z-logo
Premium
Dissolution of Aramid by Ionization of Byproduct HCl Promoted by Acetate
Author(s) -
Dai Yu,
Cheng Zheng,
Meng Chenbo,
Yuan Yihao,
Luo Longbo,
Liu Xiangyang
Publication year - 2019
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201801843
Subject(s) - dissolution , solubility , chemistry , thermogravimetric analysis , aramid , polymerization , inorganic chemistry , polyamide , chloride , amide , polymer , nuclear chemistry , polymer chemistry , organic chemistry , fiber
Poor solubility of high‐performance polymer has always been a leading bottleneck for its application. Para‐aramid fiber as a typical high‐performance fiber owns significant hydrogen‐bond interaction and chloride salts are generally needed to provide Cl − ions as hydrogen‐bond acceptors for its dissolution. In this paper, Poly‐(benzimidazole‐terephthalamide) (PABI) which complexed with by‐product HCl (PABI‐HCl) during polymerization was fabricated and by‐product HCl was regarded as potential Cl − ions donor. CH 3 COONa as cosolvent was added in DMAc to dissolve PABI‐HCl. It was confirmed that solubility of PABI‐HCl in DMAc could be improved significantly in existence of CH 3 COONa. The finding was characterized by conductivity measurement, UV‐Vis spectra, Atomic Absorbance Spectra and Thermogravimetric analysis etc. By‐product HCl as a strong acid was converted into CH 3 COOH due to existence of CH 3 COO − in solution. Then it would release Cl − ions and they could interact with secondary amide of aramid to disrupt interaction among macromolecules. Therefore, aramid was dissolved successfully by utilizing by‐product HCl and no external Cl − ions donor was needed.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom