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Charge lasers

Hamilton C E, Bierbaum V M and Leone S R 1985 Product vibrational state distributions of thermal energy charge transfer reactions determined by laser-induced fluorescence in a flowing afterglow Ar" + CC -> CC (v= 0-6) + Ar J. Chem. Rhys. 83 2284-92... [Pg.821]

Sonnenfroh D M and Leone S R 1989 A laser-induced fluorescence study of product rotational state distributions in the charge transfer reaction Ar <-i. i, ) + Ni Ar + MfXjat 0.28 and 0.40 eV J. them. Phys. 90 1677-85... [Pg.822]

Fig. 11. Electiophotogiaphic plate structure and process of use (a) laser exposure of the negatively charged photoconductor, o, sitting on the plate surface ... Fig. 11. Electiophotogiaphic plate structure and process of use (a) laser exposure of the negatively charged photoconductor, o, sitting on the plate surface ...
A unique problem arises when reducing the fissile isotope The amount of that can be reduced is limited by its critical mass. In these cases, where the charge must be kept relatively small, calcium becomes the preferred reductant, and iodine is often used as a reaction booster. This method was introduced by Baker in 1946 (54). Researchers at Los Alamos National Laboratory have recently introduced a laser-initiated modification to this reduction process that offers several advantages (55). A carbon dioxide laser is used to initiate the reaction between UF and calcium metal. This new method does not requite induction heating in a closed bomb, nor does it utilize iodine as a booster. This promising technology has been demonstrated on a 200 g scale. [Pg.321]

UV spectra, 3, 599 xanthone synthesis from, 3, 840 Xanthydryl chloride xanthone synthesis from, 3, 840 Xanthyletin synthesis, 3, 743, 804 Xanthylium laser dye synthesis, 3, 865 Xanthylium salts aromaticity, 3, 641 charge density calculations, 3, 576 C NMR, 3, 592 H NMR, 3, 585 mass spectra, 3, 620 reactions... [Pg.924]

The possible mechanism of ionization, fragmentation of studied compound as well as their desoi ption by laser radiation is discussed. It is shown that the formation of analyte ions is a result of a multi stage complex process included surface activation by laser irradiation, the adsoi ption of neutral analyte and proton donor molecules, the chemical reaction on the surface with proton or electron transfer, production of charged complexes bonded with the surface and finally laser desoi ption of such preformed molecules. [Pg.103]

Typical mass resolution values measured on the LIMA 2A range from 250 to 750 at a mass-to-charge ratio M/ Z= 100. The parameter that appears to have the most influence on the measured mass resolving power is the duration of the ionization event, which may be longer than the duration of the laser pulse (5—10 ns), along with probable time broadening effects associated with the l6-ns time resolution of the transient recorder. ... [Pg.590]


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Charge laser action from

Charge transfer Chemical lasers

Laser photolysis charge separation

Laser-induced charge transfer

Lasers multi-charged ions

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