Dresden 2017 – wissenschaftliches Programm

Bereiche | Tage | Auswahl | Suche | Aktualisierungen | Downloads | Hilfe

CPP: Fachverband Chemische Physik und Polymerphysik

CPP 22: Polymer Networks and Dynamics II: Structure and Dynamics

CPP 22.4: Vortrag

Dienstag, 21. März 2017, 10:15–10:30, ZEU 250

Tuning polymer dynamics by chain-end association — •Martin Treß¹, Kunyue Xing¹, Pengfei Cao², Shiwang Cheng², Tomonori Saito², Vladimir Novikov¹, and Alexei Sokolov^1,2 — ¹University of Tennessee Knoxville — ²Oak Ridge National Laboratory

Functional end groups in polymers are a molecular tool to reversibly connect and disconnect chains to combine properties of both short polymer and large supramolecular structures. The topology of the latter - and in turn the respective properties - can be tuned by the choice of the functional group. This is shown in a series of polydimethyl siloxanes (PDMS) of different molecular weight (MW) which are terminated by amino and carboxylic (-COOH) groups, respectively. Differential scanning calorimetry and dielectric spectroscopy measurements reveal that segmental dynamics are identical for the chains with two different end groups. In contrast, rheology unravels a mechanical reinforcement for PDMS-COOH and a rise in viscosity by ~2 decades. This is accompanied by a 2nd Tg and a corresponding dielectric relaxation process which indicates phase separation of the end groups in clusters forming a physically crosslinked network. As a consequence, the viscoelastic properties can be tuned from common short polymer chains at high temperatures to highly entangled or even crosslinked systems at T close and below the 2nd Tg. This suggests a promising route to combine easy processibility of low MW polymers with the desired mechanical performance of high MW polymers or even crosslinked networks.