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Potentiometric stripping voltammetry

42 Potentiometric stripping voltammetry. In potentiometric stripping voltammetry addition of a known amount of chemical oxidant solution replaces the potential sweep [Pg.26]


Describe clearly the principle and operation of potentiometric stripping analysis (PSA). How it is differed from anodic stripping voltammetry (ASV) What is the quantitative signal What is its advantage over ASV ... [Pg.99]

Potential of zero charge, 20, 23, 25, 66 Potential scanning detector, 92 Potential step, 7, 42, 60 Potential window, 107, 108 Potentiometry, 2, 140 Potentiometric stripping analysis, 79 Potentiostat, 104, 105 Preconcentrating surfaces, 121 Preconcentration step, 121 Pretreatment, 110, 116 Pulsed amperometric detection, 92 Pulse voltammetry, 67... [Pg.208]

Electrochemical measurements have been developed by using different electrochemical techniques (differential pulse voltammetry (DPV), cyclic voltametry (CV), potentiometric stripping analysis (PSA), square wave voltammetry (SWV), adsorptive stripping transfer voltammetry (ASTV), etc.). The abbreviations given in covalent attachment of DNA onto different transducers are water soluble carbodimide l-(3-dimethyaminopropyl)-3-ethyl-carbodimide (EDC), IV-hydroxysuccimide (NHS), mercaptohexanol (MCH), aminoethanethiol (AET), mercaptosilane (MSi), and N-cyclohexyl-lV -[2-(N-methylmorpholino)-ethyl]carbodimide-4-tolune sulfonate (CDS). [Pg.406]

SPMBE = screen-printed microband electrode, ASV = anodic stripping voltammetry, HCMV = human cytomegalovirus, PGE = pencil-graphite electrode, DPV = differential pulse voltammetry, SPEs = screen-printed electrodes, PSA = potentiometric stripping analysis, M-GECE = magnetic graphite-epoxy composite electrode. [Pg.947]

Equation (7.116) indicates that the charge-potential curves for reversible processes are only dependent on the square wave amplitude Sw and are independent of the frequency / = 1 jh and the staircase amplitude AEs. As a consequence, they are superimposable on those obtained at any differential electrochemical technique, such as DSCVC, provided that the differences between the successive potential pulses coincide (AE = 2 sw)- Moreover, when this difference is much less than RT/F (i.e., less than 25 mV at T = 198 K), the responses obtained in Cyclic Voltammetry (CV), Alternating Current Voltammetry, Potentiometric Stripping Analysis (PSA) and also in any Reciprocal Derivative Chronopotentiometry (RDCP) fulfill [5, 74, 75] ... [Pg.546]

Town, R.M. (1997) Potentiometric stripping analysis and anodic stripping voltammetry for measurement of Cu(II) and Pb(II) complexation by fulvic acid a comparative study. Electroanalysis, 9, 407-415. [Pg.234]

Electrochemical techniques anodic stripping voltammetry (ASV) and cathodic stripping voltammetry (CSV) for determining trace elements, and potentiometric sensors for determining dissolved gases (C02, N02, S02, NH3, H2S, HCN, and HF) as well as chloride, fluoride, cyanide, and sulfide. [Pg.261]

Any type of detector with a flow-through cell can be used for FIA. Photometric detectors are most often used in FIA (15-18, 25). However, many other analyses using fluorimeters (28, 29), refractometers (24), atomic absorption (30, 31), and inductively coupled plasma emission spectrometers (32) have been described. Electrochemical detectors based on potentiometry with ion-selective electrodes (15, 33), anodic stripping voltammetry (15, 34), potentiometric stripping (35), and amperometry (36) have also been used. [Pg.14]

Part IV is devoted to electrochemical methods. After an introduction to electrochemistry in Chapter 18, Chapter 19 describes the many uses of electrode potentials. Oxidation/reduction titrations are the subject of Chapter 20, while Chapter 21 presents the use of potentiometric methods to obtain concentrations of molecular and ionic species. Chapter 22 considers the bulk electrolytic methods of electrogravimetry and coulometry, while Chapter 23 discusses voltammetric methods including linear sweep and cyclic voltammetry, anodic stripping voltammetry, and polarography. [Pg.1171]

Potentiometric stripping analysis, as stated in one review,92 "is not as general an analytical technique for the determination of metal traces as is graphite-furnace atomic absorption spectroscopy." It is used as a complementary technique for assay of some toxic metals in water (zinc, cadmium, lead, and copper in potable water and wastewater,93 94 and lead and thallium in seawater.95 The advantage of anodic stripping voltammetry (ASV) is summarized in two steps, which include electrolytic preconcentration and the stripping process. There are a number of interfering ions that can affect the... [Pg.37]

Potentiometric stripping analysis (PSA) resembles conventional stripping voltammetry in that trace metal analytes are electrolytically deposited in a thin film of mercury. However, after this preconcentration, the potentiostatic circuitry is disconnected and the amalgamated elements are chemically (rather than electrochemically) oxidized by reaction with an excess of a suitable oxidant ... [Pg.133]

An integrated electronic tongue consisting of a multiple light-addressable potentiometric sensor (MLAPS) and two sets of electrochemical electrodes was developed to simultaneously detect Fe (111) and Cr (VI) ions and other heavy metals, respectively [64], The MLAPS was based on chalcogenide thin film while the electrochemical electrodes used stripping voltammetry. It has been suggested by the authors that these methods are suitable for the detection of heavy metals in wastewater or seawater. [Pg.188]

Anodic/ cathodic stripping voltammetry Adsorptive stripping voltammetry Potentiometric stripping techniques Amperometric titration... [Pg.112]


See other pages where Potentiometric stripping voltammetry is mentioned: [Pg.341]    [Pg.253]    [Pg.341]    [Pg.253]    [Pg.472]    [Pg.144]    [Pg.732]    [Pg.773]    [Pg.407]    [Pg.455]    [Pg.92]    [Pg.249]    [Pg.658]    [Pg.422]    [Pg.1545]    [Pg.142]    [Pg.142]    [Pg.361]    [Pg.449]    [Pg.449]    [Pg.289]    [Pg.201]    [Pg.276]    [Pg.135]    [Pg.146]    [Pg.231]    [Pg.428]    [Pg.436]   


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