The synthesis is described of some aromatic polyamides based on unsubstituted, and methyl-, carboxy-, and sulfo-substituted diamines by interfacial polycondensation. Some of them are crosslinked and some of them contain heterocyclic aromatic rings. Their chemical structures are characterized by IR a
Chlorination and oxidation of aromatic polyamides. II. Chlorination of some aromatic polyamides
β Scribed by Shaoyu Wu; Jing Xing; Guodong Zheng; Huiqin Lian; Lianfang Shen
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 359 KB
- Volume
- 61
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
The effects of chlorine on three kinds of aromatic polyamides: those not containing a substituent, those containing substituents, and those containing heterocyclic aromatic rings, were studied. The correlations between the chemical structures of polyamides and the reactivity to hypochlorous acid were examined by IR and 13C solid-state NMR spectra before and after chlorination. It was found that the chlorination of polyamides depends not only on their chemical structures but also on chlorination conditions such as pH value and reaction time. Their response to chlorination corresponds to four types: ring-chlorination, no reaction, N-chlorination, and chain cleavage.
π SIMILAR VOLUMES
Dielectric relaxation spectroscopy (DRS) is presented for a family of four aromatic polyamides trying to relate the structure of the lateral groups to the molecular mobility. A prominent sub-T g absorption is always seen followed in some cases by remanent dielectric activity at room temperature and