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Applications of Slow Positrons to Polymeric Surfaces and Coatings

Applications of Slow Positrons to Polymeric Surfaces and Coatings [Pg.281]

Mallon2, Renwu Zhang , Hongmin Chen1, Y.C. Wu , Ying [Pg.281]

Department of Chemistry, University of Missouri-Kansas City, USA1 [Pg.281]

For DBES data three main factors contribute to the S parameter in polymers (1) free-volume content, (2) free-volume size, and (3) chemical composition. First, larger free-volume content contributes to a larger S value. DBES measures radiation near 511 keV where a major contribution comes from p-Ps. This p-Ps contribution is only 1/3 the o-Ps intensity as that in I3 of PAL data. Second, when p-Ps is localized in a defect with a dimension fix, the momentum Ap has a dispersion according to the Heisenburg uncertainty principle AxAp h/4n. The S parameter from DBES spectra is a direct measure of the quantity of momentum dispersion. In a larger size hole where Ps is localized, there will be a larger S parameter due to smaller momentum uncertainty. Therefore, in a system with defects or voids, such as polymers, the S parameter is a qualitative measure of the defect size and defect concentration. The value of the S parameter also depends on the momentum of the valence electrons, which annihilate with the positrons. The absolute value of the S parameter therefore, may differ from polymer to polymer. Third, the S parameter depends on the electron momentum of the elements. As the atomic number of the elements increases, the electron momentum increases, and thus the S parameter decreases. Fortunately, in chemicals of [Pg.283]


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