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Laser the values

Example 1.2 The spectral resolution of a 1 m spectrograph is about 0.01 nm, which corresponds at A, = 500 nm to Aco = 27t. 12 GHz. The Doppler width of gas molecules with M = 30 at P = 300 K is, according to Vol. 1, (3.30a) 3single-mode laser the value of 8co becomes smaller than Aco and the observable signal AP/P becomes 12 times larger than in conventional spectroscopy with the same absorption cell. [Pg.4]

The value of the beam divergence angle given by equation 3 corresponds to that emerging from the laser. The beam may be collimated further by a telescope. The improvement of the coUimation is the inverse of the magnification of the telescope ... [Pg.2]

One variation in dye laser constmction is the ring dye laser. The laser cavity is a reentrant system, so that the laser light can circulate in a closed loop. The ring stmcture provides a high degree of stabiUty and a narrow spectral width. The spectral width of a conventional dye laser on the order of 40 GH2 is narrowed to a value as small as a few MH2. Such systems offer very high resolution in spectroscopic appHcations. [Pg.9]

Excitation conditions and threshold vulues for lasing in different conjugated polymers. Different resonator structures are used to achieve real lasing. Note that it is in some cases difficult to compare the values due to the different laser pulse duration used in the experiments. indicates the wavelength for excitation, r(,u< is the pulse duration of the exciting laser pulse atu A the urea of the spot on the sample. [Pg.177]

Morishima et al. [75, 76] have shown a remarkable effect of the polyelectrolyte surface potential on photoinduced ET in the laser photolysis of APh-x (8) and QPh-x (12) with viologens as electron acceptors. Decay profiles for the SPV (14) radical anion (SPV- ) generated by the photoinduced ET following a 347.1-nm laser excitation were monitored at 602 nm (Fig. 13) [75], For APh-9, the SPV- transient absorption persisted for several hundred microseconds after the laser pulse. The second-order rate constant (kb) for the back ET from SPV- to the oxidized Phen residue (Phen+) was estimated to be 8.7 x 107 M 1 s-1 for the APh-9-SPV system. For the monomer model system (AM(15)-SPV), on the other hand, kb was 2.8 x 109 M-1 s-1. This marked retardation of the back ET in the APh-9-SPV system is attributed to the electrostatic repulsion of SPV- by the electric field on the molecular surface of APh-9. The addition of NaCl decreases the electrostatic interaction. In fact, it increased the back ET rate. For example, at NaCl concentrations of 0.025 and 0.2 M, the value of kb increased to 2.5 x 108 and... [Pg.77]

From this we can see that knowledge of k f and Rf in a conventional polymerization process readily yields a value of the ratio kp fkt. In order to obtain a value for kf wc require further information on kv. Analysis of / , data obtained under non-steady state conditions (when there is no continuous source of initiator radicals) yields the ratio kvlkx. Various non-stcady state methods have been developed including the rotating sector method, spatially intermittent polymerization and pulsed laser polymerization (PLP). The classical approach for deriving the individual values of kp and kt by combining values for kp kx. with kp/k, obtained in separate experiments can, however, be problematical because the values of kx are strongly dependent on the polymerization conditions (Section... [Pg.238]


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See also in sourсe #XX -- [ Pg.198 ]




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