## Abstract With 2,2,6,6‐tetraoxo‐1,3,5,7‐tetrahydro‐2,6‐dithia‐__s__‐indacene‐4,8‐diamine (DSDA) (8), a new monomer for the synthesis of thermally crosslinkable rigid‐rod aramids was developed. DSDA was copolymerized with __p__‐phenylenediamine and terephthaloyl dichloride by a low‐temperature sol
Thermally crosslinked rigid-rod aramids, 2. Fiber spinning and fiber properties
✍ Scribed by Bernhard Glomm; Christoph Rickert; Peter Neuenschwander; Ulrich W. Suter
- Book ID
- 102939082
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 709 KB
- Volume
- 195
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
Fibers of three rigid‐rod aromatic copolymers, produced by polycondensation of 2,2,6,6‐tetraoxo‐1,3,5,7‐tetrahydro‐2,6‐dithia‐s‐indacene‐4,8‐diamine (DSDA), p‐phenylenediamine and terephthaloyl dichloride, were spun from nematic solutions and characterized by wideangle X‐ray‐diffraction (WAXD) measurements and mechanical tests. A post‐spin heat treatment was employed to improve the low degrees of orientation and crystallinity exhibited generally by the untreated fibers. The dominating crystal structures of the copolymers are similar to “modification I” of the well known fibers from poly(p‐phenyleneterephthalamide) (PPTA). Thermally induced crosslinking of the fibers in the solid state was performed simultaneously with post‐spin treatment. The influence of the annealing conditions on the mechanical fiber properties and the molecular order in the fibers was also investigated. All mechanical parameters were time‐dependent, probably due to the generation of stable radicals during heat treatment. The radicals may give rise to chain scission.
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