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Relation between the adhesion strength and interfacial width for symmetric polystyrene bilayers

✍ Scribed by Kei-Ichi Akabori; Daisuke Baba; Kazuhiro Koguchi; Keiji Tanaka; Toshihiko Nagamura


Book ID
105338490
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
251 KB
Volume
44
Category
Article
ISSN
0887-6266

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✦ Synopsis


Abstract

Polystyrene (PS) bilayers were prepared and were adhered at a temperature between the surface and bulk glass‐transition temperatures for a given time. Then, the interfacial adhesion strength (G~L~) was examined with a conventional lap‐shear measurement. G~L~ first increased with increasing adhesion time and then reached a constant value. This result implied that the segments moved across the interface, to a certain depth, even at a temperature below the bulk glass‐transition temperature. To confirm this, the interfacial evolution for the PS/deuterated PS bilayers was examined with dynamic secondary‐ion mass spectrometry. The G~L~ value was linearly proportional to the thickness of the interfacial adhesion layer. Finally, we propose a strategy for regulating the adhesion strength based on the chain‐end chemistry. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 3598–3604, 2006