Schönhals, A.; Szymoniak, P.; Kolmangadi, M.A.; Böhning, M.; Zamponi, M.; Frick, B.; Appel, M.; Günther, G.; Russina, M.; Alentiev, D.A.; Bermeshev, M.; Zorn, R.: Microscopic dynamics of highly permeable super glassy polynorbornenes revealed by quasielastic neutron scattering. Journal of Membrane Science 642 (2022), p. 119972/1-8
10.1016/j.memsci.2021.119972
Abstract:
The molecular dynamics of addition-type poly(tricyclononenes) with Si-substituted bulky side groups has been investigated by a combination of neutron time-offlight and neutron backscattering spectroscopy on a time scale from 0.1 ps to ca. 3 ns. The investigated poly(tricyclononenes) PTCNSi1 and PTCNSi2g both bear a high microporosity which makes them promising candidates for active separation layers for gas separation membranes. At least for larger gas molecules it is assumed that the pathways for diffusion require an enlargement of pre-existing micropores in terms of an activated zone. A low temperature relaxation process was found for both polymers by the performed neutron scattering experiments. This process was assigned to the methyl group rotation. It was analysed in terms of a jump diffusion in a three-fold potential. The analysis of the dependence of the elastic incoherent structure factor on the scattering vector yields the number of methyl groups which might be immobilized. For PTCNSi1 (3 methyl groups in the monomeric unit) it was found that all methyl groups take part in the methyl group rotation whereas for PTCNSi2g (6 methyl groups in monomeric unit) a considerable number of methyl groups are blocked in their rotation. This immobilization of methyl groups is due to the sterically demanding arrangement of the methyl groups in PTCNSi2g. This conclusion is further supported by the result that the activation energy for the methyl group rotation is three times higher for PTCNSi2g than that of PTCNSi1.