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180-degree Pulse

To determine the influence degree on both types of structure and volume of structural heterogeneity on the frequency spectrum characteristics of an ultrasonic pulse, research work using angle beam and straight beam probes was performed... [Pg.731]

Many optical studies have employed a quasi-static cell, through which the photolytic precursor of one of the reagents and the stable molecular reagent are slowly flowed. The reaction is then initiated by laser photolysis of the precursor, and the products are detected a short time after the photolysis event. To avoid collisional relaxation of the internal degrees of freedom of the product, the products must be detected in a shorter time when compared to the time between gas-kinetic collisions, that depends inversely upon the total pressure in the cell. In some cases, for example in case of the stable NO product from the H + NO2 reaction discussed in section B2.3.3.2. the products are not removed by collisions with the walls and may have long residence times in the apparatus. Study of such reactions are better carried out with pulsed introduction of the reagents into the cell or under crossed-beam conditions. [Pg.2080]

Calculations within tire framework of a reaction coordinate degrees of freedom coupled to a batli of oscillators (solvent) suggest tliat coherent oscillations in the electronic-state populations of an electron-transfer reaction in a polar solvent can be induced by subjecting tire system to a sequence of monocliromatic laser pulses on tire picosecond time scale. The ability to tailor electron transfer by such light fields is an ongoing area of interest [511 (figure C3.2.14). [Pg.2987]

Dick and Styrus [63] report real-time resistivity measurements on shoek-loaded silver foils. The inferred vaeaney eoneentration is 1.5 x 10 per atomie site for samples shoek loaded to 10 GPa. The eombined effect of point-defect generation and reeombination to form vaeaney clusters, for example, can be influential on pulse-duration effeets such reload, release, and recovery. This topie has not yet reeeived the degree of experimental study that it deserves. [Pg.247]

The determination of piezoelectric constants from current pulses is based on interpretation of wave shapes in the weak-coupling approximation. It is of interest to use the wave shapes to evaluate the degree of approximation involved in the various models of piezoelectric response. Such an evaluation is shown in Fig. 4.5, in which normalized current-time wave forms calculated from various models are shown for x-cut quartz and z-cut lithium niobate. In both cases the differences between the fully coupled and weakly coupled solutions are observed to be about 1%, which is within the accuracy limits of the calculations. Hence, for both quartz and lithium niobate, weakly coupled solutions appear adequate for interpretation of observed current-time waveforms. On the other hand, the adequacy of the uncoupled solution is significantly different for the two materials. For x-cut quartz the maximum error of about 1%-1.5% for the nonlinear-uncoupled solution is suitable for all but the most precise interpretation. For z-cut lithium niobate the maximum error of about 8% for the nonlinear-uncoupled solution is greater than that considered acceptable for most cases. The linear-uncoupled solution is seriously in error in each case as it neglects both strain and coupling. [Pg.81]

THE PATIENT WITH HEART BLOCK. The patient receiving atropine for third-degree heart block is placed on a cardiac monitor during and after administration of the drug. The nurse watches the monitor for a change in pulse rate or rhythm. Tachycardia, other cardiac arrhythmias, or failure of the drug to increase the heart rate must be reported to the primary health care provider immediately because other dm or medical management may be necessary. [Pg.233]

Fig. 6. The CP/MAS spectra of cellulose acetate-butyrate (CAB) and of cellulose acetate (CA, degree of substitution = 1.97), 20. The observation frequency was 50.1 MHz and the irradiation frequency 199.5 MHz. The pulse repetition time was 5 s and the contact time 2 ms. For CAB 400 scans and for CA 60 scans were collected... Fig. 6. The CP/MAS spectra of cellulose acetate-butyrate (CAB) and of cellulose acetate (CA, degree of substitution = 1.97), 20. The observation frequency was 50.1 MHz and the irradiation frequency 199.5 MHz. The pulse repetition time was 5 s and the contact time 2 ms. For CAB 400 scans and for CA 60 scans were collected...
NMR Spectroscopy. All proton-decoupled carbon-13 spectra were obtained on a General Electric GN-500 spectrometer. The vinylldene chloride isobutylene sample was run at 24 degrees centigrade. A 45 degree (3.4us) pulse was used with a Inter-pulse delay of 1.5s (prepulse delay + acquisition time). Over 2400 scans were acquired with 16k complex data points and a sweep width of +/- 5000Hz. Measured spin-lattice relaxation times (Tl) were approximately 4s for the non-protonated carbons, 3s for the methyl groups, and 0.3s for the methylene carbons. [Pg.164]

The PVA sample was run at 55 degrees centigrade. A 90 degree (6.8us) pulse was used with a inter-pulse delay of 2.1s. Exactly 800 scans were acquired with 16k complex data points and a sweep width of +/-2000 Hz. [Pg.164]

Position Feedback Encoders generate 512 pulses per revolution of the motor. One pulse correlates to the me2tsurement of 0.023 degree in angular displacement of the mandrel. [Pg.539]

Z60degree mandrel rev motor rev. 0234 degree mandrel rev ZOmotorrev 512pu/s pulse... [Pg.539]

Figure 1. HPLC analysis of product progression during hydrolysis of 0.25 % polygalacturonate by PGII. Aliquots were withdrawn from the reaction mixture at timed intervals and reactions were stopped by raising the pH of the sample to pH 8.0 by mixing with 1 volume 25 mM Na-phosphate pH 9.5. Gl to G5 indicate the oligogalacturonates with corresponding degree of polymerization. The vertical axis shows the responce of the pulsed amperometric detector and the horizontal axis the elution time. Times of sampling are indicated above the trace. Figure 1. HPLC analysis of product progression during hydrolysis of 0.25 % polygalacturonate by PGII. Aliquots were withdrawn from the reaction mixture at timed intervals and reactions were stopped by raising the pH of the sample to pH 8.0 by mixing with 1 volume 25 mM Na-phosphate pH 9.5. Gl to G5 indicate the oligogalacturonates with corresponding degree of polymerization. The vertical axis shows the responce of the pulsed amperometric detector and the horizontal axis the elution time. Times of sampling are indicated above the trace.
Catalytic activity for the fluorination of CF3CH2CI and for the alkene formation after 5 hours of CF3CH2CI pulses over chromium oxide with different degree of fluorination... [Pg.383]


See other pages where 180-degree Pulse is mentioned: [Pg.265]    [Pg.1244]    [Pg.1488]    [Pg.1489]    [Pg.2074]    [Pg.2953]    [Pg.3003]    [Pg.112]    [Pg.196]    [Pg.222]    [Pg.404]    [Pg.461]    [Pg.50]    [Pg.84]    [Pg.166]    [Pg.407]    [Pg.114]    [Pg.397]    [Pg.140]    [Pg.1837]    [Pg.124]    [Pg.600]    [Pg.220]    [Pg.25]    [Pg.96]    [Pg.206]    [Pg.303]    [Pg.163]    [Pg.60]    [Pg.115]    [Pg.436]    [Pg.215]    [Pg.231]    [Pg.190]    [Pg.13]    [Pg.15]    [Pg.16]   
See also in sourсe #XX -- [ Pg.120 ]




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