共查询到20条相似文献,搜索用时 11 毫秒
1.
抗坏血酸在普鲁士蓝修饰的丝网印刷电极上的电催化氧化 总被引:2,自引:0,他引:2
制备了普鲁士蓝修饰的丝网印刷电极,研究了该修饰电极对抗坏血酸的催化氧化作用。在pH5.0的0.2mol/L磷酸盐缓冲溶液中,修饰电极对抗坏血酸显示出快速的电化学响应,较高的稳定性、重现性和催化活性,测定的线性范围为5.0×10-6~8.0×10-3mol/L,相关系数为0.998,检出限为3.0×10-6mol/L(3σ)。已对实际样品进行了测定。 相似文献
2.
壳聚糖修饰电极上的铁氰根离子对抗坏血酸的电催化氧化作用 总被引:4,自引:0,他引:4
在玻碳电极表面滴涂一层壳聚糖膜 ,壳聚糖分子中 -NH2 在酸性溶液中发生质子化 ,靠静电引力作用吸附富集荷负电的电子介体Fe(CN) 63 -,使其固定在电极表面 ,研究了此Fe(CN) 63 - 壳聚糖 GC修饰电极对抗坏血酸的催化氧化作用。抗坏血酸的浓度在 3.0× 1 0 -6~ 5 .0× 1 0 -3 mol L范围内呈很好的线性关系 ,相关系数为 0 .998,检测限达 1 .0× 1 0 -6mol L。该法已用于测定蔬菜中抗坏血酸的含量。 相似文献
3.
溶胶-凝胶-钴-邻菲啰啉修饰电极对一氧化氮的电催化氧化及其测定 总被引:3,自引:0,他引:3
报道了溶胶 凝胶 钴 邻菲口罗啉膜修饰电极的制备方法及其在一氧化氮(NO)检测中的应用,采用循环伏安法(CV)研究修饰电极的电化学特性,差示脉冲伏安法(DPV)对NO进行检测。该修饰电极对NO的电化学氧化具有很好的催化作用,使其氧化电位负移了210mV,氧化峰电流与NO浓度在5.6×10-8~2.8×10-5mol/L范围内呈良好的线性关系,相关系数r=0.999,检测限为1.4×10-8mol/L,且生物体内常见的干扰物质如抗坏血酸、NO2-和儿茶酚胺类神经递质的代谢物等不干扰测定。 相似文献
4.
Electrocatalytic oxidation of NADH at glassy carbon electrodes modified with an electropolymerized film of nile blue A 总被引:1,自引:0,他引:1
The kinetic parameters for the electrocatalytic oxidation of di-hydronicotiamide adenine dinucleotide (NADH) at glassy carbon electrodes modified with an electropolymerized film of nile blue A (PNB) have been determined based on rotating disk electrode measurements. The rate constant for the chemical reaction between NADH and PNB is strongly influenced by NADH concentration and the pH value of solution, and it decreases with increasing NADH concentration, indicating that the electrocatalytic process proceeds via the formation of an intermediate of charge-transfer complex between NADH and PNB. 相似文献
5.
L. G. Shaidarova A. V. Gedmina I. A. Chelnokova G. K. Budnikov 《Russian Journal of Applied Chemistry》2004,77(12):1951-1957
The electrochemical behavior of methanol on graphite electrodes modified with a coating composed of (III) hexacyanoferrate and ruthenium(III) hexacyanoferrate(II) and hexacyanoruthenate(II) was studied. A method for electrochemical determination of ethanol on a carbon-paste electrode modified with a coating composed of ruthenium(III) hexacyanoruthenate(II) under stationary and flow-injection conditions was suggested.Translated from Zhurnal Prikladnoi Khimii, Vol. 77, No. 12, 2004, pp. 1974–1979.Original Russian Text Copyright © 2004 by Shaidarova, Gedmina, Chelnokova, Budnikov. 相似文献
6.
Electrocatalytic oxidation of hydrazine at cobalt hexacyanoferrate- modified glassy carbon, Pt and Au electrodes 总被引:1,自引:0,他引:1
The electrocatalytic oxidation of hydrazine has been studied on glassy carbon, Pt and Au electrodes modified by cobalt hexacyanoferrate
(CoHCF) using cyclic voltammetry and rotating disc techniques. It has been shown that the oxidation of hydrazine to nitrogen
occurs at the potential coinciding with that of Co(II) to Co(III) transformation in a CoHCF film, where no oxidation signal
is observed at a bare glassy carbon electrode. A Tafel plot, derived from RDE voltammograms, exhibits a slope of 150 mV, indicating
a one-electron charge transfer process to be the rate-limiting step. The electrocatalytic efficiency of the modified electrode
towards hydrazine oxidation depends on solution pH, and the optimum range was found to be located between pH 5 and pH 7. The
kinetic behaviour and location of the electrocatalytic process were examined using the W.J. Albery diagnosis table, and it
was concluded that the reaction has either a “surface” or a “layer” reaction mechanism. Pt- and Au-CoHCF-modified electrodes
show no significant electrocatalytic activity towards hydrazine oxidation.
Received: 25 April 1997 / Accepted: 12 August 1997 相似文献
7.
Ahmed Galal 《Journal of Solid State Electrochemistry》1998,2(1):7-15
Conducting poly(3-methylthiophene) electrodes were electrochemically prepared. The resulting polymer films were modified
with an inorganic complex, ferrocene. The incorporation of the ferrocene/ferrocenium moiety into the polymer film resulted
in enhanced charge transfer towards the oxidation of some organic molecules of biological interest. The electrochemical response
of the complex-containing polymer electrode was compared to that of the unmodified polymer electrode and that of the substrate.
Apparent diffusion coefficients of the redox species were estimated from the cyclic voltammetric data for different biological
molecules at the ferrocene-containing polymer electrode. Infra-red spectroscopic measurements for the “as-grown” films revealed
the presence of the inorganic complex within the polymer. The modified polymer electrode showed noticeable enhancement for
the charge transfer across the film interface and can be used as an electrochemical sensor for biological compounds.
Received: 3 June 1997 / Accepted: 7 July 1997 相似文献
8.
Lo Gorton Arne Torstensson Hans Jaegfeldt Gillis Johansson 《Journal of Electroanalytical Chemistry》1984,161(1):103-120
Meldola Blue (7-dimethylamino-1,2-benzophenoxazine) can be adsorbed on graphite to give chemically modified electrodes. The electrochemical redox reactions of the phenoxazine are fairly reversible at low coverages with an E′o of ?175 mV vs. SCE at pH 7.0. The electrode was most stable in acid solutions, at pH 6.0 its electrochemical activity decreased by 15% during 2h. The adsorbed compound mediated electron transfer in the electrocatalytic oxidation of the nicotinamide coenzymes (NADH and NADPH). The formation of a charge transfer complex between Meldola Blue and the coenzyme is demonstrated by experiments with a rotating disk electrode. The complex decomposes in a rate limiting step (k+2=30 s?1) to the oxidized coenzyme and the reduced Meldola Blue. The latter can be reoxidized in a fast electrochemical step. The overall result is an electrocatalytic oxidation at a voltage which is about 500 mV lower than at an unmodified electrode. 相似文献
9.
Mohammad Mazloum Ardakani Payam Ebrahimi Karami Hamid Reza Zare Mohammad Hamzehloo 《Mikrochimica acta》2007,159(1-2):165-173
The preparation and electrochemical characterization of glassy carbon electrodes modified with plumbagin were investigated
by employing cyclic voltammetry, chronoamperometry and rotating disc electrode techniques. The cyclic voltammograms of the
electroreduction of oxygen showed an enhanced current peak at approximately −0.289 V in air-saturated phosphate buffer pH
= 7 and scan rate 10 mV s−1. The thermodynamic and kinetic parameters of the reduction of oxygen at glassy carbon have been evaluated using cyclic voltammetry.
The experimental parameters were optimized and the mechanism of the catalytic process was discussed. The obtained values of
E°′ (V vs. Ag/AgCl), the apparent electron transfer rate constant ks (s−1), heterogeneous rate constant for the reduction of O2 at the surface of the modified electrode kh (M−1 s−1) and α (charge transfer coefficient of oxygen) were as follows: −0.146, 23.4, 9.9 × 103 and 0.57, respectively. In addition, plumbagin exhibited strong catalytic activity toward the reduction of H2O2. 相似文献
10.
<正>The electrocatalytic oxidation of methanol at the platinum electrode modified with Eu-Fe cyanide-bridged binuclear complexes (Eu-Fe film) was investigated for the first time by cyclic voltammetry.Compared with the bare platinum electrode,the results showed that the modified electrode had excellent electrocatalytic activity for the oxidation of methanol;the oxidation peak potential shifted more negatively and the peak current increased about twenty times.The electrooxidation of methanol at the modified electrode with Eu-Fe cyanide-bridged binuclear complexes material exhibited the better tolerance capacity to poison of intermediate species;the peak current was proportional to the concentration of methanol in the range of 0.5-2.0mol/L (R~2 = 0.9991,n =7),which was a comparatively wider linear range.Moreover,based on the linear relationship between the peak current and the square root of scan rate,electrocatalytic oxidation process of methanol was confirmed to be a diffusion control process.Furthermore,according to the counting of electron transfer number(n_α) in the rate-limiting step and the slope of linear equation between acidity of electrolyte and the oxidation peak potential(E_p),the possible mechanism of the electrooxidation of methanol at the modified electrode was primarily discussed. 相似文献
11.
Carmen Ioana Ladiu Ionel Catalin Popescu Lo Gorton 《Journal of Solid State Electrochemistry》2005,9(5):296-303
The basic electrochemistry of carbon paste electrodes modified with Meldola Blue adsorbed on zirconium phosphate (MB-ZP-CPEs) and their ability to oxidize NADH have been investigated. Three types of carbon powder (graphite and glassy carbon-type Sigradur K and G) were used to obtain MB-ZP-CPEs. On comparing cyclic voltammograms recorded at MB-ZP-CPEs, similarly prepared from the three different carbon powders, those made with Sigradur K exhibited the lowest background current, and the best MB electrochemistry, seen as the highest peak intensities and smallest peak separation. Using MB-ZP-CPEs based on Sigradur K a study on NADH oxidation was done focusing on the effect of the Ca2+ concentration in the contacting solution and on the addition of polyethyleneimine (PEI) into the paste. It can be stated that MB-ZP-CPEs based on Sigradur K and containing 1.23% (w/w) PEI exhibited the best behavior for NADH oxidation, measured by the highest electrocatalytic rate constant (8.2×103 M–1 s–1). 相似文献
12.
《Journal of Electroanalytical Chemistry》1986,199(1):153-164
Stable (polynaphthoquinone)-coated Pt, Au and graphite electrodes are prepared by electropolymerization. Stable poly(naphthoquinone)-coated Pt, Au and graphite electrodes are prepared by electropolymerization. These modified electrodes catalyse oxygen reduction. Rotating-disk studies in the case of modified Pt electrodes show that the rate-limiting factors are the substrate diffusion in the film and the cross-exchange reaction. 相似文献
13.
《中国化学快报》2019,30(9):1643-1646
A highly selective and sensitive electrochemical method was developed for the detection of serotonin (5-hydroxytryptamine, 5-HT) at gold nanoflowers (Au NFs) and overoxidized polypyrrole (OPPy) modified carbon fiber microelectrode (CFME). Carbon fiber was firstly modified with gold nanoflowers using electroless deposition method, and then modified with overoxidized polypyrrole using electrochemical polymerization and overoxidization to obtain OPPy/Au NFs/CFME. The obtained OPPy/Au NFs/CFME was characterized by field emission scanning electron microscopy and electrochemical techniques. It was found that the OPPy/Au NFs/CFME showed good sensitivity for the detection of 5-HT in the range of 10 nmol/L − 7.0 μmol/L with detection limit of 2.3 nmol/L, and negligible interferences from ascorbic acid, 5-hydroxyindole acetic acid and uric acid. The OPPy/Au NFs/CFME was successfully applied to the detection of 5-HT in human serum samples with good recovery. The work demonstrates that the electrochemical method, incorporating signal amplification of Au NFs with higher cation selection of OPPy, provides a promising tool for the detection of 5-HT in biological systems 相似文献
14.
A gold nanoflowers and overoxidized polypyrrole modified carbon fiber microelectrode (OPPy/Au NFs/CFME) was fabricated using electroless deposition and electrochemical method for highly selective and sensitive detection of 5-HT. 相似文献
15.
The electrocatalytic activities of a series of compact graphites modified with microquantities of platinum metals (Pd or Pt+Pd)
towards the electrochemical reduction of hydrogen peroxide were characterised. Operational parameters such as the optimal
working potential, the influence of temperature and the resulting electrode characteristics were examined. The benefits of
using graphite modified with Pt+Pd (mixture ratio 30%:70%) as the basic transducer in a glucose biosensor with improved sensitivity
were demonstrated. It was proven that, under the working conditions chosen, the selected electrode (whether bare or covered
with an enzyme layer) did not respond to any glutathione, uric acid or ascorbic acid (which all normally occur in biological
fluids) present. 相似文献
16.
化学修饰电极的研究 XIII.聚乙烯二茂铁薄膜电极对抗坏血酸的电催化氧化 总被引:1,自引:0,他引:1
本文表明用旋转涂层法制备的聚乙烯二茂铁(PVFc)薄膜电极在水溶液和乙腈中, 0.3~1.0V(vs.SCE)电位范围内均可呈现二茂铁(Fe)的氧化还原峰. PVFc薄膜电极对水溶液中的抗坏血酸(AH2)在较宽的pH范围和较宽的浓度范围内均有良好的电催化氧化作用,为EC平行催化过程。利用旋转圆盘电极进行了催化过程动力学分析,求出了催化反应动力学参数.PVFc薄膜电极的稳定性和催化稳定性都较好.在AH~2浓度6x10^-^2~6x10^-^6mol/L范围内,催化峰电流与AH~2浓度呈良好的线性关系,有应用于分析AH~2的意义。 相似文献
17.
T. I. Abdullin I. I. Nikitina O. V. Bondar’ 《Russian Journal of Electrochemistry》2008,44(12):1345-1349
The electrochemical behavior of nitrogen bases and their derivatives is studied on electrodes modified with carbon nanotubes. On these electrodes, the strong adsorption of purines and their oxidation is observed at potentials in the vicinity of +0.8 V for guanine and +1.0 V (vs. Ag/AgCl) for guanine nucleosides/nucleotides and adenine. At more positive potentials, the high background current prevents the detection of adenine nucleotides and pyrimidines. The peculiarities of oxidation of the most easily detectable DNA components, namely, guanine and deoxyguanosinemonophosphate, on modified electrodes are elucidated and the corresponding reaction scheme is proposed. The results can be used in the development of biosensors based on electroactive properties of nucleic acids and their components. 相似文献
18.
Electrocatalytic Properties of a Gold Nanoseed Particle‐modified Indium Tin Oxide Electrode: Comparison of the Shape and Preparation Methods
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Md. Abdul Aziz Manzar Sohail M. Nasiruzzaman Shaikh Munetaka Oyama 《Electroanalysis》2016,28(5):1119-1125
Gold nanostructures are the most commonly used nanostructures for fabricating electrochemical sensors and biosensors. In this study, we compared the catalytic performances of three types of gold nanoseed particles having two different morphologies, upon attachment to an amino‐functionalized ITO electrode surface. The ITO electrode surface was modified with 3‐aminopropyltrimethoxysilane (APTMS) and (1) gold nanoseed spheres (AuNSS), prepared using the ion capture and successive reduction method (ICR), (2) commercially available 5 nm AuNSS, and (3) a newly synthesized gold nanoseed wire (AuNSW). The electrocatalytic properties of the three electrodes were evaluated. Among the three electrodes, the AuNSW/APTMS/ITO was found to be the electrode of choice and exhibited excellent electrocatalytic properties toward the biologically important analytes glucose, uric acid, and serotonin. 相似文献
19.
本文用浓硝酸活化多层碳纳米管,将壳聚糖与活化后的碳纳米管制备成复合材料,并将其滴涂于玻碳电极表面,制备出烟酰胺腺嘌呤二核苷酸(NADH)的电化学传感器。采用循环伏安法研究了该传感器的电化学性质以及对NADH的电催化氧化行为。实验结果表明,NADH在该电极上于 0.37V(vs.SCE)左右出现一氧化峰,与未修饰的玻碳电极相比,该修饰电极明显降低了NADH的氧化峰电位,消除了反应中间产物对电极表面的污染问题。对实验条件进行了优化,建立了碳纳米管/壳聚糖修饰电极微分脉冲伏安法测定NADH的方法。本文方法具有较好的重现性和选择性,对NADH检测的线性范围为1.0×10-4~9.0×10-3mol/L,检测限为9.2×10-5mol/L。 相似文献
20.
A polyglycine chemically modified electrode shows substantial catalytic ability towards dopamine (DA). The calibration graph obtained by linear sweep voltammetry for DA is linear in the range 2.0 × 10–8~ 4.4 × 10–6 mol/L and the detection limit is ca. 5.0 × 10–9 mol/L. The catalytic ability towards DA results in the voltammetric resolution of DA and uric acid (UA) in the same solution, which is impossible at the unmodified electrode. Uric acid in less than 120-fold excess does not interfere with the determination of DA. 相似文献