Chemical sensitivity absorption

Various types of the photoconductive polymers are available now. The photoconductivity of such materials may be essentially increased by means of the chemical and spectral sensitization [12-14]. Spectral sensitization is connected with the appearance of the photosensitivity in the new spectral bands and the chemical sensitization with the increase of the proper sensitivity. As a rule both types of sensitisation may take place in the photoconductor at the same turn. The first data about chemical and spectral sensitization in organic photoconductors appeared in [19, 20]. The example of the chemical and spectral sensitization of the photoconductivity by dyes in polymeric copper-phenyl-acetylenide is presented in Fig. 2. Later on it was proposed that not only low molecular weight compounds but polyconjugated polymers could also be used as sensitizers [21] having broad absorption tends and high thermostability compared with dyes. Now it is clear that various types of molecules may be used as a photosensitizers. 

The absorption of energy by the grains produces conduction electrons and either free or trapped holes. The conduction electrons and the holes diffuse initially by a three-dimensional random walk. In chemically sensitized crystals, the holes are trapped by products of chemical sensitization which thus undergo photo-oxidation. Rapid recombination between a trapped hole and an electron is avoided by the delocalization as an interstitial Ag ion of the nonequilibrium excess positive charge created at the trapping site. Latent pre- and sub-image specks are formed by the successive combination of an interstitial Agi ion and a conduction electron at a shallow positive potential well. 

Other detection methods. Besides XPS, other chemically sensitive techniques are available to probe the reaction. Surface reflection absorption infrared spectroscopy [130] and electron-energy loss spectroscopy [131] give detailed information on the vibrational states and thus the bonds of surface species. Gas-phase mass spectroscopic techniques provide information about the desorbing species. 

If the analyte concentration is high (more than about 200 times the reciprocal sensitivity), sensitivity should be reduced. In AAS this can be done by removal of the impact bead, by burner rotation, or use of less sensitive absorption lines. However, if these are not practicable, the solution should be diluted to bring it into the best range for measurement. On the other hand, if the concentration is too low, scale expansion or some chemical pretreatment are required. 

Note that in liquid phase chromatography there are no detectors that are both sensitive and universal, that is, which respond linearly to solute concentration regardless of its chemical nature. In fact, the refractometer detects all solutes but it is not very sensitive its response depends evidently on the difference in refractive indices between solvent and solute whereas absorption and UV fluorescence methods respond only to aromatics, an advantage in numerous applications. Unfortunately, their coefficient of response (in ultraviolet, absorptivity is the term used) is highly variable among individual components. 

As discussed earlier in Section lOC.l, ultraviolet, visible and infrared absorption bands result from the absorption of electromagnetic radiation by specific valence electrons or bonds. The energy at which the absorption occurs, as well as the intensity of the absorption, is determined by the chemical environment of the absorbing moiety. Eor example, benzene has several ultraviolet absorption bands due to 7t —> 71 transitions. The position and intensity of two of these bands, 203.5 nm (8 = 7400) and 254 nm (8 = 204), are very sensitive to substitution. Eor benzoic acid, in which a carboxylic acid group replaces one of the aromatic hydrogens, the... 

These chemical effects become important in medicine because living systems operate mostly through the reactions of enzymes, which catalyze all sorts of metabolic reactions but are very sensitive to small changes in their environment. Such sensitivity can lead to preferential absorption of some deleterious isotopes in place of the more normal, beneficial ones. One example in metabolic systems can be found in the incorporation of a radioactive strontium isotope in place of calcium. 

Only slightly less accurate ( 0.3—0.5%) and more versatile in scale are other titration techniques. Plutonium maybe oxidized in aqueous solution to PuO " 2 using AgO, and then reduced to Pu" " by a known excess of Fe", which is back-titrated with Ce" ". Pu" " may be titrated complexometricaHy with EDTA and a colorimetric indicator such as Arsenazo(I), even in the presence of a large excess of UO " 2- Solution spectrophotometry (Figs. 4 and 5) can be utilized if the plutonium oxidation state is known or controlled. The spectrophotometric method is very sensitive if a colored complex such as Arsenazo(III) is used. Analytically usehil absorption maxima and molar absorption coefficients ( s) are given in Table 10. Laser photoacoustic spectroscopy has been developed for both elemental analysis and speciation (oxidation state) at concentrations of lO " — 10 M (118). Chemical extraction can also be used to enhance this technique. 

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