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Typical transients

The apparatus used for picosecond flash spectroscopy on these systems has been described before(8 10). Figure 3a and b show typical transient absorption data obtained on 2-hydroxybenzophenone and the copolymer. Summary of these spectral data are given in Table 3. The transient observed at the shortest delay time (7ps) is the first excited singlet in all systems. The spectral data (at delay times > 50ps) permit placement of upper limits on triplet yields in CH2CI2 for both 2-hydroxy benzophenone itself and the copolymerized chromophore. [Pg.33]

Fig. 3.14 Typical transient signal from the Sir Galahad instrument. Fig. 3.14 Typical transient signal from the Sir Galahad instrument.
The same model was applied to the simulation of typical transients occurring during the operation of industrial SCR monolith reactors in large power plants. In all cases it was found that the change in NO outlet concentration is considerably delayed with respect to the variation of the inlet NH3 concentration. This is unfavorable for a feedback control system using the ammonia feed as the control variable and makes... [Pg.407]

Figure 3.4 Typical transient response characteristic for hole carrier transport in a-As2Sc3 at room temperature. The behavior is displayed with both linear (a) and logarithmic (b) axes of current and time. Figure 3.4 Typical transient response characteristic for hole carrier transport in a-As2Sc3 at room temperature. The behavior is displayed with both linear (a) and logarithmic (b) axes of current and time.
Figure 4.17 A typical transient electron current waveform in an a-Se/Aso.ioSeo 90/Se triplelayer sample. d = 0.81 pm, (I2 = 0.43pm, and = 8.40pm. E = S X 10 V/cm. The inset shows the spatial distribution of photocarriers at different times. Figure 4.17 A typical transient electron current waveform in an a-Se/Aso.ioSeo 90/Se triplelayer sample. d = 0.81 pm, (I2 = 0.43pm, and = 8.40pm. E = S X 10 V/cm. The inset shows the spatial distribution of photocarriers at different times.
Two-photon absorption chemistry of 2AP, specifically photoionization processes, can be induced by intense nanosecond 308-nm XeCl excimer laser pulses [10]. Typical transient absorption spectra of 2AP in deoxygenated neutral aqueous solutions are shown in Fig. 1. The stronger (385 nm) and weaker (510 nm) absorption bands were assigned to 2AP radicals derived from the ionization of 2AP (bleaching near 310 nm) [10], whereas a structureless absorption band from -500 to 750 nm corresponds to the well-known spectrum of the hydrated electron (eh ) [41]. [Pg.133]

Fig. 22. Typical transient response of a La0 9Sr0 (Mn03 electrode to (a) a current step of 400 pA, (b) a potential step of 350 mV, located in region II. From ref. [76]. Fig. 22. Typical transient response of a La0 9Sr0 (Mn03 electrode to (a) a current step of 400 pA, (b) a potential step of 350 mV, located in region II. From ref. [76].
The stability of a FD representation deals with the behavior of the truncation error as the calculation proceeds in time or marches in space, typically, transient problems, and problems with convection-convection derivatives. A stable FD scheme will not allow the errors to grow as the solution proceeds in time or space. The issue of stability for transient problems will be analyzed in depth later in this chapter. [Pg.392]

Fig. 16.4. Typical transient spectrum showing the wavepacket dynamics in the strongly bound B state of I2. The period of 300 fs reflects the oscillatory motion between the two turning points. Adapted from Bowman, Dantus, and Zewail (1990). Fig. 16.4. Typical transient spectrum showing the wavepacket dynamics in the strongly bound B state of I2. The period of 300 fs reflects the oscillatory motion between the two turning points. Adapted from Bowman, Dantus, and Zewail (1990).
Typical transient absorption spectra are shown in Figs. 3 and 4, exhibiting the effect of alkene structure on the electron transfer — H-abstraction ratio for benzophenone as well as the influence of added salt on the SSIP-CIP ratio for benzil. [Pg.228]

Kinetic studies play a central role in the elucidation of reaction mechanisms, and when the species of primary interest are typically transients, they are also essential for the development of a solid understanding of the ways in which substituents and solvent affect reactivity. [Pg.1020]

The test method ASTM F7464 covers the determination of the resistance to either pitting or crevice corrosion of passive metals and alloys from which surgical implants are produced. The resistance of surgical implants to localized corrosion is carried out in dilute sodium chloride solution under specific conditions of potentiodynamic test method. Typical transient decay curves under potentiostatic polarization should monitor susceptibility to localized corrosion. Alloys are ranked in terms of the critical potential for pitting, the higher (more noble) this potential, the more resistant is to passive film breakdown and to localized corrosion. (Sprowls)14... [Pg.368]

The most common adverse events include flu-like symptoms and skin rashes. More serious adverse effects are less common and are typically transient. The latter may include CNS toxicity and drug-induced anaemia. [Pg.331]

Figure 92 Typical transient current pulses for holes in amorphous selenium (see Ref. 422a), illustrating the effect of temperature on the degree of the dispersion in carrier transport. Left linear current (i) and time (t) axes right normalized values in logarithmic axes log(i/io) vs. log(t/t0). The arrows indicate the position of the knee dividing the two regimes of logarithmic dependence. Similar behavior can be observed in organic solids (see e.g. Ref. 422b). Figure 92 Typical transient current pulses for holes in amorphous selenium (see Ref. 422a), illustrating the effect of temperature on the degree of the dispersion in carrier transport. Left linear current (i) and time (t) axes right normalized values in logarithmic axes log(i/io) vs. log(t/t0). The arrows indicate the position of the knee dividing the two regimes of logarithmic dependence. Similar behavior can be observed in organic solids (see e.g. Ref. 422b).
Here (and in Fig. 12K) X is the transition time required to reduce the concentration of the reactant at the electrode surface to zero. Note that this experiment must be performed in a quiescent solution. Thus, while the concentration at the surface declines to zero, the bulk concentration is essentially unchanged, as prescribed by the boundary conditions (Eq. 32K). The meaning of the transition time, T, may be clarified by considering Fig. 13K, which displays a typical transient. [Pg.207]

The measurement system developed, as shown in Figure 5, is introduced into the furnace on level SCCo i so that the ceramic tip is in the gas flow. The key elements of the measurement equipment are a suction pyrometer for the temperature measurement, a wide-range oxygen sensor (BOSCH LSU4) for the fast oxygen measurement, and a thermal conductivity detector (TCD) to measure the transient response of the Helium tracer concentration. For the determination of the transient response of the TCD measurement system itself Helium tracer was injected Just at the inlet of the suction pyrometer. In Figure 7 a typical transient response of the TCD measurement system is shown (curve with index SCCi . [Pg.577]

Figure 8. Typical transient absorption decays at 970 nm of the carotenoid radical cations of C-P-Q triads 2 and 4-6. The decays were measured in dichloromethane solution following excitation with a 590-nm laser pulse. The relative AA values reflect the relative quantum yields of C -P-Q . Figure 8. Typical transient absorption decays at 970 nm of the carotenoid radical cations of C-P-Q triads 2 and 4-6. The decays were measured in dichloromethane solution following excitation with a 590-nm laser pulse. The relative AA values reflect the relative quantum yields of C -P-Q .
Different types of set-up have been reported in the literature. A typical transient absorption set-up with a continuum probe and subpicosecond time resolution, which can be used with laser pulses of a few hundred femtoseconds of duration, is shown in Fig. 7.15. The sample is excited by the pump pulses P. The pump flu-ence (number of photons per cm ) is set to be large enough to obtain an appreciable population of the excited state, which however can be small when an excitation source of high repetition rate is used (Ti-sapphire femtosecond lasers run at 1 kHz) because it allows fast accumulation of weak amplitude signals. With low repetition lasers (10 Hz) the excitation fluence should be dose to the saturation fluence ( l/ca, where (7 is the absorption cross section of the solute at the pump wave-... [Pg.255]

Fig. 7.15. Typical transient absorption set-up using a subpicosecond laser source as the pump and a continuum of white light as the probe. For ultrashort time resolution additional stages for compensating the group velocity dispersion in both light pulses are needed. P pump, F filter. Fig. 7.15. Typical transient absorption set-up using a subpicosecond laser source as the pump and a continuum of white light as the probe. For ultrashort time resolution additional stages for compensating the group velocity dispersion in both light pulses are needed. P pump, F filter.
A typical transient NEMCA experiment, carried out in the setup depicted in Fig. la, is... [Pg.79]

The full experimental details are given elsewhere [13,14]. A typical transient absorption, due to the triplet-triplet absorption from a microcrystalline sample of benzil [16], is illustrated in figure 3, also included in this figure are the emission and baseline experimental traces which are employed in the subsequent correction of the data. [Pg.35]

In the SG/TC mode (Fig. lb), species B is electrogenerated at the substrate electrode and the reverse process, in which B is oxidized to A, occurs at the tip. In experiments hitherto, the substrate electrode has generally (1,2,6,10), but not exclusively (4,11), been macroscopic (millimeter dimensions) with a disk of micrometer dimensions serving as the collector electrode. The substrate response in the SG/TC mode is thus typically transient (2,4,6). As with the feedback and TG/SC modes discussed above, the tip/ substrate separation is a key experimental variable. Since the substrate electrode is generally large, high-resolution positioning is only required in the direction perpendicular to the surfaces of the tip and substrate. [Pg.244]

The typically transient nature of photolytically induced processes makes this area of temporally resolved crystallographic development particularly challenging, as do the many practical complications surrounding the optical excitation (see 4). High atomic resolution is commonly a prerequisite in most cases, the redistribution of electrons, following photo-induction, manifests itself in an associated alteration of bond distance between two or more atoms within a molecule. For example, a luminescent organometallic material classically becomes photo-excited... [Pg.30]


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