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LINEAR-SWEEP

CONTOUR ELEMENT END SCOPE contour s equence shift length shift direction origin dir x dir xz END  [Pg.126]

LIST OF LIST OF REF ONLY(CONTOUR ELEMENT) ANY(REAL)  [Pg.126]

All the DIRECTION, POINT and ELEMENTARY CURVE entities are located in the xy-plane. The z-value of the shift direction must not be zero. The shift length must be greater than zero. [Pg.126]


Figure Bl.28.3. Concentration profiles of an electroactive species with distance from the electrode surface during a linear sweep voltaimnogram. Figure Bl.28.3. Concentration profiles of an electroactive species with distance from the electrode surface during a linear sweep voltaimnogram.
Active electrochemical techniques are not confined to pulse and linear sweep waveforms, which are considered large ampHtude methods. A-C voltammetry, considered a small ampHtude method because an alternating voltage <10 mV is appHed to actively couple through the double-layer capacitance, can also be used (15). An excellent source of additional information concerning active electroanalytical techniques can be found in References 16—18. Reference 18, although directed toward clinical chemistry and medicine, also contains an excellent review of electroanalytical techniques (see also... [Pg.55]

The reactions are carried out under first-order conditions, i.e., the stoichiometric concentration of the antioxidant, a-tocopherol, is in large excess over that of 16-ArN, such that the concentration of a-tocopherol does not change significantly throughout the time course of the reaction. The emulsion employed was prepared by mixing the non-ionic emulsifier Brij 30, octane and HCl (3 mM, pH = 2.5). The resulting emulsion is opaque, thus values were obtained electrochemically by employing Linear Sweep Voltammetry (LSV). [Pg.139]

A simple, rapid and seleetive eleetroehemieal method is proposed as a novel and powerful analytieal teehnique for the solid phase determination of less than 4% antimony in lead-antimony alloys without any separation and ehemieal pretreatment. The proposed method is based on the surfaee antimony oxidation of Pb/Sb alloy to Sb(III) at the thin oxide layer of PbSOyPbO that is formed by oxidation of Pb and using linear sweep voltammetrie (LSV) teehnique. Determination was earried out in eoneentrate H SO solution. The influenee of reagent eoneentration and variable parameters was studied. The method has deteetion limit of 0.056% and maximum relative standard deviation of 4.26%. This method was applied for the determination of Sb in lead/aeid battery grids satisfaetory. [Pg.230]

Explain clearly the reason for the peaked response of linear sweep voltammetric experiments involving a planar macrodisk electrode and a quiescent solution. [Pg.27]

Peter studied in detail the growth of anodic CdS films on the Cd electrode in similar solutions [31], as well as the processes that occur at the Cd/solution and CdS/solution interfaces [32], According to the linear sweep voltammetry, three characteristic regions could be distinguished revealing the essential features of the anodic passivation of cadmium in alkaline sulfide solutions (a) the monolayer... [Pg.88]

Chronoamperometry Linear sweep Polarography Rotating disk electrode Faradaic impedance... [Pg.158]

In linear sweep voltammetry, a rapidly changing ramp potential is applied to the indicator electrode. The current increases to a maximum... [Pg.160]

Fig. 15. Waveforms used for in vivo electrochemical analysis. A = chronoamperometry, B = double chronoamperometry (response = SI — S2), C = linear sweep, D = differential pulse (response = S2 — SI), S = sample window... Fig. 15. Waveforms used for in vivo electrochemical analysis. A = chronoamperometry, B = double chronoamperometry (response = SI — S2), C = linear sweep, D = differential pulse (response = S2 — SI), S = sample window...
Differential pulse voltammetry has been widely used for in vivo electrochemical analysis This technique combines the linear sweep and pulsed potential... [Pg.37]

Differential pulse voltammetry provides greater voltammetric resolution than simple linear sweep voltammetry. However, again, a longer analysis time results from the more sophisticated potential waveform. At scan rates faster than 50 mV/sec the improved resolution is lost. Because it takes longer to scan the same potential window than by linear sweep, an even longer relaxation time between scans is required for differential pulse voltammetry. [Pg.37]

As with in vivo voltammetry, a variety of electrochemical techniques have been used for the stripping step. Because of its simplicity, linear sweep voltammetry has enjoyed widespread use however, the detection limit of this technique is limited by charging current. Differential pulse has become popular because it discriminates against the charging current to provide considerably lower detection limits. [Pg.40]

Here, dU/dt is the linear sweep rate of the experiment and dQjdt is the measured current. With a transfer of one electron per adsorbed H, the relation between the charge transferred per area Q, and the coverage 6 is Q = QtaiG, where gtot is e times the density of Pt atoms in the surface layer. Introducing +K for the sweep rate and i t) for the current, we obtain... [Pg.61]

Clavilier J. 1987. Pulsed linear sweep voltammetry with pulses of constant level in a potential scale, a polarization demanding condition in the study of platinum single crystal electrodes. J Electroanal Chem 236 87-94. [Pg.200]

According to Eq. (1) the steady-state current across a micro-ITIES is proportional to the bulk concentration of the transferred species. Thus, the micro-ITIES can function as an amperometric ion-selective sensor. Similarly, the peak current in a linear sweep voltam-mogram of ion egress from the micropipette obeys the Randles-Sevcik equation. Both types of measurements can be useful for analysis of small samples [18a]. [Pg.399]

Rapid DC polarography These principles can be 5. Linear-sweep 1. Polarography with 2. Oscillographic ... [Pg.151]

Linear sweep voltammetry at the dme. In linear sweep voltammetry (LSV) at the dme a continuously changing rapid voltage sweep (single or multiple) of the entire potential range to be covered is applied in one Hg drop. Originally the rapidity of the sweep (about 100 mV s 1) required the use of an oscilloscope,... [Pg.156]


See other pages where LINEAR-SWEEP is mentioned: [Pg.1926]    [Pg.1930]    [Pg.1934]    [Pg.1973]    [Pg.265]    [Pg.473]    [Pg.9]    [Pg.36]    [Pg.237]    [Pg.164]    [Pg.160]    [Pg.27]    [Pg.37]    [Pg.37]    [Pg.60]    [Pg.219]    [Pg.277]    [Pg.648]    [Pg.649]    [Pg.316]    [Pg.385]    [Pg.23]    [Pg.179]    [Pg.180]    [Pg.196]    [Pg.199]    [Pg.202]    [Pg.309]   
See also in sourсe #XX -- [ Pg.194 , Pg.282 ]

See also in sourсe #XX -- [ Pg.126 ]




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