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Continuous-scanning

Cyclic voltammograms (CV) is a kind of electrochemical analysis method and is a linear-sweep voltammetry with the scan continued in the reverse direction at the end of the first scan this cycle can be repeated a number of times. Usually it is used in the field of electrochemistry. The function of CV in electrocatalytic analysis of electrodes might be in these parts (a) kinetics (b) mechanism of electrode reactions and (c) corrosion studies. [Pg.340]

Two strategies have been adopted for kinetic measurements. Either the electrode potential can be adjusted so that only the steady-state current is measured as a function of time, or the potential might be scanned continuously with the recording of steady-state voltammograms at certain time intervals. The first strategy outlined... [Pg.540]

Because of the inferior quality of data that can be obtained from the powder XRD patterns, XRD was used as a qualitative fingerprinting technique for identification purposes and for crystallinity measurements during the kinetic studies of synthesis. If care is not taken to optimize the crystallinity and prepare the sample without any residual impurities, the qualitative data may not be erraneous but the quantitaive data will differ from sample to sample and from one person s preparation to another s. Also, the various conditions like the mode of scanning (continuous or step), scan speed, value of 20 for each step etc., have to be optimised. Correction of the interplanar distance d with respect to an internal standard such as silicon is a prerequisite for determining the lattice parameters or unit cell dimensions. [Pg.684]

Figure 6.6.2 Method for obtaining baseline for measurement of of second wave. Upper curves potential programs. Lower curves resulting voltammograms with (curve 1) potential stopped at E and (curve 2) potential scan continued. System as in Figure 6.6.1. Figure 6.6.2 Method for obtaining baseline for measurement of of second wave. Upper curves potential programs. Lower curves resulting voltammograms with (curve 1) potential stopped at E and (curve 2) potential scan continued. System as in Figure 6.6.1.
Temperature Scanning Continuously Stirred Tank Reactor... [Pg.90]

The operation and description of a temperature scanning continuously stirred tank reactor (TS-CSTR) is, in principle, much simpler than for the TS-PFR. It turns out that rates can be calculated from each individual point in each run, and that flow rates and temperature ramping do not need the same careful control as the TS-PFR. Nevertheless, the operation of die reactor should approach the perfectly mixed condition very closely. Although in practice it may be difficult to make the necessary physical arrangements for complete and instantaneous mixing within the reactor, as with other TS reactor types there are verification procedures that will reveal if proper operating conditions are not being met. [Pg.90]

As an alternative to bolus tracking, a smartscan type function can be used, in which a test bolus is administered to determine the scan delay [64]. A region of interest is selected, typically in the proximal ICA, and 10 mL of contrast is injected. This region is scanned continuously using a low mAs/kVp technique, and the prep delay is chosen as the time corresponding to... [Pg.66]

Electropolymerization A 1 x 1cm ITO glass plate (purified with soap solution, water, ethanol) was used as the working electrode. A Pt wire counter electrode was purified with H2SO4/H2O2, water and ethanol. The Ag wire as reference electrode was polished and then cleaned with water and ethanol. The solution for the electropolymerization of the phthalocyanine derivative contains 6.30 mg (10 mol) 51a (M = Ni) and 342 mg (10" mol) tetrabutylammonium perchlorate in 10 mL dry DMF, and for the electropolymerization of the porphyrin derivative 49h (M = Zn) 7.4 mg (10 mol) 49h and 342 mg (10 mol) tetrabutylammonium perchlorate in 10 mL dry methylene chloride. 4.5 mL of one of the solutions was filled into the glass cell under a stream of nitrogen. The ITO electrode was connected to a copper holder. The potential was scanned continuously between -0.4 V and +0.8 V for 51a or 0.0 and 0.9 V for 49h, respectively, vs. SCE at a rate of 10 mV/s. For calibration of the reference electrode, the porphyrin derivatives were replaced by ferrocene (E° = 0.4 V vs. SCE) in the same electrolyte. [Pg.270]

Fig. 7.2. Schematic of the model of medical image perception. Perception starts with an initial global view followed by focal scanning of potential lesion features detected in this global or gist impression. Scanning continues until the radiologist has rendered a final decision... Fig. 7.2. Schematic of the model of medical image perception. Perception starts with an initial global view followed by focal scanning of potential lesion features detected in this global or gist impression. Scanning continues until the radiologist has rendered a final decision...
Lephardt s original work was on the pyrolysis and combustion of tobacco, for which he used Ig samples. We have adapted the techniques to work with 5-lOmg samples of and have used it successfully to characterise a variety of polymers. Our standard conditions are IC C/min ramp rate, 50ml/min purge gas (usually N2), 10s data collection time (25 scans), continuous (GC mode). We use both identity and evolution profile of the evolved gases to evaluate the sample. [Pg.106]

In step scan mode the optical path difference is changed incrementally, the mirror does not scan continuously. It steps to a position, collects data, and moves to the next position. Data are collected at each step with the path difference held constant. At each step the mirror is jittered at a constant frequency, a procedure that modulates the incident beam. The ability to select a constant modulation frequency, independent of the mirror velocity and wavenumber, results in a constant probed depth over the entire spectral range. This is advantageous over the varying sampling depth observed when using rapid scanning,... [Pg.3722]

The output signal of a detector is proportional to the wavelength-dependent radiation intensity I(X) illuminating the detector element. If a monochromator scans continuously over a certain wavelength interval, the measured radiation intensity is transformed into a time-dependent signal I(t). An appropriate preamplifier modifies I(t) to an output voltage through an amplification factor g ... [Pg.4476]

The triangular potential waveform employed in cyclic voltammetry is shown in Figure 1. Typically, the potential is ramped linearly from an initial potential, Ej, to the switching potential, Emax- The direction of the potential sweep is then reversed and scanning continues until E ,in is reached. The potential sweep may be terminated at the end of the first cycle or it may continue for an arbitrary number of cycles. The primary experimental parameters are the initial potential, the switching potentials, and the potential sweep rate. Typical sweep rates for cyclic voltammetry, employing electrodes of conventional sizes (e.g.. [Pg.4926]

With 4-slice CT scanners, the entire abdomen can be scanned continuously with slices as thin as 2-3 mm. When scanning from top to bottom, the liver should be imaged during the portal venous phase and the... [Pg.30]

Time averaging is symmetrical in time, which means that it will not induce asymmetry into an otherwise symmetrical input signal. Also, the peak height is not necessarily altered. The same is valid for pointwise time averaging, that is, the determination of the arithmetic mean of accumulated data during a given time interval at constant A. After this step the scan continues with a definite increment AA, accumulation starts at A + AA, etc. Both methods are applicable if the samples are stable and not damaged by radiation. [Pg.115]

Potentiodynamic technique—The potential is changed scanned) continuously at a predetermined rate (ASTM G 5). [Pg.226]

The humidity is scanned continuously and the constant until the mass of the sample is... [Pg.160]


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See also in sourсe #XX -- [ Pg.170 , Pg.179 ]




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Computer evaluation of continually scanned

Continuous scan

Continuous scan

Continuous scan data collection

Continuous scanning mode

Continuous-scan FT-IR spectrometer

Continuous-scan porosimetry

Continuous-scanning interferometer

Figures—continued scanning tips

Interferometer continuous scan

Interferometry continuous scan

Logarithmic signals from continuous-scan porosimetry

Spectrometer continued) rapid scanning

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