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21.
Ruojun Lao Lihua Wang Ying Wan Jiong Zhang Shiping Song Zhizhou Zhang Chunhai Fan Lin He 《International journal of molecular sciences》2007,8(2):136-144
In this work, we reported the investigation on the interaction between DNA strands self-assembled at gold electrodes and an electron transfer protein, cytochrome c. We observed that cytochrome c exhibited well-defined electrochemistry in both double-stranded and single-stranded DNA films. This suggested that the electron transfer reaction of cytochrome c arose possibly due to the electron hopping along DNA strands rather than wiring along the double helix. We also compared the heterogeneous electron transfer rate of cytochrome c with that of a ruthenium complex, which further confirmed this mechanism. 相似文献
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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. 相似文献
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In this paper we report a kinetic study of the electro-oxidation of hydrazine catalyzed by vitamin B12 pre-adsorbed on an ordinary pyrolytic graphite electrode. Kinetic parameters were determined by linear sweep voltammetry and rotating-disk electrode polarization curves. The order of the reaction is 1 in OH− ions and Tafel plots give slopes of 80 mV/decade. A possible redox-catalysis mechanistic scheme is proposed. 相似文献
27.
A novel perforated bipole trickle-bed electrochemical reactor is investigated for the electro-synthesis of alkaline peroxide.
The process uses a relatively simple cell configuration in which a single electrolyte flows with oxygen gas in a flow-by graphite
felt cathode, sandwiched between a micro-porous diaphragm and a perforated bipolar electrode plate. The graphite felt cathodes
are 120 mm high by 25 mm wide and have a thickness of 3.2 mm. The reactor is operated at current densities in the range 1–5 kA m−2, ca. 800 kPa (abs) pressure and temperature (In/Out) 20–45 °C with one and two-cells. The reactor shows good performance
(current efficiency ∼78% at 2 kA m−2 and a specific energy of 5 kWh per kg of peroxide generated) with peroxide concentrations from 0.02 to 0.15 M in 1 M NaOH. 相似文献
28.
Yuehua Wen Jie Cheng Gaoping Cao Yusheng Yang 《Journal of Applied Electrochemistry》2007,37(5):543-548
For double-layer capacitors in alkaline electrolyte, the specific capacitance of the positive electrode is not equal to that
of the negative one. Thus, capacitor performance cannot be optimal with a positive/negative electrode matching ratio of 1.
In this study nanoporous glassy carbons (NPGCs) were employed as the electrodes of capacitors, and the influence of matching
ratio between positive and negative electrode on capacitor performance was systematically investigated. In aqueous KOH, the
specific capacitance of the positive electrode is lower than that of the negative electrode. The matching ratio at which a
maximum capacitance is obtained is dependent on the values of the positive and negative electrode capacitance. At low current
rate, the highest specific capacitance is achieved at a matching ratio slightly higher than 1. At high current rate, a capacitor
has the highest specific capacitance with the lowest resistance at a matching ratio of 1.5. This indicates that an optimum
matching relationship between positive and negative electrodes is attained. 相似文献
29.
Oxidation and reduction processes on coal- and mineral-pyrite surfaces have been investigated to better understand the reactions that control the hydrophobicity and flotation behavior of pyrite. The incipient oxidation and reduction reactions were studied using fresh surfaces of pyrite that were created by in situ fracturing electrodes potentiostated at a predetermined potential. Chronoamperometry immediately after fracture and subsequent cyclic voltammetry have established that fresh fracture surfaces of pyrite instantaneously assume a unique potential (referred to as the “stable” potential) at which neither oxidation nor reduction takes place. For Peruvian and Chinese pyrites, the stable potential is −0.28 V (standard hydrogen electrode, SHE) at pH 9.2 and 0 V at pH 4.6. The initial oxidation of pyrite begins at potentials slightly positive of the stable potential and is believed to produce a hydrophobic sulfur-rich species, most likely a polysulfide or metal-deficient sulfide. A rotating ring-disc electrode (RRDE) was employed to study the kinetics and mechanisms of surface reactions on pyrite over moderate potential ranges. Two distinct soluble reduction products (ferrous hydroxide and HS−) and one distinct soluble oxidation product (ferrous hydroxide) were observed on pyrite in alkaline solutions. It is concluded that the initial oxidation of pyrite and the oxidation of ferrous to ferric hydroxide occur in a similar potential range. When the electrode is oxidized, e.g. by polishing, prior to experiments, the initial oxidation of pyrite is masked by the oxidation of ferrous hydroxide, making it difficult to study the oxidation of pyrite itself. 相似文献
30.
The influence of electrode potential on pentachlorophenol (PCP) oxidation on boron doped diamond (BDD) electrodes in a 0.1 mol L–1 Britton–Robinson buffer (pH 5.5) is described. Controlled potential electrolyses were carried at 0.9, 2.0 and 3.0 V vs Ag/AgCl and the solutions analysed by square wave voltammetry, high performance liquid chromatography, chloride ion selective electrode and spectroscopy in the ultraviolet–visible region. At low positive potential (0.9 V), the formation of an adherent film on the electrode surface involving the transference of 1 electron per PCP molecule was observed. The film was identified as the dimer 2,3,4,5,6-pentachloro-4-pentachlorophenoxy-2,5-cyclohexadienone and the current efficiency was as high as 90%. At potentials close to the onset of O2 evolution (2.0 V), the formation of the corresponding quinone (p-tetrachlorobenzoquinone) was detected at the beginning of the process. This was followed by further oxidation to the hydroxy-benzoquinone with a practically quantitative yield. Electrolyses carried out well into the region of oxygen evolution (3.0 V) lead to the electrochemical combustion of PCP to CO2 and H2O as well as to the release into solution of 5 Cl– ions per PCP molecule destroyed. 相似文献