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Scanning parameters

Further, the operator must be able to choose the drop lifetime and the scan parameters, viz., the starting potential, direction (cathodic or anodic), rate and end potential, together with the sensitivity of the current measurement and the amplification in the ohmic cell resistance compensation circuit. Convenient additional facilities are (a) display of the polarogram on an oscilloscope, (b) delivery of hard copy of the polarograms on a chart recorder and (c) repeated recording of the polarographic curve for the same sample. [Pg.332]

Final image acquisition—Once the scan parameters have been determined, a scout scan performed, and scan times deemed satisfactory, the next step is to run the micro-CT scanner for the final image acquisition. [Pg.229]

In addition when it is necessary to process a large number of specimens per day, taking hours over a single specimen is clearly not a practical approach. The use of MRI to examine fresh, unfixed fetal rat and rabbit heads from embryo-fetal development (EFD) studies has already been proposed (6) (see Note 1) and the compromise between image quality and speed of acquisition that is necessary under these circumstances examined. MRI is now considered to have the potential to be an acceptable alternative to current methods after throughput was increased by scanning multiple specimens in parallel with careful optimization of scan parameters. [Pg.256]

Fig. 3. X-ray diffractogram of Class-F bituminous coal fly ash. Analytical conditions diffraction data were collected using a Philips X-ray powder diffractometer (45 kV/30-40 mA CuKa theta-compensating variable divergence slit diffracted-beam graphite monochromator scintillation detector) automated with an MDI/Radix Databox. The scan parameters were typically 0.02° step size for 1 s count times over a range of 5-60° 2-theta. All data were analysed and displayed using a data reduction and display code (JADE) from Materials Data Inc., livermore, CA. Fig. 3. X-ray diffractogram of Class-F bituminous coal fly ash. Analytical conditions diffraction data were collected using a Philips X-ray powder diffractometer (45 kV/30-40 mA CuKa theta-compensating variable divergence slit diffracted-beam graphite monochromator scintillation detector) automated with an MDI/Radix Databox. The scan parameters were typically 0.02° step size for 1 s count times over a range of 5-60° 2-theta. All data were analysed and displayed using a data reduction and display code (JADE) from Materials Data Inc., livermore, CA.
In our operations, we often establish step-scan parameters as if we were continuously scanning. Because continuous scanning requirements are more demanding, no problems arise using this approach. [Pg.180]

Figure B3.6.4 The effect of scanning parameters on the authenticity of spectra. The Raman band from Figure B3.6.1 is shown for a single scan at 1500 nm/min (dotted line) ten scans at 1500 nm/min (dashed line) and ten scans at 100 nm/min (solid line). The times required for scanning the complete baselines for these three measurements were 0.087 min, 0.87 min, and 13 min, respectively. Measurements made using a Perkin-Elmer LS50B. Figure B3.6.4 The effect of scanning parameters on the authenticity of spectra. The Raman band from Figure B3.6.1 is shown for a single scan at 1500 nm/min (dotted line) ten scans at 1500 nm/min (dashed line) and ten scans at 100 nm/min (solid line). The times required for scanning the complete baselines for these three measurements were 0.087 min, 0.87 min, and 13 min, respectively. Measurements made using a Perkin-Elmer LS50B.
In spite of the apparent sensitivity to the material properties, the direct assignment of the phase contrast to variation in the chemical composition or a specific property of the surface is hardly possible. Considerable difficulties for theoretical examination of the tapping mode result from several factors (i) the abrupt transition from an attractive force regime to strong repulsion which acts for a short moment of the oscillation period, (ii) localisation of the tip-sample interaction in a nanoscopic contact area, (iii) the non-linear variation of both attractive forces and mechanical compliance in the repulsive regime, and (iv) the interdependence of the material properties (viscoelasticity, adhesion, friction) and scanning parameters (amplitude, frequency, cantilever position). The interpretation of the phase and amplitude images becomes especially intricate for viscoelastic polymers. [Pg.86]

Fig. 12 In most parts of the scanned parameter space no possibility for an oscillatory instability was found. If the director field is only very weakly coupled to the layering (in this plot we used Bo = 200 and V = 0.4) a neutral curve for an oscillatory instability ( Fig. 12 In most parts of the scanned parameter space no possibility for an oscillatory instability was found. If the director field is only very weakly coupled to the layering (in this plot we used Bo = 200 and V = 0.4) a neutral curve for an oscillatory instability (<dashed line) appears above the stationary neutral curve solid line ). Note that the critical wave vectors are close to each other for both oscillatory and stationary instability. The inset shows the frequency along the neutral curve...
Mazzarino M et al (2010) Mass spectrometric characterization of tamoxifene metabolites in human urine utilizing different scan parameters on liquid chromatography/tandem mass spectrometry. Rapid Commun Mass Spectrom 24 749-760... [Pg.250]

Figure 8.4. Main window of Gepasi. The main window of Gepasi consists of menus (File, Options, and Help), icons, and four tabs (Model definition, Tasks, Scan, and Time course). Activation of any of the tab opens an indexed page. At the start of Gepasi, the Model definition page is opened. Enter name of the metabolic pathway to the Title box. Click Reactions button to define enzymatic reactions (e.g., E + A+B = EAB for R1, EAB = EPQ for R2, and EPQ = E + P + Q for R3 shows 3 reactions and 7 metabolites), and then click Kinetics button to select kinetic type. Activate Tasks tab to assign Time course (end time, points, simufile.dyn), Steady state (simufile.ss) and Report request. Activate Scan tab to select scan parameters. Activate Time course tab to select data to be recorded and then initiate the time course run. Figure 8.4. Main window of Gepasi. The main window of Gepasi consists of menus (File, Options, and Help), icons, and four tabs (Model definition, Tasks, Scan, and Time course). Activation of any of the tab opens an indexed page. At the start of Gepasi, the Model definition page is opened. Enter name of the metabolic pathway to the Title box. Click Reactions button to define enzymatic reactions (e.g., E + A+B = EAB for R1, EAB = EPQ for R2, and EPQ = E + P + Q for R3 shows 3 reactions and 7 metabolites), and then click Kinetics button to select kinetic type. Activate Tasks tab to assign Time course (end time, points, simufile.dyn), Steady state (simufile.ss) and Report request. Activate Scan tab to select scan parameters. Activate Time course tab to select data to be recorded and then initiate the time course run.
As with any detector, the vidicon detector has a number of limitations, many of which have not yet been thoroughly explored. To facilitate the characterization of the detector and the determination and minimization of its limitations, we wanted to place a large number of the vidicon scanning parameters under computer control. [Pg.170]

In other words, depending on the scanning parameters, but above all depending on the given writing voltage Vm the total volume can be increased. Reasons for an increase of the total volume will be discussed in Sect. 6.4. [Pg.157]

A disadvantage of DEPT is that it is a subtraction experiment and, therefore, much more sensitive to certain problems than are typical one-dimensional techniques. One remedy that is used in many experiments that suffer fi om stability problems is the employment of steady-state, or dummy, scans (parameter 2 in the foregoing list Section 2-4i). Poor signal cancelation is generally the result of difficulties in one or more of the following areas ... [Pg.237]

Before the AFM experiment is started, the scan parameters must be adjusted. First of all the tapping AFM menu must be chosen compared to CM, there are a number of changes the scan rate must be reduced (max. 1.0 Hz) and the gains are typically set to lower values (integral gain 0.5 proportional gain 1.0 differential gain 0.0). [Pg.43]

The scan parameters of the mass spectrometer need careful optimisation. In order to achieve an optimum precision for the ratio measurement a compromise has to be reached between the need to monitor several masses in quick succession, while still maintaining adequate signal levels (counts s ). This will also be governed by the amount of sample available and how much is consumed during the measurement. [Pg.19]

After acquiring the one-pass CTA of the head and neck, quantitative cine CTP can additionally be performed at 1 or 2 nonoverlapping levels, depending on the clinical need for these data in acute ischemic stroke triage. This is discussed at length in Chap. 5, along with specific scanning parameters. A sample acute ischemic... [Pg.71]

Fig. 33a-d. Resonance Raman spectra of Rps. sphaeroides reaction centers as a function of potential of the silver electrode a) 0.0 V vs SCE b) -0.2 V vs SCE c) -0.4 V vs SCE d) BPh (10" M) in CH Clj laser excitation wavelength 530.9 nm other scan parameters were identical to those in Fig. 31 (Cotton and Van Duyne, Ref. Fig. 33a-d. Resonance Raman spectra of Rps. sphaeroides reaction centers as a function of potential of the silver electrode a) 0.0 V vs SCE b) -0.2 V vs SCE c) -0.4 V vs SCE d) BPh (10" M) in CH Clj laser excitation wavelength 530.9 nm other scan parameters were identical to those in Fig. 31 (Cotton and Van Duyne, Ref.
In summary, ion mobility separations occur by a variety of methods. In all cases, there is an instrumental scan parameter that controls the separation of the ion. For example, in the drift tube spectrometers, it is the arrival time of the ion for the aspiration spectrometers, it is the position of the faraday plates for the mobility analyzers, it is the strength of the orthogonal voltage and for the DMSs, it is the compensation voltage. The relative value of these scan parameters for two ions is called the separation factor a, and the resolving power of a spectrometer is determined by the ratio of the scan parameter to the width of the scan parameters for a packet of ions. [Pg.186]

The first step is to generate a Sky Map to be fed to the subsequent modules in the Sky Generator Module and the corresponding photon noise, computed in the Sky Photon Noise Module. In parallel, given the parameters defined by the user for the instrument, an interferometric MV-map is created at the v-Map Generator Module from the position of the two telescopes. The FTS Drive module calculates the spectrometer scan parameters. Once a MV-map and the scan parameters are defined, the instrument beam is calculated at the Beam Generator Module. The sky map and the beam are then combined to recreate the observed sky map. [Pg.75]

CT, greater radiation intensities can typically be used than those applied in clinical CT. Also, because resolution and p- accuracy requirements are different, scanning parameters usually differ significantly in industrial and clinical CT scanners. [Pg.246]

Selection of scan parameters. As mentioned earher, the scan rate significantly influences the shape and quantitative features of voltammograms. Usually, a variation of v gives important information. There are, however, other scan-related parameters that may affect the current/potential curves. In computer controlled instruments, the ideal linear variation of E is often simulated using a staircase function (Fig. 7). The response from such an excitation function... [Pg.92]

However, it is often possible to design the beam and scan parameters to minimize this effect. [Pg.18]


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