Impact of Hydrogen Bonding on Dynamics of Hydroxyl-Terminated Polydimethylsiloxane

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• 作者：Kunyue Xing ; Sabornie Chatterjee ; Tomonori Saito ; Catalin Gainaru ; Alexei P. Sokolov
• 刊名：Macromolecules
• 出版年：2016
• 出版时间：April 26, 2016
• 年：2016
• 卷：49
• 期：8
• 页码：3138-3147
• 全文大小：579K
• 年卷期：0
• ISSN：1520-5835

文摘

Dielectric spectroscopy, rheology, and differential scanning calorimetry were employed to study the effect of chain-end hydrogen bonding on the dynamics of hydroxyl-terminated polydimethylsiloxane. We demonstrate that hydrogen bonding has a strong influence on both segmental and slower dynamics in the systems with low molecular weights. In particular, the decrease in the chain length leads to an increase of the glass transition temperature, viscosity, and fragility index, at variance with the usual behavior of nonassociating polymers. The supramolecular association of hydroxyl-terminated chains leads to the emergence in dielectric and mechanical relaxation spectra of the so-called Debye process traditionally observed in monohydroxy alcohols. Our analysis suggests that the hydroxyl-terminated PDMS oligomers may associate in brush-like or chain-like structures, depending on the size of their covalent chains. The effective length of the linear-associated chains was estimated from the rheological measurements.