PREPARATION AND CHARACTERIZATION OF AROMATIC POLYAMIDES FROM 4,4'-(2,6-NAPHTHYLENEDIOXY)DIBENZOIC ACID AND AROMATIC DIAMINES

Authors
Citation
Sh. Hsiao et Gs. Liou, PREPARATION AND CHARACTERIZATION OF AROMATIC POLYAMIDES FROM 4,4'-(2,6-NAPHTHYLENEDIOXY)DIBENZOIC ACID AND AROMATIC DIAMINES, Macromolecular chemistry and physics, 199(10), 1998, pp. 2321-2328
Citations number
20
Categorie Soggetti
Polymer Sciences
ISSN journal
10221352
Volume
199
Issue
10
Year of publication
1998
Pages
2321 - 2328
Database
ISI
SICI code
1022-1352(1998)199:10<2321:PACOAP>2.0.ZU;2-4
Abstract
A new aromatic dicarboxylic acid, 4,4'-(2,6-naphthylenedioxy)dibenzoic acid (3), was synthesized by the fluoro-displacement reaction of p-fl uorobenzonitrile with 2,6-naphthalenediol in the presence of potassium carbonate, followed by alkaline hydrolysis. A series of aromatic poly amides having inherent viscosities of 1.30-2.19 dL/g were prepared by the triphenyl phosphite activated polycondensation from the diacid 3 w ith sixteen aromatic diamines. Most of the resulting polymers were non crystalline and readily soluble in a variety of polar solvents such as N,N-dimethylacetamide (DMAc) and N-methyl-2-pyrrolidone (NMP). Except for those polymers derived from p-phenylenediamine, benzidine, and 4, 4'-bis(p-aminophenoxy)biphenyl, transparent, tough, and flexible films were cast from the DMAc or NMP solutions. The films had tensile stren gths ranging from 70 to 91 MPa, elongations at break from 6 to 50%, an d initial moduli from 1.35 to 2.32 GPa. The polyamides exhibit glass t ransition temperatures in the range of 178 - 300 degrees C. Almost all polymers are stable up to 400 degrees C, with 10% weight loss being r ecorded above 500 degrees C, in air and nitrogen atmosphere.