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Short-Time Dynamics of PDMS-g-PDMS Bottlebrush Polymer Melts Investigated by Quasi-Elastic Neutron Scattering
Author(s) -
Karin J. Bichler,
Bruno Jakobi,
Victoria García Sakai,
Alice Klapproth,
Richard A. Mole,
Gerald J. Schneider
Publication year - 2020
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/acs.macromol.0c01846
Subject(s) - polydimethylsiloxane , polymer , side chain , neutron scattering , relaxation (psychology) , materials science , glass transition , molecular dynamics , polymer chemistry , scattering , chemical physics , chemistry , optics , physics , composite material , computational chemistry , psychology , social psychology
We have studied the short-time dynamical behavior of polydimethylsiloxane (PDMS) bottlebrush polymers, PDMS- g -PDMS. The samples have similar backbone lengths but different side-chain lengths, resulting in a shape transition. Quasi-elastic neutron scattering was used to observe the dynamical changes inherent to these structural changes. The combination of data from three spectrometers enabled to follow the dynamics over broad frequency and temperature ranges, which included segmental relaxations and more localized motions. The latter, identified as the methyl group rotation, is described by a threefold jump model and shows higher activation energies compared to linear PDMS. The segmental relaxation times, τ s , decrease with increasing molecular weight of the side chains but increase with momentum transfer, Q , following a power law, which suggests a non-Gaussian behavior for bottlebrush polymers.

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