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Photo decay

In both examples considered it was only possible to detect the primary products of photo decay of the surface defects because they represented low-molecular radicals and could easily leave the place of their birth and can be trapped by especially chosen acceptors. [Pg.275]

The ketohydrazone tautomer of this intermediate dye can then undergo photohydrolysis to give the expected photo decayed products — a phenylhydrazine and an o-quinone. [Pg.17]

The effects of uv radiation on V/-nitroso compounds depend on the pH and the medium. Under neutral conditions and ia the absence of radical scavengers, these compounds often appear chemically stable, although the E—Z equiUbrium, with respect to rotation around the N—N bond, can be affected (70). This apparent stabiUty is due to rapid recombination of aminyl radicals and nitric oxide [10102-43-9] formed duting photolysis. In the presence of radical scavengers nitrosamines decay rapidly (71). At lower pH, a variety of photoproducts are formed, including compounds attributed to photoelimination, photoreduction, and photo-oxidation (69). Low concentrations of most nitrosamines, even at neutral pH, can be eliminated by prolonged kradiation at 366 nm. This technique is used ki the identification of /V-nitrosamines that are present ki low concentrations ki complex mixtures (72). [Pg.108]

Decay transients, photo electrodes and, 505 Degradation rate as a function of polarization time, 328 Degradation reactions simultaneous with electrode polymerization, 326 DeLevie on the density of broken bonds and the effect on the potential of zero charge, 75... [Pg.629]

It has been calculated that the decay rate of "Tc inside a star is dramatically enhanced because of /1-decay channels (Fig. 7) from thermally populated photo-excited states at high temperature [38]. The calculation was based on a simple shell model, taking into account both continum and bound state /1-decays. The... [Pg.13]

L.M. Herz and R.T. Phillips, Effects of interchain interactions, polarization anisotropy, and photo-oxidation on the ultrafast photoluminescence decay from a polyfluorene, Phys. Rev. B, 61 13691-13697, 2000. [Pg.273]

Fig. 7.15. Photophysics associated with x-ray photoelectron spectroscopy and x-ray fluorescence. As illustrated, in the XPS experiment one monitors the energy of the electron ejected from the M shell upon photoionization (process 1). In the XRF experiment, one monitors the fluorescence emitted from either the M shell after photoionization (process 2a), or from the L shell after photo ionization and radiationless decay (process 2b). Fig. 7.15. Photophysics associated with x-ray photoelectron spectroscopy and x-ray fluorescence. As illustrated, in the XPS experiment one monitors the energy of the electron ejected from the M shell upon photoionization (process 1). In the XRF experiment, one monitors the fluorescence emitted from either the M shell after photoionization (process 2a), or from the L shell after photo ionization and radiationless decay (process 2b).
Fluorescence Characterization of Ablated Polymeric Materials. In order to produce sharply etched patterns, the film was ablated with a photo-lithographically prepared mesh mask in the contact mode. The ablation was conducted with two laser shots with the laser fluence of 0.2 J/cm2. The decay curves of the ablated film was measured by a... [Pg.406]


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See also in sourсe #XX -- [ Pg.5 ]




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