Crystalline and liquid-crystalline properties of polyesters of phenyl-substituted 4,4'-biphenol. 1. Polymers from terephthalic acid and 2,6-naphthalenedicarboxylic acid

1993 ◽  
Vol 26 (3) ◽  
pp. 440-446 ◽  
Author(s):  
P. K. Bhowmik ◽  
E. D. T. Atkins ◽  
R. W. Lenz
1988 ◽  
Vol 21 (7) ◽  
pp. 2155-2160 ◽  
Author(s):  
N. D. Field ◽  
R. Baldwin ◽  
R. Layton ◽  
P. Frayer ◽  
F. Scardiglia

2018 ◽  
Vol 31 (6) ◽  
pp. 631-639 ◽  
Author(s):  
Yiheng Dai ◽  
Xiangyu Bi ◽  
Theo J Dingemans ◽  
Qingbao Guan

We have synthesized and characterized a new family of nematic all-aromatic polyesteramide thermosets based on 6-hydroxy-2-naphthoic acid (HNA), terephthalic acid (TA), and 4-acetamidophenol (AAP). In order to incorporate a high concentration of the amide-based monomer (AAP), the melt transition ( T K-N) and melt viscosity had to be lowered in order to maintain melt processable intermediates. Precursor thermoplastic reactive oligomers, end-capped with phenylethynyl functionalities, were prepared using standard melt condensation techniques with a target M n of 1000–9000 g mol−1. The reactive oligomers with 20–30 mol% AAP could easily be processed into films, and the films exhibit good tensile properties in terms of tensile strength (70–80 MPa) and elongation at break (7–10%). A glass transition of 191°C could be obtained when a 1000 g mol−1 oligomer (HNA/TA/AAP(20)–1 K) was thermally cross-linked. When the AAP concentration reaches 35 mol%, the rigidity of the backbone and the hydrogen bonding interactions are enhanced, which make HNA/TA/AAP(35) polymers difficult to process.


2020 ◽  
Vol 44 (2) ◽  
pp. 614-625
Author(s):  
Yaodong Huang ◽  
Xiaojie Zhang ◽  
Wei Cui ◽  
Xin Wang ◽  
Bin Li ◽  
...  

Terephthalic acid-based aromatic amides A1 and A2 and a terephthalaldehyde Schiff-base SB are synthesized, allowing stable gelation with numerous types of organic solvents.


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