Aramid copolymer
A technology of polymer and terephthaloyl dichloride, which is applied in the field of preparing aromatic polyamide polymers, and can solve problems such as the control of the position of monomer components that do not have
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[0067] NMP, DMAC, LiCl, CaCl 2 , DAPBI, PPD and TCl were obtained from commercial sources.
example 1
[0069] This example shows the preparation of DAPBI / PPD-T copolymers with a controlled "head-to-tail" DAPBI arrangement. DAPBI [5(6)-amino-2-(p-aminophenyl)benzimidazole] has two amine groups with very different reactivity, so-called unsymmetrical diamines. An amino group attached to a benzene ring with a fused imidazole ring reacts an order of magnitude faster than an amino group on a separate benzene ring on the opposite side of the molecule. Head and tail in this example represent faster / slower reacting amines, respectively; ie "head" is benzylamine and "tail" is azole amine.
[0070] polymer preparation :
[0071] Add 83.75 g of NMP / CaCl to a 1 L reactor equipped with frame stirrer, nitrogen inlet / outlet 2 Premix (8.3% by weight (weight of salt / total weight of salt plus solvent)), 163.30 g of NMP (N-methyl-2-pyrrolidone] and 12.288 g (0.055 mol) of DAPBI and stirred for 10 minutes. At this point DAPBI was not completely dissolved in the solvent system. Stir the content...
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