Synthesis and thermal properties of difunctional polysulfone telechelics

Synthesis and thermal properties of difunctional polysulfone telechelics Three series of dichloride and dihydroxyl-terminated polysulfone telechelics (Cl-PES-Cl and HO-PES-OH, M n = 2580–12,750 daltons) were prepared from bis(4-chlorophenyl) sulfone with bisphenol A, 4,4′-dihydroxydiphenyl ether and 4,4′-dihydroxybiphenyl. The glass transition temperatures and thermal stabilities of the 30 telechelics synthesized were evaluated as a function of molecular weights and the nature of the end groups. It was observed that the glass transition temperatures of lower molecular weighted dihydroxyl telechelics are higher, due to the capabilities of forming hydrogen bonds, than the corresponding dichloride telechelics. On the other hand, the increase in the glass transition temperatures was steeper with dichloride-terminated oligomers as compared to the corresponding dihydroxyl-terminated ones. In addition, dichloride telechelics manifest higher thermal stabilities than dihydroxyl-terminated oligomers. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Polymer Bulletin Springer Journals

Synthesis and thermal properties of difunctional polysulfone telechelics

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Publisher
Springer Berlin Heidelberg
Copyright
Copyright © 2017 by Springer-Verlag Berlin Heidelberg
Subject
Chemistry; Polymer Sciences; Soft and Granular Matter, Complex Fluids and Microfluidics; Characterization and Evaluation of Materials; Physical Chemistry; Organic Chemistry
ISSN
0170-0839
eISSN
1436-2449
D.O.I.
10.1007/s00289-017-1932-3
Publisher site
See Article on Publisher Site

Abstract

Three series of dichloride and dihydroxyl-terminated polysulfone telechelics (Cl-PES-Cl and HO-PES-OH, M n = 2580–12,750 daltons) were prepared from bis(4-chlorophenyl) sulfone with bisphenol A, 4,4′-dihydroxydiphenyl ether and 4,4′-dihydroxybiphenyl. The glass transition temperatures and thermal stabilities of the 30 telechelics synthesized were evaluated as a function of molecular weights and the nature of the end groups. It was observed that the glass transition temperatures of lower molecular weighted dihydroxyl telechelics are higher, due to the capabilities of forming hydrogen bonds, than the corresponding dichloride telechelics. On the other hand, the increase in the glass transition temperatures was steeper with dichloride-terminated oligomers as compared to the corresponding dihydroxyl-terminated ones. In addition, dichloride telechelics manifest higher thermal stabilities than dihydroxyl-terminated oligomers.

Journal

Polymer BulletinSpringer Journals

Published: Feb 7, 2017

References

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