentration in human serum ranging from 1 ng/mL to 10 µg/mL. The proposed sensor is feasible for label-free and real-time measuring of the biomarker and for point-of-care diagnosis.

  18. Reduced Graphene Oxide Modified the Interdigitated Chain Electrode for an Insulin Sensor.

    Science.gov (United States)

    Yagati, Ajay Kumar; Park, Jinsoo; Cho, Sungbo

    2016-01-01

    Insulin is a key regulator in glucose homeostasis and its deficiency or alternations in the human body causes various types of diabetic disorders. In this paper, we present the development of a reduced graphene oxide (rGO) modified interdigitated chain electrode (ICE) for direct capacitive detection of insulin. The impedance properties of rGO-ICE were characterized by equivalent circuit modeling. After an electrochemical deposition of rGO on ICE, the electrode was modified with self-assembled monolayers and insulin antibodies in order to achieve insulin binding reactions. The impedance spectra and capacitances were measured with respect to the concentrations of insulin and the capacitance change (ΔC) was analyzed to quantify insulin concentration. The antibody immobilized electrode showed an increment of ΔC according to the insulin concentration in human serum ranging from 1 ng/mL to 10 µg/mL. The proposed sensor is feasible for label-free and real-time measuring of the biomarker and for point-of-care diagnosis. PMID:26784202

  19. 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.

  20. An enzymatic glucose biosensor based on a glassy carbon electrode modified with manganese dioxide nanowires

    International Nuclear Information System (INIS)

    A glassy carbon electrode was modified with β-manganese dioxide (β-MnO2), and glucose oxidase (GOx) was immobilized on its surface. The β-MnO2 nanowires were prepared by a hydrothermal method and characterized by scanning electron microscopy and powder X-ray diffraction. They were then dispersed in Nafion solution and cast on the glassy carbon electrode (GCE) to form an electrode modified with β-MnO2 nanowires that exhibits improved sensitivity toward hydrogen peroxide. If GOx is immobilized in the surface, the β-MnO2 acts as a mediator, and Nafion as a polymer backbone. The fabrication process was characterized by electrochemical impedance spectroscopy, and the sensor and its materials were characterized by cyclic voltammetry and amperometry. The biosensor enables amperometric detection of glucose with a sensitivity of 38.2 μA · mM−1 · cm−2, and a response time of 2 nanowires. (author)

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

    Science.gov (United States)

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

    2014-08-01

    The preparation and application of a practical electrochemical sensor for environmental monitoring and assessment of heavy metal ions in samples is a subject of considerable interest. In this paper, a carbon paste electrode modified with maize tassel for the determination of Cu(II) has been proposed. Scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) were used to study morphology and identify the functional groups on the modified electrode, respectively. First, Cu(II) was adsorbed on the carbon paste electrode surface at open circuit and voltammetric techniques were used to investigate the electrochemical performances of the sensor. The electrochemical sensor showed an excellent electrocatalytic activity towards Cu(II) at pH 5.0 and by increasing the amount of maize tassel biomass, a maximum response at 1:2.5 (maize tassel:carbon paste; w/w) was obtained. The electrocatalytic redox current of Cu(II) showed a linear response in the range (1.23 μM to 0.4 mM) with the correlation coefficient of 0.9980. The limit of detection and current-concentration sensitivity were calculated to be 0.13 (±0.01) μM and 0.012 (±0.001) μA/μM, respectively. The sensor gave good recovery of Cu(II) in the range from 96.0 to 98.0 % when applied to water samples. PMID:24705875

  2. Electrocatalytic oxidation of ethanol on various metal ad-layer modified Au(111) electrodes in alkaline solution

    OpenAIRE

    DURSUN, Zekerya; KARABİBEROĞLU, Şükriye ULUBAY; GELMEZ, Buket

    2011-01-01

    Ethanol oxidation was studied on single-crystal Au(111) electrodes that were modified by platinum, palladium, and cadmium metal ad-layers. The metal ad-layer modification was carried out by the underpotential deposition process, in which controlled amounts of Pt, Pd, and Cd were electrodeposited onto the substrate as submonolayer or monolayer coverage. The activity of the metal ad-layer modified Au(111) electrodes toward ethanol oxidation was studied in alkaline media, and recorded v...

  3. Studying the ion transfer across liquid interface of thin organic-film-modified electrodes in the presence of glucose oxidase

    OpenAIRE

    Mirceski, Valentin; Mitrova, Biljana; Ivanovski, Vladimir; Mitreska, Nikolina; Aleksovska, Angela; Gulaboski, Rubin

    2015-01-01

    A coupled electron-ion transfer reaction at thin organic-film-modified electrodes (TFE) is studied in the presence of glucose oxidase (GOx) under voltammetric conditions. TFE consists of a graphite electrode modified with a nitrobenzene solution of decamethylferrocene (DMFC) as a redox mediator and tetrabuthylammonium perchlorate as an organic-supporting electrolyte, in contact with aqueous buffer solutions containing percholarte ions and GOx. The redox turnover of DMFC coupled with perchl...

  4. Reactive chemically modified piezoelectric crystal detectors: A new class of high-selectivity sensors

    International Nuclear Information System (INIS)

    A great number of works have focused on the study of properties of modified piezoelectric quartz crystal detectors (PQCDs) coated with sorbing substrates and on applying sensors based on them for the analysis of diluted gas mixtures and solutions. This work offers a new class of gravemetric sensors characterized by a reversible chemical reaction that occurs on their surface. Silica films are proposed as a sorbing coating of quartz detectors, and a chemical modification of a surface is suggested for covalent fixation of the necessary compounds. PQCDs were chemically modified with reactive diene derivatives that can also act as dienophiles. Hexachlorocyclopentadiene (HCCPD, resonater I) and cyclopentadiene (CPD, resonator II) were fixed on a PQCD surface in several stages. After treatment with the resonaters, the PQCD in a CPD gas phase exhibited time dependent frequency shifts from 20-100 Hz. The results suggest that there is a reversible chemical reaction on the electrode surface of resonators I and II when they interact with CPD vapors. Therefore, PQCDs modified with reactive dienes were prepared for the first time and may be employed as selective sensors for CPD

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

    Directory of Open Access Journals (Sweden)

    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.

  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. Gold nanoparticle-coated multiwall carbon nanotube-modified electrode for electrochemical determination of methyl parathion

    International Nuclear Information System (INIS)

    We report on an electrochemical sensor for the determination of methyl parathion. It is based on an electrode modified with multi-walled carbon nanotubes that were covered with gold nanoparticles (Au-NPs). The vertically aligned array of MWCNTs on a tantalum substrate was coated with Au-NPs by overhead magnetron sputtering deposition. Scanning and transmission electron microscopy and XRD were used to characterize the Au-NP-MWCNTs composite. Cyclic voltammetry and differential pulse voltammetry were employed to evaluate the suitability of the new electrode for the determination of methyl parathion. Under the optimal conditions, the current response of the electrode to methyl parathion is linear in the range from 0.50 to 16.0 mg mL-1, with a detection limit of 50 μg mL-1 (signal/noise = 3), and the sensitivity is 4.5 times better than that of the plain MWCNTs electrode. We conclude that this method represents a simple, rapid, effective and sensitive approach for the detection of methyl parathion. (author)

  8. Graphene-modified Electrodes for Enhancing the Performance of Microbial Fuel Cells

    OpenAIRE

    Yuan, Heyang; He, Zhen

    2014-01-01

    Graphene is an emerging material with superior physical and chemical properties, which can benefit the development of microbial fuel cells (MFC) in several aspects. Graphene-based anodes can enhance MFC performance with increased electron transfer efficiency, higher specific surface area and more active microbe-electrode-electrolyte interaction. For cathodic processes, oxygen reduction reaction is effectively catalyzed by graphene-based materials because of a favorable pathway and an increase...

  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. Biosorption of uranium by chemically modified Rhodotorula glutinis

    Energy Technology Data Exchange (ETDEWEB)

    Bai Jing, E-mail: baijing@impcas.ac.c [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); Graduate University of Chinese Academy of Sciences, Beijing 100049 (China); Yao Huijun [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); Fan Fangli; Lin Maosheng [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); Graduate University of Chinese Academy of Sciences, Beijing 100049 (China); Zhang Lina; Ding Huajie; Lei Fuan; Wu Xiaolei [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); Li, Xiaofei [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); Graduate University of Chinese Academy of Sciences, Beijing 100049 (China); Guo Junsheng; Qin Zhi [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China)

    2010-11-15

    The present paper reports the biosorption of uranium onto chemically modified yeast cells, Rhodotorula glutinis, in order to study the role played by various functional groups in the cell wall. Esterification of the carboxyl groups and methylation of the amino groups present in the cells were carried out by methanol and formaldehyde treatment, respectively. The uranium sorption capacity increased 31% for the methanol-treated biomass and 11% for the formaldehyde-treated biomass at an initial uranium concentration of 140 mg/L. The enhancement of uranium sorption capacity was investigated by Fourier transform infrared (FTIR) spectroscopy analysis, with amino and carboxyl groups were determined to be the important functional groups involved in uranium binding. The biosorption isotherms of uranium onto the raw and chemically modified biomass were also investigated with varying uranium concentrations. Langmuir and Freundlich models were well able to explain the sorption equilibrium data with satisfactory correlation coefficients higher than 0.9. -- Research highlights: {yields} Uranium biosorption on to chemically modified yeast cells {yields} Cells before and after uranium sorption were investigate by FTIR spectroscopy {yields} Amino and carboxyl groups were important functional groups involved in uranium binding {yields} The sorption equilibrium date of raw and chemically modified biomass fitted well with Langmuir and Freundlich models

  11. Double-ion imprinted polymer @magnetic nanoparticles modified screen printed carbon electrode for simultaneous analysis of cerium and gadolinium ions

    Energy Technology Data Exchange (ETDEWEB)

    Prasad, Bhim Bali, E-mail: prof.bbpd@yahoo.com; Jauhari, Darshika

    2015-05-22

    Highlights: • Synthesis of a double-ion imprinted polymer for analysis of Ce(IV) and Gd(III). • Imprinted nano-beads were grown on MNPs-modified SPCE surface. • Voltammetric determination of both templates was carried out simultaneously. • Ultra-trace analysis with LOD (ng mL{sup −1}) 0.07 for Ce(IV) and 0.19 for Gd(III) is achieved. - Abstract: A typical, reproducible, and rugged screen printed carbon electrode, modified with dual-ion imprinted beads, was fabricated employing the “surface grafting from” approach. For this, the acyl chloride functionalized magnetic nanoparticles were first immobilized and chemically attached with a typical functional monomer (but-2-enedioic acid bis-[(2-amino-ethyl)-amide]) on the electrode surface. This was subsequently subjected to the thermal polymerization in the presence of template ions (Ce(IV) and Gd(III)), cross-linker (ethylene glycol dimethacrylate), initiator (AIBN), and multiwalled carbon nanotubes. The modified sensor was used for the simultaneous analysis of both template ions in aqueous, blood serum, and waste-water samples, using differential pulse anodic stripping voltammetry which revealed two oxidation peaks for respective templates with resolution as much as 950 mV, without any cross reactivity, interferences and false-positives. The detection limits realized by the proposed sensor, under optimized conditions, were found to be as low as 0.07 ng mL{sup −1} for Ce(IV) and 0.19 ng mL{sup −1} for Gd(III) (S/N = 3) that could eventually be helpful for lanthanide estimation at stringent levels.

  12. Double-ion imprinted polymer @magnetic nanoparticles modified screen printed carbon electrode for simultaneous analysis of cerium and gadolinium ions

    International Nuclear Information System (INIS)

    Highlights: • Synthesis of a double-ion imprinted polymer for analysis of Ce(IV) and Gd(III). • Imprinted nano-beads were grown on MNPs-modified SPCE surface. • Voltammetric determination of both templates was carried out simultaneously. • Ultra-trace analysis with LOD (ng mL−1) 0.07 for Ce(IV) and 0.19 for Gd(III) is achieved. - Abstract: A typical, reproducible, and rugged screen printed carbon electrode, modified with dual-ion imprinted beads, was fabricated employing the “surface grafting from” approach. For this, the acyl chloride functionalized magnetic nanoparticles were first immobilized and chemically attached with a typical functional monomer (but-2-enedioic acid bis-[(2-amino-ethyl)-amide]) on the electrode surface. This was subsequently subjected to the thermal polymerization in the presence of template ions (Ce(IV) and Gd(III)), cross-linker (ethylene glycol dimethacrylate), initiator (AIBN), and multiwalled carbon nanotubes. The modified sensor was used for the simultaneous analysis of both template ions in aqueous, blood serum, and waste-water samples, using differential pulse anodic stripping voltammetry which revealed two oxidation peaks for respective templates with resolution as much as 950 mV, without any cross reactivity, interferences and false-positives. The detection limits realized by the proposed sensor, under optimized conditions, were found to be as low as 0.07 ng mL−1 for Ce(IV) and 0.19 ng mL−1 for Gd(III) (S/N = 3) that could eventually be helpful for lanthanide estimation at stringent levels

  13. Hydrogen peroxide biosensor based on DNA-Hb modified gold electrode

    International Nuclear Information System (INIS)

    A hydrogen peroxide (H2O2) biosensor based on DNA-hemoglobin (Hb) modified electrode is described in this paper. The sensor was designed by DNA and hemoglobin dropletting onto gold electrode surface layer by layer. The sensor based on the direct electron transfer of iron of hemoglobin showed a well electrocatalytic response to the reduction of the H2O2. This sensor offered an excellent electrochemical response for H2O2 concentration below micromole level with high sensitivity and selectivity and short response time. Experimental conditions influencing the biosensor performance such as, pH, potential were optimized and assessed. The levels of the RSD's (2O2 was observed from 10 to 120 μM with the detection limit of 0.4 μM (based on the S/N = 3)

  14. Voltammetric sensor for caffeine based on a glassy carbon electrode modified with Nafion and graphene oxide

    International Nuclear Information System (INIS)

    We report on a voltammetric sensor for caffeine that is based on a glassy carbon electrode modified with Nafion and graphene oxide (GO). It exhibits a good affinity for caffeine (resulting from the presence of Nafion), and excellent electrochemical response (resulting from the pressence of GO) for the oxidation of caffeine. The electrode enables the determination of caffeine in the range from 4.0 x 10-7 to 8.0 x 10-5 mol L-1, with a detection limit of 2.0 x 10-7 mol L-1. The sensor displays good stability, reproducibility, and high sensitivity. It was successfully applied to the quantitative determination of caffeine in beverages. (author)

  15. Third generation biosensor based on myoglobin-TiO2/MWCNTs modified glassy carbon electrode

    Institute of Scientific and Technical Information of China (English)

    Lei Zhang; Dan Bi Tian; Jun Jie Zhu

    2008-01-01

    TiO2 nanoparticles were homogeneously coated on multi-walled carbon nanotubes by hydrothermal deposition, this nano-composite may be a promising material for myoglobin immobilization in view of its high biocompatibility and large surface. The glassy carbon electrode modified with Mb-TiO2/MWCNTs films exhibited a pair of well defined, stable and nearly reversible cycle voltammetric peaks. The electron transfer between Mb and electrode surface, Ks of 3.08 s-1, was greatly facilitated in the TiO2/MWCNTs film. The electrocatalytic reductions of hydrogen peroxide were studied, the apparent Michaelis-Menten constant is calculated to be 83.10 μmol/L, which shows a large catalytic activity of Mb in the TiO2/MWCNTs film to H2O2.

  16. Voltammetric Determination of Ferulic Acid Using Polypyrrole-Multiwalled Carbon Nanotubes Modified Electrode with Sample Application

    Directory of Open Access Journals (Sweden)

    Refat Abdel-Hamid

    2015-10-01

    Full Text Available A polypyrrole-multiwalled carbon nanotubes modified glassy carbon electrode-based sensor was devised for determination of ferulic acid (FA. The fabricated sensor was prepared electrochemically using cyclic voltammetry (CV and characterized using CV and scanning electron microscope (SEM. The electrode shows an excellent electrochemical catalytic activity towards FA oxidation. Under optimal conditions, the anodic peak current correlates linearly to the FA concentration throughout the range of 3.32 × 10−6 to 2.59 × 10−5 M with a detection limit of 1.17 × 10−6 M (S/N = 3. The prepared sensor is highly selective towards ferulic acid without the interference of ascorbic acid. The sensor applicability was tested for total content determination of FA in a commercial popcorn sample and showed a robust functionality.

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

    International Nuclear Information System (INIS)

    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.

  18. Electrochemical determination of bisphenol A with a glassy carbon electrode modified with gold nanodendrites

    International Nuclear Information System (INIS)

    Three-dimensional gold nanodendrites with (111)-oriented growth were fabricated on a glassy carbon electrode by one-step electrodeposition of AuCl4− in the presence of L-asparagine. The gold nanodendrites were functionalized with 4-mercaptobenzoic acid (4-MBA), which showed the improved catalytic performance for sensitive and selective determination of bisphenol A (BPA) by differential pulse voltammetry. The oxidation peak currents of BPA at 514 mV showed linear responses to BPA concentrations from 0.05 to 55.0 μM (R2 = 0.995), with the detection limit of 1.2 nM (S/N = 3). The modified electrode was extended for trace detection of BPA in (spiked) real samples with satisfied results. (author)

  19. Acetylene black nanoparticle-modified electrode as an electrochemical sensor for rapid determination of rutin

    International Nuclear Information System (INIS)

    Acetylene black nanoparticles were homogeneously dispersed into water in the presence of hydrophobic surfactant and then used to modify the surface of a glassy carbon electrode. An examination of the electrochemistry of rutin showed that this modification of the electrodes resulted in a considerable enhancement of the surface, thus remarkably increasing the signal for rutin. As a result, a sensitive and convenient electrochemical method was developed for the determination of rutin. The linear range is from 20 μg L-1 to 5 mg L-1, and the limit of detection is 10 μg L-1. The method was successfully employed to the determination of rutin in traditional Chinese medicines. (author)

  20. Improved ceramic anodes for SOFCs with modified electrode/electrolyte interface

    DEFF Research Database (Denmark)

    Abdul Jabbar, Mohammed Hussain; Høgh, Jens Valdemar Thorvald; Zhang, Wei; Stamate, Eugen; Thydén, Karl Tor Sune; Bonanos, Nikolaos

    2012-01-01

    was deposited by magnetron sputtering. Effecting from heat treatments, Pd nanoparticles with particle sizes in the range of 5–20 nm were distributed at the interface, and throughout the backbone. The polarization resistance of the modified STN reduced to 30 Ωcm2 at 600 °C, which is three times less......The electrode performance of solid oxide fuel cell anode with Pd nanoparticles at the interface of ScYSZ electrolyte and Sr0.94Ti0.9Nb0.1O3 (STN) electrode introduced in the form of metal functional layer have been investigated at temperatures below 600 °C. A metal functional layer consisting of Pd...

  1. A glassy carbon electrode modified with porous gold nanosheets for simultaneous determination of dopamine and acetaminophen

    International Nuclear Information System (INIS)

    Porous gold nanosheets modified glassy carbon electrode (GCE) was facilely prepared by one-step electrodeposition, using N-methylimidazole as a growth-directing agent. The porous gold nanosheets modified GCE was characterized by scanning electron microscopy, transmission electron microscopy, and X-ray diffraction spectroscopy. The modified electrode displayed improved sensitivity for individual and simultaneous differential pulse voltammetric determination of dopamine (DA; at 180 mV) and acetaminophen (AC; at 450 mV vs. Ag/AgCl) even in the presence of ascorbic acid. The oxidation peak currents linearly increased with the concentrations of DA and AC in the ranges from 2.0 to 298.0 μM and 3.0 to 320.0 μM, respectively, and the detection limits are 0.28 μM for DA and 0.23 μM for AC. The relative standard deviations (n = 20) are 1.5 % for DA and 0.4 % for AC. (author)

  2. Glucose sensor based on an electrochemical reduced graphene oxide-poly(L-lysine) composite film modified GC electrode.

    Science.gov (United States)

    Hua, Liang; Wu, Xiaqin; Wang, Rong

    2012-12-21

    A convenient and environmentally friendly method of fabricating glucose biosensors is proposed. Glucose oxidase (GOD) was immobilized on electrochemically reduced graphene oxide (ERGO) which was adsorbed on the poly-L-lysine (PLL) modified glassy carbon electrode after being immersed in GO solution for 4 h. The electrochemical behaviors of GOD/ERGO/PLL/GC electrode have been investigated by cyclic voltammetry. Direct electron transfer between GOD immobilized with ERGO/PLL and GC electrode was observed. Moreover, the GOD/ERGO/PLL/GC electrode exhibited excellent electrocatalytic activity for the detection of glucose with a linear range from 0.25 to 5 mmol L(-1). PMID:23082313

  3. Part I: A comparative study of bismuth-modified screen-printed electrodes for lead detection

    Energy Technology Data Exchange (ETDEWEB)

    Calvo Quintana, Josefina [Dipartimento di Scienze e Tecnologie Chimiche, Universita di Roma Tor Vergata, Via della Ricerca Scientifica, 00133 Rome (Italy); Consorzio Interuniversitario Biostrutture e Biosistemi ' INBB' , Viale Medaglie d' Oro 305, 00136 Rome (Italy); Arduini, Fabiana, E-mail: fabiana.arduini@uniroma2.it [Dipartimento di Scienze e Tecnologie Chimiche, Universita di Roma Tor Vergata, Via della Ricerca Scientifica, 00133 Rome (Italy); Consorzio Interuniversitario Biostrutture e Biosistemi ' INBB' , Viale Medaglie d' Oro 305, 00136 Rome (Italy); Amine, Aziz [Faculte des Sciences et Techniques, B.P.146, Mohammadia, Morocco, Rome (Italy); Punzo, Francesco; Destri, Giovanni Li [LAMSUN and CSGI at Dipartimento di Scienze Chimiche, Universita degli Studi di Catania, Viale A. Doria 6, 95125, Catania (Italy); Bianchini, Chiara [Dipartimento di Ingegneria Chimica Materiali Ambienti dell' Universita degli Studi ' La Sapienza' di Roma, via Eudossiana 18, 00184 Rome (Italy); Zane, Daniela; Curulli, Antonella [Istituto per lo Studio dei Materiali Nanostrutturati (ISMN)-CNR,via del Castro Laurenziano 7, 00161 Rome (Italy); Palleschi, Giuseppe; Moscone, Danila [Dipartimento di Scienze e Tecnologie Chimiche, Universita di Roma Tor Vergata, Via della Ricerca Scientifica, 00133 Rome (Italy); Consorzio Interuniversitario Biostrutture e Biosistemi ' INBB' , Viale Medaglie d' Oro 305, 00136 Rome (Italy)

    2011-11-30

    Highlights: Black-Right-Pointing-Pointer 'In situ' Bi-SPE has higher sensitivity than 'ex situ' Bi-SPE and 'Bi{sub 2}O{sub 3} bulk' SPE. Black-Right-Pointing-Pointer Electrochemical treatment of SPE before Bi film deposition allows one to reach low LOD. Black-Right-Pointing-Pointer The linearity of Pb{sup 2+} in HCl and HClO{sub 4} is greatly affected by the ionic strength. Black-Right-Pointing-Pointer Satisfactory values of the recovery percentage were obtained in drinking water samples. - Abstract: Lead determination was carried out in the frame of the European Union project Biocop ( (www.biocop.org)) using a bismuth-modified screen-printed electrode (Bi-SPE) and the stripping analysis technique. In order to choose a sensitive Bi-SPE for lead detection, an analytical comparative study of electrodes modified by Bi using 'in situ', 'ex situ' and 'bulk' procedures was carried out. On the basis of the results obtained, we confirmed that the 'in situ' procedure resulted in better analytical performances with respect to not only 'ex situ' but also to 'Bi{sub 2}O{sub 3} bulk' modified electrodes, allowing for a linear range of lead ion concentration from 0.5 to 100 {mu}g L{sup -1} and a detection limit of 0.15 {mu}g L{sup -1}. We demonstrated that, before the Bi film deposition, an oxidative electrochemical pre-treatment of the working electrode could be useful because it eliminates traces of lead in the graphite-ink, as shown with stripping measurements. It also improves the electrochemical performance of the electrodes as demonstrated with Electrochemical Impedance Spectroscopy (EIS) measurements. The influence of different analytical parameters, such as the electrolyte solution composition (acetate buffer, chloridric acid, nitric acid, perchloric acid) and the ionic strength was investigated in order to evaluate how to treat the sample before the analysis. The morphology of

  4. 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

  5. Indium modified graphite electrodes on highly zinc containing methanesulfonate electrolyte for zinc-cerium redox flow battery

    International Nuclear Information System (INIS)

    The zinc deposition and dissolution reaction in methanesulfonic acid (2.5 mol L−1 Zn(II) in 6.5 mol L−1 MSA) on indium modified graphite electrodes aiming to suppress the competing hydrogen evolution reaction (HER), was studied on the negative electrode reaction in the zinc-cerium redox flow battery. Cyclic voltammetry, Tafel extrapolation and electrochemical impedance spectroscopy found that elevated temperatures 40 °C improved the kinetics (jo =1 × 10−2 A cm−2) of the zinc reaction and shifted the nucleation potential positively by 65 mV. The modified graphite electrodes exhibited higher coulombic efficiencies (81%) than the “as received” electrode due to the reduction of HER. Higher voltage efficiencies (84%) were found at elevated temperatures irrespective of charging time or the modification method. The highest energy efficiency was 65% at 40 °C and 600 rpm for the modified electrode treated with the highest concentration of indium (0.2 mol L−1) and longest dipping period (5 h). Scanning electron microscopy showed no signs of dendritic growth but confirmed the formation of spikes and clusters. Energy dispersive X-ray spectroscopy of the modified graphite electrodes after 340 galvanic cycles showed that indium was still present at the surface of the electrode suggesting good durability

  6. Visible light photoelectrocatalysis with salicylic acid-modified TiO2 nanotube array electrode for p-nitrophenol degradation

    International Nuclear Information System (INIS)

    This research focused on immersion method synthesis of visible light active salicylic acid (SA)-modified TiO2 nanotube array electrode and its photoelectrocatalytic (PEC) activity. The SA-modified TiO2 nanotube array electrode was synthesized by immersing in SA solution with an anodized TiO2 nanotube array electrode. Scanning electron microscope (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), infrared spectroscopy (IR), UV-vis diffuse reflectance spectrum (DRS), and Surface photovoltage (SPV) were used to characterize this electrode. It was found that SA-modified TiO2 nanotube array electrode absorbed well into visible region and exhibited enhanced visible light PEC activity on the degradation of p-nitrophenol (PNP). The degradation efficiencies increased from 63 to 100% under UV light, and 79-100% under visible light (λ > 400 nm), compared with TiO2 nanotube array electrode. The enhanced PEC activity of SA-modified TiO2 nanotube array electrode was attributed to the amount of surface hydroxyl groups introduced by SA-modification and the extension of absorption wavelength range.

  7. 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.

  8. Detection of Carbofuran with Immobilized Acetylcholinesterase Based on Carbon Nanotubes-Chitosan Modified Electrode

    Directory of Open Access Journals (Sweden)

    Shuping Zhang

    2013-01-01

    Full Text Available A sensitive and stable enzyme biosensor based on efficient immobilization of acetylcholinesterase (AChE to MWNTs-modified glassy carbon electrode (GCE with chitosan (CS by layer-by-layer (LBL technique for rapid determination of carbofuran has been devised. According to the inhibitory effect of carbamate pesticide on the enzymatic activity of AChE, we use carbofuran as a model pesticide. The inhibitory effect of carbofuran on the biosensor was proportional to concentration of carbofuran in the range from  g/L to  g/L with a detection limit of  g/L. This biosensor is a promising new method for pesticide analysis.

  9. Localized electropolymerization on oxidized boron-doped diamond electrodes modified with pyrrolyl units.

    Science.gov (United States)

    Actis, Paolo; Manesse, Mael; Nunes-Kirchner, Carolina; Wittstock, Gunther; Coffinier, Yannick; Boukherroub, Rabah; Szunerits, Sabine

    2006-11-14

    This paper describes the functionalization of oxidized boron-doped diamond (BDD) electrodes with N-(3-trimethoxysilylpropyl)pyrrole (TMPP) and the influence of this layer on the electrochemical transfer kinetics as well as on the possibility of forming strongly adhesive polypyrrole films on the BDD interface through electropolymerization. Furthermore, localized polymer formation was achieved on the TMPP-modified BDD interface using the direct mode of a scanning electrochemical microscope (SECM) as well as an electrochemical scanning near-field optical microscope (E-SNOM). Depending on the method used polypyrrole dots with diameters in the range of 1-250 microm are electrogenerated. PMID:17066183

  10. Glassy carbon electrode modified with gold nanoparticles for ractopamine and metaproterenol sensing

    Science.gov (United States)

    Duan, Jiahua; He, Dawei; Wang, Wenshuo; Liu, Yongchuan; Wu, Hongpeng; Wang, Yongsheng; Fu, Ming

    2013-06-01

    In this Letter, the gold nanoparticles (AuNPs) were used as an enhanced material for selective detection of ractopamine and metaproterenol with electrochemical methods. The morphology and size of gold nanoparticles were characterized by scanning electron microscopy and absorption spectrum. Meanwhile, the electrical properties of modified glass carbon electrode (GCE) were studied by electrochemical impedance spectroscopy. The electrochemical behaviors of ractopamine and metaproterenol were well explained by PM3 calculated method and cyclic voltammetry. Importantly, the ractopamine and metaproterenol were effectively detected. The detection range has been broadened to (10-9-10-5 M) and the detection time has been shortened to a few minutes.

  11. Voltammetric determination of Diazepam at meniscus-modified silver solid amalgam electrode

    OpenAIRE

    Samiec, Petr; Fischer, Jan; Navrátilová, Zuzana

    2014-01-01

    Voltammetric methods for determination of Diazepam (DZ) were developed. Techniques differential pulse voltammetry and DC voltammetry were used for determination of DZ at meniscus-modified silver solid amalgam electrode (m-AgSAE). The effect of the pH on the intensity of signal of DZ was studied in a mixture of Britton-Robinson buffer + methanol (9:1) and 0.1 M NaOH + methanol (9:1); the optimal medium for analysis was a mixture of 0.1 M NaOH + methanol (9:1). The developed method has been tes...

  12. Kinetics and mechanism of nitrate and nitrite electroreduction on Pt(100) electrodes modified by copper adatoms

    OpenAIRE

    Molodkina, E.B.; Botryakova, I.G.; Danilov, A.I.; Souza-Garcia, Janaina; Feliu, Juan M.

    2013-01-01

    Kinetics and mechanism of nitrate and nitrite reduction on Pt(100) electrode modified by Cu adatoms have been studied in solutions of sulfuric and perchloric acids by means of cyclic voltammetry and in situ IR-spectroscopy. It has been shown that the surface redox process with participation of ammonia or hydroxylamine at 0.5–0.9 V occurs only on the Cu-free platinum. The causes of this effect could be low adsorption energy of nitrate reduction products on copper or changes in the composition ...

  13. Determination of groundwater mercury (II) content using a disposable gold modified screen printed carbon electrode.

    Science.gov (United States)

    Somé, Issa Touridomon; Sakira, Abdoul Karim; Mertens, Dominique; Ronkart, Sebastien N; Kauffmann, Jean-Michel

    2016-05-15

    Mercury (II) measurements were performed thanks to a newly developed electrochemical method using a disposable gold modified screen printed carbon electrode. The method has a wide dynamic range (1-100µg/L), a good accuracy and a limit of detection in compliance with WHO standards. The application of the method to several groundwater samples made it possible to identify, for the first time, mercury content higher than the recommended WHO standard value in a gold mining activity area in the northern part of Burkina Faso. The accuracy of the assay was checked by ICP/MS. PMID:26992529

  14. Preparation and Electrocatalytic Performance of Bi-Modified Quartz Column Particle Electrode for Phenol Degradation

    OpenAIRE

    Jiguo Huang; Haitao Chen; Shuo Pang; Gang Liu; Huanyu Cui; Lili Dong; Xingjuan Liu

    2015-01-01

    Bismuth oxide (Bi2O3) and its composites have good electrocatalytic performance. Quartz column is a good kind of catalyst carrier with the characteristics of high mechanical strength and good stability. A novel Bi-modified quartz column particle electrode (BQP) was prepared by the dipping-calcination method. The characterization results revealed that Bi2O3 was successfully loaded on quartz column. The optimum preparation condition was calcining at 550°C for 4 h. Electrocatalytic performance w...

  15. Voltammetry of tungsten(6) on a carbon-paste electrode modified with 8-mercaptoquinoline or dimethylsulfoxide

    International Nuclear Information System (INIS)

    The voltammetric behaviour of tungsten(6) in hydrochloric acid solutions was examined using a carbon-paste electrode modified with 8-mercaptoquinoline or dimethylsulfoxide. Under the studied conditions, tungsten(6) gives a pronounced cathode peak; its height is proportional to the amount of metal from 5 x 10-4 to 3 x 10-3 M. The electrolytic reduction of tungsten is irreversible because of the diffusion-kinetic limitation of the current. A procedure for the direct voltammetric determination of tungsten from complex mixtures without matrix removal is presented. (author)

  16. Efficient degradation of rhodamine B using modified graphite felt gas diffusion electrode by electro-Fenton process.

    Science.gov (United States)

    Tian, Jiangnan; Olajuyin, Ayobami Matthew; Mu, Tingzhen; Yang, Maohua; Xing, Jianmin

    2016-06-01

    The electro-Fenton (EF) process treatment of 0.1-M (rhodamine B) RhB solution was studied with different graphite cathode materials, and graphite felt (GF) was selected as a promising material in further investigation. Then, the degradation performances of gas diffusion electrode (GDE) and graphite felt (GF) were compared, and GDE was confirmed to be more efficient in RhB removal. The operational parameters such as Fe(2+) dosage and current density were optimized, and comparison among different modified methods-polytetrafluoroethylene-carbon black (PTFE-CB), polytetrafluoroethylene-carbon nanotube (PTFE-CNT), electrodeposition-CB, and electrodeposition-CNT-showed 98.49 % RhB removal by PTFE-CB-modified cathode in 0.05 M Na2SO4 at a current density of 50 A/m(2) and an air flow rate of 1 L/min after 20 min. Meanwhile, after cathode modified by PTFE-CB, the mineralization efficiency and mineralization current efficiency performed absolutely better than the pristine one. Cyclic voltammograms, SEM images, contact angles, and BET surface area were carried out to demonstrate stronger current responses and higher hydrophilicity of GF after modified. The value of biochemical oxygen demand/chemical oxygen demand (BOD5/COD) increased from 0.049 to 0.331 after 90-min treatment, suggesting the solution was biodegradable, and the modified cathode was confirmed to be stable after ten circle runs. Finally, a proposed degradation pathway of RhB was put forward. PMID:26931661

  17. The Graphene/l-Cysteine/Gold-Modified Electrode for the Differential Pulse Stripping Voltammetry Detection of Trace Levels of Cadmium

    Directory of Open Access Journals (Sweden)

    Yu Song

    2016-06-01

    Full Text Available Cadmium(II is a common water pollutant with high toxicity. It is of significant importance for detecting aqueous contaminants accurately, as these contaminants are harmful to human health and environment. This paper describes the fabrication, characterization, and application of an environment-friendly graphene (Gr/l-cysteine/gold electrode to detect trace levels of cadmium (Cd by differential pulse stripping voltammetry (DPSV. The influence of hydrogen overflow was decreased and the current response was enhanced because the modified graphene extended the potential range of the electrode. The Gr/l-cysteine/gold electrode showed high electrochemical conductivity, producing a marked increase in anodic peak currents (vs. the glass carbon electrode (GCE and boron-doped diamond (BDD electrode. The calculated detection limits are 1.15, 0.30, and 1.42 µg/L, and the sensitivities go up to 0.18, 21.69, and 152.0 nA·mm−2·µg−1·L for, respectively, the BDD electrode, the GCE, and the Gr/l-cysteine/gold electrode. It was shown that the Gr/l-cysteine/gold-modified electrode is an effective means for obtaining highly selective and sensitive electrodes to detect trace levels of cadmium.

  18. Amperometric sensor for detection of bisphenol A using a pencil graphite electrode modified with polyaniline nanorods and multiwalled carbon nanotubes

    International Nuclear Information System (INIS)

    We report on a simple and highly sensitive amperometric method for the determination of bisphenol A (BPA) using pencil graphite electrodes modified with polyaniline nanorods and multiwalled carbon nanotubes. The modified electrodes display enhanced electroactivity for the oxidation of BPA compared to the unmodified pencil graphite electrode. Under optimized conditions, the sensor has a linear response to BPA in the 1. 0 and 400 μM concentration range, with a limit of detection of 10 nM (at S/N = 3). The modified electrode also has a remarkably stable response, and up to 95 injections are possible with a relative standard deviation of 4. 2% at 100 μM of BPA. Recoveries range from 86 to 102% for boiling water spiked with BPA from four brands of baby bottles. (author)

  19. UV/Vis Spectroelectrochemistry as a Tool for Monitoring the Fabrication of Sensors Based on Silver Nanoparticle Modified Electrodes

    Directory of Open Access Journals (Sweden)

    Aránzazu Heras

    2013-05-01

    Full Text Available A new controlled current multipulse methodology has been developed to modify the screen-printed electrode surface with silver nanoparticles (AgNPs. Spectroelectrochemistry has provided not only information about the type of nanoparticles (NPs deposited on the electrode surface, but also about the electrosynthesis process. Small NPs without plasmon band are initially generated. Next, these nuclei grow to form bigger NPs in the reduction pulses with a characteristic plasmon band centered at 400 nm. Most of the NPs are generated during the first reduction pulses and a linear growth of the absorbance at a lower reaction rate was obtained in the subsequent pulses. Oxidation pulses do not redissolve completely silver NPs but only partially, meaning that very stable NPs are generated. AgNPs-modified electrodes have been successfully used to determine hydrogen peroxide. Spectroelectrochemistry has also yielded very useful information to understand the voltammetric signal obtained during the reduction of H2O2 on silver modified electrodes.

  20. A sensor for determination of tramadol in pharmaceutical preparations and biological fluids based on multi-walled carbon nanotubes-modified glassy carbon electrode

    International Nuclear Information System (INIS)

    A chemically modified electrode is constructed based on multi-walled carbon nanotube modified glassy carbon electrode (MWCNTs/GCE). It is demonstrated that this sensor could be used for determination of pharmaceutical important compound tramadol (TRA). The measurements were carried out using differential pulse voltammetry (DPV), cyclic voltammetry (CV) and chronoamperometry (CA) methods. DPV experiments of various concentration of TRA showed two linear dynamic ranges. The first linear dynamic range was from 4 micro M to 35 micro M, and the second linear dynamic range was between 60 micro M to 550 micro M. A detection limit of 0.38 micro M (S/N = 3) was obtained. The analytical performance of this sensor has been evaluated for the detection of TRA in human serum, human urine and some pharmaceutical preparations with satisfactory results. (author)

  1. Highly sensitive determination of hydroxylamine using fused gold nanoparticles immobilized on sol-gel film modified gold electrode

    International Nuclear Information System (INIS)

    We are reporting the highly sensitive determination of hydroxylamine (HA) using 2-mercapto-4-methyl-5-thiazoleacetic acid (TAA) capped fused spherical gold nanoparticles (AuNPs) modified Au electrode. The fused TAA-AuNPs were immobilized on (3-mercaptopropyl)-trimethoxysilane (MPTS) sol-gel film, which was pre-assembled on Au electrode. The immobilization of fused TAA-AuNPs on MPTS sol-gel film was confirmed by UV-vis absorption spectroscopy and atomic force microscopy (AFM). The AFM image showed that the AuNPs retained the fused spherical morphology after immobilized on sol-gel film. The fused TAA-AuNPs on MPTS modified Au electrode were used for the determination of HA in phosphate buffer (PB) solution (pH = 7.2). When compared to bare Au electrode, the fused AuNPs modified electrode not only shifted the oxidation potential of HA towards less positive potential but also enhanced its oxidation peak current. Further, the oxidation of HA was highly stable at fused AuNPs modified electrode. Using amperometric method, determination of 17.5 nM HA was achieved for the first time. Further, the current response of HA increases linearly while increasing its concentration from 17.5 nM to 22 mM and a detection limit was found to be 0.39 nM (S/N = 3). The present modified electrode was also successfully used for the determination of 17.5 nM HA in the presence of 200-fold excess of common interferents such as urea, NO2-, NH4+, oxalate, Mn2+, Na+, K+, Mg2+, Ca2+, Ba2+ and Cu2+. The practical application of the present modified electrode was demonstrated by measuring the concentration of HA in ground water samples.

  2. Influence of temperature on natural and chemically modified zeolites

    International Nuclear Information System (INIS)

    Zeolites from Nizny Hrabovec (Slovak Republic) were modified with solutions of NaOH. The changes of zeolites in the temperature range 20-1200 deg C were studied by thermal analysis (DTA, TG, ETA), X-ray analysis and REM analysis. Thermal analysis showed that the process of dehydration started between temperatures 20 and 600 deg C, over this temperature the dealumination and structural changes have taken place. X-ray analysis and REM analysis showed the structural changes of natural zeolites and gradual loss of cristallinity of the chemically modified zeolites. (author)

  3. Chemical sensors based on molecularly modified metallic nanoparticles

    International Nuclear Information System (INIS)

    This paper presents a concise, although admittedly non-exhaustive, didactic review of some of the main concepts and approaches related to the use of molecularly modified metal nanoparticles in or as chemical sensors. This paper attempts to pull together different views and terminologies used in sensors based on molecularly modified metal nanoparticles, including those established upon electrochemical, optical, surface Plasmon resonance, piezoelectric and electrical transduction approaches. Finally, this paper discusses briefly the main advantages and disadvantages of each of the presented class of sensors. (review article)

  4. ITO electrode modified by a gold ion implantation technique for direct electrocatalytic sensing of hydrogen peroxide

    International Nuclear Information System (INIS)

    We report on a simple strategy for the fabrication of gold nanoparticles (AuNPs) on an indium tin oxide substrate using a modified ion implantation method. The morphology, structure and electrochemical features of AuNPs were characterized by atomic force microscopy, electrochemical impedance spectroscopy and cyclic voltammetry. The modified electrode has a large electrochemically active surface and enables strong loading with cytochrome c (Cyt c) proteins. It undergoes enhanced electron transfer at uncompromised electrochemical activity, and also displays good stability and repeatability. The immobilized Cyt c exhibits good electrocatalytic activity towards hydrogen peroxide (H2O2), with a linear relationship between the catalytic current during differential pulse voltammetry and the concentration of H2O2 in the 0.05 μM to 0.2 μM range. The detection limit (S/N = 3) is 0. 01 μM. (author)

  5. A sensitive and environmentally friendly method for determination of chemical oxygen demand using NiCu alloy electrode

    International Nuclear Information System (INIS)

    Highlights: ► NiCu alloy modified electrode is used to determine chemical oxygen demand. ► NiCu alloy can effectively oxidize a wide range of organic compounds. ► Compared with the existing methods, this method has wide linear range and high sensitivity. ► The results are linearly correlated to those by the classic dichromate method. ► The proposed method has an excellent practical perspective in water quality control. - Abstract: A simple, sensitive and environmentally friendly method was developed for determination of chemical oxygen demand (COD) by cyclic voltammetry using nickel–copper (NiCu) alloy electrode. The structure and the electrochemical behavior of NiCu alloy electrode were investigated by atomic force microscope, energy dispersive X-ray spectrometer, and cyclic voltammetry, respectively. The results indicated that NiCu alloy film with high quality was stably modified on the surface of glass carbon (GC) electrode, which could effectively oxidize a wide range of organic compounds. Subsequently, the parameters affecting the analytical performance were investigated, including pH, dissolved oxygen and concentration of chloride ion. Under optimized conditions, the linear range was 10–1533 mg L−1 and the detection limit was 1.0 mg L−1. The results obtained from the proposed method were linearly correlated to those by the classic dichromate method (r = 0.9978, p < 0.01, n = 13). Finally, the validated method was used to determine the COD values of surface water, reclaimed water and wastewater. It was shown that the proposed method had an excellent practical perspective on determination of COD in water quality control and pollution evaluation.

  6. Modified pulse electrodeposition of Pt nanocatalyst as high-performance electrode for PEMFC

    Science.gov (United States)

    Fouda-Onana, F.; Guillet, N.; AlMayouf, A. M.

    2014-12-01

    Low platinum loading electrode was successfully deposited by a modified pulse galvanic signal in H2PtCl6 electrolyte using carbon black as support directly on a GDL (Gas Diffusion Layer). SEM images of the deposition were composed by rough Pt particles of 50 nm leading to specific electrochemical surface area of 53 m2 g-1. In spite of large particle size and a low cathode loading of 0.12 mg cm-2, the proton exchange membrane fuel cell (PEMFC) fed with humidified H2 and O2 at 80 °C, 1.5 absolute bar reached 0.2 mA cmPt-2 and 0.1 A mg-1 at 0.9 VIR-free which were twice higher than a reference membrane electrodes assembly (MEA) with a cathode loaded at 0.4 mgPt.cm-2. Such an active cathode electrode may be ascribed to a higher utilization rate of the platinum caused by an efficient catalyst deposition by electrochemical route.

  7. Impedimetric Label-Free Immunosensor on Disposable Modified Screen-Printed Electrodes for Ochratoxin A

    Directory of Open Access Journals (Sweden)

    Francesca Malvano

    2016-06-01

    Full Text Available An impedimetric label-free immunosensor on disposable screen-printed carbon electrodes (SPCE for quantitative determination of Ochratoxin A (OTA has been developed. After modification of the SPCE surface with gold nanoparticles (AuNPs, the anti-OTA was immobilized on the working electrode through a cysteamine layer. After each coating step, the modified surfaces were characterized by cyclic voltammetry (CV and electrochemical impedance spectroscopy (EIS. The capacitance was chosen as the best parameter that describes the reproducible change in electrical properties of the electrode surface at different OTA concentrations and it was used to investigate the analytical parameters of the developed immunosensor. Under optimized conditions, the immunosensor showed a linear relationship between 0.3 and 20 ng/mL with a low detection limit of 0.25 ng/mL, making it suitable to control OTA content in many common food products. Lastly, the immunosensor was used to measure OTA in red wine samples and the results were compared with those registered with a competitive ELISA kit. The immunosensor was sensitive to OTA lower than 2 μg/kg, which represents the lower acceptable limit of OTA established by European legislation for common food products.

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

    Directory of Open Access Journals (Sweden)

    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.

  9. Synthesis of modified polymer inclusion membranes for photo-electrodeposition of cadmium using polarized electrodes

    International Nuclear Information System (INIS)

    Highlights: ► Homogeneous PIM membranes containing water soluble polymers have been obtained under new experimental conditions. ► Photoelectrodeposition of “Cd” has been carried out using WO3 and CuFeO2 as electrode. ► Using both photo-polarized electrodes enhances transference of cadmium compared to one. ► Membrane with poly-phosphoric acid (PPA) give a rise of transferred amount of Cd. - Abstract: In this work, we have developed a novel class of polymeric inclusion membranes (PIMs) for the cations separation. The membrane is made up of cellulose triacetate modified by poly-electrolytes (poly-phosphoric acid, polyvinyl pyrolidone, polyacrylic acid, polyvinyl alcohol and poly-anetholsulfonic acid) using 2-hydroxy-5-dodecylbenzaldehyde incorporated into the polymer as carrier and tris ethyl hexyl phosphate or glycerine as plasticizers. Different PIMs are synthesized and characterized by the Fourier transform infrared, X-ray diffraction, thermal analysis and scanning electron microscopy. The influence of the membrane nature is studied using supports with different physical characteristics (porosity, thickness, hydrophobia). As application, the transport of Cd2+ using PIMs coupled with photo-electrodes is investigated. The photo-catalytic results indicate that the combined system p-CuFeO2/membrane/n-WO3 enhances considerably the electrons transfer toward the delafossite CuFeO2. The position of the conduction band of CuFeO2 is looked to be the key issue for the photo electrochemical Cd2+ reduction.

  10. Temperature dependence studies on the electro-oxidation of aliphatic alcohols with modified platinum electrodes

    Indian Academy of Sciences (India)

    Panadda Katikawong; Tanakorn Ratana; Waret Veerasai

    2009-05-01

    Temperature dependence on the electro-oxidation of methanol, ethanol and 1-propanol in 0.5 M H2SO4 were investigated with Pt and PtRu electrodes. Tafel slope and apparent activation energy were evaluated from the cyclic voltammetric data in the low potential region (0.3-0.5 V vs SHE). The CV results provided Tafel slopes for alcohols in the range of 200-400 mV dec-1 which indicated a difference in the rate determining step. The decrease in Tafel slope was only observed in the case of methanol for the Ru-modified Pt electrode. This indicates that Ru improves the rate of determining step for methanol while hindering it for the other alcohols. The electrochemical impedance spectroscopy was also used to evaluate the electro-oxidation mechanism of alcohols on these electrodes. The simulated EIS results provided two important parameters: charge transfer resistance () and inductance (). The $R^{-1}_{ct}$ and -1 represent the rate of alcohol electro-oxidation and rate of desorption of intermediate species, respectively. These values increased with the increasing of temperature. The results from two techniques were well agreed that the electro-oxidation of methanol was improved by raising the temperature and ruthenium modification.

  11. Droplet-based glucosamine sensor using gold nanoparticles and polyaniline-modified electrode.

    Science.gov (United States)

    Suea-Ngam, Akkapol; Rattanarat, Poomrat; Wongravee, Kanet; Chailapakul, Orawon; Srisa-Art, Monpichar

    2016-09-01

    A droplet-based electrochemical sensor for direct measurement of D-glucosamine was developed using carbon paste electrodes (CPEs) modified with gold nanoparticles (AuNPs) and polyaniline (PANI). Central composition design (CCD) was employed as a powerful method for optimization of parameters for electrode fabrication. The optimized amounts of AuNPs and PANI obtained from the response surface were determined as 300 and 3000mgL(-1), respectively. Coupled with a droplet microfluidic system, the analysis of glucosamine was performed in a high-throughput manner with a sample throughput of at least 60 samples h(-1). In addition, the adsorption of the analyte on the electrode surface was prevented due to compartmentalization in droplets. Linearity of the proposed system was found to be in the range of 0.5-5mM with a sensitivity of 7.42×10(-3)Amol(-1)Lcm(-2) and limits of detection and quantitation of 0.45 and 1.45mM, respectively. High intraday and interday (evaluated among 3 days) precisions for the detection of 50 droplets containing glucosamine were obtained with relative standard deviation less than 3%. The system was successfully used to determine the amounts of glucosamine in supplementary products with error percentage and relative standard deviation less than 3%. In addition, the amounts of glucosamine measured using the developed sensor were in good agreement with those obtained from a CE method. These indicate high accuracy and precision of the proposed system. PMID:27343587

  12. Electrochemical sensors and biosensors based on redox polymer/carbon nanotube modified electrodes: a review.

    Science.gov (United States)

    Barsan, Madalina M; Ghica, M Emilia; Brett, Christopher M A

    2015-06-30

    The aim of this review is to present the contributions to the development of electrochemical sensors and biosensors based on polyphenazine or polytriphenylmethane redox polymers together with carbon nanotubes (CNT) during recent years. Phenazine polymers have been widely used in analytical applications due to their inherent charge transport properties and electrocatalytic effects. At the same time, since the first report on a CNT-based sensor, their application in the electroanalytical chemistry field has demonstrated that the unique structure and properties of CNT are ideal for the design of electrochemical (bio)sensors. We describe here that the specific combination of phenazine/triphenylmethane polymers with CNT leads to an improved performance of the resulting sensing devices, because of their complementary electrical, electrochemical and mechanical properties, and also due to synergistic effects. The preparation of polymer/CNT modified electrodes will be presented together with their electrochemical and surface characterization, with emphasis on the contribution of each component on the overall properties of the modified electrodes. Their importance in analytical chemistry is demonstrated by the numerous applications based on polymer/CNT-driven electrocatalytic effects, and their analytical performance as (bio) sensors is discussed. PMID:26041516

  13. Electrochemical detection of acetaminophen on the functionalized MWCNTs modified electrode using layer-by-layer technique

    Energy Technology Data Exchange (ETDEWEB)

    Manjunatha, Revanasiddappa [Chemistry Research Centre, S.S.M.R.V. Degree College, IV ' T' Block, Jayanagar, Bangalore 560041 (India); Nagaraju, Dodahalli Hanumantharayudu [Mechanical Engineering Department, National University of Singapore, 119615 (Singapore); Suresh, Gurukar Shivappa, E-mail: sureshssmrv@yahoo.co.in [Chemistry Research Centre, S.S.M.R.V. Degree College, IV ' T' Block, Jayanagar, Bangalore 560041 (India); Melo, Jose Savio; D' Souza, Stanislaus F. [Nuclear Agriculture and Biotechnology Division, Bhabha Atomic Research Centre, Mumbai 400085 (India); Venkatesha, Thimmappa Venkatarangaiah [Department of Chemistry, Kuvempu University, Jnanasahyadri, Shimoga 577451 (India)

    2011-07-30

    A selective electrochemical method is fabricated via layer-by-layer (LBL) method using both positively and negatively charged multi walled carbon nanotubes (MWCNTs) on poly (diallyldimetheylammonium chloride) (PDDA)/poly styrene sulfonate (PSS) modified graphite electrode, for the determination of acetaminophen (ACT) in the presence of dopamine (DA) and high concentration of ascorbic acid (AA). The modified electrode was characterized by cyclic voltammetry (CV) electrochemical impedance spectroscopy (EIS), atomic force microscopy (AFM) and scanning electron microscopy (SEM). Experimental conditions such as pH, accumulation potential and time, effect of potential sweep rates and interferents were studied. In CV well defined peaks for AA, ACT and DA are obtained at 24, 186 and 374 mV, respectively. The separations of peaks were 210, 188 and 398 mV between AA and DA, DA and ACT and AA and ACT, respectively. The diffusion coefficient was calculated by chronocoulometric. Chronoamperometric studies showed the linear relationship between oxidation peak current and concentration of ACT in the range 25-400 {mu}M (R = 0.9991). The detection limit was 5 x 10{sup -7} mol/L. The proposed method gave satisfactory results in the determination of ACT in pharmaceutical and human serum samples.

  14. Electrocatalytic oxidation of methanol on Ni and NiCu alloy modified glassy carbon electrode

    Energy Technology Data Exchange (ETDEWEB)

    Danaee, I.; Jafarian, M.; Forouzandeh, F.; Mahjani, M.G. [Department of Chemistry, K.N. Toosi University of Technology, P.O. Box 15875-4416, Tehran (Iran); Gobal, F. [Department of Chemistry, Sharif University of Technology, P.O. Box 11365-9516, Tehran (Iran)

    2008-08-15

    Nickel and nickel-copper alloy modified glassy carbon electrodes (GC/Ni and GC/NiCu) prepared by galvanostatic deposition were examined for their redox process and electrocatalytic activities towards the oxidation of methanol in alkaline solutions. The methods of cyclic voltammetery (CV) and chronoamperometry (CA) were employed. The cyclic voltammogram of NiCu alloy demonstrates the formation of {beta}/{beta} crystallographic forms of the nickel oxyhydroxide under prolonged repetitive potential cycling in alkaline solution. In CV studies, in the presence of methanol NiCu alloy modified electrode shows a significantly higher response for methanol oxidation. The peak current of the oxidation of nickel hydroxide increase is followed by a decrease in the corresponding cathodic current in presence of methanol. The anodic peak currents show linear dependency with the square root of scan rate. This behavior is the characteristic of a diffusion controlled process. Under the CA regime the reaction followed a Cottrellian behavior and the diffusion coefficient of methanol was found to be 2 x 10{sup -6} cm{sup 2} s{sup -1} in agreement with the values obtained from CV measurements. (author)

  15. Methionine – Au Nanoparticle Modified Glassy Carbon Electrode: a Novel Platform for Electrochemical Detection of Hydroquinone

    Directory of Open Access Journals (Sweden)

    Jiahong HE

    2014-12-01

    Full Text Available A high sensitive electrochemical sensor based on methionine/gold nanoparticles (MET/AuNPs modified glassy carbon electrode (GCE was fabricated for the quantitative detection of hydroquinone (HQ. The as-modified electrode was characterized by scanning electron microscopy (SEM and X-ray diffraction (XRD techniques. The electrochemical performance of the sensor to HQ was investigated by using cyclic and differential pulse voltammetry, which revealed its excellent electrocatalytic activity and reversibility towards HQ. The separation of anodic and cathodic peak (∆Ep was decreased from 471 mV to 75 mV. The anodic peak current achieved under the optimum conditions was linear with the HQ concentration ranging from 8 μM to 400 μM with the detection limit 0.12 μM (3σ. The as-fabricated sensor also showed a good selectivity towards HQ without demonstrating interference from other coexisting species. Furthermore, the sensor showed a good performance for HQ detection in environmental water, which suggests its potential practical application. DOI: http://dx.doi.org/10.5755/j01.ms.20.4.6477

  16. Voltammetric monitoring photodegradation of EDTA based on carbon nanotubes-modified electrode

    International Nuclear Information System (INIS)

    This work described a fast and sensitive voltammetric method developed for monitoring the photodegradation of ethylenediaminetetraacetic acid (EDTA). Due to the unique properties of carbon nanotubes (CNTs) such as negative charges, large surface area and excellent electron transfer ability, metal ion namely Fe3+ showed a pair of well-defined redox response peaks on the CNTs-modified electrode. When EDTA was present in the solution, the voltammetric response of Fe3+ was suppressed due to the chelating interaction between Fe3+ and EDTA. In acetate buffer solution, the concentration of EDTA was found to be inversely proportional to the decreased cathodic peak current in the range of 1.0 x 10-6 to 1.0 x 10-4 mol/L with a detection limit (3S/N) of 6.5 x 10-7 mol/L. While EDTA was degraded by UV irradiation, the voltammetric response on the CNTs-modified electrode was enhanced due to the reduced amount of EDTA species chelating with Fe3+. Accordingly, the concentration variation of EDTA during the photodegradation was analyzed. The effects of H2O2 and pH on the photodegradation of EDTA were investigated. Thus, the proposed CNTs-based voltammetry provided a useful analytical tool for studying the degradation of EDTA.

  17. Electrochemical detection of acetaminophen on the functionalized MWCNTs modified electrode using layer-by-layer technique

    International Nuclear Information System (INIS)

    A selective electrochemical method is fabricated via layer-by-layer (LBL) method using both positively and negatively charged multi walled carbon nanotubes (MWCNTs) on poly (diallyldimetheylammonium chloride) (PDDA)/poly styrene sulfonate (PSS) modified graphite electrode, for the determination of acetaminophen (ACT) in the presence of dopamine (DA) and high concentration of ascorbic acid (AA). The modified electrode was characterized by cyclic voltammetry (CV) electrochemical impedance spectroscopy (EIS), atomic force microscopy (AFM) and scanning electron microscopy (SEM). Experimental conditions such as pH, accumulation potential and time, effect of potential sweep rates and interferents were studied. In CV well defined peaks for AA, ACT and DA are obtained at 24, 186 and 374 mV, respectively. The separations of peaks were 210, 188 and 398 mV between AA and DA, DA and ACT and AA and ACT, respectively. The diffusion coefficient was calculated by chronocoulometric. Chronoamperometric studies showed the linear relationship between oxidation peak current and concentration of ACT in the range 25-400 μM (R = 0.9991). The detection limit was 5 x 10-7 mol/L. The proposed method gave satisfactory results in the determination of ACT in pharmaceutical and human serum samples.

  18. Electrochemical Characterization of Graphene and MWCNT Screen-Printed Electrodes Modified with AuNPs for Laccase Biosensor Development

    Directory of Open Access Journals (Sweden)

    Gabriele Favero

    2015-11-01

    Full Text Available The aim of this work is to show how the integration of gold nanoparticles (AuNPs into multi-wall-carbon-nanotubes (MWCNTs based screen-printed electrodes and into graphene-based screen-printed electrodes (GPHs could represent a potential way to further enhance the electrochemical properties of those electrodes based on nanoparticles. Laccase from Trametes versicolor (TvL was immobilized over MWCNTs and GPH previously modified with AuNPs (of 5 and 10 nm. The characterization of the modified electrode surface has been carried out by cyclic voltammetry. The results showed that the use of AuNPs for modification of both graphene and MWCNTs screen-printed electrode surfaces would increase the electrochemical performances of the electrodes. MWCNTs showed better results than GPH in terms of higher electroactive area formation after modification with AuNPs. The two modified nanostructured electrodes were successively proven to efficiently immobilize the TvL; the electrochemical sensing properties of the GPH- and MWCNT-based AuNPs-TvL biosensors were investigated by choosing 2,2′-Azino-bis(3-ethylbenzothiazoline-6-sulfonic-acid diammonium salt (ABTS, catechol and caffeic acid as laccase mediators; and the kinetic parameters of the laccase biosensor were carefully evaluated.

  19. Electrochemical synthesis of nickel–iron layered double hydroxide: Application as a novel modified electrode in electrocatalytic reduction of metronidazole

    Energy Technology Data Exchange (ETDEWEB)

    Nejati, Kamellia, E-mail: k_nejati@pnu.ac.ir [Chemistry Department, Payame Noor University, PO. Box 19395-3697 Tehran, I.R. of Iran (Iran, Islamic Republic of); Asadpour-Zeynali, Karim [Department of Analytical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz 51666-16471 (Iran, Islamic Republic of)

    2014-02-01

    A new and simple approach based on the electrochemical method was used for preparation of reproducible nanostructure thin film of Ni/Fe-layered double hydroxides (Ni/Fe-LDH) on the glassy carbon electrode (GCE). The electrochemical behavior of the Ni/Fe-LDH deposited on GCE electrode is studied. Study of the scanning electron microscopy shows the formation of a nanostructure thin film on the glassy carbon electrode. Electrochemical experiments show that Ni/Fe-LDH modified glassy carbon electrode exhibits excellent electrocatalytic reduction activity with Metronidazole. The method was successfully applied for the analysis of Metronidazole in tablets. The results were favorably compared to those obtained by the reported BP method. - Highlights: • Ni/Fe-LDH was synthesized simply via electrodeposition method on glassy carbon electrode. • The LDH modified electrode was used to electrocatalytic reduction and determination of metronidazole. • The reduction peak of Fe(III)-LDH to Fe(II)-LDH was applied to electrocatalytic reduction of Metronidazole. • The modified electrode exhibited very good analytical performance with low cost, convenient preparation and rapid detection.

  20. Electrochemical synthesis of nickel–iron layered double hydroxide: Application as a novel modified electrode in electrocatalytic reduction of metronidazole

    International Nuclear Information System (INIS)

    A new and simple approach based on the electrochemical method was used for preparation of reproducible nanostructure thin film of Ni/Fe-layered double hydroxides (Ni/Fe-LDH) on the glassy carbon electrode (GCE). The electrochemical behavior of the Ni/Fe-LDH deposited on GCE electrode is studied. Study of the scanning electron microscopy shows the formation of a nanostructure thin film on the glassy carbon electrode. Electrochemical experiments show that Ni/Fe-LDH modified glassy carbon electrode exhibits excellent electrocatalytic reduction activity with Metronidazole. The method was successfully applied for the analysis of Metronidazole in tablets. The results were favorably compared to those obtained by the reported BP method. - Highlights: • Ni/Fe-LDH was synthesized simply via electrodeposition method on glassy carbon electrode. • The LDH modified electrode was used to electrocatalytic reduction and determination of metronidazole. • The reduction peak of Fe(III)-LDH to Fe(II)-LDH was applied to electrocatalytic reduction of Metronidazole. • The modified electrode exhibited very good analytical performance with low cost, convenient preparation and rapid detection

  1. THE INDUSTRIAL UTILIZATION OF CHEMICAL MODIFIED AGRICULTURAL RESIDUES

    Institute of Scientific and Technical Information of China (English)

    FengXu; RuncangSun; HuaiyuZhan

    2004-01-01

    Various lignocellulosic materials such as wood, agricultural and forest residues has the potential to be valuable substitute for, or complement to, commercial sorbents for removing heavy metal ions or dyes from waste water or spilled oil from inland water or sea. More than 9 million tons of straw pulp are produced annually in china, which account for about 90% of the world's total straw pulp. However, huge quantity of remain straw is not used as industrial raw material and is burnt in the fields or on the side of road. These resources can be chemical modified such as acetylation. Modified straws have the characteristics of low cost, high capacity, quick uptake, and easy to desorb. This paper reviews the current status of the technology for modified agricultural residues, which focus on hemicellulose and cellulose. The potential of these natural sorbents in main industry is also indicated.

  2. THE INDUSTRIAL UTILIZATION OF CHEMICAL MODIFIED AGRICULTURAL RESIDUES

    Institute of Scientific and Technical Information of China (English)

    Feng Xu; Runcang Sun; Huaiyu Zhan

    2004-01-01

    Various lignocellulosic materials such as wood,agricultural and forest residues has the potential to be valuable substitute for, or complement to,commercial sorbents for removing heavy metal ions or dyes from waste water or spilled oil from inland water or sea. More than 9 million tons of straw pulp are produced annually in china, which account for about 90% of the world′s total straw pulp. However,huge quantity of remain straw is not used as industrial raw material and is burnt in the fields or on the side of road. These resources can be chemical modified such as acetylation. Modified straws have the characteristics of low cost, high capacity, quick uptake, and easy to desorb. This paper reviews the current status of the technology for modified agricultural residues, which focus on hemicellulose and cellulose. The potential of these natural sorbents in main industry is also indicated.

  3. Overpotential deposition of copper on an iodine-modified Au(1 1 1) electrode

    Energy Technology Data Exchange (ETDEWEB)

    Martinez-Ruiz, Alejandro [Facultad de Ciencias, Universidad Autonoma de Baja California, Ensenada, BC 22800 (Mexico)], E-mail: alejandro@uabc.mx; Palomar-Pardave, Manuel [Departamento de Materiales, Universidad Autonoma Metropolitana-Azcapotzalco, C.P. 02000 Mexico, D.F. (Mexico); Batina, Nikola [Departamento de Quimica, Universidad Autonoma Metropolitana-Iztapalapa, 09340 Mexico, D.F. (Mexico)

    2008-01-01

    Cyclic voltammetry, chronoamperometry and in situ electrochemical scanning tunneling microscopy were used to study the kinetics of nucleation and crystal growth during the initial stages of copper overpotential deposition (OPD) on a previously iodine-modified Au(1 1 1) electrode, from an aqueous solution 10{sup -3} M CuSO{sub 4} in 0.05 M H{sub 2}SO{sub 4}. The starting potential during step experiments was chosen in the region where the gold electrode was completely free of the copper deposit. The recorded current transients for copper deposition onto the iodine-modified Au(1 1 1) electrode surface appear to be very complex, with the unusual presence of two or more current maxima. A new method was used for quantitative evaluation of current transients that involves the transition UPD-OPD, developed by our group [M. Palomar-Pardave, I. Gonzalez, N. Batina, J. Phys. Chem. B 104 (2000) 3545], was used for the quantitative interpretation. Our results show that, within a single current transient, copper adsorption and two types of nucleation process: two-dimensional (2D) and three-dimensional (3D) limited by lattice incorporation of copper adatoms and diffusion of Cu(II) ion, respectively, take place simultaneously. STM images revealed the enhanced growth of 3D copper on edge of I-Au(1 1 1) during the early stages of deposition. Moreover, our results strongly suggest that the iodine adlayer is constantly present, even after the striping Cu that was overpotential deposited.

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

    Directory of Open Access Journals (Sweden)

    Koh Sing Ngai

    2015-01-01

    Full Text Available A rapid, simple, and sensitive method for the electrochemical determination of paracetamol was developed. A single-walled carbon nanotube/nickel (SWCNT/Ni nanocomposite was prepared and immobilized on a glassy carbon electrode (GCE surface via mechanical attachment. This paper reports the voltammetry study on the effect of paracetamol concentration, scan rate, pH, and temperature at a SWCNT/Ni-modified electrode in the determination of paracetamol. The characterization of the SWCNT/Ni/GCE was performed by cyclic voltammetry. Variable pressure scanning electron microscopy (VPSEM and energy dispersive X-ray (EDX spectrometer were used to examine the surface morphology and elemental profile of the modified electrode, respectively. Cyclic voltammetry showed significant enhancement in peak current for the determination of paracetamol at the SWCNT/Ni-modified electrode. A linear calibration curve was obtained for the paracetamol concentration between 0.05 and 0.50 mM. The SWCNT/Ni/GCE displayed a sensitivity of 64 mA M−1 and a detection limit of 1.17 × 10−7 M in paracetamol detection. The proposed electrode can be applied for the determination of paracetamol in real pharmaceutical samples with satisfactory performance. Results indicate that electrodes modified with SWCNT and nickel nanoparticles exhibit better electrocatalytic activity towards paracetamol.

  5. Electrocatalytic oxidation of hydrazine by copper iodide modified sol-gel derived carbon-ceramic composite Electrode

    Directory of Open Access Journals (Sweden)

    Ghasem Karim-Nezhad

    2014-03-01

    Full Text Available A new sol-gel derived ceramic-carbon composite electrode was fabricated by the use of CuI as modifier. The electrocatalytic activity of the copper iodide modified sol-gel derived ceramic-carbon composite (CIM-SGD-CCC electrode was examined for the oxidation of hydrazine. Cyclic voltammetry was employed to study the electrochemical and electrocatalytic properties of the modified electrode. Results showed that the CIM-SGD-CCC electrode has very high catalytic activity for electrooxidation of hydrazine. This proves that the copper iodide bears the main role in electro-catalytic oxidation of hydrazine. This modified electrode shows fast amperometric response with the range from 1 μ mol L-1 to 40 μ mol L-1 and the limit of detection (LOD of 0.524 μ mol L-1 for hydrazine. The relative standard deviation (R.S.D. was 0.72 % for 5 successive assays. High stability, good reproducibility, rapid response, easy surface regeneration and fabrication are the important characteristics of the proposed electrode.

  6. Sensitive determination of domperidone in biological fluids using a conductive polymer modified glassy carbon electrode

    International Nuclear Information System (INIS)

    A simple and sensitive method for domperidone (DP) determination has been developed by electropolymerizing a polymer film on the surface of glassy carbon electrode (GCE) in acidic solution using cyclic voltammetry. The modified sensor was characterized by Field Emission Scanning Electron Microscopy (FE-SEM) and Electrochemical Impedance Spectroscopy (EIS). The electrochemical measurements were carried out using square wave voltammetry and cyclic voltammetry. The modified sensor exhibited an excellent catalytic response towards the oxidation of DP with a well-defined oxidation peak at 840 mV. The modified sensor exhibited linear calibration curve for DP over a concentration range of 0.1 μM to 100 μM in phosphate buffer solution of pH 7.2 with detection limit of 12.0 nM. The sensor was capable to determine DP effectively without any interference from the common metabolites like ascorbic acid, uric acid, xanthine and hypoxanthine. The analytical utilities of the sensor have been demonstrated by determining the DP in human fluids and pharmaceutical samples. Further, the modified sensor displayed voltammetric responses with high sensitivity, good selectivity and reproducibility which make it suitable for clinical diagnosis

  7. Simultaneous Electrochemical Detection of Dopamine and Ascorbic Acid Using an Iron Oxide/Reduced Graphene Oxide Modified Glassy Carbon Electrode

    Directory of Open Access Journals (Sweden)

    Teo Peik-See

    2014-08-01

    Full Text Available The fabrication of an electrochemical sensor based on an iron oxide/graphene modified glassy carbon electrode (Fe3O4/rGO/GCE and its simultaneous detection of dopamine (DA and ascorbic acid (AA is described here. The Fe3O4/rGO nanocomposite was synthesized via a simple, one step in-situ wet chemical method and characterized by different techniques. The presence of Fe3O4 nanoparticles on the surface of rGO sheets was confirmed by FESEM and TEM images. The electrochemical behavior of Fe3O4/rGO/GCE towards electrocatalytic oxidation of DA was investigated by cyclic voltammetry (CV and differential pulse voltammetry (DPV analysis. The electrochemical studies revealed that the Fe3O4/rGO/GCE dramatically increased the current response against the DA, due to the synergistic effect emerged between Fe3O4 and rGO. This implies that Fe3O4/rGO/GCE could exhibit excellent electrocatalytic activity and remarkable electron transfer kinetics towards the oxidation of DA. Moreover, the modified sensor electrode portrayed sensitivity and selectivity for simultaneous determination of AA and DA. The observed DPVs response linearly depends on AA and DA concentration in the range of 1–9 mM and 0.5–100 µM, with correlation coefficients of 0.995 and 0.996, respectively. The detection limit of (S/N = 3 was found to be 0.42 and 0.12 µM for AA and DA, respectively.

  8. Determination of Anthracene on Ag-Au Alloy Nanoparticles/Overoxidized-Polypyrrole Composite Modified Glassy Carbon Electrodes

    Directory of Open Access Journals (Sweden)

    Emmanuel I. Iwuoha

    2010-10-01

    Full Text Available A novel electrochemical sensor for the detection of anthracene was prepared by modifying a glassy carbon electrode (GCE with over-oxidized polypyrrole (PPyox and Ag-Au (1:3 bimetallic nanoparticles (Ag-AuNPs. The composite electrode (PPyox/Ag-AuNPs/GCE was prepared by potentiodynamic polymerization of pyrrole on GCE followed by its overoxidation in 0.1 M NaOH. Ag-Au bimetallic nanoparticles were chemically prepared by the reduction of AgNO3 and HAuCl4 using C6H5O7Na3 as the reducing agent as well as the capping agent and then immobilized on the surface of the PPyox/GCE. The nanoparticles were characterized by UV-visible spectroscopy technique which confirmed the homogeneous formation of the bimetallic alloy nanoparticles. Transmission electron microscopy showed that the synthesized bimetallic nanoparticles were in the range of 20–50 nm. The electrochemical behaviour of anthracene at the PPyox/Ag-AuNPs/GCE with Ag: Au atomic ratio 25:75 (1:3 exhibited a higher electrocatalytic effect compared to that observed when GCE was modified with each constituent of the composite (i.e., PPyox, Ag-AuNPs and bare GCE. A linear relationship between anodic current and anthracene concentration was attained over the range of 3.0 × 10−6 to 3.56 × 10−4 M with a detection limit of 1.69 × 10−7 M. The proposed method was simple, less time consuming and showed a high sensitivity.

  9. Mediatorless sugar/oxygen enzymatic fuel cells based on gold nanoparticle-modified electrodes.

    Science.gov (United States)

    Wang, Xiaoju; Falk, Magnus; Ortiz, Roberto; Matsumura, Hirotoshi; Bobacka, Johan; Ludwig, Roland; Bergelin, Mikael; Gorton, Lo; Shleev, Sergey

    2012-01-15

    We report on the fabrication and characterisation of a gold-nanoparticle (AuNP)-based mediatorless sugar/oxygen biofuel cell (BFC) operating in neutral sugar-containing buffers and human physiological fluids, such as blood and plasma. First, Corynascus thermophilus cellobiose dehydrogenase (CtCDH) and Myrothecium verrucaria bilirubin oxidase (MvBOx), used as anodic and cathodic bioelements, respectively, were immobilised on gold electrodes modified with 20 nm AuNPs. Detailed characterisation and optimisation of a new CDH/AuNP-based bioanode were performed and the following fundamental parameters were obtained: (i) the redox potential of the haem-containing centre of the enzyme was measured to be 75 mV vs. NHE, (ii) the surface coverage of CtCDH was found to be 0.65 pmol cm(-2) corresponding to a sub-monolayer coverage of the thiol-modified AuNPs by the enzyme, (iii) a turnover number for CtCDH immobilised on thiol-modified AuNPs was calculated to be ca. 0.5 s(-1), and (iv) the maximal current densities as high as 40 μA cm(-2) were registered in sugar-containing neutral buffers. Second, both biomodified electrodes, namely the CtCDH/AuNP-based bioanode and the MvBOx/AuNP-based biocathode, were combined into a functional BFC and the designed biodevices were carefully investigated. The following characteristics of the mediator-, separator- and membrane-less, miniature BFC were obtained: in phosphate buffer; an open-circuit voltage of 0.68 V, a maximum power density of 15 μW cm(-2) at a cell voltage of 0.52 V and in human blood; an open-circuit voltage of 0.65 V, a maximum power density of 3 μW cm(-2) at a cell voltage of 0.45 V, respectively. The estimated half-lives of the biodevices were found to be >12, <8, and <2 h in a sugar-containing buffer, human plasma, and blood, respectively. The basic characteristics of mediatorless sugar/oxygen BFCs were significantly improved compared with previously designed biodevices, because of the usage of three-dimensional AuNP-modified

  10. Investigation of Ir-modified carbon felt as the positive electrode of an all-vanadium redox flow battery

    International Nuclear Information System (INIS)

    Porous graphite felts have been used as electrode materials for all-vanadium redox flow batteries due to their wide operating potential range, stability as both an anode and a cathode, and availability in high surface area. In this paper, the carbon felt was modified by pyrolysis of Ir reduced from H2IrCl6. ac impedance and steady-state polarization measurements showed that the Ir-modified materials have improved activity and lowered overpotential of the desired V(IV)/V(V) redox process. Ir-modification of carbon felt enhanced the electro-conductivity of electrode materials. The Ir-material, when coated on the graphite felt electrode surface, lowered the cell internal resistance. A test cell was assembled with the Ir-modified carbon felt as the activation layer of the positive electrode, the unmodified raw felt as the activation layer of the negative electrode. At an operating current density of 20 mA cm-2, a voltage efficiency of 87.5% was achieved. The resistance of the cell using Ir-modified felt decreased 25% compared to the cell using non-modified felt

  11. Electro-chemical deposition of zinc oxide nanostructures by using two electrodes

    Directory of Open Access Journals (Sweden)

    B. A. Taleatu

    2011-09-01

    Full Text Available One of the most viable ways to grow nanostructures is electro deposition. However, most electrodeposited samples are obtained by three-electrode electrochemical cell. We successfully use a much simpler two-electrode cell to grow different ZnO nanostructures from common chemical reagents. Concentration, pH of the electrolytes and growth parameters like potentials at the electrodes, are tailored to allow fast growth without complexity. Morphology and surface roughness are investigated by Scanning Electron and Air Force Microscopy (SEM and AFM respectively, crystal structure by X-Ray Diffraction measurements (XRD and ZnO stoichiometry by core level photoemission spectroscopy (XPS.

  12. Chemical composition and corrosion protection of silane films modified with CeO2 nanoparticles

    International Nuclear Information System (INIS)

    The present work aims at understanding the role of CeO2 nanoparticles (with and without activation in cerium(III) solutions) used as fillers for hybrid silane coatings applied on galvanized steel substrates. The work reports the improved corrosion protection performance of the modified silane films and discusses the chemistry of the cerium-activated nanoparticles, the mechanisms involved in the formation of the surface coatings and its corrosion inhibition ability. The anti-corrosion performance was investigated using electrochemical impedance spectroscopy (EIS), the scanning vibrating electrode technique (SVET) and d.c. potentiodynamic polarization. The chemical composition of silanised nanoparticles and the chemical changes of the silane solutions due to the presence of additives were studied using X-ray photoelectron spectroscopy (XPS) and nuclear magnetic resonance spectroscopy (NMR), respectively. The NMR and XPS data revealed that the modified silane solutions and respective coatings have enhanced cross-linking and that silane-cerium bonds are likely to occur. Electrochemical impedance spectroscopy showed that the modified coatings have improved barrier properties and the SVET measurements highlight the corrosion inhibition effect of ceria nanoparticles activated with Ce(III) ions. Potentiodynamic polarization curves demonstrate an enhanced passive domain for zinc, in the presence of nanoparticles, in solutions simulating the cathodic environment.

  13. Development of sensitive amperometric hydrogen peroxide sensor using a CuNPs/MB/MWCNT-C60-Cs-IL nanocomposite modified glassy carbon electrode.

    Science.gov (United States)

    Roushani, Mahmoud; Bakyas, Kobra; Zare Dizajdizi, Behruz

    2016-07-01

    A sensitive hydrogen peroxide (H2O2) sensor was constructed based on copper nanoparticles/methylene blue/multiwall carbon nanotubes-fullerene-chitosan-ionic liquid (CuNPs/MB/MWCNTs-C60-Cs-IL) nanocomposites. The MB/MWCNTs-C60-Cs-IL and CuNPs were modified glassy carbon electrode (GCE) by the physical adsorption and electrodeposition of copper nitrate solution, respectively. The physical morphology and chemical composition of the surface of modified electrode was investigated by scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS), respectively. The electrochemical properties of CuNPs/MB/MWCNTs-C60-Cs-IL/GCE were investigated by cyclic voltammetry (CV) and amperometry techniques and the sensor exhibited remarkably strong electrocatalytic activities toward the reduction of hydrogen peroxide. The peak currents possess a linear relationship with the concentration of H2O2 in the range of 0.2μM to 2.0mM, and the detection limit is 55.0nM (S/N=3). In addition, the modified electrode was used to determine H2O2 concentration in human blood serum sample with satisfactory results. PMID:27127028

  14. An improved biosensor for acetaldehyde determination using a bienzymatic strategy at poly(neutral red) modified carbon film electrodes

    OpenAIRE

    Ghica, Mariana Emilia; Pauliukaite, Rasa; Marchand, Nicolas; Devic, Eric; Brett, Christopher M. A.

    2007-01-01

    Improved biosensors for acetaldehyde determination have been developed using a bienzymatic strategy, based on a mediator-modified carbon film electrode and co-immobilisation of NADH oxidase and aldehyde dehydrogenase. Modification of the carbon film electrode with poly(neutral red) mediator resulted in a sensitive, low-cost and reliable NADH detector. Immobilisation of the enzymes was performed using encapsulation in a sol-gel matrix or cross-linking with glutaraldehyde. The bienzymatic biose...

  15. Application of Carbon-Microsphere-Modified Electrodes for Electrochemistry of Hemoglobin and Electrocatalytic Sensing of Trichloroacetic Acid

    OpenAIRE

    Wen-Cheng Wang; Li-Jun Yan; Fan Shi; Xue-Liang Niu; Guo-Lei Huang; Cai-Juan Zheng; Wei Sun

    2015-01-01

    By using the hydrothermal method, carbon microspheres (CMS) were fabricated and used for electrode modification. The characteristics of CMS were investigated using various techniques. The biocompatible sensing platform was built by immobilizing hemoglobin (Hb) on the micrometer-sized CMS-modified electrode with a layer of chitosan membrane. On the cyclic voltammogram, a couple of quasi-reversible cathodic and anodic peaks appeared, showing that direct electrochemistry of Hb with the working e...

  16. 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 ...

  17. Tris(2,2'-bipyridyl) Ruthenium(Ⅱ) Doped Silica Film Modified Indium Tin Oxide Electrode and Its Electrochemiluminescent Properties

    Institute of Scientific and Technical Information of China (English)

    WEI Hui; DU Yan; KANG Jian-Zhen; XU Guo-Bao; WANG Er-Kang

    2007-01-01

    An approach was reported to synthesize silica hybridized ruthenium bipyridyl complex through amidation reaction by covalent attachment of bis(bipyridyl)-4,4'-dicarboxy-2,2'-bipyridyl-ruthenium to (3-aminopropyl)-triethoxysilane.The hybrid complex then was gelatinized through acid catalytic hydrolysis method and a sol-gel modified indium tin oxide electrode was prepared via spin coating technique. As prepared indium tin oxide electrode possesses good stability therein with excellent electrochemiluminescence behavior.

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

    OpenAIRE

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

    2008-01-01

    Functionalised multi-walled carbon nanotubes (MWCNTs) were cast on glassy carbon (GC) and carbon film electrodes (CFE), and were characterised electrochemically and applied in a glucose-oxidase-based biosensor. MWCNT-modified carbon film electrodes were then used to develop an alcohol oxidase (AlcOx) biosensor, in which AlcOx-BSA was cross-linked with glutaraldehyde and attached by drop-coating. The experimental conditions, applied potential and pH, for ethanol monitoring were optimised, and ...

  19. Electrochemical Reduction of Bromate by a Pd Modified Carbon Fiber Electrode: Kinetics and Mechanism

    International Nuclear Information System (INIS)

    Highlights: • The BrO3− electroreduction proceeds with direct mechanism from 0 to -1.0 V. • The BrO3− electroreduction proceeds via atomic H* at more negative than -1.0 V. • Direct and indirect reduction result in strong and weak pH dependence respectively. • Pd facilitates oxygen atoms removal by hydrogenation without palladium-bonding. - Abstract: The electroreduction of bromate (BrO3−) was investigated at a Pd modified carbon fiber (Pd/C) electrode prepared from PdCl2 via electrodeposition method. Pd particles distributed on the carbon fiber substrate uniformly. Under various cathode potentials, electroreduction removal of BrO3− at pure carbon fiber electrode and the Pd/C electrode were firstly compared. It was observed that nearly no BrO3− removal was observed within the bias potential of -2.0 V at the carbon fiber electrode. At the Pd/C electrode, the removal efficiency of BrO3− was sharply increased from 24.0% to 58.4% at the cathode potential of -1.0 to -1.5 V, which was further increased to be 87.2% at -2.0 V. The electrochemical reduction of BrO3− was strongly pH-dependent at -0.5 V and the reduction rate could be enhanced at low pH. While at the potential of -2.0 V, a slight pH effect was observed. BrO3− electroreduction follows pseudo first-order kinetics; the rate constant k was firstly increased from 0.016 to 0.031 min−1 with the increase of the Pd loading amount from 0.31 to 0.73 mg/cm2, and then was decreased to 0.018 min−1 at a higher Pd loading amount of 1.05 mg/cm2. The Pd(0) nanoparticles played a significant role in forming atomic H* to realize indirect BrO3− reduction. The electrochemical reduction of BrO3− produces accumulated intermediates of HOBr and OBr−, which were subsequently reduced to Br− with the time evolution

  20. Electrochemical detection of rutin with a carbon ionic liquid electrode modified by Nafion, graphene oxide and ionic liquid composite

    International Nuclear Information System (INIS)

    We report on a carbon ionic liquid electrode modified with a composite made from Nafion, graphene oxide and ionic liquid, and its application to the sensitive determination of rutin. The modified electrode was characterized by cyclic voltammetry and electrochemical impedance spectroscopy. It shows excellent cyclic voltammetric and differential pulse voltammetric performance due to the presence of nanoscale graphene oxide and the ionic liquid, and their interaction. A pair of well-defined redox peaks of rutin appears at pH 3.0, and the reduction peak current is linearly related to its concentration in the range from 0.08 μM to 0.1 mM with a detection limit of 0.016 μM (at 3σ). The modified electrode displays excellent selectivity and good stability, and was successfully applied to the determination of rutin in tablets with good recovery. (author)

  1. Hydrogen peroxide sensor based on a stainless steel electrode coated with multi-walled carbon nanotubes modified with magnetite nanoparticles

    International Nuclear Information System (INIS)

    Multi-walled carbon nanotubes (MWCNTs) were decorated with magnetite (Fe3O4) nanoparticles and then used to modify a stainless steel electrode. The Fe3O4/MWCNTs composite was characterized by scanning electron microscopy, transmission electron microscopy, Raman spectroscopy and X-ray diffraction patterns. Electrochemical properties of the modified electrode revealed a substantial catalytic activity for the reduction of hydrogen peroxide. The relationship between peak current and the concentration of hydrogen peroxide was linear in the range from 0.06 mmol L-1 to 0.36 mmol L-1, and the lowest detectable concentration is 0.01 mmol.L-1 (S/N=3). The modified stainless steel electrode displays excellent stability. (author)

  2. Electrochromic properties of WO{sub 3} thin film onto gold nanoparticles modified indium tin oxide electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Deng Jiajia; Gu Ming [College of Chemistry, Chemical Engineering and Material Science, Soochow University, Suzhou Industrial Park, Suzhou, Jiangsu 215123 (China); Di Junwei, E-mail: djw@suda.edu.cn [College of Chemistry, Chemical Engineering and Material Science, Soochow University, Suzhou Industrial Park, Suzhou, Jiangsu 215123 (China)

    2011-04-15

    Gold nanoparticles (GNPs) thin films, electrochemically deposited from hydrogen tetrachloroaurate onto transparent indium tin oxide (ITO) thin film coated glass, have different color prepared by variation of the deposition condition. The color of GNP film can vary from pale red to blue due to different particle size and their interaction. The characteristic of GNPs modified ITO electrodes was studied by UV-vis spectroscopy, scanning electron microscope (SEM) images and cyclic voltammetry. WO{sub 3} thin films were fabricated by sol-gel method onto the surface of GNPs modified electrode to form the WO{sub 3}/GNPs composite films. The electrochromic properties of WO{sub 3}/GNPs composite modified ITO electrode were investigated by UV-vis spectroscopy and cyclic voltammetry. It was found that the electrochromic performance of WO{sub 3}/GNPs composite films was improved in comparison with a single component system of WO{sub 3}.

  3. Layer-by-Layer Assembly of Silicotungstate Multilayer Films Modified on Glassy Carbon Electrode and Their Electrochemical Behaviors

    International Nuclear Information System (INIS)

    A new electrode was modified by multilayer films composed of heteropolyanion (SiW12) and cationic polymer poly(diallyldimethylammonium chloride) through electrochemical growth. The modified electrode electrochemical behavior, the effect of solution ph and electrocatalytic response to the reduction of BrO3- and NO2- have been investigated. The result shows that the electrochemical process of multilayer films modified electrode including SiW12 is a reversible process by electrochemical step. One-electron process has no proton participation in the first step, and one-electron process is accompanied by one proton participation in the second step and two-electron process is accompanied by two protons participation in the third step. The films grow uniformly, and the peak currents increase with increasing layer numbers. The peak currents increase with scan rate, and the reduced potentials of multilayer films shift negatively with increasing pH. The electrochemical mechanism of multilayer films was suggested

  4. Anodic stripping voltammetric determination of arsenic(III) using a glassy carbon electrode modified with gold-palladium bimetallic nanoparticles

    International Nuclear Information System (INIS)

    A glassy carbon electrode (GC E) was modified by casting gold-palladium (Au-Pd) nanoparticles onto its surface and then used for the determination of As(III) by stripping voltammetry. The structure and electrochemical properties of the nanoparticles were characterized by UV-vis spectroscopy, high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and cyclic voltammetry. Anodic stripping voltammetry of the modified electrode was performed in solutions of pH 4.5 containing various concentrations of arsenite. The modified GC E exhibited good response towards As(III), with a limit of detection of around 0.25 ppb which is much lower than the current EPA standard of 10 ppb. The electrode is stable and not interfered by Pb(II), Cd(II), Mn(II), and Zn(II). (author)

  5. Photoelectrocatalytic analysis and electrocatalytic determination of hydroquinone by using a Cu2O-reduced graphene oxide nanocomposite modified rotating ring-disk electrode.

    Science.gov (United States)

    Xie, Hong; Duan, Kaiyue; Xue, Muyin; Du, Yongling; Wang, Chunming

    2016-08-01

    Reduced graphene oxide (rGO)-based Cu2O nanocomposites were prepared by a facile one-pot reaction process. The surface morphology, structure and chemical composition of Cu2O-rGO nanocomposites were characterized by transmission electron microscopy, X-ray photoelectron spectroscopy and X-ray diffraction. The Cu2O-rGO modified Pt rotating ring-disk electrode (RRDE) was successfully fabricated for the photoelectrocatalytic analysis of hydroquinone (HQ). The photoelectrochemical behaviors of HQ were investigated by the hydrodynamic differential pulse voltammetry technique, using the Cu2O-rGO modified Pt RRDE as the working electrode. The effects of pH values, rotation rates, illumination time and applied bias potential have been discussed. The possible electroactive intermediate product, namely hydroxyhydroquinone, was obtained through the photoelectrocatalytic degradation of HQ on the Cu2O-rGO modified Pt disk electrode, which was compulsively transported and could only be detected at the bare Pt ring electrode at around +0.02 V with an oxidation signal. We found that the peak current at +0.02 V had a good linear relationship with the HQ concentration in the range from 5.0 × 10(-6) to 1.0 × 10(-3) M, with a low limit of detection and excellent reproducibility. The present work has demonstrated that Cu2O-rGO nanocomposites have enhanced photoelectrocatalytic ability for the degradation of organic pollutants and this modified RRDE technique can be potentially applied for the in situ determination of organic pollutants. PMID:27297492

  6. Stability of [Ru(II)(tpy)(bpy)(OH(2))](2+)-modified graphite electrodes during indirect electrolyses.

    Science.gov (United States)

    Geneste, Florence; Moinet, Claude; Ababou-Girard, Soraya; Solal, Francine

    2005-06-13

    The stability of a graphite felt electrode modified by covalent attachment of [Ru(II)(tpy)(bpy)(OH(2))](2+) is investigated during the indirect electrolyses of alcohols in a flow cell. The continuous increase of the local potential of the electrode during the electrolyses attests to its degradation. Cyclic voltammetry analyses of the modified electrode after electrolyses show a total decrease of 80-90% of the wave corresponding to the Ru(III/II) couple. The concentration of remaining alcohol measured at the outlet of the cell is almost constant during all the electrolyses but increase when the potential exceeds 0.95 V(SCE). At low potentials, the electrode can be regenerated by reaction with Ru(II)Cl(2)(DMSO)(tpy) and then CF(3)SO(3)H, followed by hydrolysis, showing that the bipyridine ligand remains covalently attached to the electrode. At high potentials, the graphite is oxidized and the catalyst is partly lost in the reaction medium. XPS analyses of Ru core levels reveal that the ruthenium disappeared after electrolysis, showing that the degradation of the modified electrode is due to the demetalation of the oxidized complex. PMID:15934767

  7. DNA-modified electrodes fabricated using copper-free click chemistry for enhanced protein detection.

    Science.gov (United States)

    Furst, Ariel L; Hill, Michael G; Barton, Jacqueline K

    2013-12-31

    A method of DNA monolayer formation has been developed using copper-free click chemistry that yields enhanced surface homogeneity and enables variation in the amount of DNA assembled; extremely low-density DNA monolayers, with as little as 5% of the monolayer being DNA, have been formed. These DNA-modified electrodes (DMEs) were characterized visually, with AFM, and electrochemically, and were found to facilitate DNA-mediated reduction of a distally bound redox probe. These low-density monolayers were found to be more homogeneous than traditional thiol-modified DNA monolayers, with greater helix accessibility through an increased surface area-to-volume ratio. Protein binding efficiency of the transcriptional activator TATA-binding protein (TBP) was also investigated on these surfaces and compared to that on DNA monolayers formed with standard thiol-modified DNA. Our low-density monolayers were found to be extremely sensitive to TBP binding, with a signal decrease in excess of 75% for 150 nM protein. This protein was detectable at 4 nM, on the order of its dissociation constant, with our low-density monolayers. The improved DNA helix accessibility and sensitivity of our low-density DNA monolayers to TBP binding reflects the general utility of this method of DNA monolayer formation for DNA-based electrochemical sensor development. PMID:24328347

  8. Electrochemical sensor for Isoniazid based on the glassy carbon electrode modified with reduced graphene oxide–Au nanomaterials

    Energy Technology Data Exchange (ETDEWEB)

    Guo, Zhuo, E-mail: guozhuochina@syuct.edu.cn [Department of Materials Science and Engineering, Shenyang University of Chemical Technology, Shenyang 110142 (China); Wang, Ze-yu [Department of Materials Science and Engineering, Shenyang University of Chemical Technology, Shenyang 110142 (China); Wang, Hui-hua, E-mail: hhwang@suda.edu.cn [Shagang School of Iron and Steel, Soochow University, Suzhou 215021 (China); Huang, Guo-qing; Li, Meng-meng [Department of Materials Science and Engineering, Shenyang University of Chemical Technology, Shenyang 110142 (China)

    2015-12-01

    A sensitive electrochemical sensor has been fabricated to detect Isoniazid (INZ) using reduced graphene oxide (RGO) and Au nanocomposites (RGO–Au). RGO–Au nanocomposites were synthesized by a solution-based approach of chemical co-reduction of Au(III) and graphene oxide (GO), and were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Raman spectroscopy, and Fourier transform infrared (FT-IR). The Au nanoparticles separate the RGO sheets in the precipitate and prevent RGO sheets from aggregation upon π–π stacking interactions. RGO–Au nanocomposites were used to modify the glassy carbon electrode (GCE). The electrochemical properties of RGO–Au/GCE were investigated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), and the RGO–Au/GCE exhibited remarkably strong electrocatalytic activities towards INZ. Under the optimized conditions, there was linear relationships between the peak currents and the concentrations in the range of 1.0 × 10{sup −7} M to 1.0 × 10{sup −3} M for INZ, with the limit of detection (LOD) (based on S/N = 3) of 1.0 × 10{sup −8} M for INZ. - Highlights: • RGO–Au nanocomposites were synthesized and characterized by chemical co-reduction of Au (III) and GO. • RGO–Au/GCE was used as a sensitive electrochemical sensor to detect Isoniazid. • RGO–Au/GCE exhibited strong electrocatalytic activities towards Isoniazid.

  9. 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

  10. Film forming capacity of chemically modified corn starches.

    Science.gov (United States)

    López, Olivia V; García, María A; Zaritzky, Noemí E

    2008-09-01

    Native starch can be chemically modified to improve its functionality and to expand its uses. Modified starches were characterized and the rheological behavior of filmogenic suspensions was analyzed. The film forming capacity of different chemical modified corn starches was evaluated. Acetylated starch was selected by the characteristics of the resulted films; its optimum concentration was 5% w/w since their films exhibited the lowest water vapor permeability (WVP, 1.26×10(-10)g/msPa). The effect of glycerol as plasticizer on film properties depend on its concentration, being 1.5% w/w those that allows to obtain the lowest WVP value (1.64×10(-11)g/msPa), low film solubility in water and a more compact structure than those of unplasticized films. Mechanical behavior of plasticized acetylated starch films depends on glycerol concentration, being rigid and brittle the unplasticized ones, ductile those containing 1.5% w/w of glycerol and very flexible those with a higher plasticizer content. PMID:26048223

  11. CHEMICALLY MODIFIED ZEOLITES: SURFACES AND INTERACTION WITH Cs AND Co

    Directory of Open Access Journals (Sweden)

    Pavel Dillinger

    2007-06-01

    Full Text Available Inorganic exchangers, including zeolites, have interesting properties such as resistance to decomposition in the presence of ionizing radiation or to high temperatures, what make them applicable for the purification of low and middle polluted radioactive waste waters. The research was focused on model radioactive waste effluents and the investigated metals were cobalt (Co and cesium (Cs. The performance of natural zeolite of clinoptilolite type and zeolite chemically modified with NaOH solutions was determined by studying their surface and sorption properties using volumetric method and static radioindicator method. The measurements of zeolite´s surfaces showed the double increase of the specific surface along with an increase of mesopore’s diameter. The reason is the extraction of silicon from zeolite caused by NaOH solution what creates secondary mesoporous structure. The radioactive tracer technique was used to evaluate sorption properties of zeolites and the best sorbent was selected based on KD, μ, Γ and S values. The sorption abilities of natural and chemically modified zeolites for Cs uptake were comparable. The uptake of Co with natural zeolite was negligible and it increased up to 14 times for modified zeolites depending on the concentration of treated NaOH solution.

  12. 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...

  13. A novel electrochemical sensor of bisphenol A based on stacked graphene nanofibers/gold nanoparticles composite modified glassy carbon electrode

    International Nuclear Information System (INIS)

    In this paper, a novel and convenient electrochemical sensor based on stacked graphene nanofibers (SGNF) and gold nanoparticles (AuNPs) composite modified glassy carbon electrode (GCE) was developed for the determination of bisphenol A (BPA). The AuNPs/SGNF modified electrode showed an efficient electrocatalytic role for the oxidation of BPA, and the oxidation overpotentials of BPA were decreased significantly and the peak current increased greatly compared with bare GCE and other modified electrode. The transfer electron number (n) and the charge transfer coefficient (α) were calculated with the result as n = 4, α = 0.52 for BPA, which indicated the electrochemical oxidation of BPA on AuNPs/SGNF modified electrode was a four-electron and four-proton process. The effective surface areas of AuNPs/SGNF/GCE increased for about 1.7-fold larger than that of the bare GCE. In addition, the kinetic parameters of the modified electrode were calculated and the apparent heterogeneous electron transfer rate constant (ks) was 0.51 s−1. Linear sweep voltammetry was applied as a sensitive analytical method for the determination of BPA and a good linear relationship between the peak current and BPA concentration was obtained in the range from 0.08 to 250 μM with a detection limit of 3.5 × 10−8 M. The modified electrode exhibited a high sensitivity, long-term stability and remarkable reproducible analytical performance and was successfully applied for the determination of BPA in baby bottles with satisfying results

  14. Removal characteristics of plasma chemical vaporization machining with a pipe electrode for optical fabrication

    International Nuclear Information System (INIS)

    Plasma chemical vaporization machining (CVM) is a high-precision chemical shaping method using rf plasma generated in the proximity of an electrode in an atmospheric environment. The purpose of the present study is to clarify the removal characteristics of plasma CVM using a pipe electrode. Polished fused silica plates were processed by plasma CVM, polishing, and precision grinding under various conditions. The removal rate of plasma CVM was about 4 to 1100 times faster than that of polishing, and the maximum removal rate was almost equal to that of precision grinding. The roughness of the resultant surfaces was almost the same as that of the polished surfaces.

  15. Electrochemical Detection of Clenbuterol in Pig Liver at Pyrrole-DNA Modified Boron-doped Diamond Electrode

    Institute of Scientific and Technical Information of China (English)

    WU Jing; LI Xiao-li; WU Xu-mei; HUAN Shuang-yan; SHEN Guo-li; YU Ru-qin

    2005-01-01

    The direct detection of clenbuterol(CL) in pig liver without any extraction separation at a pyrrole-DNA modified boron-doped diamond(BDD) electrode is reported. The pyrrole-DNA modified BDD electrode has a strong electrocatalytic effect on the redox reaction of CL. One oxidization and two reduction peaks of CL appear at 340.2, 299.8 and 166.6 mV(versus SCE), respectively. The pyrrole polymer alone cannot electrocatalyze the above reaction at a BDD electrode; the electrocatalytic effect of a BDD electrode modified with DNA membrane is unsufficient for the analytical detection of CL; the replacement of boron-doped diamond by glass carbon makes the electrocatalytic reaction impossible; the redox process is pH dependent. The influences of various experimental parameters on the pyrrole-DNA modified BDD electrode were investigated. A sensitive cyclic voltammetric response for CL was obtained in a linear range from 3.4×10-6 to 5×10-4 mol/L with a detection limit of 8.5×10-7 mol/L. A mean recovery of 102.7% of CL in the pig liver sample solution and a reproducibility of 3.2% were obtained.

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

    International Nuclear Information System (INIS)

    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 × 10−8 to 2.0 × 10−4 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 × 10−8 to 2.0 × 10−4 M. • The detection limit for hydrochlorothiazide was obtained at 20.0 nM. • It resolved the voltammetric waves of hydrochlorothiazide and folic acid

  17. 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.

  18. Treatment of graphite felt by modified Hummers method for the positive electrode of vanadium redox flow battery

    International Nuclear Information System (INIS)

    A novel and highly effective treatment based on modified Hummers method was firstly used to improve the electrochemical activity of graphite felt as the positive electrode in all-vanadium redox flow battery (VRFB). The graphite felt was treated by the modified Hummers method and characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. The electrochemical performance of the prepared electrode was evaluated through cyclic voltammetry and electrochemical impedance spectroscopy. Results show that graphite felt treated by modified Hummers method exhibits excellent electrocatalytic activity and reaction rate to vanadium redox couples. In our research, the hydrogen electrode and H2 replaced the graphite felt and V2+/V3+ couple in the negative side in the VRFB performance test. The coulombic, voltage, and energy efficiencies of the VRFB with the as-prepared electrodes at 50 mA cm−2 are 95.0%, 81.3%, and 77.2%, respectively. These values are much higher than those of the cell-assembled graphite felt electrodes that were conventionally and thermally treated. The graphite felt treated by the modified Hummers method carries more hydrophilic groups, such as–OH, on its defects, which is advantageous in facilitating the redox reaction of vanadium ions, thereby improving the operation efficiency of the vanadium redox flow battery

  19. A sensitive and selective nitrite sensor based on a glassy carbon electrode modified with gold nanoparticles and sulfonated graphene

    International Nuclear Information System (INIS)

    We describe a highly sensitive and selective amperometric sensor for the determination of nitrite. A glassy carbon electrode was modified with a composite made from gold nanoparticles (AuNPs) and sulfonated graphene (SG). The modified electrode displays excellent electrocatalytic activity in terms of nitrite oxidation by giving much higher peak currents (at even lower oxidation overpotential) than those found for the bare electrode, the AuNPs-modified electrode, and the SG-modified electrode. The sensor has a linear response in the 10 μM to 3.96 mM concentration range, a very good detection sensitivity (45.44 μA mM−1), and a lower detection limit of 0.2 μM of nitrite. Most common ions and many environmental organic pollutants do not interfere. The sensor was successfully applied to the determination of nitrite in water samples, and the results were found to be consistent with the values obtained by spectrophotometry. (author)

  20. Nano-structured Ni(II)-curcumin modified glassy carbon electrode for electrocatalytic oxidation of fructose

    Energy Technology Data Exchange (ETDEWEB)

    Elahi, M. Yousef [Department of Chemistry, Faculty of Science, Tarbiat Modares University, P.O. Box 14115-175, Tehran (Iran, Islamic Republic of); Mousavi, M.F. [Department of Chemistry, Faculty of Science, Tarbiat Modares University, P.O. Box 14115-175, Tehran (Iran, Islamic Republic of)], E-mail: mousavim@modares.ac.ir; Ghasemi, S. [Department of Chemistry, Faculty of Science, Tarbiat Modares University, P.O. Box 14115-175, Tehran (Iran, Islamic Republic of)

    2008-12-30

    A nano-structured Ni(II)-curcumin (curcumin: 1,7-bis[4-hydroxy-3-methoxyphenyl]-1,6-heptadiene-3,5-dione) film is electrodeposited on a glassy carbon electrode in alkaline solution. The morphology of polyNi(II)-curcumin (NC) was investigated by scanning electron microscopy (SEM). The SEM results show NC has a nano-globular structure in the range 20-50 nm. Using cyclic voltammetry, linear sweep voltammetry, chronoamperometry, steady-state polarization measurements and electrochemical impedance spectroscopy (EIS) showed that the nano-structure NC film acts as an efficient material for the electrocatalytic oxidation of fructose. According to the voltammetric studies, the increase in the anodic peak current and subsequent decrease in the corresponding cathodic current, fructose was oxidized on the electrode surface via an electrocatalytic mechanism. The EIS results show that the charge-transfer resistance has as a function of fructose concentration, time interval and applied potential. The increase in the fructose concentration and time interval in fructose solution results in enhanced charge transfer resistance in Nyquist plots. The EIS results indicate that fructose electrooxidation at various potentials shows different impedance behaviors. At lower potentials, a semicircle is observed in the first quadrant of impedance plot. With further increase of the potential, a transition of the semicircle from the first to the second quadrant occurs. Also, the results obtained show that the rate of fructose electrooxidation depends on concentration of OH{sup -}. Electron transfer coefficient, diffusion coefficient and rate constant of the electrocatalytic oxidation reaction are obtained. The modified electrode was used as a sensor for determination of fructose with a good dynamic range and a low detection limit.

  1. DNA hybridization and phosphinothricin acetyltransferase gene sequence detection based on zirconia/nanogold film modified electrode

    Science.gov (United States)

    Zhang, Wei; Yang, Tao; Jiang, Chen; Jiao, Kui

    2008-05-01

    This study reports a novel electrochemical DNA biosensor based on zirconia (ZrO 2) and gold nanoparticles (NG) film modified glassy carbon electrode (GCE). NG was electrodeposited onto the glassy carbon electrode at 1.5 V, and then zirconia thin film on the NG/GCE was fabricated by cyclic voltammetric method (CV) in an aqueous electrolyte of ZrOCl 2 and KCl at a scan rate of 20 mV/s. DNA probes were attached onto the ZrO 2/NG/GCE due to the strong binding of the phosphate group of DNA with the zirconia film and the excellent biocompatibility of nanogold with DNA. CV and electrochemical impedance spectroscopy (EIS) were used to characterize the modification of the electrode and the probe DNA immobilization. The electrochemical response of the DNA hybridization was measured by differential pulse voltammetry (DPV) using methylene blue (MB) as the electroactive indicator. After the hybridization of DNA probe (ssDNA) with the complementary DNA (cDNA), the cathodic peak current of MB decreased obviously. The difference of the cathodic peak currents of MB between before and after the hybridization of the probe DNA was used as the signal for the detection of the target DNA. The sequence-specific DNA of phosphinothricin acetyltransferase (PAT) gene in the transgenic plants was detected with a detection range from 1.0 × 10 -10 to 1.0 × 10 -6 mol/L, and a detection limit of 3.1 × 10 -11 mol/L.

  2. Synthesis of modified polymer inclusion membranes for photo-electrodeposition of cadmium using polarized electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Yahia Cherif, Asma [Laboratory of Hydrometallurgy and Inorganic Molecular Chemistry, Faculty of Chemistry, USTHB, BP 32 El Alia, 16111, Algiers (Algeria); Arous, Omar, E-mail: omararous@yahoo.fr [Laboratory of Hydrometallurgy and Inorganic Molecular Chemistry, Faculty of Chemistry, USTHB, BP 32 El Alia, 16111, Algiers (Algeria); Center of Research in Physical and Chemical Analysis CRAPC, BP 248 Algiers, RP 16004, Algiers (Algeria); Amara, Mourad [Laboratory of Hydrometallurgy and Inorganic Molecular Chemistry, Faculty of Chemistry, USTHB, BP 32 El Alia, 16111, Algiers (Algeria); Omeiri, Said [Center of Research in Physical and Chemical Analysis CRAPC, BP 248 Algiers, RP 16004, Algiers (Algeria); Laboratory of Storage and Valorization of Renewable Energies, Faculty of Chemistry, USTHB, BP 32 El Alia, 16111, Algiers (Algeria); Kerdjoudj, Hacene [Laboratory of Hydrometallurgy and Inorganic Molecular Chemistry, Faculty of Chemistry, USTHB, BP 32 El Alia, 16111, Algiers (Algeria); Trari, Mohamed [Laboratory of Storage and Valorization of Renewable Energies, Faculty of Chemistry, USTHB, BP 32 El Alia, 16111, Algiers (Algeria)

    2012-08-15

    Highlights: Black-Right-Pointing-Pointer Homogeneous PIM membranes containing water soluble polymers have been obtained under new experimental conditions. Black-Right-Pointing-Pointer Photoelectrodeposition of 'Cd' has been carried out using WO{sub 3} and CuFeO{sub 2} as electrode. Black-Right-Pointing-Pointer Using both photo-polarized electrodes enhances transference of cadmium compared to one. Black-Right-Pointing-Pointer Membrane with poly-phosphoric acid (PPA) give a rise of transferred amount of Cd. - Abstract: In this work, we have developed a novel class of polymeric inclusion membranes (PIMs) for the cations separation. The membrane is made up of cellulose triacetate modified by poly-electrolytes (poly-phosphoric acid, polyvinyl pyrolidone, polyacrylic acid, polyvinyl alcohol and poly-anetholsulfonic acid) using 2-hydroxy-5-dodecylbenzaldehyde incorporated into the polymer as carrier and tris ethyl hexyl phosphate or glycerine as plasticizers. Different PIMs are synthesized and characterized by the Fourier transform infrared, X-ray diffraction, thermal analysis and scanning electron microscopy. The influence of the membrane nature is studied using supports with different physical characteristics (porosity, thickness, hydrophobia). As application, the transport of Cd{sup 2+} using PIMs coupled with photo-electrodes is investigated. The photo-catalytic results indicate that the combined system p-CuFeO{sub 2}/membrane/n-WO{sub 3} enhances considerably the electrons transfer toward the delafossite CuFeO{sub 2}. The position of the conduction band of CuFeO{sub 2} is looked to be the key issue for the photo electrochemical Cd{sup 2+} reduction.

  3. Nano-structured Ni(II)-curcumin modified glassy carbon electrode for electrocatalytic oxidation of fructose

    International Nuclear Information System (INIS)

    A nano-structured Ni(II)-curcumin (curcumin: 1,7-bis[4-hydroxy-3-methoxyphenyl]-1,6-heptadiene-3,5-dione) film is electrodeposited on a glassy carbon electrode in alkaline solution. The morphology of polyNi(II)-curcumin (NC) was investigated by scanning electron microscopy (SEM). The SEM results show NC has a nano-globular structure in the range 20-50 nm. Using cyclic voltammetry, linear sweep voltammetry, chronoamperometry, steady-state polarization measurements and electrochemical impedance spectroscopy (EIS) showed that the nano-structure NC film acts as an efficient material for the electrocatalytic oxidation of fructose. According to the voltammetric studies, the increase in the anodic peak current and subsequent decrease in the corresponding cathodic current, fructose was oxidized on the electrode surface via an electrocatalytic mechanism. The EIS results show that the charge-transfer resistance has as a function of fructose concentration, time interval and applied potential. The increase in the fructose concentration and time interval in fructose solution results in enhanced charge transfer resistance in Nyquist plots. The EIS results indicate that fructose electrooxidation at various potentials shows different impedance behaviors. At lower potentials, a semicircle is observed in the first quadrant of impedance plot. With further increase of the potential, a transition of the semicircle from the first to the second quadrant occurs. Also, the results obtained show that the rate of fructose electrooxidation depends on concentration of OH-. Electron transfer coefficient, diffusion coefficient and rate constant of the electrocatalytic oxidation reaction are obtained. The modified electrode was used as a sensor for determination of fructose with a good dynamic range and a low detection limit

  4. Electro-oxidation of chlorophenols at glassy carbon electrodes modified with polyNi(II)complexes

    International Nuclear Information System (INIS)

    The effect of the ligand macrocycle (phenylporphyrin (PP) or phthalocyanine (Pc)) and of the ligand substituent (-NH2 or -SO3-) on the catalytic activity for the electro-oxidation in a pH 11 buffer electrolyte of 2- and 4-chlorophenol (2-CP and 4-CP), 2,4- and 2,6-dichlorophenol (2,4-DCP and 2,6-DCP), 2,4,6-trichlorophenol (2,4,6-TCP), and pentachlorophenol (PCP) at glassy carbon electrodes modified with electropolymerized Ni(II) macrocycles was studied. The polyphenolic residue deposited at the electrode surface was characterized by cyclic voltammetry, impedance measurements, ex situ Fourier transform infrared spectroscopy (FT-IR) and X-ray Photoelectron Spectroscopy (XPS). A band of aliphatic C=O stretching in the IR spectrum of the fouling film produced by potential cycling in 2,4,6-TCP indicated that the aromatic ring had been broken, yielding ketones, aldehydes and/or carboxylic acids. The sulphonated Ni(II) polymers, which showed the Ni(III)/Ni(II) process in the CV, had XP spectra typical of paramagnetic Ni(II), indicating that they contained Ni(OH)2 clusters. On the contrary, the CVs of the amino Ni(II) did not show the Ni(III)/Ni(II) process at all, this process appearing only after previous activation by potential cycling, and only to a small extent. As was to be expected, the XP spectra of activated amino films corresponded to diamagnetic Ni(II), showing that the concentration of Ni(OH)2 clusters was very small. The amino films were less active than the sulpho films for the oxidation of chlorophenols, in agreement with the lower concentration of Ni(OH)2 clusters in the former films. For all electrodes the highest activity was observed for 2,4,6-TCP, since its oxidation yields a phenolic residue which is much more porous than those produced by the other CPs.

  5. Graphene/SnO2 nanocomposite-modified electrode for electrochemical detection of dopamine

    Directory of Open Access Journals (Sweden)

    R. Nurzulaikha

    2015-09-01

    Full Text Available A graphene-tin oxide (G-SnO2 nanocomposite was prepared via a facile hydrothermal route using graphene oxide and Sn precursor solution without addition of any surfactant. The hydrothermally synthesized G-SnO2 nanocomposite was characterized using a field emission scanning electron microscope (FESEM, high resolution transmission electron microscope (HRTEM, X-ray diffraction (XRD, and energy dispersive spectroscopy (EDS. A homogeneous deposition of SnO2 nanoparticles with an average particle size of 10 nm on the graphene was observed in the FESEM and HRTEM images. The G-SnO2 nanocomposite was used to fabricate a modified electrode for the electrochemical detection of dopamine (DA in the presence of ascorbic acid (AA. Differential pulse voltammetry (DPV showed a limit of detection (LoD of 1 μM (S/N = 3 in the presence of ascorbic acid (AA.

  6. MODIFIED SCREEN-PRINTED CARBON ELECTRODES WITH TYROSINASE FOR DETERMINATION OF PHENOLIC COMPOUNDS IN SMOKED FOOD

    Directory of Open Access Journals (Sweden)

    V. Dragancea

    2010-12-01

    Full Text Available A screen-printed carbon electrode modified with tyrosinase (SPCE-Tyr/Paa/Glut has been developed for the determination of phenol concentration in real samples. The resulting SPCE-Tyr/Paa/Glut was prepared in a one-step procedure, and was then optimized as an amperometric biosensor operating at 0 mV versus Ag/AgCl for phenol determination in flow injection mode. Phenol detection was realized by electrochemical reduction of quinone produced by tyrosinase activity. The possibility of using the developed biosensor to determine phenol concentrations in various smoked products (bacon, ham, chicken and salmon was also evaluated. Gas chromatography (GC method was used for result validation obtained in flow injection mode using amperometric biosensor. The result showed good correlation with those obtained by flowinjection analysis (FIA.

  7. The electrochemical behavior of some podands at a benzo[c]cinnoline modified glassy carbon electrode

    Energy Technology Data Exchange (ETDEWEB)

    Isbir, Aybueke A. [Ankara University, Faculty of Science, Department of Chemistry, 06100 Tandogan, Ankara (Turkey); Solak, Ali Osman [Ankara University, Faculty of Science, Department of Chemistry, 06100 Tandogan, Ankara (Turkey)]. E-mail: osolak@science.ankara.edu.tr; Uestuendag, Zafer [Ankara University, Faculty of Science, Department of Chemistry, 06100 Tandogan, Ankara (Turkey); Bilge, Selen [Ankara University, Faculty of Science, Department of Chemistry, 06100 Tandogan, Ankara (Turkey); Natsagdorj, Amgalan [Ankara University, Faculty of Science, Department of Chemistry, 06100 Tandogan, Ankara (Turkey); Kilic, Emine [Ankara University, Faculty of Science, Department of Chemistry, 06100 Tandogan, Ankara (Turkey); Kilic, Zeynel [Ankara University, Faculty of Science, Department of Chemistry, 06100 Tandogan, Ankara (Turkey)

    2005-08-15

    This paper describes the grafting of benzo[c]cinnoline (BCC) molecules on glassy carbon (GC) electrode surface. The attachment of BCC molecules to carbon substrate is induced by the electrochemical reduction of the corresponding diazonium salt. The modification of GC with BCC diazonium salt was done in aprotic solution and proved by blocking of dopamine electron transfer. The presence of BCC at the GC surface was characterized by cyclic voltammetry and X-ray photoelectron spectroscopy (XPS). On modified surface, the electrochemical behavior of two different types of podands and the catalytic effects of the GC-BCC surface were studied. The XPS was used to monitor element characteristics of the adsorbates on the GC surface and confirm the attachment of BCC molecules to the GC surface.

  8. Reaction of erythromycin with dissolved oxygen on gold nanoparticle-modified glassy carbon electrodes

    Institute of Scientific and Technical Information of China (English)

    LI Xue; FU Ying; WANG Jian-xiu; L(U) Hui-dan; XU Mao-tian

    2008-01-01

    Cyclic voltammetry was used to investigate the reaction of erythromycin (EM) with dissolved oxygen on gold nanoparticle-modified electrodes prepared via electrodeposition. A well-defined reduction peak at -0.420 V and a reoxidation peak at -0.055V were observed. With the addition of EM into the NaOH solution containing dissolved oxygen, the oxidation peak at -0.055 V was still indiscernible. However, a new oxidation peak at 0.200V appeared, which suggests the interaction between EM and dissolved oxygen. Therefore, this method can be used for the analysis of EM in tablets. The present method is simple, reproducible,and does not require complex analytical instruments.

  9. Anodic stripping voltammetry of antimony using gold nanoparticle-modified carbon screen-printed electrodes

    International Nuclear Information System (INIS)

    Carbon screen-printed electrodes (CSPE) modified with gold nanoparticles present an interesting alternative in the determination of antimony using differential pulse anodic stripping voltammetry. Metallic gold nanoparticles deposits have been obtained by direct electrochemical deposition. Scanning electron microscopy measurements show that the electrochemically synthesized gold nanoparticles are deposited in aggregated form. Any undue effects caused by the presence of foreign ions in the solution were also analyzed to ensure that common interferents in the determination of antimony by ASV. The detection limit for Sb(III) obtained was 9.44 x 10-10 M. In terms of reproducibility, the precision of the above mentioned method in %R.S.D. values was calculated at 2.69% (n = 10). The method was applied to determine levels of antimony in seawater samples and pharmaceutical preparations

  10. Sensitive determination of carbidopa through the electrochemiluminescence of luminol at graphene-modified electrodes.

    Science.gov (United States)

    Hosseini, Morteza; Mirzanasiri, Nooshin; Rezapour, Morteza; Sheikhha, Mohammad Hasan; Faridbod, Farnoush; Norouzi, Parviz; Ganjali, Mohammad Reza

    2015-06-01

    Using the concept of electrogenerated chemiluminescence (ECL), a sensitive analytical method for the determination of carbidopa is described. Electro-oxidation of carbidopa on the surface of a graphene oxide (GO)-modified gold electrode (GE) leads to enhancement of the weak emission of oxidized luminol. Under optimum experimental conditions, the ECL signal increases linearly with increasing carbidopa concentrations over a range of 1.0 × 10(-9) -1.7 × 10(-7)  M, with a detection limit of 7.4 × 10(-10)  M. The proposed ECL method was successfully used for the determination of carbidopa in urine samples. PMID:25131492

  11. Electro-oxidation of ascorbic acid catalyzed on cobalt hydroxide-modified glassy carbon electrode

    Directory of Open Access Journals (Sweden)

    GHASEM KARIM-NEZHAD

    2009-05-01

    Full Text Available The electrochemical behavior of ascorbic acid on a cobalt hydroxide modified glassy carbon (CHM–GC electrode in alkaline solution was investigated. The process of the involved oxidation and its kinetics were established using the cyclic voltammetry, chronoamperometry techniques, as well as by steady state polarization measurements. The results revealed that cobalt hydroxide promotes the rate of oxidation by increasing the peak current; hence ascorbic acid is oxidized at lower potentials, which is thermodynamically more favorable. The cyclic voltammograms and chronoamperometry indicate a catalytic EC mechanism is operative with the electrogeneration of Co(IV as the electrochemical process. Also, the process is diffusion-controlled and the current–time responses follow Cottrellian behavior. This result was confirmed by steady state measurements. The rate constants of the catalytic oxidation of ascorbic acid and the electron-transfer coefficient are reported.

  12. Detection of Carbofuran with Immobilized Acetylcholinesterase Based on Carbon Nano tubes-Chitosan Modified Electrode

    International Nuclear Information System (INIS)

    A sensitive and stable enzyme biosensor based on efficient immobilization of acetylcholinesterase (AChE) to MWNTs-modified glassy carbon electrode (GCE) with chitosan (CS) by layer-by-layer (LBL) technique for rapid determination of carbofuran has been devised. According to the inhibitory effect of carbamate pesticide on the enzymatic activity of AChE, we use carbofuran as a model pesticide. The inhibitory effect of carbofuran on the biosensor was proportional to concentration of carbofuran in the range from 10-10  g/L to 10-3 g/L with a detection limit of 10-12 g/L. This biosensor is a promising new method for pesticide analysis

  13. Biosensor based on a glassy carbon electrode modified with tyrosinase immobilized on multiwalled carbon nanotubes

    International Nuclear Information System (INIS)

    We describe a biosensor for phenolic compounds that is based on a glassy carbon electrode modified with tyrosinase immobilized on multiwalled carbon nanotubes (MWNTs). The MWNTs possess excellent inherent electrical conductivity which enhances the electron transfer rate and results in good electrochemical catalytic activity towards the reduction of benzoquinone produced by enzymatic reaction. The biosensor was characterized by cyclic voltammetry, and the experimental conditions were optimized. The cathodic current is linearly related to the concentration of the phenols between 0.4 μM and 10 μM, and the detection limit is 0.2 μM. The method was applied to the determination of phenol in water samples (author)

  14. Nanowire-Modified Three-Dimensional Electrode Enabling Low-Voltage Electroporation for Water Disinfection.

    Science.gov (United States)

    Huo, Zheng-Yang; Xie, Xing; Yu, Tong; Lu, Yun; Feng, Chao; Hu, Hong-Ying

    2016-07-19

    More than 10% of the people in the world still suffer from inadequate access to clean water. Traditional water disinfection methods (e.g., chlorination and ultraviolet radiation) include concerns about the formation of carcinogenic disinfection byproducts (DBPs), pathogen reactivation, and/or excessive energy consumption. Recently, a nanowire-assisted electroporation-disinfection method was introduced as an alternative. Here, we develop a new copper oxide nanowire (CuONW)-modified three-dimensional copper foam electrode using a facile thermal oxidation approach. An electroporation-disinfection cell (EDC) equipped with two such electrodes has achieved superior disinfection performance (>7 log removal and no detectable bacteria in the effluent). The disinfection mechanism of electroporation guarantees an exceedingly low operation voltage (1 V) and level of energy consumption (25 J L(-1)) with a short contact time (7 s). The low operation voltage avoids chlorine generation and thus reduces the potential of DBP formation. Because of irreversible electroporation damage on cell membranes, no regrowth and/or reactivation of bacteria occurs during storage after EDC treatment. Water disinfection using EDCs has great potential for practical applications. PMID:27341009

  15. Direct electrochemistry behavior of Cytochrome c on silicon dioxide nanoparticles-modified electrode

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A newfangled direct electrochemistry behavior of Cytochrome c (Cyt c) was found on glassy carbon (GC) electrode modified with the silicon dioxide (SiO2) nanoparticles by physical adsorption. A pair of stable and well-defined redox peaks of Cyt c′ quasi-reversible electrochemical reaction were obtained with a heterogeneous electron transfer rate constant of 1.66×10-3 cm/s and a formal potential of 0.069 V (vs. Ag/AgCl) (0.263 V versus NHE) in 0.1 mol/L pH 6.8 PBS. Both the size and the amount of SiO2 nanoparticles could influence the electron transfer between Cyt c and the electrode. Electrostatic interaction which is between the negative nanoparticle surface and positively charged amino acid residues on the Cyt c surface is of importance for the stability and reproducibility toward the direct electron transfer of Cyt c. It is suggested that the modification of SiO2 nanoparticles proposes a novel approach to realize the direct electrochemistry of proteins.

  16. Screen-Printed Carbon Electrodes Modified with Cobalt Phthalocyanine for Selective Sulfur Detection in Cosmetic Products

    Directory of Open Access Journals (Sweden)

    Ying Shih

    2011-06-01

    Full Text Available Cobalt phthalocyanine (CoPc films were deposited on the surface of a screen-printed carbon electrode using a simple drop coating method. The cyclic voltammogram of the resulting CoPc modified screen-printed electrode (CoPc/SPE prepared under optimum conditions shows a well-behaved redox couple due to the (CoI/CoII system. The CoPc/SPE surface demonstrates excellent electrochemical activity towards the oxidation of sulfur in a 0.01 mol·L−1 NaOH. A linear calibration curve with the detection limit (DL, S/N = 3 of 0.325 mg·L−1 was achieved by CoPc/SPE coupled with flow injection analysis of the sulfur concentration ranging from 4 to 1120 mg·L−1. The precision of the system response was evaluated (3.60% and 3.52% RSD for 12 repeated injections, in the range of 64 and 480 mg·L−1 sulfur. The applicability of the method was successfully demonstrated in a real sample analysis of sulfur in anti-acne creams, and good recovery was obtained. The CoPc/SPE displayed several advantages in sulfur determination including easy fabrication, high stability, and low cost.

  17. Preparation and Electrochemical Characterization of a Carbon Ceramic Electrode Modified with Ferrocenecarboxylic Acid

    Directory of Open Access Journals (Sweden)

    Christiana A. Pessoa

    2011-01-01

    Full Text Available The present paper describes the characterization of a carbon ceramic electrode modified with ferrocenecarboxylic acid (designated as CCE/Fc by electrochemical techniques and its detection ability for dopamine. From cyclic voltammetric experiments, it was observed that the CCE/Fc presented a redox pair at Epa = 405 mV and Epc = 335 mV (DE = 70 mV, related to the ferrocene/ferrocenium process. Studies showed a considerably increase in the redox currents at the same oxidation potential of ferrocene (Epa = 414 mV vs. Ag/AgCl in the presence of dopamine (DA, differently from those observed when using only the unmodified CCE, in which the anodic peak increase was considerably lower. From SWV experiments, it was observed that the AA (ascorbic acid oxidation at CCE/Fc occurred in a different potential than the DA oxidation (with a peak separation of approximately 200 mV. Moreover, CCE/Fc did not respond to different AA concentrations, indicating that it is possible to determine DA without the AA interference with this electrode.

  18. Voltammetry of Vitamin B12 on a thin self-assembled monolayer modified electrode

    International Nuclear Information System (INIS)

    Vitamin B12 showed three reduction waves at a thin self-assembled monolayer of mercaptoacetic acid modified gold electrode at 0.21, 0.16, -0.41 V in a 0.01 mol l-1 HCl solution at a scan rate of 100 mV s-1. The overall electrode reaction followed an ECE mechanism, leading to a total two-electron exchange. The predominant Co(III) form was reduced directly at 0.21 V by a one-electron transfer accomplished by CN- cleavage into the cyanocob(II)alamin. The latter species then equilibrated with the base-off B12r, which was immediately reduced into B12s at 0.16 V. The wave at -0.41 V might be a catalytic hydrogen wave. The cathodic peak currents at 0.21 V were controlled by the diffusion of Vitamin B12. On the base of its diffusion behavior, the semi-derivate voltammetric method for the detection of Vitamin B12 was presented. The semi-derivate voltammetric peak current of the wave at 0.21 V was linear with the content of Vitamin B12 in the range of 4.0 x 10-9 to 4.0 x 10-5 mol l-1. The detection limit was 1.0 x 10-9 mol l-1. The proposed method was applied successfully to determine the content of Vitamin B12 in pharmaceutical preparations

  19. Amperometric ascorbic acid sensor based on doped ferrites nanoparticles modified glassy carbon paste electrode.

    Science.gov (United States)

    Dimitrijević, Teodora; Vulić, Predrag; Manojlović, Dragan; Nikolić, Aleksandar S; Stanković, Dalibor M

    2016-07-01

    In this study, a novel electrochemical sensor for quantification of ascorbic acid with amperometric detection in physiological conditions was constructed. For this purpose, cobalt and nickel ferrites were synthesized using microwave and ultrasound assistance, characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, and X-ray powder diffraction (XRPD), and used for modification of glassy carbon paste electrode (GCPE). It was shown that introducing these nanoparticles to the structure of GCPE led to increasing analytical performance. Co ferrite modified GCPE (CoFeGCPE) showed better characteristics toward ascorbic acid sensing. The limit of detection (LOD) obtained by sensor was calculated to be 0.0270 mg/L, with linear range from 0.1758 to 2.6010 mg/L. This sensor was successfully applied for practical analysis, and the obtained results demonstrated that the proposed procedure could be a promising replacement for the conventional electrode materials and time-consuming and expensive separation methods. PMID:27059753

  20. Adsorption study of copper (II) by chemically modified orange peel

    International Nuclear Information System (INIS)

    An adsorbent, the chemically modified orange peel, was prepared from hydrolysis of the grafted copolymer, which was synthesized by interaction of methyl acrylate with cross-linking orange peel. The presence of poly (acrylic acid) on the biomass surface was verified by infrared spectroscopy (IR), scanning electron microscopy (SEM) and thermogravimetry (TG). Total negative charge in the biomass surface and the zeta potentials were determined. The modified biomass was found to present high adsorption capacity and fast adsorption rate for Cu (II). From Langmuir isotherm, the adsorption capacity for Cu (II) was 289.0 mg g-1, which is about 6.5 times higher than that of the unmodified biomass. The kinetics for Cu (II) adsorption followed the pseudo-second-order kinetics. The adsorbent was used to remove Cu (II) from electroplating wastewater and was suitable for repeated use for more than four cycles.

  1. Electrochemical reduction of lindane (γ-HCH) at NiCo2O4 modified electrode

    International Nuclear Information System (INIS)

    Highlights: • NiCo2O4, NiFe2O4, NiO, Co3O4, and Fe3O4 were synthesized by the hydrothermal route. • Modified electrodes based on these metal oxides were investigated in lindane reduction. • NiCo2O4 modified electrode exhibited the highest activity. • Reproducibility, stability, and interference studies were performed. -- Abstract: NiCo2O4 and NiFe2O4 were synthesized by the hydrothermal route using the molar composition, 2.2 CoCl2·6H2O:1.0 NiCl2·6H2O:9 urea:832 H2O and 2.2 FeCl2·4H2O:1.0 NiCl2·6H2O:9 urea:832 H2O, respectively. For the comparative study, NiO, Co3O4, and Fe3O4 were also prepared. Materials were characterized by a complementary combination of X-ray diffraction, nitrogen sorption, and Scanning electron microscopy. Non-enzymatic electrochemical sensors (using above-mentioned metal oxides) were constructed for the detection of lindane in the aqueous-methanol medium. Electrochemical techniques such as cyclic voltammetry, differential pulse voltammetry, and amperometry were used for the detection of lindane. Reproducibility, stability, and interference studies were performed to obtain the suitable non-enzymatic sensor. The analytical performance of the sensor was demonstrated for the detection of lindane in tap water samples

  2. Effects of reversible chemical reaction on Li diffusion and stresses in spherical composition-gradient electrodes

    International Nuclear Information System (INIS)

    Composition-gradient electrode materials have been proven to be one of the most promising materials in lithium-ion battery. To study the mechanism of mechanical degradation in spherical composition-gradient electrodes, the finite deformation theory and reversible chemical theory are adopted. In homogeneous electrodes, reversible electrochemical reaction may increase the magnitudes of stresses. However, reversible electrochemical reaction has different influences on stresses in composition-gradient electrodes, resulting from three main inhomogeneous factors—forward reaction rate, backward reaction rate, and reaction partial molar volume. The decreasing transition form of forward reaction rate, increasing transition form of backward reaction rate, and increasing transition form of reaction partial molar volume can reduce the magnitudes of stresses. As a result, capacity fading and mechanical degradation are reduced by taking advantage of the effects of inhomogeneous factors

  3. Simultaneous voltammetric determination of tramadol and acetaminophen using carbon nanoparticles modified glassy carbon electrode

    International Nuclear Information System (INIS)

    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 μL 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 μM, respectively. The resulted detection limits for ACE and TRA was 0.05 and 1 μM, 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.

  4. 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.

  5. Glassy carbon electrodes modified with multiwalled carbon nanotubes for the determination of ascorbic acid by square-wave voltammetry

    Directory of Open Access Journals (Sweden)

    Sushil Kumar

    2012-05-01

    Full Text Available Multiwalled carbon nanotubes were used to modify the surface of a glassy carbon electrode to enhance its electroactivity. Nafion served to immobilise the carbon nanotubes on the electrode surface. The modified electrode was used to develop an analytical method for the analysis of ascorbic acid (AA by square-wave voltammetry (SWV. The oxidation of ascorbic acid at the modified glassy carbon electrode showed a peak potential at 315 mV, about 80 mV lower than that observed at the bare (unmodified electrode. The peak current was about threefold higher than the response at the bare electrode. Replicate measurements of peak currents showed good precision (3% rsd. Peak currents increased with increasing ascorbic acid concentration (dynamic range = 0.0047–5.0 mmol/L and displayed good linearity (R2 = 0.994. The limit of detection was 1.4 μmol/L AA, while the limit of quantitation was 4.7 μmol/L AA. The modified electrode was applied to the determination of the amount of ascorbic acid in four brands of commercial orange-juice products. The measured content agreed well (96–104% with the product label claim for all brands tested. Recovery tests on spiked samples of orange juice showed good recovery (99–104%. The reliability of the SWV method was validated by conducting parallel experiments based on high-performance liquid chromatography (HPLC with absorbance detection. The observed mean AA contents of the commercial orange juice samples obtained by the two methods were compared statistically and were found to have no significant difference (P = 0.05.

  6. 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.

  7. Chemically modified tetracyclines: The novel host modulating agents.

    Science.gov (United States)

    Swamy, Devulapalli Narasimha; Sanivarapu, Sahitya; Moogla, Srinivas; Kapalavai, Vasavi

    2015-01-01

    Periodontal pathogens and destructive host responses are involved in the initiation and progression of periodontitis. The emergence of host response modulation as a treatment concept has resulted from our improved understanding of the pathogenesis of periodontal disease. A variety of drugs have been evaluated as host modulation agents (HMA), including Non Steroidal Anti Inflammatory Drugs (NSAIDS), bisphosphonates, tetracyclines, enamel matrix proteins and bone morphogenetic proteins. Chemically modified tetracyclines (CMTs) are one such group of drugs which have been viewed as potential host modulating agents by their anticollagenolytic property. The CMTs are designed to be more potent inhibitors of pro inflammatory mediators and can increase the levels of anti inflammatory mediators. PMID:26392682

  8. Chemically modified tetracyclines: The novel host modulating agents

    Directory of Open Access Journals (Sweden)

    Devulapalli Narasimha Swamy

    2015-01-01

    Full Text Available Periodontal pathogens and destructive host responses are involved in the initiation and progression of periodontitis. The emergence of host response modulation as a treatment concept has resulted from our improved understanding of the pathogenesis of periodontal disease. A variety of drugs have been evaluated as host modulation agents (HMA, including Non Steroidal Anti Inflammatory Drugs (NSAIDS, bisphosphonates, tetracyclines, enamel matrix proteins and bone morphogenetic proteins. Chemically modified tetracyclines (CMTs are one such group of drugs which have been viewed as potential host modulating agents by their anticollagenolytic property. The CMTs are designed to be more potent inhibitors of pro inflammatory mediators and can increase the levels of anti inflammatory mediators.

  9. A gold electrode modified with amino-modified reduced graphene oxide, ion specific DNA and DNAzyme for dual electrochemical determination of Pb(II) and Hg(II)

    International Nuclear Information System (INIS)

    Multilayered reduced graphene oxide (rGO) was functionalized with amino groups by treatment with nitrogen plasma. Raman spectroscopy showed plasma treatment not to substantially alter the chemical structure of rGO and that a wide range of functional nitrogen groups is evenly incorporated into the carbon lattice. The amino-modified rGO was used to design an electrochemical biosensor in which a DNAzyme, substrate DNA and Pb(II) and Hg(II) binding DNA were immobilized on the amino-rGO placed on a gold electrode. The high concentration of amino groups and the rough surface of the rGO favor DNA immobilization. Heavy metal ions are bound to the surface via specific interaction between DNA and the two ions which are detected by electrochemical impedance spectroscopy at a potential of 0.2 V (vs. Ag/AgCl). The detection limits for Pb(II) and Hg(II) are as low as 7.8 and 5.4 pM, respectively, and the analytical ranges extend from 0.01 to 100 nM. The sensor is highly specific and stable and therefore represents a highly promising tool for use in environmental monitoring. (author)

  10. Preparation of the Ag2O2-PbO2 Modified Electrode and Its Application towards Escherichia coli Fast Counting in Water

    Institute of Scientific and Technical Information of China (English)

    Jing GU; Wen ZHANG; Yu Feng YANG; Lei ZHENG; Zi Rong WU; Li Tong JIN

    2005-01-01

    A novel nano crystalline Ag2O2-PbO2 film chemically modified electrode (CME) was prepared and the CME was characterized by X-ray diffractometer (XRD) and atomic force microscope (AFM). By chronoamperometry, the nano Ag2O2-PbO2 CME was used as bioelectrochemical sensor to determine the population of Escherichia coli (E. coli) in water. Compared with conventional methods, it is found that the technique we used is fast and convenient in counting E.coli.

  11. Silver Solid Amalgam Electrodes as Sensors for Chemical Carcinogens

    Directory of Open Access Journals (Sweden)

    Bogdan Yosypchuk

    2006-04-01

    Full Text Available The applicability of differential pulse voltammetry (DPV and adsorptivestripping voltammetry (AdSV at a non-toxic meniscus-modified silver solid amalgamelectrode (m-AgSAE for the determination of trace amounts of genotoxic substances wasdemonstrated on the determination of micromolar and submicromolar concentrations of3-nitrofluoranthene using methanol - 0.01 mol L-1 NaOH (9:1 mixture as a base electrolyteand of Ostazine Orange using 0.01 mol L-1 NaOH as a base electrolyte.

  12. Probing Chromatin-modifying Enzymes with Chemical Tools

    KAUST Repository

    Fischle, Wolfgang

    2016-02-04

    Chromatin is the universal template of genetic information in all eukaryotic organisms. Chemical modifications of the DNA-packaging histone proteins and the DNA bases are crucial signaling events in directing the use and readout of eukaryotic genomes. The enzymes that install and remove these chromatin modifications as well as the proteins that bind these marks govern information that goes beyond the sequence of DNA. Therefore, these so-called epigenetic regulators are intensively studied and represent promising drug targets in modern medicine. We summarize and discuss recent advances in the field of chemical biology that have provided chromatin research with sophisticated tools for investigating the composition, activity, and target sites of chromatin modifying enzymes and reader proteins.

  13. Laccase on Black Pearl 2000 modified glassy carbon electrode: Characterization of direct electron transfer and biological sensing properties for pyrocatechol

    International Nuclear Information System (INIS)

    Highlights: ► Laccase can complete direct electron transfer process on BP2000 matrices. ► Laccase immobilized on BP2000 matrices has catalytic oxidation effect to pyrocatechol. ► A pyrocatechol biosensor has constructed been using Nafion/Lac-BP2000/GC electrode. ► Detection limit and linear range of the biosensor are 0.003 mM and 0.003–5.555 mM. - Abstract: In this paper, it was found that Laccase (Lac) could be stably immobilized on the glassy carbon electrode modified with Black Pearl 2000 (BP2000) and Nafion by a simple technique. The adsorption behavior of Lac immobilized on BP2000 matrix was characterized by environment scanning electron microscope (ESEM), ultraviolet–visible (UV–vis) and Fourier transform infrared (FTIR), which demonstrated that BP2000 could facilitate the electron exchange between the active center of Lac and modified electrode. The direct electrochemistry and electrocatalysis behavior of Lac on the modified electrode were characterized by cyclic voltammogram (CV) which indicated that Lac immobilized on the modified electrode displayed a direct, nearly reversible and surface-controlled redox reaction with an enhanced electron-transfer rate constant of 1.940 s−1 at the scan rate of 100 mV s−1 in 0.1 M phosphate buffer solution (PBS) (pH 7.0). Furthermore, it was also discovered that, in the presence of O2, Lac immobilized on the modified electrode exhibited the electrocatalytic response to pyrocatechol, and the kinetic apparent Michaelis-constant (KMapp) obtained from the Lineweaver–Burk equation was 1.79 mM. The detection limit, linear range and sensitivity of the Lac biosensor were 0.003 mM, 0.003–5.555 mM and 99.84 μA mM−1 cm−2, respectively.

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

    International Nuclear Information System (INIS)

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2011-10-03

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

  16. Electrochemical properties of the hexacyanoferrate(II)–ruthenium(III) complex immobilized on silica gel surface chemically modified with zirconium(IV) oxide

    Energy Technology Data Exchange (ETDEWEB)

    Panice, Lucimara B.; Oliveira, Elisangela A. de; Filho, Ricardo A.D. Molin; Oliveira, Daniela P. de [Departamento de Química, Universidade Estadual de Maringá, Av. Colombo, 5790, 87020-900 Maringá, PR (Brazil); Lazarin, Angélica M., E-mail: amlazarin2@uem.br [Departamento de Química, Universidade Estadual de Maringá, Av. Colombo, 5790, 87020-900 Maringá, PR (Brazil); Andreotti, Elza I.S.; Sernaglia, Rosana L. [Departamento de Química, Universidade Estadual de Maringá, Av. Colombo, 5790, 87020-900 Maringá, PR (Brazil); Gushikem, Yoshitaka [Instituto de Química, Universidade Estadual de Campinas, Caixa Postal 6154, 13084-971 Campinas, São Paulo (Brazil)

    2014-10-15

    Highlights: • The cyano-bridged mixed valence ruthenium composite material was synthesized. • This newly synthesized compound was incorporated into a carbon paste electrode. • The electrode did not show significant changes in response after six months of use. • The modified electrode is very stable and reproducible. • The electrode sensor was successfully applied for ascorbic acid determination. - Abstract: The chemically modified silica gel with zirconium(IV) oxide was used to immobilize the [Fe(CN){sub 6}]{sup 4−} complex ion initially. The reaction of this material with [Ru(edta)H{sub 2}O]{sup −} complex ion formed the immobilized cyano-bridged mixed valence ruthenium complex, (≡Zr){sub 5}[(edta)RuNCFe(CN){sub 5}]. This material was incorporated into a carbon paste electrode and, its electrochemical properties were investigated. However, for an ascorbic acid solution, an enhancement of the anodic peak current was detected due to electrocatalytic oxidation. The electrode presented the same response for at least 150 successive measurements, with a good repeatability. The modified electrode is very stable and reproducible. The sensor was applied for ascorbic acid determination in pharmaceutical preparation with success.

  17. Electrochemical properties of the hexacyanoferrate(II)–ruthenium(III) complex immobilized on silica gel surface chemically modified with zirconium(IV) oxide

    International Nuclear Information System (INIS)

    Highlights: • The cyano-bridged mixed valence ruthenium composite material was synthesized. • This newly synthesized compound was incorporated into a carbon paste electrode. • The electrode did not show significant changes in response after six months of use. • The modified electrode is very stable and reproducible. • The electrode sensor was successfully applied for ascorbic acid determination. - Abstract: The chemically modified silica gel with zirconium(IV) oxide was used to immobilize the [Fe(CN)6]4− complex ion initially. The reaction of this material with [Ru(edta)H2O]− complex ion formed the immobilized cyano-bridged mixed valence ruthenium complex, (≡Zr)5[(edta)RuNCFe(CN)5]. This material was incorporated into a carbon paste electrode and, its electrochemical properties were investigated. However, for an ascorbic acid solution, an enhancement of the anodic peak current was detected due to electrocatalytic oxidation. The electrode presented the same response for at least 150 successive measurements, with a good repeatability. The modified electrode is very stable and reproducible. The sensor was applied for ascorbic acid determination in pharmaceutical preparation with success

  18. 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.

  19. CdS quantum dots modified CuO inverse opal electrodes for ultrasensitive electrochemical and photoelectrochemical biosensor

    OpenAIRE

    Xia, Lei; Xu, Lin; Song, Jian; Xu, Ru; Liu, Dali; Dong, Biao; SONG, HONGWEI

    2015-01-01

    The CuO inverse opal photonic crystals (IOPCs) were synthesized by the sol-gel method and modified with CdS quantum dots by successive ionic layer adsorption and reaction (SILAR). CdS QDs modified CuO IOPCs FTO electrodes of different SILAR cycles were fabricated and their electrochemical properties were studied by cyclic voltammetry (CV) and chronoamperometry (I–t). Structure and morphology of the samples were characterized by transmission electron microscopy (TEM), scanning electron microsc...

  20. An Electrochemical Microsensor Based on a AuNPs-Modified Microband Array Electrode for Phosphate Determination in Fresh Water Samples

    Directory of Open Access Journals (Sweden)

    Fangfang Wang

    2014-12-01

    Full Text Available This work describes the fabrication, characterization, and application of a gold microband array electrode (MAE for the determination of phosphate in fresh water samples. The working principle of this MAE is based on the reduction of a molybdophosphate complex using the linear sweep voltammetric (LSV method. The calibration of this microsensor was performed with standard phosphate solutions prepared with KH2PO4 and pH adjusted to 1.0. The microsensor consists of a platinum counter electrode, a gold MAE as working electrode, and an Ag/AgCl electrode as reference electrode. The microelectrode chips were fabricated by the Micro Electro-Mechanical System (MEMS technique. To improve the sensitivity, gold nanoparticles (AuNPs were electrodeposited on the working electrode. With a linear range from 0.02 to 0.50 mg P/L, the sensitivity of the unmodified microsensor is 2.40 µA per (mg P/L (R2 = 0.99 and that of the AuNPs-modified microsensor is 7.66 µA per (mg P/L (R2 = 0.99. The experimental results showed that AuNPs-modified microelectrode had better sensitivity and a larger current response than the unmodified microelectrode.

  1. A highly performing electrochemiluminescent biosensor for glucose based on a polyelectrolyte-chitosan modified electrode

    Energy Technology Data Exchange (ETDEWEB)

    Dai Hong [Ministry of Education Key Laboratory of Analysis and Detection for Food Safety (Fuzhou University) and Department of Chemistry, Fuzhou University, 523 Gongye Road, Fuzhou, Fujian 350002 (China); Wu Xiaoping [Ministry of Education Key Laboratory of Analysis and Detection for Food Safety (Fuzhou University) and Department of Chemistry, Fuzhou University, 523 Gongye Road, Fuzhou, Fujian 350002 (China)], E-mail: wapple@fzu.edu.cn; Xu Huifeng; Wang Youmei; Chi Yuwu [Ministry of Education Key Laboratory of Analysis and Detection for Food Safety (Fuzhou University) and Department of Chemistry, Fuzhou University, 523 Gongye Road, Fuzhou, Fujian 350002 (China); Chen Guonan [Ministry of Education Key Laboratory of Analysis and Detection for Food Safety (Fuzhou University) and Department of Chemistry, Fuzhou University, 523 Gongye Road, Fuzhou, Fujian 350002 (China)], E-mail: gnchen@fzu.edu.cn

    2009-07-30

    A highly performing ECL glucose biosensor was developed by immobilizing glucose oxidase (GOD) onto a membrane modified glassy carbon electrode, which was prepared by using poly(diallyldimethylammonium chloride) (PDDA) doped with chitosan. In order to obtain the optimal performance of the ECL biosensor, the composition of modified membranes and a series of measurement conditions were investigated. Under the optimal conditions, this ECL biosensor was able to detect glucose in the range of 0.5-4.0 x 10{sup 4} nM with a detection limit of 0.1 nM (defined as the concentration that could be detected at the signal-to-noise ratio of 3). The relative standard deviation was 0.99% for 5 x 10{sup -8} mol/L glucose in repetitive measurements in the primary 12 potential cycles. This ECL biosensor offered the effectively improved stability of the electron transfer mediator and exhibited excellent properties for the ultrasensitive and selective determination of glucose with good reproducibility and stability. The present biosensor has also been used to determine the glucose concentrations in real serum samples. The recovery value for the assay of glucose ranged from 96.2 to 107% in the serum samples. The present biosensor displayed both specificity for glucose and retention of signal response even in a complex environment. Therefore, it provided an approach to the sensitive determination of glucose.

  2. DNA biosensor based on a glassy carbon electrode modified with electropolymerized Eriochrome Black T

    International Nuclear Information System (INIS)

    We report on an electrochemical DNA biosensor consisting of a glassy carbon electrode modified with a film of electropolymerized Eriochrome Black T (pEBT) that serves as a functional platform for the immobilization of probe DNA. pEBT was deposited via cyclic voltammetry, and the amino-modified DNA capture probe was covalently linked to the surface via a sulfanilamide coupling reaction. The single step of the assembly process was monitored by atomic force microscopy and electrochemistry. The surface density of DNA probe on the biosensor interface was calculated to be 1.7 × 10−10 mol cm−2 using methylene blue as an electroactive probe. Hybridization experiments showed the peak currents of methylene blue to decrease with increasing concentration of complementary sequence in the range from 5.0 f. to 5.0 pM. The detection limit is as low as 0.11 fM. Selectivity studies showed that the biosensor can discriminate a fully complementary sequence from a single-base mismatch, three-base mismatch, and a fully non-complementary sequence. The biosensor displays good stability and can be regenerated due to the beneficial effects of electropolymerization and covalent immobilization of probe DNA. (author)

  3. Highly-sensitive Detection of Salvianolic Acid B using Alumina Microfibers-modified Electrode

    International Nuclear Information System (INIS)

    Alumina microfibers with porous structures were prepared through hydrothermal reaction, and then used to modify the surface of carbon paste electrode (CPE). After modification with alumina microfibers, the electrochemical activity of CPE was found to be greatly improved. On the surface of alumina microfibers-modified CPE, the oxidation peak current of salvianolic acid B, a main bioactive compound in Danshen with anti-oxidative and anti-inflammatory effects, was remarkably increased compared with that on the bare CPE surface. The influences of pH value, amount of alumina microfibers and accumulation time were studied. Based on the strong signal amplification effects of alumina microfibers, a novel electrochemical method was developed for the detection of salvianolic acid B. The linear range was from 5 μg L-1 to 0.3 mg L-1, and the detection limit was 2 μg L-1 (2.78 nM) after 1-min accumulation. The new method was successfully used to detect salvianolic acid B in ShuangDan oral liquid samples, and the recovery was over the range from 97.4% to 102.9%

  4. Enhanced oxidation and detection of toxic ractopamine using carbon nanotube film-modified electrode

    International Nuclear Information System (INIS)

    Highlights: ► The enhanced oxidation of ractopamine on MWCNT film surface was firstly studied. ► The oxidation occurred at phenolic hydroxyl groups and transferred two electrons. ► A sensitive and effective electrochemical sensor was developed for ractopamine. ► It was used to detect ractopamine in animal tissues, the recovery was satisfactory. - Abstract: Insoluble multi-walled carbon nanotube (MWCNT) was readily dispersed into water in the presence of dihexadecyl hydrogen phosphate, and then used to modify the surface of glassy carbon electrode (GCE) by means of solvent evaporation. Scanning electron microscopy test indicated that the GCE surface was coated with uniform MWCNT film. The resulting MWCNT film-modified GCE greatly enhanced the oxidation signal of ractopamine. The oxidation mechanism was studied, and it was found that the oxidation of ractopamine occurred at two phenolic hydroxyl groups, involving two protons and two electrons. Moreover, the influences of pH value, amount of MWCNT, accumulation potential and time were investigated on the oxidation signal of ractopamine. Based on the strong enhancement effect of MWCNT, a sensitive, rapid and simple electrochemical method was developed for the detection of ractopamine. The linear range was from 50 μg L−1 to 2 mg L−1, and the detection limit was 20 μg L−1. Finally, this method was successfully used to detect the content of ractopamine in pork and liver samples, and the recovery was in the range from 93.1% to 107.2%.

  5. A highly performing electrochemiluminescent biosensor for glucose based on a polyelectrolyte-chitosan modified electrode

    International Nuclear Information System (INIS)

    A highly performing ECL glucose biosensor was developed by immobilizing glucose oxidase (GOD) onto a membrane modified glassy carbon electrode, which was prepared by using poly(diallyldimethylammonium chloride) (PDDA) doped with chitosan. In order to obtain the optimal performance of the ECL biosensor, the composition of modified membranes and a series of measurement conditions were investigated. Under the optimal conditions, this ECL biosensor was able to detect glucose in the range of 0.5-4.0 x 104 nM with a detection limit of 0.1 nM (defined as the concentration that could be detected at the signal-to-noise ratio of 3). The relative standard deviation was 0.99% for 5 x 10-8 mol/L glucose in repetitive measurements in the primary 12 potential cycles. This ECL biosensor offered the effectively improved stability of the electron transfer mediator and exhibited excellent properties for the ultrasensitive and selective determination of glucose with good reproducibility and stability. The present biosensor has also been used to determine the glucose concentrations in real serum samples. The recovery value for the assay of glucose ranged from 96.2 to 107% in the serum samples. The present biosensor displayed both specificity for glucose and retention of signal response even in a complex environment. Therefore, it provided an approach to the sensitive determination of glucose.

  6. 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.

  7. 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)

  8. Nitrogen plasma modified CVD grown graphene as counter electrodes for bifacial dye-sensitized solar cells

    International Nuclear Information System (INIS)

    In this study, we report modification of few-layer graphene grown by chemical vapour deposition via nitrogen plasma ion irradiation and its application as counter electrodes in bifacial dye-sensitized solar cells (DSSCs). The incorporation of nitrogen (N) atoms and defects are confirmed by X-ray photoelectron spectroscopy and Raman spectroscopy. Electrochemical impedance spectroscopy measurement reveals that the charge transfer resistance of graphene for triiodide reduction shows a decrease with increasing plasma treatment time, which is attributed to the increase of catalytic sites. The energy conversion efficiency of 3.12% is obtained when using the N-doped graphene films as counter electrodes, which is nearly 3 times higher than that of the pristine graphene films in DSSCs. More importantly, the DSSCs based on N-doped graphene CEs show much higher ηrear/ηfront ratio and better long-term stability than that based on Pt CEs. These results reveal the promising potential of this transparent N-doped graphene CEs in low cost and effective bifacial DSSCs

  9. Chemical treatments of the nanocrystalline porous TiO2 electrodes

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Two types of nanocrystalline porous TiO2 electrodes were prepared by the hydrothermal and painting methods. The incident photon-to-current efficiency and photoelectrical conversion efficiency were both improved by chemical treatments of titanium tetrachloride and titanium isopropoxide. The surface roughness, quantities of adsorbed dye, photocurrent-voltage curves, IR spectra and UV-visible absorption spectra were measured, and the mechanism of chemical treatments was discussed.

  10. Novel Signal-Amplified Fenitrothion Electrochemical Assay, Based on Glassy Carbon Electrode Modified with Dispersed Graphene Oxide

    Science.gov (United States)

    Wang, Limin; Dong, Jinbo; Wang, Yulong; Cheng, Qi; Yang, Mingming; Cai, Jia; Liu, Fengquan

    2016-03-01

    A novel signal-amplified electrochemical assay for the determination of fenitrothion was developed, based on the redox behaviour of organophosphorus pesticides on a glassy carbon working electrode. The electrode was modified using graphene oxide dispersion. The electrochemical response of fenitrothion at the modified electrode was investigated using cyclic voltammetry, current-time curves, and square-wave voltammetry. Experimental parameters, namely the accumulation conditions, pH value, and volume of dispersed material, were optimised. Under the optimum conditions, a good linear relationship was obtained between the oxidation peak current and the fenitrothion concentration. The linear range was 1–400 ng·mL‑1, with a detection limit of 0.1 ng·mL‑1 (signal-to-nose ratio = 3). The high sensitivity of the sensor was demonstrated by determining fenitrothion in pakchoi samples.

  11. A hydrogen peroxide sensor based on the peroxidase activity of hemoglobin immobilized on gold nanoparticles-modified ITO electrode

    International Nuclear Information System (INIS)

    A novel ITO electrode surface modified with spherical and rod-shaped gold nanoparticles was prepared by a surfactant-assisted seeding growth approach, which provided a biocompatible matrix for the immobilization of hemoglobin (Hb). By electrochemical impedance measurements, gold nanoparticles modification and Hb immobilization on the electrode surfaces were characterized using [Fe(CN)6]3-/[Fe(CN)6]4- redox probe. Owing to the promoted electron transfer of Hb by gold nanoparticles, the Hb immobilized gold nanoparticles-modified ITO (Hb/Au/ITO) electrode exhibited an effective catalytic response to the reduction of H2O2 with good reproducibility and stability. The linear relationship existed between the catalytic current and the H2O2 concentration in the range of 1 x 10-5 to 7 x 10-3 M. The detection limit (S/N = 3) was 4.5 x 10-6 M

  12. Novel Signal-Amplified Fenitrothion Electrochemical Assay, Based on Glassy Carbon Electrode Modified with Dispersed Graphene Oxide

    Science.gov (United States)

    Wang, Limin; Dong, Jinbo; Wang, Yulong; Cheng, Qi; Yang, Mingming; Cai, Jia; Liu, Fengquan

    2016-01-01

    A novel signal-amplified electrochemical assay for the determination of fenitrothion was developed, based on the redox behaviour of organophosphorus pesticides on a glassy carbon working electrode. The electrode was modified using graphene oxide dispersion. The electrochemical response of fenitrothion at the modified electrode was investigated using cyclic voltammetry, current-time curves, and square-wave voltammetry. Experimental parameters, namely the accumulation conditions, pH value, and volume of dispersed material, were optimised. Under the optimum conditions, a good linear relationship was obtained between the oxidation peak current and the fenitrothion concentration. The linear range was 1–400 ng·mL−1, with a detection limit of 0.1 ng·mL−1 (signal-to-nose ratio = 3). The high sensitivity of the sensor was demonstrated by determining fenitrothion in pakchoi samples. PMID:27003798

  13. Hollow NiO nanofibers modified by citric acid and the performances as supercapacitor electrode

    International Nuclear Information System (INIS)

    Graphical abstract: The possible formation process of NiO nanofibers without citric acid (a), and modified by citric acid (b). When the nanofibers is modified by citric acid, the nickel citrate is produced by complexing action of citric acid and nickel nitrate. Because of the larger space steric hindrance, the structure is limited by the molecular geometry. Under high temperature, the hollow nanofibers composed of NiO slices formed after the removal of PVP. Highlights: ► The method of obtaining hollow nanofibers is raised for the first time. ► The prepared NiO nanofibers are hollow tube and comprised of many NiO sheets. ► The hollow structure facilitated the electrolyte penetration. ► The hollow NiO nanofibers have good electrochemical properties. -- Abstract: NiO nanofibers modified by citric acid (NiO/CA) for supercapacitor material have been fabricated by electrospinning process. The characterizations of the nanofibers are investigated by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Electrochemical properties are characterized by cyclic voltammetry, galvanostatic charge/discharge measurements, and electrochemical impedance spectroscopy. Results show that the NiO/CA nanofibers are hollow tube and comprised of many NiO sheets. Furthermore, the NiO/CA nanofibers have good electrochemical reversibility and display superior capacitive performance with large capacitance (336 F g−1), which is 2.5 times of NiO electrodes. Moreover, the NiO/CA nanofibers show excellent cyclic performance after 1000 cycles

  14. 2D nanosheet molybdenum disulphide (MoS2) modified electrodes explored towards the hydrogen evolution reaction

    Science.gov (United States)

    Rowley-Neale, Samuel J.; Brownson, Dale A. C.; Smith, Graham C.; Sawtell, David A. G.; Kelly, Peter J.; Banks, Craig E.

    2015-10-01

    We explore the use of two-dimensional (2D) MoS2 nanosheets as an electrocatalyst for the Hydrogen Evolution Reaction (HER). Using four commonly employed commercially available carbon based electrode support materials, namely edge plane pyrolytic graphite (EPPG), glassy carbon (GC), boron-doped diamond (BDD) and screen-printed graphite electrodes (SPE), we critically evaluate the reported electrocatalytic performance of unmodified and MoS2 modified electrodes towards the HER. Surprisingly, current literature focuses almost exclusively on the use of GC as an underlying support electrode upon which HER materials are immobilised. 2D MoS2 nanosheet modified electrodes are found to exhibit a coverage dependant electrocatalytic effect towards the HER. Modification of the supporting electrode surface with an optimal mass of 2D MoS2 nanosheets results in a lowering of the HER onset potential by ca. 0.33, 0.57, 0.29 and 0.31 V at EPPG, GC, SPE and BDD electrodes compared to their unmodified counterparts respectively. The lowering of the HER onset potential is associated with each supporting electrode's individual electron transfer kinetics/properties and is thus distinct. The effect of MoS2 coverage is also explored. We reveal that its ability to catalyse the HER is dependent on the mass deposited until a critical mass of 2D MoS2 nanosheets is achieved, after which its electrocatalytic benefits and/or surface stability curtail. The active surface site density and turn over frequency for the 2D MoS2 nanosheets is determined, characterised and found to be dependent on both the coverage of 2D MoS2 nanosheets and the underlying/supporting substrate. This work is essential for those designing, fabricating and consequently electrochemically testing 2D nanosheet materials for the HER.We explore the use of two-dimensional (2D) MoS2 nanosheets as an electrocatalyst for the Hydrogen Evolution Reaction (HER). Using four commonly employed commercially available carbon based electrode

  15. 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)

  16. Microfluidic electrochemical device and process for chemical imaging and electrochemical analysis at the electrode-liquid interface in-situ

    Science.gov (United States)

    Yu, Xiao-Ying; Liu, Bingwen; Yang, Li; Zhu, Zihua; Marshall, Matthew J.

    2016-03-01

    A microfluidic electrochemical device and process are detailed that provide chemical imaging and electrochemical analysis under vacuum at the surface of the electrode-sample or electrode-liquid interface in-situ. The electrochemical device allows investigation of various surface layers including diffuse layers at selected depths populated with, e.g., adsorbed molecules in which chemical transformation in electrolyte solutions occurs.

  17. Electrochemical behavior of ruthenium-hexacyanoferrate modified glassy carbon electrode and catalytic activity towards ethanol electro oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Costa, Wendell M.; Marques, Aldalea L.B., E-mail: aldalea.ufma@hotmail.com [Universidade Federal do Maranhao (UFMA), Sao Luis, MA (Brazil). Departamento de Quimica Tecnologica; Cardoso, William S.; Marques, Edmar P.; Bezerra, Cicero W.B. [Universidade Federal do Maranhao (UFMA), Sao Luis, MA (Brazil). Departamento de Qumica; Ferreira, Antonio Ap. P. [Universidade Estadual Paulista Julio de Mesquita Filho (UNESP), Araraquara, SP (Brazil). Instituto de Quimica; Song, Chaojie; Zhang, Jiujun [Energy, Mining and Environment Portfolio, National Research Council of Canada, Vancouver, BC (Canada)

    2013-04-15

    Ruthenium-based hexacyanoferrate (RuHCF) thin film modified glassy carbon electrode was prepared by drop evaporation method. The RuHCF modified electrode exhibited four redox couples in strong acidic solution (pH 1.5) attributed to Fe(CN){sub 6}{sup 3-} ion and three ruthenium forms (Ru(II), Ru(III) and Ru(IV)), characteristic of ruthenium oxide compounds. The modified electrode displayed excellent electrocatalytic activity towards ethanol oxidation in the potential region where electrochemical processes Ru(III)-O-Ru(IV) and Ru(IV)-O-Ru(VI) occur. Impedance spectroscopy data indicated that the charge transfer resistance decreased with the increase of the applied potential and ethanol concentration, indicating the use of the RuHCF modified electrode as an ethanol sensor. Under optimized conditions, the sensor responded linearly and rapidly to ethanol concentration between 0.03 and 0.4 mol L{sup -1} with a limit of detection of 0.76 mmol L{sup -1}, suggesting an adequate sensitivity in ethanol analyses. (author)

  18. Electrocatalytic Oxidation of Hydroxylamine at a Quinizarine Modified Glassy Carbon Electrode: Application to Differential Pulse Voltammetry Detection of Hydroxylamine

    OpenAIRE

    MAZLOUMARDAKANI, Mohammad; KARAMI, Payam EBRAHIMI

    2008-01-01

    The electrocatalytic behavior of hydroxylamine was studied on a glassy carbon electrode modified by electrodeposition of quinizarine, using cyclic voltammetry, chronoamperometry, and rotating disk voltammetry as diagnostic techniques. Cyclic voltammetry showed that the catalytic current of the system depends on the concentration of hydroxylamine. The magnitude of the peak current for quinizarine increased sharply in the presence of hydroxylamine and proportional to hydroxylamine conc...

  19. Glassy carbon electrode modified with gold nanoparticles and hemoglobin in a chitosan matrix for improved pH-switchable sensing of hydrogen peroxide

    International Nuclear Information System (INIS)

    Hemoglobin (Hb) has been demonstrated to endow electrochemical sensors with pH-switchable response because of the presence of carboxyl and amino groups. Hb was deposited in a chitosan matrix on a glassy carbon electrode (GCE) that was previously coated with clustered gold nanoparticles (Au-NPs) by electrodeposition. The switching behavior is active (“on”) to the negatively charged probe [Fe(CN)63−] at pH 4.0, but inactive (“off”) to the probe at pH 8.0. This switch is fully reversible by simply changing the pH value of the solution and can be applied for pH-controlled reversible electrochemical reduction of H2O2 catalyzed by Hb. The modified electrode was tested for its response to the different electroactive probes. The response to these species strongly depends on pH which was cycled between 4 and 8. The effect is also attributed to the presence of pH dependent charges on the surface of the electrode which resulted in either electrostatic attraction or repulsion of the electroactive probes. The presence of Hb, in turn, enhances the pH-controllable response, and the electrodeposited Au-NPs improve the capability of switching. This study reveals the potential of protein based pH-switchable materials and also provides a simple and effective strategy for fabrication of switchable chemical sensors as exemplified in a pH-controllable electrode for hydrogen peroxide. (author)

  20. An amperometric bienzymatic cholesterol biosensor based on functionalized graphene modified electrode and its electrocatalytic activity towards total cholesterol determination.

    Science.gov (United States)

    Manjunatha, Revanasiddappa; Shivappa Suresh, Gurukar; Melo, Jose Savio; D'Souza, Stanislaus F; Venkatesha, Thimmappa Venkatarangaiah

    2012-09-15

    Cholesterol oxidase (ChOx) and cholesterol esterase (ChEt) have been covalently immobilized onto functionalized graphene (FG) modified graphite electrode. Enzymes modified electrodes were characterized using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). FG accelerates the electron transfer from electrode surface to the immobilized ChOx, achieving the direct electrochemistry of ChOx. A well defined redox peak was observed, corresponding to the direct electron transfer of the FAD/FADH(2) of ChOx. The electron transfer coefficient (α) and electron transfer rate constant (K(s)) were calculated and their values are found to be 0.31 and 0.78 s(-1), respectively. For the free cholesterol determination, ChOx-FG/Gr electrode exhibits a sensitive response from 50 to 350 μM (R=-0.9972) with a detection limit of 5 μM. For total cholesterol determination, co-immobilization of ChEt and ChOx on modified electrode, i.e. (ChEt/ChOx)-FG/Gr electrode showed linear range from 50 to 300 μM (R=-0.9982) with a detection limit of 15 μM. Some common interferents like glucose, ascorbic acid and uric acid did not cause any interference, due to the use of a low operating potential. The FG/Gr electrode exhibits good electrocatalytic activity towards hydrogen peroxide (H(2)O(2)). A wide linear response to H(2)O(2) ranging from 0.5 to 7 mM (R=-0.9967) with a sensitivity of 443.25 μA mM(-1) cm(-2) has been obtained. PMID:22967556

  1. Mechano-chemical degradation of flexible electrodes for optoelectronic device applications

    International Nuclear Information System (INIS)

    The electrical, optical, and structural integrity of flexible transparent electrodes is of paramount importance in the design and fabrication of optoelectronic devices such as organic light emitting diodes, liquid crystal displays, touch panels, solar cells, and solid-state lighting. The electrodes may corrode due to acid-containing pressure sensitive adhesives present in the device stacks. In addition, structural failure may occur due to external applied loading. The combined action and further accumulation of both repeated mechanical loading and corrosion can aggravate the loss of functionality of the electrodes. In this study we investigate, using the design of experimental methods, the effects of corrosion, applied mechanical strain, film thickness, and number of bending cycles on the electrical and structural integrity of indium tin oxide (ITO) and carbon nanotube (CNT) films both coated on polyethylene terephthalate (PET) substrates. In situ electrical resistance measurements suggest that fatigue-corrosion is found to be the most critical failure mode for the ITO-based coatings. For example, the change in ITO electrical resistance increase under fatigue-corrosion (1% strain, 150,000 cycles) is 5.8 times higher than that of fatigue mode alone. On the other hand, a minimum change in electrical resistance of the CNT-based electrodes is found when applying the same conditions. - Highlights: • Combined mechano-chemical effects on electrode durability. • CNT-based electrodes outperform ITO counterparts. • Importance of combined fatigue and corrosion action on device reliability

  2. Electrochemical behavior and voltammetric determination of p-methylaminophenol sulfate using LiCoO{sub 2} nanosphere modified electrode

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Wei, E-mail: swyy26@hotmail.com [College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158 (China); Deng, Ying; Liu, Jun; Liu, Weiming; Cheng, Yong; Wang, Lei; Gu, Yuanxiang [College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China)

    2014-08-01

    In this study, LiCoO{sub 2} nanoparticles were synthesized by the hydrothermal method and characterized by scanning electron microscopy, transmission electron microscopy, and X-ray diffraction analyses, which exhibited flower-like nanospheres composed of uniform nanosheets. The synthesized LiCoO{sub 2} nanospheres were further used for the modification of 1-hexylpyridinium hexafluorophosphate based carbon ionic liquid electrode (CILE). The electrochemical performance of the modified electrode, LiCoO{sub 2}/CILE, was studied by cyclic voltammetry and electrochemical impedance spectroscopy. Electrooxidation of p-methylaminophenol sulfate (metol) on the modified electrode was further tested and electrochemical responses of metol were significantly enhanced owing to the presence of LiCoO{sub 2} nanospheres with large surface area and fast electron transfer rate. The electrochemical parameters such as the charge transfer coefficient, the number of electron transferred, the standard electrode reaction rate constant, and the apparent diffusion coefficient for metol electrooxidation were calculated as 0.51, 0.91, 0.92 s{sup −1} and 7.06 × 10{sup −5} cm{sup 2}/s, respectively. Under the optimized conditions, metol can be linearly detected in the concentration range from 0.4 to 400.0 μmol/L with a detection limit of 2.46 × 10{sup −7} mol/L (3σ). The optimized method was further applied to the detection of metol content in artificial wastewater samples with satisfactory results. - Highlights: • LiCoO{sub 2} nanospheres were synthesized and characterized. • LiCoO{sub 2} nanosphere modified carbon ionic liquid electrode was fabricated. • Electrochemical behaviors of metol on the modified electrode were investigated.

  3. Electrochemical behavior and voltammetric determination of p-methylaminophenol sulfate using LiCoO2 nanosphere modified electrode

    International Nuclear Information System (INIS)

    In this study, LiCoO2 nanoparticles were synthesized by the hydrothermal method and characterized by scanning electron microscopy, transmission electron microscopy, and X-ray diffraction analyses, which exhibited flower-like nanospheres composed of uniform nanosheets. The synthesized LiCoO2 nanospheres were further used for the modification of 1-hexylpyridinium hexafluorophosphate based carbon ionic liquid electrode (CILE). The electrochemical performance of the modified electrode, LiCoO2/CILE, was studied by cyclic voltammetry and electrochemical impedance spectroscopy. Electrooxidation of p-methylaminophenol sulfate (metol) on the modified electrode was further tested and electrochemical responses of metol were significantly enhanced owing to the presence of LiCoO2 nanospheres with large surface area and fast electron transfer rate. The electrochemical parameters such as the charge transfer coefficient, the number of electron transferred, the standard electrode reaction rate constant, and the apparent diffusion coefficient for metol electrooxidation were calculated as 0.51, 0.91, 0.92 s−1 and 7.06 × 10−5 cm2/s, respectively. Under the optimized conditions, metol can be linearly detected in the concentration range from 0.4 to 400.0 μmol/L with a detection limit of 2.46 × 10−7 mol/L (3σ). The optimized method was further applied to the detection of metol content in artificial wastewater samples with satisfactory results. - Highlights: • LiCoO2 nanospheres were synthesized and characterized. • LiCoO2 nanosphere modified carbon ionic liquid electrode was fabricated. • Electrochemical behaviors of metol on the modified electrode were investigated

  4. A reference electrode based on polyvinyl butyral (PVB) polymer for decentralized chemical measurements

    Energy Technology Data Exchange (ETDEWEB)

    Guinovart, Tomàs [Departament de Química Orgànica i Química Analítica, Universitat Rovira i Virgili, Carrer Marcellí Domingo s/n 43007 Tarragona (Spain); Crespo, Gastón A. [Department of Inorganic and Analytical Chemistry, University of Geneva, Quai Ernest-Ansermet 30, CH-1211 Geneva (Switzerland); Rius, F. Xavier [Departament de Química Orgànica i Química Analítica, Universitat Rovira i Virgili, Carrer Marcellí Domingo s/n 43007 Tarragona (Spain); Andrade, Francisco J., E-mail: franciscojavier.andrade@urv.cat [Departament de Química Orgànica i Química Analítica, Universitat Rovira i Virgili, Carrer Marcellí Domingo s/n 43007 Tarragona (Spain)

    2014-04-01

    Highlights: • A disposable solid-contact reference electrode for potentiometry is presented. • The device shows unsensitivity to most ions, redox potential and light. • Low-cost and good stability, ideal to build disposable potentiometric sensors. • Nanopores formed in the membrane control the flux of ions with the solution. Abstract: A new solid-state reference electrode using a polymeric membrane of polyvinyl butyral (PVB), Ag/AgCl and NaCl to be used in decentralized chemical measurements is presented. The electrode is made by drop-casting the membrane cocktail onto a glassy carbon (GC) substrate. A stable potential (less than 1 mV dec⁻¹ over a wide range of concentrations for the several chemical species tested is obtained. No significant influence to changes in redox potential, light and pH are observed. The response of this novel electrode shows good correlation when compared with a conventional double-junction reference electrode. Also good long-term stability (90 ± 33 μV/h) and a lifetime of approximately 4 months are obtained. Aspects related to the working mechanisms are discussed. Atomic Force Microscopy (AFM) studies reveal the presence of nanopores and channels on the surface, and electrochemical impedance spectroscopy (EIS) of optimized electrodes show low bulk resistances, usually in the kΩ range, suggesting that a nanoporous polymeric structure is formed in the interface with the solution. Future applications of this electrode as a disposable device for decentralized measurements are discussed. Examples of the utilization on wearable substrates (tattoos, fabrics, etc) are provided.

  5. A reference electrode based on polyvinyl butyral (PVB) polymer for decentralized chemical measurements

    International Nuclear Information System (INIS)

    Highlights: • A disposable solid-contact reference electrode for potentiometry is presented. • The device shows unsensitivity to most ions, redox potential and light. • Low-cost and good stability, ideal to build disposable potentiometric sensors. • Nanopores formed in the membrane control the flux of ions with the solution. - Abstract: A new solid-state reference electrode using a polymeric membrane of polyvinyl butyral (PVB), Ag/AgCl and NaCl to be used in decentralized chemical measurements is presented. The electrode is made by drop-casting the membrane cocktail onto a glassy carbon (GC) substrate. A stable potential (less than 1 mV dec−1) over a wide range of concentrations for the several chemical species tested is obtained. No significant influence to changes in redox potential, light and pH are observed. The response of this novel electrode shows good correlation when compared with a conventional double-junction reference electrode. Also good long-term stability (90 ± 33 μV/h) and a lifetime of approximately 4 months are obtained. Aspects related to the working mechanisms are discussed. Atomic Force Microscopy (AFM) studies reveal the presence of nanopores and channels on the surface, and electrochemical impedance spectroscopy (EIS) of optimized electrodes show low bulk resistances, usually in the kΩ range, suggesting that a nanoporous polymeric structure is formed in the interface with the solution. Future applications of this electrode as a disposable device for decentralized measurements are discussed. Examples of the utilization on wearable substrates (tattoos, fabrics, etc) are provided

  6. Prussian Blue bulk modified screen-printed electrodes for H(2)O(2) detection and for biosensors.

    Science.gov (United States)

    O'Halloran, M P; Pravda, M; Guilbault, G G

    2001-09-13

    A sensor for H(2)O(2) amperometric detection based on a Prussian Blue (PB) bulk modified carbon screen-printed electrode was developed. It has been optimised with respect to the lowest limit of detection achieved. PB was made chemically by the reaction of FeCl(3) with K(4)[Fe(CN)(6)]. The resulting powder, obtained by forced crystallisation induced by acetone, was dried and activated at 150 degrees C for 10 h. PB microparticles (carbon ink. The limit of detection achieved was 0.4 muM with the linear range up to 100 muM of H(2)O(2) with the sensitivity of 137 muA mM(-1) cm(-2), that was comparable with sensors based on electrodeposited PB film. The transducer was applied for a glucose biosensor, that exhibited LOD of 0.22 mM, linear range up to 3 mM, K(M)(app) of 4.6 mM, and the sensitivity of 3.21+/-0.16 muA mM(-1) cm(-2). The peroxide sensor, as well as the glucose biosensor, were totally insensitive to oxygen, ascorbate, urate, and paracetamol. PMID:18968406

  7. Chemical and microstructural transformations in lithium iron phosphate battery electrodes following pulsed laser exposure

    International Nuclear Information System (INIS)

    Highlights: • Lithium iron phosphate battery electrodes are exposed to pulsed laser radiation. • Raman spectroscopy is performed on regions approaching the incisions and cuts. • Chemical and microstructural changes in the active electrode layers are limited to the visible HAZ. • Some oxidation and degradation of the olive LiFePO4 cathode active material takes place in the HAZ. • The anode polycrystalline graphite structure becomes less ordered (higher D/G ratio) in the HAZ. - Abstract: Multi-layer lithium iron phosphate (LFP) battery electrodes are exposed to nanosecond pulsed laser radiation of wavelength 1064 nm. Test parameters are chosen to achieve characteristic interaction types ranging from partial incision of the active coating layers only to complete penetration of the electrodes with high visual cut quality. Raman spectroscopy is performed on unexposed regions and at points approaching each incision, highlighting changes in chemical composition and microstructure in the heat affected zone (HAZ). Thermogravimetric analysis is performed on the unexposed electrode active materials to distinguish the development of compositional changes under conditions of slow heating below the melting and sublimation temperatures. A brief theoretical description of the physical phenomena taking place during laser exposure is provided in terms of direct ablation during each laser pulse and vaporization or thermal degradation due to conductive heat transfer on a much longer time-scale, with characteristics of the HAZ reported in terms of these changes. For all laser exposures carried out in the study, chemical and microstructural changes are limited to the visible HAZ. Some degree of oxidation and LFP olivine phase degradation is observed in the cathode, while the polycrystalline graphite structure becomes less ordered in the anode. Where complete penetration is achieved, melting of the cathode active layer and combustion of the anode active layer take place near

  8. Maltodextrins from chemically modified starches. Selected physicochemical properties.

    Science.gov (United States)

    Pycia, Karolina; Juszczak, Lesław; Gałkowska, Dorota; Witczak, Mariusz; Jaworska, Grażyna

    2016-08-01

    The aim of this work was to evaluate the effect of chemical modification of starch (cross-linking and/or stabilisation) on selected rheological and functional properties of maltodextrins of dextrose equivalent of 6, 11 and 16. It was found that values of glass transition temperatures were decreasing with dextrose equivalent of maltodextrin. The highest values of glass transition temperature (TG) were determined for maltodextrin of DE 6-obtained from distarch phosphate and acetylated distarch phosphate. Increase in DE value of maltodextrin was also accompanied by decrease and increase in values of intrinsic viscosity and the critical concentration, respectively; however, there was no significant effect of kind of chemical modification of starch on the values of these parameters. Maltodextrin solutions at concentrations of from 10 to 70 % exhibited Newtonian flow behaviour. In the case of 50% solutions of maltodextrins of DE 6 the highest viscosity was produced by maltodextrin from native potato starch, while the lowest one by maltodextrin from acetylated starch. On the other hand, among the maltodextrin of DE 11 this one produced from acetylated starch showed the highest viscosity. All the maltodextrins exhibited surfactant properties in a water-air system, with the strongest effect observed for maltodextrins produced from double chemically modified starches and from acetylated starch. The surface activity was increasing with increasing of the DE value of maltodextrin. Moreover, values of surface tension were decreasing with increasing in maltodextrin concentration in the system. PMID:27112878

  9. Electrocatalytical oxidation and sensitive determination of acetaminophen on glassy carbon electrode modified with graphene–chitosan composite

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Meixia; Gao, Feng [Department of Chemistry and Environmental Science, Zhangzhou Normal University, Zhangzhou 363000 (China); Wang, Qingxiang, E-mail: axiang236@126.com [Department of Chemistry and Environmental Science, Zhangzhou Normal University, Zhangzhou 363000 (China); Cai, Xili [Department of Chemistry and Environmental Science, Zhangzhou Normal University, Zhangzhou 363000 (China); Jiang, Shulian; Huang, Lizhang [Zhangzhou Product Quality Supervision and Inspection Institute, Zhangzhou 363000 (China); Gao, Fei [Department of Chemistry and Environmental Science, Zhangzhou Normal University, Zhangzhou 363000 (China)

    2013-04-01

    The electrochemical behaviors of acetaminophen (ACOP) on a graphene–chitosan (GR–CS) nanocomposite modified glassy carbon electrode (GCE) were investigated by cyclic voltammetry (CV), chronocoulometry (CC) and differential pulse voltammetry (DPV). Electrochemical characterization showed that the GR–CS nanocomposite had excellent electrocatalytic activity and surface area effect. As compared with bare GCE, the redox signal of ACOP on GR–CS/GCE was greatly enhanced. The values of electron transfer rate constant (k{sub s}), diffusion coefficient (D) and the surface adsorption amount (Γ{sup ⁎}) of ACOP on GR–CS/GCE were determined to be 0.25 s{sup −1}, 3.61 × 10{sup −5} cm{sup 2} s{sup −1} and 1.09 × 10{sup −9} mol cm{sup −2}, respectively. Additionally, a 2e{sup −}/2H{sup +} electrochemical reaction mechanism of ACOP was deduced based on the acidity experiment. Under the optimized conditions, the ACOP could be quantified in the range from 1.0 × 10{sup −6} to 1.0 × 10{sup −4} M with a low detection limit of 3.0 × 10{sup −7} M based on 3S/N. The interference and recovery experiments further showed that the proposed method is acceptable for the determination of ACOP in real pharmaceutical preparations. Highlights: ► A chitosan–graphene nanocomposite modified glassy carbon electrode was prepared. ► The modified electrode was electrochemically characterized by CV and EIS. ► Electro-oxidation of acetaminophen was examined on the modified electrode. ► Sensing analysis of the modified electrode toward acetaminophen was studied.

  10. 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.

  11. Electrocatalytical oxidation and sensitive determination of acetaminophen on glassy carbon electrode modified with graphene–chitosan composite

    International Nuclear Information System (INIS)

    The electrochemical behaviors of acetaminophen (ACOP) on a graphene–chitosan (GR–CS) nanocomposite modified glassy carbon electrode (GCE) were investigated by cyclic voltammetry (CV), chronocoulometry (CC) and differential pulse voltammetry (DPV). Electrochemical characterization showed that the GR–CS nanocomposite had excellent electrocatalytic activity and surface area effect. As compared with bare GCE, the redox signal of ACOP on GR–CS/GCE was greatly enhanced. The values of electron transfer rate constant (ks), diffusion coefficient (D) and the surface adsorption amount (Γ⁎) of ACOP on GR–CS/GCE were determined to be 0.25 s−1, 3.61 × 10−5 cm2 s−1 and 1.09 × 10−9 mol cm−2, respectively. Additionally, a 2e−/2H+ electrochemical reaction mechanism of ACOP was deduced based on the acidity experiment. Under the optimized conditions, the ACOP could be quantified in the range from 1.0 × 10−6 to 1.0 × 10−4 M with a low detection limit of 3.0 × 10−7 M based on 3S/N. The interference and recovery experiments further showed that the proposed method is acceptable for the determination of ACOP in real pharmaceutical preparations. Highlights: ► A chitosan–graphene nanocomposite modified glassy carbon electrode was prepared. ► The modified electrode was electrochemically characterized by CV and EIS. ► Electro-oxidation of acetaminophen was examined on the modified electrode. ► Sensing analysis of the modified electrode toward acetaminophen was studied

  12. Electro-oxidation of chlorophenols at glassy carbon electrodes modified with polyNi(II)complexes

    Energy Technology Data Exchange (ETDEWEB)

    Berrios, Cristhian [Facultad de Quimica y Biologia, Departamento de Ciencias del Ambiente, Universidad de Santiago de Chile (USACh), casilla 40, correo 33, Santiago (Chile); Marco, Jose F.; Gutierrez, Claudio [Instituto de Quimica Fisica ' Rocasolano' , CSIC, C. Serrano, 119, 28006, Madrid (Spain); Ureta-Zanartu, Maria Soledad [Facultad de Quimica y Biologia, Departamento de Ciencias del Ambiente, Universidad de Santiago de Chile (USACh), casilla 40, correo 33, Santiago (Chile)], E-mail: soledad.ureta@usach.cl

    2009-11-01

    The effect of the ligand macrocycle (phenylporphyrin (PP) or phthalocyanine (Pc)) and of the ligand substituent (-NH{sub 2} or -SO{sub 3}{sup -}) on the catalytic activity for the electro-oxidation in a pH 11 buffer electrolyte of 2- and 4-chlorophenol (2-CP and 4-CP), 2,4- and 2,6-dichlorophenol (2,4-DCP and 2,6-DCP), 2,4,6-trichlorophenol (2,4,6-TCP), and pentachlorophenol (PCP) at glassy carbon electrodes modified with electropolymerized Ni(II) macrocycles was studied. The polyphenolic residue deposited at the electrode surface was characterized by cyclic voltammetry, impedance measurements, ex situ Fourier transform infrared spectroscopy (FT-IR) and X-ray Photoelectron Spectroscopy (XPS). A band of aliphatic C=O stretching in the IR spectrum of the fouling film produced by potential cycling in 2,4,6-TCP indicated that the aromatic ring had been broken, yielding ketones, aldehydes and/or carboxylic acids. The sulphonated Ni(II) polymers, which showed the Ni(III)/Ni(II) process in the CV, had XP spectra typical of paramagnetic Ni(II), indicating that they contained Ni(OH){sub 2} clusters. On the contrary, the CVs of the amino Ni(II) did not show the Ni(III)/Ni(II) process at all, this process appearing only after previous activation by potential cycling, and only to a small extent. As was to be expected, the XP spectra of activated amino films corresponded to diamagnetic Ni(II), showing that the concentration of Ni(OH){sub 2} clusters was very small. The amino films were less active than the sulpho films for the oxidation of chlorophenols, in agreement with the lower concentration of Ni(OH){sub 2} clusters in the former films. For all electrodes the highest activity was observed for 2,4,6-TCP, since its oxidation yields a phenolic residue which is much more porous than those produced by the other CPs.

  13. Enhanced performance of a Bi-modified graphite felt as the positive electrode of a vanadium redox flow battery

    OpenAIRE

    González Arias, Zoraida; Sánchez Sánchez, Ángela; Blanco Rodríguez, Clara; Granda Ferreira, Marcos; Menéndez López, Rosa María; Santamaría Ramírez, Ricardo

    2011-01-01

    [EN] Graphite felt modified with nanodispersed bismuth was studied as electrode in the positive half-cell of a vanadium redox flow battery (VRFB). The felt was easily modified by immersion in a Bi2O3 solution followed by thermal reduction at 450 °C in air. Despite the low metal content (1 at.%) on the surface of the fibers, the Bi-modified felt showed an excellent electrochemical performance (at 1 mV s− 1) in terms of anodic and cathodic peak current densities (21 and 17 mA cm–2, respectively...

  14. Electrochemical biosensor for detection of PML/RARα fusion gene based on eriochrome cyanine R film modified glassy carbon electrode

    International Nuclear Information System (INIS)

    This communication reports on a novel biosensor to study the hybridization specificity based on eriochrome cyanine R (ECR) monolayer film modified glassy carbon electrode (GCE). Differential pulse voltammetry (DPV) was used to monitor the hybridization reaction on the ECR-modified electrode. The decrease of the peak current of methylene blue (MB), an electroactive indicator, was observed upon hybridization of the probe with the target DNA. Electrochemical investigations indicated that ECR modified biosensor displayed a wide linear range of 5.0–200 pM with a detection limit of 0.982 pM. This new biosensor exhibited good selectivity for one-base mismatch and complementary sequence after hybridization in detecting promyelocytic leukemia/retinoic acid receptor α (PML/RARα) fusion gene in acute promyelocytic leukemia (APL).

  15. Hg(2+) detection using a disposable and miniaturized screen-printed electrode modified with nanocomposite carbon black and gold nanoparticles.

    Science.gov (United States)

    Cinti, Stefano; Santella, Francesco; Moscone, Danila; Arduini, Fabiana

    2016-05-01

    A miniaturized screen-printed electrode (SPE) modified with a carbon black-gold nanoparticle (CBNP-AuNP) nanocomposite has been developed as an electrochemical sensor for the detection of inorganic mercury ions (Hg(2+)). The working electrode surface has been modified with nanocomposite constituted of CBNPs and AuNPs by an easy drop casting procedure that makes this approach extendible to an automatable mass production of modified SPEs. Square wave anodic stripping voltammetry (SWASV) was adopted to perform Hg(2+) detection, revealing satisfactory sensitivity and detection limit, equal to 14 μA ppb(-1) cm(-2) and 3 ppb, respectively. The applicability of the CBNP-AuNP-SPE for the determination of inorganic mercury has been assessed in river water by a simple filtration and acidification of the sample as well as in soil by means of a facile acidic extraction procedure assisted by ultrasound. PMID:26803751

  16. 12-Tungstophosphates Immobilized on Chemically Modified Mesoporous Silica SBA-15

    Institute of Scientific and Technical Information of China (English)

    ZHU Jing; YOU Wan-sheng; ZHU Zai-ming; SUN Zhen-gang; ZHANG Lan-cui; GU Yuan-peng

    2005-01-01

    A functionalized material, PW/SBA-15m, was prepared successfully in diluted H2SO4 aqueous solutions by immobilizing 12-tungstophosphates on chemically modified mesoporous silica SBA-15 and characterized by elemental analysis, FTIR, 31P MAS NMR, XRD and TEM. The results indicate that the framework of SBA-15 and the Keggin structure of PW12O3-40 were retained, and that 23%-33%(mass fraction) of PW12O3-40 was immobilized; the PW12O3-40 anions were finely dispersed on the pore wall of SBA-15. Having been leached in ethanol at 60 ℃ for 7 h, the loss of PW12O3-40 anions was not found.

  17. Electrocatalysis of oxygen reduction on nitrogen-containing multi-walled carbon nanotube modified glassy carbon electrodes

    International Nuclear Information System (INIS)

    Highlights: ► Pyrolysis in the presence of urea was used for nitrogen doping of carbon nanotubes. ► N-doped carbon nanotubes were used as catalysts for the oxygen reduction reaction. ► N-doped carbon material showed a high catalytic activity for ORR in alkaline media. ► N-containing CNT material is an attractive cathode catalyst for alkaline membrane fuel cells. - Abstract: The electrochemical reduction of oxygen was studied on nitrogen-doped multi-walled carbon nanotube (NCNT) modified glassy carbon (GC) electrodes employing the rotating disk electrode (RDE) method. Nitrogen doping was achieved by simple pyrolysis of the carbon nanotube material in the presence of urea. The surface morphology and composition of the NCNT samples were investigated by scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The SEM images revealed a rather uniform distribution of NCNTs on the GC electrode substrate. The XPS analysis showed a successful doping of carbon nanotubes with nitrogen species. The RDE results revealed that in alkaline solution the N-doped nanotube materials showed a remarkable electrocatalytic activity towards oxygen reduction. At low overpotentials the reduction of oxygen followed a two-electron pathway on undoped carbon nanotube modified GC electrodes, whereas on NCNT/GC electrodes a four-electron pathway of O2 reduction predominated. The results obtained are significant for the development of nitrogen-doped carbon-based cathodes for alkaline membrane fuel cells.

  18. Direct Electrochemistry and Electrocatalysis of Myoglobin with CoMoO4 Nanorods Modified Carbon Ionic Liquid Electrode

    International Nuclear Information System (INIS)

    By using ionic liquid 1-hexylpyridinium hexafluorophosphate (HPPF6) based carbon ionic liquid electrode (CILE) as the substrate electrode, a CoMoO4 nanorods and myoglobin (Mb) composite was casted on the surface of CILE with chitosan (CTS) as the film forming material to obtain the modified electrode (CTS/CoMoO4-Mb/CILE). Spectroscopic results indicated that Mb retained its native structures without any conformational changes after mixed with CoMoO4 nanorods and CTS. Electrochemical behaviors of Mb on the electrode were carefully investigated by cyclic voltammetry with a pair of well-defined redox peaks from the heme Fe(III)/Fe(II) redox center of Mb appeared, which indicated that direct electron transfer between Mb and CILE was realized. Electrochemical parameters such as the electron transfer number (n), charge transfer coefficient (α) and electron transfer rate constant (ks) were estimated by cyclic voltammetry with the results as 1.09, 0.53 and 1.16 s-1, respectively. The Mb modified electrode showed good electrocatalytic ability toward the reduction of trichloroacetic acid in the concentration range from 0.1 to 32.0 mmol L-1 with the detection limit as 0.036 mmol L-1 (3σ), and the reduction of H2O2 in the concentration range from 0.12 to 397.0 μmol L-1 with the detection limit as 0.0426 μmol L-1 (3σ)

  19. Understanding the mechanism of direct electrochemistry of mitochondria-modified electrodes from yeast, potato and bovine sources at carbon paper electrodes

    International Nuclear Information System (INIS)

    Although mitochondria have been used for bio-electrochemistry for over 5 years, little is known about their direct electrochemistry mechanism. This paper focuses on developing a better understanding of the electron transfer mechanism of mitochondria from three different organisms at carbon electrodes. Yeast, potato and bovine mitochondria have been successfully isolated and immobilized onto Toray paper electrodes via vapor deposited silica. Organelle-modified electrodes were first characterized using cyclic voltammetry. Similar electrochemical signals were obtained for all organisms. Direct electron transfer was observed when a metabolite of the Krebs cycle was present in the buffer solution. Control experiments based on the immobilization of two electron carriers contained in mitochondria, cytochrome c and a quinone (coenzyme Q10), tend to show the electron transfer mechanism to the carbon material comes from the quinone pool of the organelles. As quinones are known to be pH-dependent, we further investigated the response of the electrochemical signal of the three isolated mitochondria and the two electron carriers separately. The half wave potentials obtained from the organelles appeared to be pH-dependent and their variations are comparable to coenzyme Q10 rather than cytochrome c. Finally, extraction of both the cytochrome c and the quinone pool from intact mitochondria was performed to validate our hypothesis that direct electrochemistry of mitochondria happens via the quinone pool. Electrochemistry of immobilized quinone-depleted mitochondria validated the hypothesis that the mitochondria are communicating with the electrodes through the quinone pool

  20. Highly efficient adsorption of chlorophenols onto chemically modified chitosan

    Science.gov (United States)

    Zhou, Liang-Chun; Meng, Xiang-Guang; Fu, Jing-Wei; Yang, Yu-Chong; Yang, Peng; Mi, Chun

    2014-02-01

    A novel chemically modified chitosan CS-SA-CD with phenol and β-cyclodextrin groups was prepared. The adsorptions of phenol, 2-chlorophenol (2-CP), 4-chlorophenol (4-CP), 2,4-dichlorophenol (DCP) and 2,4,6-trichlorophenol (TCP) on the functional chitosan from aqueous solution were investigated. CS-SA-CD exhibited excellent adsorption ability for chlorophenols especially for DCP and TCP. The maximum adsorption capacities of phenol, 2-CP, 4-CP, DCP and TCP on CS-SA-CD were 59.74, 70.52, 96.43, 315.46 and 375.94 mg/g, respectively. The scanning electron microscope and Brunauer-Emmett-Teller analyses revealed that the introduction of phenol group changed the surface morphology and surface properties of chitosan. The modified chitosan CS-SA-CD possesses larger surface areas (4.72 m2/g), pore volume (7.29 × 10-3 mL/g) and average pore diameter (59.99 Å) as compared to those of chitosan 3.27 m2/g, 2.00 × 10-3 mL/g and 15.95 Å, respectively. The enhanced adsorption of chlorophenols was also attributed to the interaction of hydrogen bond between Cl atom and sbnd OH group. The adsorption of chlorophenols on CS-SA-CD followed the pseudo-second-order kinetic model. Adsorbent could be regenerated easily and the regenerated CS-SA-CD remained 80-91% adsorption efficiency.

  1. Highly efficient adsorption of chlorophenols onto chemically modified chitosan

    International Nuclear Information System (INIS)

    A novel chemically modified chitosan CS-SA-CD with phenol and β-cyclodextrin groups was prepared. The adsorptions of phenol, 2-chlorophenol (2-CP), 4-chlorophenol (4-CP), 2,4-dichlorophenol (DCP) and 2,4,6-trichlorophenol (TCP) on the functional chitosan from aqueous solution were investigated. CS-SA-CD exhibited excellent adsorption ability for chlorophenols especially for DCP and TCP. The maximum adsorption capacities of phenol, 2-CP, 4-CP, DCP and TCP on CS-SA-CD were 59.74, 70.52, 96.43, 315.46 and 375.94 mg/g, respectively. The scanning electron microscope and Brunauer–Emmett–Teller analyses revealed that the introduction of phenol group changed the surface morphology and surface properties of chitosan. The modified chitosan CS-SA-CD possesses larger surface areas (4.72 m2/g), pore volume (7.29 × 10−3 mL/g) and average pore diameter (59.99 Å) as compared to those of chitosan 3.27 m2/g, 2.00 × 10−3 mL/g and 15.95 Å, respectively. The enhanced adsorption of chlorophenols was also attributed to the interaction of hydrogen bond between Cl atom and -OH group. The adsorption of chlorophenols on CS-SA-CD followed the pseudo-second-order kinetic model. Adsorbent could be regenerated easily and the regenerated CS-SA-CD remained 80–91% adsorption efficiency.

  2. High selectivity of benzene electrochemical oxidation to p-benzoquinone on modified PbO2 electrode

    International Nuclear Information System (INIS)

    Highlights: • Uniform PbO2 surface layer with a pyramidal-angular structure. • High oxygen evolution potential of the modified electrode. • High selectivity of benzene electrochemical oxidation toward p-benzoquinone. - Abstract: In this paper, a modified Ti/SnO2–Sb2O3/PbO2 electrode was successfully synthesized. The interlayer SnO2–Sb2O3 was obtained through thermal decomposition and the surface layer by electrochemical deposition. The structures and morphology of the layers were studied by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The electrochemical property was carried out by cyclic voltammogrametry (CV) and the products obtained from electrochemical oxidation of benzene were investigated by gas chromatography and mass spectrometry (GC–MS). The results showed that the surface of the prepared electrode was mainly composed of tetragonal-shaped β-PbO2 crystal with a pyramidal-angular structure. The oxidation potential of benzene was +1.8 V vs. Ag/AgCl. The electrochemical oxidation of benzene showed the high selectivity toward p-benzoquinone on the modified Ti/SnO2–Sb2O3/PbO2 electrode. And the optimal oxidation temperature for oxidation of benzene was 75 °C and the optimal temperature was 60 min

  3. Photoamperometric flow injection analysis of glucose based on dehydrogenase modified quantum dots-carbon nanotube nanocomposite electrode.

    Science.gov (United States)

    Ertek, Bensu; Dilgin, Yusuf

    2016-12-01

    In this work, a core-shell quantum dot (QD, ZnS-CdS) was electrodeposited onto multiwalled carbon nanotube modified glassy carbon electrode (ZnS-CdS/MWCNT/GCE) and following glucose dehydrogenase (GDH) was immobilized onto QD modified electrode. The proposed electrode (GDH/ZnS-CdS/MWCNT/GCE) was effectively used for the photoelectrochemical biosensing of glucose in flow injection analysis (FIA) system using a home-made flow cell. Results from cyclic voltammetric and FI amperometric measurements have revealed that GDH/ZnS-CdS/MWCNT/GCE is capable of signaling photoelectrocatalytic activity toward NADH when the surface of enzyme modified electrode was irradiated with a light source (250W Halogen lamp). Thus, photoelectrochemical biosensing of glucose was monitored by recording current-time curve of enzymatically produced NADH at optimized conditions. The biosensor response was found linear over the range 0.010-2.0mM glucose with detection limits of 6.0 and 4.0μM for amperometric and photoamperometric methods, respectively. The relative standard deviations (n=5) for 0.5mM glucose were 5.8% and 3.8% for photoamperometric and amperometric results, respectively. The photoelectrochemical biosensor was successfully applied to the real samples. The results with this biosensor showed good selectivity, repeatability and sensitivity for monitoring glucose in amperometric and photoamperometric FIA studies. PMID:26944347

  4. Electrochemical properties of estradiol at glassy carbon electrode modified with nano-Al2O3 film

    International Nuclear Information System (INIS)

    Nano-Al2O3 is dispersed onto the surface of the glassy carbon electrode (GCE). This nanostructured film modified GCE exhibits a great enhancement to the oxidation of estradiol (E2), especially when adequate concentration of cationic surfactant such as cetyltrimethylammonium bromide (CTAB) is added into the sample solution. Due to the nanoparticle's unique properties and its inclination to selectively combine with some groups of bimolecules, as well as synergistic adsorption of E2 and CTAB on the electrode surface, E2 gives a more sensitive voltammetric response compared with bare GCE performed in the absence of CTAB. The lowest detectable concentration (3σ) of E2 is estimated to be 8x10-8 mol l-1 (accumulation for 2 min). The linear relationship between peak current and concentration of E2 holds in the range 4x10-7-4x10-5 mol l-1 (R=0.9932). The electrochemical properties of E2 on this modified electrode are investigated by linear scan voltammetry and cyclic voltammetry. Scanning electron microscope (SEM) and BET are employed to characterize the surface of the electrode modified with nano-Al2O3 film

  5. Direct determination of 5-methylcytosine based on electrochemical activation of surfactant functionalized graphene modified pyrolytic graphite electrode

    International Nuclear Information System (INIS)

    Highlights: ► Surfactant functionalized graphene modified electrode was fabricated. ► Electrochemistry activation process significantly improved the electron transfer. ► This sensor could distinguish C and 5-mC at low potentials in a mixture solution. ► 5-mC could be detected when DNA bases existed by direct electrochemical way. -- Abstract: In this paper, a simple and sensitive method was proposed for 5-methylcytosine determination based on sodium dodecyl sulfate functionalized graphene (SDS-GR) modified pyrolytic graphite electrode (PGE), where SDS-GR was synthesized by electrolyzing graphite rod in 0.01 M SDS solution containing 0.1 M KNO3. After electrochemical activation by cyclic voltammetry (CV), activated SDS-GR modified PGE (A-SDS-GR/PGE) was fabricated for discriminating 5-methylcytosine from other nucleic acid bases. The results indicated that SDS-GR could improve the conductivity of the electrode and promote the electron transfer rate. And the process of electrochemical activation significantly enhanced the amount of active sites and oxygenated groups on electrode surface. As a result, 5-methylcytosine, guanine, adenine and cytosine could be distinguished with different oxidation potentials in a mixture solution except the overlap of the oxidation potential of thymine and 5-methylcytosine. However, the interference caused by thymine could be eliminated because the content of it is equal to adenine. The fabricated A-SDS-GR/PGE provided an alternative route for 5-methylcytosine determination when cytosine existed

  6. Electrochemical removal of fluoride from water by PAOA-modified carbon felt electrodes in a continuous flow reactor.

    Science.gov (United States)

    Cui, Hao; Qian, Yan; An, Hao; Sun, Chencheng; Zhai, Jianping; Li, Qin

    2012-08-01

    A novel poly(aniline-co-o-aminophenol) (PAOA) modified carbon felt electrode reactor was designed and investigated for fluoride removal from aqueous solutions. This reactor design is innovative because it operates under a wider pH range because of coating with a copolymer PAOA ion exchange film. In addition, contaminant mass transfer from bulk solution to the electrode surface is enhanced by the porous carbon felt as an electron-conducting carrier material compared to other reactors. The electrically controlled anion exchange mechanism was investigated by X-ray photoelectron spectroscopy and cyclic voltammetry. The applicability of the reactor in the field was tested through a series of continuous flow experiments. When the flow rate and initial fluoride concentration were increased, the breakthrough curve became sharper, which lead to a decrease in the breakthrough time and the defluoridation capacity of the reactor. The terminal potential values largely influenced fluoride removal by the reactor and the optimal defluoridation efficiency was observed at around 1.2V. The breakthrough capacities were all >10mg/g over a wide pH range (pH 5-9) with an initial fluoride concentration of 10mg/L. Consecutive treatment-regeneration studies over a week (once each day) revealed that the PAOA-modified carbon felt electrode could be effectively regenerated for reuse. The PAOA-modified carbon felt electrode reactor is a promising system that could be made commercially available for fluoride removal from aqueous solutions in field applications. PMID:22595483

  7. A sensor for acetaminophen in a blood medium using a Cu(II)-conducting polymer complex modified electrode

    International Nuclear Information System (INIS)

    Complexation of Cu ions in a terthiophene carboxylic acid (TTCA) polymer film resulted an enhanced anodic current for acetaminophen oxidation when compared to polymer coated and bare glassy carbon electrodes in human blood and buffer media. Scanning electron microscopy (SEM) and ESCA experiments indicate the involvement of copper in the electrocatalytic oxidation of acetaminophen. No interference was observed from other biologically important and phenolic compounds used with this modified electrode. Especially, the non-interference from N-acetylcysteine, an antidote for the treatment of acetaminophen poisoning, reveals the proposed method's superiority in medicinal applications. In addition, the present modified electrode avoids surface fouling at higher concentrations of acetaminophen. The calibration range obtained with CV was based between 2.0x10-5 and 5.0x10-3 M [r2=0.997 (n=5, R.S.D.=2.5%); DL=5.0x10-6 M (S/N=3)]. The analytical utility of the modified electrode was achieved by analyzing the content of acetaminophen in different drugs without pretreatment using CV and amperometric techniques

  8. Fabrication of electrochemical theophylline sensor based on manganese oxide nanoparticles/ionic liquid/chitosan nanocomposite modified glassy carbon electrode

    International Nuclear Information System (INIS)

    In this study, the preparation of a glassy carbon (GC) electrode modified with chitosan/NH2-ionic liquid/manganese oxide nanoparticles (Chit/NH2-IL/MnOx) was described for electrocatalytic detection of theophylline (TP). First, chitosan hydrogel (Chit) was electrodeposited on the GC electrode surface at a constant potential (−1.5 V) in acidic solution. Then, the previously synthesized amine-terminated 1-(3-Aminopropyl)-3-methylimidazolium bromide ionic liquid (NH2-IL) was covalently attached to the modified electrode via glutaraldehyde (GA) as linking agent. Finally, manganese oxide (MnOx) nanoparticles were electrodeposited onto the Chit/NH2-IL film by potential cycling between −1.0 and 1.7 V in Mn(CH3COO)2·4H2O neutral aqueous solution. Electrochemical behavior of the modified electrode was evaluated by cyclic voltammetry (CV) technique. The charge transfer coefficient (α) and electron transfer rate constant (ks) for MnOOH/MnO2 redox couple were calculated to be 0.35 and 1.62 s−1, respectively. The resulting system brings new capabilities for electrochemical sensing through combining the advantages of IL and MnOx nanoparticles. The differential pulse voltammetric (DPV) results indicated the high ability of GC/Chit/NH2-IL/MnOx modified electrode to catalyze the oxidation of TP. DPV determination of TP in acetate buffer solution (pH 5) gave linear responses over the concentration range up to 120 μM with the detection limit of 50 nM and sensitivity of 804 nA μM−1. Furthermore, the applicability of the sensor for TP analysis in pharmaceutical samples has been successfully demonstrated

  9. Label-free, electrochemical detection of methicillin-resistant staphylococcus aureus DNA with reduced graphene oxide-modified electrodes

    KAUST Repository

    Wang, Zhijuan

    2011-05-01

    Reduced graphene oxide (rGO)-modified glassy carbon electrode is used to detect the methicillin-resistant Staphylococcus aureus (MRSA) DNA by using electrochemical impedance spectroscopy. Our experiments confirm that ssDNA, before and after hybridization with target DNA, are successfully anchored on the rGO surface. After the probe DNA, pre-adsorbed on rGO electrode, hybridizes with target DNA, the measured impedance increases dramatically. It provides a new method to detect DNA with high sensitivity (10-13M, i.e., 100 fM) and selectivity. © 2011 Elsevier B.V.

  10. Label-free immunosensing of microcystin-LR using a gold electrode modified with gold nanoparticles

    International Nuclear Information System (INIS)

    The hepatotoxic microcystins, especially microcystin-LR (MC-LR), are causing serious problems to public health and fisheries. We describe here a label-free amperometric immunosensor for rapid determination of MC-LR in water sample. The sensor was prepared by immobilizing antibody on a gold electrode coated with L-cysteine-modified gold nanoparticles. The stepwise self-assembly of the immunosensor was monitored and characterized by means of electrochemical impedance spectroscopy and differential pulse voltammetry. A 0.60 mmol L-1 solution of hydroquinone was used as the electron mediator. The immunosensor was incubated with MC-LR at 25oC for 20 min, upon which the differential pulse voltammetric current changed linearly over the concentration range from 0.05 to 15.00 μg L-1, with a detection limit of 20 ng L-1. The developed biosensor was used to determine MC-LR in spiked crude algae samples. The recovery was in the range from 95. 6 to 105%. This method is simple, economical and efficient, this making it potentially suitable for field analysis of MC-LR in crude algae and water samples. (author)

  11. Voltammetric Determination of Codeine on Glassy Carbon Electrode Modified with Nafion/MWCNTs

    Directory of Open Access Journals (Sweden)

    Robert Piech

    2015-01-01

    Full Text Available A glassy carbon electrode modified with a Nafion/MWCNTs composite is shown to enable the determination of codeine using differential pulse voltammetry in phosphate buffer of pH 3.0. At a preconcentration time of 15 s, the calibration graph is linear in the 0.5 µM (0.15 mg·L−1 to 15 µM (4.5 mg·L−1 concentration range with a correlation coefficient of 0.998. The detection limit at a preconcentration time of 120 s is as low as 4.5 μg·L−1. The repeatability of the method at a 0.6 μg·L−1 concentration level, expressed as the RSD, is 3.7% (for n=5. The method was successfully applied and validated by analyzing codeine in drug, human plasma, and urine samples.

  12. Electrochemical behaviour of different redox probes on single wall carbon nanotube buckypaper-modified electrodes

    International Nuclear Information System (INIS)

    In the present work, the electrochemical properties of single-walled carbon nanotube buckypapers (BPs) were examined in terms of carbon nanotubes nature and preparation conditions. The performance of the different free-standing single wall carbon nanotube sheets was evaluated via cyclic voltammetry of several redox probes in aqueous electrolyte. Significant differences are observed in the electron transfer kinetics of the buckypaper-modified electrodes for both the outer- and inner-sphere redox systems. These differences can be ascribed to the nature of the carbon nanotubes (nanotube diameter, chirality and aspect ratio), surface oxidation degree and type of functionalities. In the case of dopamine, ferrocene/ferrocenium, and quinone/hydroquinone redox systems the voltammetric response should be thought as a complex contribution of different tips and sidewall domains which act as mediators for the electron transfer between the adsorbate species and the molecules in solution. In the other redox systems only nanotube ends are active sites for the electron transfer. It is also interesting to point out that a higher electroactive surface area not always lead to an improvement in the electron transfer rate of various redox systems. In addition, the current densities produced by the redox reactions studied here are high enough to ensure a proper electrochemical signal, which enables the use of BPs in sensing devices

  13. Femtomolar detection of mercuric ions using polypyrrole, pectin and graphene nanocomposites modified electrode.

    Science.gov (United States)

    Arulraj, Abraham Daniel; Devasenathipathy, Rajkumar; Chen, Shen-Ming; Vasantha, Vairathevar Sivasamy; Wang, Sea-Fue

    2016-12-01

    Several nanomaterials and techniques for the detection of mercuric ions (Hg(2+)) have been developed in the past decade. However, simple, low-cost and rapid sensor for the detection of heavy metal ions yet remains an important task. Herein, we present a highly sensitive electrochemical sensor for the femtomolar detection of Hg(2+) based on polypyrrole, pectin, and graphene (PPy/Pct/GR) which was prepared by one step electrochemical potentiodyanamic method. The effect of concentration of pectin, polypyrrole and graphene were studied for the detection of Hg(2+). The influence of experimental parameters including effect of pH, accumulation time and accumulation potential were also studied. Different pulse anodic stripping voltammetry was chosen to detect Hg(2+) at PPy/Pct/GR/GCE modified electrode. The fabricated sensor achieved an excellent performance towards Hg(2+) detection such as higher sensitivity of 28.64μAμM(-1) and very low detection limit (LOD) of 4 fM at the signal to noise ratio of 3. The LOD of our sensor offered nearly 6 orders of magnitude lower than that of recommended concentration of Hg(2+) in drinking water by United States Environmental Protection Agency and World Health Organization. Compared to all previously reported electrochemical sensors towards Hg(2+) detection, our newly fabricated sensor attained a very LOD in the detection of Hg(2+). The practicality of our proposed sensor for the detection of Hg(2+) was successfully demonstrated in untreated tap water. PMID:27565958

  14. 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

  15. Freeze Drying Improves the Shelf-Life of Conductive Polymer Modified Neural Electrodes

    Directory of Open Access Journals (Sweden)

    Himadri S. Mandal

    2015-08-01

    Full Text Available Coating microelectrodes with conductive polymer is widely recognized to decrease impedance and improve performance of implantable neural devices during recording and stimulation. A concern for wide-spread use of this approach is shelf-life, i.e., the electrochemical stability of the coated microelectrodes prior to use. In this work, we investigated the possibility of using the freeze-drying process in order to retain the native low impedance state and, thereby, improve the shelf-life of conductive polymer poly(3,4-ethylenedioxythiophene (PEDOT-PSS modified neural electrodes. Control PEDOT-PSS coated microelectrodes demonstrated a significant increase in impedance at 1 kHz after 41–50 days of room temperature storage. Based on equivalent circuit modeling derived from electrochemical impedance spectroscopy, this increase in impedance could be largely attributed to a decrease in the interfacial capacitance consistent with a collapse and closing of the porous structure of the polymeric coating. Time-dependent electrochemical impedance measurements revealed higher stability of the freeze-dried coated microelectrodes compared to the controls, such that impedance values after 41–50 days appeared to be indistinguishable from the initial levels. This suggests that freeze drying PEDOT-PSS coated microelectrodes correlates with enhanced electrochemical stability during shelf storage.

  16. Development of a poly(alizarin red S)/ionic liquid film modified electrode for voltammetric determination of catechol

    International Nuclear Information System (INIS)

    Highlights: • This study is the first to conduct electroploymerization of ARS in RTILs. • BMIMBF4 was successfully mixed in polymeric ARS film. • PARS/BMIMBF4 film was tighter, smoother and better electrochemical property. • PARS/BMIMBF4/GCE showed superior performance for catechol determination. - Abstract: A novel modified electrode for voltammetric catechol determination was fabricated by electroploymerization of alizarin red S (ARS) onto a glassy carbon electrode (GCE) in one kind of room-temperature ionic liquid (1-butyl-3-methylimidazolium tetrafluoroborate, BMIMBF4). The polymeric ARS/ionic liquid (PARS/BMIMBF4) film modified electrode was characterized by using scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and electrochemical methods. The EDX, XPS and FTIR results indicated that PARS/BMIMBF4 film was successfully obtained. Compared with the GCE modified by electroploymerization of ARS in aqueous solution, the GCE modified by electroploymerization of ARS in BMIMBF4 showed smoother and more compact morphology for coating and better electroanalytical properties. Given the combined electrochemical activity of PARS and excellent conductivity of BMIMBF4, the PARS/BMIMBF4/GCE has been successfully used for catechol determination by differential pulse voltammetry (DPV) with a linear range of 0.10 to 500 μM. The sensitivity and detection limit are 42 nA/μM and 0.026 μM, respectively. The PARS/BMIMBF4 modified electrode was successfully applied to the determination of catechol in real water samples and may serve as a simple but high-performance sensor for the determination of some environmental pollutants

  17. Studies on electrochemical behaviour on NpO22+/NpO2+ redox couple at single walled carbon nanotube modified glassy carbon electrode (SWCNT-GC)

    International Nuclear Information System (INIS)

    Electrochemistry of NpO22+/NpO2+ couple in 1 M H2SO4 was studied on bare and modified glassy carbon (GC) electrodes by cyclic voltammetry (CV), differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy (EIS). The modified electrode (SWCNTs-GC) was characterized by scanning electron microscopy (SEM). Electrocatalysis of NpO22+/NpO2+ redox reaction was observed on SWCNT-GC electrode. The lower charge transfer resistance at SWCNT-GC reflects faster rate of electron transfer reaction of Np(VI)/Np(V) couple. These results are interesting to develop electroanalytical methodologies for neptunium determination using SWCNT modified electrode. To the best of our knowledge, this is the first study on the electrocatalysis of neptunium on SWCNT modified electrode.

  18. A novel hydrazine electrochemical sensor based on a carbon nanotube-wired ZnO nanoflower-modified electrode

    Energy Technology Data Exchange (ETDEWEB)

    Fang Bin, E-mail: binfang_47@yahoo.com.c [Anhui Key Laboratory of Chemo-Biosensor, College of Chemistry and Materials Science, Anhui Normal University, Beijing East Road, No. 1, Wuhu 241000 (China); Zhang Cuihong; Zhang Wei; Wang Guangfeng [Anhui Key Laboratory of Chemo-Biosensor, College of Chemistry and Materials Science, Anhui Normal University, Beijing East Road, No. 1, Wuhu 241000 (China)

    2009-12-15

    ZnO nanoflowers were synthesized by a simple process (ammonia-evaporation-induced synthetic method) and were applied to the hydrazine electrochemical sensor. The prepared material was characterized by means of scanning electron microscopy (SEM) and X-ray powder diffraction (XRD) and was then immobilized onto the surface of a glassy carbon electrode (GCE) via multi-walled carbon nanotubes (MWCNTs) to obtain ZnO/MWCNTs/GCE. The potential utility of the constructed electrodes was demonstrated by applying them to the analytical determination of hydrazine concentration. An optimized limit of detection of 0.18 muM was obtained at a signal-to-noise ratio of 3 and with a fast response time (within 3 s). Additionally, the ZnO/MWCNTs/GCE exhibited a wide linear range from 0.6 to 250 muM and higher sensitivity for hydrazine than did the ZnO modified electrode without immobilization of MWCNTs.

  19. Determination of mercury by electrochemical cold vapor generation atomic fluorescence spectrometry using polyaniline modified graphite electrode as cathode

    Energy Technology Data Exchange (ETDEWEB)

    Jiang Xianjuan [Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026 (China); Gan Wuer, E-mail: wgan@ustc.edu.c [Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026 (China); Wan Lingzhong; Zhang Hanchang; He Youzhao [Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026 (China)

    2010-02-15

    An electrochemical cold vapor generation system with polyaniline modified graphite electrode as cathode material was developed for Hg (II) determination by coupling with atomic fluorescence spectrometry. This electrochemical cold vapor generation system with polyaniline/graphite electrode exhibited higher sensitivity; excellent stability and lower memory effect compared with graphite electrode electrochemical cold vapor generation system. The relative standard deviation was 2.7% for eleven consecutive measurements of 2 ng mL{sup -1} Hg (II) standard solution and the mercury limit of detection for the sample blank solution was 1.3 rg mL{sup -1} (3sigma). The accuracy of the method was evaluated through analysis of the reference materials (GBW09101) (Human hair) and GBW (08517) (Laminaria Japonica Aresch) and the proposed method was successfully applied to the analysis of human hairs.

  20. Design and modelling of enzyme/poly-pyrrole modified electrodes for bio-catalyzed electro-synthesis processes

    International Nuclear Information System (INIS)

    This research thesis reports a study which aims at developing, analyzing and integrating an electrode-enzyme interface within an electro-enzymatic reactor to develop electrochemical biosensors. The adopted method comprises a confinement of the enzyme at the electrode surface by means of an electro-formed poly-pyrrole film. The author reports an experimental and theoretical study of the coupling between electrochemical reaction, enzymatic reaction and matter transfer in the polymer in order to better understand the operation of so-modified electrodes. Different parameters have an influence on the reaction rate. A numerical model (validated by experiments) allows the identification of the reaction limiting stages. A new elaboration protocol allows the polymer permeability to be increased. The interface is first applied to the reduction of the NAD coenzyme, and the process is also applied to the production of gluconic acid

  1. Highly efficient adsorption of chlorophenols onto chemically modified chitosan

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Liang-Chun [Key Laboratory of Green Chemistry and Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064 (China); National Center for Packaging Material Quality Supervision and Inspection, Chengdu Institute of Product Quality Supervision and Inspection, Chengdu 610064 (China); Meng, Xiang-Guang, E-mail: mengxgchem@163.com [Key Laboratory of Green Chemistry and Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064 (China); Fu, Jing-Wei [National Center for Packaging Material Quality Supervision and Inspection, Chengdu Institute of Product Quality Supervision and Inspection, Chengdu 610064 (China); Yang, Yu-Chong; Yang, Peng; Mi, Chun [Key Laboratory of Green Chemistry and Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064 (China)

    2014-02-15

    A novel chemically modified chitosan CS-SA-CD with phenol and β-cyclodextrin groups was prepared. The adsorptions of phenol, 2-chlorophenol (2-CP), 4-chlorophenol (4-CP), 2,4-dichlorophenol (DCP) and 2,4,6-trichlorophenol (TCP) on the functional chitosan from aqueous solution were investigated. CS-SA-CD exhibited excellent adsorption ability for chlorophenols especially for DCP and TCP. The maximum adsorption capacities of phenol, 2-CP, 4-CP, DCP and TCP on CS-SA-CD were 59.74, 70.52, 96.43, 315.46 and 375.94 mg/g, respectively. The scanning electron microscope and Brunauer–Emmett–Teller analyses revealed that the introduction of phenol group changed the surface morphology and surface properties of chitosan. The modified chitosan CS-SA-CD possesses larger surface areas (4.72 m{sup 2}/g), pore volume (7.29 × 10{sup −3} mL/g) and average pore diameter (59.99 Å) as compared to those of chitosan 3.27 m{sup 2}/g, 2.00 × 10{sup −3} mL/g and 15.95 Å, respectively. The enhanced adsorption of chlorophenols was also attributed to the interaction of hydrogen bond between Cl atom and -OH group. The adsorption of chlorophenols on CS-SA-CD followed the pseudo-second-order kinetic model. Adsorbent could be regenerated easily and the regenerated CS-SA-CD remained 80–91% adsorption efficiency.

  2. Amperometric detection of hydrazine utilizing synergistic action of prussian blue @ silver nanoparticles / graphite felt modified electrode

    International Nuclear Information System (INIS)

    Highlights: • Prussian Blue (PB) deposition on Ag/GF for electrochemical hydrazine sensing; • Lower detection limit of 4.9 × 10−7 mol L−1, stable over 24 days; • High sensitivity: 26.06 A mol−1 L. -- Abstract: In this study, a triple-component hydrazine sensor (PB@Ag/GF) was fabricated with freestanding graphite felt (GF), silver nanoparticles (Ag) and prussian blue (PB). The Ag nanoparticles were electrodeposited on GF ultrasonically (Ag/GF), and acted as a catalyst of the chemical deposition of PB. The electrode was characterized by scanning election microscopy (SEM), infrared spectroscopy (IR), X-ray diffraction (XRD), and energy-dispersive X-ray spectroscopy (EDS). The electrochemical behavior of PB@Ag/GF was measured by cyclic voltammetry and amperometric measurements. The sensor displayed a prominent electrocatalytic activity toward hydrazine oxidation, with a fast response time of 2 s, a low detection limit of 4.9 × 10−7 mol L−1 and very high detection sensitivity of 26.06 A mol−1 L

  3. Poly(methylene blue) functionalized graphene modified carbon ionic liquid electrode for the electrochemical detection of dopamine

    Energy Technology Data Exchange (ETDEWEB)

    Sun Wei, E-mail: swyy26@hotmail.com [College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158 (China); College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Wang Yuhua; Zhang Yuanyuan; Ju Xiaomei; Li Guangjiu [College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Sun Zhenfan [College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158 (China)

    2012-11-02

    Highlights: Black-Right-Pointing-Pointer Poly(methylene blue) functionalized graphene was electrodeposited on the electrode. Black-Right-Pointing-Pointer The fabricated electrode showed better electrochemical performances. Black-Right-Pointing-Pointer Dopamine was sensitive detected by the modified electrode. - Abstract: An ionic liquid 1-butylpyridinium hexafluorophosphate based carbon ionic liquid electrode (CILE) was used as the substrate electrode and a poly(methylene blue) (PMB) functionalized graphene (GR) composite film was co-electrodeposited on CILE surface by cyclic voltammetry. The PMB-GR/CILE exhibited better electrochemical performances with higher conductivity and lower electron transfer resistance. Electrochemical behavior of dopamine (DA) was further investigated by cyclic voltammetry and a pair of well-defined redox peaks appeared with the peak-to-peak separation ({Delta}E{sub p}) as 0.058 V in 0.1 mol L{sup -1} pH 6.0 phosphate buffer solution, which proved a fast quasi-reversible electron transfer process on the modified electrode. Electrochemical parameters of DA on PMB-GR/CILE were calculated with the electron transfer number as 1.83, the charge transfer coefficients as 0.70, the apparent heterogeneous electron transfer rate constant as 1.72 s{sup -1} and the diffusional coefficient (D) as 3.45 Multiplication-Sign 10{sup -4} cm{sup 2} s{sup -1}, respectively. Under the optimal conditions with differential pulse voltammetric measurement, the linear relationship between the oxidation peak current of DA and its concentration was obtained in the range from 0.02 to 800.0 {mu}mol L{sup -1} with the detection limit as 5.6 nmol L{sup -1} (3{sigma}). The coexisting substances exhibited no interference and PMB-GR/CILE was applied to the detection of DA injection samples and human urine samples with satisfactory results.

  4. Poly(methylene blue) functionalized graphene modified carbon ionic liquid electrode for the electrochemical detection of dopamine

    International Nuclear Information System (INIS)

    Highlights: ► Poly(methylene blue) functionalized graphene was electrodeposited on the electrode. ► The fabricated electrode showed better electrochemical performances. ► Dopamine was sensitive detected by the modified electrode. - Abstract: An ionic liquid 1-butylpyridinium hexafluorophosphate based carbon ionic liquid electrode (CILE) was used as the substrate electrode and a poly(methylene blue) (PMB) functionalized graphene (GR) composite film was co-electrodeposited on CILE surface by cyclic voltammetry. The PMB–GR/CILE exhibited better electrochemical performances with higher conductivity and lower electron transfer resistance. Electrochemical behavior of dopamine (DA) was further investigated by cyclic voltammetry and a pair of well-defined redox peaks appeared with the peak-to-peak separation (ΔEp) as 0.058 V in 0.1 mol L−1 pH 6.0 phosphate buffer solution, which proved a fast quasi-reversible electron transfer process on the modified electrode. Electrochemical parameters of DA on PMB–GR/CILE were calculated with the electron transfer number as 1.83, the charge transfer coefficients as 0.70, the apparent heterogeneous electron transfer rate constant as 1.72 s−1 and the diffusional coefficient (D) as 3.45 × 10−4 cm2 s−1, respectively. Under the optimal conditions with differential pulse voltammetric measurement, the linear relationship between the oxidation peak current of DA and its concentration was obtained in the range from 0.02 to 800.0 μmol L−1 with the detection limit as 5.6 nmol L−1 (3σ). The coexisting substances exhibited no interference and PMB–GR/CILE was applied to the detection of DA injection samples and human urine samples with satisfactory results.

  5. 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...

  6. 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

  7. A highly sensitive electrochemical biosensor for catechol using conducting polymer reduced graphene oxide-metal oxide enzyme modified electrode.

    Science.gov (United States)

    Sethuraman, V; Muthuraja, P; Anandha Raj, J; Manisankar, P

    2016-10-15

    The fabrication, characterization and analytical performances were investigated for a catechol biosensor, based on the PEDOT-rGO-Fe2O3-PPO composite modified glassy carbon (GC) electrode. The graphene oxide (GO) doped conducting polymer poly (3,4-ethylenedioxythiophene) (PEDOT) was prepared through electrochemical polymerization by potential cycling. Reduction of PEDOT-GO was carried out by amperometric method. Fe2O3 nanoparticles were synthesized in ethanol by hydrothermal method. The mixture of Fe2O3, PPO and glutaraldehyde was casted on the PEDOT-rGO electrode. The surface morphology of the modified electrodes was studied by FE-SEM and AFM. Cyclic voltammetric studies of catechol on the enzyme modified electrode revealed higher reduction peak current. Determination of catechol was carried out successfully by Differential Pulse Voltammetry (DPV) technique. The fabricated biosensor investigated shows a maximum current response at pH 6.5. The catechol biosensor exhibited wide sensing linear range from 4×10(-8) to 6.20×10(-5)M, lower detection limit of 7×10(-9)M, current maxima (Imax) of 92.55µA and Michaelis-Menten (Km) constant of 30.48µM. The activation energy (Ea) of enzyme electrode is 35.93KJmol(-1) at 50°C. There is no interference from d-glucose and l-glutamic acid, ascorbic acid and o-nitrophenol. The PEDOT-rGO-Fe2O3-PPO biosensor was stable for at least 75 days when stored in a buffer at about 4°C. PMID:26751827

  8. Electrochemical stability and restructuring and its impact on the electro-oxidation of CO: Pt modified Ru(0001) electrodes

    Science.gov (United States)

    Engstfeld, A. K.; Klein, J.; Brimaud, S.; Behm, R. J.

    2015-01-01

    Structural modifications during electrochemical measurements on well defined Pt modified Ru(0001) electrode surfaces, which were prepared and characterized under ultrahigh vacuum (UHV) conditions, and the influence of the restructuring on the CO oxidation reaction have been investigated in a set-up combining surface preparation and scanning tunneling microscopy characterization under UHV conditions (UHV-STM) and electrochemical flow cell measurements. Bare Ru(0001) and Pt monolayer island modified Ru(0001) electrodes with different Pt coverages were investigated, together with a Pt0.3Ru0.7/Ru(0001) monolayer surface alloy for comparison. Comparing bulk CO oxidation measurements performed upon cycling in base electrolyte (0.5 M H2SO4) to 0.90 VRHE with similar measurements performed after potential cycling to 1.05 VRHE, we find pronounced differences in the current-voltage characteristics, with a distinct new peak at low potentials in the positive-going scan in the latter case, which is centered at 0.67 VRHE. STM imaging performed before and after the electrocatalytic measurements revealed a distinct restructuring of the Pt monolayer island modified Ru(0001) surfaces upon potential cycling to 1.05 VRHE, while cycling to 0.90 VRHE maintains the original structure and morphology of the bimetallic surface. In contrast, for the bare Ru(0001) electrode, restructuring of steps is observed already upon potential cycling to 0.9 VRHE. Implications of these findings on the electrochemical stability of the electrodes as well as on the mechanistic understanding of the CO oxidation reaction on bimetallic PtRu electrode surfaces and on the activity of different mono- and bimetallic nanostructures are discussed.

  9. Glassy carbon electrodes modified with a film of nanodiamond-graphite/chitosan: Application to the highly sensitive electrochemical determination of Azathioprine

    International Nuclear Information System (INIS)

    A novel modified glassy carbon electrode with a film of nanodiamond-graphite/chitosan is constructed and used for the sensitive voltammetric determination of azathioprine (Aza). The surface morphology and thickness of the film modifier are characterized using atomic force microscopy. The electrochemical response characteristics of the electrode toward Aza are investigated by means of cyclic voltammetry. The modified electrode showed an efficient catalytic role for the electrochemical reduction of Aza, leading to a remarkable decrease in reduction overpotential and enhancement of the kinetics of the electrode reaction with a significant increase of peak current. The effects of experimental variables, such as the deposited amount of modifier suspension, the pH of the supporting electrolyte, the accumulation potential and time were investigated. Under optimal conditions, the modified electrode showed a wide linear response to the concentration of Aza in the range of 0.2-100 μM with a detection limit of 65 nM. The prepared modified electrode showed several advantages: simple preparation method, high stability and uniformity in the composite film, high sensitivity, excellent catalytic activity in physiological conditions and good reproducibility. The modified electrode can be successfully applied to the accurate determination of trace amounts of Aza in pharmaceutical and clinical preparations.

  10. Glassy carbon electrodes modified with a film of nanodiamond-graphite/chitosan: Application to the highly sensitive electrochemical determination of Azathioprine

    Energy Technology Data Exchange (ETDEWEB)

    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); Ghalkhani, Masoumeh [Department of Chemistry, Sharif University of Technology, Tehran 11155-9516 (Iran, Islamic Republic of)

    2010-04-15

    A novel modified glassy carbon electrode with a film of nanodiamond-graphite/chitosan is constructed and used for the sensitive voltammetric determination of azathioprine (Aza). The surface morphology and thickness of the film modifier are characterized using atomic force microscopy. The electrochemical response characteristics of the electrode toward Aza are investigated by means of cyclic voltammetry. The modified electrode showed an efficient catalytic role for the electrochemical reduction of Aza, leading to a remarkable decrease in reduction overpotential and enhancement of the kinetics of the electrode reaction with a significant increase of peak current. The effects of experimental variables, such as the deposited amount of modifier suspension, the pH of the supporting electrolyte, the accumulation potential and time were investigated. Under optimal conditions, the modified electrode showed a wide linear response to the concentration of Aza in the range of 0.2-100 muM with a detection limit of 65 nM. The prepared modified electrode showed several advantages: simple preparation method, high stability and uniformity in the composite film, high sensitivity, excellent catalytic activity in physiological conditions and good reproducibility. The modified electrode can be successfully applied to the accurate determination of trace amounts of Aza in pharmaceutical and clinical preparations.

  11. Glutathione modified screen-printed carbon nanofiber electrode for the voltammetric determination of metal ions in natural samples.

    Science.gov (United States)

    Pérez-Ràfols, Clara; Serrano, Núria; Díaz-Cruz, José Manuel; Ariño, Cristina; Esteban, Miquel

    2016-08-01

    This work reports the development of a glutathione modified electrode via electrografting on a screen-printed carbon nanofiber substrate (GSH-SPCNFE). GSH-SPCNFE was compared to a classical screen-printed carbon electrode modified with glutathione (GSH-SPCE) for the simultaneous voltammetric determination of Cd(II) and Pb(II). Their electrochemical characterization and analytical performance suggest that SPCNFE could be a much better support for GSH immobilization. The applicability of GSH-SPCNFE for the determination of low concentration levels of Pb(II) and Cd(II) ions in environmental samples was successfully tested in a certified wastewater reference material by means of stripping voltammetry with a very high reproducibility and good trueness. PMID:27216650

  12. Zinc oxide modified with benzylphosphonic acids as transparent electrodes in regular and inverted organic solar cell structures

    Energy Technology Data Exchange (ETDEWEB)

    Lange, Ilja; Reiter, Sina; Kniepert, Juliane; Piersimoni, Fortunato; Brenner, Thomas; Neher, Dieter, E-mail: neher@uni-potsdam.de [Institute of Physics and Astronomy, University of Potsdam, Karl-Liebknecht-Strasse 24-25, 14476 Potsdam (Germany); Pätzel, Michael; Hildebrandt, Jana; Hecht, Stefan [Department of Chemistry and IRIS Adlershof, Humboldt-Universität zu Berlin, Brook-Taylor-Str. 2, 12489 Berlin (Germany)

    2015-03-16

    An approach is presented to modify the work function of solution-processed sol-gel derived zinc oxide (ZnO) over an exceptionally wide range of more than 2.3 eV. This approach relies on the formation of dense and homogeneous self-assembled monolayers based on phosphonic acids with different dipole moments. This allows us to apply ZnO as charge selective bottom electrodes in either regular or inverted solar cell structures, using poly(3-hexylthiophene):phenyl-C71-butyric acid methyl ester as the active layer. These devices compete with or even surpass the performance of the reference on indium tin oxide/poly(3,4-ethylenedioxythiophene) polystyrene sulfonate. Our findings highlight the potential of properly modified ZnO as electron or hole extracting electrodes in hybrid optoelectronic devices.

  13. 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

  14. Amperometric bienzyme glucose biosensor based on carbon nanotube modified electrode with electropolymerized poly(toluidine blue O) film

    Energy Technology Data Exchange (ETDEWEB)

    Wang Wenju [Department of Chemistry, Hong Kong Baptist University, Kowloon Tong (Hong Kong); Wang Fang [Department of Chemistry, Hong Kong Baptist University, Kowloon Tong (Hong Kong)] [Department of Chemistry, Wuhan University, Wuhan 430072 (China); Yao Yanli [Department of Chemistry, Hong Kong Baptist University, Kowloon Tong (Hong Kong); Hu Shengshui [Department of Chemistry, Wuhan University, Wuhan 430072 (China); Shiu, Kwok-Keung, E-mail: kkshiu@hkbu.edu.h [Department of Chemistry, Hong Kong Baptist University, Kowloon Tong (Hong Kong)

    2010-09-30

    The amperometric bienzyme glucose biosensor utilizing horseradish peroxidase (HRP) and glucose oxidase (GOx) immobilized in poly(toluidine blue O) (PTBO) film was constructed on multi-walled carbon nanotube (MWNT) modified glassy carbon electrode. The HRP layer could be used to analyze hydrogen peroxide with toluidine blue O (TBO) mediators, while the bienzyme system (HRP + GOx) could be utilized for glucose determination. Glucose underwent biocatalytic oxidation by GOx in the presence of oxygen to yield H{sub 2}O{sub 2} which was further reduced by HRP at the MWNT-modified electrode with TBO mediators. In the absence of oxygen, glucose oxidation proceeded with electron transfer between GOx and the electrode mediated by TBO moieties without H{sub 2}O{sub 2} production. The bienzyme electrode offered high sensitivity for amperometric determination of glucose at low potential, displaying Michaelis-Menten kinetics. The bienzyme glucose biosensor displayed linear response from 0.1 to 1.2 mM with a sensitivity of 113 mA M{sup -1} cm{sup -2} at an applied potential of -0.10 V in air-saturated electrolytes.

  15. 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...

  16. EVALUATION OF ADSORPTION OF COPPER IONS IN THE PERLITE USING DIFFERENTIAL PULSE VOLTAMMETRY EMPLOYING A CHITOSAN MODIFIED GLASSY CARBON ELECTRODE

    OpenAIRE

    NOGUEIRA, James Pyetro do Amaral; CARVALHO, Araújo Daniel; MARTINEZ-HUITLE, CarlosAlberto; FERNANDES, Nedja Suely

    2011-01-01

    In this work the perlite, an aluminosilicate constituted by 72.1% of SiO2 and 18.5% of Al2O3 was evaluated as an adsorbent of copper ions in aqueous solution using the differential pulse voltammetry technique employing a chitosan modified glassy carbon electrode (EMQ). The adsorption tests performed in the range from 5 to 30 min indicated that an adsorption of copper ions around 73% at time of 30 min was achivied.

  17. Electrochemical Method for Heavy Metals Detection by Inhibition of Acetylcholinesterase Immobilized on Pt-nanoparticles Modified Graphite Electrode

    Directory of Open Access Journals (Sweden)

    Turdean G. L.

    2013-04-01

    Full Text Available The optimization and the characterization of a new amperometric biosensor based on acetylcholinestrase (AChE, immobilized on a graphite electrode modified with Pt-nanoparticles (PtNP, are reported. The G/PtNP-AChE biosensor was used for heavy metals detection. The degree of inhibition (%I, the kinetic constants of the inhibition process, as well as the influence of the PtNP presence on these parameters were estimated.

  18. Thiol anchoring and catalysis of gold nanoparticles at the liquid interface of thin-organic film-modified electrodes

    OpenAIRE

    Mirceski, Valentin; Aleksovska, Angela; Pejova, Biljana; Ivanovski, Vladimir; Mitrova, Biljana; Mitreska, Nikolina; Gulaboski, Rubin

    2014-01-01

    The deposition of in-situ formed gold nanoparticles at the liquid/liquid (L/L) interface is studied by means of thin-organic-film-modified electrodes (TFE). The degree of ordering and aggregation of gold nanoparticles can be tuned by adding a lipophilic and hydrophilic thiol in the organic and aqueous phase, respectively. The ordered thiol-anchored gold nanoparticles exhibit pronounced catalytic effect toward electron-transfer reactions across the L/L interface.

  19. Electrocatalytic oxidation of deferiprone and its determination on a carbon nanotube-modified glassy carbon electrode

    Energy Technology Data Exchange (ETDEWEB)

    Yadegari, H. [Department of Chemistry, Faculty of Science, K.N. Toosi University of Technology, P.O. Box 16315-1618, Tehran (Iran, Islamic Republic of); Jabbari, A. [Department of Chemistry, Faculty of Science, K.N. Toosi University of Technology, P.O. Box 16315-1618, Tehran (Iran, Islamic Republic of)], E-mail: jabbari@kntu.ac.ir; Heli, H.; Moosavi-Movahedi, A.A. [Institute of Biochemistry and Biophysics, University of Tehran, Tehran (Iran, Islamic Republic of); Karimian, K. [Arasto Pharmaceutical Chemicals Inc., Tehran (Iran, Islamic Republic of); Khodadadi, A. [Department of Chemical Engineering, Faculty of Engineering, University of Tehran, Tehran (Iran, Islamic Republic of)

    2008-02-15

    The electrochemical behavior of the anti-thalassemia and anti-HIV replication drug, deferiprone, was investigated on a carbon nanotube-modified glassy carbon (GC-CNT) electrode in phosphate buffer solution, pH 7.40 (PBS). During oxidation of deferiprone, two irreversible anodic peaks, with E{sub 1}{sup 0}=452 and E{sub 2}{sup 0}=906mV, appeared, using GC-CNT. Cyclic voltammetric study indicated that the oxidation process is irreversible and diffusion controlled. The number of exchanged electrons in the electro-oxidation process was obtained, and the data indicated that deferiprone is oxidized via two two-electron steps. The results revealed that carbon nanotube (CNT) promotes the rate of oxidation by increasing the peak current, so that deferiprone is oxidized at lower potentials, which thermodynamically is more favorable. This result was confirmed by impedance measurements. The diffusion coefficient, electron-transfer coefficient and heterogeneous electron-transfer rate constant of deferiprone were found to be 1.49 x 10{sup -6} cm{sup 2} s{sup -1}, 0.44, and 3.83 x 10{sup -3} cm s{sup -1}, respectively. A sensitive, simple and time-saving differential-pulse voltammetric procedure was developed for the analysis of deferiprone. Using the proposed method, deferiprone can be determined with a detection limit of 5.25 x 10{sup -7} M. The applicability of the method to direct assays of spiked human serum and urine fluids is described.

  20. Alizarin red S functionalized mesoporous silica modified glassy carbon electrode for electrochemical determination of anthracene

    International Nuclear Information System (INIS)

    Highlights: • Alizarin red S-SBA15 composite was prepared and characterized. • A novel sensing platform was constructed for anthracene determination. • The proposed sensor exhibited high sensitivity and low detection limit for detecting anthracene. • This method can be applied to the practical detection of anthracene in waste water. - Abstract: In the paper, a novel and sensitive electrochemical sensor based on modification of electroactive alizarin red S functionalized mesoporous silica material SBA15 onto glassy carbon electrode (ARS-SBA15/GCE) was developed. Alizarin red S, called electrochemical probe that can selectively recognize polycyclic aromatic hydrocarbons (PAHs), as tools for the detection of tricyclic aromatic hydrocarbon anthracene. The morphology and interface property of ARS modified SBA15 (ARS-SBA15) were examined by transmission electron microscopy (TEM) and fourier transform infrared spectroscopy (FTIR). Taking advantage of the π-π stacking force between alizarin red S and anthracene, the ARS-SBA15/GCE sensor could detect anthracene quantitatively in a wide range of 1.0 pM–10.0 nM and a low detection limit of 0.5 pM (S/N = 3). Other PAHs, such as naphthalene, phenanthrene, pyrene, and benzo[a]pyrene show little interference on the detection. Consequently, a simple and sensitive electrochemical method was proposed for the determination of anthracene, which can be used to determine anthracene in waste water samples. The electrochemical method provides a general tool that complements the commonly used spectroscopic methods and immune method for the detection of PAHs

  1. RuO2/Activated Carbon Composite Electrode Prepared by Modified Colloidal Procedure and Thermal Decomposition Method

    Science.gov (United States)

    Li, Xiang; Zheng, Feng; Gan, Weiping; Luo, Xun

    2016-01-01

    RuO2/activated carbon (AC) composite electrode was prepared by a modified colloidal procedure and a thermal decomposition method. The precursor for RuO2/AC was coated on tantalum sheet and annealed at 150°C to 190°C for 3 h to develop thin-film electrode. The microstructure and morphology of the RuO2/AC film were characterized by thermogravimetric analysis (TGA), x-ray diffraction (XRD) analysis, and scanning electron microscopy (SEM). The TGA results showed the maximum loss of RuO2/AC composite film at 410°C, with residual RuO2 of 23.17 wt.%. The amorphous phase structure of the composite was verified by XRD analysis. SEM analysis revealed that fine RuO2 particles were dispersed in an activated carbon matrix after annealing. The electrochemical properties of RuO2/AC electrode were examined by cycling voltammetry, galvanostatic charge-discharge, and cyclic behavior measurements. The specific capacitance of RuO2/AC electrode reached 245 F g-1. The cyclic behavior of RuO2/AC electrode was stable. Optimal annealing was achieved at 170°C for 3 h.

  2. Radiation modification of swollen and chemically modified cellulose

    International Nuclear Information System (INIS)

    Complete text of publication follows. Biodegradable hydrogel was produced by radiation-induced crosslinking of water soluble carboxymethyl cellulose. Mobility of the molecular chain was found to play an important role in the crosslinking reaction. In this work the role of cellulose chains' mobility in radiation-induced reactions of fibrous cellulose was studied. Mobility of chains was improved by swelling (in sodium hydroxide and tetramethylammonium hydroxide) and chemical modification (substitution of about 3 % of hydroxyl groups with carboxymethyl groups), respectively. All samples were neutralized after the treatments. Accessibility of cellulose characterized by water adsorption and retention was significantly improved by the treatments in the following order: sodium hydroxide < tetramethylammonium hydroxide < carboxymethylation. Less fibrillar structure of modified fibers was observed by electron microscope. Samples were irradiated in wet form in open air (10 kGy). Untreated sample coated with soluble CMC was also irradiated. Degree of polymerization, FTIR spectra, and water sorption of samples before and after irradiation are presented. Amount of water adsorbed on samples decreased after irradiation. It can be considered the consequence of crosslinks, which might improve the crease recovery ability of cotton fabric. High accessibility improved degradation rather than crosslinking of cellulose chains

  3. Non-enzymatic amperometric detection of hydrogen peroxide in human blood serum samples using a modified silver nanowire electrode.

    Science.gov (United States)

    Thirumalraj, Balamurugan; Zhao, Duo-Han; Chen, Shen-Ming; Palanisamy, Selvakumar

    2016-05-15

    In this paper, we report a highly sensitive amperometric H2O2 sensor based on silver nanowires (AgNWs) modified screen printed carbon electrode. The AgNWs were synthesized using polyol method. The synthesized AgNWs were characterized by scanning electron microscopy, UV-vis spectroscopy and X-ray diffraction techniques. The average diameter and length of the synthesized AgNWs were found as 86±5 and 385nm, respectively. Under optimum conditions, the AgNWs modified electrode shows a stable amperometric response for H2O2 and was linear over the concentrations ranging from 0.3 to 704.8μM. The non-enzymatic sensor showed a high sensitivity of 662.6μAmM(-1)cm(-2) with a detection limit of 29nM. The response time of the sensor was found as 2s. Furthermore, the AgNWs modified electrode exhibited a good recovery of H2O2 (94.3%) in the human blood serum samples. PMID:26939075

  4. Sensitive Detection of Haloperidol and Hydroxyzine at Multi-Walled Carbon Nanotubes-Modified Glassy Carbon Electrodes

    Directory of Open Access Journals (Sweden)

    Jilie Kong

    2008-03-01

    Full Text Available Haloperidol (i.e. HPD and hydroxyzine (i.e. HXY, two effective and important tranquilizers with low redox activity, were found to generate an irreversible anodic peak at about +0.86 V (vs. SCE or two anodic peaks at about +0.83 and +0.91 V in 0.05 M NaH2PO4-Na2HPO4 (pH=7.0 buffer solution with a multi-walled carbon nanotubes-modified glassy carbon electrode (i.e. MWNTs/GC, respectively. Their sensitive and quantitative measurement based on the first two anodic peaks was established under the optimum conditions. The anodic peak current was linear to HPD and HXY concentration from 1×10-7 to 2.5 ×10-5 M and 5×10-8 to 2.5 ×10-5 M, the detection limits obtained were 8×10-9 and 5×10-9 M, separately. The modified electrode exhibited some excellent characteristics including easy regeneration, high stability, good reproducibility and selectivity. The method proposed was successfully applied to the detection of HPD and HXY in drug tablets and proved to be reliable compared with ultraviolet spectrophotometry. The modified electrode was characterized by electrochemical methods.

  5. Aptamer biosensor for dopamine based on a gold electrode modified with carbon nanoparticles and thionine labeled gold nanoparticles as probe

    International Nuclear Information System (INIS)

    We describe a biosensor for dopamine that is based on the use of a gold electrode modified with carbon nanoparticles (CNPs) coupled to thionine labeled gold nanoparticles (AuNPs) acting as signal amplifiers. The biosensor was constructed by first modifying the CNPs on the gold electrode and adsorbing the thionine on the surface of the AuNPs, and then linking the complementary strand of the dopamine aptamer to the AuNPs via gold-thiol chemistry. Next, dopamine aptamer is added and the duplex is formed on the surface. On addition of a sample containing dopamine, it will interact with aptamer and cause the release of the electrochemical probe which then will be adsorbed on the surface of the CNP-modified gold electrode and detected by differential pulse voltammetry. The current is linearly related to the concentration of dopamine in the 30 nM to 6.0 μM ranges. The detection limit is as low as 10 nM, and the RSD is 3.1 % at a 0.3 μM level (for n = 11). The protocol was successfully applied to the determination of dopamine in spiked human urine samples. We perceive that this method holds promise as a widely applicable platform for aptamer-based electrochemical detection of small molecules. (author)

  6. Poly-glutamic acid modified carbon nanotube-doped carbon paste electrode for sensitive detection of L-tryptophan.

    Science.gov (United States)

    Liu, Xiao; Luo, Liqiang; Ding, Yaping; Ye, Daixin

    2011-08-01

    A novel poly-glutamic acid (PGA) film modified carbon paste electrode (CPE) incorporating carbon nanotubes (CNTs) was first prepared for the determination of l-tryptophan (l-Trp). Scanning electron microscopy and Fourier transform infrared spectroscopy were applied for characterization of the surface morphology of the modified electrodes and cyclic voltammetry was used to investigate the electrochemical properties of the proposed electrode towards the oxidation of l-Trp. Optimization of the experimental parameters was performed with regard to pH, ratio of CNTs, concentration of glutamic acid, electro-polymerization cycles, accumulation time and concentration of sodium dodecylbenzene sulfonate. The linearity between the oxidation peak current and the l-Trp concentration was obtained in the range of 5.0×10(-8) to 1.0×10(-4)M with a detection limit of 1.0×10(-8)M (S/N=3) and the sensitivity was calculated to be 1143.79μA∙mM(-1)∙cm(-2). In addition, the PGA modified CPE incorporating CNTs displayed high selectivity, good stability and reproducibility, making it suitable for the routine analysis of l-Trp in clinical use. PMID:21640670

  7. Determination of cadmium(II) using glassy carbon electrodes modified with cupferron, β-naphthol, and multiwalled carbon nanotubes

    International Nuclear Information System (INIS)

    We report on a simple and reliable method for the determination of trace cadmium ion using a glassy carbon electrode (GCE) modified with cupferron, β-naphthol and MWCNTs. The operational mechanism consists of several steps: first, the ligand cupferron on the modified electrode reacts with Cd2+ ion to form a chelate compound. Next, this chelate is adsorbed by the carrier β-following the principle of organic co-precipitation. Finally, the coprecipitated complex is detected by the GCE. This scheme is interesting because it combines preconcentration and electrochemical detection. Two linear responses are obtained, one in the concentration range of 5.0 x 10-11 to 1.6 x 10-8 M, the other in the range of 1.6 x 10-8 to 1.42 x 10-6 M, with a lower detection limit of 1.6 x 10-11 M. This modified GCE does not suffer from significant interferences by Cu(II), Hg(II), Ag(I), Fe(III), Pb(II), Cr(III), Zn(II), NO3-, Cl-, SO42- ions and EDTA. The response of the electrode remained constant for at least 3 weeks of successive operation. The method presented here provides a new way for the simultaneous separation, enrichment, and electrochemical detection of trace cadmium ion. (author)

  8. A reagentless non-enzymatic hydrogen peroxide sensor presented using electrochemically reduced graphene oxide modified glassy carbon electrode.

    Science.gov (United States)

    Mutyala, Sankararao; Mathiyarasu, Jayaraman

    2016-12-01

    Herein, we report a simple, facile and reproducible non-enzymatic hydrogen peroxide (H2O2) sensor using electrochemically reduced graphene oxide (ERGO) modified glassy carbon electrode (GCE). The modified electrode was characterized by Fourier transform infrared (FT-IR), UV-Visible, scanning electron microscopy (SEM) and atomic force microscopy (AFM) techniques. Cyclic voltammetric (CV) analysis revealed that ERGO/GCE exhibited virtuous charge transfer properties for a standard redox systems and showed excellent performance towards electroreduction of H2O2. Amperometric study using ERGO/GCE showed high sensitivity (0.3μA/μM) and faster response upon the addition of H2O2 at an applied potential of -0.25V vs. Ag/AgCl. The detection limit is assessed to be 0.7μM (S/N=3) and the time to reach a stable study state current is <3s for a linear range of H2O2 concentration (1-16μM). In addition, the modified electrode exhibited good reproducibility and long-term stability. PMID:27612728

  9. Effect of humic acid on the underpotential deposition-stripping voltammetry of copper in acetic acid soil extract solutions at mercaptoacetic acid-modified gold electrodes

    International Nuclear Information System (INIS)

    Electrochemical measurements were undertaken for the investigation of the underpotential deposition-stripping process of copper at bare and modified gold electrodes in 0.11 M acetic acid, the first fraction of the European Union's Bureau Communautaire de References (BCR) sequential extraction procedure for fractionating metals within soils and sediments. Gold electrodes modified with mercaptoacetic acid showed higher sensitivity for the detection of copper than bare gold electrodes, both in the absence and in the presence of humic acid in acetic acid solutions, using the underpotential deposition-stripping voltammetry (UPD-SV) method. In the presence of 50 mg l-1 of humic acid, the mercaptoacetic acid modified electrode proved to be 1.5 times more sensitive than the bare gold electrode. The mercaptoacetic acid monolayer formed on the gold surface provided efficient protection against the adsorption of humic acid onto the gold electrode surface. Variation of the humic acid concentration in the solution showed little effect on the copper stripping signal at the modified electrode. UPD-SV at the modified electrode was applied to the analysis of soil extract samples. Linear correlation of the electrochemical results with atomic spectroscopic results yielded the straight-line equation y (μg l-1) = 1.10x - 44 (ppb) (R=0.992, n=6), indicating good agreement between the two methods

  10. A nano-structured Ni(II)–chelidamic acid modified gold nanoparticle self-assembled electrode for electrocatalytic oxidation and determination of methanol

    International Nuclear Information System (INIS)

    A nano-structured Ni(II)–chelidamic acid (2,6-dicarboxy-4-hydroxypyridine) film was electrodeposited on a gold nanoparticle–cysteine–gold electrode. The morphology of Ni(II)–chelidamic acid gold nanoparticle self‐assembled electrode was investigated by scanning electron microscopy (SEM). Electrocatalytic oxidation of methanol on the surface of modified electrode was studied by cyclic voltammetry and chronoamperometry methods. The hydrodynamic amperometry at a rotating modified electrode at constant potential versus reference electrode was used for detection of methanol. Under optimized conditions the calibration plots are linear in the concentration range 0–50 mM with a detection limit of 15 μM. The formed matrix in our work possessed a 3D porous network structure with a large effective surface area, high catalytic activity and behaved like microelectrode ensembles. The modified electrode indicated reproducible behavior and a high level stability during the experiments, making it particularly suitable for analytical purposes. - Highlights: ► The Au electrode modified with thin Ni(II)/CHE-AuNP film shows stable and reproducible behavior. ► Long stability and excellent electrochemical reversibility were observed. ► This modified electrode shows excellent catalytic activity for methanol oxidation. ► Combination of unique properties of AuNP and Ni(II)/CHE resulted in improvement of current responses.

  11. Ultrathin 2D Photodetectors Utilizing Chemical Vapor Deposition Grown WS2 With Graphene Electrodes.

    Science.gov (United States)

    Tan, Haijie; Fan, Ye; Zhou, Yingqiu; Chen, Qu; Xu, Wenshuo; Warner, Jamie H

    2016-08-23

    In this report, graphene (Gr) is used as a 2D electrode and monolayer WS2 as the active semiconductor in ultrathin photodetector devices. All of the 2D materials are grown by chemical vapor deposition (CVD) and thus pose as a viable route to scalability. The monolayer thickness of both electrode and semiconductor gives these photodetectors ∼2 nm thickness. We show that graphene is different to conventional metal (Au) electrodes due to the finite density of states from the Dirac cones of the valence and conduction bands, which enables the photoresponsivity to be modulated by electrostatic gating and light input control. We demonstrate lateral Gr-WS2-Gr photodetectors with photoresponsivities reaching 3.5 A/W under illumination power densities of 2.5 × 10(7) mW/cm(2). The performance of monolayer WS2 is compared to bilayer WS2 in photodetectors and we show that increased photoresponsivity is achieved in the thicker bilayer WS2 crystals due to increased optical absorption. This approach of incorporating graphene electrodes in lateral TMD based devices provides insights on the contact engineering in 2D optoelectronics, which is crucial for the development of high performing ultrathin photodetector arrays for versatile applications. PMID:27440384

  12. FIA-automated system used to electrochemically measure nitrite and its interfering chemicals through a 1-2 DAB / Au electrode: gain of sensitivity at upper potentials

    International Nuclear Information System (INIS)

    The measurement of nitrite and its interfering-chemicals (paracetamol, ascorbic acid and uric acid) was performed employing a Flow-injection Analysis (FIA) system, which was automated using solenoid valves and air-pump. It is very important to quantify nitrite from river water, food and biologic fluids due to its antibacterial capacity in moderated concentrations, or its toxicity for human health even at low concentrations (> 20 μmol L−1 in blood fluids). Electrodes of the electrochemical planar sensor were defined by silk-screen technology. The measuring electrode was made from gold paste covered with 1-2 cis Diaminobenzene (DAB), which allowed good selectivity, linearity, repeatability, stability and optimized gain of sensitivity at 0.5 VAg/AgClNafion®117 (6.93 μA mol−1 L mm−2) compared to 0.3 VAg/AgClNafion®117. The reference electrode was obtained from silver/palladium paste modified with chloride and covered with Nafion® 117. The auxiliary electrode was made from platinum paste. It was noteworthy that nitrite response adds to the response of the studied interfering-chemicals and it is predominant for concentrations lower than 175 μmol L−1.

  13. The underlying electrode causes the reported 'electro-catalysis' observed at C{sub 60}-modified glassy carbon electrodes in the case of N-(4-hydroxyphenyl)ethanamide and salbutamol

    Energy Technology Data Exchange (ETDEWEB)

    Griese, Sebastian; Kampouris, Dimitrios K.; Kadara, Rashid O.; Banks, Craig E. [Faculty of Science and Engineering, School of Biology, Chemistry and Health Science, Division of Chemistry and Materials, Manchester Metropolitan University, Chester Street, Manchester M1 5GD, Lancs (United Kingdom)

    2008-08-20

    The reported 'electro-catalysis' of C{sub 60}-film-modified electrodes for the electrochemical oxidation of N-(4-hydroxyphenyl)ethanamide and salbutamol has been explored at boron-doped diamond and glassy carbon electrodes. Using both C{sub 60}-film-modified boron-doped diamond and glassy carbon as underlying electrode substrates no electro-catalytic response is observed using the target analytes but rather the C{sub 60} serves to block the electrode surface. A common experimental protocol used by researchers in this field is to electrochemically pre-treat the C{sub 60}-film-modified electrode. The response of employing this electrochemical pre-treatment at both bare glassy carbon and boron-doped diamond electrodes using the target analytes reveals that no effect on the electrochemical responses obtained at the boron-doped diamond electrode whereas a slight but significant effect occurs on glassy carbon which is attributed to the likely introduction of surface oxygenated species. Consequently the previously reported 'electro-catalysis' using C{sub 60}-film-modified electrode is not due to C{sub 60} itself being catalytic, but rather that substrate activation through electrode pre-treatment is responsible for the observed 'electro-catalysis' likely through the introduction of surface oxygenated species. This work clearly shows that substrate activation is an important parameter which researchers studying C{sub 60}-film-modified electrodes, especially in electro-analysis needs to be considered. (author)

  14. Electrochemical behavior of dye-linked L-proline dehydrogenase on glassy carbon electrodes modified by multi-walled carbon nanotubes

    Directory of Open Access Journals (Sweden)

    Haitao Zheng

    2010-12-01

    Full Text Available A glassy carbon electrode (GC was modified by multi-walled carbon nanotubes (MWCNTs. The modified electrode showed a pair of redox peaks that resulted from the oxygen-containing functional groups on the nanotube surface. A recombinant thermostable dye-linked L-proline dehydrogenase (L-proDH from hyperthermophilic archaeon (Thermococcus profundus was further immobilized by physical adsorption. The modified electrode (GC/MWCNTs/L-proDH exhibited an electrocatalytic signal for L-proline compared to bare GC, GC/L-proDH and GC/MWCNTs electrodes, which suggested that the presence of MWCNTs efficiently enhances electron transfer between the active site of enzyme and electrode surface. The immobilized L-proDH showed a typical Michaelis–Menten catalytic response with lower apparent constant.

  15. 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

  16. 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.

  17. Enzyme entrapment by β-cyclodextrin electropolymerization onto a carbon nanotubes-modified screen-printed electrode.

    Science.gov (United States)

    Alarcón-Ángeles, G; Guix, M; Silva, W C; Ramírez-Silva, M T; Palomar-Pardavé, M; Romero-Romo, M; Merkoçi, A

    2010-12-15

    A novel enzyme entrapment approach based on an electropolymerization process utilizing multi-walled carbon nanotubes (MWCNT), β-cyclodextrin (β-CD) and glucose oxidase (GOx) is shown. Dopamine (DA) quantification is presented using a screen-printed electrode modified by electropolymerization of cyclodextrin with glucose oxidase, SPE/MWCNT/β-CD-GOx. In order to show the relevance of the enzyme entrapment strategy controlled by electropolymerization to develop a specific and efficient biosensor, the various parts composing the electrode: SPE, SPE/β-CD, SPE/GOx, SPE/β-CD/GOx, SPE/MWCNT/β-CD, SPE/MWCNT/GOx and SPE/MWCNT/β-CD/GOx were tested separately. It was shown that although DA determination can be achieved with all of them, the electrodes modified with MWCNT presented better analytical features that those built without MWCNT, the best being the one including all components. This biosensor displayed good reproducibility, repeatability, and prolonged life-time under cold storage conditions. Its DA limit of detection (LOD) was 0.48±0.02 μA in a linear range of 10-50 μM with a sensitivity of 0.0302±0.0003 μA μM(-1) that makes it comparable or even better than many other electrodes reported in the literature. Moreover, it was also shown that using this electrode, DA quantification can be done in the presence of interfering agents such as ascorbic and uric acid. These findings demonstrate that the approach employed is feasible for enzyme entrapment and may find applications in other biosensing systems, where better sensitivity, stability and fast response are required. PMID:20863684

  18. Electrocatalytic oxidation behavior of L-cysteine at Pt microparticles modified nanofibrous polyaniline film electrode

    Institute of Scientific and Technical Information of China (English)

    MA Song-jiang; LUO Sheng-lian; ZHOU Hai-hui; KUANG Ya-fei; NING Xiao-hui

    2008-01-01

    Platinum(Pt)/nanofibrous polyaniline(PANI) electrode was prepared by pulse galvanostatic method and characterized by scanning electron microscopy. The electrochemical behavior of L-cysteine at the Pt/nanofibrous PANI electrode was investigated by cyclic voltammetry. The results indicate that the pH value of the solution and the Pt loading of the electrode have great effect on the electrocatalytic property of the Pt/nanofibrous PANI electrode; the suitable Pt loading of the electrode is 600 μg/cm2 and the suitable pH value of the solution is 4.5 for investigating L-cysteine oxidation. The L-cysteine sensor based on the Pt/nanofibrous PANI electrode has a good selectivity, reproducibility and stability. The Pt/nanofibrous PANI electrode is highly sensitive to L-cysteine, and the linear calibration curve for the oxidation of L-cysteine can be observed in the range of 0.2-5.0 mmol/L.

  19. Enhanced electrochemical stability of all-polymer redox supercapacitors with modified polypyrrole electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Hussain, A.M.P.; Kumar, A. [Department of Physics, Tezpur University, Napaam, Tezpur 784 028, Assam (India)

    2006-10-27

    Redox supercapacitors are attracting increasing attention as high power electrochemical sources and can either be coupled with batteries to provide peak power or replace batteries for memory back-up. In the present work, all-polymer solid-state supercapacitors with LiClO{sub 4} and LiCF{sub 3}SO{sub 3} doped polypyrrole electrodes and P(VDF-HFP)-PMMA based polymer gel electrolyte are fabricated. The polypyrrole electrodes are irradiated with 160MeV Ni{sup 12+} ions at 5x10{sup 10}, 5x10{sup 11} and 5x10{sup 12}ionscm{sup -2}. A comparative study is made between unirradiated and irradiated supercapacitors with polypyrrole-based electrodes. An average capacitance of about 200Fgm{sup -1} is obtained. On successive charging and discharging, the capacitance decreases for supercapacitors with unirradiated electrodes but remains stable when irradiated electrodes are used. In addition, the capacitance is slightly decreased compared with that for unirradiated electrodes. Charge-discharge studies show a decrease in total charge-discharge time for supercapacitors with irradiated electrodes. The capacitance values calculated from cyclic voltammograms are higher than those determined from charge-discharge plots due to the added contribution of a leakage current. The coulombic efficiency of all the supercapacitors is about 90%. (author)

  20. 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.

  1. Combined voltammetric and spectroscopic investigation of binding interaction between nifedipine and human serum albumin on polyelectrolyte modified ITO electrode

    International Nuclear Information System (INIS)

    Highlights: • The polyelectrolyte coated ITO surface was used as working electrode. • HSA was bounded onto modified electrode surface. • The interaction of nifedipine with HSA was studied. • Electrochemical and fluorescence techniques were used for characterization. -- Abstract: The binding interaction between the drug molecule, nifedipine (Nf), and the human serum albumin (HSA) on polyelectrolyte modified indium tin oxide (ITO) electrode has been investigated by the combination of electrochemical and fluorescence spectroscopy techniques. Surface modification has also been characterized by scanning electron microscopy (SEM) and Contact Angle (CA) measurements in each step. The cyclic voltammetry, electrochemical impedance parameters (peak potential difference (ΔEp)), peak current difference (ΔIp) and charge-transfer resistance (Rct) indicate that nifedipine strongly interacted with human serum albumin molecule on the polyelectrolyte modified ITO electrode surface. Stern–Volmer quenching constant Ka is inversely correlated with the temperature, which indicates that the probable quenching mechanism of the nifedipine-human serum albumin binding reaction is initiated by complex formation. The results obtained from these techniques showed that Nf could bind to HSA. The binding constant (Kb) and the number of binding sites (n) of the drug with HSA at different temperatures were determined. At 298 K, Kb was found as 4.04 × 10−3 and n was 1.08 for Nf-HSA. According to the van’t Hoff equation, the thermodynamic parameters, ΔG, ΔH and ΔS, were obtained, showing the involvement of hydrophobic and electrostatic force in this interaction

  2. Determination of iodine ions at poly(3-methylthiophene)-modified electrode by differential pulse stripping voltammetry

    International Nuclear Information System (INIS)

    A voltammetric electrode based on a poly(3-methylthiophene) (PMT) film for the differential pulse stripping voltammetric (DPSV) determination of iodide was developed. Gold electrodes were first coated with PMT and then iodide was doped into the polymer film by electrochemical oxidation of iodide at 0.75 V. The effects of various electrochemical parameters such as electrolyte type and its pH, deposition potential, deposition time, and precipitation time was examined. Using DPSV, the PMT electrode was found to be suitable for the measurement of iodide concentrations above 1x10-9 M

  3. 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

  4. Influence of specific surface area and microporosity-mesoporosity of pristine and Pt-nanoclusters modified carbide derived carbon electrodes on the oxygen electroreduction

    International Nuclear Information System (INIS)

    Highlights: • Oxygen electroreduction (ORR) strongly depends on the porosity and specific surface area of carbon catalysts. • There is an optimal ratio between the microporosity-mesoporosity and crystallographic ordering of the carbon structure. • Very high values of ORR current density were calculated for Pt-C(Mo2C)800 °C, and the half-wave potential is nearly 30-60 mV more positive compared with Pt-Vulcan®XC72 based catalyst. - Abstract: Oxygen electroreduction reaction (ORR) on pristine porous carbide derived carbons (CDCs) and on CDC supports modified with Pt-nanoclusters has been studied in 0.5 M H2SO4 solution using cyclic voltammetry, rotating disk electrode and electrochemical impedance spectroscopy methods. The CDCs were prepared from Mo2C (noted as C(Mo2C)) at different fixed chlorination temperatures from 600 °C to 1000 °C. The CDCs have tuneable specific surface area, micro- and mesoporosity, good electrical conductivity and corrosion stability at positive electrode potentials. Pt-nanoclusters were deposited onto/into C(Mo2C) powders using sodium borohydride reduction method. The X-ray diffraction and high-resolution transmission electron microscopy were applied for the structural and chemical characterization, and the nitrogen sorption method was used for the porosity analysis of the electrode materials studied. The cathodic current densities depend strongly on the synthesis temperature of C(Mo2C), indicating that, in addition to the specific surface area and porosity, the crystallinity (density of defects in amorphous areas) has noticeable influence on the ORR rate. Impedance data demonstrated nearly capacitive behaviour in the low AC frequency region, explained by quick cathodic ORR followed by slow adsorption step of the intermediates and reaction products at/inside microporous-mesoporous C(Mo2C) and Pt-C(Mo2C) electrodes

  5. Covalent attachment of thionine onto gold electrode modified with cadmium sulfide nanoparticles: Improvement of electrocatalytic and photelectrocatalytic reduction of hydrogen peroxide

    International Nuclear Information System (INIS)

    A newly developed strategy based on gold (Au) electrode modified with cadmium sulfide nanoparticles (CdSnp) and thionine (Th) was proposed toward electrocatalytic and photoelectrocatalytic hydrogen peroxide (H2O2) reduction. At first, a thin film of CdS nanoparticles was electrodeposited onto Au electrode. Then, the CdS/Au electrode was modified with mercaptoacetic acid (MAA), which not only acts as a stabilizing agent to prevent the chalcogenide CdS nanocrystals from aggregation but also as a linker for subsequent attachment of Th onto the CdS nanoparticles. The effective covalent immobilization of Th was achieved through amide bond formation reaction between -NH2 groups of Th and -COOH groups of MAA, using dicyclohexylcarbodiimide (DCC) as condensation agent. The Au/CdS/Th modified electrode showed a well-defined redox couple with surface confined characteristics at wide pH range (2–12). The heterogeneous electron transfer rate constant (ks) and the surface coverage of immobilized Th on the modified electrode was obtained as 0.12 s−1 and 4.35 × 10−9 mole cm−2, respectively. The electrocatalytic activity and stability of the modified electrode toward hydrogen peroxide reduction was investigated and it was found that the Au/CdS/Th electrode illustrates excellent electrocatalytic activity toward H2O2 reduction at reduced overpotential. The detection limit, sensitivity and catalytic rate constant (kcat) of the modified electrode toward H2O2 were 55 nM, 3.4 μA μM−1 cm−2 and 3.75 (±0.1) × 103 M−1 s−1, respectively, at linear concentration range up to 10 mM. Upon light irradiation, about two-fold improvements were attained in sensitivity and detection limit of the modified electrode toward H2O2 electrocatalytic determination

  6. Fabrication of ZnO Nanorod Modified Electrode and Its Application to the Direct Electrochemical Determination of Hemoglobin and Cytochrome c

    Institute of Scientific and Technical Information of China (English)

    张成林; 刘梅川; 李平; 鲜跃仲; 程欲晓; 张芬芬; 王晓丽; 金利通

    2005-01-01

    A novel electrochemical method as a sensitive and convenient technique for the determination of heme proteins based on their interaction with ZnO nanorods was developed. A ZnO nanorod modified glassy carbon electrode (ZnO/GCE) was prepared and the electrochemical behaviors of heme proteins, such as hemoglobin (HB) and cytochrome c (Cyt-c), on this modified electrode have been studied. The results showed that both HB and Cyt-c could be oxidized on the modified electrode and the oxidation currents were linear to the concentrations of the analytes in aqueous solutions. In addition, the results of flow injection analysis (FIA) further suggested the high stability and reproducibility of the ZnO nanorod modified electrode. So this method can be applied to the determination of HB and Cyt-c in biological systems.

  7. 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...

  8. Electroenzymatic Reactions With Oxygen on Laccase-Modified Electrodes in Anhydrous (Pure) Organic Solvent

    DEFF Research Database (Denmark)

    Yarapolov, A.; Shleev, S.; Zaitseva, E.;

    2007-01-01

    The electroenzymatic reactions of Trametes hirsuta laccase in the pure organic solvent dimethyl sulfoxide (DMSO) have been investigated within the framework for potential use as a catalytic reaction scheme for oxygen reduction. The bioelectrochemical characteristics of laccase were investigated in...... glassy carbon and graphite electrodes with adsorbed laccase. The influence of the time for drying the laccase solution at the electrode surface on the electroreduction of oxygen was studied. Investigating the electroenzymatic oxidation reaction of catechol and hydroquinone in DMSO reveals the formation...

  9. Direct Electrochemistry of Cytochrome bo Oxidase at a series of Gold Nanoparticles-Modified Electrodes.

    Science.gov (United States)

    Melin, Frederic; Meyer, Thomas; Lankiang, Styven; Choi, Sylvia K; Gennis, Robert B; Blanck, Christian; Schmutz, Marc; Hellwig, Petra

    2013-01-01

    New membrane-protein based electrodes were prepared incorporating cytochrome bo(3) from E. coli and gold nanoparticles. Direct electron transfer between the electrode and the immobilized enzymes was achieved, resulting in an electrocatalytic activity in presence of O(2). The size of the gold nanoparticles was shown to be important and smaller particles were shown to reduce the overpotential of the process. PMID:23335854

  10. 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...

  11. 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 ...

  12. A novel non-enzymatic hydrogen peroxide sensor based on single walled carbon nanotubes-manganese complex modified glassy carbon electrode

    Energy Technology Data Exchange (ETDEWEB)

    Salimi, Abdollah, E-mail: absalimi@uok.ac.i [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Research Center for Nanotechnology, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Mahdioun, Monierosadat; Noorbakhsh, Abdollah [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Abdolmaleki, Amir [Department of Chemistry, Isfahan University of Technology, Isfahan, 84156/83111 (Iran, Islamic Republic of); Ghavami, Raoof [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of)

    2011-03-30

    A simple procedure was developed to prepare a glassy carbon (GC) electrode modified with single wall carbon nanotubes (SWCNTs) and phenazine derivative of Mn-complex. With immersing the GC/CNTs modified electrode into Mn-complex solution for a short period of time 20-100 s, a stable thin layer of the complex was immobilized onto electrode surface. Modified electrode showed a well defined redox couples at wide pH range (1-12). The surface coverages and heterogeneous electron transfer rate constants (k{sub s}) of immobilized Mn-complex were approximately 1.58 x 10{sup -10} mole cm{sup -2} and 48.84 s{sup -1}. The modified electrode showed excellent electrocatalytic activity toward H{sub 2}O{sub 2} reduction. Detection limit, sensitivity, linear concentration range and k{sub cat} for H{sub 2}O{sub 2} were, 0.2 {mu}M and 692 nA {mu}M{sup -1} cm{sup -2}, 1 {mu}M to 1.5 mM and 7.96({+-}0.2) x 10{sup 3} M{sup -1} s{sup -1}, respectively. Compared to other modified electrodes, this electrode has many advantageous such as remarkable catalytic activity, good reproducibility, simple preparation procedure and long term stability.

  13. Electrooxidation of morin on glassy carbon electrode modified by carboxylated single-walled carbon nanotubes and surfactants

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Carboxylated SWNT/GCE modified with surfactants are tested for morin determination. • The best electrocatalytic effect observed for Cetylpyridinium bromide/SWNT-COOH/GCE. • Adsorption-controlled irreversible two electron oxidation of morin is confirmed. • Sensitive differential pulse voltammetric quantification of morin is developed. • Limits of detection and quantification are 28.9 and 96 nM, respectively. - Abstract: Voltammetric characteristics of morin on glassy carbon electrode (GCE) modified by carboxylated single-walled carbon nanotubes (SWNT-COOH) and surfactants in phosphate buffer have been found. Cationic cetylpyridium bromide (CPB), nonionic Triton X100 and anionic sodium dodecylsulfate surfactants under different concentrations have been tested as modifier of SWNT-COOH/GCE. The form of CVs and oxidation potentials are not changed significantly in the presence of all type surfactants on the electrode surface that confirms negligible influence of surfactant on electron transfer rate. Morin oxidation currents are increased on surfactant-modified electrodes. The best characteristics are observed on CPB (1 μM)/SWNT-COOH/GCE when 1.8-fold increase of oxidation currents has been observed in comparison with SWNT-COOH/GCE. Mechanism of morin oxidation on CPB/SWNT-COOH/GCE is suggested on the basis of relationship between oxidation potential and pH of supporting electrolyte. Electrooxidation is adsorption-controlled irreversible two-step process with participation of one electron and one proton on each step. The linear dynamic ranges of morin determination under conditions of differential pulse voltammetry are 0.1-100 and 100-750 μM with the limits of detection and quantification 28.9 and 96.0 nM of morin, respectively. The developed approach applied for morin quantification in mulberry leaves using preliminary extraction with ethanol

  14. Determination of 4-aminophenol using a glassy carbon electrode modified with a three-dimensionally ordered macroporous film of polycysteine

    International Nuclear Information System (INIS)

    A three-dimensionally ordered macroporous (3DOM) film of polycysteine (poly-Cys) was used to modify a glassy carbon electrode (GCE) to result in a sensor for 4-aminophenol. The new electrode was used to study the behavior of 4-aminophenol by cyclic voltammetry and differential pulse voltammetry. In comparison to a bare GCE and a GCE modified with poly-Cys without using template, this electrode displays a larger peak current which may be attributed to the structure of poly-Cys and the large surface area of the macroporous structure. The anodic peak current at a working voltage of 195 mV is linearly related to the concentration of 4-aminophenol in two concentration intervals: 0.02 to 20 μM and 20 to 200 μM, respectively. The detection limit is 8 nM (at an S/N ratio of 3). The method was successfully applied to the determination of 4-aminophenol in spiked water samples. (author)

  15. Electrocatalytic sensing of hydrogen peroxide using a screen printed carbon electrode modified with nitrogen-doped graphene nanoribbons

    International Nuclear Information System (INIS)

    We have synthesized nitrogen-doped graphene nanoribbons (N-GrNRs) by unzipping multi-walled carbon nanotubes (CNTs) under strongly oxidizing conditions and subsequent doping with nitrogen by a low-temperature hydrothermal method. The N-GNRs were characterized by transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy and Raman spectroscopy, and assembled on a disposable screen-printed carbon electrode to give a sensor for H2O2 that was characterized by cyclic voltammetry, electrochemical impedance spectroscopy, chronocoulometry and chronoamperometry. The nano-modified electrode displays enhanced electron transfer ability, and has a large active surface and a large number of catalytically active sites that originate from the presence of nitrogen atoms. This results in a catalytic activity towards H2O2 reduction at near-neutral pH values that is distinctly improved compared to electrodes modified with CNTs or unzipped (non-doped) CNTs only. At a working potential of −0.4 V (vs. Ag/AgCl), the amperometric responses to H2O2 cover the 5 to 2785 μM concentration range, with a limit of detection as low as 1.72 μM. This enzyme-free electrochemical sensor exhibits outstanding selectivity and long-term stability for H2O2 detection. (author)

  16. Amperometric sensing of anti-HIV drug zidovudine on Ag nanofilm-multiwalled carbon nanotubes modified glassy carbon electrode

    Energy Technology Data Exchange (ETDEWEB)

    Rafati, Amir Abbas, E-mail: aa_rafati@basu.ac.ir; Afraz, Ahmadreza

    2014-06-01

    The zidovudine (ZDV) is the first drug approved for the treatment of HIV virus infection. The detection and determination of this drug are very importance in human serum because of its undesirable effects. A new ZDV sensor was fabricated on the basis of nanocomposite of silver nanofilm (Ag-NF) and multiwalled carbon nanotubes (MWCNTs) immobilized on glassy carbon electrode (GCE). The modified electrodes were characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), cyclic voltammetry (CV), and linear sweep voltammetry (LSV) techniques. Results showed that the electrodeposited silver has a nanofilm structure and further electrochemical studies showed that the prepared nanocomposite has high electrocatalytic activity and is appropriate for using in sensors. The amperometric technique under optimal conditions is used for the determination of ZDV ranging from 0.1 to 400 ppm (0.37 μM–1.5 mM) with a low detection limit of 0.04 ppm (0.15 μM) (S/N = 3) and good sensitivity. The prepared sensor possessed accurate and rapid response to ZDV and shows an average recovery of 98.6% in real samples. - Highlights: • New anti-HIV drug sensor was fabricated on the basis of nanomaterials composite. • The GCE modified by prepared hydrophilic MWCNT silver nanoparticles. • Silver nanofilm electrodeposited on MWCNT/GCE and characterized by SEM, EDX, CV and LSV • Response of electrode to ZDV was thoroughly investigated by electrochemical techniques.

  17. A Metal Matrix CNTS Modified Electrode Fabricated Using Micromachining-Based Implantation Method for Improving Sensitivity and Stability

    Directory of Open Access Journals (Sweden)

    Yan Wang

    2013-01-01

    Full Text Available The metal matrix carbon nanotubes modified electrode (MCME has been fabricated by a novel process involving preparation of carbon nanotubes (CNTs/polyimide (PI composite film, wet, etching, sputtering, electroplating, and wet-etch releasing. Pretreated CNTs are dispersed in PI by mechanical ball milling and then CNTs solution is spin-coated on the substrate. The CNTs/PI composite film is etched away a layer of PI to expose tips of CNTs using buffering solution. These exposed tips of CNTs are covered by metal particles in sputtering process as metal seed layer, followed by metal supporting film formed by electroplating. The MCME is obtained after releasing PI film from the metal supporting film. The MCME shows well morphology of uniform distributional protruding tips of CNTs and increased electron transfer efficiency with strong bonding connection between CNTs and metal matrix, which greatly improves sensitivity and stability of the MCME. The oxidation peak of the MCME in cyclic voltammeter (CV test is 1.7 times more than that of CNTs suspension spin-coated metal electrode (SCME. The decline of peak current of the MCME after fifty cycles is only 1.8% much less than 67% of the SCME. Better sensitivity and stability may be helpful for CNTs modified electrodes wide application for trace test of many special materials.

  18. An amperometric sensor for nitric oxide based on a glassy carbon electrode modified with graphene, Nafion, and electrodeposited gold nanoparticles

    International Nuclear Information System (INIS)

    This article describes the fabrication of a glassy carbon electrode (GCE) modified with a film containing graphene and gold nanoparticles (AuNPs) that can be used for the determination of nitric oxide (NO) at pH 7.0. A layer of gold nanoparticles was first deposited on the GCE, this followed by coating it with a film of graphene and Nafion. The response of the electrode to NO was studied by cyclic voltammetry and amperometry. A sharp anodic peak was observed at 0.81 V, and the anodic peak current was largely increased compared to a bare GCE or a mono-film modified GCE. A negative shift of the anodic peak potential (by 220 mV) indicates that the composite film has a beneficial effect on ease of the electrochemical oxidation of NO. The electron transfer number was calculated from chronocoulometric data. The amperometric response to NO is linear in the 36 nM to 20 μM concentration range (with a correlation coefficient of 0.9981), and the detection limit is 18 nM (at a S/N of 3). The release of NO from the fish liver homogenate stimulated by L-arginine was studied with this electrode. (author)

  19. Amperometric sensing of anti-HIV drug zidovudine on Ag nanofilm-multiwalled carbon nanotubes modified glassy carbon electrode

    International Nuclear Information System (INIS)

    The zidovudine (ZDV) is the first drug approved for the treatment of HIV virus infection. The detection and determination of this drug are very importance in human serum because of its undesirable effects. A new ZDV sensor was fabricated on the basis of nanocomposite of silver nanofilm (Ag-NF) and multiwalled carbon nanotubes (MWCNTs) immobilized on glassy carbon electrode (GCE). The modified electrodes were characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), cyclic voltammetry (CV), and linear sweep voltammetry (LSV) techniques. Results showed that the electrodeposited silver has a nanofilm structure and further electrochemical studies showed that the prepared nanocomposite has high electrocatalytic activity and is appropriate for using in sensors. The amperometric technique under optimal conditions is used for the determination of ZDV ranging from 0.1 to 400 ppm (0.37 μM–1.5 mM) with a low detection limit of 0.04 ppm (0.15 μM) (S/N = 3) and good sensitivity. The prepared sensor possessed accurate and rapid response to ZDV and shows an average recovery of 98.6% in real samples. - Highlights: • New anti-HIV drug sensor was fabricated on the basis of nanomaterials composite. • The GCE modified by prepared hydrophilic MWCNT silver nanoparticles. • Silver nanofilm electrodeposited on MWCNT/GCE and characterized by SEM, EDX, CV and LSV • Response of electrode to ZDV was thoroughly investigated by electrochemical techniques

  20. Electrochemical Characterization and Determination of Phenol and Chlorophenols by Voltammetry at Single Wall Carbon Nanotube/Poly(3,4-ethylenedioxythiophene) Modified Screen Printed Carbon Electrode

    OpenAIRE

    Negash, Negussie; Alemu, Hailemichael; Tessema, Merid

    2015-01-01

    Screen printed carbon electrode (SPCE) has been modified with single wall carbon nanotube/poly(3,4-ethylenedioxythiophene) (SWCNT/PEDOT) composites for the determination of phenol and chlorophenols (phenol, 4-chlorophenol, 2,4-dichlorophenol, and 2,4,6-trichlorophenol). The effect of the modifiers on the electrode characteristics was evaluated and the responses were optimized for the voltammetric determination of phenol and chlorophenols. The parameters affecting the responses such as pH, sca...