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Basic Electrochemistry

M. B. Desiimulik, 1. Akhtar, and C. P. De, in 2nd International Symposium on Industrial and Oriented Basic Electrochemistry, Saest, India, IBH Publishing, Oxford, 1988. [Pg.246]

H. P. Agarwal and M. Saxena, in Proceedings of the 2nd International Symposium on Industrial Oriented Basic Electrochemistry, 1980, p. 1. [Pg.264]

In 1848 du Bois-Reymond [21] suggested that the surfaces of biological formations have a property similar to the electrode of a galvanic cell and that this is the source of bioelectric phenomena observed in damaged tissues. The properties of biological membranes could not, however, be explained before at least the basic electrochemistry of simple models was formulated. The thermodynamic relationships for membrane equilibria were derived by Gibbs in 1875 [29], but because the theory of electrolyte solutions was formulated first by Arrhenius as late as 1887, Gibbs does not mention either ions or electric potentials. [Pg.7]

Electrons are quantal particles and much basic electrochemistry in the past few decades has been quantal in approach, so a simplified description of the current state of this field is given. [Pg.4]

In many cases the surface of the anode is oxidized to lead oxide, which thus is the real anode material. Titanium anodes coated with lead oxide have been found to have a long lifetime [154,155]. In some cases the lead dioxide, a strong oxidant in acid solution, reacts chemically with the substrate [156] and is continuously regenerated whereas it acts as an inert electrode in other oxidations. A review of the basic electrochemistry of Pb02, mainly in relation to the lead battery, has been published [157]. [Pg.244]

The basic electrochemistry of the substrate is an important ingredient in the anodic oxidation process. The ease of doing the oxidation will definitely determine the material to be chosen for making the pattern. It appears that the two most popular substances which have been studied and used most extensively are Ti (for formation of TiO ) and H-passivated Si (for formation of Si02). [Pg.709]

Controlled-potential coulometry has also found some use in the study of basic electrochemistry. It is not always obvious how many electrons are involved in a newly studied electrochemical reaction, e.g., in polarography. Thus, coulometry at controlled potential, in which a known quantity of the substance is electrolyzed and Q is measured, is often used to determine values for n and thereby help elucidate electrode mechanisms for a wide variety of compounds, both organic and inorganic. Very slow chemical reactions coupled with the electrochemical reaction may also be studied by controlled-potential coulometry [4] other electrochemical techniques usually are suitable only for much faster chemical reactions, with time scales of jusec to sec. [Pg.102]

The basic electrochemistry of the Ni/Cd battery was given in Table 10.1 once again, however, the equations are misleading in that the reactions, particularly at... [Pg.261]

Electrochemistry of LB films of fullerenes has been widely studied and remains the subject of much research effort from both theoretical and experimental approaches. Bard etal. have studied basic electrochemistry of Ceo fullerene LB films on an electrode in acetonitrile solutions [23]. The study indicated that reduction of the fullerene films could form insoluble films with incorporated electrolyte cations or lead to dissolution. The study on Cgo LB films has become a focus of considerable interest however, it is difficult to fabricate high-quality LB films of pure Cgo due to its intrinsic hydropho-bicity. Kajiyama et al. applied a multistep creep method as an LB technique for constructing a fairly homogeneous Ceo monolayer, which is regularly packed in a hexagonal array [44]. Kunitake etal. developed the electrochemical replacement method to form epitaxial adlayers of fullerenes on Au(lll) surfaces [45]. The wet process method consists of the transfer of Langmuir films of fullerene onto iodine-modified Au(lll) surfaces at an air-water interface followed by the electrochemical removal and replacement of iodine adlayers with fullerene adlayers in solution. The fullerene adlayers prepared by this method showed excellent quality and uniformity. A visuahzing... [Pg.6395]

Introductory chapters give information on basic electrochemistry and HPLC-ED, and on the specialised area of HPLC-ED of thiols. The major portion of the book is devoted to summary details of over 400 published HPLC-ED methods that are discussed in a standard format (column, eluent, internal standard, ED conditions, extraction procedure, limit of quantitation, etc.). These data are not always available via published abstracts and, wherever possible, sufficient information is given for the reader to decide whether a particular approach is worth pursuing. Chemical structures are given for most analytes and internal standards to ensure unambiguous identification and to illustrate possible electroactive moieties. Problems and pitfalls, and alternative techniques when appropriate, are emphasised throughout. Literature coverage is comprehensive up to the end of 2003. [Pg.239]

As will be shown in this chapter, the basic electrochemistry of a fuel cell, an electrochemical gas battery, is determined by the choice of the electrolyte and... [Pg.98]

This introductory chapter will give an overview on the basic electrochemistry of some fuel cell types, developed today for dedicated technological applications. The respective electrochemistry will depend on the materials composition of the fuel cell, in particular, on the nature of the electrolyte and the temperature of operation. This further determines the choice of fuel, due to the strong influence of temperature on the mechanism of the respective electrocatalytic processes. [Pg.99]

The basic electrochemistry of the Ni-Cd battery was given in Table IIJ once again, however, the equations are misleading in that the reactions are not nearly as simple as indicated particularly at the positive electrode. In the nickel oxide paste, the oxidation state of the oxidized nickel species is uncertain and varies between - 2 and h-4 both the oxidized and reduced species exist in several crystal modifications and the important roles of water and potassium ions arc not included in the table. [Pg.566]

Strong evidence for the existence of MgH2 comes from X-ray diffraction of material scraped from the surface of a magnesium electrode surface (Perrault, 1970, 1978 Nazarov etal., 1989 Gulbrandsen, 1992 Gulbrandsen et al., 1993). This model, however, contradicts basic electrochemistry. Eq. (4-10) is a cathodic reaction, which means that the rate of the reaction decreases with increasing applied potential (or increasing applied anodic current). Hence the HER rate... [Pg.702]

The basic electrochemistry is the same for the vented pocket plate, sintered plate, fiber and plastic-bonded plate types as well as for other variations of the nickel-cadmium system. The reactions of charge and discharge can be illustrated by the following simplified equation ... [Pg.749]


See other pages where Basic Electrochemistry is mentioned: [Pg.624]    [Pg.47]    [Pg.25]    [Pg.164]    [Pg.207]    [Pg.223]    [Pg.90]    [Pg.328]    [Pg.141]    [Pg.621]    [Pg.129]    [Pg.513]    [Pg.535]    [Pg.6]    [Pg.367]    [Pg.51]    [Pg.1591]    [Pg.2798]    [Pg.42]    [Pg.6]    [Pg.7]    [Pg.9]    [Pg.11]    [Pg.13]    [Pg.15]    [Pg.17]    [Pg.19]    [Pg.232]    [Pg.624]    [Pg.276]    [Pg.289]   


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