Synthesis and properties of alpha,omega-diaminoalkane based poly(amide-imide)s
(2001) Polymer — Vol. 42, n° 17, p. 7247-7256 (2001)
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- Several regular thermoplastic poly(amide-imide)s (PAIs) were synthesized from the diacid chloride derivatives of N,N ' -alkane-alpha,omega -diylbis(trimellitimide)s and alpha,omega -diaminoaikanes. The PAI synthesized from the 1,4-diaminobutane (DAB) based bis(trimellitimide) and 1,4-diaminobutane (PAI[4,4]) yielded semi-crystalline testbars upon injection moulding, but the high melting point of ca. 346 degreesC caused degradation during processing. Surprisingly, all 1,6-diaminohexane (DAH) based PAI[6,6], prepared from the DAH based bis(trimellitimide) and DAH, with a first heating T-m of 257 degreesC, did not even crystallize from the melt at a cooling rate of 20 degreesC/min in the DSC. The same lack of crystallizability from the melt was observed for all 1,3-diaminopropane and for all 1,9-diaminononane based (odd) poly(amide-imide)s PAI[3,3] and PAI[9,9]. The PAI[6,4], based on N,N ' -butane-alpha,omega -bis(trimellitimide) and DAH, with an attractive T-m of 289 degreesC, shows an intermediate crystallization behaviour from the melt: amorphous after injection moulding, but limited crystallization from the melt at a cooling rate of 20 degreesC/min. Copoly(amide-imide)s, from the DAB based bis(trimellitimide) and mixtures of DAB and DAH, showed intermediate melting points of 290 degreesC (for 50 mol% DAB) to 317 degreesC (for 75 mol% DAB) and a better crystallizability with increasing mole percentage DAB, which is ascribed to the wider crystallization window (T-m - T-g) with increasing DAB content and to the more linear ('all-trans') configuration of DAB with respect to DAH. In spite of their amorphous character the injection moulded PAIs show some attractive physical properties. (C) 2001 Elsevier Science Ltd. All rights reserved.
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Koning, C., Teuwen, L., Lacave-Goffin, B., & Mercier, JP. (2001). Synthesis and properties of alpha,omega-diaminoalkane based poly(amide-imide)s. Polymer, 42(17), 7247-7256. https://doi.org/10.1016/S0032-3861(01)00205-1 (Original work published 2001)