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Charge distribution, after nuclear decay

The reason for bond rupture by high electric charge was clarified more clearly later. Snell and Pleasonton (1955) measured charge distribution after nuclear decay by mass spectrometry. Chemical effects of high charge in molecular systems were studied by Wexler (1961a) in detail. [Pg.1334]

A. H. Snell F. Pleasonton USA Measurement of charge distribution after nuclear decay... [Pg.1335]

As a summary of charge distribution after nuclear decay, Fig. 24.3 shows various cases in monatomic or polyatomic gases (inclusive of solid surface emission for a decay and heavy ion nuclear reaction). [Pg.1342]

Figure 9.9. Charge distribution of the ions a) after decay of Xe b) after isomeric transition of (According to A. H. Snell, F. Pleasonton, T. A. Carlson Proceedings Series, Chemical Effects of Nuclear Transformations, Vol. I. IAEA Vienna 1961, S. 147.)... Figure 9.9. Charge distribution of the ions a) after decay of Xe b) after isomeric transition of (According to A. H. Snell, F. Pleasonton, T. A. Carlson Proceedings Series, Chemical Effects of Nuclear Transformations, Vol. I. IAEA Vienna 1961, S. 147.)...
See other pages where Charge distribution, after nuclear decay is mentioned: [Pg.1343]    [Pg.1343]    [Pg.3]    [Pg.333]   
See also in sourсe #XX -- [ Pg.1334 , Pg.1343 , Pg.1396 , Pg.1398 , Pg.1399 ]



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