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Polarography definition

A definitive method for stmctural deterrnination is x-ray crystallography. Extensive x-ray crystal stmcture deterrninations have been done on a wide variety of steroids and these have been collected and Hsted (270). In addition, other analytical methods for steroid quantification or stmcture determination include, mass spectrometry (271), polarography, fluorimetry, radioimmunoassay (264), and various chromatographic techniques (272). [Pg.448]

An important feature of pulse polarography is the sampling of the current at definite points in the lifetime of the mercury drop, and it is essential to... [Pg.612]

The method of potentiostatic pulses is sometimes combined with the DME (called pulse polarography). hi this case the pulse frequency should match the drop frequency, where each pulse is used at a definite time in the drop life, hi Barker s method, large pulse amphrndes are used. Other versions of the potentiostatic pulse technique are square-wave and staircase voltammetry here smaU-amphtude pulses are used. [Pg.397]

In analytical practice, some methods using definitive measurements, in principle, are also caUbrated in an experimental way (e.g. spectrophotometry, polarography) to provide reliable estimates of S. [Pg.62]

The concept of polarization is so important that many aspects of this chapter will be discussed in terms of it. Indeed, the root polar- of polarography implies polarization. As a working definition, we say that polarization represents... [Pg.132]

Lingane was a leader in the field of - electro analytical chemistry and wrote, with Kolthoff, the definitive, two volume monograph, Polarography [i] that remains a useful reference work. He also helped develop other electroanalytical techniques, like controlled potential electrolysis, -> coulometry, -> coulometric titrations, and developed an early electromechanical (Lingane-Jones) potentiostat, He wrote the widely-used monograph in this field, Electroanalytical Chemistry (1st edn., 1953 2nd edn., 1958). Lingane received a number of awards, including the Analytical Chemistry (Fisher) Award of the American Chemical Society in 1958. Many of his Ph.D. students, e.g., -> Meites, Fred Anson, Allen Bard, Dennis Peters, and Dennis Evans, went on to academic careers in electrochemistry. [Pg.403]

Flow Indicator Recorder Controller) governing the gear-pump, and an on-line Np/Pu analyser (CoRC = Concentration Recorder Controller) (scintillation is used in the glove box experiments while polarography is under development for the hot cell plant) which discontinues the process at a definite Np/Pu concentration in the column effluent. [Pg.521]

It has been established that by definition a dropping mercury electrode is necessary for the name polarography to be used. [Pg.5]

The measurement of formal potentials allows the determination of the Gibbs free energy of amalgamation (cf Eq. 1.2.27), acidity constants (pATa values) (cf. Eq. 1.2.32), stability constants of complexes (cf. Eq. 1.2.34), solubility constants, and all other equilibrium constants, provided that there is a definite relationship between the activity of the reactants and the activity of the electrochemical active species, and provided that the electrochemical system is reversible. Today, the most frequently applied technique is cyclic voltammetry. The equations derived for the half-wave potentials in dc polarography can also be used when the mid-peak potentials derived from cyclic voltammograms are used instead. Provided that the mechanism of the electrode system is clear and the same as used for the derivation of the equations in dc polarography, and provided that the electfode kinetics is not fully different in differential pulse or square-wave voltammetry, the latter methods can also be used to measure the formal potentials. However, extreme care is advisable to first establish these prerequisites, as otherwise erroneous results will be obtained. [Pg.34]

From the definition of AdSV it follows that this method is characterized by the nature of the accumulation process, where adsorption plays an important role [28, 29]. In AdSV, the pre-concentration step is not controlled by electrolysis, but it is accomplished by anal3Ae adsorption on the working electrode surface or by reactions with chemically modihed electrodes. From the early 1960s, this technique (in connection with dc polarography and... [Pg.362]

Current-voltage curves. Nature of electrode is given, the name polarography has been definitely set aside for the mercury-dropping electrode case. [Pg.7]

Three dimensional voltammetry unites three conventional electrochemical techniques, classical polarography, pulse polarography and chronoamperometry into one very powerful experimental approach. 3D Voltammetry possess all the advantages of these methods without inheriting their limitations. Classical polarography and pulse polarography can be used to get a feel of the electrochemical behavior of a new system but both techniques suffer from a restricted time window. Both techniques discard much of the information contained in the i-t curve from each drop. Chronoamperometry possess an extended time window. However this technique can be applied once the reaction mechanism has been definitely established by some other technique, since a chronoampero-metric curve has the form of a falling transient and information is only obtained by a detailed mathematical analysis of its shape. 3D Voltammetry combines an extended time window and convenience in the analysis and interpretation of the experimental results. With 3D Voltammetry any... [Pg.496]


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See also in sourсe #XX -- [ Pg.124 ]




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