Interactions between Cytochrome c and DNA Strands Self-Assembled at Gold Electrode

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.     

三维电极处理生物难降解有机废水

介绍了三维电极电化学水处理技术的分类及其特点,着重阐述了国内外的实验研究与应用现状,及三维电极与化学催化、光催化、生物催化、超声波、絮凝和吸附法等的优化组合技术。该领域研究的主攻目标仍然是如何提高电极材料的催化性能,提高电流效率,减少电极极化,降低能耗。因此,新型三维电催化电极和高效反应器的研制,三维电极法与其他处理方法的系统集成及处理单元的有机联合将是今后的研究发展方向。     

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

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)₆^3−/4− couple in the anodic direction. Their good preconcentration efficiency at low analyte concentration highlighted their interest for electroanalytical applications.     

废水处理中的复极性固定床电解槽技术

复极性固定床电解槽（bipolar packed bed cell,BPBC)是在三维电极原理基础上发展起来的新型电化学工程技术，其在治理含氰及重金属废水、有机废水和印染废水方面具有良好的处理效果。介绍了BPBC的电化学特性，综述了国内外BPBC废水处理技术应用现状及其机理研究的概况。同时，提出了该技术目前存在的问题，并对其进一步的深入研究作了展望。     

pH玻璃电极的现状与发展

对pH玻璃电极的结构、原理以及特性进行了综述.与液体充填式玻璃电极比较,固体接触式pH玻璃电极有明显的优点.叙述了固体接触式pH玻璃电极膜的成分及其响应机理,并指出固体接触式pH玻璃电极的发展方向.     

Electro-oxidation of hydrazine on electrodes modified with vitamin B12

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.     

Alkaline peroxide generation using a novel perforated bipole trickle-bed electrochemical reactor

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.     

Matching ratio between positive and negative electrodes for double-layer capacitors

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.     

Electrochemical studies of pyrite oxidation and reduction using freshly-fractured electrodes and rotating ring-disc electrodes

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.     

Selective oxidation of pentachlorophenol on diamond electrodes

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.